From ac68f3019e055bb96fd11596b08c9507dbb51d47 Mon Sep 17 00:00:00 2001 From: Trish Whetzel Date: Thu, 23 May 2024 12:42:53 -0700 Subject: [PATCH] test build 2 the build was run as: sh run.sh make build-mondo-ingest -B --- docs/metrics/doid.md | 6 +- docs/metrics/gard.md | 2 +- docs/metrics/icd10cm.md | 2 +- docs/metrics/icd10who.md | 2 +- docs/metrics/icd11foundation.md | 2 +- docs/metrics/ncit.md | 22 +- docs/metrics/omim.md | 20 +- docs/metrics/ordo.md | 2 +- docs/reports/mapped_deprecated.md | 4 +- docs/reports/mapped_deprecated_ncit.md | 10 + docs/reports/mapped_deprecated_omim.md | 1 + docs/reports/migrate.md | 8 +- docs/reports/migrate_doid.md | 70 +- docs/reports/migrate_ncit.md | 4391 ++++++------- docs/reports/migrate_omim.md | 21 +- docs/reports/migrate_ordo.md | 27 +- docs/reports/unmapped.md | 8 +- docs/reports/unmapped_doid.md | 68 +- docs/reports/unmapped_ncit.md | 668 +- docs/reports/unmapped_omim.md | 19 +- docs/reports/unmapped_ordo.md | 9 - src/mappings/doid.sssom.tsv | 1 + src/mappings/gard.sssom.tsv | 2 +- src/mappings/icd10cm.sssom.tsv | 2 +- src/mappings/icd10who.sssom.tsv | 2 +- src/mappings/icd11foundation.sssom.tsv | 2 +- src/mappings/ncit.sssom.tsv | 4 +- src/mappings/omim.sssom.tsv | 460 +- src/ontology/external/nord.robot.owl | 787 +-- src/ontology/external/nord.robot.tsv | 147 +- src/ontology/imports/omo_import.owl | 4 +- src/ontology/imports/ro_import.owl | 46 +- src/ontology/lexmatch/README.md | 60 +- src/ontology/lexmatch/all_exact.robot.tsv | 49 +- .../mondo-only/unmapped_ncit_mondo.tsv | 4 + .../mondo-only/unmapped_ncit_mondo_exact.tsv | 5 + .../mondo-only/unmapped_omim_mondo.tsv | 1 + .../mondo-only/unmapped_ordo_mondo.tsv | 5 +- .../mondo_broadmatch_omimps.tsv | 2 - .../mondo_closematch_doid.tsv | 225 +- .../mondo_closematch_icd10cm.tsv | 9 +- .../mondo_closematch_icd11.foundation.tsv | 7 +- .../mondo_closematch_ncit.tsv | 5 +- .../mondo_closematch_omimps.tsv | 5 - .../mondo_closematch_orphanet.tsv | 6 +- .../mondo_exactmatch_doid.tsv | 44 +- .../mondo_exactmatch_icd10who.tsv | 2 +- .../mondo_exactmatch_icd11.foundation.tsv | 2 +- .../mondo_exactmatch_ncit.tsv | 25 +- .../mondo_exactmatch_omim.tsv | 1 + .../mondo_exactmatch_omimps.tsv | 3 +- .../mondo_exactmatch_orphanet.tsv | 5 +- src/ontology/lexmatch/unmapped_doid_lex.tsv | 12 - .../lexmatch/unmapped_doid_lex_exact.tsv | 32 +- .../lexmatch/unmapped_icd10who_lex.tsv | 1 + .../lexmatch/unmapped_icd10who_lex_exact.tsv | 1 - .../lexmatch/unmapped_icd11foundation_lex.tsv | 2 +- src/ontology/lexmatch/unmapped_ncit_lex.tsv | 3 + .../lexmatch/unmapped_ncit_lex_exact.tsv | 13 +- .../lexmatch/unmapped_omim_lex_exact.tsv | 3 +- src/ontology/metadata/doid-metrics.json | 18 +- src/ontology/metadata/gard-metrics.json | 2 +- src/ontology/metadata/icd10cm-metrics.json | 2 +- src/ontology/metadata/icd10who-metrics.json | 2 +- .../metadata/icd11foundation-metrics.json | 2 +- src/ontology/metadata/ncit-metrics.json | 70 +- src/ontology/metadata/omim-metrics.json | 94 +- src/ontology/metadata/ordo-metrics.json | 2 +- .../reports/component_signature-doid.tsv | 380 +- .../reports/component_signature-ncit.tsv | 399 +- .../reports/component_signature-omim.tsv | 8 +- .../doid.subclass.added-obsolete.robot.tsv | 5 +- .../reports/doid.subclass.added.robot.tsv | 56 +- .../reports/doid.subclass.confirmed.robot.tsv | 32 +- src/ontology/reports/doid_mapping_status.tsv | 104 +- src/ontology/reports/doid_unmapped_terms.tsv | 52 +- .../reports/mirror_signature-doid.tsv | 402 +- .../reports/mirror_signature-mondo.tsv | 48 +- .../reports/mirror_signature-ncit.tsv | 4000 +++++++++++- .../reports/mirror_signature-omim.tsv | 20 + .../ncit.subclass.added-obsolete.robot.tsv | 2 - .../reports/ncit.subclass.added.robot.tsv | 17 +- .../reports/ncit.subclass.confirmed.robot.tsv | 50 +- .../ncit_excluded_terms_in_mondo_xrefs.tsv | 15 +- ..._excluded_terms_in_mondo_xrefs_summary.tsv | 2 +- .../ncit_exclusion_reasons.robot.template.tsv | 3615 +++++++++- ...mapped_deprecated_terms.robot.template.tsv | 10 + src/ontology/reports/ncit_mapping_status.tsv | 4871 ++++++++++++-- src/ontology/reports/ncit_term_exclusions.txt | 3615 +++++++++- src/ontology/reports/ncit_unmapped_terms.tsv | 668 +- .../reports/omim.subclass.added.robot.tsv | 4 +- .../reports/omim.subclass.confirmed.robot.tsv | 18 +- .../omim_exclusion_reasons.robot.template.tsv | 53 +- ...mapped_deprecated_terms.robot.template.tsv | 1 + src/ontology/reports/omim_mapping_status.tsv | 212 +- src/ontology/reports/omim_term_exclusions.txt | 18 +- src/ontology/reports/omim_unmapped_terms.tsv | 15 +- .../ordo.subclass.added-obsolete.robot.tsv | 44 +- .../reports/ordo.subclass.added.robot.tsv | 10 +- .../reports/ordo.subclass.confirmed.robot.tsv | 16 +- .../ordo_exclusion_reasons.robot.template.tsv | 5 + src/ontology/reports/ordo_mapping_status.tsv | 20 +- src/ontology/reports/ordo_term_exclusions.txt | 5 + src/ontology/reports/ordo_unmapped_terms.tsv | 9 - .../sync-subClassOf.direct-in-mondo-only.tsv | 356 +- src/ontology/slurp/doid.tsv | 52 +- src/ontology/slurp/ncit.tsv | 251 +- src/ontology/slurp/omim.tsv | 15 +- src/ontology/slurp/ordo.tsv | 17 +- src/ontology/unmapped/doid-unmapped.owl | 308 +- src/ontology/unmapped/ncit-unmapped.owl | 5804 +++++++++++++---- src/ontology/unmapped/omim-unmapped.owl | 437 +- 112 files changed, 26052 insertions(+), 7532 deletions(-) delete mode 100644 src/ontology/lexmatch/split-mapping-set/mondo_broadmatch_omimps.tsv delete mode 100644 src/ontology/lexmatch/split-mapping-set/mondo_closematch_omimps.tsv diff --git a/docs/metrics/doid.md b/docs/metrics/doid.md index 530eab3e..c1bee4ab 100644 --- a/docs/metrics/doid.md +++ b/docs/metrics/doid.md @@ -2,14 +2,14 @@ **IRI:** http://purl.obolibrary.org/obo/mondo/sources/doid.owl -**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2024-05-01/doid.owl +**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2024-05-23/doid.owl ### Entities and axioms | Metric | Value | | ------ | ----- | | Annotation properties | 27 | -| Axioms | 115964 | +| Axioms | 115971 | | Logical axioms | 16110 | | Classes | 13099 | | Object properties | 2 | @@ -32,7 +32,7 @@ | Metric | Value | | ------ | ----- | -| AnnotationAssertion | 86726 | +| AnnotationAssertion | 86733 | | SubAnnotationPropertyOf | 1 | | DisjointClasses | 26 | | Declaration | 13127 | diff --git a/docs/metrics/gard.md b/docs/metrics/gard.md index 742b0cd7..16360147 100644 --- a/docs/metrics/gard.md +++ b/docs/metrics/gard.md @@ -2,7 +2,7 @@ **IRI:** http://purl.obolibrary.org/obo/mondo/sources/gard.owl -**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2024-05-01/gard.owl +**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2024-05-23/gard.owl ### Entities and axioms diff --git a/docs/metrics/icd10cm.md b/docs/metrics/icd10cm.md index 0b66702c..21c525d4 100644 --- a/docs/metrics/icd10cm.md +++ b/docs/metrics/icd10cm.md @@ -2,7 +2,7 @@ **IRI:** http://purl.obolibrary.org/obo/mondo/sources/icd10cm.owl -**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2024-05-01/icd10cm.owl +**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2024-05-23/icd10cm.owl ### Entities and axioms diff --git a/docs/metrics/icd10who.md b/docs/metrics/icd10who.md index 025d1a55..4eff889a 100644 --- a/docs/metrics/icd10who.md +++ b/docs/metrics/icd10who.md @@ -2,7 +2,7 @@ **IRI:** http://purl.obolibrary.org/obo/mondo/sources/icd10who.owl -**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2024-05-01/icd10who.owl +**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2024-05-23/icd10who.owl ### Entities and axioms diff --git a/docs/metrics/icd11foundation.md b/docs/metrics/icd11foundation.md index d2a3015e..6f170068 100644 --- a/docs/metrics/icd11foundation.md +++ b/docs/metrics/icd11foundation.md @@ -2,7 +2,7 @@ **IRI:** http://purl.obolibrary.org/obo/mondo/sources/icd11foundation.owl -**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2024-05-01/icd11foundation.owl +**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2024-05-23/icd11foundation.owl ### Entities and axioms diff --git a/docs/metrics/ncit.md b/docs/metrics/ncit.md index 07efb5b0..950880fa 100644 --- a/docs/metrics/ncit.md +++ b/docs/metrics/ncit.md @@ -2,16 +2,16 @@ **IRI:** http://purl.obolibrary.org/obo/mondo/sources/ncit.owl -**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2024-05-01/ncit.owl +**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2024-05-23/ncit.owl ### Entities and axioms | Metric | Value | | ------ | ----- | | Annotation properties | 12 | -| Axioms | 612685 | -| Logical axioms | 32780 | -| Classes | 15628 | +| Axioms | 623834 | +| Logical axioms | 33655 | +| Classes | 15971 | | Object properties | 0 | | Data properties | 0 | | Individuals | 0 | @@ -32,12 +32,12 @@ | Metric | Value | | ------ | ----- | -| AnnotationAssertion | 564246 | -| EquivalentClasses | 6027 | +| AnnotationAssertion | 574177 | +| EquivalentClasses | 6260 | | DatatypeDefinition | 19 | | AnnotationPropertyRangeOf | 1 | -| Declaration | 15658 | -| SubClassOf | 26734 | +| Declaration | 16001 | +| SubClassOf | 27376 | #### Entity namespaces: axiom counts by namespace @@ -45,7 +45,7 @@ | Metric | Value | | ------ | ----- | | prefix_unknown | 1 | -| NCIT | 15650 | +| NCIT | 15993 | | oboInOwl | 3 | | owl | 2 | | rdf | 1 | @@ -59,8 +59,8 @@ | Metric | Value | | ------ | ----- | -| Class | 88896 | -| ObjectIntersectionOf | 6027 | +| Class | 91288 | +| ObjectIntersectionOf | 6260 | More information about the source can be found [in the documentation](../sources.md). The raw data (ontology metrics) can be found [on GitHub](https://github.com/monarch-initiative/mondo-ingest/tree/main/src/ontology/metadata). diff --git a/docs/metrics/omim.md b/docs/metrics/omim.md index e1989f2b..db18c7b2 100644 --- a/docs/metrics/omim.md +++ b/docs/metrics/omim.md @@ -2,16 +2,16 @@ **IRI:** http://purl.obolibrary.org/obo/mondo/sources/omim.owl -**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2024-05-01/omim.owl +**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2024-05-23/omim.owl ### Entities and axioms | Metric | Value | | ------ | ----- | | Annotation properties | 18 | -| Axioms | 345588 | -| Logical axioms | 22689 | -| Classes | 19482 | +| Axioms | 345890 | +| Logical axioms | 22703 | +| Classes | 19488 | | Object properties | 7 | | Data properties | 0 | | Individuals | 0 | @@ -32,17 +32,17 @@ | Metric | Value | | ------ | ----- | -| AnnotationAssertion | 303395 | +| AnnotationAssertion | 303677 | | SubAnnotationPropertyOf | 1 | -| Declaration | 19503 | -| SubClassOf | 22689 | +| Declaration | 19509 | +| SubClassOf | 22703 | #### Entity namespaces: axiom counts by namespace | Metric | Value | | ------ | ----- | -| prefix_unknown | 18036 | +| prefix_unknown | 18042 | | oboInOwl | 4 | | owl | 2 | | xsd | 1 | @@ -61,8 +61,8 @@ | Metric | Value | | ------ | ----- | -| Class | 64850 | -| ObjectSomeValuesFrom | 17792 | +| Class | 64884 | +| ObjectSomeValuesFrom | 17798 | More information about the source can be found [in the documentation](../sources.md). The raw data (ontology metrics) can be found [on GitHub](https://github.com/monarch-initiative/mondo-ingest/tree/main/src/ontology/metadata). diff --git a/docs/metrics/ordo.md b/docs/metrics/ordo.md index a8db0331..e827c9a3 100644 --- a/docs/metrics/ordo.md +++ b/docs/metrics/ordo.md @@ -2,7 +2,7 @@ **IRI:** http://purl.obolibrary.org/obo/mondo/sources/ordo.owl -**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2024-05-01/ordo.owl +**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2024-05-23/ordo.owl ### Entities and axioms diff --git a/docs/reports/mapped_deprecated.md b/docs/reports/mapped_deprecated.md index 61c5a7e4..20906b61 100644 --- a/docs/reports/mapped_deprecated.md +++ b/docs/reports/mapped_deprecated.md @@ -2,9 +2,9 @@ | Ontology | Tot deprecated in Mondo | |:----------------------------------------------------------|--------------------------:| | [DOID](./mapped_deprecated_doid.md) | 5 | -| [OMIM](./mapped_deprecated_omim.md) | 45 | +| [OMIM](./mapped_deprecated_omim.md) | 46 | | [ORDO](./mapped_deprecated_ordo.md) | 225 | -| [NCIT](./mapped_deprecated_ncit.md) | 12 | +| [NCIT](./mapped_deprecated_ncit.md) | 22 | | [GARD](./mapped_deprecated_gard.md) | 0 | | [ICD11FOUNDATION](./mapped_deprecated_icd11foundation.md) | 0 | | [ICD10CM](./mapped_deprecated_icd10cm.md) | 0 | diff --git a/docs/reports/mapped_deprecated_ncit.md b/docs/reports/mapped_deprecated_ncit.md index 9525a718..4370c0a6 100644 --- a/docs/reports/mapped_deprecated_ncit.md +++ b/docs/reports/mapped_deprecated_ncit.md @@ -6,13 +6,23 @@ |:--------------|:---------------------|:-------------------------| | ID | A oboInOwl:hasDbXref | >A oboInOwl:source | | MONDO:0002063 | NCIT:C6977 | MONDO:equivalentObsolete | +| MONDO:0002938 | NCIT:C66903 | MONDO:equivalentObsolete | +| MONDO:0003222 | NCIT:C5504 | MONDO:equivalentObsolete | +| MONDO:0003450 | NCIT:C4173 | MONDO:equivalentObsolete | | MONDO:0003998 | NCIT:C40257 | MONDO:equivalentObsolete | +| MONDO:0004141 | NCIT:C9499 | MONDO:equivalentObsolete | | MONDO:0004204 | NCIT:C4462 | MONDO:equivalentObsolete | | MONDO:0004419 | NCIT:C39822 | MONDO:equivalentObsolete | | MONDO:0004819 | NCIT:C7150 | MONDO:equivalentObsolete | | MONDO:0005065 | NCIT:C3234 | MONDO:equivalentObsolete | +| MONDO:0005104 | NCIT:C9419 | MONDO:equivalentObsolete | | MONDO:0005362 | NCIT:C34801 | MONDO:equivalentObsolete | +| MONDO:0005369 | NCIT:C2915 | MONDO:equivalentObsolete | +| MONDO:0006475 | NCIT:C27892 | MONDO:equivalentObsolete | +| MONDO:0013171 | NCIT:C3963 | MONDO:equivalentObsolete | | MONDO:0015040 | NCIT:C7167 | MONDO:equivalentObsolete | +| MONDO:0015540 | NCIT:C35439 | MONDO:equivalentObsolete | +| MONDO:0016747 | NCIT:C5505 | MONDO:equivalentObsolete | | MONDO:0017308 | NCIT:C75007 | MONDO:equivalentObsolete | | MONDO:0020804 | NCIT:C7586 | MONDO:equivalentObsolete | | MONDO:0020805 | NCIT:C4743 | MONDO:equivalentObsolete | diff --git a/docs/reports/mapped_deprecated_omim.md b/docs/reports/mapped_deprecated_omim.md index b4ba95cb..1e55b632 100644 --- a/docs/reports/mapped_deprecated_omim.md +++ b/docs/reports/mapped_deprecated_omim.md @@ -16,6 +16,7 @@ | MONDO:0008126 | OMIM:164891 | MONDO:equivalentObsolete | | MONDO:0008204 | OMIM:168850 | MONDO:equivalentObsolete | | MONDO:0008415 | OMIM:181515 | MONDO:equivalentObsolete | +| MONDO:0008873 | OMIM:210730 | MONDO:equivalentObsolete | | MONDO:0009535 | OMIM:247440 | MONDO:equivalentObsolete | | MONDO:0009586 | OMIM:249660 | MONDO:equivalentObsolete | | MONDO:0009654 | OMIM:252700 | MONDO:equivalentObsolete | diff --git a/docs/reports/migrate.md b/docs/reports/migrate.md index 4de05957..9f6ecdc7 100644 --- a/docs/reports/migrate.md +++ b/docs/reports/migrate.md @@ -2,12 +2,12 @@ | Ontology | Tot | |:------------------------------------------------|:-------| | [GARD](./migrate_gard.md) | 9,370 | -| [DOID](./migrate_doid.md) | 56 | -| [NCIT](./migrate_ncit.md) | 2,176 | +| [DOID](./migrate_doid.md) | 8 | +| [OMIM](./migrate_omim.md) | 5 | +| [NCIT](./migrate_ncit.md) | 2,209 | | [ICD10WHO](./migrate_icd10who.md) | 119 | -| [ORDO](./migrate_ordo.md) | 11 | | [ICD11FOUNDATION](./migrate_icd11foundation.md) | 10,581 | -| [OMIM](./migrate_omim.md) | 10 | +| [ORDO](./migrate_ordo.md) | 10 | | [ICD10CM](./migrate_icd10cm.md) | 1,889 | ### Codebook diff --git a/docs/reports/migrate_doid.md b/docs/reports/migrate_doid.md index 692e602f..ef434615 100644 --- a/docs/reports/migrate_doid.md +++ b/docs/reports/migrate_doid.md @@ -2,62 +2,14 @@ [Interactive FlatGithub table](https://flatgithub.com/monarch-initiative/mondo-ingest?filename=src/ontology/slurp/doid.tsv) ### Migratable terms -| mondo_id | mondo_label | xref | xref_source | original_label | definition | parents | -|:--------------|:--------------------------------------------------------------------------|:---------------------|:---------------------------|:--------------------------------------------------------------------------|:-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|:------------------------------------------| -| ID | LABEL | A oboInOwl:hasDbXref | >A oboInOwl:source SPLIT=| | | A IAO:0000115 | SC % | -| MONDO:0958281 | mitochondrial complex v (atp synthase) deficiency nuclear type 4 | DOID:0060333 | MONDO:equivalentTo | mitochondrial complex V (ATP synthase) deficiency nuclear type 4 | | MONDO:0014471 | -| MONDO:0958282 | dystonia 28, childhood-onset | DOID:0060936 | MONDO:equivalentTo | dystonia 28, childhood-onset | | MONDO:0003441|MONDO:0000426 | -| MONDO:0958283 | dystonia 30 | DOID:0060937 | MONDO:equivalentTo | dystonia 30 | | MONDO:0003441|MONDO:0000426 | -| MONDO:0958284 | dystonia 31 | DOID:0060938 | MONDO:equivalentTo | dystonia 31 | | MONDO:0003441|MONDO:0006025 | -| MONDO:0958285 | dystonia 32 | DOID:0060939 | MONDO:equivalentTo | dystonia 32 | | MONDO:0003441|MONDO:0006025 | -| MONDO:0958286 | dystonia 33 | DOID:0060940 | MONDO:equivalentTo | dystonia 33 | | MONDO:0003441|MONDO:0006025|MONDO:0000426 | -| MONDO:0958287 | ullrich congenital muscular dystrophy 2 | DOID:0060944 | MONDO:equivalentTo | Ullrich congenital muscular dystrophy 2 | | MONDO:0000355 | -| MONDO:0958288 | dystonia 35, childhood-onset | DOID:0060955 | MONDO:equivalentTo | dystonia 35, childhood-onset | | MONDO:0003441|MONDO:0006025 | -| MONDO:0958289 | dystonia 37, early-onset with striatal lesions | DOID:0060956 | MONDO:equivalentTo | dystonia 37, early-onset with striatal lesions | | MONDO:0003441|MONDO:0006025 | -| MONDO:0958290 | myoclonic dystonia 34 | DOID:0060957 | MONDO:equivalentTo | myoclonic dystonia 34 | | MONDO:0003441|MONDO:0000426 | -| MONDO:0958291 | dystonia, dopa-responsive | DOID:0060963 | MONDO:equivalentTo | dystonia, DOPA-responsive | | MONDO:0006025|MONDO:0003441|MONDO:0000426 | -| MONDO:0958292 | dystonia 22, juvenile-onset | DOID:0060966 | MONDO:equivalentTo | dystonia 22, juvenile-onset | | MONDO:0003441|MONDO:0006025 | -| MONDO:0958293 | dystonia 22, adult-onset | DOID:0060967 | MONDO:equivalentTo | dystonia 22, adult-onset | | MONDO:0003441|MONDO:0006025 | -| MONDO:0958294 | halperin-birk syndrome | DOID:0070539 | MONDO:equivalentTo | Halperin-Birk syndrome | | MONDO:0006025|MONDO:0002254 | -| MONDO:0958295 | bcor itd sarcoma | DOID:0081403 | MONDO:equivalentTo | BCOR ITD sarcoma | A sarcoma with BCOR genetic alterations that is characterized by the presence of BCOR internal tandem duplication. | MONDO:0958159 | -| MONDO:0958296 | bcor-ccnb3 sarcoma | DOID:0081404 | MONDO:equivalentTo | BCOR-CCNB3 sarcoma | A sarcoma with BCOR genetic alterations that is characterized by the presence of BCOR-CCNB3 fusion gene. | MONDO:0958159 | -| MONDO:0958297 | childhood sarcoma with bcor genetic alterations | DOID:0081405 | MONDO:equivalentTo | childhood sarcoma with BCOR genetic alterations | A sarcoma with BCOR genetic alterations that occurs during childhood. | MONDO:0958159 | -| MONDO:0958298 | childhood round cell sarcoma with ewsr1-non-ets fusion | DOID:0081407 | MONDO:equivalentTo | childhood round cell sarcoma with EWSR1-non-ETS fusion | A round cell sarcoma with EWSR1-non-ETS fusion that is characterized by EWSR1-non-ETS fusion that occurs during childhood. | MONDO:0958160 | -| MONDO:0958299 | round cell sarcoma with ewsr1-nfatc2 gene fusion | DOID:0081408 | MONDO:equivalentTo | round cell sarcoma with EWSR1-NFATC2 gene fusion | A round cell sarcoma with EWSR1-non-ETS fusion that is characterized by the presence of EWSR1-NFATC2 gene fusion. | MONDO:0958160 | -| MONDO:0958300 | round cell sarcoma with ewsr1-patz1 gene fusion | DOID:0081409 | MONDO:equivalentTo | round cell sarcoma with EWSR1-PATZ1 gene fusion | A round cell sarcoma with EWSR1-non-ETS fusion that is characterized by the presence of EWSR1-PATZ1 gene fusion. | MONDO:0958160 | -| MONDO:0958301 | round cell sarcoma with fus-nfatc2 gene fusion | DOID:0081410 | MONDO:equivalentTo | round cell sarcoma with FUS-NFATC2 gene fusion | A round cell sarcoma with EWSR1-non-ETS fusion that is characterized by the presence of FUS-NFATC2 gene fusion. | MONDO:0958160 | -| MONDO:0958302 | tfeb-rearranged renal cell carcinoma | DOID:0081414 | MONDO:equivalentTo | TFEB-rearranged renal cell carcinoma | A renal cell carcinoma with MiT translocations that is characterized by the presence of the chromosomal translocation t(6;11) which fuses the TFEB transcription factor gene, located on chromosome 6, with the MALAT1 gene, located on chromosome 11. | MONDO:0017886 | -| MONDO:0958303 | childhood renal cell carcinoma with mit translocations | DOID:0081416 | MONDO:equivalentTo | childhood renal cell carcinoma with MiT translocations | A renal cell carcinoma with MiT translocations that is characterized by a TFE3 or TFEB-rearranged renal cell carcinoma that occurs during childhood. | MONDO:0017886 | -| MONDO:0958304 | microcephaly, short stature, and limb abnormalities | DOID:0081431 | MONDO:equivalentTo | microcephaly, short stature, and limb abnormalities | An osteochondrodysplasia that is characterized by intrauterine growth retardation, microcephaly, variable short stature, and limb abnormalities mainly affecting the upper limb and radial ray and that has_material_basis_in homozygous or compound heterozygous mutation in the DONSON gene on chromosome 21q22. Biallelic mutation in the DONSON gene can also cause microcephaly-micromelia syndrome, a more severe disorder that usually results in intrauterine or perinatal death. | MONDO:0005516|MONDO:0006025 | -| MONDO:0958305 | microcephaly-micromelia syndrome | DOID:0081432 | MONDO:equivalentTo | microcephaly-micromelia syndrome | A syndrome that is characterized by intrauterine growth retardation (IUGR), marked microcephaly, craniosynostosis, and severe malformation of the limbs, especially the arms and that has_material_basis_in homozygous mutation in the DONSON gene on chromosome 21q22. Biallelic mutation in the DONSON gene can also cause microcephaly, short stature, and limb abnormalities, a less severe disorder. | MONDO:0002254 | -| MONDO:0958306 | peroxisome biogenesis disorder 4b | DOID:0081433 | MONDO:equivalentTo | Peroxisome biogenesis disorder 4B | | MONDO:0019234|MONDO:0006025|MONDO:0000426 | -| MONDO:0958307 | peroxisome biogenesis disorder 5b | DOID:0081434 | MONDO:equivalentTo | Peroxisome biogenesis disorder 5B | | MONDO:0019234|MONDO:0006025 | -| MONDO:0958308 | peroxisome biogenesis disorder 6b | DOID:0081435 | MONDO:equivalentTo | Peroxisome biogenesis disorder 6B | | MONDO:0019234|MONDO:0006025 | -| MONDO:0958309 | peroxisome biogenesis disorder 7b | DOID:0081436 | MONDO:equivalentTo | Peroxisome biogenesis disorder 7B | | MONDO:0019234|MONDO:0006025 | -| MONDO:0958310 | peroxisome biogenesis disorder 8b | DOID:0081437 | MONDO:equivalentTo | Peroxisome biogenesis disorder 8B | | MONDO:0019234|MONDO:0006025 | -| MONDO:0958311 | peroxisome biogenesis disorder 9b | DOID:0081438 | MONDO:equivalentTo | Peroxisome biogenesis disorder 9B | | MONDO:0019234|MONDO:0006025 | -| MONDO:0958312 | peroxisome biogenesis disorder 11b | DOID:0081439 | MONDO:equivalentTo | Peroxisome biogenesis disorder 11B | | MONDO:0019234|MONDO:0006025 | -| MONDO:0958313 | peroxisome biogenesis disorder 10b | DOID:0081440 | MONDO:equivalentTo | Peroxisome biogenesis disorder 10B | | MONDO:0019234|MONDO:0006025 | -| MONDO:0958314 | nicolaides-baraitser syndrome | DOID:0081441 | MONDO:equivalentTo | Nicolaides-Baraitser syndrome | A syndrome that is characterized by severely impaired intellectual development, early-onset seizures, short stature, dysmorphic facial features, and sparse hair and that has_material_basis_in heterozygous mutation in the SMARCA2 gene on chromosome 9p24. | MONDO:0000426|MONDO:0002254 | -| MONDO:0958315 | blepharophimosis-impaired intellectual development syndrome | DOID:0081442 | MONDO:equivalentTo | blepharophimosis-impaired intellectual development syndrome | A syndrome that is characterized by a distinct facial appearance with blepharophimosis and global development delay and that has_material_basis_in heterozygous mutation in the SMARCA2 gene on chromosome 9p24. | MONDO:0002254|MONDO:0000426 | -| MONDO:0958316 | stolerman neurodevelopmental syndrome | DOID:0081443 | MONDO:equivalentTo | Stolerman neurodevelopmental syndrome | A syndrome that is characterized by developmental delay, often with motor and speech delay, mildly impaired intellectual development (in most patients), learning difficulties, and behavioral abnormalities, including autism spectrum disorder and that has_material_basis_in heterozygous mutation in the KDM6B gene on chromosome 17p13. | MONDO:0002254 | -| MONDO:0958317 | neurodevelopmental disorder with poor growth and behavioral abnormalities | DOID:0081444 | MONDO:equivalentTo | neurodevelopmental disorder with poor growth and behavioral abnormalities | An autosomal recessive intellectual developmental disorder that is characterized by global developmental delay, moderately to severely impaired intellectual development, often with absent speech, and behavioral abnormalities, including hyperactivity, short attention span, and ADHD and that has_material_basis_in homozygous or compound heterozygous mutation in the ATP9A gene on chromosome 20q13. | MONDO:0019502 | -| MONDO:0958318 | chronic inflammatory demyelinating polyneuritis | DOID:2536 | MONDO:equivalentTo | chronic inflammatory demyelinating polyneuritis | | MONDO:0002336 | -| MONDO:0958319 | congenital kyphosis | DOID:4668 | MONDO:equivalentTo | congenital kyphosis | | | -| MONDO:0958320 | postural kyphosis | DOID:9373 | MONDO:equivalentTo | postural kyphosis | | | -| MONDO:0958359 | childhood spinal muscular atrophy | DOID:0060160 | MONDO:equivalentTo | childhood spinal muscular atrophy | | MONDO:0001516 | -| MONDO:0958360 | cholesterol-ester transfer protein deficiency | DOID:0111368 | MONDO:equivalentTo | cholesterol-ester transfer protein deficiency | | MONDO:0002525 | -| MONDO:0968961 | interstitial lung disease 1 | DOID:0060941 | MONDO:equivalentTo | interstitial lung disease 1 | | MONDO:0000426|MONDO:0015925|MONDO:0006025 | -| MONDO:0968962 | ullrich congenital muscular dystrophy 1b | DOID:0060942 | MONDO:equivalentTo | Ullrich congenital muscular dystrophy 1B | | MONDO:0000355 | -| MONDO:0968963 | ullrich congenital muscular dystrophy 1c | DOID:0060943 | MONDO:equivalentTo | Ullrich congenital muscular dystrophy 1C | | MONDO:0000355 | -| MONDO:0968964 | amelogenesis imperfecta type 1k | DOID:0060945 | MONDO:equivalentTo | amelogenesis imperfecta type 1K | | MONDO:0019507 | -| MONDO:0968965 | ullrich congenital muscular dystrophy 1a | DOID:0060946 | MONDO:equivalentTo | Ullrich congenital muscular dystrophy 1A | An Ullrich congenital muscular dystrophy characterized by generalized muscle weakness and striking hypermobility of distal joints in conjunction with variable contractures of more proximal joints and normal intelligence that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the COL6A1 gene on chromosome 21q22. | MONDO:0000355 | -| MONDO:0968966 | autosomal recessive intellectual developmental disorder 82 | DOID:0060947 | MONDO:equivalentTo | autosomal recessive intellectual developmental disorder 82 | An autosomal recessive intellectual developmental disorder characterized by global developmental delay with motor and speech delay, variably impaired intellectual development, and behavioral abnormalities has_material_basis_in homozygous mutation in the NSUN6 gene on chromosome 10p12. | MONDO:0019502 | -| MONDO:0968967 | sickle cell disease | DOID:0081445 | MONDO:equivalentTo | sickle cell disease | A blood protein disease that is characterized by chronic hemolytic anemia and intermittent vaso-occlusive events that result in tissue ischemia leading to acute and chronic pain as well as organ damage that can affect any organ system, resulting from the replacement of one of the beta-globin subunits in hemoglobin with atypical hemoglobin molecules called hemoglobin S which can distort red blood cells into a sickle or crescent shape. Sickle cell disease subtypes should include a detailed genotypic description for the hemoglobin molecules (e.g., Hb S/S, Hb S/C, Hb S/β0-thalassemia). | MONDO:0003804 | -| MONDO:0968968 | dimethylglycine dehydrogenase deficiency | DOID:0081446 | MONDO:equivalentTo | dimethylglycine dehydrogenase deficiency | An amino acid metabolic disorder that is characterized by a fish-like odor, chronic fatigue, and increased level of the muscle form of creatine kinase in serum and that has_material_basis_in homozygous mutation in the DMGDH on chromosome 5q14. | MONDO:0004736|MONDO:0006025 | -| MONDO:0968969 | cone-rod dystrophy 21 | DOID:0081447 | MONDO:equivalentTo | cone-rod dystrophy 21 | A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the DRAM2 gene on chromosome 1p13. | MONDO:0006025|MONDO:0015993 | -| MONDO:0968970 | cone-rod dystrophy 22 | DOID:0081448 | MONDO:equivalentTo | cone-rod dystrophy 22 | A cone-rod dystrophy that is characterized by loss of central vision due to cone photoreceptor degeneration, with onset of symptoms ranging from the first to fifth decades of life and that has_material_basis_in homozygous mutation in the TLCD3B gene on chromosome 16p11. | MONDO:0006025|MONDO:0015993 | -| MONDO:0968971 | cone-rod dystrophy 24 | DOID:0081449 | MONDO:equivalentTo | cone-rod dystrophy 24 | A cone-rod dystrophy that is characterized by night blindness, defective color vision, and reduced visual acuity and that has_material_basis_in heterozygous mutation in the UNC119 gene on chromosome 17q11. | MONDO:0000426|MONDO:0015993 | -| MONDO:0968972 | hyperimmunoglobulinemia d periodic fever syndrome | DOID:0081450 | MONDO:equivalentTo | hyperimmunoglobulinemia D periodic fever syndrome | A hyperimmunoglobulin syndrome that is characterized as periodic fever from early infancy accompanied by elevated serum C-reactive protein and that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding mevalonate kinase (MVK) on chromosome 12q24. | MONDO:0002468 | -| MONDO:0968973 | pfapa syndrome | DOID:0081451 | MONDO:equivalentTo | PFAPA syndrome | An autoimmune disease that is characterized by recurrent febrile episodes associated with aphthous stomatitis, pharyngitis and cervical adenitis. | MONDO:0007179 | -| MONDO:0968974 | large b-cell lymphoma | DOID:0081452 | MONDO:equivalentTo | large B-cell lymphoma | A B-cell lymphoma that is characterized by large lymphoid cells of the B-cell lineage that by definition form sheets or clusters. | MONDO:0004095 | \ No newline at end of file +| mondo_id | mondo_label | xref | xref_source | original_label | definition | parents | +|:--------------|:-----------------------------------------------------------------|:---------------------|:---------------------------|:-----------------------------------------------------------------|:--------------|:----------------------------| +| ID | LABEL | A oboInOwl:hasDbXref | >A oboInOwl:source SPLIT=| | | A IAO:0000115 | SC % | +| MONDO:0958281 | mitochondrial complex v (atp synthase) deficiency nuclear type 4 | DOID:0060333 | MONDO:equivalentTo | mitochondrial complex V (ATP synthase) deficiency nuclear type 4 | | MONDO:0014471 | +| MONDO:0958318 | chronic inflammatory demyelinating polyneuritis | DOID:2536 | MONDO:equivalentTo | chronic inflammatory demyelinating polyneuritis | | MONDO:0002336 | +| MONDO:0958319 | congenital kyphosis | DOID:4668 | MONDO:equivalentTo | congenital kyphosis | | | +| MONDO:0958320 | postural kyphosis | DOID:9373 | MONDO:equivalentTo | postural kyphosis | | | +| MONDO:0958359 | childhood spinal muscular atrophy | DOID:0060160 | MONDO:equivalentTo | childhood spinal muscular atrophy | | MONDO:0001516 | +| MONDO:0958360 | cholesterol-ester transfer protein deficiency | DOID:0111368 | MONDO:equivalentTo | cholesterol-ester transfer protein deficiency | | MONDO:0002525 | +| MONDO:0968993 | aleutian mink disease | DOID:2934 | MONDO:equivalentTo | aleutian mink disease | | MONDO:0005108 | +| MONDO:0968994 | borna disease | DOID:5154 | MONDO:equivalentTo | borna disease | | MONDO:0005108|MONDO:0002602 | \ No newline at end of file diff --git a/docs/reports/migrate_ncit.md b/docs/reports/migrate_ncit.md index aef1c4e5..c8ede626 100644 --- a/docs/reports/migrate_ncit.md +++ b/docs/reports/migrate_ncit.md @@ -2,2182 +2,2215 @@ [Interactive FlatGithub table](https://flatgithub.com/monarch-initiative/mondo-ingest?filename=src/ontology/slurp/ncit.tsv) ### Migratable terms -| mondo_id | mondo_label | xref | xref_source | original_label | definition | parents | -|:--------------|:---------------------------------------------------------------------------------------------------------------|:---------------------|:---------------------------|:---------------------------------------------------------------------------------------------------------------|:--------------|:------------------------------------------| -| ID | LABEL | A oboInOwl:hasDbXref | >A oboInOwl:source SPLIT=| | | A IAO:0000115 | SC % | -| MONDO:0853205 | conjunctival melanocytic intraepithelial neoplasia | NCIT:C100054 | MONDO:equivalentTo | Conjunctival Melanocytic Intraepithelial Neoplasia | | MONDO:0020204 | -| MONDO:0853241 | primary central nervous system neoplasm | NCIT:C102871 | MONDO:equivalentTo | Primary Central Nervous System Neoplasm | | MONDO:0006130 | -| MONDO:0853254 | adrenal cortical carcinoma by ensat stage | NCIT:C104030 | MONDO:equivalentTo | Adrenal Cortical Carcinoma by ENSAT Stage | | MONDO:0006639 | -| MONDO:0853255 | ovarian high grade serous adenocarcinoma | NCIT:C105555 | MONDO:equivalentTo | Ovarian High Grade Serous Adenocarcinoma | | MONDO:0005211 | -| MONDO:0853256 | ovarian low grade serous adenocarcinoma | NCIT:C105556 | MONDO:equivalentTo | Ovarian Low Grade Serous Adenocarcinoma | | MONDO:0005211 | -| MONDO:0853260 | uveal melanoma by gene expression profile | NCIT:C111030 | MONDO:equivalentTo | Uveal Melanoma by Gene Expression Profile | | MONDO:0006486 | -| MONDO:0853262 | glioblastoma by gene expression profile | NCIT:C111691 | MONDO:equivalentTo | Glioblastoma by Gene Expression Profile | | MONDO:0018177 | -| MONDO:0853267 | thymoma by masaoka-koga stage | NCIT:C112006 | MONDO:equivalentTo | Thymoma by Masaoka-Koga Stage | | MONDO:0006456 | -| MONDO:0853279 | uterine carcinosarcoma, homologous type | NCIT:C113238 | MONDO:equivalentTo | Uterine Carcinosarcoma, Homologous Type | | MONDO:0006485 | -| MONDO:0853280 | uterine carcinosarcoma, heterologous type | NCIT:C113239 | MONDO:equivalentTo | Uterine Carcinosarcoma, Heterologous Type | | MONDO:0006485 | -| MONDO:0853284 | main duct pancreatic intraductal papillary-mucinous neoplasm | NCIT:C113664 | MONDO:equivalentTo | Main Duct Pancreatic Intraductal Papillary-Mucinous Neoplasm | | MONDO:0004286 | -| MONDO:0853285 | branch duct pancreatic intraductal papillary-mucinous neoplasm | NCIT:C113665 | MONDO:equivalentTo | Branch Duct Pancreatic Intraductal Papillary-Mucinous Neoplasm | | MONDO:0004286 | -| MONDO:0853286 | mixed type pancreatic intraductal papillary-mucinous neoplasm | NCIT:C113667 | MONDO:equivalentTo | Mixed Type Pancreatic Intraductal Papillary-Mucinous Neoplasm | | MONDO:0004286 | -| MONDO:0853303 | adult undifferentiated high grade pleomorphic sarcoma of bone | NCIT:C114782 | MONDO:equivalentTo | Adult Undifferentiated High Grade Pleomorphic Sarcoma of Bone | | MONDO:0002618 | -| MONDO:0853306 | metastatic malignant neoplasm in the soft tissues | NCIT:C114831 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Soft Tissues | | MONDO:0024880 | -| MONDO:0853313 | adult epithelioid hemangioendothelioma | NCIT:C114923 | MONDO:equivalentTo | Adult Epithelioid Hemangioendothelioma | | MONDO:0015523 | -| MONDO:0853316 | central nervous system hodgkin lymphoma | NCIT:C114951 | MONDO:equivalentTo | Central Nervous System Hodgkin Lymphoma | | MONDO:0004952|MONDO:0002571 | -| MONDO:0853326 | adult fibrolamellar carcinoma | NCIT:C114992 | MONDO:equivalentTo | Adult Fibrolamellar Carcinoma | | MONDO:0016216|MONDO:0006210 | -| MONDO:0853331 | hepatocellular carcinoma by bclc stage | NCIT:C115132 | MONDO:equivalentTo | Hepatocellular Carcinoma by BCLC Stage | | MONDO:0007256 | -| MONDO:0853337 | adult myelodysplastic syndrome | NCIT:C115153 | MONDO:equivalentTo | Adult Myelodysplastic Syndrome | | MONDO:0018881 | -| MONDO:0853343 | distal urethral carcinoma | NCIT:C115210 | MONDO:equivalentTo | Distal Urethral Carcinoma | | MONDO:0021327 | -| MONDO:0853344 | familial testicular germ cell tumor | NCIT:C115211 | MONDO:equivalentTo | Familial Testicular Germ Cell Tumor | | MONDO:0010108 | -| MONDO:0853348 | proximal urethral carcinoma | NCIT:C115334 | MONDO:equivalentTo | Proximal Urethral Carcinoma | | MONDO:0021327 | -| MONDO:0853359 | invasive bladder urothelial carcinoma associated with urethral carcinoma | NCIT:C115966 | MONDO:equivalentTo | Invasive Bladder Urothelial Carcinoma Associated with Urethral Carcinoma | | MONDO:0040678 | -| MONDO:0853386 | congenital cystic hygroma | NCIT:C116899 | MONDO:equivalentTo | Congenital Cystic Hygroma | | MONDO:0009761 | -| MONDO:0853405 | anaplastic plasmacytoma | NCIT:C118421 | MONDO:equivalentTo | Anaplastic Plasmacytoma | | MONDO:0005615|MONDO:0020633 | -| MONDO:0853427 | adult penile carcinoma | NCIT:C118820 | MONDO:equivalentTo | Adult Penile Carcinoma | | MONDO:0006360 | -| MONDO:0853431 | adult salivary gland carcinoma | NCIT:C118825 | MONDO:equivalentTo | Adult Salivary Gland Carcinoma | | MONDO:0000521 | -| MONDO:0853434 | orbital melanoma | NCIT:C118828 | MONDO:equivalentTo | Orbital Melanoma | | MONDO:0002889|MONDO:0005105 | -| MONDO:0853464 | malignant kidney neoplasm except pelvis | NCIT:C120456 | MONDO:equivalentTo | Malignant Kidney Neoplasm Except Pelvis | | MONDO:0002367 | -| MONDO:0853467 | mammary-type myofibroblastoma | NCIT:C121181 | MONDO:equivalentTo | Mammary-Type Myofibroblastoma | | MONDO:0040675 | -| MONDO:0853473 | leiomyosarcoma of deep soft tissue | NCIT:C121571 | MONDO:equivalentTo | Leiomyosarcoma of Deep Soft Tissue | | MONDO:0018078|MONDO:0005058 | -| MONDO:0853476 | spindle cell/sclerosing rhabdomyosarcoma | NCIT:C121654 | MONDO:equivalentTo | Spindle Cell/Sclerosing Rhabdomyosarcoma | | MONDO:0005212 | -| MONDO:0853478 | soft tissue angiosarcoma | NCIT:C121671 | MONDO:equivalentTo | Soft Tissue Angiosarcoma | | MONDO:0018078|MONDO:0016982 | -| MONDO:0853479 | conventional schwannoma | NCIT:C121677 | MONDO:equivalentTo | Conventional Schwannoma | | MONDO:0002546 | -| MONDO:0853481 | solitary circumscribed neuroma | NCIT:C121681 | MONDO:equivalentTo | Solitary Circumscribed Neuroma | | MONDO:0002547|MONDO:0000648 | -| MONDO:0853483 | hybrid nerve sheath tumor | NCIT:C121686 | MONDO:equivalentTo | Hybrid Nerve Sheath Tumor | | MONDO:0021043|MONDO:0002547|MONDO:0000648 | -| MONDO:0853491 | malignant mixed tumor, not otherwise specified | NCIT:C121787 | MONDO:equivalentTo | Malignant Mixed Tumor, Not Otherwise Specified | | MONDO:0003158|MONDO:0005853 | -| MONDO:0853492 | benign phosphaturic mesenchymal tumor | NCIT:C121788 | MONDO:equivalentTo | Benign Phosphaturic Mesenchymal Tumor | | MONDO:0006368|MONDO:0000654 | -| MONDO:0853493 | malignant phosphaturic mesenchymal tumor | NCIT:C121789 | MONDO:equivalentTo | Malignant Phosphaturic Mesenchymal Tumor | | MONDO:0006368|MONDO:0002927 | -| MONDO:0853494 | sclerosing pecoma | NCIT:C121790 | MONDO:equivalentTo | Sclerosing PEComa | | MONDO:0006359 | -| MONDO:0853495 | undifferentiated soft tissue sarcoma | NCIT:C121793 | MONDO:equivalentTo | Undifferentiated Soft Tissue Sarcoma | | MONDO:0018078 | -| MONDO:0853498 | osteochondromyxoma | NCIT:C121842 | MONDO:equivalentTo | Osteochondromyxoma | | MONDO:0024470|MONDO:0000631 | -| MONDO:0853499 | subungual exostosis | NCIT:C121844 | MONDO:equivalentTo | Subungual Exostosis | | MONDO:0024470 | -| MONDO:0853500 | bizarre parosteal osteochondromatous proliferation | NCIT:C121845 | MONDO:equivalentTo | Bizarre Parosteal Osteochondromatous Proliferation | | MONDO:0024470 | -| MONDO:0853501 | intermediate chondrogenic neoplasm | NCIT:C121846 | MONDO:equivalentTo | Intermediate Chondrogenic Neoplasm | | MONDO:0024469 | -| MONDO:0853502 | chondrosarcoma, grade 2 | NCIT:C121870 | MONDO:equivalentTo | Chondrosarcoma, Grade 2 | | MONDO:0008977 | -| MONDO:0853503 | chondrosarcoma, grade 3 | NCIT:C121871 | MONDO:equivalentTo | Chondrosarcoma, Grade 3 | | MONDO:0008977 | -| MONDO:0853504 | benign notochordal cell tumor | NCIT:C121901 | MONDO:equivalentTo | Benign Notochordal Cell Tumor | | MONDO:0002597|MONDO:0000631 | -| MONDO:0853505 | ivory exostosis | NCIT:C121923 | MONDO:equivalentTo | Ivory Exostosis | | MONDO:0005166 | -| MONDO:0853506 | enostosis | NCIT:C121924 | MONDO:equivalentTo | Enostosis | | MONDO:0005166 | -| MONDO:0853507 | intermediate osteogenic neoplasm | NCIT:C121925 | MONDO:equivalentTo | Intermediate Osteogenic Neoplasm | | MONDO:0045053 | -| MONDO:0853508 | intermediate bone neoplasm | NCIT:C121926 | MONDO:equivalentTo | Intermediate Bone Neoplasm | | MONDO:0019060 | -| MONDO:0853510 | primary bone non-hodgkin lymphoma | NCIT:C121930 | MONDO:equivalentTo | Primary Bone Non-Hodgkin Lymphoma | | MONDO:0017814|MONDO:0018908 | -| MONDO:0853512 | bone epithelioid hemangioendothelioma | NCIT:C121941 | MONDO:equivalentTo | Bone Epithelioid Hemangioendothelioma | | MONDO:0024499|MONDO:0002129|MONDO:0015523 | -| MONDO:0853515 | acute lymphoblastic leukemia by gene expression profile | NCIT:C121973 | MONDO:equivalentTo | Acute Lymphoblastic Leukemia by Gene Expression Profile | | MONDO:0004967 | -| MONDO:0853523 | borderline ovarian serous tumor/atypical proliferative ovarian serous tumor | NCIT:C122584 | MONDO:equivalentTo | Borderline Ovarian Serous Tumor/Atypical Proliferative Ovarian Serous Tumor | | MONDO:0020662 | -| MONDO:0853524 | borderline ovarian serous tumor-micropapillary variant/non-invasive low grade ovarian serous carcinoma | NCIT:C122585 | MONDO:equivalentTo | Borderline Ovarian Serous Tumor-Micropapillary Variant/Non-Invasive Low Grade Ovarian Serous Carcinoma | | MONDO:0020662 | -| MONDO:0853525 | infant leukemia | NCIT:C122603 | MONDO:equivalentTo | Infant Leukemia | | MONDO:0004355 | -| MONDO:0853528 | childhood acute myeloid leukemia not otherwise specified | NCIT:C122625 | MONDO:equivalentTo | Childhood Acute Myeloid Leukemia Not Otherwise Specified | | MONDO:0004996|MONDO:0015667 | -| MONDO:0853529 | hypoplastic myelodysplastic syndrome | NCIT:C122686 | MONDO:equivalentTo | Hypoplastic Myelodysplastic Syndrome | | MONDO:0018881 | -| MONDO:0853530 | cytogenetically normal acute myeloid leukemia | NCIT:C122687 | MONDO:equivalentTo | Cytogenetically Normal Acute Myeloid Leukemia | | MONDO:0018874 | -| MONDO:0853532 | childhood acute myeloid leukemia with abnormalities of chromosome 5q | NCIT:C122725 | MONDO:equivalentTo | Childhood Acute Myeloid Leukemia with Abnormalities of Chromosome 5q | | MONDO:0004996 | -| MONDO:0853533 | childhood acute myeloid leukemia with abnormalities of chromosome 7 | NCIT:C122726 | MONDO:equivalentTo | Childhood Acute Myeloid Leukemia with Abnormalities of Chromosome 7 | | MONDO:0004996 | -| MONDO:0853659 | childhood lymphomatoid granulomatosis | NCIT:C123392 | MONDO:equivalentTo | Childhood Lymphomatoid Granulomatosis | | MONDO:0019466 | -| MONDO:0853660 | childhood langerhans cell histiocytosis with risk organ involvement | NCIT:C123395 | MONDO:equivalentTo | Childhood Langerhans Cell Histiocytosis with Risk Organ Involvement | | MONDO:0017025 | -| MONDO:0853661 | childhood langerhans cell histiocytosis without risk organ involvement | NCIT:C123396 | MONDO:equivalentTo | Childhood Langerhans Cell Histiocytosis without Risk Organ Involvement | | MONDO:0017025 | -| MONDO:0853668 | fusion-positive rhabdomyosarcoma | NCIT:C123735 | MONDO:equivalentTo | Fusion-Positive Rhabdomyosarcoma | | MONDO:0005212 | -| MONDO:0853669 | fusion-negative rhabdomyosarcoma | NCIT:C123736 | MONDO:equivalentTo | Fusion-Negative Rhabdomyosarcoma | | MONDO:0005212 | -| MONDO:0853671 | refractory malignant germ cell tumor | NCIT:C123739 | MONDO:equivalentTo | Refractory Malignant Germ Cell Tumor | | MONDO:0006290|MONDO:0036501 | -| MONDO:0853673 | childhood germinomatous germ cell tumor | NCIT:C123838 | MONDO:equivalentTo | Childhood Germinomatous Germ Cell Tumor | | MONDO:0003751|MONDO:0020580 | -| MONDO:0853675 | childhood nongerminomatous germ cell tumor | NCIT:C123841 | MONDO:equivalentTo | Childhood Nongerminomatous Germ Cell Tumor | | MONDO:0003751|MONDO:0021656 | -| MONDO:0853680 | childhood mixed germ cell tumor | NCIT:C123848 | MONDO:equivalentTo | Childhood Mixed Germ Cell Tumor | | MONDO:0004479|MONDO:0015864|MONDO:0005853 | -| MONDO:0853693 | childhood astrocytoma | NCIT:C124275 | MONDO:equivalentTo | Childhood Astrocytoma | | MONDO:0002505|MONDO:0019781 | -| MONDO:0853694 | childhood atypical choroid plexus papilloma | NCIT:C124291 | MONDO:equivalentTo | Childhood Atypical Choroid Plexus Papilloma | | MONDO:0002684|MONDO:0024744 | -| MONDO:0853721 | ovarian adenomatoid tumor | NCIT:C126331 | MONDO:equivalentTo | Ovarian Adenomatoid Tumor | | MONDO:0004230|MONDO:0000646 | -| MONDO:0853728 | chronic eosinophilic leukemia with fip1l1-pdgfra | NCIT:C126351 | MONDO:equivalentTo | Chronic Eosinophilic Leukemia with FIP1L1-PDGFRA | | MONDO:0015689|MONDO:0001014 | -| MONDO:0853729 | primary peritoneal high grade serous adenocarcinoma | NCIT:C126353 | MONDO:equivalentTo | Primary Peritoneal High Grade Serous Adenocarcinoma | | MONDO:0006386 | -| MONDO:0853730 | primary peritoneal low grade serous adenocarcinoma | NCIT:C126354 | MONDO:equivalentTo | Primary Peritoneal Low Grade Serous Adenocarcinoma | | MONDO:0006386 | -| MONDO:0853731 | peritoneal desmoplastic small round cell tumor | NCIT:C126356 | MONDO:equivalentTo | Peritoneal Desmoplastic Small Round Cell Tumor | | MONDO:0019373|MONDO:0002087 | -| MONDO:0853732 | pelvic fibromatosis | NCIT:C126358 | MONDO:equivalentTo | Pelvic Fibromatosis | | MONDO:0007608 | -| MONDO:0853733 | abdominal inflammatory myofibroblastic tumor | NCIT:C126359 | MONDO:equivalentTo | Abdominal Inflammatory Myofibroblastic Tumor | | MONDO:0015798 | -| MONDO:0853734 | thyroid gland cribriform morular carcinoma | NCIT:C126408 | MONDO:equivalentTo | Thyroid Gland Cribriform Morular Carcinoma | | MONDO:0015075 | -| MONDO:0853735 | thyroid gland papillary carcinoma with fibromatosis/fasciitis-like/desmoid-type stroma | NCIT:C126410 | MONDO:equivalentTo | Thyroid Gland Papillary Carcinoma with Fibromatosis/Fasciitis-Like/Desmoid-Type Stroma | | MONDO:0005075 | -| MONDO:0853736 | fallopian tube high grade serous adenocarcinoma | NCIT:C126456 | MONDO:equivalentTo | Fallopian Tube High Grade Serous Adenocarcinoma | | MONDO:0006208 | -| MONDO:0853738 | fallopian tube lymphoma | NCIT:C126464 | MONDO:equivalentTo | Fallopian Tube Lymphoma | | MONDO:0002158|MONDO:0017207 | -| MONDO:0853742 | broad ligament serous adenocarcinoma | NCIT:C126479 | MONDO:equivalentTo | Broad Ligament Serous Adenocarcinoma | | MONDO:0002741|MONDO:0005278 | -| MONDO:0853743 | oropharyngeal poorly differentiated carcinoma | NCIT:C126750 | MONDO:equivalentTo | Oropharyngeal Poorly Differentiated Carcinoma | | MONDO:0044704 | -| MONDO:0853745 | endometrial dedifferentiated carcinoma | NCIT:C126769 | MONDO:equivalentTo | Endometrial Dedifferentiated Carcinoma | | MONDO:0002447 | -| MONDO:0853747 | uterine corpus neuroendocrine tumor g1 | NCIT:C126773 | MONDO:equivalentTo | Uterine Corpus Neuroendocrine Tumor G1 | | MONDO:0005369|MONDO:0021650 | -| MONDO:0853748 | uterine corpus hydropic leiomyoma | NCIT:C126975 | MONDO:equivalentTo | Uterine Corpus Hydropic Leiomyoma | | MONDO:0007886 | -| MONDO:0853749 | uterine corpus high grade endometrial stromal sarcoma | NCIT:C126998 | MONDO:equivalentTo | Uterine Corpus High Grade Endometrial Stromal Sarcoma | | MONDO:0002923 | -| MONDO:0853751 | benign uterine corpus pecoma | NCIT:C127071 | MONDO:equivalentTo | Benign Uterine Corpus PEComa | | MONDO:0004221|MONDO:0021525|MONDO:0020581 | -| MONDO:0853753 | uterine corpus germ cell tumor | NCIT:C127077 | MONDO:equivalentTo | Uterine Corpus Germ Cell Tumor | | MONDO:0021254|MONDO:0018201 | -| MONDO:0853764 | cervical neuroendocrine neoplasm | NCIT:C128041 | MONDO:equivalentTo | Cervical Neuroendocrine Neoplasm | | MONDO:0019496|MONDO:0021230 | -| MONDO:0853771 | vaginal papillary carcinoma | NCIT:C128060 | MONDO:equivalentTo | Vaginal Papillary Carcinoma | | MONDO:0002979|MONDO:0006490 | -| MONDO:0853775 | ovarian cancer by figo stage | NCIT:C128081 | MONDO:equivalentTo | Ovarian Cancer by FIGO Stage | | MONDO:0005140 | -| MONDO:0853776 | ovarian cancer by ajcc v6 and v7 stage | NCIT:C128106 | MONDO:equivalentTo | Ovarian Cancer by AJCC v6 and v7 Stage | | MONDO:0005140 | -| MONDO:0853779 | vaginal germ cell tumor | NCIT:C128112 | MONDO:equivalentTo | Vaginal Germ Cell Tumor | | MONDO:0005040|MONDO:0021050 | -| MONDO:0853781 | vulvar squamous intraepithelial lesion, hpv-associated | NCIT:C128142 | MONDO:equivalentTo | Vulvar Squamous Intraepithelial Lesion, HPV-Associated | | MONDO:0005198 | -| MONDO:0853784 | vulvar adenocarcinoma of mammary gland type | NCIT:C128162 | MONDO:equivalentTo | Vulvar Adenocarcinoma of Mammary Gland Type | | MONDO:0024336 | -| MONDO:0853787 | vulvar adenocarcinoma, intestinal-type | NCIT:C128166 | MONDO:equivalentTo | Vulvar Adenocarcinoma, Intestinal-Type | | MONDO:0024336|MONDO:0006254|MONDO:0004957 | -| MONDO:0853788 | vulvar keratoacanthoma | NCIT:C128167 | MONDO:equivalentTo | Vulvar Keratoacanthoma | | MONDO:0024609|MONDO:0002527 | -| MONDO:0853793 | vulvar merkel cell carcinoma | NCIT:C128247 | MONDO:equivalentTo | Vulvar Merkel Cell Carcinoma | | MONDO:0019210|MONDO:0056816 | -| MONDO:0853797 | vulvar germ cell tumor | NCIT:C128294 | MONDO:equivalentTo | Vulvar Germ Cell Tumor | | MONDO:0005040|MONDO:0021049 | -| MONDO:0853835 | b acute lymphoblastic leukemia, philadelphia chromosome negative | NCIT:C128629 | MONDO:equivalentTo | B Acute Lymphoblastic Leukemia, Philadelphia Chromosome Negative | | MONDO:0020511 | -| MONDO:0853837 | nk-cell lymphoma, unclassifiable | NCIT:C128697 | MONDO:equivalentTo | NK-Cell Lymphoma, Unclassifiable | | MONDO:0000430 | -| MONDO:0853840 | cutaneous malignant melanoma 2 | NCIT:C128801 | MONDO:equivalentTo | Cutaneous Malignant Melanoma 2 | | MONDO:0018961 | -| MONDO:0853846 | glioblastoma, not otherwise specified | NCIT:C129295 | MONDO:equivalentTo | Glioblastoma, Not Otherwise Specified | | MONDO:0018177 | -| MONDO:0853849 | oligodendroglioma, idh-mutant and 1p/19q-codeleted | NCIT:C129318 | MONDO:equivalentTo | Oligodendroglioma, IDH-Mutant and 1p/19q-Codeleted | | MONDO:0016695 | -| MONDO:0853850 | oligodendroglioma, not otherwise specified | NCIT:C129319 | MONDO:equivalentTo | Oligodendroglioma, Not Otherwise Specified | | MONDO:0016695 | -| MONDO:0853851 | anaplastic oligodendroglioma, idh-mutant and 1p/19q-codeleted | NCIT:C129321 | MONDO:equivalentTo | Anaplastic Oligodendroglioma, IDH-Mutant and 1p/19q-Codeleted | | MONDO:0016696 | -| MONDO:0853852 | anaplastic oligodendroglioma, not otherwise specified | NCIT:C129322 | MONDO:equivalentTo | Anaplastic Oligodendroglioma, Not Otherwise Specified | | MONDO:0016696 | -| MONDO:0853853 | oligoastrocytoma, not otherwise specified | NCIT:C129323 | MONDO:equivalentTo | Oligoastrocytoma, Not Otherwise Specified | | MONDO:0016702 | -| MONDO:0853854 | anaplastic oligoastrocytoma, not otherwise specified | NCIT:C129324 | MONDO:equivalentTo | Anaplastic Oligoastrocytoma, Not Otherwise Specified | | MONDO:0016703 | -| MONDO:0853855 | diffuse glioma | NCIT:C129325 | MONDO:equivalentTo | Diffuse Glioma | | MONDO:0021042 | -| MONDO:0853856 | anaplastic pleomorphic xanthoastrocytoma | NCIT:C129327 | MONDO:equivalentTo | Anaplastic Pleomorphic Xanthoastrocytoma | | MONDO:0019781|MONDO:0021640|MONDO:0020633 | -| MONDO:0853857 | diffuse leptomeningeal glioneuronal tumor | NCIT:C129424 | MONDO:equivalentTo | Diffuse Leptomeningeal Glioneuronal Tumor | | MONDO:0016729 | -| MONDO:0853858 | multinodular and vacuolated neuronal tumor | NCIT:C129427 | MONDO:equivalentTo | Multinodular and Vacuolated Neuronal Tumor | | MONDO:0021374|MONDO:0016729|MONDO:0021632 | -| MONDO:0853859 | medulloblastoma molecular subtypes | NCIT:C129439 | MONDO:equivalentTo | Medulloblastoma Molecular Subtypes | | MONDO:0007959 | -| MONDO:0853860 | medulloblastoma, not otherwise specified | NCIT:C129447 | MONDO:equivalentTo | Medulloblastoma, Not Otherwise Specified | | MONDO:0007959 | -| MONDO:0853861 | small cell adenocarcinoma | NCIT:C129449 | MONDO:equivalentTo | Small Cell Adenocarcinoma | | MONDO:0004970 | -| MONDO:0853862 | central nervous system solitary fibrous tumor | NCIT:C129526 | MONDO:equivalentTo | Central Nervous System Solitary Fibrous Tumor | | MONDO:0016238|MONDO:0003244 | -| MONDO:0853863 | central nervous system mesenchymal chondrosarcoma | NCIT:C129534 | MONDO:equivalentTo | Central Nervous System Mesenchymal Chondrosarcoma | | MONDO:0002217|MONDO:0006853 | -| MONDO:0853864 | central nervous system epithelioid hemangioendothelioma | NCIT:C129536 | MONDO:equivalentTo | Central Nervous System Epithelioid Hemangioendothelioma | | MONDO:0037740|MONDO:0015523 | -| MONDO:0853865 | central nervous system angiolipoma | NCIT:C129538 | MONDO:equivalentTo | Central Nervous System Angiolipoma | | MONDO:0003844|MONDO:0006085 | -| MONDO:0853866 | central nervous system undifferentiated pleomorphic sarcoma | NCIT:C129566 | MONDO:equivalentTo | Central Nervous System Undifferentiated Pleomorphic Sarcoma | | MONDO:0002217|MONDO:0002142 | -| MONDO:0853868 | central nervous system anaplastic large cell lymphoma, alk-positive | NCIT:C129598 | MONDO:equivalentTo | Central Nervous System Anaplastic Large Cell Lymphoma, ALK-Positive | | MONDO:0006128|MONDO:0017602 | -| MONDO:0853869 | central nervous system anaplastic large cell lymphoma, alk-negative | NCIT:C129599 | MONDO:equivalentTo | Central Nervous System Anaplastic Large Cell Lymphoma, ALK-Negative | | MONDO:0006128|MONDO:0017603 | -| MONDO:0853870 | central nervous system intravascular large b-cell lymphoma | NCIT:C129602 | MONDO:equivalentTo | Central Nervous System Intravascular Large B-Cell Lymphoma | | MONDO:0017596|MONDO:0020324 | -| MONDO:0853881 | acute myeloid leukemia with biallelic cebpa mutation | NCIT:C129782 | MONDO:equivalentTo | Acute Myeloid Leukemia with Biallelic CEBPA Mutation | | MONDO:0017894 | -| MONDO:0853882 | acute myeloid leukemia with monoallelic cebpa mutation | NCIT:C129783 | MONDO:equivalentTo | Acute Myeloid Leukemia with Monoallelic CEBPA Mutation | | MONDO:0017894 | -| MONDO:0853884 | b lymphoblastic leukemia/lymphoma, bcr-abl1-like | NCIT:C129787 | MONDO:equivalentTo | B Lymphoblastic Leukemia/Lymphoma, BCR-ABL1-Like | | MONDO:0035605 | -| MONDO:0853887 | metastatic transitional cell carcinoma | NCIT:C129828 | MONDO:equivalentTo | Metastatic Transitional Cell Carcinoma | | MONDO:0024879|MONDO:0006474 | -| MONDO:0853888 | chronic myelomonocytic leukemia with eosinophilia associated with t(5;12)(q31;p12) | NCIT:C129852 | MONDO:equivalentTo | Chronic Myelomonocytic Leukemia with Eosinophilia Associated with t(5;12)(q31;p12) | | MONDO:0015690 | -| MONDO:0853892 | chronic myelomonocytic leukemia-0 | NCIT:C130035 | MONDO:equivalentTo | Chronic Myelomonocytic Leukemia-0 | | MONDO:0020311 | -| MONDO:0853893 | myelodysplastic syndrome with ring sideroblasts and single lineage dysplasia | NCIT:C130037 | MONDO:equivalentTo | Myelodysplastic Syndrome with Ring Sideroblasts and Single Lineage Dysplasia | | MONDO:0019157 | -| MONDO:0853894 | b lymphoblastic leukemia/lymphoma with intrachromosomal amplification of chromosome 21 | NCIT:C130039 | MONDO:equivalentTo | B Lymphoblastic Leukemia/Lymphoma with Intrachromosomal Amplification of Chromosome 21 | | MONDO:0035605 | -| MONDO:0853943 | anastomosing hemangioma | NCIT:C131760 | MONDO:equivalentTo | Anastomosing Hemangioma | | MONDO:0002407 | -| MONDO:0853956 | acute megakaryoblastic leukemia with cbfa2t3-glis2 | NCIT:C132109 | MONDO:equivalentTo | Acute Megakaryoblastic Leukemia with CBFA2T3-GLIS2 | | MONDO:0004996 | -| MONDO:0853959 | small intestinal myeloid sarcoma | NCIT:C132260 | MONDO:equivalentTo | Small Intestinal Myeloid Sarcoma | | MONDO:0000956|MONDO:0006861 | -| MONDO:0853961 | atypical pituitary neuroendocrine tumor | NCIT:C132296 | MONDO:equivalentTo | Atypical Pituitary Neuroendocrine Tumor | | MONDO:0006373 | -| MONDO:0853963 | lip and oral cavity cancer by ajcc v8 stage | NCIT:C132728 | MONDO:equivalentTo | Lip and Oral Cavity Cancer by AJCC v8 Stage | | MONDO:0023644 | -| MONDO:0853964 | lip and oral cavity cancer by ajcc v6 and v7 stage | NCIT:C132736 | MONDO:equivalentTo | Lip and Oral Cavity Cancer by AJCC v6 and v7 Stage | | MONDO:0023644 | -| MONDO:0853965 | major salivary gland cancer by ajcc v7 stage | NCIT:C132778 | MONDO:equivalentTo | Major Salivary Gland Cancer by AJCC v7 Stage | | MONDO:0006284 | -| MONDO:0853966 | major salivary gland cancer by ajcc v8 stage | NCIT:C132779 | MONDO:equivalentTo | Major Salivary Gland Cancer by AJCC v8 Stage | | MONDO:0006284 | -| MONDO:0853968 | pharyngeal carcinoma by ajcc v8 stage | NCIT:C132814 | MONDO:equivalentTo | Pharyngeal Carcinoma by AJCC v8 Stage | | MONDO:0021345 | -| MONDO:0853973 | metastatic malignant germ cell tumor | NCIT:C132854 | MONDO:equivalentTo | Metastatic Malignant Germ Cell Tumor | | MONDO:0006290|MONDO:0024880 | -| MONDO:0853979 | sinonasal cancer by ajcc v8 stage | NCIT:C133074 | MONDO:equivalentTo | Sinonasal Cancer by AJCC v8 Stage | | MONDO:0056819 | -| MONDO:0853980 | lung adenofibroma | NCIT:C133091 | MONDO:equivalentTo | Lung Adenofibroma | | MONDO:0021043|MONDO:0002732 | -| MONDO:0853981 | laryngeal cancer by ajcc v8 stage | NCIT:C133156 | MONDO:equivalentTo | Laryngeal Cancer by AJCC v8 Stage | | MONDO:0002358 | -| MONDO:0853984 | cutaneous squamous cell carcinoma of the head and neck | NCIT:C133252 | MONDO:equivalentTo | Cutaneous Squamous Cell Carcinoma of the Head and Neck | | MONDO:0002529|MONDO:0010150 | -| MONDO:0853986 | esophageal cancer by ajcc v8 stage | NCIT:C133399 | MONDO:equivalentTo | Esophageal Cancer by AJCC v8 Stage | | MONDO:0019086 | -| MONDO:0853991 | gastroesophageal junction adenocarcinoma by ajcc v8 stage | NCIT:C133548 | MONDO:equivalentTo | Gastroesophageal Junction Adenocarcinoma by AJCC v8 Stage | | MONDO:0003219 | -| MONDO:0853993 | gastric cancer by ajcc v8 stage | NCIT:C133638 | MONDO:equivalentTo | Gastric Cancer by AJCC v8 Stage | | MONDO:0004950 | -| MONDO:0853994 | small intestinal cancer by ajcc v7 stage | NCIT:C133716 | MONDO:equivalentTo | Small Intestinal Cancer by AJCC v7 Stage | | MONDO:0005522 | -| MONDO:0853996 | appendix carcinoma by ajcc v7 stage | NCIT:C133733 | MONDO:equivalentTo | Appendix Carcinoma by AJCC v7 Stage | | MONDO:0003196 | -| MONDO:0853997 | anal canal cancer by ajcc v6 and v7 stage | NCIT:C133787 | MONDO:equivalentTo | Anal Canal Cancer by AJCC v6 and v7 Stage | | MONDO:0007108 | -| MONDO:0853998 | anal cancer by ajcc v8 stage | NCIT:C133794 | MONDO:equivalentTo | Anal Cancer by AJCC v8 Stage | | MONDO:0003199 | -| MONDO:0854000 | small intestinal adenocarcinoma by ajcc v8 stage | NCIT:C133893 | MONDO:equivalentTo | Small Intestinal Adenocarcinoma by AJCC v8 Stage | | MONDO:0003198 | -| MONDO:0854002 | appendix carcinoma by ajcc v8 stage | NCIT:C134117 | MONDO:equivalentTo | Appendix Carcinoma by AJCC v8 Stage | | MONDO:0003196 | -| MONDO:0854009 | colorectal cancer by ajcc v8 stage | NCIT:C134180 | MONDO:equivalentTo | Colorectal Cancer by AJCC v8 Stage | | MONDO:0024331 | -| MONDO:0854013 | intrahepatic cholangiocarcinoma by ajcc v7 stage | NCIT:C134514 | MONDO:equivalentTo | Intrahepatic Cholangiocarcinoma by AJCC v7 Stage | | MONDO:0003210 | -| MONDO:0854014 | hepatocellular carcinoma by ajcc v8 stage | NCIT:C134515 | MONDO:equivalentTo | Hepatocellular Carcinoma by AJCC v8 Stage | | MONDO:0007256 | -| MONDO:0854017 | intrahepatic bile duct cancer by ajcc v8 stage | NCIT:C134604 | MONDO:equivalentTo | Intrahepatic Bile Duct Cancer by AJCC v8 Stage | | MONDO:0018531 | -| MONDO:0854018 | gallbladder cancer by ajcc v8 stage | NCIT:C134660 | MONDO:equivalentTo | Gallbladder Cancer by AJCC v8 Stage | | MONDO:0003220 | -| MONDO:0854019 | hilar cholangiocarcinoma by ajcc v7 stage | NCIT:C134742 | MONDO:equivalentTo | Hilar Cholangiocarcinoma by AJCC v7 Stage | | MONDO:0003345 | -| MONDO:0854020 | hilar cholangiocarcinoma by ajcc v8 stage | NCIT:C134743 | MONDO:equivalentTo | Hilar Cholangiocarcinoma by AJCC v8 Stage | | MONDO:0003345 | -| MONDO:0854022 | distal bile duct cancer by ajcc v7 stage | NCIT:C134810 | MONDO:equivalentTo | Distal Bile Duct Cancer by AJCC v7 Stage | | MONDO:0003707 | -| MONDO:0854023 | distal bile duct cancer by ajcc v8 stage | NCIT:C134811 | MONDO:equivalentTo | Distal Bile Duct Cancer by AJCC v8 Stage | | MONDO:0003707 | -| MONDO:0854024 | ampulla of vater cancer by ajcc v7 stage | NCIT:C134863 | MONDO:equivalentTo | Ampulla of Vater Cancer by AJCC v7 Stage | | MONDO:0017590 | -| MONDO:0854025 | ampulla of vater cancer by ajcc v8 stage | NCIT:C134864 | MONDO:equivalentTo | Ampulla of Vater Cancer by AJCC v8 Stage | | MONDO:0017590 | -| MONDO:0854026 | pancreatic cancer by ajcc v6 and v7 stage | NCIT:C134902 | MONDO:equivalentTo | Pancreatic Cancer by AJCC v6 and v7 Stage | | MONDO:0005192 | -| MONDO:0854027 | pancreatic cancer by ajcc v8 stage | NCIT:C134909 | MONDO:equivalentTo | Pancreatic Cancer by AJCC v8 Stage | | MONDO:0005192 | -| MONDO:0854029 | lung non-squamous non-small cell carcinoma | NCIT:C135017 | MONDO:equivalentTo | Lung Non-Squamous Non-Small Cell Carcinoma | | MONDO:0005233 | -| MONDO:0854030 | gastric neuroendocrine tumor by ajcc v8 stage | NCIT:C135045 | MONDO:equivalentTo | Gastric Neuroendocrine Tumor by AJCC v8 Stage | | MONDO:0015062 | -| MONDO:0854031 | duodenal neuroendocrine tumor by ajcc v8 stage | NCIT:C135075 | MONDO:equivalentTo | Duodenal Neuroendocrine Tumor by AJCC v8 Stage | | MONDO:0015063 | -| MONDO:0854032 | jejunal neuroendocrine tumor by ajcc v8 stage | NCIT:C135119 | MONDO:equivalentTo | Jejunal Neuroendocrine Tumor by AJCC v8 Stage | | MONDO:0015064 | -| MONDO:0854033 | ileal neuroendocrine tumor by ajcc v8 stage | NCIT:C135124 | MONDO:equivalentTo | Ileal Neuroendocrine Tumor by AJCC v8 Stage | | MONDO:0015065 | -| MONDO:0854034 | digestive system neuroendocrine tumor by ajcc v7 stage | NCIT:C135129 | MONDO:equivalentTo | Digestive System Neuroendocrine Tumor by AJCC v7 Stage | | MONDO:0000386 | -| MONDO:0854036 | appendix neuroendocrine tumor by ajcc v8 stage | NCIT:C135156 | MONDO:equivalentTo | Appendix Neuroendocrine Tumor by AJCC v8 Stage | | MONDO:0015066 | -| MONDO:0854042 | pancreatic neuroendocrine tumor by ajcc v8 stage | NCIT:C135560 | MONDO:equivalentTo | Pancreatic Neuroendocrine Tumor by AJCC v8 Stage | | MONDO:0019954 | -| MONDO:0854043 | thymic epithelial neoplasm by ajcc v8 stage | NCIT:C136320 | MONDO:equivalentTo | Thymic Epithelial Neoplasm by AJCC v8 Stage | | MONDO:0018079 | -| MONDO:0854045 | pleural malignant mesothelioma by ajcc v7 stage | NCIT:C136374 | MONDO:equivalentTo | Pleural Malignant Mesothelioma by AJCC v7 Stage | | MONDO:0005112 | -| MONDO:0854046 | pleural malignant mesothelioma by ajcc v8 stage | NCIT:C136399 | MONDO:equivalentTo | Pleural Malignant Mesothelioma by AJCC v8 Stage | | MONDO:0005112 | -| MONDO:0854048 | lung cancer by ajcc v8 stage | NCIT:C136467 | MONDO:equivalentTo | Lung Cancer by AJCC v8 Stage | | MONDO:0005138 | -| MONDO:0854057 | bone cancer by ajcc v7 stage | NCIT:C136610 | MONDO:equivalentTo | Bone Cancer by AJCC v7 Stage | | MONDO:0002129 | -| MONDO:0854058 | bone cancer by ajcc v8 stage | NCIT:C136612 | MONDO:equivalentTo | Bone Cancer by AJCC v8 Stage | | MONDO:0002129 | -| MONDO:0854060 | soft tissue sarcoma by ajcc v8 stage | NCIT:C136693 | MONDO:equivalentTo | Soft Tissue Sarcoma by AJCC v8 Stage | | MONDO:0018078 | -| MONDO:0854061 | soft tissue sarcoma by ajcc v7 stage | NCIT:C136707 | MONDO:equivalentTo | Soft Tissue Sarcoma by AJCC v7 Stage | | MONDO:0018078 | -| MONDO:0854062 | uterine corpus sarcoma by ajcc v7 stage | NCIT:C136708 | MONDO:equivalentTo | Uterine Corpus Sarcoma by AJCC v7 Stage | | MONDO:0005210 | -| MONDO:0854063 | invasive lung mucinous adenocarcinoma | NCIT:C136709 | MONDO:equivalentTo | Invasive Lung Mucinous Adenocarcinoma | | MONDO:0040677|MONDO:0005061|MONDO:0004957 | -| MONDO:0854064 | lung enteric adenocarcinoma | NCIT:C136710 | MONDO:equivalentTo | Lung Enteric Adenocarcinoma | | MONDO:0006254|MONDO:0005061 | -| MONDO:0854065 | lung keratinizing squamous cell carcinoma | NCIT:C136713 | MONDO:equivalentTo | Lung Keratinizing Squamous Cell Carcinoma | | MONDO:0005097 | -| MONDO:0854066 | lung non-keratinizing squamous cell carcinoma | NCIT:C136714 | MONDO:equivalentTo | Lung Non-Keratinizing Squamous Cell Carcinoma | | MONDO:0005097 | -| MONDO:0854067 | lung non-mucinous adenocarcinoma in situ | NCIT:C136716 | MONDO:equivalentTo | Lung Non-Mucinous Adenocarcinoma In Situ | | MONDO:0000503 | -| MONDO:0854068 | lung mucinous adenocarcinoma in situ | NCIT:C136717 | MONDO:equivalentTo | Lung Mucinous Adenocarcinoma In Situ | | MONDO:0000503 | -| MONDO:0854069 | lung squamous cell carcinoma in situ | NCIT:C136719 | MONDO:equivalentTo | Lung Squamous Cell Carcinoma In Situ | | MONDO:0005097|MONDO:0004693 | -| MONDO:0854071 | atypical spitz nevus | NCIT:C136825 | MONDO:equivalentTo | Atypical Spitz Nevus | | MONDO:0005073|MONDO:0021583 | -| MONDO:0854072 | merkel cell carcinoma by ajcc v7 stage | NCIT:C136869 | MONDO:equivalentTo | Merkel Cell Carcinoma by AJCC v7 Stage | | MONDO:0019210 | -| MONDO:0854073 | merkel cell carcinoma by ajcc v8 stage | NCIT:C136870 | MONDO:equivalentTo | Merkel Cell Carcinoma by AJCC v8 Stage | | MONDO:0019210 | -| MONDO:0854075 | cutaneous melanoma by ajcc v8 stage | NCIT:C137645 | MONDO:equivalentTo | Cutaneous Melanoma by AJCC v8 Stage | | MONDO:0005012 | -| MONDO:0854076 | occult breast carcinoma | NCIT:C137674 | MONDO:equivalentTo | Occult Breast Carcinoma | | MONDO:0004989 | -| MONDO:0854077 | breast pleomorphic lobular carcinoma in situ | NCIT:C137839 | MONDO:equivalentTo | Breast Pleomorphic Lobular Carcinoma In Situ | | MONDO:0006270 | -| MONDO:0854089 | prostate carcinoma by gene expression profile | NCIT:C138167 | MONDO:equivalentTo | Prostate Carcinoma by Gene Expression Profile | | MONDO:0005159 | -| MONDO:0854090 | duodenal-type follicular lymphoma | NCIT:C138185 | MONDO:equivalentTo | Duodenal-Type Follicular Lymphoma | | MONDO:0018906 | -| MONDO:0854092 | high grade b-cell lymphoma with myc and bcl2 and/or bcl6 rearrangements | NCIT:C138195 | MONDO:equivalentTo | High Grade B-Cell Lymphoma with MYC and BCL2 and/or BCL6 Rearrangements | | MONDO:0044889 | -| MONDO:0854094 | double-expressor lymphoma | NCIT:C138899 | MONDO:equivalentTo | Double-Expressor Lymphoma | | MONDO:0018905 | -| MONDO:0854097 | follicular helper t-cell lymphoma | NCIT:C139005 | MONDO:equivalentTo | Follicular Helper T-Cell Lymphoma | | MONDO:0000430 | -| MONDO:0854098 | multiple myeloma myeloma by ds stage | NCIT:C139008 | MONDO:equivalentTo | Multiple Myeloma Myeloma by DS Stage | | MONDO:0009693 | -| MONDO:0854099 | multiple myeloma by iss stage | NCIT:C139009 | MONDO:equivalentTo | Multiple Myeloma by ISS Stage | | MONDO:0009693 | -| MONDO:0854100 | type d lymphomatoid papulosis | NCIT:C139014 | MONDO:equivalentTo | Type D Lymphomatoid Papulosis | | MONDO:0020326 | -| MONDO:0854101 | type e lymphomatoid papulosis | NCIT:C139015 | MONDO:equivalentTo | Type E Lymphomatoid Papulosis | | MONDO:0020326 | -| MONDO:0854102 | lymphomatoid papulosis with dusp22-irf4 gene rearrangement | NCIT:C139017 | MONDO:equivalentTo | Lymphomatoid Papulosis with DUSP22-IRF4 Gene Rearrangement | | MONDO:0020326 | -| MONDO:0854105 | breast cancer by ajcc v8 stage | NCIT:C139532 | MONDO:equivalentTo | Breast Cancer by AJCC v8 Stage | | MONDO:0004989 | -| MONDO:0854108 | fibroadenoma of anogenital mammary-type glands | NCIT:C139547 | MONDO:equivalentTo | Fibroadenoma of Anogenital Mammary-Type Glands | | MONDO:0000383|MONDO:0021045 | -| MONDO:0854109 | vulvar composite hidradenoma papilliferum and fibroadenoma | NCIT:C139548 | MONDO:equivalentTo | Vulvar Composite Hidradenoma Papilliferum and Fibroadenoma | | MONDO:0021043|MONDO:0000643 | -| MONDO:0854111 | vulvar cancer by ajcc v8 stage | NCIT:C139618 | MONDO:equivalentTo | Vulvar Cancer by AJCC v8 Stage | | MONDO:0005215 | -| MONDO:0854112 | vaginal cancer by ajcc v8 stage | NCIT:C139657 | MONDO:equivalentTo | Vaginal Cancer by AJCC v8 Stage | | MONDO:0015867 | -| MONDO:0854113 | cervical cancer by ajcc v8 stage | NCIT:C139733 | MONDO:equivalentTo | Cervical Cancer by AJCC v8 Stage | | MONDO:0005131 | -| MONDO:0854114 | uterine corpus cancer by ajcc v8 stage | NCIT:C139801 | MONDO:equivalentTo | Uterine Corpus Cancer by AJCC v8 Stage | | MONDO:0006003 | -| MONDO:0854115 | uterine corpus sarcoma by ajcc v8 stage | NCIT:C139869 | MONDO:equivalentTo | Uterine Corpus Sarcoma by AJCC v8 Stage | | MONDO:0005210 | -| MONDO:0854119 | ovarian cancer by ajcc v8 stage | NCIT:C139963 | MONDO:equivalentTo | Ovarian Cancer by AJCC v8 Stage | | MONDO:0005140 | -| MONDO:0854120 | fallopian tube cancer by ajcc v8 stage | NCIT:C139983 | MONDO:equivalentTo | Fallopian Tube Cancer by AJCC v8 Stage | | MONDO:0006206 | -| MONDO:0854121 | primary peritoneal cancer by ajcc v7 stage | NCIT:C140003 | MONDO:equivalentTo | Primary Peritoneal Cancer by AJCC v7 Stage | | MONDO:0015686 | -| MONDO:0854122 | primary peritoneal cancer by ajcc v8 stage | NCIT:C140004 | MONDO:equivalentTo | Primary Peritoneal Cancer by AJCC v8 Stage | | MONDO:0015686 | -| MONDO:0854123 | gestational trophoblastic tumor by ajcc v7 stage | NCIT:C140032 | MONDO:equivalentTo | Gestational Trophoblastic Tumor by AJCC v7 Stage | | MONDO:0018944 | -| MONDO:0854124 | penile cancer by ajcc v8 stage | NCIT:C140075 | MONDO:equivalentTo | Penile Cancer by AJCC v8 Stage | | MONDO:0006360 | -| MONDO:0854125 | prostate cancer by ajcc v8 stage | NCIT:C140163 | MONDO:equivalentTo | Prostate Cancer by AJCC v8 Stage | | MONDO:0005159 | -| MONDO:0854126 | testicular cancer by ajcc v8 stage | NCIT:C140225 | MONDO:equivalentTo | Testicular Cancer by AJCC v8 Stage | | MONDO:0005447 | -| MONDO:0854127 | testicular cancer by ajcc v6 and v7 stage | NCIT:C140241 | MONDO:equivalentTo | Testicular Cancer by AJCC v6 and v7 Stage | | MONDO:0005447 | -| MONDO:0854128 | renal cell cancer by ajcc v8 stage | NCIT:C140322 | MONDO:equivalentTo | Renal Cell Cancer by AJCC v8 Stage | | MONDO:0005549 | -| MONDO:0854130 | renal pelvis and ureter cancer by ajcc v8 stage | NCIT:C140355 | MONDO:equivalentTo | Renal Pelvis and Ureter Cancer by AJCC v8 Stage | | MONDO:0020654 | -| MONDO:0854134 | renal pelvis and ureter cancer by ajcc v7 stage | NCIT:C140376 | MONDO:equivalentTo | Renal Pelvis and Ureter Cancer by AJCC v7 Stage | | MONDO:0020654 | -| MONDO:0854137 | bladder cancer by ajcc v8 stage | NCIT:C140416 | MONDO:equivalentTo | Bladder Cancer by AJCC v8 Stage | | MONDO:0004986 | -| MONDO:0854139 | urethral cancer by ajcc v8 stage | NCIT:C140457 | MONDO:equivalentTo | Urethral Cancer by AJCC v8 Stage | | MONDO:0021327 | -| MONDO:0854141 | urethral cancer by ajcc v7 stage | NCIT:C140464 | MONDO:equivalentTo | Urethral Cancer by AJCC v7 Stage | | MONDO:0021327 | -| MONDO:0854142 | eyelid carcinoma by ajcc v7 stage | NCIT:C140511 | MONDO:equivalentTo | Eyelid Carcinoma by AJCC v7 Stage | | MONDO:0003876 | -| MONDO:0854143 | eyelid carcinoma by ajcc v8 stage | NCIT:C140513 | MONDO:equivalentTo | Eyelid Carcinoma by AJCC v8 Stage | | MONDO:0003876 | -| MONDO:0854144 | choroidal and ciliary body melanoma by ajcc v8 stage | NCIT:C140659 | MONDO:equivalentTo | Choroidal and Ciliary Body Melanoma by AJCC v8 Stage | | MONDO:0006486 | -| MONDO:0854145 | uveal melanoma by ajcc v7 stage | NCIT:C140672 | MONDO:equivalentTo | Uveal Melanoma by AJCC v7 Stage | | MONDO:0006486 | -| MONDO:0854146 | retinoblastoma by ajcc v8 stage | NCIT:C140750 | MONDO:equivalentTo | Retinoblastoma by AJCC v8 Stage | | MONDO:0008380 | -| MONDO:0854148 | differentiated thyroid gland carcinoma by ajcc v7 stage | NCIT:C140959 | MONDO:equivalentTo | Differentiated Thyroid Gland Carcinoma by AJCC v7 Stage | | MONDO:0015447 | -| MONDO:0854150 | differentiated thyroid gland carcinoma by ajcc v8 stage | NCIT:C140965 | MONDO:equivalentTo | Differentiated Thyroid Gland Carcinoma by AJCC v8 Stage | | MONDO:0015447 | -| MONDO:0854153 | thyroid gland anaplastic carcinoma by ajcc v7 stage | NCIT:C140999 | MONDO:equivalentTo | Thyroid Gland Anaplastic Carcinoma by AJCC v7 Stage | | MONDO:0006468 | -| MONDO:0854154 | thyroid gland anaplastic carcinoma by ajcc v8 stage | NCIT:C141000 | MONDO:equivalentTo | Thyroid Gland Anaplastic Carcinoma by AJCC v8 Stage | | MONDO:0006468 | -| MONDO:0854155 | thyroid gland medullary carcinoma by ajcc v7 stage | NCIT:C141041 | MONDO:equivalentTo | Thyroid Gland Medullary Carcinoma by AJCC v7 Stage | | MONDO:0015277 | -| MONDO:0854156 | thyroid gland medullary carcinoma by ajcc v8 stage | NCIT:C141042 | MONDO:equivalentTo | Thyroid Gland Medullary Carcinoma by AJCC v8 Stage | | MONDO:0015277 | -| MONDO:0854157 | adrenal cortical carcinoma by ajcc v7 stage | NCIT:C141098 | MONDO:equivalentTo | Adrenal Cortical Carcinoma by AJCC v7 Stage | | MONDO:0006639 | -| MONDO:0854158 | adrenal cortical carcinoma by ajcc v8 stage | NCIT:C141100 | MONDO:equivalentTo | Adrenal Cortical Carcinoma by AJCC v8 Stage | | MONDO:0006639 | -| MONDO:0854159 | adrenal gland pheochromocytoma and sympathetic paraganglioma by ajcc v8 stage | NCIT:C141128 | MONDO:equivalentTo | Adrenal Gland Pheochromocytoma and Sympathetic Paraganglioma by AJCC v8 Stage | | MONDO:0021072 | -| MONDO:0854166 | chronic lymphocytic leukemia- modified rai staging system | NCIT:C141206 | MONDO:equivalentTo | Chronic Lymphocytic Leukemia- Modified Rai Staging System | | MONDO:0004948 | -| MONDO:0854167 | chronic lymphocytic leukemia- binet staging system | NCIT:C141208 | MONDO:equivalentTo | Chronic Lymphocytic Leukemia- Binet Staging System | | MONDO:0004948 | -| MONDO:0854189 | multiple myeloma by riss stage | NCIT:C141393 | MONDO:equivalentTo | Multiple Myeloma by RISS Stage | | MONDO:0009693 | -| MONDO:0854192 | thoracic nut carcinoma | NCIT:C142781 | MONDO:equivalentTo | Thoracic NUT Carcinoma | | MONDO:0005563|MONDO:0003274 | -| MONDO:0854193 | benign lung pecoma | NCIT:C142784 | MONDO:equivalentTo | Benign Lung PEComa | | MONDO:0002732|MONDO:0020588|MONDO:0020581 | -| MONDO:0854200 | pulmonary artery intimal sarcoma | NCIT:C142825 | MONDO:equivalentTo | Pulmonary Artery Intimal Sarcoma | | MONDO:0006255|MONDO:0002426 | -| MONDO:0854201 | primary pulmonary myxoid sarcoma with ewsr1-creb1 fusion | NCIT:C142827 | MONDO:equivalentTo | Primary Pulmonary Myxoid Sarcoma with EWSR1-CREB1 Fusion | | MONDO:0002426 | -| MONDO:0854212 | refractory rhabdoid tumor | NCIT:C142858 | MONDO:equivalentTo | Refractory Rhabdoid Tumor | | MONDO:0002728|MONDO:0036501 | -| MONDO:0854225 | atypical type a thymoma | NCIT:C146640 | MONDO:equivalentTo | Atypical Type A Thymoma | | MONDO:0002588 | -| MONDO:0854227 | thymic hepatoid adenocarcinoma | NCIT:C146717 | MONDO:equivalentTo | Thymic Hepatoid Adenocarcinoma | | MONDO:0006243|MONDO:0003209 | -| MONDO:0854229 | malignant mediastinal germ cell tumor stage grouping of the pediatric study group | NCIT:C146848 | MONDO:equivalentTo | Malignant Mediastinal Germ Cell Tumor Stage Grouping of the Pediatric Study Group | | MONDO:0006298 | -| MONDO:0854230 | metastatic epithelioid hemangioendothelioma | NCIT:C146858 | MONDO:equivalentTo | Metastatic Epithelioid Hemangioendothelioma | | MONDO:0015523|MONDO:0024880 | -| MONDO:0854231 | mediastinal mixed germ cell tumor | NCIT:C146861 | MONDO:equivalentTo | Mediastinal Mixed Germ Cell Tumor | | MONDO:0006298|MONDO:0015864|MONDO:0005853 | -| MONDO:0854234 | mediastinal epithelioid hemangioendothelioma | NCIT:C146988 | MONDO:equivalentTo | Mediastinal Epithelioid Hemangioendothelioma | | MONDO:0037743|MONDO:0015523 | -| MONDO:0854235 | cardiac extraskeletal osteosarcoma | NCIT:C147003 | MONDO:equivalentTo | Cardiac Extraskeletal Osteosarcoma | | MONDO:0002621|MONDO:0003354 | -| MONDO:0854236 | cardiac myxofibrosarcoma | NCIT:C147004 | MONDO:equivalentTo | Cardiac Myxofibrosarcoma | | MONDO:0019202|MONDO:0003742 | -| MONDO:0854237 | cardiac yolk sac tumor | NCIT:C147006 | MONDO:equivalentTo | Cardiac Yolk Sac Tumor | | MONDO:0001991|MONDO:0005744 | -| MONDO:0854242 | pericardial sarcoma | NCIT:C147098 | MONDO:equivalentTo | Pericardial Sarcoma | | MONDO:0018078|MONDO:0001322 | -| MONDO:0854249 | recurrent lymphoproliferative disorder | NCIT:C147861 | MONDO:equivalentTo | Recurrent Lymphoproliferative Disorder | | | -| MONDO:0854250 | oropharyngeal p16ink4a-negative squamous cell carcinoma | NCIT:C147906 | MONDO:equivalentTo | Oropharyngeal p16INK4a-Negative Squamous Cell Carcinoma | | MONDO:0044704 | -| MONDO:0854251 | central nervous system b-cell non-hodgkin lymphoma | NCIT:C147948 | MONDO:equivalentTo | Central Nervous System B-Cell Non-Hodgkin Lymphoma | | MONDO:0015759|MONDO:0044887 | -| MONDO:0854253 | refractory melanoma | NCIT:C147983 | MONDO:equivalentTo | Refractory Melanoma | | MONDO:0036501|MONDO:0005105 | -| MONDO:0854257 | unresectable craniopharyngioma | NCIT:C148076 | MONDO:equivalentTo | Unresectable Craniopharyngioma | | MONDO:0018907 | -| MONDO:0854268 | refractory round cell liposarcoma | NCIT:C148299 | MONDO:equivalentTo | Refractory Round Cell Liposarcoma | | MONDO:0005238 | -| MONDO:0854269 | metastatic round cell liposarcoma | NCIT:C148300 | MONDO:equivalentTo | Metastatic Round Cell Liposarcoma | | MONDO:0005238 | -| MONDO:0854270 | refractory sarcoma | NCIT:C148301 | MONDO:equivalentTo | Refractory Sarcoma | | MONDO:0005089|MONDO:0036501 | -| MONDO:0854284 | refractory leukemia | NCIT:C148426 | MONDO:equivalentTo | Refractory Leukemia | | MONDO:0005059|MONDO:0004111 | -| MONDO:0854293 | castration-naive prostate carcinoma | NCIT:C148536 | MONDO:equivalentTo | Castration-Naive Prostate Carcinoma | | MONDO:0004956 | -| MONDO:0854294 | thoracic esophagus adenocarcinoma | NCIT:C150027 | MONDO:equivalentTo | Thoracic Esophagus Adenocarcinoma | | MONDO:0005028|MONDO:0021325 | -| MONDO:0854295 | thoracic esophagus squamous cell carcinoma | NCIT:C150029 | MONDO:equivalentTo | Thoracic Esophagus Squamous Cell Carcinoma | | MONDO:0005580|MONDO:0021325 | -| MONDO:0854296 | cervical esophagus adenocarcinoma | NCIT:C150031 | MONDO:equivalentTo | Cervical Esophagus Adenocarcinoma | | MONDO:0021326|MONDO:0005028 | -| MONDO:0854297 | cervical esophagus squamous cell carcinoma | NCIT:C150032 | MONDO:equivalentTo | Cervical Esophagus Squamous Cell Carcinoma | | MONDO:0021326|MONDO:0005580 | -| MONDO:0854298 | gastric cardia squamous cell carcinoma | NCIT:C150034 | MONDO:equivalentTo | Gastric Cardia Squamous Cell Carcinoma | | MONDO:0003834|MONDO:0006230 | -| MONDO:0854317 | high risk neuroblastoma | NCIT:C150281 | MONDO:equivalentTo | High Risk Neuroblastoma | | MONDO:0005072 | -| MONDO:0854322 | hhv8-related lymphoproliferative disorder | NCIT:C150399 | MONDO:equivalentTo | HHV8-Related Lymphoproliferative Disorder | | | -| MONDO:0854323 | hhv8-positive multicentric castleman disease | NCIT:C150404 | MONDO:equivalentTo | HHV8-Positive Multicentric Castleman Disease | | | -| MONDO:0854324 | extracavitary primary effusion lymphoma | NCIT:C150406 | MONDO:equivalentTo | Extracavitary Primary Effusion Lymphoma | | MONDO:0018842 | -| MONDO:0854325 | body cavity primary effusion lymphoma | NCIT:C150407 | MONDO:equivalentTo | Body Cavity Primary Effusion Lymphoma | | MONDO:0018842 | -| MONDO:0854332 | refractory malignant bone neoplasm | NCIT:C150525 | MONDO:equivalentTo | Refractory Malignant Bone Neoplasm | | MONDO:0002129|MONDO:0036501 | -| MONDO:0854334 | refractory malignant female reproductive system neoplasm | NCIT:C150527 | MONDO:equivalentTo | Refractory Malignant Female Reproductive System Neoplasm | | MONDO:0001416|MONDO:0036501 | -| MONDO:0854335 | refractory malignant neoplasm of multiple primary sites | NCIT:C150529 | MONDO:equivalentTo | Refractory Malignant Neoplasm of Multiple Primary Sites | | MONDO:0036501 | -| MONDO:0854339 | refractory malignant male reproductive system neoplasm | NCIT:C150534 | MONDO:equivalentTo | Refractory Malignant Male Reproductive System Neoplasm | | MONDO:0005836|MONDO:0036501 | -| MONDO:0854340 | refractory malignant mesothelioma | NCIT:C150535 | MONDO:equivalentTo | Refractory Malignant Mesothelioma | | MONDO:0006292|MONDO:0036501 | -| MONDO:0854342 | refractory malignant soft tissue neoplasm | NCIT:C150537 | MONDO:equivalentTo | Refractory Malignant Soft Tissue Neoplasm | | MONDO:0024637|MONDO:0036501 | -| MONDO:0854345 | refractory malignant endocrine neoplasm | NCIT:C150541 | MONDO:equivalentTo | Refractory Malignant Endocrine Neoplasm | | MONDO:0021069|MONDO:0036501 | -| MONDO:0854347 | refractory malignant urinary system neoplasm | NCIT:C150543 | MONDO:equivalentTo | Refractory Malignant Urinary System Neoplasm | | MONDO:0006295|MONDO:0036501 | -| MONDO:0854349 | refractory malignant skin neoplasm | NCIT:C150546 | MONDO:equivalentTo | Refractory Malignant Skin Neoplasm | | MONDO:0002898|MONDO:0036501 | -| MONDO:0854350 | prostate adenocarcinoma without neuroendocrine differentiation | NCIT:C150557 | MONDO:equivalentTo | Prostate Adenocarcinoma without Neuroendocrine Differentiation | | MONDO:0005082 | -| MONDO:0854351 | igm monoclonal gammopathy of undetermined significance | NCIT:C150566 | MONDO:equivalentTo | IgM Monoclonal Gammopathy of Undetermined Significance | | MONDO:0004225 | -| MONDO:0854352 | invasive bladder carcinoma | NCIT:C150570 | MONDO:equivalentTo | Invasive Bladder Carcinoma | | MONDO:0040677|MONDO:0004986 | -| MONDO:0854353 | localized cerebral neoplasm | NCIT:C150573 | MONDO:equivalentTo | Localized Cerebral Neoplasm | | MONDO:0021632|MONDO:0021374 | -| MONDO:0854358 | non-igm monoclonal gammopathy of undetermined significance | NCIT:C150588 | MONDO:equivalentTo | Non-IgM Monoclonal Gammopathy of Undetermined Significance | | MONDO:0004225 | -| MONDO:0854359 | testicular follicular lymphoma | NCIT:C150589 | MONDO:equivalentTo | Testicular Follicular Lymphoma | | MONDO:0001472|MONDO:0018906 | -| MONDO:0854363 | metastatic malignant neoplasm in the viscera | NCIT:C150597 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Viscera | | MONDO:0024880 | -| MONDO:0854365 | resectable malignant neoplasm | NCIT:C150602 | MONDO:equivalentTo | Resectable Malignant Neoplasm | | MONDO:0004992 | -| MONDO:0854374 | immunodeficiency-related lymphoproliferative disorder | NCIT:C150672 | MONDO:equivalentTo | Immunodeficiency-Related Lymphoproliferative Disorder | | | -| MONDO:0854376 | tumors derived from langerhans cells | NCIT:C150692 | MONDO:equivalentTo | Tumors Derived from Langerhans Cells | | MONDO:0006247 | -| MONDO:0854377 | langerhans cell histiocytosis, monostotic | NCIT:C150701 | MONDO:equivalentTo | Langerhans Cell Histiocytosis, Monostotic | | MONDO:0018310 | -| MONDO:0854378 | langerhans cell histiocytosis, polyostotic | NCIT:C150702 | MONDO:equivalentTo | Langerhans Cell Histiocytosis, Polyostotic | | MONDO:0018310 | -| MONDO:0854379 | langerhans cell histiocytosis, disseminated | NCIT:C150703 | MONDO:equivalentTo | Langerhans Cell Histiocytosis, Disseminated | | MONDO:0018310 | -| MONDO:0854381 | transformed non-hodgkin lymphoma | NCIT:C151957 | MONDO:equivalentTo | Transformed Non-Hodgkin Lymphoma | | MONDO:0018908 | -| MONDO:0854382 | acute leukemia of ambiguous lineage, not otherwise specified | NCIT:C151975 | MONDO:equivalentTo | Acute Leukemia of Ambiguous Lineage, Not Otherwise Specified | | MONDO:0019460 | -| MONDO:0854385 | abdominal rhabdomyosarcoma | NCIT:C151982 | MONDO:equivalentTo | Abdominal Rhabdomyosarcoma | | MONDO:0005212 | -| MONDO:0854388 | abdominal undifferentiated pleomorphic sarcoma | NCIT:C151985 | MONDO:equivalentTo | Abdominal Undifferentiated Pleomorphic Sarcoma | | MONDO:0002142 | -| MONDO:0854389 | mixed phenotype acute leukemia, rare types | NCIT:C151990 | MONDO:equivalentTo | Mixed Phenotype Acute Leukemia, Rare Types | | MONDO:0020743 | -| MONDO:0854394 | metastatic sarcoma | NCIT:C152076 | MONDO:equivalentTo | Metastatic Sarcoma | | MONDO:0005089|MONDO:0024880 | -| MONDO:0854395 | refractory malignant head and neck neoplasm | NCIT:C152078 | MONDO:equivalentTo | Refractory Malignant Head and Neck Neoplasm | | MONDO:0005627|MONDO:0036501 | -| MONDO:0854414 | refractory ewing sarcoma/peripheral primitive neuroectodermal tumor | NCIT:C153286 | MONDO:equivalentTo | Refractory Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor | | MONDO:0021038|MONDO:0036501 | -| MONDO:0854420 | metastatic chordoma | NCIT:C153323 | MONDO:equivalentTo | Metastatic Chordoma | | MONDO:0024880|MONDO:0008978 | -| MONDO:0854422 | castration-sensitive prostate carcinoma | NCIT:C153336 | MONDO:equivalentTo | Castration-Sensitive Prostate Carcinoma | | MONDO:0004956 | -| MONDO:0854468 | sinonasal poorly differentiated carcinoma | NCIT:C154324 | MONDO:equivalentTo | Sinonasal Poorly Differentiated Carcinoma | | MONDO:0056819 | -| MONDO:0854469 | densely granulated corticotroph pituitary neuroendocrine tumor | NCIT:C154339 | MONDO:equivalentTo | Densely Granulated Corticotroph Pituitary Neuroendocrine Tumor | | MONDO:0006068 | -| MONDO:0854470 | sparsely granulated corticotroph pituitary neuroendocrine tumor | NCIT:C154340 | MONDO:equivalentTo | Sparsely Granulated Corticotroph Pituitary Neuroendocrine Tumor | | MONDO:0006068 | -| MONDO:0854471 | crooke cell tumor | NCIT:C154342 | MONDO:equivalentTo | Crooke Cell Tumor | | MONDO:0006068 | -| MONDO:0854472 | non-functioning corticotroph pituitary neuroendocrine tumor | NCIT:C154429 | MONDO:equivalentTo | Non-Functioning Corticotroph Pituitary Neuroendocrine Tumor | | MONDO:0006068|MONDO:0019613 | -| MONDO:0854479 | anaplastic sarcoma of the kidney | NCIT:C154496 | MONDO:equivalentTo | Anaplastic Sarcoma of the Kidney | | MONDO:0002930|MONDO:0020633 | -| MONDO:0854480 | multiple synchronous pituitary neuroendocrine tumors of distinct lineages | NCIT:C154520 | MONDO:equivalentTo | Multiple Synchronous Pituitary Neuroendocrine Tumors of Distinct Lineages | | MONDO:0006373 | -| MONDO:0854485 | cutaneous melanoma of the extremity | NCIT:C155305 | MONDO:equivalentTo | Cutaneous Melanoma of the Extremity | | MONDO:0005012 | -| MONDO:0854489 | sarcoma of the extremity | NCIT:C155647 | MONDO:equivalentTo | Sarcoma of the Extremity | | MONDO:0005089 | -| MONDO:0854492 | mixed gangliocytoma-pituitary neuroendocrine tumor | NCIT:C155767 | MONDO:equivalentTo | Mixed Gangliocytoma-Pituitary Neuroendocrine Tumor | | MONDO:0021043|MONDO:0006373 | -| MONDO:0854495 | ependymal pituicytoma | NCIT:C155774 | MONDO:equivalentTo | Ependymal Pituicytoma | | MONDO:0003257 | -| MONDO:0854496 | sellar meningioma | NCIT:C155776 | MONDO:equivalentTo | Sellar Meningioma | | MONDO:0002998|MONDO:0002720 | -| MONDO:0854500 | sellar solitary fibrous tumor | NCIT:C155784 | MONDO:equivalentTo | Sellar Solitary Fibrous Tumor | | MONDO:0002720|MONDO:0003223 | -| MONDO:0854504 | pituitary gland non-hodgkin lymphoma | NCIT:C155796 | MONDO:equivalentTo | Pituitary Gland Non-Hodgkin Lymphoma | | MONDO:0002109|MONDO:0044887 | -| MONDO:0854506 | sellar germ cell tumor | NCIT:C155801 | MONDO:equivalentTo | Sellar Germ Cell Tumor | | MONDO:0003000|MONDO:0002720 | -| MONDO:0854518 | metastatic malignant pancreatic neoplasm | NCIT:C155852 | MONDO:equivalentTo | Metastatic Malignant Pancreatic Neoplasm | | MONDO:0009831|MONDO:0024880 | -| MONDO:0854521 | chest wall sarcoma | NCIT:C155873 | MONDO:equivalentTo | Chest Wall Sarcoma | | MONDO:0005089|MONDO:0021323 | -| MONDO:0854523 | unresectable desmoid fibromatosis | NCIT:C155877 | MONDO:equivalentTo | Unresectable Desmoid Fibromatosis | | MONDO:0007608 | -| MONDO:0854527 | smoldering waldenstrom macroglobulinemia | NCIT:C155910 | MONDO:equivalentTo | Smoldering Waldenstrom Macroglobulinemia | | MONDO:0100280 | -| MONDO:0854528 | metastatic malignant neoplasm in the thoracic cavity | NCIT:C155919 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Thoracic Cavity | | MONDO:0024880|MONDO:0003274 | -| MONDO:0854529 | medullary hemangioblastoma | NCIT:C155949 | MONDO:equivalentTo | Medullary Hemangioblastoma | | MONDO:0003902 | -| MONDO:0854530 | chromophobe renal cell carcinoma associated with birt-hogg-dube syndrome | NCIT:C155951 | MONDO:equivalentTo | Chromophobe Renal Cell Carcinoma Associated with Birt-Hogg-Dube Syndrome | | MONDO:0017885 | -| MONDO:0854531 | uterine ligament papillary cystadenoma | NCIT:C155952 | MONDO:equivalentTo | Uterine Ligament Papillary Cystadenoma | | MONDO:0021091|MONDO:0020582 | -| MONDO:0854533 | thyroid gland spindle cell follicular adenoma | NCIT:C155957 | MONDO:equivalentTo | Thyroid Gland Spindle Cell Follicular Adenoma | | MONDO:0005032 | -| MONDO:0854534 | thyroid gland black follicular adenoma | NCIT:C155958 | MONDO:equivalentTo | Thyroid Gland Black Follicular Adenoma | | MONDO:0005032 | -| MONDO:0854544 | third ventricle pilocytic astrocytoma | NCIT:C156037 | MONDO:equivalentTo | Third Ventricle Pilocytic Astrocytoma | | MONDO:0021631|MONDO:0016691 | -| MONDO:0854545 | hypothalamic-chiasmatic pilomyxoid astrocytoma | NCIT:C156038 | MONDO:equivalentTo | Hypothalamic-Chiasmatic Pilomyxoid Astrocytoma | | MONDO:0016692 | -| MONDO:0854546 | fourth ventricle medulloblastoma | NCIT:C156039 | MONDO:equivalentTo | Fourth Ventricle Medulloblastoma | | MONDO:0007959 | -| MONDO:0854547 | third ventricle germinoma | NCIT:C156040 | MONDO:equivalentTo | Third Ventricle Germinoma | | MONDO:0002214 | -| MONDO:0854549 | temporal lobe pleomorphic xanthoastrocytoma | NCIT:C156042 | MONDO:equivalentTo | Temporal Lobe Pleomorphic Xanthoastrocytoma | | MONDO:0016690 | -| MONDO:0854550 | spindle cell variant thyroid gland papillary carcinoma | NCIT:C156045 | MONDO:equivalentTo | Spindle Cell Variant Thyroid Gland Papillary Carcinoma | | MONDO:0005075 | -| MONDO:0854551 | hobnail variant thyroid gland papillary carcinoma | NCIT:C156050 | MONDO:equivalentTo | Hobnail Variant Thyroid Gland Papillary Carcinoma | | MONDO:0005075 | -| MONDO:0854584 | metastatic neuroblastoma | NCIT:C156101 | MONDO:equivalentTo | Metastatic Neuroblastoma | | MONDO:0024880|MONDO:0005072 | -| MONDO:0854588 | thyroid gland follicular carcinoma, encapsulated angioinvasive | NCIT:C156122 | MONDO:equivalentTo | Thyroid Gland Follicular Carcinoma, Encapsulated Angioinvasive | | MONDO:0005034 | -| MONDO:0854589 | thyroid gland follicular carcinoma, widely invasive | NCIT:C156123 | MONDO:equivalentTo | Thyroid Gland Follicular Carcinoma, Widely Invasive | | MONDO:0040677|MONDO:0005034 | -| MONDO:0854594 | thyroid gland mucinous carcinoma | NCIT:C156267 | MONDO:equivalentTo | Thyroid Gland Mucinous Carcinoma | | MONDO:0015075 | -| MONDO:0854595 | intrathyroidal thymoma | NCIT:C156268 | MONDO:equivalentTo | Intrathyroidal Thymoma | | MONDO:0015074|MONDO:0006456 | -| MONDO:0854598 | orbital alveolar soft part sarcoma | NCIT:C156276 | MONDO:equivalentTo | Orbital Alveolar Soft Part Sarcoma | | MONDO:0004943|MONDO:0011655 | -| MONDO:0854599 | bladder alveolar soft part sarcoma | NCIT:C156277 | MONDO:equivalentTo | Bladder Alveolar Soft Part Sarcoma | | MONDO:0001374|MONDO:0011655 | -| MONDO:0854600 | cellular nerve sheath myxoma | NCIT:C156278 | MONDO:equivalentTo | Cellular Nerve Sheath Myxoma | | MONDO:0006317 | -| MONDO:0854601 | colon liposarcoma | NCIT:C156279 | MONDO:equivalentTo | Colon Liposarcoma | | MONDO:0003352|MONDO:0005060 | -| MONDO:0854608 | thyroid gland schwannoma | NCIT:C156340 | MONDO:equivalentTo | Thyroid Gland Schwannoma | | MONDO:0004820|MONDO:0006107 | -| MONDO:0854609 | thyroid gland malignant peripheral nerve sheath tumor | NCIT:C156341 | MONDO:equivalentTo | Thyroid Gland Malignant Peripheral Nerve Sheath Tumor | | MONDO:0003028|MONDO:0017827 | -| MONDO:0854613 | thyroid gland leiomyoma | NCIT:C156346 | MONDO:equivalentTo | Thyroid Gland Leiomyoma | | MONDO:0006107|MONDO:0001572 | -| MONDO:0854614 | thyroid gland leiomyosarcoma | NCIT:C156347 | MONDO:equivalentTo | Thyroid Gland Leiomyosarcoma | | MONDO:0003028|MONDO:0005058 | -| MONDO:0854616 | thyroid gland solitary fibrous tumor | NCIT:C156349 | MONDO:equivalentTo | Thyroid Gland Solitary Fibrous Tumor | | MONDO:0016238|MONDO:0015074 | -| MONDO:0854625 | brain ependymoma | NCIT:C156462 | MONDO:equivalentTo | Brain Ependymoma | | MONDO:0016698|MONDO:0021632 | -| MONDO:0854631 | metastatic neuroendocrine neoplasm | NCIT:C156485 | MONDO:equivalentTo | Metastatic Neuroendocrine Neoplasm | | MONDO:0019496|MONDO:0024880 | -| MONDO:0854639 | malignant abdominal neoplasm | NCIT:C156714 | MONDO:equivalentTo | Malignant Abdominal Neoplasm | | MONDO:0004992 | -| MONDO:0854640 | malignant pelvic neoplasm | NCIT:C156715 | MONDO:equivalentTo | Malignant Pelvic Neoplasm | | MONDO:0004992 | -| MONDO:0854647 | metastatic basal cell carcinoma | NCIT:C156769 | MONDO:equivalentTo | Metastatic Basal Cell Carcinoma | | MONDO:0024879|MONDO:0020804 | -| MONDO:0854656 | adrenal cortical sex cord-stromal tumor | NCIT:C156943 | MONDO:equivalentTo | Adrenal Cortical Sex Cord-Stromal Tumor | | MONDO:0006055|MONDO:0036591 | -| MONDO:0854657 | adrenal gland schwannoma | NCIT:C156944 | MONDO:equivalentTo | Adrenal Gland Schwannoma | | MONDO:0021468|MONDO:0004820 | -| MONDO:0854658 | adrenal gland lymphoma | NCIT:C156945 | MONDO:equivalentTo | Adrenal Gland Lymphoma | | MONDO:0002817|MONDO:0001499 | -| MONDO:0854659 | adrenal gland sarcoma | NCIT:C156956 | MONDO:equivalentTo | Adrenal Gland Sarcoma | | MONDO:0002817|MONDO:0001501 | -| MONDO:0854660 | primary vitreoretinal non-hodgkin lymphoma | NCIT:C157065 | MONDO:equivalentTo | Primary Vitreoretinal Non-Hodgkin Lymphoma | | MONDO:0004351|MONDO:0044887 | -| MONDO:0854663 | unresectable paraganglioma | NCIT:C157126 | MONDO:equivalentTo | Unresectable Paraganglioma | | MONDO:0000448 | -| MONDO:0854669 | breast histiocytoid carcinoma | NCIT:C157235 | MONDO:equivalentTo | Breast Histiocytoid Carcinoma | | MONDO:0005051 | -| MONDO:0854670 | adrenal gland ganglioneuroblastoma, intermixed | NCIT:C157243 | MONDO:equivalentTo | Adrenal Gland Ganglioneuroblastoma, Intermixed | | MONDO:0004477|MONDO:0003326 | -| MONDO:0854671 | adrenal gland ganglioneuroblastoma, nodular | NCIT:C157244 | MONDO:equivalentTo | Adrenal Gland Ganglioneuroblastoma, Nodular | | MONDO:0004477|MONDO:0003325 | -| MONDO:0854672 | composite paraganglioma | NCIT:C157246 | MONDO:equivalentTo | Composite Paraganglioma | | MONDO:0000448 | -| MONDO:0854679 | peripheral hemangioblastoma | NCIT:C157450 | MONDO:equivalentTo | Peripheral Hemangioblastoma | | MONDO:0016748 | -| MONDO:0854680 | metastatic squamous cell carcinoma in the cervical lymph nodes | NCIT:C157452 | MONDO:equivalentTo | Metastatic Squamous Cell Carcinoma in the Cervical Lymph Nodes | | MONDO:0005438|MONDO:0044907 | -| MONDO:0854688 | bap1-mutant clear cell renal cell carcinoma | NCIT:C157614 | MONDO:equivalentTo | BAP1-Mutant Clear Cell Renal Cell Carcinoma | | MONDO:0005005 | -| MONDO:0854691 | transformed chronic lymphocytic leukemia to diffuse large b-cell lymphoma | NCIT:C157624 | MONDO:equivalentTo | Transformed Chronic Lymphocytic Leukemia to Diffuse Large B-Cell Lymphoma | | MONDO:0004948 | -| MONDO:0854692 | metastatic adenoid cystic carcinoma | NCIT:C157638 | MONDO:equivalentTo | Metastatic Adenoid Cystic Carcinoma | | MONDO:0024879|MONDO:0004971 | -| MONDO:0854698 | refractory lymphoproliferative disorder | NCIT:C157686 | MONDO:equivalentTo | Refractory Lymphoproliferative Disorder | | | -| MONDO:0854705 | kidney synovial sarcoma | NCIT:C157737 | MONDO:equivalentTo | Kidney Synovial Sarcoma | | MONDO:0002930|MONDO:0010434 | -| MONDO:0854706 | kidney neuroendocrine neoplasm | NCIT:C157743 | MONDO:equivalentTo | Kidney Neuroendocrine Neoplasm | | MONDO:0019496|MONDO:0021163 | -| MONDO:0854708 | metanephric tumor | NCIT:C157748 | MONDO:equivalentTo | Metanephric Tumor | | MONDO:0002513|MONDO:0036976 | -| MONDO:0854714 | bladder neuroendocrine neoplasm | NCIT:C157758 | MONDO:equivalentTo | Bladder Neuroendocrine Neoplasm | | MONDO:0019496|MONDO:0004987 | -| MONDO:0854748 | subcutaneous disorder | NCIT:C157995 | MONDO:equivalentTo | Subcutaneous Disorder | | | -| MONDO:0854749 | kidney epithelioid angiomyolipoma | NCIT:C158032 | MONDO:equivalentTo | Kidney Epithelioid Angiomyolipoma | | MONDO:0004555|MONDO:0002606 | -| MONDO:0854750 | kidney mixed epithelial and stromal tumor family | NCIT:C158046 | MONDO:equivalentTo | Kidney Mixed Epithelial and Stromal Tumor Family | | MONDO:0021163 | -| MONDO:0854756 | bladder non-invasive urothelial neoplasm | NCIT:C158374 | MONDO:equivalentTo | Bladder Non-Invasive Urothelial Neoplasm | | MONDO:0003755|MONDO:0004987 | -| MONDO:0854773 | platinum-sensitive lung small cell carcinoma | NCIT:C158495 | MONDO:equivalentTo | Platinum-Sensitive Lung Small Cell Carcinoma | | MONDO:0008433 | -| MONDO:0854780 | borderline ovarian mixed epithelial tumor/atypical proliferative ovarian mixed epithelial tumor | NCIT:C158616 | MONDO:equivalentTo | Borderline Ovarian Mixed Epithelial Tumor/Atypical Proliferative Ovarian Mixed Epithelial Tumor | | MONDO:0021043|MONDO:0016093 | -| MONDO:0854781 | endometrioid tumor, variant with squamous differentiation | NCIT:C158620 | MONDO:equivalentTo | Endometrioid Tumor, Variant with Squamous Differentiation | | MONDO:0002480 | -| MONDO:0854783 | bladder soft tissue neoplasm | NCIT:C158636 | MONDO:equivalentTo | Bladder Soft Tissue Neoplasm | | MONDO:0006424|MONDO:0004987 | -| MONDO:0854795 | early stage pancreatic ductal adenocarcinoma | NCIT:C158961 | MONDO:equivalentTo | Early Stage Pancreatic Ductal Adenocarcinoma | | MONDO:0005184 | -| MONDO:0854803 | kidney rhabdomyosarcoma | NCIT:C159206 | MONDO:equivalentTo | Kidney Rhabdomyosarcoma | | MONDO:0002930|MONDO:0005212 | -| MONDO:0854804 | kidney ewing sarcoma | NCIT:C159208 | MONDO:equivalentTo | Kidney Ewing Sarcoma | | MONDO:0018270|MONDO:0002930 | -| MONDO:0854806 | kidney hemangioma | NCIT:C159211 | MONDO:equivalentTo | Kidney Hemangioma | | MONDO:0002513|MONDO:0006500 | -| MONDO:0854807 | kidney lymphangioma | NCIT:C159214 | MONDO:equivalentTo | Kidney Lymphangioma | | MONDO:0002013|MONDO:0002513 | -| MONDO:0854808 | kidney schwannoma | NCIT:C159221 | MONDO:equivalentTo | Kidney Schwannoma | | MONDO:0002513|MONDO:0004820 | -| MONDO:0854809 | kidney solitary fibrous tumor | NCIT:C159222 | MONDO:equivalentTo | Kidney Solitary Fibrous Tumor | | MONDO:0016238|MONDO:0021163 | -| MONDO:0854812 | kidney germ cell tumor | NCIT:C159227 | MONDO:equivalentTo | Kidney Germ Cell Tumor | | MONDO:0018201|MONDO:0021163 | -| MONDO:0854813 | penile human papillomavirus-independent squamous cell carcinoma | NCIT:C159244 | MONDO:equivalentTo | Penile Human Papillomavirus-Independent Squamous Cell Carcinoma | | MONDO:0018352 | -| MONDO:0854815 | penile carcinoma cuniculatum | NCIT:C159247 | MONDO:equivalentTo | Penile Carcinoma Cuniculatum | | MONDO:0003698 | -| MONDO:0854817 | penile papillary-basaloid carcinoma | NCIT:C159249 | MONDO:equivalentTo | Penile Papillary-Basaloid Carcinoma | | MONDO:0004089 | -| MONDO:0854818 | penile warty-basaloid carcinoma | NCIT:C159250 | MONDO:equivalentTo | Penile Warty-Basaloid Carcinoma | | MONDO:0004430|MONDO:0020656 | -| MONDO:0854819 | penile lymphoepithelioma-like carcinoma | NCIT:C159252 | MONDO:equivalentTo | Penile Lymphoepithelioma-Like Carcinoma | | MONDO:0003572|MONDO:0020656 | -| MONDO:0854820 | borderline ovarian mucinous tumor/atypical proliferative ovarian mucinous tumor with microinvasion | NCIT:C159311 | MONDO:equivalentTo | Borderline Ovarian Mucinous Tumor/Atypical Proliferative Ovarian Mucinous Tumor with Microinvasion | | MONDO:0003756 | -| MONDO:0854828 | bladder rhabdomyosarcoma | NCIT:C159667 | MONDO:equivalentTo | Bladder Rhabdomyosarcoma | | MONDO:0001374|MONDO:0005212 | -| MONDO:0854831 | bladder leiomyosarcoma | NCIT:C159670 | MONDO:equivalentTo | Bladder Leiomyosarcoma | | MONDO:0001374|MONDO:0005058 | -| MONDO:0854838 | bladder hemangioma | NCIT:C159680 | MONDO:equivalentTo | Bladder Hemangioma | | MONDO:0000384|MONDO:0006500 | -| MONDO:0854839 | bladder granular cell tumor | NCIT:C159681 | MONDO:equivalentTo | Bladder Granular Cell Tumor | | MONDO:0006235|MONDO:0004987 | -| MONDO:0854840 | bladder neurofibroma | NCIT:C159682 | MONDO:equivalentTo | Bladder Neurofibroma | | MONDO:0000384|MONDO:0016755 | -| MONDO:0854841 | ebv-related lymphoproliferative disorder | NCIT:C159717 | MONDO:equivalentTo | EBV-Related Lymphoproliferative Disorder | | | -| MONDO:0854843 | platinum-sensitive ovarian carcinoma | NCIT:C159902 | MONDO:equivalentTo | Platinum-Sensitive Ovarian Carcinoma | | MONDO:0005140 | -| MONDO:0854845 | carcinoma arising in bladder diverticulum | NCIT:C160158 | MONDO:equivalentTo | Carcinoma Arising in Bladder Diverticulum | | MONDO:0004986 | -| MONDO:0854847 | metastatic nut carcinoma | NCIT:C160297 | MONDO:equivalentTo | Metastatic NUT Carcinoma | | MONDO:0005563|MONDO:0024879 | -| MONDO:0854850 | hematologic malignancy-associated skin squamous cell carcinoma | NCIT:C160666 | MONDO:equivalentTo | Hematologic Malignancy-Associated Skin Squamous Cell Carcinoma | | MONDO:0002529 | -| MONDO:0854854 | prostate acinar microcystic adenocarcinoma | NCIT:C160817 | MONDO:equivalentTo | Prostate Acinar Microcystic Adenocarcinoma | | MONDO:0002493 | -| MONDO:0854855 | prostate acinar pleomorphic giant cell adenocarcinoma | NCIT:C160818 | MONDO:equivalentTo | Prostate Acinar Pleomorphic Giant Cell Adenocarcinoma | | MONDO:0002493 | -| MONDO:0854859 | platinum-sensitive primary peritoneal carcinoma | NCIT:C160872 | MONDO:equivalentTo | Platinum-Sensitive Primary Peritoneal Carcinoma | | MONDO:0015686 | -| MONDO:0854860 | platinum-sensitive fallopian tube carcinoma | NCIT:C160873 | MONDO:equivalentTo | Platinum-Sensitive Fallopian Tube Carcinoma | | MONDO:0006206 | -| MONDO:0854866 | cribriform adenocarcinoma of minor salivary gland | NCIT:C160974 | MONDO:equivalentTo | Cribriform Adenocarcinoma of Minor Salivary Gland | | MONDO:0006304|MONDO:0006176 | -| MONDO:0854867 | sinonasal adenocarcinoma | NCIT:C160976 | MONDO:equivalentTo | Sinonasal Adenocarcinoma | | MONDO:0056819|MONDO:0004970 | -| MONDO:0854868 | head and neck sebaceous carcinoma | NCIT:C160978 | MONDO:equivalentTo | Head and Neck Sebaceous Carcinoma | | MONDO:0006962|MONDO:0002038 | -| MONDO:0854872 | prostate intraductal carcinoma | NCIT:C161022 | MONDO:equivalentTo | Prostate Intraductal Carcinoma | | MONDO:0005159 | -| MONDO:0854873 | prostate synovial sarcoma | NCIT:C161034 | MONDO:equivalentTo | Prostate Synovial Sarcoma | | MONDO:0002854|MONDO:0010434 | -| MONDO:0854874 | prostate osteosarcoma | NCIT:C161035 | MONDO:equivalentTo | Prostate Osteosarcoma | | MONDO:0002621|MONDO:0002854 | -| MONDO:0854875 | prostate undifferentiated pleomorphic sarcoma | NCIT:C161038 | MONDO:equivalentTo | Prostate Undifferentiated Pleomorphic Sarcoma | | MONDO:0002854|MONDO:0002142 | -| MONDO:0854877 | prostate soft tissue neoplasm | NCIT:C161045 | MONDO:equivalentTo | Prostate Soft Tissue Neoplasm | | MONDO:0006424|MONDO:0021259 | -| MONDO:0854881 | prostate hemangioma | NCIT:C161581 | MONDO:equivalentTo | Prostate Hemangioma | | MONDO:0021510|MONDO:0006500 | -| MONDO:0854886 | prostate carcinoma metastatic in the lymph nodes | NCIT:C161587 | MONDO:equivalentTo | Prostate Carcinoma Metastatic in the Lymph Nodes | | MONDO:0004956|MONDO:0005438 | -| MONDO:0854888 | prostate cystadenoma | NCIT:C161606 | MONDO:equivalentTo | Prostate Cystadenoma | | MONDO:0021510|MONDO:0002369 | -| MONDO:0854889 | prostate wilms tumor | NCIT:C161607 | MONDO:equivalentTo | Prostate Wilms Tumor | | MONDO:0008315|MONDO:0006058 | -| MONDO:0854891 | prostate melanoma | NCIT:C161611 | MONDO:equivalentTo | Prostate Melanoma | | MONDO:0006320|MONDO:0008315 | -| MONDO:0854893 | seminal vesicle mixed epithelial and stromal tumor | NCIT:C161636 | MONDO:equivalentTo | Seminal Vesicle Mixed Epithelial and Stromal Tumor | | MONDO:0021043|MONDO:0002790 | -| MONDO:0854895 | benign seminal vesicle neoplasm | NCIT:C161643 | MONDO:equivalentTo | Benign Seminal Vesicle Neoplasm | | MONDO:0000625|MONDO:0002790 | -| MONDO:0854896 | malignant seminal vesicle neoplasm | NCIT:C161644 | MONDO:equivalentTo | Malignant Seminal Vesicle Neoplasm | | MONDO:0005836|MONDO:0002790 | -| MONDO:0854902 | regressed testicular germ cell tumor | NCIT:C162139 | MONDO:equivalentTo | Regressed Testicular Germ Cell Tumor | | MONDO:0010108 | -| MONDO:0854909 | cervical cancer by figo stage 2018 | NCIT:C162225 | MONDO:equivalentTo | Cervical Cancer by FIGO Stage 2018 | | MONDO:0005131 | -| MONDO:0854911 | metastatic malignant digestive system neoplasm | NCIT:C162255 | MONDO:equivalentTo | Metastatic Malignant Digestive System Neoplasm | | MONDO:0002516|MONDO:0024880 | -| MONDO:0854912 | hypermutated colorectal carcinoma | NCIT:C162256 | MONDO:equivalentTo | Hypermutated Colorectal Carcinoma | | MONDO:0024331 | -| MONDO:0854925 | thymic neuroendocrine neoplasm | NCIT:C162460 | MONDO:equivalentTo | Thymic Neuroendocrine Neoplasm | | MONDO:0018079|MONDO:0019496 | -| MONDO:0854927 | intratubular large cell hyalinizing sertoli cell neoplasia | NCIT:C162466 | MONDO:equivalentTo | Intratubular Large Cell Hyalinizing Sertoli Cell Neoplasia | | MONDO:0003125 | -| MONDO:0854928 | primary diffuse large b-cell lymphoma of the testis | NCIT:C162467 | MONDO:equivalentTo | Primary Diffuse Large B-Cell Lymphoma of the Testis | | MONDO:0018905|MONDO:0001472 | -| MONDO:0854929 | testicular nasal type extranodal nk/t-cell lymphoma | NCIT:C162468 | MONDO:equivalentTo | Testicular Nasal Type Extranodal NK/T-Cell Lymphoma | | MONDO:0001472|MONDO:0019472 | -| MONDO:0854930 | testicular myeloid sarcoma | NCIT:C162469 | MONDO:equivalentTo | Testicular Myeloid Sarcoma | | MONDO:0005447|MONDO:0006861 | -| MONDO:0854931 | testicular plasmacytoma | NCIT:C162470 | MONDO:equivalentTo | Testicular Plasmacytoma | | MONDO:0005447|MONDO:0002754 | -| MONDO:0854936 | paratesticular neoplasm | NCIT:C162485 | MONDO:equivalentTo | Paratesticular Neoplasm | | MONDO:0024582 | -| MONDO:0854952 | penile melanoma | NCIT:C162547 | MONDO:equivalentTo | Penile Melanoma | | MONDO:0001325|MONDO:0005105 | -| MONDO:0854953 | penile lymphoma | NCIT:C162548 | MONDO:equivalentTo | Penile Lymphoma | | MONDO:0001325|MONDO:0017207 | -| MONDO:0854955 | primary peritoneal undifferentiated carcinoma | NCIT:C162562 | MONDO:equivalentTo | Primary Peritoneal Undifferentiated Carcinoma | | MONDO:0015686|MONDO:0005617 | -| MONDO:0854956 | primary peritoneal transitional cell carcinoma | NCIT:C162564 | MONDO:equivalentTo | Primary Peritoneal Transitional Cell Carcinoma | | MONDO:0015686|MONDO:0006474 | -| MONDO:0854959 | penile soft tissue neoplasm | NCIT:C162574 | MONDO:equivalentTo | Penile Soft Tissue Neoplasm | | MONDO:0006424|MONDO:0006895 | -| MONDO:0854966 | penile malignant peripheral nerve sheath tumor | NCIT:C162584 | MONDO:equivalentTo | Penile Malignant Peripheral Nerve Sheath Tumor | | MONDO:0001387|MONDO:0017827 | -| MONDO:0854967 | penile leiomyosarcoma | NCIT:C162585 | MONDO:equivalentTo | Penile Leiomyosarcoma | | MONDO:0001387|MONDO:0005058 | -| MONDO:0854968 | penile schwannoma | NCIT:C162586 | MONDO:equivalentTo | Penile Schwannoma | | MONDO:0004820|MONDO:0021458 | -| MONDO:0854969 | penile neurofibroma | NCIT:C162587 | MONDO:equivalentTo | Penile Neurofibroma | | MONDO:0021458|MONDO:0016755 | -| MONDO:0854970 | penile rhabdomyosarcoma | NCIT:C162588 | MONDO:equivalentTo | Penile Rhabdomyosarcoma | | MONDO:0001387|MONDO:0005212 | -| MONDO:0854971 | penile undifferentiated pleomorphic sarcoma | NCIT:C162589 | MONDO:equivalentTo | Penile Undifferentiated Pleomorphic Sarcoma | | MONDO:0001387|MONDO:0002142 | -| MONDO:0854974 | metastatic malignant neoplasm in the head and neck | NCIT:C162594 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Head and Neck | | MONDO:0005627|MONDO:0024880 | -| MONDO:0854984 | refractory childhood malignant neoplasm | NCIT:C162703 | MONDO:equivalentTo | Refractory Childhood Malignant Neoplasm | | MONDO:0006517|MONDO:0036501 | -| MONDO:0854998 | asph-positive head and neck squamous cell carcinoma | NCIT:C162770 | MONDO:equivalentTo | ASPH-Positive Head and Neck Squamous Cell Carcinoma | | MONDO:0010150 | -| MONDO:0855003 | parapharyngeal neoplasm | NCIT:C162820 | MONDO:equivalentTo | Parapharyngeal Neoplasm | | MONDO:0021351 | -| MONDO:0855006 | retropharyngeal neoplasm | NCIT:C162825 | MONDO:equivalentTo | Retropharyngeal Neoplasm | | MONDO:0021351 | -| MONDO:0855011 | digital papillary adenoma | NCIT:C162848 | MONDO:equivalentTo | Digital Papillary Adenoma | | MONDO:0024247 | -| MONDO:0855015 | non-invasive cribriform carcinoma | NCIT:C162973 | MONDO:equivalentTo | Non-Invasive Cribriform Carcinoma | | MONDO:0006176 | -| MONDO:0855016 | malignant brain glioma | NCIT:C162993 | MONDO:equivalentTo | Malignant Brain Glioma | | MONDO:0100342|MONDO:0001657|MONDO:0021632 | -| MONDO:0855017 | unresectable meningioma | NCIT:C163006 | MONDO:equivalentTo | Unresectable Meningioma | | MONDO:0016642 | -| MONDO:0855028 | micropapillary carcinoma | NCIT:C164144 | MONDO:equivalentTo | Micropapillary Carcinoma | | MONDO:0006509 | -| MONDO:0855034 | aggressive prostate adenocarcinoma | NCIT:C164185 | MONDO:equivalentTo | Aggressive Prostate Adenocarcinoma | | MONDO:0005082 | -| MONDO:0855035 | head and neck sarcoma | NCIT:C164198 | MONDO:equivalentTo | Head and Neck Sarcoma | | MONDO:0005089|MONDO:0005627 | -| MONDO:0855040 | warty carcinoma | NCIT:C164248 | MONDO:equivalentTo | Warty Carcinoma | | MONDO:0002979 | -| MONDO:0855041 | differentiated intraepithelial neoplasia | NCIT:C164249 | MONDO:equivalentTo | Differentiated Intraepithelial Neoplasia | | MONDO:0024474 | -| MONDO:0855042 | human papillomavirus-negative squamous cell carcinoma | NCIT:C164250 | MONDO:equivalentTo | Human Papillomavirus-Negative Squamous Cell Carcinoma | | MONDO:0005096 | -| MONDO:0855043 | invasive sarcomatoid urothelial carcinoma | NCIT:C164252 | MONDO:equivalentTo | Invasive Sarcomatoid Urothelial Carcinoma | | MONDO:0002837|MONDO:0040678 | -| MONDO:0855044 | mixed neuroendocrine non-neuroendocrine neoplasm | NCIT:C164255 | MONDO:equivalentTo | Mixed Neuroendocrine Non-Neuroendocrine Neoplasm | | MONDO:0021043|MONDO:0005626 | -| MONDO:0855047 | nf1-associated malignant peripheral nerve sheath tumor | NCIT:C164313 | MONDO:equivalentTo | NF1-Associated Malignant Peripheral Nerve Sheath Tumor | | MONDO:0017827 | -| MONDO:0855048 | sporadic malignant peripheral nerve sheath tumor | NCIT:C164314 | MONDO:equivalentTo | Sporadic Malignant Peripheral Nerve Sheath Tumor | | MONDO:0017827 | -| MONDO:0855049 | radiation-induced malignant peripheral nerve sheath tumor | NCIT:C164316 | MONDO:equivalentTo | Radiation-Induced Malignant Peripheral Nerve Sheath Tumor | | MONDO:0017827 | -| MONDO:0855058 | soft tissue sarcoma of the trunk and extremities | NCIT:C165190 | MONDO:equivalentTo | Soft Tissue Sarcoma of the Trunk and Extremities | | MONDO:0018078 | -| MONDO:0855059 | metastatic malignant mesothelioma | NCIT:C165252 | MONDO:equivalentTo | Metastatic Malignant Mesothelioma | | MONDO:0006292|MONDO:0024880 | -| MONDO:0855079 | skin verrucous carcinoma | NCIT:C165465 | MONDO:equivalentTo | Skin Verrucous Carcinoma | | MONDO:0002529|MONDO:0006006 | -| MONDO:0855080 | skin squamous cell carcinoma with osteoclast-like giant cells | NCIT:C165466 | MONDO:equivalentTo | Skin Squamous Cell Carcinoma with Osteoclast-Like Giant Cells | | MONDO:0002529 | -| MONDO:0855081 | skin lymphoepithelioma-like carcinoma | NCIT:C165467 | MONDO:equivalentTo | Skin Lymphoepithelioma-Like Carcinoma | | MONDO:0002529|MONDO:0003572 | -| MONDO:0855082 | skin squamous cell carcinoma with sarcomatoid differentiation | NCIT:C165468 | MONDO:equivalentTo | Skin Squamous Cell Carcinoma with Sarcomatoid Differentiation | | MONDO:0002529|MONDO:0002928 | -| MONDO:0855085 | lichen planus-like keratosis | NCIT:C165485 | MONDO:equivalentTo | Lichen Planus-Like Keratosis | | MONDO:0002093 | -| MONDO:0855087 | spitz melanoma | NCIT:C165497 | MONDO:equivalentTo | Spitz Melanoma | | MONDO:0005012 | -| MONDO:0855088 | pigmented epithelioid melanocytoma | NCIT:C165498 | MONDO:equivalentTo | Pigmented Epithelioid Melanocytoma | | MONDO:0021583 | -| MONDO:0855092 | bap1-inactivated skin melanocytic neoplasm | NCIT:C165522 | MONDO:equivalentTo | BAP1-Inactivated Skin Melanocytic Neoplasm | | MONDO:0021583 | -| MONDO:0855094 | combined nevus | NCIT:C165529 | MONDO:equivalentTo | Combined Nevus | | MONDO:0044794 | -| MONDO:0855104 | proximal gastric adenocarcinoma | NCIT:C165628 | MONDO:equivalentTo | Proximal Gastric Adenocarcinoma | | MONDO:0005036 | -| MONDO:0855106 | high-csd melanoma | NCIT:C165659 | MONDO:equivalentTo | High-CSD Melanoma | | MONDO:0005012 | -| MONDO:0855113 | mixed carcinoma | NCIT:C165723 | MONDO:equivalentTo | Mixed Carcinoma | | MONDO:0005853|MONDO:0004993 | -| MONDO:0855116 | hormone receptor-negative breast carcinoma | NCIT:C165743 | MONDO:equivalentTo | Hormone Receptor-Negative Breast Carcinoma | | MONDO:0004988 | -| MONDO:0855127 | musculoskeletal neoplasm | NCIT:C166354 | MONDO:equivalentTo | Musculoskeletal Neoplasm | | MONDO:0044334|MONDO:0002081 | -| MONDO:0855130 | mucosal nodular melanoma | NCIT:C166405 | MONDO:equivalentTo | Mucosal Nodular Melanoma | | MONDO:0000544 | -| MONDO:0855132 | pancreatobiliary carcinoma | NCIT:C166418 | MONDO:equivalentTo | Pancreatobiliary Carcinoma | | MONDO:0006181 | -| MONDO:0855139 | acute myeloid leukemia with ram immunophenotype | NCIT:C167089 | MONDO:equivalentTo | Acute Myeloid Leukemia with RAM Immunophenotype | | MONDO:0004996 | -| MONDO:0855140 | obesity-related malignant neoplasm | NCIT:C167168 | MONDO:equivalentTo | Obesity-Related Malignant Neoplasm | | MONDO:0004992 | -| MONDO:0855143 | metastatic primary peritoneal carcinoma | NCIT:C167203 | MONDO:equivalentTo | Metastatic Primary Peritoneal Carcinoma | | MONDO:0015686|MONDO:0024879 | -| MONDO:0855150 | midgut neuroendocrine tumor | NCIT:C167327 | MONDO:equivalentTo | Midgut Neuroendocrine Tumor | | MONDO:0000386 | -| MONDO:0855151 | adnexal adenocarcinoma, not otherwise specified | NCIT:C167341 | MONDO:equivalentTo | Adnexal Adenocarcinoma, Not Otherwise Specified | | MONDO:0006973|MONDO:0004970 | -| MONDO:0855152 | spiradenocylindroma | NCIT:C167342 | MONDO:equivalentTo | Spiradenocylindroma | | MONDO:0021489 | -| MONDO:0855153 | spiradenocylindrocarcinoma | NCIT:C167344 | MONDO:equivalentTo | Spiradenocylindrocarcinoma | | MONDO:0005524|MONDO:0024878 | -| MONDO:0855154 | malignant mixed tumor of the skin | NCIT:C167346 | MONDO:equivalentTo | Malignant Mixed Tumor of the Skin | | MONDO:0002206|MONDO:0005853 | -| MONDO:0855157 | syringocystadenocarcinoma papilliferum | NCIT:C167365 | MONDO:equivalentTo | Syringocystadenocarcinoma Papilliferum | | MONDO:0005524 | -| MONDO:0855158 | adnexal cribriform carcinoma | NCIT:C167366 | MONDO:equivalentTo | Adnexal Cribriform Carcinoma | | MONDO:0006973|MONDO:0006176 | -| MONDO:0855159 | adnexal secretory carcinoma | NCIT:C167368 | MONDO:equivalentTo | Adnexal Secretory Carcinoma | | MONDO:0006973|MONDO:0004970 | -| MONDO:0855160 | signet ring cell/histiocytoid carcinoma | NCIT:C167369 | MONDO:equivalentTo | Signet Ring Cell/Histiocytoid Carcinoma | | MONDO:0006973|MONDO:0004970 | -| MONDO:0855173 | resectable glioma | NCIT:C168573 | MONDO:equivalentTo | Resectable Glioma | | MONDO:0021042 | -| MONDO:0855181 | phyllodes tumor of anogenital mammary-type glands | NCIT:C168602 | MONDO:equivalentTo | Phyllodes Tumor of Anogenital Mammary-Type Glands | | MONDO:0005078 | -| MONDO:0855182 | metastatic malignant neoplasm in the digestive system | NCIT:C168669 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Digestive System | | MONDO:0002516|MONDO:0024880 | -| MONDO:0855187 | unresectable round cell liposarcoma | NCIT:C168724 | MONDO:equivalentTo | Unresectable Round Cell Liposarcoma | | MONDO:0005238 | -| MONDO:0855221 | skin soft tissue neoplasm | NCIT:C169100 | MONDO:equivalentTo | Skin Soft Tissue Neoplasm | | MONDO:0006424|MONDO:0002531 | -| MONDO:0855230 | metastatic malignant head and neck neoplasm | NCIT:C170467 | MONDO:equivalentTo | Metastatic Malignant Head and Neck Neoplasm | | MONDO:0005627|MONDO:0024880 | -| MONDO:0855232 | skin pleomorphic liposarcoma | NCIT:C170473 | MONDO:equivalentTo | Skin Pleomorphic Liposarcoma | | MONDO:0003600|MONDO:0020562 | -| MONDO:0855235 | skin angiolipoma | NCIT:C170478 | MONDO:equivalentTo | Skin Angiolipoma | | MONDO:0000964|MONDO:0006085 | -| MONDO:0855238 | benign periampullary neoplasm | NCIT:C170725 | MONDO:equivalentTo | Benign Periampullary Neoplasm | | MONDO:0006734 | -| MONDO:0855241 | metastatic malignant breast neoplasm | NCIT:C170728 | MONDO:equivalentTo | Metastatic Malignant Breast Neoplasm | | MONDO:0007254|MONDO:0024880 | -| MONDO:0855243 | primary peritoneal adenocarcinoma | NCIT:C170733 | MONDO:equivalentTo | Primary Peritoneal Adenocarcinoma | | MONDO:0015686|MONDO:0004970 | -| MONDO:0855244 | appendix mucinous neoplasm | NCIT:C170734 | MONDO:equivalentTo | Appendix Mucinous Neoplasm | | MONDO:0024338|MONDO:0001236 | -| MONDO:0855245 | pleomorphic fibroma | NCIT:C170736 | MONDO:equivalentTo | Pleomorphic Fibroma | | MONDO:0005167 | -| MONDO:0855249 | non-muscle invasive bladder urothelial carcinoma | NCIT:C170772 | MONDO:equivalentTo | Non-Muscle Invasive Bladder Urothelial Carcinoma | | MONDO:0003890|MONDO:0004200 | -| MONDO:0855250 | alveolar ridge squamous cell carcinoma | NCIT:C170774 | MONDO:equivalentTo | Alveolar Ridge Squamous Cell Carcinoma | | MONDO:0004958 | -| MONDO:0855252 | metastatic malignant skin neoplasm | NCIT:C170811 | MONDO:equivalentTo | Metastatic Malignant Skin Neoplasm | | MONDO:0024880|MONDO:0002898 | -| MONDO:0855256 | metastatic rhabdoid tumor | NCIT:C170828 | MONDO:equivalentTo | Metastatic Rhabdoid Tumor | | MONDO:0002728|MONDO:0024880 | -| MONDO:0855262 | malignant jejunal neoplasm | NCIT:C170919 | MONDO:equivalentTo | Malignant Jejunal Neoplasm | | MONDO:0002564|MONDO:0000956 | -| MONDO:0855263 | metastatic carcinosarcoma | NCIT:C170924 | MONDO:equivalentTo | Metastatic Carcinosarcoma | | MONDO:0024880|MONDO:0002928 | -| MONDO:0855266 | malignant fundus neoplasm | NCIT:C170940 | MONDO:equivalentTo | Malignant Fundus Neoplasm | | MONDO:0001056 | -| MONDO:0855281 | human papillomavirus-related mucosal head and neck squamous cell carcinoma | NCIT:C171023 | MONDO:equivalentTo | Human Papillomavirus-Related Mucosal Head and Neck Squamous Cell Carcinoma | | MONDO:0010150|MONDO:0020657 | -| MONDO:0855283 | ovarian neuroendocrine carcinoma | NCIT:C171032 | MONDO:equivalentTo | Ovarian Neuroendocrine Carcinoma | | MONDO:0002481|MONDO:0005140 | -| MONDO:0855284 | endometrial neuroendocrine carcinoma | NCIT:C171033 | MONDO:equivalentTo | Endometrial Neuroendocrine Carcinoma | | MONDO:0002447|MONDO:0021650 | -| MONDO:0855285 | mediastinal non-hodgkin lymphoma | NCIT:C171037 | MONDO:equivalentTo | Mediastinal Non-Hodgkin Lymphoma | | MONDO:0004021|MONDO:0018908 | -| MONDO:0855297 | oligometastatic prostate carcinoma | NCIT:C171265 | MONDO:equivalentTo | Oligometastatic Prostate Carcinoma | | MONDO:0004956 | -| MONDO:0855330 | acute myeloid leukemia arising from previous myeloproliferative neoplasm | NCIT:C172129 | MONDO:equivalentTo | Acute Myeloid Leukemia Arising from Previous Myeloproliferative Neoplasm | | MONDO:0019457 | -| MONDO:0855331 | acute myeloid leukemia arising from previous myelodysplastic/myeloproliferative neoplasm | NCIT:C172130 | MONDO:equivalentTo | Acute Myeloid Leukemia Arising from Previous Myelodysplastic/Myeloproliferative Neoplasm | | MONDO:0019457 | -| MONDO:0855335 | progesterone receptor-positive malignant neoplasm | NCIT:C172183 | MONDO:equivalentTo | Progesterone Receptor-Positive Malignant Neoplasm | | MONDO:0004992 | -| MONDO:0855336 | sinusoidal hemangioma | NCIT:C172206 | MONDO:equivalentTo | Sinusoidal Hemangioma | | MONDO:0006557 | -| MONDO:0855346 | refractory myeloid neoplasm | NCIT:C172281 | MONDO:equivalentTo | Refractory Myeloid Neoplasm | | MONDO:0005170|MONDO:0004111 | -| MONDO:0855368 | skin ewing sarcoma | NCIT:C172634 | MONDO:equivalentTo | Skin Ewing Sarcoma | | MONDO:0018270|MONDO:0006414 | -| MONDO:0855377 | oxyntic gland adenoma | NCIT:C172655 | MONDO:equivalentTo | Oxyntic Gland Adenoma | | MONDO:0006221 | -| MONDO:0855378 | gastroblastoma | NCIT:C172659 | MONDO:equivalentTo | Gastroblastoma | | MONDO:0001056 | -| MONDO:0855379 | digestive system neuroendocrine tumor g3 | NCIT:C172660 | MONDO:equivalentTo | Digestive System Neuroendocrine Tumor G3 | | MONDO:0000386 | -| MONDO:0855386 | colorectal conventional adenoma | NCIT:C172680 | MONDO:equivalentTo | Colorectal Conventional Adenoma | | MONDO:0005484 | -| MONDO:0855389 | colorectal poorly cohesive adenocarcinoma | NCIT:C172694 | MONDO:equivalentTo | Colorectal Poorly Cohesive Adenocarcinoma | | MONDO:0005008 | -| MONDO:0855390 | colorectal adenoma-like adenocarcinoma | NCIT:C172699 | MONDO:equivalentTo | Colorectal Adenoma-Like Adenocarcinoma | | MONDO:0005008|MONDO:0003204 | -| MONDO:0855391 | inflammatory bowel disease-associated colorectal adenocarcinoma | NCIT:C172700 | MONDO:equivalentTo | Inflammatory Bowel Disease-Associated Colorectal Adenocarcinoma | | MONDO:0005008 | -| MONDO:0855393 | steatohepatitic hepatocellular carcinoma | NCIT:C172709 | MONDO:equivalentTo | Steatohepatitic Hepatocellular Carcinoma | | MONDO:0007256 | -| MONDO:0855394 | macrotrabecular massive hepatocellular carcinoma | NCIT:C172710 | MONDO:equivalentTo | Macrotrabecular Massive Hepatocellular Carcinoma | | MONDO:0007256 | -| MONDO:0855395 | chromophobe hepatocellular carcinoma | NCIT:C172712 | MONDO:equivalentTo | Chromophobe Hepatocellular Carcinoma | | MONDO:0007256 | -| MONDO:0855396 | neutrophil-rich hepatocellular carcinoma | NCIT:C172713 | MONDO:equivalentTo | Neutrophil-Rich Hepatocellular Carcinoma | | MONDO:0007256 | -| MONDO:0855397 | small hepatocellular carcinoma | NCIT:C172714 | MONDO:equivalentTo | Small Hepatocellular Carcinoma | | MONDO:0007256 | -| MONDO:0855398 | liver mixed adenoneuroendocrine carcinoma | NCIT:C172718 | MONDO:equivalentTo | Liver Mixed Adenoneuroendocrine Carcinoma | | MONDO:0006182|MONDO:0018531 | -| MONDO:0855401 | gallbladder pyloric gland adenoma | NCIT:C172731 | MONDO:equivalentTo | Gallbladder Pyloric Gland Adenoma | | MONDO:0006216 | -| MONDO:0855408 | pancreatic poorly cohesive adenocarcinoma | NCIT:C172811 | MONDO:equivalentTo | Pancreatic Poorly Cohesive Adenocarcinoma | | MONDO:0005184 | -| MONDO:0855409 | pancreatic undifferentiated carcinoma with rhabdoid cells | NCIT:C172812 | MONDO:equivalentTo | Pancreatic Undifferentiated Carcinoma with Rhabdoid Cells | | MONDO:0006478 | -| MONDO:0855413 | conventional follicular dendritic cell sarcoma | NCIT:C172846 | MONDO:equivalentTo | Conventional Follicular Dendritic Cell Sarcoma | | MONDO:0005764 | -| MONDO:0855418 | digestive system soft tissue neoplasm | NCIT:C172852 | MONDO:equivalentTo | Digestive System Soft Tissue Neoplasm | | MONDO:0006424|MONDO:0021223 | -| MONDO:0855432 | sinonasal spindle cell squamous cell carcinoma | NCIT:C173079 | MONDO:equivalentTo | Sinonasal Spindle Cell Squamous Cell Carcinoma | | MONDO:0044787|MONDO:0021663 | -| MONDO:0855433 | sinonasal lymphoepithelial carcinoma | NCIT:C173080 | MONDO:equivalentTo | Sinonasal Lymphoepithelial Carcinoma | | MONDO:0002831|MONDO:0003572 | -| MONDO:0855435 | head and neck nut carcinoma | NCIT:C173087 | MONDO:equivalentTo | Head and Neck NUT Carcinoma | | MONDO:0005563|MONDO:0002038 | -| MONDO:0855439 | malignant sinonasal neoplasm | NCIT:C173097 | MONDO:equivalentTo | Malignant Sinonasal Neoplasm | | MONDO:0056820|MONDO:0005627 | -| MONDO:0855449 | sinonasal soft tissue neoplasm | NCIT:C173117 | MONDO:equivalentTo | Sinonasal Soft Tissue Neoplasm | | MONDO:0056820|MONDO:0006424 | -| MONDO:0855471 | peritoneal implant | NCIT:C173164 | MONDO:equivalentTo | Peritoneal Implant | | MONDO:0006901 | -| MONDO:0855472 | sinonasal ameloblastoma | NCIT:C173166 | MONDO:equivalentTo | Sinonasal Ameloblastoma | | MONDO:0056820 | -| MONDO:0855481 | microsatellite stable colorectal carcinoma | NCIT:C173324 | MONDO:equivalentTo | Microsatellite Stable Colorectal Carcinoma | | MONDO:0024331 | -| MONDO:0855487 | nasopharyngeal adenoid cystic carcinoma | NCIT:C173340 | MONDO:equivalentTo | Nasopharyngeal Adenoid Cystic Carcinoma | | MONDO:0006367|MONDO:0015459 | -| MONDO:0855489 | ectopic pituitary neuroendocrine tumor | NCIT:C173345 | MONDO:equivalentTo | Ectopic Pituitary Neuroendocrine Tumor | | MONDO:0006373 | -| MONDO:0855491 | pharyngeal lymphoma | NCIT:C173354 | MONDO:equivalentTo | Pharyngeal Lymphoma | | MONDO:0005517|MONDO:0017207 | -| MONDO:0855495 | neuroendocrine carcinoma, excluding head and neck | NCIT:C173385 | MONDO:equivalentTo | Neuroendocrine Carcinoma, Excluding Head and Neck | | MONDO:0002120 | -| MONDO:0855498 | laryngeal soft tissue neoplasm | NCIT:C173397 | MONDO:equivalentTo | Laryngeal Soft Tissue Neoplasm | | MONDO:0006424|MONDO:0021071 | -| MONDO:0855506 | laryngeal chondroma | NCIT:C173406 | MONDO:equivalentTo | Laryngeal Chondroma | | MONDO:0002360|MONDO:0002354 | -| MONDO:0855507 | laryngeal chondrosarcoma | NCIT:C173407 | MONDO:equivalentTo | Laryngeal Chondrosarcoma | | MONDO:0002448|MONDO:0008977 | -| MONDO:0855516 | oral verruca vulgaris | NCIT:C173475 | MONDO:equivalentTo | Oral Verruca Vulgaris | | MONDO:0001209 | -| MONDO:0855518 | oral cavity soft tissue neoplasm | NCIT:C173479 | MONDO:equivalentTo | Oral Cavity Soft Tissue Neoplasm | | MONDO:0021245|MONDO:0006424 | -| MONDO:0855523 | head and neck histiocytic and dendritic cell neoplasm | NCIT:C173485 | MONDO:equivalentTo | Head and Neck Histiocytic and Dendritic Cell Neoplasm | | MONDO:0006247|MONDO:0005586 | -| MONDO:0855526 | head and neck melanocytic neoplasm | NCIT:C173488 | MONDO:equivalentTo | Head and Neck Melanocytic Neoplasm | | MONDO:0021143|MONDO:0005586 | -| MONDO:0855527 | oral cavity myeloid sarcoma | NCIT:C173489 | MONDO:equivalentTo | Oral Cavity Myeloid Sarcoma | | MONDO:0005515|MONDO:0006861 | -| MONDO:0855532 | refractory primitive neuroectodermal tumor | NCIT:C173565 | MONDO:equivalentTo | Refractory Primitive Neuroectodermal Tumor | | MONDO:0005462|MONDO:0036501 | -| MONDO:0855540 | head and neck heterotopia-associated carcinoma | NCIT:C173588 | MONDO:equivalentTo | Head and Neck Heterotopia-Associated Carcinoma | | MONDO:0002038 | -| MONDO:0855551 | salivary gland poorly differentiated carcinoma | NCIT:C173649 | MONDO:equivalentTo | Salivary Gland Poorly Differentiated Carcinoma | | MONDO:0000521 | -| MONDO:0855553 | salivary gland lymphadenoma | NCIT:C173659 | MONDO:equivalentTo | Salivary Gland Lymphadenoma | | MONDO:0021460 | -| MONDO:0855556 | salivary gland hemangioma | NCIT:C173680 | MONDO:equivalentTo | Salivary Gland Hemangioma | | MONDO:0021460|MONDO:0006500 | -| MONDO:0855557 | salivary gland lipoma | NCIT:C173681 | MONDO:equivalentTo | Salivary Gland Lipoma | | MONDO:0021460|MONDO:0005106 | -| MONDO:0855558 | sialolipoma | NCIT:C173682 | MONDO:equivalentTo | Sialolipoma | | MONDO:0021460 | -| MONDO:0855561 | salivary gland nodular fasciitis | NCIT:C173687 | MONDO:equivalentTo | Salivary Gland Nodular Fasciitis | | MONDO:0021460|MONDO:0004187 | -| MONDO:0855563 | salivary gland lymphoma | NCIT:C173690 | MONDO:equivalentTo | Salivary Gland Lymphoma | | MONDO:0017207|MONDO:0004669 | -| MONDO:0855575 | appendix disorder | NCIT:C173799 | MONDO:equivalentTo | Appendix Disorder | | | -| MONDO:0855576 | retroperitoneal undifferentiated pleomorphic sarcoma | NCIT:C173808 | MONDO:equivalentTo | Retroperitoneal Undifferentiated Pleomorphic Sarcoma | | MONDO:0001501|MONDO:0002142 | -| MONDO:0855577 | lung alveolar soft part sarcoma | NCIT:C173809 | MONDO:equivalentTo | Lung Alveolar Soft Part Sarcoma | | MONDO:0002426|MONDO:0011655 | -| MONDO:0855584 | maxillofacial neoplasm | NCIT:C173845 | MONDO:equivalentTo | Maxillofacial Neoplasm | | MONDO:0019060|MONDO:0024653 | -| MONDO:0855590 | craniofacial fibrous dysplasia | NCIT:C173926 | MONDO:equivalentTo | Craniofacial Fibrous Dysplasia | | MONDO:0000845 | -| MONDO:0855591 | benign head and neck neoplasm | NCIT:C173932 | MONDO:equivalentTo | Benign Head and Neck Neoplasm | | MONDO:0005165|MONDO:0005586 | -| MONDO:0855593 | aggressive papillary tumor | NCIT:C174022 | MONDO:equivalentTo | Aggressive Papillary Tumor | | MONDO:0021096|MONDO:0021366 | -| MONDO:0855594 | benign inner ear neoplasm | NCIT:C174023 | MONDO:equivalentTo | Benign Inner Ear Neoplasm | | MONDO:0021474|MONDO:0024320 | -| MONDO:0855597 | malignant inner ear neoplasm | NCIT:C174026 | MONDO:equivalentTo | Malignant Inner Ear Neoplasm | | MONDO:0003277|MONDO:0024320 | -| MONDO:0855616 | conjunctival oncocytoma | NCIT:C174388 | MONDO:equivalentTo | Conjunctival Oncocytoma | | MONDO:0010795|MONDO:0006105 | -| MONDO:0855617 | conjunctival keratoacanthoma | NCIT:C174390 | MONDO:equivalentTo | Conjunctival Keratoacanthoma | | MONDO:0006173|MONDO:0002527 | -| MONDO:0855618 | conjunctival spindle cell carcinoma | NCIT:C174398 | MONDO:equivalentTo | Conjunctival Spindle Cell Carcinoma | | MONDO:0006173|MONDO:0021663 | -| MONDO:0855620 | conjunctival carcinoma | NCIT:C174403 | MONDO:equivalentTo | Conjunctival Carcinoma | | MONDO:0002466|MONDO:0003454 | -| MONDO:0855625 | conjunctival subepithelial nevus | NCIT:C174426 | MONDO:equivalentTo | Conjunctival Subepithelial Nevus | | MONDO:0006172 | -| MONDO:0855630 | conjunctival blue nevus | NCIT:C174452 | MONDO:equivalentTo | Conjunctival Blue Nevus | | MONDO:0006172 | -| MONDO:0855631 | atypical ewing sarcoma | NCIT:C174456 | MONDO:equivalentTo | Atypical Ewing Sarcoma | | MONDO:0012817 | -| MONDO:0855633 | conjunctival spitz nevus | NCIT:C174493 | MONDO:equivalentTo | Conjunctival Spitz Nevus | | MONDO:0006172 | -| MONDO:0855634 | metastatic malignant neoplasm in the conjunctiva | NCIT:C174496 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Conjunctiva | | MONDO:0044913|MONDO:0003454 | -| MONDO:0855635 | iris epithelioid cell melanoma | NCIT:C174498 | MONDO:equivalentTo | Iris Epithelioid Cell Melanoma | | MONDO:0004064|MONDO:0006200 | -| MONDO:0855640 | iris mixed cell melanoma | NCIT:C174506 | MONDO:equivalentTo | Iris Mixed Cell Melanoma | | MONDO:0004064|MONDO:0003910 | -| MONDO:0855641 | metastatic malignant neoplasm in the uvea | NCIT:C174507 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Uvea | | MONDO:0002659|MONDO:0044913 | -| MONDO:0855646 | retinal astrocytoma | NCIT:C174539 | MONDO:equivalentTo | Retinal Astrocytoma | | MONDO:0024649|MONDO:0021231 | -| MONDO:0855649 | adenoma of the retinal pigment epithelium | NCIT:C174550 | MONDO:equivalentTo | Adenoma of the Retinal Pigment Epithelium | | MONDO:0021453|MONDO:0004972 | -| MONDO:0855650 | retinal pigment epithelium adenocarcinoma | NCIT:C174551 | MONDO:equivalentTo | Retinal Pigment Epithelium Adenocarcinoma | | MONDO:0002466|MONDO:0003072|MONDO:0004970 | -| MONDO:0855653 | ciliary body adenoma | NCIT:C174560 | MONDO:equivalentTo | Ciliary Body Adenoma | | MONDO:0021486|MONDO:0004972 | -| MONDO:0855654 | ciliary body adenocarcinoma | NCIT:C174561 | MONDO:equivalentTo | Ciliary Body Adenocarcinoma | | MONDO:0002466|MONDO:0002969|MONDO:0004970 | -| MONDO:0855667 | incidental gallbladder carcinoma | NCIT:C175214 | MONDO:equivalentTo | Incidental Gallbladder Carcinoma | | MONDO:0003220 | -| MONDO:0855668 | metastatic malignant neoplasm in the regional lymph nodes | NCIT:C175222 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Regional Lymph Nodes | | MONDO:0005438 | -| MONDO:0855669 | lacrimal gland oncocytoma | NCIT:C175264 | MONDO:equivalentTo | Lacrimal Gland Oncocytoma | | MONDO:0010795|MONDO:0021488 | -| MONDO:0855671 | lacrimal gland myoepithelial carcinoma | NCIT:C175274 | MONDO:equivalentTo | Lacrimal Gland Myoepithelial Carcinoma | | MONDO:0003158|MONDO:0002463 | -| MONDO:0855672 | lacrimal gland carcinosarcoma | NCIT:C175279 | MONDO:equivalentTo | Lacrimal Gland Carcinosarcoma | | MONDO:0002464|MONDO:0002928 | -| MONDO:0855673 | lacrimal gland epithelial-myoepithelial carcinoma | NCIT:C175288 | MONDO:equivalentTo | Lacrimal Gland Epithelial-Myoepithelial Carcinoma | | MONDO:0002463|MONDO:0003389 | -| MONDO:0855674 | lacrimal gland acinic cell carcinoma | NCIT:C175290 | MONDO:equivalentTo | Lacrimal Gland Acinic Cell Carcinoma | | MONDO:0002475|MONDO:0004965 | -| MONDO:0855675 | lacrimal gland warthin tumor | NCIT:C175291 | MONDO:equivalentTo | Lacrimal Gland Warthin Tumor | | MONDO:0021488|MONDO:0006493 | -| MONDO:0855677 | benign lacrimal system neoplasm | NCIT:C175307 | MONDO:equivalentTo | Benign Lacrimal System Neoplasm | | MONDO:0002460|MONDO:0021454 | -| MONDO:0855678 | malignant lacrimal system neoplasm | NCIT:C175308 | MONDO:equivalentTo | Malignant Lacrimal System Neoplasm | | MONDO:0002460|MONDO:0002236 | -| MONDO:0855679 | lacrimal drainage system neoplasm | NCIT:C175316 | MONDO:equivalentTo | Lacrimal Drainage System Neoplasm | | MONDO:0002460 | -| MONDO:0855684 | lacrimal drainage system non-keratinizing squamous cell carcinoma | NCIT:C175335 | MONDO:equivalentTo | Lacrimal Drainage System Non-Keratinizing Squamous Cell Carcinoma | | MONDO:0003492 | -| MONDO:0855694 | conjunctival non-hodgkin lymphoma | NCIT:C175432 | MONDO:equivalentTo | Conjunctival Non-Hodgkin Lymphoma | | MONDO:0020646|MONDO:0003454 | -| MONDO:0855700 | primary uveal non-hodgkin lymphoma | NCIT:C175451 | MONDO:equivalentTo | Primary Uveal Non-Hodgkin Lymphoma | | MONDO:0004351|MONDO:0002659|MONDO:0017594 | -| MONDO:0855708 | conjunctival myxoma | NCIT:C175495 | MONDO:equivalentTo | Conjunctival Myxoma | | MONDO:0044784|MONDO:0006105 | -| MONDO:0855710 | conjunctival hemangioma | NCIT:C175497 | MONDO:equivalentTo | Conjunctival Hemangioma | | MONDO:0006105|MONDO:0006500 | -| MONDO:0855711 | conjunctival lymphangioma | NCIT:C175498 | MONDO:equivalentTo | Conjunctival Lymphangioma | | MONDO:0002013|MONDO:0006105 | -| MONDO:0855715 | conjunctival sarcoma | NCIT:C175502 | MONDO:equivalentTo | Conjunctival Sarcoma | | MONDO:0018078|MONDO:0003454 | -| MONDO:0855718 | malignant hypothalamic neoplasm | NCIT:C175539 | MONDO:equivalentTo | Malignant Hypothalamic Neoplasm | | MONDO:0002786|MONDO:0006799 | -| MONDO:0855721 | breast polymorphous adenocarcinoma | NCIT:C175604 | MONDO:equivalentTo | Breast Polymorphous Adenocarcinoma | | MONDO:0006256 | -| MONDO:0855722 | breast tall cell carcinoma with reversed polarity | NCIT:C175607 | MONDO:equivalentTo | Breast Tall Cell Carcinoma with Reversed Polarity | | MONDO:0006256 | -| MONDO:0855725 | metastatic malignant glomus tumor | NCIT:C175662 | MONDO:equivalentTo | Metastatic Malignant Glomus Tumor | | MONDO:0003340|MONDO:0024880 | -| MONDO:0855727 | locally invasive desmoid-type fibromatosis | NCIT:C175667 | MONDO:equivalentTo | Locally Invasive Desmoid-Type Fibromatosis | | MONDO:0007608 | -| MONDO:0855734 | metastatic malignant neoplasm in the supraclavicular lymph nodes | NCIT:C175934 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Supraclavicular Lymph Nodes | | MONDO:0005438 | -| MONDO:0855737 | breast classic lobular carcinoma in situ | NCIT:C175949 | MONDO:equivalentTo | Breast Classic Lobular Carcinoma In Situ | | MONDO:0006270 | -| MONDO:0855738 | breast florid lobular carcinoma in situ | NCIT:C175950 | MONDO:equivalentTo | Breast Florid Lobular Carcinoma In Situ | | MONDO:0006270 | -| MONDO:0855740 | breast ductal carcinoma in situ, comedo type | NCIT:C176005 | MONDO:equivalentTo | Breast Ductal Carcinoma In Situ, Comedo Type | | MONDO:0003575|MONDO:0005023 | -| MONDO:0855747 | ocular surface squamous neoplasia | NCIT:C176043 | MONDO:equivalentTo | Ocular Surface Squamous Neoplasia | | MONDO:0020204 | -| MONDO:0855748 | breast cellular fibroadenoma | NCIT:C176045 | MONDO:equivalentTo | Breast Cellular Fibroadenoma | | MONDO:0002056 | -| MONDO:0855749 | primary breast angiosarcoma | NCIT:C176251 | MONDO:equivalentTo | Primary Breast Angiosarcoma | | MONDO:0003024 | -| MONDO:0855751 | breast angiolipoma | NCIT:C176255 | MONDO:equivalentTo | Breast Angiolipoma | | MONDO:0000970|MONDO:0006085 | -| MONDO:0855753 | breast schwannoma | NCIT:C176414 | MONDO:equivalentTo | Breast Schwannoma | | MONDO:0000620|MONDO:0004820 | -| MONDO:0855754 | breast neurofibroma | NCIT:C176415 | MONDO:equivalentTo | Breast Neurofibroma | | MONDO:0000620|MONDO:0016755 | -| MONDO:0855756 | synovial chondrosarcoma | NCIT:C176467 | MONDO:equivalentTo | Synovial Chondrosarcoma | | MONDO:0018078|MONDO:0002403|MONDO:0008977 | -| MONDO:0855757 | male breast carcinoma in situ | NCIT:C176503 | MONDO:equivalentTo | Male Breast Carcinoma In Situ | | MONDO:0005628|MONDO:0004658 | -| MONDO:0855758 | invasive male breast carcinoma | NCIT:C176504 | MONDO:equivalentTo | Invasive Male Breast Carcinoma | | MONDO:0006256|MONDO:0005628 | -| MONDO:0855763 | invasive female breast carcinoma | NCIT:C176579 | MONDO:equivalentTo | Invasive Female Breast Carcinoma | | MONDO:0006256|MONDO:0004379 | -| MONDO:0855764 | female breast carcinoma in situ | NCIT:C176580 | MONDO:equivalentTo | Female Breast Carcinoma In Situ | | MONDO:0004658|MONDO:0004379 | -| MONDO:0855783 | functioning lung carcinoid tumor | NCIT:C176705 | MONDO:equivalentTo | Functioning Lung Carcinoid Tumor | | MONDO:0021120|MONDO:0006041 | -| MONDO:0855784 | non-functioning lung carcinoid tumor | NCIT:C176706 | MONDO:equivalentTo | Non-Functioning Lung Carcinoid Tumor | | MONDO:0021119|MONDO:0006041 | -| MONDO:0855809 | metastatic malignant thoracic neoplasm | NCIT:C176862 | MONDO:equivalentTo | Metastatic Malignant Thoracic Neoplasm | | MONDO:0024880|MONDO:0003274 | -| MONDO:0855811 | psammocarcinoma | NCIT:C176887 | MONDO:equivalentTo | Psammocarcinoma | | MONDO:0004970 | -| MONDO:0855812 | unresectable glioma | NCIT:C176889 | MONDO:equivalentTo | Unresectable Glioma | | MONDO:0021042 | -| MONDO:0855859 | infantile myofibromatosis 1 | NCIT:C176943 | MONDO:equivalentTo | Infantile Myofibromatosis 1 | | MONDO:0016824 | -| MONDO:0855860 | infantile myofibromatosis 2 | NCIT:C176944 | MONDO:equivalentTo | Infantile Myofibromatosis 2 | | MONDO:0016824 | -| MONDO:0855861 | lipoma-like atypical lipomatous tumor/well differentiated liposarcoma | NCIT:C176979 | MONDO:equivalentTo | Lipoma-Like Atypical Lipomatous Tumor/Well Differentiated Liposarcoma | | MONDO:0006097 | -| MONDO:0855862 | superficial atypical lipomatous tumor/well differentiated liposarcoma | NCIT:C176980 | MONDO:equivalentTo | Superficial Atypical Lipomatous Tumor/Well Differentiated Liposarcoma | | MONDO:0006097 | -| MONDO:0855863 | atypical lipomatous tumor/well differentiated liposarcoma of deep soft tissue | NCIT:C176981 | MONDO:equivalentTo | Atypical Lipomatous Tumor/Well Differentiated Liposarcoma of Deep Soft Tissue | | MONDO:0006097 | -| MONDO:0855864 | myxoid pleomorphic liposarcoma | NCIT:C176989 | MONDO:equivalentTo | Myxoid Pleomorphic Liposarcoma | | MONDO:0005060 | -| MONDO:0855883 | plaque-like dermatofibrosarcoma protuberans | NCIT:C177325 | MONDO:equivalentTo | Plaque-Like Dermatofibrosarcoma Protuberans | | MONDO:0011934 | -| MONDO:0855884 | somatic-type malignancy | NCIT:C177364 | MONDO:equivalentTo | Somatic-Type Malignancy | | MONDO:0004992 | -| MONDO:0855885 | epithelioid myxofibrosarcoma | NCIT:C177414 | MONDO:equivalentTo | Epithelioid Myxofibrosarcoma | | MONDO:0019202 | -| MONDO:0855891 | bladder flat urothelial carcinoma | NCIT:C177531 | MONDO:equivalentTo | Bladder Flat Urothelial Carcinoma | | MONDO:0005611 | -| MONDO:0855897 | epithelioid hemangioendothelioma with wwtr1-camta1 gene fusion | NCIT:C177552 | MONDO:equivalentTo | Epithelioid Hemangioendothelioma with WWTR1-CAMTA1 Gene Fusion | | MONDO:0015523 | -| MONDO:0855898 | epithelioid hemangioendothelioma with yap1-tfe3 gene fusion | NCIT:C177553 | MONDO:equivalentTo | Epithelioid Hemangioendothelioma with YAP1-TFE3 Gene Fusion | | MONDO:0015523 | -| MONDO:0855901 | sigmoid colon carcinoma | NCIT:C177680 | MONDO:equivalentTo | Sigmoid Colon Carcinoma | | MONDO:0002032 | -| MONDO:0855909 | who grade 1 glioma | NCIT:C177797 | MONDO:equivalentTo | WHO Grade 1 Glioma | | MONDO:0021637 | -| MONDO:0855911 | poorly differentiated chordoma | NCIT:C177898 | MONDO:equivalentTo | Poorly Differentiated Chordoma | | MONDO:0008978 | -| MONDO:0855914 | ebv-associated smooth muscle tumor | NCIT:C178217 | MONDO:equivalentTo | EBV-Associated Smooth Muscle Tumor | | MONDO:0006975 | -| MONDO:0855915 | pleomorphic leiomyosarcoma | NCIT:C178220 | MONDO:equivalentTo | Pleomorphic Leiomyosarcoma | | MONDO:0005058 | -| MONDO:0855916 | epithelioid schwannoma | NCIT:C178245 | MONDO:equivalentTo | Epithelioid Schwannoma | | MONDO:0002546 | -| MONDO:0855929 | round cell sarcoma with ewsr1-non-ets fusion | NCIT:C178459 | MONDO:equivalentTo | Round Cell Sarcoma with EWSR1-non-ETS Fusion | | MONDO:0006974 | -| MONDO:0855930 | sarcoma with bcor genetic alterations | NCIT:C178465 | MONDO:equivalentTo | Sarcoma with BCOR Genetic Alterations | | MONDO:0006974 | -| MONDO:0855935 | gastric melanoma | NCIT:C178519 | MONDO:equivalentTo | Gastric Melanoma | | MONDO:0001056|MONDO:0045070 | -| MONDO:0855938 | yolk sac tumor with somatic-type malignancy | NCIT:C178523 | MONDO:equivalentTo | Yolk Sac Tumor with Somatic-Type Malignancy | | MONDO:0005744 | -| MONDO:0855939 | conventional chordoma | NCIT:C178563 | MONDO:equivalentTo | Conventional Chordoma | | MONDO:0008978 | -| MONDO:0855941 | bone langerhans cell histiocytosis | NCIT:C178607 | MONDO:equivalentTo | Bone Langerhans Cell Histiocytosis | | MONDO:0019060|MONDO:0018310 | -| MONDO:0855942 | bone erdheim-chester disease | NCIT:C178609 | MONDO:equivalentTo | Bone Erdheim-Chester Disease | | MONDO:0019060|MONDO:0018153 | -| MONDO:0855961 | b-cell lymphoproliferative disorder | NCIT:C179052 | MONDO:equivalentTo | B-Cell Lymphoproliferative Disorder | | | -| MONDO:0855962 | t/nk-cell lymphoproliferative disorder | NCIT:C179053 | MONDO:equivalentTo | T/NK-Cell Lymphoproliferative Disorder | | | -| MONDO:0855976 | ovarian signet ring cell carcinoma | NCIT:C179208 | MONDO:equivalentTo | Ovarian Signet Ring Cell Carcinoma | | MONDO:0002752|MONDO:0005092 | -| MONDO:0855982 | myxoid glioneuronal tumor | NCIT:C179229 | MONDO:equivalentTo | Myxoid Glioneuronal Tumor | | MONDO:0016729 | -| MONDO:0855983 | borderline ovarian seromucinous tumor | NCIT:C179259 | MONDO:equivalentTo | Borderline Ovarian Seromucinous Tumor | | MONDO:0016093|MONDO:0003811 | -| MONDO:0855987 | mesonephric-like adenocarcinoma | NCIT:C179320 | MONDO:equivalentTo | Mesonephric-Like Adenocarcinoma | | MONDO:0001416|MONDO:0004970 | -| MONDO:0855990 | ovarian dedifferentiated carcinoma | NCIT:C179334 | MONDO:equivalentTo | Ovarian Dedifferentiated Carcinoma | | MONDO:0005140 | -| MONDO:0855991 | ovarian mixed cell adenocarcinoma | NCIT:C179339 | MONDO:equivalentTo | Ovarian Mixed Cell Adenocarcinoma | | MONDO:0002752 | -| MONDO:0855993 | giant cell-rich osteosarcoma | NCIT:C179410 | MONDO:equivalentTo | Giant Cell-Rich Osteosarcoma | | MONDO:0002631 | -| MONDO:0855995 | unresectable plexiform neurofibroma | NCIT:C179423 | MONDO:equivalentTo | Unresectable Plexiform Neurofibroma | | MONDO:0003304 | -| MONDO:0855999 | ovarian neuroectodermal-type tumor | NCIT:C179474 | MONDO:equivalentTo | Ovarian Neuroectodermal-Type Tumor | | MONDO:0008170 | -| MONDO:0856000 | ovarian wolffian tumor | NCIT:C179548 | MONDO:equivalentTo | Ovarian Wolffian Tumor | | MONDO:0002229|MONDO:0004255 | -| MONDO:0856002 | her2-low breast carcinoma | NCIT:C179553 | MONDO:equivalentTo | HER2-Low Breast Carcinoma | | MONDO:0004988 | -| MONDO:0856003 | peritoneal calcifying fibrous tumor | NCIT:C179560 | MONDO:equivalentTo | Peritoneal Calcifying Fibrous Tumor | | MONDO:0000650|MONDO:0006121 | -| MONDO:0856016 | basal ganglia neoplasm | NCIT:C179882 | MONDO:equivalentTo | Basal Ganglia Neoplasm | | MONDO:0021374 | -| MONDO:0856017 | cerebellar peduncle neoplasm | NCIT:C179883 | MONDO:equivalentTo | Cerebellar Peduncle Neoplasm | | MONDO:0002913 | -| MONDO:0856018 | corpus callosum neoplasm | NCIT:C179884 | MONDO:equivalentTo | Corpus Callosum Neoplasm | | MONDO:0021374 | -| MONDO:0856019 | oral cavity carcinoma cuniculatum | NCIT:C179894 | MONDO:equivalentTo | Oral Cavity Carcinoma Cuniculatum | | MONDO:0021538 | -| MONDO:0856021 | uterine ligament leiomyoma | NCIT:C179923 | MONDO:equivalentTo | Uterine Ligament Leiomyoma | | MONDO:0001572|MONDO:0020582 | -| MONDO:0856022 | uterine ligament adenomyoma | NCIT:C179925 | MONDO:equivalentTo | Uterine Ligament Adenomyoma | | MONDO:0005635|MONDO:0020582 | -| MONDO:0856024 | uterine ligament wolffian tumor | NCIT:C179927 | MONDO:equivalentTo | Uterine Ligament Wolffian Tumor | | MONDO:0004255|MONDO:0021629 | -| MONDO:0856025 | uterine ligament ependymoma | NCIT:C179928 | MONDO:equivalentTo | Uterine Ligament Ependymoma | | MONDO:0021629 | -| MONDO:0856026 | broad ligament neoplasm | NCIT:C179931 | MONDO:equivalentTo | Broad Ligament Neoplasm | | MONDO:0021629 | -| MONDO:0856027 | microsatellite stable ovarian carcinoma | NCIT:C180332 | MONDO:equivalentTo | Microsatellite Stable Ovarian Carcinoma | | MONDO:0005140 | -| MONDO:0856028 | microsatellite stable endometrial carcinoma | NCIT:C180335 | MONDO:equivalentTo | Microsatellite Stable Endometrial Carcinoma | | MONDO:0002447 | -| MONDO:0856030 | polymorphous low grade neuroepithelial tumor of the young | NCIT:C180378 | MONDO:equivalentTo | Polymorphous Low Grade Neuroepithelial Tumor of the Young | | MONDO:0016729|MONDO:0021632 | -| MONDO:0856033 | tectal glioma | NCIT:C180407 | MONDO:equivalentTo | Tectal Glioma | | MONDO:0021042 | -| MONDO:0856035 | pole-ultramutated endometrial endometrioid adenocarcinoma | NCIT:C180512 | MONDO:equivalentTo | POLE-Ultramutated Endometrial Endometrioid Adenocarcinoma | | MONDO:0006192 | -| MONDO:0856036 | mismatch repair-deficient endometrial endometrioid adenocarcinoma | NCIT:C180514 | MONDO:equivalentTo | Mismatch Repair-Deficient Endometrial Endometrioid Adenocarcinoma | | MONDO:0006192 | -| MONDO:0856037 | p53-mutant endometrial endometrioid adenocarcinoma | NCIT:C180515 | MONDO:equivalentTo | p53-Mutant Endometrial Endometrioid Adenocarcinoma | | MONDO:0006192 | -| MONDO:0856038 | no specific molecular profile endometrial endometrioid adenocarcinoma | NCIT:C180516 | MONDO:equivalentTo | No Specific Molecular Profile Endometrial Endometrioid Adenocarcinoma | | MONDO:0006192 | -| MONDO:0856040 | dysembryoplastic neuroepithelial-like tumor of the septum pellucidum | NCIT:C180532 | MONDO:equivalentTo | Dysembryoplastic Neuroepithelial-Like Tumor of the Septum Pellucidum | | MONDO:0016729 | -| MONDO:0856041 | endometrial mucinous adenocarcinoma, intestinal-type | NCIT:C180536 | MONDO:equivalentTo | Endometrial Mucinous Adenocarcinoma, Intestinal-Type | | MONDO:0005461|MONDO:0006254 | -| MONDO:0856042 | endometrial mucinous adenocarcinoma, gastric-type | NCIT:C180537 | MONDO:equivalentTo | Endometrial Mucinous Adenocarcinoma, Gastric-Type | | MONDO:0005461 | -| MONDO:0856044 | uterine corpus central primitive neuroectodermal tumor | NCIT:C180546 | MONDO:equivalentTo | Uterine Corpus Central Primitive Neuroectodermal Tumor | | MONDO:0005210|MONDO:0006974 | -| MONDO:0856048 | urothelial carcinoma, high grade | NCIT:C180606 | MONDO:equivalentTo | Urothelial Carcinoma, High Grade | | MONDO:0040679 | -| MONDO:0856052 | gestational trophoblastic disorder | NCIT:C180633 | MONDO:equivalentTo | Gestational Trophoblastic Disorder | | | -| MONDO:0856053 | mixed trophoblastic tumor | NCIT:C180634 | MONDO:equivalentTo | Mixed Trophoblastic Tumor | | MONDO:0018944 | -| MONDO:0856054 | metastatic hydatidiform mole | NCIT:C180635 | MONDO:equivalentTo | Metastatic Hydatidiform Mole | | MONDO:0020549 | -| MONDO:0856055 | low grade papillary schneiderian carcinoma | NCIT:C180670 | MONDO:equivalentTo | Low Grade Papillary Schneiderian Carcinoma | | MONDO:0056819 | -| MONDO:0856057 | cervical squamous cell carcinoma, not otherwise specified | NCIT:C180839 | MONDO:equivalentTo | Cervical Squamous Cell Carcinoma, Not Otherwise Specified | | MONDO:0006143 | -| MONDO:0856060 | human papillomavirus-independent cervical adenocarcinoma | NCIT:C180848 | MONDO:equivalentTo | Human Papillomavirus-Independent Cervical Adenocarcinoma | | MONDO:0005153 | -| MONDO:0856067 | cervical adenocarcinoma, not otherwise specified | NCIT:C180870 | MONDO:equivalentTo | Cervical Adenocarcinoma, Not Otherwise Specified | | MONDO:0005153 | -| MONDO:0856070 | cervical mucoepidermoid carcinoma | NCIT:C180878 | MONDO:equivalentTo | Cervical Mucoepidermoid Carcinoma | | MONDO:0005131|MONDO:0003036 | -| MONDO:0856071 | cervical germ cell tumor | NCIT:C180879 | MONDO:equivalentTo | Cervical Germ Cell Tumor | | MONDO:0005040|MONDO:0021230 | -| MONDO:0856072 | minor salivary gland intraductal papillary neoplasm | NCIT:C180880 | MONDO:equivalentTo | Minor Salivary Gland Intraductal Papillary Neoplasm | | MONDO:0021370 | -| MONDO:0856074 | adult myofibroma | NCIT:C180888 | MONDO:equivalentTo | Adult Myofibroma | | MONDO:0006312 | -| MONDO:0856077 | human papillomavirus-related vaginal squamous cell carcinoma | NCIT:C180917 | MONDO:equivalentTo | Human Papillomavirus-Related Vaginal Squamous Cell Carcinoma | | MONDO:0020657|MONDO:0006490 | -| MONDO:0856083 | vaginal adenocarcinoma of skene gland origin | NCIT:C180947 | MONDO:equivalentTo | Vaginal Adenocarcinoma of Skene Gland Origin | | MONDO:0020653|MONDO:0004173 | -| MONDO:0856100 | hybrid salivary gland tumor | NCIT:C181078 | MONDO:equivalentTo | Hybrid Salivary Gland Tumor | | MONDO:0021043|MONDO:0021357 | -| MONDO:0856104 | eyelid basal cell carcinoma | NCIT:C181159 | MONDO:equivalentTo | Eyelid Basal Cell Carcinoma | | MONDO:0003876|MONDO:0005341 | -| MONDO:0856106 | major salivary gland squamous cell carcinoma | NCIT:C181161 | MONDO:equivalentTo | Major Salivary Gland Squamous Cell Carcinoma | | MONDO:0044740|MONDO:0006284 | -| MONDO:0856110 | lung rhabdomyosarcoma | NCIT:C181201 | MONDO:equivalentTo | Lung Rhabdomyosarcoma | | MONDO:0002426|MONDO:0005212 | -| MONDO:0856111 | lung hodgkin lymphoma | NCIT:C181205 | MONDO:equivalentTo | Lung Hodgkin Lymphoma | | MONDO:0004952|MONDO:0003987 | -| MONDO:0856112 | primary bone hodgkin lymphoma | NCIT:C181207 | MONDO:equivalentTo | Primary Bone Hodgkin Lymphoma | | MONDO:0004952|MONDO:0017814 | -| MONDO:0856113 | thyroid gland hodgkin lymphoma | NCIT:C181209 | MONDO:equivalentTo | Thyroid Gland Hodgkin Lymphoma | | MONDO:0004952|MONDO:0019962 | -| MONDO:0856114 | cervical cancer by ajcc v9 stage | NCIT:C181562 | MONDO:equivalentTo | Cervical Cancer by AJCC v9 Stage | | MONDO:0005131 | -| MONDO:0856117 | epiglottic squamous cell carcinoma | NCIT:C181714 | MONDO:equivalentTo | Epiglottic Squamous Cell Carcinoma | | MONDO:0004293|MONDO:0004473 | -| MONDO:0856124 | vulvar squamous cell carcinoma, not otherwise specified | NCIT:C181902 | MONDO:equivalentTo | Vulvar Squamous Cell Carcinoma, Not Otherwise Specified | | MONDO:0024609 | -| MONDO:0856128 | endometrial mucosa-associated lymphoid tissue lymphoma | NCIT:C181910 | MONDO:equivalentTo | Endometrial Mucosa-Associated Lymphoid Tissue Lymphoma | | MONDO:0007650|MONDO:0011962 | -| MONDO:0856134 | vulvar kaposi sarcoma | NCIT:C181938 | MONDO:equivalentTo | Vulvar Kaposi Sarcoma | | MONDO:0005055|MONDO:0005214 | -| MONDO:0856136 | vulvar rhabdomyosarcoma | NCIT:C181944 | MONDO:equivalentTo | Vulvar Rhabdomyosarcoma | | MONDO:0005214|MONDO:0005212 | -| MONDO:0856137 | vulvar epithelioid sarcoma | NCIT:C181971 | MONDO:equivalentTo | Vulvar Epithelioid Sarcoma | | MONDO:0005214|MONDO:0017387 | -| MONDO:0856139 | vulvar ewing sarcoma | NCIT:C181977 | MONDO:equivalentTo | Vulvar Ewing Sarcoma | | MONDO:0018270|MONDO:0005214 | -| MONDO:0856154 | bronchiolar adenoma/ciliated muconodular papillary tumor | NCIT:C183045 | MONDO:equivalentTo | Bronchiolar Adenoma/Ciliated Muconodular Papillary Tumor | | MONDO:0003422 | -| MONDO:0856155 | invasive lung non-mucinous adenocarcinoma | NCIT:C183109 | MONDO:equivalentTo | Invasive Lung Non-Mucinous Adenocarcinoma | | MONDO:0040677|MONDO:0005061 | -| MONDO:0856156 | thoracic smarca4-deficient undifferentiated tumor | NCIT:C183115 | MONDO:equivalentTo | Thoracic SMARCA4-Deficient Undifferentiated Tumor | | MONDO:0003274 | -| MONDO:0856157 | lung hyalinizing clear cell carcinoma | NCIT:C183116 | MONDO:equivalentTo | Lung Hyalinizing Clear Cell Carcinoma | | MONDO:0005138 | -| MONDO:0856158 | lung intravascular large b-cell lymphoma | NCIT:C183121 | MONDO:equivalentTo | Lung Intravascular Large B-Cell Lymphoma | | MONDO:0006387|MONDO:0020324 | -| MONDO:0856161 | pleural mesothelioma in situ | NCIT:C183134 | MONDO:equivalentTo | Pleural Mesothelioma In Situ | | MONDO:0003308 | -| MONDO:0856165 | cardiac diffuse large b-cell lymphoma | NCIT:C183146 | MONDO:equivalentTo | Cardiac Diffuse Large B-Cell Lymphoma | | MONDO:0018905|MONDO:0003917 | -| MONDO:0856172 | pleural calcifying fibrous tumor | NCIT:C183277 | MONDO:equivalentTo | Pleural Calcifying Fibrous Tumor | | MONDO:0006121|MONDO:0021457 | -| MONDO:0856178 | thymic carcinoma with adenoid cystic carcinoma-like features | NCIT:C183313 | MONDO:equivalentTo | Thymic Carcinoma with Adenoid Cystic Carcinoma-Like Features | | MONDO:0006451 | -| MONDO:0856179 | thymic enteric-type adenocarcinoma | NCIT:C183314 | MONDO:equivalentTo | Thymic Enteric-Type Adenocarcinoma | | MONDO:0003209|MONDO:0006254 | -| MONDO:0856180 | thymic adenocarcinoma, not otherwise specified | NCIT:C183315 | MONDO:equivalentTo | Thymic Adenocarcinoma, Not Otherwise Specified | | MONDO:0003209 | -| MONDO:0856181 | thymic carcinoma, not otherwise specified | NCIT:C183316 | MONDO:equivalentTo | Thymic Carcinoma, Not Otherwise Specified | | MONDO:0006451 | -| MONDO:0856182 | mediastinal follicular dendritic cell sarcoma | NCIT:C183374 | MONDO:equivalentTo | Mediastinal Follicular Dendritic Cell Sarcoma | | MONDO:0005764|MONDO:0005843 | -| MONDO:0856183 | metastatic malignant neoplasm in the mediastinal lymph nodes | NCIT:C183510 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Mediastinal Lymph Nodes | | MONDO:0005438 | -| MONDO:0856191 | salivary gland adenoma | NCIT:C184295 | MONDO:equivalentTo | Salivary Gland Adenoma | | MONDO:0021460|MONDO:0004972 | -| MONDO:0856197 | multiple solitary plasmacytoma of bone | NCIT:C185035 | MONDO:equivalentTo | Multiple Solitary Plasmacytoma of Bone | | MONDO:0002755 | -| MONDO:0856199 | splenic plasmacytoma | NCIT:C185041 | MONDO:equivalentTo | Splenic Plasmacytoma | | MONDO:0002754|MONDO:0005966 | -| MONDO:0856204 | extramedullary disease in multiple myeloma | NCIT:C185149 | MONDO:equivalentTo | Extramedullary Disease in Multiple Myeloma | | MONDO:0009693 | -| MONDO:0856206 | astrocytoma, idh-mutant | NCIT:C185167 | MONDO:equivalentTo | Astrocytoma, IDH-Mutant | | MONDO:0019781 | -| MONDO:0856207 | astrocytoma, idh-wildtype | NCIT:C185184 | MONDO:equivalentTo | Astrocytoma, IDH-Wildtype | | MONDO:0019781 | -| MONDO:0856208 | astrocytoma, not otherwise specified | NCIT:C185185 | MONDO:equivalentTo | Astrocytoma, Not Otherwise Specified | | MONDO:0019781 | -| MONDO:0856216 | extranodal lymphoma | NCIT:C185752 | MONDO:equivalentTo | Extranodal Lymphoma | | MONDO:0017207 | -| MONDO:0856218 | high grade astrocytoma with piloid features | NCIT:C185879 | MONDO:equivalentTo | High Grade Astrocytoma with Piloid Features | | MONDO:0016684 | -| MONDO:0856232 | spinal cord ependymoma, mycn amplified | NCIT:C186494 | MONDO:equivalentTo | Spinal Cord Ependymoma, MYCN Amplified | | MONDO:0002542|MONDO:0016698 | -| MONDO:0856233 | childhood spinal cord ependymoma | NCIT:C186495 | MONDO:equivalentTo | Childhood Spinal Cord Ependymoma | | MONDO:0002716|MONDO:0003478|MONDO:0003473 | -| MONDO:0856234 | central nervous system neuroblastoma, foxr2-activated | NCIT:C186547 | MONDO:equivalentTo | Central Nervous System Neuroblastoma, FOXR2-Activated | | MONDO:0002900 | -| MONDO:0856238 | primary intracranial sarcoma, dicer1-mutant | NCIT:C186610 | MONDO:equivalentTo | Primary Intracranial Sarcoma, DICER1-Mutant | | MONDO:0002216 | -| MONDO:0856239 | central nervous system ewing sarcoma | NCIT:C186611 | MONDO:equivalentTo | Central Nervous System Ewing Sarcoma | | MONDO:0018270|MONDO:0002217|MONDO:0016713 | -| MONDO:0856240 | intracranial mesenchymal tumor, fet-creb fusion-positive | NCIT:C186614 | MONDO:equivalentTo | Intracranial Mesenchymal Tumor, FET-CREB Fusion-Positive | | MONDO:0003244|MONDO:0021632 | -| MONDO:0856241 | cervical cancer by figo stage 2009 | NCIT:C186619 | MONDO:equivalentTo | Cervical Cancer by FIGO Stage 2009 | | MONDO:0005131 | -| MONDO:0856244 | central nervous system lymphomatoid granulomatosis | NCIT:C186662 | MONDO:equivalentTo | Central Nervous System Lymphomatoid Granulomatosis | | MONDO:0019466|MONDO:0003641 | -| MONDO:0856246 | smarcb1 schwannomatosis 1 | NCIT:C186703 | MONDO:equivalentTo | SMARCB1 Schwannomatosis 1 | | MONDO:0008075 | -| MONDO:0856247 | lztr1 schwannomatosis 2 | NCIT:C186704 | MONDO:equivalentTo | LZTR1 Schwannomatosis 2 | | MONDO:0008075 | -| MONDO:0856253 | childhood acute leukemia | NCIT:C187056 | MONDO:equivalentTo | Childhood Acute Leukemia | | MONDO:0010643|MONDO:0004355 | -| MONDO:0856254 | pituitary neuroendocrine tumor of pit1-lineage | NCIT:C187086 | MONDO:equivalentTo | Pituitary Neuroendocrine Tumor of PIT1-Lineage | | MONDO:0006373 | -| MONDO:0856255 | pituitary neuroendocrine tumor of tpit-lineage | NCIT:C187087 | MONDO:equivalentTo | Pituitary Neuroendocrine Tumor of TPIT-Lineage | | MONDO:0006373 | -| MONDO:0856256 | pituitary neuroendocrine tumor of sf1-lineage | NCIT:C187088 | MONDO:equivalentTo | Pituitary Neuroendocrine Tumor of SF1-Lineage | | MONDO:0006373 | -| MONDO:0856257 | pituitary neuroendocrine tumor without distinct lineage differentiation | NCIT:C187096 | MONDO:equivalentTo | Pituitary Neuroendocrine Tumor without Distinct Lineage Differentiation | | MONDO:0006373 | -| MONDO:0856258 | pituitary neuroendocrine tumor, not otherwise specified | NCIT:C187135 | MONDO:equivalentTo | Pituitary Neuroendocrine Tumor, Not Otherwise Specified | | MONDO:0006373 | -| MONDO:0856267 | thyroid gland follicular adenoma with papillary architecture | NCIT:C187261 | MONDO:equivalentTo | Thyroid Gland Follicular Adenoma with Papillary Architecture | | MONDO:0005032 | -| MONDO:0856268 | low risk thyroid gland neoplasm | NCIT:C187273 | MONDO:equivalentTo | Low Risk Thyroid Gland Neoplasm | | MONDO:0015074 | -| MONDO:0856271 | platinum-sensitive endometrial serous adenocarcinoma | NCIT:C187374 | MONDO:equivalentTo | Platinum-Sensitive Endometrial Serous Adenocarcinoma | | MONDO:0006196 | -| MONDO:0856272 | invasive breast lobular carcinoma with extracellular mucin | NCIT:C187405 | MONDO:equivalentTo | Invasive Breast Lobular Carcinoma with Extracellular Mucin | | MONDO:0005051 | -| MONDO:0856275 | thyroid gland follicular carcinoma, signet ring cell variant | NCIT:C187643 | MONDO:equivalentTo | Thyroid Gland Follicular Carcinoma, Signet Ring Cell Variant | | MONDO:0005034 | -| MONDO:0856276 | classic thyroid gland papillary carcinoma | NCIT:C187644 | MONDO:equivalentTo | Classic Thyroid Gland Papillary Carcinoma | | MONDO:0005075 | -| MONDO:0856277 | follicular-derived thyroid gland carcinoma, high grade | NCIT:C187645 | MONDO:equivalentTo | Follicular-Derived Thyroid Gland Carcinoma, High Grade | | MONDO:0024622 | -| MONDO:0856285 | thyroid gland secretory carcinoma | NCIT:C187994 | MONDO:equivalentTo | Thyroid Gland Secretory Carcinoma | | MONDO:0024622 | -| MONDO:0856286 | thyroblastoma | NCIT:C187995 | MONDO:equivalentTo | Thyroblastoma | | MONDO:0002108|MONDO:0005564 | -| MONDO:0856287 | teratoma with endocrine differentiation | NCIT:C188013 | MONDO:equivalentTo | Teratoma with Endocrine Differentiation | | MONDO:0002601 | -| MONDO:0856289 | b-cell malignant neoplasm | NCIT:C188021 | MONDO:equivalentTo | B-Cell Malignant Neoplasm | | MONDO:0004992|MONDO:0004095 | -| MONDO:0856293 | mast cell leukemia with an associated myeloid neoplasm | NCIT:C188031 | MONDO:equivalentTo | Mast Cell Leukemia with an Associated Myeloid Neoplasm | | MONDO:0020332|MONDO:0020334 | -| MONDO:0856298 | refractory wilms tumor | NCIT:C188038 | MONDO:equivalentTo | Refractory Wilms Tumor | | MONDO:0006058|MONDO:0036501 | -| MONDO:0856302 | pleural proximal-type epithelioid sarcoma | NCIT:C188055 | MONDO:equivalentTo | Pleural Proximal-Type Epithelioid Sarcoma | | MONDO:0006294|MONDO:0004244 | -| MONDO:0856303 | lung osteosarcoma | NCIT:C188061 | MONDO:equivalentTo | Lung Osteosarcoma | | MONDO:0002621|MONDO:0002426 | -| MONDO:0856304 | pleural leiomyosarcoma | NCIT:C188063 | MONDO:equivalentTo | Pleural Leiomyosarcoma | | MONDO:0006294|MONDO:0005058 | -| MONDO:0856305 | bone malignant peripheral nerve sheath tumor | NCIT:C188064 | MONDO:equivalentTo | Bone Malignant Peripheral Nerve Sheath Tumor | | MONDO:0021054|MONDO:0017827 | -| MONDO:0856308 | lung secretory carcinoma | NCIT:C188068 | MONDO:equivalentTo | Lung Secretory Carcinoma | | MONDO:0005138 | -| MONDO:0856309 | prostate alveolar rhabdomyosarcoma | NCIT:C188070 | MONDO:equivalentTo | Prostate Alveolar Rhabdomyosarcoma | | MONDO:0006389|MONDO:0009994 | -| MONDO:0856310 | retroperitoneal rhabdomyosarcoma | NCIT:C188071 | MONDO:equivalentTo | Retroperitoneal Rhabdomyosarcoma | | MONDO:0001501|MONDO:0005212 | -| MONDO:0856312 | retroperitoneal malignant peripheral nerve sheath tumor | NCIT:C188073 | MONDO:equivalentTo | Retroperitoneal Malignant Peripheral Nerve Sheath Tumor | | MONDO:0001501|MONDO:0017827 | -| MONDO:0856313 | rectal epithelioid cell melanoma | NCIT:C188079 | MONDO:equivalentTo | Rectal Epithelioid Cell Melanoma | | MONDO:0002167|MONDO:0002973 | -| MONDO:0856316 | lung anaplastic large cell lymphoma | NCIT:C188082 | MONDO:equivalentTo | Lung Anaplastic Large Cell Lymphoma | | MONDO:0020644|MONDO:0020325 | -| MONDO:0856318 | middle ear embryonal rhabdomyosarcoma | NCIT:C188115 | MONDO:equivalentTo | Middle Ear Embryonal Rhabdomyosarcoma | | MONDO:0009993|MONDO:0003275 | -| MONDO:0856325 | adrenal cortical myxoid carcinoma | NCIT:C188182 | MONDO:equivalentTo | Adrenal Cortical Myxoid Carcinoma | | MONDO:0006639 | -| MONDO:0856326 | adrenal cortical high grade carcinoma | NCIT:C188183 | MONDO:equivalentTo | Adrenal Cortical High Grade Carcinoma | | MONDO:0006639 | -| MONDO:0856327 | adrenal cortical melanoma | NCIT:C188185 | MONDO:equivalentTo | Adrenal Cortical Melanoma | | MONDO:0021312|MONDO:0006320 | -| MONDO:0856335 | neuroendocrine tumor | NCIT:C188218 | MONDO:equivalentTo | Neuroendocrine Tumor | | MONDO:0019496 | -| MONDO:0856336 | head and neck neuroendocrine neoplasm | NCIT:C188222 | MONDO:equivalentTo | Head and Neck Neuroendocrine Neoplasm | | MONDO:0019496|MONDO:0005586 | -| MONDO:0856338 | adrenal gland lipoma | NCIT:C188250 | MONDO:equivalentTo | Adrenal Gland Lipoma | | MONDO:0021511|MONDO:0005106 | -| MONDO:0856339 | adrenal gland hemangioma | NCIT:C188251 | MONDO:equivalentTo | Adrenal Gland Hemangioma | | MONDO:0021511|MONDO:0006500 | -| MONDO:0856340 | adrenal gland lymphangioma | NCIT:C188252 | MONDO:equivalentTo | Adrenal Gland Lymphangioma | | MONDO:0002013|MONDO:0021511 | -| MONDO:0856341 | adrenal gland leiomyoma | NCIT:C188253 | MONDO:equivalentTo | Adrenal Gland Leiomyoma | | MONDO:0021511|MONDO:0001572 | -| MONDO:0856343 | multiple endocrine neoplasia type 5 | NCIT:C188257 | MONDO:equivalentTo | Multiple Endocrine Neoplasia Type 5 | | MONDO:0017169 | -| MONDO:0856349 | chronic phase primary myelofibrosis | NCIT:C188314 | MONDO:equivalentTo | Chronic Phase Primary Myelofibrosis | | MONDO:0009692 | -| MONDO:0856350 | accelerated phase myeloproliferative neoplasm | NCIT:C188315 | MONDO:equivalentTo | Accelerated Phase Myeloproliferative Neoplasm | | MONDO:0020076 | -| MONDO:0856351 | blast phase myeloproliferative neoplasm | NCIT:C188316 | MONDO:equivalentTo | Blast Phase Myeloproliferative Neoplasm | | MONDO:0020076 | -| MONDO:0856357 | intraductal hyperplasia | NCIT:C26458 | MONDO:equivalentTo | Intraductal Hyperplasia | | | -| MONDO:0856375 | reticulosarcoma involving spleen | NCIT:C26959 | MONDO:equivalentTo | Reticulosarcoma Involving Spleen | | MONDO:0009975 | -| MONDO:0856376 | lymphosarcoma involving spleen | NCIT:C26960 | MONDO:equivalentTo | Lymphosarcoma Involving Spleen | | MONDO:0004638 | -| MONDO:0856398 | nonpigmented nevus | NCIT:C27095 | MONDO:equivalentTo | Nonpigmented Nevus | | MONDO:0044794 | -| MONDO:0856421 | transplant-related disorder | NCIT:C27233 | MONDO:equivalentTo | Transplant-Related Disorder | | | -| MONDO:0856422 | familial adenomatous polyposis associated medulloblastoma | NCIT:C27237 | MONDO:equivalentTo | Familial Adenomatous Polyposis Associated Medulloblastoma | | MONDO:0007959 | -| MONDO:0856423 | lymphoma by stage | NCIT:C27268 | MONDO:equivalentTo | Lymphoma by Stage | | MONDO:0005062 | -| MONDO:0856424 | glandular cell intraepithelial neoplasia | NCIT:C27269 | MONDO:equivalentTo | Glandular Cell Intraepithelial Neoplasia | | MONDO:0024474|MONDO:0024276 | -| MONDO:0856425 | secondary myelodysplastic syndrome | NCIT:C27280 | MONDO:equivalentTo | Secondary Myelodysplastic Syndrome | | MONDO:0024881|MONDO:0018881 | -| MONDO:0856428 | metastatic ewing sarcoma/peripheral primitive neuroectodermal tumor | NCIT:C27292 | MONDO:equivalentTo | Metastatic Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor | | MONDO:0024880|MONDO:0021038 | -| MONDO:0856443 | unresectable malignant neoplasm | NCIT:C27359 | MONDO:equivalentTo | Unresectable Malignant Neoplasm | | MONDO:0004992 | -| MONDO:0856447 | mucin-producing adenocarcinoma | NCIT:C27379 | MONDO:equivalentTo | Mucin-Producing Adenocarcinoma | | MONDO:0020596|MONDO:0004970 | -| MONDO:0856451 | extraosseous/peripheral ameloblastoma | NCIT:C27396 | MONDO:equivalentTo | Extraosseous/Peripheral Ameloblastoma | | MONDO:0017795 | -| MONDO:0856452 | ampulla of vater intestinal-type adenocarcinoma | NCIT:C27415 | MONDO:equivalentTo | Ampulla of Vater Intestinal-Type Adenocarcinoma | | MONDO:0002670|MONDO:0006254 | -| MONDO:0856453 | ampulla of vater undifferentiated carcinoma | NCIT:C27419 | MONDO:equivalentTo | Ampulla of Vater Undifferentiated Carcinoma | | MONDO:0017590|MONDO:0005617 | -| MONDO:0856456 | small intestinal gastrin-producing neuroendocrine tumor | NCIT:C27450 | MONDO:equivalentTo | Small Intestinal Gastrin-Producing Neuroendocrine Tumor | | MONDO:0002995|MONDO:0003523 | -| MONDO:0856457 | small intestinal enterochromaffin cell serotonin-producing neuroendocrine tumor | NCIT:C27451 | MONDO:equivalentTo | Small Intestinal Enterochromaffin Cell Serotonin-Producing Neuroendocrine Tumor | | MONDO:0002995 | -| MONDO:0856458 | small intestinal somatostatin-producing neuroendocrine tumor | NCIT:C27453 | MONDO:equivalentTo | Small Intestinal Somatostatin-Producing Neuroendocrine Tumor | | MONDO:0002995|MONDO:0006976 | -| MONDO:0856460 | colorectal adenoma with moderate dysplasia | NCIT:C27457 | MONDO:equivalentTo | Colorectal Adenoma with Moderate Dysplasia | | MONDO:0005484 | -| MONDO:0856461 | colorectal adenoma with mild dysplasia | NCIT:C27458 | MONDO:equivalentTo | Colorectal Adenoma with Mild Dysplasia | | MONDO:0005484 | -| MONDO:0856463 | disseminated malignant neoplasm | NCIT:C27470 | MONDO:equivalentTo | Disseminated Malignant Neoplasm | | MONDO:0024880 | -| MONDO:0856464 | bone lipoma | NCIT:C27475 | MONDO:equivalentTo | Bone Lipoma | | MONDO:0000631|MONDO:0005106 | -| MONDO:0856465 | bone schwannoma | NCIT:C27476 | MONDO:equivalentTo | Bone Schwannoma | | MONDO:0000631|MONDO:0004820 | -| MONDO:0856468 | secondary chondrosarcoma | NCIT:C27482 | MONDO:equivalentTo | Secondary Chondrosarcoma | | MONDO:0021054|MONDO:0024881|MONDO:0008977 | -| MONDO:0856469 | conventional alveolar rhabdomyosarcoma | NCIT:C27492 | MONDO:equivalentTo | Conventional Alveolar Rhabdomyosarcoma | | MONDO:0009994 | -| MONDO:0856470 | solid alveolar rhabdomyosarcoma | NCIT:C27493 | MONDO:equivalentTo | Solid Alveolar Rhabdomyosarcoma | | MONDO:0009994 | -| MONDO:0856471 | lymphadenopathic kaposi sarcoma | NCIT:C27500 | MONDO:equivalentTo | Lymphadenopathic Kaposi Sarcoma | | MONDO:0001082|MONDO:0005055 | -| MONDO:0856472 | conventional extraskeletal myxoid chondrosarcoma | NCIT:C27501 | MONDO:equivalentTo | Conventional Extraskeletal Myxoid Chondrosarcoma | | MONDO:0012825 | -| MONDO:0856473 | intra-abdominal lymphangioma | NCIT:C27508 | MONDO:equivalentTo | Intra-Abdominal Lymphangioma | | MONDO:0002013 | -| MONDO:0856474 | angiosarcoma associated with lymphedema | NCIT:C27512 | MONDO:equivalentTo | Angiosarcoma Associated with Lymphedema | | MONDO:0016982 | -| MONDO:0856475 | desmoplastic fibroblastoma | NCIT:C27515 | MONDO:equivalentTo | Desmoplastic Fibroblastoma | | MONDO:0005167 | -| MONDO:0856477 | desmoplastic trichoepithelioma | NCIT:C27524 | MONDO:equivalentTo | Desmoplastic Trichoepithelioma | | MONDO:0020593 | -| MONDO:0856478 | tubular apocrine adenoma | NCIT:C27527 | MONDO:equivalentTo | Tubular Apocrine Adenoma | | MONDO:0002804 | -| MONDO:0856479 | primary cutaneous mucinous carcinoma | NCIT:C27533 | MONDO:equivalentTo | Primary Cutaneous Mucinous Carcinoma | | MONDO:0005524|MONDO:0004957 | -| MONDO:0856501 | oral cavity disorder | NCIT:C27641 | MONDO:equivalentTo | Oral Cavity Disorder | | | -| MONDO:0856504 | sinonasal disorder | NCIT:C27647 | MONDO:equivalentTo | Sinonasal Disorder | | | -| MONDO:0856509 | human papillomavirus-related verrucous carcinoma | NCIT:C27678 | MONDO:equivalentTo | Human Papillomavirus-Related Verrucous Carcinoma | | MONDO:0006006|MONDO:0020657 | -| MONDO:0856510 | human papillomavirus-related vulvar squamous cell carcinoma | NCIT:C27679 | MONDO:equivalentTo | Human Papillomavirus-Related Vulvar Squamous Cell Carcinoma | | MONDO:0024609|MONDO:0020657 | -| MONDO:0856511 | human papillomavirus-related esophageal squamous cell carcinoma | NCIT:C27680 | MONDO:equivalentTo | Human Papillomavirus-Related Esophageal Squamous Cell Carcinoma | | MONDO:0005580|MONDO:0020657 | -| MONDO:0856512 | human papillomavirus-related anal squamous cell carcinoma | NCIT:C27681 | MONDO:equivalentTo | Human Papillomavirus-Related Anal Squamous Cell Carcinoma | | MONDO:0006082|MONDO:0020657 | -| MONDO:0856518 | ebv-related post-transplant lymphoproliferative disorder | NCIT:C27696 | MONDO:equivalentTo | EBV-Related Post-Transplant Lymphoproliferative Disorder | | | -| MONDO:0856523 | extragastrointestinal gastrointestinal stromal tumor | NCIT:C27716 | MONDO:equivalentTo | Extragastrointestinal Gastrointestinal Stromal Tumor | | MONDO:0011719 | -| MONDO:0856526 | myelodysplastic syndrome with ring sideroblasts and multilineage dysplasia | NCIT:C27726 | MONDO:equivalentTo | Myelodysplastic Syndrome with Ring Sideroblasts and Multilineage Dysplasia | | MONDO:0019157 | -| MONDO:0856529 | typical acute promyelocytic leukemia | NCIT:C27756 | MONDO:equivalentTo | Typical Acute Promyelocytic Leukemia | | MONDO:0012883 | -| MONDO:0856530 | microgranular acute promyelocytic leukemia | NCIT:C27757 | MONDO:equivalentTo | Microgranular Acute Promyelocytic Leukemia | | MONDO:0012883 | -| MONDO:0856539 | myelodysplastic/myeloproliferative neoplasm, not otherwise specified | NCIT:C27780 | MONDO:equivalentTo | Myelodysplastic/Myeloproliferative Neoplasm, Not Otherwise Specified | | MONDO:0006311 | -| MONDO:0856541 | spindle cell type gastrointestinal stromal tumor | NCIT:C27792 | MONDO:equivalentTo | Spindle Cell Type Gastrointestinal Stromal Tumor | | MONDO:0011719 | -| MONDO:0856542 | mixed cell type gastrointestinal stromal tumor | NCIT:C27793 | MONDO:equivalentTo | Mixed Cell Type Gastrointestinal Stromal Tumor | | MONDO:0011719 | -| MONDO:0856545 | nodular sclerosis classic hodgkin lymphoma, syncytial variant | NCIT:C27807 | MONDO:equivalentTo | Nodular Sclerosis Classic Hodgkin Lymphoma, Syncytial Variant | | MONDO:0004665 | -| MONDO:0856546 | pigmented nevus | NCIT:C27816 | MONDO:equivalentTo | Pigmented Nevus | | MONDO:0044794 | -| MONDO:0856549 | invasive breast carcinoma by histologic grade | NCIT:C27829 | MONDO:equivalentTo | Invasive Breast Carcinoma by Histologic Grade | | MONDO:0006256 | -| MONDO:0856551 | endometrial endometrioid adenocarcinoma with clear cell change | NCIT:C27843 | MONDO:equivalentTo | Endometrial Endometrioid Adenocarcinoma with Clear Cell Change | | MONDO:0006192|MONDO:0005004 | -| MONDO:0856552 | endometrial endometrioid adenocarcinoma with a poorly differentiated carcinomatous component | NCIT:C27844 | MONDO:equivalentTo | Endometrial Endometrioid Adenocarcinoma with a Poorly Differentiated Carcinomatous Component | | MONDO:0006192 | -| MONDO:0856553 | endometrial endometrioid adenocarcinoma with an undifferentiated carcinomatous component | NCIT:C27845 | MONDO:equivalentTo | Endometrial Endometrioid Adenocarcinoma with an Undifferentiated Carcinomatous Component | | MONDO:0006192 | -| MONDO:0856554 | endometrial endometrioid adenocarcinoma, ciliated variant | NCIT:C27848 | MONDO:equivalentTo | Endometrial Endometrioid Adenocarcinoma, Ciliated Variant | | MONDO:0006192 | -| MONDO:0856567 | transitional cell intraepithelial neoplasia | NCIT:C27881 | MONDO:equivalentTo | Transitional Cell Intraepithelial Neoplasia | | MONDO:0024474|MONDO:0037254 | -| MONDO:0856569 | type 1 papillary renal cell carcinoma | NCIT:C27886 | MONDO:equivalentTo | Type 1 Papillary Renal Cell Carcinoma | | MONDO:0017884 | -| MONDO:0856570 | type 2 papillary renal cell carcinoma | NCIT:C27887 | MONDO:equivalentTo | Type 2 Papillary Renal Cell Carcinoma | | MONDO:0017884 | -| MONDO:0856571 | sporadic papillary renal cell carcinoma | NCIT:C27890 | MONDO:equivalentTo | Sporadic Papillary Renal Cell Carcinoma | | MONDO:0017884 | -| MONDO:0856577 | well differentiated prostate adenocarcinoma | NCIT:C27905 | MONDO:equivalentTo | Well Differentiated Prostate Adenocarcinoma | | MONDO:0005082 | -| MONDO:0856578 | moderately differentiated prostate adenocarcinoma | NCIT:C27906 | MONDO:equivalentTo | Moderately Differentiated Prostate Adenocarcinoma | | MONDO:0005082 | -| MONDO:0856579 | alkylating agent-related acute myeloid leukemia and myelodysplastic syndrome | NCIT:C27913 | MONDO:equivalentTo | Alkylating Agent-Related Acute Myeloid Leukemia and Myelodysplastic Syndrome | | MONDO:0006450 | -| MONDO:0856580 | sporadic burkitt lymphoma | NCIT:C27914 | MONDO:equivalentTo | Sporadic Burkitt Lymphoma | | MONDO:0007243 | -| MONDO:0856582 | poorly differentiated prostate adenocarcinoma | NCIT:C27916 | MONDO:equivalentTo | Poorly Differentiated Prostate Adenocarcinoma | | MONDO:0005082 | -| MONDO:0856592 | metaplastic carcinoma | NCIT:C27949 | MONDO:equivalentTo | Metaplastic Carcinoma | | MONDO:0004993 | -| MONDO:0856593 | squamous cell carcinoma in situ of the nipple | NCIT:C28292 | MONDO:equivalentTo | Squamous Cell Carcinoma In Situ of the Nipple | | MONDO:0003950|MONDO:0004693 | -| MONDO:0856599 | biliary system disorder | NCIT:C2899 | MONDO:equivalentTo | Biliary System Disorder | | | -| MONDO:0856602 | enchondroma | NCIT:C3007 | MONDO:equivalentTo | Enchondroma | | MONDO:0002360|MONDO:0000631 | -| MONDO:0856604 | pancreatic glucagon-producing neuroendocrine tumor | NCIT:C3062 | MONDO:equivalentTo | Pancreatic Glucagon-Producing Neuroendocrine Tumor | | MONDO:0019954 | -| MONDO:0856606 | chronic phase chronic myeloid leukemia, bcr-abl1 positive | NCIT:C3175 | MONDO:equivalentTo | Chronic Phase Chronic Myeloid Leukemia, BCR-ABL1 Positive | | MONDO:0001014|MONDO:0011996 | -| MONDO:0856607 | myeloid leukemia, philadelphia- negative | NCIT:C3176 | MONDO:equivalentTo | Myeloid Leukemia, Philadelphia- Negative | | MONDO:0004643 | -| MONDO:0856608 | neoplasm by site | NCIT:C3263 | MONDO:equivalentTo | Neoplasm by Site | | MONDO:0005070 | -| MONDO:0856610 | osteochondroma | NCIT:C3295 | MONDO:equivalentTo | Osteochondroma | | MONDO:0000631|MONDO:0024470 | -| MONDO:0856611 | extra-adrenal paraganglioma | NCIT:C3309 | MONDO:equivalentTo | Extra-Adrenal Paraganglioma | | MONDO:0000448 | -| MONDO:0856614 | supratentorial neoplasm | NCIT:C3397 | MONDO:equivalentTo | Supratentorial Neoplasm | | MONDO:0021211 | -| MONDO:0856615 | thyroid gland nodule | NCIT:C3415 | MONDO:equivalentTo | Thyroid Gland Nodule | | | -| MONDO:0856638 | grade 3 follicular lymphoma | NCIT:C3460 | MONDO:equivalentTo | Grade 3 Follicular Lymphoma | | MONDO:0018906|MONDO:0017595 | -| MONDO:0856655 | lobular capillary hemangioma | NCIT:C3480 | MONDO:equivalentTo | Lobular Capillary Hemangioma | | MONDO:0002407 | -| MONDO:0856661 | epithelioid cell type gastrointestinal stromal tumor | NCIT:C3486 | MONDO:equivalentTo | Epithelioid Cell Type Gastrointestinal Stromal Tumor | | MONDO:0011719 | -| MONDO:0856691 | uterine corpus degenerated leiomyoma | NCIT:C3511 | MONDO:equivalentTo | Uterine Corpus Degenerated Leiomyoma | | MONDO:0007886 | -| MONDO:0856703 | eyelid vascular disorder | NCIT:C35198 | MONDO:equivalentTo | Eyelid Vascular Disorder | | | -| MONDO:0856706 | placental polyp | NCIT:C3521 | MONDO:equivalentTo | Placental Polyp | | MONDO:0021498|MONDO:0005079 | -| MONDO:0856715 | chondromatosis | NCIT:C35259 | MONDO:equivalentTo | Chondromatosis | | MONDO:0024470 | -| MONDO:0856716 | malignant submandibular gland neoplasm | NCIT:C3526 | MONDO:equivalentTo | Malignant Submandibular Gland Neoplasm | | MONDO:0044743|MONDO:0021244 | -| MONDO:0856723 | malignant palate neoplasm | NCIT:C3530 | MONDO:equivalentTo | Malignant Palate Neoplasm | | MONDO:0005515|MONDO:0005286 | -| MONDO:0856758 | malignant neoplasm of multiple primary sites | NCIT:C35427 | MONDO:equivalentTo | Malignant Neoplasm of Multiple Primary Sites | | MONDO:0004992 | -| MONDO:0856764 | behavioral disorder | NCIT:C35470 | MONDO:equivalentTo | Behavioral Disorder | | | -| MONDO:0856772 | lung kaposi sarcoma | NCIT:C3551 | MONDO:equivalentTo | Lung Kaposi Sarcoma | | MONDO:0002426|MONDO:0005055 | -| MONDO:0856784 | malignant exocervical neoplasm | NCIT:C3554 | MONDO:equivalentTo | Malignant Exocervical Neoplasm | | MONDO:0002974 | -| MONDO:0856786 | malignant uterine corpus neoplasm | NCIT:C3556 | MONDO:equivalentTo | Malignant Uterine Corpus Neoplasm | | MONDO:0021254|MONDO:0002715 | -| MONDO:0856787 | complex endometrial hyperplasia with atypia | NCIT:C35560 | MONDO:equivalentTo | Complex Endometrial Hyperplasia with Atypia | | MONDO:0006169 | -| MONDO:0856809 | ocular adnexal mucosa-associated lymphoid tissue lymphoma | NCIT:C35689 | MONDO:equivalentTo | Ocular Adnexal Mucosa-Associated Lymphoid Tissue Lymphoma | | MONDO:0020646|MONDO:0007650 | -| MONDO:0856810 | mixed tumor of the salivary gland | NCIT:C35691 | MONDO:equivalentTo | Mixed Tumor of the Salivary Gland | | MONDO:0021043|MONDO:0021357 | -| MONDO:0856811 | posterior pharyngeal wall carcinoma | NCIT:C35692 | MONDO:equivalentTo | Posterior Pharyngeal Wall Carcinoma | | MONDO:0021345 | -| MONDO:0856812 | benign uvula neoplasm | NCIT:C35698 | MONDO:equivalentTo | Benign Uvula Neoplasm | | MONDO:0021480 | -| MONDO:0856814 | testicular teratoma with somatic-type malignancy | NCIT:C35711 | MONDO:equivalentTo | Testicular Teratoma with Somatic-Type Malignancy | | MONDO:0003403|MONDO:0006444|MONDO:0018193 | -| MONDO:0856818 | salivary gland lymphoepithelial carcinoma | NCIT:C35736 | MONDO:equivalentTo | Salivary Gland Lymphoepithelial Carcinoma | | MONDO:0000521|MONDO:0003572 | -| MONDO:0856830 | metastatic malignant neoplasm in the bone | NCIT:C3580 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Bone | | MONDO:0002129|MONDO:0024880 | -| MONDO:0856835 | monoblastic sarcoma | NCIT:C35816 | MONDO:equivalentTo | Monoblastic Sarcoma | | MONDO:0006861 | -| MONDO:0856836 | blastic granulocytic sarcoma | NCIT:C35817 | MONDO:equivalentTo | Blastic Granulocytic Sarcoma | | MONDO:0006237 | -| MONDO:0856837 | immature granulocytic sarcoma | NCIT:C35818 | MONDO:equivalentTo | Immature Granulocytic Sarcoma | | MONDO:0006237 | -| MONDO:0856838 | differentiated granulocytic sarcoma | NCIT:C35819 | MONDO:equivalentTo | Differentiated Granulocytic Sarcoma | | MONDO:0006237 | -| MONDO:0856840 | salivary gland cystadenoma | NCIT:C35833 | MONDO:equivalentTo | Salivary Gland Cystadenoma | | MONDO:0021460|MONDO:0036976|MONDO:0002369 | -| MONDO:0856844 | salivary gland ductal papilloma | NCIT:C35839 | MONDO:equivalentTo | Salivary Gland Ductal Papilloma | | MONDO:0002363|MONDO:0021460 | -| MONDO:0856847 | grade 1 clear cell renal cell carcinoma | NCIT:C35851 | MONDO:equivalentTo | Grade 1 Clear Cell Renal Cell Carcinoma | | MONDO:0005005 | -| MONDO:0856848 | grade 2 clear cell renal cell carcinoma | NCIT:C35852 | MONDO:equivalentTo | Grade 2 Clear Cell Renal Cell Carcinoma | | MONDO:0005005 | -| MONDO:0856849 | grade 3 clear cell renal cell carcinoma | NCIT:C35853 | MONDO:equivalentTo | Grade 3 Clear Cell Renal Cell Carcinoma | | MONDO:0005005 | -| MONDO:0856850 | grade 4 clear cell renal cell carcinoma | NCIT:C35854 | MONDO:equivalentTo | Grade 4 Clear Cell Renal Cell Carcinoma | | MONDO:0005005 | -| MONDO:0856855 | endemic african kaposi sarcoma | NCIT:C35874 | MONDO:equivalentTo | Endemic African Kaposi Sarcoma | | MONDO:0005055 | -| MONDO:0856856 | distantly metastatic malignant neoplasm | NCIT:C35933 | MONDO:equivalentTo | Distantly Metastatic Malignant Neoplasm | | MONDO:0024880 | -| MONDO:0856857 | malignant neoplasm by grade | NCIT:C36041 | MONDO:equivalentTo | Malignant Neoplasm by Grade | | MONDO:0004992 | -| MONDO:0856858 | moderately differentiated malignant neoplasm | NCIT:C36049 | MONDO:equivalentTo | Moderately Differentiated Malignant Neoplasm | | MONDO:0004992 | -| MONDO:0856859 | poorly differentiated malignant neoplasm | NCIT:C36050 | MONDO:equivalentTo | Poorly Differentiated Malignant Neoplasm | | MONDO:0004992 | -| MONDO:0856860 | undifferentiated malignant neoplasm | NCIT:C36051 | MONDO:equivalentTo | Undifferentiated Malignant Neoplasm | | MONDO:0004992 | -| MONDO:0856861 | well differentiated malignant neoplasm | NCIT:C36052 | MONDO:equivalentTo | Well Differentiated Malignant Neoplasm | | MONDO:0004992 | -| MONDO:0856862 | acute myeloid leukemia with t(11;17)(q23;q21); zbtb16-rara | NCIT:C36056 | MONDO:equivalentTo | Acute Myeloid Leukemia with t(11;17)(q23;q21); ZBTB16-RARA | | MONDO:0100375 | -| MONDO:0856863 | acute myeloid leukemia with t(5;17)(q35;q21); npm1-rara | NCIT:C36057 | MONDO:equivalentTo | Acute Myeloid Leukemia with t(5;17)(q35;q21); NPM1-RARA | | MONDO:0100375 | -| MONDO:0856864 | acute myeloid leukemia with t(11;17)(q13;q21); numa1-rara | NCIT:C36058 | MONDO:equivalentTo | Acute Myeloid Leukemia with t(11;17)(q13;q21); NUMA1-RARA | | MONDO:0100375 | -| MONDO:0856865 | chronic myelomonocytic leukemia with eosinophilia | NCIT:C36060 | MONDO:equivalentTo | Chronic Myelomonocytic Leukemia with Eosinophilia | | MONDO:0020311 | -| MONDO:0856866 | chronic myelomonocytic leukemia-1 | NCIT:C36061 | MONDO:equivalentTo | Chronic Myelomonocytic Leukemia-1 | | MONDO:0020311 | -| MONDO:0856867 | chronic myelomonocytic leukemia-2 | NCIT:C36062 | MONDO:equivalentTo | Chronic Myelomonocytic Leukemia-2 | | MONDO:0020311 | -| MONDO:0856875 | hereditary male breast carcinoma | NCIT:C36106 | MONDO:equivalentTo | Hereditary Male Breast Carcinoma | | MONDO:0016419|MONDO:0005628 | -| MONDO:0856876 | hereditary female breast carcinoma | NCIT:C36107 | MONDO:equivalentTo | Hereditary Female Breast Carcinoma | | MONDO:0016419|MONDO:0004379 | -| MONDO:0856880 | non-hereditary clear cell renal cell carcinoma | NCIT:C36261 | MONDO:equivalentTo | Non-Hereditary Clear Cell Renal Cell Carcinoma | | MONDO:0005005 | -| MONDO:0856882 | metastatic benign neoplasm | NCIT:C36264 | MONDO:equivalentTo | Metastatic Benign Neoplasm | | MONDO:0005165|MONDO:0024883 | -| MONDO:0856883 | lymphomatous adult t-cell leukemia/lymphoma | NCIT:C36266 | MONDO:equivalentTo | Lymphomatous Adult T-Cell Leukemia/Lymphoma | | MONDO:0019471 | -| MONDO:0856884 | hodgkin-like adult t-cell leukemia/lymphoma | NCIT:C36268 | MONDO:equivalentTo | Hodgkin-Like Adult T-Cell Leukemia/Lymphoma | | MONDO:0019471 | -| MONDO:0856885 | t-cell prolymphocytic leukemia, small cell variant | NCIT:C36270 | MONDO:equivalentTo | T-Cell Prolymphocytic Leukemia, Small Cell Variant | | MONDO:0019468 | -| MONDO:0856886 | t-cell prolymphocytic leukemia, cerebriform cell variant | NCIT:C36271 | MONDO:equivalentTo | T-Cell Prolymphocytic Leukemia, Cerebriform Cell Variant | | MONDO:0019468 | -| MONDO:0856887 | chronic lymphocytic leukemia with plasmacytoid differentiation | NCIT:C36272 | MONDO:equivalentTo | Chronic Lymphocytic Leukemia with Plasmacytoid Differentiation | | MONDO:0004948 | -| MONDO:0856891 | prostate carcinoma metastatic in the bone | NCIT:C36308 | MONDO:equivalentTo | Prostate Carcinoma Metastatic in the Bone | | MONDO:0004956|MONDO:0024884 | -| MONDO:0856897 | oncocytic adenocarcinoma | NCIT:C3679 | MONDO:equivalentTo | Oncocytic Adenocarcinoma | | MONDO:0004970|MONDO:0010795 | -| MONDO:0856898 | sweat gland tubular carcinoma | NCIT:C3682 | MONDO:equivalentTo | Sweat Gland Tubular Carcinoma | | MONDO:0005524|MONDO:0005606 | -| MONDO:0856899 | trabecular adenoma | NCIT:C3688 | MONDO:equivalentTo | Trabecular Adenoma | | MONDO:0004972 | -| MONDO:0856900 | carcinomatosis | NCIT:C3693 | MONDO:equivalentTo | Carcinomatosis | | MONDO:0024879 | -| MONDO:0856901 | papillary fibroelastoma | NCIT:C3695 | MONDO:equivalentTo | Papillary Fibroelastoma | | MONDO:0021505 | -| MONDO:0856902 | meningiomatosis | NCIT:C3707 | MONDO:equivalentTo | Meningiomatosis | | MONDO:0016642 | -| MONDO:0856905 | chronic lymphocytic leukemia with immunoglobulin heavy chain variable-region gene somatic hypermutation | NCIT:C37202 | MONDO:equivalentTo | Chronic Lymphocytic Leukemia with Immunoglobulin Heavy Chain Variable-Region Gene Somatic Hypermutation | | MONDO:0004152|MONDO:0004948 | -| MONDO:0856906 | chronic lymphocytic leukemia with unmutated immunoglobulin heavy chain variable-region gene | NCIT:C37205 | MONDO:equivalentTo | Chronic Lymphocytic Leukemia with Unmutated Immunoglobulin Heavy Chain Variable-Region Gene | | MONDO:0004478|MONDO:0004948 | -| MONDO:0856907 | high grade b-cell lymphoma with blastoid morphologic features | NCIT:C37209 | MONDO:equivalentTo | High Grade B-Cell Lymphoma with Blastoid Morphologic Features | | MONDO:0044889 | -| MONDO:0856911 | benign kidney mixed epithelial and stromal tumor | NCIT:C37264 | MONDO:equivalentTo | Benign Kidney Mixed Epithelial and Stromal Tumor | | MONDO:0002513|MONDO:0002386 | -| MONDO:0856912 | atypical small acinar proliferation of the prostate gland | NCIT:C37268 | MONDO:equivalentTo | Atypical Small Acinar Proliferation of the Prostate Gland | | MONDO:0021259 | -| MONDO:0856914 | head and neck basaloid carcinoma | NCIT:C37290 | MONDO:equivalentTo | Head and Neck Basaloid Carcinoma | | MONDO:0003486|MONDO:0010150 | -| MONDO:0856915 | mixed mesodermal (mullerian) tumor | NCIT:C3730 | MONDO:equivalentTo | Mixed Mesodermal (Mullerian) Tumor | | MONDO:0021148|MONDO:0021043 | -| MONDO:0856917 | abdominal (mesenteric) fibromatosis | NCIT:C3741 | MONDO:equivalentTo | Abdominal (Mesenteric) Fibromatosis | | MONDO:0007608 | -| MONDO:0856918 | adenomatous polyp | NCIT:C3764 | MONDO:equivalentTo | Adenomatous Polyp | | MONDO:0006180|MONDO:0021075 | -| MONDO:0856920 | giant cell carcinoma | NCIT:C3779 | MONDO:equivalentTo | Giant Cell Carcinoma | | MONDO:0005232|MONDO:0002402|MONDO:0005617 | -| MONDO:0856923 | renal cell carcinoma associated with t(x;1)(p11.2;q21) | NCIT:C37872 | MONDO:equivalentTo | Renal Cell Carcinoma Associated with t(X;1)(p11.2;q21) | | MONDO:0006397 | -| MONDO:0856924 | renal cell carcinoma associated with t(x;1)(p11.2;p34) | NCIT:C37874 | MONDO:equivalentTo | Renal Cell Carcinoma Associated with t(X;1)(p11.2;p34) | | MONDO:0006397 | -| MONDO:0856925 | renal cell carcinoma associated with t(x;17)(p11.2;q25) | NCIT:C37876 | MONDO:equivalentTo | Renal Cell Carcinoma Associated with t(X;17)(p11.2;q25) | | MONDO:0006397 | -| MONDO:0856927 | angiofibroma | NCIT:C3799 | MONDO:equivalentTo | Angiofibroma | | MONDO:0005167 | -| MONDO:0856930 | dermatofibrosarcoma protuberans with myoid differentiation | NCIT:C38105 | MONDO:equivalentTo | Dermatofibrosarcoma Protuberans with Myoid Differentiation | | MONDO:0011934 | -| MONDO:0856931 | myxoid dermatofibrosarcoma protuberans | NCIT:C38106 | MONDO:equivalentTo | Myxoid Dermatofibrosarcoma Protuberans | | MONDO:0011934 | -| MONDO:0856932 | dedifferentiated dermatofibrosarcoma protuberans | NCIT:C38107 | MONDO:equivalentTo | Dedifferentiated Dermatofibrosarcoma Protuberans | | MONDO:0011934 | -| MONDO:0856933 | dermatofibrosarcoma protuberans with giant cell fibroblastoma-like differentiation | NCIT:C38108 | MONDO:equivalentTo | Dermatofibrosarcoma Protuberans with Giant Cell Fibroblastoma-Like Differentiation | | MONDO:0011934 | -| MONDO:0856934 | skin basal cell carcinoma with adnexal differentiation | NCIT:C38109 | MONDO:equivalentTo | Skin Basal Cell Carcinoma with Adnexal Differentiation | | MONDO:0005341 | -| MONDO:0856938 | clear cell myomelanocytic tumor of the falciform ligament/ligamentum teres | NCIT:C38154 | MONDO:equivalentTo | Clear Cell Myomelanocytic Tumor of the Falciform Ligament/Ligamentum Teres | | MONDO:0006359 | -| MONDO:0856939 | metachronous malignant neoplasm | NCIT:C38156 | MONDO:equivalentTo | Metachronous Malignant Neoplasm | | MONDO:0004992 | -| MONDO:0856940 | plasmablastic lymphoma of mucosa site | NCIT:C38159 | MONDO:equivalentTo | Plasmablastic Lymphoma of Mucosa Site | | MONDO:0017347 | -| MONDO:0856941 | digestive system non-hodgkin lymphoma | NCIT:C38161 | MONDO:equivalentTo | Digestive System Non-Hodgkin Lymphoma | | MONDO:0004699|MONDO:0018908 | -| MONDO:0856942 | digestive system hodgkin lymphoma | NCIT:C38163 | MONDO:equivalentTo | Digestive System Hodgkin Lymphoma | | MONDO:0004952|MONDO:0004699 | -| MONDO:0856943 | acute myeloid leukemia with stat5b-rara | NCIT:C38377 | MONDO:equivalentTo | Acute Myeloid Leukemia with STAT5B-RARA | | MONDO:0100375 | -| MONDO:0856945 | traditional serrated adenoma | NCIT:C38458 | MONDO:equivalentTo | Traditional Serrated Adenoma | | MONDO:0006180 | -| MONDO:0856947 | benign female breast neoplasm | NCIT:C3848 | MONDO:equivalentTo | Benign Female Breast Neoplasm | | MONDO:0000620 | -| MONDO:0856948 | aggravated malignant neoplasm | NCIT:C3851 | MONDO:equivalentTo | Aggravated Malignant Neoplasm | | MONDO:0004992 | -| MONDO:0856949 | thyroid gland sclerosing mucoepidermoid carcinoma with eosinophilia | NCIT:C38763 | MONDO:equivalentTo | Thyroid Gland Sclerosing Mucoepidermoid Carcinoma with Eosinophilia | | MONDO:0006463 | -| MONDO:0856951 | grade 1 meningioma | NCIT:C38936 | MONDO:equivalentTo | Grade 1 Meningioma | | MONDO:0016642 | -| MONDO:0856952 | compound nevus | NCIT:C3901 | MONDO:equivalentTo | Compound Nevus | | MONDO:0005073 | -| MONDO:0856963 | t-cell large granular lymphocyte leukemia, common variant | NCIT:C39584 | MONDO:equivalentTo | T-Cell Large Granular Lymphocyte Leukemia, Common Variant | | MONDO:0019469 | -| MONDO:0856964 | t-cell large granular lymphocyte leukemia expressing the t-cell receptor gamma-delta | NCIT:C39586 | MONDO:equivalentTo | T-Cell Large Granular Lymphocyte Leukemia Expressing the T-Cell Receptor Gamma-Delta | | MONDO:0019469 | -| MONDO:0856966 | anaplastic large cell lymphoma, giant cell rich subtype | NCIT:C39674 | MONDO:equivalentTo | Anaplastic Large Cell Lymphoma, Giant Cell Rich Subtype | | MONDO:0020325 | -| MONDO:0856967 | anaplastic large cell lymphoma, sarcomatoid subtype | NCIT:C39675 | MONDO:equivalentTo | Anaplastic Large Cell Lymphoma, Sarcomatoid Subtype | | MONDO:0020325 | -| MONDO:0856968 | anaplastic large cell lymphoma, signet ring-like subtype | NCIT:C39676 | MONDO:equivalentTo | Anaplastic Large Cell Lymphoma, Signet Ring-Like Subtype | | MONDO:0020325 | -| MONDO:0856969 | pleomorphic variant mantle cell lymphoma | NCIT:C39747 | MONDO:equivalentTo | Pleomorphic Variant Mantle Cell Lymphoma | | MONDO:0018876 | -| MONDO:0856970 | type ii endometrial adenocarcinoma | NCIT:C39749 | MONDO:equivalentTo | Type II Endometrial Adenocarcinoma | | MONDO:0005461 | -| MONDO:0856971 | glioblastoma, idh-wildtype | NCIT:C39750 | MONDO:equivalentTo | Glioblastoma, IDH-Wildtype | | MONDO:0018177 | -| MONDO:0856972 | secondary glioblastoma | NCIT:C39751 | MONDO:equivalentTo | Secondary Glioblastoma | | MONDO:0018177 | -| MONDO:0856973 | solid/multicystic ameloblastoma | NCIT:C39755 | MONDO:equivalentTo | Solid/Multicystic Ameloblastoma | | MONDO:0017795 | -| MONDO:0856974 | unicystic ameloblastoma | NCIT:C39756 | MONDO:equivalentTo | Unicystic Ameloblastoma | | MONDO:0021077|MONDO:0017795 | -| MONDO:0856975 | renal cell carcinoma with constitutional chromosome 3 translocations | NCIT:C39790 | MONDO:equivalentTo | Renal Cell Carcinoma with Constitutional Chromosome 3 Translocations | | MONDO:0003008 | -| MONDO:0856976 | renal cell carcinoma associated with inv(x)(p11;q12) | NCIT:C39802 | MONDO:equivalentTo | Renal Cell Carcinoma Associated with inv(X)(p11;q12) | | MONDO:0006397 | -| MONDO:0856980 | invasive bladder sarcomatoid urothelial carcinoma with heterologous elements | NCIT:C39825 | MONDO:equivalentTo | Invasive Bladder Sarcomatoid Urothelial Carcinoma with Heterologous Elements | | MONDO:0004278 | -| MONDO:0856981 | invasive bladder sarcomatoid urothelial carcinoma without heterologous elements | NCIT:C39826 | MONDO:equivalentTo | Invasive Bladder Sarcomatoid Urothelial Carcinoma without Heterologous Elements | | MONDO:0004278 | -| MONDO:0856984 | bladder adenocarcinoma, not otherwise specified | NCIT:C39836 | MONDO:equivalentTo | Bladder Adenocarcinoma, Not Otherwise Specified | | MONDO:0002751 | -| MONDO:0856986 | human papillomavirus-related urethral squamous cell carcinoma | NCIT:C39862 | MONDO:equivalentTo | Human Papillomavirus-Related Urethral Squamous Cell Carcinoma | | MONDO:0002764|MONDO:0020657 | -| MONDO:0856987 | bladder mucosa-associated lymphoid tissue lymphoma | NCIT:C39878 | MONDO:equivalentTo | Bladder Mucosa-Associated Lymphoid Tissue Lymphoma | | MONDO:0001381|MONDO:0007650 | -| MONDO:0856988 | prostate acinar adenocarcinoma, atrophic pattern | NCIT:C39880 | MONDO:equivalentTo | Prostate Acinar Adenocarcinoma, Atrophic Pattern | | MONDO:0002493 | -| MONDO:0856989 | prostate acinar pseudohyperplastic adenocarcinoma | NCIT:C39881 | MONDO:equivalentTo | Prostate Acinar Pseudohyperplastic Adenocarcinoma | | MONDO:0002493 | -| MONDO:0856991 | prostatic duct urothelial carcinoma | NCIT:C39901 | MONDO:equivalentTo | Prostatic Duct Urothelial Carcinoma | | MONDO:0002834 | -| MONDO:0856992 | testicular seminoma with syncytiotrophoblastic cells | NCIT:C39919 | MONDO:equivalentTo | Testicular Seminoma with Syncytiotrophoblastic Cells | | MONDO:0003669 | -| MONDO:0856994 | testicular seminoma with high mitotic index | NCIT:C39920 | MONDO:equivalentTo | Testicular Seminoma with High Mitotic Index | | MONDO:0020633|MONDO:0003669 | -| MONDO:0856995 | testicular spermatocytic tumor with sarcoma | NCIT:C39922 | MONDO:equivalentTo | Testicular Spermatocytic Tumor with Sarcoma | | MONDO:0020513 | -| MONDO:0856996 | monodermal testicular teratoma | NCIT:C39936 | MONDO:equivalentTo | Monodermal Testicular Teratoma | | MONDO:0018193 | -| MONDO:0856997 | testicular sertoli cell tumor, lipid rich variant | NCIT:C39943 | MONDO:equivalentTo | Testicular Sertoli Cell Tumor, Lipid Rich Variant | | MONDO:0020813 | -| MONDO:0856998 | testicular large cell calcifying sertoli cell tumor | NCIT:C39944 | MONDO:equivalentTo | Testicular Large Cell Calcifying Sertoli Cell Tumor | | MONDO:0020808 | -| MONDO:0856999 | testicular sclerosing sertoli cell tumor | NCIT:C39945 | MONDO:equivalentTo | Testicular Sclerosing Sertoli Cell Tumor | | MONDO:0020813 | -| MONDO:0857002 | tumor of the thecoma/fibroma group | NCIT:C39950 | MONDO:equivalentTo | Tumor of the Thecoma/Fibroma Group | | MONDO:0006055 | -| MONDO:0857004 | moderately differentiated ovarian sertoli-leydig cell tumor | NCIT:C39968 | MONDO:equivalentTo | Moderately Differentiated Ovarian Sertoli-Leydig Cell Tumor | | MONDO:0036595 | -| MONDO:0857005 | ovarian sertoli-leydig cell tumor with heterologous elements | NCIT:C39970 | MONDO:equivalentTo | Ovarian Sertoli-Leydig Cell Tumor with Heterologous Elements | | MONDO:0036595 | -| MONDO:0857006 | ovarian retiform sertoli-leydig cell tumor | NCIT:C39971 | MONDO:equivalentTo | Ovarian Retiform Sertoli-Leydig Cell Tumor | | MONDO:0036595 | -| MONDO:0857007 | ovarian sertoli-leydig cell tumor with retiform elements | NCIT:C39974 | MONDO:equivalentTo | Ovarian Sertoli-Leydig Cell Tumor with Retiform Elements | | MONDO:0036595 | -| MONDO:0857008 | ovarian stromal-leydig cell tumor | NCIT:C39977 | MONDO:equivalentTo | Ovarian Stromal-Leydig Cell Tumor | | MONDO:0024387|MONDO:0020807 | -| MONDO:0857009 | ovarian sex cord-stromal tumor, not otherwise specified | NCIT:C39978 | MONDO:equivalentTo | Ovarian Sex Cord-Stromal Tumor, Not Otherwise Specified | | MONDO:0021657 | -| MONDO:0857012 | malignant ovarian teratoma | NCIT:C39995 | MONDO:equivalentTo | Malignant Ovarian Teratoma | | MONDO:0018171|MONDO:0003514|MONDO:0003821 | -| MONDO:0857014 | borderline ovarian serous tumor/atypical proliferative ovarian serous tumor with microinvasion | NCIT:C40027 | MONDO:equivalentTo | Borderline Ovarian Serous Tumor/Atypical Proliferative Ovarian Serous Tumor with Microinvasion | | MONDO:0037255 | -| MONDO:0857015 | borderline ovarian serous adenofibroma | NCIT:C40028 | MONDO:equivalentTo | Borderline Ovarian Serous Adenofibroma | | MONDO:0024886|MONDO:0003462|MONDO:0020662 | -| MONDO:0857016 | borderline ovarian mucinous tumor | NCIT:C40036 | MONDO:equivalentTo | Borderline Ovarian Mucinous Tumor | | MONDO:0003756|MONDO:0016093 | -| MONDO:0857017 | ovarian mucinous cystic tumor with mural nodules | NCIT:C40042 | MONDO:equivalentTo | Ovarian Mucinous Cystic Tumor with Mural Nodules | | MONDO:0003756 | -| MONDO:0857018 | ovarian mucinous cystic tumor associated with pseudomyxoma peritonei | NCIT:C40043 | MONDO:equivalentTo | Ovarian Mucinous Cystic Tumor Associated with Pseudomyxoma Peritonei | | MONDO:0003756 | -| MONDO:0857022 | borderline ovarian clear cell tumor | NCIT:C40080 | MONDO:equivalentTo | Borderline Ovarian Clear Cell Tumor | | MONDO:0021144|MONDO:0016093 | -| MONDO:0857025 | fallopian tube serous neoplasm | NCIT:C40102 | MONDO:equivalentTo | Fallopian Tube Serous Neoplasm | | MONDO:0037256|MONDO:0021092 | -| MONDO:0857028 | fallopian tube endometrioid polyp | NCIT:C40115 | MONDO:equivalentTo | Fallopian Tube Endometrioid Polyp | | MONDO:0021075|MONDO:0021576 | -| MONDO:0857029 | fallopian tube metaplastic papillary tumor | NCIT:C40116 | MONDO:equivalentTo | Fallopian Tube Metaplastic Papillary Tumor | | MONDO:0021096|MONDO:0000645|MONDO:0036976 | -| MONDO:0857030 | fallopian tube soft tissue neoplasm | NCIT:C40126 | MONDO:equivalentTo | Fallopian Tube Soft Tissue Neoplasm | | MONDO:0006424|MONDO:0021092 | -| MONDO:0857031 | type i endometrial adenocarcinoma | NCIT:C40145 | MONDO:equivalentTo | Type I Endometrial Adenocarcinoma | | MONDO:0005461 | -| MONDO:0857033 | figo grade 1 endometrial mucinous adenocarcinoma | NCIT:C40149 | MONDO:equivalentTo | FIGO Grade 1 Endometrial Mucinous Adenocarcinoma | | MONDO:0002747 | -| MONDO:0857034 | figo grade 2 endometrial mucinous adenocarcinoma | NCIT:C40150 | MONDO:equivalentTo | FIGO Grade 2 Endometrial Mucinous Adenocarcinoma | | MONDO:0002747 | -| MONDO:0857035 | figo grade 3 endometrial mucinous adenocarcinoma | NCIT:C40151 | MONDO:equivalentTo | FIGO Grade 3 Endometrial Mucinous Adenocarcinoma | | MONDO:0002747 | -| MONDO:0857036 | uterine corpus leiomyoma, mitotically active variant | NCIT:C40162 | MONDO:equivalentTo | Uterine Corpus Leiomyoma, Mitotically Active Variant | | MONDO:0007886 | -| MONDO:0857037 | uterine corpus soft tissue neoplasm | NCIT:C40179 | MONDO:equivalentTo | Uterine Corpus Soft Tissue Neoplasm | | MONDO:0021254|MONDO:0006424 | -| MONDO:0857039 | cervical squamous neoplasm | NCIT:C40195 | MONDO:equivalentTo | Cervical Squamous Neoplasm | | MONDO:0002532|MONDO:0021230 | -| MONDO:0857040 | cervical glandular neoplasm | NCIT:C40210 | MONDO:equivalentTo | Cervical Glandular Neoplasm | | MONDO:0024276|MONDO:0021230 | -| MONDO:0857041 | cervical soft tissue neoplasm | NCIT:C40216 | MONDO:equivalentTo | Cervical Soft Tissue Neoplasm | | MONDO:0006424|MONDO:0021230 | -| MONDO:0857043 | cervical mixed epithelial and mesenchymal neoplasm | NCIT:C40226 | MONDO:equivalentTo | Cervical Mixed Epithelial and Mesenchymal Neoplasm | | MONDO:0021043|MONDO:0021230 | -| MONDO:0857045 | vaginal keratinizing squamous cell carcinoma | NCIT:C40243 | MONDO:equivalentTo | Vaginal Keratinizing Squamous Cell Carcinoma | | MONDO:0005056|MONDO:0006490 | -| MONDO:0857046 | vaginal basaloid carcinoma | NCIT:C40245 | MONDO:equivalentTo | Vaginal Basaloid Carcinoma | | MONDO:0003486|MONDO:0006490 | -| MONDO:0857047 | vaginal endometrioid adenocarcinoma | NCIT:C40251 | MONDO:equivalentTo | Vaginal Endometrioid Adenocarcinoma | | MONDO:0020653|MONDO:0005026 | -| MONDO:0857048 | vaginal mucinous adenocarcinoma | NCIT:C40252 | MONDO:equivalentTo | Vaginal Mucinous Adenocarcinoma | | MONDO:0020653|MONDO:0004957 | -| MONDO:0857049 | vaginal mesonephric adenocarcinoma | NCIT:C40253 | MONDO:equivalentTo | Vaginal Mesonephric Adenocarcinoma | | MONDO:0020653|MONDO:0005613 | -| MONDO:0857050 | vaginal adenosquamous carcinoma | NCIT:C40260 | MONDO:equivalentTo | Vaginal Adenosquamous Carcinoma | | MONDO:0015867|MONDO:0006074 | -| MONDO:0857051 | vaginal adenoid basal carcinoma | NCIT:C40262 | MONDO:equivalentTo | Vaginal Adenoid Basal Carcinoma | | MONDO:0015867 | -| MONDO:0857052 | vaginal undifferentiated carcinoma | NCIT:C40264 | MONDO:equivalentTo | Vaginal Undifferentiated Carcinoma | | MONDO:0015867|MONDO:0005617 | -| MONDO:0857053 | vaginal soft tissue neoplasm | NCIT:C40265 | MONDO:equivalentTo | Vaginal Soft Tissue Neoplasm | | MONDO:0021050|MONDO:0006424 | -| MONDO:0857056 | vaginal mixed epithelial and mesenchymal neoplasm | NCIT:C40274 | MONDO:equivalentTo | Vaginal Mixed Epithelial and Mesenchymal Neoplasm | | MONDO:0021043|MONDO:0021050 | -| MONDO:0857057 | malignant vaginal mixed tumor resembling synovial sarcoma | NCIT:C40279 | MONDO:equivalentTo | Malignant Vaginal Mixed Tumor Resembling Synovial Sarcoma | | MONDO:0037746 | -| MONDO:0857058 | vulvar squamous cell carcinoma with tumor giant cells | NCIT:C40289 | MONDO:equivalentTo | Vulvar Squamous Cell Carcinoma with Tumor Giant Cells | | MONDO:0024609 | -| MONDO:0857059 | vulvar neoplasm of skin appendage origin | NCIT:C40303 | MONDO:equivalentTo | Vulvar Neoplasm of Skin Appendage Origin | | MONDO:0002297|MONDO:0021049 | -| MONDO:0857061 | vulvar soft tissue neoplasm | NCIT:C40316 | MONDO:equivalentTo | Vulvar Soft Tissue Neoplasm | | MONDO:0021049|MONDO:0006424 | -| MONDO:0857062 | superficial angiomyxoma | NCIT:C40323 | MONDO:equivalentTo | Superficial Angiomyxoma | | MONDO:0006086 | -| MONDO:0857067 | vulvar melanocytic neoplasm | NCIT:C40335 | MONDO:equivalentTo | Vulvar Melanocytic Neoplasm | | MONDO:0021143|MONDO:0021049 | -| MONDO:0857071 | breast carcinoma with osteoclast-like stromal giant cells | NCIT:C40349 | MONDO:equivalentTo | Breast Carcinoma with Osteoclast-Like Stromal Giant Cells | | MONDO:0004953 | -| MONDO:0857072 | breast carcinoma with choriocarcinomatous features | NCIT:C40350 | MONDO:equivalentTo | Breast Carcinoma with Choriocarcinomatous Features | | MONDO:0004953 | -| MONDO:0857073 | breast carcinoma with melanotic features | NCIT:C40351 | MONDO:equivalentTo | Breast Carcinoma with Melanotic Features | | MONDO:0004953 | -| MONDO:0857075 | low grade breast adenosquamous carcinoma | NCIT:C40362 | MONDO:equivalentTo | Low Grade Breast Adenosquamous Carcinoma | | MONDO:0003548 | -| MONDO:0857076 | acute myeloid leukemia arising from previous myelodysplastic syndrome | NCIT:C4037 | MONDO:equivalentTo | Acute Myeloid Leukemia Arising from Previous Myelodysplastic Syndrome | | MONDO:0019457 | -| MONDO:0857078 | postradiation breast angiosarcoma | NCIT:C40378 | MONDO:equivalentTo | Postradiation Breast Angiosarcoma | | MONDO:0003024 | -| MONDO:0857080 | salivary gland myoepithelial tumor | NCIT:C40393 | MONDO:equivalentTo | Salivary Gland Myoepithelial Tumor | | MONDO:0002380|MONDO:0021357 | -| MONDO:0857083 | breast soft tissue neoplasm | NCIT:C40406 | MONDO:equivalentTo | Breast Soft Tissue Neoplasm | | MONDO:0006424|MONDO:0021100 | -| MONDO:0857084 | breast pleomorphic adenoma | NCIT:C40408 | MONDO:equivalentTo | Breast Pleomorphic Adenoma | | MONDO:0008401|MONDO:0002058 | -| MONDO:0857089 | ovarian sex cord-stromal tumor associated with peutz-jeghers syndrome | NCIT:C40436 | MONDO:equivalentTo | Ovarian Sex Cord-Stromal Tumor Associated with Peutz-Jeghers Syndrome | | MONDO:0021657 | -| MONDO:0857091 | esophageal polyp | NCIT:C4057 | MONDO:equivalentTo | Esophageal Polyp | | MONDO:0021459|MONDO:0024292 | -| MONDO:0857095 | polycythemia vera, polycythemic phase | NCIT:C41232 | MONDO:equivalentTo | Polycythemia Vera, Polycythemic Phase | | MONDO:0009891 | -| MONDO:0857096 | polycythemia vera, post-polycythemic myelofibrosis phase | NCIT:C41233 | MONDO:equivalentTo | Polycythemia Vera, Post-Polycythemic Myelofibrosis Phase | | MONDO:0009891 | -| MONDO:0857097 | overt primary myelofibrosis | NCIT:C41238 | MONDO:equivalentTo | Overt Primary Myelofibrosis | | MONDO:0009692 | -| MONDO:0857098 | metastatic adenocarcinoma | NCIT:C4124 | MONDO:equivalentTo | Metastatic Adenocarcinoma | | MONDO:0004970|MONDO:0024879 | -| MONDO:0857100 | solid carcinoma | NCIT:C4137 | MONDO:equivalentTo | Solid Carcinoma | | MONDO:0004993 | -| MONDO:0857101 | basophilic adenocarcinoma | NCIT:C4150 | MONDO:equivalentTo | Basophilic Adenocarcinoma | | MONDO:0004970 | -| MONDO:0857102 | juxtaglomerular cell tumor | NCIT:C4162 | MONDO:equivalentTo | Juxtaglomerular Cell Tumor | | MONDO:0002513 | -| MONDO:0857103 | adrenal cortical compact cell adenoma | NCIT:C4163 | MONDO:equivalentTo | Adrenal Cortical Compact Cell Adenoma | | MONDO:0003924 | -| MONDO:0857104 | pigmented adrenal cortical adenoma | NCIT:C4164 | MONDO:equivalentTo | Pigmented Adrenal Cortical Adenoma | | MONDO:0003924 | -| MONDO:0857105 | adrenal cortical clear cell adenoma | NCIT:C4165 | MONDO:equivalentTo | Adrenal Cortical Clear Cell Adenoma | | MONDO:0003924|MONDO:0003426 | -| MONDO:0857106 | adrenal cortical glomerulosa cell adenoma | NCIT:C4166 | MONDO:equivalentTo | Adrenal Cortical Glomerulosa Cell Adenoma | | MONDO:0003924 | -| MONDO:0857107 | adrenal cortical mixed cell adenoma | NCIT:C4167 | MONDO:equivalentTo | Adrenal Cortical Mixed Cell Adenoma | | MONDO:0003421|MONDO:0003924 | -| MONDO:0857109 | papillary serous cystadenoma | NCIT:C4180 | MONDO:equivalentTo | Papillary Serous Cystadenoma | | MONDO:0005177|MONDO:0021091 | -| MONDO:0857110 | serous surface papillary carcinoma | NCIT:C4182 | MONDO:equivalentTo | Serous Surface Papillary Carcinoma | | MONDO:0005278|MONDO:0002512 | -| MONDO:0857111 | papillary mucinous cystadenoma | NCIT:C4184 | MONDO:equivalentTo | Papillary Mucinous Cystadenoma | | MONDO:0021091|MONDO:0006859 | -| MONDO:0857112 | gliomatosis cerebri type i | NCIT:C41842 | MONDO:equivalentTo | Gliomatosis Cerebri Type I | | MONDO:0016683 | -| MONDO:0857113 | gliomatosis cerebri type ii | NCIT:C41843 | MONDO:equivalentTo | Gliomatosis Cerebri Type II | | MONDO:0016683 | -| MONDO:0857115 | thyroid gland medullary carcinoma with amyloid stroma | NCIT:C4193 | MONDO:equivalentTo | Thyroid Gland Medullary Carcinoma with Amyloid Stroma | | MONDO:0015277 | -| MONDO:0857117 | acinar cell neoplasm | NCIT:C4197 | MONDO:equivalentTo | Acinar Cell Neoplasm | | MONDO:0024276 | -| MONDO:0857118 | ovarian luteinized thecoma | NCIT:C4203 | MONDO:equivalentTo | Ovarian Luteinized Thecoma | | MONDO:0037253 | -| MONDO:0857119 | undifferentiated neuroblastoma | NCIT:C42046 | MONDO:equivalentTo | Undifferentiated Neuroblastoma | | MONDO:0005072 | -| MONDO:0857120 | poorly differentiated neuroblastoma | NCIT:C42047 | MONDO:equivalentTo | Poorly Differentiated Neuroblastoma | | MONDO:0005072 | -| MONDO:0857121 | malignant granulosa cell tumor | NCIT:C4205 | MONDO:equivalentTo | Malignant Granulosa Cell Tumor | | MONDO:0006036 | -| MONDO:0857122 | maturing ganglioneuroma | NCIT:C42064 | MONDO:equivalentTo | Maturing Ganglioneuroma | | MONDO:0005033 | -| MONDO:0857123 | mature ganglioneuroma | NCIT:C42065 | MONDO:equivalentTo | Mature Ganglioneuroma | | MONDO:0005033 | -| MONDO:0857125 | ovarian sex cord tumor with annular tubules | NCIT:C4208 | MONDO:equivalentTo | Ovarian Sex Cord Tumor with Annular Tubules | | MONDO:0021657 | -| MONDO:0857126 | well differentiated ovarian sertoli-leydig cell tumor | NCIT:C4209 | MONDO:equivalentTo | Well Differentiated Ovarian Sertoli-Leydig Cell Tumor | | MONDO:0036595 | -| MONDO:0857127 | poorly differentiated ovarian sertoli-leydig cell tumor | NCIT:C4210 | MONDO:equivalentTo | Poorly Differentiated Ovarian Sertoli-Leydig Cell Tumor | | MONDO:0018172|MONDO:0036595 | -| MONDO:0857128 | ovarian steroid cell tumor | NCIT:C4215 | MONDO:equivalentTo | Ovarian Steroid Cell Tumor | | MONDO:0021657 | -| MONDO:0857129 | balloon cell nevus | NCIT:C4226 | MONDO:equivalentTo | Balloon Cell Nevus | | MONDO:0044794 | -| MONDO:0857130 | regressing melanoma | NCIT:C4228 | MONDO:equivalentTo | Regressing Melanoma | | MONDO:0005105 | -| MONDO:0857131 | neuronevus | NCIT:C4229 | MONDO:equivalentTo | Neuronevus | | MONDO:0006813 | -| MONDO:0857132 | junctional nevus | NCIT:C4231 | MONDO:equivalentTo | Junctional Nevus | | MONDO:0005073 | -| MONDO:0857133 | melanoma in junctional nevus | NCIT:C4232 | MONDO:equivalentTo | Melanoma in Junctional Nevus | | MONDO:0005012 | -| MONDO:0857134 | type a spindle cell melanoma | NCIT:C4238 | MONDO:equivalentTo | Type A Spindle Cell Melanoma | | MONDO:0006427 | -| MONDO:0857135 | type b spindle cell melanoma | NCIT:C4239 | MONDO:equivalentTo | Type B Spindle Cell Melanoma | | MONDO:0006427 | -| MONDO:0857136 | melanoma arising from blue nevus | NCIT:C4240 | MONDO:equivalentTo | Melanoma Arising from Blue Nevus | | MONDO:0005012 | -| MONDO:0857137 | cellular blue nevus | NCIT:C4241 | MONDO:equivalentTo | Cellular Blue Nevus | | MONDO:0006680 | -| MONDO:0857138 | fibrolipoma | NCIT:C4249 | MONDO:equivalentTo | Fibrolipoma | | MONDO:0005106 | -| MONDO:0857139 | fibromyxolipoma | NCIT:C4251 | MONDO:equivalentTo | Fibromyxolipoma | | MONDO:0005106 | -| MONDO:0857140 | lipoblastomatosis | NCIT:C4255 | MONDO:equivalentTo | Lipoblastomatosis | | MONDO:0044983 | -| MONDO:0857141 | sporadic retinoblastoma | NCIT:C42596 | MONDO:equivalentTo | Sporadic Retinoblastoma | | MONDO:0008380 | -| MONDO:0857142 | low grade endometrioid stromal sarcoma | NCIT:C4263 | MONDO:equivalentTo | Low Grade Endometrioid Stromal Sarcoma | | MONDO:0006745 | -| MONDO:0857144 | acute myelomonocytic leukemia without abnormal eosinophils | NCIT:C42779 | MONDO:equivalentTo | Acute Myelomonocytic Leukemia without Abnormal Eosinophils | | MONDO:0018871 | -| MONDO:0857145 | pericardial solitary fibrous tumor | NCIT:C4281 | MONDO:equivalentTo | Pericardial Solitary Fibrous Tumor | | MONDO:0016238|MONDO:0021381 | -| MONDO:0857146 | benign hemangiopericytoma | NCIT:C4300 | MONDO:equivalentTo | Benign Hemangiopericytoma | | MONDO:0005094 | -| MONDO:0857147 | benign odontogenic neoplasm | NCIT:C4306 | MONDO:equivalentTo | Benign Odontogenic Neoplasm | | MONDO:0021445|MONDO:0021192 | -| MONDO:0857152 | pure cutaneous mastocytosis | NCIT:C43277 | MONDO:equivalentTo | Pure Cutaneous Mastocytosis | | MONDO:0019023 | -| MONDO:0857155 | germinative follicular epithelium neoplasm | NCIT:C43311 | MONDO:equivalentTo | Germinative Follicular Epithelium Neoplasm | | MONDO:0003413|MONDO:0021634 | -| MONDO:0857156 | mixed epithelial and mesenchymal hair follicle neoplasm | NCIT:C43312 | MONDO:equivalentTo | Mixed Epithelial and Mesenchymal Hair Follicle Neoplasm | | MONDO:0003413|MONDO:0021043 | -| MONDO:0857160 | outer hair sheath and infundibulum neoplasm | NCIT:C43324 | MONDO:equivalentTo | Outer Hair Sheath and Infundibulum Neoplasm | | MONDO:0003413 | -| MONDO:0857163 | superficial epithelioma with sebaceous differentiation | NCIT:C43334 | MONDO:equivalentTo | Superficial Epithelioma with Sebaceous Differentiation | | MONDO:0021490 | -| MONDO:0857164 | sebaceoma | NCIT:C43336 | MONDO:equivalentTo | Sebaceoma | | MONDO:0021490 | -| MONDO:0857165 | extraocular cutaneous sebaceous carcinoma | NCIT:C43341 | MONDO:equivalentTo | Extraocular Cutaneous Sebaceous Carcinoma | | MONDO:0006962 | -| MONDO:0857166 | apocrine hidrocystoma | NCIT:C43342 | MONDO:equivalentTo | Apocrine Hidrocystoma | | MONDO:0002804|MONDO:0006787 | -| MONDO:0857167 | cylindrocarcinoma | NCIT:C43344 | MONDO:equivalentTo | Cylindrocarcinoma | | MONDO:0005524|MONDO:0024878 | -| MONDO:0857168 | ductal eccrine carcinoma with spindle cell elements | NCIT:C43346 | MONDO:equivalentTo | Ductal Eccrine Carcinoma with Spindle Cell Elements | | MONDO:0024245 | -| MONDO:0857169 | squamoid eccrine ductal carcinoma | NCIT:C43347 | MONDO:equivalentTo | Squamoid Eccrine Ductal Carcinoma | | MONDO:0024245 | -| MONDO:0857170 | ductal eccrine carcinoma with abundant fibromyxoid stroma | NCIT:C43349 | MONDO:equivalentTo | Ductal Eccrine Carcinoma with Abundant Fibromyxoid Stroma | | MONDO:0024245 | -| MONDO:0857171 | sporadic cylindroma | NCIT:C43351 | MONDO:equivalentTo | Sporadic Cylindroma | | MONDO:0021812 | -| MONDO:0857172 | classical poroma | NCIT:C43353 | MONDO:equivalentTo | Classical Poroma | | MONDO:0006738 | -| MONDO:0857173 | porocarcinoma in situ | NCIT:C43354 | MONDO:equivalentTo | Porocarcinoma In Situ | | MONDO:0006189 | -| MONDO:0857174 | aleukemic lymphoid leukemia | NCIT:C4343 | MONDO:equivalentTo | Aleukemic Lymphoid Leukemia | | MONDO:0005402|MONDO:0003730 | -| MONDO:0857175 | sporadic gastric adenocarcinoma | NCIT:C43527 | MONDO:equivalentTo | Sporadic Gastric Adenocarcinoma | | MONDO:0005036 | -| MONDO:0857177 | small intestinal adenosquamous carcinoma | NCIT:C43535 | MONDO:equivalentTo | Small Intestinal Adenosquamous Carcinoma | | MONDO:0005522|MONDO:0006074 | -| MONDO:0857178 | small intestinal mucinous adenocarcinoma | NCIT:C43536 | MONDO:equivalentTo | Small Intestinal Mucinous Adenocarcinoma | | MONDO:0003198|MONDO:0004957 | -| MONDO:0857179 | small intestinal medullary carcinoma | NCIT:C43537 | MONDO:equivalentTo | Small Intestinal Medullary Carcinoma | | MONDO:0005522 | -| MONDO:0857180 | small intestinal undifferentiated carcinoma | NCIT:C43538 | MONDO:equivalentTo | Small Intestinal Undifferentiated Carcinoma | | MONDO:0005522|MONDO:0005617 | -| MONDO:0857181 | pituitary neuroendocrine tumor/microadenoma | NCIT:C43541 | MONDO:equivalentTo | Pituitary Neuroendocrine Tumor/Microadenoma | | MONDO:0006373 | -| MONDO:0857182 | pituitary neuroendocrine tumor/macroadenoma | NCIT:C43542 | MONDO:equivalentTo | Pituitary Neuroendocrine Tumor/Macroadenoma | | MONDO:0006373 | -| MONDO:0857183 | small intestinal signet ring cell carcinoma | NCIT:C43543 | MONDO:equivalentTo | Small Intestinal Signet Ring Cell Carcinoma | | MONDO:0003198|MONDO:0005092 | -| MONDO:0857184 | appendix tubular adenoma | NCIT:C43546 | MONDO:equivalentTo | Appendix Tubular Adenoma | | MONDO:0006088|MONDO:0024660 | -| MONDO:0857185 | appendix tubulovillous adenoma | NCIT:C43547 | MONDO:equivalentTo | Appendix Tubulovillous Adenoma | | MONDO:0006088|MONDO:0024661 | -| MONDO:0857187 | eyelid squamous papilloma | NCIT:C4355 | MONDO:equivalentTo | Eyelid Squamous Papilloma | | MONDO:0021275|MONDO:0001825 | -| MONDO:0857188 | small intestinal villous adenoma | NCIT:C43551 | MONDO:equivalentTo | Small Intestinal Villous Adenoma | | MONDO:0000502|MONDO:0021303 | -| MONDO:0857189 | appendix signet ring cell carcinoma | NCIT:C43554 | MONDO:equivalentTo | Appendix Signet Ring Cell Carcinoma | | MONDO:0006087|MONDO:0005092 | -| MONDO:0857190 | appendix undifferentiated carcinoma | NCIT:C43556 | MONDO:equivalentTo | Appendix Undifferentiated Carcinoma | | MONDO:0003196|MONDO:0005617 | -| MONDO:0857191 | appendix mixed adenoneuroendocrine carcinoma | NCIT:C43564 | MONDO:equivalentTo | Appendix Mixed Adenoneuroendocrine Carcinoma | | MONDO:0006182|MONDO:0003196 | -| MONDO:0857192 | appendix tubular carcinoid | NCIT:C43565 | MONDO:equivalentTo | Appendix Tubular Carcinoid | | MONDO:0015066 | -| MONDO:0857194 | rectosigmoid adenocarcinoma | NCIT:C43584 | MONDO:equivalentTo | Rectosigmoid Adenocarcinoma | | MONDO:0002424|MONDO:0005008 | -| MONDO:0857195 | colorectal mucinous adenocarcinoma | NCIT:C43585 | MONDO:equivalentTo | Colorectal Mucinous Adenocarcinoma | | MONDO:0005008|MONDO:0004957 | -| MONDO:0857196 | colorectal undifferentiated carcinoma | NCIT:C43591 | MONDO:equivalentTo | Colorectal Undifferentiated Carcinoma | | MONDO:0005617|MONDO:0024331 | -| MONDO:0857198 | gallbladder adenocarcinoma, intestinal-type | NCIT:C43604 | MONDO:equivalentTo | Gallbladder Adenocarcinoma, Intestinal-Type | | MONDO:0006215|MONDO:0006254 | -| MONDO:0857199 | gallbladder clear cell adenocarcinoma | NCIT:C43605 | MONDO:equivalentTo | Gallbladder Clear Cell Adenocarcinoma | | MONDO:0006215|MONDO:0005004 | -| MONDO:0857200 | gallbladder flat biliary intraepithelial neoplasia | NCIT:C43607 | MONDO:equivalentTo | Gallbladder Flat Biliary Intraepithelial Neoplasia | | MONDO:0006218 | -| MONDO:0857201 | gallbladder papillary biliary intraepithelial neoplasia | NCIT:C43609 | MONDO:equivalentTo | Gallbladder Papillary Biliary Intraepithelial Neoplasia | | MONDO:0006218 | -| MONDO:0857202 | pleomorphic hepatocellular carcinoma | NCIT:C43625 | MONDO:equivalentTo | Pleomorphic Hepatocellular Carcinoma | | MONDO:0007256 | -| MONDO:0857203 | sarcomatoid hepatocellular carcinoma | NCIT:C43627 | MONDO:equivalentTo | Sarcomatoid Hepatocellular Carcinoma | | MONDO:0007256 | -| MONDO:0857205 | cherry hemangioma of lip | NCIT:C4372 | MONDO:equivalentTo | Cherry Hemangioma of Lip | | MONDO:0002323|MONDO:0021496 | -| MONDO:0857206 | accessory urethral gland neoplasm | NCIT:C4378 | MONDO:equivalentTo | Accessory Urethral Gland Neoplasm | | MONDO:0021239 | -| MONDO:0857208 | clear cell intrahepatic cholangiocarcinoma | NCIT:C43848 | MONDO:equivalentTo | Clear Cell Intrahepatic Cholangiocarcinoma | | MONDO:0005004|MONDO:0003210 | -| MONDO:0857210 | anogenital papillomaviral intraepithelial neoplasia | NCIT:C4394 | MONDO:equivalentTo | Anogenital Papillomaviral Intraepithelial Neoplasia | | MONDO:0024475 | -| MONDO:0857211 | posterior tongue neoplasm | NCIT:C4400 | MONDO:equivalentTo | Posterior Tongue Neoplasm | | MONDO:0021240 | -| MONDO:0857212 | pyriform fossa neoplasm | NCIT:C4424 | MONDO:equivalentTo | Pyriform Fossa Neoplasm | | MONDO:0021358 | -| MONDO:0857213 | gastric pylorus carcinoma in situ ajcc v6 and v7 | NCIT:C4431 | MONDO:equivalentTo | Gastric Pylorus Carcinoma In Situ AJCC v6 and v7 | | MONDO:0004716|MONDO:0003971 | -| MONDO:0857215 | lung epithelioid hemangioendothelioma | NCIT:C4453 | MONDO:equivalentTo | Lung Epithelioid Hemangioendothelioma | | MONDO:0008903|MONDO:0015523 | -| MONDO:0857216 | dermal duct tumor | NCIT:C4473 | MONDO:equivalentTo | Dermal Duct Tumor | | MONDO:0006738 | -| MONDO:0857217 | cutaneous neural neoplasm | NCIT:C4479 | MONDO:equivalentTo | Cutaneous Neural Neoplasm | | MONDO:0002300|MONDO:0001406 | -| MONDO:0857219 | malignant skin hemangiopericytoma | NCIT:C4493 | MONDO:equivalentTo | Malignant Skin Hemangiopericytoma | | MONDO:0021424|MONDO:0009330 | -| MONDO:0857220 | cockade nevus | NCIT:C4495 | MONDO:equivalentTo | Cockade Nevus | | MONDO:0044794 | -| MONDO:0857222 | common blue nevus | NCIT:C4496 | MONDO:equivalentTo | Common Blue Nevus | | MONDO:0006680 | -| MONDO:0857223 | nevus spilus | NCIT:C4498 | MONDO:equivalentTo | Nevus Spilus | | MONDO:0044794 | -| MONDO:0857224 | benign ovarian epithelial tumor | NCIT:C4510 | MONDO:equivalentTo | Benign Ovarian Epithelial Tumor | | MONDO:0002229|MONDO:0036976|MONDO:0000646 | -| MONDO:0857229 | classical low grade fibromyxoid sarcoma | NCIT:C45210 | MONDO:equivalentTo | Classical Low Grade Fibromyxoid Sarcoma | | MONDO:0006272 | -| MONDO:0857233 | cutaneous hematopoietic and lymphoid cell neoplasm | NCIT:C45240 | MONDO:equivalentTo | Cutaneous Hematopoietic and Lymphoid Cell Neoplasm | | MONDO:0002531|MONDO:0044881 | -| MONDO:0857240 | lacrimal gland pleomorphic adenoma | NCIT:C4542 | MONDO:equivalentTo | Lacrimal Gland Pleomorphic Adenoma | | MONDO:0008401|MONDO:0021488 | -| MONDO:0857244 | orbit capillary hemangioma | NCIT:C4545 | MONDO:equivalentTo | Orbit Capillary Hemangioma | | MONDO:0002407|MONDO:0001974 | -| MONDO:0857245 | orbit hemangiopericytoma | NCIT:C4547 | MONDO:equivalentTo | Orbit Hemangiopericytoma | | MONDO:0005094 | -| MONDO:0857247 | lymphangioma circumscriptum | NCIT:C45485 | MONDO:equivalentTo | Lymphangioma Circumscriptum | | MONDO:0002013 | -| MONDO:0857248 | lung squamous cell carcinoma, papillary variant | NCIT:C45502 | MONDO:equivalentTo | Lung Squamous Cell Carcinoma, Papillary Variant | | MONDO:0005056|MONDO:0002979|MONDO:0056806 | -| MONDO:0857249 | lung squamous cell carcinoma, clear cell variant | NCIT:C45503 | MONDO:equivalentTo | Lung Squamous Cell Carcinoma, Clear Cell Variant | | MONDO:0005056|MONDO:0056806 | -| MONDO:0857250 | lung squamous cell carcinoma, small cell variant | NCIT:C45504 | MONDO:equivalentTo | Lung Squamous Cell Carcinoma, Small Cell Variant | | MONDO:0005056|MONDO:0005097 | -| MONDO:0857251 | lung basaloid squamous cell carcinoma | NCIT:C45507 | MONDO:equivalentTo | Lung Basaloid Squamous Cell Carcinoma | | MONDO:0003486|MONDO:0005056|MONDO:0005097 | -| MONDO:0857252 | lung spindle cell carcinoma | NCIT:C45541 | MONDO:equivalentTo | Lung Spindle Cell Carcinoma | | MONDO:0006279 | -| MONDO:0857253 | lung pleomorphic carcinoma | NCIT:C45542 | MONDO:equivalentTo | Lung Pleomorphic Carcinoma | | MONDO:0006279|MONDO:0003573 | -| MONDO:0857254 | lung carcinosarcoma | NCIT:C45543 | MONDO:equivalentTo | Lung Carcinosarcoma | | MONDO:0006279|MONDO:0002928 | -| MONDO:0857255 | lung typical carcinoid tumor | NCIT:C45550 | MONDO:equivalentTo | Lung Typical Carcinoid Tumor | | MONDO:0006041 | -| MONDO:0857256 | lung atypical carcinoid tumor | NCIT:C45551 | MONDO:equivalentTo | Lung Atypical Carcinoid Tumor | | MONDO:0006041|MONDO:0006095 | -| MONDO:0857259 | ciliary body malignant medulloepithelioma | NCIT:C4557 | MONDO:equivalentTo | Ciliary Body Malignant Medulloepithelioma | | MONDO:0017050|MONDO:0002969 | -| MONDO:0857260 | lung squamous papilloma | NCIT:C45573 | MONDO:equivalentTo | Lung Squamous Papilloma | | MONDO:0006278|MONDO:0001825 | -| MONDO:0857262 | bronchial glandular papilloma | NCIT:C45601 | MONDO:equivalentTo | Bronchial Glandular Papilloma | | MONDO:0006278|MONDO:0021078 | -| MONDO:0857263 | bronchial mixed squamous cell and glandular papilloma | NCIT:C45602 | MONDO:equivalentTo | Bronchial Mixed Squamous Cell and Glandular Papilloma | | MONDO:0021043|MONDO:0006278 | -| MONDO:0857264 | lung pleomorphic adenoma | NCIT:C45603 | MONDO:equivalentTo | Lung Pleomorphic Adenoma | | MONDO:0008401|MONDO:0003422 | -| MONDO:0857265 | lung mucinous cystadenoma | NCIT:C45604 | MONDO:equivalentTo | Lung Mucinous Cystadenoma | | MONDO:0003422|MONDO:0006859 | -| MONDO:0857267 | lung soft tissue neoplasm | NCIT:C45612 | MONDO:equivalentTo | Lung Soft Tissue Neoplasm | | MONDO:0006424|MONDO:0021117 | -| MONDO:0857268 | malignant lung and pleural neoplasm | NCIT:C45625 | MONDO:equivalentTo | Malignant Lung and Pleural Neoplasm | | MONDO:0003274 | -| MONDO:0857270 | lung synovial sarcoma | NCIT:C45631 | MONDO:equivalentTo | Lung Synovial Sarcoma | | MONDO:0002426|MONDO:0010434 | -| MONDO:0857273 | intrapulmonary thymoma | NCIT:C45638 | MONDO:equivalentTo | Intrapulmonary Thymoma | | MONDO:0006456|MONDO:0021117 | -| MONDO:0857274 | mediastinal thymoma | NCIT:C45639 | MONDO:equivalentTo | Mediastinal Thymoma | | MONDO:0006456|MONDO:0021386 | -| MONDO:0857275 | lung melanoma | NCIT:C45652 | MONDO:equivalentTo | Lung Melanoma | | MONDO:0006320|MONDO:0008903 | -| MONDO:0857276 | pleural well differentiated papillary mesothelial tumor | NCIT:C45660 | MONDO:equivalentTo | Pleural Well Differentiated Papillary Mesothelial Tumor | | MONDO:0003308|MONDO:0003688 | -| MONDO:0857278 | pleural lymphoma | NCIT:C45687 | MONDO:equivalentTo | Pleural Lymphoma | | MONDO:0017207|MONDO:0006294 | -| MONDO:0857279 | pleural epithelioid hemangioendothelioma | NCIT:C45695 | MONDO:equivalentTo | Pleural Epithelioid Hemangioendothelioma | | MONDO:0015523|MONDO:0006294 | -| MONDO:0857280 | pleural synovial sarcoma | NCIT:C45696 | MONDO:equivalentTo | Pleural Synovial Sarcoma | | MONDO:0006294|MONDO:0010434 | -| MONDO:0857282 | micronodular thymoma with lymphoid stroma | NCIT:C45706 | MONDO:equivalentTo | Micronodular Thymoma with Lymphoid Stroma | | MONDO:0006456 | -| MONDO:0857283 | metaplastic thymoma | NCIT:C45707 | MONDO:equivalentTo | Metaplastic Thymoma | | MONDO:0006456 | -| MONDO:0857284 | microscopic thymoma | NCIT:C45708 | MONDO:equivalentTo | Microscopic Thymoma | | MONDO:0006456 | -| MONDO:0857285 | sclerosing thymoma | NCIT:C45709 | MONDO:equivalentTo | Sclerosing Thymoma | | MONDO:0006456 | -| MONDO:0857286 | malignant respiratory system neoplasm | NCIT:C4571 | MONDO:equivalentTo | Malignant Respiratory System Neoplasm | | MONDO:0020641|MONDO:0004992 | -| MONDO:0857287 | thymus lipofibroadenoma | NCIT:C45710 | MONDO:equivalentTo | Thymus Lipofibroadenoma | | MONDO:0021512 | -| MONDO:0857289 | combined thymic epithelial neoplasm | NCIT:C45722 | MONDO:equivalentTo | Combined Thymic Epithelial Neoplasm | | MONDO:0018079|MONDO:0002586 | -| MONDO:0857290 | malignant skin appendage neoplasm | NCIT:C4573 | MONDO:equivalentTo | Malignant Skin Appendage Neoplasm | | MONDO:0002297|MONDO:0002898 | -| MONDO:0857291 | mediastinal germ cell tumor with somatic-type malignancy | NCIT:C45732 | MONDO:equivalentTo | Mediastinal Germ Cell Tumor with Somatic-Type Malignancy | | MONDO:0006298 | -| MONDO:0857292 | mediastinal t lymphoblastic leukemia/lymphoma | NCIT:C45738 | MONDO:equivalentTo | Mediastinal T Lymphoblastic Leukemia/Lymphoma | | MONDO:0003537|MONDO:0005843 | -| MONDO:0857294 | mediastinal myeloid sarcoma | NCIT:C45741 | MONDO:equivalentTo | Mediastinal Myeloid Sarcoma | | MONDO:0005843|MONDO:0006861 | -| MONDO:0857295 | mediastinal paraganglioma | NCIT:C45743 | MONDO:equivalentTo | Mediastinal Paraganglioma | | MONDO:0003098|MONDO:0021052 | -| MONDO:0857296 | mediastinal solitary fibrous tumor | NCIT:C45744 | MONDO:equivalentTo | Mediastinal Solitary Fibrous Tumor | | MONDO:0016238|MONDO:0003512 | -| MONDO:0857297 | adult cardiac cellular rhabdomyoma | NCIT:C45747 | MONDO:equivalentTo | Adult Cardiac Cellular Rhabdomyoma | | MONDO:0006123 | -| MONDO:0857298 | cardiac hemangioma | NCIT:C45749 | MONDO:equivalentTo | Cardiac Hemangioma | | MONDO:0021450|MONDO:0006500 | -| MONDO:0857300 | cardiac inflammatory myofibroblastic tumor | NCIT:C45753 | MONDO:equivalentTo | Cardiac Inflammatory Myofibroblastic Tumor | | MONDO:0015798|MONDO:0021209 | -| MONDO:0857301 | cystic tumor of the atrioventricular node | NCIT:C45754 | MONDO:equivalentTo | Cystic Tumor of the Atrioventricular Node | | MONDO:0021450 | -| MONDO:0857302 | cardiac undifferentiated pleomorphic sarcoma | NCIT:C45755 | MONDO:equivalentTo | Cardiac Undifferentiated Pleomorphic Sarcoma | | MONDO:0003354|MONDO:0002142 | -| MONDO:0857303 | cardiac synovial sarcoma | NCIT:C45756 | MONDO:equivalentTo | Cardiac Synovial Sarcoma | | MONDO:0003354|MONDO:0010434 | -| MONDO:0857305 | cardiac rhabdomyosarcoma | NCIT:C45759 | MONDO:equivalentTo | Cardiac Rhabdomyosarcoma | | MONDO:0003354|MONDO:0005212 | -| MONDO:0857306 | pericardial germ cell tumor | NCIT:C45761 | MONDO:equivalentTo | Pericardial Germ Cell Tumor | | MONDO:0021381|MONDO:0018201 | -| MONDO:0857308 | corneal kaposi sarcoma | NCIT:C4579 | MONDO:equivalentTo | Corneal Kaposi Sarcoma | | MONDO:0005055|MONDO:0003802 | -| MONDO:0857310 | metastatic malignant neoplasm in the bone marrow | NCIT:C4582 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Bone Marrow | | MONDO:0024880|MONDO:0021138 | -| MONDO:0857311 | pancreatic neuroendocrine microtumor | NCIT:C45834 | MONDO:equivalentTo | Pancreatic Neuroendocrine Microtumor | | MONDO:0004334 | -| MONDO:0857315 | sellar gangliocytoma | NCIT:C45917 | MONDO:equivalentTo | Sellar Gangliocytoma | | MONDO:0016730|MONDO:0002720 | -| MONDO:0857316 | hypothalamic gangliocytoma | NCIT:C45918 | MONDO:equivalentTo | Hypothalamic Gangliocytoma | | MONDO:0016730|MONDO:0006799 | -| MONDO:0857317 | anterior pituitary gland neoplasm | NCIT:C45921 | MONDO:equivalentTo | Anterior Pituitary Gland Neoplasm | | MONDO:0017611 | -| MONDO:0857319 | densely granulated somatotroph pituitary neuroendocrine tumor | NCIT:C45925 | MONDO:equivalentTo | Densely Granulated Somatotroph Pituitary Neuroendocrine Tumor | | MONDO:0006238 | -| MONDO:0857320 | sparsely granulated somatotroph pituitary neuroendocrine tumor | NCIT:C45926 | MONDO:equivalentTo | Sparsely Granulated Somatotroph Pituitary Neuroendocrine Tumor | | MONDO:0006238 | -| MONDO:0857321 | densely granulated lactotroph pituitary neuroendocrine tumor | NCIT:C45931 | MONDO:equivalentTo | Densely Granulated Lactotroph Pituitary Neuroendocrine Tumor | | MONDO:0010911 | -| MONDO:0857322 | sparsely granulated lactotroph pituitary neuroendocrine tumor | NCIT:C45932 | MONDO:equivalentTo | Sparsely Granulated Lactotroph Pituitary Neuroendocrine Tumor | | MONDO:0010911 | -| MONDO:0857324 | benign palate neoplasm | NCIT:C4599 | MONDO:equivalentTo | Benign Palate Neoplasm | | MONDO:0005286 | -| MONDO:0857325 | thyroid gland oncocytic neoplasm | NCIT:C46068 | MONDO:equivalentTo | Thyroid Gland Oncocytic Neoplasm | | MONDO:0015074|MONDO:0010795 | -| MONDO:0857326 | unilateral breast carcinoma | NCIT:C46073 | MONDO:equivalentTo | Unilateral Breast Carcinoma | | MONDO:0004989 | -| MONDO:0857327 | nonestrogen-dependent malignant neoplasm | NCIT:C46080 | MONDO:equivalentTo | Nonestrogen-Dependent Malignant Neoplasm | | MONDO:0004992 | -| MONDO:0857330 | macrofollicular variant thyroid gland papillary carcinoma | NCIT:C46092 | MONDO:equivalentTo | Macrofollicular Variant Thyroid Gland Papillary Carcinoma | | MONDO:0005075 | -| MONDO:0857331 | clear cell variant thyroid gland papillary carcinoma | NCIT:C46094 | MONDO:equivalentTo | Clear Cell Variant Thyroid Gland Papillary Carcinoma | | MONDO:0005075|MONDO:0005004 | -| MONDO:0857333 | thyroid gland follicular carcinoma, clear cell variant | NCIT:C46096 | MONDO:equivalentTo | Thyroid Gland Follicular Carcinoma, Clear Cell Variant | | MONDO:0005034|MONDO:0005004 | -| MONDO:0857334 | sporadic thyroid gland medullary carcinoma | NCIT:C46098 | MONDO:equivalentTo | Sporadic Thyroid Gland Medullary Carcinoma | | MONDO:0015277 | -| MONDO:0857336 | thyroid gland mixed medullary and follicular cell-derived carcinoma | NCIT:C46104 | MONDO:equivalentTo | Thyroid Gland Mixed Medullary and Follicular Cell-Derived Carcinoma | | MONDO:0015075|MONDO:0021069 | -| MONDO:0857337 | intrathyroid thymic carcinoma | NCIT:C46106 | MONDO:equivalentTo | Intrathyroid Thymic Carcinoma | | MONDO:0015075 | -| MONDO:0857338 | thyroid gland follicular adenoma with papillary hyperplasia | NCIT:C46111 | MONDO:equivalentTo | Thyroid Gland Follicular Adenoma with Papillary Hyperplasia | | MONDO:0002533|MONDO:0005032 | -| MONDO:0857339 | thyroid gland signet ring cell follicular adenoma | NCIT:C46115 | MONDO:equivalentTo | Thyroid Gland Signet Ring Cell Follicular Adenoma | | MONDO:0005032 | -| MONDO:0857340 | thyroid gland mucinous follicular adenoma | NCIT:C46116 | MONDO:equivalentTo | Thyroid Gland Mucinous Follicular Adenoma | | MONDO:0005032 | -| MONDO:0857341 | thyroid gland lipoadenoma | NCIT:C46118 | MONDO:equivalentTo | Thyroid Gland Lipoadenoma | | MONDO:0003431|MONDO:0005032 | -| MONDO:0857342 | thyroid gland clear cell follicular adenoma | NCIT:C46119 | MONDO:equivalentTo | Thyroid Gland Clear Cell Follicular Adenoma | | MONDO:0003426|MONDO:0005032 | -| MONDO:0857343 | thyroid gland hyperfunctioning adenoma | NCIT:C46122 | MONDO:equivalentTo | Thyroid Gland Hyperfunctioning Adenoma | | MONDO:0005032 | -| MONDO:0857345 | thyroid gland paraganglioma | NCIT:C46125 | MONDO:equivalentTo | Thyroid Gland Paraganglioma | | MONDO:0006239|MONDO:0015074 | -| MONDO:0857346 | benign skin appendage neoplasm | NCIT:C4615 | MONDO:equivalentTo | Benign Skin Appendage Neoplasm | | MONDO:0002297|MONDO:0021440 | -| MONDO:0857349 | pineal region germ cell tumor | NCIT:C4659 | MONDO:equivalentTo | Pineal Region Germ Cell Tumor | | MONDO:0003000|MONDO:0021232 | -| MONDO:0857356 | adenocarcinoma with metaplasia | NCIT:C4712 | MONDO:equivalentTo | Adenocarcinoma with Metaplasia | | MONDO:0004970 | -| MONDO:0857357 | atypical meningioma | NCIT:C4723 | MONDO:equivalentTo | Atypical Meningioma | | MONDO:0045056 | -| MONDO:0857358 | neoplasm by morphology | NCIT:C4741 | MONDO:equivalentTo | Neoplasm by Morphology | | MONDO:0005070 | -| MONDO:0857359 | benign squamous cell neoplasm | NCIT:C4742 | MONDO:equivalentTo | Benign Squamous Cell Neoplasm | | MONDO:0036976|MONDO:0002532 | -| MONDO:0857360 | skin cavernous hemangioma | NCIT:C4750 | MONDO:equivalentTo | Skin Cavernous Hemangioma | | MONDO:0003110|MONDO:0003155 | -| MONDO:0857361 | malignant olfactory nerve neoplasm | NCIT:C4768 | MONDO:equivalentTo | Malignant Olfactory Nerve Neoplasm | | MONDO:0002722|MONDO:0002433 | -| MONDO:0857362 | benign extrahepatic bile duct neoplasm | NCIT:C4776 | MONDO:equivalentTo | Benign Extrahepatic Bile Duct Neoplasm | | MONDO:0000385|MONDO:0021385 | -| MONDO:0857363 | breast carcinoma with chondroid metaplasia | NCIT:C47847 | MONDO:equivalentTo | Breast Carcinoma with Chondroid Metaplasia | | MONDO:0004274 | -| MONDO:0857364 | breast carcinoma with osseous metaplasia | NCIT:C47848 | MONDO:equivalentTo | Breast Carcinoma with Osseous Metaplasia | | MONDO:0004274 | -| MONDO:0857365 | breast paget disease without invasive carcinoma | NCIT:C47858 | MONDO:equivalentTo | Breast Paget Disease without Invasive Carcinoma | | MONDO:0002648 | -| MONDO:0857366 | breast hyperplasia | NCIT:C4804 | MONDO:equivalentTo | Breast Hyperplasia | | MONDO:0005043|MONDO:0021100 | -| MONDO:0857367 | malignant odontogenic neoplasm | NCIT:C4812 | MONDO:equivalentTo | Malignant Odontogenic Neoplasm | | MONDO:0021192|MONDO:0005515 | -| MONDO:0857369 | tongue carcinoma | NCIT:C4824 | MONDO:equivalentTo | Tongue Carcinoma | | MONDO:0004631|MONDO:0044925 | -| MONDO:0857370 | parathyroid gland lipoadenoma | NCIT:C48283 | MONDO:equivalentTo | Parathyroid Gland Lipoadenoma | | MONDO:0003431|MONDO:0006890 | -| MONDO:0857371 | atypical parathyroid gland tumor | NCIT:C48285 | MONDO:equivalentTo | Atypical Parathyroid Gland Tumor | | MONDO:0021360 | -| MONDO:0857375 | non-metastatic paraganglioma | NCIT:C48314 | MONDO:equivalentTo | Non-Metastatic Paraganglioma | | MONDO:0000448 | -| MONDO:0857376 | nasopharyngeal paraganglioma | NCIT:C48316 | MONDO:equivalentTo | Nasopharyngeal Paraganglioma | | MONDO:0006239|MONDO:0005375 | -| MONDO:0857377 | primary bone osteosarcoma | NCIT:C4834 | MONDO:equivalentTo | Primary Bone Osteosarcoma | | MONDO:0002629 | -| MONDO:0857378 | adrenal cortical oncocytic adenoma | NCIT:C48447 | MONDO:equivalentTo | Adrenal Cortical Oncocytic Adenoma | | MONDO:0003924|MONDO:0003424 | -| MONDO:0857379 | androgen-producing adrenal cortical adenoma | NCIT:C48454 | MONDO:equivalentTo | Androgen-Producing Adrenal Cortical Adenoma | | MONDO:0006408 | -| MONDO:0857380 | estrogen-producing adrenal cortical adenoma | NCIT:C48456 | MONDO:equivalentTo | Estrogen-Producing Adrenal Cortical Adenoma | | MONDO:0006408 | -| MONDO:0857382 | invasive prostate carcinoma | NCIT:C48596 | MONDO:equivalentTo | Invasive Prostate Carcinoma | | MONDO:0040677|MONDO:0005159 | -| MONDO:0857383 | minimal deviation melanoma | NCIT:C48612 | MONDO:equivalentTo | Minimal Deviation Melanoma | | MONDO:0005012 | -| MONDO:0857384 | melanoma in congenital melanocytic nevus | NCIT:C48613 | MONDO:equivalentTo | Melanoma in Congenital Melanocytic Nevus | | MONDO:0005012 | -| MONDO:0857385 | desmoplastic neurotropic melanoma | NCIT:C48614 | MONDO:equivalentTo | Desmoplastic Neurotropic Melanoma | | MONDO:0044785 | -| MONDO:0857386 | mucosal lentiginous melanoma | NCIT:C48622 | MONDO:equivalentTo | Mucosal Lentiginous Melanoma | | MONDO:0000544 | -| MONDO:0857388 | metastatic malignant neoplasm in the trachea | NCIT:C4887 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Trachea | | MONDO:0001407|MONDO:0024880 | -| MONDO:0857389 | splenic lymphoma | NCIT:C48873 | MONDO:equivalentTo | Splenic Lymphoma | | MONDO:0017207|MONDO:0005966 | -| MONDO:0857390 | dedifferentiated chordoma | NCIT:C48876 | MONDO:equivalentTo | Dedifferentiated Chordoma | | MONDO:0008978 | -| MONDO:0857391 | benign lung hilum neoplasm | NCIT:C4888 | MONDO:equivalentTo | Benign Lung Hilum Neoplasm | | MONDO:0003639|MONDO:0002732 | -| MONDO:0857393 | hiv lipodystrophy | NCIT:C48899 | MONDO:equivalentTo | HIV Lipodystrophy | | MONDO:0006573|MONDO:0006574 | -| MONDO:0857394 | gardner fibroma | NCIT:C49017 | MONDO:equivalentTo | Gardner Fibroma | | MONDO:0005167 | -| MONDO:0857397 | skin fibrous histiocytoma, fibroblastic variant | NCIT:C49076 | MONDO:equivalentTo | Skin Fibrous Histiocytoma, Fibroblastic Variant | | MONDO:0006717 | -| MONDO:0857398 | skin fibrous histiocytoma, histiocytic variant | NCIT:C49077 | MONDO:equivalentTo | Skin Fibrous Histiocytoma, Histiocytic Variant | | MONDO:0006717 | -| MONDO:0857399 | skin fibrous histiocytoma, cellular variant | NCIT:C49078 | MONDO:equivalentTo | Skin Fibrous Histiocytoma, Cellular Variant | | MONDO:0006717 | -| MONDO:0857400 | skin fibrous histiocytoma, epithelioid variant | NCIT:C49079 | MONDO:equivalentTo | Skin Fibrous Histiocytoma, Epithelioid Variant | | MONDO:0006717 | -| MONDO:0857401 | solid angioleiomyoma | NCIT:C49110 | MONDO:equivalentTo | Solid Angioleiomyoma | | MONDO:0006646 | -| MONDO:0857402 | venous angioleiomyoma | NCIT:C49111 | MONDO:equivalentTo | Venous Angioleiomyoma | | MONDO:0006646 | -| MONDO:0857403 | cavernous angioleiomyoma | NCIT:C49115 | MONDO:equivalentTo | Cavernous Angioleiomyoma | | MONDO:0006646 | -| MONDO:0857404 | conventional cardiac rhabdomyoma | NCIT:C49179 | MONDO:equivalentTo | Conventional Cardiac Rhabdomyoma | | MONDO:0006123 | -| MONDO:0857405 | anaplastic embryonal rhabdomyosarcoma | NCIT:C49204 | MONDO:equivalentTo | Anaplastic Embryonal Rhabdomyosarcoma | | MONDO:0009993 | -| MONDO:0857407 | duodenal adenoma | NCIT:C4932 | MONDO:equivalentTo | Duodenal Adenoma | | MONDO:0021303|MONDO:0006734 | -| MONDO:0857409 | benign lymphoproliferative disorder | NCIT:C4939 | MONDO:equivalentTo | Benign Lymphoproliferative Disorder | | | -| MONDO:0857412 | intracranial neoplasm | NCIT:C4953 | MONDO:equivalentTo | Intracranial Neoplasm | | MONDO:0006130 | -| MONDO:0857413 | leptomeningeal neoplasm | NCIT:C4958 | MONDO:equivalentTo | Leptomeningeal Neoplasm | | MONDO:0016743 | -| MONDO:0857415 | benign infratentorial neoplasm | NCIT:C4965 | MONDO:equivalentTo | Benign Infratentorial Neoplasm | | MONDO:0021451|MONDO:0037736 | -| MONDO:0857417 | primary brain stem neoplasm | NCIT:C4975 | MONDO:equivalentTo | Primary Brain Stem Neoplasm | | MONDO:0021228|MONDO:0021632 | -| MONDO:0857419 | carcinoma unspecified site | NCIT:C4979 | MONDO:equivalentTo | Carcinoma Unspecified Site | | MONDO:0004993 | -| MONDO:0857430 | verrucous lesion | NCIT:C5028 | MONDO:equivalentTo | Verrucous Lesion | | MONDO:0002532 | -| MONDO:0857438 | primary cerebral diffuse large b-cell lymphoma | NCIT:C5054 | MONDO:equivalentTo | Primary Cerebral Diffuse Large B-Cell Lymphoma | | MONDO:0003655|MONDO:0017596 | -| MONDO:0857466 | renomedullary interstitial cell tumor | NCIT:C5100 | MONDO:equivalentTo | Renomedullary Interstitial Cell Tumor | | MONDO:0002513 | -| MONDO:0857469 | solid glomus tumor | NCIT:C51133 | MONDO:equivalentTo | Solid Glomus Tumor | | MONDO:0018327 | -| MONDO:0857473 | adult central nervous system neoplasm | NCIT:C5131 | MONDO:equivalentTo | Adult Central Nervous System Neoplasm | | MONDO:0006130 | -| MONDO:0857476 | breast ductal carcinoma in situ, non-comedo type | NCIT:C5137 | MONDO:equivalentTo | Breast Ductal Carcinoma In Situ, Non-Comedo Type | | MONDO:0005023 | -| MONDO:0857477 | invasive breast cribriform carcinoma | NCIT:C5142 | MONDO:equivalentTo | Invasive Breast Cribriform Carcinoma | | MONDO:0006256|MONDO:0004988|MONDO:0006176 | -| MONDO:0857478 | malignant breast adenomyoepithelioma | NCIT:C5143 | MONDO:equivalentTo | Malignant Breast Adenomyoepithelioma | | MONDO:0007254|MONDO:0002066 | -| MONDO:0857479 | infratentorial glioblastoma | NCIT:C5148 | MONDO:equivalentTo | Infratentorial Glioblastoma | | MONDO:0003107|MONDO:0002501 | -| MONDO:0857480 | supratentorial glioblastoma | NCIT:C5149 | MONDO:equivalentTo | Supratentorial Glioblastoma | | MONDO:0002071|MONDO:0002501 | -| MONDO:0857482 | high grade breast mucoepidermoid carcinoma | NCIT:C5167 | MONDO:equivalentTo | High Grade Breast Mucoepidermoid Carcinoma | | MONDO:0003087 | -| MONDO:0857483 | low grade breast mucoepidermoid carcinoma | NCIT:C5168 | MONDO:equivalentTo | Low Grade Breast Mucoepidermoid Carcinoma | | MONDO:0003087 | -| MONDO:0857486 | breast non-hodgkin lymphoma | NCIT:C5181 | MONDO:equivalentTo | Breast Non-Hodgkin Lymphoma | | MONDO:0003661|MONDO:0018908 | -| MONDO:0857487 | breast complex fibroadenoma | NCIT:C5194 | MONDO:equivalentTo | Breast Complex Fibroadenoma | | MONDO:0002056 | -| MONDO:0857488 | benign nipple neoplasm | NCIT:C5197 | MONDO:equivalentTo | Benign Nipple Neoplasm | | MONDO:0002482|MONDO:0000620 | -| MONDO:0857490 | breast papillary neoplasm | NCIT:C5206 | MONDO:equivalentTo | Breast Papillary Neoplasm | | MONDO:0021096|MONDO:0021100 | -| MONDO:0857492 | malignant nipple neoplasm | NCIT:C5213 | MONDO:equivalentTo | Malignant Nipple Neoplasm | | MONDO:0007254|MONDO:0002482 | -| MONDO:0857493 | benign ovarian thecoma | NCIT:C5219 | MONDO:equivalentTo | Benign Ovarian Thecoma | | MONDO:0024387|MONDO:0037253 | -| MONDO:0857496 | ovarian soft tissue neoplasm | NCIT:C5244 | MONDO:equivalentTo | Ovarian Soft Tissue Neoplasm | | MONDO:0021068|MONDO:0006424 | -| MONDO:0857498 | gastric burkitt lymphoma | NCIT:C5251 | MONDO:equivalentTo | Gastric Burkitt Lymphoma | | MONDO:0007243|MONDO:0042493 | -| MONDO:0857499 | gastric t-cell non-hodgkin lymphoma | NCIT:C5254 | MONDO:equivalentTo | Gastric T-Cell Non-Hodgkin Lymphoma | | MONDO:0015760|MONDO:0042493 | -| MONDO:0857502 | deletion of the short arm of chromosome 1 (1p) associated meningioma | NCIT:C5294 | MONDO:equivalentTo | Deletion of the Short Arm of Chromosome 1 (1p) Associated Meningioma | | MONDO:0016642 | -| MONDO:0857503 | deletion of chromosome 22 associated meningioma | NCIT:C5305 | MONDO:equivalentTo | Deletion of Chromosome 22 Associated Meningioma | | MONDO:0016642 | -| MONDO:0857504 | deletion of chromosome 3p associated meningioma | NCIT:C5306 | MONDO:equivalentTo | Deletion of Chromosome 3p Associated Meningioma | | MONDO:0016642 | -| MONDO:0857507 | extra-adrenal retroperitoneal paraganglioma | NCIT:C5328 | MONDO:equivalentTo | Extra-Adrenal Retroperitoneal Paraganglioma | | MONDO:0000550|MONDO:0024645 | -| MONDO:0857508 | hereditary paraganglioma | NCIT:C5329 | MONDO:equivalentTo | Hereditary Paraganglioma | | MONDO:0000448 | -| MONDO:0857513 | great vessel neoplasm | NCIT:C5348 | MONDO:equivalentTo | Great Vessel Neoplasm | | MONDO:0024757 | -| MONDO:0857514 | mesenchymal chondrosarcoma of bone | NCIT:C53493 | MONDO:equivalentTo | Mesenchymal Chondrosarcoma of Bone | | MONDO:0021054|MONDO:0006853 | -| MONDO:0857518 | cardiac schwannoma | NCIT:C5358 | MONDO:equivalentTo | Cardiac Schwannoma | | MONDO:0004820|MONDO:0021450 | -| MONDO:0857519 | cardiac epithelioid hemangioendothelioma | NCIT:C5362 | MONDO:equivalentTo | Cardiac Epithelioid Hemangioendothelioma | | MONDO:0015523|MONDO:0001340 | -| MONDO:0857520 | cardiac kaposi sarcoma | NCIT:C5363 | MONDO:equivalentTo | Cardiac Kaposi Sarcoma | | MONDO:0005055|MONDO:0003354 | -| MONDO:0857524 | cardiac myeloid sarcoma | NCIT:C5370 | MONDO:equivalentTo | Cardiac Myeloid Sarcoma | | MONDO:0001340|MONDO:0006861 | -| MONDO:0857525 | secondary osteosarcoma | NCIT:C53704 | MONDO:equivalentTo | Secondary Osteosarcoma | | MONDO:0002629|MONDO:0024881 | -| MONDO:0857526 | malignant inferior vena cava neoplasm | NCIT:C5377 | MONDO:equivalentTo | Malignant Inferior Vena Cava Neoplasm | | MONDO:0040676 | -| MONDO:0857527 | malignant superior vena cava neoplasm | NCIT:C5379 | MONDO:equivalentTo | Malignant Superior Vena Cava Neoplasm | | MONDO:0040676 | -| MONDO:0857528 | malignant pulmonary artery neoplasm | NCIT:C5380 | MONDO:equivalentTo | Malignant Pulmonary Artery Neoplasm | | MONDO:0040676 | -| MONDO:0857529 | malignant pulmonary vein neoplasm | NCIT:C5383 | MONDO:equivalentTo | Malignant Pulmonary Vein Neoplasm | | MONDO:0040676 | -| MONDO:0857532 | leiomyosarcoma of vessels | NCIT:C5387 | MONDO:equivalentTo | Leiomyosarcoma of Vessels | | MONDO:0005058 | -| MONDO:0857533 | benign atrial neoplasm | NCIT:C5389 | MONDO:equivalentTo | Benign Atrial Neoplasm | | MONDO:0021450 | -| MONDO:0857534 | parotid gland lymphangioma | NCIT:C5393 | MONDO:equivalentTo | Parotid Gland Lymphangioma | | MONDO:0002013|MONDO:0021494 | -| MONDO:0857535 | solitary adult fibroma | NCIT:C5394 | MONDO:equivalentTo | Solitary Adult Fibroma | | MONDO:0005167 | -| MONDO:0857536 | fibrous histiocytoma of bone | NCIT:C53963 | MONDO:equivalentTo | Fibrous Histiocytoma of Bone | | MONDO:0000631|MONDO:0002989 | -| MONDO:0857537 | bone leiomyoma | NCIT:C53964 | MONDO:equivalentTo | Bone Leiomyoma | | MONDO:0001572 | -| MONDO:0857541 | undifferentiated stromal sarcoma | NCIT:C53994 | MONDO:equivalentTo | Undifferentiated Stromal Sarcoma | | MONDO:0037742|MONDO:0044337|MONDO:0001416 | -| MONDO:0857542 | benign gastrointestinal stromal tumor | NCIT:C53998 | MONDO:equivalentTo | Benign Gastrointestinal Stromal Tumor | | MONDO:0044335|MONDO:0011719 | -| MONDO:0857543 | malignant gastrointestinal stromal tumor | NCIT:C53999 | MONDO:equivalentTo | Malignant Gastrointestinal Stromal Tumor | | MONDO:0011719|MONDO:0044337 | -| MONDO:0857546 | region 17p13 allelic loss associated medulloblastoma | NCIT:C5402 | MONDO:equivalentTo | Region 17p13 Allelic Loss Associated Medulloblastoma | | MONDO:0007959 | -| MONDO:0857547 | nevoid basal cell carcinoma syndrome associated medulloblastoma | NCIT:C5405 | MONDO:equivalentTo | Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma | | MONDO:0007959 | -| MONDO:0857548 | central nervous system t-cell non-hodgkin lymphoma | NCIT:C5409 | MONDO:equivalentTo | Central Nervous System T-Cell Non-Hodgkin Lymphoma | | MONDO:0015760|MONDO:0044887 | -| MONDO:0857549 | gastric granular cell tumor | NCIT:C54094 | MONDO:equivalentTo | Gastric Granular Cell Tumor | | MONDO:0006235|MONDO:0021085 | -| MONDO:0857550 | malignant central nervous system germ cell tumor | NCIT:C54099 | MONDO:equivalentTo | Malignant Central Nervous System Germ Cell Tumor | | MONDO:0003113|MONDO:0003000|MONDO:0002714 | -| MONDO:0857552 | breast columnar cell lesion | NCIT:C54180 | MONDO:equivalentTo | Breast Columnar Cell Lesion | | MONDO:0021100 | -| MONDO:0857556 | head and neck keratinizing squamous cell carcinoma | NCIT:C54283 | MONDO:equivalentTo | Head and Neck Keratinizing Squamous Cell Carcinoma | | MONDO:0005056|MONDO:0010150 | -| MONDO:0857559 | metastasizing ameloblastoma | NCIT:C54297 | MONDO:equivalentTo | Metastasizing Ameloblastoma | | MONDO:0024883|MONDO:0017795 | -| MONDO:0857561 | primary intraosseous squamous cell carcinoma derived from keratocystic odontogenic tumor | NCIT:C54303 | MONDO:equivalentTo | Primary Intraosseous Squamous Cell Carcinoma Derived From Keratocystic Odontogenic Tumor | | MONDO:0006385|MONDO:0024878 | -| MONDO:0857562 | lipomatosis of nerve | NCIT:C5431 | MONDO:equivalentTo | Lipomatosis of Nerve | | MONDO:0000648|MONDO:0001406|MONDO:0006574 | -| MONDO:0857564 | laryngeal papillary squamous cell carcinoma | NCIT:C54335 | MONDO:equivalentTo | Laryngeal Papillary Squamous Cell Carcinoma | | MONDO:0002979|MONDO:0005595 | -| MONDO:0857565 | laryngeal squamous cell carcinoma, spindle cell variant | NCIT:C54336 | MONDO:equivalentTo | Laryngeal Squamous Cell Carcinoma, Spindle Cell Variant | | MONDO:0005595|MONDO:0021663 | -| MONDO:0857566 | laryngeal acantholytic squamous cell carcinoma | NCIT:C54337 | MONDO:equivalentTo | Laryngeal Acantholytic Squamous Cell Carcinoma | | MONDO:0003487|MONDO:0005595 | -| MONDO:0857567 | laryngeal adenosquamous carcinoma | NCIT:C54338 | MONDO:equivalentTo | Laryngeal Adenosquamous Carcinoma | | MONDO:0002358|MONDO:0006074 | -| MONDO:0857568 | laryngeal undifferentiated carcinoma | NCIT:C54339 | MONDO:equivalentTo | Laryngeal Undifferentiated Carcinoma | | MONDO:0002358|MONDO:0005617 | -| MONDO:0857570 | kadish stage c olfactory neuroblastoma | NCIT:C5435 | MONDO:equivalentTo | Kadish Stage C Olfactory Neuroblastoma | | MONDO:0006329 | -| MONDO:0857571 | drop metastasis in the spinal cord | NCIT:C5439 | MONDO:equivalentTo | Drop Metastasis in the Spinal Cord | | MONDO:0044912 | -| MONDO:0857572 | nasopharyngeal papillary adenocarcinoma | NCIT:C54400 | MONDO:equivalentTo | Nasopharyngeal Papillary Adenocarcinoma | | MONDO:0015459|MONDO:0002512 | -| MONDO:0857574 | meningeal gliomatosis | NCIT:C5446 | MONDO:equivalentTo | Meningeal Gliomatosis | | MONDO:0100342|MONDO:0021322 | -| MONDO:0857575 | invasive breast apocrine carcinoma | NCIT:C5457 | MONDO:equivalentTo | Invasive Breast Apocrine Carcinoma | | MONDO:0006256|MONDO:0003934 | -| MONDO:0857576 | breast nevus | NCIT:C54658 | MONDO:equivalentTo | Breast Nevus | | MONDO:0044794|MONDO:0000620 | -| MONDO:0857577 | acral nevus | NCIT:C54659 | MONDO:equivalentTo | Acral Nevus | | MONDO:0044794 | -| MONDO:0857578 | flexural skin nevus | NCIT:C54660 | MONDO:equivalentTo | Flexural Skin Nevus | | MONDO:0044794 | -| MONDO:0857580 | nevoid melanoma | NCIT:C54662 | MONDO:equivalentTo | Nevoid Melanoma | | MONDO:0005012 | -| MONDO:0857581 | signet ring melanoma | NCIT:C54663 | MONDO:equivalentTo | Signet Ring Melanoma | | MONDO:0005012 | -| MONDO:0857582 | skin keratotic basal cell carcinoma | NCIT:C54665 | MONDO:equivalentTo | Skin Keratotic Basal Cell Carcinoma | | MONDO:0005341 | -| MONDO:0857583 | invasive breast lobular carcinoma, signet ring variant | NCIT:C54691 | MONDO:equivalentTo | Invasive Breast Lobular Carcinoma, Signet Ring Variant | | MONDO:0005051|MONDO:0002671 | -| MONDO:0857587 | central nervous system dermoid cyst | NCIT:C5508 | MONDO:equivalentTo | Central Nervous System Dermoid Cyst | | MONDO:0002378|MONDO:0003733 | -| MONDO:0857589 | appendix mucinous cystadenoma | NCIT:C5510 | MONDO:equivalentTo | Appendix Mucinous Cystadenoma | | MONDO:0006088|MONDO:0006859 | -| MONDO:0857592 | prostate kaposi sarcoma | NCIT:C5523 | MONDO:equivalentTo | Prostate Kaposi Sarcoma | | MONDO:0005055|MONDO:0002854 | -| MONDO:0857593 | prostate myeloid sarcoma | NCIT:C5527 | MONDO:equivalentTo | Prostate Myeloid Sarcoma | | MONDO:0008315|MONDO:0006861 | -| MONDO:0857595 | prostate non-hodgkin lymphoma | NCIT:C5534 | MONDO:equivalentTo | Prostate Non-Hodgkin Lymphoma | | MONDO:0000996|MONDO:0018908 | -| MONDO:0857596 | ceruminous neoplasm | NCIT:C5558 | MONDO:equivalentTo | Ceruminous Neoplasm | | MONDO:0003686|MONDO:0021235 | -| MONDO:0857599 | stage i skin cancer | NCIT:C5581 | MONDO:equivalentTo | Stage I Skin Cancer | | MONDO:0002656 | -| MONDO:0857600 | stage ii skin cancer | NCIT:C5582 | MONDO:equivalentTo | Stage II Skin Cancer | | MONDO:0002656 | -| MONDO:0857601 | stage iii skin cancer | NCIT:C5583 | MONDO:equivalentTo | Stage III Skin Cancer | | MONDO:0002656 | -| MONDO:0857602 | stage iv skin cancer | NCIT:C5584 | MONDO:equivalentTo | Stage IV Skin Cancer | | MONDO:0002656 | -| MONDO:0857604 | jugular foramen neoplasm | NCIT:C5589 | MONDO:equivalentTo | Jugular Foramen Neoplasm | | MONDO:0021351 | -| MONDO:0857607 | benign anal granular cell tumor | NCIT:C5607 | MONDO:equivalentTo | Benign Anal Granular Cell Tumor | | MONDO:0021469|MONDO:0003250 | -| MONDO:0857611 | metastatic malignant neoplasm in the skin | NCIT:C5629 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Skin | | MONDO:0002898|MONDO:0024880 | -| MONDO:0857613 | occult lung carcinoma | NCIT:C5641 | MONDO:equivalentTo | Occult Lung Carcinoma | | MONDO:0005138 | -| MONDO:0857614 | endobronchial hamartoma | NCIT:C5662 | MONDO:equivalentTo | Endobronchial Hamartoma | | MONDO:0021540 | -| MONDO:0857615 | multiple pulmonary hamartomas | NCIT:C5663 | MONDO:equivalentTo | Multiple Pulmonary Hamartomas | | MONDO:0021540 | -| MONDO:0857619 | colorectal adenoma with severe dysplasia | NCIT:C5685 | MONDO:equivalentTo | Colorectal Adenoma with Severe Dysplasia | | MONDO:0005484 | -| MONDO:0857623 | esophageal schwannoma | NCIT:C5703 | MONDO:equivalentTo | Esophageal Schwannoma | | MONDO:0004820|MONDO:0021459 | -| MONDO:0857629 | extrahepatic bile duct undifferentiated carcinoma | NCIT:C5780 | MONDO:equivalentTo | Extrahepatic Bile Duct Undifferentiated Carcinoma | | MONDO:0003090|MONDO:0005617 | -| MONDO:0857635 | esophageal neuroendocrine neoplasm | NCIT:C5821 | MONDO:equivalentTo | Esophageal Neuroendocrine Neoplasm | | MONDO:0021355|MONDO:0024503 | -| MONDO:0857638 | extrahepatic bile duct tubular adenoma | NCIT:C5850 | MONDO:equivalentTo | Extrahepatic Bile Duct Tubular Adenoma | | MONDO:0003445|MONDO:0024660 | -| MONDO:0857646 | oral cavity granular cell tumor | NCIT:C5912 | MONDO:equivalentTo | Oral Cavity Granular Cell Tumor | | MONDO:0021245|MONDO:0006235 | -| MONDO:0857647 | oral cavity adenoma | NCIT:C5913 | MONDO:equivalentTo | Oral Cavity Adenoma | | MONDO:0021445|MONDO:0036976|MONDO:0004972 | -| MONDO:0857648 | oral cavity adenocarcinoma | NCIT:C5914 | MONDO:equivalentTo | Oral Cavity Adenocarcinoma | | MONDO:0044925|MONDO:0004970 | -| MONDO:0857660 | minor salivary gland mucoepidermoid carcinoma | NCIT:C5953 | MONDO:equivalentTo | Minor Salivary Gland Mucoepidermoid Carcinoma | | MONDO:0045069|MONDO:0021009 | -| MONDO:0857661 | minor salivary gland small cell neuroendocrine carcinoma | NCIT:C5956 | MONDO:equivalentTo | Minor Salivary Gland Small Cell Neuroendocrine Carcinoma | | MONDO:0045069|MONDO:0006405 | -| MONDO:0857663 | minor salivary gland squamous cell carcinoma | NCIT:C5959 | MONDO:equivalentTo | Minor Salivary Gland Squamous Cell Carcinoma | | MONDO:0044740|MONDO:0045069 | -| MONDO:0857665 | ear polyp | NCIT:C5971 | MONDO:equivalentTo | Ear Polyp | | MONDO:0021474|MONDO:0021075 | -| MONDO:0857671 | oropharyngeal polyp | NCIT:C5988 | MONDO:equivalentTo | Oropharyngeal Polyp | | MONDO:0021479|MONDO:0005079 | -| MONDO:0857679 | lung mature b-cell neoplasm | NCIT:C60310 | MONDO:equivalentTo | Lung Mature B-Cell Neoplasm | | MONDO:0021117|MONDO:0004949 | -| MONDO:0857682 | nasopharyngeal polyp | NCIT:C6034 | MONDO:equivalentTo | Nasopharyngeal Polyp | | MONDO:0021478|MONDO:0005079 | -| MONDO:0857683 | stage 0 nasopharyngeal undifferentiated carcinoma ajcc v6, v7, and v8 | NCIT:C6035 | MONDO:equivalentTo | Stage 0 Nasopharyngeal Undifferentiated Carcinoma AJCC v6, v7, and v8 | | MONDO:0021297|MONDO:0021537 | -| MONDO:0857685 | nasopharyngeal squamous papilloma | NCIT:C6037 | MONDO:equivalentTo | Nasopharyngeal Squamous Papilloma | | MONDO:0001825|MONDO:0021478 | -| MONDO:0857686 | oropharyngeal squamous papilloma | NCIT:C6038 | MONDO:equivalentTo | Oropharyngeal Squamous Papilloma | | MONDO:0021479|MONDO:0001825 | -| MONDO:0857687 | stage 0 oropharyngeal squamous cell carcinoma ajcc v6 and v7 | NCIT:C6039 | MONDO:equivalentTo | Stage 0 Oropharyngeal Squamous Cell Carcinoma AJCC v6 and v7 | | MONDO:0044704|MONDO:0021298 | -| MONDO:0857688 | thyroid gland non-hodgkin lymphoma | NCIT:C6044 | MONDO:equivalentTo | Thyroid Gland Non-Hodgkin Lymphoma | | MONDO:0019962|MONDO:0018908 | -| MONDO:0857689 | stage 0 hypopharyngeal squamous cell carcinoma ajcc v6, v7, and v8 | NCIT:C6048 | MONDO:equivalentTo | Stage 0 Hypopharyngeal Squamous Cell Carcinoma AJCC v6, v7, and v8 | | MONDO:0021288|MONDO:0044638 | -| MONDO:0857690 | stage 0 oral cavity squamous cell carcinoma ajcc v6 and v7 | NCIT:C6052 | MONDO:equivalentTo | Stage 0 Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7 | | MONDO:0004958|MONDO:0000371|MONDO:0004693 | -| MONDO:0857692 | anterior tongue neoplasm | NCIT:C6062 | MONDO:equivalentTo | Anterior Tongue Neoplasm | | MONDO:0021240 | -| MONDO:0857697 | neck carcinoma | NCIT:C6077 | MONDO:equivalentTo | Neck Carcinoma | | MONDO:0021310|MONDO:0002038 | -| MONDO:0857698 | external ear actinic keratosis | NCIT:C6080 | MONDO:equivalentTo | External Ear Actinic Keratosis | | MONDO:0021235|MONDO:0005173 | -| MONDO:0857700 | middle ear paraganglioma | NCIT:C6085 | MONDO:equivalentTo | Middle Ear Paraganglioma | | MONDO:0021366|MONDO:0021064 | -| MONDO:0857702 | benign uveal neoplasm | NCIT:C6104 | MONDO:equivalentTo | Benign Uveal Neoplasm | | MONDO:0021454|MONDO:0021225 | -| MONDO:0857703 | stage 0 laryngeal squamous cell carcinoma ajcc v6, v7, and v8 | NCIT:C6121 | MONDO:equivalentTo | Stage 0 Laryngeal Squamous Cell Carcinoma AJCC v6, v7, and v8 | | MONDO:0004696|MONDO:0005595|MONDO:0004693 | -| MONDO:0857715 | testicular typical seminoma | NCIT:C61383 | MONDO:equivalentTo | Testicular Typical Seminoma | | MONDO:0003669 | -| MONDO:0857719 | ureter undifferentiated carcinoma | NCIT:C6159 | MONDO:equivalentTo | Ureter Undifferentiated Carcinoma | | MONDO:0006481|MONDO:0005617 | -| MONDO:0857720 | urethral undifferentiated carcinoma | NCIT:C6168 | MONDO:equivalentTo | Urethral Undifferentiated Carcinoma | | MONDO:0021327|MONDO:0005617 | -| MONDO:0857725 | hard palate mucoepidermoid carcinoma | NCIT:C6214 | MONDO:equivalentTo | Hard Palate Mucoepidermoid Carcinoma | | MONDO:0021339|MONDO:0044964 | -| MONDO:0857728 | salivary gland clear cell carcinoma | NCIT:C62191 | MONDO:equivalentTo | Salivary Gland Clear Cell Carcinoma | | MONDO:0000521 | -| MONDO:0857729 | breast tubular adenoma | NCIT:C62210 | MONDO:equivalentTo | Breast Tubular Adenoma | | MONDO:0002058 | -| MONDO:0857730 | conjunctival squamous papilloma | NCIT:C6224 | MONDO:equivalentTo | Conjunctival Squamous Papilloma | | MONDO:0001825|MONDO:0006105 | -| MONDO:0857731 | skin nodular basal cell carcinoma | NCIT:C62282 | MONDO:equivalentTo | Skin Nodular Basal Cell Carcinoma | | MONDO:0005341 | -| MONDO:0857732 | superficial basal cell carcinoma | NCIT:C62284 | MONDO:equivalentTo | Superficial Basal Cell Carcinoma | | MONDO:0005341 | -| MONDO:0857734 | minor salivary gland acinic cell carcinoma | NCIT:C6243 | MONDO:equivalentTo | Minor Salivary Gland Acinic Cell Carcinoma | | MONDO:0006400|MONDO:0006304 | -| MONDO:0857736 | ovarian endometrioid tumor | NCIT:C6257 | MONDO:equivalentTo | Ovarian Endometrioid Tumor | | MONDO:0002480|MONDO:0002229 | -| MONDO:0857738 | childhood cerebral ependymoma, not otherwise specified | NCIT:C6268 | MONDO:equivalentTo | Childhood Cerebral Ependymoma, Not Otherwise Specified | | MONDO:0004249 | -| MONDO:0857739 | fallopian tube undifferentiated carcinoma | NCIT:C6281 | MONDO:equivalentTo | Fallopian Tube Undifferentiated Carcinoma | | MONDO:0006206|MONDO:0005617 | -| MONDO:0857740 | vaginal verrucous carcinoma | NCIT:C6325 | MONDO:equivalentTo | Vaginal Verrucous Carcinoma | | MONDO:0006006|MONDO:0006490 | -| MONDO:0857743 | benign uterine corpus mixed epithelial and mesenchymal neoplasm | NCIT:C6335 | MONDO:equivalentTo | Benign Uterine Corpus Mixed Epithelial and Mesenchymal Neoplasm | | MONDO:0016255|MONDO:0021525 | -| MONDO:0857744 | cervical undifferentiated carcinoma | NCIT:C6345 | MONDO:equivalentTo | Cervical Undifferentiated Carcinoma | | MONDO:0005131|MONDO:0005617 | -| MONDO:0857745 | testicular mixed embryonal carcinoma and seminoma | NCIT:C6350 | MONDO:equivalentTo | Testicular Mixed Embryonal Carcinoma and Seminoma | | MONDO:0003120 | -| MONDO:0857746 | testicular mixed embryonal carcinoma and teratoma | NCIT:C6351 | MONDO:equivalentTo | Testicular Mixed Embryonal Carcinoma and Teratoma | | MONDO:0003120|MONDO:0003403|MONDO:0002599 | -| MONDO:0857747 | testicular mixed embryonal carcinoma and teratoma with seminoma | NCIT:C6352 | MONDO:equivalentTo | Testicular Mixed Embryonal Carcinoma and Teratoma with Seminoma | | MONDO:0003120 | -| MONDO:0857748 | kidney lymphoma | NCIT:C63532 | MONDO:equivalentTo | Kidney Lymphoma | | MONDO:0002367|MONDO:0017207 | -| MONDO:0857750 | testicular mature teratoma | NCIT:C6355 | MONDO:equivalentTo | Testicular Mature Teratoma | | MONDO:0003517|MONDO:0018193|MONDO:0021447 | -| MONDO:0857752 | undifferentiated carcinoma with osteoclast-like giant cells | NCIT:C63622 | MONDO:equivalentTo | Undifferentiated Carcinoma with Osteoclast-Like Giant Cells | | MONDO:0005617 | -| MONDO:0857753 | penile kaposi sarcoma | NCIT:C6377 | MONDO:equivalentTo | Penile Kaposi Sarcoma | | MONDO:0005055|MONDO:0001387|MONDO:0022293 | -| MONDO:0857758 | orbit paraganglioma | NCIT:C6408 | MONDO:equivalentTo | Orbit Paraganglioma | | MONDO:0006239|MONDO:0024611 | -| MONDO:0857759 | laryngeal paraganglioma | NCIT:C6409 | MONDO:equivalentTo | Laryngeal Paraganglioma | | MONDO:0015070|MONDO:0006239|MONDO:0021052 | -| MONDO:0857760 | intrathoracic paravertebral paraganglioma | NCIT:C6411 | MONDO:equivalentTo | Intrathoracic Paravertebral Paraganglioma | | MONDO:0000550|MONDO:0021350 | -| MONDO:0857763 | foregut neuroendocrine tumor g1 | NCIT:C6421 | MONDO:equivalentTo | Foregut Neuroendocrine Tumor G1 | | MONDO:0005369 | -| MONDO:0857765 | hindgut neuroendocrine tumor g1 | NCIT:C6423 | MONDO:equivalentTo | Hindgut Neuroendocrine Tumor G1 | | MONDO:0005369 | -| MONDO:0857767 | malignant mediastinal nongerminomatous germ cell tumor | NCIT:C6439 | MONDO:equivalentTo | Malignant Mediastinal Nongerminomatous Germ Cell Tumor | | MONDO:0003578|MONDO:0006298 | -| MONDO:0857768 | gastric germ cell tumor | NCIT:C6448 | MONDO:equivalentTo | Gastric Germ Cell Tumor | | MONDO:0018201|MONDO:0021085 | -| MONDO:0857769 | benign germ cell tumor | NCIT:C6449 | MONDO:equivalentTo | Benign Germ Cell Tumor | | MONDO:0005040|MONDO:0005165 | -| MONDO:0857770 | invasive thymoma | NCIT:C6453 | MONDO:equivalentTo | Invasive Thymoma | | MONDO:0006456 | -| MONDO:0857771 | bone hemangioma | NCIT:C6477 | MONDO:equivalentTo | Bone Hemangioma | | MONDO:0024499|MONDO:0000631|MONDO:0006500 | -| MONDO:0857772 | bone glomus tumor | NCIT:C6480 | MONDO:equivalentTo | Bone Glomus Tumor | | MONDO:0019060|MONDO:0018327 | -| MONDO:0857773 | extraabdominal fibromatosis | NCIT:C6489 | MONDO:equivalentTo | Extraabdominal Fibromatosis | | MONDO:0007608 | -| MONDO:0857774 | deep lipoma | NCIT:C6498 | MONDO:equivalentTo | Deep Lipoma | | MONDO:0005106 | -| MONDO:0857775 | benign skeletal muscle neoplasm | NCIT:C6515 | MONDO:equivalentTo | Benign Skeletal Muscle Neoplasm | | MONDO:0002848|MONDO:0003061 | -| MONDO:0857776 | non-small cell carcinoma | NCIT:C65151 | MONDO:equivalentTo | Non-Small Cell Carcinoma | | MONDO:0004993 | -| MONDO:0857777 | malignant neoplasm, uncertain whether primary or metastatic | NCIT:C65153 | MONDO:equivalentTo | Malignant Neoplasm, Uncertain Whether Primary or Metastatic | | MONDO:0004992 | -| MONDO:0857778 | papillary carcinoma in situ | NCIT:C65163 | MONDO:equivalentTo | Papillary Carcinoma In Situ | | MONDO:0004647|MONDO:0006509 | -| MONDO:0857779 | non-invasive papillary squamous cell carcinoma | NCIT:C65164 | MONDO:equivalentTo | Non-Invasive Papillary Squamous Cell Carcinoma | | MONDO:0002979 | -| MONDO:0857780 | inverted squamous papilloma | NCIT:C65165 | MONDO:equivalentTo | Inverted Squamous Papilloma | | MONDO:0002537|MONDO:0001825 | -| MONDO:0857781 | non-keratinizing large cell squamous cell carcinoma | NCIT:C65173 | MONDO:equivalentTo | Non-Keratinizing Large Cell Squamous Cell Carcinoma | | MONDO:0005096 | -| MONDO:0857782 | non-keratinizing small cell squamous cell carcinoma | NCIT:C65175 | MONDO:equivalentTo | Non-Keratinizing Small Cell Squamous Cell Carcinoma | | MONDO:0005096 | -| MONDO:0857783 | squamous cell carcinoma in situ with questionable stromal invasion | NCIT:C65176 | MONDO:equivalentTo | Squamous Cell Carcinoma In Situ with Questionable Stromal Invasion | | MONDO:0005096 | -| MONDO:0857785 | squamous cell carcinoma with horn formation | NCIT:C65179 | MONDO:equivalentTo | Squamous Cell Carcinoma with Horn Formation | | MONDO:0005056 | -| MONDO:0857786 | squamous cell carcinoma, clear cell type | NCIT:C65180 | MONDO:equivalentTo | Squamous Cell Carcinoma, Clear Cell Type | | MONDO:0005096 | -| MONDO:0857787 | non-invasive papillary transitional cell carcinoma | NCIT:C65181 | MONDO:equivalentTo | Non-Invasive Papillary Transitional Cell Carcinoma | | MONDO:0006350 | -| MONDO:0857789 | malignant pancreatic insulinoma | NCIT:C65186 | MONDO:equivalentTo | Malignant Pancreatic Insulinoma | | MONDO:0024677 | -| MONDO:0857790 | malignant pancreatic glucagonoma | NCIT:C65187 | MONDO:equivalentTo | Malignant Pancreatic Glucagonoma | | MONDO:0019959 | -| MONDO:0857791 | malignant gastrinoma | NCIT:C65188 | MONDO:equivalentTo | Malignant Gastrinoma | | MONDO:0003523 | -| MONDO:0857792 | malignant vipoma | NCIT:C65189 | MONDO:equivalentTo | Malignant Vipoma | | MONDO:0019960 | -| MONDO:0857793 | malignant somatostatinoma | NCIT:C65190 | MONDO:equivalentTo | Malignant Somatostatinoma | | MONDO:0006976 | -| MONDO:0857794 | flat adenoma | NCIT:C65193 | MONDO:equivalentTo | Flat Adenoma | | MONDO:0006180 | -| MONDO:0857795 | glandular papillomatosis | NCIT:C65198 | MONDO:equivalentTo | Glandular Papillomatosis | | MONDO:0021098 | -| MONDO:0857796 | thyroid gland follicular carcinoma, minimally invasive | NCIT:C65200 | MONDO:equivalentTo | Thyroid Gland Follicular Carcinoma, Minimally Invasive | | MONDO:0040677|MONDO:0005034 | -| MONDO:0857797 | papillary mucinous cystadenocarcinoma | NCIT:C65204 | MONDO:equivalentTo | Papillary Mucinous Cystadenocarcinoma | | MONDO:0005858|MONDO:0005074 | -| MONDO:0857798 | malignant testicular sertoli cell tumor | NCIT:C6523 | MONDO:equivalentTo | Malignant Testicular Sertoli Cell Tumor | | MONDO:0000378|MONDO:0020808 | -| MONDO:0857799 | malignant pericytic neoplasm | NCIT:C6530 | MONDO:equivalentTo | Malignant Pericytic Neoplasm | | MONDO:0002604|MONDO:0024637 | -| MONDO:0857802 | ancient schwannoma | NCIT:C6556 | MONDO:equivalentTo | Ancient Schwannoma | | MONDO:0002546 | -| MONDO:0857803 | extraskeletal cartilaginous and osseous neoplasm | NCIT:C6570 | MONDO:equivalentTo | Extraskeletal Cartilaginous and Osseous Neoplasm | | MONDO:0006424 | -| MONDO:0857804 | intramuscular myxoma | NCIT:C6579 | MONDO:equivalentTo | Intramuscular Myxoma | | MONDO:0044784 | -| MONDO:0857805 | juxta-articular myxoma | NCIT:C6580 | MONDO:equivalentTo | Juxta-Articular Myxoma | | MONDO:0044784 | -| MONDO:0857806 | peripheral neuroblastoma | NCIT:C6591 | MONDO:equivalentTo | Peripheral Neuroblastoma | | MONDO:0002749|MONDO:0021089 | -| MONDO:0857807 | benign mediastinal soft tissue neoplasm | NCIT:C6593 | MONDO:equivalentTo | Benign Mediastinal Soft Tissue Neoplasm | | MONDO:0003512|MONDO:0044335|MONDO:0021521 | -| MONDO:0857810 | soft tissue fibrosarcoma | NCIT:C6605 | MONDO:equivalentTo | Soft Tissue Fibrosarcoma | | MONDO:0018078|MONDO:0005164 | -| MONDO:0857811 | mediastinal malignant peripheral nerve sheath tumor | NCIT:C6626 | MONDO:equivalentTo | Mediastinal Malignant Peripheral Nerve Sheath Tumor | | MONDO:0003098|MONDO:0002852|MONDO:0017827 | -| MONDO:0857812 | mediastinal ganglioneuroma | NCIT:C6632 | MONDO:equivalentTo | Mediastinal Ganglioneuroma | | MONDO:0003098|MONDO:0021521|MONDO:0005033 | -| MONDO:0857813 | mediastinal hodgkin lymphoma | NCIT:C6634 | MONDO:equivalentTo | Mediastinal Hodgkin Lymphoma | | MONDO:0004952|MONDO:0004021 | -| MONDO:0857814 | stage 1 neuroblastoma | NCIT:C6638 | MONDO:equivalentTo | Stage 1 Neuroblastoma | | MONDO:0005072 | -| MONDO:0857815 | stage 2 neuroblastoma | NCIT:C6639 | MONDO:equivalentTo | Stage 2 Neuroblastoma | | MONDO:0005072 | -| MONDO:0857816 | stage 3 neuroblastoma | NCIT:C6640 | MONDO:equivalentTo | Stage 3 Neuroblastoma | | MONDO:0005072 | -| MONDO:0857817 | stage 4 neuroblastoma | NCIT:C6641 | MONDO:equivalentTo | Stage 4 Neuroblastoma | | MONDO:0005072 | -| MONDO:0857821 | breast atypical medullary carcinoma | NCIT:C66719 | MONDO:equivalentTo | Breast Atypical Medullary Carcinoma | | MONDO:0004953 | -| MONDO:0857822 | adenocarcinoma with neuroendocrine differentiation | NCIT:C66745 | MONDO:equivalentTo | Adenocarcinoma with Neuroendocrine Differentiation | | MONDO:0004970 | -| MONDO:0857823 | testicular sex cord-stromal tumor, not otherwise specified | NCIT:C66748 | MONDO:equivalentTo | Testicular Sex Cord-Stromal Tumor, Not Otherwise Specified | | MONDO:0003125 | -| MONDO:0857824 | ovarian stromal tumor with minor sex cord elements | NCIT:C66749 | MONDO:equivalentTo | Ovarian Stromal Tumor with Minor Sex Cord Elements | | MONDO:0021657 | -| MONDO:0857825 | adult granulosa cell tumor | NCIT:C66750 | MONDO:equivalentTo | Adult Granulosa Cell Tumor | | MONDO:0006036 | -| MONDO:0857826 | malignant melanoma in precancerous melanosis | NCIT:C66753 | MONDO:equivalentTo | Malignant Melanoma in Precancerous Melanosis | | MONDO:0005012 | -| MONDO:0857827 | small congenital melanocytic nevus | NCIT:C66754 | MONDO:equivalentTo | Small Congenital Melanocytic Nevus | | MONDO:0044792 | -| MONDO:0857828 | proliferative nodules in congenital melanocytic nevus | NCIT:C66755 | MONDO:equivalentTo | Proliferative Nodules in Congenital Melanocytic Nevus | | MONDO:0044792 | -| MONDO:0857829 | periosteal fibroma | NCIT:C66761 | MONDO:equivalentTo | Periosteal Fibroma | | MONDO:0000631|MONDO:0005167 | -| MONDO:0857830 | fascial fibroma | NCIT:C66764 | MONDO:equivalentTo | Fascial Fibroma | | MONDO:0005167 | -| MONDO:0857831 | fascial fibrosarcoma | NCIT:C66765 | MONDO:equivalentTo | Fascial Fibrosarcoma | | MONDO:0005164 | -| MONDO:0857834 | choriocarcinoma combined with other germ cell elements | NCIT:C66777 | MONDO:equivalentTo | Choriocarcinoma Combined with Other Germ Cell Elements | | MONDO:0015864|MONDO:0005853 | -| MONDO:0857835 | hemolymphangioma | NCIT:C66792 | MONDO:equivalentTo | Hemolymphangioma | | MONDO:0002013 | -| MONDO:0857836 | ganglioneuromatosis | NCIT:C66804 | MONDO:equivalentTo | Ganglioneuromatosis | | MONDO:0005033 | -| MONDO:0857837 | ciliary body benign medulloepithelioma | NCIT:C66807 | MONDO:equivalentTo | Ciliary Body Benign Medulloepithelioma | | MONDO:0021486|MONDO:0017050 | -| MONDO:0857838 | ciliary body teratoid medulloepithelioma | NCIT:C66810 | MONDO:equivalentTo | Ciliary Body Teratoid Medulloepithelioma | | MONDO:0017050 | -| MONDO:0857839 | retinocytoma | NCIT:C66812 | MONDO:equivalentTo | Retinocytoma | | MONDO:0021453|MONDO:0024341 | -| MONDO:0857840 | differentiated retinoblastoma | NCIT:C66813 | MONDO:equivalentTo | Differentiated Retinoblastoma | | MONDO:0008380 | -| MONDO:0857841 | undifferentiated retinoblastoma | NCIT:C66814 | MONDO:equivalentTo | Undifferentiated Retinoblastoma | | MONDO:0008380 | -| MONDO:0857842 | diffuse retinoblastoma | NCIT:C66815 | MONDO:equivalentTo | Diffuse Retinoblastoma | | MONDO:0008380 | -| MONDO:0857844 | melanotic neurofibroma | NCIT:C66841 | MONDO:equivalentTo | Melanotic Neurofibroma | | MONDO:0016755 | -| MONDO:0857846 | testicular mixed sex cord-stromal tumor | NCIT:C66991 | MONDO:equivalentTo | Testicular Mixed Sex Cord-Stromal Tumor | | MONDO:0003125 | -| MONDO:0857847 | pyriform fossa carcinoma | NCIT:C6700 | MONDO:equivalentTo | Pyriform Fossa Carcinoma | | MONDO:0005216 | -| MONDO:0857848 | ovarian serous adenocarcinofibroma | NCIT:C67092 | MONDO:equivalentTo | Ovarian Serous Adenocarcinofibroma | | MONDO:0024885|MONDO:0002991 | -| MONDO:0857849 | sternal chondromyxoid fibroma | NCIT:C6714 | MONDO:equivalentTo | Sternal Chondromyxoid Fibroma | | MONDO:0021456|MONDO:0018447 | -| MONDO:0857850 | olfactory neurogenic tumor | NCIT:C67155 | MONDO:equivalentTo | Olfactory Neurogenic Tumor | | MONDO:0002722 | -| MONDO:0857852 | nodular sclerosis classic hodgkin lymphoma, cellular phase | NCIT:C67171 | MONDO:equivalentTo | Nodular Sclerosis Classic Hodgkin Lymphoma, Cellular Phase | | MONDO:0004665 | -| MONDO:0857853 | sternal intraosseous schwannoma | NCIT:C6718 | MONDO:equivalentTo | Sternal Intraosseous Schwannoma | | MONDO:0021456|MONDO:0004820 | -| MONDO:0857854 | peripheral primitive neuroectodermal tumor of the kidney | NCIT:C67214 | MONDO:equivalentTo | Peripheral Primitive Neuroectodermal Tumor of the Kidney | | MONDO:0018271|MONDO:0002367 | -| MONDO:0857855 | chest wall hodgkin lymphoma | NCIT:C6723 | MONDO:equivalentTo | Chest Wall Hodgkin Lymphoma | | MONDO:0004952|MONDO:0003985 | -| MONDO:0857858 | benign glomus tumor | NCIT:C6748 | MONDO:equivalentTo | Benign Glomus Tumor | | MONDO:0003342|MONDO:0018327 | -| MONDO:0857859 | malignant sex cord-stromal tumor | NCIT:C67561 | MONDO:equivalentTo | Malignant Sex Cord-Stromal Tumor | | MONDO:0006055|MONDO:0002149 | -| MONDO:0857860 | myxoid leiomyoma | NCIT:C67563 | MONDO:equivalentTo | Myxoid Leiomyoma | | MONDO:0001572 | -| MONDO:0857862 | stromal neoplasm | NCIT:C6781 | MONDO:equivalentTo | Stromal Neoplasm | | MONDO:0002616|MONDO:0006424 | -| MONDO:0857864 | benign apocrine neoplasm | NCIT:C6799 | MONDO:equivalentTo | Benign Apocrine Neoplasm | | MONDO:0003686|MONDO:0021489 | -| MONDO:0857866 | benign external ear neoplasm | NCIT:C6807 | MONDO:equivalentTo | Benign External Ear Neoplasm | | MONDO:0021474|MONDO:0021235 | -| MONDO:0857867 | prostate ductal adenocarcinoma | NCIT:C6813 | MONDO:equivalentTo | Prostate Ductal Adenocarcinoma | | MONDO:0005082 | -| MONDO:0857870 | high grade paranasal sinus sarcoma | NCIT:C6850 | MONDO:equivalentTo | High Grade Paranasal Sinus Sarcoma | | MONDO:0001758 | -| MONDO:0857871 | low grade paranasal sinus sarcoma | NCIT:C6851 | MONDO:equivalentTo | Low Grade Paranasal Sinus Sarcoma | | MONDO:0001758 | -| MONDO:0857872 | kadish stage a olfactory neuroblastoma | NCIT:C6853 | MONDO:equivalentTo | Kadish Stage A Olfactory Neuroblastoma | | MONDO:0006329 | -| MONDO:0857873 | kadish stage b olfactory neuroblastoma | NCIT:C6854 | MONDO:equivalentTo | Kadish Stage B Olfactory Neuroblastoma | | MONDO:0006329 | -| MONDO:0857874 | oropharyngeal undifferentiated carcinoma | NCIT:C68610 | MONDO:equivalentTo | Oropharyngeal Undifferentiated Carcinoma | | MONDO:0044704|MONDO:0003572 | -| MONDO:0857876 | childhood extracranial germ cell tumor | NCIT:C68627 | MONDO:equivalentTo | Childhood Extracranial Germ Cell Tumor | | MONDO:0003751 | -| MONDO:0857879 | childhood extragonadal malignant germ cell tumor | NCIT:C68632 | MONDO:equivalentTo | Childhood Extragonadal Malignant Germ Cell Tumor | | MONDO:0003113|MONDO:0004479 | -| MONDO:0857881 | adrenal cortical low grade carcinoma | NCIT:C68635 | MONDO:equivalentTo | Adrenal Cortical Low Grade Carcinoma | | MONDO:0006639 | -| MONDO:0857882 | adrenal cortical sarcomatoid carcinoma | NCIT:C68644 | MONDO:equivalentTo | Adrenal Cortical Sarcomatoid Carcinoma | | MONDO:0006639|MONDO:0006406 | -| MONDO:0857884 | hodgkin lymphoma by clinical course | NCIT:C68666 | MONDO:equivalentTo | Hodgkin Lymphoma by Clinical Course | | MONDO:0004952 | -| MONDO:0857892 | adult gliosarcoma | NCIT:C68701 | MONDO:equivalentTo | Adult Gliosarcoma | | MONDO:0020690|MONDO:0016681 | -| MONDO:0857893 | adult giant cell glioblastoma | NCIT:C68702 | MONDO:equivalentTo | Adult Giant Cell Glioblastoma | | MONDO:0020690|MONDO:0016682 | -| MONDO:0857895 | pancreatic mixed acinar-neuroendocrine carcinoma | NCIT:C6878 | MONDO:equivalentTo | Pancreatic Mixed Acinar-Neuroendocrine Carcinoma | | MONDO:0044727 | -| MONDO:0857896 | cellular fibroma | NCIT:C6892 | MONDO:equivalentTo | Cellular Fibroma | | MONDO:0005167 | -| MONDO:0857897 | malignant solitary fibrous tumor | NCIT:C6894 | MONDO:equivalentTo | Malignant Solitary Fibrous Tumor | | MONDO:0016238|MONDO:0004992 | -| MONDO:0857899 | atypical burkitt/burkitt-like lymphoma | NCIT:C6917 | MONDO:equivalentTo | Atypical Burkitt/Burkitt-Like Lymphoma | | MONDO:0007243 | -| MONDO:0857900 | acute myeloid leukemia with a variant kmt2a rearrangement | NCIT:C6924 | MONDO:equivalentTo | Acute Myeloid Leukemia with a Variant KMT2A Rearrangement | | MONDO:0100404 | -| MONDO:0857901 | malignant ovarian thecoma | NCIT:C6929 | MONDO:equivalentTo | Malignant Ovarian Thecoma | | MONDO:0018172|MONDO:0037253 | -| MONDO:0857902 | solitary plasmacytoma | NCIT:C6932 | MONDO:equivalentTo | Solitary Plasmacytoma | | MONDO:0005615 | -| MONDO:0857903 | deep (aggressive) angiomyxoma | NCIT:C6936 | MONDO:equivalentTo | Deep (Aggressive) Angiomyxoma | | MONDO:0006086 | -| MONDO:0857904 | cardiac fibroma | NCIT:C6947 | MONDO:equivalentTo | Cardiac Fibroma | | MONDO:0021450|MONDO:0005167 | -| MONDO:0857906 | anaplastic kidney wilms tumor | NCIT:C6952 | MONDO:equivalentTo | Anaplastic Kidney Wilms Tumor | | MONDO:0019004|MONDO:0020633 | -| MONDO:0857907 | simple endometrial hyperplasia with atypia | NCIT:C6991 | MONDO:equivalentTo | Simple Endometrial Hyperplasia with Atypia | | MONDO:0006410 | -| MONDO:0857910 | central nervous system kaposi sarcoma | NCIT:C7006 | MONDO:equivalentTo | Central Nervous System Kaposi Sarcoma | | MONDO:0005055|MONDO:0002217 | -| MONDO:0857913 | central nervous system inflammatory myofibroblastic tumor | NCIT:C7020 | MONDO:equivalentTo | Central Nervous System Inflammatory Myofibroblastic Tumor | | MONDO:0015798|MONDO:0003244 | -| MONDO:0857914 | refractory multiple myeloma | NCIT:C7024 | MONDO:equivalentTo | Refractory Multiple Myeloma | | MONDO:0004816|MONDO:0009693 | -| MONDO:0857918 | meningioma by site | NCIT:C7051 | MONDO:equivalentTo | Meningioma by Site | | MONDO:0016642 | -| MONDO:0857919 | mature b-cell non-hodgkin lymphoma | NCIT:C7056 | MONDO:equivalentTo | Mature B-Cell Non-Hodgkin Lymphoma | | MONDO:0015759|MONDO:0004949 | -| MONDO:0857921 | neoplasm by special category | NCIT:C7062 | MONDO:equivalentTo | Neoplasm by Special Category | | MONDO:0005070 | -| MONDO:0857925 | megakaryocytic neoplasm | NCIT:C7066 | MONDO:equivalentTo | Megakaryocytic Neoplasm | | MONDO:0005170|MONDO:0021138 | -| MONDO:0857926 | prostate cancer by whitmore-jewett stage | NCIT:C7079 | MONDO:equivalentTo | Prostate Cancer by Whitmore-Jewett Stage | | MONDO:0005159 | -| MONDO:0857931 | metastatic non-cutaneous melanoma | NCIT:C7092 | MONDO:equivalentTo | Metastatic Non-Cutaneous Melanoma | | MONDO:0005191|MONDO:0006320 | -| MONDO:0857935 | teratoid hepatoblastoma | NCIT:C7098 | MONDO:equivalentTo | Teratoid Hepatoblastoma | | MONDO:0003650 | -| MONDO:0857937 | adult pilocytic astrocytoma | NCIT:C71016 | MONDO:equivalentTo | Adult Pilocytic Astrocytoma | | MONDO:0002503|MONDO:0016691 | -| MONDO:0857938 | adult subependymal giant cell astrocytoma | NCIT:C71017 | MONDO:equivalentTo | Adult Subependymal Giant Cell Astrocytoma | | MONDO:0002503|MONDO:0016693 | -| MONDO:0857940 | liver non-epithelial neoplasm | NCIT:C7107 | MONDO:equivalentTo | Liver Non-Epithelial Neoplasm | | MONDO:0024477 | -| MONDO:0857943 | stage i liver cancer | NCIT:C7116 | MONDO:equivalentTo | Stage I Liver Cancer | | MONDO:0018531 | -| MONDO:0857944 | stage ii liver cancer | NCIT:C7117 | MONDO:equivalentTo | Stage II Liver Cancer | | MONDO:0018531 | -| MONDO:0857945 | stage iii liver cancer | NCIT:C7118 | MONDO:equivalentTo | Stage III Liver Cancer | | MONDO:0018531 | -| MONDO:0857946 | stage iv liver cancer | NCIT:C7121 | MONDO:equivalentTo | Stage IV Liver Cancer | | MONDO:0018531 | -| MONDO:0857947 | intrahepatic bile duct microcystic adenoma | NCIT:C7127 | MONDO:equivalentTo | Intrahepatic Bile Duct Microcystic Adenoma | | MONDO:0003444|MONDO:0003435 | -| MONDO:0857948 | gallbladder benign non-epithelial neoplasm | NCIT:C7129 | MONDO:equivalentTo | Gallbladder Benign Non-Epithelial Neoplasm | | MONDO:0021503 | -| MONDO:0857950 | childhood grade 2 meningioma | NCIT:C71301 | MONDO:equivalentTo | Childhood Grade 2 Meningioma | | MONDO:0003057|MONDO:0045056 | -| MONDO:0857952 | ovarian sertoli cell tumor | NCIT:C7133 | MONDO:equivalentTo | Ovarian Sertoli Cell Tumor | | MONDO:0002696|MONDO:0020807 | -| MONDO:0857961 | benign fibroblastic neoplasm | NCIT:C7147 | MONDO:equivalentTo | Benign Fibroblastic Neoplasm | | MONDO:0006209|MONDO:0044335 | -| MONDO:0857962 | soft tissue tumor of uncertain differentiation | NCIT:C7148 | MONDO:equivalentTo | Soft Tissue Tumor of Uncertain Differentiation | | MONDO:0006424 | -| MONDO:0857963 | monoclonal immunoglobulin deposition disease | NCIT:C7151 | MONDO:equivalentTo | Monoclonal Immunoglobulin Deposition Disease | | MONDO:0004949 | -| MONDO:0857964 | erythroleukemia | NCIT:C7152 | MONDO:equivalentTo | Erythroleukemia | | MONDO:0017858 | -| MONDO:0857965 | primary central chondrosarcoma | NCIT:C7155 | MONDO:equivalentTo | Primary Central Chondrosarcoma | | MONDO:0008977|MONDO:0021054 | -| MONDO:0857966 | benign dermal neoplasm | NCIT:C7158 | MONDO:equivalentTo | Benign Dermal Neoplasm | | MONDO:0002300|MONDO:0021440 | -| MONDO:0857967 | grade 1 nodular sclerosis classic hodgkin lymphoma | NCIT:C7165 | MONDO:equivalentTo | Grade 1 Nodular Sclerosis Classic Hodgkin Lymphoma | | MONDO:0004665 | -| MONDO:0857968 | grade 2 nodular sclerosis classic hodgkin lymphoma | NCIT:C7166 | MONDO:equivalentTo | Grade 2 Nodular Sclerosis Classic Hodgkin Lymphoma | | MONDO:0004665 | -| MONDO:0857971 | adult diffuse astrocytoma | NCIT:C7174 | MONDO:equivalentTo | Adult Diffuse Astrocytoma | | MONDO:0004320|MONDO:0016686 | -| MONDO:0857972 | spindle cell/pleomorphic lipoma | NCIT:C7180 | MONDO:equivalentTo | Spindle Cell/Pleomorphic Lipoma | | MONDO:0005106 | -| MONDO:0857973 | classical burkitt lymphoma | NCIT:C7188 | MONDO:equivalentTo | Classical Burkitt Lymphoma | | MONDO:0007243 | -| MONDO:0857974 | burkitt lymphoma with plasmacytoid differentiation | NCIT:C7189 | MONDO:equivalentTo | Burkitt Lymphoma with Plasmacytoid Differentiation | | MONDO:0007243 | -| MONDO:0857975 | type b lymphomatoid papulosis | NCIT:C7198 | MONDO:equivalentTo | Type B Lymphomatoid Papulosis | | MONDO:0020326 | -| MONDO:0857976 | lymphoepithelioid variant peripheral t-cell lymphoma, not otherwise specified | NCIT:C7205 | MONDO:equivalentTo | Lymphoepithelioid Variant Peripheral T-Cell Lymphoma, Not Otherwise Specified | | MONDO:0004964 | -| MONDO:0857977 | common variant anaplastic large cell lymphoma | NCIT:C7206 | MONDO:equivalentTo | Common Variant Anaplastic Large Cell Lymphoma | | MONDO:0020325 | -| MONDO:0857978 | lymphohistiocytic variant anaplastic large cell lymphoma | NCIT:C7207 | MONDO:equivalentTo | Lymphohistiocytic Variant Anaplastic Large Cell Lymphoma | | MONDO:0020325 | -| MONDO:0857981 | non-hodgkin lymphoma by clinical course | NCIT:C7215 | MONDO:equivalentTo | Non-Hodgkin Lymphoma by Clinical Course | | MONDO:0018908 | -| MONDO:0857982 | primary cutaneous hodgkin lymphoma | NCIT:C7221 | MONDO:equivalentTo | Primary Cutaneous Hodgkin Lymphoma | | MONDO:0004952|MONDO:0018898 | -| MONDO:0857984 | blastoid variant mantle cell lymphoma | NCIT:C7229 | MONDO:equivalentTo | Blastoid Variant Mantle Cell Lymphoma | | MONDO:0018876 | -| MONDO:0857995 | follicular lymphoma with predominantly diffuse growth pattern | NCIT:C7264 | MONDO:equivalentTo | Follicular Lymphoma with Predominantly Diffuse Growth Pattern | | MONDO:0018906 | -| MONDO:0857996 | minimally invasive lung mucinous adenocarcinoma | NCIT:C7268 | MONDO:equivalentTo | Minimally Invasive Lung Mucinous Adenocarcinoma | | MONDO:0004991 | -| MONDO:0857997 | minimally invasive lung non-mucinous adenocarcinoma | NCIT:C7269 | MONDO:equivalentTo | Minimally Invasive Lung Non-Mucinous Adenocarcinoma | | MONDO:0004991 | -| MONDO:0857998 | ovarian dermoid cyst with secondary tumor | NCIT:C7284 | MONDO:equivalentTo | Ovarian Dermoid Cyst with Secondary Tumor | | MONDO:0003331 | -| MONDO:0857999 | ovarian granulosa-stromal cell tumor | NCIT:C7287 | MONDO:equivalentTo | Ovarian Granulosa-Stromal Cell Tumor | | MONDO:0021657 | -| MONDO:0858001 | malignant splenic soft tissue neoplasm | NCIT:C7292 | MONDO:equivalentTo | Malignant Splenic Soft Tissue Neoplasm | | MONDO:0024637|MONDO:0005966 | -| MONDO:0858002 | splenic manifestation of t-cell prolymphocytic leukemia | NCIT:C7298 | MONDO:equivalentTo | Splenic Manifestation of T-Cell Prolymphocytic Leukemia | | MONDO:0002966|MONDO:0019468 | -| MONDO:0858003 | splenic manifestation of b-cell prolymphocytic leukemia | NCIT:C7299 | MONDO:equivalentTo | Splenic Manifestation of B-Cell Prolymphocytic Leukemia | | MONDO:0002966|MONDO:0019461 | -| MONDO:0858004 | splenic manifestation of chronic lymphocytic leukemia | NCIT:C7300 | MONDO:equivalentTo | Splenic Manifestation of Chronic Lymphocytic Leukemia | | MONDO:0004107|MONDO:0004948 | -| MONDO:0858005 | splenic manifestation of t-cell large granular lymphocyte leukemia | NCIT:C7302 | MONDO:equivalentTo | Splenic Manifestation of T-Cell Large Granular Lymphocyte Leukemia | | MONDO:0004107|MONDO:0019469 | -| MONDO:0858006 | splenic manifestation of chronic myeloid leukemia, bcr-abl1 positive | NCIT:C7303 | MONDO:equivalentTo | Splenic Manifestation of Chronic Myeloid Leukemia, BCR-ABL1 Positive | | MONDO:0004107|MONDO:0011996 | -| MONDO:0858007 | splenic lymphoplasmacytic lymphoma | NCIT:C7305 | MONDO:equivalentTo | Splenic Lymphoplasmacytic Lymphoma | | MONDO:0000432 | -| MONDO:0858008 | splenic lymphoblastic lymphoma | NCIT:C7312 | MONDO:equivalentTo | Splenic Lymphoblastic Lymphoma | | MONDO:0000873 | -| MONDO:0858010 | acute monoblastic and monocytic leukemia | NCIT:C7318 | MONDO:equivalentTo | Acute Monoblastic and Monocytic Leukemia | | MONDO:0015667 | -| MONDO:0858011 | childhood chronic myeloid leukemia, bcr-abl1 positive | NCIT:C7320 | MONDO:equivalentTo | Childhood Chronic Myeloid Leukemia, BCR-ABL1 Positive | | MONDO:0011996|MONDO:0004355 | -| MONDO:0858012 | ovarian mixed germ cell-sex cord-stromal tumor | NCIT:C7321 | MONDO:equivalentTo | Ovarian Mixed Germ Cell-Sex Cord-Stromal Tumor | | MONDO:0002478|MONDO:0021068 | -| MONDO:0858013 | testicular mixed germ cell-sex cord-stromal tumor | NCIT:C7322 | MONDO:equivalentTo | Testicular Mixed Germ Cell-Sex Cord-Stromal Tumor | | MONDO:0002478|MONDO:0021348 | -| MONDO:0858016 | reproductive endocrine neoplasm | NCIT:C7335 | MONDO:equivalentTo | Reproductive Endocrine Neoplasm | | MONDO:0006054|MONDO:0002082|MONDO:0002259 | -| MONDO:0858017 | high grade intraepithelial neoplasia | NCIT:C7348 | MONDO:equivalentTo | High Grade Intraepithelial Neoplasia | | MONDO:0024474 | -| MONDO:0858019 | cerebellar glioneuronal and neuronal tumors | NCIT:C7372 | MONDO:equivalentTo | Cerebellar Glioneuronal and Neuronal Tumors | | MONDO:0016729|MONDO:0002913 | -| MONDO:0858020 | benign vascular neoplasm | NCIT:C7389 | MONDO:equivalentTo | Benign Vascular Neoplasm | | MONDO:0024296|MONDO:0000654 | -| MONDO:0858021 | malignant vascular neoplasm | NCIT:C7390 | MONDO:equivalentTo | Malignant Vascular Neoplasm | | MONDO:0024296|MONDO:0002100 | -| MONDO:0858024 | precancerous condition by site | NCIT:C7422 | MONDO:equivalentTo | Precancerous Condition by Site | | | -| MONDO:0858025 | oral cavity and lip precancerous condition | NCIT:C7425 | MONDO:equivalentTo | Oral Cavity and Lip Precancerous Condition | | | -| MONDO:0858029 | invasive papillary adenocarcinoma | NCIT:C7438 | MONDO:equivalentTo | Invasive Papillary Adenocarcinoma | | MONDO:0040677|MONDO:0002512 | -| MONDO:0858030 | benign myoepithelioma | NCIT:C7442 | MONDO:equivalentTo | Benign Myoepithelioma | | MONDO:0044335|MONDO:0002380 | -| MONDO:0858036 | pure erythroid leukemia | NCIT:C7467 | MONDO:equivalentTo | Pure Erythroid Leukemia | | MONDO:0017858 | -| MONDO:0858037 | anal extramucosal (perianal) adenocarcinoma | NCIT:C7474 | MONDO:equivalentTo | Anal Extramucosal (Perianal) Adenocarcinoma | | MONDO:0002652 | -| MONDO:0858041 | primary intraosseous squamous cell carcinoma-solid type | NCIT:C7491 | MONDO:equivalentTo | Primary Intraosseous Squamous Cell Carcinoma-Solid Type | | MONDO:0006385 | -| MONDO:0858042 | ameloblastic carcinoma-primary type | NCIT:C7493 | MONDO:equivalentTo | Ameloblastic Carcinoma-Primary Type | | MONDO:0006079 | -| MONDO:0858043 | ameloblastic carcinoma-secondary type (dedifferentiated) | NCIT:C7496 | MONDO:equivalentTo | Ameloblastic Carcinoma-Secondary Type (Dedifferentiated) | | MONDO:0006079|MONDO:0024878 | -| MONDO:0858044 | ameloblastic carcinoma derived from odontogenic cyst | NCIT:C7497 | MONDO:equivalentTo | Ameloblastic Carcinoma Derived From Odontogenic Cyst | | MONDO:0006079|MONDO:0024878 | -| MONDO:0858045 | primary intraosseous squamous cell carcinoma derived from odontogenic cyst | NCIT:C7500 | MONDO:equivalentTo | Primary Intraosseous Squamous Cell Carcinoma Derived From Odontogenic Cyst | | MONDO:0006385|MONDO:0024878 | -| MONDO:0858049 | metastatic malignant neoplasm in the breast | NCIT:C7511 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Breast | | MONDO:0007254|MONDO:0024880 | -| MONDO:0858050 | malignant esophageal neoplasm by anatomic region | NCIT:C7512 | MONDO:equivalentTo | Malignant Esophageal Neoplasm by Anatomic Region | | MONDO:0007576 | -| MONDO:0858051 | malignant esophageal neoplasm by topographic region | NCIT:C7513 | MONDO:equivalentTo | Malignant Esophageal Neoplasm by Topographic Region | | MONDO:0007576 | -| MONDO:0858052 | kidney and ureter neoplasm | NCIT:C7514 | MONDO:equivalentTo | Kidney and Ureter Neoplasm | | MONDO:0021066 | -| MONDO:0858059 | atypical adenoma | NCIT:C7559 | MONDO:equivalentTo | Atypical Adenoma | | MONDO:0004972 | -| MONDO:0858060 | eccrine hidrocystoma | NCIT:C7565 | MONDO:equivalentTo | Eccrine Hidrocystoma | | MONDO:0024247|MONDO:0006787 | -| MONDO:0858062 | deep penetrating nevus | NCIT:C7576 | MONDO:equivalentTo | Deep Penetrating Nevus | | MONDO:0044794 | -| MONDO:0858064 | nevus of female genitalia | NCIT:C7578 | MONDO:equivalentTo | Nevus of Female Genitalia | | MONDO:0005073|MONDO:0021148 | -| MONDO:0858066 | regressing nevus | NCIT:C7603 | MONDO:equivalentTo | Regressing Nevus | | MONDO:0044794 | -| MONDO:0858068 | cerebral non-hodgkin lymphoma | NCIT:C7609 | MONDO:equivalentTo | Cerebral Non-Hodgkin Lymphoma | | MONDO:0003655|MONDO:0044887 | -| MONDO:0858069 | malignant thymoma | NCIT:C7612 | MONDO:equivalentTo | Malignant Thymoma | | MONDO:0002586|MONDO:0006456 | -| MONDO:0858070 | cutaneous lymphoproliferative disorder | NCIT:C7614 | MONDO:equivalentTo | Cutaneous Lymphoproliferative Disorder | | | -| MONDO:0858074 | bilateral malignant neoplasm | NCIT:C7627 | MONDO:equivalentTo | Bilateral Malignant Neoplasm | | MONDO:0004992 | -| MONDO:0858078 | regional malignant urethral neoplasm | NCIT:C7639 | MONDO:equivalentTo | Regional Malignant Urethral Neoplasm | | MONDO:0004192 | -| MONDO:0858080 | intermediate soft tissue neoplasm | NCIT:C7653 | MONDO:equivalentTo | Intermediate Soft Tissue Neoplasm | | MONDO:0006424 | -| MONDO:0858081 | carcinoma in a polyp | NCIT:C7682 | MONDO:equivalentTo | Carcinoma in a Polyp | | MONDO:0004993 | -| MONDO:0858082 | invasive breast ductal carcinoma and lobular carcinoma in situ | NCIT:C7689 | MONDO:equivalentTo | Invasive Breast Ductal Carcinoma and Lobular Carcinoma In Situ | | MONDO:0005050 | -| MONDO:0858083 | breast ductal carcinoma in situ and lobular carcinoma | NCIT:C7690 | MONDO:equivalentTo | Breast Ductal Carcinoma In Situ and Lobular Carcinoma | | MONDO:0006306 | -| MONDO:0858086 | adult hodgkin lymphoma | NCIT:C7702 | MONDO:equivalentTo | Adult Hodgkin Lymphoma | | MONDO:0004952|MONDO:0003660 | -| MONDO:0858087 | adult non-hodgkin lymphoma | NCIT:C7704 | MONDO:equivalentTo | Adult Non-Hodgkin Lymphoma | | MONDO:0003660|MONDO:0018908 | -| MONDO:0858088 | childhood non-hodgkin lymphoma | NCIT:C7706 | MONDO:equivalentTo | Childhood Non-Hodgkin Lymphoma | | MONDO:0003659|MONDO:0018908 | -| MONDO:0858089 | adult soft tissue sarcoma | NCIT:C7707 | MONDO:equivalentTo | Adult Soft Tissue Sarcoma | | MONDO:0018078 | -| MONDO:0858090 | digestive system neuroendocrine tumor g1 | NCIT:C7709 | MONDO:equivalentTo | Digestive System Neuroendocrine Tumor G1 | | MONDO:0000386|MONDO:0005369 | -| MONDO:0858091 | adult liver carcinoma | NCIT:C7711 | MONDO:equivalentTo | Adult Liver Carcinoma | | MONDO:0018531 | -| MONDO:0858092 | childhood hodgkin lymphoma | NCIT:C7714 | MONDO:equivalentTo | Childhood Hodgkin Lymphoma | | MONDO:0004952|MONDO:0003659 | -| MONDO:0858094 | gingival carcinoma | NCIT:C7721 | MONDO:equivalentTo | Gingival Carcinoma | | MONDO:0005507|MONDO:0044925 | -| MONDO:0858095 | vaginal clear cell adenocarcinoma | NCIT:C7735 | MONDO:equivalentTo | Vaginal Clear Cell Adenocarcinoma | | MONDO:0020653|MONDO:0005004 | -| MONDO:0858096 | digestive system hemangioma | NCIT:C7741 | MONDO:equivalentTo | Digestive System Hemangioma | | MONDO:0000385|MONDO:0006500 | -| MONDO:0858097 | mucous membrane hemangioma | NCIT:C7744 | MONDO:equivalentTo | Mucous Membrane Hemangioma | | MONDO:0006500 | -| MONDO:0858099 | cardiac myxoma | NCIT:C7748 | MONDO:equivalentTo | Cardiac Myxoma | | MONDO:0044784|MONDO:0021505 | -| MONDO:0858100 | malignant pericarditis | NCIT:C7753 | MONDO:equivalentTo | Malignant Pericarditis | | MONDO:0001322|MONDO:0005904 | -| MONDO:0858108 | adult leiomyosarcoma | NCIT:C7810 | MONDO:equivalentTo | Adult Leiomyosarcoma | | MONDO:0005058 | -| MONDO:0858116 | regional neuroblastoma | NCIT:C7836 | MONDO:equivalentTo | Regional Neuroblastoma | | MONDO:0005072 | -| MONDO:0858119 | stage i kidney wilms tumor | NCIT:C7840 | MONDO:equivalentTo | Stage I Kidney Wilms Tumor | | MONDO:0019004 | -| MONDO:0858120 | stage ii kidney wilms tumor | NCIT:C7841 | MONDO:equivalentTo | Stage II Kidney Wilms Tumor | | MONDO:0019004 | -| MONDO:0858121 | stage iii kidney wilms tumor | NCIT:C7842 | MONDO:equivalentTo | Stage III Kidney Wilms Tumor | | MONDO:0019004 | -| MONDO:0858122 | stage iv kidney wilms tumor | NCIT:C7843 | MONDO:equivalentTo | Stage IV Kidney Wilms Tumor | | MONDO:0019004 | -| MONDO:0858123 | stage v kidney wilms tumor | NCIT:C7844 | MONDO:equivalentTo | Stage V Kidney Wilms Tumor | | MONDO:0019004 | -| MONDO:0858126 | limited stage lung small cell carcinoma | NCIT:C7853 | MONDO:equivalentTo | Limited Stage Lung Small Cell Carcinoma | | MONDO:0008433 | -| MONDO:0858151 | grade i lymphomatoid granulomatosis | NCIT:C7931 | MONDO:equivalentTo | Grade I Lymphomatoid Granulomatosis | | MONDO:0019466 | -| MONDO:0858152 | grade ii lymphomatoid granulomatosis | NCIT:C7932 | MONDO:equivalentTo | Grade II Lymphomatoid Granulomatosis | | MONDO:0019466 | -| MONDO:0858155 | breast ductal carcinoma in situ, high grade | NCIT:C7949 | MONDO:equivalentTo | Breast Ductal Carcinoma In Situ, High Grade | | MONDO:0005023 | -| MONDO:0858156 | breast paget disease with invasive ductal carcinoma | NCIT:C7951 | MONDO:equivalentTo | Breast Paget Disease with Invasive Ductal Carcinoma | | MONDO:0006256|MONDO:0002648 | -| MONDO:0858161 | childhood acute promyelocytic leukemia with t(15;17)(q24.1;q21.2); pml-rara | NCIT:C7968 | MONDO:equivalentTo | Childhood Acute Promyelocytic Leukemia with t(15;17)(q24.1;q21.2); PML-RARA | | MONDO:0012883|MONDO:0004996 | -| MONDO:0858166 | distal bile duct adenocarcinoma | NCIT:C7976 | MONDO:equivalentTo | Distal Bile Duct Adenocarcinoma | | MONDO:0002665|MONDO:0003707|MONDO:0019087 | -| MONDO:0858169 | carcinoma arising from craniopharyngioma | NCIT:C79949 | MONDO:equivalentTo | Carcinoma Arising from Craniopharyngioma | | MONDO:0024878 | -| MONDO:0858170 | testicular mixed embryonal carcinoma and yolk sac tumor | NCIT:C8001 | MONDO:equivalentTo | Testicular Mixed Embryonal Carcinoma and Yolk Sac Tumor | | MONDO:0003120|MONDO:0003403 | -| MONDO:0858171 | testicular mixed yolk sac tumor and teratoma | NCIT:C8002 | MONDO:equivalentTo | Testicular Mixed Yolk Sac Tumor and Teratoma | | MONDO:0003120|MONDO:0003403 | -| MONDO:0858172 | testicular mixed yolk sac tumor and teratoma with seminoma | NCIT:C8003 | MONDO:equivalentTo | Testicular Mixed Yolk Sac Tumor and Teratoma with Seminoma | | MONDO:0003120 | -| MONDO:0858173 | pancreatic somatostatin-producing neuroendocrine tumor | NCIT:C8006 | MONDO:equivalentTo | Pancreatic Somatostatin-Producing Neuroendocrine Tumor | | MONDO:0006976|MONDO:0002994 | -| MONDO:0858174 | low grade salivary gland carcinoma | NCIT:C8012 | MONDO:equivalentTo | Low Grade Salivary Gland Carcinoma | | MONDO:0000521 | -| MONDO:0858175 | lip basal cell carcinoma | NCIT:C8014 | MONDO:equivalentTo | Lip Basal Cell Carcinoma | | MONDO:0005341|MONDO:0021333 | -| MONDO:0858176 | intermediate grade salivary gland mucoepidermoid carcinoma | NCIT:C8017 | MONDO:equivalentTo | Intermediate Grade Salivary Gland Mucoepidermoid Carcinoma | | MONDO:0021009 | -| MONDO:0858177 | high grade salivary gland carcinoma | NCIT:C8018 | MONDO:equivalentTo | High Grade Salivary Gland Carcinoma | | MONDO:0000521 | -| MONDO:0858178 | salivary gland adenocarcinoma | NCIT:C8021 | MONDO:equivalentTo | Salivary Gland Adenocarcinoma | | MONDO:0000521|MONDO:0004970 | -| MONDO:0858179 | salivary gland poorly differentiated squamous cell carcinoma | NCIT:C8022 | MONDO:equivalentTo | Salivary Gland Poorly Differentiated Squamous Cell Carcinoma | | MONDO:0044740 | -| MONDO:0858180 | salivary gland undifferentiated carcinoma | NCIT:C8024 | MONDO:equivalentTo | Salivary Gland Undifferentiated Carcinoma | | MONDO:0000521|MONDO:0005617 | -| MONDO:0858182 | diffuse large b-cell lymphoma, not otherwise specified | NCIT:C80280 | MONDO:equivalentTo | Diffuse Large B-Cell Lymphoma, Not Otherwise Specified | | MONDO:0018905 | -| MONDO:0858183 | diffuse large b-cell lymphoma associated with chronic inflammation | NCIT:C80289 | MONDO:equivalentTo | Diffuse Large B-Cell Lymphoma Associated with Chronic Inflammation | | MONDO:0018905 | -| MONDO:0858184 | progressive hairy cell leukemia initial treatment | NCIT:C8029 | MONDO:equivalentTo | Progressive Hairy Cell Leukemia Initial Treatment | | MONDO:0018935 | -| MONDO:0858185 | high grade b-cell lymphoma, not otherwise specified | NCIT:C80291 | MONDO:equivalentTo | High Grade B-Cell Lymphoma, Not Otherwise Specified | | MONDO:0044889 | -| MONDO:0858186 | pediatric-type follicular lymphoma | NCIT:C80297 | MONDO:equivalentTo | Pediatric-Type Follicular Lymphoma | | MONDO:0018906 | -| MONDO:0858189 | monoclonal b-cell lymphocytosis | NCIT:C80310 | MONDO:equivalentTo | Monoclonal B-Cell Lymphocytosis | | MONDO:0004949 | -| MONDO:0858190 | b lymphoblastic leukemia/lymphoma, not otherwise specified | NCIT:C80326 | MONDO:equivalentTo | B Lymphoblastic Leukemia/Lymphoma, Not Otherwise Specified | | MONDO:0004947 | -| MONDO:0858191 | b lymphoblastic leukemia/lymphoma with t(1;19)(q23;p13.3); tcf3-pbx1 | NCIT:C80341 | MONDO:equivalentTo | B Lymphoblastic Leukemia/Lymphoma with t(1;19)(q23;p13.3); TCF3-PBX1 | | MONDO:0035605 | -| MONDO:0858205 | regional adrenal gland pheochromocytoma | NCIT:C8045 | MONDO:equivalentTo | Regional Adrenal Gland Pheochromocytoma | | MONDO:0004974 | -| MONDO:0858211 | stage i ovarian germ cell tumor ajcc v6 and v7 | NCIT:C8083 | MONDO:equivalentTo | Stage I Ovarian Germ Cell Tumor AJCC v6 and v7 | | MONDO:0018171 | -| MONDO:0858212 | stage ii ovarian germ cell tumor ajcc v6 and v7 | NCIT:C8084 | MONDO:equivalentTo | Stage II Ovarian Germ Cell Tumor AJCC v6 and v7 | | MONDO:0018171 | -| MONDO:0858213 | stage iii ovarian germ cell tumor ajcc v6 and v7 | NCIT:C8085 | MONDO:equivalentTo | Stage III Ovarian Germ Cell Tumor AJCC v6 and v7 | | MONDO:0018171 | -| MONDO:0858214 | stage iv ovarian germ cell tumor ajcc v6 and v7 | NCIT:C8086 | MONDO:equivalentTo | Stage IV Ovarian Germ Cell Tumor AJCC v6 and v7 | | MONDO:0018171 | -| MONDO:0858219 | regional renal pelvis and ureter urothelial carcinoma | NCIT:C8168 | MONDO:equivalentTo | Regional Renal Pelvis and Ureter Urothelial Carcinoma | | MONDO:0020654 | -| MONDO:0858221 | buccal mucosa verrucous carcinoma | NCIT:C8175 | MONDO:equivalentTo | Buccal Mucosa Verrucous Carcinoma | | MONDO:0021538|MONDO:0021431 | -| MONDO:0858222 | fibroblastic reticular cell sarcoma | NCIT:C81758 | MONDO:equivalentTo | Fibroblastic Reticular Cell Sarcoma | | MONDO:0006247|MONDO:0004992 | -| MONDO:0858224 | disseminated juvenile xanthogranuloma | NCIT:C81772 | MONDO:equivalentTo | Disseminated Juvenile Xanthogranuloma | | MONDO:0006247 | -| MONDO:0858225 | oral cavity adenoid cystic carcinoma | NCIT:C8179 | MONDO:equivalentTo | Oral Cavity Adenoid Cystic Carcinoma | | MONDO:0044925|MONDO:0004971 | -| MONDO:0858240 | mixed phenotype acute leukemia, b/myeloid | NCIT:C82212 | MONDO:equivalentTo | Mixed Phenotype Acute Leukemia, B/Myeloid | | MONDO:0020743 | -| MONDO:0858241 | mixed phenotype acute leukemia, t/myeloid | NCIT:C82213 | MONDO:equivalentTo | Mixed Phenotype Acute Leukemia, T/Myeloid | | MONDO:0020743 | -| MONDO:0858242 | natural killer cell lymphoblastic leukemia/lymphoma | NCIT:C82217 | MONDO:equivalentTo | Natural Killer Cell Lymphoblastic Leukemia/Lymphoma | | MONDO:0003538 | -| MONDO:0858245 | myelodysplastic/myeloproliferative neoplasm post cytotoxic therapy | NCIT:C82397 | MONDO:equivalentTo | Myelodysplastic/Myeloproliferative Neoplasm Post Cytotoxic Therapy | | MONDO:0006450|MONDO:0006311 | -| MONDO:0858246 | acute myeloid leukemia with myelodysplasia-related gene mutations | NCIT:C82430 | MONDO:equivalentTo | Acute Myeloid Leukemia with Myelodysplasia-Related Gene Mutations | | MONDO:0100409 | -| MONDO:0858249 | de novo myelodysplastic syndrome | NCIT:C8253 | MONDO:equivalentTo | de novo Myelodysplastic Syndrome | | MONDO:0018881 | -| MONDO:0858251 | adult anaplastic astrocytoma | NCIT:C8257 | MONDO:equivalentTo | Adult Anaplastic Astrocytoma | | MONDO:0016684|MONDO:0004320 | -| MONDO:0858252 | refractory neutropenia | NCIT:C82593 | MONDO:equivalentTo | Refractory Neutropenia | | MONDO:0005272 | -| MONDO:0858253 | refractory thrombocytopenia | NCIT:C82594 | MONDO:equivalentTo | Refractory Thrombocytopenia | | MONDO:0005272 | -| MONDO:0858254 | myelodysplastic syndrome with excess blasts and fibrosis | NCIT:C82595 | MONDO:equivalentTo | Myelodysplastic Syndrome with Excess Blasts and Fibrosis | | MONDO:0019454 | -| MONDO:0858256 | myelodysplastic/myeloproliferative neoplasm with ring sideroblasts and thrombocytosis, not otherwise specified | NCIT:C82616 | MONDO:equivalentTo | Myelodysplastic/Myeloproliferative Neoplasm with Ring Sideroblasts and Thrombocytosis, Not Otherwise Specified | | MONDO:0006311 | -| MONDO:0858257 | adult cholangiocarcinoma | NCIT:C8265 | MONDO:equivalentTo | Adult Cholangiocarcinoma | | MONDO:0019087 | -| MONDO:0858258 | meyerson nevus | NCIT:C82862 | MONDO:equivalentTo | Meyerson Nevus | | MONDO:0044794 | -| MONDO:0858259 | cystic oncocytic neoplasm | NCIT:C82890 | MONDO:equivalentTo | Cystic Oncocytic Neoplasm | | MONDO:0010795 | -| MONDO:0858265 | duodenal extraskeletal osteosarcoma | NCIT:C82972 | MONDO:equivalentTo | Duodenal Extraskeletal Osteosarcoma | | MONDO:0000920|MONDO:0002621|MONDO:0003361 | -| MONDO:0858272 | cellular pleomorphic adenoma | NCIT:C83174 | MONDO:equivalentTo | Cellular Pleomorphic Adenoma | | MONDO:0008401 | -| MONDO:0858275 | atypical hyperplasia | NCIT:C8355 | MONDO:equivalentTo | Atypical Hyperplasia | | | -| MONDO:0858277 | low grade intraepithelial neoplasia | NCIT:C8367 | MONDO:equivalentTo | Low Grade Intraepithelial Neoplasia | | MONDO:0024474 | -| MONDO:0858280 | lymphangiomatosis | NCIT:C8373 | MONDO:equivalentTo | Lymphangiomatosis | | MONDO:0036870 | -| MONDO:0858283 | fibrohistiocytic neoplasm | NCIT:C8402 | MONDO:equivalentTo | Fibrohistiocytic Neoplasm | | MONDO:0002616 | -| MONDO:0858284 | benign supraglottis neoplasm | NCIT:C8414 | MONDO:equivalentTo | Benign Supraglottis Neoplasm | | MONDO:0004427|MONDO:0002354 | -| MONDO:0858285 | benign bartholin gland neoplasm | NCIT:C8418 | MONDO:equivalentTo | Benign Bartholin Gland Neoplasm | | MONDO:0021114|MONDO:0000643 | -| MONDO:0858286 | diffuse malignant mesothelioma | NCIT:C8420 | MONDO:equivalentTo | Diffuse Malignant Mesothelioma | | MONDO:0006292 | -| MONDO:0858287 | renal benign mesenchymoma | NCIT:C84256 | MONDO:equivalentTo | Renal Benign Mesenchymoma | | MONDO:0002382 | -| MONDO:0858288 | diffuse neurofibroma | NCIT:C8426 | MONDO:equivalentTo | Diffuse Neurofibroma | | MONDO:0016755 | -| MONDO:0858289 | anaplastic astroblastoma, mn1-altered | NCIT:C84347 | MONDO:equivalentTo | Anaplastic Astroblastoma, MN1-Altered | | MONDO:0016707 | -| MONDO:0858299 | asbestos-related lung disorder | NCIT:C84472 | MONDO:equivalentTo | Asbestos-Related Lung Disorder | | | -| MONDO:0858304 | central nervous system cavernous hemangioma | NCIT:C84621 | MONDO:equivalentTo | Central Nervous System Cavernous Hemangioma | | MONDO:0003241|MONDO:0003155 | -| MONDO:0858314 | invasive malignant neoplasm | NCIT:C8505 | MONDO:equivalentTo | Invasive Malignant Neoplasm | | MONDO:0004992 | -| MONDO:0858316 | refractory carcinoma | NCIT:C8511 | MONDO:equivalentTo | Refractory Carcinoma | | MONDO:0036501|MONDO:0004993 | -| MONDO:0858321 | locally advanced malignant neoplasm | NCIT:C8524 | MONDO:equivalentTo | Locally Advanced Malignant Neoplasm | | MONDO:0024880 | -| MONDO:0858324 | benign respiratory system neoplasm | NCIT:C8531 | MONDO:equivalentTo | Benign Respiratory System Neoplasm | | MONDO:0005165|MONDO:0020641 | -| MONDO:0858330 | metastatic malignant neoplasm in the nervous system | NCIT:C8547 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Nervous System | | MONDO:0005872|MONDO:0024880 | -| MONDO:0858334 | metastatic malignant neoplasm in the retina | NCIT:C8555 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Retina | | MONDO:0044913|MONDO:0003072 | -| MONDO:0858337 | metastatic malignant neoplasm of unknown primary | NCIT:C8566 | MONDO:equivalentTo | Metastatic Malignant Neoplasm of Unknown Primary | | MONDO:0024880 | -| MONDO:0858339 | invasive cervical carcinoma | NCIT:C8577 | MONDO:equivalentTo | Invasive Cervical Carcinoma | | MONDO:0040677|MONDO:0005131 | -| MONDO:0858341 | precancerous polyp | NCIT:C8587 | MONDO:equivalentTo | Precancerous Polyp | | MONDO:0021075 | -| MONDO:0858342 | leukemic phase of lymphoma | NCIT:C8594 | MONDO:equivalentTo | Leukemic Phase of Lymphoma | | MONDO:0005402|MONDO:0018908 | -| MONDO:0858343 | postcricoid carcinoma | NCIT:C8595 | MONDO:equivalentTo | Postcricoid Carcinoma | | MONDO:0005216|MONDO:0004635 | -| MONDO:0858346 | anaplastic (malignant) intraspinal meningioma | NCIT:C8605 | MONDO:equivalentTo | Anaplastic (Malignant) Intraspinal Meningioma | | MONDO:0001279|MONDO:0020635 | -| MONDO:0858350 | malignant hepatobiliary neoplasm | NCIT:C8609 | MONDO:equivalentTo | Malignant Hepatobiliary Neoplasm | | MONDO:0002514|MONDO:0002516 | -| MONDO:0858351 | metastatic malignant neoplasm in the adrenal gland | NCIT:C8610 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Adrenal Gland | | MONDO:0002817|MONDO:0024880 | -| MONDO:0858363 | stage i t lymphoblastic leukemia/lymphoma | NCIT:C8697 | MONDO:equivalentTo | Stage I T Lymphoblastic Leukemia/Lymphoma | | MONDO:0003537 | -| MONDO:0858364 | stage ii t lymphoblastic leukemia/lymphoma | NCIT:C8698 | MONDO:equivalentTo | Stage II T Lymphoblastic Leukemia/Lymphoma | | MONDO:0003537 | -| MONDO:0858365 | stage iii t lymphoblastic leukemia/lymphoma | NCIT:C8699 | MONDO:equivalentTo | Stage III T Lymphoblastic Leukemia/Lymphoma | | MONDO:0003537 | -| MONDO:0858366 | stage iv t lymphoblastic leukemia/lymphoma | NCIT:C8700 | MONDO:equivalentTo | Stage IV T Lymphoblastic Leukemia/Lymphoma | | MONDO:0003537 | -| MONDO:0858370 | metastatic malignant hemangiopericytoma | NCIT:C8709 | MONDO:equivalentTo | Metastatic Malignant Hemangiopericytoma | | MONDO:0009330 | -| MONDO:0858371 | primary malignant hemangiopericytoma | NCIT:C8710 | MONDO:equivalentTo | Primary Malignant Hemangiopericytoma | | MONDO:0009330 | -| MONDO:0858372 | regional malignant ureter neoplasm | NCIT:C8716 | MONDO:equivalentTo | Regional Malignant Ureter Neoplasm | | MONDO:0008627 | -| MONDO:0858381 | stage i ovarian choriocarcinoma | NCIT:C8730 | MONDO:equivalentTo | Stage I Ovarian Choriocarcinoma | | MONDO:0003507 | -| MONDO:0858382 | stage ii ovarian choriocarcinoma | NCIT:C8731 | MONDO:equivalentTo | Stage II Ovarian Choriocarcinoma | | MONDO:0003507 | -| MONDO:0858383 | stage iii ovarian choriocarcinoma | NCIT:C8732 | MONDO:equivalentTo | Stage III Ovarian Choriocarcinoma | | MONDO:0003507 | -| MONDO:0858384 | stage iv ovarian choriocarcinoma | NCIT:C8733 | MONDO:equivalentTo | Stage IV Ovarian Choriocarcinoma | | MONDO:0003507 | -| MONDO:0858395 | stage i pharyngeal cancer | NCIT:C8768 | MONDO:equivalentTo | Stage I Pharyngeal Cancer | | MONDO:0021345 | -| MONDO:0858396 | stage ii pharyngeal cancer | NCIT:C8769 | MONDO:equivalentTo | Stage II Pharyngeal Cancer | | MONDO:0021345 | -| MONDO:0858397 | stage iii pharyngeal cancer | NCIT:C8770 | MONDO:equivalentTo | Stage III Pharyngeal Cancer | | MONDO:0021345 | -| MONDO:0858398 | stage iv pharyngeal cancer | NCIT:C8771 | MONDO:equivalentTo | Stage IV Pharyngeal Cancer | | MONDO:0021345 | -| MONDO:0858443 | b lymphoblastic lymphoma | NCIT:C8868 | MONDO:equivalentTo | B Lymphoblastic Lymphoma | | MONDO:0000873|MONDO:0017595|MONDO:0004947 | -| MONDO:0858446 | extragonadal embryonal carcinoma | NCIT:C8880 | MONDO:equivalentTo | Extragonadal Embryonal Carcinoma | | MONDO:0003578|MONDO:0005440 | -| MONDO:0858459 | pediatric disorder | NCIT:C89328 | MONDO:equivalentTo | Pediatric Disorder | | | -| MONDO:0858464 | fundic gland polyp | NCIT:C8961 | MONDO:equivalentTo | Fundic Gland Polyp | | MONDO:0006221|MONDO:0036976 | -| MONDO:0858471 | oral neoplasm | NCIT:C8989 | MONDO:equivalentTo | Oral Neoplasm | | MONDO:0006858|MONDO:0005586 | -| MONDO:0858472 | malignant mastocytosis | NCIT:C8991 | MONDO:equivalentTo | Malignant Mastocytosis | | MONDO:0004992|MONDO:0016586 | -| MONDO:0858473 | benign adrenal cortical neoplasm | NCIT:C9004 | MONDO:equivalentTo | Benign Adrenal Cortical Neoplasm | | MONDO:0021511|MONDO:0036591 | -| MONDO:0858474 | acute myelomonocytic leukemia with abnormal eosinophils | NCIT:C9020 | MONDO:equivalentTo | Acute Myelomonocytic Leukemia with Abnormal Eosinophils | | MONDO:0018871 | -| MONDO:0858475 | sarcoma by fnclcc grade | NCIT:C9023 | MONDO:equivalentTo | Sarcoma by FNCLCC Grade | | MONDO:0005089 | -| MONDO:0858476 | low grade malignant peripheral nerve sheath tumor | NCIT:C9026 | MONDO:equivalentTo | Low Grade Malignant Peripheral Nerve Sheath Tumor | | MONDO:0017827 | -| MONDO:0858477 | atypical cartilaginous tumor/chondrosarcoma, grade 1 | NCIT:C9027 | MONDO:equivalentTo | Atypical Cartilaginous Tumor/Chondrosarcoma, Grade 1 | | MONDO:0008977 | -| MONDO:0858478 | high grade malignant peripheral nerve sheath tumor | NCIT:C9030 | MONDO:equivalentTo | High Grade Malignant Peripheral Nerve Sheath Tumor | | MONDO:0017827 | -| MONDO:0858479 | renal cell cancer by ajcc v6 stage | NCIT:C90343 | MONDO:equivalentTo | Renal Cell Cancer by AJCC v6 Stage | | MONDO:0005549 | -| MONDO:0858480 | bladder cancer by ajcc v6 stage | NCIT:C90344 | MONDO:equivalentTo | Bladder Cancer by AJCC v6 Stage | | MONDO:0004986 | -| MONDO:0858481 | vulvar cancer by ajcc v6 stage | NCIT:C90345 | MONDO:equivalentTo | Vulvar Cancer by AJCC v6 Stage | | MONDO:0005215 | -| MONDO:0858482 | vaginal cancer by ajcc v6 stage | NCIT:C90347 | MONDO:equivalentTo | Vaginal Cancer by AJCC v6 Stage | | MONDO:0015867 | -| MONDO:0858483 | adult angiosarcoma | NCIT:C9040 | MONDO:equivalentTo | Adult Angiosarcoma | | MONDO:0016982 | -| MONDO:0858485 | extensive stage lung small cell carcinoma | NCIT:C9049 | MONDO:equivalentTo | Extensive Stage Lung Small Cell Carcinoma | | MONDO:0008433 | -| MONDO:0858486 | cervical cancer by ajcc v6 stage | NCIT:C90493 | MONDO:equivalentTo | Cervical Cancer by AJCC v6 Stage | | MONDO:0005131 | -| MONDO:0858487 | uterine corpus cancer by ajcc v6 stage | NCIT:C90494 | MONDO:equivalentTo | Uterine Corpus Cancer by AJCC v6 Stage | | MONDO:0006003 | -| MONDO:0858488 | fallopian tube cancer by ajcc v6 stage | NCIT:C90499 | MONDO:equivalentTo | Fallopian Tube Cancer by AJCC v6 Stage | | MONDO:0006206 | -| MONDO:0858489 | esophageal cancer by ajcc v6 stage | NCIT:C90500 | MONDO:equivalentTo | Esophageal Cancer by AJCC v6 Stage | | MONDO:0019086 | -| MONDO:0858490 | gastric cancer by ajcc v6 stage | NCIT:C90503 | MONDO:equivalentTo | Gastric Cancer by AJCC v6 Stage | | MONDO:0004950 | -| MONDO:0858491 | colorectal cancer by ajcc v6 stage | NCIT:C90506 | MONDO:equivalentTo | Colorectal Cancer by AJCC v6 Stage | | MONDO:0024331 | -| MONDO:0858493 | hepatocellular carcinoma by ajcc v6 stage | NCIT:C90510 | MONDO:equivalentTo | Hepatocellular Carcinoma by AJCC v6 Stage | | MONDO:0007256 | -| MONDO:0858494 | gallbladder cancer by ajcc v6 stage | NCIT:C90512 | MONDO:equivalentTo | Gallbladder Cancer by AJCC v6 Stage | | MONDO:0003220 | -| MONDO:0858495 | breast cancer by ajcc v6 stage | NCIT:C90513 | MONDO:equivalentTo | Breast Cancer by AJCC v6 Stage | | MONDO:0004989 | -| MONDO:0858496 | cutaneous melanoma by ajcc v6 stage | NCIT:C90514 | MONDO:equivalentTo | Cutaneous Melanoma by AJCC v6 Stage | | MONDO:0005012 | -| MONDO:0858497 | lung cancer by ajcc v6 stage | NCIT:C90519 | MONDO:equivalentTo | Lung Cancer by AJCC v6 Stage | | MONDO:0005138 | -| MONDO:0858498 | penile cancer by ajcc v6 stage | NCIT:C90520 | MONDO:equivalentTo | Penile Cancer by AJCC v6 Stage | | MONDO:0006360 | -| MONDO:0858499 | prostate cancer by ajcc v6 stage | NCIT:C90521 | MONDO:equivalentTo | Prostate Cancer by AJCC v6 Stage | | MONDO:0005159 | -| MONDO:0858502 | pharyngeal carcinoma by ajcc v6 stage | NCIT:C90525 | MONDO:equivalentTo | Pharyngeal Carcinoma by AJCC v6 Stage | | MONDO:0021345 | -| MONDO:0858503 | laryngeal cancer by ajcc v6 stage | NCIT:C90527 | MONDO:equivalentTo | Laryngeal Cancer by AJCC v6 Stage | | MONDO:0002358 | -| MONDO:0858504 | sinonasal cancer by ajcc v6 stage | NCIT:C90528 | MONDO:equivalentTo | Sinonasal Cancer by AJCC v6 Stage | | MONDO:0056819 | -| MONDO:0858510 | kaposi sarcoma related to immunosuppressive treatment | NCIT:C9113 | MONDO:equivalentTo | Kaposi Sarcoma Related to Immunosuppressive Treatment | | MONDO:0005188 | -| MONDO:0858511 | renal cell cancer by ajcc v7 stage | NCIT:C91201 | MONDO:equivalentTo | Renal Cell Cancer by AJCC v7 Stage | | MONDO:0005549 | -| MONDO:0858512 | bladder cancer by ajcc v7 stage | NCIT:C91202 | MONDO:equivalentTo | Bladder Cancer by AJCC v7 Stage | | MONDO:0004986 | -| MONDO:0858513 | vulvar cancer by ajcc v7 stage | NCIT:C91203 | MONDO:equivalentTo | Vulvar Cancer by AJCC v7 Stage | | MONDO:0005215 | -| MONDO:0858514 | vaginal cancer by ajcc v7 stage | NCIT:C91204 | MONDO:equivalentTo | Vaginal Cancer by AJCC v7 Stage | | MONDO:0015867 | -| MONDO:0858515 | cervical cancer by ajcc v7 stage | NCIT:C91208 | MONDO:equivalentTo | Cervical Cancer by AJCC v7 Stage | | MONDO:0005131 | -| MONDO:0858516 | uterine corpus cancer by ajcc v7 stage | NCIT:C91218 | MONDO:equivalentTo | Uterine Corpus Cancer by AJCC v7 Stage | | MONDO:0006003 | -| MONDO:0858517 | fallopian tube cancer by ajcc v7 stage | NCIT:C91219 | MONDO:equivalentTo | Fallopian Tube Cancer by AJCC v7 Stage | | MONDO:0006206 | -| MONDO:0858518 | esophageal cancer by ajcc v7 stage | NCIT:C91221 | MONDO:equivalentTo | Esophageal Cancer by AJCC v7 Stage | | MONDO:0019086 | -| MONDO:0858519 | gastric cancer by ajcc v7 stage | NCIT:C91222 | MONDO:equivalentTo | Gastric Cancer by AJCC v7 Stage | | MONDO:0004950 | -| MONDO:0858520 | colorectal cancer by ajcc v7 stage | NCIT:C91223 | MONDO:equivalentTo | Colorectal Cancer by AJCC v7 Stage | | MONDO:0024331 | -| MONDO:0858522 | hepatocellular carcinoma by ajcc v7 stage | NCIT:C91228 | MONDO:equivalentTo | Hepatocellular Carcinoma by AJCC v7 Stage | | MONDO:0007256 | -| MONDO:0858523 | gallbladder cancer by ajcc v7 stage | NCIT:C91229 | MONDO:equivalentTo | Gallbladder Cancer by AJCC v7 Stage | | MONDO:0003220 | -| MONDO:0858524 | breast cancer by ajcc v7 stage | NCIT:C91230 | MONDO:equivalentTo | Breast Cancer by AJCC v7 Stage | | MONDO:0004989 | -| MONDO:0858525 | cutaneous melanoma by ajcc v7 stage | NCIT:C91231 | MONDO:equivalentTo | Cutaneous Melanoma by AJCC v7 Stage | | MONDO:0005012 | -| MONDO:0858526 | lung cancer by ajcc v7 stage | NCIT:C91232 | MONDO:equivalentTo | Lung Cancer by AJCC v7 Stage | | MONDO:0005138 | -| MONDO:0858527 | prostate cancer by ajcc v7 stage | NCIT:C91233 | MONDO:equivalentTo | Prostate Cancer by AJCC v7 Stage | | MONDO:0005159 | -| MONDO:0858528 | penile cancer by ajcc v7 stage | NCIT:C91234 | MONDO:equivalentTo | Penile Cancer by AJCC v7 Stage | | MONDO:0006360 | -| MONDO:0858531 | pharyngeal carcinoma by ajcc v7 stage | NCIT:C91252 | MONDO:equivalentTo | Pharyngeal Carcinoma by AJCC v7 Stage | | MONDO:0021345 | -| MONDO:0858532 | sinonasal cancer by ajcc v7 stage | NCIT:C91255 | MONDO:equivalentTo | Sinonasal Cancer by AJCC v7 Stage | | MONDO:0056819 | -| MONDO:0858533 | laryngeal cancer by ajcc v7 stage | NCIT:C91256 | MONDO:equivalentTo | Laryngeal Cancer by AJCC v7 Stage | | MONDO:0002358 | -| MONDO:0858534 | chronic myeloid leukemia, philadelphia chromosome positive, bcr-abl1 positive | NCIT:C9128 | MONDO:equivalentTo | Chronic Myeloid Leukemia, Philadelphia Chromosome Positive, BCR-ABL1 Positive | | MONDO:0024685|MONDO:0011996 | -| MONDO:0858535 | adult rhabdomyosarcoma | NCIT:C9130 | MONDO:equivalentTo | Adult Rhabdomyosarcoma | | MONDO:0005212 | -| MONDO:0858536 | invasive breast carcinoma of no special type with predominant intraductal component | NCIT:C9132 | MONDO:equivalentTo | Invasive Breast Carcinoma of No Special Type with Predominant Intraductal Component | | MONDO:0004953 | -| MONDO:0858537 | invasive breast lobular carcinoma with predominant in situ component | NCIT:C9136 | MONDO:equivalentTo | Invasive Breast Lobular Carcinoma with Predominant In Situ Component | | MONDO:0005051 | -| MONDO:0858538 | adult acute myeloid leukemia | NCIT:C9154 | MONDO:equivalentTo | Adult Acute Myeloid Leukemia | | MONDO:0018874 | -| MONDO:0858543 | testicular mixed embryonal carcinoma and yolk sac tumor with seminoma | NCIT:C9172 | MONDO:equivalentTo | Testicular Mixed Embryonal Carcinoma and Yolk Sac Tumor with Seminoma | | MONDO:0003120 | -| MONDO:0858544 | middle ear carcinoma in situ | NCIT:C91741 | MONDO:equivalentTo | Middle Ear Carcinoma In Situ | | MONDO:0003190|MONDO:0004647 | -| MONDO:0858546 | good prognosis metastatic gestational trophoblastic tumor | NCIT:C9177 | MONDO:equivalentTo | Good Prognosis Metastatic Gestational Trophoblastic Tumor | | MONDO:0018944 | -| MONDO:0858547 | poor prognosis metastatic gestational trophoblastic tumor | NCIT:C9178 | MONDO:equivalentTo | Poor Prognosis Metastatic Gestational Trophoblastic Tumor | | MONDO:0018944 | -| MONDO:0858549 | intraocular schwannoma | NCIT:C92182 | MONDO:equivalentTo | Intraocular Schwannoma | | MONDO:0021454|MONDO:0004820 | -| MONDO:0858550 | esophageal malignant peripheral nerve sheath tumor | NCIT:C92185 | MONDO:equivalentTo | Esophageal Malignant Peripheral Nerve Sheath Tumor | | MONDO:0001204|MONDO:0017827 | -| MONDO:0858551 | intraocular malignant peripheral nerve sheath tumor | NCIT:C92186 | MONDO:equivalentTo | Intraocular Malignant Peripheral Nerve Sheath Tumor | | MONDO:0002236|MONDO:0017827 | -| MONDO:0858558 | non-hematologic malignancy | NCIT:C9226 | MONDO:equivalentTo | Non-Hematologic Malignancy | | MONDO:0004992 | -| MONDO:0858562 | recurrent malignant hemangiopericytoma | NCIT:C9254 | MONDO:equivalentTo | Recurrent Malignant Hemangiopericytoma | | MONDO:0009330 | -| MONDO:0858563 | multifocal glioblastomas | NCIT:C92549 | MONDO:equivalentTo | Multifocal Glioblastomas | | MONDO:0018177 | -| MONDO:0858565 | glioneuronal tumor with neuropil-like islands | NCIT:C92550 | MONDO:equivalentTo | Glioneuronal Tumor with Neuropil-Like Islands | | MONDO:0019781 | -| MONDO:0858569 | anaplastic medulloblastoma | NCIT:C92625 | MONDO:equivalentTo | Anaplastic Medulloblastoma | | MONDO:0007959 | -| MONDO:0858573 | malignant peripheral nerve sheath tumor with mesenchymal differentiation | NCIT:C92647 | MONDO:equivalentTo | Malignant Peripheral Nerve Sheath Tumor with Mesenchymal Differentiation | | MONDO:0017827 | -| MONDO:0858574 | mycosis fungoides and sezary syndrome | NCIT:C9265 | MONDO:equivalentTo | Mycosis Fungoides and Sezary Syndrome | | MONDO:0000430 | -| MONDO:0858580 | advanced malignant neoplasm | NCIT:C9270 | MONDO:equivalentTo | Advanced Malignant Neoplasm | | MONDO:0024880 | -| MONDO:0858584 | lymphocyte-depleted classic hodgkin lymphoma | NCIT:C9283 | MONDO:equivalentTo | Lymphocyte-Depleted Classic Hodgkin Lymphoma | | MONDO:0009348 | -| MONDO:0858585 | central nervous system histiocytic and dendritic cell neoplasm | NCIT:C92944 | MONDO:equivalentTo | Central Nervous System Histiocytic and Dendritic Cell Neoplasm | | MONDO:0006247|MONDO:0003641 | -| MONDO:0858588 | peritoneal malignant mesothelioma | NCIT:C9350 | MONDO:equivalentTo | Peritoneal Malignant Mesothelioma | | MONDO:0006292|MONDO:0002087|MONDO:0006362 | -| MONDO:0858595 | combined lung small cell carcinoma and lung adenocarcinoma | NCIT:C9379 | MONDO:equivalentTo | Combined Lung Small Cell Carcinoma and Lung Adenocarcinoma | | MONDO:0003438 | -| MONDO:0858596 | sarcoma by nci grade | NCIT:C9387 | MONDO:equivalentTo | Sarcoma by NCI Grade | | MONDO:0005089 | -| MONDO:0858597 | well differentiated malignant hemangiopericytoma | NCIT:C9392 | MONDO:equivalentTo | Well Differentiated Malignant Hemangiopericytoma | | MONDO:0009330 | -| MONDO:0858598 | malignant hemangiopericytoma nci grade 2 | NCIT:C9393 | MONDO:equivalentTo | Malignant Hemangiopericytoma NCI Grade 2 | | MONDO:0002789 | -| MONDO:0858599 | malignant hemangiopericytoma nci grade 3 | NCIT:C9394 | MONDO:equivalentTo | Malignant Hemangiopericytoma NCI Grade 3 | | MONDO:0002789 | -| MONDO:0858600 | round cell liposarcoma nci grade 2 | NCIT:C9401 | MONDO:equivalentTo | Round Cell Liposarcoma NCI Grade 2 | | MONDO:0005238 | -| MONDO:0858601 | round cell liposarcoma nci grade 3 | NCIT:C9402 | MONDO:equivalentTo | Round Cell Liposarcoma NCI Grade 3 | | MONDO:0005238 | -| MONDO:0858602 | sarcoma by ajcc grade | NCIT:C9416 | MONDO:equivalentTo | Sarcoma by AJCC Grade | | MONDO:0005089 | -| MONDO:0858603 | childhood hematopoietic and lymphoid cell neoplasm | NCIT:C9431 | MONDO:equivalentTo | Childhood Hematopoietic and Lymphoid Cell Neoplasm | | MONDO:0021079|MONDO:0044881 | -| MONDO:0858619 | grade 1 colorectal adenocarcinoma | NCIT:C9446 | MONDO:equivalentTo | Grade 1 Colorectal Adenocarcinoma | | MONDO:0005008 | -| MONDO:0858620 | grade 2 colorectal adenocarcinoma | NCIT:C9447 | MONDO:equivalentTo | Grade 2 Colorectal Adenocarcinoma | | MONDO:0005008 | -| MONDO:0858621 | grade 3 colorectal adenocarcinoma | NCIT:C9448 | MONDO:equivalentTo | Grade 3 Colorectal Adenocarcinoma | | MONDO:0005008 | -| MONDO:0858623 | spindle cell oncocytoma | NCIT:C94537 | MONDO:equivalentTo | Spindle Cell Oncocytoma | | MONDO:0003257|MONDO:0010795 | -| MONDO:0858625 | breast ductal carcinoma in situ, intermediate grade | NCIT:C9456 | MONDO:equivalentTo | Breast Ductal Carcinoma In Situ, Intermediate Grade | | MONDO:0005023 | -| MONDO:0858626 | breast ductal carcinoma in situ, low grade | NCIT:C9457 | MONDO:equivalentTo | Breast Ductal Carcinoma In Situ, Low Grade | | MONDO:0005023 | -| MONDO:0858627 | borderline ovarian brenner tumor | NCIT:C9459 | MONDO:equivalentTo | Borderline Ovarian Brenner Tumor | | MONDO:0016093|MONDO:0002370 | -| MONDO:0858628 | systemic anaplastic large cell lymphoma | NCIT:C9470 | MONDO:equivalentTo | Systemic Anaplastic Large Cell Lymphoma | | MONDO:0020325 | -| MONDO:0858630 | meningeal leukemia | NCIT:C94754 | MONDO:equivalentTo | Meningeal Leukemia | | MONDO:0001606|MONDO:0700219 | -| MONDO:0858631 | meningeal lymphoma | NCIT:C94756 | MONDO:equivalentTo | Meningeal Lymphoma | | MONDO:0002571|MONDO:0021322 | -| MONDO:0858632 | multifocal breast carcinoma | NCIT:C94770 | MONDO:equivalentTo | Multifocal Breast Carcinoma | | MONDO:0004989 | -| MONDO:0858633 | multicentric breast carcinoma | NCIT:C94772 | MONDO:equivalentTo | Multicentric Breast Carcinoma | | MONDO:0004989 | -| MONDO:0858634 | early stage breast carcinoma | NCIT:C94774 | MONDO:equivalentTo | Early Stage Breast Carcinoma | | MONDO:0004989 | -| MONDO:0858635 | hereditary malignant neoplasm | NCIT:C9479 | MONDO:equivalentTo | Hereditary Malignant Neoplasm | | MONDO:0004992 | -| MONDO:0858637 | stage i borderline ovarian surface epithelial-stromal tumor | NCIT:C94821 | MONDO:equivalentTo | Stage I Borderline Ovarian Surface Epithelial-Stromal Tumor | | MONDO:0016093 | -| MONDO:0858638 | stage ii borderline ovarian surface epithelial-stromal tumor | NCIT:C94822 | MONDO:equivalentTo | Stage II Borderline Ovarian Surface Epithelial-Stromal Tumor | | MONDO:0016093 | -| MONDO:0858639 | stage iii borderline ovarian surface epithelial-stromal tumor | NCIT:C94824 | MONDO:equivalentTo | Stage III Borderline Ovarian Surface Epithelial-Stromal Tumor | | MONDO:0016093 | -| MONDO:0858640 | stage iv borderline ovarian surface epithelial-stromal tumor | NCIT:C94825 | MONDO:equivalentTo | Stage IV Borderline Ovarian Surface Epithelial-Stromal Tumor | | MONDO:0016093 | -| MONDO:0858648 | melanocytoma | NCIT:C9498 | MONDO:equivalentTo | Melanocytoma | | MONDO:0021143 | -| MONDO:0858649 | myolipoma | NCIT:C9502 | MONDO:equivalentTo | Myolipoma | | MONDO:0005106 | -| MONDO:0858650 | thymoliposarcoma | NCIT:C95038 | MONDO:equivalentTo | Thymoliposarcoma | | MONDO:0003601|MONDO:0002586 | -| MONDO:0858651 | ectopic cervical thymoma | NCIT:C95048 | MONDO:equivalentTo | Ectopic Cervical Thymoma | | MONDO:0006456|MONDO:0021351 | -| MONDO:0858656 | intramucosal adenocarcinoma | NCIT:C95397 | MONDO:equivalentTo | Intramucosal Adenocarcinoma | | MONDO:0004970 | -| MONDO:0858658 | pancreatic well differentiated ductal adenocarcinoma | NCIT:C95426 | MONDO:equivalentTo | Pancreatic Well Differentiated Ductal Adenocarcinoma | | MONDO:0005184 | -| MONDO:0858659 | pancreatic moderately differentiated ductal adenocarcinoma | NCIT:C95427 | MONDO:equivalentTo | Pancreatic Moderately Differentiated Ductal Adenocarcinoma | | MONDO:0005184 | -| MONDO:0858660 | pancreatic poorly differentiated ductal adenocarcinoma | NCIT:C95428 | MONDO:equivalentTo | Pancreatic Poorly Differentiated Ductal Adenocarcinoma | | MONDO:0005184 | -| MONDO:0858661 | pancreatic mixed acinar-ductal carcinoma | NCIT:C95458 | MONDO:equivalentTo | Pancreatic Mixed Acinar-Ductal Carcinoma | | MONDO:0006047 | -| MONDO:0858662 | pancreatic mixed acinar-ductal neuroendocrine carcinoma | NCIT:C95460 | MONDO:equivalentTo | Pancreatic Mixed Acinar-Ductal Neuroendocrine Carcinoma | | MONDO:0044727 | -| MONDO:0858663 | pancreatic hepatoid adenocarcinoma | NCIT:C95465 | MONDO:equivalentTo | Pancreatic Hepatoid Adenocarcinoma | | MONDO:0005184|MONDO:0006243 | -| MONDO:0858664 | pancreatic medullary carcinoma | NCIT:C95466 | MONDO:equivalentTo | Pancreatic Medullary Carcinoma | | MONDO:0005184 | -| MONDO:0858665 | pancreatic serous adenoma | NCIT:C95470 | MONDO:equivalentTo | Pancreatic Serous Adenoma | | MONDO:0021441|MONDO:0002810|MONDO:0036976 | -| MONDO:0858666 | pancreatic intraductal neoplasm | NCIT:C95505 | MONDO:equivalentTo | Pancreatic Intraductal Neoplasm | | MONDO:0024276|MONDO:0021076 | -| MONDO:0858667 | pancreatic intraductal papillary mucinous neoplasm, gastric-type | NCIT:C95508 | MONDO:equivalentTo | Pancreatic Intraductal Papillary Mucinous Neoplasm, Gastric-Type | | MONDO:0004286 | -| MONDO:0858668 | pancreatic intraductal papillary mucinous neoplasm, intestinal-type | NCIT:C95510 | MONDO:equivalentTo | Pancreatic Intraductal Papillary Mucinous Neoplasm, Intestinal-Type | | MONDO:0004286 | -| MONDO:0858669 | pancreatic intraductal papillary mucinous neoplasm, pancreatobiliary-type | NCIT:C95512 | MONDO:equivalentTo | Pancreatic Intraductal Papillary Mucinous Neoplasm, Pancreatobiliary-Type | | MONDO:0004286 | -| MONDO:0858675 | non-functioning pancreatic neuroendocrine tumor g1 | NCIT:C95585 | MONDO:equivalentTo | Non-Functioning Pancreatic Neuroendocrine Tumor G1 | | MONDO:0021535|MONDO:0004334 | -| MONDO:0858676 | pancreatic vipoma | NCIT:C95599 | MONDO:equivalentTo | Pancreatic Vipoma | | MONDO:0023206|MONDO:0003622 | -| MONDO:0858677 | esophageal spindle cell carcinoma | NCIT:C95608 | MONDO:equivalentTo | Esophageal Spindle Cell Carcinoma | | MONDO:0005580|MONDO:0021663 | -| MONDO:0858678 | esophageal well differentiated squamous cell carcinoma | NCIT:C95610 | MONDO:equivalentTo | Esophageal Well Differentiated Squamous Cell Carcinoma | | MONDO:0005580 | -| MONDO:0858679 | esophageal moderately differentiated squamous cell carcinoma | NCIT:C95611 | MONDO:equivalentTo | Esophageal Moderately Differentiated Squamous Cell Carcinoma | | MONDO:0005580 | -| MONDO:0858680 | esophageal poorly differentiated squamous cell carcinoma | NCIT:C95612 | MONDO:equivalentTo | Esophageal Poorly Differentiated Squamous Cell Carcinoma | | MONDO:0005580 | -| MONDO:0858681 | esophageal mixed adenoneuroendocrine carcinoma | NCIT:C95621 | MONDO:equivalentTo | Esophageal Mixed Adenoneuroendocrine Carcinoma | | MONDO:0006182|MONDO:0019086 | -| MONDO:0858683 | esophageal synovial sarcoma | NCIT:C95624 | MONDO:equivalentTo | Esophageal Synovial Sarcoma | | MONDO:0001204|MONDO:0010434 | -| MONDO:0858686 | gastric adenoma, gastric-type | NCIT:C95775 | MONDO:equivalentTo | Gastric Adenoma, Gastric-Type | | MONDO:0006221 | -| MONDO:0858689 | gastric mixed adenoneuroendocrine carcinoma | NCIT:C95886 | MONDO:equivalentTo | Gastric Mixed Adenoneuroendocrine Carcinoma | | MONDO:0006182|MONDO:0004950 | -| MONDO:0858691 | gastric schwannoma | NCIT:C95901 | MONDO:equivalentTo | Gastric Schwannoma | | MONDO:0004820|MONDO:0021449 | -| MONDO:0858693 | ampulla of vater pancreatobiliary type adenocarcinoma | NCIT:C95963 | MONDO:equivalentTo | Ampulla of Vater Pancreatobiliary Type Adenocarcinoma | | MONDO:0002670 | -| MONDO:0858694 | ampulla of vater hepatoid adenocarcinoma | NCIT:C95966 | MONDO:equivalentTo | Ampulla of Vater Hepatoid Adenocarcinoma | | MONDO:0006243|MONDO:0002670 | -| MONDO:0858695 | ampulla of vater neuroendocrine neoplasm | NCIT:C95980 | MONDO:equivalentTo | Ampulla of Vater Neuroendocrine Neoplasm | | MONDO:0000921|MONDO:0024503 | -| MONDO:0858696 | ampulla of vater mixed adenoneuroendocrine carcinoma | NCIT:C95986 | MONDO:equivalentTo | Ampulla of Vater Mixed Adenoneuroendocrine Carcinoma | | MONDO:0006182|MONDO:0017590 | -| MONDO:0858702 | intestinal neuroendocrine tumor | NCIT:C96062 | MONDO:equivalentTo | Intestinal Neuroendocrine Tumor | | MONDO:0000386|MONDO:0002883 | -| MONDO:0858703 | small intestinal mixed adenoneuroendocrine carcinoma | NCIT:C96066 | MONDO:equivalentTo | Small Intestinal Mixed Adenoneuroendocrine Carcinoma | | MONDO:0006182|MONDO:0005522 | -| MONDO:0858705 | colorectal neuroendocrine neoplasm | NCIT:C96152 | MONDO:equivalentTo | Colorectal Neuroendocrine Neoplasm | | MONDO:0002883|MONDO:0005335 | -| MONDO:0858706 | colorectal mixed adenoneuroendocrine carcinoma | NCIT:C96158 | MONDO:equivalentTo | Colorectal Mixed Adenoneuroendocrine Carcinoma | | MONDO:0006182|MONDO:0024331 | -| MONDO:0858707 | digestive system neuroendocrine tumor g2 | NCIT:C96166 | MONDO:equivalentTo | Digestive System Neuroendocrine Tumor G2 | | MONDO:0000386 | -| MONDO:0858715 | serrated lesions and polyps | NCIT:C96414 | MONDO:equivalentTo | Serrated Lesions and Polyps | | MONDO:0006180 | -| MONDO:0858717 | appendix enterochromaffin cell serotonin-producing neuroendocrine tumor | NCIT:C96424 | MONDO:equivalentTo | Appendix Enterochromaffin Cell Serotonin-Producing Neuroendocrine Tumor | | MONDO:0015066 | -| MONDO:0858721 | rectal serrated lesions and polyps | NCIT:C96465 | MONDO:equivalentTo | Rectal Serrated Lesions and Polyps | | MONDO:0006164|MONDO:0000530|MONDO:0021398 | -| MONDO:0858725 | colon serrated adenocarcinoma | NCIT:C96486 | MONDO:equivalentTo | Colon Serrated Adenocarcinoma | | MONDO:0006163|MONDO:0002271 | -| MONDO:0858726 | rectal serrated adenocarcinoma | NCIT:C96487 | MONDO:equivalentTo | Rectal Serrated Adenocarcinoma | | MONDO:0006163|MONDO:0002169 | -| MONDO:0858729 | colorectal sarcomatoid carcinoma | NCIT:C96494 | MONDO:equivalentTo | Colorectal Sarcomatoid Carcinoma | | MONDO:0024331|MONDO:0006406 | -| MONDO:0858735 | colorectal schwannoma | NCIT:C96512 | MONDO:equivalentTo | Colorectal Schwannoma | | MONDO:0021444|MONDO:0004820 | -| MONDO:0858736 | colorectal ganglioneuroma | NCIT:C96514 | MONDO:equivalentTo | Colorectal Ganglioneuroma | | MONDO:0021444|MONDO:0005033 | -| MONDO:0858737 | colorectal benign granular cell tumor | NCIT:C96516 | MONDO:equivalentTo | Colorectal Benign Granular Cell Tumor | | MONDO:0021444|MONDO:0003250 | -| MONDO:0858738 | anal canal undifferentiated carcinoma | NCIT:C96529 | MONDO:equivalentTo | Anal Canal Undifferentiated Carcinoma | | MONDO:0007108|MONDO:0005617 | -| MONDO:0858741 | anal canal mixed adenoneuroendocrine carcinoma | NCIT:C96553 | MONDO:equivalentTo | Anal Canal Mixed Adenoneuroendocrine Carcinoma | | MONDO:0006182|MONDO:0007108 | -| MONDO:0858742 | anal canal squamous papilloma | NCIT:C96554 | MONDO:equivalentTo | Anal Canal Squamous Papilloma | | MONDO:0021469|MONDO:0060766|MONDO:0001825 | -| MONDO:0858743 | anal hidradenoma papilliferum | NCIT:C96699 | MONDO:equivalentTo | Anal Hidradenoma Papilliferum | | MONDO:0021469|MONDO:0003446 | -| MONDO:0858745 | hnf1alpha-inactivated hepatocellular adenoma | NCIT:C96758 | MONDO:equivalentTo | HNF1alpha-Inactivated Hepatocellular Adenoma | | MONDO:0018902 | -| MONDO:0858746 | beta-catenin-activated hepatocellular adenoma | NCIT:C96759 | MONDO:equivalentTo | Beta-Catenin-Activated Hepatocellular Adenoma | | MONDO:0018902 | -| MONDO:0858747 | inflammatory hepatocellular adenoma | NCIT:C96760 | MONDO:equivalentTo | Inflammatory Hepatocellular Adenoma | | MONDO:0018902 | -| MONDO:0858748 | unclassified hepatocellular adenoma | NCIT:C96761 | MONDO:equivalentTo | Unclassified Hepatocellular Adenoma | | MONDO:0018902 | -| MONDO:0858750 | liver neuroendocrine neoplasm | NCIT:C96786 | MONDO:equivalentTo | Liver Neuroendocrine Neoplasm | | MONDO:0024477|MONDO:0024503 | -| MONDO:0858751 | lymphocyte-rich hepatocellular carcinoma | NCIT:C96788 | MONDO:equivalentTo | Lymphocyte-Rich Hepatocellular Carcinoma | | MONDO:0007256 | -| MONDO:0858752 | well differentiated hepatocellular carcinoma | NCIT:C96789 | MONDO:equivalentTo | Well Differentiated Hepatocellular Carcinoma | | MONDO:0007256 | -| MONDO:0858753 | moderately differentiated hepatocellular carcinoma | NCIT:C96790 | MONDO:equivalentTo | Moderately Differentiated Hepatocellular Carcinoma | | MONDO:0007256 | -| MONDO:0858754 | poorly differentiated hepatocellular carcinoma | NCIT:C96791 | MONDO:equivalentTo | Poorly Differentiated Hepatocellular Carcinoma | | MONDO:0007256 | -| MONDO:0858755 | liver undifferentiated carcinoma | NCIT:C96792 | MONDO:equivalentTo | Liver Undifferentiated Carcinoma | | MONDO:0018531|MONDO:0005617 | -| MONDO:0858756 | small duct intrahepatic cholangiocarcinoma | NCIT:C96805 | MONDO:equivalentTo | Small Duct Intrahepatic Cholangiocarcinoma | | MONDO:0003210 | -| MONDO:0858757 | bile duct intraductal papillary neoplasm with an associated invasive carcinoma | NCIT:C96810 | MONDO:equivalentTo | Bile Duct Intraductal Papillary Neoplasm with an Associated Invasive Carcinoma | | MONDO:0003455|MONDO:0003193 | -| MONDO:0858758 | extrahepatic bile duct tubulopapillary adenoma | NCIT:C96811 | MONDO:equivalentTo | Extrahepatic Bile Duct Tubulopapillary Adenoma | | MONDO:0003445|MONDO:0024661 | -| MONDO:0858760 | liver synovial sarcoma | NCIT:C96845 | MONDO:equivalentTo | Liver Synovial Sarcoma | | MONDO:0002397|MONDO:0010434 | -| MONDO:0858761 | liver carcinosarcoma | NCIT:C96848 | MONDO:equivalentTo | Liver Carcinosarcoma | | MONDO:0018531|MONDO:0002928 | -| MONDO:0858765 | gallbladder mucinous cystic neoplasm | NCIT:C96881 | MONDO:equivalentTo | Gallbladder Mucinous Cystic Neoplasm | | MONDO:0021253 | -| MONDO:0858766 | gallbladder carcinosarcoma | NCIT:C96888 | MONDO:equivalentTo | Gallbladder Carcinosarcoma | | MONDO:0003220|MONDO:0002928 | -| MONDO:0858767 | gallbladder hepatoid adenocarcinoma | NCIT:C96890 | MONDO:equivalentTo | Gallbladder Hepatoid Adenocarcinoma | | MONDO:0006215|MONDO:0006243 | -| MONDO:0858768 | gallbladder cribriform carcinoma | NCIT:C96891 | MONDO:equivalentTo | Gallbladder Cribriform Carcinoma | | MONDO:0006215|MONDO:0006176 | -| MONDO:0858769 | gallbladder adenocarcinoma, biliary type | NCIT:C96915 | MONDO:equivalentTo | Gallbladder Adenocarcinoma, Biliary Type | | MONDO:0006215|MONDO:0005606 | -| MONDO:0858770 | gallbladder adenocarcinoma, gastric foveolar type | NCIT:C96916 | MONDO:equivalentTo | Gallbladder Adenocarcinoma, Gastric Foveolar Type | | MONDO:0006215 | -| MONDO:0858774 | gallbladder mixed adenoneuroendocrine carcinoma | NCIT:C96927 | MONDO:equivalentTo | Gallbladder Mixed Adenoneuroendocrine Carcinoma | | MONDO:0006182|MONDO:0003220 | -| MONDO:0858775 | gallbladder tubular carcinoid | NCIT:C96930 | MONDO:equivalentTo | Gallbladder Tubular Carcinoid | | MONDO:0015073 | -| MONDO:0858776 | extrahepatic bile duct adenocarcinoma, biliary type | NCIT:C96936 | MONDO:equivalentTo | Extrahepatic Bile Duct Adenocarcinoma, Biliary Type | | MONDO:0002665|MONDO:0005606 | -| MONDO:0858777 | extrahepatic bile duct adenocarcinoma, gastric foveolar type | NCIT:C96937 | MONDO:equivalentTo | Extrahepatic Bile Duct Adenocarcinoma, Gastric Foveolar Type | | MONDO:0002665 | -| MONDO:0858778 | extrahepatic bile duct adenocarcinoma, intestinal type | NCIT:C96938 | MONDO:equivalentTo | Extrahepatic Bile Duct Adenocarcinoma, Intestinal Type | | MONDO:0002665 | -| MONDO:0858779 | extrahepatic bile duct carcinosarcoma | NCIT:C96939 | MONDO:equivalentTo | Extrahepatic Bile Duct Carcinosarcoma | | MONDO:0003090|MONDO:0002928 | -| MONDO:0858780 | extrahepatic bile duct mucinous cystic neoplasm with an associated invasive carcinoma | NCIT:C96946 | MONDO:equivalentTo | Extrahepatic Bile Duct Mucinous Cystic Neoplasm with an Associated Invasive Carcinoma | | MONDO:0002665|MONDO:0004462|MONDO:0002868 | -| MONDO:0858781 | intrahepatic bile duct mucinous cystic neoplasm with an associated invasive carcinoma | NCIT:C96947 | MONDO:equivalentTo | Intrahepatic Bile Duct Mucinous Cystic Neoplasm with an Associated Invasive Carcinoma | | MONDO:0003979|MONDO:0018531|MONDO:0002868 | -| MONDO:0858783 | extrahepatic bile duct lymphoma | NCIT:C96952 | MONDO:equivalentTo | Extrahepatic Bile Duct Lymphoma | | MONDO:0021321|MONDO:0004699 | -| MONDO:0858785 | extrahepatic bile duct neuroendocrine neoplasm | NCIT:C96954 | MONDO:equivalentTo | Extrahepatic Bile Duct Neuroendocrine Neoplasm | | MONDO:0021385|MONDO:0024503 | -| MONDO:0858786 | extrahepatic bile duct mixed adenoneuroendocrine carcinoma | NCIT:C96959 | MONDO:equivalentTo | Extrahepatic Bile Duct Mixed Adenoneuroendocrine Carcinoma | | MONDO:0006182|MONDO:0003090 | -| MONDO:0858788 | invasive breast lobular carcinoma, alveolar variant | NCIT:C97049 | MONDO:equivalentTo | Invasive Breast Lobular Carcinoma, Alveolar Variant | | MONDO:0005051 | -| MONDO:0858789 | invasive breast lobular carcinoma, pleomorphic variant | NCIT:C97051 | MONDO:equivalentTo | Invasive Breast Lobular Carcinoma, Pleomorphic Variant | | MONDO:0005051 | -| MONDO:0858790 | invasive breast lobular carcinoma, solid variant | NCIT:C97052 | MONDO:equivalentTo | Invasive Breast Lobular Carcinoma, Solid Variant | | MONDO:0005051 | -| MONDO:0858791 | invasive breast lobular carcinoma, tubulolobular variant | NCIT:C97053 | MONDO:equivalentTo | Invasive Breast Lobular Carcinoma, Tubulolobular Variant | | MONDO:0005051 | -| MONDO:0858792 | mixed congenital mesoblastic nephroma | NCIT:C97058 | MONDO:equivalentTo | Mixed Congenital Mesoblastic Nephroma | | MONDO:0017043|MONDO:0005853 | -| MONDO:0858804 | sclerosing polycystic adenosis | NCIT:C97135 | MONDO:equivalentTo | Sclerosing Polycystic Adenosis | | MONDO:0021460 | -| MONDO:0858851 | contralateral breast carcinoma | NCIT:C99390 | MONDO:equivalentTo | Contralateral Breast Carcinoma | | MONDO:0003982 | -| MONDO:0859471 | neoplastic medium-sized lymphocyte | NCIT:C37004 | MONDO:equivalentTo | Neoplastic Medium-Sized Lymphocyte | | | -| MONDO:0859472 | neoplastic b-lymphocyte | NCIT:C38640 | MONDO:equivalentTo | Neoplastic B-Lymphocyte | | | -| MONDO:0859554 | medaka melanoma | NCIT:C134572 | MONDO:equivalentTo | Medaka Melanoma | | MONDO:0700196 | -| MONDO:0859555 | xiphophorus melanoma | NCIT:C134575 | MONDO:equivalentTo | Xiphophorus Melanoma | | MONDO:0700196 | -| MONDO:0859556 | non-human or experimental organism neoplasm | NCIT:C134576 | MONDO:equivalentTo | Non-Human or Experimental Organism Neoplasm | | | -| MONDO:0859560 | tubulostromal adenoma | NCIT:C79953 | MONDO:equivalentTo | Tubulostromal Adenoma | | | -| MONDO:0859561 | tubulostromal adenocarcinoma | NCIT:C80356 | MONDO:equivalentTo | Tubulostromal Adenocarcinoma | | | -| MONDO:0859730 | vaginal non-keratinizing squamous cell carcinoma | NCIT:C40244 | MONDO:equivalentTo | Vaginal Non-Keratinizing Squamous Cell Carcinoma | | MONDO:0006490 | -| MONDO:0860042 | lymphoproliferative disease associated with primary immune disorder | NCIT:C150673 | MONDO:equivalentTo | Lymphoproliferative Disease Associated with Primary Immune Disorder | | | -| MONDO:0860043 | genitourinary system disorder | NCIT:C156660 | MONDO:equivalentTo | Genitourinary System Disorder | | | -| MONDO:0860044 | recurrent hiv-related lymphoproliferative disorder | NCIT:C157685 | MONDO:equivalentTo | Recurrent HIV-Related Lymphoproliferative Disorder | | | -| MONDO:0860045 | refractory hiv-related lymphoproliferative disorder | NCIT:C157687 | MONDO:equivalentTo | Refractory HIV-Related Lymphoproliferative Disorder | | | -| MONDO:0860046 | hiv-related lymphoproliferative disorder | NCIT:C157709 | MONDO:equivalentTo | HIV-Related Lymphoproliferative Disorder | | | -| MONDO:0860047 | ebv-related lymphoproliferative disease with primary immunodeficiency | NCIT:C160150 | MONDO:equivalentTo | EBV-Related Lymphoproliferative Disease with Primary Immunodeficiency | | | -| MONDO:0860048 | recurrent ebv-related lymphoproliferative disease with primary immunodeficiency | NCIT:C160151 | MONDO:equivalentTo | Recurrent EBV-Related Lymphoproliferative Disease with Primary Immunodeficiency | | | -| MONDO:0860049 | refractory ebv-related lymphoproliferative disease with primary immunodeficiency | NCIT:C160152 | MONDO:equivalentTo | Refractory EBV-Related Lymphoproliferative Disease with Primary Immunodeficiency | | | -| MONDO:0860050 | tonsillar disorder | NCIT:C173797 | MONDO:equivalentTo | Tonsillar Disorder | | | -| MONDO:0860051 | soft tissue disorder | NCIT:C27042 | MONDO:equivalentTo | Soft Tissue Disorder | | | -| MONDO:0860052 | connective and soft tissue disorder | NCIT:C27574 | MONDO:equivalentTo | Connective and Soft Tissue Disorder | | | -| MONDO:0860053 | neck disorder | NCIT:C27648 | MONDO:equivalentTo | Neck Disorder | | | -| MONDO:0860054 | peritoneal and retroperitoneal disorder | NCIT:C27664 | MONDO:equivalentTo | Peritoneal and Retroperitoneal Disorder | | | -| MONDO:0860055 | female reproductive system precancerous condition | NCIT:C27788 | MONDO:equivalentTo | Female Reproductive System Precancerous Condition | | | -| MONDO:0860056 | tobacco use disorder | NCIT:C35074 | MONDO:equivalentTo | Tobacco Use Disorder | | | -| MONDO:0860057 | sternal disorder | NCIT:C35744 | MONDO:equivalentTo | Sternal Disorder | | | -| MONDO:0860058 | chest wall disorder | NCIT:C35745 | MONDO:equivalentTo | Chest Wall Disorder | | | -| MONDO:0860059 | axillary disorder | NCIT:C35746 | MONDO:equivalentTo | Axillary Disorder | | | -| MONDO:0860060 | hematopoietic and lymphoid system disorder | NCIT:C35814 | MONDO:equivalentTo | Hematopoietic and Lymphoid System Disorder | | | -| MONDO:0860062 | anal precancerous condition | NCIT:C7407 | MONDO:equivalentTo | Anal Precancerous Condition | | | -| MONDO:0860063 | esophageal precancerous condition | NCIT:C7423 | MONDO:equivalentTo | Esophageal Precancerous Condition | | | -| MONDO:0860064 | gastric precancerous condition | NCIT:C7424 | MONDO:equivalentTo | Gastric Precancerous Condition | | | -| MONDO:0860065 | pulmonary precancerous condition | NCIT:C7435 | MONDO:equivalentTo | Pulmonary Precancerous Condition | | | -| MONDO:0860066 | hepatobiliary precancerous condition | NCIT:C7655 | MONDO:equivalentTo | Hepatobiliary Precancerous Condition | | | -| MONDO:0860067 | intestinal precancerous condition | NCIT:C7657 | MONDO:equivalentTo | Intestinal Precancerous Condition | | | -| MONDO:0860068 | digestive system precancerous condition | NCIT:C7659 | MONDO:equivalentTo | Digestive System Precancerous Condition | | | -| MONDO:0860069 | cutaneous precancerous condition | NCIT:C8957 | MONDO:equivalentTo | Cutaneous Precancerous Condition | | | -| MONDO:0860070 | neonatal disorder | NCIT:C98996 | MONDO:equivalentTo | Neonatal Disorder | | | -| MONDO:0950158 | core binding factor acute myeloid leukemia | NCIT:C122688 | MONDO:equivalentTo | Core Binding Factor Acute Myeloid Leukemia | | MONDO:0020078 | -| MONDO:0955884 | adult acute eosinophilic leukemia | NCIT:C7963 | MONDO:equivalentTo | Adult Acute Eosinophilic Leukemia | | MONDO:0043881 | -| MONDO:0956044 | acute myeloid leukemia (megakaryoblastic) with t(1;22)(p13.3;q13.1); rbm15-mkl1 | NCIT:C82427 | MONDO:equivalentTo | Acute Myeloid Leukemia (Megakaryoblastic) with t(1;22)(p13.3;q13.1); RBM15-MKL1 | | MONDO:0020078 | -| MONDO:0956704 | childhood acute eosinophilic leukemia | NCIT:C9165 | MONDO:equivalentTo | Childhood Acute Eosinophilic Leukemia | | MONDO:0043881 | -| MONDO:0956756 | acute myeloid leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22); cbfb-myh11 | NCIT:C9287 | MONDO:equivalentTo | Acute Myeloid Leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22); CBFB-MYH11 | | MONDO:0020078 | -| MONDO:0956757 | acute myeloid leukemia with t(8;21)(q22; q22.1); runx1-runx1t1 | NCIT:C9288 | MONDO:equivalentTo | Acute Myeloid Leukemia with t(8;21)(q22; q22.1); RUNX1-RUNX1T1 | | MONDO:0020078 | -| MONDO:0957380 | cic-rearranged sarcoma | NCIT:C120224 | MONDO:equivalentTo | CIC-Rearranged Sarcoma | | MONDO:0858921 | -| MONDO:0957623 | smoldering systemic mastocytosis | NCIT:C115460 | MONDO:equivalentTo | Smoldering Systemic Mastocytosis | | MONDO:0016586 | -| MONDO:0957624 | indolent clonal t-cell lymphoproliferative disorder of the gastrointestinal tract | NCIT:C139021 | MONDO:equivalentTo | Indolent Clonal T-Cell Lymphoproliferative Disorder of the Gastrointestinal Tract | | MONDO:0005169 | -| MONDO:0957625 | penile adenosquamous carcinoma | NCIT:C159248 | MONDO:equivalentTo | Penile Adenosquamous Carcinoma | | MONDO:0006360|MONDO:0006074 | -| MONDO:0957626 | seminal vesicle soft tissue neoplasm | NCIT:C161637 | MONDO:equivalentTo | Seminal Vesicle Soft Tissue Neoplasm | | MONDO:0002790|MONDO:0006424 | -| MONDO:0957627 | hepatocellular malignant neoplasm, not otherwise specified | NCIT:C161838 | MONDO:equivalentTo | Hepatocellular Malignant Neoplasm, Not Otherwise Specified | | MONDO:0018666 | -| MONDO:0957628 | epididymal melanotic neuroectodermal tumor | NCIT:C162488 | MONDO:equivalentTo | Epididymal Melanotic Neuroectodermal Tumor | | MONDO:0002072|MONDO:0021473 | -| MONDO:0957629 | systemic mastocytosis with an associated germ cell tumor | NCIT:C186735 | MONDO:equivalentTo | Systemic Mastocytosis with an Associated Germ Cell Tumor | | MONDO:0016586 | -| MONDO:0957630 | estrogen receptor-positive breast carcinoma | NCIT:C188366 | MONDO:equivalentTo | Estrogen Receptor-Positive Breast Carcinoma | | | -| MONDO:0957631 | childhood myelodysplastic syndrome with excess blasts | NCIT:C188449 | MONDO:equivalentTo | Childhood Myelodysplastic Syndrome with Excess Blasts | | MONDO:0019454|MONDO:0044873 | -| MONDO:0957632 | childhood acute myeloid leukemia with t(9;11)(p21.3;q23.3); mllt3-kmt2a | NCIT:C188451 | MONDO:equivalentTo | Childhood Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A | | MONDO:0004996|MONDO:0020317 | -| MONDO:0957633 | lung small cell carcinoma neuroendocrine subtype | NCIT:C188753 | MONDO:equivalentTo | Lung Small Cell Carcinoma Neuroendocrine Subtype | | MONDO:0008433 | -| MONDO:0957634 | lung small cell carcinoma molecular subtypes | NCIT:C188756 | MONDO:equivalentTo | Lung Small Cell Carcinoma Molecular Subtypes | | MONDO:0008433 | -| MONDO:0957635 | adult ganglioneuroma | NCIT:C188947 | MONDO:equivalentTo | Adult Ganglioneuroma | | MONDO:0005033 | -| MONDO:0957636 | childhood nervous system neoplasm | NCIT:C188950 | MONDO:equivalentTo | Childhood Nervous System Neoplasm | | MONDO:0021079|MONDO:0021248 | -| MONDO:0957637 | choroidal ganglioneuroma | NCIT:C188956 | MONDO:equivalentTo | Choroidal Ganglioneuroma | | MONDO:0021487|MONDO:0005033 | -| MONDO:0957638 | childhood connective and soft tissue neoplasm | NCIT:C188963 | MONDO:equivalentTo | Childhood Connective and Soft Tissue Neoplasm | | MONDO:0021079|MONDO:0044334 | -| MONDO:0957639 | childhood low grade fibromyxoid sarcoma | NCIT:C188970 | MONDO:equivalentTo | Childhood Low Grade Fibromyxoid Sarcoma | | MONDO:0002678|MONDO:0006272 | -| MONDO:0957640 | extragonadal teratoma | NCIT:C189045 | MONDO:equivalentTo | Extragonadal Teratoma | | MONDO:0018201|MONDO:0002601 | -| MONDO:0957641 | testicular teratoma, postpubertal-type | NCIT:C189057 | MONDO:equivalentTo | Testicular Teratoma, Postpubertal-Type | | MONDO:0003510|MONDO:0018193 | -| MONDO:0957642 | kidney carcinoma molecular subtypes | NCIT:C189241 | MONDO:equivalentTo | Kidney Carcinoma Molecular Subtypes | | MONDO:0005206 | -| MONDO:0957643 | eosinophilic solid and cystic renal cell carcinoma | NCIT:C189254 | MONDO:equivalentTo | Eosinophilic Solid and Cystic Renal Cell Carcinoma | | MONDO:0005549 | -| MONDO:0957644 | ovarian sertoli-leydig cell tumor molecular subtypes | NCIT:C189319 | MONDO:equivalentTo | Ovarian Sertoli-Leydig Cell Tumor Molecular Subtypes | | MONDO:0036595 | -| MONDO:0957645 | mullerian papilloma | NCIT:C189336 | MONDO:equivalentTo | Mullerian Papilloma | | MONDO:0021078 | -| MONDO:0957646 | childhood breast neoplasm | NCIT:C189338 | MONDO:equivalentTo | Childhood Breast Neoplasm | | MONDO:0021079|MONDO:0021100 | -| MONDO:0957647 | childhood digestive system neoplasm | NCIT:C189869 | MONDO:equivalentTo | Childhood Digestive System Neoplasm | | MONDO:0021079|MONDO:0021223 | -| MONDO:0957648 | epithelial hepatoblastoma | NCIT:C189923 | MONDO:equivalentTo | Epithelial Hepatoblastoma | | MONDO:0018666 | -| MONDO:0957649 | non-teratoid hepatoblastoma | NCIT:C189926 | MONDO:equivalentTo | Non-Teratoid Hepatoblastoma | | MONDO:0003650 | -| MONDO:0957650 | hepatoblastoma by pretext stage | NCIT:C189927 | MONDO:equivalentTo | Hepatoblastoma by PRETEXT Stage | | MONDO:0018666 | -| MONDO:0957651 | hepatoblastoma by postsurgical stage | NCIT:C189929 | MONDO:equivalentTo | Hepatoblastoma by Postsurgical Stage | | MONDO:0018666 | -| MONDO:0957652 | childhood fibrolamellar carcinoma | NCIT:C189932 | MONDO:equivalentTo | Childhood Fibrolamellar Carcinoma | | MONDO:0018055|MONDO:0006210 | -| MONDO:0957653 | childhood endocrine neoplasm | NCIT:C190056 | MONDO:equivalentTo | Childhood Endocrine Neoplasm | | MONDO:0021079|MONDO:0002082 | -| MONDO:0957654 | childhood thoracic neoplasm | NCIT:C190090 | MONDO:equivalentTo | Childhood Thoracic Neoplasm | | MONDO:0021079|MONDO:0021350 | -| MONDO:0957655 | childhood head and neck neoplasm | NCIT:C190119 | MONDO:equivalentTo | Childhood Head and Neck Neoplasm | | MONDO:0021079|MONDO:0005586 | -| MONDO:0957656 | childhood skin neoplasm | NCIT:C190123 | MONDO:equivalentTo | Childhood Skin Neoplasm | | MONDO:0021079|MONDO:0002531 | -| MONDO:0957657 | childhood carcinoma | NCIT:C190275 | MONDO:equivalentTo | Childhood Carcinoma | | MONDO:0004993|MONDO:0036491 | -| MONDO:0957658 | refractory t/nk-cell lymphoproliferative disorder | NCIT:C190397 | MONDO:equivalentTo | Refractory T/NK-Cell Lymphoproliferative Disorder | | | -| MONDO:0957659 | recurrent t/nk-cell lymphoproliferative disorder | NCIT:C190398 | MONDO:equivalentTo | Recurrent T/NK-Cell Lymphoproliferative Disorder | | | -| MONDO:0957660 | ebv-related t/nk-cell lymphoproliferative disorder | NCIT:C190402 | MONDO:equivalentTo | EBV-Related T/NK-Cell Lymphoproliferative Disorder | | | -| MONDO:0957661 | childhood benign neoplasm | NCIT:C190573 | MONDO:equivalentTo | Childhood Benign Neoplasm | | MONDO:0021079|MONDO:0005165 | -| MONDO:0957662 | benign liver neoplasm | NCIT:C190592 | MONDO:equivalentTo | Benign Liver Neoplasm | | MONDO:0024477|MONDO:0000385 | -| MONDO:0957663 | high grade endometrial carcinoma | NCIT:C190680 | MONDO:equivalentTo | High Grade Endometrial Carcinoma | | MONDO:0002447 | -| MONDO:0957664 | iridociliary melanoma | NCIT:C190746 | MONDO:equivalentTo | Iridociliary Melanoma | | MONDO:0006486 | -| MONDO:0957665 | b acute lymphoblastic leukemia associated with down syndrome | NCIT:C190847 | MONDO:equivalentTo | B Acute Lymphoblastic Leukemia Associated with Down Syndrome | | MONDO:0020511 | -| MONDO:0957666 | androgen receptor-positive breast carcinoma | NCIT:C190851 | MONDO:equivalentTo | Androgen Receptor-Positive Breast Carcinoma | | | -| MONDO:0957667 | b lymphoblastic leukemia/lymphoma with etv6-runx1-like features | NCIT:C190956 | MONDO:equivalentTo | B Lymphoblastic Leukemia/Lymphoma with ETV6-RUNX1-Like Features | | MONDO:0035605 | -| MONDO:0957668 | renal cell carcinoma, not otherwise specified | NCIT:C191370 | MONDO:equivalentTo | Renal Cell Carcinoma, Not Otherwise Specified | | MONDO:0005549 | -| MONDO:0957669 | kidney classic angiomyolipoma | NCIT:C191391 | MONDO:equivalentTo | Kidney Classic Angiomyolipoma | | MONDO:0002513|MONDO:0004555 | -| MONDO:0957670 | secondary plasma cell leukemia | NCIT:C191432 | MONDO:equivalentTo | Secondary Plasma Cell Leukemia | | MONDO:0024881|MONDO:0018689 | -| MONDO:0957671 | papillary urothelial neoplasm of low malignant potential | NCIT:C191672 | MONDO:equivalentTo | Papillary Urothelial Neoplasm of Low Malignant Potential | | MONDO:0003755|MONDO:0003443 | -| MONDO:0957672 | invasive lymphoepithelioma-like urothelial carcinoma | NCIT:C191678 | MONDO:equivalentTo | Invasive Lymphoepithelioma-Like Urothelial Carcinoma | | MONDO:0003572|MONDO:0040678 | -| MONDO:0957673 | invasive giant cell urothelial carcinoma | NCIT:C191679 | MONDO:equivalentTo | Invasive Giant Cell Urothelial Carcinoma | | MONDO:0040678 | -| MONDO:0957674 | invasive urothelial carcinoma with glandular differentiation | NCIT:C191680 | MONDO:equivalentTo | Invasive Urothelial Carcinoma with Glandular Differentiation | | MONDO:0040678 | -| MONDO:0957675 | invasive urothelial carcinoma with squamous differentiation | NCIT:C191681 | MONDO:equivalentTo | Invasive Urothelial Carcinoma with Squamous Differentiation | | MONDO:0040678 | -| MONDO:0957676 | invasive urothelial carcinoma with trophoblastic differentiation | NCIT:C191682 | MONDO:equivalentTo | Invasive Urothelial Carcinoma with Trophoblastic Differentiation | | MONDO:0040678 | -| MONDO:0957677 | invasive clear cell (glycogen-rich) urothelial carcinoma | NCIT:C191683 | MONDO:equivalentTo | Invasive Clear Cell (Glycogen-Rich) Urothelial Carcinoma | | MONDO:0040678 | -| MONDO:0957678 | invasive lipid-rich urothelial carcinoma | NCIT:C191684 | MONDO:equivalentTo | Invasive Lipid-Rich Urothelial Carcinoma | | MONDO:0040678 | -| MONDO:0957679 | invasive microcystic urothelial carcinoma | NCIT:C191685 | MONDO:equivalentTo | Invasive Microcystic Urothelial Carcinoma | | MONDO:0040678 | -| MONDO:0957680 | invasive nested urothelial carcinoma | NCIT:C191687 | MONDO:equivalentTo | Invasive Nested Urothelial Carcinoma | | MONDO:0040678 | -| MONDO:0957681 | invasive plasmacytoid urothelial carcinoma | NCIT:C191688 | MONDO:equivalentTo | Invasive Plasmacytoid Urothelial Carcinoma | | MONDO:0040678 | -| MONDO:0957682 | invasive large nested urothelial carcinoma | NCIT:C191725 | MONDO:equivalentTo | Invasive Large Nested Urothelial Carcinoma | | MONDO:0040678 | -| MONDO:0957683 | invasive tubular urothelial carcinoma | NCIT:C191728 | MONDO:equivalentTo | Invasive Tubular Urothelial Carcinoma | | MONDO:0040678 | -| MONDO:0957684 | invasive poorly differentiated urothelial carcinoma | NCIT:C191730 | MONDO:equivalentTo | Invasive Poorly Differentiated Urothelial Carcinoma | | MONDO:0040678 | -| MONDO:0957685 | invasive conventional urothelial carcinoma | NCIT:C191734 | MONDO:equivalentTo | Invasive Conventional Urothelial Carcinoma | | MONDO:0040678 | -| MONDO:0957686 | prostatic intraepithelial neoplasia-like adenocarcinoma | NCIT:C191961 | MONDO:equivalentTo | Prostatic Intraepithelial Neoplasia-Like Adenocarcinoma | | MONDO:0002493 | -| MONDO:0957687 | extrapulmonary neuroendocrine carcinoma | NCIT:C191977 | MONDO:equivalentTo | Extrapulmonary Neuroendocrine Carcinoma | | MONDO:0002120 | -| MONDO:0957688 | intratubular embryonal carcinoma | NCIT:C192096 | MONDO:equivalentTo | Intratubular Embryonal Carcinoma | | MONDO:0004520|MONDO:0006446 | -| MONDO:0957689 | testicular yolk sac tumor, postpubertal-type | NCIT:C192099 | MONDO:equivalentTo | Testicular Yolk Sac Tumor, Postpubertal-Type | | MONDO:0003402 | -| MONDO:0957690 | cystic trophoblastic tumor | NCIT:C192105 | MONDO:equivalentTo | Cystic Trophoblastic Tumor | | MONDO:0021077|MONDO:0002872 | -| MONDO:0957691 | testicular teratoma, prepubertal-type | NCIT:C192107 | MONDO:equivalentTo | Testicular Teratoma, Prepubertal-Type | | MONDO:0018193 | -| MONDO:0957692 | gonadal myoid stromal tumor | NCIT:C192116 | MONDO:equivalentTo | Gonadal Myoid Stromal Tumor | | MONDO:0021447 | -| MONDO:0957693 | penile squamous cell carcinoma, not otherwise specified | NCIT:C192222 | MONDO:equivalentTo | Penile Squamous Cell Carcinoma, Not Otherwise Specified | | MONDO:0018352 | -| MONDO:0957694 | penile mucoepidermoid carcinoma | NCIT:C192223 | MONDO:equivalentTo | Penile Mucoepidermoid Carcinoma | | MONDO:0006360|MONDO:0003036 | -| MONDO:0957695 | urinary tract neoplasm | NCIT:C192666 | MONDO:equivalentTo | Urinary Tract Neoplasm | | MONDO:0021066 | -| MONDO:0957696 | benign cranial nerve neoplasm | NCIT:C193416 | MONDO:equivalentTo | Benign Cranial Nerve Neoplasm | | MONDO:0000648|MONDO:0002633 | -| MONDO:0957697 | benign spinal meningioma | NCIT:C193417 | MONDO:equivalentTo | Benign Spinal Meningioma | | MONDO:0001279|MONDO:0003054 | -| MONDO:0957698 | rectal gastrointestinal stromal tumor | NCIT:C193420 | MONDO:equivalentTo | Rectal Gastrointestinal Stromal Tumor | | MONDO:0002165|MONDO:0006159 | -| MONDO:0957699 | malignant ileal neoplasm | NCIT:C193425 | MONDO:equivalentTo | Malignant Ileal Neoplasm | | MONDO:0006801|MONDO:0000956 | -| MONDO:0957700 | refractory malignant phyllodes tumor | NCIT:C193453 | MONDO:equivalentTo | Refractory Malignant Phyllodes Tumor | | MONDO:0037003|MONDO:0036501 | -| MONDO:0957701 | childhood cancer stage by toronto guidelines v2 | NCIT:C198027 | MONDO:equivalentTo | Childhood Cancer Stage by Toronto Guidelines v2 | | MONDO:0006517 | -| MONDO:0957702 | myeloproliferative neoplasm, bcr-abl1 negative | NCIT:C198555 | MONDO:equivalentTo | Myeloproliferative Neoplasm, BCR-ABL1 Negative | | MONDO:0020076 | -| MONDO:0957703 | myeloid/lymphoid neoplasms with flt3 rearrangement | NCIT:C198559 | MONDO:equivalentTo | Myeloid/Lymphoid Neoplasms with FLT3 Rearrangement | | MONDO:0015688 | -| MONDO:0957704 | myeloid/lymphoid neoplasms with etv6-abl1 | NCIT:C198565 | MONDO:equivalentTo | Myeloid/Lymphoid Neoplasms with ETV6-ABL1 | | MONDO:0015688 | -| MONDO:0957705 | bone marrow mastocytosis | NCIT:C198573 | MONDO:equivalentTo | Bone Marrow Mastocytosis | | MONDO:0020331 | -| MONDO:0957706 | clonal monocytosis of undetermined significance | NCIT:C198580 | MONDO:equivalentTo | Clonal Monocytosis of Undetermined Significance | | MONDO:0006311 | -| MONDO:0957707 | myelodysplastic/myeloproliferative neoplasm with sf3b1 mutation and thrombocytosis | NCIT:C198581 | MONDO:equivalentTo | Myelodysplastic/Myeloproliferative Neoplasm with SF3B1 Mutation and Thrombocytosis | | MONDO:0006311 | -| MONDO:0957708 | clonal cytopenia with monocytosis of undetermined significance | NCIT:C198582 | MONDO:equivalentTo | Clonal Cytopenia with Monocytosis of Undetermined Significance | | MONDO:0006311 | -| MONDO:0957709 | myeloid neoplasm with mutated tp53 | NCIT:C198593 | MONDO:equivalentTo | Myeloid Neoplasm with Mutated TP53 | | MONDO:0005170 | -| MONDO:0957710 | myelodysplastic syndrome/acute myeloid leukemia, not otherwise specified | NCIT:C198597 | MONDO:equivalentTo | Myelodysplastic Syndrome/Acute Myeloid Leukemia, Not Otherwise Specified | | MONDO:0015041 | -| MONDO:0957711 | pediatric and/or germline mutation-associated myeloid disorders | NCIT:C198663 | MONDO:equivalentTo | Pediatric and/or Germline Mutation-Associated Myeloid Disorders | | MONDO:0005170 | -| MONDO:0957712 | b acute lymphoblastic leukemia with germline predisposition | NCIT:C198683 | MONDO:equivalentTo | B Acute Lymphoblastic Leukemia with Germline Predisposition | | MONDO:0020511 | -| MONDO:0957713 | acute myeloid leukemia with stat3-rara | NCIT:C198827 | MONDO:equivalentTo | Acute Myeloid Leukemia with STAT3-RARA | | MONDO:0100375 | -| MONDO:0957714 | acute myeloid leukemia with t(1;17)(q42.3;q21.2); irf2bp2-rara | NCIT:C198831 | MONDO:equivalentTo | Acute Myeloid Leukemia with t(1;17)(q42.3;q21.2); IRF2BP2-RARA | | MONDO:0100375 | -| MONDO:0957715 | acute myeloid leukemia with tbl1xr1-rara | NCIT:C198834 | MONDO:equivalentTo | Acute Myeloid Leukemia with TBL1XR1-RARA | | MONDO:0100375 | -| MONDO:0957716 | acute myeloid leukemia with fip1l1-rara | NCIT:C198839 | MONDO:equivalentTo | Acute Myeloid Leukemia with FIP1L1-RARA | | MONDO:0100375 | -| MONDO:0957717 | acute myeloid leukemia with bcor-rara | NCIT:C198841 | MONDO:equivalentTo | Acute Myeloid Leukemia with BCOR-RARA | | MONDO:0100375 | -| MONDO:0957718 | acute myeloid leukemia with in-frame bzip cebpa mutation | NCIT:C198891 | MONDO:equivalentTo | Acute Myeloid Leukemia with In-Frame bZIP CEBPA Mutation | | MONDO:0017894 | -| MONDO:0957719 | acute myeloid leukemia with myelodysplasia-related cytogenetic abnormalities | NCIT:C198957 | MONDO:equivalentTo | Acute Myeloid Leukemia with Myelodysplasia-Related Cytogenetic Abnormalities | | MONDO:0100409 | -| MONDO:0957720 | low grade endometrioid adenocarcinoma | NCIT:C199146 | MONDO:equivalentTo | Low Grade Endometrioid Adenocarcinoma | | MONDO:0005026 | -| MONDO:0957721 | high grade endometrioid adenocarcinoma | NCIT:C199149 | MONDO:equivalentTo | High Grade Endometrioid Adenocarcinoma | | MONDO:0005026 | -| MONDO:0957722 | early t precursor lymphoblastic leukemia/lymphoma | NCIT:C199170 | MONDO:equivalentTo | Early T Precursor Lymphoblastic Leukemia/Lymphoma | | MONDO:0003537 | -| MONDO:0957723 | early t precursor acute lymphoblastic leukemia with bcl11b rearrangement | NCIT:C199171 | MONDO:equivalentTo | Early T Precursor Acute Lymphoblastic Leukemia with BCL11B Rearrangement | | MONDO:0100291 | -| MONDO:0957724 | early t precursor acute lymphoblastic leukemia, not otherwise specified | NCIT:C199172 | MONDO:equivalentTo | Early T Precursor Acute Lymphoblastic Leukemia, Not Otherwise Specified | | MONDO:0100291 | -| MONDO:0957725 | t lymphoblastic leukemia/lymphoma, not otherwise specified | NCIT:C199173 | MONDO:equivalentTo | T Lymphoblastic Leukemia/Lymphoma, Not Otherwise Specified | | MONDO:0003537 | -| MONDO:0957726 | b acute lymphoblastic leukemia with recurrent genetic abnormalities | NCIT:C199202 | MONDO:equivalentTo | B Acute Lymphoblastic Leukemia with Recurrent Genetic Abnormalities | | MONDO:0020511|MONDO:0035605 | -| MONDO:0957727 | b lymphoblastic leukemia/lymphoma with myc rearrangement | NCIT:C199231 | MONDO:equivalentTo | B Lymphoblastic Leukemia/Lymphoma with MYC Rearrangement | | MONDO:0035605 | -| MONDO:0957728 | primary cold agglutinin disease | NCIT:C199387 | MONDO:equivalentTo | Primary Cold Agglutinin Disease | | MONDO:0004949 | -| MONDO:0957729 | multiple myeloma with recurrent genetic abnormalities | NCIT:C199392 | MONDO:equivalentTo | Multiple Myeloma with Recurrent Genetic Abnormalities | | MONDO:0009693 | -| MONDO:0957730 | multiple myeloma, not otherwise specified | NCIT:C199418 | MONDO:equivalentTo | Multiple Myeloma, Not Otherwise Specified | | MONDO:0009693 | -| MONDO:0957731 | heavy chain class-switched primary cutaneous marginal zone lymphoproliferative disorder | NCIT:C199457 | MONDO:equivalentTo | Heavy Chain Class-Switched Primary Cutaneous Marginal Zone Lymphoproliferative Disorder | | MONDO:0015813 | -| MONDO:0957732 | igm-positive primary cutaneous marginal zone lymphoproliferative disorder | NCIT:C199460 | MONDO:equivalentTo | IgM-Positive Primary Cutaneous Marginal Zone Lymphoproliferative Disorder | | MONDO:0015813 | -| MONDO:0957733 | bcl2-r-negative, cd23-positive follicle center lymphoma | NCIT:C199467 | MONDO:equivalentTo | BCL2-R-Negative, CD23-Positive Follicle Center Lymphoma | | MONDO:0018906 | -| MONDO:0957734 | cyclin d1-positive mantle cell lymphoma | NCIT:C199481 | MONDO:equivalentTo | Cyclin D1-Positive Mantle Cell Lymphoma | | MONDO:0018876 | -| MONDO:0957735 | hhv-8 and ebv-negative primary effusion-based lymphoma | NCIT:C199576 | MONDO:equivalentTo | HHV-8 and EBV-Negative Primary Effusion-Based Lymphoma | | MONDO:0018905 | -| MONDO:0957736 | classic hydroa vacciniforme lymphoproliferative disorder | NCIT:C199676 | MONDO:equivalentTo | Classic Hydroa Vacciniforme Lymphoproliferative Disorder | | MONDO:0018224 | -| MONDO:0957737 | systemic hydroa vacciniforme lymphoproliferative disorder | NCIT:C199677 | MONDO:equivalentTo | Systemic Hydroa Vacciniforme Lymphoproliferative Disorder | | MONDO:0018224 | -| MONDO:0957738 | indolent nk-cell lymphoproliferative disorder of the gastrointestinal tract | NCIT:C200037 | MONDO:equivalentTo | Indolent NK-Cell Lymphoproliferative Disorder of the Gastrointestinal Tract | | MONDO:0005169 | -| MONDO:0957739 | peripheral t-cell lymphoma-gata3 | NCIT:C200073 | MONDO:equivalentTo | Peripheral T-Cell Lymphoma-GATA3 | | MONDO:0004964 | -| MONDO:0957740 | peripheral t-cell lymphoma-tbx21 | NCIT:C200074 | MONDO:equivalentTo | Peripheral T-Cell Lymphoma-TBX21 | | MONDO:0004964 | -| MONDO:0957741 | alk-positive histiocytosis | NCIT:C200105 | MONDO:equivalentTo | ALK-Positive Histiocytosis | | MONDO:0006247 | -| MONDO:0957742 | vulvar tubulovillous adenoma | NCIT:C200207 | MONDO:equivalentTo | Vulvar Tubulovillous Adenoma | | MONDO:0002198|MONDO:0000643 | -| MONDO:0957743 | pancreatic cystic neoplasm | NCIT:C200227 | MONDO:equivalentTo | Pancreatic Cystic Neoplasm | | MONDO:0021077|MONDO:0021076 | -| MONDO:0957744 | myelodysplastic syndrome with low blasts | NCIT:C200389 | MONDO:equivalentTo | Myelodysplastic Syndrome with Low Blasts | | MONDO:0018881 | -| MONDO:0957745 | myelodysplastic syndrome with genetic abnormalities | NCIT:C200390 | MONDO:equivalentTo | Myelodysplastic Syndrome with Genetic Abnormalities | | MONDO:0018881 | -| MONDO:0957746 | myelodysplastic syndrome/acute myeloid leukemia with myelodysplasia-related gene mutations | NCIT:C200400 | MONDO:equivalentTo | Myelodysplastic Syndrome/Acute Myeloid Leukemia with Myelodysplasia-Related Gene Mutations | | MONDO:0015041 | -| MONDO:0957747 | myelodysplastic syndrome/acute myeloid leukemia with myelodysplasia-related cytogenetic abnormalities | NCIT:C200402 | MONDO:equivalentTo | Myelodysplastic Syndrome/Acute Myeloid Leukemia with Myelodysplasia-Related Cytogenetic Abnormalities | | MONDO:0015041 | -| MONDO:0957748 | acute myeloid leukemia with mecom rearrangement | NCIT:C200407 | MONDO:equivalentTo | Acute Myeloid Leukemia with MECOM Rearrangement | | MONDO:0020078 | -| MONDO:0957749 | acute myeloid leukemia with nup98 rearrangement | NCIT:C200411 | MONDO:equivalentTo | Acute Myeloid Leukemia with NUP98 Rearrangement | | MONDO:0020078 | -| MONDO:0957750 | acute myeloid leukemia with fus-erg | NCIT:C200419 | MONDO:equivalentTo | Acute Myeloid Leukemia with FUS-ERG | | MONDO:0020078 | -| MONDO:0957751 | acute myeloid leukemia with npm1-mlf1 | NCIT:C200420 | MONDO:equivalentTo | Acute Myeloid Leukemia with NPM1-MLF1 | | MONDO:0020078 | -| MONDO:0957752 | acute myeloid leukemia with kat6a-crebbp | NCIT:C200421 | MONDO:equivalentTo | Acute Myeloid Leukemia with KAT6A-CREBBP | | MONDO:0020078 | -| MONDO:0957753 | acute leukemia of ambiguous lineage with defining genetic abnormalities | NCIT:C200494 | MONDO:equivalentTo | Acute Leukemia of Ambiguous Lineage with Defining Genetic Abnormalities | | MONDO:0019460 | -| MONDO:0957754 | mature plasmacytoid dendritic cell proliferation associated with myeloid neoplasm | NCIT:C200513 | MONDO:equivalentTo | Mature Plasmacytoid Dendritic Cell Proliferation Associated with Myeloid Neoplasm | | MONDO:0006247 | -| MONDO:0957755 | b lymphoblastic leukemia/lymphoma with tcf3-hlf rearrangement | NCIT:C200587 | MONDO:equivalentTo | B Lymphoblastic Leukemia/Lymphoma with TCF3-HLF Rearrangement | | MONDO:0035605 | -| MONDO:0957756 | atypical teratoid/rhabdoid tumor molecular subtypes | NCIT:C200597 | MONDO:equivalentTo | Atypical Teratoid/Rhabdoid Tumor Molecular Subtypes | | MONDO:0020560 | -| MONDO:0957757 | classic follicular lymphoma | NCIT:C200669 | MONDO:equivalentTo | Classic Follicular Lymphoma | | MONDO:0018906 | -| MONDO:0957758 | follicular lymphoma with unusual cytological features | NCIT:C200684 | MONDO:equivalentTo | Follicular Lymphoma with Unusual Cytological Features | | MONDO:0018906 | -| MONDO:0957759 | cyclin d1-negative mantle cell lymphoma | NCIT:C200685 | MONDO:equivalentTo | Cyclin D1-Negative Mantle Cell Lymphoma | | MONDO:0018876 | -| MONDO:0957760 | primary large b-cell lymphoma of immune-privileged site | NCIT:C200687 | MONDO:equivalentTo | Primary Large B-Cell Lymphoma of Immune-Privileged Site | | MONDO:0018905 | -| MONDO:0957761 | ebv-negative burkitt lymphoma | NCIT:C200688 | MONDO:equivalentTo | EBV-Negative Burkitt Lymphoma | | MONDO:0007243 | -| MONDO:0957762 | plasma cell neoplasm with associated paraneoplastic syndrome | NCIT:C200738 | MONDO:equivalentTo | Plasma Cell Neoplasm with Associated Paraneoplastic Syndrome | | MONDO:0004959 | -| MONDO:0957763 | who grade 4 glioma | NCIT:C200758 | MONDO:equivalentTo | WHO Grade 4 Glioma | | MONDO:0100342 | -| MONDO:0957764 | primary cutaneous peripheral t-cell lymphoma, not otherwise specified | NCIT:C201080 | MONDO:equivalentTo | Primary Cutaneous Peripheral T-Cell Lymphoma, Not Otherwise Specified | | MONDO:0000607 | -| MONDO:0957765 | cribriform comedo-type adenocarcinoma | NCIT:C201124 | MONDO:equivalentTo | Cribriform Comedo-Type Adenocarcinoma | | MONDO:0003575 | -| MONDO:0957766 | aleukemic myeloid leukemia | NCIT:C201127 | MONDO:equivalentTo | Aleukemic Myeloid leukemia | | MONDO:0003730|MONDO:0004643 | -| MONDO:0957767 | solid pseudopapillary neoplasm | NCIT:C201136 | MONDO:equivalentTo | Solid Pseudopapillary Neoplasm | | MONDO:0004992 | -| MONDO:0957768 | endemic burkitt lymphoma | NCIT:C27122 | MONDO:equivalentTo | Endemic Burkitt Lymphoma | | MONDO:0007243 | -| MONDO:0957769 | multicystic mesothelioma | NCIT:C3765 | MONDO:equivalentTo | Multicystic Mesothelioma | | MONDO:0006856|MONDO:0021077 | -| MONDO:0957770 | low grade myofibroblastic sarcoma | NCIT:C49024 | MONDO:equivalentTo | Low Grade Myofibroblastic Sarcoma | | MONDO:0005164 | -| MONDO:0957771 | sclerosing epithelioid fibrosarcoma | NCIT:C49027 | MONDO:equivalentTo | Sclerosing Epithelioid Fibrosarcoma | | MONDO:0005164 | -| MONDO:0957772 | meningothelial cell neoplasm | NCIT:C6971 | MONDO:equivalentTo | Meningothelial Cell Neoplasm | | MONDO:0002616 | -| MONDO:0957773 | type a lymphomatoid papulosis | NCIT:C7197 | MONDO:equivalentTo | Type A Lymphomatoid Papulosis | | MONDO:0020326 | -| MONDO:0957774 | type c lymphomatoid papulosis | NCIT:C7199 | MONDO:equivalentTo | Type C Lymphomatoid Papulosis | | MONDO:0020326 | -| MONDO:0957775 | pancreatic intraductal papillary mucinous neoplasm, oncocytic-type | NCIT:C95514 | MONDO:equivalentTo | Pancreatic Intraductal Papillary Mucinous Neoplasm, Oncocytic-Type | | MONDO:0004286|MONDO:0010795 | -| MONDO:0957850 | post-essential thrombocythemia myelofibrosis | NCIT:C126806 | MONDO:equivalentTo | Post-Essential Thrombocythemia Myelofibrosis | | MONDO:0005029 | -| MONDO:0957851 | recurrent myelofibrosis | NCIT:C162424 | MONDO:equivalentTo | Recurrent Myelofibrosis | | | -| MONDO:0957852 | refractory myelofibrosis | NCIT:C162425 | MONDO:equivalentTo | Refractory Myelofibrosis | | | -| MONDO:0957853 | bone rosai-dorfman-destombes disease | NCIT:C178613 | MONDO:equivalentTo | Bone Rosai-Dorfman-Destombes Disease | | MONDO:0019060|MONDO:0006412 | -| MONDO:0957854 | stage m0 medulloblastoma | NCIT:C186521 | MONDO:equivalentTo | Stage M0 Medulloblastoma | | MONDO:0007959 | -| MONDO:0957855 | stage m1 medulloblastoma | NCIT:C186522 | MONDO:equivalentTo | Stage M1 Medulloblastoma | | MONDO:0007959 | -| MONDO:0957856 | stage m2 medulloblastoma | NCIT:C186523 | MONDO:equivalentTo | Stage M2 Medulloblastoma | | MONDO:0007959 | -| MONDO:0957857 | stage m3 medulloblastoma | NCIT:C186524 | MONDO:equivalentTo | Stage M3 Medulloblastoma | | MONDO:0007959 | -| MONDO:0957858 | stage m4 medulloblastoma | NCIT:C186525 | MONDO:equivalentTo | Stage M4 Medulloblastoma | | MONDO:0007959 | -| MONDO:0957859 | stage m0 atypical teratoid/rhabdoid tumor | NCIT:C186528 | MONDO:equivalentTo | Stage M0 Atypical Teratoid/Rhabdoid Tumor | | MONDO:0020560 | -| MONDO:0957860 | stage m1 atypical teratoid/rhabdoid tumor | NCIT:C186529 | MONDO:equivalentTo | Stage M1 Atypical Teratoid/Rhabdoid Tumor | | MONDO:0020560 | -| MONDO:0957861 | stage m2 atypical teratoid/rhabdoid tumor | NCIT:C186530 | MONDO:equivalentTo | Stage M2 Atypical Teratoid/Rhabdoid Tumor | | MONDO:0020560 | -| MONDO:0957862 | stage m3 atypical teratoid/rhabdoid tumor | NCIT:C186531 | MONDO:equivalentTo | Stage M3 Atypical Teratoid/Rhabdoid Tumor | | MONDO:0020560 | -| MONDO:0957863 | stage m4 atypical teratoid/rhabdoid tumor | NCIT:C186532 | MONDO:equivalentTo | Stage M4 Atypical Teratoid/Rhabdoid Tumor | | MONDO:0020560 | -| MONDO:0957864 | stage m0 pineoblastoma | NCIT:C186568 | MONDO:equivalentTo | Stage M0 Pineoblastoma | | MONDO:0016722 | -| MONDO:0957865 | stage m1 pineoblastoma | NCIT:C186569 | MONDO:equivalentTo | Stage M1 Pineoblastoma | | MONDO:0016722 | -| MONDO:0957866 | stage m2 pineoblastoma | NCIT:C186570 | MONDO:equivalentTo | Stage M2 Pineoblastoma | | MONDO:0016722 | -| MONDO:0957867 | stage m3 pineoblastoma | NCIT:C186571 | MONDO:equivalentTo | Stage M3 Pineoblastoma | | MONDO:0016722 | -| MONDO:0957868 | stage m4 pineoblastoma | NCIT:C186572 | MONDO:equivalentTo | Stage M4 Pineoblastoma | | MONDO:0016722 | -| MONDO:0958220 | colorectal perineurioma | NCIT:C96513 | MONDO:equivalentTo | Colorectal Perineurioma | | MONDO:0015031|MONDO:0021444 | \ No newline at end of file +| mondo_id | mondo_label | xref | xref_source | original_label | definition | parents | +|:--------------|:---------------------------------------------------------------------------------------------------------------|:---------------------|:---------------------------|:---------------------------------------------------------------------------------------------------------------|:--------------|:--------------------------------------------------------| +| ID | LABEL | A oboInOwl:hasDbXref | >A oboInOwl:source SPLIT=| | | A IAO:0000115 | SC % | +| MONDO:0853241 | primary central nervous system neoplasm | NCIT:C102871 | MONDO:equivalentTo | Primary Central Nervous System Neoplasm | | MONDO:0006130 | +| MONDO:0853254 | adrenal cortical carcinoma by ensat stage | NCIT:C104030 | MONDO:equivalentTo | Adrenal Cortical Carcinoma by ENSAT Stage | | MONDO:0006639 | +| MONDO:0853255 | ovarian high grade serous adenocarcinoma | NCIT:C105555 | MONDO:equivalentTo | Ovarian High Grade Serous Adenocarcinoma | | MONDO:0005211 | +| MONDO:0853256 | ovarian low grade serous adenocarcinoma | NCIT:C105556 | MONDO:equivalentTo | Ovarian Low Grade Serous Adenocarcinoma | | MONDO:0005211 | +| MONDO:0853260 | uveal melanoma by gene expression profile | NCIT:C111030 | MONDO:equivalentTo | Uveal Melanoma by Gene Expression Profile | | MONDO:0006486 | +| MONDO:0853262 | glioblastoma by gene expression profile | NCIT:C111691 | MONDO:equivalentTo | Glioblastoma by Gene Expression Profile | | MONDO:0018177 | +| MONDO:0853267 | thymoma by masaoka-koga stage | NCIT:C112006 | MONDO:equivalentTo | Thymoma by Masaoka-Koga Stage | | MONDO:0006456 | +| MONDO:0853279 | uterine carcinosarcoma, homologous type | NCIT:C113238 | MONDO:equivalentTo | Uterine Carcinosarcoma, Homologous Type | | MONDO:0006485 | +| MONDO:0853280 | uterine carcinosarcoma, heterologous type | NCIT:C113239 | MONDO:equivalentTo | Uterine Carcinosarcoma, Heterologous Type | | MONDO:0006485 | +| MONDO:0853284 | main duct pancreatic intraductal papillary-mucinous neoplasm | NCIT:C113664 | MONDO:equivalentTo | Main Duct Pancreatic Intraductal Papillary-Mucinous Neoplasm | | MONDO:0004286 | +| MONDO:0853285 | branch duct pancreatic intraductal papillary-mucinous neoplasm | NCIT:C113665 | MONDO:equivalentTo | Branch Duct Pancreatic Intraductal Papillary-Mucinous Neoplasm | | MONDO:0004286 | +| MONDO:0853286 | mixed type pancreatic intraductal papillary-mucinous neoplasm | NCIT:C113667 | MONDO:equivalentTo | Mixed Type Pancreatic Intraductal Papillary-Mucinous Neoplasm | | MONDO:0004286 | +| MONDO:0853303 | adult undifferentiated high grade pleomorphic sarcoma of bone | NCIT:C114782 | MONDO:equivalentTo | Adult Undifferentiated High Grade Pleomorphic Sarcoma of Bone | | MONDO:0002618 | +| MONDO:0853306 | metastatic malignant neoplasm in the soft tissues | NCIT:C114831 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Soft Tissues | | MONDO:0024880 | +| MONDO:0853313 | adult epithelioid hemangioendothelioma | NCIT:C114923 | MONDO:equivalentTo | Adult Epithelioid Hemangioendothelioma | | MONDO:0015523 | +| MONDO:0853316 | central nervous system hodgkin lymphoma | NCIT:C114951 | MONDO:equivalentTo | Central Nervous System Hodgkin Lymphoma | | MONDO:0004952|MONDO:0002571 | +| MONDO:0853326 | adult fibrolamellar carcinoma | NCIT:C114992 | MONDO:equivalentTo | Adult Fibrolamellar Carcinoma | | MONDO:0016216|MONDO:0006210 | +| MONDO:0853331 | hepatocellular carcinoma by bclc stage | NCIT:C115132 | MONDO:equivalentTo | Hepatocellular Carcinoma by BCLC Stage | | MONDO:0007256 | +| MONDO:0853337 | adult myelodysplastic syndrome | NCIT:C115153 | MONDO:equivalentTo | Adult Myelodysplastic Syndrome | | MONDO:0018881 | +| MONDO:0853343 | distal urethral carcinoma | NCIT:C115210 | MONDO:equivalentTo | Distal Urethral Carcinoma | | MONDO:0021327 | +| MONDO:0853344 | familial testicular germ cell tumor | NCIT:C115211 | MONDO:equivalentTo | Familial Testicular Germ Cell Tumor | | MONDO:0010108 | +| MONDO:0853348 | proximal urethral carcinoma | NCIT:C115334 | MONDO:equivalentTo | Proximal Urethral Carcinoma | | MONDO:0021327 | +| MONDO:0853359 | invasive bladder urothelial carcinoma associated with urethral carcinoma | NCIT:C115966 | MONDO:equivalentTo | Invasive Bladder Urothelial Carcinoma Associated with Urethral Carcinoma | | MONDO:0040678 | +| MONDO:0853386 | congenital cystic hygroma | NCIT:C116899 | MONDO:equivalentTo | Congenital Cystic Hygroma | | MONDO:0009761 | +| MONDO:0853405 | anaplastic plasmacytoma | NCIT:C118421 | MONDO:equivalentTo | Anaplastic Plasmacytoma | | MONDO:0005615|MONDO:0020633 | +| MONDO:0853427 | adult penile carcinoma | NCIT:C118820 | MONDO:equivalentTo | Adult Penile Carcinoma | | MONDO:0006360 | +| MONDO:0853431 | adult salivary gland carcinoma | NCIT:C118825 | MONDO:equivalentTo | Adult Salivary Gland Carcinoma | | MONDO:0000521 | +| MONDO:0853434 | orbital melanoma | NCIT:C118828 | MONDO:equivalentTo | Orbital Melanoma | | MONDO:0002889|MONDO:0005105 | +| MONDO:0853464 | malignant kidney neoplasm except pelvis | NCIT:C120456 | MONDO:equivalentTo | Malignant Kidney Neoplasm Except Pelvis | | MONDO:0002367 | +| MONDO:0853467 | mammary-type myofibroblastoma | NCIT:C121181 | MONDO:equivalentTo | Mammary-Type Myofibroblastoma | | MONDO:0040675 | +| MONDO:0853473 | leiomyosarcoma of deep soft tissue | NCIT:C121571 | MONDO:equivalentTo | Leiomyosarcoma of Deep Soft Tissue | | MONDO:0018078|MONDO:0005058 | +| MONDO:0853476 | spindle cell/sclerosing rhabdomyosarcoma | NCIT:C121654 | MONDO:equivalentTo | Spindle Cell/Sclerosing Rhabdomyosarcoma | | MONDO:0005212 | +| MONDO:0853478 | soft tissue angiosarcoma | NCIT:C121671 | MONDO:equivalentTo | Soft Tissue Angiosarcoma | | MONDO:0018078|MONDO:0016982 | +| MONDO:0853479 | conventional schwannoma | NCIT:C121677 | MONDO:equivalentTo | Conventional Schwannoma | | MONDO:0002546 | +| MONDO:0853481 | solitary circumscribed neuroma | NCIT:C121681 | MONDO:equivalentTo | Solitary Circumscribed Neuroma | | MONDO:0002547|MONDO:0000648 | +| MONDO:0853483 | hybrid nerve sheath tumor | NCIT:C121686 | MONDO:equivalentTo | Hybrid Nerve Sheath Tumor | | MONDO:0021043|MONDO:0002547|MONDO:0000648 | +| MONDO:0853491 | malignant mixed tumor, not otherwise specified | NCIT:C121787 | MONDO:equivalentTo | Malignant Mixed Tumor, Not Otherwise Specified | | MONDO:0003158|MONDO:0005853 | +| MONDO:0853492 | benign phosphaturic mesenchymal tumor | NCIT:C121788 | MONDO:equivalentTo | Benign Phosphaturic Mesenchymal Tumor | | MONDO:0006368|MONDO:0000654 | +| MONDO:0853493 | malignant phosphaturic mesenchymal tumor | NCIT:C121789 | MONDO:equivalentTo | Malignant Phosphaturic Mesenchymal Tumor | | MONDO:0006368|MONDO:0002927 | +| MONDO:0853494 | sclerosing pecoma | NCIT:C121790 | MONDO:equivalentTo | Sclerosing PEComa | | MONDO:0006359 | +| MONDO:0853495 | undifferentiated soft tissue sarcoma | NCIT:C121793 | MONDO:equivalentTo | Undifferentiated Soft Tissue Sarcoma | | MONDO:0018078 | +| MONDO:0853498 | osteochondromyxoma | NCIT:C121842 | MONDO:equivalentTo | Osteochondromyxoma | | MONDO:0024470|MONDO:0000631 | +| MONDO:0853499 | subungual exostosis | NCIT:C121844 | MONDO:equivalentTo | Subungual Exostosis | | MONDO:0024470 | +| MONDO:0853500 | bizarre parosteal osteochondromatous proliferation | NCIT:C121845 | MONDO:equivalentTo | Bizarre Parosteal Osteochondromatous Proliferation | | MONDO:0024470 | +| MONDO:0853501 | intermediate chondrogenic neoplasm | NCIT:C121846 | MONDO:equivalentTo | Intermediate Chondrogenic Neoplasm | | MONDO:0024469 | +| MONDO:0853502 | chondrosarcoma, grade 2 | NCIT:C121870 | MONDO:equivalentTo | Chondrosarcoma, Grade 2 | | MONDO:0008977 | +| MONDO:0853503 | chondrosarcoma, grade 3 | NCIT:C121871 | MONDO:equivalentTo | Chondrosarcoma, Grade 3 | | MONDO:0008977 | +| MONDO:0853504 | benign notochordal cell tumor | NCIT:C121901 | MONDO:equivalentTo | Benign Notochordal Cell Tumor | | MONDO:0002597|MONDO:0000631 | +| MONDO:0853507 | intermediate osteogenic neoplasm | NCIT:C121925 | MONDO:equivalentTo | Intermediate Osteogenic Neoplasm | | MONDO:0045053 | +| MONDO:0853508 | intermediate bone neoplasm | NCIT:C121926 | MONDO:equivalentTo | Intermediate Bone Neoplasm | | MONDO:0019060 | +| MONDO:0853510 | primary bone non-hodgkin lymphoma | NCIT:C121930 | MONDO:equivalentTo | Primary Bone Non-Hodgkin Lymphoma | | MONDO:0017814|MONDO:0018908 | +| MONDO:0853512 | bone epithelioid hemangioendothelioma | NCIT:C121941 | MONDO:equivalentTo | Bone Epithelioid Hemangioendothelioma | | MONDO:0024499|MONDO:0002129|MONDO:0015523 | +| MONDO:0853515 | acute lymphoblastic leukemia by gene expression profile | NCIT:C121973 | MONDO:equivalentTo | Acute Lymphoblastic Leukemia by Gene Expression Profile | | MONDO:0004967 | +| MONDO:0853523 | borderline ovarian serous tumor/atypical proliferative ovarian serous tumor | NCIT:C122584 | MONDO:equivalentTo | Borderline Ovarian Serous Tumor/Atypical Proliferative Ovarian Serous Tumor | | MONDO:0020662 | +| MONDO:0853524 | borderline ovarian serous tumor-micropapillary variant/non-invasive low grade ovarian serous carcinoma | NCIT:C122585 | MONDO:equivalentTo | Borderline Ovarian Serous Tumor-Micropapillary Variant/Non-Invasive Low Grade Ovarian Serous Carcinoma | | MONDO:0020662 | +| MONDO:0853525 | infant leukemia | NCIT:C122603 | MONDO:equivalentTo | Infant Leukemia | | MONDO:0004355 | +| MONDO:0853528 | childhood acute myeloid leukemia not otherwise specified | NCIT:C122625 | MONDO:equivalentTo | Childhood Acute Myeloid Leukemia Not Otherwise Specified | | MONDO:0004996|MONDO:0015667 | +| MONDO:0853529 | hypoplastic myelodysplastic syndrome | NCIT:C122686 | MONDO:equivalentTo | Hypoplastic Myelodysplastic Syndrome | | MONDO:0018881 | +| MONDO:0853530 | cytogenetically normal acute myeloid leukemia | NCIT:C122687 | MONDO:equivalentTo | Cytogenetically Normal Acute Myeloid Leukemia | | MONDO:0018874 | +| MONDO:0853532 | childhood acute myeloid leukemia with abnormalities of chromosome 5q | NCIT:C122725 | MONDO:equivalentTo | Childhood Acute Myeloid Leukemia with Abnormalities of Chromosome 5q | | MONDO:0004996 | +| MONDO:0853533 | childhood acute myeloid leukemia with abnormalities of chromosome 7 | NCIT:C122726 | MONDO:equivalentTo | Childhood Acute Myeloid Leukemia with Abnormalities of Chromosome 7 | | MONDO:0004996 | +| MONDO:0853659 | childhood lymphomatoid granulomatosis | NCIT:C123392 | MONDO:equivalentTo | Childhood Lymphomatoid Granulomatosis | | MONDO:0019466 | +| MONDO:0853660 | childhood langerhans cell histiocytosis with risk organ involvement | NCIT:C123395 | MONDO:equivalentTo | Childhood Langerhans Cell Histiocytosis with Risk Organ Involvement | | MONDO:0017025 | +| MONDO:0853661 | childhood langerhans cell histiocytosis without risk organ involvement | NCIT:C123396 | MONDO:equivalentTo | Childhood Langerhans Cell Histiocytosis without Risk Organ Involvement | | MONDO:0017025 | +| MONDO:0853668 | fusion-positive rhabdomyosarcoma | NCIT:C123735 | MONDO:equivalentTo | Fusion-Positive Rhabdomyosarcoma | | MONDO:0005212 | +| MONDO:0853669 | fusion-negative rhabdomyosarcoma | NCIT:C123736 | MONDO:equivalentTo | Fusion-Negative Rhabdomyosarcoma | | MONDO:0005212 | +| MONDO:0853671 | refractory malignant germ cell tumor | NCIT:C123739 | MONDO:equivalentTo | Refractory Malignant Germ Cell Tumor | | MONDO:0006290|MONDO:0036501 | +| MONDO:0853673 | childhood germinomatous germ cell tumor | NCIT:C123838 | MONDO:equivalentTo | Childhood Germinomatous Germ Cell Tumor | | MONDO:0003751|MONDO:0020580 | +| MONDO:0853675 | childhood nongerminomatous germ cell tumor | NCIT:C123841 | MONDO:equivalentTo | Childhood Nongerminomatous Germ Cell Tumor | | MONDO:0003751|MONDO:0021656 | +| MONDO:0853680 | childhood mixed germ cell tumor | NCIT:C123848 | MONDO:equivalentTo | Childhood Mixed Germ Cell Tumor | | MONDO:0004479|MONDO:0015864|MONDO:0005853 | +| MONDO:0853693 | childhood astrocytoma | NCIT:C124275 | MONDO:equivalentTo | Childhood Astrocytoma | | MONDO:0002505|MONDO:0019781 | +| MONDO:0853694 | childhood atypical choroid plexus papilloma | NCIT:C124291 | MONDO:equivalentTo | Childhood Atypical Choroid Plexus Papilloma | | MONDO:0002684|MONDO:0024744 | +| MONDO:0853721 | ovarian adenomatoid tumor | NCIT:C126331 | MONDO:equivalentTo | Ovarian Adenomatoid Tumor | | MONDO:0004230|MONDO:0000646 | +| MONDO:0853728 | chronic eosinophilic leukemia with fip1l1-pdgfra | NCIT:C126351 | MONDO:equivalentTo | Chronic Eosinophilic Leukemia with FIP1L1-PDGFRA | | MONDO:0015689|MONDO:0001014 | +| MONDO:0853729 | primary peritoneal high grade serous adenocarcinoma | NCIT:C126353 | MONDO:equivalentTo | Primary Peritoneal High Grade Serous Adenocarcinoma | | MONDO:0006386 | +| MONDO:0853730 | primary peritoneal low grade serous adenocarcinoma | NCIT:C126354 | MONDO:equivalentTo | Primary Peritoneal Low Grade Serous Adenocarcinoma | | MONDO:0006386 | +| MONDO:0853731 | peritoneal desmoplastic small round cell tumor | NCIT:C126356 | MONDO:equivalentTo | Peritoneal Desmoplastic Small Round Cell Tumor | | MONDO:0019373|MONDO:0002087 | +| MONDO:0853732 | pelvic fibromatosis | NCIT:C126358 | MONDO:equivalentTo | Pelvic Fibromatosis | | MONDO:0007608 | +| MONDO:0853733 | abdominal inflammatory myofibroblastic tumor | NCIT:C126359 | MONDO:equivalentTo | Abdominal Inflammatory Myofibroblastic Tumor | | MONDO:0015798 | +| MONDO:0853734 | thyroid gland cribriform morular carcinoma | NCIT:C126408 | MONDO:equivalentTo | Thyroid Gland Cribriform Morular Carcinoma | | MONDO:0015075 | +| MONDO:0853735 | thyroid gland papillary carcinoma with fibromatosis/fasciitis-like/desmoid-type stroma | NCIT:C126410 | MONDO:equivalentTo | Thyroid Gland Papillary Carcinoma with Fibromatosis/Fasciitis-Like/Desmoid-Type Stroma | | MONDO:0005075 | +| MONDO:0853736 | fallopian tube high grade serous adenocarcinoma | NCIT:C126456 | MONDO:equivalentTo | Fallopian Tube High Grade Serous Adenocarcinoma | | MONDO:0006208 | +| MONDO:0853738 | fallopian tube lymphoma | NCIT:C126464 | MONDO:equivalentTo | Fallopian Tube Lymphoma | | MONDO:0002158|MONDO:0017207 | +| MONDO:0853742 | broad ligament serous adenocarcinoma | NCIT:C126479 | MONDO:equivalentTo | Broad Ligament Serous Adenocarcinoma | | MONDO:0002741|MONDO:0005278 | +| MONDO:0853743 | oropharyngeal poorly differentiated carcinoma | NCIT:C126750 | MONDO:equivalentTo | Oropharyngeal Poorly Differentiated Carcinoma | | MONDO:0044704 | +| MONDO:0853745 | endometrial dedifferentiated carcinoma | NCIT:C126769 | MONDO:equivalentTo | Endometrial Dedifferentiated Carcinoma | | MONDO:0002447 | +| MONDO:0853748 | uterine corpus hydropic leiomyoma | NCIT:C126975 | MONDO:equivalentTo | Uterine Corpus Hydropic Leiomyoma | | MONDO:0007886 | +| MONDO:0853749 | uterine corpus high grade endometrial stromal sarcoma | NCIT:C126998 | MONDO:equivalentTo | Uterine Corpus High Grade Endometrial Stromal Sarcoma | | MONDO:0002923 | +| MONDO:0853751 | benign uterine corpus pecoma | NCIT:C127071 | MONDO:equivalentTo | Benign Uterine Corpus PEComa | | MONDO:0004221|MONDO:0021525|MONDO:0020581 | +| MONDO:0853753 | uterine corpus germ cell tumor | NCIT:C127077 | MONDO:equivalentTo | Uterine Corpus Germ Cell Tumor | | MONDO:0021254|MONDO:0018201 | +| MONDO:0853764 | cervical neuroendocrine neoplasm | NCIT:C128041 | MONDO:equivalentTo | Cervical Neuroendocrine Neoplasm | | MONDO:0019496|MONDO:0021230 | +| MONDO:0853771 | vaginal papillary carcinoma | NCIT:C128060 | MONDO:equivalentTo | Vaginal Papillary Carcinoma | | MONDO:0002979|MONDO:0006490 | +| MONDO:0853775 | ovarian cancer by figo stage | NCIT:C128081 | MONDO:equivalentTo | Ovarian Cancer by FIGO Stage | | MONDO:0005140 | +| MONDO:0853776 | ovarian cancer by ajcc v6 and v7 stage | NCIT:C128106 | MONDO:equivalentTo | Ovarian Cancer by AJCC v6 and v7 Stage | | MONDO:0005140 | +| MONDO:0853779 | vaginal germ cell tumor | NCIT:C128112 | MONDO:equivalentTo | Vaginal Germ Cell Tumor | | MONDO:0005040|MONDO:0021050 | +| MONDO:0853781 | vulvar squamous intraepithelial lesion, hpv-associated | NCIT:C128142 | MONDO:equivalentTo | Vulvar Squamous Intraepithelial Lesion, HPV-Associated | | MONDO:0005198 | +| MONDO:0853784 | vulvar adenocarcinoma of mammary gland type | NCIT:C128162 | MONDO:equivalentTo | Vulvar Adenocarcinoma of Mammary Gland Type | | MONDO:0024336 | +| MONDO:0853787 | vulvar mucinous adenocarcinoma, intestinal-type | NCIT:C128166 | MONDO:equivalentTo | Vulvar Mucinous Adenocarcinoma, Intestinal-Type | | MONDO:0024336|MONDO:0006254|MONDO:0004957 | +| MONDO:0853788 | vulvar keratoacanthoma | NCIT:C128167 | MONDO:equivalentTo | Vulvar Keratoacanthoma | | MONDO:0024609|MONDO:0002527 | +| MONDO:0853797 | vulvar germ cell tumor | NCIT:C128294 | MONDO:equivalentTo | Vulvar Germ Cell Tumor | | MONDO:0005040|MONDO:0021049 | +| MONDO:0853835 | b acute lymphoblastic leukemia, philadelphia chromosome negative | NCIT:C128629 | MONDO:equivalentTo | B Acute Lymphoblastic Leukemia, Philadelphia Chromosome Negative | | MONDO:0020511 | +| MONDO:0853837 | nk-cell lymphoma, unclassifiable | NCIT:C128697 | MONDO:equivalentTo | NK-Cell Lymphoma, Unclassifiable | | MONDO:0000430 | +| MONDO:0853840 | cutaneous malignant melanoma 2 | NCIT:C128801 | MONDO:equivalentTo | Cutaneous Malignant Melanoma 2 | | MONDO:0018961 | +| MONDO:0853846 | glioblastoma, not otherwise specified | NCIT:C129295 | MONDO:equivalentTo | Glioblastoma, Not Otherwise Specified | | MONDO:0018177 | +| MONDO:0853849 | oligodendroglioma, idh-mutant and 1p/19q-codeleted | NCIT:C129318 | MONDO:equivalentTo | Oligodendroglioma, IDH-Mutant and 1p/19q-Codeleted | | MONDO:0016695 | +| MONDO:0853850 | oligodendroglioma, not otherwise specified | NCIT:C129319 | MONDO:equivalentTo | Oligodendroglioma, Not Otherwise Specified | | MONDO:0016695 | +| MONDO:0853851 | anaplastic oligodendroglioma, idh-mutant and 1p/19q-codeleted | NCIT:C129321 | MONDO:equivalentTo | Anaplastic Oligodendroglioma, IDH-Mutant and 1p/19q-Codeleted | | MONDO:0016696 | +| MONDO:0853852 | anaplastic oligodendroglioma, not otherwise specified | NCIT:C129322 | MONDO:equivalentTo | Anaplastic Oligodendroglioma, Not Otherwise Specified | | MONDO:0016696 | +| MONDO:0853853 | oligoastrocytoma, not otherwise specified | NCIT:C129323 | MONDO:equivalentTo | Oligoastrocytoma, Not Otherwise Specified | | MONDO:0016702 | +| MONDO:0853854 | anaplastic oligoastrocytoma, not otherwise specified | NCIT:C129324 | MONDO:equivalentTo | Anaplastic Oligoastrocytoma, Not Otherwise Specified | | MONDO:0016703 | +| MONDO:0853855 | diffuse glioma | NCIT:C129325 | MONDO:equivalentTo | Diffuse Glioma | | MONDO:0021042 | +| MONDO:0853856 | anaplastic pleomorphic xanthoastrocytoma | NCIT:C129327 | MONDO:equivalentTo | Anaplastic Pleomorphic Xanthoastrocytoma | | MONDO:0019781|MONDO:0021640|MONDO:0020633 | +| MONDO:0853857 | diffuse leptomeningeal glioneuronal tumor | NCIT:C129424 | MONDO:equivalentTo | Diffuse Leptomeningeal Glioneuronal Tumor | | MONDO:0016729 | +| MONDO:0853858 | multinodular and vacuolated neuronal tumor | NCIT:C129427 | MONDO:equivalentTo | Multinodular and Vacuolated Neuronal Tumor | | MONDO:0021374|MONDO:0016729|MONDO:0021632 | +| MONDO:0853859 | medulloblastoma molecular subtypes | NCIT:C129439 | MONDO:equivalentTo | Medulloblastoma Molecular Subtypes | | MONDO:0007959 | +| MONDO:0853860 | medulloblastoma, not otherwise specified | NCIT:C129447 | MONDO:equivalentTo | Medulloblastoma, Not Otherwise Specified | | MONDO:0007959 | +| MONDO:0853861 | small cell adenocarcinoma | NCIT:C129449 | MONDO:equivalentTo | Small Cell Adenocarcinoma | | MONDO:0004970 | +| MONDO:0853862 | central nervous system solitary fibrous tumor | NCIT:C129526 | MONDO:equivalentTo | Central Nervous System Solitary Fibrous Tumor | | MONDO:0016238|MONDO:0003244 | +| MONDO:0853863 | central nervous system mesenchymal chondrosarcoma | NCIT:C129534 | MONDO:equivalentTo | Central Nervous System Mesenchymal Chondrosarcoma | | MONDO:0002217|MONDO:0006853 | +| MONDO:0853864 | central nervous system epithelioid hemangioendothelioma | NCIT:C129536 | MONDO:equivalentTo | Central Nervous System Epithelioid Hemangioendothelioma | | MONDO:0037740|MONDO:0015523 | +| MONDO:0853865 | central nervous system angiolipoma | NCIT:C129538 | MONDO:equivalentTo | Central Nervous System Angiolipoma | | MONDO:0003844|MONDO:0006085 | +| MONDO:0853866 | central nervous system undifferentiated pleomorphic sarcoma | NCIT:C129566 | MONDO:equivalentTo | Central Nervous System Undifferentiated Pleomorphic Sarcoma | | MONDO:0002217|MONDO:0002142 | +| MONDO:0853868 | central nervous system anaplastic large cell lymphoma, alk-positive | NCIT:C129598 | MONDO:equivalentTo | Central Nervous System Anaplastic Large Cell Lymphoma, ALK-Positive | | MONDO:0006128|MONDO:0017602 | +| MONDO:0853869 | central nervous system anaplastic large cell lymphoma, alk-negative | NCIT:C129599 | MONDO:equivalentTo | Central Nervous System Anaplastic Large Cell Lymphoma, ALK-Negative | | MONDO:0006128|MONDO:0017603 | +| MONDO:0853870 | central nervous system intravascular large b-cell lymphoma | NCIT:C129602 | MONDO:equivalentTo | Central Nervous System Intravascular Large B-Cell Lymphoma | | MONDO:0017596|MONDO:0020324 | +| MONDO:0853881 | acute myeloid leukemia with biallelic cebpa mutation | NCIT:C129782 | MONDO:equivalentTo | Acute Myeloid Leukemia with Biallelic CEBPA Mutation | | MONDO:0017894 | +| MONDO:0853882 | acute myeloid leukemia with monoallelic cebpa mutation | NCIT:C129783 | MONDO:equivalentTo | Acute Myeloid Leukemia with Monoallelic CEBPA Mutation | | MONDO:0017894 | +| MONDO:0853884 | b lymphoblastic leukemia/lymphoma, bcr-abl1-like | NCIT:C129787 | MONDO:equivalentTo | B Lymphoblastic Leukemia/Lymphoma, BCR-ABL1-Like | | MONDO:0035605 | +| MONDO:0853887 | metastatic transitional cell carcinoma | NCIT:C129828 | MONDO:equivalentTo | Metastatic Transitional Cell Carcinoma | | MONDO:0024879|MONDO:0006474 | +| MONDO:0853888 | chronic myelomonocytic leukemia with eosinophilia associated with t(5;12)(q31;p12) | NCIT:C129852 | MONDO:equivalentTo | Chronic Myelomonocytic Leukemia with Eosinophilia Associated with t(5;12)(q31;p12) | | MONDO:0015690 | +| MONDO:0853892 | chronic myelomonocytic leukemia-0 | NCIT:C130035 | MONDO:equivalentTo | Chronic Myelomonocytic Leukemia-0 | | MONDO:0020311 | +| MONDO:0853893 | myelodysplastic syndrome with ring sideroblasts and single lineage dysplasia | NCIT:C130037 | MONDO:equivalentTo | Myelodysplastic Syndrome with Ring Sideroblasts and Single Lineage Dysplasia | | MONDO:0019157 | +| MONDO:0853894 | b lymphoblastic leukemia/lymphoma with intrachromosomal amplification of chromosome 21 | NCIT:C130039 | MONDO:equivalentTo | B Lymphoblastic Leukemia/Lymphoma with Intrachromosomal Amplification of Chromosome 21 | | MONDO:0035605 | +| MONDO:0853943 | anastomosing hemangioma | NCIT:C131760 | MONDO:equivalentTo | Anastomosing Hemangioma | | MONDO:0002407 | +| MONDO:0853956 | acute megakaryoblastic leukemia with cbfa2t3-glis2 | NCIT:C132109 | MONDO:equivalentTo | Acute Megakaryoblastic Leukemia with CBFA2T3-GLIS2 | | MONDO:0004996 | +| MONDO:0853959 | small intestinal myeloid sarcoma | NCIT:C132260 | MONDO:equivalentTo | Small Intestinal Myeloid Sarcoma | | MONDO:0000956|MONDO:0006861 | +| MONDO:0853961 | atypical pituitary neuroendocrine tumor | NCIT:C132296 | MONDO:equivalentTo | Atypical Pituitary Neuroendocrine Tumor | | MONDO:0006373 | +| MONDO:0853963 | lip and oral cavity cancer by ajcc v8 stage | NCIT:C132728 | MONDO:equivalentTo | Lip and Oral Cavity Cancer by AJCC v8 Stage | | MONDO:0023644 | +| MONDO:0853964 | lip and oral cavity cancer by ajcc v6 and v7 stage | NCIT:C132736 | MONDO:equivalentTo | Lip and Oral Cavity Cancer by AJCC v6 and v7 Stage | | MONDO:0023644 | +| MONDO:0853965 | major salivary gland cancer by ajcc v7 stage | NCIT:C132778 | MONDO:equivalentTo | Major Salivary Gland Cancer by AJCC v7 Stage | | MONDO:0006284 | +| MONDO:0853966 | major salivary gland cancer by ajcc v8 stage | NCIT:C132779 | MONDO:equivalentTo | Major Salivary Gland Cancer by AJCC v8 Stage | | MONDO:0006284 | +| MONDO:0853968 | pharyngeal carcinoma by ajcc v8 stage | NCIT:C132814 | MONDO:equivalentTo | Pharyngeal Carcinoma by AJCC v8 Stage | | MONDO:0021345 | +| MONDO:0853973 | metastatic malignant germ cell tumor | NCIT:C132854 | MONDO:equivalentTo | Metastatic Malignant Germ Cell Tumor | | MONDO:0006290|MONDO:0024880 | +| MONDO:0853979 | sinonasal cancer by ajcc v8 stage | NCIT:C133074 | MONDO:equivalentTo | Sinonasal Cancer by AJCC v8 Stage | | MONDO:0056819 | +| MONDO:0853980 | lung adenofibroma | NCIT:C133091 | MONDO:equivalentTo | Lung Adenofibroma | | MONDO:0021043|MONDO:0002732 | +| MONDO:0853981 | laryngeal cancer by ajcc v8 stage | NCIT:C133156 | MONDO:equivalentTo | Laryngeal Cancer by AJCC v8 Stage | | MONDO:0002358 | +| MONDO:0853984 | cutaneous squamous cell carcinoma of the head and neck | NCIT:C133252 | MONDO:equivalentTo | Cutaneous Squamous Cell Carcinoma of the Head and Neck | | MONDO:0002529|MONDO:0010150 | +| MONDO:0853986 | esophageal cancer by ajcc v8 stage | NCIT:C133399 | MONDO:equivalentTo | Esophageal Cancer by AJCC v8 Stage | | MONDO:0019086 | +| MONDO:0853991 | gastroesophageal junction adenocarcinoma by ajcc v8 stage | NCIT:C133548 | MONDO:equivalentTo | Gastroesophageal Junction Adenocarcinoma by AJCC v8 Stage | | MONDO:0003219 | +| MONDO:0853993 | gastric cancer by ajcc v8 stage | NCIT:C133638 | MONDO:equivalentTo | Gastric Cancer by AJCC v8 Stage | | MONDO:0004950 | +| MONDO:0853994 | small intestinal cancer by ajcc v7 stage | NCIT:C133716 | MONDO:equivalentTo | Small Intestinal Cancer by AJCC v7 Stage | | MONDO:0005522 | +| MONDO:0853996 | appendix carcinoma by ajcc v7 stage | NCIT:C133733 | MONDO:equivalentTo | Appendix Carcinoma by AJCC v7 Stage | | MONDO:0003196 | +| MONDO:0853997 | anal canal cancer by ajcc v6 and v7 stage | NCIT:C133787 | MONDO:equivalentTo | Anal Canal Cancer by AJCC v6 and v7 Stage | | MONDO:0007108 | +| MONDO:0853998 | anal cancer by ajcc v8 stage | NCIT:C133794 | MONDO:equivalentTo | Anal Cancer by AJCC v8 Stage | | MONDO:0003199 | +| MONDO:0854000 | small intestinal adenocarcinoma by ajcc v8 stage | NCIT:C133893 | MONDO:equivalentTo | Small Intestinal Adenocarcinoma by AJCC v8 Stage | | MONDO:0003198 | +| MONDO:0854002 | appendix carcinoma by ajcc v8 stage | NCIT:C134117 | MONDO:equivalentTo | Appendix Carcinoma by AJCC v8 Stage | | MONDO:0003196 | +| MONDO:0854009 | colorectal cancer by ajcc v8 stage | NCIT:C134180 | MONDO:equivalentTo | Colorectal Cancer by AJCC v8 Stage | | MONDO:0024331 | +| MONDO:0854013 | intrahepatic cholangiocarcinoma by ajcc v7 stage | NCIT:C134514 | MONDO:equivalentTo | Intrahepatic Cholangiocarcinoma by AJCC v7 Stage | | MONDO:0003210 | +| MONDO:0854014 | hepatocellular carcinoma by ajcc v8 stage | NCIT:C134515 | MONDO:equivalentTo | Hepatocellular Carcinoma by AJCC v8 Stage | | MONDO:0007256 | +| MONDO:0854017 | intrahepatic bile duct cancer by ajcc v8 stage | NCIT:C134604 | MONDO:equivalentTo | Intrahepatic Bile Duct Cancer by AJCC v8 Stage | | MONDO:0018531 | +| MONDO:0854018 | gallbladder cancer by ajcc v8 stage | NCIT:C134660 | MONDO:equivalentTo | Gallbladder Cancer by AJCC v8 Stage | | MONDO:0003220 | +| MONDO:0854019 | hilar cholangiocarcinoma by ajcc v7 stage | NCIT:C134742 | MONDO:equivalentTo | Hilar Cholangiocarcinoma by AJCC v7 Stage | | MONDO:0003345 | +| MONDO:0854020 | hilar cholangiocarcinoma by ajcc v8 stage | NCIT:C134743 | MONDO:equivalentTo | Hilar Cholangiocarcinoma by AJCC v8 Stage | | MONDO:0003345 | +| MONDO:0854022 | distal bile duct cancer by ajcc v7 stage | NCIT:C134810 | MONDO:equivalentTo | Distal Bile Duct Cancer by AJCC v7 Stage | | MONDO:0003707 | +| MONDO:0854023 | distal bile duct cancer by ajcc v8 stage | NCIT:C134811 | MONDO:equivalentTo | Distal Bile Duct Cancer by AJCC v8 Stage | | MONDO:0003707 | +| MONDO:0854024 | ampulla of vater cancer by ajcc v7 stage | NCIT:C134863 | MONDO:equivalentTo | Ampulla of Vater Cancer by AJCC v7 Stage | | MONDO:0017590 | +| MONDO:0854025 | ampulla of vater cancer by ajcc v8 stage | NCIT:C134864 | MONDO:equivalentTo | Ampulla of Vater Cancer by AJCC v8 Stage | | MONDO:0017590 | +| MONDO:0854026 | pancreatic cancer by ajcc v6 and v7 stage | NCIT:C134902 | MONDO:equivalentTo | Pancreatic Cancer by AJCC v6 and v7 Stage | | MONDO:0005192 | +| MONDO:0854027 | pancreatic cancer by ajcc v8 stage | NCIT:C134909 | MONDO:equivalentTo | Pancreatic Cancer by AJCC v8 Stage | | MONDO:0005192 | +| MONDO:0854029 | lung non-squamous non-small cell carcinoma | NCIT:C135017 | MONDO:equivalentTo | Lung Non-Squamous Non-Small Cell Carcinoma | | MONDO:0005233 | +| MONDO:0854030 | gastric neuroendocrine tumor by ajcc v8 stage | NCIT:C135045 | MONDO:equivalentTo | Gastric Neuroendocrine Tumor by AJCC v8 Stage | | MONDO:0015062 | +| MONDO:0854031 | duodenal neuroendocrine tumor by ajcc v8 stage | NCIT:C135075 | MONDO:equivalentTo | Duodenal Neuroendocrine Tumor by AJCC v8 Stage | | MONDO:0015063 | +| MONDO:0854032 | jejunal neuroendocrine tumor by ajcc v8 stage | NCIT:C135119 | MONDO:equivalentTo | Jejunal Neuroendocrine Tumor by AJCC v8 Stage | | MONDO:0015064 | +| MONDO:0854033 | ileal neuroendocrine tumor by ajcc v8 stage | NCIT:C135124 | MONDO:equivalentTo | Ileal Neuroendocrine Tumor by AJCC v8 Stage | | MONDO:0015065 | +| MONDO:0854034 | digestive system neuroendocrine tumor by ajcc v7 stage | NCIT:C135129 | MONDO:equivalentTo | Digestive System Neuroendocrine Tumor by AJCC v7 Stage | | MONDO:0000386 | +| MONDO:0854036 | appendix neuroendocrine tumor by ajcc v8 stage | NCIT:C135156 | MONDO:equivalentTo | Appendix Neuroendocrine Tumor by AJCC v8 Stage | | MONDO:0015066 | +| MONDO:0854042 | pancreatic neuroendocrine tumor by ajcc v8 stage | NCIT:C135560 | MONDO:equivalentTo | Pancreatic Neuroendocrine Tumor by AJCC v8 Stage | | MONDO:0019954 | +| MONDO:0854043 | thymic epithelial neoplasm by ajcc v8 stage | NCIT:C136320 | MONDO:equivalentTo | Thymic Epithelial Neoplasm by AJCC v8 Stage | | MONDO:0018079 | +| MONDO:0854045 | pleural malignant mesothelioma by ajcc v7 stage | NCIT:C136374 | MONDO:equivalentTo | Pleural Malignant Mesothelioma by AJCC v7 Stage | | MONDO:0005112 | +| MONDO:0854046 | pleural malignant mesothelioma by ajcc v8 stage | NCIT:C136399 | MONDO:equivalentTo | Pleural Malignant Mesothelioma by AJCC v8 Stage | | MONDO:0005112 | +| MONDO:0854048 | lung cancer by ajcc v8 stage | NCIT:C136467 | MONDO:equivalentTo | Lung Cancer by AJCC v8 Stage | | MONDO:0005138 | +| MONDO:0854057 | bone cancer by ajcc v7 stage | NCIT:C136610 | MONDO:equivalentTo | Bone Cancer by AJCC v7 Stage | | MONDO:0002129 | +| MONDO:0854058 | bone cancer by ajcc v8 stage | NCIT:C136612 | MONDO:equivalentTo | Bone Cancer by AJCC v8 Stage | | MONDO:0002129 | +| MONDO:0854060 | soft tissue sarcoma by ajcc v8 stage | NCIT:C136693 | MONDO:equivalentTo | Soft Tissue Sarcoma by AJCC v8 Stage | | MONDO:0018078 | +| MONDO:0854061 | soft tissue sarcoma by ajcc v7 stage | NCIT:C136707 | MONDO:equivalentTo | Soft Tissue Sarcoma by AJCC v7 Stage | | MONDO:0018078 | +| MONDO:0854062 | uterine corpus sarcoma by ajcc v7 stage | NCIT:C136708 | MONDO:equivalentTo | Uterine Corpus Sarcoma by AJCC v7 Stage | | MONDO:0005210 | +| MONDO:0854063 | invasive lung mucinous adenocarcinoma | NCIT:C136709 | MONDO:equivalentTo | Invasive Lung Mucinous Adenocarcinoma | | MONDO:0040677|MONDO:0005061|MONDO:0004957 | +| MONDO:0854064 | lung enteric adenocarcinoma | NCIT:C136710 | MONDO:equivalentTo | Lung Enteric Adenocarcinoma | | MONDO:0006254|MONDO:0005061 | +| MONDO:0854065 | lung keratinizing squamous cell carcinoma | NCIT:C136713 | MONDO:equivalentTo | Lung Keratinizing Squamous Cell Carcinoma | | MONDO:0005097 | +| MONDO:0854066 | lung non-keratinizing squamous cell carcinoma | NCIT:C136714 | MONDO:equivalentTo | Lung Non-Keratinizing Squamous Cell Carcinoma | | MONDO:0005097 | +| MONDO:0854067 | lung non-mucinous adenocarcinoma in situ | NCIT:C136716 | MONDO:equivalentTo | Lung Non-Mucinous Adenocarcinoma In Situ | | MONDO:0000503 | +| MONDO:0854068 | lung mucinous adenocarcinoma in situ | NCIT:C136717 | MONDO:equivalentTo | Lung Mucinous Adenocarcinoma In Situ | | MONDO:0000503 | +| MONDO:0854069 | lung squamous cell carcinoma in situ | NCIT:C136719 | MONDO:equivalentTo | Lung Squamous Cell Carcinoma In Situ | | MONDO:0005097|MONDO:0004693 | +| MONDO:0854075 | cutaneous melanoma by ajcc v8 stage | NCIT:C137645 | MONDO:equivalentTo | Cutaneous Melanoma by AJCC v8 Stage | | MONDO:0005012 | +| MONDO:0854076 | occult breast carcinoma | NCIT:C137674 | MONDO:equivalentTo | Occult Breast Carcinoma | | MONDO:0004989 | +| MONDO:0854077 | breast pleomorphic lobular carcinoma in situ | NCIT:C137839 | MONDO:equivalentTo | Breast Pleomorphic Lobular Carcinoma In Situ | | MONDO:0006270 | +| MONDO:0854089 | prostate carcinoma by gene expression profile | NCIT:C138167 | MONDO:equivalentTo | Prostate Carcinoma by Gene Expression Profile | | MONDO:0005159 | +| MONDO:0854090 | duodenal-type follicular lymphoma | NCIT:C138185 | MONDO:equivalentTo | Duodenal-Type Follicular Lymphoma | | MONDO:0018906 | +| MONDO:0854092 | high grade b-cell lymphoma with myc and bcl2 and/or bcl6 rearrangements | NCIT:C138195 | MONDO:equivalentTo | High Grade B-Cell Lymphoma with MYC and BCL2 and/or BCL6 Rearrangements | | MONDO:0044889 | +| MONDO:0854094 | double-expressor lymphoma | NCIT:C138899 | MONDO:equivalentTo | Double-Expressor Lymphoma | | MONDO:0018905 | +| MONDO:0854097 | follicular helper t-cell lymphoma | NCIT:C139005 | MONDO:equivalentTo | Follicular Helper T-Cell Lymphoma | | MONDO:0000430 | +| MONDO:0854098 | multiple myeloma myeloma by ds stage | NCIT:C139008 | MONDO:equivalentTo | Multiple Myeloma Myeloma by DS Stage | | MONDO:0009693 | +| MONDO:0854099 | multiple myeloma by iss stage | NCIT:C139009 | MONDO:equivalentTo | Multiple Myeloma by ISS Stage | | MONDO:0009693 | +| MONDO:0854100 | type d lymphomatoid papulosis | NCIT:C139014 | MONDO:equivalentTo | Type D Lymphomatoid Papulosis | | MONDO:0020326 | +| MONDO:0854101 | type e lymphomatoid papulosis | NCIT:C139015 | MONDO:equivalentTo | Type E Lymphomatoid Papulosis | | MONDO:0020326 | +| MONDO:0854102 | lymphomatoid papulosis with dusp22-irf4 gene rearrangement | NCIT:C139017 | MONDO:equivalentTo | Lymphomatoid Papulosis with DUSP22-IRF4 Gene Rearrangement | | MONDO:0020326 | +| MONDO:0854105 | breast cancer by ajcc v8 stage | NCIT:C139532 | MONDO:equivalentTo | Breast Cancer by AJCC v8 Stage | | MONDO:0004989 | +| MONDO:0854108 | fibroadenoma of anogenital mammary-type glands | NCIT:C139547 | MONDO:equivalentTo | Fibroadenoma of Anogenital Mammary-Type Glands | | MONDO:0000383|MONDO:0021045 | +| MONDO:0854109 | vulvar composite hidradenoma papilliferum and fibroadenoma | NCIT:C139548 | MONDO:equivalentTo | Vulvar Composite Hidradenoma Papilliferum and Fibroadenoma | | MONDO:0021043|MONDO:0000643 | +| MONDO:0854111 | vulvar cancer by ajcc v8 stage | NCIT:C139618 | MONDO:equivalentTo | Vulvar Cancer by AJCC v8 Stage | | MONDO:0005215 | +| MONDO:0854112 | vaginal cancer by ajcc v8 stage | NCIT:C139657 | MONDO:equivalentTo | Vaginal Cancer by AJCC v8 Stage | | MONDO:0015867 | +| MONDO:0854113 | cervical cancer by ajcc v8 stage | NCIT:C139733 | MONDO:equivalentTo | Cervical Cancer by AJCC v8 Stage | | MONDO:0005131 | +| MONDO:0854114 | uterine corpus cancer by ajcc v8 stage | NCIT:C139801 | MONDO:equivalentTo | Uterine Corpus Cancer by AJCC v8 Stage | | MONDO:0006003 | +| MONDO:0854115 | uterine corpus sarcoma by ajcc v8 stage | NCIT:C139869 | MONDO:equivalentTo | Uterine Corpus Sarcoma by AJCC v8 Stage | | MONDO:0005210 | +| MONDO:0854119 | ovarian cancer by ajcc v8 stage | NCIT:C139963 | MONDO:equivalentTo | Ovarian Cancer by AJCC v8 Stage | | MONDO:0005140 | +| MONDO:0854120 | fallopian tube cancer by ajcc v8 stage | NCIT:C139983 | MONDO:equivalentTo | Fallopian Tube Cancer by AJCC v8 Stage | | MONDO:0006206 | +| MONDO:0854121 | primary peritoneal cancer by ajcc v7 stage | NCIT:C140003 | MONDO:equivalentTo | Primary Peritoneal Cancer by AJCC v7 Stage | | MONDO:0015686 | +| MONDO:0854122 | primary peritoneal cancer by ajcc v8 stage | NCIT:C140004 | MONDO:equivalentTo | Primary Peritoneal Cancer by AJCC v8 Stage | | MONDO:0015686 | +| MONDO:0854123 | gestational trophoblastic tumor by ajcc v7 stage | NCIT:C140032 | MONDO:equivalentTo | Gestational Trophoblastic Tumor by AJCC v7 Stage | | MONDO:0018944 | +| MONDO:0854124 | penile cancer by ajcc v8 stage | NCIT:C140075 | MONDO:equivalentTo | Penile Cancer by AJCC v8 Stage | | MONDO:0006360 | +| MONDO:0854125 | prostate cancer by ajcc v8 stage | NCIT:C140163 | MONDO:equivalentTo | Prostate Cancer by AJCC v8 Stage | | MONDO:0005159 | +| MONDO:0854126 | testicular cancer by ajcc v8 stage | NCIT:C140225 | MONDO:equivalentTo | Testicular Cancer by AJCC v8 Stage | | MONDO:0005447 | +| MONDO:0854127 | testicular cancer by ajcc v6 and v7 stage | NCIT:C140241 | MONDO:equivalentTo | Testicular Cancer by AJCC v6 and v7 Stage | | MONDO:0005447 | +| MONDO:0854128 | renal cell cancer by ajcc v8 stage | NCIT:C140322 | MONDO:equivalentTo | Renal Cell Cancer by AJCC v8 Stage | | MONDO:0005549 | +| MONDO:0854130 | renal pelvis and ureter cancer by ajcc v8 stage | NCIT:C140355 | MONDO:equivalentTo | Renal Pelvis and Ureter Cancer by AJCC v8 Stage | | MONDO:0020654 | +| MONDO:0854134 | renal pelvis and ureter cancer by ajcc v7 stage | NCIT:C140376 | MONDO:equivalentTo | Renal Pelvis and Ureter Cancer by AJCC v7 Stage | | MONDO:0020654 | +| MONDO:0854137 | bladder cancer by ajcc v8 stage | NCIT:C140416 | MONDO:equivalentTo | Bladder Cancer by AJCC v8 Stage | | MONDO:0004986 | +| MONDO:0854139 | urethral cancer by ajcc v8 stage | NCIT:C140457 | MONDO:equivalentTo | Urethral Cancer by AJCC v8 Stage | | MONDO:0021327 | +| MONDO:0854141 | urethral cancer by ajcc v7 stage | NCIT:C140464 | MONDO:equivalentTo | Urethral Cancer by AJCC v7 Stage | | MONDO:0021327 | +| MONDO:0854142 | eyelid carcinoma by ajcc v7 stage | NCIT:C140511 | MONDO:equivalentTo | Eyelid Carcinoma by AJCC v7 Stage | | MONDO:0003876 | +| MONDO:0854143 | eyelid carcinoma by ajcc v8 stage | NCIT:C140513 | MONDO:equivalentTo | Eyelid Carcinoma by AJCC v8 Stage | | MONDO:0003876 | +| MONDO:0854144 | choroidal and ciliary body melanoma by ajcc v8 stage | NCIT:C140659 | MONDO:equivalentTo | Choroidal and Ciliary Body Melanoma by AJCC v8 Stage | | MONDO:0006486 | +| MONDO:0854145 | uveal melanoma by ajcc v7 stage | NCIT:C140672 | MONDO:equivalentTo | Uveal Melanoma by AJCC v7 Stage | | MONDO:0006486 | +| MONDO:0854146 | retinoblastoma by ajcc v8 stage | NCIT:C140750 | MONDO:equivalentTo | Retinoblastoma by AJCC v8 Stage | | MONDO:0008380 | +| MONDO:0854148 | differentiated thyroid gland carcinoma by ajcc v7 stage | NCIT:C140959 | MONDO:equivalentTo | Differentiated Thyroid Gland Carcinoma by AJCC v7 Stage | | MONDO:0015447 | +| MONDO:0854150 | differentiated thyroid gland carcinoma by ajcc v8 stage | NCIT:C140965 | MONDO:equivalentTo | Differentiated Thyroid Gland Carcinoma by AJCC v8 Stage | | MONDO:0015447 | +| MONDO:0854153 | thyroid gland anaplastic carcinoma by ajcc v7 stage | NCIT:C140999 | MONDO:equivalentTo | Thyroid Gland Anaplastic Carcinoma by AJCC v7 Stage | | MONDO:0006468 | +| MONDO:0854154 | thyroid gland anaplastic carcinoma by ajcc v8 stage | NCIT:C141000 | MONDO:equivalentTo | Thyroid Gland Anaplastic Carcinoma by AJCC v8 Stage | | MONDO:0006468 | +| MONDO:0854155 | thyroid gland medullary carcinoma by ajcc v7 stage | NCIT:C141041 | MONDO:equivalentTo | Thyroid Gland Medullary Carcinoma by AJCC v7 Stage | | MONDO:0015277 | +| MONDO:0854156 | thyroid gland medullary carcinoma by ajcc v8 stage | NCIT:C141042 | MONDO:equivalentTo | Thyroid Gland Medullary Carcinoma by AJCC v8 Stage | | MONDO:0015277 | +| MONDO:0854157 | adrenal cortical carcinoma by ajcc v7 stage | NCIT:C141098 | MONDO:equivalentTo | Adrenal Cortical Carcinoma by AJCC v7 Stage | | MONDO:0006639 | +| MONDO:0854158 | adrenal cortical carcinoma by ajcc v8 stage | NCIT:C141100 | MONDO:equivalentTo | Adrenal Cortical Carcinoma by AJCC v8 Stage | | MONDO:0006639 | +| MONDO:0854159 | adrenal gland pheochromocytoma and sympathetic paraganglioma by ajcc v8 stage | NCIT:C141128 | MONDO:equivalentTo | Adrenal Gland Pheochromocytoma and Sympathetic Paraganglioma by AJCC v8 Stage | | MONDO:0021072 | +| MONDO:0854166 | chronic lymphocytic leukemia- modified rai staging system | NCIT:C141206 | MONDO:equivalentTo | Chronic Lymphocytic Leukemia- Modified Rai Staging System | | MONDO:0004948 | +| MONDO:0854167 | chronic lymphocytic leukemia- binet staging system | NCIT:C141208 | MONDO:equivalentTo | Chronic Lymphocytic Leukemia- Binet Staging System | | MONDO:0004948 | +| MONDO:0854189 | multiple myeloma by riss stage | NCIT:C141393 | MONDO:equivalentTo | Multiple Myeloma by RISS Stage | | MONDO:0009693 | +| MONDO:0854192 | thoracic nut carcinoma | NCIT:C142781 | MONDO:equivalentTo | Thoracic NUT Carcinoma | | MONDO:0005563|MONDO:0003274 | +| MONDO:0854193 | benign lung pecoma | NCIT:C142784 | MONDO:equivalentTo | Benign Lung PEComa | | MONDO:0002732|MONDO:0020588|MONDO:0020581 | +| MONDO:0854200 | pulmonary artery intimal sarcoma | NCIT:C142825 | MONDO:equivalentTo | Pulmonary Artery Intimal Sarcoma | | MONDO:0006255|MONDO:0002426 | +| MONDO:0854201 | primary pulmonary myxoid sarcoma with ewsr1-creb1 fusion | NCIT:C142827 | MONDO:equivalentTo | Primary Pulmonary Myxoid Sarcoma with EWSR1-CREB1 Fusion | | MONDO:0002426 | +| MONDO:0854212 | refractory rhabdoid tumor | NCIT:C142858 | MONDO:equivalentTo | Refractory Rhabdoid Tumor | | MONDO:0002728|MONDO:0036501 | +| MONDO:0854225 | atypical type a thymoma | NCIT:C146640 | MONDO:equivalentTo | Atypical Type A Thymoma | | MONDO:0002588 | +| MONDO:0854227 | thymic hepatoid adenocarcinoma | NCIT:C146717 | MONDO:equivalentTo | Thymic Hepatoid Adenocarcinoma | | MONDO:0006243|MONDO:0003209 | +| MONDO:0854229 | malignant mediastinal germ cell tumor stage grouping of the pediatric study group | NCIT:C146848 | MONDO:equivalentTo | Malignant Mediastinal Germ Cell Tumor Stage Grouping of the Pediatric Study Group | | MONDO:0006298 | +| MONDO:0854230 | metastatic epithelioid hemangioendothelioma | NCIT:C146858 | MONDO:equivalentTo | Metastatic Epithelioid Hemangioendothelioma | | MONDO:0015523|MONDO:0024880 | +| MONDO:0854231 | mediastinal mixed germ cell tumor | NCIT:C146861 | MONDO:equivalentTo | Mediastinal Mixed Germ Cell Tumor | | MONDO:0006298|MONDO:0015864|MONDO:0005853 | +| MONDO:0854234 | mediastinal epithelioid hemangioendothelioma | NCIT:C146988 | MONDO:equivalentTo | Mediastinal Epithelioid Hemangioendothelioma | | MONDO:0037743|MONDO:0015523 | +| MONDO:0854235 | cardiac extraskeletal osteosarcoma | NCIT:C147003 | MONDO:equivalentTo | Cardiac Extraskeletal Osteosarcoma | | MONDO:0002621|MONDO:0003354 | +| MONDO:0854236 | cardiac myxofibrosarcoma | NCIT:C147004 | MONDO:equivalentTo | Cardiac Myxofibrosarcoma | | MONDO:0019202|MONDO:0003742 | +| MONDO:0854237 | cardiac yolk sac tumor | NCIT:C147006 | MONDO:equivalentTo | Cardiac Yolk Sac Tumor | | MONDO:0001991|MONDO:0005744 | +| MONDO:0854242 | pericardial sarcoma | NCIT:C147098 | MONDO:equivalentTo | Pericardial Sarcoma | | MONDO:0018078|MONDO:0001322 | +| MONDO:0854249 | recurrent lymphoproliferative disorder | NCIT:C147861 | MONDO:equivalentTo | Recurrent Lymphoproliferative Disorder | | | +| MONDO:0854250 | oropharyngeal p16ink4a-negative squamous cell carcinoma | NCIT:C147906 | MONDO:equivalentTo | Oropharyngeal p16INK4a-Negative Squamous Cell Carcinoma | | MONDO:0044704 | +| MONDO:0854251 | central nervous system b-cell non-hodgkin lymphoma | NCIT:C147948 | MONDO:equivalentTo | Central Nervous System B-Cell Non-Hodgkin Lymphoma | | MONDO:0015759|MONDO:0044887 | +| MONDO:0854253 | refractory melanoma | NCIT:C147983 | MONDO:equivalentTo | Refractory Melanoma | | MONDO:0036501|MONDO:0005105 | +| MONDO:0854268 | refractory round cell liposarcoma | NCIT:C148299 | MONDO:equivalentTo | Refractory Round Cell Liposarcoma | | MONDO:0005238 | +| MONDO:0854269 | metastatic round cell liposarcoma | NCIT:C148300 | MONDO:equivalentTo | Metastatic Round Cell Liposarcoma | | MONDO:0005238 | +| MONDO:0854270 | refractory sarcoma | NCIT:C148301 | MONDO:equivalentTo | Refractory Sarcoma | | MONDO:0005089|MONDO:0036501 | +| MONDO:0854284 | refractory leukemia | NCIT:C148426 | MONDO:equivalentTo | Refractory Leukemia | | MONDO:0005059|MONDO:0004111 | +| MONDO:0854293 | castration-naive prostate carcinoma | NCIT:C148536 | MONDO:equivalentTo | Castration-Naive Prostate Carcinoma | | MONDO:0004956 | +| MONDO:0854294 | thoracic esophagus adenocarcinoma | NCIT:C150027 | MONDO:equivalentTo | Thoracic Esophagus Adenocarcinoma | | MONDO:0005028|MONDO:0021325 | +| MONDO:0854295 | thoracic esophagus squamous cell carcinoma | NCIT:C150029 | MONDO:equivalentTo | Thoracic Esophagus Squamous Cell Carcinoma | | MONDO:0005580|MONDO:0021325 | +| MONDO:0854296 | cervical esophagus adenocarcinoma | NCIT:C150031 | MONDO:equivalentTo | Cervical Esophagus Adenocarcinoma | | MONDO:0021326|MONDO:0005028 | +| MONDO:0854297 | cervical esophagus squamous cell carcinoma | NCIT:C150032 | MONDO:equivalentTo | Cervical Esophagus Squamous Cell Carcinoma | | MONDO:0021326|MONDO:0005580 | +| MONDO:0854298 | gastric cardia squamous cell carcinoma | NCIT:C150034 | MONDO:equivalentTo | Gastric Cardia Squamous Cell Carcinoma | | MONDO:0003834|MONDO:0006230 | +| MONDO:0854317 | high risk neuroblastoma | NCIT:C150281 | MONDO:equivalentTo | High Risk Neuroblastoma | | MONDO:0005072 | +| MONDO:0854322 | hhv8-related lymphoproliferative disorder | NCIT:C150399 | MONDO:equivalentTo | HHV8-Related Lymphoproliferative Disorder | | | +| MONDO:0854323 | hhv8-positive multicentric castleman disease | NCIT:C150404 | MONDO:equivalentTo | HHV8-Positive Multicentric Castleman Disease | | | +| MONDO:0854324 | extracavitary primary effusion lymphoma | NCIT:C150406 | MONDO:equivalentTo | Extracavitary Primary Effusion Lymphoma | | MONDO:0018842 | +| MONDO:0854325 | body cavity primary effusion lymphoma | NCIT:C150407 | MONDO:equivalentTo | Body Cavity Primary Effusion Lymphoma | | MONDO:0018842 | +| MONDO:0854332 | refractory malignant bone neoplasm | NCIT:C150525 | MONDO:equivalentTo | Refractory Malignant Bone Neoplasm | | MONDO:0002129|MONDO:0036501 | +| MONDO:0854334 | refractory malignant female reproductive system neoplasm | NCIT:C150527 | MONDO:equivalentTo | Refractory Malignant Female Reproductive System Neoplasm | | MONDO:0001416|MONDO:0036501 | +| MONDO:0854335 | refractory malignant neoplasm of multiple primary sites | NCIT:C150529 | MONDO:equivalentTo | Refractory Malignant Neoplasm of Multiple Primary Sites | | MONDO:0036501 | +| MONDO:0854339 | refractory malignant male reproductive system neoplasm | NCIT:C150534 | MONDO:equivalentTo | Refractory Malignant Male Reproductive System Neoplasm | | MONDO:0005836|MONDO:0036501 | +| MONDO:0854340 | refractory malignant mesothelioma | NCIT:C150535 | MONDO:equivalentTo | Refractory Malignant Mesothelioma | | MONDO:0006292|MONDO:0036501 | +| MONDO:0854342 | refractory malignant soft tissue neoplasm | NCIT:C150537 | MONDO:equivalentTo | Refractory Malignant Soft Tissue Neoplasm | | MONDO:0024637|MONDO:0036501 | +| MONDO:0854345 | refractory malignant endocrine neoplasm | NCIT:C150541 | MONDO:equivalentTo | Refractory Malignant Endocrine Neoplasm | | MONDO:0021069|MONDO:0036501 | +| MONDO:0854347 | refractory malignant urinary system neoplasm | NCIT:C150543 | MONDO:equivalentTo | Refractory Malignant Urinary System Neoplasm | | MONDO:0006295|MONDO:0036501 | +| MONDO:0854349 | refractory malignant skin neoplasm | NCIT:C150546 | MONDO:equivalentTo | Refractory Malignant Skin Neoplasm | | MONDO:0002898|MONDO:0036501 | +| MONDO:0854350 | prostate adenocarcinoma without neuroendocrine differentiation | NCIT:C150557 | MONDO:equivalentTo | Prostate Adenocarcinoma without Neuroendocrine Differentiation | | MONDO:0005082 | +| MONDO:0854351 | igm monoclonal gammopathy of undetermined significance | NCIT:C150566 | MONDO:equivalentTo | IgM Monoclonal Gammopathy of Undetermined Significance | | MONDO:0004225 | +| MONDO:0854352 | invasive bladder carcinoma | NCIT:C150570 | MONDO:equivalentTo | Invasive Bladder Carcinoma | | MONDO:0040677|MONDO:0004986 | +| MONDO:0854353 | localized cerebral neoplasm | NCIT:C150573 | MONDO:equivalentTo | Localized Cerebral Neoplasm | | MONDO:0021632|MONDO:0021374 | +| MONDO:0854358 | non-igm monoclonal gammopathy of undetermined significance | NCIT:C150588 | MONDO:equivalentTo | Non-IgM Monoclonal Gammopathy of Undetermined Significance | | MONDO:0004225 | +| MONDO:0854359 | testicular follicular lymphoma | NCIT:C150589 | MONDO:equivalentTo | Testicular Follicular Lymphoma | | MONDO:0001472|MONDO:0018906 | +| MONDO:0854363 | metastatic malignant neoplasm in the viscera | NCIT:C150597 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Viscera | | MONDO:0024880 | +| MONDO:0854365 | resectable malignant neoplasm | NCIT:C150602 | MONDO:equivalentTo | Resectable Malignant Neoplasm | | MONDO:0004992 | +| MONDO:0854374 | immunodeficiency-related lymphoproliferative disorder | NCIT:C150672 | MONDO:equivalentTo | Immunodeficiency-Related Lymphoproliferative Disorder | | | +| MONDO:0854376 | tumors derived from langerhans cells | NCIT:C150692 | MONDO:equivalentTo | Tumors Derived from Langerhans Cells | | MONDO:0006247 | +| MONDO:0854377 | langerhans cell histiocytosis, monostotic | NCIT:C150701 | MONDO:equivalentTo | Langerhans Cell Histiocytosis, Monostotic | | MONDO:0018310 | +| MONDO:0854378 | langerhans cell histiocytosis, polyostotic | NCIT:C150702 | MONDO:equivalentTo | Langerhans Cell Histiocytosis, Polyostotic | | MONDO:0018310 | +| MONDO:0854379 | langerhans cell histiocytosis, disseminated | NCIT:C150703 | MONDO:equivalentTo | Langerhans Cell Histiocytosis, Disseminated | | MONDO:0018310 | +| MONDO:0854381 | transformed non-hodgkin lymphoma | NCIT:C151957 | MONDO:equivalentTo | Transformed Non-Hodgkin Lymphoma | | MONDO:0018908 | +| MONDO:0854382 | acute leukemia of ambiguous lineage, not otherwise specified | NCIT:C151975 | MONDO:equivalentTo | Acute Leukemia of Ambiguous Lineage, Not Otherwise Specified | | MONDO:0019460 | +| MONDO:0854385 | abdominal rhabdomyosarcoma | NCIT:C151982 | MONDO:equivalentTo | Abdominal Rhabdomyosarcoma | | MONDO:0005212 | +| MONDO:0854388 | abdominal undifferentiated pleomorphic sarcoma | NCIT:C151985 | MONDO:equivalentTo | Abdominal Undifferentiated Pleomorphic Sarcoma | | MONDO:0002142 | +| MONDO:0854389 | mixed phenotype acute leukemia, rare types | NCIT:C151990 | MONDO:equivalentTo | Mixed Phenotype Acute Leukemia, Rare Types | | MONDO:0020743 | +| MONDO:0854394 | metastatic sarcoma | NCIT:C152076 | MONDO:equivalentTo | Metastatic Sarcoma | | MONDO:0005089|MONDO:0024880 | +| MONDO:0854395 | refractory malignant head and neck neoplasm | NCIT:C152078 | MONDO:equivalentTo | Refractory Malignant Head and Neck Neoplasm | | MONDO:0005627|MONDO:0036501 | +| MONDO:0854414 | refractory ewing sarcoma/peripheral primitive neuroectodermal tumor | NCIT:C153286 | MONDO:equivalentTo | Refractory Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor | | MONDO:0021038|MONDO:0036501 | +| MONDO:0854420 | metastatic chordoma | NCIT:C153323 | MONDO:equivalentTo | Metastatic Chordoma | | MONDO:0024880|MONDO:0008978 | +| MONDO:0854422 | castration-sensitive prostate carcinoma | NCIT:C153336 | MONDO:equivalentTo | Castration-Sensitive Prostate Carcinoma | | MONDO:0004956 | +| MONDO:0854468 | sinonasal poorly differentiated carcinoma | NCIT:C154324 | MONDO:equivalentTo | Sinonasal Poorly Differentiated Carcinoma | | MONDO:0056819 | +| MONDO:0854469 | densely granulated corticotroph pituitary neuroendocrine tumor | NCIT:C154339 | MONDO:equivalentTo | Densely Granulated Corticotroph Pituitary Neuroendocrine Tumor | | MONDO:0006068 | +| MONDO:0854470 | sparsely granulated corticotroph pituitary neuroendocrine tumor | NCIT:C154340 | MONDO:equivalentTo | Sparsely Granulated Corticotroph Pituitary Neuroendocrine Tumor | | MONDO:0006068 | +| MONDO:0854471 | crooke cell tumor | NCIT:C154342 | MONDO:equivalentTo | Crooke Cell Tumor | | MONDO:0006068 | +| MONDO:0854472 | non-functioning corticotroph pituitary neuroendocrine tumor | NCIT:C154429 | MONDO:equivalentTo | Non-Functioning Corticotroph Pituitary Neuroendocrine Tumor | | MONDO:0006068|MONDO:0019613 | +| MONDO:0854479 | anaplastic sarcoma of the kidney | NCIT:C154496 | MONDO:equivalentTo | Anaplastic Sarcoma of the Kidney | | MONDO:0002930|MONDO:0020633 | +| MONDO:0854480 | multiple synchronous pituitary neuroendocrine tumors of distinct lineages | NCIT:C154520 | MONDO:equivalentTo | Multiple Synchronous Pituitary Neuroendocrine Tumors of Distinct Lineages | | MONDO:0006373 | +| MONDO:0854485 | cutaneous melanoma of the extremity | NCIT:C155305 | MONDO:equivalentTo | Cutaneous Melanoma of the Extremity | | MONDO:0005012 | +| MONDO:0854489 | sarcoma of the extremity | NCIT:C155647 | MONDO:equivalentTo | Sarcoma of the Extremity | | MONDO:0005089 | +| MONDO:0854492 | mixed gangliocytoma-pituitary neuroendocrine tumor | NCIT:C155767 | MONDO:equivalentTo | Mixed Gangliocytoma-Pituitary Neuroendocrine Tumor | | MONDO:0021043|MONDO:0006373 | +| MONDO:0854495 | ependymal pituicytoma | NCIT:C155774 | MONDO:equivalentTo | Ependymal Pituicytoma | | MONDO:0003257 | +| MONDO:0854496 | sellar meningioma | NCIT:C155776 | MONDO:equivalentTo | Sellar Meningioma | | MONDO:0002998|MONDO:0002720 | +| MONDO:0854500 | sellar solitary fibrous tumor | NCIT:C155784 | MONDO:equivalentTo | Sellar Solitary Fibrous Tumor | | MONDO:0002720|MONDO:0003223 | +| MONDO:0854518 | metastatic malignant pancreatic neoplasm | NCIT:C155852 | MONDO:equivalentTo | Metastatic Malignant Pancreatic Neoplasm | | MONDO:0009831|MONDO:0024880 | +| MONDO:0854521 | chest wall sarcoma | NCIT:C155873 | MONDO:equivalentTo | Chest Wall Sarcoma | | MONDO:0005089|MONDO:0021323 | +| MONDO:0854523 | unresectable desmoid fibromatosis | NCIT:C155877 | MONDO:equivalentTo | Unresectable Desmoid Fibromatosis | | MONDO:0007608 | +| MONDO:0854527 | smoldering waldenstrom macroglobulinemia | NCIT:C155910 | MONDO:equivalentTo | Smoldering Waldenstrom Macroglobulinemia | | MONDO:0100280 | +| MONDO:0854528 | metastatic malignant neoplasm in the thoracic cavity | NCIT:C155919 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Thoracic Cavity | | MONDO:0024880|MONDO:0003274 | +| MONDO:0854529 | medullary hemangioblastoma | NCIT:C155949 | MONDO:equivalentTo | Medullary Hemangioblastoma | | MONDO:0003902 | +| MONDO:0854530 | chromophobe renal cell carcinoma associated with birt-hogg-dube syndrome | NCIT:C155951 | MONDO:equivalentTo | Chromophobe Renal Cell Carcinoma Associated with Birt-Hogg-Dube Syndrome | | MONDO:0017885 | +| MONDO:0854531 | uterine ligament papillary cystadenoma | NCIT:C155952 | MONDO:equivalentTo | Uterine Ligament Papillary Cystadenoma | | MONDO:0021091|MONDO:0020582 | +| MONDO:0854533 | thyroid gland spindle cell follicular adenoma | NCIT:C155957 | MONDO:equivalentTo | Thyroid Gland Spindle Cell Follicular Adenoma | | MONDO:0005032 | +| MONDO:0854534 | thyroid gland black follicular adenoma | NCIT:C155958 | MONDO:equivalentTo | Thyroid Gland Black Follicular Adenoma | | MONDO:0005032 | +| MONDO:0854545 | hypothalamic-chiasmatic pilomyxoid astrocytoma | NCIT:C156038 | MONDO:equivalentTo | Hypothalamic-Chiasmatic Pilomyxoid Astrocytoma | | MONDO:0016692 | +| MONDO:0854546 | fourth ventricle medulloblastoma | NCIT:C156039 | MONDO:equivalentTo | Fourth Ventricle Medulloblastoma | | MONDO:0007959 | +| MONDO:0854547 | third ventricle germinoma | NCIT:C156040 | MONDO:equivalentTo | Third Ventricle Germinoma | | MONDO:0002214 | +| MONDO:0854549 | temporal lobe pleomorphic xanthoastrocytoma | NCIT:C156042 | MONDO:equivalentTo | Temporal Lobe Pleomorphic Xanthoastrocytoma | | MONDO:0016690 | +| MONDO:0854550 | spindle cell variant thyroid gland papillary carcinoma | NCIT:C156045 | MONDO:equivalentTo | Spindle Cell Variant Thyroid Gland Papillary Carcinoma | | MONDO:0005075 | +| MONDO:0854551 | hobnail variant thyroid gland papillary carcinoma | NCIT:C156050 | MONDO:equivalentTo | Hobnail Variant Thyroid Gland Papillary Carcinoma | | MONDO:0005075 | +| MONDO:0854584 | metastatic neuroblastoma | NCIT:C156101 | MONDO:equivalentTo | Metastatic Neuroblastoma | | MONDO:0024880|MONDO:0005072 | +| MONDO:0854588 | thyroid gland follicular carcinoma, encapsulated angioinvasive | NCIT:C156122 | MONDO:equivalentTo | Thyroid Gland Follicular Carcinoma, Encapsulated Angioinvasive | | MONDO:0005034 | +| MONDO:0854589 | thyroid gland follicular carcinoma, widely invasive | NCIT:C156123 | MONDO:equivalentTo | Thyroid Gland Follicular Carcinoma, Widely Invasive | | MONDO:0040677|MONDO:0005034 | +| MONDO:0854594 | thyroid gland mucinous carcinoma | NCIT:C156267 | MONDO:equivalentTo | Thyroid Gland Mucinous Carcinoma | | MONDO:0015075 | +| MONDO:0854595 | intrathyroidal thymoma | NCIT:C156268 | MONDO:equivalentTo | Intrathyroidal Thymoma | | MONDO:0015074|MONDO:0006456 | +| MONDO:0854598 | orbital alveolar soft part sarcoma | NCIT:C156276 | MONDO:equivalentTo | Orbital Alveolar Soft Part Sarcoma | | MONDO:0004943|MONDO:0011655 | +| MONDO:0854599 | bladder alveolar soft part sarcoma | NCIT:C156277 | MONDO:equivalentTo | Bladder Alveolar Soft Part Sarcoma | | MONDO:0001374|MONDO:0011655 | +| MONDO:0854600 | cellular nerve sheath myxoma | NCIT:C156278 | MONDO:equivalentTo | Cellular Nerve Sheath Myxoma | | MONDO:0006317 | +| MONDO:0854601 | colon liposarcoma | NCIT:C156279 | MONDO:equivalentTo | Colon Liposarcoma | | MONDO:0003352|MONDO:0005060 | +| MONDO:0854608 | thyroid gland schwannoma | NCIT:C156340 | MONDO:equivalentTo | Thyroid Gland Schwannoma | | MONDO:0004820|MONDO:0006107 | +| MONDO:0854616 | thyroid gland solitary fibrous tumor | NCIT:C156349 | MONDO:equivalentTo | Thyroid Gland Solitary Fibrous Tumor | | MONDO:0016238|MONDO:0015074 | +| MONDO:0854631 | metastatic neuroendocrine neoplasm | NCIT:C156485 | MONDO:equivalentTo | Metastatic Neuroendocrine Neoplasm | | MONDO:0019496|MONDO:0024880 | +| MONDO:0854639 | malignant abdominal neoplasm | NCIT:C156714 | MONDO:equivalentTo | Malignant Abdominal Neoplasm | | MONDO:0004992 | +| MONDO:0854640 | malignant pelvic neoplasm | NCIT:C156715 | MONDO:equivalentTo | Malignant Pelvic Neoplasm | | MONDO:0004992 | +| MONDO:0854647 | metastatic basal cell carcinoma | NCIT:C156769 | MONDO:equivalentTo | Metastatic Basal Cell Carcinoma | | MONDO:0024879|MONDO:0020804 | +| MONDO:0854656 | adrenal cortical sex cord-stromal tumor | NCIT:C156943 | MONDO:equivalentTo | Adrenal Cortical Sex Cord-Stromal Tumor | | MONDO:0006055|MONDO:0036591 | +| MONDO:0854657 | adrenal gland schwannoma | NCIT:C156944 | MONDO:equivalentTo | Adrenal Gland Schwannoma | | MONDO:0021468|MONDO:0004820 | +| MONDO:0854658 | adrenal gland lymphoma | NCIT:C156945 | MONDO:equivalentTo | Adrenal Gland Lymphoma | | MONDO:0002817|MONDO:0001499 | +| MONDO:0854659 | adrenal gland sarcoma | NCIT:C156956 | MONDO:equivalentTo | Adrenal Gland Sarcoma | | MONDO:0002817|MONDO:0001501 | +| MONDO:0854660 | primary vitreoretinal non-hodgkin lymphoma | NCIT:C157065 | MONDO:equivalentTo | Primary Vitreoretinal Non-Hodgkin Lymphoma | | MONDO:0004351|MONDO:0044887 | +| MONDO:0854663 | unresectable paraganglioma | NCIT:C157126 | MONDO:equivalentTo | Unresectable Paraganglioma | | MONDO:0000448 | +| MONDO:0854669 | breast histiocytoid carcinoma | NCIT:C157235 | MONDO:equivalentTo | Breast Histiocytoid Carcinoma | | MONDO:0005051 | +| MONDO:0854670 | adrenal gland ganglioneuroblastoma, intermixed | NCIT:C157243 | MONDO:equivalentTo | Adrenal Gland Ganglioneuroblastoma, Intermixed | | MONDO:0004477|MONDO:0003326 | +| MONDO:0854671 | adrenal gland ganglioneuroblastoma, nodular | NCIT:C157244 | MONDO:equivalentTo | Adrenal Gland Ganglioneuroblastoma, Nodular | | MONDO:0004477|MONDO:0003325 | +| MONDO:0854672 | composite paraganglioma | NCIT:C157246 | MONDO:equivalentTo | Composite Paraganglioma | | MONDO:0000448 | +| MONDO:0854679 | peripheral hemangioblastoma | NCIT:C157450 | MONDO:equivalentTo | Peripheral Hemangioblastoma | | MONDO:0016748 | +| MONDO:0854680 | metastatic squamous cell carcinoma in the cervical lymph nodes | NCIT:C157452 | MONDO:equivalentTo | Metastatic Squamous Cell Carcinoma in the Cervical Lymph Nodes | | MONDO:0005438|MONDO:0044907 | +| MONDO:0854688 | bap1-mutant clear cell renal cell carcinoma | NCIT:C157614 | MONDO:equivalentTo | BAP1-Mutant Clear Cell Renal Cell Carcinoma | | MONDO:0005005 | +| MONDO:0854691 | transformed chronic lymphocytic leukemia to diffuse large b-cell lymphoma | NCIT:C157624 | MONDO:equivalentTo | Transformed Chronic Lymphocytic Leukemia to Diffuse Large B-Cell Lymphoma | | MONDO:0004948 | +| MONDO:0854692 | metastatic adenoid cystic carcinoma | NCIT:C157638 | MONDO:equivalentTo | Metastatic Adenoid Cystic Carcinoma | | MONDO:0024879|MONDO:0004971 | +| MONDO:0854698 | refractory lymphoproliferative disorder | NCIT:C157686 | MONDO:equivalentTo | Refractory Lymphoproliferative Disorder | | | +| MONDO:0854705 | kidney synovial sarcoma | NCIT:C157737 | MONDO:equivalentTo | Kidney Synovial Sarcoma | | MONDO:0002930|MONDO:0010434 | +| MONDO:0854706 | kidney neuroendocrine neoplasm | NCIT:C157743 | MONDO:equivalentTo | Kidney Neuroendocrine Neoplasm | | MONDO:0019496|MONDO:0021163 | +| MONDO:0854708 | metanephric tumor | NCIT:C157748 | MONDO:equivalentTo | Metanephric Tumor | | MONDO:0002513|MONDO:0036976 | +| MONDO:0854714 | bladder neuroendocrine neoplasm | NCIT:C157758 | MONDO:equivalentTo | Bladder Neuroendocrine Neoplasm | | MONDO:0019496|MONDO:0004987 | +| MONDO:0854748 | subcutaneous disorder | NCIT:C157995 | MONDO:equivalentTo | Subcutaneous Disorder | | | +| MONDO:0854749 | kidney epithelioid angiomyolipoma | NCIT:C158032 | MONDO:equivalentTo | Kidney Epithelioid Angiomyolipoma | | MONDO:0004555|MONDO:0002606 | +| MONDO:0854750 | kidney mixed epithelial and stromal tumor family | NCIT:C158046 | MONDO:equivalentTo | Kidney Mixed Epithelial and Stromal Tumor Family | | MONDO:0021163 | +| MONDO:0854756 | bladder non-invasive urothelial neoplasm | NCIT:C158374 | MONDO:equivalentTo | Bladder Non-Invasive Urothelial Neoplasm | | MONDO:0003755|MONDO:0004987 | +| MONDO:0854773 | platinum-sensitive lung small cell carcinoma | NCIT:C158495 | MONDO:equivalentTo | Platinum-Sensitive Lung Small Cell Carcinoma | | MONDO:0008433 | +| MONDO:0854780 | borderline ovarian mixed epithelial tumor/atypical proliferative ovarian mixed epithelial tumor | NCIT:C158616 | MONDO:equivalentTo | Borderline Ovarian Mixed Epithelial Tumor/Atypical Proliferative Ovarian Mixed Epithelial Tumor | | MONDO:0021043|MONDO:0016093 | +| MONDO:0854781 | endometrioid tumor, variant with squamous differentiation | NCIT:C158620 | MONDO:equivalentTo | Endometrioid Tumor, Variant with Squamous Differentiation | | MONDO:0002480 | +| MONDO:0854783 | bladder soft tissue neoplasm | NCIT:C158636 | MONDO:equivalentTo | Bladder Soft Tissue Neoplasm | | MONDO:0006424|MONDO:0004987 | +| MONDO:0854795 | early stage pancreatic ductal adenocarcinoma | NCIT:C158961 | MONDO:equivalentTo | Early Stage Pancreatic Ductal Adenocarcinoma | | MONDO:0005184 | +| MONDO:0854803 | kidney rhabdomyosarcoma | NCIT:C159206 | MONDO:equivalentTo | Kidney Rhabdomyosarcoma | | MONDO:0002930|MONDO:0005212 | +| MONDO:0854804 | kidney ewing sarcoma | NCIT:C159208 | MONDO:equivalentTo | Kidney Ewing Sarcoma | | MONDO:0018270|MONDO:0002930 | +| MONDO:0854806 | kidney hemangioma | NCIT:C159211 | MONDO:equivalentTo | Kidney Hemangioma | | MONDO:0002513|MONDO:0006500 | +| MONDO:0854807 | kidney lymphangioma | NCIT:C159214 | MONDO:equivalentTo | Kidney Lymphangioma | | MONDO:0002013|MONDO:0002513 | +| MONDO:0854808 | kidney schwannoma | NCIT:C159221 | MONDO:equivalentTo | Kidney Schwannoma | | MONDO:0002513|MONDO:0004820 | +| MONDO:0854809 | kidney solitary fibrous tumor | NCIT:C159222 | MONDO:equivalentTo | Kidney Solitary Fibrous Tumor | | MONDO:0016238|MONDO:0021163 | +| MONDO:0854812 | kidney germ cell tumor | NCIT:C159227 | MONDO:equivalentTo | Kidney Germ Cell Tumor | | MONDO:0018201|MONDO:0021163 | +| MONDO:0854813 | penile human papillomavirus-independent squamous cell carcinoma | NCIT:C159244 | MONDO:equivalentTo | Penile Human Papillomavirus-Independent Squamous Cell Carcinoma | | MONDO:0018352 | +| MONDO:0854815 | penile carcinoma cuniculatum | NCIT:C159247 | MONDO:equivalentTo | Penile Carcinoma Cuniculatum | | MONDO:0003698 | +| MONDO:0854817 | penile papillary-basaloid carcinoma | NCIT:C159249 | MONDO:equivalentTo | Penile Papillary-Basaloid Carcinoma | | MONDO:0004089 | +| MONDO:0854818 | penile warty-basaloid carcinoma | NCIT:C159250 | MONDO:equivalentTo | Penile Warty-Basaloid Carcinoma | | MONDO:0004430|MONDO:0020656 | +| MONDO:0854819 | penile lymphoepithelioma-like carcinoma | NCIT:C159252 | MONDO:equivalentTo | Penile Lymphoepithelioma-Like Carcinoma | | MONDO:0003572|MONDO:0020656 | +| MONDO:0854820 | borderline ovarian mucinous tumor/atypical proliferative ovarian mucinous tumor with microinvasion | NCIT:C159311 | MONDO:equivalentTo | Borderline Ovarian Mucinous Tumor/Atypical Proliferative Ovarian Mucinous Tumor with Microinvasion | | MONDO:0003756 | +| MONDO:0854828 | bladder rhabdomyosarcoma | NCIT:C159667 | MONDO:equivalentTo | Bladder Rhabdomyosarcoma | | MONDO:0001374|MONDO:0005212 | +| MONDO:0854831 | bladder leiomyosarcoma | NCIT:C159670 | MONDO:equivalentTo | Bladder Leiomyosarcoma | | MONDO:0001374|MONDO:0005058 | +| MONDO:0854838 | bladder hemangioma | NCIT:C159680 | MONDO:equivalentTo | Bladder Hemangioma | | MONDO:0000384|MONDO:0006500 | +| MONDO:0854839 | bladder granular cell tumor | NCIT:C159681 | MONDO:equivalentTo | Bladder Granular Cell Tumor | | MONDO:0006235|MONDO:0004987 | +| MONDO:0854840 | bladder neurofibroma | NCIT:C159682 | MONDO:equivalentTo | Bladder Neurofibroma | | MONDO:0000384|MONDO:0016755 | +| MONDO:0854841 | ebv-related lymphoproliferative disorder | NCIT:C159717 | MONDO:equivalentTo | EBV-Related Lymphoproliferative Disorder | | | +| MONDO:0854843 | platinum-sensitive ovarian carcinoma | NCIT:C159902 | MONDO:equivalentTo | Platinum-Sensitive Ovarian Carcinoma | | MONDO:0005140 | +| MONDO:0854845 | carcinoma arising in bladder diverticulum | NCIT:C160158 | MONDO:equivalentTo | Carcinoma Arising in Bladder Diverticulum | | MONDO:0004986 | +| MONDO:0854847 | metastatic nut carcinoma | NCIT:C160297 | MONDO:equivalentTo | Metastatic NUT Carcinoma | | MONDO:0005563|MONDO:0024879 | +| MONDO:0854850 | hematologic malignancy-associated skin squamous cell carcinoma | NCIT:C160666 | MONDO:equivalentTo | Hematologic Malignancy-Associated Skin Squamous Cell Carcinoma | | MONDO:0002529 | +| MONDO:0854854 | prostate acinar microcystic adenocarcinoma | NCIT:C160817 | MONDO:equivalentTo | Prostate Acinar Microcystic Adenocarcinoma | | MONDO:0002493 | +| MONDO:0854855 | prostate acinar pleomorphic giant cell adenocarcinoma | NCIT:C160818 | MONDO:equivalentTo | Prostate Acinar Pleomorphic Giant Cell Adenocarcinoma | | MONDO:0002493 | +| MONDO:0854859 | platinum-sensitive primary peritoneal carcinoma | NCIT:C160872 | MONDO:equivalentTo | Platinum-Sensitive Primary Peritoneal Carcinoma | | MONDO:0015686 | +| MONDO:0854860 | platinum-sensitive fallopian tube carcinoma | NCIT:C160873 | MONDO:equivalentTo | Platinum-Sensitive Fallopian Tube Carcinoma | | MONDO:0006206 | +| MONDO:0854866 | cribriform adenocarcinoma of minor salivary gland | NCIT:C160974 | MONDO:equivalentTo | Cribriform Adenocarcinoma of Minor Salivary Gland | | MONDO:0006304|MONDO:0006176 | +| MONDO:0854867 | sinonasal adenocarcinoma | NCIT:C160976 | MONDO:equivalentTo | Sinonasal Adenocarcinoma | | MONDO:0056819|MONDO:0004970 | +| MONDO:0854868 | head and neck sebaceous carcinoma | NCIT:C160978 | MONDO:equivalentTo | Head and Neck Sebaceous Carcinoma | | MONDO:0006962|MONDO:0002038 | +| MONDO:0854872 | prostate intraductal carcinoma | NCIT:C161022 | MONDO:equivalentTo | Prostate Intraductal Carcinoma | | MONDO:0005159 | +| MONDO:0854873 | prostate synovial sarcoma | NCIT:C161034 | MONDO:equivalentTo | Prostate Synovial Sarcoma | | MONDO:0002854|MONDO:0010434 | +| MONDO:0854874 | prostate osteosarcoma | NCIT:C161035 | MONDO:equivalentTo | Prostate Osteosarcoma | | MONDO:0002621|MONDO:0002854 | +| MONDO:0854875 | prostate undifferentiated pleomorphic sarcoma | NCIT:C161038 | MONDO:equivalentTo | Prostate Undifferentiated Pleomorphic Sarcoma | | MONDO:0002854|MONDO:0002142 | +| MONDO:0854877 | prostate soft tissue neoplasm | NCIT:C161045 | MONDO:equivalentTo | Prostate Soft Tissue Neoplasm | | MONDO:0006424|MONDO:0021259 | +| MONDO:0854881 | prostate hemangioma | NCIT:C161581 | MONDO:equivalentTo | Prostate Hemangioma | | MONDO:0021510|MONDO:0006500 | +| MONDO:0854886 | prostate carcinoma metastatic in the lymph nodes | NCIT:C161587 | MONDO:equivalentTo | Prostate Carcinoma Metastatic in the Lymph Nodes | | MONDO:0004956|MONDO:0005438 | +| MONDO:0854888 | prostate cystadenoma | NCIT:C161606 | MONDO:equivalentTo | Prostate Cystadenoma | | MONDO:0021510|MONDO:0002369 | +| MONDO:0854889 | prostate wilms tumor | NCIT:C161607 | MONDO:equivalentTo | Prostate Wilms Tumor | | MONDO:0008315|MONDO:0006058 | +| MONDO:0854891 | prostate melanoma | NCIT:C161611 | MONDO:equivalentTo | Prostate Melanoma | | MONDO:0006320|MONDO:0008315 | +| MONDO:0854893 | seminal vesicle mixed epithelial and stromal tumor | NCIT:C161636 | MONDO:equivalentTo | Seminal Vesicle Mixed Epithelial and Stromal Tumor | | MONDO:0021043|MONDO:0002790 | +| MONDO:0854895 | benign seminal vesicle neoplasm | NCIT:C161643 | MONDO:equivalentTo | Benign Seminal Vesicle Neoplasm | | MONDO:0000625|MONDO:0002790 | +| MONDO:0854896 | malignant seminal vesicle neoplasm | NCIT:C161644 | MONDO:equivalentTo | Malignant Seminal Vesicle Neoplasm | | MONDO:0005836|MONDO:0002790 | +| MONDO:0854902 | regressed testicular germ cell tumor | NCIT:C162139 | MONDO:equivalentTo | Regressed Testicular Germ Cell Tumor | | MONDO:0010108 | +| MONDO:0854909 | cervical cancer by figo stage 2018 | NCIT:C162225 | MONDO:equivalentTo | Cervical Cancer by FIGO Stage 2018 | | MONDO:0005131 | +| MONDO:0854911 | metastatic malignant digestive system neoplasm | NCIT:C162255 | MONDO:equivalentTo | Metastatic Malignant Digestive System Neoplasm | | MONDO:0002516|MONDO:0024880 | +| MONDO:0854912 | hypermutated colorectal carcinoma | NCIT:C162256 | MONDO:equivalentTo | Hypermutated Colorectal Carcinoma | | MONDO:0024331 | +| MONDO:0854925 | thymic neuroendocrine neoplasm | NCIT:C162460 | MONDO:equivalentTo | Thymic Neuroendocrine Neoplasm | | MONDO:0018079|MONDO:0019496 | +| MONDO:0854927 | intratubular large cell hyalinizing sertoli cell neoplasia | NCIT:C162466 | MONDO:equivalentTo | Intratubular Large Cell Hyalinizing Sertoli Cell Neoplasia | | MONDO:0003125 | +| MONDO:0854928 | testicular diffuse large b-cell lymphoma | NCIT:C162467 | MONDO:equivalentTo | Testicular Diffuse Large B-Cell Lymphoma | | MONDO:0018905|MONDO:0001472 | +| MONDO:0854929 | testicular nasal type extranodal nk/t-cell lymphoma | NCIT:C162468 | MONDO:equivalentTo | Testicular Nasal Type Extranodal NK/T-Cell Lymphoma | | MONDO:0001472|MONDO:0019472 | +| MONDO:0854930 | testicular myeloid sarcoma | NCIT:C162469 | MONDO:equivalentTo | Testicular Myeloid Sarcoma | | MONDO:0005447|MONDO:0006861 | +| MONDO:0854931 | testicular plasmacytoma | NCIT:C162470 | MONDO:equivalentTo | Testicular Plasmacytoma | | MONDO:0005447|MONDO:0002754 | +| MONDO:0854936 | paratesticular neoplasm | NCIT:C162485 | MONDO:equivalentTo | Paratesticular Neoplasm | | MONDO:0024582 | +| MONDO:0854952 | penile melanoma | NCIT:C162547 | MONDO:equivalentTo | Penile Melanoma | | MONDO:0001325|MONDO:0005105 | +| MONDO:0854953 | penile lymphoma | NCIT:C162548 | MONDO:equivalentTo | Penile Lymphoma | | MONDO:0001325|MONDO:0017207 | +| MONDO:0854955 | primary peritoneal undifferentiated carcinoma | NCIT:C162562 | MONDO:equivalentTo | Primary Peritoneal Undifferentiated Carcinoma | | MONDO:0015686|MONDO:0005617 | +| MONDO:0854956 | primary peritoneal transitional cell carcinoma | NCIT:C162564 | MONDO:equivalentTo | Primary Peritoneal Transitional Cell Carcinoma | | MONDO:0015686|MONDO:0006474 | +| MONDO:0854959 | penile soft tissue neoplasm | NCIT:C162574 | MONDO:equivalentTo | Penile Soft Tissue Neoplasm | | MONDO:0006424|MONDO:0006895 | +| MONDO:0854966 | penile malignant peripheral nerve sheath tumor | NCIT:C162584 | MONDO:equivalentTo | Penile Malignant Peripheral Nerve Sheath Tumor | | MONDO:0001387|MONDO:0017827 | +| MONDO:0854967 | penile leiomyosarcoma | NCIT:C162585 | MONDO:equivalentTo | Penile Leiomyosarcoma | | MONDO:0001387|MONDO:0005058 | +| MONDO:0854968 | penile schwannoma | NCIT:C162586 | MONDO:equivalentTo | Penile Schwannoma | | MONDO:0004820|MONDO:0021458 | +| MONDO:0854969 | penile neurofibroma | NCIT:C162587 | MONDO:equivalentTo | Penile Neurofibroma | | MONDO:0021458|MONDO:0016755 | +| MONDO:0854970 | penile rhabdomyosarcoma | NCIT:C162588 | MONDO:equivalentTo | Penile Rhabdomyosarcoma | | MONDO:0001387|MONDO:0005212 | +| MONDO:0854971 | penile undifferentiated pleomorphic sarcoma | NCIT:C162589 | MONDO:equivalentTo | Penile Undifferentiated Pleomorphic Sarcoma | | MONDO:0001387|MONDO:0002142 | +| MONDO:0854974 | metastatic malignant neoplasm in the head and neck | NCIT:C162594 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Head and Neck | | MONDO:0005627|MONDO:0024880 | +| MONDO:0854984 | refractory childhood malignant neoplasm | NCIT:C162703 | MONDO:equivalentTo | Refractory Childhood Malignant Neoplasm | | MONDO:0006517|MONDO:0036501 | +| MONDO:0854998 | asph-positive head and neck squamous cell carcinoma | NCIT:C162770 | MONDO:equivalentTo | ASPH-Positive Head and Neck Squamous Cell Carcinoma | | MONDO:0010150 | +| MONDO:0855003 | parapharyngeal neoplasm | NCIT:C162820 | MONDO:equivalentTo | Parapharyngeal Neoplasm | | MONDO:0021351 | +| MONDO:0855006 | retropharyngeal neoplasm | NCIT:C162825 | MONDO:equivalentTo | Retropharyngeal Neoplasm | | MONDO:0021351 | +| MONDO:0855015 | non-invasive cribriform carcinoma | NCIT:C162973 | MONDO:equivalentTo | Non-Invasive Cribriform Carcinoma | | MONDO:0006176 | +| MONDO:0855016 | malignant brain glioma | NCIT:C162993 | MONDO:equivalentTo | Malignant Brain Glioma | | MONDO:0100342|MONDO:0001657|MONDO:0021632 | +| MONDO:0855028 | micropapillary carcinoma | NCIT:C164144 | MONDO:equivalentTo | Micropapillary Carcinoma | | MONDO:0006509 | +| MONDO:0855034 | aggressive prostate adenocarcinoma | NCIT:C164185 | MONDO:equivalentTo | Aggressive Prostate Adenocarcinoma | | MONDO:0005082 | +| MONDO:0855035 | head and neck sarcoma | NCIT:C164198 | MONDO:equivalentTo | Head and Neck Sarcoma | | MONDO:0005089|MONDO:0005627 | +| MONDO:0855040 | warty carcinoma | NCIT:C164248 | MONDO:equivalentTo | Warty Carcinoma | | MONDO:0002979 | +| MONDO:0855041 | differentiated intraepithelial neoplasia | NCIT:C164249 | MONDO:equivalentTo | Differentiated Intraepithelial Neoplasia | | MONDO:0024474 | +| MONDO:0855042 | human papillomavirus-independent squamous cell carcinoma | NCIT:C164250 | MONDO:equivalentTo | Human Papillomavirus-Independent Squamous Cell Carcinoma | | MONDO:0005096 | +| MONDO:0855043 | invasive sarcomatoid urothelial carcinoma | NCIT:C164252 | MONDO:equivalentTo | Invasive Sarcomatoid Urothelial Carcinoma | | MONDO:0002837|MONDO:0040678 | +| MONDO:0855044 | mixed neuroendocrine non-neuroendocrine neoplasm | NCIT:C164255 | MONDO:equivalentTo | Mixed Neuroendocrine Non-Neuroendocrine Neoplasm | | MONDO:0021043|MONDO:0005626 | +| MONDO:0855047 | nf1-associated malignant peripheral nerve sheath tumor | NCIT:C164313 | MONDO:equivalentTo | NF1-Associated Malignant Peripheral Nerve Sheath Tumor | | MONDO:0017827 | +| MONDO:0855048 | sporadic malignant peripheral nerve sheath tumor | NCIT:C164314 | MONDO:equivalentTo | Sporadic Malignant Peripheral Nerve Sheath Tumor | | MONDO:0017827 | +| MONDO:0855049 | radiation-induced malignant peripheral nerve sheath tumor | NCIT:C164316 | MONDO:equivalentTo | Radiation-Induced Malignant Peripheral Nerve Sheath Tumor | | MONDO:0017827 | +| MONDO:0855058 | soft tissue sarcoma of the trunk and extremities | NCIT:C165190 | MONDO:equivalentTo | Soft Tissue Sarcoma of the Trunk and Extremities | | MONDO:0018078 | +| MONDO:0855059 | metastatic malignant mesothelioma | NCIT:C165252 | MONDO:equivalentTo | Metastatic Malignant Mesothelioma | | MONDO:0006292|MONDO:0024880 | +| MONDO:0855079 | skin verrucous carcinoma | NCIT:C165465 | MONDO:equivalentTo | Skin Verrucous Carcinoma | | MONDO:0002529|MONDO:0006006 | +| MONDO:0855080 | skin squamous cell carcinoma with osteoclast-like giant cells | NCIT:C165466 | MONDO:equivalentTo | Skin Squamous Cell Carcinoma with Osteoclast-Like Giant Cells | | MONDO:0002529 | +| MONDO:0855081 | skin lymphoepithelial carcinoma | NCIT:C165467 | MONDO:equivalentTo | Skin Lymphoepithelial Carcinoma | | MONDO:0002529|MONDO:0003572 | +| MONDO:0855082 | skin squamous cell carcinoma with sarcomatoid differentiation | NCIT:C165468 | MONDO:equivalentTo | Skin Squamous Cell Carcinoma with Sarcomatoid Differentiation | | MONDO:0002529|MONDO:0002928 | +| MONDO:0855085 | lichen planus-like keratosis | NCIT:C165485 | MONDO:equivalentTo | Lichen Planus-Like Keratosis | | MONDO:0002093 | +| MONDO:0855094 | combined nevus | NCIT:C165529 | MONDO:equivalentTo | Combined Nevus | | MONDO:0044794 | +| MONDO:0855104 | proximal gastric adenocarcinoma | NCIT:C165628 | MONDO:equivalentTo | Proximal Gastric Adenocarcinoma | | MONDO:0005036 | +| MONDO:0855113 | mixed carcinoma | NCIT:C165723 | MONDO:equivalentTo | Mixed Carcinoma | | MONDO:0005853|MONDO:0004993 | +| MONDO:0855116 | hormone receptor-negative breast carcinoma | NCIT:C165743 | MONDO:equivalentTo | Hormone Receptor-Negative Breast Carcinoma | | MONDO:0004988 | +| MONDO:0855127 | musculoskeletal neoplasm | NCIT:C166354 | MONDO:equivalentTo | Musculoskeletal Neoplasm | | MONDO:0044334|MONDO:0002081 | +| MONDO:0855132 | pancreatobiliary carcinoma | NCIT:C166418 | MONDO:equivalentTo | Pancreatobiliary Carcinoma | | MONDO:0006181 | +| MONDO:0855139 | acute myeloid leukemia with ram immunophenotype | NCIT:C167089 | MONDO:equivalentTo | Acute Myeloid Leukemia with RAM Immunophenotype | | MONDO:0004996 | +| MONDO:0855140 | obesity-related malignant neoplasm | NCIT:C167168 | MONDO:equivalentTo | Obesity-Related Malignant Neoplasm | | MONDO:0004992 | +| MONDO:0855143 | metastatic primary peritoneal carcinoma | NCIT:C167203 | MONDO:equivalentTo | Metastatic Primary Peritoneal Carcinoma | | MONDO:0015686|MONDO:0024879 | +| MONDO:0855150 | midgut neuroendocrine tumor | NCIT:C167327 | MONDO:equivalentTo | Midgut Neuroendocrine Tumor | | MONDO:0000386 | +| MONDO:0855151 | adnexal adenocarcinoma, not otherwise specified | NCIT:C167341 | MONDO:equivalentTo | Adnexal Adenocarcinoma, Not Otherwise Specified | | MONDO:0006973|MONDO:0004970 | +| MONDO:0855152 | spiradenocylindroma | NCIT:C167342 | MONDO:equivalentTo | Spiradenocylindroma | | MONDO:0021489 | +| MONDO:0855153 | spiradenocylindrocarcinoma | NCIT:C167344 | MONDO:equivalentTo | Spiradenocylindrocarcinoma | | MONDO:0005524|MONDO:0024878 | +| MONDO:0855154 | malignant mixed tumor of the skin | NCIT:C167346 | MONDO:equivalentTo | Malignant Mixed Tumor of the Skin | | MONDO:0002206|MONDO:0005853 | +| MONDO:0855157 | syringocystadenocarcinoma papilliferum | NCIT:C167365 | MONDO:equivalentTo | Syringocystadenocarcinoma Papilliferum | | MONDO:0005524 | +| MONDO:0855158 | adnexal cribriform carcinoma | NCIT:C167366 | MONDO:equivalentTo | Adnexal Cribriform Carcinoma | | MONDO:0006973|MONDO:0006176 | +| MONDO:0855159 | adnexal secretory carcinoma | NCIT:C167368 | MONDO:equivalentTo | Adnexal Secretory Carcinoma | | MONDO:0006973|MONDO:0004970 | +| MONDO:0855160 | signet ring cell/histiocytoid carcinoma | NCIT:C167369 | MONDO:equivalentTo | Signet Ring Cell/Histiocytoid Carcinoma | | MONDO:0006973|MONDO:0004970 | +| MONDO:0855173 | resectable glioma | NCIT:C168573 | MONDO:equivalentTo | Resectable Glioma | | MONDO:0021042 | +| MONDO:0855181 | phyllodes tumor of anogenital mammary-type glands | NCIT:C168602 | MONDO:equivalentTo | Phyllodes Tumor of Anogenital Mammary-Type Glands | | MONDO:0005078 | +| MONDO:0855182 | metastatic malignant neoplasm in the digestive system | NCIT:C168669 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Digestive System | | MONDO:0002516|MONDO:0024880 | +| MONDO:0855187 | unresectable round cell liposarcoma | NCIT:C168724 | MONDO:equivalentTo | Unresectable Round Cell Liposarcoma | | MONDO:0005238 | +| MONDO:0855221 | skin soft tissue neoplasm | NCIT:C169100 | MONDO:equivalentTo | Skin Soft Tissue Neoplasm | | MONDO:0006424|MONDO:0002531 | +| MONDO:0855230 | metastatic malignant head and neck neoplasm | NCIT:C170467 | MONDO:equivalentTo | Metastatic Malignant Head and Neck Neoplasm | | MONDO:0005627|MONDO:0024880 | +| MONDO:0855232 | skin pleomorphic liposarcoma | NCIT:C170473 | MONDO:equivalentTo | Skin Pleomorphic Liposarcoma | | MONDO:0003600|MONDO:0020562 | +| MONDO:0855235 | skin angiolipoma | NCIT:C170478 | MONDO:equivalentTo | Skin Angiolipoma | | MONDO:0000964|MONDO:0006085 | +| MONDO:0855238 | benign periampullary neoplasm | NCIT:C170725 | MONDO:equivalentTo | Benign Periampullary Neoplasm | | MONDO:0006734 | +| MONDO:0855241 | metastatic malignant breast neoplasm | NCIT:C170728 | MONDO:equivalentTo | Metastatic Malignant Breast Neoplasm | | MONDO:0007254|MONDO:0024880 | +| MONDO:0855243 | primary peritoneal adenocarcinoma | NCIT:C170733 | MONDO:equivalentTo | Primary Peritoneal Adenocarcinoma | | MONDO:0015686|MONDO:0004970 | +| MONDO:0855244 | appendix mucinous neoplasm | NCIT:C170734 | MONDO:equivalentTo | Appendix Mucinous Neoplasm | | MONDO:0024338|MONDO:0001236 | +| MONDO:0855245 | pleomorphic fibroma | NCIT:C170736 | MONDO:equivalentTo | Pleomorphic Fibroma | | MONDO:0005167 | +| MONDO:0855249 | non-muscle invasive bladder urothelial carcinoma | NCIT:C170772 | MONDO:equivalentTo | Non-Muscle Invasive Bladder Urothelial Carcinoma | | MONDO:0003890|MONDO:0004200 | +| MONDO:0855250 | alveolar ridge squamous cell carcinoma | NCIT:C170774 | MONDO:equivalentTo | Alveolar Ridge Squamous Cell Carcinoma | | MONDO:0004958 | +| MONDO:0855252 | metastatic malignant skin neoplasm | NCIT:C170811 | MONDO:equivalentTo | Metastatic Malignant Skin Neoplasm | | MONDO:0024880|MONDO:0002898 | +| MONDO:0855256 | metastatic rhabdoid tumor | NCIT:C170828 | MONDO:equivalentTo | Metastatic Rhabdoid Tumor | | MONDO:0002728|MONDO:0024880 | +| MONDO:0855262 | malignant jejunal neoplasm | NCIT:C170919 | MONDO:equivalentTo | Malignant Jejunal Neoplasm | | MONDO:0002564|MONDO:0000956 | +| MONDO:0855263 | metastatic carcinosarcoma | NCIT:C170924 | MONDO:equivalentTo | Metastatic Carcinosarcoma | | MONDO:0024880|MONDO:0002928 | +| MONDO:0855266 | malignant fundus neoplasm | NCIT:C170940 | MONDO:equivalentTo | Malignant Fundus Neoplasm | | MONDO:0001056 | +| MONDO:0855281 | human papillomavirus-related mucosal head and neck squamous cell carcinoma | NCIT:C171023 | MONDO:equivalentTo | Human Papillomavirus-Related Mucosal Head and Neck Squamous Cell Carcinoma | | MONDO:0010150|MONDO:0020657 | +| MONDO:0855283 | ovarian neuroendocrine carcinoma | NCIT:C171032 | MONDO:equivalentTo | Ovarian Neuroendocrine Carcinoma | | MONDO:0002481|MONDO:0005140 | +| MONDO:0855284 | endometrial neuroendocrine carcinoma | NCIT:C171033 | MONDO:equivalentTo | Endometrial Neuroendocrine Carcinoma | | MONDO:0002447|MONDO:0021650 | +| MONDO:0855285 | mediastinal non-hodgkin lymphoma | NCIT:C171037 | MONDO:equivalentTo | Mediastinal Non-Hodgkin Lymphoma | | MONDO:0004021|MONDO:0018908 | +| MONDO:0855297 | oligometastatic prostate carcinoma | NCIT:C171265 | MONDO:equivalentTo | Oligometastatic Prostate Carcinoma | | MONDO:0004956 | +| MONDO:0855330 | acute myeloid leukemia arising from previous myeloproliferative neoplasm | NCIT:C172129 | MONDO:equivalentTo | Acute Myeloid Leukemia Arising from Previous Myeloproliferative Neoplasm | | MONDO:0019457 | +| MONDO:0855331 | acute myeloid leukemia arising from previous myelodysplastic/myeloproliferative neoplasm | NCIT:C172130 | MONDO:equivalentTo | Acute Myeloid Leukemia Arising from Previous Myelodysplastic/Myeloproliferative Neoplasm | | MONDO:0019457 | +| MONDO:0855335 | progesterone receptor-positive malignant neoplasm | NCIT:C172183 | MONDO:equivalentTo | Progesterone Receptor-Positive Malignant Neoplasm | | MONDO:0004992 | +| MONDO:0855336 | sinusoidal hemangioma | NCIT:C172206 | MONDO:equivalentTo | Sinusoidal Hemangioma | | MONDO:0006557 | +| MONDO:0855346 | refractory myeloid neoplasm | NCIT:C172281 | MONDO:equivalentTo | Refractory Myeloid Neoplasm | | MONDO:0005170|MONDO:0004111 | +| MONDO:0855368 | skin ewing sarcoma | NCIT:C172634 | MONDO:equivalentTo | Skin Ewing Sarcoma | | MONDO:0018270|MONDO:0006414 | +| MONDO:0855377 | oxyntic gland adenoma | NCIT:C172655 | MONDO:equivalentTo | Oxyntic Gland Adenoma | | MONDO:0006221 | +| MONDO:0855378 | gastroblastoma | NCIT:C172659 | MONDO:equivalentTo | Gastroblastoma | | MONDO:0001056 | +| MONDO:0855386 | colorectal conventional adenoma | NCIT:C172680 | MONDO:equivalentTo | Colorectal Conventional Adenoma | | MONDO:0005484 | +| MONDO:0855389 | colorectal poorly cohesive adenocarcinoma | NCIT:C172694 | MONDO:equivalentTo | Colorectal Poorly Cohesive Adenocarcinoma | | MONDO:0005008 | +| MONDO:0855390 | colorectal adenoma-like adenocarcinoma | NCIT:C172699 | MONDO:equivalentTo | Colorectal Adenoma-Like Adenocarcinoma | | MONDO:0005008|MONDO:0003204 | +| MONDO:0855391 | inflammatory bowel disease-associated colorectal adenocarcinoma | NCIT:C172700 | MONDO:equivalentTo | Inflammatory Bowel Disease-Associated Colorectal Adenocarcinoma | | MONDO:0005008 | +| MONDO:0855393 | steatohepatitic hepatocellular carcinoma | NCIT:C172709 | MONDO:equivalentTo | Steatohepatitic Hepatocellular Carcinoma | | MONDO:0007256 | +| MONDO:0855394 | macrotrabecular massive hepatocellular carcinoma | NCIT:C172710 | MONDO:equivalentTo | Macrotrabecular Massive Hepatocellular Carcinoma | | MONDO:0007256 | +| MONDO:0855395 | chromophobe hepatocellular carcinoma | NCIT:C172712 | MONDO:equivalentTo | Chromophobe Hepatocellular Carcinoma | | MONDO:0007256 | +| MONDO:0855396 | neutrophil-rich hepatocellular carcinoma | NCIT:C172713 | MONDO:equivalentTo | Neutrophil-Rich Hepatocellular Carcinoma | | MONDO:0007256 | +| MONDO:0855397 | small hepatocellular carcinoma | NCIT:C172714 | MONDO:equivalentTo | Small Hepatocellular Carcinoma | | MONDO:0007256 | +| MONDO:0855398 | liver mixed adenoneuroendocrine carcinoma | NCIT:C172718 | MONDO:equivalentTo | Liver Mixed Adenoneuroendocrine Carcinoma | | MONDO:0006182|MONDO:0018531 | +| MONDO:0855401 | gallbladder pyloric gland adenoma | NCIT:C172731 | MONDO:equivalentTo | Gallbladder Pyloric Gland Adenoma | | MONDO:0006216 | +| MONDO:0855408 | pancreatic poorly cohesive adenocarcinoma | NCIT:C172811 | MONDO:equivalentTo | Pancreatic Poorly Cohesive Adenocarcinoma | | MONDO:0005184 | +| MONDO:0855409 | pancreatic undifferentiated carcinoma with rhabdoid cells | NCIT:C172812 | MONDO:equivalentTo | Pancreatic Undifferentiated Carcinoma with Rhabdoid Cells | | MONDO:0006478 | +| MONDO:0855413 | conventional follicular dendritic cell sarcoma | NCIT:C172846 | MONDO:equivalentTo | Conventional Follicular Dendritic Cell Sarcoma | | MONDO:0005764 | +| MONDO:0855418 | digestive system soft tissue neoplasm | NCIT:C172852 | MONDO:equivalentTo | Digestive System Soft Tissue Neoplasm | | MONDO:0006424|MONDO:0021223 | +| MONDO:0855432 | sinonasal spindle cell squamous carcinoma | NCIT:C173079 | MONDO:equivalentTo | Sinonasal Spindle Cell Squamous Carcinoma | | MONDO:0044787|MONDO:0021663 | +| MONDO:0855433 | sinonasal lymphoepithelial carcinoma | NCIT:C173080 | MONDO:equivalentTo | Sinonasal Lymphoepithelial Carcinoma | | MONDO:0002831|MONDO:0003572 | +| MONDO:0855435 | head and neck nut carcinoma | NCIT:C173087 | MONDO:equivalentTo | Head and Neck NUT Carcinoma | | MONDO:0005563|MONDO:0002038 | +| MONDO:0855439 | malignant sinonasal neoplasm | NCIT:C173097 | MONDO:equivalentTo | Malignant Sinonasal Neoplasm | | MONDO:0056820|MONDO:0005627 | +| MONDO:0855471 | peritoneal implant | NCIT:C173164 | MONDO:equivalentTo | Peritoneal Implant | | MONDO:0006901 | +| MONDO:0855472 | sinonasal ameloblastoma | NCIT:C173166 | MONDO:equivalentTo | Sinonasal Ameloblastoma | | MONDO:0056820 | +| MONDO:0855481 | microsatellite stable colorectal carcinoma | NCIT:C173324 | MONDO:equivalentTo | Microsatellite Stable Colorectal Carcinoma | | MONDO:0024331 | +| MONDO:0855487 | nasopharyngeal adenoid cystic carcinoma | NCIT:C173340 | MONDO:equivalentTo | Nasopharyngeal Adenoid Cystic Carcinoma | | MONDO:0006367|MONDO:0015459 | +| MONDO:0855489 | ectopic pituitary neuroendocrine tumor | NCIT:C173345 | MONDO:equivalentTo | Ectopic Pituitary Neuroendocrine Tumor | | MONDO:0006373 | +| MONDO:0855495 | cutaneous merkel cell carcinoma | NCIT:C173385 | MONDO:equivalentTo | Cutaneous Merkel Cell Carcinoma | | MONDO:0019210|MONDO:0002656 | +| MONDO:0855506 | laryngeal chondroma | NCIT:C173406 | MONDO:equivalentTo | Laryngeal Chondroma | | MONDO:0002360|MONDO:0002354 | +| MONDO:0855507 | laryngeal chondrosarcoma | NCIT:C173407 | MONDO:equivalentTo | Laryngeal Chondrosarcoma | | MONDO:0002448|MONDO:0008977 | +| MONDO:0855526 | head and neck melanocytic neoplasm | NCIT:C173488 | MONDO:equivalentTo | Head and Neck Melanocytic Neoplasm | | MONDO:0021143|MONDO:0005586 | +| MONDO:0855532 | refractory primitive neuroectodermal tumor | NCIT:C173565 | MONDO:equivalentTo | Refractory Primitive Neuroectodermal Tumor | | MONDO:0005462|MONDO:0036501 | +| MONDO:0855540 | head and neck heterotopia-associated carcinoma | NCIT:C173588 | MONDO:equivalentTo | Head and Neck Heterotopia-Associated Carcinoma | | MONDO:0002038 | +| MONDO:0855551 | salivary gland poorly differentiated carcinoma | NCIT:C173649 | MONDO:equivalentTo | Salivary Gland Poorly Differentiated Carcinoma | | MONDO:0000521 | +| MONDO:0855553 | salivary gland lymphadenoma | NCIT:C173659 | MONDO:equivalentTo | Salivary Gland Lymphadenoma | | MONDO:0021460 | +| MONDO:0855558 | sialolipoma | NCIT:C173682 | MONDO:equivalentTo | Sialolipoma | | MONDO:0021460 | +| MONDO:0855575 | appendix disorder | NCIT:C173799 | MONDO:equivalentTo | Appendix Disorder | | | +| MONDO:0855576 | retroperitoneal undifferentiated pleomorphic sarcoma | NCIT:C173808 | MONDO:equivalentTo | Retroperitoneal Undifferentiated Pleomorphic Sarcoma | | MONDO:0001501|MONDO:0002142 | +| MONDO:0855577 | lung alveolar soft part sarcoma | NCIT:C173809 | MONDO:equivalentTo | Lung Alveolar Soft Part Sarcoma | | MONDO:0002426|MONDO:0011655 | +| MONDO:0855584 | maxillofacial neoplasm | NCIT:C173845 | MONDO:equivalentTo | Maxillofacial Neoplasm | | MONDO:0019060|MONDO:0024653 | +| MONDO:0855590 | craniofacial fibrous dysplasia | NCIT:C173926 | MONDO:equivalentTo | Craniofacial Fibrous Dysplasia | | MONDO:0000845 | +| MONDO:0855591 | benign head and neck neoplasm | NCIT:C173932 | MONDO:equivalentTo | Benign Head and Neck Neoplasm | | MONDO:0005165|MONDO:0005586 | +| MONDO:0855593 | aggressive papillary tumor | NCIT:C174022 | MONDO:equivalentTo | Aggressive Papillary Tumor | | MONDO:0021096|MONDO:0021366 | +| MONDO:0855594 | benign inner ear neoplasm | NCIT:C174023 | MONDO:equivalentTo | Benign Inner Ear Neoplasm | | MONDO:0021474|MONDO:0024320 | +| MONDO:0855597 | malignant inner ear neoplasm | NCIT:C174026 | MONDO:equivalentTo | Malignant Inner Ear Neoplasm | | MONDO:0003277|MONDO:0024320 | +| MONDO:0855616 | conjunctival oncocytoma | NCIT:C174388 | MONDO:equivalentTo | Conjunctival Oncocytoma | | MONDO:0010795|MONDO:0006105 | +| MONDO:0855617 | conjunctival keratoacanthoma | NCIT:C174390 | MONDO:equivalentTo | Conjunctival Keratoacanthoma | | MONDO:0006173|MONDO:0002527 | +| MONDO:0855618 | conjunctival spindle cell carcinoma | NCIT:C174398 | MONDO:equivalentTo | Conjunctival Spindle Cell Carcinoma | | MONDO:0006173|MONDO:0021663 | +| MONDO:0855620 | conjunctival carcinoma | NCIT:C174403 | MONDO:equivalentTo | Conjunctival Carcinoma | | MONDO:0002466|MONDO:0003454 | +| MONDO:0855625 | conjunctival subepithelial (stromal) nevus | NCIT:C174426 | MONDO:equivalentTo | Conjunctival Subepithelial (Stromal) Nevus | | MONDO:0006172 | +| MONDO:0855630 | conjunctival blue nevus | NCIT:C174452 | MONDO:equivalentTo | Conjunctival Blue Nevus | | MONDO:0006172 | +| MONDO:0855631 | atypical ewing sarcoma | NCIT:C174456 | MONDO:equivalentTo | Atypical Ewing Sarcoma | | MONDO:0012817 | +| MONDO:0855633 | conjunctival spitz nevus | NCIT:C174493 | MONDO:equivalentTo | Conjunctival Spitz Nevus | | MONDO:0006172 | +| MONDO:0855634 | metastatic malignant neoplasm in the conjunctiva | NCIT:C174496 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Conjunctiva | | MONDO:0044913|MONDO:0003454 | +| MONDO:0855635 | iris epithelioid cell melanoma | NCIT:C174498 | MONDO:equivalentTo | Iris Epithelioid Cell Melanoma | | MONDO:0004064|MONDO:0006200 | +| MONDO:0855640 | iris mixed epithelioid and spindle cell melanoma | NCIT:C174506 | MONDO:equivalentTo | Iris Mixed Epithelioid and Spindle Cell Melanoma | | MONDO:0004064|MONDO:0003910 | +| MONDO:0855641 | metastatic malignant neoplasm in the uvea | NCIT:C174507 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Uvea | | MONDO:0002659|MONDO:0044913 | +| MONDO:0855646 | retinal astrocytoma | NCIT:C174539 | MONDO:equivalentTo | Retinal Astrocytoma | | MONDO:0024649|MONDO:0021231 | +| MONDO:0855649 | adenoma of the retinal pigment epithelium | NCIT:C174550 | MONDO:equivalentTo | Adenoma of the Retinal Pigment Epithelium | | MONDO:0021453|MONDO:0004972 | +| MONDO:0855650 | retinal pigment epithelium adenocarcinoma | NCIT:C174551 | MONDO:equivalentTo | Retinal Pigment Epithelium Adenocarcinoma | | MONDO:0002466|MONDO:0003072|MONDO:0004970 | +| MONDO:0855653 | ciliary body adenoma | NCIT:C174560 | MONDO:equivalentTo | Ciliary Body Adenoma | | MONDO:0021486|MONDO:0004972 | +| MONDO:0855654 | ciliary body adenocarcinoma | NCIT:C174561 | MONDO:equivalentTo | Ciliary Body Adenocarcinoma | | MONDO:0002466|MONDO:0002969|MONDO:0004970 | +| MONDO:0855667 | incidental gallbladder carcinoma | NCIT:C175214 | MONDO:equivalentTo | Incidental Gallbladder Carcinoma | | MONDO:0003220 | +| MONDO:0855668 | metastatic malignant neoplasm in the regional lymph nodes | NCIT:C175222 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Regional Lymph Nodes | | MONDO:0005438 | +| MONDO:0855669 | lacrimal gland oncocytoma | NCIT:C175264 | MONDO:equivalentTo | Lacrimal Gland Oncocytoma | | MONDO:0010795|MONDO:0021488 | +| MONDO:0855671 | lacrimal gland myoepithelial carcinoma | NCIT:C175274 | MONDO:equivalentTo | Lacrimal Gland Myoepithelial Carcinoma | | MONDO:0003158|MONDO:0002463 | +| MONDO:0855672 | lacrimal gland carcinosarcoma | NCIT:C175279 | MONDO:equivalentTo | Lacrimal Gland Carcinosarcoma | | MONDO:0002464|MONDO:0002928 | +| MONDO:0855673 | lacrimal gland epithelial-myoepithelial carcinoma | NCIT:C175288 | MONDO:equivalentTo | Lacrimal Gland Epithelial-Myoepithelial Carcinoma | | MONDO:0002463|MONDO:0003389 | +| MONDO:0855674 | lacrimal gland acinic cell carcinoma | NCIT:C175290 | MONDO:equivalentTo | Lacrimal Gland Acinic Cell Carcinoma | | MONDO:0002475|MONDO:0004965 | +| MONDO:0855675 | lacrimal gland warthin tumor | NCIT:C175291 | MONDO:equivalentTo | Lacrimal Gland Warthin Tumor | | MONDO:0021488|MONDO:0006493 | +| MONDO:0855677 | benign lacrimal system neoplasm | NCIT:C175307 | MONDO:equivalentTo | Benign Lacrimal System Neoplasm | | MONDO:0002460|MONDO:0021454 | +| MONDO:0855678 | malignant lacrimal system neoplasm | NCIT:C175308 | MONDO:equivalentTo | Malignant Lacrimal System Neoplasm | | MONDO:0002460|MONDO:0002236 | +| MONDO:0855679 | lacrimal drainage system neoplasm | NCIT:C175316 | MONDO:equivalentTo | Lacrimal Drainage System Neoplasm | | MONDO:0002460 | +| MONDO:0855684 | lacrimal drainage system non-keratinizing squamous cell carcinoma | NCIT:C175335 | MONDO:equivalentTo | Lacrimal Drainage System Non-Keratinizing Squamous Cell Carcinoma | | MONDO:0003492 | +| MONDO:0855694 | conjunctival non-hodgkin lymphoma | NCIT:C175432 | MONDO:equivalentTo | Conjunctival Non-Hodgkin Lymphoma | | MONDO:0004034|MONDO:0003454 | +| MONDO:0855700 | primary uveal non-hodgkin lymphoma | NCIT:C175451 | MONDO:equivalentTo | Primary Uveal Non-Hodgkin Lymphoma | | MONDO:0004351|MONDO:0002659|MONDO:0017594 | +| MONDO:0855708 | conjunctival myxoma | NCIT:C175495 | MONDO:equivalentTo | Conjunctival Myxoma | | MONDO:0044784|MONDO:0006105 | +| MONDO:0855710 | conjunctival hemangioma | NCIT:C175497 | MONDO:equivalentTo | Conjunctival Hemangioma | | MONDO:0006105|MONDO:0006500 | +| MONDO:0855711 | conjunctival lymphangioma | NCIT:C175498 | MONDO:equivalentTo | Conjunctival Lymphangioma | | MONDO:0002013|MONDO:0006105 | +| MONDO:0855715 | conjunctival sarcoma | NCIT:C175502 | MONDO:equivalentTo | Conjunctival Sarcoma | | MONDO:0018078|MONDO:0003454 | +| MONDO:0855718 | malignant hypothalamic neoplasm | NCIT:C175539 | MONDO:equivalentTo | Malignant Hypothalamic Neoplasm | | MONDO:0002786|MONDO:0006799 | +| MONDO:0855721 | breast polymorphous adenocarcinoma | NCIT:C175604 | MONDO:equivalentTo | Breast Polymorphous Adenocarcinoma | | MONDO:0006256 | +| MONDO:0855722 | breast tall cell carcinoma with reversed polarity | NCIT:C175607 | MONDO:equivalentTo | Breast Tall Cell Carcinoma with Reversed Polarity | | MONDO:0006256 | +| MONDO:0855725 | metastatic malignant glomus tumor | NCIT:C175662 | MONDO:equivalentTo | Metastatic Malignant Glomus Tumor | | MONDO:0003340|MONDO:0024880 | +| MONDO:0855727 | locally invasive desmoid-type fibromatosis | NCIT:C175667 | MONDO:equivalentTo | Locally Invasive Desmoid-Type Fibromatosis | | MONDO:0007608 | +| MONDO:0855734 | metastatic malignant neoplasm in the supraclavicular lymph nodes | NCIT:C175934 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Supraclavicular Lymph Nodes | | MONDO:0005438 | +| MONDO:0855737 | breast classic lobular carcinoma in situ | NCIT:C175949 | MONDO:equivalentTo | Breast Classic Lobular Carcinoma In Situ | | MONDO:0006270 | +| MONDO:0855738 | breast florid lobular carcinoma in situ | NCIT:C175950 | MONDO:equivalentTo | Breast Florid Lobular Carcinoma In Situ | | MONDO:0006270 | +| MONDO:0855740 | breast ductal carcinoma in situ, comedo type | NCIT:C176005 | MONDO:equivalentTo | Breast Ductal Carcinoma In Situ, Comedo Type | | MONDO:0003575|MONDO:0005023 | +| MONDO:0855747 | ocular surface squamous neoplasia | NCIT:C176043 | MONDO:equivalentTo | Ocular Surface Squamous Neoplasia | | MONDO:0020204 | +| MONDO:0855748 | breast cellular fibroadenoma | NCIT:C176045 | MONDO:equivalentTo | Breast Cellular Fibroadenoma | | MONDO:0002056 | +| MONDO:0855749 | primary breast angiosarcoma | NCIT:C176251 | MONDO:equivalentTo | Primary Breast Angiosarcoma | | MONDO:0003024 | +| MONDO:0855751 | breast angiolipoma | NCIT:C176255 | MONDO:equivalentTo | Breast Angiolipoma | | MONDO:0000970|MONDO:0006085 | +| MONDO:0855753 | breast schwannoma | NCIT:C176414 | MONDO:equivalentTo | Breast Schwannoma | | MONDO:0000620|MONDO:0004820 | +| MONDO:0855754 | breast neurofibroma | NCIT:C176415 | MONDO:equivalentTo | Breast Neurofibroma | | MONDO:0000620|MONDO:0016755 | +| MONDO:0855756 | synovial chondrosarcoma | NCIT:C176467 | MONDO:equivalentTo | Synovial Chondrosarcoma | | MONDO:0018078|MONDO:0002403|MONDO:0008977 | +| MONDO:0855757 | male breast carcinoma in situ | NCIT:C176503 | MONDO:equivalentTo | Male Breast Carcinoma In Situ | | MONDO:0005628|MONDO:0004658 | +| MONDO:0855758 | invasive male breast carcinoma | NCIT:C176504 | MONDO:equivalentTo | Invasive Male Breast Carcinoma | | MONDO:0006256|MONDO:0005628 | +| MONDO:0855763 | invasive female breast carcinoma | NCIT:C176579 | MONDO:equivalentTo | Invasive Female Breast Carcinoma | | MONDO:0006256|MONDO:0004379 | +| MONDO:0855764 | female breast carcinoma in situ | NCIT:C176580 | MONDO:equivalentTo | Female Breast Carcinoma In Situ | | MONDO:0004658|MONDO:0004379 | +| MONDO:0855783 | functioning lung neuroendocrine tumor | NCIT:C176705 | MONDO:equivalentTo | Functioning Lung Neuroendocrine Tumor | | MONDO:0021120|MONDO:0006041 | +| MONDO:0855784 | non-functioning lung neuroendocrine tumor | NCIT:C176706 | MONDO:equivalentTo | Non-Functioning Lung Neuroendocrine Tumor | | MONDO:0021119|MONDO:0006041 | +| MONDO:0855809 | metastatic malignant thoracic neoplasm | NCIT:C176862 | MONDO:equivalentTo | Metastatic Malignant Thoracic Neoplasm | | MONDO:0024880|MONDO:0003274 | +| MONDO:0855811 | psammocarcinoma | NCIT:C176887 | MONDO:equivalentTo | Psammocarcinoma | | MONDO:0004970 | +| MONDO:0855859 | infantile myofibromatosis 1 | NCIT:C176943 | MONDO:equivalentTo | Infantile Myofibromatosis 1 | | MONDO:0016824 | +| MONDO:0855860 | infantile myofibromatosis 2 | NCIT:C176944 | MONDO:equivalentTo | Infantile Myofibromatosis 2 | | MONDO:0016824 | +| MONDO:0855861 | lipoma-like atypical lipomatous tumor/well differentiated liposarcoma | NCIT:C176979 | MONDO:equivalentTo | Lipoma-Like Atypical Lipomatous Tumor/Well Differentiated Liposarcoma | | MONDO:0006097 | +| MONDO:0855862 | superficial atypical lipomatous tumor/well differentiated liposarcoma | NCIT:C176980 | MONDO:equivalentTo | Superficial Atypical Lipomatous Tumor/Well Differentiated Liposarcoma | | MONDO:0006097 | +| MONDO:0855863 | atypical lipomatous tumor/well differentiated liposarcoma of deep soft tissue | NCIT:C176981 | MONDO:equivalentTo | Atypical Lipomatous Tumor/Well Differentiated Liposarcoma of Deep Soft Tissue | | MONDO:0006097 | +| MONDO:0855864 | myxoid pleomorphic liposarcoma | NCIT:C176989 | MONDO:equivalentTo | Myxoid Pleomorphic Liposarcoma | | MONDO:0005060 | +| MONDO:0855883 | plaque-like dermatofibrosarcoma protuberans | NCIT:C177325 | MONDO:equivalentTo | Plaque-Like Dermatofibrosarcoma Protuberans | | MONDO:0011934 | +| MONDO:0855884 | somatic-type malignancy | NCIT:C177364 | MONDO:equivalentTo | Somatic-Type Malignancy | | MONDO:0004992 | +| MONDO:0855885 | epithelioid myxofibrosarcoma | NCIT:C177414 | MONDO:equivalentTo | Epithelioid Myxofibrosarcoma | | MONDO:0019202 | +| MONDO:0855891 | bladder flat urothelial carcinoma | NCIT:C177531 | MONDO:equivalentTo | Bladder Flat Urothelial Carcinoma | | MONDO:0005611 | +| MONDO:0855897 | epithelioid hemangioendothelioma with wwtr1-camta1 gene fusion | NCIT:C177552 | MONDO:equivalentTo | Epithelioid Hemangioendothelioma with WWTR1-CAMTA1 Gene Fusion | | MONDO:0015523 | +| MONDO:0855898 | epithelioid hemangioendothelioma with yap1-tfe3 gene fusion | NCIT:C177553 | MONDO:equivalentTo | Epithelioid Hemangioendothelioma with YAP1-TFE3 Gene Fusion | | MONDO:0015523 | +| MONDO:0855909 | who grade 1 glioma | NCIT:C177797 | MONDO:equivalentTo | WHO Grade 1 Glioma | | MONDO:0021637 | +| MONDO:0855911 | poorly differentiated chordoma | NCIT:C177898 | MONDO:equivalentTo | Poorly Differentiated Chordoma | | MONDO:0008978 | +| MONDO:0855914 | ebv-associated smooth muscle tumor | NCIT:C178217 | MONDO:equivalentTo | EBV-Associated Smooth Muscle Tumor | | MONDO:0006975 | +| MONDO:0855915 | pleomorphic leiomyosarcoma | NCIT:C178220 | MONDO:equivalentTo | Pleomorphic Leiomyosarcoma | | MONDO:0005058 | +| MONDO:0855916 | epithelioid schwannoma | NCIT:C178245 | MONDO:equivalentTo | Epithelioid Schwannoma | | MONDO:0002546 | +| MONDO:0855929 | round cell sarcoma with ewsr1-non-ets fusion | NCIT:C178459 | MONDO:equivalentTo | Round Cell Sarcoma with EWSR1-non-ETS Fusion | | MONDO:0006974 | +| MONDO:0855930 | sarcoma with bcor genetic alterations | NCIT:C178465 | MONDO:equivalentTo | Sarcoma with BCOR Genetic Alterations | | MONDO:0006974 | +| MONDO:0855935 | gastric melanoma | NCIT:C178519 | MONDO:equivalentTo | Gastric Melanoma | | MONDO:0001056|MONDO:0045070 | +| MONDO:0855938 | yolk sac tumor with somatic-type malignancy | NCIT:C178523 | MONDO:equivalentTo | Yolk Sac Tumor with Somatic-Type Malignancy | | MONDO:0005744 | +| MONDO:0855939 | conventional chordoma | NCIT:C178563 | MONDO:equivalentTo | Conventional Chordoma | | MONDO:0008978 | +| MONDO:0855941 | bone langerhans cell histiocytosis | NCIT:C178607 | MONDO:equivalentTo | Bone Langerhans Cell Histiocytosis | | MONDO:0019060|MONDO:0018310 | +| MONDO:0855942 | bone erdheim-chester disease | NCIT:C178609 | MONDO:equivalentTo | Bone Erdheim-Chester Disease | | MONDO:0019060|MONDO:0018153 | +| MONDO:0855961 | b-cell lymphoproliferative disorder | NCIT:C179052 | MONDO:equivalentTo | B-Cell Lymphoproliferative Disorder | | | +| MONDO:0855962 | t/nk-cell lymphoproliferative disorder | NCIT:C179053 | MONDO:equivalentTo | T/NK-Cell Lymphoproliferative Disorder | | | +| MONDO:0855976 | ovarian signet ring cell carcinoma | NCIT:C179208 | MONDO:equivalentTo | Ovarian Signet Ring Cell Carcinoma | | MONDO:0002752|MONDO:0005092 | +| MONDO:0855982 | myxoid glioneuronal tumor | NCIT:C179229 | MONDO:equivalentTo | Myxoid Glioneuronal Tumor | | MONDO:0016729 | +| MONDO:0855983 | borderline ovarian seromucinous tumor | NCIT:C179259 | MONDO:equivalentTo | Borderline Ovarian Seromucinous Tumor | | MONDO:0016093|MONDO:0003811 | +| MONDO:0855987 | mesonephric-like adenocarcinoma | NCIT:C179320 | MONDO:equivalentTo | Mesonephric-Like Adenocarcinoma | | MONDO:0001416|MONDO:0004970 | +| MONDO:0855990 | ovarian dedifferentiated carcinoma | NCIT:C179334 | MONDO:equivalentTo | Ovarian Dedifferentiated Carcinoma | | MONDO:0005140 | +| MONDO:0855991 | ovarian mixed cell adenocarcinoma | NCIT:C179339 | MONDO:equivalentTo | Ovarian Mixed Cell Adenocarcinoma | | MONDO:0002752 | +| MONDO:0855993 | giant cell-rich osteosarcoma | NCIT:C179410 | MONDO:equivalentTo | Giant Cell-Rich Osteosarcoma | | MONDO:0002631 | +| MONDO:0855995 | unresectable plexiform neurofibroma | NCIT:C179423 | MONDO:equivalentTo | Unresectable Plexiform Neurofibroma | | MONDO:0003304 | +| MONDO:0855999 | ovarian neuroectodermal-type tumor | NCIT:C179474 | MONDO:equivalentTo | Ovarian Neuroectodermal-Type Tumor | | MONDO:0008170 | +| MONDO:0856000 | ovarian wolffian tumor | NCIT:C179548 | MONDO:equivalentTo | Ovarian Wolffian Tumor | | MONDO:0002229|MONDO:0004255 | +| MONDO:0856002 | her2-low breast carcinoma | NCIT:C179553 | MONDO:equivalentTo | HER2-Low Breast Carcinoma | | MONDO:0004988 | +| MONDO:0856003 | peritoneal calcifying fibrous tumor | NCIT:C179560 | MONDO:equivalentTo | Peritoneal Calcifying Fibrous Tumor | | MONDO:0000650|MONDO:0006121 | +| MONDO:0856016 | basal ganglia neoplasm | NCIT:C179882 | MONDO:equivalentTo | Basal Ganglia Neoplasm | | MONDO:0021374 | +| MONDO:0856017 | cerebellar peduncle neoplasm | NCIT:C179883 | MONDO:equivalentTo | Cerebellar Peduncle Neoplasm | | MONDO:0002913 | +| MONDO:0856018 | corpus callosum neoplasm | NCIT:C179884 | MONDO:equivalentTo | Corpus Callosum Neoplasm | | MONDO:0021374 | +| MONDO:0856019 | oral cavity carcinoma cuniculatum | NCIT:C179894 | MONDO:equivalentTo | Oral Cavity Carcinoma Cuniculatum | | MONDO:0021538 | +| MONDO:0856021 | uterine ligament leiomyoma | NCIT:C179923 | MONDO:equivalentTo | Uterine Ligament Leiomyoma | | MONDO:0001572|MONDO:0020582 | +| MONDO:0856022 | uterine ligament adenomyoma | NCIT:C179925 | MONDO:equivalentTo | Uterine Ligament Adenomyoma | | MONDO:0005635|MONDO:0020582 | +| MONDO:0856024 | uterine ligament wolffian tumor | NCIT:C179927 | MONDO:equivalentTo | Uterine Ligament Wolffian Tumor | | MONDO:0004255|MONDO:0021629 | +| MONDO:0856025 | uterine ligament ependymoma | NCIT:C179928 | MONDO:equivalentTo | Uterine Ligament Ependymoma | | MONDO:0021629 | +| MONDO:0856026 | broad ligament neoplasm | NCIT:C179931 | MONDO:equivalentTo | Broad Ligament Neoplasm | | MONDO:0021629 | +| MONDO:0856027 | microsatellite stable ovarian carcinoma | NCIT:C180332 | MONDO:equivalentTo | Microsatellite Stable Ovarian Carcinoma | | MONDO:0005140 | +| MONDO:0856028 | microsatellite stable endometrial carcinoma | NCIT:C180335 | MONDO:equivalentTo | Microsatellite Stable Endometrial Carcinoma | | MONDO:0002447 | +| MONDO:0856030 | polymorphous low grade neuroepithelial tumor of the young | NCIT:C180378 | MONDO:equivalentTo | Polymorphous Low Grade Neuroepithelial Tumor of the Young | | MONDO:0016729|MONDO:0021632 | +| MONDO:0856033 | tectal glioma | NCIT:C180407 | MONDO:equivalentTo | Tectal Glioma | | MONDO:0021042 | +| MONDO:0856035 | pole-ultramutated endometrial endometrioid adenocarcinoma | NCIT:C180512 | MONDO:equivalentTo | POLE-Ultramutated Endometrial Endometrioid Adenocarcinoma | | MONDO:0006192 | +| MONDO:0856036 | mismatch repair-deficient endometrial endometrioid adenocarcinoma | NCIT:C180514 | MONDO:equivalentTo | Mismatch Repair-Deficient Endometrial Endometrioid Adenocarcinoma | | MONDO:0006192 | +| MONDO:0856037 | p53-mutant endometrial endometrioid adenocarcinoma | NCIT:C180515 | MONDO:equivalentTo | p53-Mutant Endometrial Endometrioid Adenocarcinoma | | MONDO:0006192 | +| MONDO:0856038 | no specific molecular profile endometrial endometrioid adenocarcinoma | NCIT:C180516 | MONDO:equivalentTo | No Specific Molecular Profile Endometrial Endometrioid Adenocarcinoma | | MONDO:0006192 | +| MONDO:0856040 | dysembryoplastic neuroepithelial-like tumor of the septum pellucidum | NCIT:C180532 | MONDO:equivalentTo | Dysembryoplastic Neuroepithelial-Like Tumor of the Septum Pellucidum | | MONDO:0016729 | +| MONDO:0856041 | endometrial mucinous adenocarcinoma, intestinal-type | NCIT:C180536 | MONDO:equivalentTo | Endometrial Mucinous Adenocarcinoma, Intestinal-Type | | MONDO:0005461|MONDO:0006254 | +| MONDO:0856042 | endometrial mucinous adenocarcinoma, gastric-type | NCIT:C180537 | MONDO:equivalentTo | Endometrial Mucinous Adenocarcinoma, Gastric-Type | | MONDO:0005461 | +| MONDO:0856044 | uterine corpus central primitive neuroectodermal tumor | NCIT:C180546 | MONDO:equivalentTo | Uterine Corpus Central Primitive Neuroectodermal Tumor | | MONDO:0005210|MONDO:0006974 | +| MONDO:0856048 | urothelial carcinoma, high grade | NCIT:C180606 | MONDO:equivalentTo | Urothelial Carcinoma, High Grade | | MONDO:0040679 | +| MONDO:0856052 | gestational trophoblastic disorder | NCIT:C180633 | MONDO:equivalentTo | Gestational Trophoblastic Disorder | | | +| MONDO:0856053 | mixed trophoblastic tumor | NCIT:C180634 | MONDO:equivalentTo | Mixed Trophoblastic Tumor | | MONDO:0018944 | +| MONDO:0856054 | metastatic hydatidiform mole | NCIT:C180635 | MONDO:equivalentTo | Metastatic Hydatidiform Mole | | MONDO:0020549 | +| MONDO:0856055 | low grade papillary schneiderian carcinoma | NCIT:C180670 | MONDO:equivalentTo | Low Grade Papillary Schneiderian Carcinoma | | MONDO:0056819 | +| MONDO:0856057 | cervical squamous cell carcinoma, not otherwise specified | NCIT:C180839 | MONDO:equivalentTo | Cervical Squamous Cell Carcinoma, Not Otherwise Specified | | MONDO:0006143 | +| MONDO:0856060 | human papillomavirus-independent cervical adenocarcinoma | NCIT:C180848 | MONDO:equivalentTo | Human Papillomavirus-Independent Cervical Adenocarcinoma | | MONDO:0005153 | +| MONDO:0856067 | cervical adenocarcinoma, not otherwise specified | NCIT:C180870 | MONDO:equivalentTo | Cervical Adenocarcinoma, Not Otherwise Specified | | MONDO:0005153 | +| MONDO:0856070 | cervical mucoepidermoid carcinoma | NCIT:C180878 | MONDO:equivalentTo | Cervical Mucoepidermoid Carcinoma | | MONDO:0005131|MONDO:0003036 | +| MONDO:0856071 | cervical germ cell tumor | NCIT:C180879 | MONDO:equivalentTo | Cervical Germ Cell Tumor | | MONDO:0005040|MONDO:0021230 | +| MONDO:0856072 | minor salivary gland intraductal papillary neoplasm | NCIT:C180880 | MONDO:equivalentTo | Minor Salivary Gland Intraductal Papillary Neoplasm | | MONDO:0021370 | +| MONDO:0856074 | adult myofibroma | NCIT:C180888 | MONDO:equivalentTo | Adult Myofibroma | | MONDO:0006312 | +| MONDO:0856077 | human papillomavirus-related vaginal squamous cell carcinoma | NCIT:C180917 | MONDO:equivalentTo | Human Papillomavirus-Related Vaginal Squamous Cell Carcinoma | | MONDO:0020657|MONDO:0006490 | +| MONDO:0856083 | vaginal adenocarcinoma of skene gland origin | NCIT:C180947 | MONDO:equivalentTo | Vaginal Adenocarcinoma of Skene Gland Origin | | MONDO:0020653|MONDO:0004173 | +| MONDO:0856100 | hybrid salivary gland tumor | NCIT:C181078 | MONDO:equivalentTo | Hybrid Salivary Gland Tumor | | MONDO:0021043|MONDO:0021357 | +| MONDO:0856104 | eyelid basal cell carcinoma | NCIT:C181159 | MONDO:equivalentTo | Eyelid Basal Cell Carcinoma | | MONDO:0003876|MONDO:0005341 | +| MONDO:0856106 | major salivary gland squamous cell carcinoma | NCIT:C181161 | MONDO:equivalentTo | Major Salivary Gland Squamous Cell Carcinoma | | MONDO:0044740|MONDO:0006284 | +| MONDO:0856110 | lung rhabdomyosarcoma | NCIT:C181201 | MONDO:equivalentTo | Lung Rhabdomyosarcoma | | MONDO:0002426|MONDO:0005212 | +| MONDO:0856111 | lung hodgkin lymphoma | NCIT:C181205 | MONDO:equivalentTo | Lung Hodgkin Lymphoma | | MONDO:0004952|MONDO:0003987 | +| MONDO:0856112 | primary bone hodgkin lymphoma | NCIT:C181207 | MONDO:equivalentTo | Primary Bone Hodgkin Lymphoma | | MONDO:0004952|MONDO:0017814 | +| MONDO:0856114 | cervical cancer by ajcc v9 stage | NCIT:C181562 | MONDO:equivalentTo | Cervical Cancer by AJCC v9 Stage | | MONDO:0005131 | +| MONDO:0856117 | epiglottic squamous cell carcinoma | NCIT:C181714 | MONDO:equivalentTo | Epiglottic Squamous Cell Carcinoma | | MONDO:0004293|MONDO:0004473 | +| MONDO:0856124 | vulvar squamous cell carcinoma, not otherwise specified | NCIT:C181902 | MONDO:equivalentTo | Vulvar Squamous Cell Carcinoma, Not Otherwise Specified | | MONDO:0024609 | +| MONDO:0856128 | endometrial mucosa-associated lymphoid tissue lymphoma | NCIT:C181910 | MONDO:equivalentTo | Endometrial Mucosa-Associated Lymphoid Tissue Lymphoma | | MONDO:0007650|MONDO:0011962 | +| MONDO:0856134 | vulvar kaposi sarcoma | NCIT:C181938 | MONDO:equivalentTo | Vulvar Kaposi Sarcoma | | MONDO:0005055|MONDO:0005214 | +| MONDO:0856136 | vulvar rhabdomyosarcoma | NCIT:C181944 | MONDO:equivalentTo | Vulvar Rhabdomyosarcoma | | MONDO:0005214|MONDO:0005212 | +| MONDO:0856137 | vulvar epithelioid sarcoma | NCIT:C181971 | MONDO:equivalentTo | Vulvar Epithelioid Sarcoma | | MONDO:0005214|MONDO:0017387 | +| MONDO:0856139 | vulvar ewing sarcoma | NCIT:C181977 | MONDO:equivalentTo | Vulvar Ewing Sarcoma | | MONDO:0018270|MONDO:0005214 | +| MONDO:0856154 | bronchiolar adenoma/ciliated muconodular papillary tumor | NCIT:C183045 | MONDO:equivalentTo | Bronchiolar Adenoma/Ciliated Muconodular Papillary Tumor | | MONDO:0003422 | +| MONDO:0856155 | invasive lung non-mucinous adenocarcinoma | NCIT:C183109 | MONDO:equivalentTo | Invasive Lung Non-Mucinous Adenocarcinoma | | MONDO:0040677|MONDO:0005061 | +| MONDO:0856156 | thoracic smarca4-deficient undifferentiated tumor | NCIT:C183115 | MONDO:equivalentTo | Thoracic SMARCA4-Deficient Undifferentiated Tumor | | MONDO:0003274 | +| MONDO:0856158 | lung intravascular large b-cell lymphoma | NCIT:C183121 | MONDO:equivalentTo | Lung Intravascular Large B-Cell Lymphoma | | MONDO:0006387|MONDO:0020324 | +| MONDO:0856161 | pleural mesothelioma in situ | NCIT:C183134 | MONDO:equivalentTo | Pleural Mesothelioma In Situ | | MONDO:0003308 | +| MONDO:0856165 | cardiac diffuse large b-cell lymphoma | NCIT:C183146 | MONDO:equivalentTo | Cardiac Diffuse Large B-Cell Lymphoma | | MONDO:0018905|MONDO:0003917 | +| MONDO:0856172 | pleural calcifying fibrous tumor | NCIT:C183277 | MONDO:equivalentTo | Pleural Calcifying Fibrous Tumor | | MONDO:0006121|MONDO:0021457 | +| MONDO:0856178 | thymic carcinoma with adenoid cystic carcinoma-like features | NCIT:C183313 | MONDO:equivalentTo | Thymic Carcinoma with Adenoid Cystic Carcinoma-Like Features | | MONDO:0006451 | +| MONDO:0856179 | thymic enteric-type adenocarcinoma | NCIT:C183314 | MONDO:equivalentTo | Thymic Enteric-Type Adenocarcinoma | | MONDO:0003209|MONDO:0006254 | +| MONDO:0856180 | thymic adenocarcinoma, not otherwise specified | NCIT:C183315 | MONDO:equivalentTo | Thymic Adenocarcinoma, Not Otherwise Specified | | MONDO:0003209 | +| MONDO:0856181 | thymic carcinoma, not otherwise specified | NCIT:C183316 | MONDO:equivalentTo | Thymic Carcinoma, Not Otherwise Specified | | MONDO:0006451 | +| MONDO:0856182 | mediastinal follicular dendritic cell sarcoma | NCIT:C183374 | MONDO:equivalentTo | Mediastinal Follicular Dendritic Cell Sarcoma | | MONDO:0005764|MONDO:0005843 | +| MONDO:0856183 | metastatic malignant neoplasm in the mediastinal lymph nodes | NCIT:C183510 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Mediastinal Lymph Nodes | | MONDO:0005438 | +| MONDO:0856191 | salivary gland adenoma | NCIT:C184295 | MONDO:equivalentTo | Salivary Gland Adenoma | | MONDO:0021460|MONDO:0004972 | +| MONDO:0856197 | multiple solitary plasmacytoma of bone | NCIT:C185035 | MONDO:equivalentTo | Multiple Solitary Plasmacytoma of Bone | | MONDO:0002755 | +| MONDO:0856199 | splenic plasmacytoma | NCIT:C185041 | MONDO:equivalentTo | Splenic Plasmacytoma | | MONDO:0002754|MONDO:0005966 | +| MONDO:0856204 | extramedullary disease in multiple myeloma | NCIT:C185149 | MONDO:equivalentTo | Extramedullary Disease in Multiple Myeloma | | MONDO:0009693 | +| MONDO:0856206 | astrocytoma, idh-mutant | NCIT:C185167 | MONDO:equivalentTo | Astrocytoma, IDH-Mutant | | MONDO:0019781 | +| MONDO:0856207 | astrocytoma, idh-wildtype | NCIT:C185184 | MONDO:equivalentTo | Astrocytoma, IDH-Wildtype | | MONDO:0019781 | +| MONDO:0856208 | astrocytoma, not otherwise specified | NCIT:C185185 | MONDO:equivalentTo | Astrocytoma, Not Otherwise Specified | | MONDO:0019781 | +| MONDO:0856216 | extranodal lymphoma | NCIT:C185752 | MONDO:equivalentTo | Extranodal Lymphoma | | MONDO:0017207 | +| MONDO:0856218 | high grade astrocytoma with piloid features | NCIT:C185879 | MONDO:equivalentTo | High Grade Astrocytoma with Piloid Features | | MONDO:0016684 | +| MONDO:0856232 | spinal cord ependymoma, mycn amplified | NCIT:C186494 | MONDO:equivalentTo | Spinal Cord Ependymoma, MYCN Amplified | | MONDO:0002542|MONDO:0016698 | +| MONDO:0856233 | childhood spinal cord ependymoma | NCIT:C186495 | MONDO:equivalentTo | Childhood Spinal Cord Ependymoma | | MONDO:0002716|MONDO:0003478|MONDO:0003473 | +| MONDO:0856234 | central nervous system neuroblastoma, foxr2-activated | NCIT:C186547 | MONDO:equivalentTo | Central Nervous System Neuroblastoma, FOXR2-Activated | | MONDO:0002900 | +| MONDO:0856238 | primary intracranial sarcoma, dicer1-mutant | NCIT:C186610 | MONDO:equivalentTo | Primary Intracranial Sarcoma, DICER1-Mutant | | MONDO:0002216 | +| MONDO:0856239 | central nervous system ewing sarcoma | NCIT:C186611 | MONDO:equivalentTo | Central Nervous System Ewing Sarcoma | | MONDO:0018270|MONDO:0002217|MONDO:0016713 | +| MONDO:0856240 | intracranial mesenchymal tumor, fet-creb fusion-positive | NCIT:C186614 | MONDO:equivalentTo | Intracranial Mesenchymal Tumor, FET-CREB Fusion-Positive | | MONDO:0003244|MONDO:0021632 | +| MONDO:0856241 | cervical cancer by figo stage 2009 | NCIT:C186619 | MONDO:equivalentTo | Cervical Cancer by FIGO Stage 2009 | | MONDO:0005131 | +| MONDO:0856244 | central nervous system lymphomatoid granulomatosis | NCIT:C186662 | MONDO:equivalentTo | Central Nervous System Lymphomatoid Granulomatosis | | MONDO:0019466|MONDO:0003641 | +| MONDO:0856246 | smarcb1 schwannomatosis 1 | NCIT:C186703 | MONDO:equivalentTo | SMARCB1 Schwannomatosis 1 | | MONDO:0008075 | +| MONDO:0856247 | lztr1 schwannomatosis 2 | NCIT:C186704 | MONDO:equivalentTo | LZTR1 Schwannomatosis 2 | | MONDO:0008075 | +| MONDO:0856253 | childhood acute leukemia | NCIT:C187056 | MONDO:equivalentTo | Childhood Acute Leukemia | | MONDO:0010643|MONDO:0004355 | +| MONDO:0856254 | pituitary neuroendocrine tumor of pit1-lineage | NCIT:C187086 | MONDO:equivalentTo | Pituitary Neuroendocrine Tumor of PIT1-Lineage | | MONDO:0006373 | +| MONDO:0856255 | pituitary neuroendocrine tumor of tpit-lineage | NCIT:C187087 | MONDO:equivalentTo | Pituitary Neuroendocrine Tumor of TPIT-Lineage | | MONDO:0006373 | +| MONDO:0856256 | pituitary neuroendocrine tumor of sf1-lineage | NCIT:C187088 | MONDO:equivalentTo | Pituitary Neuroendocrine Tumor of SF1-Lineage | | MONDO:0006373 | +| MONDO:0856257 | pituitary neuroendocrine tumor without distinct lineage differentiation | NCIT:C187096 | MONDO:equivalentTo | Pituitary Neuroendocrine Tumor without Distinct Lineage Differentiation | | MONDO:0006373 | +| MONDO:0856258 | pituitary neuroendocrine tumor, not otherwise specified | NCIT:C187135 | MONDO:equivalentTo | Pituitary Neuroendocrine Tumor, Not Otherwise Specified | | MONDO:0006373 | +| MONDO:0856267 | thyroid gland follicular adenoma with papillary architecture | NCIT:C187261 | MONDO:equivalentTo | Thyroid Gland Follicular Adenoma with Papillary Architecture | | MONDO:0005032 | +| MONDO:0856268 | low risk thyroid gland neoplasm | NCIT:C187273 | MONDO:equivalentTo | Low Risk Thyroid Gland Neoplasm | | MONDO:0015074 | +| MONDO:0856272 | invasive breast lobular carcinoma with extracellular mucin | NCIT:C187405 | MONDO:equivalentTo | Invasive Breast Lobular Carcinoma with Extracellular Mucin | | MONDO:0005051 | +| MONDO:0856275 | thyroid gland follicular carcinoma, signet ring cell variant | NCIT:C187643 | MONDO:equivalentTo | Thyroid Gland Follicular Carcinoma, Signet Ring Cell Variant | | MONDO:0005034 | +| MONDO:0856276 | classic thyroid gland papillary carcinoma | NCIT:C187644 | MONDO:equivalentTo | Classic Thyroid Gland Papillary Carcinoma | | MONDO:0005075 | +| MONDO:0856277 | high grade follicular cell-derived non-anaplastic thyroid gland carcinoma | NCIT:C187645 | MONDO:equivalentTo | High Grade Follicular Cell-Derived Non-Anaplastic Thyroid Gland Carcinoma | | MONDO:0024622 | +| MONDO:0856285 | thyroid gland secretory carcinoma | NCIT:C187994 | MONDO:equivalentTo | Thyroid Gland Secretory Carcinoma | | MONDO:0024622 | +| MONDO:0856286 | thyroblastoma | NCIT:C187995 | MONDO:equivalentTo | Thyroblastoma | | MONDO:0002108|MONDO:0005564 | +| MONDO:0856287 | teratoma with endocrine differentiation | NCIT:C188013 | MONDO:equivalentTo | Teratoma with Endocrine Differentiation | | MONDO:0002601 | +| MONDO:0856289 | b-cell malignant neoplasm | NCIT:C188021 | MONDO:equivalentTo | B-Cell Malignant Neoplasm | | MONDO:0004992|MONDO:0004095 | +| MONDO:0856293 | mast cell leukemia with an associated myeloid neoplasm | NCIT:C188031 | MONDO:equivalentTo | Mast Cell Leukemia with an Associated Myeloid Neoplasm | | MONDO:0020332|MONDO:0020334 | +| MONDO:0856298 | refractory wilms tumor | NCIT:C188038 | MONDO:equivalentTo | Refractory Wilms Tumor | | MONDO:0006058|MONDO:0036501 | +| MONDO:0856302 | pleural proximal-type epithelioid sarcoma | NCIT:C188055 | MONDO:equivalentTo | Pleural Proximal-Type Epithelioid Sarcoma | | MONDO:0006294|MONDO:0004244 | +| MONDO:0856303 | lung osteosarcoma | NCIT:C188061 | MONDO:equivalentTo | Lung Osteosarcoma | | MONDO:0002621|MONDO:0002426 | +| MONDO:0856304 | pleural leiomyosarcoma | NCIT:C188063 | MONDO:equivalentTo | Pleural Leiomyosarcoma | | MONDO:0006294|MONDO:0005058 | +| MONDO:0856305 | bone malignant peripheral nerve sheath tumor | NCIT:C188064 | MONDO:equivalentTo | Bone Malignant Peripheral Nerve Sheath Tumor | | MONDO:0021054|MONDO:0017827 | +| MONDO:0856308 | lung secretory carcinoma | NCIT:C188068 | MONDO:equivalentTo | Lung Secretory Carcinoma | | MONDO:0005138 | +| MONDO:0856309 | prostate alveolar rhabdomyosarcoma | NCIT:C188070 | MONDO:equivalentTo | Prostate Alveolar Rhabdomyosarcoma | | MONDO:0006389|MONDO:0009994 | +| MONDO:0856310 | retroperitoneal rhabdomyosarcoma | NCIT:C188071 | MONDO:equivalentTo | Retroperitoneal Rhabdomyosarcoma | | MONDO:0001501|MONDO:0005212 | +| MONDO:0856312 | retroperitoneal malignant peripheral nerve sheath tumor | NCIT:C188073 | MONDO:equivalentTo | Retroperitoneal Malignant Peripheral Nerve Sheath Tumor | | MONDO:0001501|MONDO:0017827 | +| MONDO:0856313 | rectal epithelioid cell melanoma | NCIT:C188079 | MONDO:equivalentTo | Rectal Epithelioid Cell Melanoma | | MONDO:0002167|MONDO:0002973 | +| MONDO:0856316 | lung anaplastic large cell lymphoma | NCIT:C188082 | MONDO:equivalentTo | Lung Anaplastic Large Cell Lymphoma | | MONDO:0020644|MONDO:0020325 | +| MONDO:0856325 | adrenal cortical myxoid carcinoma | NCIT:C188182 | MONDO:equivalentTo | Adrenal Cortical Myxoid Carcinoma | | MONDO:0006639 | +| MONDO:0856326 | adrenal cortical high grade carcinoma | NCIT:C188183 | MONDO:equivalentTo | Adrenal Cortical High Grade Carcinoma | | MONDO:0006639 | +| MONDO:0856327 | adrenal cortical melanoma | NCIT:C188185 | MONDO:equivalentTo | Adrenal Cortical Melanoma | | MONDO:0021312|MONDO:0006320 | +| MONDO:0856335 | neuroendocrine tumor | NCIT:C188218 | MONDO:equivalentTo | Neuroendocrine Tumor | | MONDO:0019496 | +| MONDO:0856336 | head and neck neuroendocrine neoplasm | NCIT:C188222 | MONDO:equivalentTo | Head and Neck Neuroendocrine Neoplasm | | MONDO:0019496|MONDO:0005586 | +| MONDO:0856338 | adrenal gland lipoma | NCIT:C188250 | MONDO:equivalentTo | Adrenal Gland Lipoma | | MONDO:0021511|MONDO:0005106 | +| MONDO:0856339 | adrenal gland hemangioma | NCIT:C188251 | MONDO:equivalentTo | Adrenal Gland Hemangioma | | MONDO:0021511|MONDO:0006500 | +| MONDO:0856340 | adrenal gland lymphangioma | NCIT:C188252 | MONDO:equivalentTo | Adrenal Gland Lymphangioma | | MONDO:0002013|MONDO:0021511 | +| MONDO:0856341 | adrenal gland leiomyoma | NCIT:C188253 | MONDO:equivalentTo | Adrenal Gland Leiomyoma | | MONDO:0021511|MONDO:0001572 | +| MONDO:0856343 | multiple endocrine neoplasia type 5 | NCIT:C188257 | MONDO:equivalentTo | Multiple Endocrine Neoplasia Type 5 | | MONDO:0017169 | +| MONDO:0856349 | chronic phase primary myelofibrosis | NCIT:C188314 | MONDO:equivalentTo | Chronic Phase Primary Myelofibrosis | | MONDO:0009692 | +| MONDO:0856350 | accelerated phase myeloproliferative neoplasm | NCIT:C188315 | MONDO:equivalentTo | Accelerated Phase Myeloproliferative Neoplasm | | MONDO:0020076 | +| MONDO:0856351 | blast phase myeloproliferative neoplasm | NCIT:C188316 | MONDO:equivalentTo | Blast Phase Myeloproliferative Neoplasm | | MONDO:0020076 | +| MONDO:0856357 | intraductal hyperplasia | NCIT:C26458 | MONDO:equivalentTo | Intraductal Hyperplasia | | | +| MONDO:0856375 | reticulosarcoma involving spleen | NCIT:C26959 | MONDO:equivalentTo | Reticulosarcoma Involving Spleen | | MONDO:0009975 | +| MONDO:0856376 | lymphosarcoma involving spleen | NCIT:C26960 | MONDO:equivalentTo | Lymphosarcoma Involving Spleen | | MONDO:0004638 | +| MONDO:0856398 | nonpigmented nevus | NCIT:C27095 | MONDO:equivalentTo | Nonpigmented Nevus | | MONDO:0044794 | +| MONDO:0856421 | transplant-related disorder | NCIT:C27233 | MONDO:equivalentTo | Transplant-Related Disorder | | | +| MONDO:0856422 | familial adenomatous polyposis associated medulloblastoma | NCIT:C27237 | MONDO:equivalentTo | Familial Adenomatous Polyposis Associated Medulloblastoma | | MONDO:0007959 | +| MONDO:0856423 | lymphoma by stage | NCIT:C27268 | MONDO:equivalentTo | Lymphoma by Stage | | MONDO:0005062 | +| MONDO:0856424 | glandular cell intraepithelial neoplasia | NCIT:C27269 | MONDO:equivalentTo | Glandular Cell Intraepithelial Neoplasia | | MONDO:0024474|MONDO:0024276 | +| MONDO:0856425 | secondary myelodysplastic syndrome | NCIT:C27280 | MONDO:equivalentTo | Secondary Myelodysplastic Syndrome | | MONDO:0024881|MONDO:0018881 | +| MONDO:0856428 | metastatic ewing sarcoma/peripheral primitive neuroectodermal tumor | NCIT:C27292 | MONDO:equivalentTo | Metastatic Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor | | MONDO:0024880|MONDO:0021038 | +| MONDO:0856443 | unresectable malignant neoplasm | NCIT:C27359 | MONDO:equivalentTo | Unresectable Malignant Neoplasm | | MONDO:0004992 | +| MONDO:0856447 | mucin-producing adenocarcinoma | NCIT:C27379 | MONDO:equivalentTo | Mucin-Producing Adenocarcinoma | | MONDO:0020596|MONDO:0004970 | +| MONDO:0856451 | extraosseous/peripheral ameloblastoma | NCIT:C27396 | MONDO:equivalentTo | Extraosseous/Peripheral Ameloblastoma | | MONDO:0017795 | +| MONDO:0856452 | ampulla of vater intestinal-type adenocarcinoma | NCIT:C27415 | MONDO:equivalentTo | Ampulla of Vater Intestinal-Type Adenocarcinoma | | MONDO:0002670|MONDO:0006254 | +| MONDO:0856453 | ampulla of vater undifferentiated carcinoma | NCIT:C27419 | MONDO:equivalentTo | Ampulla of Vater Undifferentiated Carcinoma | | MONDO:0017590|MONDO:0005617 | +| MONDO:0856456 | small intestinal gastrin-producing neuroendocrine tumor | NCIT:C27450 | MONDO:equivalentTo | Small Intestinal Gastrin-Producing Neuroendocrine Tumor | | MONDO:0002995|MONDO:0003523 | +| MONDO:0856457 | small intestinal enterochromaffin cell serotonin-producing neuroendocrine tumor | NCIT:C27451 | MONDO:equivalentTo | Small Intestinal Enterochromaffin Cell Serotonin-Producing Neuroendocrine Tumor | | MONDO:0002995 | +| MONDO:0856458 | small intestinal somatostatin-producing neuroendocrine tumor | NCIT:C27453 | MONDO:equivalentTo | Small Intestinal Somatostatin-Producing Neuroendocrine Tumor | | MONDO:0002995|MONDO:0006976 | +| MONDO:0856460 | colorectal adenoma with moderate dysplasia | NCIT:C27457 | MONDO:equivalentTo | Colorectal Adenoma with Moderate Dysplasia | | MONDO:0005484 | +| MONDO:0856461 | colorectal adenoma with mild dysplasia | NCIT:C27458 | MONDO:equivalentTo | Colorectal Adenoma with Mild Dysplasia | | MONDO:0005484 | +| MONDO:0856463 | disseminated malignant neoplasm | NCIT:C27470 | MONDO:equivalentTo | Disseminated Malignant Neoplasm | | MONDO:0024880 | +| MONDO:0856464 | bone lipoma | NCIT:C27475 | MONDO:equivalentTo | Bone Lipoma | | MONDO:0000631|MONDO:0005106 | +| MONDO:0856465 | bone schwannoma | NCIT:C27476 | MONDO:equivalentTo | Bone Schwannoma | | MONDO:0000631|MONDO:0004820 | +| MONDO:0856468 | secondary chondrosarcoma | NCIT:C27482 | MONDO:equivalentTo | Secondary Chondrosarcoma | | MONDO:0021054|MONDO:0024881|MONDO:0008977 | +| MONDO:0856469 | conventional alveolar rhabdomyosarcoma | NCIT:C27492 | MONDO:equivalentTo | Conventional Alveolar Rhabdomyosarcoma | | MONDO:0009994 | +| MONDO:0856470 | solid alveolar rhabdomyosarcoma | NCIT:C27493 | MONDO:equivalentTo | Solid Alveolar Rhabdomyosarcoma | | MONDO:0009994 | +| MONDO:0856471 | lymphadenopathic kaposi sarcoma | NCIT:C27500 | MONDO:equivalentTo | Lymphadenopathic Kaposi Sarcoma | | MONDO:0001082|MONDO:0005055 | +| MONDO:0856472 | conventional extraskeletal myxoid chondrosarcoma | NCIT:C27501 | MONDO:equivalentTo | Conventional Extraskeletal Myxoid Chondrosarcoma | | MONDO:0012825 | +| MONDO:0856473 | intra-abdominal lymphangioma | NCIT:C27508 | MONDO:equivalentTo | Intra-Abdominal Lymphangioma | | MONDO:0002013 | +| MONDO:0856474 | angiosarcoma associated with lymphedema | NCIT:C27512 | MONDO:equivalentTo | Angiosarcoma Associated with Lymphedema | | MONDO:0016982 | +| MONDO:0856475 | desmoplastic fibroblastoma | NCIT:C27515 | MONDO:equivalentTo | Desmoplastic Fibroblastoma | | MONDO:0005167 | +| MONDO:0856477 | columnar trichoblastoma | NCIT:C27524 | MONDO:equivalentTo | Columnar Trichoblastoma | | MONDO:0020593 | +| MONDO:0856478 | tubular apocrine adenoma | NCIT:C27527 | MONDO:equivalentTo | Tubular Apocrine Adenoma | | MONDO:0002804 | +| MONDO:0856479 | primary cutaneous mucinous carcinoma | NCIT:C27533 | MONDO:equivalentTo | Primary Cutaneous Mucinous Carcinoma | | MONDO:0005524|MONDO:0004957 | +| MONDO:0856501 | oral cavity disorder | NCIT:C27641 | MONDO:equivalentTo | Oral Cavity Disorder | | | +| MONDO:0856504 | sinonasal disorder | NCIT:C27647 | MONDO:equivalentTo | Sinonasal Disorder | | | +| MONDO:0856509 | human papillomavirus-related verrucous carcinoma | NCIT:C27678 | MONDO:equivalentTo | Human Papillomavirus-Related Verrucous Carcinoma | | MONDO:0006006|MONDO:0020657 | +| MONDO:0856510 | human papillomavirus-related vulvar squamous cell carcinoma | NCIT:C27679 | MONDO:equivalentTo | Human Papillomavirus-Related Vulvar Squamous Cell Carcinoma | | MONDO:0024609|MONDO:0020657 | +| MONDO:0856511 | human papillomavirus-related esophageal squamous cell carcinoma | NCIT:C27680 | MONDO:equivalentTo | Human Papillomavirus-Related Esophageal Squamous Cell Carcinoma | | MONDO:0005580|MONDO:0020657 | +| MONDO:0856512 | human papillomavirus-related anal squamous cell carcinoma | NCIT:C27681 | MONDO:equivalentTo | Human Papillomavirus-Related Anal Squamous Cell Carcinoma | | MONDO:0006082|MONDO:0020657 | +| MONDO:0856518 | ebv-related post-transplant lymphoproliferative disorder | NCIT:C27696 | MONDO:equivalentTo | EBV-Related Post-Transplant Lymphoproliferative Disorder | | | +| MONDO:0856523 | extragastrointestinal gastrointestinal stromal tumor | NCIT:C27716 | MONDO:equivalentTo | Extragastrointestinal Gastrointestinal Stromal Tumor | | MONDO:0011719 | +| MONDO:0856526 | myelodysplastic syndrome with ring sideroblasts and multilineage dysplasia | NCIT:C27726 | MONDO:equivalentTo | Myelodysplastic Syndrome with Ring Sideroblasts and Multilineage Dysplasia | | MONDO:0019157 | +| MONDO:0856529 | typical acute promyelocytic leukemia | NCIT:C27756 | MONDO:equivalentTo | Typical Acute Promyelocytic Leukemia | | MONDO:0012883 | +| MONDO:0856530 | microgranular acute promyelocytic leukemia | NCIT:C27757 | MONDO:equivalentTo | Microgranular Acute Promyelocytic Leukemia | | MONDO:0012883 | +| MONDO:0856539 | myelodysplastic/myeloproliferative neoplasm, not otherwise specified | NCIT:C27780 | MONDO:equivalentTo | Myelodysplastic/Myeloproliferative Neoplasm, Not Otherwise Specified | | MONDO:0006311 | +| MONDO:0856541 | spindle cell type gastrointestinal stromal tumor | NCIT:C27792 | MONDO:equivalentTo | Spindle Cell Type Gastrointestinal Stromal Tumor | | MONDO:0011719 | +| MONDO:0856542 | mixed cell type gastrointestinal stromal tumor | NCIT:C27793 | MONDO:equivalentTo | Mixed Cell Type Gastrointestinal Stromal Tumor | | MONDO:0011719 | +| MONDO:0856545 | nodular sclerosis classic hodgkin lymphoma, syncytial variant | NCIT:C27807 | MONDO:equivalentTo | Nodular Sclerosis Classic Hodgkin Lymphoma, Syncytial Variant | | MONDO:0004665 | +| MONDO:0856546 | pigmented nevus | NCIT:C27816 | MONDO:equivalentTo | Pigmented Nevus | | MONDO:0044794 | +| MONDO:0856549 | invasive breast carcinoma by histologic grade | NCIT:C27829 | MONDO:equivalentTo | Invasive Breast Carcinoma by Histologic Grade | | MONDO:0006256 | +| MONDO:0856551 | endometrial endometrioid adenocarcinoma with clear cell change | NCIT:C27843 | MONDO:equivalentTo | Endometrial Endometrioid Adenocarcinoma with Clear Cell Change | | MONDO:0006192|MONDO:0005004 | +| MONDO:0856552 | endometrial endometrioid adenocarcinoma with a poorly differentiated carcinomatous component | NCIT:C27844 | MONDO:equivalentTo | Endometrial Endometrioid Adenocarcinoma with a Poorly Differentiated Carcinomatous Component | | MONDO:0006192 | +| MONDO:0856553 | endometrial endometrioid adenocarcinoma with an undifferentiated carcinomatous component | NCIT:C27845 | MONDO:equivalentTo | Endometrial Endometrioid Adenocarcinoma with an Undifferentiated Carcinomatous Component | | MONDO:0006192 | +| MONDO:0856554 | endometrial endometrioid adenocarcinoma, ciliated variant | NCIT:C27848 | MONDO:equivalentTo | Endometrial Endometrioid Adenocarcinoma, Ciliated Variant | | MONDO:0006192 | +| MONDO:0856567 | transitional cell intraepithelial neoplasia | NCIT:C27881 | MONDO:equivalentTo | Transitional Cell Intraepithelial Neoplasia | | MONDO:0024474|MONDO:0037254 | +| MONDO:0856569 | type 1 papillary renal cell carcinoma | NCIT:C27886 | MONDO:equivalentTo | Type 1 Papillary Renal Cell Carcinoma | | MONDO:0017884 | +| MONDO:0856570 | type 2 papillary renal cell carcinoma | NCIT:C27887 | MONDO:equivalentTo | Type 2 Papillary Renal Cell Carcinoma | | MONDO:0017884 | +| MONDO:0856571 | sporadic papillary renal cell carcinoma | NCIT:C27890 | MONDO:equivalentTo | Sporadic Papillary Renal Cell Carcinoma | | MONDO:0017884 | +| MONDO:0856577 | well differentiated prostate adenocarcinoma | NCIT:C27905 | MONDO:equivalentTo | Well Differentiated Prostate Adenocarcinoma | | MONDO:0005082 | +| MONDO:0856578 | moderately differentiated prostate adenocarcinoma | NCIT:C27906 | MONDO:equivalentTo | Moderately Differentiated Prostate Adenocarcinoma | | MONDO:0005082 | +| MONDO:0856579 | alkylating agent-related acute myeloid leukemia and myelodysplastic syndrome | NCIT:C27913 | MONDO:equivalentTo | Alkylating Agent-Related Acute Myeloid Leukemia and Myelodysplastic Syndrome | | MONDO:0006450 | +| MONDO:0856580 | sporadic burkitt lymphoma | NCIT:C27914 | MONDO:equivalentTo | Sporadic Burkitt Lymphoma | | MONDO:0007243 | +| MONDO:0856582 | poorly differentiated prostate adenocarcinoma | NCIT:C27916 | MONDO:equivalentTo | Poorly Differentiated Prostate Adenocarcinoma | | MONDO:0005082 | +| MONDO:0856592 | metaplastic carcinoma | NCIT:C27949 | MONDO:equivalentTo | Metaplastic Carcinoma | | MONDO:0004993 | +| MONDO:0856593 | squamous cell carcinoma in situ of the nipple | NCIT:C28292 | MONDO:equivalentTo | Squamous Cell Carcinoma In Situ of the Nipple | | MONDO:0003950|MONDO:0004693 | +| MONDO:0856599 | biliary system disorder | NCIT:C2899 | MONDO:equivalentTo | Biliary System Disorder | | | +| MONDO:0856602 | enchondroma | NCIT:C3007 | MONDO:equivalentTo | Enchondroma | | MONDO:0002360|MONDO:0000631 | +| MONDO:0856604 | pancreatic glucagon-producing neuroendocrine tumor | NCIT:C3062 | MONDO:equivalentTo | Pancreatic Glucagon-Producing Neuroendocrine Tumor | | MONDO:0019954 | +| MONDO:0856606 | chronic phase chronic myeloid leukemia, bcr-abl1 positive | NCIT:C3175 | MONDO:equivalentTo | Chronic Phase Chronic Myeloid Leukemia, BCR-ABL1 Positive | | MONDO:0001014|MONDO:0011996 | +| MONDO:0856607 | myeloid leukemia, philadelphia-negative | NCIT:C3176 | MONDO:equivalentTo | Myeloid Leukemia, Philadelphia-Negative | | MONDO:0004643 | +| MONDO:0856608 | neoplasm by site | NCIT:C3263 | MONDO:equivalentTo | Neoplasm by Site | | MONDO:0005070 | +| MONDO:0856610 | osteochondroma | NCIT:C3295 | MONDO:equivalentTo | Osteochondroma | | MONDO:0000631|MONDO:0024470 | +| MONDO:0856611 | extra-adrenal paraganglioma | NCIT:C3309 | MONDO:equivalentTo | Extra-Adrenal Paraganglioma | | MONDO:0000448 | +| MONDO:0856614 | supratentorial neoplasm | NCIT:C3397 | MONDO:equivalentTo | Supratentorial Neoplasm | | MONDO:0021211 | +| MONDO:0856615 | thyroid gland nodule | NCIT:C3415 | MONDO:equivalentTo | Thyroid Gland Nodule | | | +| MONDO:0856638 | grade 3 follicular lymphoma | NCIT:C3460 | MONDO:equivalentTo | Grade 3 Follicular Lymphoma | | MONDO:0018906|MONDO:0017595 | +| MONDO:0856655 | lobular capillary hemangioma | NCIT:C3480 | MONDO:equivalentTo | Lobular Capillary Hemangioma | | MONDO:0002407 | +| MONDO:0856661 | epithelioid cell type gastrointestinal stromal tumor | NCIT:C3486 | MONDO:equivalentTo | Epithelioid Cell Type Gastrointestinal Stromal Tumor | | MONDO:0011719 | +| MONDO:0856691 | uterine corpus degenerated leiomyoma | NCIT:C3511 | MONDO:equivalentTo | Uterine Corpus Degenerated Leiomyoma | | MONDO:0007886 | +| MONDO:0856703 | eyelid vascular disorder | NCIT:C35198 | MONDO:equivalentTo | Eyelid Vascular Disorder | | | +| MONDO:0856706 | placental polyp | NCIT:C3521 | MONDO:equivalentTo | Placental Polyp | | MONDO:0021498|MONDO:0005079 | +| MONDO:0856715 | chondromatosis | NCIT:C35259 | MONDO:equivalentTo | Chondromatosis | | MONDO:0024470 | +| MONDO:0856716 | malignant submandibular gland neoplasm | NCIT:C3526 | MONDO:equivalentTo | Malignant Submandibular Gland Neoplasm | | MONDO:0021244|MONDO:0044743 | +| MONDO:0856723 | malignant palate neoplasm | NCIT:C3530 | MONDO:equivalentTo | Malignant Palate Neoplasm | | MONDO:0005515|MONDO:0005286 | +| MONDO:0856758 | malignant neoplasm of multiple primary sites | NCIT:C35427 | MONDO:equivalentTo | Malignant Neoplasm of Multiple Primary Sites | | MONDO:0004992 | +| MONDO:0856764 | behavioral disorder | NCIT:C35470 | MONDO:equivalentTo | Behavioral Disorder | | | +| MONDO:0856772 | lung kaposi sarcoma | NCIT:C3551 | MONDO:equivalentTo | Lung Kaposi Sarcoma | | MONDO:0002426|MONDO:0005055 | +| MONDO:0856784 | malignant exocervical neoplasm | NCIT:C3554 | MONDO:equivalentTo | Malignant Exocervical Neoplasm | | MONDO:0002974 | +| MONDO:0856786 | malignant uterine corpus neoplasm | NCIT:C3556 | MONDO:equivalentTo | Malignant Uterine Corpus Neoplasm | | MONDO:0021254|MONDO:0002715 | +| MONDO:0856787 | complex endometrial hyperplasia with atypia | NCIT:C35560 | MONDO:equivalentTo | Complex Endometrial Hyperplasia with Atypia | | MONDO:0006169 | +| MONDO:0856810 | mixed tumor of the salivary gland | NCIT:C35691 | MONDO:equivalentTo | Mixed Tumor of the Salivary Gland | | MONDO:0021043|MONDO:0021357 | +| MONDO:0856811 | posterior pharyngeal wall carcinoma | NCIT:C35692 | MONDO:equivalentTo | Posterior Pharyngeal Wall Carcinoma | | MONDO:0021345 | +| MONDO:0856812 | benign uvula neoplasm | NCIT:C35698 | MONDO:equivalentTo | Benign Uvula Neoplasm | | MONDO:0021480 | +| MONDO:0856814 | testicular teratoma with somatic-type malignancy | NCIT:C35711 | MONDO:equivalentTo | Testicular Teratoma with Somatic-Type Malignancy | | MONDO:0003403|MONDO:0006444|MONDO:0018193 | +| MONDO:0856818 | salivary gland lymphoepithelial carcinoma | NCIT:C35736 | MONDO:equivalentTo | Salivary Gland Lymphoepithelial Carcinoma | | MONDO:0000521|MONDO:0003572 | +| MONDO:0856830 | metastatic malignant neoplasm in the bone | NCIT:C3580 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Bone | | MONDO:0002129|MONDO:0024880 | +| MONDO:0856835 | monoblastic sarcoma | NCIT:C35816 | MONDO:equivalentTo | Monoblastic Sarcoma | | MONDO:0006861 | +| MONDO:0856836 | blastic granulocytic sarcoma | NCIT:C35817 | MONDO:equivalentTo | Blastic Granulocytic Sarcoma | | MONDO:0006237 | +| MONDO:0856837 | immature granulocytic sarcoma | NCIT:C35818 | MONDO:equivalentTo | Immature Granulocytic Sarcoma | | MONDO:0006237 | +| MONDO:0856838 | differentiated granulocytic sarcoma | NCIT:C35819 | MONDO:equivalentTo | Differentiated Granulocytic Sarcoma | | MONDO:0006237 | +| MONDO:0856840 | salivary gland cystadenoma | NCIT:C35833 | MONDO:equivalentTo | Salivary Gland Cystadenoma | | MONDO:0021460|MONDO:0036976|MONDO:0002369 | +| MONDO:0856844 | salivary gland ductal papilloma | NCIT:C35839 | MONDO:equivalentTo | Salivary Gland Ductal Papilloma | | MONDO:0002363|MONDO:0021460 | +| MONDO:0856847 | grade 1 clear cell renal cell carcinoma | NCIT:C35851 | MONDO:equivalentTo | Grade 1 Clear Cell Renal Cell Carcinoma | | MONDO:0005005 | +| MONDO:0856848 | grade 2 clear cell renal cell carcinoma | NCIT:C35852 | MONDO:equivalentTo | Grade 2 Clear Cell Renal Cell Carcinoma | | MONDO:0005005 | +| MONDO:0856849 | grade 3 clear cell renal cell carcinoma | NCIT:C35853 | MONDO:equivalentTo | Grade 3 Clear Cell Renal Cell Carcinoma | | MONDO:0005005 | +| MONDO:0856850 | grade 4 clear cell renal cell carcinoma | NCIT:C35854 | MONDO:equivalentTo | Grade 4 Clear Cell Renal Cell Carcinoma | | MONDO:0005005 | +| MONDO:0856855 | endemic african kaposi sarcoma | NCIT:C35874 | MONDO:equivalentTo | Endemic African Kaposi Sarcoma | | MONDO:0005055 | +| MONDO:0856856 | distantly metastatic malignant neoplasm | NCIT:C35933 | MONDO:equivalentTo | Distantly Metastatic Malignant Neoplasm | | MONDO:0024880 | +| MONDO:0856857 | malignant neoplasm by grade | NCIT:C36041 | MONDO:equivalentTo | Malignant Neoplasm by Grade | | MONDO:0004992 | +| MONDO:0856858 | moderately differentiated malignant neoplasm | NCIT:C36049 | MONDO:equivalentTo | Moderately Differentiated Malignant Neoplasm | | MONDO:0004992 | +| MONDO:0856859 | poorly differentiated malignant neoplasm | NCIT:C36050 | MONDO:equivalentTo | Poorly Differentiated Malignant Neoplasm | | MONDO:0004992 | +| MONDO:0856860 | undifferentiated malignant neoplasm | NCIT:C36051 | MONDO:equivalentTo | Undifferentiated Malignant Neoplasm | | MONDO:0004992 | +| MONDO:0856861 | well differentiated malignant neoplasm | NCIT:C36052 | MONDO:equivalentTo | Well Differentiated Malignant Neoplasm | | MONDO:0004992 | +| MONDO:0856862 | acute myeloid leukemia with t(11;17)(q23;q21); zbtb16-rara | NCIT:C36056 | MONDO:equivalentTo | Acute Myeloid Leukemia with t(11;17)(q23;q21); ZBTB16-RARA | | MONDO:0100375 | +| MONDO:0856863 | acute myeloid leukemia with t(5;17)(q35;q21); npm1-rara | NCIT:C36057 | MONDO:equivalentTo | Acute Myeloid Leukemia with t(5;17)(q35;q21); NPM1-RARA | | MONDO:0100375 | +| MONDO:0856864 | acute myeloid leukemia with t(11;17)(q13;q21); numa1-rara | NCIT:C36058 | MONDO:equivalentTo | Acute Myeloid Leukemia with t(11;17)(q13;q21); NUMA1-RARA | | MONDO:0100375 | +| MONDO:0856865 | chronic myelomonocytic leukemia with eosinophilia | NCIT:C36060 | MONDO:equivalentTo | Chronic Myelomonocytic Leukemia with Eosinophilia | | MONDO:0020311 | +| MONDO:0856866 | chronic myelomonocytic leukemia-1 | NCIT:C36061 | MONDO:equivalentTo | Chronic Myelomonocytic Leukemia-1 | | MONDO:0020311 | +| MONDO:0856867 | chronic myelomonocytic leukemia-2 | NCIT:C36062 | MONDO:equivalentTo | Chronic Myelomonocytic Leukemia-2 | | MONDO:0020311 | +| MONDO:0856875 | hereditary male breast carcinoma | NCIT:C36106 | MONDO:equivalentTo | Hereditary Male Breast Carcinoma | | MONDO:0016419|MONDO:0005628 | +| MONDO:0856876 | hereditary female breast carcinoma | NCIT:C36107 | MONDO:equivalentTo | Hereditary Female Breast Carcinoma | | MONDO:0016419|MONDO:0004379 | +| MONDO:0856880 | non-hereditary clear cell renal cell carcinoma | NCIT:C36261 | MONDO:equivalentTo | Non-Hereditary Clear Cell Renal Cell Carcinoma | | MONDO:0005005 | +| MONDO:0856882 | metastatic benign neoplasm | NCIT:C36264 | MONDO:equivalentTo | Metastatic Benign Neoplasm | | MONDO:0005165|MONDO:0024883 | +| MONDO:0856883 | lymphomatous adult t-cell leukemia/lymphoma | NCIT:C36266 | MONDO:equivalentTo | Lymphomatous Adult T-Cell Leukemia/Lymphoma | | MONDO:0019471 | +| MONDO:0856884 | hodgkin-like adult t-cell leukemia/lymphoma | NCIT:C36268 | MONDO:equivalentTo | Hodgkin-Like Adult T-Cell Leukemia/Lymphoma | | MONDO:0019471 | +| MONDO:0856885 | t-cell prolymphocytic leukemia, small cell variant | NCIT:C36270 | MONDO:equivalentTo | T-Cell Prolymphocytic Leukemia, Small Cell Variant | | MONDO:0019468 | +| MONDO:0856886 | t-cell prolymphocytic leukemia, cerebriform cell variant | NCIT:C36271 | MONDO:equivalentTo | T-Cell Prolymphocytic Leukemia, Cerebriform Cell Variant | | MONDO:0019468 | +| MONDO:0856887 | chronic lymphocytic leukemia with plasmacytoid differentiation | NCIT:C36272 | MONDO:equivalentTo | Chronic Lymphocytic Leukemia with Plasmacytoid Differentiation | | MONDO:0004948 | +| MONDO:0856891 | prostate carcinoma metastatic in the bone | NCIT:C36308 | MONDO:equivalentTo | Prostate Carcinoma Metastatic in the Bone | | MONDO:0004956|MONDO:0024884 | +| MONDO:0856897 | oncocytic adenocarcinoma | NCIT:C3679 | MONDO:equivalentTo | Oncocytic Adenocarcinoma | | MONDO:0004970|MONDO:0010795 | +| MONDO:0856898 | sweat gland tubular carcinoma | NCIT:C3682 | MONDO:equivalentTo | Sweat Gland Tubular Carcinoma | | MONDO:0005524|MONDO:0005606 | +| MONDO:0856899 | trabecular adenoma | NCIT:C3688 | MONDO:equivalentTo | Trabecular Adenoma | | MONDO:0004972 | +| MONDO:0856900 | carcinomatosis | NCIT:C3693 | MONDO:equivalentTo | Carcinomatosis | | MONDO:0024879 | +| MONDO:0856901 | papillary fibroelastoma | NCIT:C3695 | MONDO:equivalentTo | Papillary Fibroelastoma | | MONDO:0021505 | +| MONDO:0856902 | meningiomatosis | NCIT:C3707 | MONDO:equivalentTo | Meningiomatosis | | MONDO:0016642 | +| MONDO:0856905 | chronic lymphocytic leukemia with immunoglobulin heavy chain variable-region gene somatic hypermutation | NCIT:C37202 | MONDO:equivalentTo | Chronic Lymphocytic Leukemia with Immunoglobulin Heavy Chain Variable-Region Gene Somatic Hypermutation | | MONDO:0004152|MONDO:0004948 | +| MONDO:0856906 | chronic lymphocytic leukemia with unmutated immunoglobulin heavy chain variable-region gene | NCIT:C37205 | MONDO:equivalentTo | Chronic Lymphocytic Leukemia with Unmutated Immunoglobulin Heavy Chain Variable-Region Gene | | MONDO:0004478|MONDO:0004948 | +| MONDO:0856907 | high grade b-cell lymphoma with blastoid morphologic features | NCIT:C37209 | MONDO:equivalentTo | High Grade B-Cell Lymphoma with Blastoid Morphologic Features | | MONDO:0044889 | +| MONDO:0856911 | benign kidney mixed epithelial and stromal tumor | NCIT:C37264 | MONDO:equivalentTo | Benign Kidney Mixed Epithelial and Stromal Tumor | | MONDO:0002513|MONDO:0002386 | +| MONDO:0856912 | atypical small acinar proliferation of the prostate gland | NCIT:C37268 | MONDO:equivalentTo | Atypical Small Acinar Proliferation of the Prostate Gland | | MONDO:0021259 | +| MONDO:0856914 | head and neck basaloid squamous cell carcinoma | NCIT:C37290 | MONDO:equivalentTo | Head and Neck Basaloid Squamous Cell Carcinoma | | MONDO:0003486|MONDO:0010150 | +| MONDO:0856915 | mixed mesodermal (mullerian) tumor | NCIT:C3730 | MONDO:equivalentTo | Mixed Mesodermal (Mullerian) Tumor | | MONDO:0021148|MONDO:0021043 | +| MONDO:0856917 | abdominal (mesenteric) fibromatosis | NCIT:C3741 | MONDO:equivalentTo | Abdominal (Mesenteric) Fibromatosis | | MONDO:0007608 | +| MONDO:0856918 | adenomatous polyp | NCIT:C3764 | MONDO:equivalentTo | Adenomatous Polyp | | MONDO:0006180|MONDO:0021075 | +| MONDO:0856920 | giant cell carcinoma | NCIT:C3779 | MONDO:equivalentTo | Giant Cell Carcinoma | | MONDO:0005232|MONDO:0002402|MONDO:0005617 | +| MONDO:0856923 | renal cell carcinoma associated with t(x;1)(p11.2;q21) | NCIT:C37872 | MONDO:equivalentTo | Renal Cell Carcinoma Associated with t(X;1)(p11.2;q21) | | MONDO:0006397 | +| MONDO:0856924 | renal cell carcinoma associated with t(x;1)(p11.2;p34) | NCIT:C37874 | MONDO:equivalentTo | Renal Cell Carcinoma Associated with t(X;1)(p11.2;p34) | | MONDO:0006397 | +| MONDO:0856925 | renal cell carcinoma associated with t(x;17)(p11.2;q25) | NCIT:C37876 | MONDO:equivalentTo | Renal Cell Carcinoma Associated with t(X;17)(p11.2;q25) | | MONDO:0006397 | +| MONDO:0856927 | angiofibroma | NCIT:C3799 | MONDO:equivalentTo | Angiofibroma | | MONDO:0005167 | +| MONDO:0856930 | dermatofibrosarcoma protuberans with myoid differentiation | NCIT:C38105 | MONDO:equivalentTo | Dermatofibrosarcoma Protuberans with Myoid Differentiation | | MONDO:0011934 | +| MONDO:0856931 | myxoid dermatofibrosarcoma protuberans | NCIT:C38106 | MONDO:equivalentTo | Myxoid Dermatofibrosarcoma Protuberans | | MONDO:0011934 | +| MONDO:0856932 | dedifferentiated dermatofibrosarcoma protuberans | NCIT:C38107 | MONDO:equivalentTo | Dedifferentiated Dermatofibrosarcoma Protuberans | | MONDO:0011934 | +| MONDO:0856933 | dermatofibrosarcoma protuberans with giant cell fibroblastoma-like differentiation | NCIT:C38108 | MONDO:equivalentTo | Dermatofibrosarcoma Protuberans with Giant Cell Fibroblastoma-Like Differentiation | | MONDO:0011934 | +| MONDO:0856934 | skin basal cell carcinoma with adnexal differentiation | NCIT:C38109 | MONDO:equivalentTo | Skin Basal Cell Carcinoma with Adnexal Differentiation | | MONDO:0005341 | +| MONDO:0856938 | clear cell myomelanocytic tumor of the falciform ligament/ligamentum teres | NCIT:C38154 | MONDO:equivalentTo | Clear Cell Myomelanocytic Tumor of the Falciform Ligament/Ligamentum Teres | | MONDO:0006359 | +| MONDO:0856939 | metachronous malignant neoplasm | NCIT:C38156 | MONDO:equivalentTo | Metachronous Malignant Neoplasm | | MONDO:0004992 | +| MONDO:0856940 | plasmablastic lymphoma of mucosa site | NCIT:C38159 | MONDO:equivalentTo | Plasmablastic Lymphoma of Mucosa Site | | MONDO:0017347 | +| MONDO:0856941 | digestive system non-hodgkin lymphoma | NCIT:C38161 | MONDO:equivalentTo | Digestive System Non-Hodgkin Lymphoma | | MONDO:0004699|MONDO:0018908 | +| MONDO:0856942 | digestive system hodgkin lymphoma | NCIT:C38163 | MONDO:equivalentTo | Digestive System Hodgkin Lymphoma | | MONDO:0004952|MONDO:0004699 | +| MONDO:0856943 | acute myeloid leukemia with stat5b-rara | NCIT:C38377 | MONDO:equivalentTo | Acute Myeloid Leukemia with STAT5B-RARA | | MONDO:0100375 | +| MONDO:0856945 | traditional serrated adenoma | NCIT:C38458 | MONDO:equivalentTo | Traditional Serrated Adenoma | | MONDO:0006180 | +| MONDO:0856947 | benign female breast neoplasm | NCIT:C3848 | MONDO:equivalentTo | Benign Female Breast Neoplasm | | MONDO:0000620 | +| MONDO:0856948 | aggravated malignant neoplasm | NCIT:C3851 | MONDO:equivalentTo | Aggravated Malignant Neoplasm | | MONDO:0004992 | +| MONDO:0856949 | thyroid gland sclerosing mucoepidermoid carcinoma with eosinophilia | NCIT:C38763 | MONDO:equivalentTo | Thyroid Gland Sclerosing Mucoepidermoid Carcinoma with Eosinophilia | | MONDO:0006463 | +| MONDO:0856951 | grade 1 meningioma | NCIT:C38936 | MONDO:equivalentTo | Grade 1 Meningioma | | MONDO:0016642 | +| MONDO:0856952 | compound nevus | NCIT:C3901 | MONDO:equivalentTo | Compound Nevus | | MONDO:0005073 | +| MONDO:0856963 | t-cell large granular lymphocyte leukemia, common variant | NCIT:C39584 | MONDO:equivalentTo | T-Cell Large Granular Lymphocyte Leukemia, Common Variant | | MONDO:0019469 | +| MONDO:0856964 | t-cell large granular lymphocyte leukemia expressing the t-cell receptor gamma-delta | NCIT:C39586 | MONDO:equivalentTo | T-Cell Large Granular Lymphocyte Leukemia Expressing the T-Cell Receptor Gamma-Delta | | MONDO:0019469 | +| MONDO:0856966 | anaplastic large cell lymphoma, giant cell rich subtype | NCIT:C39674 | MONDO:equivalentTo | Anaplastic Large Cell Lymphoma, Giant Cell Rich Subtype | | MONDO:0020325 | +| MONDO:0856967 | anaplastic large cell lymphoma, sarcomatoid subtype | NCIT:C39675 | MONDO:equivalentTo | Anaplastic Large Cell Lymphoma, Sarcomatoid Subtype | | MONDO:0020325 | +| MONDO:0856968 | anaplastic large cell lymphoma, signet ring-like subtype | NCIT:C39676 | MONDO:equivalentTo | Anaplastic Large Cell Lymphoma, Signet Ring-Like Subtype | | MONDO:0020325 | +| MONDO:0856969 | pleomorphic variant mantle cell lymphoma | NCIT:C39747 | MONDO:equivalentTo | Pleomorphic Variant Mantle Cell Lymphoma | | MONDO:0018876 | +| MONDO:0856970 | type ii endometrial adenocarcinoma | NCIT:C39749 | MONDO:equivalentTo | Type II Endometrial Adenocarcinoma | | MONDO:0005461 | +| MONDO:0856971 | glioblastoma, idh-wildtype | NCIT:C39750 | MONDO:equivalentTo | Glioblastoma, IDH-Wildtype | | MONDO:0018177 | +| MONDO:0856972 | secondary glioblastoma | NCIT:C39751 | MONDO:equivalentTo | Secondary Glioblastoma | | MONDO:0018177 | +| MONDO:0856973 | conventional ameloblastoma | NCIT:C39755 | MONDO:equivalentTo | Conventional Ameloblastoma | | MONDO:0017795 | +| MONDO:0856974 | unicystic ameloblastoma | NCIT:C39756 | MONDO:equivalentTo | Unicystic Ameloblastoma | | MONDO:0021077|MONDO:0017795 | +| MONDO:0856975 | renal cell carcinoma with constitutional chromosome 3 translocations | NCIT:C39790 | MONDO:equivalentTo | Renal Cell Carcinoma with Constitutional Chromosome 3 Translocations | | MONDO:0003008 | +| MONDO:0856976 | renal cell carcinoma associated with inv(x)(p11;q12) | NCIT:C39802 | MONDO:equivalentTo | Renal Cell Carcinoma Associated with inv(X)(p11;q12) | | MONDO:0006397 | +| MONDO:0856980 | invasive bladder sarcomatoid urothelial carcinoma with heterologous elements | NCIT:C39825 | MONDO:equivalentTo | Invasive Bladder Sarcomatoid Urothelial Carcinoma with Heterologous Elements | | MONDO:0004278 | +| MONDO:0856981 | invasive bladder sarcomatoid urothelial carcinoma without heterologous elements | NCIT:C39826 | MONDO:equivalentTo | Invasive Bladder Sarcomatoid Urothelial Carcinoma without Heterologous Elements | | MONDO:0004278 | +| MONDO:0856984 | bladder adenocarcinoma, not otherwise specified | NCIT:C39836 | MONDO:equivalentTo | Bladder Adenocarcinoma, Not Otherwise Specified | | MONDO:0002751 | +| MONDO:0856986 | human papillomavirus-related urethral squamous cell carcinoma | NCIT:C39862 | MONDO:equivalentTo | Human Papillomavirus-Related Urethral Squamous Cell Carcinoma | | MONDO:0002764|MONDO:0020657 | +| MONDO:0856987 | bladder mucosa-associated lymphoid tissue lymphoma | NCIT:C39878 | MONDO:equivalentTo | Bladder Mucosa-Associated Lymphoid Tissue Lymphoma | | MONDO:0001381|MONDO:0007650 | +| MONDO:0856988 | prostate acinar adenocarcinoma, atrophic pattern | NCIT:C39880 | MONDO:equivalentTo | Prostate Acinar Adenocarcinoma, Atrophic Pattern | | MONDO:0002493 | +| MONDO:0856989 | prostate acinar pseudohyperplastic adenocarcinoma | NCIT:C39881 | MONDO:equivalentTo | Prostate Acinar Pseudohyperplastic Adenocarcinoma | | MONDO:0002493 | +| MONDO:0856991 | prostatic duct urothelial carcinoma | NCIT:C39901 | MONDO:equivalentTo | Prostatic Duct Urothelial Carcinoma | | MONDO:0002834 | +| MONDO:0856992 | testicular seminoma with syncytiotrophoblastic cells | NCIT:C39919 | MONDO:equivalentTo | Testicular Seminoma with Syncytiotrophoblastic Cells | | MONDO:0003669 | +| MONDO:0856994 | testicular seminoma with high mitotic index | NCIT:C39920 | MONDO:equivalentTo | Testicular Seminoma with High Mitotic Index | | MONDO:0020633|MONDO:0003669 | +| MONDO:0856995 | testicular spermatocytic tumor with sarcoma | NCIT:C39922 | MONDO:equivalentTo | Testicular Spermatocytic Tumor with Sarcoma | | MONDO:0020513 | +| MONDO:0856996 | monodermal testicular teratoma | NCIT:C39936 | MONDO:equivalentTo | Monodermal Testicular Teratoma | | MONDO:0018193 | +| MONDO:0856997 | testicular sertoli cell tumor, lipid rich variant | NCIT:C39943 | MONDO:equivalentTo | Testicular Sertoli Cell Tumor, Lipid Rich Variant | | MONDO:0020813 | +| MONDO:0856998 | testicular large cell calcifying sertoli cell tumor | NCIT:C39944 | MONDO:equivalentTo | Testicular Large Cell Calcifying Sertoli Cell Tumor | | MONDO:0020808 | +| MONDO:0856999 | testicular sclerosing sertoli cell tumor | NCIT:C39945 | MONDO:equivalentTo | Testicular Sclerosing Sertoli Cell Tumor | | MONDO:0020813 | +| MONDO:0857002 | tumor of the thecoma/fibroma group | NCIT:C39950 | MONDO:equivalentTo | Tumor of the Thecoma/Fibroma Group | | MONDO:0006055 | +| MONDO:0857004 | moderately differentiated ovarian sertoli-leydig cell tumor | NCIT:C39968 | MONDO:equivalentTo | Moderately Differentiated Ovarian Sertoli-Leydig Cell Tumor | | MONDO:0036595 | +| MONDO:0857005 | ovarian sertoli-leydig cell tumor with heterologous elements | NCIT:C39970 | MONDO:equivalentTo | Ovarian Sertoli-Leydig Cell Tumor with Heterologous Elements | | MONDO:0036595 | +| MONDO:0857006 | ovarian retiform sertoli-leydig cell tumor | NCIT:C39971 | MONDO:equivalentTo | Ovarian Retiform Sertoli-Leydig Cell Tumor | | MONDO:0036595 | +| MONDO:0857007 | ovarian sertoli-leydig cell tumor with retiform elements | NCIT:C39974 | MONDO:equivalentTo | Ovarian Sertoli-Leydig Cell Tumor with Retiform Elements | | MONDO:0036595 | +| MONDO:0857008 | ovarian stromal-leydig cell tumor | NCIT:C39977 | MONDO:equivalentTo | Ovarian Stromal-Leydig Cell Tumor | | MONDO:0024387|MONDO:0020807 | +| MONDO:0857009 | ovarian sex cord-stromal tumor, not otherwise specified | NCIT:C39978 | MONDO:equivalentTo | Ovarian Sex Cord-Stromal Tumor, Not Otherwise Specified | | MONDO:0021657 | +| MONDO:0857012 | malignant ovarian teratoma | NCIT:C39995 | MONDO:equivalentTo | Malignant Ovarian Teratoma | | MONDO:0018171|MONDO:0003514|MONDO:0003821 | +| MONDO:0857014 | borderline ovarian serous tumor/atypical proliferative ovarian serous tumor with microinvasion | NCIT:C40027 | MONDO:equivalentTo | Borderline Ovarian Serous Tumor/Atypical Proliferative Ovarian Serous Tumor with Microinvasion | | MONDO:0037255 | +| MONDO:0857015 | borderline ovarian serous adenofibroma | NCIT:C40028 | MONDO:equivalentTo | Borderline Ovarian Serous Adenofibroma | | MONDO:0024886|MONDO:0003462|MONDO:0020662 | +| MONDO:0857016 | borderline ovarian mucinous tumor | NCIT:C40036 | MONDO:equivalentTo | Borderline Ovarian Mucinous Tumor | | MONDO:0003756|MONDO:0016093 | +| MONDO:0857017 | ovarian mucinous cystic tumor with mural nodules | NCIT:C40042 | MONDO:equivalentTo | Ovarian Mucinous Cystic Tumor with Mural Nodules | | MONDO:0003756 | +| MONDO:0857018 | ovarian mucinous cystic tumor associated with pseudomyxoma peritonei | NCIT:C40043 | MONDO:equivalentTo | Ovarian Mucinous Cystic Tumor Associated with Pseudomyxoma Peritonei | | MONDO:0003756 | +| MONDO:0857022 | borderline ovarian clear cell tumor | NCIT:C40080 | MONDO:equivalentTo | Borderline Ovarian Clear Cell Tumor | | MONDO:0021144|MONDO:0016093 | +| MONDO:0857025 | fallopian tube serous neoplasm | NCIT:C40102 | MONDO:equivalentTo | Fallopian Tube Serous Neoplasm | | MONDO:0037256|MONDO:0021092 | +| MONDO:0857028 | fallopian tube endometrioid polyp | NCIT:C40115 | MONDO:equivalentTo | Fallopian Tube Endometrioid Polyp | | MONDO:0021075|MONDO:0021576 | +| MONDO:0857029 | fallopian tube metaplastic papillary tumor | NCIT:C40116 | MONDO:equivalentTo | Fallopian Tube Metaplastic Papillary Tumor | | MONDO:0021096|MONDO:0000645|MONDO:0036976 | +| MONDO:0857030 | fallopian tube soft tissue neoplasm | NCIT:C40126 | MONDO:equivalentTo | Fallopian Tube Soft Tissue Neoplasm | | MONDO:0006424|MONDO:0021092 | +| MONDO:0857031 | type i endometrial adenocarcinoma | NCIT:C40145 | MONDO:equivalentTo | Type I Endometrial Adenocarcinoma | | MONDO:0005461 | +| MONDO:0857033 | figo grade 1 endometrial mucinous adenocarcinoma | NCIT:C40149 | MONDO:equivalentTo | FIGO Grade 1 Endometrial Mucinous Adenocarcinoma | | MONDO:0002747 | +| MONDO:0857034 | figo grade 2 endometrial mucinous adenocarcinoma | NCIT:C40150 | MONDO:equivalentTo | FIGO Grade 2 Endometrial Mucinous Adenocarcinoma | | MONDO:0002747 | +| MONDO:0857035 | figo grade 3 endometrial mucinous adenocarcinoma | NCIT:C40151 | MONDO:equivalentTo | FIGO Grade 3 Endometrial Mucinous Adenocarcinoma | | MONDO:0002747 | +| MONDO:0857036 | uterine corpus leiomyoma, mitotically active variant | NCIT:C40162 | MONDO:equivalentTo | Uterine Corpus Leiomyoma, Mitotically Active Variant | | MONDO:0007886 | +| MONDO:0857037 | uterine corpus soft tissue neoplasm | NCIT:C40179 | MONDO:equivalentTo | Uterine Corpus Soft Tissue Neoplasm | | MONDO:0021254|MONDO:0006424 | +| MONDO:0857039 | cervical squamous neoplasm | NCIT:C40195 | MONDO:equivalentTo | Cervical Squamous Neoplasm | | MONDO:0002532|MONDO:0021230 | +| MONDO:0857040 | cervical glandular neoplasm | NCIT:C40210 | MONDO:equivalentTo | Cervical Glandular Neoplasm | | MONDO:0024276|MONDO:0021230 | +| MONDO:0857041 | cervical soft tissue neoplasm | NCIT:C40216 | MONDO:equivalentTo | Cervical Soft Tissue Neoplasm | | MONDO:0006424|MONDO:0021230 | +| MONDO:0857043 | cervical mixed epithelial and mesenchymal neoplasm | NCIT:C40226 | MONDO:equivalentTo | Cervical Mixed Epithelial and Mesenchymal Neoplasm | | MONDO:0021043|MONDO:0021230 | +| MONDO:0857045 | vaginal keratinizing squamous cell carcinoma | NCIT:C40243 | MONDO:equivalentTo | Vaginal Keratinizing Squamous Cell Carcinoma | | MONDO:0005056|MONDO:0006490 | +| MONDO:0857046 | vaginal basaloid squamous cell carcinoma | NCIT:C40245 | MONDO:equivalentTo | Vaginal Basaloid Squamous Cell Carcinoma | | MONDO:0003486|MONDO:0006490 | +| MONDO:0857047 | vaginal endometrioid adenocarcinoma | NCIT:C40251 | MONDO:equivalentTo | Vaginal Endometrioid Adenocarcinoma | | MONDO:0020653|MONDO:0005026 | +| MONDO:0857048 | vaginal mucinous adenocarcinoma | NCIT:C40252 | MONDO:equivalentTo | Vaginal Mucinous Adenocarcinoma | | MONDO:0020653|MONDO:0004957 | +| MONDO:0857049 | vaginal mesonephric adenocarcinoma | NCIT:C40253 | MONDO:equivalentTo | Vaginal Mesonephric Adenocarcinoma | | MONDO:0020653|MONDO:0005613 | +| MONDO:0857050 | vaginal adenosquamous carcinoma | NCIT:C40260 | MONDO:equivalentTo | Vaginal Adenosquamous Carcinoma | | MONDO:0015867|MONDO:0006074 | +| MONDO:0857051 | vaginal adenoid basal carcinoma | NCIT:C40262 | MONDO:equivalentTo | Vaginal Adenoid Basal Carcinoma | | MONDO:0015867 | +| MONDO:0857052 | vaginal undifferentiated carcinoma | NCIT:C40264 | MONDO:equivalentTo | Vaginal Undifferentiated Carcinoma | | MONDO:0015867|MONDO:0005617 | +| MONDO:0857053 | vaginal soft tissue neoplasm | NCIT:C40265 | MONDO:equivalentTo | Vaginal Soft Tissue Neoplasm | | MONDO:0021050|MONDO:0006424 | +| MONDO:0857056 | vaginal mixed epithelial and mesenchymal neoplasm | NCIT:C40274 | MONDO:equivalentTo | Vaginal Mixed Epithelial and Mesenchymal Neoplasm | | MONDO:0021043|MONDO:0021050 | +| MONDO:0857057 | malignant vaginal mixed tumor resembling synovial sarcoma | NCIT:C40279 | MONDO:equivalentTo | Malignant Vaginal Mixed Tumor Resembling Synovial Sarcoma | | MONDO:0037746 | +| MONDO:0857058 | vulvar squamous cell carcinoma with tumor giant cells | NCIT:C40289 | MONDO:equivalentTo | Vulvar Squamous Cell Carcinoma with Tumor Giant Cells | | MONDO:0024609 | +| MONDO:0857059 | vulvar neoplasm of skin appendage origin | NCIT:C40303 | MONDO:equivalentTo | Vulvar Neoplasm of Skin Appendage Origin | | MONDO:0002297|MONDO:0021049 | +| MONDO:0857061 | vulvar soft tissue neoplasm | NCIT:C40316 | MONDO:equivalentTo | Vulvar Soft Tissue Neoplasm | | MONDO:0021049|MONDO:0006424 | +| MONDO:0857062 | superficial angiomyxoma | NCIT:C40323 | MONDO:equivalentTo | Superficial Angiomyxoma | | MONDO:0006086 | +| MONDO:0857067 | vulvar melanocytic neoplasm | NCIT:C40335 | MONDO:equivalentTo | Vulvar Melanocytic Neoplasm | | MONDO:0021143|MONDO:0021049 | +| MONDO:0857071 | breast carcinoma with osteoclast-like stromal giant cells | NCIT:C40349 | MONDO:equivalentTo | Breast Carcinoma with Osteoclast-Like Stromal Giant Cells | | MONDO:0004953 | +| MONDO:0857072 | breast carcinoma with choriocarcinomatous features | NCIT:C40350 | MONDO:equivalentTo | Breast Carcinoma with Choriocarcinomatous Features | | MONDO:0004953 | +| MONDO:0857073 | breast carcinoma with melanotic features | NCIT:C40351 | MONDO:equivalentTo | Breast Carcinoma with Melanotic Features | | MONDO:0004953 | +| MONDO:0857075 | low grade breast adenosquamous carcinoma | NCIT:C40362 | MONDO:equivalentTo | Low Grade Breast Adenosquamous Carcinoma | | MONDO:0003548 | +| MONDO:0857076 | acute myeloid leukemia arising from previous myelodysplastic syndrome | NCIT:C4037 | MONDO:equivalentTo | Acute Myeloid Leukemia Arising from Previous Myelodysplastic Syndrome | | MONDO:0019457 | +| MONDO:0857078 | postradiation breast angiosarcoma | NCIT:C40378 | MONDO:equivalentTo | Postradiation Breast Angiosarcoma | | MONDO:0003024 | +| MONDO:0857080 | salivary gland myoepithelial tumor | NCIT:C40393 | MONDO:equivalentTo | Salivary Gland Myoepithelial Tumor | | MONDO:0002380|MONDO:0021357 | +| MONDO:0857083 | breast soft tissue neoplasm | NCIT:C40406 | MONDO:equivalentTo | Breast Soft Tissue Neoplasm | | MONDO:0006424|MONDO:0021100 | +| MONDO:0857084 | breast pleomorphic adenoma | NCIT:C40408 | MONDO:equivalentTo | Breast Pleomorphic Adenoma | | MONDO:0008401|MONDO:0002058 | +| MONDO:0857089 | ovarian sex cord-stromal tumor associated with peutz-jeghers syndrome | NCIT:C40436 | MONDO:equivalentTo | Ovarian Sex Cord-Stromal Tumor Associated with Peutz-Jeghers Syndrome | | MONDO:0021657 | +| MONDO:0857091 | esophageal polyp | NCIT:C4057 | MONDO:equivalentTo | Esophageal Polyp | | MONDO:0021459|MONDO:0024292 | +| MONDO:0857095 | polycythemia vera, polycythemic phase | NCIT:C41232 | MONDO:equivalentTo | Polycythemia Vera, Polycythemic Phase | | MONDO:0009891 | +| MONDO:0857096 | polycythemia vera, post-polycythemic myelofibrosis phase | NCIT:C41233 | MONDO:equivalentTo | Polycythemia Vera, Post-Polycythemic Myelofibrosis Phase | | MONDO:0009891 | +| MONDO:0857097 | overt primary myelofibrosis | NCIT:C41238 | MONDO:equivalentTo | Overt Primary Myelofibrosis | | MONDO:0009692 | +| MONDO:0857098 | metastatic adenocarcinoma | NCIT:C4124 | MONDO:equivalentTo | Metastatic Adenocarcinoma | | MONDO:0004970|MONDO:0024879 | +| MONDO:0857100 | solid carcinoma | NCIT:C4137 | MONDO:equivalentTo | Solid Carcinoma | | MONDO:0004993 | +| MONDO:0857101 | basophilic adenocarcinoma | NCIT:C4150 | MONDO:equivalentTo | Basophilic Adenocarcinoma | | MONDO:0004970 | +| MONDO:0857102 | juxtaglomerular cell tumor | NCIT:C4162 | MONDO:equivalentTo | Juxtaglomerular Cell Tumor | | MONDO:0002513 | +| MONDO:0857103 | adrenal cortical compact cell adenoma | NCIT:C4163 | MONDO:equivalentTo | Adrenal Cortical Compact Cell Adenoma | | MONDO:0003924 | +| MONDO:0857104 | pigmented adrenal cortical adenoma | NCIT:C4164 | MONDO:equivalentTo | Pigmented Adrenal Cortical Adenoma | | MONDO:0003924 | +| MONDO:0857105 | adrenal cortical clear cell adenoma | NCIT:C4165 | MONDO:equivalentTo | Adrenal Cortical Clear Cell Adenoma | | MONDO:0003924|MONDO:0003426 | +| MONDO:0857106 | adrenal cortical glomerulosa cell adenoma | NCIT:C4166 | MONDO:equivalentTo | Adrenal Cortical Glomerulosa Cell Adenoma | | MONDO:0003924 | +| MONDO:0857107 | adrenal cortical mixed cell adenoma | NCIT:C4167 | MONDO:equivalentTo | Adrenal Cortical Mixed Cell Adenoma | | MONDO:0003421|MONDO:0003924 | +| MONDO:0857109 | papillary serous cystadenoma | NCIT:C4180 | MONDO:equivalentTo | Papillary Serous Cystadenoma | | MONDO:0005177|MONDO:0021091 | +| MONDO:0857110 | serous surface papillary carcinoma | NCIT:C4182 | MONDO:equivalentTo | Serous Surface Papillary Carcinoma | | MONDO:0005278|MONDO:0002512 | +| MONDO:0857111 | papillary mucinous cystadenoma | NCIT:C4184 | MONDO:equivalentTo | Papillary Mucinous Cystadenoma | | MONDO:0021091|MONDO:0006859 | +| MONDO:0857112 | gliomatosis cerebri type i | NCIT:C41842 | MONDO:equivalentTo | Gliomatosis Cerebri Type I | | MONDO:0016683 | +| MONDO:0857113 | gliomatosis cerebri type ii | NCIT:C41843 | MONDO:equivalentTo | Gliomatosis Cerebri Type II | | MONDO:0016683 | +| MONDO:0857115 | thyroid gland medullary carcinoma with amyloid stroma | NCIT:C4193 | MONDO:equivalentTo | Thyroid Gland Medullary Carcinoma with Amyloid Stroma | | MONDO:0015277 | +| MONDO:0857117 | acinar cell neoplasm | NCIT:C4197 | MONDO:equivalentTo | Acinar Cell Neoplasm | | MONDO:0024276 | +| MONDO:0857118 | ovarian luteinized thecoma | NCIT:C4203 | MONDO:equivalentTo | Ovarian Luteinized Thecoma | | MONDO:0037253 | +| MONDO:0857119 | undifferentiated neuroblastoma | NCIT:C42046 | MONDO:equivalentTo | Undifferentiated Neuroblastoma | | MONDO:0005072 | +| MONDO:0857120 | poorly differentiated neuroblastoma | NCIT:C42047 | MONDO:equivalentTo | Poorly Differentiated Neuroblastoma | | MONDO:0005072 | +| MONDO:0857121 | malignant granulosa cell tumor | NCIT:C4205 | MONDO:equivalentTo | Malignant Granulosa Cell Tumor | | MONDO:0006036 | +| MONDO:0857122 | maturing ganglioneuroma | NCIT:C42064 | MONDO:equivalentTo | Maturing Ganglioneuroma | | MONDO:0005033 | +| MONDO:0857123 | mature ganglioneuroma | NCIT:C42065 | MONDO:equivalentTo | Mature Ganglioneuroma | | MONDO:0005033 | +| MONDO:0857125 | ovarian sex cord tumor with annular tubules | NCIT:C4208 | MONDO:equivalentTo | Ovarian Sex Cord Tumor with Annular Tubules | | MONDO:0021657 | +| MONDO:0857126 | well differentiated ovarian sertoli-leydig cell tumor | NCIT:C4209 | MONDO:equivalentTo | Well Differentiated Ovarian Sertoli-Leydig Cell Tumor | | MONDO:0036595 | +| MONDO:0857127 | poorly differentiated ovarian sertoli-leydig cell tumor | NCIT:C4210 | MONDO:equivalentTo | Poorly Differentiated Ovarian Sertoli-Leydig Cell Tumor | | MONDO:0018172|MONDO:0036595 | +| MONDO:0857128 | ovarian steroid cell tumor | NCIT:C4215 | MONDO:equivalentTo | Ovarian Steroid Cell Tumor | | MONDO:0021657 | +| MONDO:0857129 | balloon cell nevus | NCIT:C4226 | MONDO:equivalentTo | Balloon Cell Nevus | | MONDO:0044794 | +| MONDO:0857130 | regressing melanoma | NCIT:C4228 | MONDO:equivalentTo | Regressing Melanoma | | MONDO:0005105 | +| MONDO:0857131 | neuronevus | NCIT:C4229 | MONDO:equivalentTo | Neuronevus | | MONDO:0006813 | +| MONDO:0857132 | junctional nevus | NCIT:C4231 | MONDO:equivalentTo | Junctional Nevus | | MONDO:0005073 | +| MONDO:0857133 | melanoma in junctional nevus | NCIT:C4232 | MONDO:equivalentTo | Melanoma in Junctional Nevus | | MONDO:0005012 | +| MONDO:0857134 | type a spindle cell melanoma | NCIT:C4238 | MONDO:equivalentTo | Type A Spindle Cell Melanoma | | MONDO:0006427 | +| MONDO:0857135 | type b spindle cell melanoma | NCIT:C4239 | MONDO:equivalentTo | Type B Spindle Cell Melanoma | | MONDO:0006427 | +| MONDO:0857136 | melanoma arising in blue nevus | NCIT:C4240 | MONDO:equivalentTo | Melanoma Arising in Blue Nevus | | MONDO:0005012 | +| MONDO:0857137 | cellular blue nevus | NCIT:C4241 | MONDO:equivalentTo | Cellular Blue Nevus | | MONDO:0006680 | +| MONDO:0857138 | fibrolipoma | NCIT:C4249 | MONDO:equivalentTo | Fibrolipoma | | MONDO:0005106 | +| MONDO:0857139 | fibromyxolipoma | NCIT:C4251 | MONDO:equivalentTo | Fibromyxolipoma | | MONDO:0005106 | +| MONDO:0857140 | lipoblastomatosis | NCIT:C4255 | MONDO:equivalentTo | Lipoblastomatosis | | MONDO:0044983 | +| MONDO:0857141 | sporadic retinoblastoma | NCIT:C42596 | MONDO:equivalentTo | Sporadic Retinoblastoma | | MONDO:0008380 | +| MONDO:0857144 | acute myelomonocytic leukemia without abnormal eosinophils | NCIT:C42779 | MONDO:equivalentTo | Acute Myelomonocytic Leukemia without Abnormal Eosinophils | | MONDO:0018871 | +| MONDO:0857145 | pericardial solitary fibrous tumor | NCIT:C4281 | MONDO:equivalentTo | Pericardial Solitary Fibrous Tumor | | MONDO:0016238|MONDO:0021381 | +| MONDO:0857146 | benign hemangiopericytoma | NCIT:C4300 | MONDO:equivalentTo | Benign Hemangiopericytoma | | MONDO:0005094 | +| MONDO:0857147 | benign odontogenic neoplasm | NCIT:C4306 | MONDO:equivalentTo | Benign Odontogenic Neoplasm | | MONDO:0021445|MONDO:0021192 | +| MONDO:0857152 | pure cutaneous mastocytosis | NCIT:C43277 | MONDO:equivalentTo | Pure Cutaneous Mastocytosis | | MONDO:0019023 | +| MONDO:0857155 | germinative follicular epithelium neoplasm | NCIT:C43311 | MONDO:equivalentTo | Germinative Follicular Epithelium Neoplasm | | MONDO:0003413|MONDO:0021634 | +| MONDO:0857156 | adamantinoid trichoblastoma | NCIT:C43312 | MONDO:equivalentTo | Adamantinoid Trichoblastoma | | MONDO:0020593 | +| MONDO:0857160 | outer hair sheath and infundibulum neoplasm | NCIT:C43324 | MONDO:equivalentTo | Outer Hair Sheath and Infundibulum Neoplasm | | MONDO:0003413 | +| MONDO:0857163 | superficial epithelioma with sebaceous differentiation | NCIT:C43334 | MONDO:equivalentTo | Superficial Epithelioma with Sebaceous Differentiation | | MONDO:0021490 | +| MONDO:0857164 | sebaceoma | NCIT:C43336 | MONDO:equivalentTo | Sebaceoma | | MONDO:0021490 | +| MONDO:0857165 | extraocular cutaneous sebaceous carcinoma | NCIT:C43341 | MONDO:equivalentTo | Extraocular Cutaneous Sebaceous Carcinoma | | MONDO:0006962 | +| MONDO:0857166 | apocrine hidrocystoma | NCIT:C43342 | MONDO:equivalentTo | Apocrine Hidrocystoma | | MONDO:0002804|MONDO:0006787 | +| MONDO:0857167 | cylindrocarcinoma | NCIT:C43344 | MONDO:equivalentTo | Cylindrocarcinoma | | MONDO:0005524|MONDO:0024878 | +| MONDO:0857168 | ductal eccrine carcinoma with spindle cell elements | NCIT:C43346 | MONDO:equivalentTo | Ductal Eccrine Carcinoma with Spindle Cell Elements | | MONDO:0024245 | +| MONDO:0857169 | squamoid eccrine ductal carcinoma | NCIT:C43347 | MONDO:equivalentTo | Squamoid Eccrine Ductal Carcinoma | | MONDO:0024245 | +| MONDO:0857170 | ductal eccrine carcinoma with abundant fibromyxoid stroma | NCIT:C43349 | MONDO:equivalentTo | Ductal Eccrine Carcinoma with Abundant Fibromyxoid Stroma | | MONDO:0024245 | +| MONDO:0857171 | sporadic cylindroma | NCIT:C43351 | MONDO:equivalentTo | Sporadic Cylindroma | | MONDO:0021812 | +| MONDO:0857172 | classic poroma | NCIT:C43353 | MONDO:equivalentTo | Classic Poroma | | MONDO:0006738 | +| MONDO:0857173 | porocarcinoma in situ | NCIT:C43354 | MONDO:equivalentTo | Porocarcinoma In Situ | | MONDO:0006189 | +| MONDO:0857174 | aleukemic lymphoid leukemia | NCIT:C4343 | MONDO:equivalentTo | Aleukemic Lymphoid Leukemia | | MONDO:0005402|MONDO:0003730 | +| MONDO:0857175 | sporadic gastric adenocarcinoma | NCIT:C43527 | MONDO:equivalentTo | Sporadic Gastric Adenocarcinoma | | MONDO:0005036 | +| MONDO:0857177 | small intestinal adenosquamous carcinoma | NCIT:C43535 | MONDO:equivalentTo | Small Intestinal Adenosquamous Carcinoma | | MONDO:0005522|MONDO:0006074 | +| MONDO:0857178 | small intestinal mucinous adenocarcinoma | NCIT:C43536 | MONDO:equivalentTo | Small Intestinal Mucinous Adenocarcinoma | | MONDO:0003198|MONDO:0004957 | +| MONDO:0857179 | small intestinal medullary carcinoma | NCIT:C43537 | MONDO:equivalentTo | Small Intestinal Medullary Carcinoma | | MONDO:0005522 | +| MONDO:0857180 | small intestinal undifferentiated carcinoma | NCIT:C43538 | MONDO:equivalentTo | Small Intestinal Undifferentiated Carcinoma | | MONDO:0005522|MONDO:0005617 | +| MONDO:0857181 | pituitary neuroendocrine tumor/microadenoma | NCIT:C43541 | MONDO:equivalentTo | Pituitary Neuroendocrine Tumor/Microadenoma | | MONDO:0006373 | +| MONDO:0857182 | pituitary neuroendocrine tumor/macroadenoma | NCIT:C43542 | MONDO:equivalentTo | Pituitary Neuroendocrine Tumor/Macroadenoma | | MONDO:0006373 | +| MONDO:0857183 | small intestinal signet ring cell carcinoma | NCIT:C43543 | MONDO:equivalentTo | Small Intestinal Signet Ring Cell Carcinoma | | MONDO:0003198|MONDO:0005092 | +| MONDO:0857184 | appendix tubular adenoma | NCIT:C43546 | MONDO:equivalentTo | Appendix Tubular Adenoma | | MONDO:0006088|MONDO:0024660 | +| MONDO:0857185 | appendix tubulovillous adenoma | NCIT:C43547 | MONDO:equivalentTo | Appendix Tubulovillous Adenoma | | MONDO:0006088|MONDO:0024661 | +| MONDO:0857187 | eyelid squamous papilloma | NCIT:C4355 | MONDO:equivalentTo | Eyelid Squamous Papilloma | | MONDO:0021275|MONDO:0001825 | +| MONDO:0857188 | small intestinal villous adenoma | NCIT:C43551 | MONDO:equivalentTo | Small Intestinal Villous Adenoma | | MONDO:0000502|MONDO:0021303 | +| MONDO:0857189 | appendix signet ring cell carcinoma | NCIT:C43554 | MONDO:equivalentTo | Appendix Signet Ring Cell Carcinoma | | MONDO:0006087|MONDO:0005092 | +| MONDO:0857190 | appendix undifferentiated carcinoma | NCIT:C43556 | MONDO:equivalentTo | Appendix Undifferentiated Carcinoma | | MONDO:0003196|MONDO:0005617 | +| MONDO:0857191 | appendix mixed adenoneuroendocrine carcinoma | NCIT:C43564 | MONDO:equivalentTo | Appendix Mixed Adenoneuroendocrine Carcinoma | | MONDO:0006182|MONDO:0003196 | +| MONDO:0857192 | appendix tubular carcinoid | NCIT:C43565 | MONDO:equivalentTo | Appendix Tubular Carcinoid | | MONDO:0015066 | +| MONDO:0857194 | rectosigmoid adenocarcinoma | NCIT:C43584 | MONDO:equivalentTo | Rectosigmoid Adenocarcinoma | | MONDO:0002424|MONDO:0005008 | +| MONDO:0857195 | colorectal mucinous adenocarcinoma | NCIT:C43585 | MONDO:equivalentTo | Colorectal Mucinous Adenocarcinoma | | MONDO:0005008|MONDO:0004957 | +| MONDO:0857196 | colorectal undifferentiated carcinoma | NCIT:C43591 | MONDO:equivalentTo | Colorectal Undifferentiated Carcinoma | | MONDO:0005617|MONDO:0024331 | +| MONDO:0857198 | gallbladder adenocarcinoma, intestinal-type | NCIT:C43604 | MONDO:equivalentTo | Gallbladder Adenocarcinoma, Intestinal-Type | | MONDO:0006215|MONDO:0006254 | +| MONDO:0857199 | gallbladder clear cell adenocarcinoma | NCIT:C43605 | MONDO:equivalentTo | Gallbladder Clear Cell Adenocarcinoma | | MONDO:0006215|MONDO:0005004 | +| MONDO:0857200 | gallbladder flat biliary intraepithelial neoplasia | NCIT:C43607 | MONDO:equivalentTo | Gallbladder Flat Biliary Intraepithelial Neoplasia | | MONDO:0006218 | +| MONDO:0857201 | gallbladder papillary biliary intraepithelial neoplasia | NCIT:C43609 | MONDO:equivalentTo | Gallbladder Papillary Biliary Intraepithelial Neoplasia | | MONDO:0006218 | +| MONDO:0857202 | pleomorphic hepatocellular carcinoma | NCIT:C43625 | MONDO:equivalentTo | Pleomorphic Hepatocellular Carcinoma | | MONDO:0007256 | +| MONDO:0857203 | sarcomatoid hepatocellular carcinoma | NCIT:C43627 | MONDO:equivalentTo | Sarcomatoid Hepatocellular Carcinoma | | MONDO:0007256 | +| MONDO:0857206 | accessory urethral gland neoplasm | NCIT:C4378 | MONDO:equivalentTo | Accessory Urethral Gland Neoplasm | | MONDO:0021239 | +| MONDO:0857208 | clear cell intrahepatic cholangiocarcinoma | NCIT:C43848 | MONDO:equivalentTo | Clear Cell Intrahepatic Cholangiocarcinoma | | MONDO:0005004|MONDO:0003210 | +| MONDO:0857210 | anogenital papillomaviral intraepithelial neoplasia | NCIT:C4394 | MONDO:equivalentTo | Anogenital Papillomaviral Intraepithelial Neoplasia | | MONDO:0024475 | +| MONDO:0857211 | posterior tongue neoplasm | NCIT:C4400 | MONDO:equivalentTo | Posterior Tongue Neoplasm | | MONDO:0021240 | +| MONDO:0857212 | pyriform fossa neoplasm | NCIT:C4424 | MONDO:equivalentTo | Pyriform Fossa Neoplasm | | MONDO:0021358 | +| MONDO:0857213 | gastric pylorus carcinoma in situ ajcc v6 and v7 | NCIT:C4431 | MONDO:equivalentTo | Gastric Pylorus Carcinoma In Situ AJCC v6 and v7 | | MONDO:0004716|MONDO:0003971 | +| MONDO:0857215 | lung epithelioid hemangioendothelioma | NCIT:C4453 | MONDO:equivalentTo | Lung Epithelioid Hemangioendothelioma | | MONDO:0008903|MONDO:0015523 | +| MONDO:0857216 | dermal duct tumor | NCIT:C4473 | MONDO:equivalentTo | Dermal Duct Tumor | | MONDO:0006738 | +| MONDO:0857217 | cutaneous neural neoplasm | NCIT:C4479 | MONDO:equivalentTo | Cutaneous Neural Neoplasm | | MONDO:0002300|MONDO:0001406 | +| MONDO:0857219 | malignant skin hemangiopericytoma | NCIT:C4493 | MONDO:equivalentTo | Malignant Skin Hemangiopericytoma | | MONDO:0021424|MONDO:0009330 | +| MONDO:0857220 | cockade nevus | NCIT:C4495 | MONDO:equivalentTo | Cockade Nevus | | MONDO:0044794 | +| MONDO:0857222 | common blue nevus | NCIT:C4496 | MONDO:equivalentTo | Common Blue Nevus | | MONDO:0006680 | +| MONDO:0857223 | nevus spilus | NCIT:C4498 | MONDO:equivalentTo | Nevus Spilus | | MONDO:0044792 | +| MONDO:0857224 | benign ovarian epithelial tumor | NCIT:C4510 | MONDO:equivalentTo | Benign Ovarian Epithelial Tumor | | MONDO:0002229|MONDO:0036976|MONDO:0000646 | +| MONDO:0857229 | classical low grade fibromyxoid sarcoma | NCIT:C45210 | MONDO:equivalentTo | Classical Low Grade Fibromyxoid Sarcoma | | MONDO:0006272 | +| MONDO:0857233 | cutaneous hematopoietic and lymphoid cell neoplasm | NCIT:C45240 | MONDO:equivalentTo | Cutaneous Hematopoietic and Lymphoid Cell Neoplasm | | MONDO:0002531|MONDO:0044881 | +| MONDO:0857240 | lacrimal gland pleomorphic adenoma | NCIT:C4542 | MONDO:equivalentTo | Lacrimal Gland Pleomorphic Adenoma | | MONDO:0008401|MONDO:0021488 | +| MONDO:0857244 | orbit capillary hemangioma | NCIT:C4545 | MONDO:equivalentTo | Orbit Capillary Hemangioma | | MONDO:0002407|MONDO:0001974 | +| MONDO:0857245 | orbit hemangiopericytoma | NCIT:C4547 | MONDO:equivalentTo | Orbit Hemangiopericytoma | | MONDO:0005094 | +| MONDO:0857247 | lymphangioma circumscriptum | NCIT:C45485 | MONDO:equivalentTo | Lymphangioma Circumscriptum | | MONDO:0002013 | +| MONDO:0857248 | lung squamous cell carcinoma, papillary variant | NCIT:C45502 | MONDO:equivalentTo | Lung Squamous Cell Carcinoma, Papillary Variant | | MONDO:0005056|MONDO:0002979|MONDO:0056806 | +| MONDO:0857249 | lung squamous cell carcinoma, clear cell variant | NCIT:C45503 | MONDO:equivalentTo | Lung Squamous Cell Carcinoma, Clear Cell Variant | | MONDO:0005056|MONDO:0056806 | +| MONDO:0857250 | lung squamous cell carcinoma, small cell variant | NCIT:C45504 | MONDO:equivalentTo | Lung Squamous Cell Carcinoma, Small Cell Variant | | MONDO:0005056|MONDO:0005097 | +| MONDO:0857251 | lung basaloid squamous cell carcinoma | NCIT:C45507 | MONDO:equivalentTo | Lung Basaloid Squamous Cell Carcinoma | | MONDO:0003486|MONDO:0005056|MONDO:0005097 | +| MONDO:0857252 | lung spindle cell carcinoma | NCIT:C45541 | MONDO:equivalentTo | Lung Spindle Cell Carcinoma | | MONDO:0006279 | +| MONDO:0857253 | lung pleomorphic carcinoma | NCIT:C45542 | MONDO:equivalentTo | Lung Pleomorphic Carcinoma | | MONDO:0006279|MONDO:0003573 | +| MONDO:0857254 | lung carcinosarcoma | NCIT:C45543 | MONDO:equivalentTo | Lung Carcinosarcoma | | MONDO:0006279|MONDO:0002928 | +| MONDO:0857256 | lung neuroendocrine tumor g2 | NCIT:C45551 | MONDO:equivalentTo | Lung Neuroendocrine Tumor G2 | | MONDO:0006041|MONDO:0006095 | +| MONDO:0857259 | ciliary body malignant medulloepithelioma | NCIT:C4557 | MONDO:equivalentTo | Ciliary Body Malignant Medulloepithelioma | | MONDO:0017050|MONDO:0002969 | +| MONDO:0857260 | lung squamous papilloma | NCIT:C45573 | MONDO:equivalentTo | Lung Squamous Papilloma | | MONDO:0006278|MONDO:0001825 | +| MONDO:0857262 | bronchial glandular papilloma | NCIT:C45601 | MONDO:equivalentTo | Bronchial Glandular Papilloma | | MONDO:0006278|MONDO:0021078 | +| MONDO:0857263 | bronchial mixed squamous cell and glandular papilloma | NCIT:C45602 | MONDO:equivalentTo | Bronchial Mixed Squamous Cell and Glandular Papilloma | | MONDO:0021043|MONDO:0006278 | +| MONDO:0857264 | lung pleomorphic adenoma | NCIT:C45603 | MONDO:equivalentTo | Lung Pleomorphic Adenoma | | MONDO:0008401|MONDO:0003422 | +| MONDO:0857265 | lung mucinous cystadenoma | NCIT:C45604 | MONDO:equivalentTo | Lung Mucinous Cystadenoma | | MONDO:0003422|MONDO:0006859 | +| MONDO:0857267 | lung soft tissue neoplasm | NCIT:C45612 | MONDO:equivalentTo | Lung Soft Tissue Neoplasm | | MONDO:0006424|MONDO:0021117 | +| MONDO:0857268 | malignant lung and pleural neoplasm | NCIT:C45625 | MONDO:equivalentTo | Malignant Lung and Pleural Neoplasm | | MONDO:0003274 | +| MONDO:0857270 | lung synovial sarcoma | NCIT:C45631 | MONDO:equivalentTo | Lung Synovial Sarcoma | | MONDO:0002426|MONDO:0010434 | +| MONDO:0857273 | intrapulmonary thymoma | NCIT:C45638 | MONDO:equivalentTo | Intrapulmonary Thymoma | | MONDO:0006456|MONDO:0021117 | +| MONDO:0857274 | mediastinal thymoma | NCIT:C45639 | MONDO:equivalentTo | Mediastinal Thymoma | | MONDO:0006456|MONDO:0021386 | +| MONDO:0857275 | lung melanoma | NCIT:C45652 | MONDO:equivalentTo | Lung Melanoma | | MONDO:0006320|MONDO:0008903 | +| MONDO:0857276 | pleural well differentiated papillary mesothelial tumor | NCIT:C45660 | MONDO:equivalentTo | Pleural Well Differentiated Papillary Mesothelial Tumor | | MONDO:0003308|MONDO:0003688 | +| MONDO:0857278 | pleural lymphoma | NCIT:C45687 | MONDO:equivalentTo | Pleural Lymphoma | | MONDO:0017207|MONDO:0006294 | +| MONDO:0857279 | pleural epithelioid hemangioendothelioma | NCIT:C45695 | MONDO:equivalentTo | Pleural Epithelioid Hemangioendothelioma | | MONDO:0015523|MONDO:0006294 | +| MONDO:0857280 | pleural synovial sarcoma | NCIT:C45696 | MONDO:equivalentTo | Pleural Synovial Sarcoma | | MONDO:0006294|MONDO:0010434 | +| MONDO:0857282 | micronodular thymoma with lymphoid stroma | NCIT:C45706 | MONDO:equivalentTo | Micronodular Thymoma with Lymphoid Stroma | | MONDO:0006456 | +| MONDO:0857283 | metaplastic thymoma | NCIT:C45707 | MONDO:equivalentTo | Metaplastic Thymoma | | MONDO:0006456 | +| MONDO:0857284 | microscopic thymoma | NCIT:C45708 | MONDO:equivalentTo | Microscopic Thymoma | | MONDO:0006456 | +| MONDO:0857285 | sclerosing thymoma | NCIT:C45709 | MONDO:equivalentTo | Sclerosing Thymoma | | MONDO:0006456 | +| MONDO:0857286 | malignant respiratory system neoplasm | NCIT:C4571 | MONDO:equivalentTo | Malignant Respiratory System Neoplasm | | MONDO:0020641|MONDO:0004992 | +| MONDO:0857287 | thymus lipofibroadenoma | NCIT:C45710 | MONDO:equivalentTo | Thymus Lipofibroadenoma | | MONDO:0021512 | +| MONDO:0857289 | combined thymic epithelial neoplasm | NCIT:C45722 | MONDO:equivalentTo | Combined Thymic Epithelial Neoplasm | | MONDO:0018079|MONDO:0002586 | +| MONDO:0857290 | malignant skin appendage neoplasm | NCIT:C4573 | MONDO:equivalentTo | Malignant Skin Appendage Neoplasm | | MONDO:0002297|MONDO:0002898 | +| MONDO:0857291 | mediastinal germ cell tumor with somatic-type malignancy | NCIT:C45732 | MONDO:equivalentTo | Mediastinal Germ Cell Tumor with Somatic-Type Malignancy | | MONDO:0006298 | +| MONDO:0857292 | mediastinal t lymphoblastic leukemia/lymphoma | NCIT:C45738 | MONDO:equivalentTo | Mediastinal T Lymphoblastic Leukemia/Lymphoma | | MONDO:0003537|MONDO:0005843 | +| MONDO:0857294 | mediastinal myeloid sarcoma | NCIT:C45741 | MONDO:equivalentTo | Mediastinal Myeloid Sarcoma | | MONDO:0005843|MONDO:0006861 | +| MONDO:0857295 | mediastinal paraganglioma | NCIT:C45743 | MONDO:equivalentTo | Mediastinal Paraganglioma | | MONDO:0003098|MONDO:0021052 | +| MONDO:0857296 | mediastinal solitary fibrous tumor | NCIT:C45744 | MONDO:equivalentTo | Mediastinal Solitary Fibrous Tumor | | MONDO:0016238|MONDO:0003512 | +| MONDO:0857297 | adult cardiac cellular rhabdomyoma | NCIT:C45747 | MONDO:equivalentTo | Adult Cardiac Cellular Rhabdomyoma | | MONDO:0006123 | +| MONDO:0857298 | cardiac hemangioma | NCIT:C45749 | MONDO:equivalentTo | Cardiac Hemangioma | | MONDO:0021450|MONDO:0006500 | +| MONDO:0857300 | cardiac inflammatory myofibroblastic tumor | NCIT:C45753 | MONDO:equivalentTo | Cardiac Inflammatory Myofibroblastic Tumor | | MONDO:0015798|MONDO:0021209 | +| MONDO:0857301 | cystic tumor of the atrioventricular node | NCIT:C45754 | MONDO:equivalentTo | Cystic Tumor of the Atrioventricular Node | | MONDO:0021450 | +| MONDO:0857302 | cardiac undifferentiated pleomorphic sarcoma | NCIT:C45755 | MONDO:equivalentTo | Cardiac Undifferentiated Pleomorphic Sarcoma | | MONDO:0003354|MONDO:0002142 | +| MONDO:0857303 | cardiac synovial sarcoma | NCIT:C45756 | MONDO:equivalentTo | Cardiac Synovial Sarcoma | | MONDO:0003354|MONDO:0010434 | +| MONDO:0857305 | cardiac rhabdomyosarcoma | NCIT:C45759 | MONDO:equivalentTo | Cardiac Rhabdomyosarcoma | | MONDO:0003354|MONDO:0005212 | +| MONDO:0857306 | pericardial germ cell tumor | NCIT:C45761 | MONDO:equivalentTo | Pericardial Germ Cell Tumor | | MONDO:0021381|MONDO:0018201 | +| MONDO:0857308 | corneal kaposi sarcoma | NCIT:C4579 | MONDO:equivalentTo | Corneal Kaposi Sarcoma | | MONDO:0005055|MONDO:0003802 | +| MONDO:0857310 | metastatic malignant neoplasm in the bone marrow | NCIT:C4582 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Bone Marrow | | MONDO:0024880|MONDO:0021138 | +| MONDO:0857311 | pancreatic neuroendocrine microtumor | NCIT:C45834 | MONDO:equivalentTo | Pancreatic Neuroendocrine Microtumor | | MONDO:0004334 | +| MONDO:0857315 | sellar gangliocytoma | NCIT:C45917 | MONDO:equivalentTo | Sellar Gangliocytoma | | MONDO:0016730|MONDO:0002720 | +| MONDO:0857316 | hypothalamic gangliocytoma | NCIT:C45918 | MONDO:equivalentTo | Hypothalamic Gangliocytoma | | MONDO:0016730|MONDO:0006799 | +| MONDO:0857317 | anterior pituitary gland neoplasm | NCIT:C45921 | MONDO:equivalentTo | Anterior Pituitary Gland Neoplasm | | MONDO:0017611 | +| MONDO:0857319 | densely granulated somatotroph pituitary neuroendocrine tumor | NCIT:C45925 | MONDO:equivalentTo | Densely Granulated Somatotroph Pituitary Neuroendocrine Tumor | | MONDO:0006238 | +| MONDO:0857320 | sparsely granulated somatotroph pituitary neuroendocrine tumor | NCIT:C45926 | MONDO:equivalentTo | Sparsely Granulated Somatotroph Pituitary Neuroendocrine Tumor | | MONDO:0006238 | +| MONDO:0857321 | densely granulated lactotroph pituitary neuroendocrine tumor | NCIT:C45931 | MONDO:equivalentTo | Densely Granulated Lactotroph Pituitary Neuroendocrine Tumor | | MONDO:0010911 | +| MONDO:0857322 | sparsely granulated lactotroph pituitary neuroendocrine tumor | NCIT:C45932 | MONDO:equivalentTo | Sparsely Granulated Lactotroph Pituitary Neuroendocrine Tumor | | MONDO:0010911 | +| MONDO:0857324 | benign palate neoplasm | NCIT:C4599 | MONDO:equivalentTo | Benign Palate Neoplasm | | MONDO:0005286 | +| MONDO:0857325 | thyroid gland oncocytic neoplasm | NCIT:C46068 | MONDO:equivalentTo | Thyroid Gland Oncocytic Neoplasm | | MONDO:0015074|MONDO:0010795 | +| MONDO:0857326 | unilateral breast carcinoma | NCIT:C46073 | MONDO:equivalentTo | Unilateral Breast Carcinoma | | MONDO:0004989 | +| MONDO:0857327 | nonestrogen-dependent malignant neoplasm | NCIT:C46080 | MONDO:equivalentTo | Nonestrogen-Dependent Malignant Neoplasm | | MONDO:0004992 | +| MONDO:0857330 | macrofollicular variant thyroid gland papillary carcinoma | NCIT:C46092 | MONDO:equivalentTo | Macrofollicular Variant Thyroid Gland Papillary Carcinoma | | MONDO:0005075 | +| MONDO:0857331 | clear cell variant thyroid gland papillary carcinoma | NCIT:C46094 | MONDO:equivalentTo | Clear Cell Variant Thyroid Gland Papillary Carcinoma | | MONDO:0005075|MONDO:0005004 | +| MONDO:0857333 | thyroid gland follicular carcinoma, clear cell variant | NCIT:C46096 | MONDO:equivalentTo | Thyroid Gland Follicular Carcinoma, Clear Cell Variant | | MONDO:0005034|MONDO:0005004 | +| MONDO:0857334 | sporadic thyroid gland medullary carcinoma | NCIT:C46098 | MONDO:equivalentTo | Sporadic Thyroid Gland Medullary Carcinoma | | MONDO:0015277 | +| MONDO:0857336 | thyroid gland mixed medullary and follicular cell-derived carcinoma | NCIT:C46104 | MONDO:equivalentTo | Thyroid Gland Mixed Medullary and Follicular Cell-Derived Carcinoma | | MONDO:0015075|MONDO:0021069 | +| MONDO:0857337 | intrathyroid thymic carcinoma | NCIT:C46106 | MONDO:equivalentTo | Intrathyroid Thymic Carcinoma | | MONDO:0015075 | +| MONDO:0857338 | thyroid gland follicular adenoma with papillary hyperplasia | NCIT:C46111 | MONDO:equivalentTo | Thyroid Gland Follicular Adenoma with Papillary Hyperplasia | | MONDO:0002533|MONDO:0005032 | +| MONDO:0857339 | thyroid gland signet ring cell follicular adenoma | NCIT:C46115 | MONDO:equivalentTo | Thyroid Gland Signet Ring Cell Follicular Adenoma | | MONDO:0005032 | +| MONDO:0857340 | thyroid gland mucinous follicular adenoma | NCIT:C46116 | MONDO:equivalentTo | Thyroid Gland Mucinous Follicular Adenoma | | MONDO:0005032 | +| MONDO:0857341 | thyroid gland lipoadenoma | NCIT:C46118 | MONDO:equivalentTo | Thyroid Gland Lipoadenoma | | MONDO:0003431|MONDO:0005032 | +| MONDO:0857342 | thyroid gland clear cell follicular adenoma | NCIT:C46119 | MONDO:equivalentTo | Thyroid Gland Clear Cell Follicular Adenoma | | MONDO:0003426|MONDO:0005032 | +| MONDO:0857343 | thyroid gland hyperfunctioning adenoma | NCIT:C46122 | MONDO:equivalentTo | Thyroid Gland Hyperfunctioning Adenoma | | MONDO:0005032 | +| MONDO:0857345 | thyroid gland paraganglioma | NCIT:C46125 | MONDO:equivalentTo | Thyroid Gland Paraganglioma | | MONDO:0006239|MONDO:0015074 | +| MONDO:0857346 | benign skin appendage neoplasm | NCIT:C4615 | MONDO:equivalentTo | Benign Skin Appendage Neoplasm | | MONDO:0002297|MONDO:0021440 | +| MONDO:0857349 | pineal region germ cell tumor | NCIT:C4659 | MONDO:equivalentTo | Pineal Region Germ Cell Tumor | | MONDO:0003000|MONDO:0021232 | +| MONDO:0857356 | adenocarcinoma with metaplasia | NCIT:C4712 | MONDO:equivalentTo | Adenocarcinoma with Metaplasia | | MONDO:0004970 | +| MONDO:0857357 | atypical meningioma | NCIT:C4723 | MONDO:equivalentTo | Atypical Meningioma | | MONDO:0045056 | +| MONDO:0857358 | neoplasm by morphology | NCIT:C4741 | MONDO:equivalentTo | Neoplasm by Morphology | | MONDO:0005070 | +| MONDO:0857359 | benign squamous cell neoplasm | NCIT:C4742 | MONDO:equivalentTo | Benign Squamous Cell Neoplasm | | MONDO:0036976|MONDO:0002532 | +| MONDO:0857360 | skin cavernous hemangioma | NCIT:C4750 | MONDO:equivalentTo | Skin Cavernous Hemangioma | | MONDO:0003110|MONDO:0003155 | +| MONDO:0857361 | malignant olfactory nerve neoplasm | NCIT:C4768 | MONDO:equivalentTo | Malignant Olfactory Nerve Neoplasm | | MONDO:0002722|MONDO:0002433 | +| MONDO:0857362 | benign extrahepatic bile duct neoplasm | NCIT:C4776 | MONDO:equivalentTo | Benign Extrahepatic Bile Duct Neoplasm | | MONDO:0000385|MONDO:0021385 | +| MONDO:0857363 | breast carcinoma with chondroid metaplasia | NCIT:C47847 | MONDO:equivalentTo | Breast Carcinoma with Chondroid Metaplasia | | MONDO:0004274 | +| MONDO:0857364 | breast carcinoma with osseous metaplasia | NCIT:C47848 | MONDO:equivalentTo | Breast Carcinoma with Osseous Metaplasia | | MONDO:0004274 | +| MONDO:0857365 | breast paget disease without invasive carcinoma | NCIT:C47858 | MONDO:equivalentTo | Breast Paget Disease without Invasive Carcinoma | | MONDO:0002648 | +| MONDO:0857366 | breast hyperplasia | NCIT:C4804 | MONDO:equivalentTo | Breast Hyperplasia | | MONDO:0005043|MONDO:0021100 | +| MONDO:0857367 | malignant odontogenic neoplasm | NCIT:C4812 | MONDO:equivalentTo | Malignant Odontogenic Neoplasm | | MONDO:0021192|MONDO:0005515 | +| MONDO:0857369 | tongue carcinoma | NCIT:C4824 | MONDO:equivalentTo | Tongue Carcinoma | | MONDO:0004631|MONDO:0044925 | +| MONDO:0857370 | parathyroid gland lipoadenoma | NCIT:C48283 | MONDO:equivalentTo | Parathyroid Gland Lipoadenoma | | MONDO:0003431|MONDO:0006890 | +| MONDO:0857371 | atypical parathyroid gland tumor | NCIT:C48285 | MONDO:equivalentTo | Atypical Parathyroid Gland Tumor | | MONDO:0021360 | +| MONDO:0857375 | non-metastatic paraganglioma | NCIT:C48314 | MONDO:equivalentTo | Non-Metastatic Paraganglioma | | MONDO:0000448 | +| MONDO:0857376 | nasopharyngeal paraganglioma | NCIT:C48316 | MONDO:equivalentTo | Nasopharyngeal Paraganglioma | | MONDO:0006239|MONDO:0005375 | +| MONDO:0857377 | primary bone osteosarcoma | NCIT:C4834 | MONDO:equivalentTo | Primary Bone Osteosarcoma | | MONDO:0002629 | +| MONDO:0857378 | adrenal cortical oncocytic adenoma | NCIT:C48447 | MONDO:equivalentTo | Adrenal Cortical Oncocytic Adenoma | | MONDO:0003924|MONDO:0003424 | +| MONDO:0857379 | androgen-producing adrenal cortical adenoma | NCIT:C48454 | MONDO:equivalentTo | Androgen-Producing Adrenal Cortical Adenoma | | MONDO:0006408 | +| MONDO:0857380 | estrogen-producing adrenal cortical adenoma | NCIT:C48456 | MONDO:equivalentTo | Estrogen-Producing Adrenal Cortical Adenoma | | MONDO:0006408 | +| MONDO:0857382 | invasive prostate carcinoma | NCIT:C48596 | MONDO:equivalentTo | Invasive Prostate Carcinoma | | MONDO:0040677|MONDO:0005159 | +| MONDO:0857383 | minimal deviation melanoma | NCIT:C48612 | MONDO:equivalentTo | Minimal Deviation Melanoma | | MONDO:0005012 | +| MONDO:0857384 | melanoma arising in congenital melanocytic nevus | NCIT:C48613 | MONDO:equivalentTo | Melanoma Arising in Congenital Melanocytic Nevus | | MONDO:0005012 | +| MONDO:0857385 | desmoplastic neurotropic melanoma | NCIT:C48614 | MONDO:equivalentTo | Desmoplastic Neurotropic Melanoma | | MONDO:0044785 | +| MONDO:0857386 | mucosal lentiginous melanoma | NCIT:C48622 | MONDO:equivalentTo | Mucosal Lentiginous Melanoma | | MONDO:0000544 | +| MONDO:0857388 | metastatic malignant neoplasm in the trachea | NCIT:C4887 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Trachea | | MONDO:0001407|MONDO:0024880 | +| MONDO:0857389 | splenic lymphoma | NCIT:C48873 | MONDO:equivalentTo | Splenic Lymphoma | | MONDO:0017207|MONDO:0005966 | +| MONDO:0857390 | dedifferentiated chordoma | NCIT:C48876 | MONDO:equivalentTo | Dedifferentiated Chordoma | | MONDO:0008978 | +| MONDO:0857391 | benign lung hilum neoplasm | NCIT:C4888 | MONDO:equivalentTo | Benign Lung Hilum Neoplasm | | MONDO:0003639|MONDO:0002732 | +| MONDO:0857393 | hiv lipodystrophy | NCIT:C48899 | MONDO:equivalentTo | HIV Lipodystrophy | | MONDO:0006573|MONDO:0006574 | +| MONDO:0857394 | gardner fibroma | NCIT:C49017 | MONDO:equivalentTo | Gardner Fibroma | | MONDO:0005167 | +| MONDO:0857397 | skin fibrous histiocytoma, fibroblastic variant | NCIT:C49076 | MONDO:equivalentTo | Skin Fibrous Histiocytoma, Fibroblastic Variant | | MONDO:0006717 | +| MONDO:0857398 | skin fibrous histiocytoma, histiocytic variant | NCIT:C49077 | MONDO:equivalentTo | Skin Fibrous Histiocytoma, Histiocytic Variant | | MONDO:0006717 | +| MONDO:0857399 | skin fibrous histiocytoma, cellular variant | NCIT:C49078 | MONDO:equivalentTo | Skin Fibrous Histiocytoma, Cellular Variant | | MONDO:0006717 | +| MONDO:0857400 | skin fibrous histiocytoma, epithelioid variant | NCIT:C49079 | MONDO:equivalentTo | Skin Fibrous Histiocytoma, Epithelioid Variant | | MONDO:0006717 | +| MONDO:0857401 | solid angioleiomyoma | NCIT:C49110 | MONDO:equivalentTo | Solid Angioleiomyoma | | MONDO:0006646 | +| MONDO:0857402 | venous angioleiomyoma | NCIT:C49111 | MONDO:equivalentTo | Venous Angioleiomyoma | | MONDO:0006646 | +| MONDO:0857403 | cavernous angioleiomyoma | NCIT:C49115 | MONDO:equivalentTo | Cavernous Angioleiomyoma | | MONDO:0006646 | +| MONDO:0857404 | conventional cardiac rhabdomyoma | NCIT:C49179 | MONDO:equivalentTo | Conventional Cardiac Rhabdomyoma | | MONDO:0006123 | +| MONDO:0857405 | anaplastic embryonal rhabdomyosarcoma | NCIT:C49204 | MONDO:equivalentTo | Anaplastic Embryonal Rhabdomyosarcoma | | MONDO:0009993 | +| MONDO:0857407 | duodenal adenoma | NCIT:C4932 | MONDO:equivalentTo | Duodenal Adenoma | | MONDO:0021303|MONDO:0006734 | +| MONDO:0857409 | benign lymphoproliferative disorder | NCIT:C4939 | MONDO:equivalentTo | Benign Lymphoproliferative Disorder | | | +| MONDO:0857412 | intracranial neoplasm | NCIT:C4953 | MONDO:equivalentTo | Intracranial Neoplasm | | MONDO:0006130 | +| MONDO:0857413 | leptomeningeal neoplasm | NCIT:C4958 | MONDO:equivalentTo | Leptomeningeal Neoplasm | | MONDO:0016743 | +| MONDO:0857415 | benign infratentorial neoplasm | NCIT:C4965 | MONDO:equivalentTo | Benign Infratentorial Neoplasm | | MONDO:0021451|MONDO:0037736 | +| MONDO:0857417 | primary brain stem neoplasm | NCIT:C4975 | MONDO:equivalentTo | Primary Brain Stem Neoplasm | | MONDO:0021228|MONDO:0021632 | +| MONDO:0857419 | carcinoma unspecified site | NCIT:C4979 | MONDO:equivalentTo | Carcinoma Unspecified Site | | MONDO:0004993 | +| MONDO:0857430 | verrucous lesion | NCIT:C5028 | MONDO:equivalentTo | Verrucous Lesion | | MONDO:0002532 | +| MONDO:0857438 | primary cerebral diffuse large b-cell lymphoma | NCIT:C5054 | MONDO:equivalentTo | Primary Cerebral Diffuse Large B-Cell Lymphoma | | MONDO:0003655|MONDO:0017596 | +| MONDO:0857466 | renomedullary interstitial cell tumor | NCIT:C5100 | MONDO:equivalentTo | Renomedullary Interstitial Cell Tumor | | MONDO:0002513 | +| MONDO:0857469 | solid glomus tumor | NCIT:C51133 | MONDO:equivalentTo | Solid Glomus Tumor | | MONDO:0018327 | +| MONDO:0857473 | adult central nervous system neoplasm | NCIT:C5131 | MONDO:equivalentTo | Adult Central Nervous System Neoplasm | | MONDO:0006130 | +| MONDO:0857476 | breast ductal carcinoma in situ, non-comedo type | NCIT:C5137 | MONDO:equivalentTo | Breast Ductal Carcinoma In Situ, Non-Comedo Type | | MONDO:0005023 | +| MONDO:0857477 | invasive breast cribriform carcinoma | NCIT:C5142 | MONDO:equivalentTo | Invasive Breast Cribriform Carcinoma | | MONDO:0006256|MONDO:0004988|MONDO:0006176 | +| MONDO:0857478 | malignant breast adenomyoepithelioma | NCIT:C5143 | MONDO:equivalentTo | Malignant Breast Adenomyoepithelioma | | MONDO:0007254|MONDO:0002066 | +| MONDO:0857479 | infratentorial glioblastoma | NCIT:C5148 | MONDO:equivalentTo | Infratentorial Glioblastoma | | MONDO:0003107|MONDO:0002501 | +| MONDO:0857480 | supratentorial glioblastoma | NCIT:C5149 | MONDO:equivalentTo | Supratentorial Glioblastoma | | MONDO:0002071|MONDO:0002501 | +| MONDO:0857482 | breast high grade mucoepidermoid carcinoma | NCIT:C5167 | MONDO:equivalentTo | Breast High Grade Mucoepidermoid Carcinoma | | MONDO:0003087 | +| MONDO:0857483 | breast low grade mucoepidermoid carcinoma | NCIT:C5168 | MONDO:equivalentTo | Breast Low Grade Mucoepidermoid Carcinoma | | MONDO:0003087 | +| MONDO:0857486 | breast non-hodgkin lymphoma | NCIT:C5181 | MONDO:equivalentTo | Breast Non-Hodgkin Lymphoma | | MONDO:0003661|MONDO:0018908 | +| MONDO:0857487 | breast complex fibroadenoma | NCIT:C5194 | MONDO:equivalentTo | Breast Complex Fibroadenoma | | MONDO:0002056 | +| MONDO:0857488 | benign nipple neoplasm | NCIT:C5197 | MONDO:equivalentTo | Benign Nipple Neoplasm | | MONDO:0002482|MONDO:0000620 | +| MONDO:0857490 | breast papillary neoplasm | NCIT:C5206 | MONDO:equivalentTo | Breast Papillary Neoplasm | | MONDO:0021096|MONDO:0021100 | +| MONDO:0857492 | malignant nipple neoplasm | NCIT:C5213 | MONDO:equivalentTo | Malignant Nipple Neoplasm | | MONDO:0007254|MONDO:0002482 | +| MONDO:0857493 | benign ovarian thecoma | NCIT:C5219 | MONDO:equivalentTo | Benign Ovarian Thecoma | | MONDO:0024387|MONDO:0037253 | +| MONDO:0857496 | ovarian soft tissue neoplasm | NCIT:C5244 | MONDO:equivalentTo | Ovarian Soft Tissue Neoplasm | | MONDO:0021068|MONDO:0006424 | +| MONDO:0857498 | gastric burkitt lymphoma | NCIT:C5251 | MONDO:equivalentTo | Gastric Burkitt Lymphoma | | MONDO:0007243|MONDO:0042493 | +| MONDO:0857499 | gastric t-cell non-hodgkin lymphoma | NCIT:C5254 | MONDO:equivalentTo | Gastric T-Cell Non-Hodgkin Lymphoma | | MONDO:0015760|MONDO:0042493 | +| MONDO:0857502 | deletion of the short arm of chromosome 1 (1p) associated meningioma | NCIT:C5294 | MONDO:equivalentTo | Deletion of the Short Arm of Chromosome 1 (1p) Associated Meningioma | | MONDO:0016642 | +| MONDO:0857503 | deletion of chromosome 22 associated meningioma | NCIT:C5305 | MONDO:equivalentTo | Deletion of Chromosome 22 Associated Meningioma | | MONDO:0016642 | +| MONDO:0857504 | deletion of chromosome 3p associated meningioma | NCIT:C5306 | MONDO:equivalentTo | Deletion of Chromosome 3p Associated Meningioma | | MONDO:0016642 | +| MONDO:0857507 | extra-adrenal retroperitoneal paraganglioma | NCIT:C5328 | MONDO:equivalentTo | Extra-Adrenal Retroperitoneal Paraganglioma | | MONDO:0000550|MONDO:0024645 | +| MONDO:0857508 | hereditary paraganglioma | NCIT:C5329 | MONDO:equivalentTo | Hereditary Paraganglioma | | MONDO:0000448 | +| MONDO:0857513 | great vessel neoplasm | NCIT:C5348 | MONDO:equivalentTo | Great Vessel Neoplasm | | MONDO:0024757 | +| MONDO:0857514 | mesenchymal chondrosarcoma of bone | NCIT:C53493 | MONDO:equivalentTo | Mesenchymal Chondrosarcoma of Bone | | MONDO:0021054|MONDO:0006853 | +| MONDO:0857518 | cardiac schwannoma | NCIT:C5358 | MONDO:equivalentTo | Cardiac Schwannoma | | MONDO:0004820|MONDO:0021450 | +| MONDO:0857519 | cardiac epithelioid hemangioendothelioma | NCIT:C5362 | MONDO:equivalentTo | Cardiac Epithelioid Hemangioendothelioma | | MONDO:0015523|MONDO:0001340 | +| MONDO:0857520 | cardiac kaposi sarcoma | NCIT:C5363 | MONDO:equivalentTo | Cardiac Kaposi Sarcoma | | MONDO:0005055|MONDO:0003354 | +| MONDO:0857524 | cardiac myeloid sarcoma | NCIT:C5370 | MONDO:equivalentTo | Cardiac Myeloid Sarcoma | | MONDO:0001340|MONDO:0006861 | +| MONDO:0857525 | secondary osteosarcoma | NCIT:C53704 | MONDO:equivalentTo | Secondary Osteosarcoma | | MONDO:0002629|MONDO:0024881 | +| MONDO:0857526 | malignant inferior vena cava neoplasm | NCIT:C5377 | MONDO:equivalentTo | Malignant Inferior Vena Cava Neoplasm | | MONDO:0040676 | +| MONDO:0857527 | malignant superior vena cava neoplasm | NCIT:C5379 | MONDO:equivalentTo | Malignant Superior Vena Cava Neoplasm | | MONDO:0040676 | +| MONDO:0857528 | malignant pulmonary artery neoplasm | NCIT:C5380 | MONDO:equivalentTo | Malignant Pulmonary Artery Neoplasm | | MONDO:0040676 | +| MONDO:0857529 | malignant pulmonary vein neoplasm | NCIT:C5383 | MONDO:equivalentTo | Malignant Pulmonary Vein Neoplasm | | MONDO:0040676 | +| MONDO:0857532 | leiomyosarcoma of vessels | NCIT:C5387 | MONDO:equivalentTo | Leiomyosarcoma of Vessels | | MONDO:0005058 | +| MONDO:0857533 | benign atrial neoplasm | NCIT:C5389 | MONDO:equivalentTo | Benign Atrial Neoplasm | | MONDO:0021450 | +| MONDO:0857535 | solitary adult fibroma | NCIT:C5394 | MONDO:equivalentTo | Solitary Adult Fibroma | | MONDO:0005167 | +| MONDO:0857536 | fibrous histiocytoma of bone | NCIT:C53963 | MONDO:equivalentTo | Fibrous Histiocytoma of Bone | | MONDO:0000631|MONDO:0002989 | +| MONDO:0857537 | bone leiomyoma | NCIT:C53964 | MONDO:equivalentTo | Bone Leiomyoma | | MONDO:0001572 | +| MONDO:0857542 | benign gastrointestinal stromal tumor | NCIT:C53998 | MONDO:equivalentTo | Benign Gastrointestinal Stromal Tumor | | MONDO:0044335|MONDO:0011719 | +| MONDO:0857543 | malignant gastrointestinal stromal tumor | NCIT:C53999 | MONDO:equivalentTo | Malignant Gastrointestinal Stromal Tumor | | MONDO:0011719|MONDO:0044337 | +| MONDO:0857546 | region 17p13 allelic loss associated medulloblastoma | NCIT:C5402 | MONDO:equivalentTo | Region 17p13 Allelic Loss Associated Medulloblastoma | | MONDO:0007959 | +| MONDO:0857547 | nevoid basal cell carcinoma syndrome associated medulloblastoma | NCIT:C5405 | MONDO:equivalentTo | Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma | | MONDO:0007959 | +| MONDO:0857548 | central nervous system t-cell non-hodgkin lymphoma | NCIT:C5409 | MONDO:equivalentTo | Central Nervous System T-Cell Non-Hodgkin Lymphoma | | MONDO:0015760|MONDO:0044887 | +| MONDO:0857549 | gastric granular cell tumor | NCIT:C54094 | MONDO:equivalentTo | Gastric Granular Cell Tumor | | MONDO:0006235|MONDO:0021085 | +| MONDO:0857550 | malignant central nervous system germ cell tumor | NCIT:C54099 | MONDO:equivalentTo | Malignant Central Nervous System Germ Cell Tumor | | MONDO:0003113|MONDO:0003000|MONDO:0002714 | +| MONDO:0857552 | breast columnar cell lesion | NCIT:C54180 | MONDO:equivalentTo | Breast Columnar Cell Lesion | | MONDO:0021100 | +| MONDO:0857556 | head and neck keratinizing squamous cell carcinoma | NCIT:C54283 | MONDO:equivalentTo | Head and Neck Keratinizing Squamous Cell Carcinoma | | MONDO:0005056|MONDO:0010150 | +| MONDO:0857559 | metastasizing ameloblastoma | NCIT:C54297 | MONDO:equivalentTo | Metastasizing Ameloblastoma | | MONDO:0024883|MONDO:0017795 | +| MONDO:0857562 | lipomatosis of nerve | NCIT:C5431 | MONDO:equivalentTo | Lipomatosis of Nerve | | MONDO:0000648|MONDO:0001406|MONDO:0006574 | +| MONDO:0857564 | laryngeal papillary squamous cell carcinoma | NCIT:C54335 | MONDO:equivalentTo | Laryngeal Papillary Squamous Cell Carcinoma | | MONDO:0002979|MONDO:0005595 | +| MONDO:0857565 | laryngeal spindle cell squamous carcinoma | NCIT:C54336 | MONDO:equivalentTo | Laryngeal Spindle Cell Squamous Carcinoma | | MONDO:0005595|MONDO:0021663 | +| MONDO:0857566 | laryngeal acantholytic squamous cell carcinoma | NCIT:C54337 | MONDO:equivalentTo | Laryngeal Acantholytic Squamous Cell Carcinoma | | MONDO:0003487|MONDO:0005595 | +| MONDO:0857567 | laryngeal adenosquamous carcinoma | NCIT:C54338 | MONDO:equivalentTo | Laryngeal Adenosquamous Carcinoma | | MONDO:0002358|MONDO:0006074 | +| MONDO:0857568 | laryngeal undifferentiated carcinoma | NCIT:C54339 | MONDO:equivalentTo | Laryngeal Undifferentiated Carcinoma | | MONDO:0002358|MONDO:0005617 | +| MONDO:0857570 | kadish stage c olfactory neuroblastoma | NCIT:C5435 | MONDO:equivalentTo | Kadish Stage C Olfactory Neuroblastoma | | MONDO:0006329 | +| MONDO:0857571 | drop metastasis in the spinal cord | NCIT:C5439 | MONDO:equivalentTo | Drop Metastasis in the Spinal Cord | | MONDO:0044912 | +| MONDO:0857572 | nasopharyngeal low grade papillary adenocarcinoma | NCIT:C54400 | MONDO:equivalentTo | Nasopharyngeal Low Grade Papillary Adenocarcinoma | | MONDO:0015459|MONDO:0002512 | +| MONDO:0857574 | meningeal gliomatosis | NCIT:C5446 | MONDO:equivalentTo | Meningeal Gliomatosis | | MONDO:0100342|MONDO:0021322 | +| MONDO:0857575 | invasive breast apocrine carcinoma | NCIT:C5457 | MONDO:equivalentTo | Invasive Breast Apocrine Carcinoma | | MONDO:0006256|MONDO:0003934 | +| MONDO:0857576 | breast nevus | NCIT:C54658 | MONDO:equivalentTo | Breast Nevus | | MONDO:0044794|MONDO:0000620 | +| MONDO:0857577 | acral nevus | NCIT:C54659 | MONDO:equivalentTo | Acral Nevus | | MONDO:0044794 | +| MONDO:0857578 | flexural skin nevus | NCIT:C54660 | MONDO:equivalentTo | Flexural Skin Nevus | | MONDO:0044794 | +| MONDO:0857580 | nevoid melanoma | NCIT:C54662 | MONDO:equivalentTo | Nevoid Melanoma | | MONDO:0005012 | +| MONDO:0857581 | signet ring melanoma | NCIT:C54663 | MONDO:equivalentTo | Signet Ring Melanoma | | MONDO:0005012 | +| MONDO:0857583 | invasive breast lobular carcinoma, signet ring variant | NCIT:C54691 | MONDO:equivalentTo | Invasive Breast Lobular Carcinoma, Signet Ring Variant | | MONDO:0005051|MONDO:0002671 | +| MONDO:0857587 | central nervous system dermoid cyst | NCIT:C5508 | MONDO:equivalentTo | Central Nervous System Dermoid Cyst | | MONDO:0002378|MONDO:0003733 | +| MONDO:0857589 | appendix mucinous cystadenoma | NCIT:C5510 | MONDO:equivalentTo | Appendix Mucinous Cystadenoma | | MONDO:0006088|MONDO:0006859 | +| MONDO:0857592 | prostate kaposi sarcoma | NCIT:C5523 | MONDO:equivalentTo | Prostate Kaposi Sarcoma | | MONDO:0005055|MONDO:0002854 | +| MONDO:0857593 | prostate myeloid sarcoma | NCIT:C5527 | MONDO:equivalentTo | Prostate Myeloid Sarcoma | | MONDO:0008315|MONDO:0006861 | +| MONDO:0857595 | prostate non-hodgkin lymphoma | NCIT:C5534 | MONDO:equivalentTo | Prostate Non-Hodgkin Lymphoma | | MONDO:0000996|MONDO:0018908 | +| MONDO:0857596 | ceruminous neoplasm | NCIT:C5558 | MONDO:equivalentTo | Ceruminous Neoplasm | | MONDO:0003686|MONDO:0021235 | +| MONDO:0857599 | stage i skin cancer | NCIT:C5581 | MONDO:equivalentTo | Stage I Skin Cancer | | MONDO:0002656 | +| MONDO:0857600 | stage ii skin cancer | NCIT:C5582 | MONDO:equivalentTo | Stage II Skin Cancer | | MONDO:0002656 | +| MONDO:0857601 | stage iii skin cancer | NCIT:C5583 | MONDO:equivalentTo | Stage III Skin Cancer | | MONDO:0002656 | +| MONDO:0857602 | stage iv skin cancer | NCIT:C5584 | MONDO:equivalentTo | Stage IV Skin Cancer | | MONDO:0002656 | +| MONDO:0857604 | jugular foramen neoplasm | NCIT:C5589 | MONDO:equivalentTo | Jugular Foramen Neoplasm | | MONDO:0021351 | +| MONDO:0857607 | benign anal granular cell tumor | NCIT:C5607 | MONDO:equivalentTo | Benign Anal Granular Cell Tumor | | MONDO:0021469|MONDO:0003250 | +| MONDO:0857611 | metastatic malignant neoplasm in the skin | NCIT:C5629 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Skin | | MONDO:0002898|MONDO:0024880 | +| MONDO:0857613 | occult lung carcinoma | NCIT:C5641 | MONDO:equivalentTo | Occult Lung Carcinoma | | MONDO:0005138 | +| MONDO:0857614 | endobronchial hamartoma | NCIT:C5662 | MONDO:equivalentTo | Endobronchial Hamartoma | | MONDO:0021540 | +| MONDO:0857615 | multiple pulmonary hamartomas | NCIT:C5663 | MONDO:equivalentTo | Multiple Pulmonary Hamartomas | | MONDO:0021540 | +| MONDO:0857619 | colorectal adenoma with severe dysplasia | NCIT:C5685 | MONDO:equivalentTo | Colorectal Adenoma with Severe Dysplasia | | MONDO:0005484 | +| MONDO:0857623 | esophageal schwannoma | NCIT:C5703 | MONDO:equivalentTo | Esophageal Schwannoma | | MONDO:0004820|MONDO:0021459 | +| MONDO:0857629 | extrahepatic bile duct undifferentiated carcinoma | NCIT:C5780 | MONDO:equivalentTo | Extrahepatic Bile Duct Undifferentiated Carcinoma | | MONDO:0003090|MONDO:0005617 | +| MONDO:0857635 | esophageal neuroendocrine neoplasm | NCIT:C5821 | MONDO:equivalentTo | Esophageal Neuroendocrine Neoplasm | | MONDO:0021355|MONDO:0024503 | +| MONDO:0857638 | extrahepatic bile duct tubular adenoma | NCIT:C5850 | MONDO:equivalentTo | Extrahepatic Bile Duct Tubular Adenoma | | MONDO:0003445|MONDO:0024660 | +| MONDO:0857646 | oral cavity granular cell tumor | NCIT:C5912 | MONDO:equivalentTo | Oral Cavity Granular Cell Tumor | | MONDO:0021245|MONDO:0006235 | +| MONDO:0857647 | oral cavity adenoma | NCIT:C5913 | MONDO:equivalentTo | Oral Cavity Adenoma | | MONDO:0021445|MONDO:0036976|MONDO:0004972 | +| MONDO:0857648 | oral cavity adenocarcinoma | NCIT:C5914 | MONDO:equivalentTo | Oral Cavity Adenocarcinoma | | MONDO:0044925|MONDO:0004970 | +| MONDO:0857660 | minor salivary gland mucoepidermoid carcinoma | NCIT:C5953 | MONDO:equivalentTo | Minor Salivary Gland Mucoepidermoid Carcinoma | | MONDO:0045069|MONDO:0021009 | +| MONDO:0857661 | minor salivary gland small cell neuroendocrine carcinoma | NCIT:C5956 | MONDO:equivalentTo | Minor Salivary Gland Small Cell Neuroendocrine Carcinoma | | MONDO:0045069|MONDO:0006405 | +| MONDO:0857663 | minor salivary gland squamous cell carcinoma | NCIT:C5959 | MONDO:equivalentTo | Minor Salivary Gland Squamous Cell Carcinoma | | MONDO:0044740|MONDO:0045069 | +| MONDO:0857671 | oropharyngeal polyp | NCIT:C5988 | MONDO:equivalentTo | Oropharyngeal Polyp | | MONDO:0021479|MONDO:0005079 | +| MONDO:0857679 | lung mature b-cell neoplasm | NCIT:C60310 | MONDO:equivalentTo | Lung Mature B-Cell Neoplasm | | MONDO:0021117|MONDO:0004949 | +| MONDO:0857682 | nasopharyngeal polyp | NCIT:C6034 | MONDO:equivalentTo | Nasopharyngeal Polyp | | MONDO:0021478|MONDO:0005079 | +| MONDO:0857683 | stage 0 nasopharyngeal undifferentiated carcinoma ajcc v6, v7, and v8 | NCIT:C6035 | MONDO:equivalentTo | Stage 0 Nasopharyngeal Undifferentiated Carcinoma AJCC v6, v7, and v8 | | MONDO:0021297|MONDO:0021537 | +| MONDO:0857685 | nasopharyngeal squamous papilloma | NCIT:C6037 | MONDO:equivalentTo | Nasopharyngeal Squamous Papilloma | | MONDO:0001825|MONDO:0021478 | +| MONDO:0857686 | oropharyngeal squamous papilloma | NCIT:C6038 | MONDO:equivalentTo | Oropharyngeal Squamous Papilloma | | MONDO:0021479|MONDO:0001825 | +| MONDO:0857687 | stage 0 oropharyngeal squamous cell carcinoma ajcc v6 and v7 | NCIT:C6039 | MONDO:equivalentTo | Stage 0 Oropharyngeal Squamous Cell Carcinoma AJCC v6 and v7 | | MONDO:0044704|MONDO:0021298 | +| MONDO:0857689 | stage 0 hypopharyngeal squamous cell carcinoma ajcc v6, v7, and v8 | NCIT:C6048 | MONDO:equivalentTo | Stage 0 Hypopharyngeal Squamous Cell Carcinoma AJCC v6, v7, and v8 | | MONDO:0021288|MONDO:0044638 | +| MONDO:0857690 | stage 0 oral cavity squamous cell carcinoma ajcc v6 and v7 | NCIT:C6052 | MONDO:equivalentTo | Stage 0 Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7 | | MONDO:0004958|MONDO:0000371|MONDO:0004693 | +| MONDO:0857692 | anterior tongue neoplasm | NCIT:C6062 | MONDO:equivalentTo | Anterior Tongue Neoplasm | | MONDO:0021240 | +| MONDO:0857697 | neck carcinoma | NCIT:C6077 | MONDO:equivalentTo | Neck Carcinoma | | MONDO:0021310|MONDO:0002038 | +| MONDO:0857698 | external ear actinic keratosis | NCIT:C6080 | MONDO:equivalentTo | External Ear Actinic Keratosis | | MONDO:0021235|MONDO:0005173 | +| MONDO:0857700 | middle ear paraganglioma | NCIT:C6085 | MONDO:equivalentTo | Middle Ear Paraganglioma | | MONDO:0021366|MONDO:0021064 | +| MONDO:0857702 | benign uveal neoplasm | NCIT:C6104 | MONDO:equivalentTo | Benign Uveal Neoplasm | | MONDO:0021454|MONDO:0021225 | +| MONDO:0857703 | stage 0 laryngeal squamous cell carcinoma ajcc v6, v7, and v8 | NCIT:C6121 | MONDO:equivalentTo | Stage 0 Laryngeal Squamous Cell Carcinoma AJCC v6, v7, and v8 | | MONDO:0004696|MONDO:0005595|MONDO:0004693 | +| MONDO:0857715 | testicular typical seminoma | NCIT:C61383 | MONDO:equivalentTo | Testicular Typical Seminoma | | MONDO:0003669 | +| MONDO:0857719 | ureter undifferentiated carcinoma | NCIT:C6159 | MONDO:equivalentTo | Ureter Undifferentiated Carcinoma | | MONDO:0006481|MONDO:0005617 | +| MONDO:0857720 | urethral undifferentiated carcinoma | NCIT:C6168 | MONDO:equivalentTo | Urethral Undifferentiated Carcinoma | | MONDO:0021327|MONDO:0005617 | +| MONDO:0857725 | hard palate mucoepidermoid carcinoma | NCIT:C6214 | MONDO:equivalentTo | Hard Palate Mucoepidermoid Carcinoma | | MONDO:0021339|MONDO:0044964 | +| MONDO:0857728 | salivary gland clear cell carcinoma | NCIT:C62191 | MONDO:equivalentTo | Salivary Gland Clear Cell Carcinoma | | MONDO:0000521 | +| MONDO:0857729 | breast tubular adenoma | NCIT:C62210 | MONDO:equivalentTo | Breast Tubular Adenoma | | MONDO:0002058 | +| MONDO:0857730 | conjunctival squamous papilloma | NCIT:C6224 | MONDO:equivalentTo | Conjunctival Squamous Papilloma | | MONDO:0001825|MONDO:0006105 | +| MONDO:0857731 | skin nodular basal cell carcinoma | NCIT:C62282 | MONDO:equivalentTo | Skin Nodular Basal Cell Carcinoma | | MONDO:0005341 | +| MONDO:0857732 | superficial basal cell carcinoma | NCIT:C62284 | MONDO:equivalentTo | Superficial Basal Cell Carcinoma | | MONDO:0005341 | +| MONDO:0857734 | minor salivary gland acinic cell carcinoma | NCIT:C6243 | MONDO:equivalentTo | Minor Salivary Gland Acinic Cell Carcinoma | | MONDO:0006400|MONDO:0006304 | +| MONDO:0857736 | ovarian endometrioid tumor | NCIT:C6257 | MONDO:equivalentTo | Ovarian Endometrioid Tumor | | MONDO:0002480|MONDO:0002229 | +| MONDO:0857738 | childhood cerebral ependymoma, not otherwise specified | NCIT:C6268 | MONDO:equivalentTo | Childhood Cerebral Ependymoma, Not Otherwise Specified | | MONDO:0004249 | +| MONDO:0857739 | fallopian tube undifferentiated carcinoma | NCIT:C6281 | MONDO:equivalentTo | Fallopian Tube Undifferentiated Carcinoma | | MONDO:0006206|MONDO:0005617 | +| MONDO:0857740 | vaginal verrucous carcinoma | NCIT:C6325 | MONDO:equivalentTo | Vaginal Verrucous Carcinoma | | MONDO:0006006|MONDO:0006490 | +| MONDO:0857743 | benign uterine corpus mixed epithelial and mesenchymal neoplasm | NCIT:C6335 | MONDO:equivalentTo | Benign Uterine Corpus Mixed Epithelial and Mesenchymal Neoplasm | | MONDO:0016255|MONDO:0021525 | +| MONDO:0857744 | cervical undifferentiated carcinoma | NCIT:C6345 | MONDO:equivalentTo | Cervical Undifferentiated Carcinoma | | MONDO:0005131|MONDO:0005617 | +| MONDO:0857745 | testicular mixed embryonal carcinoma and seminoma | NCIT:C6350 | MONDO:equivalentTo | Testicular Mixed Embryonal Carcinoma and Seminoma | | MONDO:0003120 | +| MONDO:0857746 | testicular mixed embryonal carcinoma and teratoma | NCIT:C6351 | MONDO:equivalentTo | Testicular Mixed Embryonal Carcinoma and Teratoma | | MONDO:0003120|MONDO:0003403|MONDO:0002599 | +| MONDO:0857747 | testicular mixed embryonal carcinoma and teratoma with seminoma | NCIT:C6352 | MONDO:equivalentTo | Testicular Mixed Embryonal Carcinoma and Teratoma with Seminoma | | MONDO:0003120 | +| MONDO:0857748 | kidney lymphoma | NCIT:C63532 | MONDO:equivalentTo | Kidney Lymphoma | | MONDO:0002367|MONDO:0017207 | +| MONDO:0857750 | testicular mature teratoma | NCIT:C6355 | MONDO:equivalentTo | Testicular Mature Teratoma | | MONDO:0003517|MONDO:0018193|MONDO:0021447 | +| MONDO:0857752 | undifferentiated carcinoma with osteoclast-like giant cells | NCIT:C63622 | MONDO:equivalentTo | Undifferentiated Carcinoma with Osteoclast-Like Giant Cells | | MONDO:0005617 | +| MONDO:0857753 | penile kaposi sarcoma | NCIT:C6377 | MONDO:equivalentTo | Penile Kaposi Sarcoma | | MONDO:0005055|MONDO:0001387|MONDO:0022293 | +| MONDO:0857758 | orbit paraganglioma | NCIT:C6408 | MONDO:equivalentTo | Orbit Paraganglioma | | MONDO:0006239|MONDO:0024611 | +| MONDO:0857759 | laryngeal paraganglioma | NCIT:C6409 | MONDO:equivalentTo | Laryngeal Paraganglioma | | MONDO:0015070|MONDO:0006239|MONDO:0021052 | +| MONDO:0857760 | intrathoracic paravertebral paraganglioma | NCIT:C6411 | MONDO:equivalentTo | Intrathoracic Paravertebral Paraganglioma | | MONDO:0000550|MONDO:0021350 | +| MONDO:0857763 | foregut neuroendocrine tumor | NCIT:C6421 | MONDO:equivalentTo | Foregut Neuroendocrine Tumor | | MONDO:0000386 | +| MONDO:0857765 | hindgut neuroendocrine tumor | NCIT:C6423 | MONDO:equivalentTo | Hindgut Neuroendocrine Tumor | | MONDO:0000386 | +| MONDO:0857767 | malignant mediastinal nongerminomatous germ cell tumor | NCIT:C6439 | MONDO:equivalentTo | Malignant Mediastinal Nongerminomatous Germ Cell Tumor | | MONDO:0003578|MONDO:0006298 | +| MONDO:0857768 | gastric germ cell tumor | NCIT:C6448 | MONDO:equivalentTo | Gastric Germ Cell Tumor | | MONDO:0018201|MONDO:0021085 | +| MONDO:0857769 | benign germ cell tumor | NCIT:C6449 | MONDO:equivalentTo | Benign Germ Cell Tumor | | MONDO:0005040|MONDO:0005165 | +| MONDO:0857770 | invasive thymoma | NCIT:C6453 | MONDO:equivalentTo | Invasive Thymoma | | MONDO:0006456 | +| MONDO:0857771 | bone hemangioma | NCIT:C6477 | MONDO:equivalentTo | Bone Hemangioma | | MONDO:0024499|MONDO:0000631|MONDO:0006500 | +| MONDO:0857772 | bone glomus tumor | NCIT:C6480 | MONDO:equivalentTo | Bone Glomus Tumor | | MONDO:0019060|MONDO:0018327 | +| MONDO:0857773 | extraabdominal fibromatosis | NCIT:C6489 | MONDO:equivalentTo | Extraabdominal Fibromatosis | | MONDO:0007608 | +| MONDO:0857774 | deep lipoma | NCIT:C6498 | MONDO:equivalentTo | Deep Lipoma | | MONDO:0005106 | +| MONDO:0857775 | benign skeletal muscle neoplasm | NCIT:C6515 | MONDO:equivalentTo | Benign Skeletal Muscle Neoplasm | | MONDO:0002848|MONDO:0003061 | +| MONDO:0857776 | non-small cell carcinoma | NCIT:C65151 | MONDO:equivalentTo | Non-Small Cell Carcinoma | | MONDO:0004993 | +| MONDO:0857777 | malignant neoplasm, uncertain whether primary or metastatic | NCIT:C65153 | MONDO:equivalentTo | Malignant Neoplasm, Uncertain Whether Primary or Metastatic | | MONDO:0004992 | +| MONDO:0857778 | papillary carcinoma in situ | NCIT:C65163 | MONDO:equivalentTo | Papillary Carcinoma In Situ | | MONDO:0004647|MONDO:0006509 | +| MONDO:0857779 | non-invasive papillary squamous cell carcinoma | NCIT:C65164 | MONDO:equivalentTo | Non-Invasive Papillary Squamous Cell Carcinoma | | MONDO:0002979 | +| MONDO:0857780 | inverted squamous papilloma | NCIT:C65165 | MONDO:equivalentTo | Inverted Squamous Papilloma | | MONDO:0002537|MONDO:0001825 | +| MONDO:0857781 | non-keratinizing large cell squamous cell carcinoma | NCIT:C65173 | MONDO:equivalentTo | Non-Keratinizing Large Cell Squamous Cell Carcinoma | | MONDO:0005096 | +| MONDO:0857782 | non-keratinizing small cell squamous cell carcinoma | NCIT:C65175 | MONDO:equivalentTo | Non-Keratinizing Small Cell Squamous Cell Carcinoma | | MONDO:0005096 | +| MONDO:0857783 | squamous cell carcinoma in situ with questionable stromal invasion | NCIT:C65176 | MONDO:equivalentTo | Squamous Cell Carcinoma In Situ with Questionable Stromal Invasion | | MONDO:0005096 | +| MONDO:0857785 | squamous cell carcinoma with horn formation | NCIT:C65179 | MONDO:equivalentTo | Squamous Cell Carcinoma with Horn Formation | | MONDO:0005056 | +| MONDO:0857786 | squamous cell carcinoma, clear cell type | NCIT:C65180 | MONDO:equivalentTo | Squamous Cell Carcinoma, Clear Cell Type | | MONDO:0005096 | +| MONDO:0857787 | non-invasive papillary transitional cell carcinoma | NCIT:C65181 | MONDO:equivalentTo | Non-Invasive Papillary Transitional Cell Carcinoma | | MONDO:0006350 | +| MONDO:0857789 | malignant pancreatic insulinoma | NCIT:C65186 | MONDO:equivalentTo | Malignant Pancreatic Insulinoma | | MONDO:0024677 | +| MONDO:0857790 | malignant pancreatic glucagonoma | NCIT:C65187 | MONDO:equivalentTo | Malignant Pancreatic Glucagonoma | | MONDO:0019959 | +| MONDO:0857791 | malignant gastrinoma | NCIT:C65188 | MONDO:equivalentTo | Malignant Gastrinoma | | MONDO:0003523 | +| MONDO:0857792 | malignant vipoma | NCIT:C65189 | MONDO:equivalentTo | Malignant Vipoma | | MONDO:0019960 | +| MONDO:0857793 | malignant somatostatinoma | NCIT:C65190 | MONDO:equivalentTo | Malignant Somatostatinoma | | MONDO:0006976 | +| MONDO:0857794 | flat adenoma | NCIT:C65193 | MONDO:equivalentTo | Flat Adenoma | | MONDO:0006180 | +| MONDO:0857795 | glandular papillomatosis | NCIT:C65198 | MONDO:equivalentTo | Glandular Papillomatosis | | MONDO:0021098 | +| MONDO:0857796 | thyroid gland follicular carcinoma, minimally invasive | NCIT:C65200 | MONDO:equivalentTo | Thyroid Gland Follicular Carcinoma, Minimally Invasive | | MONDO:0040677|MONDO:0005034 | +| MONDO:0857797 | papillary mucinous cystadenocarcinoma | NCIT:C65204 | MONDO:equivalentTo | Papillary Mucinous Cystadenocarcinoma | | MONDO:0005858|MONDO:0005074 | +| MONDO:0857798 | malignant testicular sertoli cell tumor | NCIT:C6523 | MONDO:equivalentTo | Malignant Testicular Sertoli Cell Tumor | | MONDO:0000378|MONDO:0020808 | +| MONDO:0857799 | malignant pericytic neoplasm | NCIT:C6530 | MONDO:equivalentTo | Malignant Pericytic Neoplasm | | MONDO:0002604|MONDO:0024637 | +| MONDO:0857802 | ancient schwannoma | NCIT:C6556 | MONDO:equivalentTo | Ancient Schwannoma | | MONDO:0002546 | +| MONDO:0857803 | extraskeletal cartilaginous and osseous neoplasm | NCIT:C6570 | MONDO:equivalentTo | Extraskeletal Cartilaginous and Osseous Neoplasm | | MONDO:0006424 | +| MONDO:0857804 | intramuscular myxoma | NCIT:C6579 | MONDO:equivalentTo | Intramuscular Myxoma | | MONDO:0044784 | +| MONDO:0857805 | juxta-articular myxoma | NCIT:C6580 | MONDO:equivalentTo | Juxta-Articular Myxoma | | MONDO:0044784 | +| MONDO:0857806 | peripheral neuroblastoma | NCIT:C6591 | MONDO:equivalentTo | Peripheral Neuroblastoma | | MONDO:0002749|MONDO:0021089 | +| MONDO:0857807 | benign mediastinal soft tissue neoplasm | NCIT:C6593 | MONDO:equivalentTo | Benign Mediastinal Soft Tissue Neoplasm | | MONDO:0003512|MONDO:0044335|MONDO:0021521 | +| MONDO:0857810 | soft tissue fibrosarcoma | NCIT:C6605 | MONDO:equivalentTo | Soft Tissue Fibrosarcoma | | MONDO:0018078|MONDO:0005164 | +| MONDO:0857811 | mediastinal malignant peripheral nerve sheath tumor | NCIT:C6626 | MONDO:equivalentTo | Mediastinal Malignant Peripheral Nerve Sheath Tumor | | MONDO:0003098|MONDO:0002852|MONDO:0017827 | +| MONDO:0857812 | mediastinal ganglioneuroma | NCIT:C6632 | MONDO:equivalentTo | Mediastinal Ganglioneuroma | | MONDO:0003098|MONDO:0021521|MONDO:0005033 | +| MONDO:0857813 | mediastinal hodgkin lymphoma | NCIT:C6634 | MONDO:equivalentTo | Mediastinal Hodgkin Lymphoma | | MONDO:0004952|MONDO:0004021 | +| MONDO:0857814 | stage 1 neuroblastoma | NCIT:C6638 | MONDO:equivalentTo | Stage 1 Neuroblastoma | | MONDO:0005072 | +| MONDO:0857815 | stage 2 neuroblastoma | NCIT:C6639 | MONDO:equivalentTo | Stage 2 Neuroblastoma | | MONDO:0005072 | +| MONDO:0857816 | stage 3 neuroblastoma | NCIT:C6640 | MONDO:equivalentTo | Stage 3 Neuroblastoma | | MONDO:0005072 | +| MONDO:0857817 | stage 4 neuroblastoma | NCIT:C6641 | MONDO:equivalentTo | Stage 4 Neuroblastoma | | MONDO:0005072 | +| MONDO:0857821 | breast atypical medullary carcinoma | NCIT:C66719 | MONDO:equivalentTo | Breast Atypical Medullary Carcinoma | | MONDO:0004953 | +| MONDO:0857822 | adenocarcinoma with neuroendocrine differentiation | NCIT:C66745 | MONDO:equivalentTo | Adenocarcinoma with Neuroendocrine Differentiation | | MONDO:0004970 | +| MONDO:0857823 | testicular sex cord-stromal tumor, not otherwise specified | NCIT:C66748 | MONDO:equivalentTo | Testicular Sex Cord-Stromal Tumor, Not Otherwise Specified | | MONDO:0003125 | +| MONDO:0857824 | ovarian stromal tumor with minor sex cord elements | NCIT:C66749 | MONDO:equivalentTo | Ovarian Stromal Tumor with Minor Sex Cord Elements | | MONDO:0021657 | +| MONDO:0857825 | adult granulosa cell tumor | NCIT:C66750 | MONDO:equivalentTo | Adult Granulosa Cell Tumor | | MONDO:0006036 | +| MONDO:0857826 | melanoma in precancerous melanosis | NCIT:C66753 | MONDO:equivalentTo | Melanoma in Precancerous Melanosis | | MONDO:0005012 | +| MONDO:0857827 | small congenital melanocytic nevus | NCIT:C66754 | MONDO:equivalentTo | Small Congenital Melanocytic Nevus | | MONDO:0044792 | +| MONDO:0857828 | proliferative nodules in congenital melanocytic nevus | NCIT:C66755 | MONDO:equivalentTo | Proliferative Nodules in Congenital Melanocytic Nevus | | MONDO:0044792 | +| MONDO:0857829 | periosteal fibroma | NCIT:C66761 | MONDO:equivalentTo | Periosteal Fibroma | | MONDO:0000631|MONDO:0005167 | +| MONDO:0857830 | fascial fibroma | NCIT:C66764 | MONDO:equivalentTo | Fascial Fibroma | | MONDO:0005167 | +| MONDO:0857831 | fascial fibrosarcoma | NCIT:C66765 | MONDO:equivalentTo | Fascial Fibrosarcoma | | MONDO:0005164 | +| MONDO:0857834 | choriocarcinoma combined with other germ cell elements | NCIT:C66777 | MONDO:equivalentTo | Choriocarcinoma Combined with Other Germ Cell Elements | | MONDO:0015864|MONDO:0005853 | +| MONDO:0857835 | hemolymphangioma | NCIT:C66792 | MONDO:equivalentTo | Hemolymphangioma | | MONDO:0002013 | +| MONDO:0857836 | ganglioneuromatosis | NCIT:C66804 | MONDO:equivalentTo | Ganglioneuromatosis | | MONDO:0005033 | +| MONDO:0857837 | ciliary body benign medulloepithelioma | NCIT:C66807 | MONDO:equivalentTo | Ciliary Body Benign Medulloepithelioma | | MONDO:0021486|MONDO:0017050 | +| MONDO:0857838 | ciliary body teratoid medulloepithelioma | NCIT:C66810 | MONDO:equivalentTo | Ciliary Body Teratoid Medulloepithelioma | | MONDO:0017050 | +| MONDO:0857839 | retinocytoma | NCIT:C66812 | MONDO:equivalentTo | Retinocytoma | | MONDO:0021453|MONDO:0024341 | +| MONDO:0857840 | differentiated retinoblastoma | NCIT:C66813 | MONDO:equivalentTo | Differentiated Retinoblastoma | | MONDO:0008380 | +| MONDO:0857841 | undifferentiated retinoblastoma | NCIT:C66814 | MONDO:equivalentTo | Undifferentiated Retinoblastoma | | MONDO:0008380 | +| MONDO:0857842 | diffuse retinoblastoma | NCIT:C66815 | MONDO:equivalentTo | Diffuse Retinoblastoma | | MONDO:0008380 | +| MONDO:0857844 | melanotic neurofibroma | NCIT:C66841 | MONDO:equivalentTo | Melanotic Neurofibroma | | MONDO:0016755 | +| MONDO:0857846 | testicular mixed sex cord-stromal tumor | NCIT:C66991 | MONDO:equivalentTo | Testicular Mixed Sex Cord-Stromal Tumor | | MONDO:0003125 | +| MONDO:0857847 | pyriform fossa carcinoma | NCIT:C6700 | MONDO:equivalentTo | Pyriform Fossa Carcinoma | | MONDO:0005216 | +| MONDO:0857848 | ovarian serous adenocarcinofibroma | NCIT:C67092 | MONDO:equivalentTo | Ovarian Serous Adenocarcinofibroma | | MONDO:0024885|MONDO:0002991 | +| MONDO:0857849 | sternal chondromyxoid fibroma | NCIT:C6714 | MONDO:equivalentTo | Sternal Chondromyxoid Fibroma | | MONDO:0021456|MONDO:0018447 | +| MONDO:0857850 | olfactory neurogenic tumor | NCIT:C67155 | MONDO:equivalentTo | Olfactory Neurogenic Tumor | | MONDO:0002722 | +| MONDO:0857852 | nodular sclerosis classic hodgkin lymphoma, cellular phase | NCIT:C67171 | MONDO:equivalentTo | Nodular Sclerosis Classic Hodgkin Lymphoma, Cellular Phase | | MONDO:0004665 | +| MONDO:0857853 | sternal intraosseous schwannoma | NCIT:C6718 | MONDO:equivalentTo | Sternal Intraosseous Schwannoma | | MONDO:0021456|MONDO:0004820 | +| MONDO:0857854 | peripheral primitive neuroectodermal tumor of the kidney | NCIT:C67214 | MONDO:equivalentTo | Peripheral Primitive Neuroectodermal Tumor of the Kidney | | MONDO:0018271|MONDO:0002367 | +| MONDO:0857855 | chest wall hodgkin lymphoma | NCIT:C6723 | MONDO:equivalentTo | Chest Wall Hodgkin Lymphoma | | MONDO:0004952|MONDO:0003985 | +| MONDO:0857858 | benign glomus tumor | NCIT:C6748 | MONDO:equivalentTo | Benign Glomus Tumor | | MONDO:0003342|MONDO:0018327 | +| MONDO:0857859 | malignant sex cord-stromal tumor | NCIT:C67561 | MONDO:equivalentTo | Malignant Sex Cord-Stromal Tumor | | MONDO:0006055|MONDO:0002149 | +| MONDO:0857860 | myxoid leiomyoma | NCIT:C67563 | MONDO:equivalentTo | Myxoid Leiomyoma | | MONDO:0001572 | +| MONDO:0857862 | stromal neoplasm | NCIT:C6781 | MONDO:equivalentTo | Stromal Neoplasm | | MONDO:0002616|MONDO:0006424 | +| MONDO:0857864 | benign apocrine neoplasm | NCIT:C6799 | MONDO:equivalentTo | Benign Apocrine Neoplasm | | MONDO:0003686|MONDO:0021489 | +| MONDO:0857866 | benign external ear neoplasm | NCIT:C6807 | MONDO:equivalentTo | Benign External Ear Neoplasm | | MONDO:0021474|MONDO:0021235 | +| MONDO:0857867 | prostate ductal adenocarcinoma | NCIT:C6813 | MONDO:equivalentTo | Prostate Ductal Adenocarcinoma | | MONDO:0005082 | +| MONDO:0857872 | kadish stage a olfactory neuroblastoma | NCIT:C6853 | MONDO:equivalentTo | Kadish Stage A Olfactory Neuroblastoma | | MONDO:0006329 | +| MONDO:0857873 | kadish stage b olfactory neuroblastoma | NCIT:C6854 | MONDO:equivalentTo | Kadish Stage B Olfactory Neuroblastoma | | MONDO:0006329 | +| MONDO:0857874 | oropharyngeal undifferentiated carcinoma | NCIT:C68610 | MONDO:equivalentTo | Oropharyngeal Undifferentiated Carcinoma | | MONDO:0044704|MONDO:0003572 | +| MONDO:0857876 | childhood extracranial germ cell tumor | NCIT:C68627 | MONDO:equivalentTo | Childhood Extracranial Germ Cell Tumor | | MONDO:0003751 | +| MONDO:0857879 | childhood extragonadal malignant germ cell tumor | NCIT:C68632 | MONDO:equivalentTo | Childhood Extragonadal Malignant Germ Cell Tumor | | MONDO:0003113|MONDO:0004479 | +| MONDO:0857881 | adrenal cortical low grade carcinoma | NCIT:C68635 | MONDO:equivalentTo | Adrenal Cortical Low Grade Carcinoma | | MONDO:0006639 | +| MONDO:0857882 | adrenal cortical sarcomatoid carcinoma | NCIT:C68644 | MONDO:equivalentTo | Adrenal Cortical Sarcomatoid Carcinoma | | MONDO:0006639|MONDO:0006406 | +| MONDO:0857884 | hodgkin lymphoma by clinical course | NCIT:C68666 | MONDO:equivalentTo | Hodgkin Lymphoma by Clinical Course | | MONDO:0004952 | +| MONDO:0857892 | adult gliosarcoma | NCIT:C68701 | MONDO:equivalentTo | Adult Gliosarcoma | | MONDO:0020690|MONDO:0016681 | +| MONDO:0857893 | adult giant cell glioblastoma | NCIT:C68702 | MONDO:equivalentTo | Adult Giant Cell Glioblastoma | | MONDO:0020690|MONDO:0016682 | +| MONDO:0857895 | pancreatic mixed acinar carcinoma-neuroendocrine carcinoma | NCIT:C6878 | MONDO:equivalentTo | Pancreatic Mixed Acinar Carcinoma-Neuroendocrine Carcinoma | | MONDO:0044727 | +| MONDO:0857896 | cellular fibroma | NCIT:C6892 | MONDO:equivalentTo | Cellular Fibroma | | MONDO:0005167 | +| MONDO:0857897 | malignant solitary fibrous tumor | NCIT:C6894 | MONDO:equivalentTo | Malignant Solitary Fibrous Tumor | | MONDO:0016238|MONDO:0004992 | +| MONDO:0857899 | atypical burkitt/burkitt-like lymphoma | NCIT:C6917 | MONDO:equivalentTo | Atypical Burkitt/Burkitt-Like Lymphoma | | MONDO:0007243 | +| MONDO:0857900 | acute myeloid leukemia with a variant kmt2a rearrangement | NCIT:C6924 | MONDO:equivalentTo | Acute Myeloid Leukemia with a Variant KMT2A Rearrangement | | MONDO:0100404 | +| MONDO:0857901 | malignant ovarian thecoma | NCIT:C6929 | MONDO:equivalentTo | Malignant Ovarian Thecoma | | MONDO:0018172|MONDO:0037253 | +| MONDO:0857902 | solitary plasmacytoma | NCIT:C6932 | MONDO:equivalentTo | Solitary Plasmacytoma | | MONDO:0005615 | +| MONDO:0857903 | deep (aggressive) angiomyxoma | NCIT:C6936 | MONDO:equivalentTo | Deep (Aggressive) Angiomyxoma | | MONDO:0006086 | +| MONDO:0857904 | cardiac fibroma | NCIT:C6947 | MONDO:equivalentTo | Cardiac Fibroma | | MONDO:0021450|MONDO:0005167 | +| MONDO:0857906 | anaplastic kidney wilms tumor | NCIT:C6952 | MONDO:equivalentTo | Anaplastic Kidney Wilms Tumor | | MONDO:0019004|MONDO:0020633 | +| MONDO:0857907 | simple endometrial hyperplasia with atypia | NCIT:C6991 | MONDO:equivalentTo | Simple Endometrial Hyperplasia with Atypia | | MONDO:0006410 | +| MONDO:0857910 | central nervous system kaposi sarcoma | NCIT:C7006 | MONDO:equivalentTo | Central Nervous System Kaposi Sarcoma | | MONDO:0005055|MONDO:0002217 | +| MONDO:0857913 | central nervous system inflammatory myofibroblastic tumor | NCIT:C7020 | MONDO:equivalentTo | Central Nervous System Inflammatory Myofibroblastic Tumor | | MONDO:0015798|MONDO:0003244 | +| MONDO:0857918 | meningioma by site | NCIT:C7051 | MONDO:equivalentTo | Meningioma by Site | | MONDO:0016642 | +| MONDO:0857919 | mature b-cell non-hodgkin lymphoma | NCIT:C7056 | MONDO:equivalentTo | Mature B-Cell Non-Hodgkin Lymphoma | | MONDO:0015759|MONDO:0004949 | +| MONDO:0857921 | neoplasm by special category | NCIT:C7062 | MONDO:equivalentTo | Neoplasm by Special Category | | MONDO:0005070 | +| MONDO:0857925 | megakaryocytic neoplasm | NCIT:C7066 | MONDO:equivalentTo | Megakaryocytic Neoplasm | | MONDO:0005170|MONDO:0021138 | +| MONDO:0857926 | prostate cancer by whitmore-jewett stage | NCIT:C7079 | MONDO:equivalentTo | Prostate Cancer by Whitmore-Jewett Stage | | MONDO:0005159 | +| MONDO:0857931 | metastatic non-cutaneous melanoma | NCIT:C7092 | MONDO:equivalentTo | Metastatic Non-Cutaneous Melanoma | | MONDO:0005191|MONDO:0006320 | +| MONDO:0857935 | teratoid hepatoblastoma | NCIT:C7098 | MONDO:equivalentTo | Teratoid Hepatoblastoma | | MONDO:0003650 | +| MONDO:0857937 | adult pilocytic astrocytoma | NCIT:C71016 | MONDO:equivalentTo | Adult Pilocytic Astrocytoma | | MONDO:0002503|MONDO:0016691 | +| MONDO:0857940 | liver non-epithelial neoplasm | NCIT:C7107 | MONDO:equivalentTo | Liver Non-Epithelial Neoplasm | | MONDO:0024477 | +| MONDO:0857943 | stage i liver cancer | NCIT:C7116 | MONDO:equivalentTo | Stage I Liver Cancer | | MONDO:0018531 | +| MONDO:0857944 | stage ii liver cancer | NCIT:C7117 | MONDO:equivalentTo | Stage II Liver Cancer | | MONDO:0018531 | +| MONDO:0857945 | stage iii liver cancer | NCIT:C7118 | MONDO:equivalentTo | Stage III Liver Cancer | | MONDO:0018531 | +| MONDO:0857946 | stage iv liver cancer | NCIT:C7121 | MONDO:equivalentTo | Stage IV Liver Cancer | | MONDO:0018531 | +| MONDO:0857947 | intrahepatic bile duct microcystic adenoma | NCIT:C7127 | MONDO:equivalentTo | Intrahepatic Bile Duct Microcystic Adenoma | | MONDO:0003444|MONDO:0003435 | +| MONDO:0857948 | gallbladder benign non-epithelial neoplasm | NCIT:C7129 | MONDO:equivalentTo | Gallbladder Benign Non-Epithelial Neoplasm | | MONDO:0021503 | +| MONDO:0857950 | childhood grade 2 meningioma | NCIT:C71301 | MONDO:equivalentTo | Childhood Grade 2 Meningioma | | MONDO:0003057|MONDO:0045056 | +| MONDO:0857952 | ovarian sertoli cell tumor | NCIT:C7133 | MONDO:equivalentTo | Ovarian Sertoli Cell Tumor | | MONDO:0002696|MONDO:0020807 | +| MONDO:0857961 | benign fibroblastic neoplasm | NCIT:C7147 | MONDO:equivalentTo | Benign Fibroblastic Neoplasm | | MONDO:0006209|MONDO:0044335 | +| MONDO:0857962 | soft tissue tumor of uncertain differentiation | NCIT:C7148 | MONDO:equivalentTo | Soft Tissue Tumor of Uncertain Differentiation | | MONDO:0006424 | +| MONDO:0857963 | monoclonal immunoglobulin deposition disease | NCIT:C7151 | MONDO:equivalentTo | Monoclonal Immunoglobulin Deposition Disease | | MONDO:0004949 | +| MONDO:0857964 | erythroleukemia | NCIT:C7152 | MONDO:equivalentTo | Erythroleukemia | | MONDO:0017858 | +| MONDO:0857965 | primary central chondrosarcoma | NCIT:C7155 | MONDO:equivalentTo | Primary Central Chondrosarcoma | | MONDO:0008977|MONDO:0021054 | +| MONDO:0857966 | benign dermal neoplasm | NCIT:C7158 | MONDO:equivalentTo | Benign Dermal Neoplasm | | MONDO:0002300|MONDO:0021440 | +| MONDO:0857967 | grade 1 nodular sclerosis classic hodgkin lymphoma | NCIT:C7165 | MONDO:equivalentTo | Grade 1 Nodular Sclerosis Classic Hodgkin Lymphoma | | MONDO:0004665 | +| MONDO:0857968 | grade 2 nodular sclerosis classic hodgkin lymphoma | NCIT:C7166 | MONDO:equivalentTo | Grade 2 Nodular Sclerosis Classic Hodgkin Lymphoma | | MONDO:0004665 | +| MONDO:0857971 | adult diffuse astrocytoma | NCIT:C7174 | MONDO:equivalentTo | Adult Diffuse Astrocytoma | | MONDO:0004320|MONDO:0016686 | +| MONDO:0857972 | spindle cell/pleomorphic lipoma | NCIT:C7180 | MONDO:equivalentTo | Spindle Cell/Pleomorphic Lipoma | | MONDO:0005106 | +| MONDO:0857973 | classical burkitt lymphoma | NCIT:C7188 | MONDO:equivalentTo | Classical Burkitt Lymphoma | | MONDO:0007243 | +| MONDO:0857974 | burkitt lymphoma with plasmacytoid differentiation | NCIT:C7189 | MONDO:equivalentTo | Burkitt Lymphoma with Plasmacytoid Differentiation | | MONDO:0007243 | +| MONDO:0857975 | type b lymphomatoid papulosis | NCIT:C7198 | MONDO:equivalentTo | Type B Lymphomatoid Papulosis | | MONDO:0020326 | +| MONDO:0857976 | lymphoepithelioid variant peripheral t-cell lymphoma, not otherwise specified | NCIT:C7205 | MONDO:equivalentTo | Lymphoepithelioid Variant Peripheral T-Cell Lymphoma, Not Otherwise Specified | | MONDO:0004964 | +| MONDO:0857977 | common variant anaplastic large cell lymphoma | NCIT:C7206 | MONDO:equivalentTo | Common Variant Anaplastic Large Cell Lymphoma | | MONDO:0020325 | +| MONDO:0857978 | lymphohistiocytic variant anaplastic large cell lymphoma | NCIT:C7207 | MONDO:equivalentTo | Lymphohistiocytic Variant Anaplastic Large Cell Lymphoma | | MONDO:0020325 | +| MONDO:0857981 | non-hodgkin lymphoma by clinical course | NCIT:C7215 | MONDO:equivalentTo | Non-Hodgkin Lymphoma by Clinical Course | | MONDO:0018908 | +| MONDO:0857982 | primary cutaneous hodgkin lymphoma | NCIT:C7221 | MONDO:equivalentTo | Primary Cutaneous Hodgkin Lymphoma | | MONDO:0004952|MONDO:0018898 | +| MONDO:0857984 | blastoid variant mantle cell lymphoma | NCIT:C7229 | MONDO:equivalentTo | Blastoid Variant Mantle Cell Lymphoma | | MONDO:0018876 | +| MONDO:0857995 | follicular lymphoma with predominantly diffuse growth pattern | NCIT:C7264 | MONDO:equivalentTo | Follicular Lymphoma with Predominantly Diffuse Growth Pattern | | MONDO:0018906 | +| MONDO:0857996 | minimally invasive lung mucinous adenocarcinoma | NCIT:C7268 | MONDO:equivalentTo | Minimally Invasive Lung Mucinous Adenocarcinoma | | MONDO:0004991 | +| MONDO:0857997 | minimally invasive lung non-mucinous adenocarcinoma | NCIT:C7269 | MONDO:equivalentTo | Minimally Invasive Lung Non-Mucinous Adenocarcinoma | | MONDO:0004991 | +| MONDO:0857998 | ovarian dermoid cyst with secondary tumor | NCIT:C7284 | MONDO:equivalentTo | Ovarian Dermoid Cyst with Secondary Tumor | | MONDO:0003331 | +| MONDO:0857999 | ovarian granulosa-stromal cell tumor | NCIT:C7287 | MONDO:equivalentTo | Ovarian Granulosa-Stromal Cell Tumor | | MONDO:0021657 | +| MONDO:0858001 | malignant splenic soft tissue neoplasm | NCIT:C7292 | MONDO:equivalentTo | Malignant Splenic Soft Tissue Neoplasm | | MONDO:0024637|MONDO:0005966 | +| MONDO:0858002 | splenic manifestation of t-cell prolymphocytic leukemia | NCIT:C7298 | MONDO:equivalentTo | Splenic Manifestation of T-Cell Prolymphocytic Leukemia | | MONDO:0002966|MONDO:0019468 | +| MONDO:0858003 | splenic manifestation of b-cell prolymphocytic leukemia | NCIT:C7299 | MONDO:equivalentTo | Splenic Manifestation of B-Cell Prolymphocytic Leukemia | | MONDO:0002966|MONDO:0019461 | +| MONDO:0858004 | splenic manifestation of chronic lymphocytic leukemia | NCIT:C7300 | MONDO:equivalentTo | Splenic Manifestation of Chronic Lymphocytic Leukemia | | MONDO:0004107|MONDO:0004948 | +| MONDO:0858005 | splenic manifestation of t-cell large granular lymphocyte leukemia | NCIT:C7302 | MONDO:equivalentTo | Splenic Manifestation of T-Cell Large Granular Lymphocyte Leukemia | | MONDO:0004107|MONDO:0019469 | +| MONDO:0858006 | splenic manifestation of chronic myeloid leukemia, bcr-abl1 positive | NCIT:C7303 | MONDO:equivalentTo | Splenic Manifestation of Chronic Myeloid Leukemia, BCR-ABL1 Positive | | MONDO:0004107|MONDO:0011996 | +| MONDO:0858007 | splenic lymphoplasmacytic lymphoma | NCIT:C7305 | MONDO:equivalentTo | Splenic Lymphoplasmacytic Lymphoma | | MONDO:0000432 | +| MONDO:0858008 | splenic lymphoblastic lymphoma | NCIT:C7312 | MONDO:equivalentTo | Splenic Lymphoblastic Lymphoma | | MONDO:0000873 | +| MONDO:0858010 | acute monoblastic and monocytic leukemia | NCIT:C7318 | MONDO:equivalentTo | Acute Monoblastic and Monocytic Leukemia | | MONDO:0015667 | +| MONDO:0858011 | childhood chronic myeloid leukemia, bcr-abl1 positive | NCIT:C7320 | MONDO:equivalentTo | Childhood Chronic Myeloid Leukemia, BCR-ABL1 Positive | | MONDO:0011996|MONDO:0004355 | +| MONDO:0858012 | ovarian mixed germ cell-sex cord-stromal tumor | NCIT:C7321 | MONDO:equivalentTo | Ovarian Mixed Germ Cell-Sex Cord-Stromal Tumor | | MONDO:0002478|MONDO:0021068 | +| MONDO:0858013 | testicular mixed germ cell-sex cord-stromal tumor | NCIT:C7322 | MONDO:equivalentTo | Testicular Mixed Germ Cell-Sex Cord-Stromal Tumor | | MONDO:0002478|MONDO:0021348 | +| MONDO:0858016 | reproductive endocrine neoplasm | NCIT:C7335 | MONDO:equivalentTo | Reproductive Endocrine Neoplasm | | MONDO:0006054|MONDO:0002082|MONDO:0002259 | +| MONDO:0858017 | high grade intraepithelial neoplasia | NCIT:C7348 | MONDO:equivalentTo | High Grade Intraepithelial Neoplasia | | MONDO:0024474 | +| MONDO:0858019 | cerebellar glioneuronal and neuronal tumors | NCIT:C7372 | MONDO:equivalentTo | Cerebellar Glioneuronal and Neuronal Tumors | | MONDO:0016729|MONDO:0002913 | +| MONDO:0858020 | benign vascular neoplasm | NCIT:C7389 | MONDO:equivalentTo | Benign Vascular Neoplasm | | MONDO:0024296|MONDO:0000654 | +| MONDO:0858021 | malignant vascular neoplasm | NCIT:C7390 | MONDO:equivalentTo | Malignant Vascular Neoplasm | | MONDO:0024296|MONDO:0002100 | +| MONDO:0858024 | precancerous condition by site | NCIT:C7422 | MONDO:equivalentTo | Precancerous Condition by Site | | | +| MONDO:0858025 | oral cavity and lip precancerous condition | NCIT:C7425 | MONDO:equivalentTo | Oral Cavity and Lip Precancerous Condition | | | +| MONDO:0858029 | invasive papillary adenocarcinoma | NCIT:C7438 | MONDO:equivalentTo | Invasive Papillary Adenocarcinoma | | MONDO:0040677|MONDO:0002512 | +| MONDO:0858030 | benign myoepithelioma | NCIT:C7442 | MONDO:equivalentTo | Benign Myoepithelioma | | MONDO:0044335|MONDO:0002380 | +| MONDO:0858036 | pure erythroid leukemia | NCIT:C7467 | MONDO:equivalentTo | Pure Erythroid Leukemia | | MONDO:0017858 | +| MONDO:0858037 | anal extramucosal (perianal) adenocarcinoma | NCIT:C7474 | MONDO:equivalentTo | Anal Extramucosal (Perianal) Adenocarcinoma | | MONDO:0002652 | +| MONDO:0858042 | ameloblastic carcinoma-primary type | NCIT:C7493 | MONDO:equivalentTo | Ameloblastic Carcinoma-Primary Type | | MONDO:0006079 | +| MONDO:0858043 | ameloblastic carcinoma-secondary type (dedifferentiated) | NCIT:C7496 | MONDO:equivalentTo | Ameloblastic Carcinoma-Secondary Type (Dedifferentiated) | | MONDO:0006079|MONDO:0024878 | +| MONDO:0858044 | ameloblastic carcinoma derived from odontogenic cyst | NCIT:C7497 | MONDO:equivalentTo | Ameloblastic Carcinoma Derived From Odontogenic Cyst | | MONDO:0006079|MONDO:0024878 | +| MONDO:0858045 | primary intraosseous carcinoma, not otherwise specified, derived from odontogenic cyst | NCIT:C7500 | MONDO:equivalentTo | Primary Intraosseous Carcinoma, Not Otherwise Specified, Derived from Odontogenic Cyst | | MONDO:0006385 | +| MONDO:0858049 | metastatic malignant neoplasm in the breast | NCIT:C7511 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Breast | | MONDO:0007254|MONDO:0024880 | +| MONDO:0858050 | malignant esophageal neoplasm by anatomic region | NCIT:C7512 | MONDO:equivalentTo | Malignant Esophageal Neoplasm by Anatomic Region | | MONDO:0007576 | +| MONDO:0858051 | malignant esophageal neoplasm by topographic region | NCIT:C7513 | MONDO:equivalentTo | Malignant Esophageal Neoplasm by Topographic Region | | MONDO:0007576 | +| MONDO:0858052 | kidney and ureter neoplasm | NCIT:C7514 | MONDO:equivalentTo | Kidney and Ureter Neoplasm | | MONDO:0021066 | +| MONDO:0858059 | atypical adenoma | NCIT:C7559 | MONDO:equivalentTo | Atypical Adenoma | | MONDO:0004972 | +| MONDO:0858060 | eccrine hidrocystoma | NCIT:C7565 | MONDO:equivalentTo | Eccrine Hidrocystoma | | MONDO:0024247|MONDO:0006787 | +| MONDO:0858066 | regressing nevus | NCIT:C7603 | MONDO:equivalentTo | Regressing Nevus | | MONDO:0044794 | +| MONDO:0858068 | cerebral non-hodgkin lymphoma | NCIT:C7609 | MONDO:equivalentTo | Cerebral Non-Hodgkin Lymphoma | | MONDO:0003655|MONDO:0044887 | +| MONDO:0858069 | malignant thymoma | NCIT:C7612 | MONDO:equivalentTo | Malignant Thymoma | | MONDO:0002586|MONDO:0006456 | +| MONDO:0858070 | cutaneous lymphoproliferative disorder | NCIT:C7614 | MONDO:equivalentTo | Cutaneous Lymphoproliferative Disorder | | | +| MONDO:0858074 | bilateral malignant neoplasm | NCIT:C7627 | MONDO:equivalentTo | Bilateral Malignant Neoplasm | | MONDO:0004992 | +| MONDO:0858080 | intermediate soft tissue neoplasm | NCIT:C7653 | MONDO:equivalentTo | Intermediate Soft Tissue Neoplasm | | MONDO:0006424 | +| MONDO:0858081 | carcinoma in a polyp | NCIT:C7682 | MONDO:equivalentTo | Carcinoma in a Polyp | | MONDO:0004993 | +| MONDO:0858082 | invasive breast ductal carcinoma and lobular carcinoma in situ | NCIT:C7689 | MONDO:equivalentTo | Invasive Breast Ductal Carcinoma and Lobular Carcinoma In Situ | | MONDO:0005050 | +| MONDO:0858083 | breast ductal carcinoma in situ and lobular carcinoma | NCIT:C7690 | MONDO:equivalentTo | Breast Ductal Carcinoma In Situ and Lobular Carcinoma | | MONDO:0006306 | +| MONDO:0858086 | adult hodgkin lymphoma | NCIT:C7702 | MONDO:equivalentTo | Adult Hodgkin Lymphoma | | MONDO:0004952|MONDO:0003660 | +| MONDO:0858087 | adult non-hodgkin lymphoma | NCIT:C7704 | MONDO:equivalentTo | Adult Non-Hodgkin Lymphoma | | MONDO:0003660|MONDO:0018908 | +| MONDO:0858088 | childhood non-hodgkin lymphoma | NCIT:C7706 | MONDO:equivalentTo | Childhood Non-Hodgkin Lymphoma | | MONDO:0003659|MONDO:0018908 | +| MONDO:0858089 | adult soft tissue sarcoma | NCIT:C7707 | MONDO:equivalentTo | Adult Soft Tissue Sarcoma | | MONDO:0018078 | +| MONDO:0858091 | adult liver carcinoma | NCIT:C7711 | MONDO:equivalentTo | Adult Liver Carcinoma | | MONDO:0018531 | +| MONDO:0858092 | childhood hodgkin lymphoma | NCIT:C7714 | MONDO:equivalentTo | Childhood Hodgkin Lymphoma | | MONDO:0004952|MONDO:0003659 | +| MONDO:0858094 | gingival carcinoma | NCIT:C7721 | MONDO:equivalentTo | Gingival Carcinoma | | MONDO:0005507|MONDO:0044925 | +| MONDO:0858095 | vaginal clear cell adenocarcinoma | NCIT:C7735 | MONDO:equivalentTo | Vaginal Clear Cell Adenocarcinoma | | MONDO:0020653|MONDO:0005004 | +| MONDO:0858096 | digestive system hemangioma | NCIT:C7741 | MONDO:equivalentTo | Digestive System Hemangioma | | MONDO:0000385|MONDO:0006500 | +| MONDO:0858097 | mucous membrane hemangioma | NCIT:C7744 | MONDO:equivalentTo | Mucous Membrane Hemangioma | | MONDO:0006500 | +| MONDO:0858099 | cardiac myxoma | NCIT:C7748 | MONDO:equivalentTo | Cardiac Myxoma | | MONDO:0044784|MONDO:0021505 | +| MONDO:0858100 | malignant pericarditis | NCIT:C7753 | MONDO:equivalentTo | Malignant Pericarditis | | MONDO:0001322|MONDO:0005904 | +| MONDO:0858108 | adult leiomyosarcoma | NCIT:C7810 | MONDO:equivalentTo | Adult Leiomyosarcoma | | MONDO:0005058 | +| MONDO:0858116 | regional neuroblastoma | NCIT:C7836 | MONDO:equivalentTo | Regional Neuroblastoma | | MONDO:0005072 | +| MONDO:0858119 | stage i kidney wilms tumor | NCIT:C7840 | MONDO:equivalentTo | Stage I Kidney Wilms Tumor | | MONDO:0019004 | +| MONDO:0858120 | stage ii kidney wilms tumor | NCIT:C7841 | MONDO:equivalentTo | Stage II Kidney Wilms Tumor | | MONDO:0019004 | +| MONDO:0858121 | stage iii kidney wilms tumor | NCIT:C7842 | MONDO:equivalentTo | Stage III Kidney Wilms Tumor | | MONDO:0019004 | +| MONDO:0858122 | stage iv kidney wilms tumor | NCIT:C7843 | MONDO:equivalentTo | Stage IV Kidney Wilms Tumor | | MONDO:0019004 | +| MONDO:0858123 | stage v kidney wilms tumor | NCIT:C7844 | MONDO:equivalentTo | Stage V Kidney Wilms Tumor | | MONDO:0019004 | +| MONDO:0858126 | limited stage lung small cell carcinoma | NCIT:C7853 | MONDO:equivalentTo | Limited Stage Lung Small Cell Carcinoma | | MONDO:0008433 | +| MONDO:0858151 | grade i lymphomatoid granulomatosis | NCIT:C7931 | MONDO:equivalentTo | Grade I Lymphomatoid Granulomatosis | | MONDO:0019466 | +| MONDO:0858152 | grade ii lymphomatoid granulomatosis | NCIT:C7932 | MONDO:equivalentTo | Grade II Lymphomatoid Granulomatosis | | MONDO:0019466 | +| MONDO:0858155 | breast ductal carcinoma in situ, high grade | NCIT:C7949 | MONDO:equivalentTo | Breast Ductal Carcinoma In Situ, High Grade | | MONDO:0005023 | +| MONDO:0858156 | breast paget disease with invasive ductal carcinoma | NCIT:C7951 | MONDO:equivalentTo | Breast Paget Disease with Invasive Ductal Carcinoma | | MONDO:0006256|MONDO:0002648 | +| MONDO:0858161 | childhood acute promyelocytic leukemia with t(15;17)(q24.1;q21.2); pml-rara | NCIT:C7968 | MONDO:equivalentTo | Childhood Acute Promyelocytic Leukemia with t(15;17)(q24.1;q21.2); PML-RARA | | MONDO:0012883|MONDO:0004996 | +| MONDO:0858166 | distal bile duct adenocarcinoma | NCIT:C7976 | MONDO:equivalentTo | Distal Bile Duct Adenocarcinoma | | MONDO:0002665|MONDO:0003707|MONDO:0019087 | +| MONDO:0858169 | carcinoma arising from craniopharyngioma | NCIT:C79949 | MONDO:equivalentTo | Carcinoma Arising from Craniopharyngioma | | MONDO:0024878 | +| MONDO:0858170 | testicular mixed embryonal carcinoma and yolk sac tumor | NCIT:C8001 | MONDO:equivalentTo | Testicular Mixed Embryonal Carcinoma and Yolk Sac Tumor | | MONDO:0003120|MONDO:0003403 | +| MONDO:0858171 | testicular mixed yolk sac tumor and teratoma | NCIT:C8002 | MONDO:equivalentTo | Testicular Mixed Yolk Sac Tumor and Teratoma | | MONDO:0003120|MONDO:0003403 | +| MONDO:0858172 | testicular mixed yolk sac tumor and teratoma with seminoma | NCIT:C8003 | MONDO:equivalentTo | Testicular Mixed Yolk Sac Tumor and Teratoma with Seminoma | | MONDO:0003120 | +| MONDO:0858173 | pancreatic somatostatin-producing neuroendocrine tumor | NCIT:C8006 | MONDO:equivalentTo | Pancreatic Somatostatin-Producing Neuroendocrine Tumor | | MONDO:0006976|MONDO:0002994 | +| MONDO:0858174 | salivary gland low grade carcinoma | NCIT:C8012 | MONDO:equivalentTo | Salivary Gland Low Grade Carcinoma | | MONDO:0000521 | +| MONDO:0858175 | lip basal cell carcinoma | NCIT:C8014 | MONDO:equivalentTo | Lip Basal Cell Carcinoma | | MONDO:0005341|MONDO:0021333 | +| MONDO:0858176 | salivary gland intermediate grade mucoepidermoid carcinoma | NCIT:C8017 | MONDO:equivalentTo | Salivary Gland Intermediate Grade Mucoepidermoid Carcinoma | | MONDO:0021009 | +| MONDO:0858177 | salivary gland high grade carcinoma | NCIT:C8018 | MONDO:equivalentTo | Salivary Gland High Grade Carcinoma | | MONDO:0000521 | +| MONDO:0858178 | salivary gland adenocarcinoma | NCIT:C8021 | MONDO:equivalentTo | Salivary Gland Adenocarcinoma | | MONDO:0000521|MONDO:0004970 | +| MONDO:0858179 | salivary gland poorly differentiated squamous cell carcinoma | NCIT:C8022 | MONDO:equivalentTo | Salivary Gland Poorly Differentiated Squamous Cell Carcinoma | | MONDO:0044740 | +| MONDO:0858180 | salivary gland undifferentiated carcinoma | NCIT:C8024 | MONDO:equivalentTo | Salivary Gland Undifferentiated Carcinoma | | MONDO:0000521|MONDO:0005617 | +| MONDO:0858182 | diffuse large b-cell lymphoma, not otherwise specified | NCIT:C80280 | MONDO:equivalentTo | Diffuse Large B-Cell Lymphoma, Not Otherwise Specified | | MONDO:0018905 | +| MONDO:0858183 | diffuse large b-cell lymphoma associated with chronic inflammation | NCIT:C80289 | MONDO:equivalentTo | Diffuse Large B-Cell Lymphoma Associated with Chronic Inflammation | | MONDO:0018905 | +| MONDO:0858184 | progressive hairy cell leukemia initial treatment | NCIT:C8029 | MONDO:equivalentTo | Progressive Hairy Cell Leukemia Initial Treatment | | MONDO:0018935 | +| MONDO:0858185 | high grade b-cell lymphoma, not otherwise specified | NCIT:C80291 | MONDO:equivalentTo | High Grade B-Cell Lymphoma, Not Otherwise Specified | | MONDO:0044889 | +| MONDO:0858186 | pediatric-type follicular lymphoma | NCIT:C80297 | MONDO:equivalentTo | Pediatric-Type Follicular Lymphoma | | MONDO:0018906 | +| MONDO:0858189 | monoclonal b-cell lymphocytosis | NCIT:C80310 | MONDO:equivalentTo | Monoclonal B-Cell Lymphocytosis | | MONDO:0004949 | +| MONDO:0858190 | b lymphoblastic leukemia/lymphoma, not otherwise specified | NCIT:C80326 | MONDO:equivalentTo | B Lymphoblastic Leukemia/Lymphoma, Not Otherwise Specified | | MONDO:0004947 | +| MONDO:0858191 | b lymphoblastic leukemia/lymphoma with t(1;19)(q23;p13.3); tcf3-pbx1 | NCIT:C80341 | MONDO:equivalentTo | B Lymphoblastic Leukemia/Lymphoma with t(1;19)(q23;p13.3); TCF3-PBX1 | | MONDO:0035605 | +| MONDO:0858205 | regional adrenal gland pheochromocytoma | NCIT:C8045 | MONDO:equivalentTo | Regional Adrenal Gland Pheochromocytoma | | MONDO:0004974 | +| MONDO:0858211 | stage i ovarian germ cell tumor ajcc v6 and v7 | NCIT:C8083 | MONDO:equivalentTo | Stage I Ovarian Germ Cell Tumor AJCC v6 and v7 | | MONDO:0018171 | +| MONDO:0858212 | stage ii ovarian germ cell tumor ajcc v6 and v7 | NCIT:C8084 | MONDO:equivalentTo | Stage II Ovarian Germ Cell Tumor AJCC v6 and v7 | | MONDO:0018171 | +| MONDO:0858213 | stage iii ovarian germ cell tumor ajcc v6 and v7 | NCIT:C8085 | MONDO:equivalentTo | Stage III Ovarian Germ Cell Tumor AJCC v6 and v7 | | MONDO:0018171 | +| MONDO:0858214 | stage iv ovarian germ cell tumor ajcc v6 and v7 | NCIT:C8086 | MONDO:equivalentTo | Stage IV Ovarian Germ Cell Tumor AJCC v6 and v7 | | MONDO:0018171 | +| MONDO:0858219 | regional renal pelvis and ureter urothelial carcinoma | NCIT:C8168 | MONDO:equivalentTo | Regional Renal Pelvis and Ureter Urothelial Carcinoma | | MONDO:0020654 | +| MONDO:0858221 | buccal mucosa verrucous carcinoma | NCIT:C8175 | MONDO:equivalentTo | Buccal Mucosa Verrucous Carcinoma | | MONDO:0021538|MONDO:0021431 | +| MONDO:0858222 | fibroblastic reticular cell sarcoma | NCIT:C81758 | MONDO:equivalentTo | Fibroblastic Reticular Cell Sarcoma | | MONDO:0006247|MONDO:0004992 | +| MONDO:0858224 | disseminated juvenile xanthogranuloma | NCIT:C81772 | MONDO:equivalentTo | Disseminated Juvenile Xanthogranuloma | | MONDO:0006247 | +| MONDO:0858225 | oral cavity adenoid cystic carcinoma | NCIT:C8179 | MONDO:equivalentTo | Oral Cavity Adenoid Cystic Carcinoma | | MONDO:0044925|MONDO:0004971 | +| MONDO:0858240 | mixed phenotype acute leukemia, b/myeloid | NCIT:C82212 | MONDO:equivalentTo | Mixed Phenotype Acute Leukemia, B/Myeloid | | MONDO:0020743 | +| MONDO:0858241 | mixed phenotype acute leukemia, t/myeloid | NCIT:C82213 | MONDO:equivalentTo | Mixed Phenotype Acute Leukemia, T/Myeloid | | MONDO:0020743 | +| MONDO:0858242 | natural killer cell lymphoblastic leukemia/lymphoma | NCIT:C82217 | MONDO:equivalentTo | Natural Killer Cell Lymphoblastic Leukemia/Lymphoma | | MONDO:0003538 | +| MONDO:0858245 | myelodysplastic/myeloproliferative neoplasm post cytotoxic therapy | NCIT:C82397 | MONDO:equivalentTo | Myelodysplastic/Myeloproliferative Neoplasm Post Cytotoxic Therapy | | MONDO:0006450|MONDO:0006311 | +| MONDO:0858246 | acute myeloid leukemia with myelodysplasia-related gene mutations | NCIT:C82430 | MONDO:equivalentTo | Acute Myeloid Leukemia with Myelodysplasia-Related Gene Mutations | | MONDO:0100409 | +| MONDO:0858249 | de novo myelodysplastic syndrome | NCIT:C8253 | MONDO:equivalentTo | de novo Myelodysplastic Syndrome | | MONDO:0018881 | +| MONDO:0858251 | adult anaplastic astrocytoma | NCIT:C8257 | MONDO:equivalentTo | Adult Anaplastic Astrocytoma | | MONDO:0016684|MONDO:0004320 | +| MONDO:0858252 | refractory neutropenia | NCIT:C82593 | MONDO:equivalentTo | Refractory Neutropenia | | MONDO:0005272 | +| MONDO:0858253 | refractory thrombocytopenia | NCIT:C82594 | MONDO:equivalentTo | Refractory Thrombocytopenia | | MONDO:0005272 | +| MONDO:0858254 | myelodysplastic syndrome with excess blasts and fibrosis | NCIT:C82595 | MONDO:equivalentTo | Myelodysplastic Syndrome with Excess Blasts and Fibrosis | | MONDO:0019454 | +| MONDO:0858256 | myelodysplastic/myeloproliferative neoplasm with ring sideroblasts and thrombocytosis, not otherwise specified | NCIT:C82616 | MONDO:equivalentTo | Myelodysplastic/Myeloproliferative Neoplasm with Ring Sideroblasts and Thrombocytosis, Not Otherwise Specified | | MONDO:0006311 | +| MONDO:0858257 | adult cholangiocarcinoma | NCIT:C8265 | MONDO:equivalentTo | Adult Cholangiocarcinoma | | MONDO:0019087 | +| MONDO:0858258 | meyerson nevus | NCIT:C82862 | MONDO:equivalentTo | Meyerson Nevus | | MONDO:0044794 | +| MONDO:0858259 | cystic oncocytic neoplasm | NCIT:C82890 | MONDO:equivalentTo | Cystic Oncocytic Neoplasm | | MONDO:0010795 | +| MONDO:0858265 | duodenal extraskeletal osteosarcoma | NCIT:C82972 | MONDO:equivalentTo | Duodenal Extraskeletal Osteosarcoma | | MONDO:0000920|MONDO:0002621|MONDO:0003361 | +| MONDO:0858272 | cellular pleomorphic adenoma | NCIT:C83174 | MONDO:equivalentTo | Cellular Pleomorphic Adenoma | | MONDO:0008401 | +| MONDO:0858275 | atypical hyperplasia | NCIT:C8355 | MONDO:equivalentTo | Atypical Hyperplasia | | | +| MONDO:0858277 | low grade intraepithelial neoplasia | NCIT:C8367 | MONDO:equivalentTo | Low Grade Intraepithelial Neoplasia | | MONDO:0024474 | +| MONDO:0858280 | lymphangiomatosis | NCIT:C8373 | MONDO:equivalentTo | Lymphangiomatosis | | MONDO:0036870 | +| MONDO:0858283 | fibrohistiocytic neoplasm | NCIT:C8402 | MONDO:equivalentTo | Fibrohistiocytic Neoplasm | | MONDO:0002616 | +| MONDO:0858284 | benign supraglottis neoplasm | NCIT:C8414 | MONDO:equivalentTo | Benign Supraglottis Neoplasm | | MONDO:0004427|MONDO:0002354 | +| MONDO:0858285 | benign bartholin gland neoplasm | NCIT:C8418 | MONDO:equivalentTo | Benign Bartholin Gland Neoplasm | | MONDO:0021114|MONDO:0000643 | +| MONDO:0858286 | diffuse malignant mesothelioma | NCIT:C8420 | MONDO:equivalentTo | Diffuse Malignant Mesothelioma | | MONDO:0006292 | +| MONDO:0858287 | renal benign mesenchymoma | NCIT:C84256 | MONDO:equivalentTo | Renal Benign Mesenchymoma | | MONDO:0002382 | +| MONDO:0858288 | diffuse neurofibroma | NCIT:C8426 | MONDO:equivalentTo | Diffuse Neurofibroma | | MONDO:0016755 | +| MONDO:0858289 | anaplastic astroblastoma, mn1-altered | NCIT:C84347 | MONDO:equivalentTo | Anaplastic Astroblastoma, MN1-Altered | | MONDO:0016707 | +| MONDO:0858299 | asbestos-related lung disorder | NCIT:C84472 | MONDO:equivalentTo | Asbestos-Related Lung Disorder | | | +| MONDO:0858304 | central nervous system cavernous hemangioma | NCIT:C84621 | MONDO:equivalentTo | Central Nervous System Cavernous Hemangioma | | MONDO:0003241|MONDO:0003155 | +| MONDO:0858314 | invasive malignant neoplasm | NCIT:C8505 | MONDO:equivalentTo | Invasive Malignant Neoplasm | | MONDO:0004992 | +| MONDO:0858316 | refractory carcinoma | NCIT:C8511 | MONDO:equivalentTo | Refractory Carcinoma | | MONDO:0036501|MONDO:0004993 | +| MONDO:0858321 | locally advanced malignant neoplasm | NCIT:C8524 | MONDO:equivalentTo | Locally Advanced Malignant Neoplasm | | MONDO:0024880 | +| MONDO:0858324 | benign respiratory system neoplasm | NCIT:C8531 | MONDO:equivalentTo | Benign Respiratory System Neoplasm | | MONDO:0005165|MONDO:0020641 | +| MONDO:0858330 | metastatic malignant neoplasm in the nervous system | NCIT:C8547 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Nervous System | | MONDO:0005872|MONDO:0024880 | +| MONDO:0858334 | metastatic malignant neoplasm in the retina | NCIT:C8555 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Retina | | MONDO:0044913|MONDO:0003072 | +| MONDO:0858337 | metastatic malignant neoplasm of unknown primary | NCIT:C8566 | MONDO:equivalentTo | Metastatic Malignant Neoplasm of Unknown Primary | | MONDO:0024880 | +| MONDO:0858339 | invasive cervical carcinoma | NCIT:C8577 | MONDO:equivalentTo | Invasive Cervical Carcinoma | | MONDO:0040677|MONDO:0005131 | +| MONDO:0858341 | precancerous polyp | NCIT:C8587 | MONDO:equivalentTo | Precancerous Polyp | | MONDO:0021075 | +| MONDO:0858342 | leukemic phase of lymphoma | NCIT:C8594 | MONDO:equivalentTo | Leukemic Phase of Lymphoma | | MONDO:0005402|MONDO:0018908 | +| MONDO:0858343 | postcricoid carcinoma | NCIT:C8595 | MONDO:equivalentTo | Postcricoid Carcinoma | | MONDO:0005216|MONDO:0004635 | +| MONDO:0858346 | anaplastic (malignant) intraspinal meningioma | NCIT:C8605 | MONDO:equivalentTo | Anaplastic (Malignant) Intraspinal Meningioma | | MONDO:0001279|MONDO:0020635 | +| MONDO:0858350 | malignant hepatobiliary neoplasm | NCIT:C8609 | MONDO:equivalentTo | Malignant Hepatobiliary Neoplasm | | MONDO:0002514|MONDO:0002516 | +| MONDO:0858351 | metastatic malignant neoplasm in the adrenal gland | NCIT:C8610 | MONDO:equivalentTo | Metastatic Malignant Neoplasm in the Adrenal Gland | | MONDO:0002817|MONDO:0024880 | +| MONDO:0858363 | stage i t lymphoblastic leukemia/lymphoma | NCIT:C8697 | MONDO:equivalentTo | Stage I T Lymphoblastic Leukemia/Lymphoma | | MONDO:0003537 | +| MONDO:0858364 | stage ii t lymphoblastic leukemia/lymphoma | NCIT:C8698 | MONDO:equivalentTo | Stage II T Lymphoblastic Leukemia/Lymphoma | | MONDO:0003537 | +| MONDO:0858365 | stage iii t lymphoblastic leukemia/lymphoma | NCIT:C8699 | MONDO:equivalentTo | Stage III T Lymphoblastic Leukemia/Lymphoma | | MONDO:0003537 | +| MONDO:0858366 | stage iv t lymphoblastic leukemia/lymphoma | NCIT:C8700 | MONDO:equivalentTo | Stage IV T Lymphoblastic Leukemia/Lymphoma | | MONDO:0003537 | +| MONDO:0858370 | metastatic malignant hemangiopericytoma | NCIT:C8709 | MONDO:equivalentTo | Metastatic Malignant Hemangiopericytoma | | MONDO:0009330 | +| MONDO:0858371 | primary malignant hemangiopericytoma | NCIT:C8710 | MONDO:equivalentTo | Primary Malignant Hemangiopericytoma | | MONDO:0009330 | +| MONDO:0858381 | stage i ovarian choriocarcinoma | NCIT:C8730 | MONDO:equivalentTo | Stage I Ovarian Choriocarcinoma | | MONDO:0003507 | +| MONDO:0858382 | stage ii ovarian choriocarcinoma | NCIT:C8731 | MONDO:equivalentTo | Stage II Ovarian Choriocarcinoma | | MONDO:0003507 | +| MONDO:0858383 | stage iii ovarian choriocarcinoma | NCIT:C8732 | MONDO:equivalentTo | Stage III Ovarian Choriocarcinoma | | MONDO:0003507 | +| MONDO:0858384 | stage iv ovarian choriocarcinoma | NCIT:C8733 | MONDO:equivalentTo | Stage IV Ovarian Choriocarcinoma | | MONDO:0003507 | +| MONDO:0858395 | stage i pharyngeal cancer | NCIT:C8768 | MONDO:equivalentTo | Stage I Pharyngeal Cancer | | MONDO:0021345 | +| MONDO:0858396 | stage ii pharyngeal cancer | NCIT:C8769 | MONDO:equivalentTo | Stage II Pharyngeal Cancer | | MONDO:0021345 | +| MONDO:0858397 | stage iii pharyngeal cancer | NCIT:C8770 | MONDO:equivalentTo | Stage III Pharyngeal Cancer | | MONDO:0021345 | +| MONDO:0858398 | stage iv pharyngeal cancer | NCIT:C8771 | MONDO:equivalentTo | Stage IV Pharyngeal Cancer | | MONDO:0021345 | +| MONDO:0858443 | b lymphoblastic lymphoma | NCIT:C8868 | MONDO:equivalentTo | B Lymphoblastic Lymphoma | | MONDO:0000873|MONDO:0017595|MONDO:0004947 | +| MONDO:0858446 | extragonadal embryonal carcinoma | NCIT:C8880 | MONDO:equivalentTo | Extragonadal Embryonal Carcinoma | | MONDO:0003578|MONDO:0005440 | +| MONDO:0858459 | pediatric disorder | NCIT:C89328 | MONDO:equivalentTo | Pediatric Disorder | | | +| MONDO:0858464 | fundic gland polyp | NCIT:C8961 | MONDO:equivalentTo | Fundic Gland Polyp | | MONDO:0006221|MONDO:0036976 | +| MONDO:0858471 | oral neoplasm | NCIT:C8989 | MONDO:equivalentTo | Oral Neoplasm | | MONDO:0006858|MONDO:0005586 | +| MONDO:0858472 | malignant mastocytosis | NCIT:C8991 | MONDO:equivalentTo | Malignant Mastocytosis | | MONDO:0004992|MONDO:0016586 | +| MONDO:0858473 | benign adrenal cortical neoplasm | NCIT:C9004 | MONDO:equivalentTo | Benign Adrenal Cortical Neoplasm | | MONDO:0021511|MONDO:0036591 | +| MONDO:0858474 | acute myelomonocytic leukemia with abnormal eosinophils | NCIT:C9020 | MONDO:equivalentTo | Acute Myelomonocytic Leukemia with Abnormal Eosinophils | | MONDO:0018871 | +| MONDO:0858475 | sarcoma by fnclcc grade | NCIT:C9023 | MONDO:equivalentTo | Sarcoma by FNCLCC Grade | | MONDO:0005089 | +| MONDO:0858477 | atypical cartilaginous tumor/chondrosarcoma, grade 1 | NCIT:C9027 | MONDO:equivalentTo | Atypical Cartilaginous Tumor/Chondrosarcoma, Grade 1 | | MONDO:0008977 | +| MONDO:0858479 | renal cell cancer by ajcc v6 stage | NCIT:C90343 | MONDO:equivalentTo | Renal Cell Cancer by AJCC v6 Stage | | MONDO:0005549 | +| MONDO:0858480 | bladder cancer by ajcc v6 stage | NCIT:C90344 | MONDO:equivalentTo | Bladder Cancer by AJCC v6 Stage | | MONDO:0004986 | +| MONDO:0858481 | vulvar cancer by ajcc v6 stage | NCIT:C90345 | MONDO:equivalentTo | Vulvar Cancer by AJCC v6 Stage | | MONDO:0005215 | +| MONDO:0858482 | vaginal cancer by ajcc v6 stage | NCIT:C90347 | MONDO:equivalentTo | Vaginal Cancer by AJCC v6 Stage | | MONDO:0015867 | +| MONDO:0858483 | adult angiosarcoma | NCIT:C9040 | MONDO:equivalentTo | Adult Angiosarcoma | | MONDO:0016982 | +| MONDO:0858485 | extensive stage lung small cell carcinoma | NCIT:C9049 | MONDO:equivalentTo | Extensive Stage Lung Small Cell Carcinoma | | MONDO:0008433 | +| MONDO:0858486 | cervical cancer by ajcc v6 stage | NCIT:C90493 | MONDO:equivalentTo | Cervical Cancer by AJCC v6 Stage | | MONDO:0005131 | +| MONDO:0858487 | uterine corpus cancer by ajcc v6 stage | NCIT:C90494 | MONDO:equivalentTo | Uterine Corpus Cancer by AJCC v6 Stage | | MONDO:0006003 | +| MONDO:0858488 | fallopian tube cancer by ajcc v6 stage | NCIT:C90499 | MONDO:equivalentTo | Fallopian Tube Cancer by AJCC v6 Stage | | MONDO:0006206 | +| MONDO:0858489 | esophageal cancer by ajcc v6 stage | NCIT:C90500 | MONDO:equivalentTo | Esophageal Cancer by AJCC v6 Stage | | MONDO:0019086 | +| MONDO:0858490 | gastric cancer by ajcc v6 stage | NCIT:C90503 | MONDO:equivalentTo | Gastric Cancer by AJCC v6 Stage | | MONDO:0004950 | +| MONDO:0858491 | colorectal cancer by ajcc v6 stage | NCIT:C90506 | MONDO:equivalentTo | Colorectal Cancer by AJCC v6 Stage | | MONDO:0024331 | +| MONDO:0858493 | hepatocellular carcinoma by ajcc v6 stage | NCIT:C90510 | MONDO:equivalentTo | Hepatocellular Carcinoma by AJCC v6 Stage | | MONDO:0007256 | +| MONDO:0858494 | gallbladder cancer by ajcc v6 stage | NCIT:C90512 | MONDO:equivalentTo | Gallbladder Cancer by AJCC v6 Stage | | MONDO:0003220 | +| MONDO:0858495 | breast cancer by ajcc v6 stage | NCIT:C90513 | MONDO:equivalentTo | Breast Cancer by AJCC v6 Stage | | MONDO:0004989 | +| MONDO:0858496 | cutaneous melanoma by ajcc v6 stage | NCIT:C90514 | MONDO:equivalentTo | Cutaneous Melanoma by AJCC v6 Stage | | MONDO:0005012 | +| MONDO:0858497 | lung cancer by ajcc v6 stage | NCIT:C90519 | MONDO:equivalentTo | Lung Cancer by AJCC v6 Stage | | MONDO:0005138 | +| MONDO:0858498 | penile cancer by ajcc v6 stage | NCIT:C90520 | MONDO:equivalentTo | Penile Cancer by AJCC v6 Stage | | MONDO:0006360 | +| MONDO:0858499 | prostate cancer by ajcc v6 stage | NCIT:C90521 | MONDO:equivalentTo | Prostate Cancer by AJCC v6 Stage | | MONDO:0005159 | +| MONDO:0858502 | pharyngeal carcinoma by ajcc v6 stage | NCIT:C90525 | MONDO:equivalentTo | Pharyngeal Carcinoma by AJCC v6 Stage | | MONDO:0021345 | +| MONDO:0858503 | laryngeal cancer by ajcc v6 stage | NCIT:C90527 | MONDO:equivalentTo | Laryngeal Cancer by AJCC v6 Stage | | MONDO:0002358 | +| MONDO:0858504 | sinonasal cancer by ajcc v6 stage | NCIT:C90528 | MONDO:equivalentTo | Sinonasal Cancer by AJCC v6 Stage | | MONDO:0056819 | +| MONDO:0858510 | kaposi sarcoma related to immunosuppressive treatment | NCIT:C9113 | MONDO:equivalentTo | Kaposi Sarcoma Related to Immunosuppressive Treatment | | MONDO:0005188 | +| MONDO:0858511 | renal cell cancer by ajcc v7 stage | NCIT:C91201 | MONDO:equivalentTo | Renal Cell Cancer by AJCC v7 Stage | | MONDO:0005549 | +| MONDO:0858512 | bladder cancer by ajcc v7 stage | NCIT:C91202 | MONDO:equivalentTo | Bladder Cancer by AJCC v7 Stage | | MONDO:0004986 | +| MONDO:0858513 | vulvar cancer by ajcc v7 stage | NCIT:C91203 | MONDO:equivalentTo | Vulvar Cancer by AJCC v7 Stage | | MONDO:0005215 | +| MONDO:0858514 | vaginal cancer by ajcc v7 stage | NCIT:C91204 | MONDO:equivalentTo | Vaginal Cancer by AJCC v7 Stage | | MONDO:0015867 | +| MONDO:0858515 | cervical cancer by ajcc v7 stage | NCIT:C91208 | MONDO:equivalentTo | Cervical Cancer by AJCC v7 Stage | | MONDO:0005131 | +| MONDO:0858516 | uterine corpus cancer by ajcc v7 stage | NCIT:C91218 | MONDO:equivalentTo | Uterine Corpus Cancer by AJCC v7 Stage | | MONDO:0006003 | +| MONDO:0858517 | fallopian tube cancer by ajcc v7 stage | NCIT:C91219 | MONDO:equivalentTo | Fallopian Tube Cancer by AJCC v7 Stage | | MONDO:0006206 | +| MONDO:0858518 | esophageal cancer by ajcc v7 stage | NCIT:C91221 | MONDO:equivalentTo | Esophageal Cancer by AJCC v7 Stage | | MONDO:0019086 | +| MONDO:0858519 | gastric cancer by ajcc v7 stage | NCIT:C91222 | MONDO:equivalentTo | Gastric Cancer by AJCC v7 Stage | | MONDO:0004950 | +| MONDO:0858520 | colorectal cancer by ajcc v7 stage | NCIT:C91223 | MONDO:equivalentTo | Colorectal Cancer by AJCC v7 Stage | | MONDO:0024331 | +| MONDO:0858522 | hepatocellular carcinoma by ajcc v7 stage | NCIT:C91228 | MONDO:equivalentTo | Hepatocellular Carcinoma by AJCC v7 Stage | | MONDO:0007256 | +| MONDO:0858523 | gallbladder cancer by ajcc v7 stage | NCIT:C91229 | MONDO:equivalentTo | Gallbladder Cancer by AJCC v7 Stage | | MONDO:0003220 | +| MONDO:0858524 | breast cancer by ajcc v7 stage | NCIT:C91230 | MONDO:equivalentTo | Breast Cancer by AJCC v7 Stage | | MONDO:0004989 | +| MONDO:0858525 | cutaneous melanoma by ajcc v7 stage | NCIT:C91231 | MONDO:equivalentTo | Cutaneous Melanoma by AJCC v7 Stage | | MONDO:0005012 | +| MONDO:0858526 | lung cancer by ajcc v7 stage | NCIT:C91232 | MONDO:equivalentTo | Lung Cancer by AJCC v7 Stage | | MONDO:0005138 | +| MONDO:0858527 | prostate cancer by ajcc v7 stage | NCIT:C91233 | MONDO:equivalentTo | Prostate Cancer by AJCC v7 Stage | | MONDO:0005159 | +| MONDO:0858528 | penile cancer by ajcc v7 stage | NCIT:C91234 | MONDO:equivalentTo | Penile Cancer by AJCC v7 Stage | | MONDO:0006360 | +| MONDO:0858531 | pharyngeal carcinoma by ajcc v7 stage | NCIT:C91252 | MONDO:equivalentTo | Pharyngeal Carcinoma by AJCC v7 Stage | | MONDO:0021345 | +| MONDO:0858532 | sinonasal cancer by ajcc v7 stage | NCIT:C91255 | MONDO:equivalentTo | Sinonasal Cancer by AJCC v7 Stage | | MONDO:0056819 | +| MONDO:0858533 | laryngeal cancer by ajcc v7 stage | NCIT:C91256 | MONDO:equivalentTo | Laryngeal Cancer by AJCC v7 Stage | | MONDO:0002358 | +| MONDO:0858534 | chronic myeloid leukemia, philadelphia chromosome positive, bcr-abl1 positive | NCIT:C9128 | MONDO:equivalentTo | Chronic Myeloid Leukemia, Philadelphia Chromosome Positive, BCR-ABL1 Positive | | MONDO:0024685|MONDO:0011996 | +| MONDO:0858535 | adult rhabdomyosarcoma | NCIT:C9130 | MONDO:equivalentTo | Adult Rhabdomyosarcoma | | MONDO:0005212 | +| MONDO:0858536 | invasive breast carcinoma of no special type with predominant intraductal component | NCIT:C9132 | MONDO:equivalentTo | Invasive Breast Carcinoma of No Special Type with Predominant Intraductal Component | | MONDO:0004953 | +| MONDO:0858537 | invasive breast lobular carcinoma with predominant in situ component | NCIT:C9136 | MONDO:equivalentTo | Invasive Breast Lobular Carcinoma with Predominant In Situ Component | | MONDO:0005051 | +| MONDO:0858538 | adult acute myeloid leukemia | NCIT:C9154 | MONDO:equivalentTo | Adult Acute Myeloid Leukemia | | MONDO:0018874 | +| MONDO:0858543 | testicular mixed embryonal carcinoma and yolk sac tumor with seminoma | NCIT:C9172 | MONDO:equivalentTo | Testicular Mixed Embryonal Carcinoma and Yolk Sac Tumor with Seminoma | | MONDO:0003120 | +| MONDO:0858546 | good prognosis metastatic gestational trophoblastic tumor | NCIT:C9177 | MONDO:equivalentTo | Good Prognosis Metastatic Gestational Trophoblastic Tumor | | MONDO:0018944 | +| MONDO:0858547 | poor prognosis metastatic gestational trophoblastic tumor | NCIT:C9178 | MONDO:equivalentTo | Poor Prognosis Metastatic Gestational Trophoblastic Tumor | | MONDO:0018944 | +| MONDO:0858549 | intraocular schwannoma | NCIT:C92182 | MONDO:equivalentTo | Intraocular Schwannoma | | MONDO:0021454|MONDO:0004820 | +| MONDO:0858550 | esophageal malignant peripheral nerve sheath tumor | NCIT:C92185 | MONDO:equivalentTo | Esophageal Malignant Peripheral Nerve Sheath Tumor | | MONDO:0001204|MONDO:0017827 | +| MONDO:0858551 | intraocular malignant peripheral nerve sheath tumor | NCIT:C92186 | MONDO:equivalentTo | Intraocular Malignant Peripheral Nerve Sheath Tumor | | MONDO:0002236|MONDO:0017827 | +| MONDO:0858558 | non-hematologic malignancy | NCIT:C9226 | MONDO:equivalentTo | Non-Hematologic Malignancy | | MONDO:0004992 | +| MONDO:0858562 | recurrent malignant hemangiopericytoma | NCIT:C9254 | MONDO:equivalentTo | Recurrent Malignant Hemangiopericytoma | | MONDO:0009330 | +| MONDO:0858563 | multifocal glioblastomas | NCIT:C92549 | MONDO:equivalentTo | Multifocal Glioblastomas | | MONDO:0018177 | +| MONDO:0858565 | glioneuronal tumor with neuropil-like islands | NCIT:C92550 | MONDO:equivalentTo | Glioneuronal Tumor with Neuropil-Like Islands | | MONDO:0019781 | +| MONDO:0858569 | anaplastic medulloblastoma | NCIT:C92625 | MONDO:equivalentTo | Anaplastic Medulloblastoma | | MONDO:0007959 | +| MONDO:0858573 | malignant peripheral nerve sheath tumor with mesenchymal differentiation | NCIT:C92647 | MONDO:equivalentTo | Malignant Peripheral Nerve Sheath Tumor with Mesenchymal Differentiation | | MONDO:0017827 | +| MONDO:0858574 | mycosis fungoides and sezary syndrome | NCIT:C9265 | MONDO:equivalentTo | Mycosis Fungoides and Sezary Syndrome | | MONDO:0000430 | +| MONDO:0858580 | advanced malignant neoplasm | NCIT:C9270 | MONDO:equivalentTo | Advanced Malignant Neoplasm | | MONDO:0024880 | +| MONDO:0858584 | lymphocyte-depleted classic hodgkin lymphoma | NCIT:C9283 | MONDO:equivalentTo | Lymphocyte-Depleted Classic Hodgkin Lymphoma | | MONDO:0009348 | +| MONDO:0858585 | central nervous system histiocytic and dendritic cell neoplasm | NCIT:C92944 | MONDO:equivalentTo | Central Nervous System Histiocytic and Dendritic Cell Neoplasm | | MONDO:0006247|MONDO:0003641 | +| MONDO:0858588 | peritoneal malignant mesothelioma | NCIT:C9350 | MONDO:equivalentTo | Peritoneal Malignant Mesothelioma | | MONDO:0006292|MONDO:0002087|MONDO:0006362 | +| MONDO:0858595 | combined lung small cell carcinoma and lung adenocarcinoma | NCIT:C9379 | MONDO:equivalentTo | Combined Lung Small Cell Carcinoma and Lung Adenocarcinoma | | MONDO:0003438 | +| MONDO:0858597 | well differentiated malignant hemangiopericytoma | NCIT:C9392 | MONDO:equivalentTo | Well Differentiated Malignant Hemangiopericytoma | | MONDO:0009330 | +| MONDO:0858598 | malignant hemangiopericytoma nci grade 2 | NCIT:C9393 | MONDO:equivalentTo | Malignant Hemangiopericytoma NCI Grade 2 | | MONDO:0002789 | +| MONDO:0858599 | malignant hemangiopericytoma nci grade 3 | NCIT:C9394 | MONDO:equivalentTo | Malignant Hemangiopericytoma NCI Grade 3 | | MONDO:0002789 | +| MONDO:0858600 | round cell liposarcoma nci grade 2 | NCIT:C9401 | MONDO:equivalentTo | Round Cell Liposarcoma NCI Grade 2 | | MONDO:0005238 | +| MONDO:0858601 | round cell liposarcoma nci grade 3 | NCIT:C9402 | MONDO:equivalentTo | Round Cell Liposarcoma NCI Grade 3 | | MONDO:0005238 | +| MONDO:0858603 | childhood hematopoietic and lymphoid cell neoplasm | NCIT:C9431 | MONDO:equivalentTo | Childhood Hematopoietic and Lymphoid Cell Neoplasm | | MONDO:0021079|MONDO:0044881 | +| MONDO:0858619 | grade 1 colorectal adenocarcinoma | NCIT:C9446 | MONDO:equivalentTo | Grade 1 Colorectal Adenocarcinoma | | MONDO:0005008 | +| MONDO:0858620 | grade 2 colorectal adenocarcinoma | NCIT:C9447 | MONDO:equivalentTo | Grade 2 Colorectal Adenocarcinoma | | MONDO:0005008 | +| MONDO:0858621 | grade 3 colorectal adenocarcinoma | NCIT:C9448 | MONDO:equivalentTo | Grade 3 Colorectal Adenocarcinoma | | MONDO:0005008 | +| MONDO:0858623 | spindle cell oncocytoma | NCIT:C94537 | MONDO:equivalentTo | Spindle Cell Oncocytoma | | MONDO:0003257|MONDO:0010795 | +| MONDO:0858625 | breast ductal carcinoma in situ, intermediate grade | NCIT:C9456 | MONDO:equivalentTo | Breast Ductal Carcinoma In Situ, Intermediate Grade | | MONDO:0005023 | +| MONDO:0858626 | breast ductal carcinoma in situ, low grade | NCIT:C9457 | MONDO:equivalentTo | Breast Ductal Carcinoma In Situ, Low Grade | | MONDO:0005023 | +| MONDO:0858627 | borderline ovarian brenner tumor | NCIT:C9459 | MONDO:equivalentTo | Borderline Ovarian Brenner Tumor | | MONDO:0016093|MONDO:0002370 | +| MONDO:0858628 | systemic anaplastic large cell lymphoma | NCIT:C9470 | MONDO:equivalentTo | Systemic Anaplastic Large Cell Lymphoma | | MONDO:0020325 | +| MONDO:0858630 | meningeal leukemia | NCIT:C94754 | MONDO:equivalentTo | Meningeal Leukemia | | MONDO:0001606|MONDO:0700219 | +| MONDO:0858631 | meningeal lymphoma | NCIT:C94756 | MONDO:equivalentTo | Meningeal Lymphoma | | MONDO:0002571|MONDO:0021322 | +| MONDO:0858632 | multifocal breast carcinoma | NCIT:C94770 | MONDO:equivalentTo | Multifocal Breast Carcinoma | | MONDO:0004989 | +| MONDO:0858633 | multicentric breast carcinoma | NCIT:C94772 | MONDO:equivalentTo | Multicentric Breast Carcinoma | | MONDO:0004989 | +| MONDO:0858634 | early stage breast carcinoma | NCIT:C94774 | MONDO:equivalentTo | Early Stage Breast Carcinoma | | MONDO:0004989 | +| MONDO:0858635 | hereditary malignant neoplasm | NCIT:C9479 | MONDO:equivalentTo | Hereditary Malignant Neoplasm | | MONDO:0004992 | +| MONDO:0858637 | stage i borderline ovarian surface epithelial-stromal tumor | NCIT:C94821 | MONDO:equivalentTo | Stage I Borderline Ovarian Surface Epithelial-Stromal Tumor | | MONDO:0016093 | +| MONDO:0858638 | stage ii borderline ovarian surface epithelial-stromal tumor | NCIT:C94822 | MONDO:equivalentTo | Stage II Borderline Ovarian Surface Epithelial-Stromal Tumor | | MONDO:0016093 | +| MONDO:0858639 | stage iii borderline ovarian surface epithelial-stromal tumor | NCIT:C94824 | MONDO:equivalentTo | Stage III Borderline Ovarian Surface Epithelial-Stromal Tumor | | MONDO:0016093 | +| MONDO:0858640 | stage iv borderline ovarian surface epithelial-stromal tumor | NCIT:C94825 | MONDO:equivalentTo | Stage IV Borderline Ovarian Surface Epithelial-Stromal Tumor | | MONDO:0016093 | +| MONDO:0858648 | melanocytoma | NCIT:C9498 | MONDO:equivalentTo | Melanocytoma | | MONDO:0021143 | +| MONDO:0858649 | myolipoma | NCIT:C9502 | MONDO:equivalentTo | Myolipoma | | MONDO:0005106 | +| MONDO:0858650 | thymoliposarcoma | NCIT:C95038 | MONDO:equivalentTo | Thymoliposarcoma | | MONDO:0003601|MONDO:0002586 | +| MONDO:0858651 | ectopic cervical thymoma | NCIT:C95048 | MONDO:equivalentTo | Ectopic Cervical Thymoma | | MONDO:0006456|MONDO:0021351 | +| MONDO:0858656 | intramucosal adenocarcinoma | NCIT:C95397 | MONDO:equivalentTo | Intramucosal Adenocarcinoma | | MONDO:0004970 | +| MONDO:0858658 | pancreatic well differentiated ductal adenocarcinoma | NCIT:C95426 | MONDO:equivalentTo | Pancreatic Well Differentiated Ductal Adenocarcinoma | | MONDO:0005184 | +| MONDO:0858659 | pancreatic moderately differentiated ductal adenocarcinoma | NCIT:C95427 | MONDO:equivalentTo | Pancreatic Moderately Differentiated Ductal Adenocarcinoma | | MONDO:0005184 | +| MONDO:0858660 | pancreatic poorly differentiated ductal adenocarcinoma | NCIT:C95428 | MONDO:equivalentTo | Pancreatic Poorly Differentiated Ductal Adenocarcinoma | | MONDO:0005184 | +| MONDO:0858661 | pancreatic mixed acinar-ductal carcinoma | NCIT:C95458 | MONDO:equivalentTo | Pancreatic Mixed Acinar-Ductal Carcinoma | | MONDO:0006047 | +| MONDO:0858662 | pancreatic mixed ductal adenocarcinoma-acinar carcinoma-neuroendocrine carcinoma | NCIT:C95460 | MONDO:equivalentTo | Pancreatic Mixed Ductal Adenocarcinoma-Acinar Carcinoma-Neuroendocrine Carcinoma | | MONDO:0044727 | +| MONDO:0858663 | pancreatic hepatoid adenocarcinoma | NCIT:C95465 | MONDO:equivalentTo | Pancreatic Hepatoid Adenocarcinoma | | MONDO:0005184|MONDO:0006243 | +| MONDO:0858664 | pancreatic medullary carcinoma | NCIT:C95466 | MONDO:equivalentTo | Pancreatic Medullary Carcinoma | | MONDO:0005184 | +| MONDO:0858665 | pancreatic serous adenoma | NCIT:C95470 | MONDO:equivalentTo | Pancreatic Serous Adenoma | | MONDO:0021441|MONDO:0002810|MONDO:0036976 | +| MONDO:0858666 | pancreatic intraductal neoplasm | NCIT:C95505 | MONDO:equivalentTo | Pancreatic Intraductal Neoplasm | | MONDO:0024276|MONDO:0021076 | +| MONDO:0858667 | pancreatic intraductal papillary mucinous neoplasm, gastric-type | NCIT:C95508 | MONDO:equivalentTo | Pancreatic Intraductal Papillary Mucinous Neoplasm, Gastric-Type | | MONDO:0004286 | +| MONDO:0858668 | pancreatic intraductal papillary mucinous neoplasm, intestinal-type | NCIT:C95510 | MONDO:equivalentTo | Pancreatic Intraductal Papillary Mucinous Neoplasm, Intestinal-Type | | MONDO:0004286 | +| MONDO:0858669 | pancreatic intraductal papillary mucinous neoplasm, pancreatobiliary-type | NCIT:C95512 | MONDO:equivalentTo | Pancreatic Intraductal Papillary Mucinous Neoplasm, Pancreatobiliary-Type | | MONDO:0004286 | +| MONDO:0858675 | non-functioning pancreatic neuroendocrine tumor g1 | NCIT:C95585 | MONDO:equivalentTo | Non-Functioning Pancreatic Neuroendocrine Tumor G1 | | MONDO:0021535|MONDO:0004334 | +| MONDO:0858676 | pancreatic vipoma | NCIT:C95599 | MONDO:equivalentTo | Pancreatic Vipoma | | MONDO:0023206|MONDO:0003622 | +| MONDO:0858677 | esophageal spindle cell carcinoma | NCIT:C95608 | MONDO:equivalentTo | Esophageal Spindle Cell Carcinoma | | MONDO:0005580|MONDO:0021663 | +| MONDO:0858678 | esophageal well differentiated squamous cell carcinoma | NCIT:C95610 | MONDO:equivalentTo | Esophageal Well Differentiated Squamous Cell Carcinoma | | MONDO:0005580 | +| MONDO:0858679 | esophageal moderately differentiated squamous cell carcinoma | NCIT:C95611 | MONDO:equivalentTo | Esophageal Moderately Differentiated Squamous Cell Carcinoma | | MONDO:0005580 | +| MONDO:0858680 | esophageal poorly differentiated squamous cell carcinoma | NCIT:C95612 | MONDO:equivalentTo | Esophageal Poorly Differentiated Squamous Cell Carcinoma | | MONDO:0005580 | +| MONDO:0858681 | esophageal mixed adenoneuroendocrine carcinoma | NCIT:C95621 | MONDO:equivalentTo | Esophageal Mixed Adenoneuroendocrine Carcinoma | | MONDO:0006182|MONDO:0019086 | +| MONDO:0858683 | esophageal synovial sarcoma | NCIT:C95624 | MONDO:equivalentTo | Esophageal Synovial Sarcoma | | MONDO:0001204|MONDO:0010434 | +| MONDO:0858686 | gastric adenoma, gastric-type | NCIT:C95775 | MONDO:equivalentTo | Gastric Adenoma, Gastric-Type | | MONDO:0006221 | +| MONDO:0858689 | gastric mixed adenoneuroendocrine carcinoma | NCIT:C95886 | MONDO:equivalentTo | Gastric Mixed Adenoneuroendocrine Carcinoma | | MONDO:0006182|MONDO:0004950 | +| MONDO:0858691 | gastric schwannoma | NCIT:C95901 | MONDO:equivalentTo | Gastric Schwannoma | | MONDO:0004820|MONDO:0021449 | +| MONDO:0858693 | ampulla of vater pancreatobiliary type adenocarcinoma | NCIT:C95963 | MONDO:equivalentTo | Ampulla of Vater Pancreatobiliary Type Adenocarcinoma | | MONDO:0002670 | +| MONDO:0858694 | ampulla of vater hepatoid adenocarcinoma | NCIT:C95966 | MONDO:equivalentTo | Ampulla of Vater Hepatoid Adenocarcinoma | | MONDO:0006243|MONDO:0002670 | +| MONDO:0858695 | ampulla of vater neuroendocrine neoplasm | NCIT:C95980 | MONDO:equivalentTo | Ampulla of Vater Neuroendocrine Neoplasm | | MONDO:0000921|MONDO:0024503 | +| MONDO:0858696 | ampulla of vater mixed adenoneuroendocrine carcinoma | NCIT:C95986 | MONDO:equivalentTo | Ampulla of Vater Mixed Adenoneuroendocrine Carcinoma | | MONDO:0006182|MONDO:0017590 | +| MONDO:0858702 | intestinal neuroendocrine tumor | NCIT:C96062 | MONDO:equivalentTo | Intestinal Neuroendocrine Tumor | | MONDO:0000386|MONDO:0002883 | +| MONDO:0858703 | small intestinal mixed adenoneuroendocrine carcinoma | NCIT:C96066 | MONDO:equivalentTo | Small Intestinal Mixed Adenoneuroendocrine Carcinoma | | MONDO:0006182|MONDO:0005522 | +| MONDO:0858705 | colorectal neuroendocrine neoplasm | NCIT:C96152 | MONDO:equivalentTo | Colorectal Neuroendocrine Neoplasm | | MONDO:0002883|MONDO:0005335 | +| MONDO:0858706 | colorectal mixed adenoneuroendocrine carcinoma | NCIT:C96158 | MONDO:equivalentTo | Colorectal Mixed Adenoneuroendocrine Carcinoma | | MONDO:0006182|MONDO:0024331 | +| MONDO:0858707 | digestive system neuroendocrine tumor g2 | NCIT:C96166 | MONDO:equivalentTo | Digestive System Neuroendocrine Tumor G2 | | MONDO:0000386|MONDO:0006095 | +| MONDO:0858715 | serrated lesions and polyps | NCIT:C96414 | MONDO:equivalentTo | Serrated Lesions and Polyps | | MONDO:0006180 | +| MONDO:0858717 | appendix enterochromaffin cell serotonin-producing neuroendocrine tumor | NCIT:C96424 | MONDO:equivalentTo | Appendix Enterochromaffin Cell Serotonin-Producing Neuroendocrine Tumor | | MONDO:0015066 | +| MONDO:0858721 | rectal serrated lesions and polyps | NCIT:C96465 | MONDO:equivalentTo | Rectal Serrated Lesions and Polyps | | MONDO:0006164|MONDO:0000530|MONDO:0021398 | +| MONDO:0858725 | colon serrated adenocarcinoma | NCIT:C96486 | MONDO:equivalentTo | Colon Serrated Adenocarcinoma | | MONDO:0006163|MONDO:0002271 | +| MONDO:0858726 | rectal serrated adenocarcinoma | NCIT:C96487 | MONDO:equivalentTo | Rectal Serrated Adenocarcinoma | | MONDO:0006163|MONDO:0002169 | +| MONDO:0858729 | colorectal sarcomatoid carcinoma | NCIT:C96494 | MONDO:equivalentTo | Colorectal Sarcomatoid Carcinoma | | MONDO:0024331|MONDO:0006406 | +| MONDO:0858735 | colorectal schwannoma | NCIT:C96512 | MONDO:equivalentTo | Colorectal Schwannoma | | MONDO:0021444|MONDO:0004820 | +| MONDO:0858736 | colorectal ganglioneuroma | NCIT:C96514 | MONDO:equivalentTo | Colorectal Ganglioneuroma | | MONDO:0021444|MONDO:0005033 | +| MONDO:0858737 | colorectal benign granular cell tumor | NCIT:C96516 | MONDO:equivalentTo | Colorectal Benign Granular Cell Tumor | | MONDO:0021444|MONDO:0003250 | +| MONDO:0858738 | anal canal undifferentiated carcinoma | NCIT:C96529 | MONDO:equivalentTo | Anal Canal Undifferentiated Carcinoma | | MONDO:0007108|MONDO:0005617 | +| MONDO:0858741 | anal canal mixed adenoneuroendocrine carcinoma | NCIT:C96553 | MONDO:equivalentTo | Anal Canal Mixed Adenoneuroendocrine Carcinoma | | MONDO:0006182|MONDO:0007108 | +| MONDO:0858742 | anal canal squamous papilloma | NCIT:C96554 | MONDO:equivalentTo | Anal Canal Squamous Papilloma | | MONDO:0021469|MONDO:0060766|MONDO:0001825 | +| MONDO:0858743 | anal hidradenoma papilliferum | NCIT:C96699 | MONDO:equivalentTo | Anal Hidradenoma Papilliferum | | MONDO:0021469|MONDO:0003446 | +| MONDO:0858745 | hnf1alpha-inactivated hepatocellular adenoma | NCIT:C96758 | MONDO:equivalentTo | HNF1alpha-Inactivated Hepatocellular Adenoma | | MONDO:0018902 | +| MONDO:0858746 | beta-catenin-activated hepatocellular adenoma | NCIT:C96759 | MONDO:equivalentTo | Beta-Catenin-Activated Hepatocellular Adenoma | | MONDO:0018902 | +| MONDO:0858747 | inflammatory hepatocellular adenoma | NCIT:C96760 | MONDO:equivalentTo | Inflammatory Hepatocellular Adenoma | | MONDO:0018902 | +| MONDO:0858748 | unclassified hepatocellular adenoma | NCIT:C96761 | MONDO:equivalentTo | Unclassified Hepatocellular Adenoma | | MONDO:0018902 | +| MONDO:0858750 | liver neuroendocrine neoplasm | NCIT:C96786 | MONDO:equivalentTo | Liver Neuroendocrine Neoplasm | | MONDO:0024477|MONDO:0024503 | +| MONDO:0858751 | lymphocyte-rich hepatocellular carcinoma | NCIT:C96788 | MONDO:equivalentTo | Lymphocyte-Rich Hepatocellular Carcinoma | | MONDO:0007256 | +| MONDO:0858752 | well differentiated hepatocellular carcinoma | NCIT:C96789 | MONDO:equivalentTo | Well Differentiated Hepatocellular Carcinoma | | MONDO:0007256 | +| MONDO:0858753 | moderately differentiated hepatocellular carcinoma | NCIT:C96790 | MONDO:equivalentTo | Moderately Differentiated Hepatocellular Carcinoma | | MONDO:0007256 | +| MONDO:0858754 | poorly differentiated hepatocellular carcinoma | NCIT:C96791 | MONDO:equivalentTo | Poorly Differentiated Hepatocellular Carcinoma | | MONDO:0007256 | +| MONDO:0858755 | liver undifferentiated carcinoma | NCIT:C96792 | MONDO:equivalentTo | Liver Undifferentiated Carcinoma | | MONDO:0018531|MONDO:0005617 | +| MONDO:0858756 | small duct intrahepatic cholangiocarcinoma | NCIT:C96805 | MONDO:equivalentTo | Small Duct Intrahepatic Cholangiocarcinoma | | MONDO:0003210 | +| MONDO:0858757 | bile duct intraductal papillary neoplasm with an associated invasive carcinoma | NCIT:C96810 | MONDO:equivalentTo | Bile Duct Intraductal Papillary Neoplasm with an Associated Invasive Carcinoma | | MONDO:0003455|MONDO:0003193 | +| MONDO:0858758 | extrahepatic bile duct tubulopapillary adenoma | NCIT:C96811 | MONDO:equivalentTo | Extrahepatic Bile Duct Tubulopapillary Adenoma | | MONDO:0003445|MONDO:0024661 | +| MONDO:0858760 | liver synovial sarcoma | NCIT:C96845 | MONDO:equivalentTo | Liver Synovial Sarcoma | | MONDO:0002397|MONDO:0010434 | +| MONDO:0858761 | liver carcinosarcoma | NCIT:C96848 | MONDO:equivalentTo | Liver Carcinosarcoma | | MONDO:0018531|MONDO:0002928 | +| MONDO:0858765 | gallbladder mucinous cystic neoplasm | NCIT:C96881 | MONDO:equivalentTo | Gallbladder Mucinous Cystic Neoplasm | | MONDO:0021253 | +| MONDO:0858766 | gallbladder carcinosarcoma | NCIT:C96888 | MONDO:equivalentTo | Gallbladder Carcinosarcoma | | MONDO:0003220|MONDO:0002928 | +| MONDO:0858767 | gallbladder hepatoid adenocarcinoma | NCIT:C96890 | MONDO:equivalentTo | Gallbladder Hepatoid Adenocarcinoma | | MONDO:0006215|MONDO:0006243 | +| MONDO:0858768 | gallbladder cribriform carcinoma | NCIT:C96891 | MONDO:equivalentTo | Gallbladder Cribriform Carcinoma | | MONDO:0006215|MONDO:0006176 | +| MONDO:0858769 | gallbladder adenocarcinoma, biliary type | NCIT:C96915 | MONDO:equivalentTo | Gallbladder Adenocarcinoma, Biliary Type | | MONDO:0006215|MONDO:0005606 | +| MONDO:0858770 | gallbladder adenocarcinoma, gastric foveolar type | NCIT:C96916 | MONDO:equivalentTo | Gallbladder Adenocarcinoma, Gastric Foveolar Type | | MONDO:0006215 | +| MONDO:0858774 | gallbladder mixed adenoneuroendocrine carcinoma | NCIT:C96927 | MONDO:equivalentTo | Gallbladder Mixed Adenoneuroendocrine Carcinoma | | MONDO:0006182|MONDO:0003220 | +| MONDO:0858775 | gallbladder tubular carcinoid | NCIT:C96930 | MONDO:equivalentTo | Gallbladder Tubular Carcinoid | | MONDO:0015073 | +| MONDO:0858776 | extrahepatic bile duct adenocarcinoma, biliary type | NCIT:C96936 | MONDO:equivalentTo | Extrahepatic Bile Duct Adenocarcinoma, Biliary Type | | MONDO:0002665|MONDO:0005606 | +| MONDO:0858777 | extrahepatic bile duct adenocarcinoma, gastric foveolar type | NCIT:C96937 | MONDO:equivalentTo | Extrahepatic Bile Duct Adenocarcinoma, Gastric Foveolar Type | | MONDO:0002665 | +| MONDO:0858778 | extrahepatic bile duct adenocarcinoma, intestinal type | NCIT:C96938 | MONDO:equivalentTo | Extrahepatic Bile Duct Adenocarcinoma, Intestinal Type | | MONDO:0002665 | +| MONDO:0858779 | extrahepatic bile duct carcinosarcoma | NCIT:C96939 | MONDO:equivalentTo | Extrahepatic Bile Duct Carcinosarcoma | | MONDO:0003090|MONDO:0002928 | +| MONDO:0858780 | extrahepatic bile duct mucinous cystic neoplasm with an associated invasive carcinoma | NCIT:C96946 | MONDO:equivalentTo | Extrahepatic Bile Duct Mucinous Cystic Neoplasm with an Associated Invasive Carcinoma | | MONDO:0002665|MONDO:0004462|MONDO:0002868 | +| MONDO:0858781 | intrahepatic bile duct mucinous cystic neoplasm with an associated invasive carcinoma | NCIT:C96947 | MONDO:equivalentTo | Intrahepatic Bile Duct Mucinous Cystic Neoplasm with an Associated Invasive Carcinoma | | MONDO:0003979|MONDO:0018531|MONDO:0002868 | +| MONDO:0858783 | extrahepatic bile duct lymphoma | NCIT:C96952 | MONDO:equivalentTo | Extrahepatic Bile Duct Lymphoma | | MONDO:0021321|MONDO:0004699 | +| MONDO:0858785 | extrahepatic bile duct neuroendocrine neoplasm | NCIT:C96954 | MONDO:equivalentTo | Extrahepatic Bile Duct Neuroendocrine Neoplasm | | MONDO:0021385|MONDO:0024503 | +| MONDO:0858786 | extrahepatic bile duct mixed adenoneuroendocrine carcinoma | NCIT:C96959 | MONDO:equivalentTo | Extrahepatic Bile Duct Mixed Adenoneuroendocrine Carcinoma | | MONDO:0006182|MONDO:0003090 | +| MONDO:0858788 | invasive breast lobular carcinoma, alveolar variant | NCIT:C97049 | MONDO:equivalentTo | Invasive Breast Lobular Carcinoma, Alveolar Variant | | MONDO:0005051 | +| MONDO:0858789 | invasive breast lobular carcinoma, pleomorphic variant | NCIT:C97051 | MONDO:equivalentTo | Invasive Breast Lobular Carcinoma, Pleomorphic Variant | | MONDO:0005051 | +| MONDO:0858790 | invasive breast lobular carcinoma, solid variant | NCIT:C97052 | MONDO:equivalentTo | Invasive Breast Lobular Carcinoma, Solid Variant | | MONDO:0005051 | +| MONDO:0858791 | invasive breast lobular carcinoma, tubulolobular variant | NCIT:C97053 | MONDO:equivalentTo | Invasive Breast Lobular Carcinoma, Tubulolobular Variant | | MONDO:0005051 | +| MONDO:0858792 | mixed congenital mesoblastic nephroma | NCIT:C97058 | MONDO:equivalentTo | Mixed Congenital Mesoblastic Nephroma | | MONDO:0017043|MONDO:0005853 | +| MONDO:0858851 | contralateral breast carcinoma | NCIT:C99390 | MONDO:equivalentTo | Contralateral Breast Carcinoma | | MONDO:0003982 | +| MONDO:0859471 | neoplastic medium-sized lymphocyte | NCIT:C37004 | MONDO:equivalentTo | Neoplastic Medium-Sized Lymphocyte | | | +| MONDO:0859472 | neoplastic b-lymphocyte | NCIT:C38640 | MONDO:equivalentTo | Neoplastic B-Lymphocyte | | | +| MONDO:0859554 | medaka melanoma | NCIT:C134572 | MONDO:equivalentTo | Medaka Melanoma | | MONDO:0700196 | +| MONDO:0859555 | xiphophorus melanoma | NCIT:C134575 | MONDO:equivalentTo | Xiphophorus Melanoma | | MONDO:0700196 | +| MONDO:0859556 | non-human or experimental organism neoplasm | NCIT:C134576 | MONDO:equivalentTo | Non-Human or Experimental Organism Neoplasm | | | +| MONDO:0859560 | tubulostromal adenoma | NCIT:C79953 | MONDO:equivalentTo | Tubulostromal Adenoma | | | +| MONDO:0859561 | tubulostromal adenocarcinoma | NCIT:C80356 | MONDO:equivalentTo | Tubulostromal Adenocarcinoma | | | +| MONDO:0859730 | vaginal non-keratinizing squamous cell carcinoma | NCIT:C40244 | MONDO:equivalentTo | Vaginal Non-Keratinizing Squamous Cell Carcinoma | | MONDO:0006490 | +| MONDO:0860042 | lymphoproliferative disease associated with primary immune disorder | NCIT:C150673 | MONDO:equivalentTo | Lymphoproliferative Disease Associated with Primary Immune Disorder | | | +| MONDO:0860043 | genitourinary system disorder | NCIT:C156660 | MONDO:equivalentTo | Genitourinary System Disorder | | | +| MONDO:0860044 | recurrent hiv-related lymphoproliferative disorder | NCIT:C157685 | MONDO:equivalentTo | Recurrent HIV-Related Lymphoproliferative Disorder | | | +| MONDO:0860045 | refractory hiv-related lymphoproliferative disorder | NCIT:C157687 | MONDO:equivalentTo | Refractory HIV-Related Lymphoproliferative Disorder | | | +| MONDO:0860046 | hiv-related lymphoproliferative disorder | NCIT:C157709 | MONDO:equivalentTo | HIV-Related Lymphoproliferative Disorder | | | +| MONDO:0860047 | ebv-related lymphoproliferative disease with primary immunodeficiency | NCIT:C160150 | MONDO:equivalentTo | EBV-Related Lymphoproliferative Disease with Primary Immunodeficiency | | | +| MONDO:0860048 | recurrent ebv-related lymphoproliferative disease with primary immunodeficiency | NCIT:C160151 | MONDO:equivalentTo | Recurrent EBV-Related Lymphoproliferative Disease with Primary Immunodeficiency | | | +| MONDO:0860049 | refractory ebv-related lymphoproliferative disease with primary immunodeficiency | NCIT:C160152 | MONDO:equivalentTo | Refractory EBV-Related Lymphoproliferative Disease with Primary Immunodeficiency | | | +| MONDO:0860050 | tonsillar disorder | NCIT:C173797 | MONDO:equivalentTo | Tonsillar Disorder | | | +| MONDO:0860051 | soft tissue disorder | NCIT:C27042 | MONDO:equivalentTo | Soft Tissue Disorder | | | +| MONDO:0860052 | connective and soft tissue disorder | NCIT:C27574 | MONDO:equivalentTo | Connective and Soft Tissue Disorder | | | +| MONDO:0860053 | neck disorder | NCIT:C27648 | MONDO:equivalentTo | Neck Disorder | | | +| MONDO:0860054 | peritoneal and retroperitoneal disorder | NCIT:C27664 | MONDO:equivalentTo | Peritoneal and Retroperitoneal Disorder | | | +| MONDO:0860055 | female reproductive system precancerous condition | NCIT:C27788 | MONDO:equivalentTo | Female Reproductive System Precancerous Condition | | | +| MONDO:0860056 | tobacco use disorder | NCIT:C35074 | MONDO:equivalentTo | Tobacco Use Disorder | | | +| MONDO:0860057 | sternal disorder | NCIT:C35744 | MONDO:equivalentTo | Sternal Disorder | | | +| MONDO:0860058 | chest wall disorder | NCIT:C35745 | MONDO:equivalentTo | Chest Wall Disorder | | | +| MONDO:0860059 | axillary disorder | NCIT:C35746 | MONDO:equivalentTo | Axillary Disorder | | | +| MONDO:0860060 | hematopoietic and lymphatic system disorder | NCIT:C35814 | MONDO:equivalentTo | Hematopoietic and Lymphatic System Disorder | | | +| MONDO:0860062 | anal precancerous condition | NCIT:C7407 | MONDO:equivalentTo | Anal Precancerous Condition | | | +| MONDO:0860063 | esophageal precancerous condition | NCIT:C7423 | MONDO:equivalentTo | Esophageal Precancerous Condition | | | +| MONDO:0860064 | gastric precancerous condition | NCIT:C7424 | MONDO:equivalentTo | Gastric Precancerous Condition | | | +| MONDO:0860065 | pulmonary precancerous condition | NCIT:C7435 | MONDO:equivalentTo | Pulmonary Precancerous Condition | | | +| MONDO:0860066 | hepatobiliary precancerous condition | NCIT:C7655 | MONDO:equivalentTo | Hepatobiliary Precancerous Condition | | | +| MONDO:0860067 | intestinal precancerous condition | NCIT:C7657 | MONDO:equivalentTo | Intestinal Precancerous Condition | | | +| MONDO:0860068 | digestive system precancerous condition | NCIT:C7659 | MONDO:equivalentTo | Digestive System Precancerous Condition | | | +| MONDO:0860069 | cutaneous precancerous condition | NCIT:C8957 | MONDO:equivalentTo | Cutaneous Precancerous Condition | | | +| MONDO:0860070 | neonatal disorder | NCIT:C98996 | MONDO:equivalentTo | Neonatal Disorder | | | +| MONDO:0950158 | core binding factor acute myeloid leukemia | NCIT:C122688 | MONDO:equivalentTo | Core Binding Factor Acute Myeloid Leukemia | | MONDO:0020078 | +| MONDO:0955884 | adult acute eosinophilic leukemia | NCIT:C7963 | MONDO:equivalentTo | Adult Acute Eosinophilic Leukemia | | MONDO:0043881 | +| MONDO:0956044 | acute myeloid leukemia (megakaryoblastic) with t(1;22)(p13.3;q13.1); rbm15-mkl1 | NCIT:C82427 | MONDO:equivalentTo | Acute Myeloid Leukemia (Megakaryoblastic) with t(1;22)(p13.3;q13.1); RBM15-MKL1 | | MONDO:0020078 | +| MONDO:0956704 | childhood acute eosinophilic leukemia | NCIT:C9165 | MONDO:equivalentTo | Childhood Acute Eosinophilic Leukemia | | MONDO:0043881 | +| MONDO:0956756 | acute myeloid leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22); cbfb-myh11 | NCIT:C9287 | MONDO:equivalentTo | Acute Myeloid Leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22); CBFB-MYH11 | | MONDO:0020078 | +| MONDO:0956757 | acute myeloid leukemia with t(8;21)(q22; q22.1); runx1-runx1t1 | NCIT:C9288 | MONDO:equivalentTo | Acute Myeloid Leukemia with t(8;21)(q22; q22.1); RUNX1-RUNX1T1 | | MONDO:0020078 | +| MONDO:0957380 | cic-rearranged sarcoma | NCIT:C120224 | MONDO:equivalentTo | CIC-Rearranged Sarcoma | | MONDO:0858921 | +| MONDO:0957623 | smoldering systemic mastocytosis | NCIT:C115460 | MONDO:equivalentTo | Smoldering Systemic Mastocytosis | | MONDO:0016586 | +| MONDO:0957624 | indolent clonal t-cell lymphoproliferative disorder of the gastrointestinal tract | NCIT:C139021 | MONDO:equivalentTo | Indolent Clonal T-Cell Lymphoproliferative Disorder of the Gastrointestinal Tract | | MONDO:0005169 | +| MONDO:0957625 | penile adenosquamous carcinoma | NCIT:C159248 | MONDO:equivalentTo | Penile Adenosquamous Carcinoma | | MONDO:0006360|MONDO:0006074 | +| MONDO:0957626 | seminal vesicle soft tissue neoplasm | NCIT:C161637 | MONDO:equivalentTo | Seminal Vesicle Soft Tissue Neoplasm | | MONDO:0002790|MONDO:0006424 | +| MONDO:0957627 | hepatocellular malignant neoplasm, not otherwise specified | NCIT:C161838 | MONDO:equivalentTo | Hepatocellular Malignant Neoplasm, Not Otherwise Specified | | MONDO:0018666 | +| MONDO:0957628 | epididymal melanotic neuroectodermal tumor | NCIT:C162488 | MONDO:equivalentTo | Epididymal Melanotic Neuroectodermal Tumor | | MONDO:0002072|MONDO:0021473 | +| MONDO:0957629 | systemic mastocytosis with an associated germ cell tumor | NCIT:C186735 | MONDO:equivalentTo | Systemic Mastocytosis with an Associated Germ Cell Tumor | | MONDO:0016586 | +| MONDO:0957630 | estrogen receptor-positive breast carcinoma | NCIT:C188366 | MONDO:equivalentTo | Estrogen Receptor-Positive Breast Carcinoma | | | +| MONDO:0957631 | childhood myelodysplastic syndrome with excess blasts | NCIT:C188449 | MONDO:equivalentTo | Childhood Myelodysplastic Syndrome with Excess Blasts | | MONDO:0019454|MONDO:0044873 | +| MONDO:0957632 | childhood acute myeloid leukemia with t(9;11)(p21.3;q23.3); mllt3-kmt2a | NCIT:C188451 | MONDO:equivalentTo | Childhood Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A | | MONDO:0004996|MONDO:0020317 | +| MONDO:0957633 | lung small cell carcinoma neuroendocrine subtype | NCIT:C188753 | MONDO:equivalentTo | Lung Small Cell Carcinoma Neuroendocrine Subtype | | MONDO:0008433 | +| MONDO:0957634 | lung small cell carcinoma molecular subtypes | NCIT:C188756 | MONDO:equivalentTo | Lung Small Cell Carcinoma Molecular Subtypes | | MONDO:0008433 | +| MONDO:0957635 | adult ganglioneuroma | NCIT:C188947 | MONDO:equivalentTo | Adult Ganglioneuroma | | MONDO:0005033 | +| MONDO:0957636 | childhood nervous system neoplasm | NCIT:C188950 | MONDO:equivalentTo | Childhood Nervous System Neoplasm | | MONDO:0021079|MONDO:0021248 | +| MONDO:0957637 | choroidal ganglioneuroma | NCIT:C188956 | MONDO:equivalentTo | Choroidal Ganglioneuroma | | MONDO:0021487|MONDO:0005033 | +| MONDO:0957638 | childhood connective and soft tissue neoplasm | NCIT:C188963 | MONDO:equivalentTo | Childhood Connective and Soft Tissue Neoplasm | | MONDO:0021079|MONDO:0044334 | +| MONDO:0957639 | childhood low grade fibromyxoid sarcoma | NCIT:C188970 | MONDO:equivalentTo | Childhood Low Grade Fibromyxoid Sarcoma | | MONDO:0002678|MONDO:0006272 | +| MONDO:0957640 | extragonadal teratoma | NCIT:C189045 | MONDO:equivalentTo | Extragonadal Teratoma | | MONDO:0018201|MONDO:0002601 | +| MONDO:0957641 | testicular teratoma, postpubertal-type | NCIT:C189057 | MONDO:equivalentTo | Testicular Teratoma, Postpubertal-Type | | MONDO:0003510|MONDO:0018193 | +| MONDO:0957642 | kidney carcinoma molecular subtypes | NCIT:C189241 | MONDO:equivalentTo | Kidney Carcinoma Molecular Subtypes | | MONDO:0005206 | +| MONDO:0957644 | ovarian sertoli-leydig cell tumor molecular subtypes | NCIT:C189319 | MONDO:equivalentTo | Ovarian Sertoli-Leydig Cell Tumor Molecular Subtypes | | MONDO:0036595 | +| MONDO:0957645 | mullerian papilloma | NCIT:C189336 | MONDO:equivalentTo | Mullerian Papilloma | | MONDO:0021078 | +| MONDO:0957646 | childhood breast neoplasm | NCIT:C189338 | MONDO:equivalentTo | Childhood Breast Neoplasm | | MONDO:0021079|MONDO:0021100 | +| MONDO:0957647 | childhood digestive system neoplasm | NCIT:C189869 | MONDO:equivalentTo | Childhood Digestive System Neoplasm | | MONDO:0021079|MONDO:0021223 | +| MONDO:0957648 | epithelial hepatoblastoma | NCIT:C189923 | MONDO:equivalentTo | Epithelial Hepatoblastoma | | MONDO:0018666 | +| MONDO:0957649 | non-teratoid hepatoblastoma | NCIT:C189926 | MONDO:equivalentTo | Non-Teratoid Hepatoblastoma | | MONDO:0003650 | +| MONDO:0957650 | hepatoblastoma by pretext stage | NCIT:C189927 | MONDO:equivalentTo | Hepatoblastoma by PRETEXT Stage | | MONDO:0018666 | +| MONDO:0957651 | hepatoblastoma by postsurgical stage | NCIT:C189929 | MONDO:equivalentTo | Hepatoblastoma by Postsurgical Stage | | MONDO:0018666 | +| MONDO:0957652 | childhood fibrolamellar carcinoma | NCIT:C189932 | MONDO:equivalentTo | Childhood Fibrolamellar Carcinoma | | MONDO:0018055|MONDO:0006210 | +| MONDO:0957653 | childhood endocrine neoplasm | NCIT:C190056 | MONDO:equivalentTo | Childhood Endocrine Neoplasm | | MONDO:0021079|MONDO:0002082 | +| MONDO:0957654 | childhood thoracic neoplasm | NCIT:C190090 | MONDO:equivalentTo | Childhood Thoracic Neoplasm | | MONDO:0021079|MONDO:0021350 | +| MONDO:0957655 | childhood head and neck neoplasm | NCIT:C190119 | MONDO:equivalentTo | Childhood Head and Neck Neoplasm | | MONDO:0021079|MONDO:0005586 | +| MONDO:0957656 | childhood skin neoplasm | NCIT:C190123 | MONDO:equivalentTo | Childhood Skin Neoplasm | | MONDO:0021079|MONDO:0002531 | +| MONDO:0957657 | childhood carcinoma | NCIT:C190275 | MONDO:equivalentTo | Childhood Carcinoma | | MONDO:0004993|MONDO:0036491 | +| MONDO:0957658 | refractory t/nk-cell lymphoproliferative disorder | NCIT:C190397 | MONDO:equivalentTo | Refractory T/NK-Cell Lymphoproliferative Disorder | | | +| MONDO:0957659 | recurrent t/nk-cell lymphoproliferative disorder | NCIT:C190398 | MONDO:equivalentTo | Recurrent T/NK-Cell Lymphoproliferative Disorder | | | +| MONDO:0957660 | ebv-related t/nk-cell lymphoproliferative disorder | NCIT:C190402 | MONDO:equivalentTo | EBV-Related T/NK-Cell Lymphoproliferative Disorder | | | +| MONDO:0957661 | childhood benign neoplasm | NCIT:C190573 | MONDO:equivalentTo | Childhood Benign Neoplasm | | MONDO:0021079|MONDO:0005165 | +| MONDO:0957662 | benign liver neoplasm | NCIT:C190592 | MONDO:equivalentTo | Benign Liver Neoplasm | | MONDO:0024477|MONDO:0000385 | +| MONDO:0957663 | high grade endometrial carcinoma | NCIT:C190680 | MONDO:equivalentTo | High Grade Endometrial Carcinoma | | MONDO:0002447 | +| MONDO:0957664 | iridociliary melanoma | NCIT:C190746 | MONDO:equivalentTo | Iridociliary Melanoma | | MONDO:0006486 | +| MONDO:0957665 | b acute lymphoblastic leukemia associated with down syndrome | NCIT:C190847 | MONDO:equivalentTo | B Acute Lymphoblastic Leukemia Associated with Down Syndrome | | MONDO:0020511 | +| MONDO:0957666 | androgen receptor-positive breast carcinoma | NCIT:C190851 | MONDO:equivalentTo | Androgen Receptor-Positive Breast Carcinoma | | | +| MONDO:0957667 | b lymphoblastic leukemia/lymphoma with etv6-runx1-like features | NCIT:C190956 | MONDO:equivalentTo | B Lymphoblastic Leukemia/Lymphoma with ETV6-RUNX1-Like Features | | MONDO:0035605 | +| MONDO:0957668 | renal cell carcinoma, not otherwise specified | NCIT:C191370 | MONDO:equivalentTo | Renal Cell Carcinoma, Not Otherwise Specified | | MONDO:0005549 | +| MONDO:0957669 | kidney classic angiomyolipoma | NCIT:C191391 | MONDO:equivalentTo | Kidney Classic Angiomyolipoma | | MONDO:0002513|MONDO:0004555 | +| MONDO:0957670 | secondary plasma cell leukemia | NCIT:C191432 | MONDO:equivalentTo | Secondary Plasma Cell Leukemia | | MONDO:0024881|MONDO:0018689 | +| MONDO:0957671 | papillary urothelial neoplasm of low malignant potential | NCIT:C191672 | MONDO:equivalentTo | Papillary Urothelial Neoplasm of Low Malignant Potential | | MONDO:0003755|MONDO:0003443 | +| MONDO:0957672 | invasive lymphoepithelioma-like urothelial carcinoma | NCIT:C191678 | MONDO:equivalentTo | Invasive Lymphoepithelioma-Like Urothelial Carcinoma | | MONDO:0003572|MONDO:0040678 | +| MONDO:0957673 | invasive giant cell urothelial carcinoma | NCIT:C191679 | MONDO:equivalentTo | Invasive Giant Cell Urothelial Carcinoma | | MONDO:0040678 | +| MONDO:0957674 | invasive urothelial carcinoma with glandular differentiation | NCIT:C191680 | MONDO:equivalentTo | Invasive Urothelial Carcinoma with Glandular Differentiation | | MONDO:0040678 | +| MONDO:0957675 | invasive urothelial carcinoma with squamous differentiation | NCIT:C191681 | MONDO:equivalentTo | Invasive Urothelial Carcinoma with Squamous Differentiation | | MONDO:0040678 | +| MONDO:0957676 | invasive urothelial carcinoma with trophoblastic differentiation | NCIT:C191682 | MONDO:equivalentTo | Invasive Urothelial Carcinoma with Trophoblastic Differentiation | | MONDO:0040678 | +| MONDO:0957677 | invasive clear cell (glycogen-rich) urothelial carcinoma | NCIT:C191683 | MONDO:equivalentTo | Invasive Clear Cell (Glycogen-Rich) Urothelial Carcinoma | | MONDO:0040678 | +| MONDO:0957678 | invasive lipid-rich urothelial carcinoma | NCIT:C191684 | MONDO:equivalentTo | Invasive Lipid-Rich Urothelial Carcinoma | | MONDO:0040678 | +| MONDO:0957679 | invasive microcystic urothelial carcinoma | NCIT:C191685 | MONDO:equivalentTo | Invasive Microcystic Urothelial Carcinoma | | MONDO:0040678 | +| MONDO:0957680 | invasive nested urothelial carcinoma | NCIT:C191687 | MONDO:equivalentTo | Invasive Nested Urothelial Carcinoma | | MONDO:0040678 | +| MONDO:0957681 | invasive plasmacytoid urothelial carcinoma | NCIT:C191688 | MONDO:equivalentTo | Invasive Plasmacytoid Urothelial Carcinoma | | MONDO:0040678 | +| MONDO:0957682 | invasive large nested urothelial carcinoma | NCIT:C191725 | MONDO:equivalentTo | Invasive Large Nested Urothelial Carcinoma | | MONDO:0040678 | +| MONDO:0957683 | invasive tubular urothelial carcinoma | NCIT:C191728 | MONDO:equivalentTo | Invasive Tubular Urothelial Carcinoma | | MONDO:0040678 | +| MONDO:0957684 | invasive poorly differentiated urothelial carcinoma | NCIT:C191730 | MONDO:equivalentTo | Invasive Poorly Differentiated Urothelial Carcinoma | | MONDO:0040678 | +| MONDO:0957685 | invasive conventional urothelial carcinoma | NCIT:C191734 | MONDO:equivalentTo | Invasive Conventional Urothelial Carcinoma | | MONDO:0040678 | +| MONDO:0957686 | prostatic intraepithelial neoplasia-like adenocarcinoma | NCIT:C191961 | MONDO:equivalentTo | Prostatic Intraepithelial Neoplasia-Like Adenocarcinoma | | MONDO:0002493 | +| MONDO:0957687 | extrapulmonary neuroendocrine carcinoma | NCIT:C191977 | MONDO:equivalentTo | Extrapulmonary Neuroendocrine Carcinoma | | MONDO:0002120 | +| MONDO:0957688 | intratubular embryonal carcinoma | NCIT:C192096 | MONDO:equivalentTo | Intratubular Embryonal Carcinoma | | MONDO:0004520|MONDO:0006446 | +| MONDO:0957689 | testicular yolk sac tumor, postpubertal-type | NCIT:C192099 | MONDO:equivalentTo | Testicular Yolk Sac Tumor, Postpubertal-Type | | MONDO:0003402 | +| MONDO:0957690 | cystic trophoblastic tumor | NCIT:C192105 | MONDO:equivalentTo | Cystic Trophoblastic Tumor | | MONDO:0021077|MONDO:0002872 | +| MONDO:0957691 | testicular teratoma, prepubertal-type | NCIT:C192107 | MONDO:equivalentTo | Testicular Teratoma, Prepubertal-Type | | MONDO:0018193 | +| MONDO:0957692 | gonadal myoid stromal tumor | NCIT:C192116 | MONDO:equivalentTo | Gonadal Myoid Stromal Tumor | | MONDO:0021447 | +| MONDO:0957693 | penile squamous cell carcinoma, not otherwise specified | NCIT:C192222 | MONDO:equivalentTo | Penile Squamous Cell Carcinoma, Not Otherwise Specified | | MONDO:0018352 | +| MONDO:0957694 | penile mucoepidermoid carcinoma | NCIT:C192223 | MONDO:equivalentTo | Penile Mucoepidermoid Carcinoma | | MONDO:0006360|MONDO:0003036 | +| MONDO:0957695 | urinary tract neoplasm | NCIT:C192666 | MONDO:equivalentTo | Urinary Tract Neoplasm | | MONDO:0021066 | +| MONDO:0957696 | benign cranial nerve neoplasm | NCIT:C193416 | MONDO:equivalentTo | Benign Cranial Nerve Neoplasm | | MONDO:0000648|MONDO:0002633 | +| MONDO:0957697 | benign spinal meningioma | NCIT:C193417 | MONDO:equivalentTo | Benign Spinal Meningioma | | MONDO:0001279|MONDO:0003054 | +| MONDO:0957698 | rectal gastrointestinal stromal tumor | NCIT:C193420 | MONDO:equivalentTo | Rectal Gastrointestinal Stromal Tumor | | MONDO:0002165|MONDO:0006159 | +| MONDO:0957699 | malignant ileal neoplasm | NCIT:C193425 | MONDO:equivalentTo | Malignant Ileal Neoplasm | | MONDO:0006801|MONDO:0000956 | +| MONDO:0957700 | refractory malignant phyllodes tumor | NCIT:C193453 | MONDO:equivalentTo | Refractory Malignant Phyllodes Tumor | | MONDO:0037003|MONDO:0036501 | +| MONDO:0957701 | childhood cancer stage by toronto guidelines v2 | NCIT:C198027 | MONDO:equivalentTo | Childhood Cancer Stage by Toronto Guidelines v2 | | MONDO:0006517 | +| MONDO:0957702 | myeloproliferative neoplasm, bcr-abl1 negative | NCIT:C198555 | MONDO:equivalentTo | Myeloproliferative Neoplasm, BCR-ABL1 Negative | | MONDO:0020076 | +| MONDO:0957703 | myeloid/lymphoid neoplasms with flt3 rearrangement | NCIT:C198559 | MONDO:equivalentTo | Myeloid/Lymphoid Neoplasms with FLT3 Rearrangement | | MONDO:0015688 | +| MONDO:0957704 | myeloid/lymphoid neoplasms with etv6-abl1 | NCIT:C198565 | MONDO:equivalentTo | Myeloid/Lymphoid Neoplasms with ETV6-ABL1 | | MONDO:0015688 | +| MONDO:0957705 | bone marrow mastocytosis | NCIT:C198573 | MONDO:equivalentTo | Bone Marrow Mastocytosis | | MONDO:0020331 | +| MONDO:0957706 | clonal monocytosis of undetermined significance | NCIT:C198580 | MONDO:equivalentTo | Clonal Monocytosis of Undetermined Significance | | MONDO:0006311 | +| MONDO:0957707 | myelodysplastic/myeloproliferative neoplasm with sf3b1 mutation and thrombocytosis | NCIT:C198581 | MONDO:equivalentTo | Myelodysplastic/Myeloproliferative Neoplasm with SF3B1 Mutation and Thrombocytosis | | MONDO:0006311 | +| MONDO:0957708 | clonal cytopenia with monocytosis of undetermined significance | NCIT:C198582 | MONDO:equivalentTo | Clonal Cytopenia with Monocytosis of Undetermined Significance | | MONDO:0006311 | +| MONDO:0957709 | myeloid neoplasm with mutated tp53 | NCIT:C198593 | MONDO:equivalentTo | Myeloid Neoplasm with Mutated TP53 | | MONDO:0005170 | +| MONDO:0957710 | myelodysplastic syndrome/acute myeloid leukemia, not otherwise specified | NCIT:C198597 | MONDO:equivalentTo | Myelodysplastic Syndrome/Acute Myeloid Leukemia, Not Otherwise Specified | | MONDO:0015041 | +| MONDO:0957711 | pediatric and/or germline mutation-associated myeloid disorders | NCIT:C198663 | MONDO:equivalentTo | Pediatric and/or Germline Mutation-Associated Myeloid Disorders | | MONDO:0005170 | +| MONDO:0957712 | b acute lymphoblastic leukemia with germline predisposition | NCIT:C198683 | MONDO:equivalentTo | B Acute Lymphoblastic Leukemia with Germline Predisposition | | MONDO:0020511 | +| MONDO:0957713 | acute myeloid leukemia with stat3-rara | NCIT:C198827 | MONDO:equivalentTo | Acute Myeloid Leukemia with STAT3-RARA | | MONDO:0100375 | +| MONDO:0957714 | acute myeloid leukemia with t(1;17)(q42.3;q21.2); irf2bp2-rara | NCIT:C198831 | MONDO:equivalentTo | Acute Myeloid Leukemia with t(1;17)(q42.3;q21.2); IRF2BP2-RARA | | MONDO:0100375 | +| MONDO:0957715 | acute myeloid leukemia with tbl1xr1-rara | NCIT:C198834 | MONDO:equivalentTo | Acute Myeloid Leukemia with TBL1XR1-RARA | | MONDO:0100375 | +| MONDO:0957716 | acute myeloid leukemia with fip1l1-rara | NCIT:C198839 | MONDO:equivalentTo | Acute Myeloid Leukemia with FIP1L1-RARA | | MONDO:0100375 | +| MONDO:0957717 | acute myeloid leukemia with bcor-rara | NCIT:C198841 | MONDO:equivalentTo | Acute Myeloid Leukemia with BCOR-RARA | | MONDO:0100375 | +| MONDO:0957718 | acute myeloid leukemia with in-frame bzip cebpa mutation | NCIT:C198891 | MONDO:equivalentTo | Acute Myeloid Leukemia with In-Frame bZIP CEBPA Mutation | | MONDO:0017894 | +| MONDO:0957719 | acute myeloid leukemia with myelodysplasia-related cytogenetic abnormalities | NCIT:C198957 | MONDO:equivalentTo | Acute Myeloid Leukemia with Myelodysplasia-Related Cytogenetic Abnormalities | | MONDO:0100409 | +| MONDO:0957720 | low grade endometrioid adenocarcinoma | NCIT:C199146 | MONDO:equivalentTo | Low Grade Endometrioid Adenocarcinoma | | MONDO:0005026 | +| MONDO:0957721 | high grade endometrioid adenocarcinoma | NCIT:C199149 | MONDO:equivalentTo | High Grade Endometrioid Adenocarcinoma | | MONDO:0005026 | +| MONDO:0957722 | early t precursor lymphoblastic leukemia/lymphoma | NCIT:C199170 | MONDO:equivalentTo | Early T Precursor Lymphoblastic Leukemia/Lymphoma | | MONDO:0003537 | +| MONDO:0957724 | early t precursor acute lymphoblastic leukemia, not otherwise specified | NCIT:C199172 | MONDO:equivalentTo | Early T Precursor Acute Lymphoblastic Leukemia, Not Otherwise Specified | | MONDO:0100291 | +| MONDO:0957725 | t lymphoblastic leukemia/lymphoma, not otherwise specified | NCIT:C199173 | MONDO:equivalentTo | T Lymphoblastic Leukemia/Lymphoma, Not Otherwise Specified | | MONDO:0003537 | +| MONDO:0957726 | b acute lymphoblastic leukemia with recurrent genetic abnormalities | NCIT:C199202 | MONDO:equivalentTo | B Acute Lymphoblastic Leukemia with Recurrent Genetic Abnormalities | | MONDO:0020511|MONDO:0035605 | +| MONDO:0957727 | b lymphoblastic leukemia/lymphoma with myc rearrangement | NCIT:C199231 | MONDO:equivalentTo | B Lymphoblastic Leukemia/Lymphoma with MYC Rearrangement | | MONDO:0035605 | +| MONDO:0957728 | primary cold agglutinin disease | NCIT:C199387 | MONDO:equivalentTo | Primary Cold Agglutinin Disease | | MONDO:0004949 | +| MONDO:0957729 | multiple myeloma with recurrent genetic abnormalities | NCIT:C199392 | MONDO:equivalentTo | Multiple Myeloma with Recurrent Genetic Abnormalities | | MONDO:0009693 | +| MONDO:0957730 | multiple myeloma, not otherwise specified | NCIT:C199418 | MONDO:equivalentTo | Multiple Myeloma, Not Otherwise Specified | | MONDO:0009693 | +| MONDO:0957731 | heavy chain class-switched primary cutaneous marginal zone lymphoproliferative disorder | NCIT:C199457 | MONDO:equivalentTo | Heavy Chain Class-Switched Primary Cutaneous Marginal Zone Lymphoproliferative Disorder | | MONDO:0015813 | +| MONDO:0957732 | igm-positive primary cutaneous marginal zone lymphoproliferative disorder | NCIT:C199460 | MONDO:equivalentTo | IgM-Positive Primary Cutaneous Marginal Zone Lymphoproliferative Disorder | | MONDO:0015813 | +| MONDO:0957733 | bcl2-r-negative, cd23-positive follicle center lymphoma | NCIT:C199467 | MONDO:equivalentTo | BCL2-R-Negative, CD23-Positive Follicle Center Lymphoma | | MONDO:0018906 | +| MONDO:0957734 | cyclin d1-positive mantle cell lymphoma | NCIT:C199481 | MONDO:equivalentTo | Cyclin D1-Positive Mantle Cell Lymphoma | | MONDO:0018876 | +| MONDO:0957735 | hhv-8 and ebv-negative primary effusion-based lymphoma | NCIT:C199576 | MONDO:equivalentTo | HHV-8 and EBV-Negative Primary Effusion-Based Lymphoma | | MONDO:0018905 | +| MONDO:0957736 | classic hydroa vacciniforme lymphoproliferative disorder | NCIT:C199676 | MONDO:equivalentTo | Classic Hydroa Vacciniforme Lymphoproliferative Disorder | | MONDO:0018224 | +| MONDO:0957737 | systemic hydroa vacciniforme lymphoproliferative disorder | NCIT:C199677 | MONDO:equivalentTo | Systemic Hydroa Vacciniforme Lymphoproliferative Disorder | | MONDO:0018224 | +| MONDO:0957738 | indolent nk-cell lymphoproliferative disorder of the gastrointestinal tract | NCIT:C200037 | MONDO:equivalentTo | Indolent NK-Cell Lymphoproliferative Disorder of the Gastrointestinal Tract | | MONDO:0005169 | +| MONDO:0957739 | peripheral t-cell lymphoma-gata3 | NCIT:C200073 | MONDO:equivalentTo | Peripheral T-Cell Lymphoma-GATA3 | | MONDO:0004964 | +| MONDO:0957740 | peripheral t-cell lymphoma-tbx21 | NCIT:C200074 | MONDO:equivalentTo | Peripheral T-Cell Lymphoma-TBX21 | | MONDO:0004964 | +| MONDO:0957741 | alk-positive histiocytosis | NCIT:C200105 | MONDO:equivalentTo | ALK-Positive Histiocytosis | | MONDO:0006247 | +| MONDO:0957742 | vulvar tubulovillous adenoma | NCIT:C200207 | MONDO:equivalentTo | Vulvar Tubulovillous Adenoma | | MONDO:0002198|MONDO:0000643 | +| MONDO:0957743 | pancreatic cystic neoplasm | NCIT:C200227 | MONDO:equivalentTo | Pancreatic Cystic Neoplasm | | MONDO:0021077|MONDO:0021076 | +| MONDO:0957744 | myelodysplastic syndrome with low blasts | NCIT:C200389 | MONDO:equivalentTo | Myelodysplastic Syndrome with Low Blasts | | MONDO:0018881 | +| MONDO:0957745 | myelodysplastic syndrome with genetic abnormalities | NCIT:C200390 | MONDO:equivalentTo | Myelodysplastic Syndrome with Genetic Abnormalities | | MONDO:0018881 | +| MONDO:0957746 | myelodysplastic syndrome/acute myeloid leukemia with myelodysplasia-related gene mutations | NCIT:C200400 | MONDO:equivalentTo | Myelodysplastic Syndrome/Acute Myeloid Leukemia with Myelodysplasia-Related Gene Mutations | | MONDO:0015041 | +| MONDO:0957747 | myelodysplastic syndrome/acute myeloid leukemia with myelodysplasia-related cytogenetic abnormalities | NCIT:C200402 | MONDO:equivalentTo | Myelodysplastic Syndrome/Acute Myeloid Leukemia with Myelodysplasia-Related Cytogenetic Abnormalities | | MONDO:0015041 | +| MONDO:0957748 | acute myeloid leukemia with mecom rearrangement | NCIT:C200407 | MONDO:equivalentTo | Acute Myeloid Leukemia with MECOM Rearrangement | | MONDO:0020078 | +| MONDO:0957749 | acute myeloid leukemia with nup98 rearrangement | NCIT:C200411 | MONDO:equivalentTo | Acute Myeloid Leukemia with NUP98 Rearrangement | | MONDO:0020078 | +| MONDO:0957750 | acute myeloid leukemia with fus-erg | NCIT:C200419 | MONDO:equivalentTo | Acute Myeloid Leukemia with FUS-ERG | | MONDO:0020078 | +| MONDO:0957751 | acute myeloid leukemia with npm1-mlf1 | NCIT:C200420 | MONDO:equivalentTo | Acute Myeloid Leukemia with NPM1-MLF1 | | MONDO:0020078 | +| MONDO:0957752 | acute myeloid leukemia with kat6a-crebbp | NCIT:C200421 | MONDO:equivalentTo | Acute Myeloid Leukemia with KAT6A-CREBBP | | MONDO:0020078 | +| MONDO:0957753 | acute leukemia of ambiguous lineage with defining genetic abnormalities | NCIT:C200494 | MONDO:equivalentTo | Acute Leukemia of Ambiguous Lineage with Defining Genetic Abnormalities | | MONDO:0019460 | +| MONDO:0957754 | mature plasmacytoid dendritic cell proliferation associated with myeloid neoplasm | NCIT:C200513 | MONDO:equivalentTo | Mature Plasmacytoid Dendritic Cell Proliferation Associated with Myeloid Neoplasm | | MONDO:0006247 | +| MONDO:0957755 | b lymphoblastic leukemia/lymphoma with tcf3-hlf rearrangement | NCIT:C200587 | MONDO:equivalentTo | B Lymphoblastic Leukemia/Lymphoma with TCF3-HLF Rearrangement | | MONDO:0035605 | +| MONDO:0957756 | atypical teratoid/rhabdoid tumor molecular subtypes | NCIT:C200597 | MONDO:equivalentTo | Atypical Teratoid/Rhabdoid Tumor Molecular Subtypes | | MONDO:0020560 | +| MONDO:0957757 | classic follicular lymphoma | NCIT:C200669 | MONDO:equivalentTo | Classic Follicular Lymphoma | | MONDO:0018906 | +| MONDO:0957758 | follicular lymphoma with unusual cytological features | NCIT:C200684 | MONDO:equivalentTo | Follicular Lymphoma with Unusual Cytological Features | | MONDO:0018906 | +| MONDO:0957759 | cyclin d1-negative mantle cell lymphoma | NCIT:C200685 | MONDO:equivalentTo | Cyclin D1-Negative Mantle Cell Lymphoma | | MONDO:0018876 | +| MONDO:0957760 | primary large b-cell lymphoma of immune-privileged site | NCIT:C200687 | MONDO:equivalentTo | Primary Large B-Cell Lymphoma of Immune-Privileged Site | | MONDO:0018905 | +| MONDO:0957761 | ebv-negative burkitt lymphoma | NCIT:C200688 | MONDO:equivalentTo | EBV-Negative Burkitt Lymphoma | | MONDO:0007243 | +| MONDO:0957762 | plasma cell neoplasm with associated paraneoplastic syndrome | NCIT:C200738 | MONDO:equivalentTo | Plasma Cell Neoplasm with Associated Paraneoplastic Syndrome | | MONDO:0004959 | +| MONDO:0957763 | who grade 4 glioma | NCIT:C200758 | MONDO:equivalentTo | WHO Grade 4 Glioma | | MONDO:0100342 | +| MONDO:0957764 | primary cutaneous peripheral t-cell lymphoma, not otherwise specified | NCIT:C201080 | MONDO:equivalentTo | Primary Cutaneous Peripheral T-Cell Lymphoma, Not Otherwise Specified | | MONDO:0000607 | +| MONDO:0957765 | cribriform comedo-type adenocarcinoma | NCIT:C201124 | MONDO:equivalentTo | Cribriform Comedo-Type Adenocarcinoma | | MONDO:0003575|MONDO:0006176 | +| MONDO:0957766 | aleukemic myeloid leukemia | NCIT:C201127 | MONDO:equivalentTo | Aleukemic Myeloid leukemia | | MONDO:0003730|MONDO:0004643 | +| MONDO:0957767 | solid pseudopapillary neoplasm | NCIT:C201136 | MONDO:equivalentTo | Solid Pseudopapillary Neoplasm | | MONDO:0004992 | +| MONDO:0957768 | endemic burkitt lymphoma | NCIT:C27122 | MONDO:equivalentTo | Endemic Burkitt Lymphoma | | MONDO:0007243 | +| MONDO:0957769 | multicystic mesothelioma | NCIT:C3765 | MONDO:equivalentTo | Multicystic Mesothelioma | | MONDO:0006856|MONDO:0021077 | +| MONDO:0957770 | low grade myofibroblastic sarcoma | NCIT:C49024 | MONDO:equivalentTo | Low Grade Myofibroblastic Sarcoma | | MONDO:0005164 | +| MONDO:0957771 | sclerosing epithelioid fibrosarcoma | NCIT:C49027 | MONDO:equivalentTo | Sclerosing Epithelioid Fibrosarcoma | | MONDO:0005164 | +| MONDO:0957772 | meningothelial cell neoplasm | NCIT:C6971 | MONDO:equivalentTo | Meningothelial Cell Neoplasm | | MONDO:0002616 | +| MONDO:0957773 | type a lymphomatoid papulosis | NCIT:C7197 | MONDO:equivalentTo | Type A Lymphomatoid Papulosis | | MONDO:0020326 | +| MONDO:0957774 | type c lymphomatoid papulosis | NCIT:C7199 | MONDO:equivalentTo | Type C Lymphomatoid Papulosis | | MONDO:0020326 | +| MONDO:0957775 | pancreatic intraductal papillary mucinous neoplasm, oncocytic-type | NCIT:C95514 | MONDO:equivalentTo | Pancreatic Intraductal Papillary Mucinous Neoplasm, Oncocytic-Type | | MONDO:0004286|MONDO:0010795 | +| MONDO:0957850 | post-essential thrombocythemia myelofibrosis | NCIT:C126806 | MONDO:equivalentTo | Post-Essential Thrombocythemia Myelofibrosis | | MONDO:0005029 | +| MONDO:0957851 | recurrent myelofibrosis | NCIT:C162424 | MONDO:equivalentTo | Recurrent Myelofibrosis | | | +| MONDO:0957852 | refractory myelofibrosis | NCIT:C162425 | MONDO:equivalentTo | Refractory Myelofibrosis | | | +| MONDO:0957853 | bone rosai-dorfman-destombes disease | NCIT:C178613 | MONDO:equivalentTo | Bone Rosai-Dorfman-Destombes Disease | | MONDO:0019060|MONDO:0006412 | +| MONDO:0957854 | stage m0 medulloblastoma | NCIT:C186521 | MONDO:equivalentTo | Stage M0 Medulloblastoma | | MONDO:0007959 | +| MONDO:0957855 | stage m1 medulloblastoma | NCIT:C186522 | MONDO:equivalentTo | Stage M1 Medulloblastoma | | MONDO:0007959 | +| MONDO:0957856 | stage m2 medulloblastoma | NCIT:C186523 | MONDO:equivalentTo | Stage M2 Medulloblastoma | | MONDO:0007959 | +| MONDO:0957857 | stage m3 medulloblastoma | NCIT:C186524 | MONDO:equivalentTo | Stage M3 Medulloblastoma | | MONDO:0007959 | +| MONDO:0957858 | stage m4 medulloblastoma | NCIT:C186525 | MONDO:equivalentTo | Stage M4 Medulloblastoma | | MONDO:0007959 | +| MONDO:0957859 | stage m0 atypical teratoid/rhabdoid tumor | NCIT:C186528 | MONDO:equivalentTo | Stage M0 Atypical Teratoid/Rhabdoid Tumor | | MONDO:0020560 | +| MONDO:0957860 | stage m1 atypical teratoid/rhabdoid tumor | NCIT:C186529 | MONDO:equivalentTo | Stage M1 Atypical Teratoid/Rhabdoid Tumor | | MONDO:0020560 | +| MONDO:0957861 | stage m2 atypical teratoid/rhabdoid tumor | NCIT:C186530 | MONDO:equivalentTo | Stage M2 Atypical Teratoid/Rhabdoid Tumor | | MONDO:0020560 | +| MONDO:0957862 | stage m3 atypical teratoid/rhabdoid tumor | NCIT:C186531 | MONDO:equivalentTo | Stage M3 Atypical Teratoid/Rhabdoid Tumor | | MONDO:0020560 | +| MONDO:0957863 | stage m4 atypical teratoid/rhabdoid tumor | NCIT:C186532 | MONDO:equivalentTo | Stage M4 Atypical Teratoid/Rhabdoid Tumor | | MONDO:0020560 | +| MONDO:0957864 | stage m0 pineoblastoma | NCIT:C186568 | MONDO:equivalentTo | Stage M0 Pineoblastoma | | MONDO:0016722 | +| MONDO:0957865 | stage m1 pineoblastoma | NCIT:C186569 | MONDO:equivalentTo | Stage M1 Pineoblastoma | | MONDO:0016722 | +| MONDO:0957866 | stage m2 pineoblastoma | NCIT:C186570 | MONDO:equivalentTo | Stage M2 Pineoblastoma | | MONDO:0016722 | +| MONDO:0957867 | stage m3 pineoblastoma | NCIT:C186571 | MONDO:equivalentTo | Stage M3 Pineoblastoma | | MONDO:0016722 | +| MONDO:0957868 | stage m4 pineoblastoma | NCIT:C186572 | MONDO:equivalentTo | Stage M4 Pineoblastoma | | MONDO:0016722 | +| MONDO:0958220 | colorectal perineurioma | NCIT:C96513 | MONDO:equivalentTo | Colorectal Perineurioma | | MONDO:0015031|MONDO:0021444 | +| MONDO:0968996 | platinum-resistant primary peritoneal carcinoma | NCIT:C157622 | MONDO:equivalentTo | Platinum-Resistant Primary Peritoneal Carcinoma | | MONDO:0015686 | +| MONDO:0968997 | platinum-resistant malignant female reproductive system neoplasm | NCIT:C169021 | MONDO:equivalentTo | Platinum-Resistant Malignant Female Reproductive System Neoplasm | | MONDO:0001416 | +| MONDO:0968998 | extracutaneous merkel cell carcinoma | NCIT:C173586 | MONDO:equivalentTo | Extracutaneous Merkel Cell Carcinoma | | MONDO:0019210 | +| MONDO:0968999 | non-neoplastic tonsillar disorder | NCIT:C173798 | MONDO:equivalentTo | Non-Neoplastic Tonsillar Disorder | | | +| MONDO:0969000 | swi/snf complex-deficient sinonasal carcinoma | NCIT:C201634 | MONDO:equivalentTo | SWI/SNF Complex-Deficient Sinonasal Carcinoma | | MONDO:0056819 | +| MONDO:0969001 | tracheal verrucous carcinoma | NCIT:C201742 | MONDO:equivalentTo | Tracheal Verrucous Carcinoma | | MONDO:0001419|MONDO:0006006 | +| MONDO:0969002 | hypopharyngeal verrucous carcinoma | NCIT:C201743 | MONDO:equivalentTo | Hypopharyngeal Verrucous Carcinoma | | MONDO:0044638|MONDO:0006006 | +| MONDO:0969003 | hypopharyngeal papillary squamous cell carcinoma | NCIT:C201748 | MONDO:equivalentTo | Hypopharyngeal Papillary Squamous Cell Carcinoma | | MONDO:0002979|MONDO:0044638 | +| MONDO:0969004 | hypopharyngeal spindle cell squamous carcinoma | NCIT:C201749 | MONDO:equivalentTo | Hypopharyngeal Spindle Cell Squamous Carcinoma | | MONDO:0044638|MONDO:0021663 | +| MONDO:0969005 | parotid gland keratocystoma | NCIT:C201770 | MONDO:equivalentTo | Parotid Gland Keratocystoma | | MONDO:0021460 | +| MONDO:0969006 | hyalinizing clear cell carcinoma | NCIT:C201821 | MONDO:equivalentTo | Hyalinizing Clear Cell Carcinoma | | MONDO:0004993 | +| MONDO:0969007 | tongue verrucous carcinoma | NCIT:C201878 | MONDO:equivalentTo | Tongue Verrucous Carcinoma | | MONDO:0021538|MONDO:0000500 | +| MONDO:0969008 | palatine tonsil hamartomatous polyp | NCIT:C201900 | MONDO:equivalentTo | Palatine Tonsil Hamartomatous Polyp | | | +| MONDO:0969009 | transformed chronic lymphocytic leukemia to hodgkin lymphoma | NCIT:C201960 | MONDO:equivalentTo | Transformed Chronic Lymphocytic Leukemia to Hodgkin Lymphoma | | MONDO:0004948 | +| MONDO:0969010 | pineoblastoma molecular subtypes | NCIT:C201966 | MONDO:equivalentTo | Pineoblastoma Molecular Subtypes | | MONDO:0016722 | +| MONDO:0969011 | spinal cord pilocytic astrocytoma | NCIT:C201976 | MONDO:equivalentTo | Spinal Cord Pilocytic Astrocytoma | | MONDO:0003174|MONDO:0016691 | +| MONDO:0969012 | brain low grade glioma | NCIT:C201977 | MONDO:equivalentTo | Brain Low Grade Glioma | | MONDO:0021632|MONDO:0021637 | +| MONDO:0969013 | clear cell calcifying epithelial odontogenic tumor | NCIT:C202057 | MONDO:equivalentTo | Clear Cell Calcifying Epithelial Odontogenic Tumor | | MONDO:0022057 | +| MONDO:0969014 | cystic/microcystic calcifying epithelial odontogenic tumor | NCIT:C202058 | MONDO:equivalentTo | Cystic/Microcystic Calcifying Epithelial Odontogenic Tumor | | MONDO:0022057 | +| MONDO:0969015 | non-calcifying/langerhans cell-rich calcifying epithelial odontogenic tumor | NCIT:C202059 | MONDO:equivalentTo | Non-Calcifying/Langerhans Cell-Rich Calcifying Epithelial Odontogenic Tumor | | MONDO:0022057 | +| MONDO:0969016 | adenoid ameloblastoma | NCIT:C202061 | MONDO:equivalentTo | Adenoid Ameloblastoma | | MONDO:0017795 | +| MONDO:0969017 | egfr-positive lung non-small cell carcinoma | NCIT:C202131 | MONDO:equivalentTo | EGFR-Positive Lung Non-Small Cell Carcinoma | | MONDO:0005233 | +| MONDO:0969018 | juvenile trabecular ossifying fibroma | NCIT:C202205 | MONDO:equivalentTo | Juvenile Trabecular Ossifying Fibroma | | MONDO:0002119 | +| MONDO:0969019 | psammomatoid ossifying fibroma | NCIT:C202209 | MONDO:equivalentTo | Psammomatoid Ossifying Fibroma | | MONDO:0002119 | +| MONDO:0969020 | surface osteoma | NCIT:C202252 | MONDO:equivalentTo | Surface Osteoma | | MONDO:0005166 | +| MONDO:0969021 | central osteoma | NCIT:C202253 | MONDO:equivalentTo | Central Osteoma | | MONDO:0005166 | +| MONDO:0969022 | rhabdomyosarcoma with tfcp2 rearrangement | NCIT:C202263 | MONDO:equivalentTo | Rhabdomyosarcoma with TFCP2 Rearrangement | | MONDO:0005212 | +| MONDO:0969023 | non-clear cell renal cell carcinoma | NCIT:C202497 | MONDO:equivalentTo | Non-Clear Cell Renal Cell Carcinoma | | MONDO:0005549 | +| MONDO:0969024 | middle ear papilloma | NCIT:C202582 | MONDO:equivalentTo | Middle Ear Papilloma | | MONDO:0021078|MONDO:0021482 | +| MONDO:0969025 | external auditory canal squamous cell carcinoma | NCIT:C202594 | MONDO:equivalentTo | External Auditory Canal Squamous Cell Carcinoma | | MONDO:0003501 | +| MONDO:0969026 | orbit solitary fibrous tumor | NCIT:C202620 | MONDO:equivalentTo | Orbit Solitary Fibrous Tumor | | MONDO:0016238|MONDO:0024611 | +| MONDO:0969027 | head and neck soft tissue neoplasm | NCIT:C202623 | MONDO:equivalentTo | Head and Neck Soft Tissue Neoplasm | | MONDO:0006424|MONDO:0005586 | +| MONDO:0969028 | proximal colon carcinoma | NCIT:C202633 | MONDO:equivalentTo | Proximal Colon Carcinoma | | MONDO:0002032 | +| MONDO:0969029 | distal colon carcinoma | NCIT:C202634 | MONDO:equivalentTo | Distal Colon Carcinoma | | MONDO:0002032 | +| MONDO:0969030 | oral cavity neurofibroma | NCIT:C202860 | MONDO:equivalentTo | Oral Cavity Neurofibroma | | MONDO:0021445|MONDO:0016755 | +| MONDO:0969031 | oral cavity schwannoma | NCIT:C202876 | MONDO:equivalentTo | Oral Cavity Schwannoma | | MONDO:0021445|MONDO:0004820 | +| MONDO:0969032 | head and neck phosphaturic mesenchymal tumor | NCIT:C202879 | MONDO:equivalentTo | Head and Neck Phosphaturic Mesenchymal Tumor | | MONDO:0006368|MONDO:0005586 | +| MONDO:0969033 | appendicular skeleton phosphaturic mesenchymal tumor | NCIT:C202880 | MONDO:equivalentTo | Appendicular Skeleton Phosphaturic Mesenchymal Tumor | | MONDO:0019060|MONDO:0006368 | +| MONDO:0969034 | poorly differentiated synovial sarcoma | NCIT:C202883 | MONDO:equivalentTo | Poorly Differentiated Synovial Sarcoma | | MONDO:0010434 | +| MONDO:0969035 | primary cd30-positive t-cell lymphoproliferative disorder | NCIT:C202952 | MONDO:equivalentTo | Primary CD30-Positive T-Cell Lymphoproliferative Disorder | | MONDO:0005169 | +| MONDO:0969036 | head and neck hematopoietic and lymphoid cell neoplasm | NCIT:C202954 | MONDO:equivalentTo | Head and Neck Hematopoietic and Lymphoid Cell Neoplasm | | MONDO:0005586|MONDO:0044881 | +| MONDO:0969037 | head and neck germ cell tumor | NCIT:C202977 | MONDO:equivalentTo | Head and Neck Germ Cell Tumor | | MONDO:0018201|MONDO:0005586 | +| MONDO:0969038 | cecum neuroendocrine tumor | NCIT:C203386 | MONDO:equivalentTo | Cecum Neuroendocrine Tumor | | MONDO:0005694|MONDO:0015067 | +| MONDO:0969039 | ascending colon neuroendocrine tumor | NCIT:C203387 | MONDO:equivalentTo | Ascending Colon Neuroendocrine Tumor | | MONDO:0015067 | +| MONDO:0969040 | descending colon neuroendocrine tumor | NCIT:C203388 | MONDO:equivalentTo | Descending Colon Neuroendocrine Tumor | | MONDO:0015067 | +| MONDO:0969041 | sigmoid colon neuroendocrine tumor | NCIT:C203389 | MONDO:equivalentTo | Sigmoid Colon Neuroendocrine Tumor | | MONDO:0015067 | +| MONDO:0969042 | transverse colon neuroendocrine tumor | NCIT:C203390 | MONDO:equivalentTo | Transverse Colon Neuroendocrine Tumor | | MONDO:0015067 | +| MONDO:0969043 | histiocytic disorder | NCIT:C203422 | MONDO:equivalentTo | Histiocytic Disorder | | | +| MONDO:0969044 | myelodysplastic chronic myelomonocytic leukemia | NCIT:C203443 | MONDO:equivalentTo | Myelodysplastic Chronic Myelomonocytic Leukemia | | MONDO:0020311 | +| MONDO:0969045 | myeloproliferative chronic myelomonocytic leukemia | NCIT:C203444 | MONDO:equivalentTo | Myeloproliferative Chronic Myelomonocytic Leukemia | | MONDO:0020311 | +| MONDO:0969046 | t acute lymphoblastic leukemia with recurrent genetic abnormalities | NCIT:C203469 | MONDO:equivalentTo | T Acute Lymphoblastic Leukemia with Recurrent Genetic Abnormalities | | MONDO:0004963 | +| MONDO:0969047 | esophageal and gastroesophageal junction carcinoma | NCIT:C203673 | MONDO:equivalentTo | Esophageal and Gastroesophageal Junction Carcinoma | | MONDO:0006181 | +| MONDO:0969048 | low grade mucinous carcinoma peritonei | NCIT:C203946 | MONDO:equivalentTo | Low Grade Mucinous Carcinoma Peritonei | | MONDO:0017048 | +| MONDO:0969049 | high grade mucinous carcinoma peritonei | NCIT:C203948 | MONDO:equivalentTo | High Grade Mucinous Carcinoma Peritonei | | MONDO:0017048 | +| MONDO:0969050 | merkel cell polyoma virus-positive merkel cell carcinoma | NCIT:C204383 | MONDO:equivalentTo | Merkel Cell Polyoma Virus-Positive Merkel Cell Carcinoma | | MONDO:0019210 | +| MONDO:0969051 | merkel cell polyoma virus-negative merkel cell carcinoma | NCIT:C204385 | MONDO:equivalentTo | Merkel Cell Polyoma Virus-Negative Merkel Cell Carcinoma | | MONDO:0019210 | +| MONDO:0969052 | lentiginous melanocytic nevus | NCIT:C204482 | MONDO:equivalentTo | Lentiginous Melanocytic Nevus | | MONDO:0044794 | +| MONDO:0969053 | mitf pathway-activated melanocytic tumor | NCIT:C204739 | MONDO:equivalentTo | MITF Pathway-Activated Melanocytic Tumor | | MONDO:0021583 | +| MONDO:0969054 | dermal spitz nevus | NCIT:C204789 | MONDO:equivalentTo | Dermal Spitz Nevus | | MONDO:0006813|MONDO:0044793 | +| MONDO:0969055 | spitz tumor | NCIT:C204790 | MONDO:equivalentTo | Spitz Tumor | | MONDO:0021583 | +| MONDO:0969056 | melanoma in intermittently sun-exposed skin | NCIT:C204840 | MONDO:equivalentTo | Melanoma in Intermittently Sun-Exposed Skin | | MONDO:0005012 | +| MONDO:0969057 | low-csd melanoma, superficial spreading melanoma subtype | NCIT:C204843 | MONDO:equivalentTo | Low-CSD Melanoma, Superficial Spreading Melanoma Subtype | | MONDO:0020638 | +| MONDO:0969058 | melanoma in chronically sun-exposed skin | NCIT:C204864 | MONDO:equivalentTo | Melanoma in Chronically Sun-Exposed Skin | | MONDO:0005012 | +| MONDO:0969059 | mucosal nevus | NCIT:C204907 | MONDO:equivalentTo | Mucosal Nevus | | MONDO:0005073 | +| MONDO:0969060 | dendritic blue nevus | NCIT:C204910 | MONDO:equivalentTo | Dendritic Blue Nevus | | MONDO:0006680 | +| MONDO:0969061 | intermediate congenital melanocytic nevus | NCIT:C204976 | MONDO:equivalentTo | Intermediate Congenital Melanocytic Nevus | | MONDO:0044792 | +| MONDO:0969062 | conjunctival melanocytic neoplasm | NCIT:C204977 | MONDO:equivalentTo | Conjunctival Melanocytic Neoplasm | | MONDO:0021143|MONDO:0020204 | +| MONDO:0969063 | uveal melanocytic neoplasm | NCIT:C205057 | MONDO:equivalentTo | Uveal Melanocytic Neoplasm | | MONDO:0021143|MONDO:0021225 | +| MONDO:0969064 | nodular melanoma | NCIT:C205125 | MONDO:equivalentTo | Nodular Melanoma | | MONDO:0005105 | +| MONDO:0969065 | dermal melanoma | NCIT:C205129 | MONDO:equivalentTo | Dermal Melanoma | | MONDO:0005012 | +| MONDO:0969066 | metastatic melanoma in the lymph nodes | NCIT:C205131 | MONDO:equivalentTo | Metastatic Melanoma in the Lymph Nodes | | MONDO:0005191|MONDO:0005438 | +| MONDO:0969067 | platinum-sensitive endometrial carcinoma | NCIT:C205187 | MONDO:equivalentTo | Platinum-Sensitive Endometrial Carcinoma | | MONDO:0002447 | +| MONDO:0969068 | early stage cervical carcinoma | NCIT:C205287 | MONDO:equivalentTo | Early Stage Cervical Carcinoma | | MONDO:0005131 | +| MONDO:0969069 | early stage clear cell renal cell carcinoma | NCIT:C205289 | MONDO:equivalentTo | Early Stage Clear Cell Renal Cell Carcinoma | | MONDO:0005005 | +| MONDO:0969070 | early stage colorectal carcinoma | NCIT:C205290 | MONDO:equivalentTo | Early Stage Colorectal Carcinoma | | MONDO:0024331 | +| MONDO:0969071 | early stage endometrial carcinoma | NCIT:C205295 | MONDO:equivalentTo | Early Stage Endometrial Carcinoma | | MONDO:0002447 | +| MONDO:0969072 | early stage esophageal carcinoma | NCIT:C205298 | MONDO:equivalentTo | Early Stage Esophageal Carcinoma | | MONDO:0019086 | +| MONDO:0969073 | early stage hepatocellular carcinoma | NCIT:C205301 | MONDO:equivalentTo | Early Stage Hepatocellular Carcinoma | | MONDO:0007256 | +| MONDO:0969074 | early stage lung non-small cell carcinoma | NCIT:C205303 | MONDO:equivalentTo | Early Stage Lung Non-Small Cell Carcinoma | | MONDO:0005233 | +| MONDO:0969075 | early stage malignant skin neoplasm | NCIT:C205307 | MONDO:equivalentTo | Early Stage Malignant Skin Neoplasm | | MONDO:0002898 | +| MONDO:0969076 | primary cutaneous nut adnexal carcinoma | NCIT:C205357 | MONDO:equivalentTo | Primary Cutaneous NUT Adnexal Carcinoma | | MONDO:0005563|MONDO:0006973 | +| MONDO:0969077 | trichogerminoma | NCIT:C205371 | MONDO:equivalentTo | Trichogerminoma | | MONDO:0020593 | +| MONDO:0969078 | apocrine cystadenoma | NCIT:C205459 | MONDO:equivalentTo | Apocrine Cystadenoma | | MONDO:0002804|MONDO:0002369 | +| MONDO:0969079 | eccrine poroma | NCIT:C205462 | MONDO:equivalentTo | Eccrine Poroma | | MONDO:0006738|MONDO:0024247 | +| MONDO:0969080 | hidroacanthoma simplex | NCIT:C205475 | MONDO:equivalentTo | Hidroacanthoma Simplex | | MONDO:0006738 | +| MONDO:0969081 | solid cystic hidradenoma | NCIT:C205539 | MONDO:equivalentTo | Solid Cystic Hidradenoma | | MONDO:0002805 | +| MONDO:0969082 | sialoblastoma | NCIT:C35837 | MONDO:equivalentTo | Sialoblastoma | | MONDO:0004669 | +| MONDO:0969083 | cribriform trichoblastoma | NCIT:C43322 | MONDO:equivalentTo | Cribriform Trichoblastoma | | MONDO:0020593 | +| MONDO:0969084 | lung neuroendocrine carcinoma | NCIT:C45569 | MONDO:equivalentTo | Lung Neuroendocrine Carcinoma | | MONDO:0005454|MONDO:0005138|MONDO:0002120 | +| MONDO:0969085 | branchioma | NCIT:C53595 | MONDO:equivalentTo | Branchioma | | MONDO:0021455 | +| MONDO:0969086 | ear carcinoma | NCIT:C54262 | MONDO:equivalentTo | Ear Carcinoma | | MONDO:0003277|MONDO:0002038 | +| MONDO:0969087 | intracranial melanoma | NCIT:C5442 | MONDO:equivalentTo | Intracranial Melanoma | | MONDO:0003761|MONDO:0001657|MONDO:0021632 | +| MONDO:0969088 | meckel diverticulum neuroendocrine tumor g1 | NCIT:C6424 | MONDO:equivalentTo | Meckel Diverticulum Neuroendocrine Tumor G1 | | MONDO:0021533 | +| MONDO:0969089 | duodenal neuroendocrine tumor g1 | NCIT:C6425 | MONDO:equivalentTo | Duodenal Neuroendocrine Tumor G1 | | MONDO:0000540|MONDO:0015063 | +| MONDO:0969090 | intracranial myeloid sarcoma | NCIT:C7008 | MONDO:equivalentTo | Intracranial Myeloid Sarcoma | | MONDO:0003641|MONDO:0001657|MONDO:0006861|MONDO:0021632 | +| MONDO:0969091 | hamartomatous polyp | NCIT:C8372 | MONDO:equivalentTo | Hamartomatous Polyp | | | +| MONDO:0969092 | well differentiated fibrosarcoma | NCIT:C9025 | MONDO:equivalentTo | Well Differentiated Fibrosarcoma | | MONDO:0005164 | +| MONDO:0969093 | poorly differentiated angiosarcoma | NCIT:C9031 | MONDO:equivalentTo | Poorly Differentiated Angiosarcoma | | MONDO:0016982 | +| MONDO:0969094 | well differentiated leiomyosarcoma | NCIT:C9389 | MONDO:equivalentTo | Well Differentiated Leiomyosarcoma | | MONDO:0005058 | +| MONDO:0969095 | poorly differentiated fibrosarcoma | NCIT:C9404 | MONDO:equivalentTo | Poorly Differentiated Fibrosarcoma | | MONDO:0005164 | +| MONDO:0969096 | low grade sarcoma | NCIT:C9417 | MONDO:equivalentTo | Low Grade Sarcoma | | MONDO:0005089 | +| MONDO:0969097 | high grade sarcoma | NCIT:C9418 | MONDO:equivalentTo | High Grade Sarcoma | | MONDO:0005089 | \ No newline at end of file diff --git a/docs/reports/migrate_omim.md b/docs/reports/migrate_omim.md index 70eb9f84..e620077b 100644 --- a/docs/reports/migrate_omim.md +++ b/docs/reports/migrate_omim.md @@ -2,16 +2,11 @@ [Interactive FlatGithub table](https://flatgithub.com/monarch-initiative/mondo-ingest?filename=src/ontology/slurp/omim.tsv) ### Migratable terms -| mondo_id | mondo_label | xref | xref_source | original_label | definition | parents | -|:--------------|:--------------------------------------------------------------------|:---------------------|:---------------------------|:--------------------------------------------------------------------|:--------------|:--------------| -| ID | LABEL | A oboInOwl:hasDbXref | >A oboInOwl:source SPLIT=| | | A IAO:0000115 | SC % | -| MONDO:0968950 | li-fraumeni syndrome | OMIMPS:151623 | MONDO:equivalentTo | Li-Fraumeni syndrome | | | -| MONDO:0968976 | neurodevelopmental disorder with progressive movement abnormalities | OMIM:620785 | MONDO:equivalentTo | neurodevelopmental disorder with progressive movement abnormalities | | | -| MONDO:0968977 | basal ganglia calcification, idiopathic, 9, autosomal recessive | OMIM:620786 | MONDO:equivalentTo | basal ganglia calcification, idiopathic, 9, autosomal recessive | | | -| MONDO:0968978 | aplasia cutis-enamel dysplasia syndrome | OMIM:620789 | MONDO:equivalentTo | aplasia cutis-enamel dysplasia syndrome | | | -| MONDO:0968979 | neurodevelopmental disorder with hypotonia and seizures | OMIM:620790 | MONDO:equivalentTo | neurodevelopmental disorder with hypotonia and seizures | | | -| MONDO:0968980 | otosclerosis 12 | OMIM:620792 | MONDO:equivalentTo | otosclerosis 12 | | MONDO:0005349 | -| MONDO:0968981 | deafness, autosomal recessive 124 | OMIM:620794 | MONDO:equivalentTo | deafness, autosomal recessive 124 | | MONDO:0019588 | -| MONDO:0968982 | autoinflammation with episodic fever and immune dysregulation | OMIM:620795 | MONDO:equivalentTo | autoinflammation with episodic fever and immune dysregulation | | | -| MONDO:0968983 | proteasome-associated autoinflammatory syndrome 6 | OMIM:620796 | MONDO:equivalentTo | proteasome-associated autoinflammatory syndrome 6 | | MONDO:0009726 | -| MONDO:0968984 | citrullinemia | OMIMPS:215700 | MONDO:equivalentTo | Citrullinemia | | | \ No newline at end of file +| mondo_id | mondo_label | xref | xref_source | original_label | definition | parents | +|:--------------|:-----------------------------------------------|:---------------------|:---------------------------|:-----------------------------------------------|:--------------|:--------------| +| ID | LABEL | A oboInOwl:hasDbXref | >A oboInOwl:source SPLIT=| | | A IAO:0000115 | SC % | +| MONDO:0969099 | leigh syndrome, mitochondrial | OMIM:500017 | MONDO:equivalentTo | leigh syndrome, mitochondrial | | | +| MONDO:0969100 | developmental and epileptic encephalopathy 116 | OMIM:620806 | MONDO:equivalentTo | developmental and epileptic encephalopathy 116 | | MONDO:0100062 | +| MONDO:0969101 | rothmund-thomson syndrome, type 4 | OMIM:620819 | MONDO:equivalentTo | rothmund-thomson syndrome, type 4 | | MONDO:0010002 | +| MONDO:0969102 | el hayek-chahrour neurodevelopmental syndrome | OMIM:620820 | MONDO:equivalentTo | el hayek-chahrour neurodevelopmental syndrome | | | +| MONDO:0969103 | neuroocular syndrome | OMIMPS:619539 | MONDO:equivalentTo | Neuroocular syndrome | | | \ No newline at end of file diff --git a/docs/reports/migrate_ordo.md b/docs/reports/migrate_ordo.md index 9ee305c6..2333d305 100644 --- a/docs/reports/migrate_ordo.md +++ b/docs/reports/migrate_ordo.md @@ -2,17 +2,16 @@ [Interactive FlatGithub table](https://flatgithub.com/monarch-initiative/mondo-ingest?filename=src/ontology/slurp/ordo.tsv) ### Migratable terms -| mondo_id | mondo_label | xref | xref_source | original_label | definition | parents | -|:--------------|:----------------------------------------------------|:---------------------|:---------------------------|:----------------------------------------------------|:-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|:------------------------------------------| -| ID | LABEL | A oboInOwl:hasDbXref | >A oboInOwl:source SPLIT=| | | A IAO:0000115 | SC % | -| MONDO:0958337 | disorder with optic nerve compression | Orphanet:519337 | MONDO:equivalentTo | Disorder with optic nerve compression | | MONDO:8000033 | -| MONDO:0958338 | congenital optic disc excavation of genetic origin | Orphanet:522514 | MONDO:equivalentTo | Congenital optic disc excavation of genetic origin | | MONDO:8000033|MONDO:0026186 | -| MONDO:0958339 | syndromic genetic disorder with strabismus | Orphanet:522520 | MONDO:equivalentTo | Syndromic genetic disorder with strabismus | | MONDO:8000033 | -| MONDO:0958340 | rare genetic disorder with entropion | Orphanet:522530 | MONDO:equivalentTo | Rare genetic disorder with entropion | | MONDO:8000033 | -| MONDO:0958341 | genetic superficial corneal dystrophy | Orphanet:522562 | MONDO:equivalentTo | Genetic superficial corneal dystrophy | | MONDO:8000033 | -| MONDO:0968986 | chaotic conus spinal cord lipoma | Orphanet:645285 | MONDO:equivalentTo | Chaotic conus spinal cord lipoma | A rare dysraphic spinal cord lipoma characterized by the lipomatous mass extending ventrally to the dorsal root entry zone, indicating a more severe malformation of the spinal cord. The diagnosis can be suggested on imaging but usually confirmed during surgery. | MONDO:0958350|MONDO:8000034|MONDO:8000030 | -| MONDO:0968987 | extramedullary conus spinal cord lipoma | Orphanet:645297 | MONDO:equivalentTo | Extramedullary conus spinal cord lipoma | A rare closed lipomatous, dysraphic malformation of the lower spinal cord characterized by extramedullary lipomatous mass attached to the conus region. The conus is dysplastic and poorly delineated. Various morphological subtypes are recognized. Possible symptoms include bowel and bladder dysfunction and neuro-orthopedic deformity of the lower limbs. | MONDO:0958350|MONDO:8000034|MONDO:8000030 | -| MONDO:0968988 | saccular spinal dysraphism with a stalk to the dome | Orphanet:645319 | MONDO:equivalentTo | Saccular spinal dysraphism with a stalk to the dome | A rare spinal dysraphism characterized by a meningocele, containing a stalk, that is attached to the inner surface of the meningocele. The stalk can be posteriorly fibroneural (saccular limited dorsal myeloschisis) or the spinal cord itself (myelic limited dorsal malformation). | MONDO:0958345|MONDO:8000033|MONDO:0017069 | -| MONDO:0968989 | non-saccular limited dorsal myeloschisis | Orphanet:645343 | MONDO:equivalentTo | Non-saccular limited dorsal myeloschisis | A rare form of limited dorsal myeloschisis (LDM), characterized by a non saccular cutaneous stigmata (midline skin abnormality classically dimple, pit or sometimes angioma), the stalk is attached to this cutaneous stigmata. Fibroneural stalk varies in thickness and complexity. | MONDO:0958345|MONDO:8000030|MONDO:8000034 | -| MONDO:0968990 | genetic central precocious puberty in male | Orphanet:650097 | MONDO:equivalentTo | Genetic central precocious puberty in male | | MONDO:8000031|MONDO:0958356 | -| MONDO:0968991 | non-genetic central precocious puberty in male | Orphanet:650102 | MONDO:equivalentTo | Non-genetic central precocious puberty in male | | MONDO:0958356|MONDO:8000031 | \ No newline at end of file +| mondo_id | mondo_label | xref | xref_source | original_label | definition | parents | +|:--------------|:-----------------------------------------------------|:---------------------|:---------------------------|:-----------------------------------------------------|:---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|:--------------------------------------------------------| +| ID | LABEL | A oboInOwl:hasDbXref | >A oboInOwl:source SPLIT=| | | A IAO:0000115 | SC % | +| MONDO:0968990 | genetic central precocious puberty in male | Orphanet:650097 | MONDO:equivalentTo | Genetic central precocious puberty in male | | MONDO:8000031|MONDO:0958356 | +| MONDO:0968991 | non-genetic central precocious puberty in male | Orphanet:650102 | MONDO:equivalentTo | Non-genetic central precocious puberty in male | | MONDO:0958356|MONDO:8000031 | +| MONDO:0969105 | terminal extramedullary conus spinal cord lipoma | Orphanet:645288 | MONDO:equivalentTo | Terminal extramedullary conus spinal cord lipoma | A rare form of extramedullary conus region spinal cord lipoma characterized by its location, extending from the poorly delineated tip of the conus. | MONDO:0968987|MONDO:8000031 | +| MONDO:0969106 | transitional extramedullary conus spinal cord lipoma | Orphanet:645291 | MONDO:equivalentTo | Transitional extramedullary conus spinal cord lipoma | A rare form of extramedullary conus region spinal cord lipoma characterized by a location at the posterior surface of the conus and its tip. i.e-"transitional" between posterior and terminal conus region spinal cord lipoma. | MONDO:0968987|MONDO:8000031 | +| MONDO:0969107 | posterior extramedullary conus spinal cord lipoma | Orphanet:645294 | MONDO:equivalentTo | Posterior extramedullary conus spinal cord lipoma | A rare form of conus region spinal cord lipoma characterized by its location where the interface between the lipoma and the spinal cord is strictcly above the level of the tip of the conus. The tip of the conus is readily delineated. | MONDO:0968987|MONDO:8000031 | +| MONDO:0969108 | lipomatous non-saccular limited dorsal myeloschisis | Orphanet:645300 | MONDO:equivalentTo | Lipomatous non-saccular limited dorsal myeloschisis | A rare non-saccular limited dorsal myeloschisis histologically characterized by skin tissue with a jagged depression of squamous epithelium continued to subcutaneous mature adipose tissue with loose connective tissue. GFAP-immunopositive glial cells are embedded in the subcutaneous lipoma. The extradural and intradural stalk have cord-like fibrocollagenous tissue containing adipose tissue, peripheral nerve fibers, clusters of melanocytes, and skeletal muscle fibers. | MONDO:0968989|MONDO:8000031 | +| MONDO:0969109 | fibroneural non-saccular limited dorsal myeloschisis | Orphanet:645310 | MONDO:equivalentTo | Fibroneural non-saccular limited dorsal myeloschisis | A rare non-saccular limited dorsal myeloschisis, in which the stalk histology is characterized by skin tissue with dermo-epidermal epithelium in continuity with a subcutaneous fibrocollagenous tract containing various ectopic tissues. | MONDO:8000031|MONDO:0968989 | +| MONDO:0969110 | terminal myelocystocele | Orphanet:645337 | MONDO:equivalentTo | Terminal myelocystocele | A rare closed spinal dysraphism characterized by a myelocystocele at the termination of the spinal cord. It may be an isolated anomaly or be associated with other defects, including sacral agenesis, anorectal and genitourinary anomalies. The conus is not identifiable. The myelocystocele sac may have a significant lipomatous component (terminal lipomyelocystocele). | MONDO:0968988|MONDO:8000034|MONDO:8000030|MONDO:0017077 | +| MONDO:0969111 | saccular limited dorsal myeloschisis | Orphanet:645354 | MONDO:equivalentTo | Saccular limited dorsal myeloschisis | A rare form of limited dorsal myeloschisis (LDM), characterized by the stalk attached to the apex of a fully epithelialized meningocele. Chiari II malformation is not present. | MONDO:0968988|MONDO:8000034|MONDO:8000030 | +| MONDO:0969112 | myelic limited dorsal malformation | Orphanet:645378 | MONDO:equivalentTo | Myelic limited dorsal malformation | A rare intermediate form of open dysraphism between myelomeningocele and saccular limited dorsal myeloschisis without fulfilling the characteristics of one of these two diagnosis, characterized by stretched neurulated spinal cord attached at the dome of a sac. Partial cerebral signs of open dysraphism can be observed and the meningocele is usually poorly epithelialized. | MONDO:0968988|MONDO:8000034|MONDO:8000030 | \ No newline at end of file diff --git a/docs/reports/unmapped.md b/docs/reports/unmapped.md index 1d4965e7..91ed7693 100644 --- a/docs/reports/unmapped.md +++ b/docs/reports/unmapped.md @@ -3,12 +3,12 @@ |:-------------------------------------------------|:------------|:---------------|:-----------------|:--------------------------|:------------------------------------------|:--------------------------|:----------------------------|:--------------------------| | [ICD10WHO](./unmapped_icd10who.md) | 12,542 | 0 | 0 | 0 | 12,542 | 18 | 12,524 | 99.9% | | [ICD10CM](./unmapped_icd10cm.md) | 95,847 | 15,452 | 0 | 0 | 80,395 | 1,162 | 79,233 | 98.6% | -| [NCIT](./unmapped_ncit.md) | 187,170 | 166,382 | 5,166 | 5,154 | 15,622 | 3,686 | 11,936 | 76.4% | +| [NCIT](./unmapped_ncit.md) | 191,123 | 169,937 | 5,221 | 5,199 | 15,965 | 3,675 | 12,290 | 77.0% | | [ICD11FOUNDATION](./unmapped_icd11foundation.md) | 100,003 | 12,464 | 6,311 | 6,311 | 81,232 | 0 | 81,232 | 100.0% | | [GARD](./unmapped_gard.md) | 12,004 | 0 | 0 | 0 | 12,004 | 0 | 12,004 | 100.0% | -| [ORDO](./unmapped_ordo.md) | 15,402 | 6,207 | 1,391 | 1,166 | 9,195 | 9,123 | 72 | 0.8% | -| [DOID](./unmapped_doid.md) | 14,033 | 2,655 | 2,483 | 2,468 | 11,376 | 11,320 | 56 | 0.5% | -| [OMIM](./unmapped_omim.md) | 29,307 | 19,232 | 1,362 | 1,317 | 8,714 | 8,704 | 10 | 0.1% | +| [ORDO](./unmapped_ordo.md) | 15,402 | 6,212 | 1,391 | 1,166 | 9,190 | 9,127 | 63 | 0.7% | +| [DOID](./unmapped_doid.md) | 14,033 | 2,655 | 2,483 | 2,468 | 11,376 | 11,368 | 8 | 0.1% | +| [OMIM](./unmapped_omim.md) | 29,327 | 19,248 | 1,363 | 1,317 | 8,717 | 8,712 | 5 | 0.1% | `Ontology`: Name of ontology `Tot terms`: Total terms in ontology diff --git a/docs/reports/unmapped_doid.md b/docs/reports/unmapped_doid.md index f4454232..6c58be99 100644 --- a/docs/reports/unmapped_doid.md +++ b/docs/reports/unmapped_doid.md @@ -2,61 +2,13 @@ [Interactive FlatGithub table](https://flatgithub.com/monarch-initiative/mondo-ingest?filename=src/ontology/reports/doid_mapping_status.tsv) ### Unmapped mappable terms _(!excluded, !deprecated)_ -| subject_id | subject_label | -|:-------------|:--------------------------------------------------------------------------| -| DOID:0081403 | BCOR ITD sarcoma | -| DOID:0081404 | BCOR-CCNB3 sarcoma | -| DOID:0070539 | Halperin-Birk syndrome | -| DOID:0081441 | Nicolaides-Baraitser syndrome | -| DOID:0081451 | PFAPA syndrome | -| DOID:0081440 | Peroxisome biogenesis disorder 10B | -| DOID:0081439 | Peroxisome biogenesis disorder 11B | -| DOID:0081433 | Peroxisome biogenesis disorder 4B | -| DOID:0081434 | Peroxisome biogenesis disorder 5B | -| DOID:0081435 | Peroxisome biogenesis disorder 6B | -| DOID:0081436 | Peroxisome biogenesis disorder 7B | -| DOID:0081437 | Peroxisome biogenesis disorder 8B | -| DOID:0081438 | Peroxisome biogenesis disorder 9B | -| DOID:0081443 | Stolerman neurodevelopmental syndrome | -| DOID:0081414 | TFEB-rearranged renal cell carcinoma | -| DOID:0060946 | Ullrich congenital muscular dystrophy 1A | -| DOID:0060942 | Ullrich congenital muscular dystrophy 1B | -| DOID:0060943 | Ullrich congenital muscular dystrophy 1C | -| DOID:0060944 | Ullrich congenital muscular dystrophy 2 | -| DOID:0060945 | amelogenesis imperfecta type 1K | -| DOID:0060947 | autosomal recessive intellectual developmental disorder 82 | -| DOID:0081442 | blepharophimosis-impaired intellectual development syndrome | -| DOID:0081416 | childhood renal cell carcinoma with MiT translocations | -| DOID:0081407 | childhood round cell sarcoma with EWSR1-non-ETS fusion | -| DOID:0081405 | childhood sarcoma with BCOR genetic alterations | -| DOID:0060160 | childhood spinal muscular atrophy | -| DOID:0111368 | cholesterol-ester transfer protein deficiency | -| DOID:2536 | chronic inflammatory demyelinating polyneuritis | -| DOID:0081447 | cone-rod dystrophy 21 | -| DOID:0081448 | cone-rod dystrophy 22 | -| DOID:0081449 | cone-rod dystrophy 24 | -| DOID:4668 | congenital kyphosis | -| DOID:0081446 | dimethylglycine dehydrogenase deficiency | -| DOID:0060967 | dystonia 22, adult-onset | -| DOID:0060966 | dystonia 22, juvenile-onset | -| DOID:0060936 | dystonia 28, childhood-onset | -| DOID:0060937 | dystonia 30 | -| DOID:0060938 | dystonia 31 | -| DOID:0060939 | dystonia 32 | -| DOID:0060940 | dystonia 33 | -| DOID:0060955 | dystonia 35, childhood-onset | -| DOID:0060956 | dystonia 37, early-onset with striatal lesions | -| DOID:0060963 | dystonia, DOPA-responsive | -| DOID:0081450 | hyperimmunoglobulinemia D periodic fever syndrome | -| DOID:0060941 | interstitial lung disease 1 | -| DOID:0081452 | large B-cell lymphoma | -| DOID:0081431 | microcephaly, short stature, and limb abnormalities | -| DOID:0081432 | microcephaly-micromelia syndrome | -| DOID:0060333 | mitochondrial complex V (ATP synthase) deficiency nuclear type 4 | -| DOID:0060957 | myoclonic dystonia 34 | -| DOID:0081444 | neurodevelopmental disorder with poor growth and behavioral abnormalities | -| DOID:9373 | postural kyphosis | -| DOID:0081408 | round cell sarcoma with EWSR1-NFATC2 gene fusion | -| DOID:0081409 | round cell sarcoma with EWSR1-PATZ1 gene fusion | -| DOID:0081410 | round cell sarcoma with FUS-NFATC2 gene fusion | -| DOID:0081445 | sickle cell disease | \ No newline at end of file +| subject_id | subject_label | +|:-------------|:-----------------------------------------------------------------| +| DOID:2934 | aleutian mink disease | +| DOID:5154 | borna disease | +| DOID:0060160 | childhood spinal muscular atrophy | +| DOID:0111368 | cholesterol-ester transfer protein deficiency | +| DOID:2536 | chronic inflammatory demyelinating polyneuritis | +| DOID:4668 | congenital kyphosis | +| DOID:0060333 | mitochondrial complex V (ATP synthase) deficiency nuclear type 4 | +| DOID:9373 | postural kyphosis | \ No newline at end of file diff --git a/docs/reports/unmapped_ncit.md b/docs/reports/unmapped_ncit.md index 67888512..6bd69a88 100644 --- a/docs/reports/unmapped_ncit.md +++ b/docs/reports/unmapped_ncit.md @@ -32,13 +32,11 @@ | NCIT:C4046 | AIDS-Related Malignant Neoplasm | | NCIT:C5051 | AIDS-Related Non-Hodgkin Lymphoma | | NCIT:C7434 | AIDS-Related Non-Hodgkin Lymphoma of the Cervix | +| NCIT:C9016 | AIDS-Related Oral Cavity Plasmablastic Lymphoma | | NCIT:C27859 | AIDS-Related Plasmablastic Lymphoma | | NCIT:C38160 | AIDS-Related Plasmablastic Lymphoma of Mucosa Site | -| NCIT:C9016 | AIDS-Related Plasmablastic Lymphoma of the Oral Mucosa | | NCIT:C186660 | AIDS-Related Primary Diffuse Large B-Cell Lymphoma of the Central Nervous System | | NCIT:C9017 | AIDS-Related Primary Effusion Lymphoma | -| NCIT:C9420 | AJCC Grade 2 Sarcoma | -| NCIT:C9421 | AJCC Grade 3 Sarcoma | | NCIT:C9422 | AJCC Grade 4 Sarcoma | | NCIT:C200105 | ALK-Positive Histiocytosis | | NCIT:C189249 | ALK-Rearranged Renal Cell Carcinoma | @@ -70,9 +68,11 @@ | NCIT:C23141 | Acinic Cell Carcinoma of the Mouse Salivary Glands | | NCIT:C22944 | Acquired Tufted Hemangioma of the Mouse Blood Vessel | | NCIT:C121713 | Acral Fibromyxoma | +| NCIT:C204883 | Acral Melanoma | | NCIT:C54659 | Acral Nevus | | NCIT:C36265 | Acute Adult T-Cell Leukemia/Lymphoma | | NCIT:C22079 | Acute Enteritis of the Mouse Intestinal Tract | +| NCIT:C203437 | Acute Leukemia of Ambiguous Lineage with BCL11B Rearrangement | | NCIT:C200494 | Acute Leukemia of Ambiguous Lineage with Defining Genetic Abnormalities | | NCIT:C151975 | Acute Leukemia of Ambiguous Lineage, Not Otherwise Specified | | NCIT:C121973 | Acute Lymphoblastic Leukemia by Gene Expression Profile | @@ -137,6 +137,7 @@ | NCIT:C9020 | Acute Myelomonocytic Leukemia with Abnormal Eosinophils | | NCIT:C42779 | Acute Myelomonocytic Leukemia without Abnormal Eosinophils | | NCIT:C22086 | Acute Ulcerative Enteritis of the Mouse Intestinal Tract | +| NCIT:C43312 | Adamantinoid Trichoblastoma | | NCIT:C64005 | Adenocarcinoma Arising In Fibroadenoma of the Rat Mammary Gland | | NCIT:C7678 | Adenocarcinoma In Situ in Adenomatous Polyp | | NCIT:C7679 | Adenocarcinoma In Situ in Tubular Adenoma | @@ -199,6 +200,7 @@ | NCIT:C7684 | Adenocarcinoma with Osseous Metaplasia | | NCIT:C4201 | Adenocarcinoma with Spindle Cell Metaplasia | | NCIT:C4200 | Adenocarcinoma with Squamous Metaplasia | +| NCIT:C202061 | Adenoid Ameloblastoma | | NCIT:C23115 | Adenoid Cystic Carcinoma of the Mouse Larynx | | NCIT:C23142 | Adenoid Cystic Carcinoma of the Mouse Salivary Glands | | NCIT:C64015 | Adenolipoma of the Rat Mammary Gland | @@ -322,6 +324,7 @@ | NCIT:C7954 | Adult Burkitt Leukemia | | NCIT:C9062 | Adult Burkitt Lymphoma | | NCIT:C45747 | Adult Cardiac Cellular Rhabdomyoma | +| NCIT:C115253 | Adult Central Nervous System Melanocytic Neoplasm | | NCIT:C5131 | Adult Central Nervous System Neoplasm | | NCIT:C8265 | Adult Cholangiocarcinoma | | NCIT:C69138 | Adult Classic Hodgkin Lymphoma | @@ -394,7 +397,6 @@ | NCIT:C188945 | Adult Posterior Fossa Ependymoma | | NCIT:C114599 | Adult Pre-B Acute Lymphoblastic Leukemia | | NCIT:C27365 | Adult Primary Cutaneous Anaplastic Large Cell Lymphoma | -| NCIT:C115253 | Adult Primary Meningeal Melanocytic Neoplasm | | NCIT:C68693 | Adult Pure Erythroid Leukemia | | NCIT:C9130 | Adult Rhabdomyosarcoma | | NCIT:C118825 | Adult Salivary Gland Carcinoma | @@ -437,7 +439,6 @@ | NCIT:C165700 | Advanced Breast Adenocarcinoma | | NCIT:C162648 | Advanced Breast Carcinoma | | NCIT:C180922 | Advanced Bronchogenic Carcinoma | -| NCIT:C156487 | Advanced Carcinoid Tumor | | NCIT:C153171 | Advanced Carcinoma | | NCIT:C170960 | Advanced Carcinoma Of Unknown Primary | | NCIT:C170928 | Advanced Carcinosarcoma | @@ -445,8 +446,8 @@ | NCIT:C174032 | Advanced Cervical Adenosquamous Carcinoma | | NCIT:C156294 | Advanced Cervical Carcinoma | | NCIT:C174030 | Advanced Cervical Squamous Cell Carcinoma | -| NCIT:C187213 | Advanced Childhood Malignant Brain Neoplasm | | NCIT:C187210 | Advanced Childhood Malignant Solid Neoplasm | +| NCIT:C187213 | Advanced Childhood Primary Malignant Brain Neoplasm | | NCIT:C162752 | Advanced Cholangiocarcinoma | | NCIT:C173333 | Advanced Chordoma | | NCIT:C171579 | Advanced Chromophobe Renal Cell Carcinoma | @@ -463,9 +464,12 @@ | NCIT:C173980 | Advanced Differentiated Thyroid Gland Carcinoma | | NCIT:C171264 | Advanced Diffuse Large B-Cell Lymphoma | | NCIT:C156746 | Advanced Digestive System Carcinoma | +| NCIT:C203253 | Advanced Digestive System Neuroendocrine Carcinoma | | NCIT:C158089 | Advanced Digestive System Neuroendocrine Neoplasm | +| NCIT:C204036 | Advanced Digestive System Neuroendocrine Tumor | | NCIT:C179418 | Advanced Digestive System Neuroendocrine Tumor G1 | | NCIT:C190711 | Advanced Digestive System Neuroendocrine Tumor G2 | +| NCIT:C203252 | Advanced Digestive System Neuroendocrine Tumor G3 | | NCIT:C176888 | Advanced Distal Bile Duct Adenocarcinoma | | NCIT:C170805 | Advanced Endometrial Adenocarcinoma | | NCIT:C159676 | Advanced Endometrial Carcinoma | @@ -487,6 +491,7 @@ | NCIT:C191982 | Advanced Extrapulmonary Neuroendocrine Carcinoma | | NCIT:C191993 | Advanced Extrapulmonary Small Cell Neuroendocrine Carcinoma | | NCIT:C167395 | Advanced Fallopian Tube Carcinoma | +| NCIT:C203311 | Advanced Fallopian Tube High Grade Serous Adenocarcinoma | | NCIT:C68662 | Advanced Favorable Hodgkin Lymphoma | | NCIT:C53283 | Advanced Favorable Non-Hodgkin Lymphoma | | NCIT:C185067 | Advanced Fibrolamellar Carcinoma | @@ -523,11 +528,11 @@ | NCIT:C168701 | Advanced Liposarcoma | | NCIT:C176727 | Advanced Lung Adenocarcinoma | | NCIT:C181967 | Advanced Lung Adenosquamous Carcinoma | -| NCIT:C177245 | Advanced Lung Carcinoid Tumor | | NCIT:C153203 | Advanced Lung Carcinoma | | NCIT:C187163 | Advanced Lung Large Cell Neuroendocrine Carcinoma | | NCIT:C192798 | Advanced Lung Neuroendocrine Carcinoma | | NCIT:C165446 | Advanced Lung Neuroendocrine Neoplasm | +| NCIT:C177245 | Advanced Lung Neuroendocrine Tumor | | NCIT:C162158 | Advanced Lung Non-Small Cell Carcinoma | | NCIT:C153201 | Advanced Lung Non-Small Cell Squamous Carcinoma | | NCIT:C147924 | Advanced Lung Non-Squamous Non-Small Cell Carcinoma | @@ -581,6 +586,7 @@ | NCIT:C170937 | Advanced Ovarian Serous Adenocarcinoma | | NCIT:C187235 | Advanced Ovarian Serous Cystadenocarcinoma | | NCIT:C162153 | Advanced Pancreatic Adenocarcinoma | +| NCIT:C204035 | Advanced Pancreatic Adenosquamous Carcinoma | | NCIT:C165452 | Advanced Pancreatic Carcinoma | | NCIT:C164214 | Advanced Pancreatic Ductal Adenocarcinoma | | NCIT:C165448 | Advanced Pancreatic Neuroendocrine Neoplasm | @@ -594,6 +600,7 @@ | NCIT:C8703 | Advanced Pericardial Malignant Mesothelioma | | NCIT:C170784 | Advanced Pharyngeal Carcinoma | | NCIT:C173694 | Advanced Pharyngeal Squamous Cell Carcinoma | +| NCIT:C204866 | Advanced Platinum-Refractory Ovarian Carcinoma | | NCIT:C170958 | Advanced Platinum-Resistant Malignant Germ Cell Tumor | | NCIT:C189977 | Advanced Platinum-Resistant Ovarian Carcinoma | | NCIT:C182026 | Advanced Pleomorphic Liposarcoma | @@ -602,15 +609,18 @@ | NCIT:C175549 | Advanced Primary Malignant Brain Neoplasm | | NCIT:C170966 | Advanced Primary Malignant Central Nervous System Neoplasm | | NCIT:C167396 | Advanced Primary Peritoneal Carcinoma | +| NCIT:C203312 | Advanced Primary Peritoneal High Grade Serous Adenocarcinoma | | NCIT:C200573 | Advanced Progesterone Receptor-Positive Breast Carcinoma | | NCIT:C156286 | Advanced Prostate Adenocarcinoma | | NCIT:C186456 | Advanced Prostate Adenocarcinoma with Neuroendocrine Differentiation | | NCIT:C156284 | Advanced Prostate Carcinoma | +| NCIT:C202894 | Advanced Prostate Small Cell Neuroendocrine Carcinoma | | NCIT:C192677 | Advanced Rare Malignant Solid Neoplasm | | NCIT:C175363 | Advanced Rectal Adenocarcinoma | | NCIT:C170777 | Advanced Rectal Carcinoma | | NCIT:C170780 | Advanced Rectal Squamous Cell Carcinoma | | NCIT:C153170 | Advanced Renal Cell Carcinoma | +| NCIT:C171582 | Advanced Renal Cell Carcinoma, Not Otherwise Specified | | NCIT:C163966 | Advanced Renal Pelvis Carcinoma | | NCIT:C172278 | Advanced Renal Pelvis Urothelial Carcinoma | | NCIT:C172276 | Advanced Renal Pelvis and Ureter Urothelial Carcinoma | @@ -638,11 +648,10 @@ | NCIT:C172361 | Advanced Transformed Non-Hodgkin Lymphoma | | NCIT:C172091 | Advanced Transitional Cell Carcinoma | | NCIT:C175236 | Advanced Triple-Negative Breast Carcinoma | -| NCIT:C171582 | Advanced Unclassified Renal Cell Carcinoma | | NCIT:C165781 | Advanced Undifferentiated Pleomorphic Sarcoma | | NCIT:C68665 | Advanced Unfavorable Hodgkin Lymphoma | | NCIT:C53284 | Advanced Unfavorable Non-Hodgkin Lymphoma | -| NCIT:C153317 | Advanced Unresectable Gastric Adenocarcinoma | +| NCIT:C8716 | Advanced Ureter Carcinoma | | NCIT:C163955 | Advanced Ureter Urothelial Carcinoma | | NCIT:C163963 | Advanced Urethral Urothelial Carcinoma | | NCIT:C148493 | Advanced Urothelial Carcinoma | @@ -688,10 +697,10 @@ | NCIT:C54298 | Ameloblastic Carcinoma-Secondary Type (Dedifferentiated), Intraosseous | | NCIT:C54299 | Ameloblastic Carcinoma-Secondary Type (Dedifferentiated), Peripheral | | NCIT:C3710 | Ameloblastic Fibro-Odontoma | +| NCIT:C173740 | Ameloblastic Fibro-Odontosarcoma | | NCIT:C66800 | Ameloblastic Fibrodentinoma | | NCIT:C173739 | Ameloblastic Fibrodentinosarcoma | | NCIT:C4316 | Ameloblastic Fibroma | -| NCIT:C173740 | Ameloblastic Fibroodontosarcoma | | NCIT:C4317 | Ameloblastic Fibrosarcoma | | NCIT:C63901 | Amphophilic Focus of Cellular Alteration of the Rat | | NCIT:C6657 | Ampulla of Vater Adenoma, Intestinal-Type | @@ -1030,8 +1039,11 @@ | NCIT:C8169 | Anterior Tongue Squamous Cell Carcinoma | | NCIT:C21646 | Aplasia of the Mouse Mammary Gland | | NCIT:C21705 | Aplasia of the Mouse Prostate Gland | +| NCIT:C205459 | Apocrine Cystadenoma | | NCIT:C43342 | Apocrine Hidrocystoma | | NCIT:C21828 | Apocrine Neoplasms of the Mouse Skin | +| NCIT:C205463 | Apocrine Poroma | +| NCIT:C202880 | Appendicular Skeleton Phosphaturic Mesenchymal Tumor | | NCIT:C133733 | Appendix Carcinoma by AJCC v7 Stage | | NCIT:C134117 | Appendix Carcinoma by AJCC v8 Stage | | NCIT:C173799 | Appendix Disorder | @@ -1063,6 +1075,8 @@ | NCIT:C84472 | Asbestos-Related Lung Disorder | | NCIT:C27926 | Asbestos-Related Malignant Mesothelioma | | NCIT:C27774 | Asbestos-Related Malignant Neoplasm | +| NCIT:C203387 | Ascending Colon Neuroendocrine Tumor | +| NCIT:C203391 | Ascending Colon Neuroendocrine Tumor G2 | | NCIT:C36202 | Astler-Coller A Colon Carcinoma | | NCIT:C5927 | Astler-Coller A Colorectal Carcinoma | | NCIT:C5924 | Astler-Coller A Rectal Carcinoma | @@ -1110,7 +1124,6 @@ | NCIT:C48285 | Atypical Parathyroid Gland Tumor | | NCIT:C132296 | Atypical Pituitary Neuroendocrine Tumor | | NCIT:C37268 | Atypical Small Acinar Proliferation of the Prostate Gland | -| NCIT:C136825 | Atypical Spitz Nevus | | NCIT:C200597 | Atypical Teratoid/Rhabdoid Tumor Molecular Subtypes | | NCIT:C200599 | Atypical Teratoid/Rhabdoid Tumor-MYC | | NCIT:C200598 | Atypical Teratoid/Rhabdoid Tumor-SHH | @@ -1172,7 +1185,6 @@ | NCIT:C21850 | B-cell Lymphomas of the Mouse Skin | | NCIT:C16317 | B16 Malignant Melanoma | | NCIT:C165525 | BAP1-Inactivated Melanocytoma | -| NCIT:C165522 | BAP1-Inactivated Skin Melanocytic Neoplasm | | NCIT:C157614 | BAP1-Mutant Clear Cell Renal Cell Carcinoma | | NCIT:C199467 | BCL2-R-Negative, CD23-Positive Follicle Center Lymphoma | | NCIT:C115139 | BCLC Stage 0 Adult Hepatocellular Carcinoma | @@ -1259,6 +1271,7 @@ | NCIT:C8539 | Benign Great Vessel Neoplasm | | NCIT:C27520 | Benign Hair Follicle Neoplasm | | NCIT:C173932 | Benign Head and Neck Neoplasm | +| NCIT:C202624 | Benign Head and Neck Soft Tissue Neoplasm | | NCIT:C66779 | Benign Hemangioendothelioma | | NCIT:C4300 | Benign Hemangiopericytoma | | NCIT:C21857 | Benign Histiocytic Neoplasms of the Mouse Skin | @@ -1289,7 +1302,6 @@ | NCIT:C64106 | Benign Mesothelioma of the Rat Pericardium | | NCIT:C64107 | Benign Mesothelioma of the Rat Peritoneum | | NCIT:C64108 | Benign Mesothelioma of the Rat Pleura | -| NCIT:C43322 | Benign Mixed Epithelial and Mesenchymal Hair Follicle Neoplasm | | NCIT:C64034 | Benign Mixed Glioma of the Rat Spinal Cord | | NCIT:C63968 | Benign Mixed Muellerian Tumor of the Rat Uterine Cervix | | NCIT:C63969 | Benign Mixed Muellerian Tumor of the Rat Uterus | @@ -1511,8 +1523,11 @@ | NCIT:C181907 | Borderline Vulvar Phyllodes Tumor | | NCIT:C45163 | Borrelia Burgdoferi-Associated Primary Cutaneous Marginal Zone Lymphoproliferative Disorder | | NCIT:C156462 | Brain Ependymoma | +| NCIT:C201977 | Brain Low Grade Glioma | +| NCIT:C201975 | Brain Pilocytic Astrocytoma | | NCIT:C5097 | Brain Stem Glioblastoma | | NCIT:C113665 | Branch Duct Pancreatic Intraductal Papillary-Mucinous Neoplasm | +| NCIT:C53595 | Branchioma | | NCIT:C40360 | Breast Adenocarcinoma with Spindle Cell Metaplasia | | NCIT:C5163 | Breast Adenocarcinoma with Squamous Metaplasia | | NCIT:C176255 | Breast Angiolipoma | @@ -1526,12 +1541,6 @@ | NCIT:C139533 | Breast Cancer by AJCC v8 Anatomic Stage | | NCIT:C139554 | Breast Cancer by AJCC v8 Prognostic Stage | | NCIT:C139532 | Breast Cancer by AJCC v8 Stage | -| NCIT:C36303 | Breast Carcinoma Metastatic in the Bone | -| NCIT:C36301 | Breast Carcinoma Metastatic in the Brain | -| NCIT:C133501 | Breast Carcinoma Metastatic in the Central Nervous System | -| NCIT:C36302 | Breast Carcinoma Metastatic in the Liver | -| NCIT:C36300 | Breast Carcinoma Metastatic in the Lung | -| NCIT:C153227 | Breast Carcinoma Metastatic in the Lymph Nodes | | NCIT:C153226 | Breast Carcinoma Metastatic in the Spine | | NCIT:C47847 | Breast Carcinoma with Chondroid Metaplasia | | NCIT:C40350 | Breast Carcinoma with Choriocarcinomatous Features | @@ -1558,11 +1567,13 @@ | NCIT:C9492 | Breast Ductal Hyperplasia | | NCIT:C175950 | Breast Florid Lobular Carcinoma In Situ | | NCIT:C40377 | Breast Follicular Lymphoma | +| NCIT:C5167 | Breast High Grade Mucoepidermoid Carcinoma | | NCIT:C157235 | Breast Histiocytoid Carcinoma | | NCIT:C4804 | Breast Hyperplasia | | NCIT:C139012 | Breast Implant-Associated Anaplastic Large Cell Lymphoma | | NCIT:C40398 | Breast Inflammatory Myofibroblastic Tumor | | NCIT:C7645 | Breast Intracystic Papillary Carcinoma | +| NCIT:C5168 | Breast Low Grade Mucoepidermoid Carcinoma | | NCIT:C5139 | Breast Micropapillary Ductal Carcinoma In Situ | | NCIT:C40347 | Breast Mixed Carcinoma | | NCIT:C175581 | Breast Neuroendocrine Carcinoma | @@ -1607,6 +1618,7 @@ | NCIT:C7436 | Bronchial Intraepithelial Neoplasia | | NCIT:C45602 | Bronchial Mixed Squamous Cell and Glandular Papilloma | | NCIT:C183045 | Bronchiolar Adenoma/Ciliated Muconodular Papillary Tumor | +| NCIT:C202609 | Buccal Mucosa Lipoma | | NCIT:C8175 | Buccal Mucosa Verrucous Carcinoma | | NCIT:C134943 | Budgerigar Fibrosarcoma | | NCIT:C135003 | Budgerigar Testicular Carcinoma | @@ -1682,6 +1694,8 @@ | NCIT:C5324 | Cauda Equina Neuroendocrine Tumor | | NCIT:C49115 | Cavernous Angioleiomyoma | | NCIT:C22922 | Cavernous Hemangioma of the Mouse Blood Vessel | +| NCIT:C203386 | Cecum Neuroendocrine Tumor | +| NCIT:C203392 | Cecum Neuroendocrine Tumor G2 | | NCIT:C5521 | Cecum Non-Hodgkin Lymphoma | | NCIT:C27257 | Cellular Angiofibroma | | NCIT:C4241 | Cellular Blue Nevus | @@ -1723,6 +1737,7 @@ | NCIT:C129806 | Central Nervous System Langerhans Cell Histiocytosis | | NCIT:C186662 | Central Nervous System Lymphomatoid Granulomatosis | | NCIT:C129600 | Central Nervous System Mature T-Cell and NK-Cell Non-Hodgkin Lymphoma | +| NCIT:C4661 | Central Nervous System Melanocytic Neoplasm | | NCIT:C129534 | Central Nervous System Mesenchymal Chondrosarcoma | | NCIT:C129551 | Central Nervous System Myofibroblastoma | | NCIT:C186547 | Central Nervous System Neuroblastoma, FOXR2-Activated | @@ -1739,6 +1754,8 @@ | NCIT:C7015 | Central Nervous System Teratoma with Malignant Transformation | | NCIT:C186556 | Central Nervous System Tumor with BCOR Internal Tandem Duplication | | NCIT:C129566 | Central Nervous System Undifferentiated Pleomorphic Sarcoma | +| NCIT:C202077 | Central Odontogenic Fibroma | +| NCIT:C202253 | Central Osteoma | | NCIT:C22955 | Central Osteosarcoma of the Mouse Skeletal System | | NCIT:C21913 | Centroblastic Diffuse Large B Cell Lymphoma of the Mouse Hematologic System | | NCIT:C4074 | Centroblastic Lymphoma | @@ -2023,6 +2040,7 @@ | NCIT:C189934 | Childhood Liver Embryonal Sarcoma | | NCIT:C27368 | Childhood Liver Neoplasm | | NCIT:C188970 | Childhood Low Grade Fibromyxoid Sarcoma | +| NCIT:C202299 | Childhood Low Grade Glioma | | NCIT:C188973 | Childhood Low Grade Myofibroblastic Sarcoma | | NCIT:C190095 | Childhood Lung Neoplasm | | NCIT:C118814 | Childhood Lung Non-Small Cell Carcinoma | @@ -2040,6 +2058,7 @@ | NCIT:C189870 | Childhood Malignant Digestive System Neoplasm | | NCIT:C190070 | Childhood Malignant Endocrine Neoplasm | | NCIT:C189269 | Childhood Malignant Genitourinary System Neoplasm | +| NCIT:C202298 | Childhood Malignant Glioma | | NCIT:C190121 | Childhood Malignant Head and Neck Neoplasm | | NCIT:C198104 | Childhood Malignant Kidney Neoplasm Excluding Renal Cell Carcinoma by Toronto Guidelines v2 Stage | | NCIT:C198085 | Childhood Malignant Kidney Neoplasm Excluding Renal Cell Carcinoma by Toronto Guidelines v2 Stage, Children's Oncology Group (COG) Protocol | @@ -2261,6 +2280,7 @@ | NCIT:C36061 | Chronic Myelomonocytic Leukemia-1 | | NCIT:C36062 | Chronic Myelomonocytic Leukemia-2 | | NCIT:C3175 | Chronic Phase Chronic Myeloid Leukemia, BCR-ABL1 Positive | +| NCIT:C203904 | Chronic Phase Chronic Myeloid Leukemia, Philadelphia Chromosome Positive, BCR-ABL1 Positive | | NCIT:C188314 | Chronic Phase Primary Myelofibrosis | | NCIT:C22094 | Chronic Ulcerative Enteritis of the Mouse Intestinal Tract | | NCIT:C27772 | Cigarette Smoking-Related Carcinoma | @@ -2278,6 +2298,7 @@ | NCIT:C200669 | Classic Follicular Lymphoma | | NCIT:C7243 | Classic Hodgkin Lymphoma Post-Transplant Lymphoproliferative Disorder | | NCIT:C199676 | Classic Hydroa Vacciniforme Lymphoproliferative Disorder | +| NCIT:C43353 | Classic Poroma | | NCIT:C27480 | Classic Rhabdomyoma | | NCIT:C187644 | Classic Thyroid Gland Papillary Carcinoma | | NCIT:C27545 | Classic Type Atypical Fibroxanthoma | @@ -2285,9 +2306,9 @@ | NCIT:C27523 | Classic Type Trichoepithelioma | | NCIT:C7188 | Classical Burkitt Lymphoma | | NCIT:C45210 | Classical Low Grade Fibromyxoid Sarcoma | -| NCIT:C43353 | Classical Poroma | | NCIT:C191768 | Clear Cell Adenocarcinoma of the Urinary Tract | | NCIT:C23134 | Clear Cell Adenoma of the Mouse Salivary Glands | +| NCIT:C202057 | Clear Cell Calcifying Epithelial Odontogenic Tumor | | NCIT:C22976 | Clear Cell Chondrosarcoma of the Mouse Skeletal System | | NCIT:C63900 | Clear Cell Focus of Cellular Alteration of the Rat | | NCIT:C43848 | Clear Cell Intrahepatic Cholangiocarcinoma | @@ -2296,57 +2317,61 @@ | NCIT:C66752 | Clear Cell Neoplasm | | NCIT:C54300 | Clear Cell Odontogenic Carcinoma | | NCIT:C121955 | Clear Cell Papillary Renal Tumor | +| NCIT:C204755 | Clear Cell Tumor with Melanocytic Differentiation and ACTB-MITF Translocation | +| NCIT:C204756 | Clear Cell Tumor with Melanocytic Differentiation and ACTG1-MITF Translocation | +| NCIT:C204740 | Clear Cell Tumor with Melanocytic Differentiation and ACTIN-MITF Translocation | +| NCIT:C204741 | Clear Cell Tumor with Melanocytic Differentiation and MITF-CREM Translocation | | NCIT:C46094 | Clear Cell Variant Thyroid Gland Papillary Carcinoma | | NCIT:C137647 | Clinical Stage 0 Cutaneous Melanoma AJCC v8 | +| NCIT:C136872 | Clinical Stage 0 Cutaneous Merkel Cell Carcinoma AJCC v8 | | NCIT:C133402 | Clinical Stage 0 Esophageal Adenocarcinoma AJCC v8 | | NCIT:C133447 | Clinical Stage 0 Esophageal Squamous Cell Carcinoma AJCC v8 | | NCIT:C133647 | Clinical Stage 0 Gastric Cancer AJCC v8 | | NCIT:C133550 | Clinical Stage 0 Gastroesophageal Junction Adenocarcinoma AJCC v8 | -| NCIT:C136872 | Clinical Stage 0 Merkel Cell Carcinoma AJCC v8 | | NCIT:C137648 | Clinical Stage I Cutaneous Melanoma AJCC v8 | +| NCIT:C136873 | Clinical Stage I Cutaneous Merkel Cell Carcinoma AJCC v8 | | NCIT:C133403 | Clinical Stage I Esophageal Adenocarcinoma AJCC v8 | | NCIT:C133448 | Clinical Stage I Esophageal Squamous Cell Carcinoma AJCC v8 | | NCIT:C133648 | Clinical Stage I Gastric Cancer AJCC v8 | | NCIT:C133552 | Clinical Stage I Gastroesophageal Junction Adenocarcinoma AJCC v8 | | NCIT:C132885 | Clinical Stage I HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8 | -| NCIT:C136873 | Clinical Stage I Merkel Cell Carcinoma AJCC v8 | | NCIT:C140752 | Clinical Stage I Retinoblastoma AJCC v8 | | NCIT:C137649 | Clinical Stage IA Cutaneous Melanoma AJCC v8 | | NCIT:C137650 | Clinical Stage IB Cutaneous Melanoma AJCC v8 | | NCIT:C137651 | Clinical Stage II Cutaneous Melanoma AJCC v8 | +| NCIT:C136874 | Clinical Stage II Cutaneous Merkel Cell Carcinoma AJCC v8 | | NCIT:C133404 | Clinical Stage II Esophageal Adenocarcinoma AJCC v8 | | NCIT:C133449 | Clinical Stage II Esophageal Squamous Cell Carcinoma AJCC v8 | | NCIT:C133649 | Clinical Stage II Gastric Cancer AJCC v8 | | NCIT:C133553 | Clinical Stage II Gastroesophageal Junction Adenocarcinoma AJCC v8 | | NCIT:C132886 | Clinical Stage II HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8 | -| NCIT:C136874 | Clinical Stage II Merkel Cell Carcinoma AJCC v8 | | NCIT:C140753 | Clinical Stage II Retinoblastoma AJCC v8 | | NCIT:C137652 | Clinical Stage IIA Cutaneous Melanoma AJCC v8 | +| NCIT:C136875 | Clinical Stage IIA Cutaneous Merkel Cell Carcinoma AJCC v8 | | NCIT:C133405 | Clinical Stage IIA Esophageal Adenocarcinoma AJCC v8 | | NCIT:C133681 | Clinical Stage IIA Gastric Cancer AJCC v8 | | NCIT:C133554 | Clinical Stage IIA Gastroesophageal Junction Adenocarcinoma AJCC v8 | -| NCIT:C136875 | Clinical Stage IIA Merkel Cell Carcinoma AJCC v8 | | NCIT:C137653 | Clinical Stage IIB Cutaneous Melanoma AJCC v8 | +| NCIT:C136876 | Clinical Stage IIB Cutaneous Merkel Cell Carcinoma AJCC v8 | | NCIT:C133406 | Clinical Stage IIB Esophageal Adenocarcinoma AJCC v8 | | NCIT:C133682 | Clinical Stage IIB Gastric Cancer AJCC v8 | | NCIT:C133555 | Clinical Stage IIB Gastroesophageal Junction Adenocarcinoma AJCC v8 | -| NCIT:C136876 | Clinical Stage IIB Merkel Cell Carcinoma AJCC v8 | | NCIT:C137654 | Clinical Stage IIC Cutaneous Melanoma AJCC v8 | | NCIT:C137655 | Clinical Stage III Cutaneous Melanoma AJCC v8 | +| NCIT:C136877 | Clinical Stage III Cutaneous Merkel Cell Carcinoma AJCC v8 | | NCIT:C133407 | Clinical Stage III Esophageal Adenocarcinoma AJCC v8 | | NCIT:C133450 | Clinical Stage III Esophageal Squamous Cell Carcinoma AJCC v8 | | NCIT:C133650 | Clinical Stage III Gastric Cancer AJCC v8 | | NCIT:C133556 | Clinical Stage III Gastroesophageal Junction Adenocarcinoma AJCC v8 | | NCIT:C132891 | Clinical Stage III HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8 | -| NCIT:C136877 | Clinical Stage III Merkel Cell Carcinoma AJCC v8 | | NCIT:C140754 | Clinical Stage III Retinoblastoma AJCC v8 | | NCIT:C137656 | Clinical Stage IV Cutaneous Melanoma AJCC v8 | +| NCIT:C136878 | Clinical Stage IV Cutaneous Merkel Cell Carcinoma AJCC v8 | | NCIT:C133408 | Clinical Stage IV Esophageal Adenocarcinoma AJCC v8 | | NCIT:C133451 | Clinical Stage IV Esophageal Squamous Cell Carcinoma AJCC v8 | | NCIT:C133651 | Clinical Stage IV Gastric Cancer AJCC v8 | | NCIT:C133557 | Clinical Stage IV Gastroesophageal Junction Adenocarcinoma AJCC v8 | | NCIT:C132893 | Clinical Stage IV HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8 | -| NCIT:C136878 | Clinical Stage IV Merkel Cell Carcinoma AJCC v8 | | NCIT:C140755 | Clinical Stage IV Retinoblastoma AJCC v8 | | NCIT:C133409 | Clinical Stage IVA Esophageal Adenocarcinoma AJCC v8 | | NCIT:C133452 | Clinical Stage IVA Esophageal Squamous Cell Carcinoma AJCC v8 | @@ -2380,6 +2405,7 @@ | NCIT:C156279 | Colon Liposarcoma | | NCIT:C27411 | Colon Mantle Cell Lymphoma | | NCIT:C96492 | Colon Micropapillary Adenocarcinoma | +| NCIT:C203384 | Colon Neuroendocrine Carcinoma | | NCIT:C160443 | Colon Neuroendocrine Tumor G2 | | NCIT:C172702 | Colon Neuroendocrine Tumor G3 | | NCIT:C135214 | Colon Neuroendocrine Tumor by AJCC v8 Stage | @@ -2441,7 +2467,8 @@ | NCIT:C5676 | Colorectal Villous Adenoma | | NCIT:C54181 | Columnar Cell Change of the Breast | | NCIT:C54182 | Columnar Cell Change of the Breast with Atypia | -| NCIT:C165523 | Combined BAP1-Inactivated Nevus | +| NCIT:C27524 | Columnar Trichoblastoma | +| NCIT:C165523 | Combined BAP1-Inactivated Melanocytoma | | NCIT:C21727 | Combined Epithelial / Stromal Atypical Hyperplasia of the Mouse Prostate Gland | | NCIT:C21714 | Combined Epithelial / Stromal Diffuse Hyperplasia of the Mouse Prostate Gland | | NCIT:C21720 | Combined Epithelial / Stromal Focal Hyperplasia of the Mouse Prostate Gland | @@ -2457,6 +2484,7 @@ | NCIT:C157246 | Composite Paraganglioma | | NCIT:C21785 | Compound Melanocytic Hyperplasia of Mouse | | NCIT:C3901 | Compound Nevus | +| NCIT:C204787 | Compound Spitz Nevus | | NCIT:C2960 | Condyloma Acuminatum | | NCIT:C97057 | Condyloma Acuminatum with Dysplasia | | NCIT:C116899 | Congenital Cystic Hygroma | @@ -2464,6 +2492,7 @@ | NCIT:C22105 | Congestion of the Mouse Intestinal Tract | | NCIT:C174402 | Conjunctival Adenosquamous Carcinoma | | NCIT:C175499 | Conjunctival Angiosarcoma | +| NCIT:C204978 | Conjunctival Balloon Cell Nevus | | NCIT:C174452 | Conjunctival Blue Nevus | | NCIT:C174403 | Conjunctival Carcinoma | | NCIT:C174418 | Conjunctival Compound Nevus | @@ -2475,7 +2504,9 @@ | NCIT:C174390 | Conjunctival Keratoacanthoma | | NCIT:C175500 | Conjunctival Leiomyosarcoma | | NCIT:C175498 | Conjunctival Lymphangioma | -| NCIT:C100054 | Conjunctival Melanocytic Intraepithelial Neoplasia | +| NCIT:C100054 | Conjunctival Melanocytic Intraepithelial Lesion | +| NCIT:C204977 | Conjunctival Melanocytic Neoplasm | +| NCIT:C204981 | Conjunctival Melanoma In Situ | | NCIT:C175431 | Conjunctival Mucosa-Associated Lymphoid Tissue Lymphoma | | NCIT:C175495 | Conjunctival Myxoma | | NCIT:C175432 | Conjunctival Non-Hodgkin Lymphoma | @@ -2487,11 +2518,12 @@ | NCIT:C174493 | Conjunctival Spitz Nevus | | NCIT:C6224 | Conjunctival Squamous Papilloma | | NCIT:C175494 | Conjunctival Stromal Tumor | -| NCIT:C174426 | Conjunctival Subepithelial Nevus | +| NCIT:C174426 | Conjunctival Subepithelial (Stromal) Nevus | | NCIT:C27574 | Connective and Soft Tissue Disorder | | NCIT:C62277 | Connective and Soft Tissue Neoplasm (Antiquated) | | NCIT:C99390 | Contralateral Breast Carcinoma | | NCIT:C27492 | Conventional Alveolar Rhabdomyosarcoma | +| NCIT:C39755 | Conventional Ameloblastoma | | NCIT:C49179 | Conventional Cardiac Rhabdomyoma | | NCIT:C178563 | Conventional Chordoma | | NCIT:C49104 | Conventional Dermatofibrosarcoma Protuberans | @@ -2506,6 +2538,7 @@ | NCIT:C201124 | Cribriform Comedo-Type Adenocarcinoma | | NCIT:C21683 | Cribriform Mammary Carcinoma of Mouse | | NCIT:C121963 | Cribriform Neuroepithelial Tumor | +| NCIT:C43322 | Cribriform Trichoblastoma | | NCIT:C96497 | Crohn Disease-Associated Colorectal Adenocarcinoma | | NCIT:C154342 | Crooke Cell Tumor | | NCIT:C45272 | Cutaneous Adult T-Cell Leukemia/Lymphoma | @@ -2518,6 +2551,7 @@ | NCIT:C45240 | Cutaneous Hematopoietic and Lymphoid Cell Neoplasm | | NCIT:C168980 | Cutaneous Histiocytic and Dendritic Cell Neoplasm | | NCIT:C168984 | Cutaneous Indeterminate Dendritic Cell Histiocytosis | +| NCIT:C202966 | Cutaneous Juvenile Xanthogranuloma | | NCIT:C168983 | Cutaneous Langerhans Cell Histiocytosis | | NCIT:C171101 | Cutaneous Lymphoma | | NCIT:C45267 | Cutaneous Lymphomatoid Granulomatosis | @@ -2532,6 +2566,11 @@ | NCIT:C137657 | Cutaneous Melanoma by AJCC v8 Pathologic Stage | | NCIT:C137645 | Cutaneous Melanoma by AJCC v8 Stage | | NCIT:C155305 | Cutaneous Melanoma of the Extremity | +| NCIT:C173385 | Cutaneous Merkel Cell Carcinoma | +| NCIT:C136869 | Cutaneous Merkel Cell Carcinoma by AJCC v7 Stage | +| NCIT:C136871 | Cutaneous Merkel Cell Carcinoma by AJCC v8 Clinical Stage | +| NCIT:C136880 | Cutaneous Merkel Cell Carcinoma by AJCC v8 Pathologic Stage | +| NCIT:C136870 | Cutaneous Merkel Cell Carcinoma by AJCC v8 Stage | | NCIT:C45268 | Cutaneous Nasal Type Extranodal NK/T-Cell Lymphoma | | NCIT:C4479 | Cutaneous Neural Neoplasm | | NCIT:C128451 | Cutaneous Neurofibroma | @@ -2553,6 +2592,7 @@ | NCIT:C82890 | Cystic Oncocytic Neoplasm | | NCIT:C192105 | Cystic Trophoblastic Tumor | | NCIT:C45754 | Cystic Tumor of the Atrioventricular Node | +| NCIT:C202058 | Cystic/Microcystic Calcifying Epithelial Odontogenic Tumor | | NCIT:C122687 | Cytogenetically Normal Acute Myeloid Leukemia | | NCIT:C186730 | Cytogenetically Normal Acute Myeloid Leukemia Post Cytotoxic Therapy | | NCIT:C21900 | Cytopenia with Increased Blasts of Mouse | @@ -2569,6 +2609,7 @@ | NCIT:C181865 | DS Stage IIIA Multiple Myeloma | | NCIT:C181866 | DS Stage IIIB Multiple Myeloma | | NCIT:C200050 | DUSP22-R Anaplastic Large Cell Lymphoma, ALK-Negative | +| NCIT:C205127 | De Novo Nodular Melanoma | | NCIT:C63978 | Decidual Reaction of the Rat Uterine Cervix | | NCIT:C63979 | Decidual Reaction of the Rat Uterus | | NCIT:C22977 | Dedifferentiated Chondrosarcoma of the Mouse Skeletal System | @@ -2578,10 +2619,11 @@ | NCIT:C178222 | Dedifferentiated Leiomyosarcoma | | NCIT:C6936 | Deep (Aggressive) Angiomyxoma | | NCIT:C6498 | Deep Lipoma | -| NCIT:C7576 | Deep Penetrating Nevus | +| NCIT:C7576 | Deep Penetrating Melanocytoma | | NCIT:C5305 | Deletion of Chromosome 22 Associated Meningioma | | NCIT:C5306 | Deletion of Chromosome 3p Associated Meningioma | | NCIT:C5294 | Deletion of the Short Arm of Chromosome 1 (1p) Associated Meningioma | +| NCIT:C204910 | Dendritic Blue Nevus | | NCIT:C154339 | Densely Granulated Corticotroph Pituitary Neuroendocrine Tumor | | NCIT:C45931 | Densely Granulated Lactotroph Pituitary Neuroendocrine Tumor | | NCIT:C45925 | Densely Granulated Somatotroph Pituitary Neuroendocrine Tumor | @@ -2589,18 +2631,21 @@ | NCIT:C4473 | Dermal Duct Tumor | | NCIT:C6484 | Dermal Fibroma | | NCIT:C21784 | Dermal Melanocytic Hyperplasia of Mouse | +| NCIT:C205129 | Dermal Melanoma | | NCIT:C121680 | Dermal Nerve Sheath Myxoma | +| NCIT:C204789 | Dermal Spitz Nevus | | NCIT:C38108 | Dermatofibrosarcoma Protuberans with Giant Cell Fibroblastoma-Like Differentiation | | NCIT:C38105 | Dermatofibrosarcoma Protuberans with Myoid Differentiation | | NCIT:C170888 | Dermatomyofibroma | +| NCIT:C203388 | Descending Colon Neuroendocrine Tumor | | NCIT:C6428 | Descending Colon Neuroendocrine Tumor G1 | +| NCIT:C203393 | Descending Colon Neuroendocrine Tumor G2 | | NCIT:C27515 | Desmoplastic Fibroblastoma | | NCIT:C3740 | Desmoplastic Fibroma | | NCIT:C6747 | Desmoplastic Mesothelioma | | NCIT:C178507 | Desmoplastic Myxoid Tumor of the Pineal Region, SMARCB1-Mutant | | NCIT:C48614 | Desmoplastic Neurotropic Melanoma | | NCIT:C27522 | Desmoplastic Trichilemmoma | -| NCIT:C27524 | Desmoplastic Trichoepithelioma | | NCIT:C136978 | Devil Facial Tumor Disease | | NCIT:C176223 | Devil Facial Tumor Disease 1 | | NCIT:C176224 | Devil Facial Tumor Disease 2 | @@ -2650,6 +2695,7 @@ | NCIT:C27822 | Diffuse Malignant Lymphoma | | NCIT:C8420 | Diffuse Malignant Mesothelioma | | NCIT:C22052 | Diffuse Melanocytosis of the Mouse Nervous System | +| NCIT:C205069 | Diffuse Meningeal Melanocytic Neoplasm | | NCIT:C182151 | Diffuse Midline Glioma | | NCIT:C185370 | Diffuse Midline Glioma with EZHIP Overexpression | | NCIT:C185369 | Diffuse Midline Glioma, EGFR-Mutant | @@ -2665,7 +2711,6 @@ | NCIT:C185467 | Diffuse Pediatric-Type High Grade Glioma, H3-Wildtype and IDH-Wildtype | | NCIT:C45630 | Diffuse Pulmonary Lymphangiomatosis | | NCIT:C66815 | Diffuse Retinoblastoma | -| NCIT:C182357 | Diffusion Restriction | | NCIT:C35180 | Digestive System Carcinoma In Situ | | NCIT:C172850 | Digestive System Diffuse Large B-Cell Lymphoma | | NCIT:C96466 | Digestive System Filiform Serrated Adenoma | @@ -2690,7 +2735,6 @@ | NCIT:C154641 | Digestive System Small Cell Neuroendocrine Carcinoma | | NCIT:C172852 | Digestive System Soft Tissue Neoplasm | | NCIT:C172940 | Digestive System Solitary Fibrous Tumor | -| NCIT:C162848 | Digital Papillary Adenoma | | NCIT:C21864 | Disorders of Pigmentation of the Mouse Skin | | NCIT:C21865 | Disorders of the Mouse Hair Follicle | | NCIT:C21863 | Disorders of the Squamous Epithelium of the Mouse Skin | @@ -2702,6 +2746,7 @@ | NCIT:C7976 | Distal Bile Duct Adenocarcinoma | | NCIT:C134810 | Distal Bile Duct Cancer by AJCC v7 Stage | | NCIT:C134811 | Distal Bile Duct Cancer by AJCC v8 Stage | +| NCIT:C202634 | Distal Colon Carcinoma | | NCIT:C152036 | Distal Esophagus Adenocarcinoma | | NCIT:C150037 | Distal Esophagus Squamous Cell Carcinoma | | NCIT:C115210 | Distal Urethral Carcinoma | @@ -2749,6 +2794,8 @@ | NCIT:C27696 | EBV-Related Post-Transplant Lymphoproliferative Disorder | | NCIT:C162305 | EBV-Related Sarcoma | | NCIT:C190402 | EBV-Related T/NK-Cell Lymphoproliferative Disorder | +| NCIT:C202130 | EGFR-Positive Lung Adenocarcinoma | +| NCIT:C202131 | EGFR-Positive Lung Non-Small Cell Carcinoma | | NCIT:C191375 | ELOC-Mutated Renal Cell Carcinoma | | NCIT:C186591 | ELP1-Associated Medulloblastoma | | NCIT:C104031 | ENSAT Stage I Adrenal Cortical Carcinoma | @@ -2758,13 +2805,22 @@ | NCIT:C177278 | EWSR1-SMAD3-Positive Fibroblastic Tumor | | NCIT:C148398 | EZB Diffuse Large B-Cell Lymphoma | | NCIT:C54262 | Ear Carcinoma | -| NCIT:C5971 | Ear Polyp | +| NCIT:C202574 | Ear Osteoma | | NCIT:C68661 | Early Favorable Hodgkin Lymphoma | | NCIT:C53280 | Early Favorable Non-Hodgkin Lymphoma | | NCIT:C96772 | Early Hepatocellular Carcinoma | | NCIT:C180374 | Early Primary Cutaneous T-Cell Non-Hodgkin Lymphoma | +| NCIT:C205286 | Early Stage Bladder Urothelial Carcinoma | | NCIT:C94774 | Early Stage Breast Carcinoma | +| NCIT:C205287 | Early Stage Cervical Carcinoma | +| NCIT:C205289 | Early Stage Clear Cell Renal Cell Carcinoma | +| NCIT:C205290 | Early Stage Colorectal Carcinoma | +| NCIT:C205295 | Early Stage Endometrial Carcinoma | +| NCIT:C205298 | Early Stage Esophageal Carcinoma | | NCIT:C190215 | Early Stage HER2-Negative Breast Carcinoma | +| NCIT:C205301 | Early Stage Hepatocellular Carcinoma | +| NCIT:C205303 | Early Stage Lung Non-Small Cell Carcinoma | +| NCIT:C205307 | Early Stage Malignant Skin Neoplasm | | NCIT:C158961 | Early Stage Pancreatic Ductal Adenocarcinoma | | NCIT:C181081 | Early Stage Triple-Negative Breast Carcinoma | | NCIT:C199171 | Early T Precursor Acute Lymphoblastic Leukemia with BCL11B Rearrangement | @@ -2773,15 +2829,16 @@ | NCIT:C68664 | Early Unfavorable Hodgkin Lymphoma | | NCIT:C53282 | Early Unfavorable Non-Hodgkin Lymphoma | | NCIT:C7565 | Eccrine Hidrocystoma | +| NCIT:C205462 | Eccrine Poroma | | NCIT:C121785 | Ectomesenchymal Chondromyxoid Tumor | | NCIT:C95048 | Ectopic Cervical Thymoma | -| NCIT:C53595 | Ectopic Hamartomatous Thymoma | | NCIT:C5308 | Ectopic Meningioma | | NCIT:C173345 | Ectopic Pituitary Neuroendocrine Tumor | | NCIT:C22064 | Embryonal Carcinoma of the Mouse Nervous System | | NCIT:C23108 | Embryonal Rhabdomyosarcoma of the Mouse Nose and Paranasal Sinuses | | NCIT:C23078 | Embryonal Rhabdomyosarcoma of the Mouse Pharynx | | NCIT:C186534 | Embryonal Tumor with Multilayered Rosettes | +| NCIT:C202010 | Embryonal Tumor with Multilayered Rosettes of the Fourth Ventricle | | NCIT:C129499 | Embryonal Tumor with Multilayered Rosettes without C19MC Alteration | | NCIT:C186535 | Embryonal Tumor with Multilayered Rosettes, DICER1-Mutated | | NCIT:C176009 | Encapsulated Breast Papillary Carcinoma | @@ -2806,7 +2863,9 @@ | NCIT:C27845 | Endometrial Endometrioid Adenocarcinoma with an Undifferentiated Carcinomatous Component | | NCIT:C27848 | Endometrial Endometrioid Adenocarcinoma, Ciliated Variant | | NCIT:C6290 | Endometrial Endometrioid Adenocarcinoma, Variant with Squamous Differentiation | +| NCIT:C40148 | Endometrial High Grade Endometrioid Adenocarcinoma | | NCIT:C126772 | Endometrial Large Cell Neuroendocrine Carcinoma | +| NCIT:C180510 | Endometrial Low Grade Endometrioid Adenocarcinoma | | NCIT:C179322 | Endometrial Mesonephric-Like Adenocarcinoma | | NCIT:C180537 | Endometrial Mucinous Adenocarcinoma, Gastric-Type | | NCIT:C180536 | Endometrial Mucinous Adenocarcinoma, Intestinal-Type | @@ -2823,7 +2882,6 @@ | NCIT:C158620 | Endometrioid Tumor, Variant with Squamous Differentiation | | NCIT:C63887 | Endophytic Squamous Cell Carcinoma of the Rat Esophagus | | NCIT:C22935 | Endovascular Papillary Angioendothelioma of the Mouse Blood Vessel | -| NCIT:C121924 | Enostosis | | NCIT:C27252 | Enterochromaffin-Like Cell Neuroendocrine Tumor G1 | | NCIT:C66925 | Enteroglucagonoma | | NCIT:C141295 | Enteropathy-Associated T-Cell Lymphoma by Ann Arbor Stage | @@ -2927,11 +2985,14 @@ | NCIT:C27423 | Esophageal Squamous Intraepithelial Neoplasia | | NCIT:C95624 | Esophageal Synovial Sarcoma | | NCIT:C95610 | Esophageal Well Differentiated Squamous Cell Carcinoma | +| NCIT:C203673 | Esophageal and Gastroesophageal Junction Carcinoma | | NCIT:C188366 | Estrogen Receptor-Positive Breast Carcinoma | | NCIT:C48456 | Estrogen-Producing Adrenal Cortical Adenoma | | NCIT:C63888 | Exophytic Squamous Cell Carcinoma of the Rat Esophagus | | NCIT:C16835 | Experimental Malignant Melanoma | | NCIT:C9049 | Extensive Stage Lung Small Cell Carcinoma | +| NCIT:C202594 | External Auditory Canal Squamous Cell Carcinoma | +| NCIT:C91741 | External Auditory Canal Squamous Cell Carcinoma In Situ | | NCIT:C6080 | External Ear Actinic Keratosis | | NCIT:C3309 | Extra-Adrenal Paraganglioma | | NCIT:C5328 | Extra-Adrenal Retroperitoneal Paraganglioma | @@ -3034,9 +3095,6 @@ | NCIT:C6406 | FIGO Stage IVB Gestational Trophoblastic Tumor | | NCIT:C128095 | FIGO Stage IVB Ovarian Cancer | | NCIT:C6407 | FIGO Stage IVC Gestational Trophoblastic Tumor | -| NCIT:C9024 | FNCLCC Sarcoma Grade 1 | -| NCIT:C9028 | FNCLCC Sarcoma Grade 2 | -| NCIT:C9029 | FNCLCC Sarcoma Grade 3 | | NCIT:C189329 | FOXL2 c.402C>G (p.Cys134Trp)-Mutant Ovarian Sertoli-Leydig Cell Tumor | | NCIT:C121152 | FSH-Producing Pituitary Neuroendocrine Tumor | | NCIT:C90499 | Fallopian Tube Cancer by AJCC v6 Stage | @@ -3119,15 +3177,17 @@ | NCIT:C200684 | Follicular Lymphoma with Unusual Cytological Features | | NCIT:C27526 | Follicular Myxoma | | NCIT:C21813 | Follicular Neoplasms of the Mouse Skin | -| NCIT:C187645 | Follicular-Derived Thyroid Gland Carcinoma, High Grade | -| NCIT:C6421 | Foregut Neuroendocrine Tumor G1 | +| NCIT:C6421 | Foregut Neuroendocrine Tumor | +| NCIT:C203258 | Foregut Neuroendocrine Tumor G1 | +| NCIT:C203259 | Foregut Neuroendocrine Tumor G2 | +| NCIT:C203260 | Foregut Neuroendocrine Tumor G3 | | NCIT:C156039 | Fourth Ventricle Medulloblastoma | | NCIT:C95779 | Foveolar-Type Adenoma | | NCIT:C134771 | Frog Pronephric Kidney Tumor | | NCIT:C156035 | Frontal Lobe Anaplastic Astrocytoma | | NCIT:C156120 | Frontal Lobe Anaplastic Oligodendroglioma | | NCIT:C164156 | Fumarate Hydratase-Deficient Renal Cell Carcinoma | -| NCIT:C176705 | Functioning Lung Carcinoid Tumor | +| NCIT:C176705 | Functioning Lung Neuroendocrine Tumor | | NCIT:C45841 | Functioning Pancreatic Neuroendocrine Tumor G2 | | NCIT:C121720 | Functioning Pituitary Neuroendocrine Tumor/Macroadenoma | | NCIT:C121679 | Functioning Pituitary Neuroendocrine Tumor/Microadenoma | @@ -3136,6 +3196,7 @@ | NCIT:C123736 | Fusion-Negative Rhabdomyosarcoma | | NCIT:C123731 | Fusion-Positive Alveolar Rhabdomyosarcoma | | NCIT:C123735 | Fusion-Positive Rhabdomyosarcoma | +| NCIT:C202896 | GLI1-Altered Soft Tissue Tumor | | NCIT:C9169 | Gallbladder Adenocarcinoma with Squamous Metaplasia | | NCIT:C96915 | Gallbladder Adenocarcinoma, Biliary Type | | NCIT:C96916 | Gallbladder Adenocarcinoma, Gastric Foveolar Type | @@ -3229,6 +3290,7 @@ | NCIT:C133563 | Gastroesophageal Junction Adenocarcinoma by AJCC v8 Pathologic Stage | | NCIT:C133583 | Gastroesophageal Junction Adenocarcinoma by AJCC v8 Postneoadjuvant Therapy Stage | | NCIT:C133548 | Gastroesophageal Junction Adenocarcinoma by AJCC v8 Stage | +| NCIT:C203675 | Gastroesophageal Junction Carcinoma | | NCIT:C126323 | Gastroesophageal Junction Large Cell Neuroendocrine Carcinoma | | NCIT:C126324 | Gastroesophageal Junction Neuroendocrine Carcinoma | | NCIT:C126325 | Gastroesophageal Junction Small Cell Neuroendocrine Carcinoma | @@ -3271,6 +3333,7 @@ | NCIT:C134774 | Gibbon Lymphosarcoma | | NCIT:C27478 | Gingival Angiofibroma | | NCIT:C7721 | Gingival Carcinoma | +| NCIT:C202622 | Gingival Low Grade Myofibroblastic Sarcoma | | NCIT:C129289 | Gingival Spindle Cell Carcinoma | | NCIT:C129857 | Gingival Squamous Cell Carcinoma | | NCIT:C27269 | Glandular Cell Intraepithelial Neoplasia | @@ -3373,6 +3436,7 @@ | NCIT:C132882 | HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma by AJCC v8 Stage | | NCIT:C27685 | HTLV-1-Related Malignant Neoplasm | | NCIT:C22104 | Hamartoma of the Mouse Intestinal Tract | +| NCIT:C8372 | Hamartomatous Polyp | | NCIT:C134990 | Hamster Adrenal Carcinoma | | NCIT:C134565 | Hamster Buccal Pouch Carcinoma | | NCIT:C134566 | Hamster Cholangiocarcinoma | @@ -3397,16 +3461,45 @@ | NCIT:C6212 | Hard Palate Pleomorphic Adenoma | | NCIT:C8170 | Hard Palate Squamous Cell Carcinoma | | NCIT:C16662 | Harding-Passey Malignant Melanoma | -| NCIT:C37290 | Head and Neck Basaloid Carcinoma | +| NCIT:C202656 | Head and Neck Angiosarcoma | +| NCIT:C37290 | Head and Neck Basaloid Squamous Cell Carcinoma | +| NCIT:C202935 | Head and Neck Burkitt Lymphoma | | NCIT:C162595 | Head and Neck Carcinoma of Unknown Primary | +| NCIT:C202975 | Head and Neck Dermoid Cyst | +| NCIT:C202930 | Head and Neck Diffuse Large B-Cell Lymphoma | +| NCIT:C202849 | Head and Neck EBV-Associated Smooth Muscle Tumor | +| NCIT:C202655 | Head and Neck Epithelioid Hemangioendothelioma | +| NCIT:C202652 | Head and Neck Epithelioid Hemangioma | +| NCIT:C202972 | Head and Neck Erdheim-Chester Disease | +| NCIT:C202904 | Head and Neck Ewing Sarcoma | +| NCIT:C202924 | Head and Neck Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue | +| NCIT:C202881 | Head and Neck Extraskeletal Myxoid Chondrosarcoma | | NCIT:C173580 | Head and Neck Follicular Dendritic Cell Sarcoma | +| NCIT:C202926 | Head and Neck Follicular Lymphoma | +| NCIT:C202897 | Head and Neck GLI1-Altered Soft Tissue Tumor | +| NCIT:C202977 | Head and Neck Germ Cell Tumor | +| NCIT:C202647 | Head and Neck Hemangioma | +| NCIT:C202954 | Head and Neck Hematopoietic and Lymphoid Cell Neoplasm | | NCIT:C173588 | Head and Neck Heterotopia-Associated Carcinoma | | NCIT:C173485 | Head and Neck Histiocytic and Dendritic Cell Neoplasm | +| NCIT:C202922 | Head and Neck Hodgkin Lymphoma | +| NCIT:C202635 | Head and Neck Inflammatory Myofibroblastic Tumor | +| NCIT:C202967 | Head and Neck Juvenile Xanthogranuloma | | NCIT:C54283 | Head and Neck Keratinizing Squamous Cell Carcinoma | | NCIT:C173486 | Head and Neck Langerhans Cell Histiocytosis | +| NCIT:C202929 | Head and Neck Large B-Cell Lymphoma with IRF4 Rearrangement | | NCIT:C160982 | Head and Neck Large Cell Neuroendocrine Carcinoma | +| NCIT:C202711 | Head and Neck Leiomyoma | +| NCIT:C202853 | Head and Neck Leiomyosarcoma | +| NCIT:C202646 | Head and Neck Lipoma | +| NCIT:C202611 | Head and Neck Liposarcoma | +| NCIT:C202654 | Head and Neck Lymphangioma | +| NCIT:C202921 | Head and Neck Lymphoma | +| NCIT:C202878 | Head and Neck Malignant Peripheral Nerve Sheath Tumor | +| NCIT:C202925 | Head and Neck Mantle Cell Lymphoma | | NCIT:C173488 | Head and Neck Melanocytic Neoplasm | | NCIT:C173587 | Head and Neck Merkel Cell Carcinoma | +| NCIT:C202914 | Head and Neck Myeloid Sarcoma | | NCIT:C173087 | Head and Neck NUT Carcinoma | | NCIT:C160980 | Head and Neck Neuroendocrine Carcinoma | | NCIT:C188222 | Head and Neck Neuroendocrine Neoplasm | @@ -3414,9 +3507,22 @@ | NCIT:C188224 | Head and Neck Neuroendocrine Tumor G1 | | NCIT:C173388 | Head and Neck Neuroendocrine Tumor G2 | | NCIT:C54661 | Head and Neck Nevus | +| NCIT:C202613 | Head and Neck Nodular Fasciitis | +| NCIT:C202923 | Head and Neck Non-Hodgkin Lymphoma | +| NCIT:C202927 | Head and Neck Pediatric-Type Follicular Lymphoma | +| NCIT:C202879 | Head and Neck Phosphaturic Mesenchymal Tumor | +| NCIT:C202936 | Head and Neck Plasmablastic Lymphoma | +| NCIT:C202973 | Head and Neck Plasmacytoma | +| NCIT:C202858 | Head and Neck Rhabdomyoma | +| NCIT:C202859 | Head and Neck Rhabdomyosarcoma | +| NCIT:C202971 | Head and Neck Rosai-Dorfman-Destombes Disease | | NCIT:C164198 | Head and Neck Sarcoma | | NCIT:C160978 | Head and Neck Sebaceous Carcinoma | | NCIT:C160981 | Head and Neck Small Cell Neuroendocrine Carcinoma | +| NCIT:C202623 | Head and Neck Soft Tissue Neoplasm | +| NCIT:C202884 | Head and Neck Synovial Sarcoma | +| NCIT:C202980 | Head and Neck Teratoma | +| NCIT:C202901 | Head and Neck Undifferentiated Pleomorphic Sarcoma | | NCIT:C199457 | Heavy Chain Class-Switched Primary Cutaneous Marginal Zone Lymphoproliferative Disorder | | NCIT:C27763 | Helicobacter Pylori-Associated Gastric Mucosa-Associated Lymphoid Tissue Lymphoma | | NCIT:C27764 | Helicobacter Pylori-Related Carcinoma | @@ -3460,8 +3566,8 @@ | NCIT:C23063 | Hematopoietic Neoplasms of the Mouse Oral Cavity | | NCIT:C23083 | Hematopoietic Neoplasms of the Mouse Pharynx | | NCIT:C23147 | Hematopoietic Neoplasms of the Mouse Salivary Glands | +| NCIT:C35814 | Hematopoietic and Lymphatic System Disorder | | NCIT:C7340 | Hematopoietic and Lymphoid Neoplasm (Antiquated) | -| NCIT:C35814 | Hematopoietic and Lymphoid System Disorder | | NCIT:C5123 | Hemispheric Anaplastic Astrocytoma | | NCIT:C66792 | Hemolymphangioma | | NCIT:C121752 | Hemosiderotic Fibrolipomatous Tumor | @@ -3495,6 +3601,7 @@ | NCIT:C46099 | Hereditary Thyroid Gland Medullary Carcinoma | | NCIT:C22032 | Hibernoma of the Mouse Nervous System | | NCIT:C21835 | Hibernoma of the Mouse Skin | +| NCIT:C205475 | Hidroacanthoma Simplex | | NCIT:C9109 | High Grade Adult Non-Hodgkin's Lymphoma | | NCIT:C27275 | High Grade Anal Canal Intraepithelial Neoplasia | | NCIT:C172706 | High Grade Anal Intraepithelial Neoplasia | @@ -3509,21 +3616,21 @@ | NCIT:C131913 | High Grade B-Cell Lymphoma with MYC, BCL2, and BCL6 Rearrangements | | NCIT:C80291 | High Grade B-Cell Lymphoma, Not Otherwise Specified | | NCIT:C6817 | High Grade B-Cell Non-Hodgkin's Lymphoma | -| NCIT:C5167 | High Grade Breast Mucoepidermoid Carcinoma | | NCIT:C5005 | High Grade Burkitt-Like Lymphoma | | NCIT:C7675 | High Grade Cervical Glandular Intraepithelial Neoplasia | | NCIT:C7670 | High Grade Cervical Intraepithelial Neoplasia | | NCIT:C40197 | High Grade Cervical Squamous Intraepithelial Neoplasia | +| NCIT:C204980 | High Grade Conjunctival Melanocytic Intraepithelial Lesion | | NCIT:C7668 | High Grade Conjunctival Squamous Intraepithelial Neoplasia | | NCIT:C7669 | High Grade Corneal Squamous Intraepithelial Neoplasia | | NCIT:C190680 | High Grade Endometrial Carcinoma | -| NCIT:C40148 | High Grade Endometrial Endometrioid Adenocarcinoma | | NCIT:C199149 | High Grade Endometrioid Adenocarcinoma | | NCIT:C27429 | High Grade Esophageal Glandular Intraepithelial Neoplasia | | NCIT:C27426 | High Grade Esophageal Squamous Intraepithelial Neoplasia | | NCIT:C22132 | High Grade Flat Tubular Dysplasia of the Mouse Intestinal Tract | | NCIT:C22138 | High Grade Flat Tubulovillous Dysplasia of the Mouse Intestinal Tract | | NCIT:C22135 | High Grade Flat Villous Dysplasia of the Mouse Intestinal Tract | +| NCIT:C187645 | High Grade Follicular Cell-Derived Non-Anaplastic Thyroid Gland Carcinoma | | NCIT:C27437 | High Grade Gastric Intraepithelial Neoplasia | | NCIT:C7662 | High Grade Glandular Intraepithelial Neoplasia | | NCIT:C7348 | High Grade Intraepithelial Neoplasia | @@ -3532,9 +3639,10 @@ | NCIT:C9030 | High Grade Malignant Peripheral Nerve Sheath Tumor | | NCIT:C21676 | High Grade Mouse MIN | | NCIT:C21730 | High Grade Mouse Prostatic Intraepithelial Neoplasia | +| NCIT:C203948 | High Grade Mucinous Carcinoma Peritonei | +| NCIT:C203949 | High Grade Mucinous Carcinoma Peritonei with Signet Ring Cells | | NCIT:C23139 | High Grade Mucoepidermoid Tumor of the Mouse Salivary Glands | | NCIT:C197813 | High Grade Osteosarcoma | -| NCIT:C199166 | High Grade Ovarian Endometrioid Adenocarcinoma | | NCIT:C95432 | High Grade Pancreatic Intraepithelial Neoplasia | | NCIT:C6850 | High Grade Paranasal Sinus Sarcoma | | NCIT:C22142 | High Grade Pedunculated Tubular Dysplasia of the Mouse Intestinal Tract | @@ -3546,8 +3654,6 @@ | NCIT:C39888 | High Grade Prostatic Intraepithelial Neoplasia, Mucinous Variant | | NCIT:C39887 | High Grade Prostatic Intraepithelial Neoplasia, Signet Ring Variant | | NCIT:C39891 | High Grade Prostatic Intraepithelial Neoplasia, Small Cell Neuroendocrine Variant | -| NCIT:C8018 | High Grade Salivary Gland Carcinoma | -| NCIT:C8019 | High Grade Salivary Gland Mucoepidermoid Carcinoma | | NCIT:C9418 | High Grade Sarcoma | | NCIT:C22122 | High Grade Sessile Tubular Dysplasia of the Mouse Intestinal Tract | | NCIT:C22128 | High Grade Sessile Tubulovillous Dysplasia of the Mouse Intestinal Tract | @@ -3568,8 +3674,12 @@ | NCIT:C67493 | High-Grade Biliary Intraepithelial Neoplasia | | NCIT:C134742 | Hilar Cholangiocarcinoma by AJCC v7 Stage | | NCIT:C134743 | Hilar Cholangiocarcinoma by AJCC v8 Stage | -| NCIT:C6423 | Hindgut Neuroendocrine Tumor G1 | +| NCIT:C6423 | Hindgut Neuroendocrine Tumor | +| NCIT:C203262 | Hindgut Neuroendocrine Tumor G1 | +| NCIT:C203265 | Hindgut Neuroendocrine Tumor G2 | +| NCIT:C203266 | Hindgut Neuroendocrine Tumor G3 | | NCIT:C21915 | Histiocyte-Associated Diffuse Large B Cell Lymphoma of the Mouse Hematologic System | +| NCIT:C203422 | Histiocytic Disorder | | NCIT:C23121 | Histiocytic Neoplasms of the Mouse Larynx | | NCIT:C21856 | Histiocytic Neoplasms of the Mouse Skin | | NCIT:C21874 | Histiocytosis in Association with a Hematopoietic Neoplasm of Mouse | @@ -3591,10 +3701,10 @@ | NCIT:C180848 | Human Papillomavirus-Independent Cervical Adenocarcinoma | | NCIT:C180846 | Human Papillomavirus-Independent Cervical Adenocarcinoma In Situ | | NCIT:C180841 | Human Papillomavirus-Independent Cervical Squamous Cell Carcinoma | +| NCIT:C164250 | Human Papillomavirus-Independent Squamous Cell Carcinoma | | NCIT:C180919 | Human Papillomavirus-Independent Vaginal Squamous Cell Carcinoma | | NCIT:C181903 | Human Papillomavirus-Independent Vulvar Squamous Cell Carcinoma | -| NCIT:C190149 | Human Papillomavirus-Negative Head and Neck Squamous Cell Carcinoma of Unknown Primary | -| NCIT:C164250 | Human Papillomavirus-Negative Squamous Cell Carcinoma | +| NCIT:C190149 | Human Papillomavirus-Negative Neck Squamous Cell Carcinoma of Unknown Primary | | NCIT:C27684 | Human Papillomavirus-Related Adenocarcinoma | | NCIT:C97046 | Human Papillomavirus-Related Adenosquamous Carcinoma | | NCIT:C27681 | Human Papillomavirus-Related Anal Squamous Cell Carcinoma | @@ -3604,18 +3714,20 @@ | NCIT:C27675 | Human Papillomavirus-Related Cervical Carcinoma | | NCIT:C27676 | Human Papillomavirus-Related Cervical Squamous Cell Carcinoma | | NCIT:C27680 | Human Papillomavirus-Related Esophageal Squamous Cell Carcinoma | -| NCIT:C187051 | Human Papillomavirus-Related Head and Neck Squamous Cell Carcinoma of Unknown Primary | | NCIT:C27718 | Human Papillomavirus-Related Malignant Neoplasm | | NCIT:C102884 | Human Papillomavirus-Related Malignant Neoplasm in AIDS Patient | | NCIT:C171023 | Human Papillomavirus-Related Mucosal Head and Neck Squamous Cell Carcinoma | +| NCIT:C187051 | Human Papillomavirus-Related Neck Squamous Cell Carcinoma of Unknown Primary | | NCIT:C162541 | Human Papillomavirus-Related Penile Intraepithelial Neoplasia | | NCIT:C39862 | Human Papillomavirus-Related Urethral Squamous Cell Carcinoma | | NCIT:C180943 | Human Papillomavirus-Related Vaginal Adenocarcinoma | | NCIT:C180917 | Human Papillomavirus-Related Vaginal Squamous Cell Carcinoma | | NCIT:C27678 | Human Papillomavirus-Related Verrucous Carcinoma | | NCIT:C27679 | Human Papillomavirus-Related Vulvar Squamous Cell Carcinoma | +| NCIT:C201821 | Hyalinizing Clear Cell Carcinoma | | NCIT:C121686 | Hybrid Nerve Sheath Tumor | | NCIT:C7448 | Hybrid Odontogenic Fibroma | +| NCIT:C202081 | Hybrid Odontogenic Fibroma with Central Giant Cell Granuloma | | NCIT:C181079 | Hybrid Salivary Gland Carcinoma | | NCIT:C181078 | Hybrid Salivary Gland Tumor | | NCIT:C80344 | Hyperdiploid B Acute Lymphoblastic Leukemia | @@ -3625,9 +3737,13 @@ | NCIT:C21708 | Hyperplasia of the Mouse Prostate Gland | | NCIT:C21756 | Hyperplasia of the Mouse Pulmonary System | | NCIT:C80345 | Hypodiploid B Acute Lymphoblastic Leukemia | +| NCIT:C201746 | Hypopharyngeal Basaloid Squamous Cell Carcinoma | | NCIT:C90524 | Hypopharyngeal Carcinoma by AJCC v6 Stage | | NCIT:C91251 | Hypopharyngeal Carcinoma by AJCC v7 Stage | | NCIT:C133003 | Hypopharyngeal Carcinoma by AJCC v8 Stage | +| NCIT:C201748 | Hypopharyngeal Papillary Squamous Cell Carcinoma | +| NCIT:C201749 | Hypopharyngeal Spindle Cell Squamous Carcinoma | +| NCIT:C201743 | Hypopharyngeal Verrucous Carcinoma | | NCIT:C21647 | Hypoplasia of the Mouse Mammary Gland | | NCIT:C21706 | Hypoplasia of the Mouse Prostate Gland | | NCIT:C122686 | Hypoplastic Myelodysplastic Syndrome | @@ -3699,13 +3815,13 @@ | NCIT:C9408 | Inflammatory Malignant Fibrous Histiocytoma NCI Grade 3 | | NCIT:C21657 | Inflammatory Nodule of the Mouse Mammary Gland | | NCIT:C5148 | Infratentorial Glioblastoma | -| NCIT:C7201 | Infrequent Neoplasm | | NCIT:C45473 | Intermediate (Locally Aggressive) Blood Vessel Neoplasm | | NCIT:C45474 | Intermediate (Rarely Metastasizing) Blood Vessel Neoplasm | | NCIT:C136972 | Intermediate Atypical Prostate Carcinoma | | NCIT:C7391 | Intermediate Blood Vessel Neoplasm | | NCIT:C121926 | Intermediate Bone Neoplasm | | NCIT:C121846 | Intermediate Chondrogenic Neoplasm | +| NCIT:C204976 | Intermediate Congenital Melanocytic Nevus | | NCIT:C7333 | Intermediate Fibroblastic Neoplasm | | NCIT:C6491 | Intermediate Fibrohistiocytic Neoplasm | | NCIT:C9108 | Intermediate Grade Adult Non-Hodgkin's Lymphoma | @@ -3714,7 +3830,6 @@ | NCIT:C3459 | Intermediate Grade Lymphoma | | NCIT:C36047 | Intermediate Grade Malignant Neoplasm | | NCIT:C197814 | Intermediate Grade Osteosarcoma | -| NCIT:C8017 | Intermediate Grade Salivary Gland Mucoepidermoid Carcinoma | | NCIT:C7630 | Intermediate Lipomatous Neoplasm | | NCIT:C121931 | Intermediate Osteoclastic Giant Cell-Rich Tumor of Bone | | NCIT:C121925 | Intermediate Osteogenic Neoplasm | @@ -3847,10 +3962,15 @@ | NCIT:C27930 | Ionizing Radiation-Related Malignant Neoplasm | | NCIT:C190746 | Iridociliary Melanoma | | NCIT:C174498 | Iris Epithelioid Cell Melanoma | -| NCIT:C174506 | Iris Mixed Cell Melanoma | +| NCIT:C174506 | Iris Mixed Epithelioid and Spindle Cell Melanoma | | NCIT:C4556 | Iris Nevus | | NCIT:C65184 | Islet Cell Adenoma | -| NCIT:C121923 | Ivory Exostosis | +| NCIT:C202257 | Jaw Chondromyxoid Fibroma | +| NCIT:C202258 | Jaw Desmoplastic Fibroma | +| NCIT:C202256 | Jaw Osteoblastoma | +| NCIT:C202254 | Jaw Osteoma | +| NCIT:C202261 | Jaw Osteosarcoma | +| NCIT:C202265 | Jaw Rhabdomyosarcoma with TFCP2 Rearrangement | | NCIT:C181157 | Jejunal Carcinoma | | NCIT:C188067 | Jejunal Melanoma | | NCIT:C160437 | Jejunal Neuroendocrine Tumor G2 | @@ -3859,6 +3979,7 @@ | NCIT:C5589 | Jugular Foramen Neoplasm | | NCIT:C21783 | Junctional Melanocytic Hyperplasia of Mouse | | NCIT:C4231 | Junctional Nevus | +| NCIT:C204788 | Junctional Spitz Nevus | | NCIT:C40434 | Juvenile Bilateral Ovarian Granulosa Cell Tumor | | NCIT:C4276 | Juvenile Breast Fibroadenoma | | NCIT:C4207 | Juvenile Granulosa Cell Tumor | @@ -3866,6 +3987,7 @@ | NCIT:C198682 | Juvenile Myelomonocytic Leukemia Associated with Noonan Syndrome-Like Disorder | | NCIT:C198661 | Juvenile Myelomonocytic Leukemia-Like Neoplasm | | NCIT:C7289 | Juvenile Ovarian Granulosa Cell Tumor | +| NCIT:C202205 | Juvenile Trabecular Ossifying Fibroma | | NCIT:C6580 | Juxta-Articular Myxoma | | NCIT:C22969 | Juxtacortical Chondroma of the Mouse Skeletal System | | NCIT:C22970 | Juxtacortical Chondrosarcoma of the Mouse Skeletal System | @@ -3953,7 +4075,7 @@ | NCIT:C21926 | Large Cell Anaplastic Lymphoma of the Mouse Hematologic System | | NCIT:C54337 | Laryngeal Acantholytic Squamous Cell Carcinoma | | NCIT:C54338 | Laryngeal Adenosquamous Carcinoma | -| NCIT:C54334 | Laryngeal Basaloid Carcinoma | +| NCIT:C54334 | Laryngeal Basaloid Squamous Cell Carcinoma | | NCIT:C90527 | Laryngeal Cancer by AJCC v6 Stage | | NCIT:C91256 | Laryngeal Cancer by AJCC v7 Stage | | NCIT:C133156 | Laryngeal Cancer by AJCC v8 Stage | @@ -3974,7 +4096,7 @@ | NCIT:C173412 | Laryngeal Pleomorphic Adenoma | | NCIT:C173397 | Laryngeal Soft Tissue Neoplasm | | NCIT:C173408 | Laryngeal Soft Tissue Sarcoma | -| NCIT:C54336 | Laryngeal Squamous Cell Carcinoma, Spindle Cell Variant | +| NCIT:C54336 | Laryngeal Spindle Cell Squamous Carcinoma | | NCIT:C54339 | Laryngeal Undifferentiated Carcinoma | | NCIT:C4791 | Left Atrial Myxoma | | NCIT:C22147 | Leiomyoma of the Mouse Intestinal Tract | @@ -3990,6 +4112,7 @@ | NCIT:C23055 | Leiomyosarcoma of the Mouse Oral Cavity | | NCIT:C21749 | Leiomyosarcoma of the Mouse Prostate Gland | | NCIT:C21844 | Leiomyosarcoma of the Mouse Skin | +| NCIT:C204482 | Lentiginous Melanocytic Nevus | | NCIT:C43372 | Lentigo Maligna | | NCIT:C123160 | Lepidic Adenocarcinoma | | NCIT:C134530 | Leporine Experimental Organism Diagnosis | @@ -4115,7 +4238,9 @@ | NCIT:C27353 | Localized Peripheral Primitive Neuroectodermal Tumor of Bone | | NCIT:C45666 | Localized Pleural Malignant Mesothelioma | | NCIT:C27294 | Localized Primitive Neuroectodermal Tumor | +| NCIT:C201849 | Localized Prostate Adenocarcinoma | | NCIT:C176517 | Localized Prostate Carcinoma | +| NCIT:C205361 | Localized Renal Cell Carcinoma | | NCIT:C8167 | Localized Renal Pelvis and Ureter Urothelial Carcinoma | | NCIT:C9064 | Localized Resectable Adult Hepatocellular Carcinoma | | NCIT:C7877 | Localized Resectable Adult Liver Carcinoma | @@ -4134,15 +4259,18 @@ | NCIT:C171327 | Locally Advanced Ampulla of Vater Carcinoma | | NCIT:C168977 | Locally Advanced Anal Carcinoma | | NCIT:C146856 | Locally Advanced Angiosarcoma | +| NCIT:C203618 | Locally Advanced Appendix Adenocarcinoma | | NCIT:C156770 | Locally Advanced Basal Cell Carcinoma | | NCIT:C151971 | Locally Advanced Bile Duct Carcinoma | | NCIT:C168981 | Locally Advanced Biliary Tract Carcinoma | +| NCIT:C203407 | Locally Advanced Bladder Adenocarcinoma | | NCIT:C167071 | Locally Advanced Bladder Carcinoma | +| NCIT:C203415 | Locally Advanced Bladder Small Cell Neuroendocrine Carcinoma | +| NCIT:C203410 | Locally Advanced Bladder Squamous Cell Carcinoma | | NCIT:C162618 | Locally Advanced Bladder Urothelial Carcinoma | | NCIT:C153070 | Locally Advanced Bone Sarcoma | | NCIT:C165699 | Locally Advanced Breast Adenocarcinoma | | NCIT:C160920 | Locally Advanced Breast Carcinoma | -| NCIT:C187328 | Locally Advanced Carcinoid Tumor | | NCIT:C148130 | Locally Advanced Carcinoma | | NCIT:C156297 | Locally Advanced Cervical Adenocarcinoma | | NCIT:C156295 | Locally Advanced Cervical Carcinoma | @@ -4164,6 +4292,7 @@ | NCIT:C153358 | Locally Advanced Digestive System Carcinoma | | NCIT:C155934 | Locally Advanced Digestive System Neuroendocrine Carcinoma | | NCIT:C178271 | Locally Advanced Digestive System Neuroendocrine Neoplasm | +| NCIT:C204038 | Locally Advanced Digestive System Neuroendocrine Tumor | | NCIT:C187332 | Locally Advanced Digestive System Neuroendocrine Tumor G1 | | NCIT:C187341 | Locally Advanced Digestive System Neuroendocrine Tumor G2 | | NCIT:C192773 | Locally Advanced Digestive System Neuroendocrine Tumor G3 | @@ -4183,6 +4312,7 @@ | NCIT:C191991 | Locally Advanced Extrapulmonary Large Cell Neuroendocrine Carcinoma | | NCIT:C191983 | Locally Advanced Extrapulmonary Neuroendocrine Carcinoma | | NCIT:C191992 | Locally Advanced Extrapulmonary Small Cell Neuroendocrine Carcinoma | +| NCIT:C201951 | Locally Advanced Extraskeletal Myxoid Chondrosarcoma | | NCIT:C167202 | Locally Advanced Fallopian Tube Carcinoma | | NCIT:C171317 | Locally Advanced Fibrosarcoma | | NCIT:C170462 | Locally Advanced Gallbladder Carcinoma | @@ -4193,6 +4323,7 @@ | NCIT:C167069 | Locally Advanced Genitourinary System Carcinoma | | NCIT:C170980 | Locally Advanced Glioblastoma | | NCIT:C180876 | Locally Advanced Glioma | +| NCIT:C204437 | Locally Advanced HER2-Low Breast Carcinoma | | NCIT:C178348 | Locally Advanced HER2-Negative Breast Carcinoma | | NCIT:C181793 | Locally Advanced HER2-Positive Breast Carcinoma | | NCIT:C153213 | Locally Advanced Head and Neck Carcinoma | @@ -4204,6 +4335,7 @@ | NCIT:C165701 | Locally Advanced Hypopharyngeal Squamous Cell Carcinoma | | NCIT:C173814 | Locally Advanced Intrahepatic Cholangiocarcinoma | | NCIT:C172618 | Locally Advanced Kidney Carcinoma | +| NCIT:C203412 | Locally Advanced Kidney Medullary Carcinoma | | NCIT:C158910 | Locally Advanced Large Cell Neuroendocrine Carcinoma | | NCIT:C165560 | Locally Advanced Laryngeal Carcinoma | | NCIT:C165473 | Locally Advanced Laryngeal Squamous Cell Carcinoma | @@ -4240,12 +4372,14 @@ | NCIT:C168671 | Locally Advanced Myxofibrosarcoma | | NCIT:C185350 | Locally Advanced Nasal Cavity Squamous Cell Carcinoma | | NCIT:C167352 | Locally Advanced Nasopharyngeal Squamous Cell Carcinoma | +| NCIT:C203526 | Locally Advanced Neuroblastoma | | NCIT:C158909 | Locally Advanced Neuroendocrine Carcinoma | | NCIT:C167332 | Locally Advanced Neuroendocrine Neoplasm | | NCIT:C167333 | Locally Advanced Neuroendocrine Tumor | | NCIT:C171297 | Locally Advanced Non-Cutaneous Melanoma | | NCIT:C190773 | Locally Advanced Non-Muscle Invasive Bladder Carcinoma | | NCIT:C171296 | Locally Advanced Ocular Melanoma | +| NCIT:C203513 | Locally Advanced Olfactory Neuroblastoma | | NCIT:C171281 | Locally Advanced Oral Cavity Carcinoma | | NCIT:C165472 | Locally Advanced Oral Cavity Squamous Cell Carcinoma | | NCIT:C170782 | Locally Advanced Oropharyngeal Carcinoma | @@ -4268,8 +4402,10 @@ | NCIT:C185351 | Locally Advanced Paranasal Sinus Squamous Cell Carcinoma | | NCIT:C163958 | Locally Advanced Parathyroid Gland Carcinoma | | NCIT:C170789 | Locally Advanced Penile Carcinoma | +| NCIT:C203413 | Locally Advanced Penile Squamous Cell Carcinoma | | NCIT:C165561 | Locally Advanced Pharyngeal Carcinoma | | NCIT:C163956 | Locally Advanced Pituitary Neuroendocrine Tumor | +| NCIT:C204868 | Locally Advanced Platinum-Refractory Ovarian Carcinoma | | NCIT:C189978 | Locally Advanced Platinum-Resistant Ovarian Carcinoma | | NCIT:C175936 | Locally Advanced Pleural Malignant Mesothelioma | | NCIT:C180874 | Locally Advanced Primary Malignant Brain Neoplasm | @@ -4282,6 +4418,7 @@ | NCIT:C170778 | Locally Advanced Rectal Carcinoma | | NCIT:C170781 | Locally Advanced Rectal Squamous Cell Carcinoma | | NCIT:C168995 | Locally Advanced Renal Cell Carcinoma | +| NCIT:C172222 | Locally Advanced Renal Cell Carcinoma, Not Otherwise Specified | | NCIT:C172277 | Locally Advanced Renal Pelvis Carcinoma | | NCIT:C162617 | Locally Advanced Renal Pelvis Urothelial Carcinoma | | NCIT:C164159 | Locally Advanced Renal Pelvis and Ureter Urothelial Carcinoma | @@ -4289,6 +4426,7 @@ | NCIT:C158464 | Locally Advanced Salivary Gland Carcinoma | | NCIT:C153071 | Locally Advanced Sarcoma | | NCIT:C172219 | Locally Advanced Sarcomatoid Renal Cell Carcinoma | +| NCIT:C203515 | Locally Advanced Sinonasal Carcinoma | | NCIT:C154322 | Locally Advanced Sinonasal Squamous Cell Carcinoma | | NCIT:C153182 | Locally Advanced Skin Squamous Cell Carcinoma | | NCIT:C158915 | Locally Advanced Small Cell Neuroendocrine Carcinoma | @@ -4306,7 +4444,6 @@ | NCIT:C175507 | Locally Advanced Thyroid Gland Oncocytic Carcinoma | | NCIT:C175493 | Locally Advanced Transitional Cell Carcinoma | | NCIT:C175237 | Locally Advanced Triple-Negative Breast Carcinoma | -| NCIT:C172222 | Locally Advanced Unclassified Renal Cell Carcinoma | | NCIT:C160919 | Locally Advanced Undifferentiated Pleomorphic Sarcoma | | NCIT:C156789 | Locally Advanced Unresectable Basal Cell Carcinoma | | NCIT:C153475 | Locally Advanced Unresectable Bone Sarcoma | @@ -4317,6 +4454,7 @@ | NCIT:C187412 | Locally Advanced Unresectable Cholangiocarcinoma | | NCIT:C162271 | Locally Advanced Unresectable Colon Adenocarcinoma | | NCIT:C162270 | Locally Advanced Unresectable Colorectal Adenocarcinoma | +| NCIT:C202500 | Locally Advanced Unresectable Digestive System Adenocarcinoma | | NCIT:C158090 | Locally Advanced Unresectable Digestive System Neuroendocrine Neoplasm | | NCIT:C187406 | Locally Advanced Unresectable Endometrial Carcinoma | | NCIT:C162113 | Locally Advanced Unresectable Esophageal Adenocarcinoma | @@ -4332,6 +4470,7 @@ | NCIT:C164247 | Locally Advanced Unresectable Malignant PEComa | | NCIT:C187393 | Locally Advanced Unresectable Ovarian High Grade Serous Adenocarcinoma | | NCIT:C155743 | Locally Advanced Unresectable Pancreatic Adenocarcinoma | +| NCIT:C205226 | Locally Advanced Unresectable Pancreatic Ductal Adenocarcinoma | | NCIT:C176728 | Locally Advanced Unresectable Primary Central Chondrosarcoma | | NCIT:C187389 | Locally Advanced Unresectable Primary Peritoneal Carcinoma | | NCIT:C156289 | Locally Advanced Unresectable Prostate Adenocarcinoma | @@ -4343,6 +4482,7 @@ | NCIT:C187402 | Locally Advanced Unresectable Triple-Negative Breast Carcinoma | | NCIT:C190138 | Locally Advanced Unresectable Uveal Melanoma | | NCIT:C162616 | Locally Advanced Ureter Urothelial Carcinoma | +| NCIT:C7639 | Locally Advanced Urethral Carcinoma | | NCIT:C162619 | Locally Advanced Urethral Urothelial Carcinoma | | NCIT:C157636 | Locally Advanced Urothelial Carcinoma | | NCIT:C188208 | Locally Advanced Uterine Corpus Leiomyosarcoma | @@ -4376,14 +4516,13 @@ | NCIT:C6816 | Low Grade B-Cell Non-Hodgkin's Lymphoma | | NCIT:C172804 | Low Grade Biliary Intraepithelial Neoplasia | | NCIT:C40362 | Low Grade Breast Adenosquamous Carcinoma | -| NCIT:C5168 | Low Grade Breast Mucoepidermoid Carcinoma | | NCIT:C126480 | Low Grade Broad Ligament Serous Adenocarcinoma | | NCIT:C7674 | Low Grade Cervical Glandular Intraepithelial Neoplasia | | NCIT:C4630 | Low Grade Cervical Intraepithelial Neoplasia | | NCIT:C40196 | Low Grade Cervical Squamous Intraepithelial Neoplasia | +| NCIT:C204979 | Low Grade Conjunctival Melanocytic Intraepithelial Lesion | | NCIT:C6097 | Low Grade Conjunctival Squamous Intraepithelial Neoplasia | | NCIT:C6094 | Low Grade Corneal Squamous Intraepithelial Neoplasia | -| NCIT:C180510 | Low Grade Endometrial Endometrioid Adenocarcinoma | | NCIT:C199146 | Low Grade Endometrioid Adenocarcinoma | | NCIT:C4263 | Low Grade Endometrioid Stromal Sarcoma | | NCIT:C27428 | Low Grade Esophageal Glandular Intraepithelial Neoplasia | @@ -4402,10 +4541,10 @@ | NCIT:C9026 | Low Grade Malignant Peripheral Nerve Sheath Tumor | | NCIT:C21668 | Low Grade Mouse MIN | | NCIT:C21729 | Low Grade Mouse Prostatic Intraepithelial Neoplasia | +| NCIT:C203946 | Low Grade Mucinous Carcinoma Peritonei | | NCIT:C23138 | Low Grade Mucoepidermoid Tumor of the Mouse Salivary Glands | | NCIT:C49024 | Low Grade Myofibroblastic Sarcoma | | NCIT:C197815 | Low Grade Osteosarcoma | -| NCIT:C199159 | Low Grade Ovarian Endometrioid Adenocarcinoma | | NCIT:C172803 | Low Grade Pancreatic Intraepithelial Neoplasia | | NCIT:C180670 | Low Grade Papillary Schneiderian Carcinoma | | NCIT:C6851 | Low Grade Paranasal Sinus Sarcoma | @@ -4413,8 +4552,6 @@ | NCIT:C22144 | Low Grade Pedunculated Tubulovillous Dysplasia of the Mouse Intestinal Tract | | NCIT:C7666 | Low Grade Penile Intraepithelial Neoplasia | | NCIT:C5542 | Low Grade Prostatic Intraepithelial Neoplasia | -| NCIT:C8012 | Low Grade Salivary Gland Carcinoma | -| NCIT:C8015 | Low Grade Salivary Gland Mucoepidermoid Carcinoma | | NCIT:C9417 | Low Grade Sarcoma | | NCIT:C22121 | Low Grade Sessile Tubular Dysplasia of the Mouse Intestinal Tract | | NCIT:C22127 | Low Grade Sessile Tubulovillous Dysplasia of the Mouse Intestinal Tract | @@ -4428,6 +4565,7 @@ | NCIT:C27242 | Low Risk Gastrointestinal Stromal Tumor | | NCIT:C27244 | Low Risk Small Intestinal Gastrointestinal Stromal Tumor | | NCIT:C187273 | Low Risk Thyroid Gland Neoplasm | +| NCIT:C204843 | Low-CSD Melanoma, Superficial Spreading Melanoma Subtype | | NCIT:C199213 | Low-Hypodiploid B Acute Lymphoblastic Leukemia | | NCIT:C170776 | Lower Alveolar Ridge Squamous Cell Carcinoma | | NCIT:C8393 | Lower Gingival Carcinoma | @@ -4490,16 +4628,11 @@ | NCIT:C136492 | Lung Adenosquamous Carcinoma by AJCC v7 Stage | | NCIT:C173809 | Lung Alveolar Soft Part Sarcoma | | NCIT:C188082 | Lung Anaplastic Large Cell Lymphoma | -| NCIT:C45551 | Lung Atypical Carcinoid Tumor | | NCIT:C45507 | Lung Basaloid Squamous Cell Carcinoma | | NCIT:C45632 | Lung Biphasic Synovial Sarcoma | | NCIT:C90519 | Lung Cancer by AJCC v6 Stage | | NCIT:C91232 | Lung Cancer by AJCC v7 Stage | | NCIT:C136467 | Lung Cancer by AJCC v8 Stage | -| NCIT:C36305 | Lung Carcinoma Metastatic in the Bone | -| NCIT:C36304 | Lung Carcinoma Metastatic in the Brain | -| NCIT:C133503 | Lung Carcinoma Metastatic in the Central Nervous System | -| NCIT:C36306 | Lung Carcinoma Metastatic in the Liver | | NCIT:C45543 | Lung Carcinosarcoma | | NCIT:C45629 | Lung Chondroma | | NCIT:C45516 | Lung Clear Cell Adenocarcinoma | @@ -4525,6 +4658,8 @@ | NCIT:C142829 | Lung Myoepithelioma | | NCIT:C5657 | Lung Myolipoma | | NCIT:C45569 | Lung Neuroendocrine Carcinoma | +| NCIT:C45550 | Lung Neuroendocrine Tumor G1 | +| NCIT:C45551 | Lung Neuroendocrine Tumor G2 | | NCIT:C136714 | Lung Non-Keratinizing Squamous Cell Carcinoma | | NCIT:C136716 | Lung Non-Mucinous Adenocarcinoma In Situ | | NCIT:C136491 | Lung Non-Small Cell Cancer by AJCC v7 Stage | @@ -4555,7 +4690,6 @@ | NCIT:C45573 | Lung Squamous Papilloma | | NCIT:C45631 | Lung Synovial Sarcoma | | NCIT:C45637 | Lung Teratoma | -| NCIT:C45550 | Lung Typical Carcinoid Tumor | | NCIT:C27500 | Lymphadenopathic Kaposi Sarcoma | | NCIT:C45485 | Lymphangioma Circumscriptum | | NCIT:C8373 | Lymphangiomatosis | @@ -4594,6 +4728,7 @@ | NCIT:C148394 | MCD Diffuse Large B-Cell Lymphoma | | NCIT:C154335 | MGMT-Methylated Glioblastoma | | NCIT:C132902 | MGMT-Unmethylated Glioblastoma | +| NCIT:C204739 | MITF Pathway-Activated Melanocytic Tumor | | NCIT:C198069 | MS Childhood Neuroblastoma by Toronto Guidelines v2 | | NCIT:C178235 | MYOD1-Mutant Spindle Cell/Sclerosing Rhabdomyosarcoma | | NCIT:C182077 | Macaca mulatta Hepatocellular Carcinoma | @@ -4644,6 +4779,8 @@ | NCIT:C4205 | Malignant Granulosa Cell Tumor | | NCIT:C63986 | Malignant Granulosa Cell Tumor of the Rat Ovary | | NCIT:C43310 | Malignant Hair Follicle Neoplasm | +| NCIT:C202983 | Malignant Head and Neck Germ Cell Tumor | +| NCIT:C202625 | Malignant Head and Neck Soft Tissue Neoplasm | | NCIT:C9393 | Malignant Hemangiopericytoma NCI Grade 2 | | NCIT:C9394 | Malignant Hemangiopericytoma NCI Grade 3 | | NCIT:C8609 | Malignant Hepatobiliary Neoplasm | @@ -4654,7 +4791,6 @@ | NCIT:C174026 | Malignant Inner Ear Neoplasm | | NCIT:C5403 | Malignant Intracranial Germ Cell Tumor | | NCIT:C5114 | Malignant Intracranial Neoplasm | -| NCIT:C7045 | Malignant Intracranial Neoplasm by Morphology | | NCIT:C64047 | Malignant Intraocular Schwannoma of the Rat Eyeball | | NCIT:C170919 | Malignant Jejunal Neoplasm | | NCIT:C120456 | Malignant Kidney Neoplasm Except Pelvis | @@ -4677,11 +4813,11 @@ | NCIT:C27266 | Malignant Lymphoma, Non-Cleaved, Diffuse | | NCIT:C22059 | Malignant Lymphomas of the Mouse Nervous System | | NCIT:C8991 | Malignant Mastocytosis | +| NCIT:C202262 | Malignant Maxillofacial Neoplasm | | NCIT:C146848 | Malignant Mediastinal Germ Cell Tumor Stage Grouping of the Pediatric Study Group | | NCIT:C45733 | Malignant Mediastinal Germ Cell Tumor with Associated Hematologic Malignancy | | NCIT:C6439 | Malignant Mediastinal Nongerminomatous Germ Cell Tumor | | NCIT:C63917 | Malignant Medullary Tumor of the Rat Adrenal Gland | -| NCIT:C66753 | Malignant Melanoma in Precancerous Melanosis | | NCIT:C22054 | Malignant Melanoma of the Mouse Nervous System | | NCIT:C64048 | Malignant Melanoma of the Rat Cerebral Meninx | | NCIT:C64123 | Malignant Melanoma of the Rat Skin | @@ -4730,13 +4866,13 @@ | NCIT:C24087 | Malignant Mouse Uterine Corpus Neoplasm | | NCIT:C24066 | Malignant Mouse Uterine Neoplasms | | NCIT:C166357 | Malignant Musculoskeletal Neoplasm | +| NCIT:C202985 | Malignant Nasopharyngeal Germ Cell Tumor | | NCIT:C36041 | Malignant Neoplasm by Grade | | NCIT:C139565 | Malignant Neoplasm of Lung - Multiple Primary Sites | | NCIT:C35427 | Malignant Neoplasm of Multiple Primary Sites | | NCIT:C3535 | Malignant Neoplasm of the Lower Third of the Esophagus | | NCIT:C3534 | Malignant Neoplasm of the Middle Third of the Esophagus | | NCIT:C3533 | Malignant Neoplasm of the Upper Third of the Esophagus | -| NCIT:C8512 | Malignant Neoplasm with Regional Lymph Node Involvement | | NCIT:C65153 | Malignant Neoplasm, Uncertain Whether Primary or Metastatic | | NCIT:C38772 | Malignant Neoplasms of Mouse Liver | | NCIT:C22151 | Malignant Neoplasms of the Mouse Intestinal Tract | @@ -4796,6 +4932,7 @@ | NCIT:C63989 | Malignant Sertoli Cell Tumor of the Rat Ovary | | NCIT:C64058 | Malignant Sertoli Cell Tumor of the Rat Testis | | NCIT:C67561 | Malignant Sex Cord-Stromal Tumor | +| NCIT:C202984 | Malignant Sinonasal Germ Cell Tumor | | NCIT:C173097 | Malignant Sinonasal Neoplasm | | NCIT:C173176 | Malignant Sinonasal Soft Tissue Neoplasm | | NCIT:C4573 | Malignant Skin Appendage Neoplasm | @@ -4867,9 +5004,11 @@ | NCIT:C173843 | Maxillofacial Mesenchymal Chondrosarcoma | | NCIT:C173845 | Maxillofacial Neoplasm | | NCIT:C173899 | Maxillofacial Osteoblastoma | +| NCIT:C202260 | Maxillofacial Osteochondroma | | NCIT:C173898 | Maxillofacial Osteoid Osteoma | | NCIT:C173894 | Maxillofacial Osteoma | | NCIT:C173844 | Maxillofacial Osteosarcoma | +| NCIT:C202264 | Maxillofacial Rhabdomyosarcoma with TFCP2 Rearrangement | | NCIT:C173841 | Maxillofacial Sarcoma | | NCIT:C6424 | Meckel Diverticulum Neuroendocrine Tumor G1 | | NCIT:C134571 | Medaka Hepatoma | @@ -4925,12 +5064,13 @@ | NCIT:C21782 | Melanocytic Proliferative Disorders of Mouse | | NCIT:C9498 | Melanocytoma | | NCIT:C22053 | Melanocytoma of the Mouse Nervous System | -| NCIT:C4240 | Melanoma Arising from Blue Nevus | +| NCIT:C4240 | Melanoma Arising in Blue Nevus | +| NCIT:C48613 | Melanoma Arising in Congenital Melanocytic Nevus | | NCIT:C4235 | Melanoma Arising in Giant Congenital Nevus | -| NCIT:C179206 | Melanoma Metastatic in the Brain | -| NCIT:C133504 | Melanoma Metastatic in the Central Nervous System | -| NCIT:C48613 | Melanoma in Congenital Melanocytic Nevus | +| NCIT:C204864 | Melanoma in Chronically Sun-Exposed Skin | +| NCIT:C204840 | Melanoma in Intermittently Sun-Exposed Skin | | NCIT:C4232 | Melanoma in Junctional Nevus | +| NCIT:C66753 | Melanoma in Precancerous Melanosis | | NCIT:C154473 | Melanoma of Unknown Primary | | NCIT:C23098 | Melanoma of the Mouse Nose and Paranasal Sinuses | | NCIT:C23062 | Melanoma of the Mouse Oral Cavity | @@ -4948,10 +5088,8 @@ | NCIT:C7051 | Meningioma by Site | | NCIT:C3707 | Meningiomatosis | | NCIT:C6971 | Meningothelial Cell Neoplasm | -| NCIT:C136869 | Merkel Cell Carcinoma by AJCC v7 Stage | -| NCIT:C136871 | Merkel Cell Carcinoma by AJCC v8 Clinical Stage | -| NCIT:C136880 | Merkel Cell Carcinoma by AJCC v8 Pathologic Stage | -| NCIT:C136870 | Merkel Cell Carcinoma by AJCC v8 Stage | +| NCIT:C204385 | Merkel Cell Polyoma Virus-Negative Merkel Cell Carcinoma | +| NCIT:C204383 | Merkel Cell Polyoma Virus-Positive Merkel Cell Carcinoma | | NCIT:C53493 | Mesenchymal Chondrosarcoma of Bone | | NCIT:C22974 | Mesenchymal Chondrosarcoma of the Mouse Skeletal System | | NCIT:C22029 | Mesenchymal Non-meningothelial Tumours of the Mouse Nervous System | @@ -4998,6 +5136,7 @@ | NCIT:C36264 | Metastatic Benign Neoplasm | | NCIT:C142869 | Metastatic Bile Duct Carcinoma | | NCIT:C162751 | Metastatic Biliary Tract Carcinoma | +| NCIT:C203406 | Metastatic Bladder Adenocarcinoma | | NCIT:C156062 | Metastatic Bladder Carcinoma | | NCIT:C157768 | Metastatic Bladder Clear Cell (Glycogen-Rich) Urothelial Carcinoma | | NCIT:C157769 | Metastatic Bladder Giant Cell Urothelial Carcinoma | @@ -5015,6 +5154,12 @@ | NCIT:C153073 | Metastatic Bone Sarcoma | | NCIT:C165698 | Metastatic Breast Adenocarcinoma | | NCIT:C153238 | Metastatic Breast Carcinoma | +| NCIT:C36303 | Metastatic Breast Carcinoma in the Bone | +| NCIT:C36301 | Metastatic Breast Carcinoma in the Brain | +| NCIT:C133501 | Metastatic Breast Carcinoma in the Central Nervous System | +| NCIT:C36302 | Metastatic Breast Carcinoma in the Liver | +| NCIT:C36300 | Metastatic Breast Carcinoma in the Lung | +| NCIT:C153227 | Metastatic Breast Carcinoma in the Lymph Nodes | | NCIT:C28311 | Metastatic Breast Carcinoma in the Skin | | NCIT:C76326 | Metastatic Breast Ductal Carcinoma | | NCIT:C181787 | Metastatic Breast Inflammatory Carcinoma | @@ -5023,7 +5168,6 @@ | NCIT:C5171 | Metastatic Breast Neuroendocrine Tumor G1 | | NCIT:C5176 | Metastatic Breast Signet Ring Cell Carcinoma | | NCIT:C5178 | Metastatic Breast Squamous Cell Carcinoma | -| NCIT:C6431 | Metastatic Carcinoid Tumor | | NCIT:C27381 | Metastatic Carcinoma in the Adrenal Cortex | | NCIT:C96767 | Metastatic Carcinoma in the Liver | | NCIT:C27408 | Metastatic Carcinoma in the Lung | @@ -5047,7 +5191,6 @@ | NCIT:C198189 | Metastatic Childhood Hepatoblastoma by Toronto Guidelines v2, Tier 1 | | NCIT:C198192 | Metastatic Childhood Hepatoblastoma by Toronto Guidelines v2, Tier 2 | | NCIT:C198173 | Metastatic Childhood Malignant Bone Neoplasm by Toronto Guidelines v2 | -| NCIT:C187212 | Metastatic Childhood Malignant Brain Neoplasm | | NCIT:C198088 | Metastatic Childhood Malignant Kidney Neoplasm Excluding Renal Cell Carcinoma by Toronto Guidelines v2, Children's Oncology Group (COG) Protocol | | NCIT:C198079 | Metastatic Childhood Malignant Kidney Neoplasm Excluding Renal Cell Carcinoma by Toronto Guidelines v2, International Society of Pediatric Oncology (SIOP) Protocol | | NCIT:C187211 | Metastatic Childhood Malignant Neoplasm in the Brain | @@ -5055,6 +5198,7 @@ | NCIT:C198067 | Metastatic Childhood Neuroblastoma by Toronto Guidelines v2 | | NCIT:C198163 | Metastatic Childhood Non-Rhabdomyosarcoma Soft Tissue Sarcoma by Toronto Guidelines v2 | | NCIT:C198441 | Metastatic Childhood Ovarian Germ Cell Tumor by Toronto Guidelines v2 | +| NCIT:C187212 | Metastatic Childhood Primary Malignant Brain Neoplasm | | NCIT:C198178 | Metastatic Childhood Retinoblastoma by Toronto Guidelines v2 | | NCIT:C198154 | Metastatic Childhood Rhabdomyosarcoma by Toronto Guidelines v2 | | NCIT:C8066 | Metastatic Childhood Soft Tissue Sarcoma | @@ -5082,6 +5226,7 @@ | NCIT:C163967 | Metastatic Digestive System Mixed Adenoneuroendocrine Carcinoma | | NCIT:C155936 | Metastatic Digestive System Neuroendocrine Carcinoma | | NCIT:C156492 | Metastatic Digestive System Neuroendocrine Neoplasm | +| NCIT:C204037 | Metastatic Digestive System Neuroendocrine Tumor | | NCIT:C115245 | Metastatic Digestive System Neuroendocrine Tumor G1 | | NCIT:C179415 | Metastatic Digestive System Neuroendocrine Tumor G2 | | NCIT:C192769 | Metastatic Digestive System Neuroendocrine Tumor G3 | @@ -5165,11 +5310,15 @@ | NCIT:C178558 | Metastatic Low Grade Glioma | | NCIT:C155908 | Metastatic Lung Adenocarcinoma | | NCIT:C156093 | Metastatic Lung Adenosquamous Carcinoma | -| NCIT:C177243 | Metastatic Lung Carcinoid Tumor | | NCIT:C153202 | Metastatic Lung Carcinoma | +| NCIT:C36305 | Metastatic Lung Carcinoma in the Bone | +| NCIT:C36304 | Metastatic Lung Carcinoma in the Brain | +| NCIT:C133503 | Metastatic Lung Carcinoma in the Central Nervous System | +| NCIT:C36306 | Metastatic Lung Carcinoma in the Liver | | NCIT:C177799 | Metastatic Lung Large Cell Neuroendocrine Carcinoma | | NCIT:C192797 | Metastatic Lung Neuroendocrine Carcinoma | | NCIT:C157602 | Metastatic Lung Neuroendocrine Neoplasm | +| NCIT:C177243 | Metastatic Lung Neuroendocrine Tumor | | NCIT:C156094 | Metastatic Lung Non-Small Cell Carcinoma | | NCIT:C157364 | Metastatic Lung Non-Small Cell Squamous Carcinoma | | NCIT:C128798 | Metastatic Lung Non-Squamous Non-Small Cell Carcinoma | @@ -5282,6 +5431,11 @@ | NCIT:C25771 | Metastatic Malignant Testicular Germ Cell Tumor | | NCIT:C176862 | Metastatic Malignant Thoracic Neoplasm | | NCIT:C177725 | Metastatic Medulloblastoma | +| NCIT:C179206 | Metastatic Melanoma in the Brain | +| NCIT:C133504 | Metastatic Melanoma in the Central Nervous System | +| NCIT:C205131 | Metastatic Melanoma in the Lymph Nodes | +| NCIT:C205130 | Metastatic Melanoma in the Skin | +| NCIT:C205132 | Metastatic Melanoma in the Viscera | | NCIT:C5274 | Metastatic Meningioma | | NCIT:C162572 | Metastatic Merkel Cell Carcinoma | | NCIT:C185381 | Metastatic Mesonephric Adenocarcinoma | @@ -5301,7 +5455,7 @@ | NCIT:C167236 | Metastatic Nasal Cavity Squamous Cell Carcinoma | | NCIT:C156079 | Metastatic Nasopharyngeal Carcinoma | | NCIT:C156077 | Metastatic Nasopharyngeal Keratinizing Squamous Cell Carcinoma | -| NCIT:C177153 | Metastatic Nasopharyngeal Nonkeratinizing Carcinoma | +| NCIT:C177153 | Metastatic Nasopharyngeal Non-Keratinizing Carcinoma | | NCIT:C150209 | Metastatic Nasopharyngeal Squamous Cell Carcinoma | | NCIT:C156078 | Metastatic Nasopharyngeal Undifferentiated Carcinoma | | NCIT:C24162 | Metastatic Neoplasm to the Mouse Gallbladder | @@ -5316,6 +5470,7 @@ | NCIT:C190772 | Metastatic Non-Muscle Invasive Bladder Carcinoma | | NCIT:C165537 | Metastatic Non-Small Cell Carcinoma | | NCIT:C171295 | Metastatic Ocular Melanoma | +| NCIT:C203511 | Metastatic Olfactory Neuroblastoma | | NCIT:C156089 | Metastatic Oral Cavity Adenoid Cystic Carcinoma | | NCIT:C156087 | Metastatic Oral Cavity Carcinoma | | NCIT:C156090 | Metastatic Oral Cavity Mucoepidermoid Carcinoma | @@ -5361,8 +5516,11 @@ | NCIT:C156080 | Metastatic Pharyngeal Carcinoma | | NCIT:C173685 | Metastatic Pharyngeal Squamous Cell Carcinoma | | NCIT:C191697 | Metastatic Plasmacytoid Urothelial Carcinoma | +| NCIT:C204865 | Metastatic Platinum-Refractory Ovarian Carcinoma | +| NCIT:C203313 | Metastatic Platinum-Resistant Fallopian Tube Carcinoma | | NCIT:C170957 | Metastatic Platinum-Resistant Malignant Germ Cell Tumor | | NCIT:C179460 | Metastatic Platinum-Resistant Ovarian Carcinoma | +| NCIT:C203314 | Metastatic Platinum-Resistant Primary Peritoneal Carcinoma | | NCIT:C182025 | Metastatic Pleomorphic Liposarcoma | | NCIT:C168545 | Metastatic Pleural Malignant Mesothelioma | | NCIT:C174046 | Metastatic Poorly Differentiated Thyroid Gland Carcinoma | @@ -5383,6 +5541,7 @@ | NCIT:C156098 | Metastatic Rectal Carcinoma | | NCIT:C170779 | Metastatic Rectal Squamous Cell Carcinoma | | NCIT:C150595 | Metastatic Renal Cell Carcinoma | +| NCIT:C171583 | Metastatic Renal Cell Carcinoma, Not Otherwise Specified | | NCIT:C163965 | Metastatic Renal Pelvis Carcinoma | | NCIT:C150514 | Metastatic Renal Pelvis Urothelial Carcinoma | | NCIT:C8064 | Metastatic Renal Pelvis and Ureter Urothelial Carcinoma | @@ -5393,6 +5552,7 @@ | NCIT:C199665 | Metastatic Salivary Gland Adenocarcinoma | | NCIT:C199664 | Metastatic Salivary Gland Adenocarcinoma, Not Otherwise Specified | | NCIT:C158463 | Metastatic Salivary Gland Carcinoma | +| NCIT:C203380 | Metastatic Salivary Gland Secretory Carcinoma | | NCIT:C172649 | Metastatic Salivary Gland Squamous Cell Carcinoma | | NCIT:C152076 | Metastatic Sarcoma | | NCIT:C179657 | Metastatic Sarcoma in the Peritoneum | @@ -5426,7 +5586,6 @@ | NCIT:C153348 | Metastatic Triple-Negative Breast Carcinoma | | NCIT:C185954 | Metastatic Triple-Negative Breast Inflammatory Carcinoma | | NCIT:C22077 | Metastatic Tumours of the Mouse Nervous System | -| NCIT:C171583 | Metastatic Unclassified Renal Cell Carcinoma | | NCIT:C4926 | Metastatic Undifferentiated Pleomorphic Sarcoma | | NCIT:C156788 | Metastatic Unresectable Basal Cell Carcinoma | | NCIT:C153315 | Metastatic Unresectable Carcinoma | @@ -5475,8 +5634,11 @@ | NCIT:C180332 | Microsatellite Stable Ovarian Carcinoma | | NCIT:C177776 | Microsatellite Stable Rectal Carcinoma | | NCIT:C45708 | Microscopic Thymoma | -| NCIT:C91741 | Middle Ear Carcinoma In Situ | | NCIT:C188115 | Middle Ear Embryonal Rhabdomyosarcoma | +| NCIT:C202584 | Middle Ear Exophytic Sinonasal-Type Papilloma | +| NCIT:C202583 | Middle Ear Inverted Sinonasal-Type Papilloma | +| NCIT:C202585 | Middle Ear Oncocytic Sinonasal-Type Papilloma | +| NCIT:C202582 | Middle Ear Papilloma | | NCIT:C6085 | Middle Ear Paraganglioma | | NCIT:C167327 | Midgut Neuroendocrine Tumor | | NCIT:C6422 | Midgut Neuroendocrine Tumor G1 | @@ -5491,6 +5653,7 @@ | NCIT:C180880 | Minor Salivary Gland Intraductal Papillary Neoplasm | | NCIT:C180881 | Minor Salivary Gland Intraductal Papillary-Mucinous Neoplasm | | NCIT:C5953 | Minor Salivary Gland Mucoepidermoid Carcinoma | +| NCIT:C201832 | Minor Salivary Gland Sclerosing Microcystic Adenocarcinoma | | NCIT:C5956 | Minor Salivary Gland Small Cell Neuroendocrine Carcinoma | | NCIT:C5959 | Minor Salivary Gland Squamous Cell Carcinoma | | NCIT:C5954 | Minor Salivary Gland Undifferentiated Carcinoma | @@ -5502,7 +5665,6 @@ | NCIT:C27793 | Mixed Cell Type Gastrointestinal Stromal Tumor | | NCIT:C141224 | Mixed Cellularity Classic Hodgkin Lymphoma by Ann Arbor Stage | | NCIT:C97058 | Mixed Congenital Mesoblastic Nephroma | -| NCIT:C43312 | Mixed Epithelial and Mesenchymal Hair Follicle Neoplasm | | NCIT:C63903 | Mixed Focus of Cellular Alteration of the Rat | | NCIT:C155767 | Mixed Gangliocytoma-Pituitary Neuroendocrine Tumor | | NCIT:C22071 | Mixed Germ Cell Tumours of the Mouse Nervous System | @@ -6030,6 +6192,7 @@ | NCIT:C133187 | Mucosal Melanoma of the Head and Neck | | NCIT:C133186 | Mucosal Melanoma of the Head and Neck by AJCC v7 Stage | | NCIT:C178453 | Mucosal Melanoma of the Urinary System | +| NCIT:C204907 | Mucosal Nevus | | NCIT:C166405 | Mucosal Nodular Melanoma | | NCIT:C7744 | Mucous Membrane Hemangioma | | NCIT:C64296 | Mucus Cell Hyperplasia of the Rat Bronchiole | @@ -6070,6 +6233,7 @@ | NCIT:C141142 | Mycosis Fungoides and Sezary Syndrome by AJCC v7 Stage | | NCIT:C141346 | Mycosis Fungoides and Sezary Syndrome by AJCC v8 Stage | | NCIT:C141143 | Mycosis Fungoides by AJCC v7 Stage | +| NCIT:C203443 | Myelodysplastic Chronic Myelomonocytic Leukemia | | NCIT:C27722 | Myelodysplastic Syndrome Post Cytotoxic Therapy | | NCIT:C200376 | Myelodysplastic Syndrome with Biallelic TP53 Inactivation | | NCIT:C200381 | Myelodysplastic Syndrome with Biallelic TP53 Mutation | @@ -6099,10 +6263,11 @@ | NCIT:C27780 | Myelodysplastic/Myeloproliferative Neoplasm, Not Otherwise Specified | | NCIT:C21898 | Myeloid Dysplasia of Mouse | | NCIT:C43223 | Myeloid Leukemia Associated with Down Syndrome | -| NCIT:C3176 | Myeloid Leukemia, Philadelphia- Negative | +| NCIT:C3176 | Myeloid Leukemia, Philadelphia-Negative | | NCIT:C198593 | Myeloid Neoplasm with Mutated TP53 | | NCIT:C198565 | Myeloid/Lymphoid Neoplasms with ETV6-ABL1 | | NCIT:C198559 | Myeloid/Lymphoid Neoplasms with FLT3 Rearrangement | +| NCIT:C203444 | Myeloproliferative Chronic Myelomonocytic Leukemia | | NCIT:C198555 | Myeloproliferative Neoplasm, BCR-ABL1 Negative | | NCIT:C21687 | Myoepithelial Carcinoma of the Mouse Mammary Gland | | NCIT:C21688 | Myoepithelial and Mixed Glandular Myoepithelial Carcinoma of the Mouse Mammary Gland | @@ -6121,36 +6286,48 @@ | NCIT:C164313 | NF1-Associated Malignant Peripheral Nerve Sheath Tumor | | NCIT:C128697 | NK-Cell Lymphoma, Unclassifiable | | NCIT:C178426 | NTRK-Rearranged Spindle Cell Neoplasm | +| NCIT:C204889 | Nail Apparatus Melanoma | | NCIT:C165662 | Nail Matrix Nevus | | NCIT:C188081 | Nasal Cavity Diffuse Large B-Cell Lymphoma | | NCIT:C54347 | Nasal Cavity Exophytic Papilloma | | NCIT:C173173 | Nasal Cavity Extranodal NK/T-Cell Lymphoma | | NCIT:C54285 | Nasal Cavity Keratinizing Squamous Cell Carcinoma | +| NCIT:C203005 | Nasal Cavity Large Cell Neuroendocrine Carcinoma | +| NCIT:C202996 | Nasal Cavity Neuroendocrine Carcinoma | +| NCIT:C202992 | Nasal Cavity Neuroendocrine Neoplasm | +| NCIT:C202994 | Nasal Cavity Neuroendocrine Tumor | +| NCIT:C203008 | Nasal Cavity Neuroendocrine Tumor G1 | +| NCIT:C203011 | Nasal Cavity Neuroendocrine Tumor G2 | | NCIT:C6075 | Nasal Cavity Non-Hodgkin Lymphoma | | NCIT:C164256 | Nasal Cavity Papilloma | +| NCIT:C203002 | Nasal Cavity Small Cell Neuroendocrine Carcinoma | | NCIT:C141296 | Nasal Type NK/T-Cell Lymphoma by Ann Arbor Stage | | NCIT:C175259 | Nasolacrimal Duct Neoplasm | | NCIT:C173340 | Nasopharyngeal Adenoid Cystic Carcinoma | -| NCIT:C54360 | Nasopharyngeal Basaloid Carcinoma | +| NCIT:C54360 | Nasopharyngeal Basaloid Squamous Cell Carcinoma | | NCIT:C90522 | Nasopharyngeal Carcinoma by AJCC v6 Stage | | NCIT:C91244 | Nasopharyngeal Carcinoma by AJCC v7 Stage | | NCIT:C132816 | Nasopharyngeal Carcinoma by AJCC v8 Stage | | NCIT:C54389 | Nasopharyngeal Differentiated Carcinoma | +| NCIT:C202979 | Nasopharyngeal Germ Cell Tumor | | NCIT:C173361 | Nasopharyngeal Hodgkin Lymphoma | | NCIT:C7992 | Nasopharyngeal Keratinizing Squamous Cell Carcinoma | +| NCIT:C203015 | Nasopharyngeal Large Cell Neuroendocrine Carcinoma | +| NCIT:C54400 | Nasopharyngeal Low Grade Papillary Adenocarcinoma | | NCIT:C173357 | Nasopharyngeal Lymphoma | | NCIT:C178522 | Nasopharyngeal Melanoma | +| NCIT:C203013 | Nasopharyngeal Neuroendocrine Carcinoma | | NCIT:C173359 | Nasopharyngeal Non-Hodgkin Lymphoma | -| NCIT:C7373 | Nasopharyngeal Nonkeratinizing Carcinoma | -| NCIT:C54400 | Nasopharyngeal Papillary Adenocarcinoma | +| NCIT:C7373 | Nasopharyngeal Non-Keratinizing Carcinoma | | NCIT:C48316 | Nasopharyngeal Paraganglioma | | NCIT:C173352 | Nasopharyngeal Pituitary Neuroendocrine Tumor | | NCIT:C6034 | Nasopharyngeal Polyp | +| NCIT:C203014 | Nasopharyngeal Small Cell Neuroendocrine Carcinoma | | NCIT:C6037 | Nasopharyngeal Squamous Papilloma | +| NCIT:C202982 | Nasopharyngeal Teratoma | | NCIT:C82217 | Natural Killer Cell Lymphoblastic Leukemia/Lymphoma | | NCIT:C199215 | Near-Haploid B Acute Lymphoblastic Leukemia | | NCIT:C6077 | Neck Carcinoma | -| NCIT:C173585 | Neck Carcinoma of Unknown Primary | | NCIT:C27648 | Neck Disorder | | NCIT:C7713 | Neck Squamous Cell Carcinoma of Unknown Primary | | NCIT:C36029 | Necrotic Neoplasm | @@ -6182,13 +6359,14 @@ | NCIT:C22150 | Neuroendocrine Adenoma of the Mouse Intestinal Tract | | NCIT:C163975 | Neuroendocrine Carcinoma of Unknown Primary | | NCIT:C21778 | Neuroendocrine Carcinoma of the Mouse Pulmonary System | -| NCIT:C173385 | Neuroendocrine Carcinoma, Excluding Head and Neck | | NCIT:C22163 | Neuroendocrine Cell Carcinoma of the Mouse Intestinal Tract | | NCIT:C22101 | Neuroendocrine Cell Hyperplasia of the Mouse Intestinal Tract | | NCIT:C63890 | Neuroendocrine Cell Hyperplasia of the Rat Glandular Stomach | | NCIT:C21758 | Neuroendocrine Hyperplasia of the Mouse Pulmonary System | | NCIT:C23123 | Neuroendocrine Neoplasms of the Mouse Larynx | | NCIT:C188218 | Neuroendocrine Tumor | +| NCIT:C203250 | Neuroendocrine Tumor G1 | +| NCIT:C203251 | Neuroendocrine Tumor G3 | | NCIT:C35562 | Neuroepithelial, Perineurial, and Schwann Cell Neoplasm | | NCIT:C23058 | Neurofibroma of the Mouse Oral Cavity | | NCIT:C21837 | Neurofibroma of the Mouse Skin | @@ -6203,16 +6381,19 @@ | NCIT:C180516 | No Specific Molecular Profile Endometrial Endometrioid Adenocarcinoma | | NCIT:C141261 | Nodal Marginal Zone Lymphoma by Ann Arbor Stage | | NCIT:C141225 | Nodular Lymphocyte Predominant B-Cell Lymphoma by Ann Arbor Stage | +| NCIT:C205125 | Nodular Melanoma | | NCIT:C36012 | Nodular Neoplasm | | NCIT:C141223 | Nodular Sclerosis Classic Hodgkin Lymphoma by Ann Arbor Stage | | NCIT:C67171 | Nodular Sclerosis Classic Hodgkin Lymphoma, Cellular Phase | | NCIT:C27807 | Nodular Sclerosis Classic Hodgkin Lymphoma, Syncytial Variant | | NCIT:C7187 | Non-Burkitt's Lymphoma | +| NCIT:C202059 | Non-Calcifying/Langerhans Cell-Rich Calcifying Epithelial Odontogenic Tumor | +| NCIT:C202497 | Non-Clear Cell Renal Cell Carcinoma | | NCIT:C121583 | Non-Cutaneous Leiomyosarcoma | | NCIT:C36036 | Non-Encapsulated Neoplasm | | NCIT:C154429 | Non-Functioning Corticotroph Pituitary Neuroendocrine Tumor | | NCIT:C154431 | Non-Functioning Densely Granulated Corticotroph Pituitary Neuroendocrine Tumor | -| NCIT:C176706 | Non-Functioning Lung Carcinoid Tumor | +| NCIT:C176706 | Non-Functioning Lung Neuroendocrine Tumor | | NCIT:C95585 | Non-Functioning Pancreatic Neuroendocrine Tumor G1 | | NCIT:C45838 | Non-Functioning Pancreatic Neuroendocrine Tumor G2 | | NCIT:C121721 | Non-Functioning Pituitary Neuroendocrine Tumor/Macroadenoma | @@ -6239,7 +6420,7 @@ | NCIT:C23072 | Non-Keratinizing Carcinoma of the Mouse Pharynx Without Lymphoid Stroma | | NCIT:C64125 | Non-Keratinizing Epithelioma of the Rat Lung | | NCIT:C65173 | Non-Keratinizing Large Cell Squamous Cell Carcinoma | -| NCIT:C7499 | Non-Keratinizing Primary Intraosseous Squamous Cell Carcinoma -Solid Type | +| NCIT:C7499 | Non-Keratinizing Primary Intraosseous Squamous Cell Carcinoma-Solid Type | | NCIT:C65175 | Non-Keratinizing Small Cell Squamous Cell Carcinoma | | NCIT:C21883 | Non-Lymphoid Hematopoietic Neoplasm of Mouse | | NCIT:C163003 | Non-Malignant Neoplasm | @@ -6256,6 +6437,7 @@ | NCIT:C38752 | Non-Neoplastic Proliferation of the Mouse Liver | | NCIT:C21651 | Non-Neoplastic Proliferation of the Mouse Mammary Gland | | NCIT:C21870 | Non-Neoplastic Splenic Myeloid Hyperplasia of Mouse | +| NCIT:C173798 | Non-Neoplastic Tonsillar Disorder | | NCIT:C121929 | Non-Ossifying Fibroma | | NCIT:C27745 | Non-Small Cell Adenocarcinoma | | NCIT:C65151 | Non-Small Cell Carcinoma | @@ -6293,6 +6475,9 @@ | NCIT:C173720 | Odontogenic Carcinoma | | NCIT:C173735 | Odontogenic Carcinosarcoma | | NCIT:C4314 | Odontogenic Fibroma | +| NCIT:C202078 | Odontogenic Fibroma, Amyloid Subtype | +| NCIT:C202079 | Odontogenic Fibroma, Granular Cell Subtype | +| NCIT:C202080 | Odontogenic Fibroma, Ossifying Subtype | | NCIT:C7452 | Odontogenic Myxofibroma | | NCIT:C7501 | Odontogenic Myxoma | | NCIT:C173738 | Odontogenic Sarcoma | @@ -6319,6 +6504,7 @@ | NCIT:C40340 | Omentum Gastrointestinal Stromal Tumor | | NCIT:C3679 | Oncocytic Adenocarcinoma | | NCIT:C46093 | Oncocytic Variant Thyroid Gland Papillary Carcinoma | +| NCIT:C201839 | Oncocytic Variant of Chromophobe Renal Cell Carcinoma | | NCIT:C27769 | Opisthorchis Viverrini-Related Cholangiocarcinoma | | NCIT:C179886 | Optic Chiasm Neoplasm | | NCIT:C4230 | Optic Disc Melanocytoma | @@ -6338,8 +6524,11 @@ | NCIT:C6845 | Oral Cavity Monomorphic Adenoma | | NCIT:C5915 | Oral Cavity Mucosal Melanoma | | NCIT:C173489 | Oral Cavity Myeloid Sarcoma | +| NCIT:C202860 | Oral Cavity Neurofibroma | +| NCIT:C80290 | Oral Cavity Plasmablastic Lymphoma | | NCIT:C6242 | Oral Cavity Pleomorphic Adenoma | | NCIT:C5916 | Oral Cavity Sarcoma | +| NCIT:C202876 | Oral Cavity Schwannoma | | NCIT:C173479 | Oral Cavity Soft Tissue Neoplasm | | NCIT:C173481 | Oral Cavity Soft Tissue Sarcoma | | NCIT:C7425 | Oral Cavity and Lip Precancerous Condition | @@ -6351,24 +6540,33 @@ | NCIT:C173476 | Oral Squamous Papilloma | | NCIT:C173475 | Oral Verruca Vulgaris | | NCIT:C4545 | Orbit Capillary Hemangioma | +| NCIT:C202882 | Orbit Extraskeletal Myxoid Chondrosarcoma | | NCIT:C4547 | Orbit Hemangiopericytoma | | NCIT:C6408 | Orbit Paraganglioma | +| NCIT:C202620 | Orbit Solitary Fibrous Tumor | | NCIT:C156276 | Orbital Alveolar Soft Part Sarcoma | | NCIT:C118828 | Orbital Melanoma | | NCIT:C60317 | Organ not Available for Histological Examination | | NCIT:C132994 | Oropharyngeal (p16-Negative) Carcinoma by AJCC v8 Stage | -| NCIT:C126751 | Oropharyngeal Basaloid Carcinoma | +| NCIT:C126751 | Oropharyngeal Basaloid Squamous Cell Carcinoma | | NCIT:C90523 | Oropharyngeal Carcinoma by AJCC v6 Stage | | NCIT:C91248 | Oropharyngeal Carcinoma by AJCC v7 Stage | | NCIT:C173578 | Oropharyngeal Hodgkin Lymphoma | -| NCIT:C173414 | Oropharyngeal Human Papillomavirus-Negative Squamous Cell Carcinoma | -| NCIT:C87055 | Oropharyngeal Human Papillomavirus-Positive Squamous Cell Carcinoma | +| NCIT:C201905 | Oropharyngeal Human Papillomavirus-Independent Keratinizing Squamous Cell Carcinoma | +| NCIT:C173414 | Oropharyngeal Human Papillomavirus-Independent Squamous Cell Carcinoma | +| NCIT:C201906 | Oropharyngeal Human Papillomavirus-Related Keratinizing Squamous Cell Carcinoma | +| NCIT:C201907 | Oropharyngeal Human Papillomavirus-Related Non-Keratinizing Squamous Cell Carcinoma | +| NCIT:C87055 | Oropharyngeal Human Papillomavirus-Related Squamous Cell Carcinoma | +| NCIT:C201904 | Oropharyngeal Keratinizing Squamous Cell Carcinoma | +| NCIT:C203018 | Oropharyngeal Large Cell Neuroendocrine Carcinoma | | NCIT:C173577 | Oropharyngeal Lymphoma | +| NCIT:C203016 | Oropharyngeal Neuroendocrine Carcinoma | | NCIT:C173579 | Oropharyngeal Non-Hodgkin Lymphoma | | NCIT:C173575 | Oropharyngeal Pleomorphic Adenoma | | NCIT:C173576 | Oropharyngeal Polymorphous Adenocarcinoma | | NCIT:C5988 | Oropharyngeal Polyp | | NCIT:C126750 | Oropharyngeal Poorly Differentiated Carcinoma | +| NCIT:C203017 | Oropharyngeal Small Cell Neuroendocrine Carcinoma | | NCIT:C6038 | Oropharyngeal Squamous Papilloma | | NCIT:C68610 | Oropharyngeal Undifferentiated Carcinoma | | NCIT:C147906 | Oropharyngeal p16INK4a-Negative Squamous Cell Carcinoma | @@ -6408,7 +6606,6 @@ | NCIT:C128106 | Ovarian Cancer by AJCC v6 and v7 Stage | | NCIT:C139963 | Ovarian Cancer by AJCC v8 Stage | | NCIT:C128081 | Ovarian Cancer by FIGO Stage | -| NCIT:C5229 | Ovarian Carcinoid Tumor | | NCIT:C7291 | Ovarian Cellular Fibroma | | NCIT:C179334 | Ovarian Dedifferentiated Carcinoma | | NCIT:C39999 | Ovarian Dermoid Cyst with Adenocarcinoma | @@ -6431,6 +6628,7 @@ | NCIT:C6257 | Ovarian Endometrioid Tumor | | NCIT:C5233 | Ovarian Fibrosarcoma | | NCIT:C7287 | Ovarian Granulosa-Stromal Cell Tumor | +| NCIT:C199166 | Ovarian High Grade Endometrioid Adenocarcinoma | | NCIT:C105555 | Ovarian High Grade Serous Adenocarcinoma | | NCIT:C4214 | Ovarian Hilus Cell Tumor | | NCIT:C40013 | Ovarian Insular Carcinoid Tumor | @@ -6438,6 +6636,7 @@ | NCIT:C5231 | Ovarian Leydig Cell Tumor | | NCIT:C39983 | Ovarian Leydig Cell Tumor, Non-Hilar Type | | NCIT:C39984 | Ovarian Leydig Cell Tumor, Not Otherwise Specified | +| NCIT:C199159 | Ovarian Low Grade Endometrioid Adenocarcinoma | | NCIT:C40063 | Ovarian Low Grade Endometrioid Stromal Sarcoma | | NCIT:C105556 | Ovarian Low Grade Serous Adenocarcinoma | | NCIT:C4203 | Ovarian Luteinized Thecoma | @@ -6452,6 +6651,7 @@ | NCIT:C5245 | Ovarian Myxoma | | NCIT:C179474 | Ovarian Neuroectodermal-Type Tumor | | NCIT:C171032 | Ovarian Neuroendocrine Carcinoma | +| NCIT:C5229 | Ovarian Neuroendocrine Tumor | | NCIT:C39971 | Ovarian Retiform Sertoli-Leydig Cell Tumor | | NCIT:C126322 | Ovarian Retiform Sertoli-Leydig Cell Tumor, Variant with Heterologous Elements | | NCIT:C4204 | Ovarian Sclerosing Stromal Tumor | @@ -6493,9 +6693,11 @@ | NCIT:C7140 | PRETEXT II Hepatoblastoma | | NCIT:C7141 | PRETEXT III Hepatoblastoma | | NCIT:C7142 | PRETEXT IV Hepatoblastoma | +| NCIT:C204574 | PRKAR1A-Inactivated Pigmented Epithelioid Melanocytoma | | NCIT:C8463 | Palate Carcinoma | | NCIT:C6749 | Palate Kaposi Sarcoma | | NCIT:C4649 | Palate Squamous Cell Carcinoma | +| NCIT:C201900 | Palatine Tonsil Hamartomatous Polyp | | NCIT:C95542 | Pancreatic Acinar Cell Neoplasm | | NCIT:C67455 | Pancreatic Alpha Cell Adenoma | | NCIT:C67457 | Pancreatic Beta Cell Adenoma | @@ -6523,10 +6725,11 @@ | NCIT:C95471 | Pancreatic Macrocystic Serous Cystadenoma | | NCIT:C95559 | Pancreatic Mature Teratoma | | NCIT:C95466 | Pancreatic Medullary Carcinoma | +| NCIT:C6878 | Pancreatic Mixed Acinar Carcinoma-Neuroendocrine Carcinoma | | NCIT:C95458 | Pancreatic Mixed Acinar-Ductal Carcinoma | -| NCIT:C95460 | Pancreatic Mixed Acinar-Ductal Neuroendocrine Carcinoma | -| NCIT:C6878 | Pancreatic Mixed Acinar-Neuroendocrine Carcinoma | -| NCIT:C188217 | Pancreatic Mixed Ductal-Neuroendocrine Neoplasm | +| NCIT:C95460 | Pancreatic Mixed Ductal Adenocarcinoma-Acinar Carcinoma-Neuroendocrine Carcinoma | +| NCIT:C188217 | Pancreatic Mixed Ductal Adenocarcinoma-Neuroendocrine Neoplasm | +| NCIT:C203795 | Pancreatic Mixed Ductal Adenocarcinoma-Neuroendocrine Tumor | | NCIT:C95427 | Pancreatic Moderately Differentiated Ductal Adenocarcinoma | | NCIT:C6883 | Pancreatic Mucinous-Cystic Neoplasm with Intermediate Grade Dysplasia | | NCIT:C95493 | Pancreatic Mucinous-Cystic Neoplasm, High Grade | @@ -6575,8 +6778,15 @@ | NCIT:C6073 | Paranasal Sinus Diffuse Large B-Cell Lymphoma | | NCIT:C8195 | Paranasal Sinus Inverted Papilloma | | NCIT:C54284 | Paranasal Sinus Keratinizing Squamous Cell Carcinoma | +| NCIT:C203006 | Paranasal Sinus Large Cell Neuroendocrine Carcinoma | +| NCIT:C202997 | Paranasal Sinus Neuroendocrine Carcinoma | +| NCIT:C202993 | Paranasal Sinus Neuroendocrine Neoplasm | +| NCIT:C202995 | Paranasal Sinus Neuroendocrine Tumor | +| NCIT:C203009 | Paranasal Sinus Neuroendocrine Tumor G1 | +| NCIT:C203012 | Paranasal Sinus Neuroendocrine Tumor G2 | | NCIT:C6069 | Paranasal Sinus Non-Hodgkin Lymphoma | | NCIT:C6016 | Paranasal Sinus Olfactory Neuroblastoma | +| NCIT:C203004 | Paranasal Sinus Small Cell Neuroendocrine Carcinoma | | NCIT:C162820 | Parapharyngeal Neoplasm | | NCIT:C27767 | Parasite-Related Carcinoma | | NCIT:C27766 | Parasite-Related Malignant Neoplasm | @@ -6619,6 +6829,7 @@ | NCIT:C173716 | Parotid Gland Follicular Lymphoma | | NCIT:C5397 | Parotid Gland Hemangioma | | NCIT:C5952 | Parotid Gland Kaposi Sarcoma | +| NCIT:C201770 | Parotid Gland Keratocystoma | | NCIT:C5982 | Parotid Gland Lipoma | | NCIT:C156281 | Parotid Gland Liposarcoma | | NCIT:C5393 | Parotid Gland Lymphangioma | @@ -6634,18 +6845,18 @@ | NCIT:C5946 | Parotid Gland Undifferentiated Carcinoma | | NCIT:C66865 | Parotid Gland Warthin Tumor | | NCIT:C137662 | Pathologic Stage 0 Cutaneous Melanoma AJCC v8 | +| NCIT:C136881 | Pathologic Stage 0 Cutaneous Merkel Cell Carcinoma AJCC v8 | | NCIT:C133413 | Pathologic Stage 0 Esophageal Adenocarcinoma AJCC v8 | | NCIT:C133519 | Pathologic Stage 0 Esophageal Squamous Cell Carcinoma AJCC v8 | | NCIT:C133654 | Pathologic Stage 0 Gastric Cancer AJCC v8 | | NCIT:C133564 | Pathologic Stage 0 Gastroesophageal Junction Adenocarcinoma AJCC v8 | -| NCIT:C136881 | Pathologic Stage 0 Merkel Cell Carcinoma AJCC v8 | | NCIT:C137663 | Pathologic Stage I Cutaneous Melanoma AJCC v8 | +| NCIT:C136882 | Pathologic Stage I Cutaneous Merkel Cell Carcinoma AJCC v8 | | NCIT:C133414 | Pathologic Stage I Esophageal Adenocarcinoma AJCC v8 | | NCIT:C133521 | Pathologic Stage I Esophageal Squamous Cell Carcinoma AJCC v8 | | NCIT:C133655 | Pathologic Stage I Gastric Cancer AJCC v8 | | NCIT:C133565 | Pathologic Stage I Gastroesophageal Junction Adenocarcinoma AJCC v8 | | NCIT:C132898 | Pathologic Stage I HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8 | -| NCIT:C136882 | Pathologic Stage I Merkel Cell Carcinoma AJCC v8 | | NCIT:C140757 | Pathologic Stage I Retinoblastoma AJCC v8 | | NCIT:C137664 | Pathologic Stage IA Cutaneous Melanoma AJCC v8 | | NCIT:C133415 | Pathologic Stage IA Esophageal Adenocarcinoma AJCC v8 | @@ -6660,56 +6871,56 @@ | NCIT:C133417 | Pathologic Stage IC Esophageal Adenocarcinoma AJCC v8 | | NCIT:C133568 | Pathologic Stage IC Gastroesophageal Junction Adenocarcinoma AJCC v8 | | NCIT:C137666 | Pathologic Stage II Cutaneous Melanoma AJCC v8 | +| NCIT:C136883 | Pathologic Stage II Cutaneous Merkel Cell Carcinoma AJCC v8 | | NCIT:C133418 | Pathologic Stage II Esophageal Adenocarcinoma AJCC v8 | | NCIT:C133532 | Pathologic Stage II Esophageal Squamous Cell Carcinoma AJCC v8 | | NCIT:C133659 | Pathologic Stage II Gastric Cancer AJCC v8 | | NCIT:C133570 | Pathologic Stage II Gastroesophageal Junction Adenocarcinoma AJCC v8 | | NCIT:C132899 | Pathologic Stage II HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8 | -| NCIT:C136883 | Pathologic Stage II Merkel Cell Carcinoma AJCC v8 | | NCIT:C140758 | Pathologic Stage II Retinoblastoma AJCC v8 | | NCIT:C137667 | Pathologic Stage IIA Cutaneous Melanoma AJCC v8 | +| NCIT:C136884 | Pathologic Stage IIA Cutaneous Merkel Cell Carcinoma AJCC v8 | | NCIT:C133419 | Pathologic Stage IIA Esophageal Adenocarcinoma AJCC v8 | | NCIT:C133534 | Pathologic Stage IIA Esophageal Squamous Cell Carcinoma AJCC v8 | | NCIT:C133660 | Pathologic Stage IIA Gastric Cancer AJCC v8 | | NCIT:C133572 | Pathologic Stage IIA Gastroesophageal Junction Adenocarcinoma AJCC v8 | -| NCIT:C136884 | Pathologic Stage IIA Merkel Cell Carcinoma AJCC v8 | | NCIT:C137668 | Pathologic Stage IIB Cutaneous Melanoma AJCC v8 | +| NCIT:C136885 | Pathologic Stage IIB Cutaneous Merkel Cell Carcinoma AJCC v8 | | NCIT:C133420 | Pathologic Stage IIB Esophageal Adenocarcinoma AJCC v8 | | NCIT:C133535 | Pathologic Stage IIB Esophageal Squamous Cell Carcinoma AJCC v8 | | NCIT:C133662 | Pathologic Stage IIB Gastric Cancer AJCC v8 | | NCIT:C133573 | Pathologic Stage IIB Gastroesophageal Junction Adenocarcinoma AJCC v8 | -| NCIT:C136885 | Pathologic Stage IIB Merkel Cell Carcinoma AJCC v8 | | NCIT:C137669 | Pathologic Stage IIC Cutaneous Melanoma AJCC v8 | | NCIT:C137670 | Pathologic Stage III Cutaneous Melanoma AJCC v8 | +| NCIT:C136886 | Pathologic Stage III Cutaneous Merkel Cell Carcinoma AJCC v8 | | NCIT:C133421 | Pathologic Stage III Esophageal Adenocarcinoma AJCC v8 | | NCIT:C133536 | Pathologic Stage III Esophageal Squamous Cell Carcinoma AJCC v8 | | NCIT:C133663 | Pathologic Stage III Gastric Cancer AJCC v8 | | NCIT:C133575 | Pathologic Stage III Gastroesophageal Junction Adenocarcinoma AJCC v8 | | NCIT:C132900 | Pathologic Stage III HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8 | -| NCIT:C136886 | Pathologic Stage III Merkel Cell Carcinoma AJCC v8 | | NCIT:C140759 | Pathologic Stage III Retinoblastoma AJCC v8 | | NCIT:C137671 | Pathologic Stage IIIA Cutaneous Melanoma AJCC v8 | +| NCIT:C136887 | Pathologic Stage IIIA Cutaneous Merkel Cell Carcinoma AJCC v8 | | NCIT:C133422 | Pathologic Stage IIIA Esophageal Adenocarcinoma AJCC v8 | | NCIT:C133537 | Pathologic Stage IIIA Esophageal Squamous Cell Carcinoma AJCC v8 | | NCIT:C133665 | Pathologic Stage IIIA Gastric Cancer AJCC v8 | | NCIT:C133577 | Pathologic Stage IIIA Gastroesophageal Junction Adenocarcinoma AJCC v8 | -| NCIT:C136887 | Pathologic Stage IIIA Merkel Cell Carcinoma AJCC v8 | | NCIT:C137672 | Pathologic Stage IIIB Cutaneous Melanoma AJCC v8 | +| NCIT:C136888 | Pathologic Stage IIIB Cutaneous Merkel Cell Carcinoma AJCC v8 | | NCIT:C133423 | Pathologic Stage IIIB Esophageal Adenocarcinoma AJCC v8 | | NCIT:C133538 | Pathologic Stage IIIB Esophageal Squamous Cell Carcinoma AJCC v8 | | NCIT:C133666 | Pathologic Stage IIIB Gastric Cancer AJCC v8 | | NCIT:C133579 | Pathologic Stage IIIB Gastroesophageal Junction Adenocarcinoma AJCC v8 | -| NCIT:C136888 | Pathologic Stage IIIB Merkel Cell Carcinoma AJCC v8 | | NCIT:C137673 | Pathologic Stage IIIC Cutaneous Melanoma AJCC v8 | | NCIT:C133667 | Pathologic Stage IIIC Gastric Cancer AJCC v8 | | NCIT:C137675 | Pathologic Stage IIID Cutaneous Melanoma AJCC v8 | | NCIT:C137677 | Pathologic Stage IV Cutaneous Melanoma AJCC v8 | +| NCIT:C136889 | Pathologic Stage IV Cutaneous Merkel Cell Carcinoma AJCC v8 | | NCIT:C133424 | Pathologic Stage IV Esophageal Adenocarcinoma AJCC v8 | | NCIT:C133539 | Pathologic Stage IV Esophageal Squamous Cell Carcinoma AJCC v8 | | NCIT:C133668 | Pathologic Stage IV Gastric Cancer AJCC v8 | | NCIT:C133580 | Pathologic Stage IV Gastroesophageal Junction Adenocarcinoma AJCC v8 | | NCIT:C132901 | Pathologic Stage IV HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8 | -| NCIT:C136889 | Pathologic Stage IV Merkel Cell Carcinoma AJCC v8 | | NCIT:C140760 | Pathologic Stage IV Retinoblastoma AJCC v8 | | NCIT:C133425 | Pathologic Stage IVA Esophageal Adenocarcinoma AJCC v8 | | NCIT:C133541 | Pathologic Stage IVA Esophageal Squamous Cell Carcinoma AJCC v8 | @@ -6824,8 +7035,14 @@ | NCIT:C43313 | Pilar-Associated Mesenchyme Neoplasm | | NCIT:C21815 | Pilomatrixoma Type of Basaloid Follicular Neoplasm of the Mouse Skin | | NCIT:C4659 | Pineal Region Germ Cell Tumor | +| NCIT:C201966 | Pineoblastoma Molecular Subtypes | +| NCIT:C201967 | Pineoblastoma miRNA Processing Altered 1 | +| NCIT:C201968 | Pineoblastoma miRNA Processing Altered 2 | +| NCIT:C201973 | Pineoblastoma, MYC/FOXR2-Activated | +| NCIT:C201969 | Pineoblastoma, RB1-Altered | | NCIT:C4147 | Pituitary Gland Acidophil Carcinoma | | NCIT:C155304 | Pituitary Gland Blastoma | +| NCIT:C155797 | Pituitary Gland Diffuse Large B-Cell Lymphoma | | NCIT:C4149 | Pituitary Gland Mixed Acidophil-Basophil Carcinoma | | NCIT:C45922 | Pituitary Gland Neoplasm (Antiquated) | | NCIT:C155796 | Pituitary Gland Non-Hodgkin Lymphoma | @@ -6849,7 +7066,6 @@ | NCIT:C21853 | Plasma Cell Neoplasms of the Mouse Skin | | NCIT:C7240 | Plasma Cell Post-Transplant Lymphoproliferative Disorder | | NCIT:C38159 | Plasmablastic Lymphoma of Mucosa Site | -| NCIT:C80290 | Plasmablastic Lymphoma of the Oral Mucosa | | NCIT:C21919 | Plasmacytoma of the Mouse Hematologic System | | NCIT:C22060 | Plasmacytoma of the Mouse Nervous System | | NCIT:C23104 | Plasmacytoma of the Mouse Nose and Paranasal Sinuses | @@ -6858,10 +7074,14 @@ | NCIT:C23151 | Plasmacytoma of the Mouse Salivary Glands | | NCIT:C7241 | Plasmacytoma-Like Post-Transplant Lymphoproliferative Disorder | | NCIT:C178698 | Platinum-Refractory Fallopian Tube Carcinoma | +| NCIT:C204988 | Platinum-Refractory Fallopian Tube High Grade Serous Adenocarcinoma | | NCIT:C178697 | Platinum-Refractory Malignant Female Reproductive System Neoplasm | | NCIT:C178700 | Platinum-Refractory Ovarian Carcinoma | +| NCIT:C204987 | Platinum-Refractory Ovarian High Grade Serous Adenocarcinoma | | NCIT:C178702 | Platinum-Refractory Primary Peritoneal Carcinoma | +| NCIT:C204991 | Platinum-Refractory Primary Peritoneal High Grade Serous Adenocarcinoma | | NCIT:C157621 | Platinum-Resistant Fallopian Tube Carcinoma | +| NCIT:C204982 | Platinum-Resistant Fallopian Tube High Grade Serous Adenocarcinoma | | NCIT:C179151 | Platinum-Resistant Head and Neck Carcinoma | | NCIT:C158493 | Platinum-Resistant Lung Small Cell Carcinoma | | NCIT:C169021 | Platinum-Resistant Malignant Female Reproductive System Neoplasm | @@ -6869,7 +7089,9 @@ | NCIT:C147561 | Platinum-Resistant Ovarian Carcinoma | | NCIT:C199567 | Platinum-Resistant Ovarian High Grade Serous Adenocarcinoma | | NCIT:C157622 | Platinum-Resistant Primary Peritoneal Carcinoma | +| NCIT:C204985 | Platinum-Resistant Primary Peritoneal High Grade Serous Adenocarcinoma | | NCIT:C150365 | Platinum-Resistant Urothelial Carcinoma | +| NCIT:C205187 | Platinum-Sensitive Endometrial Carcinoma | | NCIT:C187374 | Platinum-Sensitive Endometrial Serous Adenocarcinoma | | NCIT:C160873 | Platinum-Sensitive Fallopian Tube Carcinoma | | NCIT:C158495 | Platinum-Sensitive Lung Small Cell Carcinoma | @@ -6897,6 +7119,7 @@ | NCIT:C45696 | Pleural Synovial Sarcoma | | NCIT:C45660 | Pleural Well Differentiated Papillary Mesothelial Tumor | | NCIT:C6493 | Plexiform Fibrohistiocytic Tumor | +| NCIT:C204516 | Plexiform Spindle Cell Melanocytoma | | NCIT:C45916 | Plurihormonal Pituitary Neuroendocrine Tumor | | NCIT:C154505 | Plurimorphous Plurihormonal Pituitary Neuroendocrine Tumor | | NCIT:C134962 | Poeciliopsis Lucida Hepatocellular Carcinoma | @@ -6920,8 +7143,10 @@ | NCIT:C4210 | Poorly Differentiated Ovarian Sertoli-Leydig Cell Tumor | | NCIT:C39973 | Poorly Differentiated Ovarian Sertoli-Leydig Cell Tumor, Variant with Heterologous Elements | | NCIT:C27916 | Poorly Differentiated Prostate Adenocarcinoma | +| NCIT:C202883 | Poorly Differentiated Synovial Sarcoma | | NCIT:C21809 | Poorly-differentiated Squamous Cell Carcinoma of the Mouse Skin | | NCIT:C43354 | Porocarcinoma In Situ | +| NCIT:C205476 | Poroid Hidradenoma | | NCIT:C126806 | Post-Essential Thrombocythemia Myelofibrosis | | NCIT:C8595 | Postcricoid Carcinoma | | NCIT:C8185 | Postcricoid Squamous Cell Carcinoma | @@ -6991,6 +7216,7 @@ | NCIT:C4834 | Primary Bone Osteosarcoma | | NCIT:C4975 | Primary Brain Stem Neoplasm | | NCIT:C176251 | Primary Breast Angiosarcoma | +| NCIT:C202952 | Primary CD30-Positive T-Cell Lymphoproliferative Disorder | | NCIT:C178476 | Primary Central Atypical Cartilaginous Tumor/Chondrosarcoma, Grade 1 | | NCIT:C7155 | Primary Central Chondrosarcoma | | NCIT:C102871 | Primary Central Nervous System Neoplasm | @@ -7010,15 +7236,16 @@ | NCIT:C7221 | Primary Cutaneous Hodgkin Lymphoma | | NCIT:C45214 | Primary Cutaneous Intravascular Large B-Cell Lymphoma | | NCIT:C27533 | Primary Cutaneous Mucinous Carcinoma | +| NCIT:C205357 | Primary Cutaneous NUT Adnexal Carcinoma | | NCIT:C188114 | Primary Cutaneous Non-Hodgkin Lymphoma | | NCIT:C201080 | Primary Cutaneous Peripheral T-Cell Lymphoma, Not Otherwise Specified | | NCIT:C45332 | Primary Cutaneous Peripheral T-Cell Lymphoma, Rare Subtype | | NCIT:C45216 | Primary Cutaneous Plasmablastic Lymphoma | | NCIT:C45215 | Primary Cutaneous T-Cell/Histiocyte-Rich Large B-Cell Lymphoma | -| NCIT:C162467 | Primary Diffuse Large B-Cell Lymphoma of the Testis | +| NCIT:C202953 | Primary Head and Neck Mucosal CD30-Positive T-Cell Lymphoproliferative Disorder | | NCIT:C186610 | Primary Intracranial Sarcoma, DICER1-Mutant | -| NCIT:C54303 | Primary Intraosseous Squamous Cell Carcinoma Derived From Keratocystic Odontogenic Tumor | -| NCIT:C7500 | Primary Intraosseous Squamous Cell Carcinoma Derived From Odontogenic Cyst | +| NCIT:C7500 | Primary Intraosseous Carcinoma, Not Otherwise Specified, Derived from Odontogenic Cyst | +| NCIT:C54303 | Primary Intraosseous Carcinoma, Not Otherwise Specified, Derived from Odontogenic Keratocyst | | NCIT:C7491 | Primary Intraosseous Squamous Cell Carcinoma-Solid Type | | NCIT:C175467 | Primary Iris Non-Hodgkin Lymphoma | | NCIT:C200687 | Primary Large B-Cell Lymphoma of Immune-Privileged Site | @@ -7030,11 +7257,11 @@ | NCIT:C141262 | Primary Mediastinal Large B-Cell Lymphoma by Ann Arbor Stage | | NCIT:C21916 | Primary Mediastinal Thymic Diffuse Large B Cell Lymphoma of the Mouse Hematologic System | | NCIT:C22051 | Primary Melanocytic Lesions of the Mouse Nervous System | -| NCIT:C4661 | Primary Meningeal Melanocytic Neoplasm | | NCIT:C174033 | Primary Middle Ear Meningioma | | NCIT:C24238 | Primary Mouse Gastric Non-Hodgkin's Lymphoma | | NCIT:C8509 | Primary Neoplasm | | NCIT:C139288 | Primary Nodal EBV-Positive T-Cell/NK-Cell Lymphoma | +| NCIT:C202955 | Primary Oral Cavity CD30-Positive T-Cell Lymphoproliferative Disorder | | NCIT:C170733 | Primary Peritoneal Adenocarcinoma | | NCIT:C140003 | Primary Peritoneal Cancer by AJCC v7 Stage | | NCIT:C140004 | Primary Peritoneal Cancer by AJCC v8 Stage | @@ -7045,7 +7272,6 @@ | NCIT:C126354 | Primary Peritoneal Low Grade Serous Adenocarcinoma | | NCIT:C162564 | Primary Peritoneal Transitional Cell Carcinoma | | NCIT:C162562 | Primary Peritoneal Undifferentiated Carcinoma | -| NCIT:C155797 | Primary Pituitary Gland Diffuse Large B-Cell Lymphoma | | NCIT:C142827 | Primary Pulmonary Myxoid Sarcoma with EWSR1-CREB1 Fusion | | NCIT:C173163 | Primary Sinonasal Meningioma | | NCIT:C175451 | Primary Uveal Non-Hodgkin Lymphoma | @@ -7135,14 +7361,17 @@ | NCIT:C39901 | Prostatic Duct Urothelial Carcinoma | | NCIT:C21728 | Prostatic Intraepithelial Neoplasia of the Mouse Prostate Gland | | NCIT:C191961 | Prostatic Intraepithelial Neoplasia-Like Adenocarcinoma | +| NCIT:C202633 | Proximal Colon Carcinoma | | NCIT:C165628 | Proximal Gastric Adenocarcinoma | | NCIT:C115334 | Proximal Urethral Carcinoma | | NCIT:C176887 | Psammocarcinoma | +| NCIT:C202209 | Psammomatoid Ossifying Fibroma | | NCIT:C121668 | Pseudomyogenic Hemangioendothelioma | | NCIT:C3763 | Pulmonary Adenomatosis | | NCIT:C6746 | Pulmonary Artery Angiosarcoma | | NCIT:C142825 | Pulmonary Artery Intimal Sarcoma | | NCIT:C45607 | Pulmonary Lymphomatoid Granulomatosis | +| NCIT:C201978 | Pulmonary Mucinous Cystic Tumor of Borderline Malignancy | | NCIT:C7435 | Pulmonary Precancerous Condition | | NCIT:C28620 | Pulmonary Proliferative Lesions of the Mouse | | NCIT:C43277 | Pure Cutaneous Mastocytosis | @@ -7175,6 +7404,7 @@ | NCIT:C134573 | Rainbow Trout Hepatoma | | NCIT:C136977 | Rainbow Trout Mesothelioma | | NCIT:C192672 | Rare Malignant Solid Neoplasm | +| NCIT:C7201 | Rare Neoplasm | | NCIT:C63820 | Rat Acanthomatous Ameloblastoma | | NCIT:C60318 | Rat Acinar Cell Adenocarcinoma | | NCIT:C60319 | Rat Acinar Cell Adenoma | @@ -7445,6 +7675,7 @@ | NCIT:C193420 | Rectal Gastrointestinal Stromal Tumor | | NCIT:C176697 | Rectal Large Cell Neuroendocrine Carcinoma | | NCIT:C96493 | Rectal Micropapillary Adenocarcinoma | +| NCIT:C203385 | Rectal Neuroendocrine Carcinoma | | NCIT:C160451 | Rectal Neuroendocrine Tumor G2 | | NCIT:C172703 | Rectal Neuroendocrine Tumor G3 | | NCIT:C135527 | Rectal Neuroendocrine Tumor by AJCC v8 Stage | @@ -7535,6 +7766,7 @@ | NCIT:C153802 | Recurrent Appendix Carcinoma | | NCIT:C153579 | Recurrent Appendix Mucinous Adenocarcinoma | | NCIT:C27900 | Recurrent Askin Tumor | +| NCIT:C203274 | Recurrent Astrocytic Tumor | | NCIT:C188127 | Recurrent Astrocytoma, IDH-Mutant | | NCIT:C191197 | Recurrent Astrocytoma, IDH-Mutant, Grade 3 | | NCIT:C182018 | Recurrent Astrocytoma, IDH-Mutant, Grade 4 | @@ -7546,6 +7778,7 @@ | NCIT:C134834 | Recurrent B Acute Lymphoblastic Leukemia, BCR-ABL1-Like | | NCIT:C189042 | Recurrent B Acute Lymphoblastic Leukemia, Philadelphia Chromosome Negative | | NCIT:C8869 | Recurrent B Lymphoblastic Lymphoma | +| NCIT:C204124 | Recurrent B-Cell Malignant Neoplasm | | NCIT:C8841 | Recurrent B-Cell Non-Hodgkin Lymphoma | | NCIT:C158081 | Recurrent B-Cell Prolymphocytic Leukemia | | NCIT:C148025 | Recurrent BRCA- Associated Ovarian Carcinoma | @@ -7554,6 +7787,7 @@ | NCIT:C156782 | Recurrent Biliary Tract Carcinoma | | NCIT:C4995 | Recurrent Bladder Adenocarcinoma | | NCIT:C7899 | Recurrent Bladder Carcinoma | +| NCIT:C203815 | Recurrent Bladder Non-Invasive Papillary Urothelial Carcinoma, Low Grade | | NCIT:C191860 | Recurrent Bladder Small Cell Neuroendocrine Carcinoma | | NCIT:C8902 | Recurrent Bladder Squamous Cell Carcinoma | | NCIT:C126307 | Recurrent Bladder Urothelial Carcinoma | @@ -7566,16 +7800,22 @@ | NCIT:C175588 | Recurrent Breast Adenocarcinoma | | NCIT:C133092 | Recurrent Breast Angiosarcoma | | NCIT:C7771 | Recurrent Breast Carcinoma | +| NCIT:C203339 | Recurrent Breast Ductal Carcinoma In Situ | | NCIT:C176680 | Recurrent Breast Implant-Associated Anaplastic Large Cell Lymphoma | | NCIT:C8607 | Recurrent Breast Inflammatory Carcinoma | | NCIT:C138023 | Recurrent Breast Lymphoma | +| NCIT:C203341 | Recurrent Breast Medullary Carcinoma | +| NCIT:C203342 | Recurrent Breast Mucinous Carcinoma | | NCIT:C153588 | Recurrent Breast Paget Disease | +| NCIT:C203344 | Recurrent Breast Papillary Carcinoma | | NCIT:C170727 | Recurrent Breast Sarcoma | +| NCIT:C203362 | Recurrent Breast Tubular Carcinoma | | NCIT:C180923 | Recurrent Bronchogenic Carcinoma | | NCIT:C151976 | Recurrent Burkitt Leukemia | | NCIT:C5008 | Recurrent Burkitt Lymphoma | | NCIT:C7619 | Recurrent Carcinoma | | NCIT:C9181 | Recurrent Carcinoma of Unknown Primary | +| NCIT:C205238 | Recurrent Castration-Sensitive Prostate Carcinoma | | NCIT:C138019 | Recurrent Central Nervous System Lymphoma | | NCIT:C146990 | Recurrent Central Nervous System Non-Hodgkin Lymphoma | | NCIT:C8926 | Recurrent Centroblastic Lymphoma | @@ -7666,12 +7906,15 @@ | NCIT:C158426 | Recurrent Desmoplastic Small Round Cell Tumor | | NCIT:C165611 | Recurrent Differentiated Thyroid Gland Carcinoma | | NCIT:C167081 | Recurrent Diffuse Astrocytoma | +| NCIT:C203285 | Recurrent Diffuse Glioma | +| NCIT:C203273 | Recurrent Diffuse Hemispheric Glioma, H3 G34-Mutant | | NCIT:C136518 | Recurrent Diffuse Intrinsic Pontine Glioma | | NCIT:C8852 | Recurrent Diffuse Large B-Cell Lymphoma | | NCIT:C160231 | Recurrent Diffuse Large B-Cell Lymphoma Activated B-Cell Type | | NCIT:C183140 | Recurrent Diffuse Large B-Cell Lymphoma Associated with Chronic Inflammation | | NCIT:C160230 | Recurrent Diffuse Large B-Cell Lymphoma Germinal Center B-Cell Type | | NCIT:C165240 | Recurrent Diffuse Large B-Cell Lymphoma, Not Otherwise Specified | +| NCIT:C203267 | Recurrent Diffuse Midline Glioma | | NCIT:C179222 | Recurrent Diffuse Midline Glioma, H3 K27M-Mutant | | NCIT:C7622 | Recurrent Digestive System Carcinoma | | NCIT:C155938 | Recurrent Digestive System Neuroendocrine Carcinoma | @@ -7690,6 +7933,8 @@ | NCIT:C155816 | Recurrent Endometrial Clear Cell Adenocarcinoma | | NCIT:C165282 | Recurrent Endometrial Dedifferentiated Carcinoma | | NCIT:C150097 | Recurrent Endometrial Endometrioid Adenocarcinoma | +| NCIT:C199156 | Recurrent Endometrial High Grade Endometrioid Adenocarcinoma | +| NCIT:C199153 | Recurrent Endometrial Low Grade Endometrioid Adenocarcinoma | | NCIT:C155819 | Recurrent Endometrial Mixed Cell Adenocarcinoma | | NCIT:C165291 | Recurrent Endometrial Mucinous Adenocarcinoma | | NCIT:C132294 | Recurrent Endometrial Serous Adenocarcinoma | @@ -7754,6 +7999,7 @@ | NCIT:C182019 | Recurrent Glioblastoma, IDH-Wildtype | | NCIT:C132506 | Recurrent Glioma | | NCIT:C179221 | Recurrent Gliomatosis Cerebri | +| NCIT:C203302 | Recurrent Glioneuronal and Neuronal Tumors | | NCIT:C131209 | Recurrent Gliosarcoma | | NCIT:C8155 | Recurrent Grade 1 Follicular Lymphoma | | NCIT:C8156 | Recurrent Grade 2 Follicular Lymphoma | @@ -7766,6 +8012,7 @@ | NCIT:C138013 | Recurrent Gray-Zone Lymphoma | | NCIT:C168783 | Recurrent HER2-Negative Breast Carcinoma | | NCIT:C182108 | Recurrent HER2-Positive Breast Carcinoma | +| NCIT:C202986 | Recurrent HHV8-Positive Diffuse Large B-Cell Lymphoma, Not Otherwise Specified | | NCIT:C157685 | Recurrent HIV-Related Lymphoproliferative Disorder | | NCIT:C142882 | Recurrent Hairy Cell Leukemia | | NCIT:C171065 | Recurrent Hairy Cell Leukemia Variant | @@ -7782,9 +8029,7 @@ | NCIT:C162451 | Recurrent High Grade B-Cell Lymphoma with MYC, BCL2, and BCL6 Rearrangements | | NCIT:C188788 | Recurrent High Grade B-Cell Lymphoma, Not Otherwise Specified | | NCIT:C5004 | Recurrent High Grade Burkitt-Like Lymphoma | -| NCIT:C199156 | Recurrent High Grade Endometrial Endometrioid Adenocarcinoma | | NCIT:C199152 | Recurrent High Grade Endometrioid Adenocarcinoma | -| NCIT:C199168 | Recurrent High Grade Ovarian Endometrioid Adenocarcinoma | | NCIT:C134172 | Recurrent Histiocytic and Dendritic Cell Neoplasm | | NCIT:C4937 | Recurrent Hodgkin Lymphoma | | NCIT:C8828 | Recurrent Hodgkin's Disease Lymphocyte Predominance Type | @@ -7824,11 +8069,9 @@ | NCIT:C153584 | Recurrent Lobular Breast Carcinoma | | NCIT:C8153 | Recurrent Low Grade Adult Non-Hodgkin's Lymphoma | | NCIT:C176464 | Recurrent Low Grade Astrocytoma | -| NCIT:C199153 | Recurrent Low Grade Endometrial Endometrioid Adenocarcinoma | | NCIT:C199150 | Recurrent Low Grade Endometrioid Adenocarcinoma | | NCIT:C156456 | Recurrent Low Grade Fallopian Tube Serous Adenocarcinoma | | NCIT:C177794 | Recurrent Low Grade Glioma | -| NCIT:C199167 | Recurrent Low Grade Ovarian Endometrioid Adenocarcinoma | | NCIT:C8757 | Recurrent Lung Adenocarcinoma | | NCIT:C8747 | Recurrent Lung Adenosquamous Carcinoma | | NCIT:C8953 | Recurrent Lung Carcinoma | @@ -7982,7 +8225,9 @@ | NCIT:C153617 | Recurrent Ovarian Cystadenocarcinoma | | NCIT:C150095 | Recurrent Ovarian Endometrioid Adenocarcinoma | | NCIT:C8087 | Recurrent Ovarian Germ Cell Tumor | +| NCIT:C199168 | Recurrent Ovarian High Grade Endometrioid Adenocarcinoma | | NCIT:C165262 | Recurrent Ovarian High Grade Serous Adenocarcinoma | +| NCIT:C199167 | Recurrent Ovarian Low Grade Endometrioid Adenocarcinoma | | NCIT:C156455 | Recurrent Ovarian Low Grade Serous Adenocarcinoma | | NCIT:C153616 | Recurrent Ovarian Mucinous Adenocarcinoma | | NCIT:C178669 | Recurrent Ovarian Seromucinous Carcinoma | @@ -8021,9 +8266,12 @@ | NCIT:C172289 | Recurrent Plasma Cell Neoplasm | | NCIT:C157683 | Recurrent Plasmablastic Lymphoma | | NCIT:C170750 | Recurrent Platinum-Resistant Fallopian Tube Carcinoma | +| NCIT:C204984 | Recurrent Platinum-Resistant Fallopian Tube High Grade Serous Adenocarcinoma | | NCIT:C170748 | Recurrent Platinum-Resistant Ovarian Carcinoma | | NCIT:C200719 | Recurrent Platinum-Resistant Ovarian High Grade Serous Adenocarcinoma | | NCIT:C170751 | Recurrent Platinum-Resistant Primary Peritoneal Carcinoma | +| NCIT:C204986 | Recurrent Platinum-Resistant Primary Peritoneal High Grade Serous Adenocarcinoma | +| NCIT:C205188 | Recurrent Platinum-Sensitive Endometrial Carcinoma | | NCIT:C191395 | Recurrent Platinum-Sensitive Fallopian Tube Carcinoma | | NCIT:C188391 | Recurrent Platinum-Sensitive Ovarian Carcinoma | | NCIT:C191407 | Recurrent Platinum-Sensitive Primary Peritoneal Carcinoma | @@ -8036,6 +8284,7 @@ | NCIT:C71700 | Recurrent Primary Central Nervous System Neoplasm | | NCIT:C181044 | Recurrent Primary Cutaneous Anaplastic Large Cell Lymphoma | | NCIT:C191823 | Recurrent Primary Cutaneous CD8-Positive Aggressive Epidermotropic Cytotoxic T-Cell Lymphoma | +| NCIT:C203667 | Recurrent Primary Cutaneous Diffuse Large B-Cell Lymphoma | | NCIT:C138027 | Recurrent Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type | | NCIT:C191818 | Recurrent Primary Cutaneous Gamma-Delta T-Cell Lymphoma | | NCIT:C142876 | Recurrent Primary Cutaneous Lymphoma | @@ -8079,6 +8328,7 @@ | NCIT:C199666 | Recurrent Salivary Gland Adenocarcinoma | | NCIT:C199663 | Recurrent Salivary Gland Adenocarcinoma, Not Otherwise Specified | | NCIT:C7926 | Recurrent Salivary Gland Carcinoma | +| NCIT:C203381 | Recurrent Salivary Gland Mucoepidermoid Carcinoma | | NCIT:C172650 | Recurrent Salivary Gland Squamous Cell Carcinoma | | NCIT:C148302 | Recurrent Sarcoma | | NCIT:C155648 | Recurrent Sarcoma of the Extremity | @@ -8212,6 +8462,7 @@ | NCIT:C134835 | Refractory B Acute Lymphoblastic Leukemia, BCR-ABL1-Like | | NCIT:C189043 | Refractory B Acute Lymphoblastic Leukemia, Philadelphia Chromosome Negative | | NCIT:C8870 | Refractory B Lymphoblastic Lymphoma | +| NCIT:C204126 | Refractory B-Cell Malignant Neoplasm | | NCIT:C8842 | Refractory B-Cell Non-Hodgkin Lymphoma | | NCIT:C157697 | Refractory B-Cell Prolymphocytic Leukemia | | NCIT:C199640 | Refractory Basal Cell Carcinoma | @@ -8348,6 +8599,7 @@ | NCIT:C138014 | Refractory Gray-Zone Lymphoma | | NCIT:C168784 | Refractory HER2-Negative Breast Carcinoma | | NCIT:C182110 | Refractory HER2-Positive Breast Carcinoma | +| NCIT:C202987 | Refractory HHV8-Positive Diffuse Large B-Cell Lymphoma, Not Otherwise Specified | | NCIT:C157687 | Refractory HIV-Related Lymphoproliferative Disorder | | NCIT:C171064 | Refractory Hairy Cell Leukemia Variant | | NCIT:C151907 | Refractory Head and Neck Carcinoma | @@ -8374,6 +8626,7 @@ | NCIT:C183515 | Refractory Indolent T-Cell Non-Hodgkin Lymphoma | | NCIT:C174247 | Refractory Intrahepatic Cholangiocarcinoma | | NCIT:C138026 | Refractory Intravascular Large B-Cell Lymphoma | +| NCIT:C203523 | Refractory Juvenile Myelomonocytic Leukemia | | NCIT:C156474 | Refractory Kaposi Sarcoma | | NCIT:C172623 | Refractory Kidney Carcinoma | | NCIT:C162727 | Refractory Kidney Medullary Carcinoma | @@ -8398,6 +8651,7 @@ | NCIT:C8650 | Refractory Lymphocyte-Depleted Classic Hodgkin Lymphoma | | NCIT:C142982 | Refractory Lymphocyte-Rich Classic Hodgkin Lymphoma | | NCIT:C134154 | Refractory Lymphoma | +| NCIT:C202989 | Refractory Lymphomatoid Granulomatosis | | NCIT:C8652 | Refractory Lymphoplasmacytic Lymphoma | | NCIT:C157686 | Refractory Lymphoproliferative Disorder | | NCIT:C177149 | Refractory Male Reproductive System Carcinoma | @@ -8475,6 +8729,7 @@ | NCIT:C8838 | Refractory Nodular Sclerosis Classic Hodgkin Lymphoma | | NCIT:C173328 | Refractory Non-Cutaneous Melanoma | | NCIT:C8701 | Refractory Non-Hodgkin Lymphoma | +| NCIT:C202899 | Refractory Non-Muscle Invasive Bladder Carcinoma | | NCIT:C180530 | Refractory Non-Muscle Invasive Bladder Urothelial Carcinoma | | NCIT:C173329 | Refractory Ocular Melanoma | | NCIT:C148384 | Refractory Oral Cavity Squamous Cell Carcinoma | @@ -8514,6 +8769,7 @@ | NCIT:C71701 | Refractory Primary Central Nervous System Neoplasm | | NCIT:C181045 | Refractory Primary Cutaneous Anaplastic Large Cell Lymphoma | | NCIT:C191824 | Refractory Primary Cutaneous CD8-Positive Aggressive Epidermotropic Cytotoxic T-Cell Lymphoma | +| NCIT:C203669 | Refractory Primary Cutaneous Diffuse Large B-Cell Lymphoma | | NCIT:C138028 | Refractory Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type | | NCIT:C191820 | Refractory Primary Cutaneous Gamma-Delta T-Cell Lymphoma | | NCIT:C142877 | Refractory Primary Cutaneous Lymphoma | @@ -8612,6 +8868,7 @@ | NCIT:C177798 | Refractory WHO Grade 1 Glioma | | NCIT:C158104 | Refractory WHO Grade 2 Glioma | | NCIT:C153865 | Refractory WHO Grade 3 Glioma | +| NCIT:C203369 | Refractory WHO Grade 4 Glioma | | NCIT:C142149 | Refractory Waldenstrom Macroglobulinemia | | NCIT:C188038 | Refractory Wilms Tumor | | NCIT:C5402 | Region 17p13 Allelic Loss Associated Medulloblastoma | @@ -8620,8 +8877,6 @@ | NCIT:C198177 | Regional Childhood Retinoblastoma by Toronto Guidelines v2 | | NCIT:C198416 | Regional Childhood Testicular Germ Cell Tumor by Toronto Guidelines v2 | | NCIT:C7862 | Regional Digestive System Neuroendocrine Tumor G1 | -| NCIT:C8716 | Regional Malignant Ureter Neoplasm | -| NCIT:C7639 | Regional Malignant Urethral Neoplasm | | NCIT:C7836 | Regional Neuroblastoma | | NCIT:C8168 | Regional Renal Pelvis and Ureter Urothelial Carcinoma | | NCIT:C162139 | Regressed Testicular Germ Cell Tumor | @@ -8658,7 +8913,9 @@ | NCIT:C188035 | Resectable Breast Carcinoma | | NCIT:C150604 | Resectable Carcinoma | | NCIT:C170961 | Resectable Carcinoma of Unknown Primary | +| NCIT:C205308 | Resectable Cervical Carcinoma | | NCIT:C27326 | Resectable Cholangiocarcinoma | +| NCIT:C205309 | Resectable Clear Cell Renal Cell Carcinoma | | NCIT:C167237 | Resectable Colon Carcinoma | | NCIT:C162257 | Resectable Colorectal Carcinoma | | NCIT:C190240 | Resectable Cutaneous Melanoma | @@ -8666,7 +8923,9 @@ | NCIT:C150607 | Resectable Dedifferentiated Liposarcoma | | NCIT:C156909 | Resectable Digestive System Carcinoma | | NCIT:C27323 | Resectable Duodenal Carcinoma | +| NCIT:C205310 | Resectable Endometrial Carcinoma | | NCIT:C198615 | Resectable Esophageal Adenocarcinoma | +| NCIT:C205311 | Resectable Esophageal Carcinoma | | NCIT:C156911 | Resectable Extrahepatic Bile Duct Adenocarcinoma | | NCIT:C8640 | Resectable Extrahepatic Bile Duct Carcinoma | | NCIT:C198617 | Resectable Gallbladder Adenocarcinoma | @@ -8680,7 +8939,7 @@ | NCIT:C156908 | Resectable Intrahepatic Cholangiocarcinoma | | NCIT:C175505 | Resectable Leiomyosarcoma | | NCIT:C150606 | Resectable Liposarcoma | -| NCIT:C165293 | Resectable Liver and Intrahepatic Bile Duct Carcinoma | +| NCIT:C165293 | Resectable Liver Carcinoma | | NCIT:C190954 | Resectable Lung Adenocarcinoma | | NCIT:C190952 | Resectable Lung Carcinoma | | NCIT:C165767 | Resectable Lung Non-Small Cell Carcinoma | @@ -8690,6 +8949,7 @@ | NCIT:C7692 | Resectable Malignant Liver Neoplasm | | NCIT:C154442 | Resectable Malignant Mesothelioma | | NCIT:C150602 | Resectable Malignant Neoplasm | +| NCIT:C205313 | Resectable Malignant Solid Neoplasm | | NCIT:C190239 | Resectable Melanoma | | NCIT:C193450 | Resectable Merkel Cell Carcinoma | | NCIT:C150620 | Resectable Neuroblastoma | @@ -8711,6 +8971,8 @@ | NCIT:C170464 | Resectable Skin Squamous Cell Carcinoma | | NCIT:C8639 | Resectable Small Intestinal Carcinoma | | NCIT:C153086 | Resectable Soft Tissue Sarcoma | +| NCIT:C201952 | Resectable Soft Tissue Sarcoma of the Trunk and Extremities | +| NCIT:C205314 | Resectable Triple-Negative Breast Carcinoma | | NCIT:C150611 | Resectable Undifferentiated Pleomorphic Sarcoma | | NCIT:C26959 | Reticulosarcoma Involving Spleen | | NCIT:C174539 | Retinal Astrocytoma | @@ -8733,6 +8995,7 @@ | NCIT:C22040 | Rhabdomyosarcoma of the Mouse Nervous System | | NCIT:C21750 | Rhabdomyosarcoma of the Mouse Prostate Gland | | NCIT:C21845 | Rhabdomyosarcoma of the Mouse Skin | +| NCIT:C202263 | Rhabdomyosarcoma with TFCP2 Rearrangement | | NCIT:C134783 | Rhesus Monkey Lymphoma | | NCIT:C134784 | Rhesus Monkey Mammary Tumor | | NCIT:C4792 | Right Atrial Myxoma | @@ -8746,8 +9009,12 @@ | NCIT:C168746 | SAMD9-Associated Hereditary Myelodysplastic Syndrome | | NCIT:C168747 | SAMD9L-Associated Hereditary Myelodysplastic Syndrome | | NCIT:C21880 | SJL Disease of the Mouse Hematologic System | +| NCIT:C201637 | SMARCA4 -Deficient Sinonasal Carcinoma | | NCIT:C186703 | SMARCB1 Schwannomatosis 1 | +| NCIT:C201636 | SMARCB1-Deficient Sinonasal Adenocarcinoma | +| NCIT:C201635 | SMARCB1-Deficient Sinonasal Carcinoma | | NCIT:C187445 | ST2 Diffuse Large B-Cell Lymphoma | +| NCIT:C201634 | SWI/SNF Complex-Deficient Sinonasal Carcinoma | | NCIT:C129927 | Sacral Chordoma | | NCIT:C168674 | Sacral Spine Neoplasm | | NCIT:C8021 | Salivary Gland Adenocarcinoma | @@ -8762,15 +9029,27 @@ | NCIT:C35839 | Salivary Gland Ductal Papilloma | | NCIT:C173715 | Salivary Gland Follicular Lymphoma | | NCIT:C173680 | Salivary Gland Hemangioma | +| NCIT:C203370 | Salivary Gland High Grade Adenocarcinoma, Not Otherwise Specified | +| NCIT:C8018 | Salivary Gland High Grade Carcinoma | +| NCIT:C8019 | Salivary Gland High Grade Mucoepidermoid Carcinoma | | NCIT:C173692 | Salivary Gland Hodgkin Lymphoma | +| NCIT:C201823 | Salivary Gland Hyalinizing Clear Cell Carcinoma | +| NCIT:C201764 | Salivary Gland Intercalated Duct Adenoma | +| NCIT:C203375 | Salivary Gland Intermediate Grade Adenocarcinoma, Not Otherwise Specified | +| NCIT:C8017 | Salivary Gland Intermediate Grade Mucoepidermoid Carcinoma | +| NCIT:C203376 | Salivary Gland Intestinal-Type Adenocarcinoma | | NCIT:C62192 | Salivary Gland Intraductal Carcinoma | | NCIT:C35834 | Salivary Gland Intraductal Papilloma | | NCIT:C35835 | Salivary Gland Inverted Ductal Papilloma | | NCIT:C173650 | Salivary Gland Large Cell Neuroendocrine Carcinoma | | NCIT:C173681 | Salivary Gland Lipoma | +| NCIT:C203374 | Salivary Gland Low Grade Adenocarcinoma, Not Otherwise Specified | +| NCIT:C8012 | Salivary Gland Low Grade Carcinoma | +| NCIT:C8015 | Salivary Gland Low Grade Mucoepidermoid Carcinoma | | NCIT:C173659 | Salivary Gland Lymphadenoma | | NCIT:C35736 | Salivary Gland Lymphoepithelial Carcinoma | | NCIT:C173690 | Salivary Gland Lymphoma | +| NCIT:C201772 | Salivary Gland Microsecretory Adenocarcinoma | | NCIT:C3686 | Salivary Gland Monomorphic Adenoma | | NCIT:C62193 | Salivary Gland Mucinous Adenocarcinoma | | NCIT:C173693 | Salivary Gland Mucosa-Associated Lymphoid Tissue Lymphoma | @@ -8780,10 +9059,12 @@ | NCIT:C173653 | Salivary Gland Neuroendocrine Carcinoma | | NCIT:C173687 | Salivary Gland Nodular Fasciitis | | NCIT:C173691 | Salivary Gland Non-Hodgkin Lymphoma | -| NCIT:C62194 | Salivary Gland Oncocytic Carcinoma | +| NCIT:C62194 | Salivary Gland Oncocytic Adenocarcinoma | | NCIT:C5932 | Salivary Gland Oncocytoma | | NCIT:C40409 | Salivary Gland Pleomorphic Adenoma | | NCIT:C35702 | Salivary Gland Polymorphous Adenocarcinoma | +| NCIT:C201781 | Salivary Gland Polymorphous Adenocarcinoma, Conventional Subtype | +| NCIT:C201786 | Salivary Gland Polymorphous Adenocarcinoma, Cribriform Subtype | | NCIT:C173649 | Salivary Gland Poorly Differentiated Carcinoma | | NCIT:C8022 | Salivary Gland Poorly Differentiated Squamous Cell Carcinoma | | NCIT:C35738 | Salivary Gland Sebaceous Adenoma | @@ -8793,11 +9074,14 @@ | NCIT:C35836 | Salivary Gland Sialadenoma Papilliferum | | NCIT:C200313 | Salivary Gland Striated Duct Adenoma | | NCIT:C8024 | Salivary Gland Undifferentiated Carcinoma | +| NCIT:C9024 | Sarcoma G1 | +| NCIT:C9028 | Sarcoma G2 | +| NCIT:C9029 | Sarcoma G3 | +| NCIT:C203583 | Sarcoma GX | | NCIT:C9388 | Sarcoma NCI Grade 1 | | NCIT:C9400 | Sarcoma NCI Grade 2 | | NCIT:C9415 | Sarcoma NCI Grade 3 | | NCIT:C21753 | Sarcoma NOS of the Mouse Prostate Gland | -| NCIT:C9416 | Sarcoma by AJCC Grade | | NCIT:C9023 | Sarcoma by FNCLCC Grade | | NCIT:C9387 | Sarcoma by NCI Grade | | NCIT:C155647 | Sarcoma of the Extremity | @@ -8810,10 +9094,11 @@ | NCIT:C21836 | Schwannoma of the Mouse Skin | | NCIT:C188213 | Schwannoma of the Seventh Cranial Nerve | | NCIT:C200533 | Sclerosing Angiomatoid Nodular Transformation of Spleen | +| NCIT:C204911 | Sclerosing Blue Nevus | | NCIT:C49027 | Sclerosing Epithelioid Fibrosarcoma | | NCIT:C173733 | Sclerosing Odontogenic Carcinoma | | NCIT:C121790 | Sclerosing PEComa | -| NCIT:C97135 | Sclerosing Polycystic Adenosis | +| NCIT:C97135 | Sclerosing Polycystic Adenoma | | NCIT:C121655 | Sclerosing Rhabdomyosarcoma | | NCIT:C45709 | Sclerosing Thymoma | | NCIT:C156282 | Scrotal Liposarcoma | @@ -8899,7 +9184,9 @@ | NCIT:C35837 | Sialoblastoma | | NCIT:C173682 | Sialolipoma | | NCIT:C177680 | Sigmoid Colon Carcinoma | +| NCIT:C203389 | Sigmoid Colon Neuroendocrine Tumor | | NCIT:C188043 | Sigmoid Colon Neuroendocrine Tumor G1 | +| NCIT:C203394 | Sigmoid Colon Neuroendocrine Tumor G2 | | NCIT:C22156 | Signet Ring Cell Adenocarcinoma of the Mouse Intestinal Tract | | NCIT:C63891 | Signet Ring Cell Adenocarcinoma of the Rat Glandular Stomach | | NCIT:C167369 | Signet Ring Cell/Histiocytoid Carcinoma | @@ -8924,13 +9211,14 @@ | NCIT:C173133 | Sinonasal Desmoid Fibromatosis | | NCIT:C27647 | Sinonasal Disorder | | NCIT:C173138 | Sinonasal Epithelioid Hemangioendothelioma | -| NCIT:C173175 | Sinonasal Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor | +| NCIT:C173175 | Sinonasal Ewing Sarcoma | | NCIT:C164251 | Sinonasal Exophytic Papilloma | | NCIT:C173172 | Sinonasal Extranodal NK/T-Cell Lymphoma | | NCIT:C173120 | Sinonasal Fibrosarcoma | +| NCIT:C202978 | Sinonasal Germ Cell Tumor | | NCIT:C173136 | Sinonasal Glomangiopericytoma | | NCIT:C173142 | Sinonasal Hemangioma | -| NCIT:C173078 | Sinonasal Human Papillomavirus-Related Carcinoma with Adenoid Cystic-Like Features | +| NCIT:C173078 | Sinonasal Human Papillomavirus-Related Multiphenotypic Carcinoma | | NCIT:C6871 | Sinonasal Inverted Papilloma | | NCIT:C173077 | Sinonasal Keratinizing Squamous Cell Carcinoma | | NCIT:C173091 | Sinonasal Large Cell Neuroendocrine Carcinoma | @@ -8942,6 +9230,10 @@ | NCIT:C166399 | Sinonasal Mucosal Melanoma | | NCIT:C173088 | Sinonasal NUT Carcinoma | | NCIT:C173089 | Sinonasal Neuroendocrine Carcinoma | +| NCIT:C202990 | Sinonasal Neuroendocrine Neoplasm | +| NCIT:C202991 | Sinonasal Neuroendocrine Tumor | +| NCIT:C203007 | Sinonasal Neuroendocrine Tumor G1 | +| NCIT:C203010 | Sinonasal Neuroendocrine Tumor G2 | | NCIT:C173144 | Sinonasal Neurofibroma | | NCIT:C173171 | Sinonasal Non-Hodgkin Lymphoma | | NCIT:C173174 | Sinonasal Olfactory Neuroblastoma | @@ -8954,11 +9246,13 @@ | NCIT:C173118 | Sinonasal Sarcoma | | NCIT:C173143 | Sinonasal Schwannoma | | NCIT:C116318 | Sinonasal Small Cell Neuroendocrine Carcinoma | +| NCIT:C202852 | Sinonasal Smooth Muscle Tumor of Uncertain Malignant Potential | | NCIT:C173117 | Sinonasal Soft Tissue Neoplasm | | NCIT:C173137 | Sinonasal Solitary Fibrous Tumor | -| NCIT:C173079 | Sinonasal Spindle Cell Squamous Cell Carcinoma | +| NCIT:C173079 | Sinonasal Spindle Cell Squamous Carcinoma | | NCIT:C173128 | Sinonasal Synovial Sarcoma | | NCIT:C173094 | Sinonasal Teratocarcinosarcoma | +| NCIT:C202981 | Sinonasal Teratoma | | NCIT:C190160 | Sinonasal Tract Myxoma | | NCIT:C173121 | Sinonasal Undifferentiated Pleomorphic Sarcoma | | NCIT:C21873 | Sinus Histiocytosis of Mouse | @@ -8985,12 +9279,13 @@ | NCIT:C54665 | Skin Keratotic Basal Cell Carcinoma | | NCIT:C5566 | Skin Lipomatous Neoplasm | | NCIT:C4370 | Skin Lymphangioleiomyomatosis | -| NCIT:C165467 | Skin Lymphoepithelioma-Like Carcinoma | +| NCIT:C165467 | Skin Lymphoepithelial Carcinoma | | NCIT:C167370 | Skin Myoepithelioma | | NCIT:C172632 | Skin Myxofibrosarcoma | | NCIT:C6578 | Skin Myxoma | | NCIT:C62282 | Skin Nodular Basal Cell Carcinoma | | NCIT:C5616 | Skin Nodular Solid Basal Cell Carcinoma | +| NCIT:C204355 | Skin Nodulocystic Basal Cell Carcinoma | | NCIT:C170476 | Skin Pleomorphic Lipoma | | NCIT:C170473 | Skin Pleomorphic Liposarcoma | | NCIT:C27719 | Skin Radiation-Related Angiosarcoma | @@ -9000,6 +9295,7 @@ | NCIT:C170474 | Skin Spindle Cell/Pleomorphic Lipoma | | NCIT:C165466 | Skin Squamous Cell Carcinoma with Osteoclast-Like Giant Cells | | NCIT:C165468 | Skin Squamous Cell Carcinoma with Sarcomatoid Differentiation | +| NCIT:C205551 | Skin Syncytial Myoepithelioma | | NCIT:C5354 | Skin Vascular Neoplasm | | NCIT:C165465 | Skin Verrucous Carcinoma | | NCIT:C192732 | Skull Base Carcinoma | @@ -9063,6 +9359,7 @@ | NCIT:C155910 | Smoldering Waldenstrom Macroglobulinemia | | NCIT:C23105 | Smooth Muscle Neoplasms of the Mouse Nose and Paranasal Sinuses | | NCIT:C23053 | Smooth Muscle Neoplasms of the Mouse Oral Cavity | +| NCIT:C202851 | Smooth Muscle Tumor of Uncertain Malignant Potential | | NCIT:C6210 | Soft Palate Benign Granular Cell Tumor | | NCIT:C6211 | Soft Palate Pleomorphic Adenoma | | NCIT:C4941 | Soft Palate Squamous Cell Carcinoma | @@ -9082,6 +9379,7 @@ | NCIT:C27493 | Solid Alveolar Rhabdomyosarcoma | | NCIT:C49110 | Solid Angioleiomyoma | | NCIT:C4137 | Solid Carcinoma | +| NCIT:C205539 | Solid Cystic Hidradenoma | | NCIT:C51133 | Solid Glomus Tumor | | NCIT:C5651 | Solid Lung Adenocarcinoma | | NCIT:C21685 | Solid Mammary Carcinoma of Mouse | @@ -9089,7 +9387,6 @@ | NCIT:C9292 | Solid Neoplasm | | NCIT:C201136 | Solid Pseudopapillary Neoplasm | | NCIT:C165261 | Solid Pseudopapillary Neoplasm of the Ovary | -| NCIT:C39755 | Solid/Multicystic Ameloblastoma | | NCIT:C46095 | Solid/Trabecular Variant Thyroid Gland Papillary Carcinoma | | NCIT:C5394 | Solitary Adult Fibroma | | NCIT:C121681 | Solitary Circumscribed Neuroma | @@ -9102,6 +9399,7 @@ | NCIT:C45932 | Sparsely Granulated Lactotroph Pituitary Neuroendocrine Tumor | | NCIT:C45926 | Sparsely Granulated Somatotroph Pituitary Neuroendocrine Tumor | | NCIT:C186494 | Spinal Cord Ependymoma, MYCN Amplified | +| NCIT:C201976 | Spinal Cord Pilocytic Astrocytoma | | NCIT:C155948 | Spinal Hemangioblastoma | | NCIT:C168693 | Spinal Neoplasm | | NCIT:C21745 | Spindle Cell / Sarcomatoid Carcinoma of the Mouse Prostate Gland | @@ -9118,7 +9416,9 @@ | NCIT:C167344 | Spiradenocylindrocarcinoma | | NCIT:C167342 | Spiradenocylindroma | | NCIT:C21820 | Spiradenoma Type of Basaloid Follicular Neoplasm of the Mouse Skin | +| NCIT:C136825 | Spitz Melanocytoma | | NCIT:C165497 | Spitz Melanoma | +| NCIT:C204790 | Spitz Tumor | | NCIT:C7310 | Splenic B Lymphoblastic Lymphoma | | NCIT:C80308 | Splenic B-Cell Lymphoma/Leukemia, Unclassifiable | | NCIT:C7309 | Splenic Burkitt Lymphoma | @@ -9274,6 +9574,7 @@ | NCIT:C8932 | Stage 0 Colorectal Cancer AJCC v6 and v7 | | NCIT:C134182 | Stage 0 Colorectal Cancer AJCC v8 | | NCIT:C8423 | Stage 0 Cutaneous Melanoma AJCC v6 and v7 | +| NCIT:C85887 | Stage 0 Cutaneous Merkel Cell Carcinoma AJCC v7 | | NCIT:C133255 | Stage 0 Cutaneous Squamous Cell Carcinoma of the Head and Neck AJCC v8 | | NCIT:C88027 | Stage 0 Digestive System Neuroendocrine Tumor AJCC v7 | | NCIT:C88089 | Stage 0 Distal Bile Duct Cancer AJCC v7 | @@ -9304,7 +9605,6 @@ | NCIT:C9104 | Stage 0 Lung Non-Small Cell Cancer AJCC v6 and v7 | | NCIT:C8763 | Stage 0 Lung Squamous Cell Carcinoma AJCC v6 and v7 | | NCIT:C132783 | Stage 0 Major Salivary Gland Cancer AJCC v8 | -| NCIT:C85887 | Stage 0 Merkel Cell Carcinoma AJCC v7 | | NCIT:C6036 | Stage 0 Nasopharyngeal Keratinizing Squamous Cell Carcinoma AJCC v6, v7, and v8 | | NCIT:C6035 | Stage 0 Nasopharyngeal Undifferentiated Carcinoma AJCC v6, v7, and v8 | | NCIT:C6052 | Stage 0 Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7 | @@ -9424,6 +9724,7 @@ | NCIT:C135206 | Stage I Colorectal Neuroendocrine Tumor AJCC v8 | | NCIT:C7916 | Stage I Cutaneous Melanoma AJCC v6 | | NCIT:C88414 | Stage I Cutaneous Melanoma AJCC v7 | +| NCIT:C85889 | Stage I Cutaneous Merkel Cell Carcinoma AJCC v7 | | NCIT:C133256 | Stage I Cutaneous Squamous Cell Carcinoma of the Head and Neck AJCC v8 | | NCIT:C7795 | Stage I Cutaneous T-Cell Non-Hodgkin Lymphoma | | NCIT:C101540 | Stage I Differentiated Thyroid Gland Carcinoma 45 Years and Older AJCC v7 | @@ -9496,7 +9797,6 @@ | NCIT:C5895 | Stage I Major Salivary Gland Cancer AJCC v7 | | NCIT:C132781 | Stage I Major Salivary Gland Cancer AJCC v8 | | NCIT:C146849 | Stage I Malignant Mediastinal Germ Cell Tumor | -| NCIT:C85889 | Stage I Merkel Cell Carcinoma AJCC v7 | | NCIT:C7796 | Stage I Mycosis Fungoides AJCC v7 | | NCIT:C88150 | Stage I Mycosis Fungoides and Sezary Syndrome AJCC v7 | | NCIT:C141347 | Stage I Mycosis Fungoides and Sezary Syndrome AJCC v8 | @@ -9617,6 +9917,7 @@ | NCIT:C198043 | Stage IA Childhood Hodgkin Lymphoma by Toronto Guidelines v2 | | NCIT:C198420 | Stage IA Childhood Testicular Germ Cell Tumor by Toronto Guidelines v2 | | NCIT:C86026 | Stage IA Cutaneous Melanoma AJCC v7 | +| NCIT:C85890 | Stage IA Cutaneous Merkel Cell Carcinoma AJCC v7 | | NCIT:C88090 | Stage IA Distal Bile Duct Cancer AJCC v7 | | NCIT:C87782 | Stage IA Esophageal Adenocarcinoma AJCC v7 | | NCIT:C115117 | Stage IA Esophageal Cancer AJCC v7 | @@ -9639,7 +9940,6 @@ | NCIT:C5652 | Stage IA Lung Non-Small Cell Carcinoma AJCC v7 | | NCIT:C6674 | Stage IA Lung Small Cell Carcinoma AJCC v7 | | NCIT:C6687 | Stage IA Lung Squamous Cell Carcinoma AJCC v7 | -| NCIT:C85890 | Stage IA Merkel Cell Carcinoma AJCC v7 | | NCIT:C130951 | Stage IA Mycosis Fungoides AJCC v7 | | NCIT:C88151 | Stage IA Mycosis Fungoides and Sezary Syndrome AJCC v7 | | NCIT:C141348 | Stage IA Mycosis Fungoides and Sezary Syndrome AJCC v8 | @@ -9695,6 +9995,7 @@ | NCIT:C198044 | Stage IB Childhood Hodgkin Lymphoma by Toronto Guidelines v2 | | NCIT:C198421 | Stage IB Childhood Testicular Germ Cell Tumor by Toronto Guidelines v2 | | NCIT:C86030 | Stage IB Cutaneous Melanoma AJCC v7 | +| NCIT:C85892 | Stage IB Cutaneous Merkel Cell Carcinoma AJCC v7 | | NCIT:C88091 | Stage IB Distal Bile Duct Cancer AJCC v7 | | NCIT:C87783 | Stage IB Esophageal Adenocarcinoma AJCC v7 | | NCIT:C115118 | Stage IB Esophageal Cancer AJCC v7 | @@ -9718,7 +10019,6 @@ | NCIT:C5653 | Stage IB Lung Non-Small Cell Carcinoma AJCC v7 | | NCIT:C6675 | Stage IB Lung Small Cell Carcinoma AJCC v7 | | NCIT:C6692 | Stage IB Lung Squamous Cell Carcinoma AJCC v7 | -| NCIT:C85892 | Stage IB Merkel Cell Carcinoma AJCC v7 | | NCIT:C130237 | Stage IB Mycosis Fungoides AJCC v7 | | NCIT:C88152 | Stage IB Mycosis Fungoides and Sezary Syndrome AJCC v7 | | NCIT:C141349 | Stage IB Mycosis Fungoides and Sezary Syndrome AJCC v8 | @@ -9824,6 +10124,7 @@ | NCIT:C8474 | Stage II Contiguous Adult Diffuse Mixed Cell Lymphoma | | NCIT:C8471 | Stage II Contiguous Adult Diffuse Small Cleaved Cell Lymphoma | | NCIT:C7917 | Stage II Cutaneous Melanoma AJCC v6 and v7 | +| NCIT:C85893 | Stage II Cutaneous Merkel Cell Carcinoma AJCC v7 | | NCIT:C133257 | Stage II Cutaneous Squamous Cell Carcinoma of the Head and Neck AJCC v8 | | NCIT:C7797 | Stage II Cutaneous T-Cell Non-Hodgkin Lymphoma | | NCIT:C101542 | Stage II Differentiated Thyroid Gland Carcinoma 45 Years and Older AJCC v7 | @@ -9896,7 +10197,6 @@ | NCIT:C5896 | Stage II Major Salivary Gland Cancer AJCC v7 | | NCIT:C132785 | Stage II Major Salivary Gland Cancer AJCC v8 | | NCIT:C146850 | Stage II Malignant Mediastinal Germ Cell Tumor | -| NCIT:C85893 | Stage II Merkel Cell Carcinoma AJCC v7 | | NCIT:C7798 | Stage II Mycosis Fungoides AJCC v7 | | NCIT:C88153 | Stage II Mycosis Fungoides and Sezary Syndrome AJCC v7 | | NCIT:C141350 | Stage II Mycosis Fungoides and Sezary Syndrome AJCC v8 | @@ -10034,6 +10334,7 @@ | NCIT:C134187 | Stage IIA Colorectal Cancer AJCC v8 | | NCIT:C135207 | Stage IIA Colorectal Neuroendocrine Tumor AJCC v8 | | NCIT:C86033 | Stage IIA Cutaneous Melanoma AJCC v6 and v7 | +| NCIT:C85894 | Stage IIA Cutaneous Merkel Cell Carcinoma AJCC v7 | | NCIT:C88029 | Stage IIA Digestive System Neuroendocrine Tumor AJCC v7 | | NCIT:C88092 | Stage IIA Distal Bile Duct Cancer AJCC v7 | | NCIT:C134815 | Stage IIA Distal Bile Duct Cancer AJCC v8 | @@ -10054,7 +10355,6 @@ | NCIT:C5655 | Stage IIA Lung Non-Small Cell Carcinoma AJCC v7 | | NCIT:C6677 | Stage IIA Lung Small Cell Carcinoma AJCC v7 | | NCIT:C6688 | Stage IIA Lung Squamous Cell Carcinoma AJCC v7 | -| NCIT:C85894 | Stage IIA Merkel Cell Carcinoma AJCC v7 | | NCIT:C88154 | Stage IIA Mycosis Fungoides and Sezary Syndrome AJCC v7 | | NCIT:C141351 | Stage IIA Mycosis Fungoides and Sezary Syndrome AJCC v8 | | NCIT:C5998 | Stage IIA Nasopharyngeal Carcinoma | @@ -10118,6 +10418,7 @@ | NCIT:C134188 | Stage IIB Colorectal Cancer AJCC v8 | | NCIT:C135208 | Stage IIB Colorectal Neuroendocrine Tumor AJCC v8 | | NCIT:C27742 | Stage IIB Cutaneous Melanoma AJCC v6 and v7 | +| NCIT:C85895 | Stage IIB Cutaneous Merkel Cell Carcinoma AJCC v7 | | NCIT:C88030 | Stage IIB Digestive System Neuroendocrine Tumor AJCC v7 | | NCIT:C88093 | Stage IIB Distal Bile Duct Cancer AJCC v7 | | NCIT:C134816 | Stage IIB Distal Bile Duct Cancer AJCC v8 | @@ -10138,7 +10439,6 @@ | NCIT:C5654 | Stage IIB Lung Non-Small Cell Carcinoma AJCC v7 | | NCIT:C6676 | Stage IIB Lung Small Cell Carcinoma AJCC v7 | | NCIT:C6691 | Stage IIB Lung Squamous Cell Carcinoma AJCC v7 | -| NCIT:C85895 | Stage IIB Merkel Cell Carcinoma AJCC v7 | | NCIT:C88155 | Stage IIB Mycosis Fungoides and Sezary Syndrome AJCC v7 | | NCIT:C141352 | Stage IIB Mycosis Fungoides and Sezary Syndrome AJCC v8 | | NCIT:C5999 | Stage IIB Nasopharyngeal Carcinoma | @@ -10175,8 +10475,8 @@ | NCIT:C87815 | Stage IIC Colorectal Cancer AJCC v7 | | NCIT:C134190 | Stage IIC Colorectal Cancer AJCC v8 | | NCIT:C86034 | Stage IIC Cutaneous Melanoma AJCC v6 and v7 | +| NCIT:C85896 | Stage IIC Cutaneous Merkel Cell Carcinoma AJCC v7 | | NCIT:C6276 | Stage IIC Fallopian Tube Cancer AJCC v6 and v7 | -| NCIT:C85896 | Stage IIC Merkel Cell Carcinoma AJCC v7 | | NCIT:C5225 | Stage IIC Ovarian Cancer AJCC v6 and v7 | | NCIT:C6294 | Stage IIC Ovarian Germ Cell Tumor AJCC v6 and v7 | | NCIT:C140168 | Stage IIC Prostate Cancer AJCC v8 | @@ -10240,6 +10540,7 @@ | NCIT:C134191 | Stage III Colorectal Cancer AJCC v8 | | NCIT:C7918 | Stage III Cutaneous Melanoma AJCC v6 | | NCIT:C88415 | Stage III Cutaneous Melanoma AJCC v7 | +| NCIT:C85897 | Stage III Cutaneous Merkel Cell Carcinoma AJCC v7 | | NCIT:C133258 | Stage III Cutaneous Squamous Cell Carcinoma of the Head and Neck AJCC v8 | | NCIT:C7799 | Stage III Cutaneous T-Cell Non-Hodgkin Lymphoma | | NCIT:C87545 | Stage III Differentiated Thyroid Gland Carcinoma AJCC v7 | @@ -10310,7 +10611,6 @@ | NCIT:C5897 | Stage III Major Salivary Gland Cancer AJCC v7 | | NCIT:C132786 | Stage III Major Salivary Gland Cancer AJCC v8 | | NCIT:C146851 | Stage III Malignant Mediastinal Germ Cell Tumor | -| NCIT:C85897 | Stage III Merkel Cell Carcinoma AJCC v7 | | NCIT:C87532 | Stage III Mucosal Melanoma of the Head and Neck AJCC v7 | | NCIT:C7800 | Stage III Mycosis Fungoides AJCC v7 | | NCIT:C88157 | Stage III Mycosis Fungoides and Sezary Syndrome AJCC v7 | @@ -10440,6 +10740,7 @@ | NCIT:C134192 | Stage IIIA Colorectal Cancer AJCC v8 | | NCIT:C135209 | Stage IIIA Colorectal Neuroendocrine Tumor AJCC v8 | | NCIT:C86049 | Stage IIIA Cutaneous Melanoma AJCC v7 | +| NCIT:C85898 | Stage IIIA Cutaneous Merkel Cell Carcinoma AJCC v7 | | NCIT:C88031 | Stage IIIA Digestive System Neuroendocrine Tumor AJCC v7 | | NCIT:C134818 | Stage IIIA Distal Bile Duct Cancer AJCC v8 | | NCIT:C87784 | Stage IIIA Esophageal Adenocarcinoma AJCC v7 | @@ -10469,7 +10770,6 @@ | NCIT:C9102 | Stage IIIA Lung Non-Small Cell Cancer AJCC v7 | | NCIT:C6680 | Stage IIIA Lung Small Cell Carcinoma AJCC v7 | | NCIT:C6689 | Stage IIIA Lung Squamous Cell Carcinoma AJCC v7 | -| NCIT:C85898 | Stage IIIA Merkel Cell Carcinoma AJCC v7 | | NCIT:C88158 | Stage IIIA Mycosis Fungoides and Sezary Syndrome AJCC v7 | | NCIT:C141354 | Stage IIIA Mycosis Fungoides and Sezary Syndrome AJCC v8 | | NCIT:C6258 | Stage IIIA Ovarian Cancer AJCC v6 and v7 | @@ -10531,6 +10831,7 @@ | NCIT:C134193 | Stage IIIB Colorectal Cancer AJCC v8 | | NCIT:C135210 | Stage IIIB Colorectal Neuroendocrine Tumor AJCC v8 | | NCIT:C86051 | Stage IIIB Cutaneous Melanoma AJCC v7 | +| NCIT:C85899 | Stage IIIB Cutaneous Merkel Cell Carcinoma AJCC v7 | | NCIT:C88032 | Stage IIIB Digestive System Neuroendocrine Tumor AJCC v7 | | NCIT:C134819 | Stage IIIB Distal Bile Duct Cancer AJCC v8 | | NCIT:C87785 | Stage IIIB Esophageal Adenocarcinoma AJCC v7 | @@ -10562,7 +10863,6 @@ | NCIT:C35756 | Stage IIIB Lung Small Cell Carcinoma with Pleural Effusion AJCC v7 | | NCIT:C35757 | Stage IIIB Lung Small Cell Carcinoma without Pleural Effusion AJCC v7 | | NCIT:C6690 | Stage IIIB Lung Squamous Cell Carcinoma AJCC v7 | -| NCIT:C85899 | Stage IIIB Merkel Cell Carcinoma AJCC v7 | | NCIT:C88159 | Stage IIIB Mycosis Fungoides and Sezary Syndrome AJCC v7 | | NCIT:C141355 | Stage IIIB Mycosis Fungoides and Sezary Syndrome AJCC v8 | | NCIT:C6259 | Stage IIIB Ovarian Cancer AJCC v6 and v7 | @@ -10709,6 +11009,7 @@ | NCIT:C134195 | Stage IV Colorectal Cancer AJCC v8 | | NCIT:C135211 | Stage IV Colorectal Neuroendocrine Tumor AJCC v8 | | NCIT:C9096 | Stage IV Cutaneous Melanoma AJCC v6 and v7 | +| NCIT:C85900 | Stage IV Cutaneous Merkel Cell Carcinoma AJCC v7 | | NCIT:C133259 | Stage IV Cutaneous Squamous Cell Carcinoma of the Head and Neck AJCC v8 | | NCIT:C7801 | Stage IV Cutaneous T-Cell Non-Hodgkin Lymphoma | | NCIT:C140973 | Stage IV Differentiated Thyroid Gland Carcinoma AJCC v8 | @@ -10783,7 +11084,6 @@ | NCIT:C5899 | Stage IV Major Salivary Gland Carcinoma with Metastasis | | NCIT:C5900 | Stage IV Major Salivary Gland Carcinoma without Metastasis | | NCIT:C146852 | Stage IV Malignant Mediastinal Germ Cell Tumor | -| NCIT:C85900 | Stage IV Merkel Cell Carcinoma AJCC v7 | | NCIT:C7802 | Stage IV Mycosis Fungoides AJCC v7 | | NCIT:C88160 | Stage IV Mycosis Fungoides and Sezary Syndrome AJCC v7 | | NCIT:C141356 | Stage IV Mycosis Fungoides and Sezary Syndrome AJCC v8 | @@ -11184,6 +11484,7 @@ | NCIT:C5947 | Submandibular Gland Undifferentiated Carcinoma | | NCIT:C23002 | Subtypes of Diffuse Large B Cell Lymphoma of the Mouse Hematologic System | | NCIT:C121844 | Subungual Exostosis | +| NCIT:C204887 | Subungual Melanoma | | NCIT:C156464 | Succinate Dehydrogenase-Deficient Renal Cell Carcinoma | | NCIT:C134951 | Suncus Murinus Mammary Tumor | | NCIT:C40323 | Superficial Angiomyxoma | @@ -11208,6 +11509,7 @@ | NCIT:C7048 | Supratentorial Meningioma | | NCIT:C3397 | Supratentorial Neoplasm | | NCIT:C156041 | Supratentorial Pleomorphic Xanthoastrocytoma | +| NCIT:C202252 | Surface Osteoma | | NCIT:C3682 | Sweat Gland Tubular Carcinoma | | NCIT:C200087 | Synchronous Ipsilateral Breast Carcinoma | | NCIT:C176467 | Synovial Chondrosarcoma | @@ -11222,6 +11524,14 @@ | NCIT:C37195 | Systemic Anaplastic Large Cell Lymphoma, ALK-Positive | | NCIT:C199677 | Systemic Hydroa Vacciniforme Lymphoproliferative Disorder | | NCIT:C186735 | Systemic Mastocytosis with an Associated Germ Cell Tumor | +| NCIT:C203434 | T Acute Lymphoblastic Leukemia with LMO1 Rearrangement | +| NCIT:C203435 | T Acute Lymphoblastic Leukemia with LMO2 Rearrangement | +| NCIT:C203469 | T Acute Lymphoblastic Leukemia with Recurrent Genetic Abnormalities | +| NCIT:C203428 | T Acute Lymphoblastic Leukemia with SPI1 Rearrangement | +| NCIT:C203433 | T Acute Lymphoblastic Leukemia with TAL1 Rearrangement | +| NCIT:C203431 | T Acute Lymphoblastic Leukemia with TLX1 Rearrangement | +| NCIT:C203432 | T Acute Lymphoblastic Leukemia with TLX3 Rearrangement | +| NCIT:C203426 | T Acute Lymphoblastic Leukemia, HOXA Dysregulated | | NCIT:C199174 | T Acute Lymphoblastic Leukemia, Not Otherwise Specified | | NCIT:C22999 | T Cell Neoplasms of Undetermined Character of the Mouse Hematologic System | | NCIT:C21923 | T Cell Neoplasms of the Mouse Hematologic System | @@ -11254,6 +11564,7 @@ | NCIT:C140225 | Testicular Cancer by AJCC v8 Stage | | NCIT:C192106 | Testicular Cystic Trophoblastic Tumor | | NCIT:C36092 | Testicular Dermoid Cyst | +| NCIT:C162467 | Testicular Diffuse Large B-Cell Lymphoma | | NCIT:C150589 | Testicular Follicular Lymphoma | | NCIT:C40345 | Testicular Germ Cell Neoplasia In Situ | | NCIT:C7326 | Testicular Germ Cell Neoplasia In Situ with Extratubular Extension | @@ -11306,8 +11617,6 @@ | NCIT:C168672 | Thoracic Spine Neoplasm | | NCIT:C35506 | Throat Carcinoma | | NCIT:C183315 | Thymic Adenocarcinoma, Not Otherwise Specified | -| NCIT:C45719 | Thymic Atypical Carcinoid Tumor | -| NCIT:C6430 | Thymic Carcinoid Tumor | | NCIT:C183313 | Thymic Carcinoma with Adenoid Cystic Carcinoma-Like Features | | NCIT:C183316 | Thymic Carcinoma, Not Otherwise Specified | | NCIT:C183314 | Thymic Enteric-Type Adenocarcinoma | @@ -11316,7 +11625,9 @@ | NCIT:C95057 | Thymic Hodgkin Lymphoma | | NCIT:C45380 | Thymic Mucosa-Associated Lymphoid Tissue Lymphoma | | NCIT:C162460 | Thymic Neuroendocrine Neoplasm | -| NCIT:C45720 | Thymic Typical Carcinoid Tumor | +| NCIT:C6430 | Thymic Neuroendocrine Tumor | +| NCIT:C45720 | Thymic Neuroendocrine Tumor G1 | +| NCIT:C45719 | Thymic Neuroendocrine Tumor G2 | | NCIT:C95038 | Thymoliposarcoma | | NCIT:C136345 | Thymoma by AJCC v8 Stage | | NCIT:C112006 | Thymoma by Masaoka-Koga Stage | @@ -11388,19 +11699,31 @@ | NCIT:C173807 | Tongue Adenosquamous Carcinoma | | NCIT:C156273 | Tongue Alveolar Soft Part Sarcoma' | | NCIT:C4824 | Tongue Carcinoma | +| NCIT:C201880 | Tongue Ectomesenchymal Chondromyxoid Tumor | +| NCIT:C202898 | Tongue GLI1-Altered Soft Tissue Tumor | | NCIT:C7734 | Tongue Lipoma | | NCIT:C173404 | Tongue Liposarcoma | +| NCIT:C202621 | Tongue Low Grade Myofibroblastic Sarcoma | | NCIT:C181160 | Tongue Mucoepidermoid Carcinoma | +| NCIT:C202861 | Tongue Neurofibroma | | NCIT:C156274 | Tongue Sarcoma | +| NCIT:C202877 | Tongue Schwannoma | +| NCIT:C201878 | Tongue Verrucous Carcinoma | | NCIT:C188072 | Tonsillar Diffuse Large B-Cell Lymphoma | | NCIT:C173797 | Tonsillar Disorder | | NCIT:C188080 | Tonsillar Mantle Cell Lymphoma | | NCIT:C8184 | Tonsillar Undifferentiated Carcinoma | | NCIT:C27755 | Topoisomerase II Inhibitor-Related Acute Myeloid Leukemia | | NCIT:C3688 | Trabecular Adenoma | +| NCIT:C201747 | Tracheal Basaloid Squamous Cell Carcinoma | +| NCIT:C201742 | Tracheal Verrucous Carcinoma | | NCIT:C38458 | Traditional Serrated Adenoma | | NCIT:C179721 | Transformed B-Cell Lymphoma, Unclassifiable, with Features Intermediate between Diffuse Large B-Cell Lymphoma and Classic Hodgkin Lymphoma to Diffuse Large B-Cell Lymphoma | | NCIT:C157624 | Transformed Chronic Lymphocytic Leukemia to Diffuse Large B-Cell Lymphoma | +| NCIT:C201960 | Transformed Chronic Lymphocytic Leukemia to Hodgkin Lymphoma | +| NCIT:C202133 | Transformed EGFR-Positive Lung Adenocarcinoma to Small Cell Carcinoma | +| NCIT:C202128 | Transformed EGFR-Positive Lung Adenocarcinoma to Squamous Cell Carcinoma | +| NCIT:C202132 | Transformed EGFR-Positive Lung Non-Small Cell Carcinoma to Small Cell Carcinoma | | NCIT:C139681 | Transformed Follicular Lymphoma to Diffuse Large B-Cell Lymphoma | | NCIT:C179717 | Transformed Indolent B-Cell Non-Hodgkin Lymphoma to Diffuse Large B-Cell Lymphoma | | NCIT:C185134 | Transformed Lymphoplasmacytic Lymphoma to Diffuse Large B-Cell Lymphoma | @@ -11408,6 +11731,7 @@ | NCIT:C165783 | Transformed Mycosis Fungoides | | NCIT:C151957 | Transformed Non-Hodgkin Lymphoma | | NCIT:C157625 | Transformed Small Lymphocytic Lymphoma to Diffuse Large B-Cell Lymphoma | +| NCIT:C201961 | Transformed Small Lymphocytic Lymphoma to Hodgkin Lymphoma | | NCIT:C185135 | Transformed Waldenstrom Macroglobulinemia to Diffuse Large B-Cell Lymphoma | | NCIT:C64158 | Transitional Cell Carcinoma of the Rat Renal Pelvis | | NCIT:C64159 | Transitional Cell Carcinoma of the Rat Ureter | @@ -11433,7 +11757,9 @@ | NCIT:C27638 | Transplant-Related Renal Cell Carcinoma | | NCIT:C27636 | Transplant-Related Skin Squamous Cell Carcinoma | | NCIT:C154700 | Transplant-Related Squamous Cell Carcinoma | +| NCIT:C203390 | Transverse Colon Neuroendocrine Tumor | | NCIT:C6426 | Transverse Colon Neuroendocrine Tumor G1 | +| NCIT:C203395 | Transverse Colon Neuroendocrine Tumor G2 | | NCIT:C191963 | Treatment-Related Prostate Neuroendocrine Carcinoma | | NCIT:C43326 | Trichilemmal Carcinoma | | NCIT:C4113 | Trichilemmoma | @@ -11445,6 +11771,7 @@ | NCIT:C21817 | Trichoepithelioma Type of Basaloid Follicular Neoplasm of the Mouse Skin | | NCIT:C43329 | Trichofollicular Carcinoma | | NCIT:C21818 | Trichofolliculoma Type of Basaloid Follicular Neoplasm of the Mouse Skin | +| NCIT:C205371 | Trichogerminoma | | NCIT:C178375 | Triple-Class Refractory Multiple Myeloma | | NCIT:C35382 | True Histiocytic Lymphoma | | NCIT:C22153 | Tubular Adenocarcinoma of the Mouse Intestinal Tract | @@ -11514,13 +11841,19 @@ | NCIT:C175384 | Unresectable Anal Canal Squamous Cell Carcinoma | | NCIT:C173156 | Unresectable Anal Squamous Cell Carcinoma | | NCIT:C168718 | Unresectable Angiosarcoma | +| NCIT:C203619 | Unresectable Appendix Adenocarcinoma | +| NCIT:C203282 | Unresectable Astrocytic Tumor | +| NCIT:C203269 | Unresectable Astrocytoma, IDH-Mutant | | NCIT:C157330 | Unresectable Basal Cell Carcinoma | | NCIT:C171322 | Unresectable Bile Duct Carcinoma | | NCIT:C176042 | Unresectable Biliary Tract Carcinoma | +| NCIT:C203409 | Unresectable Bladder Adenocarcinoma | | NCIT:C167075 | Unresectable Bladder Carcinoma | | NCIT:C191857 | Unresectable Bladder Small Cell Neuroendocrine Carcinoma | +| NCIT:C203411 | Unresectable Bladder Squamous Cell Carcinoma | | NCIT:C158586 | Unresectable Bladder Urothelial Carcinoma | | NCIT:C153072 | Unresectable Bone Sarcoma | +| NCIT:C203331 | Unresectable Breast Adenocarcinoma | | NCIT:C158752 | Unresectable Breast Carcinoma | | NCIT:C158751 | Unresectable Breast Inflammatory Carcinoma | | NCIT:C148124 | Unresectable Carcinoma | @@ -11531,6 +11864,7 @@ | NCIT:C174025 | Unresectable Cervical Squamous Cell Carcinoma | | NCIT:C27324 | Unresectable Cholangiocarcinoma | | NCIT:C153325 | Unresectable Chordoma | +| NCIT:C201953 | Unresectable Chromophobe Renal Cell Carcinoma | | NCIT:C165449 | Unresectable Clear Cell Renal Cell Carcinoma | | NCIT:C162116 | Unresectable Colon Adenocarcinoma | | NCIT:C180406 | Unresectable Colon Carcinoma | @@ -11543,6 +11877,10 @@ | NCIT:C155877 | Unresectable Desmoid Fibromatosis | | NCIT:C170826 | Unresectable Desmoplastic Small Round Cell Tumor | | NCIT:C168572 | Unresectable Differentiated Thyroid Gland Carcinoma | +| NCIT:C203286 | Unresectable Diffuse Glioma | +| NCIT:C203272 | Unresectable Diffuse Hemispheric Glioma, H3 G34-Mutant | +| NCIT:C203263 | Unresectable Diffuse Midline Glioma | +| NCIT:C203271 | Unresectable Diffuse Midline Glioma, H3 K27M-Mutant | | NCIT:C129654 | Unresectable Digestive System Adenocarcinoma | | NCIT:C155903 | Unresectable Digestive System Carcinoma | | NCIT:C172808 | Unresectable Digestive System Mixed Adenoneuroendocrine Carcinoma | @@ -11581,6 +11919,8 @@ | NCIT:C190783 | Unresectable Genitourinary System Carcinoma | | NCIT:C176890 | Unresectable Glioblastoma | | NCIT:C176889 | Unresectable Glioma | +| NCIT:C203308 | Unresectable Glioneuronal and Neuronal Tumors | +| NCIT:C203700 | Unresectable HER2-Low Breast Carcinoma | | NCIT:C187161 | Unresectable HER2-Negative Breast Carcinoma | | NCIT:C186284 | Unresectable HER2-Positive Breast Carcinoma | | NCIT:C165174 | Unresectable Head and Neck Carcinoma | @@ -11599,14 +11939,14 @@ | NCIT:C172645 | Unresectable Laryngeal Squamous Cell Carcinoma | | NCIT:C132147 | Unresectable Leiomyosarcoma | | NCIT:C132148 | Unresectable Liposarcoma | -| NCIT:C165171 | Unresectable Liver and Intrahepatic Bile Duct Carcinoma | +| NCIT:C165171 | Unresectable Liver Carcinoma | | NCIT:C155829 | Unresectable Low Grade Glioma | | NCIT:C174510 | Unresectable Lung Adenocarcinoma | -| NCIT:C177246 | Unresectable Lung Carcinoid Tumor | | NCIT:C155902 | Unresectable Lung Carcinoma | | NCIT:C187162 | Unresectable Lung Large Cell Neuroendocrine Carcinoma | | NCIT:C192018 | Unresectable Lung Neuroendocrine Carcinoma | | NCIT:C165454 | Unresectable Lung Neuroendocrine Neoplasm | +| NCIT:C177246 | Unresectable Lung Neuroendocrine Tumor | | NCIT:C155901 | Unresectable Lung Non-Small Cell Carcinoma | | NCIT:C171612 | Unresectable Lung Non-Small Cell Squamous Carcinoma | | NCIT:C162642 | Unresectable Lung Non-Squamous Non-Small Cell Carcinoma | @@ -11639,6 +11979,8 @@ | NCIT:C168973 | Unresectable Neuroendocrine Neoplasm | | NCIT:C165453 | Unresectable Neuroendocrine Tumor | | NCIT:C153080 | Unresectable Neuroendocrine Tumor G1 | +| NCIT:C203284 | Unresectable Oligodendroglioma | +| NCIT:C203270 | Unresectable Oligodendroglioma, IDH-Mutant and 1p/19q-Codeleted | | NCIT:C172644 | Unresectable Oral Cavity Squamous Cell Carcinoma | | NCIT:C162833 | Unresectable Oropharyngeal Squamous Cell Carcinoma | | NCIT:C190632 | Unresectable Oropharyngeal Undifferentiated Carcinoma | @@ -11663,12 +12005,18 @@ | NCIT:C173609 | Unresectable Paratesticular Epithelioid Mesothelioma | | NCIT:C173608 | Unresectable Paratesticular Malignant Mesothelioma | | NCIT:C173610 | Unresectable Paratesticular Sarcomatoid Mesothelioma | +| NCIT:C201837 | Unresectable Penile Carcinoma | +| NCIT:C201838 | Unresectable Penile Squamous Cell Carcinoma | | NCIT:C165173 | Unresectable Periampullary Adenocarcinoma | | NCIT:C173615 | Unresectable Peritoneal Biphasic Mesothelioma | | NCIT:C173613 | Unresectable Peritoneal Epithelioid Mesothelioma | | NCIT:C173612 | Unresectable Peritoneal Malignant Mesothelioma | | NCIT:C173614 | Unresectable Peritoneal Sarcomatoid Mesothelioma | +| NCIT:C203283 | Unresectable Pilocytic Astrocytoma | +| NCIT:C204867 | Unresectable Platinum-Refractory Ovarian Carcinoma | +| NCIT:C203315 | Unresectable Platinum-Resistant Fallopian Tube Carcinoma | | NCIT:C179459 | Unresectable Platinum-Resistant Ovarian Carcinoma | +| NCIT:C203316 | Unresectable Platinum-Resistant Primary Peritoneal Carcinoma | | NCIT:C182028 | Unresectable Pleomorphic Liposarcoma | | NCIT:C173618 | Unresectable Pleural Biphasic Mesothelioma | | NCIT:C173616 | Unresectable Pleural Epithelioid Mesothelioma | @@ -11677,6 +12025,8 @@ | NCIT:C179423 | Unresectable Plexiform Neurofibroma | | NCIT:C174569 | Unresectable Poorly Differentiated Thyroid Gland Carcinoma | | NCIT:C171070 | Unresectable Primary Central Chondrosarcoma | +| NCIT:C203309 | Unresectable Primary Central Nervous System Neoplasm | +| NCIT:C203310 | Unresectable Primary Malignant Central Nervous System Neoplasm | | NCIT:C170974 | Unresectable Primary Peritoneal Adenocarcinoma | | NCIT:C170973 | Unresectable Primary Peritoneal Carcinoma | | NCIT:C186276 | Unresectable Primary Peritoneal Endometrioid Adenocarcinoma | @@ -11686,6 +12036,7 @@ | NCIT:C191856 | Unresectable Prostate Small Cell Neuroendocrine Carcinoma | | NCIT:C162117 | Unresectable Rectal Adenocarcinoma | | NCIT:C154545 | Unresectable Renal Cell Carcinoma | +| NCIT:C190508 | Unresectable Renal Cell Carcinoma, Not Otherwise Specified | | NCIT:C158588 | Unresectable Renal Pelvis Urothelial Carcinoma | | NCIT:C164160 | Unresectable Renal Pelvis and Ureter Urothelial Carcinoma | | NCIT:C170829 | Unresectable Rhabdoid Tumor | @@ -11717,7 +12068,6 @@ | NCIT:C174570 | Unresectable Thyroid Gland Papillary Carcinoma | | NCIT:C129827 | Unresectable Transitional Cell Carcinoma | | NCIT:C165491 | Unresectable Triple-Negative Breast Carcinoma | -| NCIT:C190508 | Unresectable Unclassified Renal Cell Carcinoma | | NCIT:C150610 | Unresectable Undifferentiated Pleomorphic Sarcoma | | NCIT:C158587 | Unresectable Ureter Urothelial Carcinoma | | NCIT:C158585 | Unresectable Urethral Urothelial Carcinoma | @@ -11787,6 +12137,7 @@ | NCIT:C111022 | Uveal Class 1a Melanoma | | NCIT:C111023 | Uveal Class 1b Melanoma | | NCIT:C111021 | Uveal Class 2 Melanoma | +| NCIT:C205057 | Uveal Melanocytic Neoplasm | | NCIT:C174503 | Uveal Melanocytoma | | NCIT:C150130 | Uveal Melanoma Metastatic in the Liver | | NCIT:C140672 | Uveal Melanoma by AJCC v7 Stage | @@ -11798,7 +12149,7 @@ | NCIT:C40262 | Vaginal Adenoid Basal Carcinoma | | NCIT:C40260 | Vaginal Adenosquamous Carcinoma | | NCIT:C45445 | Vaginal Angiomyofibroblastoma | -| NCIT:C40245 | Vaginal Basaloid Carcinoma | +| NCIT:C40245 | Vaginal Basaloid Squamous Cell Carcinoma | | NCIT:C40282 | Vaginal Blue Nevus | | NCIT:C90347 | Vaginal Cancer by AJCC v6 Stage | | NCIT:C91204 | Vaginal Cancer by AJCC v7 Stage | @@ -11835,6 +12186,8 @@ | NCIT:C49111 | Venous Angioleiomyoma | | NCIT:C22923 | Venous Hemangioma of the Mouse Blood Vessel | | NCIT:C45748 | Ventricular Myxoma | +| NCIT:C203968 | Verruca Palmaris | +| NCIT:C203969 | Verruca Plana | | NCIT:C23093 | Verrucous Carcinoma of the Mouse Nose and Paranasal Sinuses | | NCIT:C23051 | Verrucous Carcinoma of the Mouse Oral Cavity | | NCIT:C22939 | Verrucous Keratotic Hemangioma of the Mouse Blood Vessel | @@ -11846,7 +12199,6 @@ | NCIT:C27734 | Very Low Risk Small Intestinal Gastrointestinal Stromal Tumor | | NCIT:C22155 | Villous Adenocarcinoma of the Mouse Intestinal Tract | | NCIT:C191750 | Villous Adenoma of the Urinary Tract | -| NCIT:C36034 | Villous Neoplasm | | NCIT:C27698 | Virus-Related Carcinoma | | NCIT:C27699 | Virus-Related Lymphoma | | NCIT:C27673 | Virus-Related Malignant Neoplasm | @@ -11855,11 +12207,11 @@ | NCIT:C175225 | Visual Pathway Medulloepithelioma | | NCIT:C175224 | Visual Pathway Melanocytoma | | NCIT:C6262 | Visual Pathway Neoplasm | +| NCIT:C204888 | Volar Melanoma | | NCIT:C95476 | Von Hippel Lindau Syndrome-Associated Pancreatic Serous Adenoma | | NCIT:C40331 | Vulvar Acquired Melanocytic Nevus | | NCIT:C128162 | Vulvar Adenocarcinoma of Mammary Gland Type | | NCIT:C128164 | Vulvar Adenocarcinoma of Sweat Gland Origin | -| NCIT:C128166 | Vulvar Adenocarcinoma, Intestinal-Type | | NCIT:C128273 | Vulvar Alveolar Rhabdomyosarcoma | | NCIT:C45446 | Vulvar Angiomyofibroblastoma | | NCIT:C40325 | Vulvar Angiomyxoma | @@ -11890,6 +12242,7 @@ | NCIT:C40335 | Vulvar Melanocytic Neoplasm | | NCIT:C128289 | Vulvar Melanocytic Nevus | | NCIT:C128247 | Vulvar Merkel Cell Carcinoma | +| NCIT:C128166 | Vulvar Mucinous Adenocarcinoma, Intestinal-Type | | NCIT:C40303 | Vulvar Neoplasm of Skin Appendage Origin | | NCIT:C181905 | Vulvar Phyllodes Tumor | | NCIT:C181926 | Vulvar Prepubertal Fibroma | @@ -11909,6 +12262,7 @@ | NCIT:C128295 | Vulvar Yolk Sac Tumor | | NCIT:C177797 | WHO Grade 1 Glioma | | NCIT:C200758 | WHO Grade 4 Glioma | +| NCIT:C204514 | WNT-Activated Deep Penetrating/Plexiform Melanocytoma (Nevus) | | NCIT:C135002 | Walleye Dermal Sarcoma | | NCIT:C23132 | Warthin's Tumor of the Mouse Salivary Glands | | NCIT:C126409 | Warthin-Like Variant Thyroid Gland Papillary Carcinoma | diff --git a/docs/reports/unmapped_omim.md b/docs/reports/unmapped_omim.md index 2bccf7a0..46fa2018 100644 --- a/docs/reports/unmapped_omim.md +++ b/docs/reports/unmapped_omim.md @@ -2,15 +2,10 @@ [Interactive FlatGithub table](https://flatgithub.com/monarch-initiative/mondo-ingest?filename=src/ontology/reports/omim_mapping_status.tsv) ### Unmapped mappable terms _(!excluded, !deprecated)_ -| subject_id | subject_label | -|:--------------|:--------------------------------------------------------------------| -| OMIMPS:215700 | Citrullinemia | -| OMIMPS:151623 | Li-Fraumeni syndrome | -| OMIM:620789 | aplasia cutis-enamel dysplasia syndrome | -| OMIM:620795 | autoinflammation with episodic fever and immune dysregulation | -| OMIM:620786 | basal ganglia calcification, idiopathic, 9, autosomal recessive | -| OMIM:620794 | deafness, autosomal recessive 124 | -| OMIM:620790 | neurodevelopmental disorder with hypotonia and seizures | -| OMIM:620785 | neurodevelopmental disorder with progressive movement abnormalities | -| OMIM:620792 | otosclerosis 12 | -| OMIM:620796 | proteasome-associated autoinflammatory syndrome 6 | \ No newline at end of file +| subject_id | subject_label | +|:--------------|:-----------------------------------------------| +| OMIMPS:619539 | Neuroocular syndrome | +| OMIM:620806 | developmental and epileptic encephalopathy 116 | +| OMIM:620820 | el hayek-chahrour neurodevelopmental syndrome | +| OMIM:500017 | leigh syndrome, mitochondrial | +| OMIM:620819 | rothmund-thomson syndrome, type 4 | \ No newline at end of file diff --git a/docs/reports/unmapped_ordo.md b/docs/reports/unmapped_ordo.md index 546991d4..617150af 100644 --- a/docs/reports/unmapped_ordo.md +++ b/docs/reports/unmapped_ordo.md @@ -10,22 +10,13 @@ | Orphanet:409978 | 6-9 / 10 000 | | Orphanet:409979 | <1 / 1 000 000 | | Orphanet:409980 | >1 / 1000 | -| Orphanet:645285 | Chaotic conus spinal cord lipoma | -| Orphanet:522514 | Congenital optic disc excavation of genetic origin | -| Orphanet:519337 | Disorder with optic nerve compression | -| Orphanet:645297 | Extramedullary conus spinal cord lipoma | | Orphanet:645310 | Fibroneural non-saccular limited dorsal myeloschisis | | Orphanet:650097 | Genetic central precocious puberty in male | -| Orphanet:522562 | Genetic superficial corneal dystrophy | | Orphanet:645300 | Lipomatous non-saccular limited dorsal myeloschisis | | Orphanet:645378 | Myelic limited dorsal malformation | | Orphanet:650102 | Non-genetic central precocious puberty in male | -| Orphanet:645343 | Non-saccular limited dorsal myeloschisis | | Orphanet:645294 | Posterior extramedullary conus spinal cord lipoma | -| Orphanet:522530 | Rare genetic disorder with entropion | | Orphanet:645354 | Saccular limited dorsal myeloschisis | -| Orphanet:645319 | Saccular spinal dysraphism with a stalk to the dome | -| Orphanet:522520 | Syndromic genetic disorder with strabismus | | Orphanet:645288 | Terminal extramedullary conus spinal cord lipoma | | Orphanet:645337 | Terminal myelocystocele | | Orphanet:645291 | Transitional extramedullary conus spinal cord lipoma | diff --git a/src/mappings/doid.sssom.tsv b/src/mappings/doid.sssom.tsv index 5d5cb75c..354da4e4 100644 --- a/src/mappings/doid.sssom.tsv +++ b/src/mappings/doid.sssom.tsv @@ -38678,6 +38678,7 @@ DOID:9997 peripartum cardiomyopathy oboInOwl:hasDbXref NCI:C171602 semapv:Unspec DOID:9997 peripartum cardiomyopathy oboInOwl:hasDbXref UMLS:C0877208 semapv:UnspecifiedMatching ExO:0000013 acid rain oboInOwl:hasDbXref ENVO:03000127 semapv:UnspecifiedMatching ExO:0000013 acid rain oboInOwl:hasDbXref OMIT:0016047 semapv:UnspecifiedMatching +SYMP:0000022 depression oboInOwl:hasDbXref MESH:D003863 semapv:UnspecifiedMatching SYMP:0000178 weight loss oboInOwl:hasDbXref ICD9CM:783.21 semapv:UnspecifiedMatching SYMP:0000178 weight loss oboInOwl:hasDbXref UMLS:C0043096 semapv:UnspecifiedMatching SYMP:0000448 epistaxis oboInOwl:hasDbXref ICD9CM:784.7 semapv:UnspecifiedMatching diff --git a/src/mappings/gard.sssom.tsv b/src/mappings/gard.sssom.tsv index c17c7422..82d0b845 100644 --- a/src/mappings/gard.sssom.tsv +++ b/src/mappings/gard.sssom.tsv @@ -9,7 +9,7 @@ # skos: http://www.w3.org/2004/02/skos/core# # sssom: https://w3id.org/sssom/ # license: https://w3id.org/sssom/license/unspecified -# mapping_set_id: https://w3id.org/sssom/mappings/71aecb40-1bdc-40d5-bec3-1b64a1ec71a7 +# mapping_set_id: https://w3id.org/sssom/mappings/025ad2c4-3f38-45cc-ba91-f390ae223112 subject_id subject_label predicate_id object_id mapping_justification obo:GARD_1 GRACILE syndrome skos:exactMatch Orphanet:53693 semapv:UnspecifiedMatching obo:GARD_1 GRACILE syndrome skos:narrowMatch OMIM:603358 semapv:UnspecifiedMatching diff --git a/src/mappings/icd10cm.sssom.tsv b/src/mappings/icd10cm.sssom.tsv index 98012aa8..3850374a 100644 --- a/src/mappings/icd10cm.sssom.tsv +++ b/src/mappings/icd10cm.sssom.tsv @@ -6,6 +6,6 @@ # skos: http://www.w3.org/2004/02/skos/core# # sssom: https://w3id.org/sssom/ # license: https://w3id.org/sssom/license/unspecified -# mapping_set_id: https://w3id.org/sssom/mappings/b064d8ea-3112-4b16-98b9-794ca754bd61 +# mapping_set_id: https://w3id.org/sssom/mappings/c51de1ba-1d4f-4fd0-91e8-9925aaf2da78 diff --git a/src/mappings/icd10who.sssom.tsv b/src/mappings/icd10who.sssom.tsv index 6ae3ef82..37035ce7 100644 --- a/src/mappings/icd10who.sssom.tsv +++ b/src/mappings/icd10who.sssom.tsv @@ -6,6 +6,6 @@ # skos: http://www.w3.org/2004/02/skos/core# # sssom: https://w3id.org/sssom/ # license: https://w3id.org/sssom/license/unspecified -# mapping_set_id: https://w3id.org/sssom/mappings/3e569ce5-eb04-419a-8d48-097e42219a53 +# mapping_set_id: https://w3id.org/sssom/mappings/00f8067a-13c3-4116-9c18-497d77264cd3 diff --git a/src/mappings/icd11foundation.sssom.tsv b/src/mappings/icd11foundation.sssom.tsv index 441850fa..482a7e20 100644 --- a/src/mappings/icd11foundation.sssom.tsv +++ b/src/mappings/icd11foundation.sssom.tsv @@ -6,6 +6,6 @@ # skos: http://www.w3.org/2004/02/skos/core# # sssom: https://w3id.org/sssom/ # license: https://w3id.org/sssom/license/unspecified -# mapping_set_id: https://w3id.org/sssom/mappings/6fb59218-8678-4fd0-b82a-be2fed364df3 +# mapping_set_id: https://w3id.org/sssom/mappings/16d351b5-40bb-4cf4-b2c7-1965afc5a849 diff --git a/src/mappings/ncit.sssom.tsv b/src/mappings/ncit.sssom.tsv index b6728c9f..2e2df807 100644 --- a/src/mappings/ncit.sssom.tsv +++ b/src/mappings/ncit.sssom.tsv @@ -9,7 +9,7 @@ # skos: http://www.w3.org/2004/02/skos/core# # sssom: https://w3id.org/sssom/ # license: https://w3id.org/sssom/license/unspecified -# mapping_set_id: https://w3id.org/sssom/mappings/56a6cd2b-5cec-4616-ac7a-43a778be54d4 +# mapping_set_id: https://w3id.org/sssom/mappings/b2264d8c-3b9d-491a-a650-727383e233f7 subject_id subject_label predicate_id object_id mapping_justification NCIT:C103222 Popliteal Fossa oboInOwl:hasDbXref UBERON:0013069 semapv:UnspecifiedMatching NCIT:C103384 Common Iliac Lymph Node oboInOwl:hasDbXref UBERON:0015878 semapv:UnspecifiedMatching @@ -209,9 +209,9 @@ NCIT:C177768 Temporal Lobe Cortex oboInOwl:hasDbXref UBERON:0016538 semapv:Unspe NCIT:C185194 Cerebrospinal Fluid Sample oboInOwl:hasDbXref UBERON:0001359 semapv:UnspecifiedMatching NCIT:C186102 Anorectum oboInOwl:hasDbXref UBERON:8410050 semapv:UnspecifiedMatching NCIT:C199220 Carotid Artery Segment oboInOwl:hasDbXref UBERON:0005396 semapv:UnspecifiedMatching +NCIT:C204859 Mammary Region oboInOwl:hasDbXref UBERON:0001443 semapv:UnspecifiedMatching NCIT:C25203 Shoulder oboInOwl:hasDbXref UBERON:0001467 semapv:UnspecifiedMatching NCIT:C25264 Carina oboInOwl:hasDbXref UBERON:0006679 semapv:UnspecifiedMatching -NCIT:C25389 Chest oboInOwl:hasDbXref UBERON:0001443 semapv:UnspecifiedMatching NCIT:C26470 Maxilla oboInOwl:hasDbXref UBERON:0002397 semapv:UnspecifiedMatching NCIT:C32042 Acetabulum oboInOwl:hasDbXref UBERON:0001269 semapv:UnspecifiedMatching NCIT:C32078 Ankle Joint oboInOwl:hasDbXref UBERON:0001488 semapv:UnspecifiedMatching diff --git a/src/mappings/omim.sssom.tsv b/src/mappings/omim.sssom.tsv index 9429662c..05c65805 100644 --- a/src/mappings/omim.sssom.tsv +++ b/src/mappings/omim.sssom.tsv @@ -31,6 +31,7 @@ MONDO:0000049 skos:exactMatch omim.ps:610799 semapv:UnspecifiedMatching MONDO:0000050 skos:exactMatch omim.ps:262400 Isolated growth hormone deficiency semapv:UnspecifiedMatching MONDO:0000062 skos:exactMatch omim.ps:251600 Microphthalmia, isolated semapv:UnspecifiedMatching MONDO:0000065 skos:exactMatch omim.ps:603933 Microvascular complications of diabetes semapv:UnspecifiedMatching +MONDO:0000070 skos:exactMatch OMIM:607948 mycobacterium tuberculosis, susceptibility to semapv:UnspecifiedMatching MONDO:0000079 skos:exactMatch omim.ps:612286 Nephrolithiasis/osteoporosis, hypophosphatemic semapv:UnspecifiedMatching MONDO:0000090 skos:exactMatch omim.ps:157640 Progressive external ophthalmoplegia with mtDNA deletions semapv:UnspecifiedMatching MONDO:0000104 skos:exactMatch omim.ps:206100 Anemia, hypochromic microcytic, with iron overload semapv:UnspecifiedMatching @@ -183,6 +184,7 @@ MONDO:0006536 skos:exactMatch omim.ps:608594 Lipodystrophy, congenital generali MONDO:0006602 skos:exactMatch omim.ps:175800 Porokeratosis semapv:UnspecifiedMatching MONDO:0006664 skos:exactMatch omim.ps:108800 Atrial septal defect semapv:UnspecifiedMatching MONDO:0006761 skos:exactMatch OMIM:135580 fibromuscular dysplasia, arterial semapv:UnspecifiedMatching +MONDO:0007029 skos:exactMatch omim.ps:113650 Branchiootorenal syndrome semapv:UnspecifiedMatching MONDO:0007030 skos:exactMatch OMIM:100050 aarskog syndrome, autosomal dominant semapv:UnspecifiedMatching MONDO:0007031 skos:exactMatch omim.ps:100070 Aortic aneurysm, familial abdominal semapv:UnspecifiedMatching MONDO:0007032 skos:exactMatch OMIM:100100 prune belly syndrome semapv:UnspecifiedMatching @@ -287,7 +289,7 @@ MONDO:0007138 skos:exactMatch OMIM:107250 anterior segment dysgenesis 1 semapv: MONDO:0007139 skos:exactMatch OMIM:107290 antipyrine metabolism semapv:UnspecifiedMatching MONDO:0007141 skos:exactMatch OMIM:107440 antiviral state repressor, regulator of semapv:UnspecifiedMatching MONDO:0007142 skos:exactMatch omim.ps:107480 Townes-Brocks syndrome semapv:UnspecifiedMatching -MONDO:0007143 skos:exactMatch OMIM:107500 aortic arch anomaly with peculiar facies and mental retardation semapv:UnspecifiedMatching +MONDO:0007143 skos:exactMatch OMIM:107500 aortic arch anomaly with peculiar facies and impaired intellectual development semapv:UnspecifiedMatching MONDO:0007144 skos:exactMatch OMIM:107550 aortic arch interruption, facial palsy, and retinal coloboma semapv:UnspecifiedMatching MONDO:0007145 skos:exactMatch OMIM:107600 aplasia cutis congenita, nonsyndromic semapv:UnspecifiedMatching MONDO:0007147 skos:exactMatch OMIM:107650 apnea, obstructive sleep semapv:UnspecifiedMatching @@ -380,6 +382,7 @@ MONDO:0007234 skos:exactMatch OMIM:113610 branchial myoclonus with spastic para MONDO:0007235 skos:exactMatch OMIM:113620 branchiooculofacial syndrome semapv:UnspecifiedMatching MONDO:0007236 skos:exactMatch OMIM:113650 branchiootorenal syndrome 1 semapv:UnspecifiedMatching MONDO:0007237 skos:exactMatch OMIM:113670 hypertrophy of the breast, juvenile semapv:UnspecifiedMatching +MONDO:0007239 skos:exactMatch omim.ps:113800 Epidermolytic hyperkeratosis semapv:UnspecifiedMatching MONDO:0007240 skos:exactMatch OMIM:113900 progressive familial heart block, type 1a semapv:UnspecifiedMatching MONDO:0007241 skos:exactMatch OMIM:113950 bundle branch block, familial isolated complete right semapv:UnspecifiedMatching MONDO:0007242 skos:exactMatch OMIM:113960 butyrylesterase 1 semapv:UnspecifiedMatching @@ -512,7 +515,7 @@ MONDO:0007378 skos:exactMatch OMIM:122000 corneal dystrophy, posterior polymorp MONDO:0007379 skos:exactMatch omim.ps:122100 Corneal dystrophy, Meesmann semapv:UnspecifiedMatching MONDO:0007380 skos:exactMatch OMIM:122200 corneal dystrophy, lattice type 1 semapv:UnspecifiedMatching MONDO:0007381 skos:exactMatch OMIM:122400 epithelial recurrent erosion dystrophy semapv:UnspecifiedMatching -MONDO:0007382 skos:exactMatch OMIM:122430 corneal hypesthesia with retinal abnormalities, sensorineural deafness, unusual facies, persistent ductus arteriosus, and mental retardation semapv:UnspecifiedMatching +MONDO:0007382 skos:exactMatch OMIM:122430 ramos-arroyo syndrome semapv:UnspecifiedMatching MONDO:0007383 skos:exactMatch OMIM:122440 corneodermatoosseous syndrome semapv:UnspecifiedMatching MONDO:0007384 skos:exactMatch OMIM:122450 corneal hypesthesia, familial semapv:UnspecifiedMatching MONDO:0007385 skos:exactMatch OMIM:122455 coronary artery dissection, spontaneous semapv:UnspecifiedMatching @@ -830,7 +833,7 @@ MONDO:0007720 skos:exactMatch OMIM:142350 hernia, double inguinal semapv:Unspec MONDO:0007721 skos:exactMatch OMIM:142400 hernia, hiatus semapv:UnspecifiedMatching MONDO:0007722 skos:exactMatch OMIM:142500 heterochromia iridis semapv:UnspecifiedMatching MONDO:0007723 skos:exactMatch OMIM:142623 hirschsprung disease, susceptibility to, 1 semapv:UnspecifiedMatching -MONDO:0007724 skos:exactMatch OMIM:142625 hirsutism, skeletal dysplasia, and mental retardation semapv:UnspecifiedMatching +MONDO:0007724 skos:exactMatch OMIM:142625 hirsutism, skeletal dysplasia, and impaired intellectual development semapv:UnspecifiedMatching MONDO:0007725 skos:exactMatch OMIM:142630 histiocytosis, progressive mucinous semapv:UnspecifiedMatching MONDO:0007726 skos:exactMatch OMIM:142669 beukes hip dysplasia semapv:UnspecifiedMatching MONDO:0007727 skos:exactMatch OMIM:142680 periodic fever, familial, autosomal dominant semapv:UnspecifiedMatching @@ -1278,7 +1281,7 @@ MONDO:0008202 skos:exactMatch OMIM:168800 parotidomegaly, hereditary bilateral MONDO:0008203 skos:exactMatch OMIM:168830 passovoy factor defect semapv:UnspecifiedMatching MONDO:0008204 skos:exactMatch OMIM:168850 semapv:UnspecifiedMatching MONDO:0008205 skos:exactMatch OMIM:168860 patella aplasia-hypoplasia semapv:UnspecifiedMatching -MONDO:0008206 skos:exactMatch OMIM:168885 paroxysmal tonic upgaze, benign childhood, with ataxia semapv:UnspecifiedMatching +MONDO:0008206 skos:exactMatch OMIM:168885 neuroocular syndrome 2, paroxysmal type semapv:UnspecifiedMatching MONDO:0008207 skos:exactMatch OMIM:168900 patella, chondromalacia of semapv:UnspecifiedMatching MONDO:0008208 skos:exactMatch OMIM:169000 patella, familial recurrent dislocation of semapv:UnspecifiedMatching MONDO:0008209 skos:exactMatch OMIM:169100 char syndrome semapv:UnspecifiedMatching @@ -1484,7 +1487,6 @@ MONDO:0008427 skos:exactMatch OMIM:182220 sister chromatid exchange, frequency MONDO:0008428 skos:exactMatch OMIM:182230 septooptic dysplasia semapv:UnspecifiedMatching MONDO:0008429 skos:exactMatch omim.ps:182250 Singleton-Merten syndrome semapv:UnspecifiedMatching MONDO:0008430 skos:exactMatch OMIM:182255 skeletal dysplasia with delayed epiphyseal and carpal bone ossification semapv:UnspecifiedMatching -MONDO:0008431 skos:exactMatch OMIM:182260 slipped femoral capital epiphyses semapv:UnspecifiedMatching MONDO:0008432 skos:exactMatch OMIM:182270 ketone compounds, ability to smell semapv:UnspecifiedMatching MONDO:0008433 skos:exactMatch OMIM:182280 small cell cancer of the lung semapv:UnspecifiedMatching MONDO:0008434 skos:exactMatch OMIM:182290 smith-magenis syndrome semapv:UnspecifiedMatching @@ -1492,8 +1494,8 @@ MONDO:0008435 skos:exactMatch OMIM:182400 somatomedin, embryonic semapv:Unspeci MONDO:0008436 skos:exactMatch OMIM:182410 sneddon syndrome semapv:UnspecifiedMatching MONDO:0008437 skos:exactMatch OMIM:182600 spastic paraplegia 3, autosomal dominant semapv:UnspecifiedMatching MONDO:0008438 skos:exactMatch OMIM:182601 spastic paraplegia 4, autosomal dominant semapv:UnspecifiedMatching -MONDO:0008439 skos:exactMatch OMIM:182610 spastic paraplegia, epilepsy, and mental retardation semapv:UnspecifiedMatching -MONDO:0008440 skos:exactMatch OMIM:182690 spastic paraplegia, sensorineural deafness, mental retardation, and progressive nephropathy semapv:UnspecifiedMatching +MONDO:0008439 skos:exactMatch OMIM:182610 spastic paraplegia, epilepsy, and impaired intellectual development semapv:UnspecifiedMatching +MONDO:0008440 skos:exactMatch OMIM:182690 spastic paraplegia, sensorineural deafness, impaired intellectual development, and progressive nephropathy semapv:UnspecifiedMatching MONDO:0008441 skos:exactMatch OMIM:182800 spastic paraplegia with associated extrapyramidal signs semapv:UnspecifiedMatching MONDO:0008442 skos:exactMatch OMIM:182815 spastic paraplegia with neuropathy and poikiloderma semapv:UnspecifiedMatching MONDO:0008443 skos:exactMatch OMIM:182820 spastic paraplegia with precocious puberty semapv:UnspecifiedMatching @@ -1732,7 +1734,7 @@ MONDO:0008690 skos:exactMatch OMIM:194400 xeroderma pigmentosum, autosomal domi MONDO:0008691 skos:exactMatch OMIM:194470 zinc, elevated plasma semapv:UnspecifiedMatching MONDO:0008692 skos:exactMatch OMIM:200100 abetalipoproteinemia semapv:UnspecifiedMatching MONDO:0008693 skos:exactMatch OMIM:200110 ablepharon-macrostomia syndrome semapv:UnspecifiedMatching -MONDO:0008694 skos:exactMatch OMIM:200130 absent eyebrows and eyelashes with mental retardation semapv:UnspecifiedMatching +MONDO:0008694 skos:exactMatch OMIM:200130 absent eyebrows and eyelashes with impaired intellectual development semapv:UnspecifiedMatching MONDO:0008695 skos:exactMatch OMIM:200150 choreoacanthocytosis semapv:UnspecifiedMatching MONDO:0008696 skos:exactMatch OMIM:200170 acanthosis nigricans with muscle cramps and acral enlargement semapv:UnspecifiedMatching MONDO:0008697 skos:exactMatch OMIM:200300 acetophenetidin sensitivity semapv:UnspecifiedMatching @@ -1788,7 +1790,7 @@ MONDO:0008750 skos:exactMatch OMIM:203340 albinism-microcephaly-digital anomali MONDO:0008751 skos:exactMatch OMIM:203400 corticosterone methyloxidase type 1 deficiency semapv:UnspecifiedMatching MONDO:0008752 skos:exactMatch OMIM:203450 alexander disease semapv:UnspecifiedMatching MONDO:0008753 skos:exactMatch OMIM:203500 alkaptonuria semapv:UnspecifiedMatching -MONDO:0008754 skos:exactMatch OMIM:203550 alopecia-contractures-dwarfism mental retardation syndrome semapv:UnspecifiedMatching +MONDO:0008754 skos:exactMatch OMIM:203550 intellectual developmental syndrome with alopecia, contractures, and dwarfism semapv:UnspecifiedMatching MONDO:0008755 skos:exactMatch OMIM:203600 alopecia-epilepsy-oligophrenia syndrome of moynahan semapv:UnspecifiedMatching MONDO:0008756 skos:exactMatch omim.ps:203650 Alopecia-intellectual disability syndrome semapv:UnspecifiedMatching MONDO:0008757 skos:exactMatch OMIM:203655 alopecia universalis congenita semapv:UnspecifiedMatching @@ -1878,7 +1880,7 @@ MONDO:0008846 skos:exactMatch OMIM:209300 atransferrinemia semapv:UnspecifiedMa MONDO:0008847 skos:exactMatch OMIM:209500 atrichia with papular lesions semapv:UnspecifiedMatching MONDO:0008848 skos:exactMatch OMIM:209600 atrioventricular dissociation semapv:UnspecifiedMatching MONDO:0008849 skos:exactMatch OMIM:209700 atrophoderma vermiculata semapv:UnspecifiedMatching -MONDO:0008850 skos:exactMatch OMIM:209770 aural atresia, multiple congenital anomalies, and mental retardation semapv:UnspecifiedMatching +MONDO:0008850 skos:exactMatch OMIM:209770 aural atresia, multiple congenital anomalies, and impaired intellectual development semapv:UnspecifiedMatching MONDO:0008853 skos:exactMatch OMIM:209885 barber-say syndrome semapv:UnspecifiedMatching MONDO:0008854 skos:exactMatch OMIM:209900 bardet-biedl syndrome 1 semapv:UnspecifiedMatching MONDO:0008855 skos:exactMatch OMIM:209920 bare lymphocyte syndrome, type 2 semapv:UnspecifiedMatching @@ -1898,7 +1900,7 @@ MONDO:0008869 skos:exactMatch OMIM:210600 seckel syndrome 1 semapv:UnspecifiedM MONDO:0008870 skos:exactMatch OMIM:210700 microcephalic primordial dwarfism, montreal type semapv:UnspecifiedMatching MONDO:0008871 skos:exactMatch OMIM:210710 microcephalic osteodysplastic primordial dwarfism, type 1 semapv:UnspecifiedMatching MONDO:0008872 skos:exactMatch OMIM:210720 microcephalic osteodysplastic primordial dwarfism, type 2 semapv:UnspecifiedMatching -MONDO:0008873 skos:exactMatch OMIM:210730 microcephalic osteodysplastic primordial dwarfism, type 3 semapv:UnspecifiedMatching +MONDO:0008873 skos:exactMatch OMIM:210730 semapv:UnspecifiedMatching MONDO:0008874 skos:exactMatch OMIM:210740 bangstad syndrome semapv:UnspecifiedMatching MONDO:0008875 skos:exactMatch OMIM:210745 blepharophimosis with ptosis, syndactyly, and short stature semapv:UnspecifiedMatching MONDO:0008876 skos:exactMatch OMIM:210900 bloom syndrome semapv:UnspecifiedMatching @@ -1999,7 +2001,7 @@ MONDO:0008977 skos:exactMatch OMIM:215300 chondrosarcoma semapv:UnspecifiedMatc MONDO:0008978 skos:exactMatch OMIM:215400 chordoma, susceptibility to semapv:UnspecifiedMatching MONDO:0008979 skos:exactMatch OMIM:215450 chorea, benign familial semapv:UnspecifiedMatching MONDO:0008980 skos:exactMatch OMIM:215470 boucher-neuhauser syndrome semapv:UnspecifiedMatching -MONDO:0008981 skos:exactMatch OMIM:215480 choroid plexus calcification and mental retardation semapv:UnspecifiedMatching +MONDO:0008981 skos:exactMatch OMIM:215480 choroid plexus calcification and impaired intellectual development semapv:UnspecifiedMatching MONDO:0008982 skos:exactMatch omim.ps:215500 Choroidal dystrophy, central areolar semapv:UnspecifiedMatching MONDO:0008983 skos:exactMatch OMIM:215510 chromosomal instability with tissue-specific radiosensitivity semapv:UnspecifiedMatching MONDO:0008984 skos:exactMatch OMIM:215518 ciliary discoordination due to random ciliary orientation semapv:UnspecifiedMatching @@ -2050,8 +2052,8 @@ MONDO:0009036 skos:exactMatch OMIM:218450 craniostenosis, sagittal, with congen MONDO:0009037 skos:exactMatch OMIM:218530 craniosynostosis with anomalies of the cranial base and digits semapv:UnspecifiedMatching MONDO:0009038 skos:exactMatch OMIM:218550 craniosynostosis with fibular aplasia semapv:UnspecifiedMatching MONDO:0009039 skos:exactMatch OMIM:218600 baller-gerold syndrome semapv:UnspecifiedMatching -MONDO:0009040 skos:exactMatch OMIM:218649 craniosynostosis-mental retardation syndrome of 51n and gettig semapv:UnspecifiedMatching -MONDO:0009041 skos:exactMatch OMIM:218650 craniosynostosis-mental retardation-clefting syndrome semapv:UnspecifiedMatching +MONDO:0009040 skos:exactMatch OMIM:218649 lin-getting syndrome semapv:UnspecifiedMatching +MONDO:0009041 skos:exactMatch OMIM:218650 craniosynostosis-impaired intellectual development-clefting syndrome semapv:UnspecifiedMatching MONDO:0009042 skos:exactMatch OMIM:218670 craniotelencephalic dysplasia semapv:UnspecifiedMatching MONDO:0009045 skos:exactMatch OMIM:218900 crome syndrome semapv:UnspecifiedMatching MONDO:0009046 skos:exactMatch omim.ps:219000 Fraser syndrome semapv:UnspecifiedMatching @@ -2062,13 +2064,13 @@ MONDO:0009051 skos:exactMatch OMIM:219095 cutaneous photosensitivity and coliti MONDO:0009052 skos:exactMatch OMIM:219100 cutis laxa, autosomal recessive, type 1a semapv:UnspecifiedMatching MONDO:0009053 skos:exactMatch OMIM:219150 cutis laxa, autosomal recessive, type 3a semapv:UnspecifiedMatching MONDO:0009055 skos:exactMatch OMIM:219250 cutis marmorata telangiectatica congenita semapv:UnspecifiedMatching -MONDO:0009056 skos:exactMatch OMIM:219300 cutis verticis gyrata and mental retardation semapv:UnspecifiedMatching +MONDO:0009056 skos:exactMatch OMIM:219300 cutis verticis gyrata and impaired intellectual development semapv:UnspecifiedMatching MONDO:0009057 skos:exactMatch OMIM:219400 cyanosis and hepatic disease semapv:UnspecifiedMatching MONDO:0009058 skos:exactMatch OMIM:219500 cystathioninuria semapv:UnspecifiedMatching MONDO:0009059 skos:exactMatch OMIM:219550 cysteine peptiduria semapv:UnspecifiedMatching MONDO:0009060 skos:exactMatch OMIM:219600 polycystic lung disease semapv:UnspecifiedMatching MONDO:0009061 skos:exactMatch OMIM:219700 cystic fibrosis semapv:UnspecifiedMatching -MONDO:0009062 skos:exactMatch OMIM:219721 cystic fibrosis with helicobacter pylori gastritis, megaloblastic anemia, and mental retardation semapv:UnspecifiedMatching +MONDO:0009062 skos:exactMatch OMIM:219721 cystic fibrosis with helicobacter pylori gastritis, megaloblastic anemia, and impaired intellectual development semapv:UnspecifiedMatching MONDO:0009063 skos:exactMatch OMIM:219730 ventriculomegaly with cystic kidney disease semapv:UnspecifiedMatching MONDO:0009064 skos:exactMatch OMIM:219750 cystinosis, adult nonnephropathic semapv:UnspecifiedMatching MONDO:0009066 skos:exactMatch OMIM:219900 cystinosis, late-onset juvenile or adolescent nephropathic type semapv:UnspecifiedMatching @@ -2077,7 +2079,7 @@ MONDO:0009069 skos:exactMatch OMIM:220111 mitochondrial complex 4 deficiency, n MONDO:0009070 skos:exactMatch OMIM:220120 d-glyceric aciduria semapv:UnspecifiedMatching MONDO:0009072 skos:exactMatch OMIM:220200 dandy-walker syndrome semapv:UnspecifiedMatching MONDO:0009073 skos:exactMatch OMIM:220210 ritscher-schinzel syndrome 1 semapv:UnspecifiedMatching -MONDO:0009074 skos:exactMatch OMIM:220219 dandy-walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy semapv:UnspecifiedMatching +MONDO:0009074 skos:exactMatch OMIM:220219 dandy-walker malformation with impaired intellectual development, macrocephaly, myopia, and brachytelephalangy semapv:UnspecifiedMatching MONDO:0009075 skos:exactMatch OMIM:220220 dandy-walker malformation with postaxial polydactyly semapv:UnspecifiedMatching MONDO:0009076 skos:exactMatch OMIM:220290 deafness, autosomal recessive 1a semapv:UnspecifiedMatching MONDO:0009077 skos:exactMatch OMIM:220300 deafness, congenital, and familial myoclonic epilepsy semapv:UnspecifiedMatching @@ -2100,7 +2102,7 @@ MONDO:0009094 skos:exactMatch OMIM:221800 dermochondrocorneal dystrophy semapv: MONDO:0009095 skos:exactMatch OMIM:221810 dermatoosteolysis, kirghizian type semapv:UnspecifiedMatching MONDO:0009097 skos:exactMatch OMIM:221900 persistent hyperplastic primary vitreous, autosomal recessive semapv:UnspecifiedMatching MONDO:0009098 skos:exactMatch OMIM:221950 dextrocardia with unusual facies and microphthalmia semapv:UnspecifiedMatching -MONDO:0009099 skos:exactMatch OMIM:221995 diabetes insipidus, nephrogenic, with mental retardation and intracerebral calcification semapv:UnspecifiedMatching +MONDO:0009099 skos:exactMatch OMIM:221995 diabetes insipidus, nephrogenic, with impaired intellectual development and intracerebral calcification semapv:UnspecifiedMatching MONDO:0009101 skos:exactMatch OMIM:222300 wolfram syndrome 1 semapv:UnspecifiedMatching MONDO:0009102 skos:exactMatch OMIM:222350 diaminopentanuria semapv:UnspecifiedMatching MONDO:0009103 skos:exactMatch OMIM:222400 diaphragmatic hernia 2 semapv:UnspecifiedMatching @@ -2127,7 +2129,7 @@ MONDO:0009124 skos:exactMatch OMIM:223370 dubowitz syndrome semapv:UnspecifiedM MONDO:0009125 skos:exactMatch OMIM:223380 dopamine beta-hydroxylase, plasma, thermolability of semapv:UnspecifiedMatching MONDO:0009126 skos:exactMatch OMIM:223400 duodenal atresia semapv:UnspecifiedMatching MONDO:0009127 skos:exactMatch OMIM:223500 dwarfism, low-birth-weight type, with unresponsiveness to growth hormone semapv:UnspecifiedMatching -MONDO:0009128 skos:exactMatch OMIM:223540 dwarfism, mental retardation, and eye abnormality semapv:UnspecifiedMatching +MONDO:0009128 skos:exactMatch OMIM:223540 mollica syndrome semapv:UnspecifiedMatching MONDO:0009129 skos:exactMatch OMIM:223550 dwarfism, proportionate, with hip dislocation semapv:UnspecifiedMatching MONDO:0009130 skos:exactMatch OMIM:223800 dyggve-melchior-clausen disease semapv:UnspecifiedMatching MONDO:0009131 skos:exactMatch OMIM:223900 neuropathy, hereditary sensory and autonomic, type 3 semapv:UnspecifiedMatching @@ -2174,7 +2176,7 @@ MONDO:0009172 skos:exactMatch OMIM:226150 enterocolitis semapv:UnspecifiedMatch MONDO:0009173 skos:exactMatch OMIM:226200 enterokinase deficiency semapv:UnspecifiedMatching MONDO:0009174 skos:exactMatch OMIM:226300 complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy semapv:UnspecifiedMatching MONDO:0009175 skos:exactMatch OMIM:226350 eosinophilic fasciitis semapv:UnspecifiedMatching -MONDO:0009177 skos:exactMatch OMIM:226440 epidermolysis bullosa, late-onset localized junctional, with mental retardation semapv:UnspecifiedMatching +MONDO:0009177 skos:exactMatch OMIM:226440 epidermolysis bullosa, late-onset localized junctional, with impaired intellectual development semapv:UnspecifiedMatching MONDO:0009178 skos:exactMatch OMIM:226500 epidermolysis bullosa dystrophica neurotrophica semapv:UnspecifiedMatching MONDO:0009179 skos:exactMatch OMIM:226600 epidermolysis bullosa dystrophica, autosomal recessive semapv:UnspecifiedMatching MONDO:0009180 skos:exactMatch OMIM:226650 epidermolysis bullosa, junctional 1a, intermediate semapv:UnspecifiedMatching @@ -2183,7 +2185,7 @@ MONDO:0009182 skos:exactMatch OMIM:226700 epidermolysis bullosa, junctional 1b, MONDO:0009183 skos:exactMatch OMIM:226730 epidermolysis bullosa, junctional 5b, with pyloric atresia semapv:UnspecifiedMatching MONDO:0009184 skos:exactMatch OMIM:226735 epidermolysis bullosa with diaphragmatic hernia semapv:UnspecifiedMatching MONDO:0009185 skos:exactMatch OMIM:226750 kohlschutter-tonz syndrome semapv:UnspecifiedMatching -MONDO:0009186 skos:exactMatch OMIM:226800 epilepsy, photogenic, with spastic diplegia and mental retardation semapv:UnspecifiedMatching +MONDO:0009186 skos:exactMatch OMIM:226800 epilepsy, photogenic, with spastic diplegia and impaired intellectual development semapv:UnspecifiedMatching MONDO:0009187 skos:exactMatch OMIM:226810 epilepsy with bilateral occipital calcifications semapv:UnspecifiedMatching MONDO:0009188 skos:exactMatch OMIM:226850 epilepsy-telangiectasia semapv:UnspecifiedMatching MONDO:0009189 skos:exactMatch OMIM:226900 epiphyseal dysplasia, multiple, 4 semapv:UnspecifiedMatching @@ -2198,7 +2200,7 @@ MONDO:0009197 skos:exactMatch OMIM:227050 transient erythroblastopenia of child MONDO:0009198 skos:exactMatch OMIM:227090 erythroderma, lethal congenital semapv:UnspecifiedMatching MONDO:0009199 skos:exactMatch OMIM:227150 ethanolaminosis semapv:UnspecifiedMatching MONDO:0009200 skos:exactMatch OMIM:227210 eyebrows, duplication of, with stretchable skin and syndactyly semapv:UnspecifiedMatching -MONDO:0009201 skos:exactMatch OMIM:227250 facial abnormalities, kyphoscoliosis, and mental retardation semapv:UnspecifiedMatching +MONDO:0009201 skos:exactMatch OMIM:227250 facial abnormalities, kyphoscoliosis, and impaired intellectual development semapv:UnspecifiedMatching MONDO:0009202 skos:exactMatch OMIM:227255 facial dysmorphism with multiple malformations semapv:UnspecifiedMatching MONDO:0009203 skos:exactMatch OMIM:227260 focal facial dermal dysplasia 3, setleis type semapv:UnspecifiedMatching MONDO:0009204 skos:exactMatch OMIM:227270 faciocardiomelic dysplasia, lethal semapv:UnspecifiedMatching @@ -2422,7 +2424,7 @@ MONDO:0009431 skos:exactMatch OMIM:241530 hypophosphatemic rickets with hyperca MONDO:0009432 skos:exactMatch OMIM:241540 hypopituitarism, congenital, with central diabetes insipidus semapv:UnspecifiedMatching MONDO:0009433 skos:exactMatch OMIM:241550 hypoplastic left heart syndrome 1 semapv:UnspecifiedMatching MONDO:0009434 skos:exactMatch OMIM:241600 immunodeficiency 43 semapv:UnspecifiedMatching -MONDO:0009435 skos:exactMatch OMIM:241760 hypospadias-mental retardation syndrome semapv:UnspecifiedMatching +MONDO:0009435 skos:exactMatch OMIM:241760 hypospadias-impaired intellectual development syndrome semapv:UnspecifiedMatching MONDO:0009436 skos:exactMatch OMIM:241800 pallister-hall-like syndrome semapv:UnspecifiedMatching MONDO:0009437 skos:exactMatch OMIM:241850 bamforth-lazarus syndrome semapv:UnspecifiedMatching MONDO:0009438 skos:exactMatch OMIM:242050 hypouricemia, hypercalcinuria, and decreased bone density semapv:UnspecifiedMatching @@ -2431,9 +2433,9 @@ MONDO:0009440 skos:exactMatch OMIM:242150 keratitis-ichthyosis-deafness syndrom MONDO:0009441 skos:exactMatch OMIM:242300 ichthyosis, congenital, autosomal recessive 1 semapv:UnspecifiedMatching MONDO:0009442 skos:exactMatch OMIM:242400 ichthyosis congenita with biliary atresia semapv:UnspecifiedMatching MONDO:0009443 skos:exactMatch OMIM:242500 ichthyosis, congenital, autosomal recessive 4b semapv:UnspecifiedMatching -MONDO:0009444 skos:exactMatch OMIM:242510 ichthyosis with alopecia, eclabium, ectropion, and mental retardation semapv:UnspecifiedMatching +MONDO:0009444 skos:exactMatch OMIM:242510 ichthyosis with alopecia, eclabium, ectropion, and impaired intellectual development semapv:UnspecifiedMatching MONDO:0009445 skos:exactMatch OMIM:242520 ichthyosis, hepatosplenomegaly, and cerebellar degeneration semapv:UnspecifiedMatching -MONDO:0009446 skos:exactMatch OMIM:242530 ichthyosis, mental retardation, dwarfism, and renal impairment semapv:UnspecifiedMatching +MONDO:0009446 skos:exactMatch OMIM:242530 ichthyosis, impaired intellectual development, dwarfism, and renal impairment semapv:UnspecifiedMatching MONDO:0009447 skos:exactMatch OMIM:242550 ichthyosis, split hairs, and amino aciduria semapv:UnspecifiedMatching MONDO:0009448 skos:exactMatch OMIM:242600 iminoglycinuria semapv:UnspecifiedMatching MONDO:0009449 skos:exactMatch OMIM:242670 ciliary dyskinesia with defective radial spokes semapv:UnspecifiedMatching @@ -2447,7 +2449,7 @@ MONDO:0009456 skos:exactMatch OMIM:242880 immunoerythromyeloid hypoplasia semap MONDO:0009457 skos:exactMatch OMIM:242890 immunoglobulin d level 1n plasma, low semapv:UnspecifiedMatching MONDO:0009458 skos:exactMatch OMIM:242900 schimke immunoosseous dysplasia semapv:UnspecifiedMatching MONDO:0009459 skos:exactMatch OMIM:243000 indifference to pain, congenital, autosomal recessive semapv:UnspecifiedMatching -MONDO:0009460 skos:exactMatch OMIM:243050 indolylacroyl glycinuria with mental retardation semapv:UnspecifiedMatching +MONDO:0009460 skos:exactMatch OMIM:243050 indolylacroyl glycinuria with impaired intellectual development semapv:UnspecifiedMatching MONDO:0009461 skos:exactMatch OMIM:243060 spermatogenic failure 5 semapv:UnspecifiedMatching MONDO:0009462 skos:exactMatch OMIM:243080 inosine phosphorylase deficiency, immune defect due to semapv:UnspecifiedMatching MONDO:0009463 skos:exactMatch OMIM:243100 internal carotid arteries, hypoplasia of semapv:UnspecifiedMatching @@ -2505,9 +2507,9 @@ MONDO:0009518 skos:exactMatch OMIM:246300 leprosy, susceptibility to, 3 semapv: MONDO:0009519 skos:exactMatch OMIM:246400 letterer-siwe disease semapv:UnspecifiedMatching MONDO:0009520 skos:exactMatch OMIM:246450 3-hydroxy-3-methylglutaryl-coa lyase deficiency semapv:UnspecifiedMatching MONDO:0009521 skos:exactMatch OMIM:246470 leukemia, acute myelocytic, with polyposis coli and colon cancer semapv:UnspecifiedMatching -MONDO:0009522 skos:exactMatch OMIM:246500 leukomelanoderma, infantilism, mental retardation, hypodontia, hypotrichosis semapv:UnspecifiedMatching +MONDO:0009522 skos:exactMatch OMIM:246500 leukomelanoderma, infantilism, impaired intellectual development, hypodontia, hypotrichosis semapv:UnspecifiedMatching MONDO:0009523 skos:exactMatch OMIM:246550 lichtenstein syndrome semapv:UnspecifiedMatching -MONDO:0009524 skos:exactMatch OMIM:246555 limb defects, distal transverse, with mental retardation and spasticity semapv:UnspecifiedMatching +MONDO:0009524 skos:exactMatch OMIM:246555 limb defects, distal transverse, with impaired intellectual development and spasticity semapv:UnspecifiedMatching MONDO:0009525 skos:exactMatch OMIM:246560 split-hand/foot malformation 3 semapv:UnspecifiedMatching MONDO:0009526 skos:exactMatch OMIM:246570 fibular aplasia, tibial campomelia, and oligosyndactyly syndrome semapv:UnspecifiedMatching MONDO:0009527 skos:exactMatch OMIM:246650 lipase deficiency, combined semapv:UnspecifiedMatching @@ -2542,14 +2544,14 @@ MONDO:0009555 skos:exactMatch OMIM:248350 malocclusion and short stature semapv MONDO:0009556 skos:exactMatch OMIM:248360 malonyl-coa decarboxylase deficiency semapv:UnspecifiedMatching MONDO:0009557 skos:exactMatch OMIM:248370 mandibuloacral dysplasia with type a lipodystrophy semapv:UnspecifiedMatching MONDO:0009558 skos:exactMatch OMIM:248390 treacher collins syndrome 3 semapv:UnspecifiedMatching -MONDO:0009559 skos:exactMatch OMIM:248400 mandibulofacial dysostosis with mental retardation semapv:UnspecifiedMatching +MONDO:0009559 skos:exactMatch OMIM:248400 mandibulofacial dysostosis with impaired intellectual development semapv:UnspecifiedMatching MONDO:0009560 skos:exactMatch OMIM:248450 manitoba oculotrichoanal syndrome semapv:UnspecifiedMatching MONDO:0009561 skos:exactMatch OMIM:248500 mannosidosis, alpha b, lysosomal semapv:UnspecifiedMatching MONDO:0009562 skos:exactMatch OMIM:248510 mannosidosis, beta a, lysosomal semapv:UnspecifiedMatching MONDO:0009563 skos:exactMatch omim.ps:248600 Maple syrup urine disease semapv:UnspecifiedMatching MONDO:0009564 skos:exactMatch OMIM:248700 marden-walker syndrome semapv:UnspecifiedMatching MONDO:0009565 skos:exactMatch OMIM:248760 marfanoid habitus with microcephaly and glomerulonephritis semapv:UnspecifiedMatching -MONDO:0009566 skos:exactMatch OMIM:248770 marfanoid mental retardation syndrome, autosomal semapv:UnspecifiedMatching +MONDO:0009566 skos:exactMatch OMIM:248770 marfanoid impaired intellectual developmental syndrome, autosomal semapv:UnspecifiedMatching MONDO:0009567 skos:exactMatch OMIM:248800 marinesco-sjogren syndrome semapv:UnspecifiedMatching MONDO:0009568 skos:exactMatch OMIM:248900 mast syndrome semapv:UnspecifiedMatching MONDO:0009569 skos:exactMatch OMIM:248910 cutaneous mastocytosis, conductive hearing loss and microtia semapv:UnspecifiedMatching @@ -2564,10 +2566,10 @@ MONDO:0009577 skos:exactMatch OMIM:249310 neuhauser syndrome semapv:Unspecified MONDO:0009578 skos:exactMatch OMIM:249400 melanosis, neurocutaneous semapv:UnspecifiedMatching MONDO:0009579 skos:exactMatch OMIM:249420 frank-ter haar syndrome semapv:UnspecifiedMatching MONDO:0009580 skos:exactMatch OMIM:249500 intellectual developmental disorder, autosomal recessive 1 semapv:UnspecifiedMatching -MONDO:0009581 skos:exactMatch OMIM:249599 mental retardation syndrome, belgian type semapv:UnspecifiedMatching +MONDO:0009581 skos:exactMatch OMIM:249599 intellectual developmental disorder, belgian type semapv:UnspecifiedMatching MONDO:0009582 skos:exactMatch OMIM:249600 mental retardation syndrome, mietens-weber type semapv:UnspecifiedMatching MONDO:0009583 skos:exactMatch OMIM:249620 ohdo syndrome semapv:UnspecifiedMatching -MONDO:0009584 skos:exactMatch OMIM:249630 mental retardation, buenos aires type semapv:UnspecifiedMatching +MONDO:0009584 skos:exactMatch OMIM:249630 mutchinick syndrome semapv:UnspecifiedMatching MONDO:0009585 skos:exactMatch OMIM:249650 mercaptolactate-cysteine disulfiduria semapv:UnspecifiedMatching MONDO:0009586 skos:exactMatch OMIM:249660 semapv:UnspecifiedMatching MONDO:0009587 skos:exactMatch OMIM:249670 mesoaxial hexadactyly and cardiac malformation semapv:UnspecifiedMatching @@ -2622,8 +2624,8 @@ MONDO:0009635 skos:exactMatch OMIM:251850 diarrhea 2, with microvillus atrophy, MONDO:0009636 skos:exactMatch OMIM:251880 mitochondrial DNA depletion syndrome 3 (hepatocerebral type) semapv:UnspecifiedMatching MONDO:0009638 skos:exactMatch OMIM:251945 mitochondrial myopathy with a defect 1n mitochondrial-protein transport semapv:UnspecifiedMatching MONDO:0009642 skos:exactMatch OMIM:252100 orofaciodigital syndrome 2 semapv:UnspecifiedMatching -MONDO:0009643 skos:exactMatch OMIM:252150 molybdenum cofactor deficiency, complementation group a semapv:UnspecifiedMatching -MONDO:0009644 skos:exactMatch OMIM:252160 molybdenum cofactor deficiency, complementation group B semapv:UnspecifiedMatching +MONDO:0009643 skos:exactMatch OMIM:252150 molybdenum cofactor deficiency, type a semapv:UnspecifiedMatching +MONDO:0009644 skos:exactMatch OMIM:252160 molybdenum cofactor deficiency, type B semapv:UnspecifiedMatching MONDO:0009645 skos:exactMatch OMIM:252250 monocyte chemotactic disorder semapv:UnspecifiedMatching MONDO:0009646 skos:exactMatch OMIM:252270 monosomy 7 myelodysplasia and leukemia syndrome 1 semapv:UnspecifiedMatching MONDO:0009647 skos:exactMatch OMIM:252300 morquio syndrome c semapv:UnspecifiedMatching @@ -2649,7 +2651,7 @@ MONDO:0009667 skos:exactMatch OMIM:253280 muscular dystrophy-dystroglycanopathy MONDO:0009668 skos:exactMatch OMIM:253290 multiple pterygium syndrome, lethal type semapv:UnspecifiedMatching MONDO:0009669 skos:exactMatch OMIM:253300 spinal muscular atrophy, type 1 semapv:UnspecifiedMatching MONDO:0009670 skos:exactMatch OMIM:253310 lethal congenital contracture syndrome 1 semapv:UnspecifiedMatching -MONDO:0009671 skos:exactMatch OMIM:253320 multicore myopathy with mental retardation, short stature, and hypogonadotropic hypogonadism semapv:UnspecifiedMatching +MONDO:0009671 skos:exactMatch OMIM:253320 chudley syndrome semapv:UnspecifiedMatching MONDO:0009672 skos:exactMatch OMIM:253400 spinal muscular atrophy, type 3 semapv:UnspecifiedMatching MONDO:0009673 skos:exactMatch OMIM:253550 spinal muscular atrophy, type 2 semapv:UnspecifiedMatching MONDO:0009674 skos:exactMatch OMIM:253590 muscular dystrophy, adult-onset, with leukoencephalopathy semapv:UnspecifiedMatching @@ -2691,13 +2693,13 @@ MONDO:0009712 skos:exactMatch OMIM:255320 congenital myopathy 1b, autosomal rec MONDO:0009713 skos:exactMatch OMIM:255500 myopia 18, autosomal recessive semapv:UnspecifiedMatching MONDO:0009714 skos:exactMatch OMIM:255600 myosclerosis, autosomal recessive semapv:UnspecifiedMatching MONDO:0009715 skos:exactMatch OMIM:255700 myotonia congenita, autosomal recessive semapv:UnspecifiedMatching -MONDO:0009716 skos:exactMatch OMIM:255710 myotonia with skeletal abnormalities and mental retardation semapv:UnspecifiedMatching +MONDO:0009716 skos:exactMatch OMIM:255710 myotonia with skeletal abnormalities and impaired intellectual development semapv:UnspecifiedMatching MONDO:0009718 skos:exactMatch OMIM:255900 myxedema semapv:UnspecifiedMatching MONDO:0009719 skos:exactMatch OMIM:255960 myxoma, intracardiac semapv:UnspecifiedMatching MONDO:0009720 skos:exactMatch OMIM:301026 keipert syndrome semapv:UnspecifiedMatching MONDO:0009721 skos:exactMatch OMIM:255990 nathalie syndrome semapv:UnspecifiedMatching MONDO:0009722 skos:exactMatch OMIM:255995 congenital myopathy 13 semapv:UnspecifiedMatching -MONDO:0009723 skos:exactMatch OMIM:256000 leigh syndrome semapv:UnspecifiedMatching +MONDO:0009723 skos:exactMatch OMIM:256000 leigh syndrome, nuclear semapv:UnspecifiedMatching MONDO:0009724 skos:exactMatch OMIM:256020 focal segmental glomerulosclerosis 10 semapv:UnspecifiedMatching MONDO:0009725 skos:exactMatch OMIM:256030 nemaline myopathy 2 semapv:UnspecifiedMatching MONDO:0009726 skos:exactMatch omim.ps:256040 Proteosome-associated autoinflammatory syndrome semapv:UnspecifiedMatching @@ -2878,7 +2880,7 @@ MONDO:0009909 skos:exactMatch OMIM:264080 progesterone resistance semapv:Unspec MONDO:0009910 skos:exactMatch OMIM:264090 wiedemann-rautenstrauch syndrome semapv:UnspecifiedMatching MONDO:0009911 skos:exactMatch OMIM:264110 prolactin deficiency, isolated semapv:UnspecifiedMatching MONDO:0009912 skos:exactMatch OMIM:264120 prolactin deficiency with obesity and enlarged testes semapv:UnspecifiedMatching -MONDO:0009913 skos:exactMatch OMIM:264140 prune belly syndrome with pulmonic stenosis, mental retardation, and deafness semapv:UnspecifiedMatching +MONDO:0009913 skos:exactMatch OMIM:264140 prune belly syndrome with pulmonic stenosis, impaired intellectual development, and deafness semapv:UnspecifiedMatching MONDO:0009914 skos:exactMatch OMIM:264180 pseudodiastrophic dysplasia semapv:UnspecifiedMatching MONDO:0009915 skos:exactMatch OMIM:264270 pseudohermaphroditism, female, with skeletal anomalies semapv:UnspecifiedMatching MONDO:0009916 skos:exactMatch OMIM:264300 17-beta hydroxysteroid dehydrogenase 3 deficiency semapv:UnspecifiedMatching @@ -2944,7 +2946,7 @@ MONDO:0009978 skos:exactMatch OMIM:267760 retinal degeneration with nanophthalm MONDO:0009979 skos:exactMatch OMIM:179840 reticular dystrophy of retinal pigment epithelium semapv:UnspecifiedMatching MONDO:0009980 skos:exactMatch OMIM:267900 retinal telangiectasia and hypogammaglobulinemia semapv:UnspecifiedMatching MONDO:0009982 skos:exactMatch OMIM:268010 retinitis pigmentosa inversa with deafness semapv:UnspecifiedMatching -MONDO:0009983 skos:exactMatch OMIM:268020 retinitis pigmentosa, deafness, mental retardation, and hypogonadism semapv:UnspecifiedMatching +MONDO:0009983 skos:exactMatch OMIM:268020 retinitis pigmentosa, deafness, impaired intellectual development, and hypogonadism semapv:UnspecifiedMatching MONDO:0009984 skos:exactMatch OMIM:268025 retinitis pigmentosa, late-adult onset semapv:UnspecifiedMatching MONDO:0009985 skos:exactMatch OMIM:268040 retinohepatoendocrinologic syndrome semapv:UnspecifiedMatching MONDO:0009986 skos:exactMatch OMIM:268050 mirhosseini-holmes-walton syndrome semapv:UnspecifiedMatching @@ -2995,7 +2997,7 @@ MONDO:0010036 skos:exactMatch OMIM:270420 diarrhea 3, secretory sodium, congeni MONDO:0010037 skos:exactMatch OMIM:270425 sodium-potassium-atpase activity of red cell semapv:UnspecifiedMatching MONDO:0010038 skos:exactMatch OMIM:270450 insulin-like growth factor i, resistance to semapv:UnspecifiedMatching MONDO:0010039 skos:exactMatch OMIM:270460 sonoda syndrome semapv:UnspecifiedMatching -MONDO:0010040 skos:exactMatch OMIM:270500 ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and mental retardation semapv:UnspecifiedMatching +MONDO:0010040 skos:exactMatch OMIM:270500 ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and impaired intellectual development semapv:UnspecifiedMatching MONDO:0010041 skos:exactMatch OMIM:270550 spastic ataxia, charlevoix-saguenay type semapv:UnspecifiedMatching MONDO:0010042 skos:exactMatch OMIM:270600 spastic diplegia and impaired intellectual development semapv:UnspecifiedMatching MONDO:0010043 skos:exactMatch OMIM:270685 spastic paraplegia 17, autosomal dominant semapv:UnspecifiedMatching @@ -3004,13 +3006,13 @@ MONDO:0010045 skos:exactMatch OMIM:270710 semapv:UnspecifiedMatching MONDO:0010046 skos:exactMatch OMIM:270750 spastic paraplegia 23, autosomal recessive semapv:UnspecifiedMatching MONDO:0010047 skos:exactMatch OMIM:270800 spastic paraplegia 5a, autosomal recessive semapv:UnspecifiedMatching MONDO:0010048 skos:exactMatch OMIM:270805 spastic paraplegia with myoclonic epilepsy semapv:UnspecifiedMatching -MONDO:0010049 skos:exactMatch OMIM:270850 spastic paresis, glaucoma, and mental retardation semapv:UnspecifiedMatching +MONDO:0010049 skos:exactMatch OMIM:270850 spastic paresis, glaucoma, and impaired intellectual development semapv:UnspecifiedMatching MONDO:0010050 skos:exactMatch OMIM:270900 spastic pseudosclerosis semapv:UnspecifiedMatching -MONDO:0010051 skos:exactMatch OMIM:270950 spastic quadriplegia, retinitis pigmentosa, and mental retardation semapv:UnspecifiedMatching +MONDO:0010051 skos:exactMatch OMIM:270950 spastic quadriplegia, retinitis pigmentosa, and impaired intellectual development semapv:UnspecifiedMatching MONDO:0010052 skos:exactMatch OMIM:270960 spermatogenic failure 4 semapv:UnspecifiedMatching MONDO:0010053 skos:exactMatch OMIM:270970 spherocytosis, type 3 semapv:UnspecifiedMatching -MONDO:0010054 skos:exactMatch OMIM:271109 spinal muscular atrophy with mental retardation semapv:UnspecifiedMatching -MONDO:0010055 skos:exactMatch OMIM:271110 spinal muscular atrophy with microcephaly and mental subnormality semapv:UnspecifiedMatching +MONDO:0010054 skos:exactMatch OMIM:271109 spinal muscular atrophy with impaired intellectual development semapv:UnspecifiedMatching +MONDO:0010055 skos:exactMatch OMIM:271110 spinal muscular atrophy with microcephaly and impaired intellectual development semapv:UnspecifiedMatching MONDO:0010056 skos:exactMatch OMIM:271150 spinal muscular atrophy, type 4 semapv:UnspecifiedMatching MONDO:0010057 skos:exactMatch OMIM:271200 spinal muscular atrophy, ryukyuan type semapv:UnspecifiedMatching MONDO:0010058 skos:exactMatch OMIM:271220 spinal muscular atrophy, scapuloperoneal semapv:UnspecifiedMatching @@ -3026,7 +3028,7 @@ MONDO:0010068 skos:exactMatch OMIM:271510 spondyloepimetaphyseal dysplasia, spo MONDO:0010069 skos:exactMatch OMIM:271520 spondylocostal dysostosis with anal atresia and urogenital anomalies semapv:UnspecifiedMatching MONDO:0010070 skos:exactMatch OMIM:271530 brachyolmia type 1, hobaek type semapv:UnspecifiedMatching MONDO:0010072 skos:exactMatch OMIM:271600 spondyloepiphyseal dysplasia tarda, autosomal recessive semapv:UnspecifiedMatching -MONDO:0010073 skos:exactMatch OMIM:271620 spondyloepiphyseal dysplasia tarda with mental retardation semapv:UnspecifiedMatching +MONDO:0010073 skos:exactMatch OMIM:271620 spondyloepiphyseal dysplasia tarda with impaired intellectual development semapv:UnspecifiedMatching MONDO:0010074 skos:exactMatch OMIM:271630 brachyolmia type 1, toledo type semapv:UnspecifiedMatching MONDO:0010075 skos:exactMatch OMIM:271640 spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures semapv:UnspecifiedMatching MONDO:0010076 skos:exactMatch OMIM:271650 spondyloepimetaphyseal dysplasia, irapa type semapv:UnspecifiedMatching @@ -3113,7 +3115,7 @@ MONDO:0010161 skos:exactMatch OMIM:276700 tyrosinemia, type 1 semapv:Unspecifie MONDO:0010162 skos:exactMatch OMIM:276710 tyrosinemia, type 3 semapv:UnspecifiedMatching MONDO:0010163 skos:exactMatch OMIM:276800 tyrosinosis semapv:UnspecifiedMatching MONDO:0010164 skos:exactMatch OMIM:276820 ulna and fibula, absence of, with severe limb deficiency semapv:UnspecifiedMatching -MONDO:0010165 skos:exactMatch OMIM:276821 ulnar hypoplasia with mental retardation semapv:UnspecifiedMatching +MONDO:0010165 skos:exactMatch OMIM:276821 ulnar hypoplasia with impaired intellectual development semapv:UnspecifiedMatching MONDO:0010166 skos:exactMatch OMIM:276822 ulnar agenesis and endocardial fibroelastosis semapv:UnspecifiedMatching MONDO:0010167 skos:exactMatch OMIM:276880 urocanase deficiency semapv:UnspecifiedMatching MONDO:0010169 skos:exactMatch OMIM:276901 usher syndrome, type 2a semapv:UnspecifiedMatching @@ -3135,7 +3137,7 @@ MONDO:0010185 skos:exactMatch OMIM:277410 methylmalonic aciduria and homocystin MONDO:0010186 skos:exactMatch OMIM:277440 vitamin d-dependent rickets, type 2a semapv:UnspecifiedMatching MONDO:0010187 skos:exactMatch OMIM:277450 vitamin k-dependent clotting factors, combined deficiency of, 1 semapv:UnspecifiedMatching MONDO:0010188 skos:exactMatch OMIM:277460 ataxia with vitamin e deficiency semapv:UnspecifiedMatching -MONDO:0010189 skos:exactMatch OMIM:277465 vitiligo, progressive, with mental retardation and urethral duplication semapv:UnspecifiedMatching +MONDO:0010189 skos:exactMatch OMIM:277465 vitiligo, progressive, with impaired intellectual development and urethral duplication semapv:UnspecifiedMatching MONDO:0010190 skos:exactMatch OMIM:277470 pontocerebellar hypoplasia, type 2a semapv:UnspecifiedMatching MONDO:0010191 skos:exactMatch OMIM:277480 von willebrand disease, type 3 semapv:UnspecifiedMatching MONDO:0010192 skos:exactMatch OMIM:277580 waardenburg syndrome, type 4a semapv:UnspecifiedMatching @@ -3147,7 +3149,7 @@ MONDO:0010198 skos:exactMatch OMIM:277730 wernicke-korsakoff syndrome semapv:Un MONDO:0010199 skos:exactMatch OMIM:277740 white forelock with malformations semapv:UnspecifiedMatching MONDO:0010200 skos:exactMatch OMIM:277900 wilson disease semapv:UnspecifiedMatching MONDO:0010201 skos:exactMatch OMIM:277950 winchester syndrome semapv:UnspecifiedMatching -MONDO:0010203 skos:exactMatch OMIM:277990 wolff mental retardation syndrome semapv:UnspecifiedMatching +MONDO:0010203 skos:exactMatch OMIM:277990 wolff syndrome semapv:UnspecifiedMatching MONDO:0010206 skos:exactMatch OMIM:278150 hypotrichosis 8 semapv:UnspecifiedMatching MONDO:0010207 skos:exactMatch OMIM:278200 woolly hair, hypotrichosis, everted lower lip, and outstanding ears semapv:UnspecifiedMatching MONDO:0010208 skos:exactMatch OMIM:278250 wrinkly skin syndrome semapv:UnspecifiedMatching @@ -3178,7 +3180,7 @@ MONDO:0010232 skos:exactMatch OMIM:300048 intestinal pseudoobstruction, neurona MONDO:0010233 skos:exactMatch OMIM:300049 periventricular nodular heterotopia 1 semapv:UnspecifiedMatching MONDO:0010235 skos:exactMatch OMIM:300055 intellectual developmental disorder, x-linked, syndromic 13 semapv:UnspecifiedMatching MONDO:0010236 skos:exactMatch OMIM:300062 intellectual developmental disorder, X-linked 14 semapv:UnspecifiedMatching -MONDO:0010237 skos:exactMatch OMIM:300064 mental retardation, x-linked, with craniofacial dysmorphism semapv:UnspecifiedMatching +MONDO:0010237 skos:exactMatch OMIM:300064 hyde-forster syndrome semapv:UnspecifiedMatching MONDO:0010238 skos:exactMatch OMIM:300066 deafness, X-linked 4 semapv:UnspecifiedMatching MONDO:0010239 skos:exactMatch OMIM:300067 lissencephaly, x-linked, 1 semapv:UnspecifiedMatching MONDO:0010241 skos:exactMatch OMIM:300071 night blindness, congenital stationary, type 2a semapv:UnspecifiedMatching @@ -3352,7 +3354,7 @@ MONDO:0010421 skos:exactMatch OMIM:300755 agammaglobulinemia, X-linked semapv:U MONDO:0010422 skos:exactMatch OMIM:300756 alzheimer disease 16 semapv:UnspecifiedMatching MONDO:0010423 skos:exactMatch OMIM:300758 hypospadias 2, X-linked semapv:UnspecifiedMatching MONDO:0010424 skos:exactMatch OMIM:300770 surfactant metabolism dysfunction, pulmonary, 4 semapv:UnspecifiedMatching -MONDO:0010425 skos:exactMatch OMIM:300778 semapv:UnspecifiedMatching +MONDO:0010425 skos:exactMatch OMIM:620763 corneal dystrophy, lisch epithelial semapv:UnspecifiedMatching MONDO:0010426 skos:exactMatch OMIM:300779 corneal dystrophy, endothelial, X-linked semapv:UnspecifiedMatching MONDO:0010427 skos:exactMatch OMIM:300799 intellectual developmental disorder, x-linked, syndromic, raymond type semapv:UnspecifiedMatching MONDO:0010428 skos:exactMatch OMIM:300801 chromosome xp11.23-p11.22 duplication syndrome semapv:UnspecifiedMatching @@ -3494,7 +3496,7 @@ MONDO:0010569 skos:exactMatch OMIM:304100 corpus callosum, partial agenesis of, MONDO:0010570 skos:exactMatch OMIM:304110 craniofrontonasal syndrome semapv:UnspecifiedMatching MONDO:0010571 skos:exactMatch OMIM:304120 otopalatodigital syndrome, type 2 semapv:UnspecifiedMatching MONDO:0010572 skos:exactMatch OMIM:304150 occipital horn syndrome semapv:UnspecifiedMatching -MONDO:0010573 skos:exactMatch OMIM:304200 cutis verticis gyrata, thyroid aplasia, and mental retardation semapv:UnspecifiedMatching +MONDO:0010573 skos:exactMatch OMIM:304200 cutis verticis gyrata, thyroid aplasia, and impaired intellectual development semapv:UnspecifiedMatching MONDO:0010574 skos:exactMatch OMIM:304340 pettigrew syndrome semapv:UnspecifiedMatching MONDO:0010575 skos:exactMatch OMIM:304350 deafness-hypogonadism syndrome semapv:UnspecifiedMatching MONDO:0010576 skos:exactMatch OMIM:304400 deafness, X-linked 2 semapv:UnspecifiedMatching @@ -3534,7 +3536,7 @@ MONDO:0010612 skos:exactMatch OMIM:307010 hydrocephalus with cerebellar agenesi MONDO:0010613 skos:exactMatch OMIM:307030 glycerol kinase deficiency semapv:UnspecifiedMatching MONDO:0010614 skos:exactMatch OMIM:307150 hypertrichosis, congenital generalized, 2 semapv:UnspecifiedMatching MONDO:0010615 skos:exactMatch OMIM:307200 isolated growth hormone deficiency, type iii, with agammaglobulinemia semapv:UnspecifiedMatching -MONDO:0010617 skos:exactMatch OMIM:307500 hypogonadism, male, with mental retardation and skeletal anomalies semapv:UnspecifiedMatching +MONDO:0010617 skos:exactMatch OMIM:307500 hypogonadism, male, with impaired intellectual development and skeletal anomalies semapv:UnspecifiedMatching MONDO:0010618 skos:exactMatch OMIM:307700 hypoparathyroidism, X-linked semapv:UnspecifiedMatching MONDO:0010619 skos:exactMatch OMIM:307800 hypophosphatemic rickets, X-linked dominant semapv:UnspecifiedMatching MONDO:0010620 skos:exactMatch OMIM:307830 hypouricemia, familial renal, due to tubular hypersecretion semapv:UnspecifiedMatching @@ -3566,7 +3568,7 @@ MONDO:0010648 skos:exactMatch OMIM:309200 major affective disorder 2 semapv:Uns MONDO:0010649 skos:exactMatch OMIM:309300 megalocornea semapv:UnspecifiedMatching MONDO:0010650 skos:exactMatch OMIM:309350 melnick-needles syndrome semapv:UnspecifiedMatching MONDO:0010651 skos:exactMatch OMIM:309400 menkes disease semapv:UnspecifiedMatching -MONDO:0010652 skos:exactMatch OMIM:309480 mental retardation and psoriasis semapv:UnspecifiedMatching +MONDO:0010652 skos:exactMatch OMIM:309480 impaired intellectual development and psoriasis semapv:UnspecifiedMatching MONDO:0010653 skos:exactMatch OMIM:309500 renpenning syndrome 1 semapv:UnspecifiedMatching MONDO:0010654 skos:exactMatch OMIM:309510 partington syndrome semapv:UnspecifiedMatching MONDO:0010655 skos:exactMatch OMIM:309520 intellectual developmental disorder, x-linked, syndromic, lujan-fryns type semapv:UnspecifiedMatching @@ -3576,13 +3578,13 @@ MONDO:0010658 skos:exactMatch OMIM:309545 intellectual developmental disorder, MONDO:0010659 skos:exactMatch OMIM:309548 intellectual developmental disorder, X-linked 109 semapv:UnspecifiedMatching MONDO:0010660 skos:exactMatch OMIM:309549 intellectual developmental disorder, X-linked 9 semapv:UnspecifiedMatching MONDO:0010661 skos:exactMatch OMIM:309555 intellectual developmental disorder, x-linked, syndromic, gustavson type semapv:UnspecifiedMatching -MONDO:0010662 skos:exactMatch OMIM:309560 mental retardation with spastic paraplegia and palmoplantar hyperkeratosis semapv:UnspecifiedMatching +MONDO:0010662 skos:exactMatch OMIM:309560 impaired intellectual development with spastic paraplegia and palmoplantar hyperkeratosis semapv:UnspecifiedMatching MONDO:0010663 skos:exactMatch OMIM:309580 intellectual disability-hypotonic facies syndrome, x-linked, 1 semapv:UnspecifiedMatching MONDO:0010664 skos:exactMatch OMIM:309583 intellectual developmental disorder, x-linked, syndromic, snyder-robinson type semapv:UnspecifiedMatching MONDO:0010665 skos:exactMatch OMIM:309585 intellectual developmental disorder, x-linked, syndromic, wilson-turner type semapv:UnspecifiedMatching MONDO:0010666 skos:exactMatch OMIM:309605 semapv:UnspecifiedMatching MONDO:0010667 skos:exactMatch OMIM:309610 prieto syndrome semapv:UnspecifiedMatching -MONDO:0010668 skos:exactMatch OMIM:309620 mental retardation, skeletal dysplasia, and abducens palsy semapv:UnspecifiedMatching +MONDO:0010668 skos:exactMatch OMIM:309620 christian syndrome semapv:UnspecifiedMatching MONDO:0010669 skos:exactMatch OMIM:309630 metacarpal 4-5 fusion semapv:UnspecifiedMatching MONDO:0010670 skos:exactMatch OMIM:309640 mental retardation with spastic paraplegia semapv:UnspecifiedMatching MONDO:0010671 skos:exactMatch OMIM:309800 microphthalmia, syndromic 1 semapv:UnspecifiedMatching @@ -3639,7 +3641,7 @@ MONDO:0010725 skos:exactMatch OMIM:312700 retinoschisis 1, x-linked, juvenile s MONDO:0010726 skos:exactMatch OMIM:312750 rett syndrome semapv:UnspecifiedMatching MONDO:0010727 skos:exactMatch OMIM:312780 russell-silver syndrome, X-linked semapv:UnspecifiedMatching MONDO:0010728 skos:exactMatch OMIM:312830 scarf syndrome semapv:UnspecifiedMatching -MONDO:0010729 skos:exactMatch OMIM:312840 schimke X-linked mental retardation syndrome semapv:UnspecifiedMatching +MONDO:0010729 skos:exactMatch OMIM:312840 schimke syndrome semapv:UnspecifiedMatching MONDO:0010730 skos:exactMatch OMIM:312863 combined immunodeficiency, X-linked semapv:UnspecifiedMatching MONDO:0010732 skos:exactMatch OMIM:312910 spastic paraparesis and deafness semapv:UnspecifiedMatching MONDO:0010733 skos:exactMatch OMIM:312920 spastic paraplegia 2, X-linked semapv:UnspecifiedMatching @@ -3729,7 +3731,7 @@ MONDO:0010820 skos:exactMatch OMIM:600116 parkinson disease 2, autosomal recess MONDO:0010821 skos:exactMatch OMIM:600117 dysphasia, familial developmental semapv:UnspecifiedMatching MONDO:0010822 skos:exactMatch OMIM:600118 warburg micro syndrome 1 semapv:UnspecifiedMatching MONDO:0010823 skos:exactMatch OMIM:600121 rhizomelic chondrodysplasia punctata, type 3 semapv:UnspecifiedMatching -MONDO:0010824 skos:exactMatch OMIM:600122 male pseudohermaphroditism/mental retardation syndrome, verloes type semapv:UnspecifiedMatching +MONDO:0010824 skos:exactMatch OMIM:600122 verloes syndrome semapv:UnspecifiedMatching MONDO:0010825 skos:exactMatch OMIM:600123 atrioventricular septal defect with blepharophimosis and anal and radial defects semapv:UnspecifiedMatching MONDO:0010826 skos:exactMatch omim.ps:600131 Epilepsy, childhood absence semapv:UnspecifiedMatching MONDO:0010827 skos:exactMatch OMIM:600132 retinitis pigmentosa 14 semapv:UnspecifiedMatching @@ -3740,7 +3742,7 @@ MONDO:0010831 skos:exactMatch OMIM:600145 sacral defect with anterior meningoce MONDO:0010832 skos:exactMatch OMIM:600151 bardet-biedl syndrome 3 semapv:UnspecifiedMatching MONDO:0010833 skos:exactMatch OMIM:600155 hirschsprung disease, susceptibility to, 2 semapv:UnspecifiedMatching MONDO:0010834 skos:exactMatch OMIM:600156 hirschsprung disease, susceptibility to, 5 semapv:UnspecifiedMatching -MONDO:0010835 skos:exactMatch OMIM:600159 pterygium colli and mental retardation with facial and digital anomalies semapv:UnspecifiedMatching +MONDO:0010835 skos:exactMatch OMIM:600159 pterygium colli and impaired intellectual development with facial and digital anomalies semapv:UnspecifiedMatching MONDO:0010836 skos:exactMatch OMIM:600165 nanophthalmos 1 semapv:UnspecifiedMatching MONDO:0010838 skos:exactMatch OMIM:600171 gonadal agenesis semapv:UnspecifiedMatching MONDO:0010839 skos:exactMatch OMIM:600175 neuronopathy, distal hereditary motor, autosomal dominant 8 semapv:UnspecifiedMatching @@ -3852,7 +3854,7 @@ MONDO:0010951 skos:exactMatch OMIM:600884 cardiomyopathy, dilated, 1b semapv:Un MONDO:0010952 skos:exactMatch OMIM:600886 hyperferritinemia with or without cataract semapv:UnspecifiedMatching MONDO:0010953 skos:exactMatch OMIM:600901 fanconi anemia, complementation group e semapv:UnspecifiedMatching MONDO:0010954 skos:exactMatch OMIM:600903 wiskott-aldrich syndrome, autosomal dominant semapv:UnspecifiedMatching -MONDO:0010955 skos:exactMatch OMIM:600906 ectodermal dysplasia with mental retardation and syndactyly semapv:UnspecifiedMatching +MONDO:0010955 skos:exactMatch OMIM:600906 ectodermal dysplasia with impaired intellectual development and syndactyly semapv:UnspecifiedMatching MONDO:0010956 skos:exactMatch OMIM:600907 enamel hypoplasia, cataracts, and aqueductal stenosis semapv:UnspecifiedMatching MONDO:0010958 skos:exactMatch OMIM:600919 cardiac arrhythmia, ankyrin-b-related semapv:UnspecifiedMatching MONDO:0010959 skos:exactMatch OMIM:600920 van den ende-gupta syndrome semapv:UnspecifiedMatching @@ -3877,7 +3879,7 @@ MONDO:0010978 skos:exactMatch OMIM:601004 portal vein, cavernous transformation MONDO:0010979 skos:exactMatch OMIM:601005 timothy syndrome semapv:UnspecifiedMatching MONDO:0010980 skos:exactMatch OMIM:601016 midline malformations, multiple, with limb abnormalities and hypopituitarism semapv:UnspecifiedMatching MONDO:0010981 skos:exactMatch OMIM:601027 tibia, absence or hypoplasia of, with polydactyly, retrocerebellar arachnoid cyst, and other anomalies semapv:UnspecifiedMatching -MONDO:0010982 skos:exactMatch OMIM:601039 ichthyosis-mental retardation syndrome with large keratohyalin granules 1n the skin semapv:UnspecifiedMatching +MONDO:0010982 skos:exactMatch OMIM:601039 ichthyosis-impaired intellectual developmental syndrome with large keratohyalin granules 1n the skin semapv:UnspecifiedMatching MONDO:0010983 skos:exactMatch OMIM:601042 dystonia 9 semapv:UnspecifiedMatching MONDO:0010984 skos:exactMatch OMIM:601067 usher syndrome, type 1d semapv:UnspecifiedMatching MONDO:0010985 skos:exactMatch OMIM:601068 epilepsy, familial adult myoclonic, 1 semapv:UnspecifiedMatching @@ -3914,7 +3916,7 @@ MONDO:0011015 skos:exactMatch OMIM:601202 cataract 24 semapv:UnspecifiedMatchin MONDO:0011016 skos:exactMatch OMIM:601208 type 1 diabetes mellitus 11 semapv:UnspecifiedMatching MONDO:0011017 skos:exactMatch OMIM:601214 naxos disease semapv:UnspecifiedMatching MONDO:0011018 skos:exactMatch OMIM:601216 dental anomalies and short stature semapv:UnspecifiedMatching -MONDO:0011019 skos:exactMatch OMIM:601217 alopecia-mental retardation syndrome with convulsions and hypergonadotropic hypogonadism semapv:UnspecifiedMatching +MONDO:0011019 skos:exactMatch OMIM:601217 alopecia-impaired intellectual developmental syndrome with convulsions and hypergonadotropic hypogonadism semapv:UnspecifiedMatching MONDO:0011020 skos:exactMatch OMIM:601220 osteoporosis and oculocutaneous hypopigmentation syndrome semapv:UnspecifiedMatching MONDO:0011021 skos:exactMatch OMIM:601223 neuronal intestinal dysplasia, type B semapv:UnspecifiedMatching MONDO:0011022 skos:exactMatch OMIM:601224 potocki-shaffer syndrome semapv:UnspecifiedMatching @@ -3943,7 +3945,7 @@ MONDO:0011044 skos:exactMatch OMIM:601348 ectrodactyly of lower limbs, congenit MONDO:0011045 skos:exactMatch OMIM:601349 microphthalmia, syndromic 8 semapv:UnspecifiedMatching MONDO:0011046 skos:exactMatch OMIM:601350 short stature syndrome, brussels type semapv:UnspecifiedMatching MONDO:0011047 skos:exactMatch OMIM:601351 growth retardation, deafness, femoral epiphyseal dysplasia, and lacrimal duct obstruction semapv:UnspecifiedMatching -MONDO:0011048 skos:exactMatch OMIM:601352 mental retardation, microcephaly, epilepsy, and coarse face semapv:UnspecifiedMatching +MONDO:0011048 skos:exactMatch OMIM:601352 impaired intellectual development, microcephaly, epilepsy, and coarse face semapv:UnspecifiedMatching MONDO:0011049 skos:exactMatch OMIM:601353 brachycephaly, deafness, cataract, microstomia, and impaired intellectual development semapv:UnspecifiedMatching MONDO:0011050 skos:exactMatch OMIM:601355 microcephaly, congenital heart disease, unilateral renal agenesis, and hyposegmented lungs semapv:UnspecifiedMatching MONDO:0011051 skos:exactMatch OMIM:601356 lethal short-limb skeletal dysplasia, al gazali type semapv:UnspecifiedMatching @@ -4028,7 +4030,7 @@ MONDO:0011139 skos:exactMatch OMIM:601759 preaxial hallucal polydactyly semapv: MONDO:0011141 skos:exactMatch OMIM:601775 megaloblastic anemia, folate-responsive semapv:UnspecifiedMatching MONDO:0011143 skos:exactMatch OMIM:601777 cone-rod dystrophy 6 semapv:UnspecifiedMatching MONDO:0011144 skos:exactMatch OMIM:601780 ceroid lipofuscinosis, neuronal, 6a semapv:UnspecifiedMatching -MONDO:0011145 skos:exactMatch OMIM:601794 coloboma-obesity-hypogenitalism-mental retardation syndrome semapv:UnspecifiedMatching +MONDO:0011145 skos:exactMatch OMIM:601794 coloboma-obesity-hypogenitalism-impaired intellectual development syndrome semapv:UnspecifiedMatching MONDO:0011146 skos:exactMatch OMIM:601803 pallister-killian syndrome semapv:UnspecifiedMatching MONDO:0011147 skos:exactMatch OMIM:601808 chromosome 18q deletion syndrome semapv:UnspecifiedMatching MONDO:0011148 skos:exactMatch OMIM:601809 spondylospinal thoracic dysostosis semapv:UnspecifiedMatching @@ -4131,24 +4133,24 @@ MONDO:0011246 skos:exactMatch OMIM:602541 muscular dystrophy, congenital, megac MONDO:0011247 skos:exactMatch OMIM:602551 jejunal atresia with renal adysplasia semapv:UnspecifiedMatching MONDO:0011248 skos:exactMatch OMIM:602553 anal atresia, hypospadias, and penoscrotal inversion semapv:UnspecifiedMatching MONDO:0011249 skos:exactMatch OMIM:602554 torsion dystonia with onset 1n infancy semapv:UnspecifiedMatching -MONDO:0011250 skos:exactMatch OMIM:602555 microcephaly, macrotia, and mental retardation semapv:UnspecifiedMatching +MONDO:0011250 skos:exactMatch OMIM:602555 microcephaly, macrotia, and impaired intellectual development semapv:UnspecifiedMatching MONDO:0011251 skos:exactMatch OMIM:602556 facial dysmorphism, cleft palate, hearing loss, and camptodactyly semapv:UnspecifiedMatching MONDO:0011252 skos:exactMatch OMIM:602557 spondyloepimetaphyseal dysplasia, shohat type semapv:UnspecifiedMatching MONDO:0011253 skos:exactMatch OMIM:602558 craniomicromelic syndrome semapv:UnspecifiedMatching MONDO:0011254 skos:exactMatch OMIM:602561 brachydactyly, intraventricular septal defect, and deafness semapv:UnspecifiedMatching MONDO:0011255 skos:exactMatch OMIM:602562 mandibulofacial dysostosis with macroblepharon and macrostomia semapv:UnspecifiedMatching -MONDO:0011256 skos:exactMatch OMIM:602564 emphysema, congenital, with deafness, penoscrotal web, and mental retardation semapv:UnspecifiedMatching +MONDO:0011256 skos:exactMatch OMIM:602564 emphysema, congenital, with deafness, penoscrotal web, and intellectual developmental disorder semapv:UnspecifiedMatching MONDO:0011257 skos:exactMatch OMIM:602579 congenital disorder of glycosylation, type ib semapv:UnspecifiedMatching MONDO:0011258 skos:exactMatch OMIM:602588 branchiootic syndrome 1 semapv:UnspecifiedMatching MONDO:0011259 skos:exactMatch OMIM:602594 retinitis pigmentosa 22 semapv:UnspecifiedMatching MONDO:0011260 skos:exactMatch OMIM:602596 pancreatic lymphoma, familial semapv:UnspecifiedMatching -MONDO:0011261 skos:exactMatch OMIM:602611 spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and mental retardation semapv:UnspecifiedMatching +MONDO:0011261 skos:exactMatch OMIM:602611 spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and impaired intellectual development semapv:UnspecifiedMatching MONDO:0011262 skos:exactMatch OMIM:602612 camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye semapv:UnspecifiedMatching MONDO:0011263 skos:exactMatch OMIM:602613 skeletal dysplasia and progressive central nervous system degeneration, lethal semapv:UnspecifiedMatching MONDO:0011264 skos:exactMatch OMIM:602629 dystonia 6, torsion semapv:UnspecifiedMatching MONDO:0011265 skos:exactMatch OMIM:602639 tooth agenesis, selective, 2 semapv:UnspecifiedMatching MONDO:0011266 skos:exactMatch OMIM:602668 myotonic dystrophy 2 semapv:UnspecifiedMatching -MONDO:0011267 skos:exactMatch OMIM:602685 mental retardation, severe, with spasticity and pigmentary tapetoretinal degeneration semapv:UnspecifiedMatching +MONDO:0011267 skos:exactMatch OMIM:602685 intellectual developmental disorder with spasticity and pigmentary tapetoretinal degeneration semapv:UnspecifiedMatching MONDO:0011268 skos:exactMatch OMIM:602722 renal tubular acidosis, distal, 3, with or without sensorineural hearing loss semapv:UnspecifiedMatching MONDO:0011269 skos:exactMatch OMIM:602723 psoriasis 2 semapv:UnspecifiedMatching MONDO:0011270 skos:exactMatch OMIM:602759 prostate cancer, hereditary, 8 semapv:UnspecifiedMatching @@ -4170,7 +4172,7 @@ MONDO:0011286 skos:exactMatch OMIM:603098 deafness, autosomal recessive 13 sema MONDO:0011287 skos:exactMatch OMIM:603116 cdags syndrome semapv:UnspecifiedMatching MONDO:0011288 skos:exactMatch OMIM:603117 spastic paraplegia, optic atrophy, microcephaly, and 10y sex reversal semapv:UnspecifiedMatching MONDO:0011289 skos:exactMatch OMIM:603119 apraxia of eyelid opening semapv:UnspecifiedMatching -MONDO:0011290 skos:exactMatch OMIM:603133 dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and mental retardation semapv:UnspecifiedMatching +MONDO:0011290 skos:exactMatch OMIM:603133 dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and impaired intellectual development semapv:UnspecifiedMatching MONDO:0011291 skos:exactMatch OMIM:603147 congenital disorder of glycosylation, type ic semapv:UnspecifiedMatching MONDO:0011292 skos:exactMatch OMIM:603165 dermatitis, atopic semapv:UnspecifiedMatching MONDO:0011294 skos:exactMatch OMIM:603175 schizophrenia 5 semapv:UnspecifiedMatching @@ -4199,7 +4201,7 @@ MONDO:0011316 skos:exactMatch OMIM:603393 osteosclerotic chondrodysplasia, leth MONDO:0011317 skos:exactMatch OMIM:603394 microcephaly, severe, with skeletal anomalies including posterior rib-gap defects semapv:UnspecifiedMatching MONDO:0011318 skos:exactMatch OMIM:603396 tonoki syndrome semapv:UnspecifiedMatching MONDO:0011319 skos:exactMatch OMIM:603416 ribosomal protein l21 pseudogene 1 semapv:UnspecifiedMatching -MONDO:0011320 skos:exactMatch OMIM:603438 radioulnar synostosis with microcephaly, short stature, scoliosis, and mental retardation semapv:UnspecifiedMatching +MONDO:0011320 skos:exactMatch OMIM:603438 tsukahara syndrome semapv:UnspecifiedMatching MONDO:0011321 skos:exactMatch OMIM:603439 expansile bone lesions semapv:UnspecifiedMatching MONDO:0011322 skos:exactMatch OMIM:603446 oroacral syndrome, verloes-koulischer type semapv:UnspecifiedMatching MONDO:0011323 skos:exactMatch OMIM:603457 bosma arhinia microphthalmia syndrome semapv:UnspecifiedMatching @@ -4216,7 +4218,7 @@ MONDO:0011337 skos:exactMatch OMIM:603553 hemophagocytic lymphohistiocytosis, f MONDO:0011338 skos:exactMatch OMIM:603554 omenn syndrome semapv:UnspecifiedMatching MONDO:0011339 skos:exactMatch OMIM:603563 spastic paraplegia 8, autosomal dominant semapv:UnspecifiedMatching MONDO:0011340 skos:exactMatch OMIM:603569 tracheobronchial stenosis, congenital semapv:UnspecifiedMatching -MONDO:0011341 skos:exactMatch OMIM:603572 microcephaly, facial abnormalities, micromelia, and mental retardation semapv:UnspecifiedMatching +MONDO:0011341 skos:exactMatch OMIM:603572 microcephaly, facial abnormalities, micromelia, and impaired intellectual development semapv:UnspecifiedMatching MONDO:0011342 skos:exactMatch OMIM:603585 congenital disorder of glycosylation, type iif semapv:UnspecifiedMatching MONDO:0011343 skos:exactMatch OMIM:603587 follicular atrophoderma, perioral pigmented, with milia and epidermoid cysts semapv:UnspecifiedMatching MONDO:0011344 skos:exactMatch OMIM:603588 parotitis, juvenile recurrent semapv:UnspecifiedMatching @@ -4301,7 +4303,7 @@ MONDO:0011428 skos:exactMatch OMIM:604292 ectrodactyly, ectodermal dysplasia, a MONDO:0011429 skos:exactMatch OMIM:604302 rheumatoid arthritis, systemic juvenile semapv:UnspecifiedMatching MONDO:0011431 skos:exactMatch OMIM:604308 mass syndrome semapv:UnspecifiedMatching MONDO:0011432 skos:exactMatch OMIM:604314 blepharophimosis with facial and genital anomalies and impaired intellectual development semapv:UnspecifiedMatching -MONDO:0011433 skos:exactMatch OMIM:604315 anemia, congenital hypoplastic, with multiple congenital anomalies/mental retardation syndrome semapv:UnspecifiedMatching +MONDO:0011433 skos:exactMatch OMIM:604315 anemia, congenital hypoplastic, with multiple congenital anomalies/impaired intellectual development syndrome semapv:UnspecifiedMatching MONDO:0011434 skos:exactMatch OMIM:604316 psoriasis 5, susceptibility to semapv:UnspecifiedMatching MONDO:0011435 skos:exactMatch OMIM:604317 microcephaly 2, primary, autosomal recessive, with or without cortical malformations semapv:UnspecifiedMatching MONDO:0011436 skos:exactMatch OMIM:604320 neuronopathy, distal hereditary motor, autosomal recessive 1 semapv:UnspecifiedMatching @@ -4411,7 +4413,7 @@ MONDO:0011546 skos:exactMatch OMIM:605376 heterotaxy, visceral, 2, autosomal se MONDO:0011547 skos:exactMatch OMIM:605387 cataract 31, multiple types semapv:UnspecifiedMatching MONDO:0011548 skos:exactMatch OMIM:605388 cerebral palsy, ataxic, autosomal recessive semapv:UnspecifiedMatching MONDO:0011549 skos:exactMatch OMIM:605389 hypotrichosis 1 semapv:UnspecifiedMatching -MONDO:0011550 skos:exactMatch OMIM:605400 fibromatosis, gingival, with hypertrichosis and mental retardation semapv:UnspecifiedMatching +MONDO:0011550 skos:exactMatch OMIM:605400 fibromatosis, gingival, with hypertrichosis and impaired intellectual development semapv:UnspecifiedMatching MONDO:0011551 skos:exactMatch OMIM:605407 segawa syndrome, autosomal recessive semapv:UnspecifiedMatching MONDO:0011552 skos:exactMatch OMIM:605419 schizophrenia 10 semapv:UnspecifiedMatching MONDO:0011553 skos:exactMatch OMIM:605428 deafness, autosomal recessive 26 semapv:UnspecifiedMatching @@ -4510,7 +4512,7 @@ MONDO:0011650 skos:exactMatch OMIM:606217 atrioventricular septal defect, susce MONDO:0011651 skos:exactMatch OMIM:606220 intellectual developmental disorder with short stature, facial anomalies, and speech defects semapv:UnspecifiedMatching MONDO:0011652 skos:exactMatch OMIM:606232 phelan-mcdermid syndrome semapv:UnspecifiedMatching MONDO:0011653 skos:exactMatch OMIM:606240 thyroid cancer, nonmedullary, 3 semapv:UnspecifiedMatching -MONDO:0011654 skos:exactMatch OMIM:606242 mental retardation, microcephaly, growth retardation, joint contractures, and facial dysmorphism semapv:UnspecifiedMatching +MONDO:0011654 skos:exactMatch OMIM:606242 kondoh syndrome semapv:UnspecifiedMatching MONDO:0011655 skos:exactMatch OMIM:606243 alveolar soft part sarcoma semapv:UnspecifiedMatching MONDO:0011656 skos:exactMatch OMIM:606263 paget disease of bone 4 semapv:UnspecifiedMatching MONDO:0011657 skos:exactMatch OMIM:606282 deafness, autosomal dominant 24 semapv:UnspecifiedMatching @@ -4587,7 +4589,7 @@ MONDO:0011732 skos:exactMatch OMIM:606835 digital arthropathy-brachydactyly, fa MONDO:0011733 skos:exactMatch OMIM:606840 parasomnia, sleep bruxism type semapv:UnspecifiedMatching MONDO:0011734 skos:exactMatch OMIM:606842 cardioneuromyopathy with hyaline masses and nemaline rods semapv:UnspecifiedMatching MONDO:0011735 skos:exactMatch OMIM:606843 immunodeficiency with hyper-igm, type 3 semapv:UnspecifiedMatching -MONDO:0011736 skos:exactMatch OMIM:606851 cree mental retardation syndrome semapv:UnspecifiedMatching +MONDO:0011736 skos:exactMatch OMIM:606851 cree impaired intellectual development syndrome semapv:UnspecifiedMatching MONDO:0011737 skos:exactMatch OMIM:606852 parkinson disease 10 semapv:UnspecifiedMatching MONDO:0011738 skos:exactMatch OMIM:606854 cortical dysplasia, complex, with other brain malformations 14a (bilateral frontoparietal) semapv:UnspecifiedMatching MONDO:0011739 skos:exactMatch OMIM:606856 pancreatic cancer, susceptibility to, 1 semapv:UnspecifiedMatching @@ -4703,7 +4705,7 @@ MONDO:0011854 skos:exactMatch OMIM:607540 secretory diarrhea, myopathy, and dea MONDO:0011855 skos:exactMatch OMIM:607541 corneal dystrophy, avellino type semapv:UnspecifiedMatching MONDO:0011856 skos:exactMatch OMIM:607543 spondylometaphyseal dysplasia with bowed forearms and facial dysmorphism semapv:UnspecifiedMatching MONDO:0011857 skos:exactMatch OMIM:607554 atrial fibrillation, familial, 3 semapv:UnspecifiedMatching -MONDO:0011858 skos:exactMatch OMIM:607565 spastic paraplegia, ataxia, and mental retardation semapv:UnspecifiedMatching +MONDO:0011858 skos:exactMatch OMIM:607565 spastic paraplegia, ataxia, and impaired intellectual development semapv:UnspecifiedMatching MONDO:0011860 skos:exactMatch OMIM:607572 leprosy, susceptibility to, 2 semapv:UnspecifiedMatching MONDO:0011861 skos:exactMatch OMIM:607578 breath-holding spells semapv:UnspecifiedMatching MONDO:0011862 skos:exactMatch OMIM:607584 spastic paraplegia 24, autosomal recessive semapv:UnspecifiedMatching @@ -4779,7 +4781,6 @@ MONDO:0011936 skos:exactMatch OMIM:607932 microphthalmia, syndromic 6 semapv:Un MONDO:0011937 skos:exactMatch OMIM:607936 peeling skin syndrome 4 semapv:UnspecifiedMatching MONDO:0011938 skos:exactMatch OMIM:607941 atrial septal defect 2 semapv:UnspecifiedMatching MONDO:0011939 skos:exactMatch OMIM:607944 spondyloenchondrodysplasia with immune dysregulation semapv:UnspecifiedMatching -MONDO:0011940 skos:exactMatch OMIM:607948 mycobacterium tuberculosis, susceptibility to semapv:UnspecifiedMatching MONDO:0011941 skos:exactMatch OMIM:607949 mycobacterium tuberculosis, susceptibility to, 1 semapv:UnspecifiedMatching MONDO:0011942 skos:exactMatch OMIM:607965 systemic lupus erythematosus with nephritis, susceptibility to, 1 semapv:UnspecifiedMatching MONDO:0011943 skos:exactMatch OMIM:607966 systemic lupus erythematosus with nephritis, susceptibility to, 2 semapv:UnspecifiedMatching @@ -4814,7 +4815,7 @@ MONDO:0011972 skos:exactMatch OMIM:608115 ovarian hyperstimulation syndrome sem MONDO:0011973 skos:exactMatch OMIM:608118 zinc deficiency, transient neonatal semapv:UnspecifiedMatching MONDO:0011974 skos:exactMatch OMIM:608133 retinitis pigmentosa 7 semapv:UnspecifiedMatching MONDO:0011975 skos:exactMatch OMIM:608149 kagami-ogata syndrome semapv:UnspecifiedMatching -MONDO:0011976 skos:exactMatch OMIM:608154 lipodystrophy, generalized, with mental retardation, deafness, short stature, and slender bones semapv:UnspecifiedMatching +MONDO:0011976 skos:exactMatch OMIM:608154 lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones semapv:UnspecifiedMatching MONDO:0011977 skos:exactMatch OMIM:608156 nablus mask-like facial syndrome semapv:UnspecifiedMatching MONDO:0011978 skos:exactMatch OMIM:608158 coq-responsive oxphos deficiency semapv:UnspecifiedMatching MONDO:0011980 skos:exactMatch OMIM:608173 autoimmune thyroid disease, susceptibility to, 1 semapv:UnspecifiedMatching @@ -4841,7 +4842,7 @@ MONDO:0012001 skos:exactMatch OMIM:608257 mandibulofacial dysostosis with ptosi MONDO:0012002 skos:exactMatch OMIM:608264 deafness, autosomal recessive 40 semapv:UnspecifiedMatching MONDO:0012003 skos:exactMatch OMIM:608265 deafness, autosomal recessive 39 semapv:UnspecifiedMatching MONDO:0012004 skos:exactMatch OMIM:608266 parathyroid carcinoma semapv:UnspecifiedMatching -MONDO:0012005 skos:exactMatch OMIM:608278 growth failure, microcephaly, mental retardation, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy semapv:UnspecifiedMatching +MONDO:0012005 skos:exactMatch OMIM:608278 growth failure, microcephaly, impaired intellectual development, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy semapv:UnspecifiedMatching MONDO:0012006 skos:exactMatch OMIM:608279 craniosynostosis with ocular abnormalities and hallucal defects semapv:UnspecifiedMatching MONDO:0012007 skos:exactMatch OMIM:608281 scimitar anomaly, multiple cardiac malformations, and craniofacial and central nervous system abnormalities semapv:UnspecifiedMatching MONDO:0012008 skos:exactMatch OMIM:608290 lelis syndrome semapv:UnspecifiedMatching @@ -5007,7 +5008,7 @@ MONDO:0012174 skos:exactMatch OMIM:609021 peripheral cone dystrophy semapv:Unsp MONDO:0012175 skos:exactMatch OMIM:609026 cataract 28 semapv:UnspecifiedMatching MONDO:0012176 skos:exactMatch OMIM:609029 emanuel syndrome semapv:UnspecifiedMatching MONDO:0012177 skos:exactMatch OMIM:609033 posterior column ataxia with retinitis pigmentosa semapv:UnspecifiedMatching -MONDO:0012178 skos:exactMatch OMIM:609037 mental retardation with optic atrophy, facial dysmorphism, microcephaly, and short stature semapv:UnspecifiedMatching +MONDO:0012178 skos:exactMatch OMIM:609037 intellectual developmental disorder with optic atrophy, facial dysmorphism, microcephaly, and short stature semapv:UnspecifiedMatching MONDO:0012179 skos:exactMatch OMIM:609039 narcolepsy 3 semapv:UnspecifiedMatching MONDO:0012180 skos:exactMatch OMIM:609040 arrhythmogenic right ventricular dysplasia, familial, 9 semapv:UnspecifiedMatching MONDO:0012181 skos:exactMatch OMIM:609041 spastic paraplegia 27, autosomal recessive semapv:UnspecifiedMatching @@ -5096,7 +5097,7 @@ MONDO:0012267 skos:exactMatch OMIM:609408 holoprosencephaly 8 semapv:Unspecifie MONDO:0012269 skos:exactMatch OMIM:609425 chromosome 3q29 deletion syndrome semapv:UnspecifiedMatching MONDO:0012270 skos:exactMatch OMIM:609428 tukel syndrome semapv:UnspecifiedMatching MONDO:0012271 skos:exactMatch OMIM:609432 syndactyly, mesoaxial synostotic, with phalangeal reduction semapv:UnspecifiedMatching -MONDO:0012272 skos:exactMatch OMIM:609438 mental retardation, keratoconus, febrile seizures, and sinoatrial block semapv:UnspecifiedMatching +MONDO:0012272 skos:exactMatch OMIM:609438 intellectual developmental disorder with keratoconus, febrile seizures, and sinoatrial block semapv:UnspecifiedMatching MONDO:0012273 skos:exactMatch OMIM:609439 deafness, autosomal recessive 48 semapv:UnspecifiedMatching MONDO:0012274 skos:exactMatch OMIM:609441 acromesomelic dysplasia 3 semapv:UnspecifiedMatching MONDO:0012275 skos:exactMatch OMIM:609442 valproate embryopathy, susceptibility to semapv:UnspecifiedMatching @@ -5864,7 +5865,7 @@ MONDO:0013051 skos:exactMatch OMIM:612940 cutis laxa, autosomal recessive, type MONDO:0013052 skos:exactMatch OMIM:612943 retinitis pigmentosa 42 semapv:UnspecifiedMatching MONDO:0013053 skos:exactMatch OMIM:612946 hadziselimovic syndrome semapv:UnspecifiedMatching MONDO:0013054 skos:exactMatch OMIM:612947 microcephaly, growth retardation, cataract, hearing loss, and unusual appearance semapv:UnspecifiedMatching -MONDO:0013055 skos:exactMatch OMIM:612948 stargardt macular degeneration, absent or hypoplastic corpus callosum, mental retardation, and dysmorphic facial features semapv:UnspecifiedMatching +MONDO:0013055 skos:exactMatch OMIM:612948 stargardt macular degeneration, absent or hypoplastic corpus callosum, impaired intellectual development, and dysmorphic facial features semapv:UnspecifiedMatching MONDO:0013056 skos:exactMatch OMIM:612949 developmental and epileptic encephalopathy 39 with leukodystrophy semapv:UnspecifiedMatching MONDO:0013057 skos:exactMatch OMIM:612950 psoriasis 12, susceptibility to semapv:UnspecifiedMatching MONDO:0013058 skos:exactMatch OMIM:612951 leukoencephalopathy, cystic, without megalencephaly semapv:UnspecifiedMatching @@ -6133,7 +6134,7 @@ MONDO:0013328 skos:exactMatch OMIM:613617 retinitis pigmentosa 58 semapv:Unspec MONDO:0013329 skos:exactMatch OMIM:613618 chromosome 17q23.1-q23.2 duplication syndrome semapv:UnspecifiedMatching MONDO:0013330 skos:exactMatch OMIM:613623 agenesis of the corpus callosum and congenital lymphedema semapv:UnspecifiedMatching MONDO:0013331 skos:exactMatch OMIM:613625 factor 5 and factor viii, combined deficiency of, 2 semapv:UnspecifiedMatching -MONDO:0013332 skos:exactMatch OMIM:613627 brachydactyly, type a1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation semapv:UnspecifiedMatching +MONDO:0013332 skos:exactMatch OMIM:613627 tsukahara syndrome semapv:UnspecifiedMatching MONDO:0013333 skos:exactMatch OMIM:613628 odontoid hypoplasia semapv:UnspecifiedMatching MONDO:0013334 skos:exactMatch OMIM:613630 fetal encasement syndrome semapv:UnspecifiedMatching MONDO:0013335 skos:exactMatch OMIM:613636 tuberculin skin test reactivity, absence of semapv:UnspecifiedMatching @@ -6637,7 +6638,7 @@ MONDO:0013852 skos:exactMatch OMIM:614676 cardiomyopathy, familial hypertrophic MONDO:0013853 skos:exactMatch OMIM:614678 pontocerebellar hypoplasia, type 1b semapv:UnspecifiedMatching MONDO:0013854 skos:exactMatch OMIM:614679 ciliary dyskinesia, primary, 17 semapv:UnspecifiedMatching MONDO:0013855 skos:exactMatch OMIM:614680 influenza, severe, susceptibility to semapv:UnspecifiedMatching -MONDO:0013856 skos:exactMatch OMIM:614684 hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, mental retardation, and recurrent inflammatory episodes semapv:UnspecifiedMatching +MONDO:0013856 skos:exactMatch OMIM:614684 hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes semapv:UnspecifiedMatching MONDO:0013857 skos:exactMatch OMIM:614687 alar cleft, isolated semapv:UnspecifiedMatching MONDO:0013858 skos:exactMatch OMIM:614688 pontine tegmental cap dysplasia semapv:UnspecifiedMatching MONDO:0013859 skos:exactMatch OMIM:614691 cataract 38 semapv:UnspecifiedMatching @@ -6984,7 +6985,7 @@ MONDO:0014208 skos:exactMatch OMIM:615490 charcot-marie-tooth disease, axonal, MONDO:0014209 skos:exactMatch OMIM:615491 spastic paraplegia 79b, autosomal recessive semapv:UnspecifiedMatching MONDO:0014210 skos:exactMatch OMIM:615493 intellectual developmental disorder, autosomal recessive 37 semapv:UnspecifiedMatching MONDO:0014211 skos:exactMatch OMIM:615500 ciliary dyskinesia, primary, 26 semapv:UnspecifiedMatching -MONDO:0014212 skos:exactMatch OMIM:615501 molybdenum cofactor deficiency, complementation group c semapv:UnspecifiedMatching +MONDO:0014212 skos:exactMatch OMIM:615501 molybdenum cofactor deficiency, type c semapv:UnspecifiedMatching MONDO:0014213 skos:exactMatch OMIM:615502 intellectual developmental disorder, autosomal dominant 21 semapv:UnspecifiedMatching MONDO:0014214 skos:exactMatch OMIM:615503 short-rib thoracic dysplasia 8 with or without polydactyly semapv:UnspecifiedMatching MONDO:0014215 skos:exactMatch OMIM:615504 ciliary dyskinesia, primary, 27 semapv:UnspecifiedMatching @@ -7116,7 +7117,7 @@ MONDO:0014343 skos:exactMatch OMIM:615777 desbuquois dysplasia 2 semapv:Unspeci MONDO:0014344 skos:exactMatch OMIM:615779 congenital heart defects, multiple types, 4 semapv:UnspecifiedMatching MONDO:0014345 skos:exactMatch OMIM:615780 retinitis pigmentosa 69 semapv:UnspecifiedMatching MONDO:0014346 skos:exactMatch OMIM:615785 white sponge nevus 2 semapv:UnspecifiedMatching -MONDO:0014347 skos:exactMatch OMIM:615789 short stature with microcephaly and distinctive facies semapv:UnspecifiedMatching +MONDO:0014347 skos:exactMatch OMIM:615789 rothmund-thomson syndrome, type 3 semapv:UnspecifiedMatching MONDO:0014348 skos:exactMatch OMIM:615802 neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities semapv:UnspecifiedMatching MONDO:0014349 skos:exactMatch OMIM:615803 pontocerebellar hypoplasia, type 10 semapv:UnspecifiedMatching MONDO:0014350 skos:exactMatch OMIM:615807 seckel syndrome 8 semapv:UnspecifiedMatching @@ -7890,6 +7891,7 @@ MONDO:0017138 skos:exactMatch omim.ps:300000 semapv:UnspecifiedMatching MONDO:0017148 skos:exactMatch omim.ps:178600 Pulmonary hypertension, primary semapv:UnspecifiedMatching MONDO:0017161 skos:exactMatch omim.ps:105550 Frontotemporal dementia and/or amyotrophic lateral sclerosis semapv:UnspecifiedMatching MONDO:0017169 skos:exactMatch omim.ps:131100 Multiple endocrine neoplasia semapv:UnspecifiedMatching +MONDO:0017195 skos:exactMatch omim.ps:259450 Bruck syndrome semapv:UnspecifiedMatching MONDO:0017265 skos:exactMatch omim.ps:242300 Ichthyosis, congenital, autosomal recessive semapv:UnspecifiedMatching MONDO:0017312 skos:exactMatch omim.ps:233400 Perrault syndrome semapv:UnspecifiedMatching MONDO:0017329 skos:exactMatch omim.ps:193000 Vesicoureteral reflux semapv:UnspecifiedMatching @@ -7952,6 +7954,7 @@ MONDO:0018310 skos:exactMatch OMIM:604856 langerhans cell histiocytosis semapv: MONDO:0018319 skos:exactMatch omim.ps:615040 Familial episodic pain syndrome semapv:UnspecifiedMatching MONDO:0018346 skos:exactMatch OMIM:301072 neurodevelopmental disorder with epilepsy and hemochromatosis semapv:UnspecifiedMatching MONDO:0018363 skos:exactMatch omim.ps:136500 Focal facial dermal dysplasia semapv:UnspecifiedMatching +MONDO:0018382 skos:exactMatch OMIM:182260 slipped femoral capital epiphyses semapv:UnspecifiedMatching MONDO:0018445 skos:exactMatch OMIM:618272 global developmental delay, lung cysts, overgrowth, and wilms tumor semapv:UnspecifiedMatching MONDO:0018458 skos:exactMatch omim.ps:145980 Hypocalciuric hypercalcemia semapv:UnspecifiedMatching MONDO:0018470 skos:exactMatch omim.ps:191830 Renal hypodysplasia/aplasia semapv:UnspecifiedMatching @@ -7987,6 +7990,7 @@ MONDO:0018866 skos:exactMatch omim.ps:225750 Aicardi-Goutieres syndrome semapv: MONDO:0018870 skos:exactMatch omim.ps:208000 Generalized arterial calcification of infancy semapv:UnspecifiedMatching MONDO:0018874 skos:exactMatch OMIM:601626 leukemia, acute myeloid semapv:UnspecifiedMatching MONDO:0018875 skos:exactMatch OMIM:151623 li-fraumeni syndrome semapv:UnspecifiedMatching +MONDO:0018878 skos:exactMatch omim.ps:602588 Branchiootic syndrome semapv:UnspecifiedMatching MONDO:0018881 skos:exactMatch OMIM:614286 myelodysplastic syndrome semapv:UnspecifiedMatching MONDO:0018901 skos:exactMatch omim.ps:604169 Left ventricular noncompaction semapv:UnspecifiedMatching MONDO:0018910 skos:exactMatch omim.ps:203100 Oculocutaneous albinism semapv:UnspecifiedMatching @@ -8263,7 +8267,7 @@ MONDO:0021582 skos:exactMatch OMIM:150900 lentigines semapv:UnspecifiedMatching MONDO:0021944 skos:exactMatch omim.ps:609129 Auditory neuropathy semapv:UnspecifiedMatching MONDO:0022109 skos:exactMatch OMIM:116850 catatrichy semapv:UnspecifiedMatching MONDO:0022113 skos:exactMatch OMIM:618352 central centrifugal cicatricial alopecia semapv:UnspecifiedMatching -MONDO:0022316 skos:exactMatch OMIM:234030 hair defect with photosensitivity and mental retardation semapv:UnspecifiedMatching +MONDO:0022316 skos:exactMatch OMIM:234030 hair defect with photosensitivity and impaired intellectual development semapv:UnspecifiedMatching MONDO:0023122 skos:exactMatch OMIM:176807 prostate cancer semapv:UnspecifiedMatching MONDO:0023655 skos:exactMatch OMIM:619281 immunodeficiency 14b, autosomal recessive semapv:UnspecifiedMatching MONDO:0023657 skos:exactMatch OMIM:619320 intellectual developmental disorder, autosomal dominant 65 semapv:UnspecifiedMatching @@ -9918,7 +9922,7 @@ MONDO:0859189 skos:exactMatch OMIM:619518 muscular dystrophy, congenital hearin MONDO:0859190 skos:exactMatch OMIM:619522 neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities semapv:UnspecifiedMatching MONDO:0859191 skos:exactMatch OMIM:619534 biliary, renal, neurologic, and skeletal syndrome semapv:UnspecifiedMatching MONDO:0859192 skos:exactMatch OMIM:619538 cerebral cavernous malformations 4 semapv:UnspecifiedMatching -MONDO:0859193 skos:exactMatch OMIM:619539 neuroocular syndrome semapv:UnspecifiedMatching +MONDO:0859193 skos:exactMatch OMIM:619539 neuroocular syndrome 1 semapv:UnspecifiedMatching MONDO:0859194 skos:exactMatch OMIM:619543 boudin-mortier syndrome semapv:UnspecifiedMatching MONDO:0859196 skos:exactMatch OMIM:619548 usmani-riazuddin syndrome, autosomal recessive semapv:UnspecifiedMatching MONDO:0859197 skos:exactMatch OMIM:619556 intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies semapv:UnspecifiedMatching @@ -10182,7 +10186,6 @@ MONDO:0957307 skos:exactMatch OMIM:620415 woolly hair-skin fragility syndrome s MONDO:0957308 skos:exactMatch OMIM:620416 spastic paraplegia 90a, autosomal dominant semapv:UnspecifiedMatching MONDO:0957309 skos:exactMatch OMIM:620417 spastic paraplegia 90b, autosomal recessive semapv:UnspecifiedMatching MONDO:0957314 skos:exactMatch OMIM:620422 retinitis pigmentosa 97 semapv:UnspecifiedMatching -MONDO:0957316 skos:exactMatch omim.ps:113800 Epidermolytic hyperkeratosis semapv:UnspecifiedMatching MONDO:0957317 skos:exactMatch omim.ps:141200 Hematuria, benign familial semapv:UnspecifiedMatching MONDO:0957318 skos:exactMatch omim.ps:167030 Nephrolithiasis, calcium oxalate semapv:UnspecifiedMatching MONDO:0957319 skos:exactMatch omim.ps:177735 Pseudohypoaldosteronism, type I semapv:UnspecifiedMatching @@ -10352,6 +10355,25 @@ MONDO:0958242 skos:exactMatch OMIM:620744 spermatogenic failure 90 semapv:Unspe MONDO:0958277 skos:exactMatch OMIM:620745 deafness, autosomal recessive 123 semapv:UnspecifiedMatching MONDO:0958278 skos:exactMatch OMIM:620746 neurodevelopmental disorder with hypotonia and characteristic brain abnormalities semapv:UnspecifiedMatching MONDO:0958279 skos:exactMatch OMIM:620748 megalencephaly-polydactyly syndrome semapv:UnspecifiedMatching +MONDO:0958322 skos:exactMatch OMIM:301118 intellectual developmental disorder, x-linked, syndromic 37 semapv:UnspecifiedMatching +MONDO:0958323 skos:exactMatch OMIM:620747 neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities semapv:UnspecifiedMatching +MONDO:0958324 skos:exactMatch OMIM:620755 generalized epilepsy with febrile seizures plus, type 12 semapv:UnspecifiedMatching +MONDO:0958325 skos:exactMatch OMIM:620757 thrombocytopenia 12 with or without myopathy semapv:UnspecifiedMatching +MONDO:0958326 skos:exactMatch OMIM:620762 macular dystrophy with or without cone dysfunction semapv:UnspecifiedMatching +MONDO:0958328 skos:exactMatch OMIM:620767 seckel syndrome 11 semapv:UnspecifiedMatching +MONDO:0958329 skos:exactMatch OMIM:620771 jeffries-lakhani neurodevelopmental syndrome semapv:UnspecifiedMatching +MONDO:0958330 skos:exactMatch OMIM:620772 developmental and epileptic encephalopathy 113 semapv:UnspecifiedMatching +MONDO:0958331 skos:exactMatch OMIM:620774 developmental and epileptic encephalopathy 114 semapv:UnspecifiedMatching +MONDO:0958332 skos:exactMatch OMIM:620775 neuromuscular disorder, congenital, with dysmorphic facies semapv:UnspecifiedMatching +MONDO:0958333 skos:exactMatch OMIM:620776 thrombocytopenia 13, syndromic semapv:UnspecifiedMatching +MONDO:0958334 skos:exactMatch OMIM:620777 pulmonary hypertension, primary, 6 semapv:UnspecifiedMatching +MONDO:0958335 skos:exactMatch OMIM:620780 cutis laxa, autosomal recessive, type 1d semapv:UnspecifiedMatching +MONDO:0968944 skos:exactMatch OMIM:620779 intellectual developmental disorder, autosomal recessive 82 semapv:UnspecifiedMatching +MONDO:0968945 skos:exactMatch OMIM:620782 neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder semapv:UnspecifiedMatching +MONDO:0968946 skos:exactMatch OMIM:620783 developmental and epileptic encephalopathy 115 semapv:UnspecifiedMatching +MONDO:0968947 skos:exactMatch OMIM:620784 neurodevelopmental disorder plus optic atrophy semapv:UnspecifiedMatching +MONDO:0968949 skos:exactMatch omim.ps:144200 Palmoplantar keratoderma, epidermolytic semapv:UnspecifiedMatching +MONDO:0968951 skos:exactMatch omim.ps:220150 Hypouricemia, renal semapv:UnspecifiedMatching MONDO:1030001 skos:exactMatch omim.ps:607631 Epilepsy, juvenile absence semapv:UnspecifiedMatching MONDO:8000006 skos:exactMatch OMIM:193670 whim syndrome 1 semapv:UnspecifiedMatching MONDO:8000008 skos:exactMatch OMIM:212720 martsolf syndrome 1 semapv:UnspecifiedMatching @@ -10992,7 +11014,7 @@ OMIM:107470 IFNGR1 skos:exactMatch hgnc.symbol:5439 semapv:UnspecifiedMatching OMIM:107470 IFNGR1 skos:exactMatch hgnc.symbol:IFNGR1 semapv:UnspecifiedMatching OMIM:107470 IFNGR1 skos:exactMatch ncbigene:3459 semapv:UnspecifiedMatching OMIM:107480 townes-brocks syndrome 1 skos:exactMatch MONDO:0054581 semapv:UnspecifiedMatching -OMIM:107500 aortic arch anomaly with peculiar facies and mental retardation skos:exactMatch MONDO:0007143 semapv:UnspecifiedMatching +OMIM:107500 aortic arch anomaly with peculiar facies and impaired intellectual development skos:exactMatch MONDO:0007143 semapv:UnspecifiedMatching OMIM:107550 aortic arch interruption, facial palsy, and retinal coloboma skos:exactMatch MONDO:0007144 semapv:UnspecifiedMatching OMIM:107580 TFAP2A skos:exactMatch hgnc.symbol:11742 semapv:UnspecifiedMatching OMIM:107580 TFAP2A skos:exactMatch hgnc.symbol:TFAP2A semapv:UnspecifiedMatching @@ -12623,7 +12645,7 @@ OMIM:122200 corneal dystrophy, lattice type 1 skos:exactMatch MONDO:0007380 sem OMIM:122200 corneal dystrophy, lattice type 1 skos:exactMatch Orphanet:98964 semapv:UnspecifiedMatching OMIM:122200 corneal dystrophy, lattice type 1 skos:exactMatch UMLS:C1690006 semapv:UnspecifiedMatching OMIM:122400 epithelial recurrent erosion dystrophy skos:exactMatch MONDO:0007381 semapv:UnspecifiedMatching -OMIM:122430 corneal hypesthesia with retinal abnormalities, sensorineural deafness, unusual facies, persistent ductus arteriosus, and mental retardation skos:exactMatch MONDO:0007382 semapv:UnspecifiedMatching +OMIM:122430 ramos-arroyo syndrome skos:exactMatch MONDO:0007382 semapv:UnspecifiedMatching OMIM:122440 corneodermatoosseous syndrome skos:exactMatch MONDO:0007383 semapv:UnspecifiedMatching OMIM:122450 corneal hypesthesia, familial skos:exactMatch MONDO:0007384 semapv:UnspecifiedMatching OMIM:122455 coronary artery dissection, spontaneous skos:exactMatch MONDO:0007385 semapv:UnspecifiedMatching @@ -14776,7 +14798,7 @@ OMIM:142622 HPCA skos:exactMatch hgnc.symbol:5144 semapv:UnspecifiedMatching OMIM:142622 HPCA skos:exactMatch hgnc.symbol:HPCA semapv:UnspecifiedMatching OMIM:142622 HPCA skos:exactMatch ncbigene:3208 semapv:UnspecifiedMatching OMIM:142623 hirschsprung disease, susceptibility to, 1 skos:exactMatch MONDO:0007723 semapv:UnspecifiedMatching -OMIM:142625 hirsutism, skeletal dysplasia, and mental retardation skos:exactMatch MONDO:0007724 semapv:UnspecifiedMatching +OMIM:142625 hirsutism, skeletal dysplasia, and impaired intellectual development skos:exactMatch MONDO:0007724 semapv:UnspecifiedMatching OMIM:142630 histiocytosis, progressive mucinous skos:exactMatch MONDO:0007725 semapv:UnspecifiedMatching OMIM:142640 HRG skos:exactMatch hgnc.symbol:5181 semapv:UnspecifiedMatching OMIM:142640 HRG skos:exactMatch hgnc.symbol:HRG semapv:UnspecifiedMatching @@ -17663,7 +17685,7 @@ OMIM:168840 PRB3 skos:exactMatch hgnc.symbol:PRB3 semapv:UnspecifiedMatching OMIM:168840 PRB3 skos:exactMatch ncbigene:5544 semapv:UnspecifiedMatching OMIM:168850 skos:exactMatch MONDO:0008204 semapv:UnspecifiedMatching OMIM:168860 patella aplasia-hypoplasia skos:exactMatch MONDO:0008205 semapv:UnspecifiedMatching -OMIM:168885 paroxysmal tonic upgaze, benign childhood, with ataxia skos:exactMatch MONDO:0008206 semapv:UnspecifiedMatching +OMIM:168885 neuroocular syndrome 2, paroxysmal type skos:exactMatch MONDO:0008206 semapv:UnspecifiedMatching OMIM:168890 PVALB skos:exactMatch hgnc.symbol:9704 semapv:UnspecifiedMatching OMIM:168890 PVALB skos:exactMatch hgnc.symbol:PVALB semapv:UnspecifiedMatching OMIM:168890 PVALB skos:exactMatch ncbigene:5816 semapv:UnspecifiedMatching @@ -19287,7 +19309,7 @@ OMIM:182255 skeletal dysplasia with delayed epiphyseal and carpal bone ossificat OMIM:182257 PI3 skos:exactMatch hgnc.symbol:8947 semapv:UnspecifiedMatching OMIM:182257 PI3 skos:exactMatch hgnc.symbol:PI3 semapv:UnspecifiedMatching OMIM:182257 PI3 skos:exactMatch ncbigene:5266 semapv:UnspecifiedMatching -OMIM:182260 slipped femoral capital epiphyses skos:exactMatch MONDO:0008431 semapv:UnspecifiedMatching +OMIM:182260 slipped femoral capital epiphyses skos:exactMatch MONDO:0018382 semapv:UnspecifiedMatching OMIM:182265 SPRR1A skos:exactMatch hgnc.symbol:11259 semapv:UnspecifiedMatching OMIM:182265 SPRR1A skos:exactMatch hgnc.symbol:SPRR1A semapv:UnspecifiedMatching OMIM:182265 SPRR1A skos:exactMatch ncbigene:6698 semapv:UnspecifiedMatching @@ -19442,8 +19464,8 @@ OMIM:182600 spastic paraplegia 3, autosomal dominant skos:exactMatch MONDO:00084 OMIM:182600 spastic paraplegia 3, autosomal dominant skos:exactMatch Orphanet:100984 semapv:UnspecifiedMatching OMIM:182600 spastic paraplegia 3, autosomal dominant skos:exactMatch UMLS:C2931355 semapv:UnspecifiedMatching OMIM:182601 spastic paraplegia 4, autosomal dominant skos:exactMatch MONDO:0008438 semapv:UnspecifiedMatching -OMIM:182610 spastic paraplegia, epilepsy, and mental retardation skos:exactMatch MONDO:0008439 semapv:UnspecifiedMatching -OMIM:182690 spastic paraplegia, sensorineural deafness, mental retardation, and progressive nephropathy skos:exactMatch MONDO:0008440 semapv:UnspecifiedMatching +OMIM:182610 spastic paraplegia, epilepsy, and impaired intellectual development skos:exactMatch MONDO:0008439 semapv:UnspecifiedMatching +OMIM:182690 spastic paraplegia, sensorineural deafness, impaired intellectual development, and progressive nephropathy skos:exactMatch MONDO:0008440 semapv:UnspecifiedMatching OMIM:182790 SPTBN1 skos:exactMatch hgnc.symbol:11275 semapv:UnspecifiedMatching OMIM:182790 SPTBN1 skos:exactMatch hgnc.symbol:SPTBN1 semapv:UnspecifiedMatching OMIM:182790 SPTBN1 skos:exactMatch ncbigene:6711 semapv:UnspecifiedMatching @@ -20898,7 +20920,7 @@ OMIM:195000 ZP1 skos:exactMatch hgnc.symbol:ZP1 semapv:UnspecifiedMatching OMIM:195000 ZP1 skos:exactMatch ncbigene:22917 semapv:UnspecifiedMatching OMIM:200100 abetalipoproteinemia skos:exactMatch MONDO:0008692 semapv:UnspecifiedMatching OMIM:200110 ablepharon-macrostomia syndrome skos:exactMatch MONDO:0008693 semapv:UnspecifiedMatching -OMIM:200130 absent eyebrows and eyelashes with mental retardation skos:exactMatch MONDO:0008694 semapv:UnspecifiedMatching +OMIM:200130 absent eyebrows and eyelashes with impaired intellectual development skos:exactMatch MONDO:0008694 semapv:UnspecifiedMatching OMIM:200150 choreoacanthocytosis skos:exactMatch MONDO:0008695 semapv:UnspecifiedMatching OMIM:200170 acanthosis nigricans with muscle cramps and acral enlargement skos:exactMatch MONDO:0008696 semapv:UnspecifiedMatching OMIM:200300 acetophenetidin sensitivity skos:exactMatch MONDO:0008697 semapv:UnspecifiedMatching @@ -20977,7 +20999,7 @@ OMIM:203450 alexander disease skos:exactMatch Orphanet:363722 semapv:Unspecifie OMIM:203450 alexander disease skos:exactMatch Orphanet:58 semapv:UnspecifiedMatching OMIM:203450 alexander disease skos:exactMatch UMLS:C0270726 semapv:UnspecifiedMatching OMIM:203500 alkaptonuria skos:exactMatch MONDO:0008753 semapv:UnspecifiedMatching -OMIM:203550 alopecia-contractures-dwarfism mental retardation syndrome skos:exactMatch MONDO:0008754 semapv:UnspecifiedMatching +OMIM:203550 intellectual developmental syndrome with alopecia, contractures, and dwarfism skos:exactMatch MONDO:0008754 semapv:UnspecifiedMatching OMIM:203600 alopecia-epilepsy-oligophrenia syndrome of moynahan skos:exactMatch MONDO:0008755 semapv:UnspecifiedMatching OMIM:203650 alopecia-intellectual disability syndrome 1 skos:exactMatch MONDO:0021035 semapv:UnspecifiedMatching OMIM:203650 alopecia-intellectual disability syndrome 1 skos:exactMatch Orphanet:2850 semapv:UnspecifiedMatching @@ -21106,7 +21128,7 @@ OMIM:209300 atransferrinemia skos:exactMatch MONDO:0008846 semapv:UnspecifiedMa OMIM:209500 atrichia with papular lesions skos:exactMatch MONDO:0008847 semapv:UnspecifiedMatching OMIM:209600 atrioventricular dissociation skos:exactMatch MONDO:0008848 semapv:UnspecifiedMatching OMIM:209700 atrophoderma vermiculata skos:exactMatch MONDO:0008849 semapv:UnspecifiedMatching -OMIM:209770 aural atresia, multiple congenital anomalies, and mental retardation skos:exactMatch MONDO:0008850 semapv:UnspecifiedMatching +OMIM:209770 aural atresia, multiple congenital anomalies, and impaired intellectual development skos:exactMatch MONDO:0008850 semapv:UnspecifiedMatching OMIM:209800 australia antigen skos:exactMatch MONDO:0044251 semapv:UnspecifiedMatching OMIM:209850 autism skos:exactMatch MONDO:0005260 semapv:UnspecifiedMatching OMIM:209850 autism skos:exactMatch UMLS:C0004352 semapv:UnspecifiedMatching @@ -21152,7 +21174,7 @@ OMIM:210710 microcephalic osteodysplastic primordial dwarfism, type 1 skos:exact OMIM:210710 microcephalic osteodysplastic primordial dwarfism, type 1 skos:exactMatch Orphanet:2636 semapv:UnspecifiedMatching OMIM:210710 microcephalic osteodysplastic primordial dwarfism, type 1 skos:exactMatch UMLS:C1859452 semapv:UnspecifiedMatching OMIM:210720 microcephalic osteodysplastic primordial dwarfism, type 2 skos:exactMatch MONDO:0008872 semapv:UnspecifiedMatching -OMIM:210730 microcephalic osteodysplastic primordial dwarfism, type 3 skos:exactMatch MONDO:0008873 semapv:UnspecifiedMatching +OMIM:210730 skos:exactMatch MONDO:0008873 semapv:UnspecifiedMatching OMIM:210740 bangstad syndrome skos:exactMatch MONDO:0008874 semapv:UnspecifiedMatching OMIM:210745 blepharophimosis with ptosis, syndactyly, and short stature skos:exactMatch MONDO:0008875 semapv:UnspecifiedMatching OMIM:210750 skin/hair/eye pigmentation, variation in, 6 skos:exactMatch MONDO:0044252 semapv:UnspecifiedMatching @@ -21294,7 +21316,7 @@ OMIM:215300 chondrosarcoma skos:exactMatch UMLS:C0008479 semapv:UnspecifiedMatc OMIM:215400 chordoma, susceptibility to skos:exactMatch MONDO:0008978 semapv:UnspecifiedMatching OMIM:215450 chorea, benign familial skos:exactMatch MONDO:0008979 semapv:UnspecifiedMatching OMIM:215470 boucher-neuhauser syndrome skos:exactMatch MONDO:0008980 semapv:UnspecifiedMatching -OMIM:215480 choroid plexus calcification and mental retardation skos:exactMatch MONDO:0008981 semapv:UnspecifiedMatching +OMIM:215480 choroid plexus calcification and impaired intellectual development skos:exactMatch MONDO:0008981 semapv:UnspecifiedMatching OMIM:215500 choroidal dystrophy, central areolar, 1 skos:exactMatch MONDO:0024539 semapv:UnspecifiedMatching OMIM:215510 chromosomal instability with tissue-specific radiosensitivity skos:exactMatch MONDO:0008983 semapv:UnspecifiedMatching OMIM:215518 ciliary discoordination due to random ciliary orientation skos:exactMatch MONDO:0008984 semapv:UnspecifiedMatching @@ -21381,8 +21403,8 @@ OMIM:218450 craniostenosis, sagittal, with congenital heart disease, mental defi OMIM:218530 craniosynostosis with anomalies of the cranial base and digits skos:exactMatch MONDO:0009037 semapv:UnspecifiedMatching OMIM:218550 craniosynostosis with fibular aplasia skos:exactMatch MONDO:0009038 semapv:UnspecifiedMatching OMIM:218600 baller-gerold syndrome skos:exactMatch MONDO:0009039 semapv:UnspecifiedMatching -OMIM:218649 craniosynostosis-mental retardation syndrome of 51n and gettig skos:exactMatch MONDO:0009040 semapv:UnspecifiedMatching -OMIM:218650 craniosynostosis-mental retardation-clefting syndrome skos:exactMatch MONDO:0009041 semapv:UnspecifiedMatching +OMIM:218649 lin-getting syndrome skos:exactMatch MONDO:0009040 semapv:UnspecifiedMatching +OMIM:218650 craniosynostosis-impaired intellectual development-clefting syndrome skos:exactMatch MONDO:0009041 semapv:UnspecifiedMatching OMIM:218670 craniotelencephalic dysplasia skos:exactMatch MONDO:0009042 semapv:UnspecifiedMatching OMIM:218700 hypothyroidism, congenital, nongoitrous, 2 skos:exactMatch MONDO:0024264 semapv:UnspecifiedMatching OMIM:218800 crigler-najjar syndrome, type 1 skos:exactMatch MONDO:0021020 semapv:UnspecifiedMatching @@ -21397,7 +21419,7 @@ OMIM:219100 cutis laxa, autosomal recessive, type 1a skos:exactMatch MONDO:00090 OMIM:219150 cutis laxa, autosomal recessive, type 3a skos:exactMatch MONDO:0009053 semapv:UnspecifiedMatching OMIM:219200 cutis laxa, autosomal recessive, type 2a skos:exactMatch MONDO:0018163 semapv:UnspecifiedMatching OMIM:219250 cutis marmorata telangiectatica congenita skos:exactMatch MONDO:0009055 semapv:UnspecifiedMatching -OMIM:219300 cutis verticis gyrata and mental retardation skos:exactMatch MONDO:0009056 semapv:UnspecifiedMatching +OMIM:219300 cutis verticis gyrata and impaired intellectual development skos:exactMatch MONDO:0009056 semapv:UnspecifiedMatching OMIM:219400 cyanosis and hepatic disease skos:exactMatch MONDO:0009057 semapv:UnspecifiedMatching OMIM:219500 cystathioninuria skos:exactMatch MONDO:0009058 semapv:UnspecifiedMatching OMIM:219500 cystathioninuria skos:exactMatch Orphanet:212 semapv:UnspecifiedMatching @@ -21408,7 +21430,7 @@ OMIM:219600 polycystic lung disease skos:exactMatch MONDO:0009060 semapv:Unspec OMIM:219700 cystic fibrosis skos:exactMatch MONDO:0009061 semapv:UnspecifiedMatching OMIM:219700 cystic fibrosis skos:exactMatch Orphanet:586 semapv:UnspecifiedMatching OMIM:219700 cystic fibrosis skos:exactMatch UMLS:C0010674 semapv:UnspecifiedMatching -OMIM:219721 cystic fibrosis with helicobacter pylori gastritis, megaloblastic anemia, and mental retardation skos:exactMatch MONDO:0009062 semapv:UnspecifiedMatching +OMIM:219721 cystic fibrosis with helicobacter pylori gastritis, megaloblastic anemia, and impaired intellectual development skos:exactMatch MONDO:0009062 semapv:UnspecifiedMatching OMIM:219730 ventriculomegaly with cystic kidney disease skos:exactMatch MONDO:0009063 semapv:UnspecifiedMatching OMIM:219750 cystinosis, adult nonnephropathic skos:exactMatch MONDO:0009064 semapv:UnspecifiedMatching OMIM:219800 cystinosis, nephropathic skos:exactMatch MONDO:0100151 semapv:UnspecifiedMatching @@ -21428,7 +21450,7 @@ OMIM:220210 ritscher-schinzel syndrome 1 skos:exactMatch MONDO:0009073 semapv:U OMIM:220210 ritscher-schinzel syndrome 1 skos:exactMatch Orphanet:7 semapv:UnspecifiedMatching OMIM:220210 ritscher-schinzel syndrome 1 skos:exactMatch UMLS:C0796137 semapv:UnspecifiedMatching OMIM:220210 ritscher-schinzel syndrome 1 skos:exactMatch UMLS:C4551776 semapv:UnspecifiedMatching -OMIM:220219 dandy-walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy skos:exactMatch MONDO:0009074 semapv:UnspecifiedMatching +OMIM:220219 dandy-walker malformation with impaired intellectual development, macrocephaly, myopia, and brachytelephalangy skos:exactMatch MONDO:0009074 semapv:UnspecifiedMatching OMIM:220220 dandy-walker malformation with postaxial polydactyly skos:exactMatch MONDO:0009075 semapv:UnspecifiedMatching OMIM:220290 deafness, autosomal recessive 1a skos:exactMatch MONDO:0009076 semapv:UnspecifiedMatching OMIM:220300 deafness, congenital, and familial myoclonic epilepsy skos:exactMatch MONDO:0009077 semapv:UnspecifiedMatching @@ -21455,7 +21477,7 @@ OMIM:221810 dermatoosteolysis, kirghizian type skos:exactMatch MONDO:0009095 se OMIM:221820 leukoencephalopathy, hereditary diffuse, with spheroids 1 skos:exactMatch MONDO:0800027 semapv:UnspecifiedMatching OMIM:221900 persistent hyperplastic primary vitreous, autosomal recessive skos:exactMatch MONDO:0009097 semapv:UnspecifiedMatching OMIM:221950 dextrocardia with unusual facies and microphthalmia skos:exactMatch MONDO:0009098 semapv:UnspecifiedMatching -OMIM:221995 diabetes insipidus, nephrogenic, with mental retardation and intracerebral calcification skos:exactMatch MONDO:0009099 semapv:UnspecifiedMatching +OMIM:221995 diabetes insipidus, nephrogenic, with impaired intellectual development and intracerebral calcification skos:exactMatch MONDO:0009099 semapv:UnspecifiedMatching OMIM:222100 type 1 diabetes mellitus skos:exactMatch MONDO:0005147 semapv:UnspecifiedMatching OMIM:222100 type 1 diabetes mellitus skos:exactMatch UMLS:C0011854 semapv:UnspecifiedMatching OMIM:222100 type 1 diabetes mellitus skos:exactMatch UMLS:C5435660 semapv:UnspecifiedMatching @@ -21497,7 +21519,7 @@ OMIM:223370 dubowitz syndrome skos:exactMatch MONDO:0009124 semapv:UnspecifiedM OMIM:223380 dopamine beta-hydroxylase, plasma, thermolability of skos:exactMatch MONDO:0009125 semapv:UnspecifiedMatching OMIM:223400 duodenal atresia skos:exactMatch MONDO:0009126 semapv:UnspecifiedMatching OMIM:223500 dwarfism, low-birth-weight type, with unresponsiveness to growth hormone skos:exactMatch MONDO:0009127 semapv:UnspecifiedMatching -OMIM:223540 dwarfism, mental retardation, and eye abnormality skos:exactMatch MONDO:0009128 semapv:UnspecifiedMatching +OMIM:223540 mollica syndrome skos:exactMatch MONDO:0009128 semapv:UnspecifiedMatching OMIM:223550 dwarfism, proportionate, with hip dislocation skos:exactMatch MONDO:0009129 semapv:UnspecifiedMatching OMIM:223800 dyggve-melchior-clausen disease skos:exactMatch MONDO:0009130 semapv:UnspecifiedMatching OMIM:223800 dyggve-melchior-clausen disease skos:exactMatch Orphanet:239 semapv:UnspecifiedMatching @@ -21570,7 +21592,7 @@ OMIM:226300 complement hyperactivation, angiopathic thrombosis, and protein-losi OMIM:226300 complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy skos:exactMatch UMLS:C4538570 semapv:UnspecifiedMatching OMIM:226350 eosinophilic fasciitis skos:exactMatch MONDO:0009175 semapv:UnspecifiedMatching OMIM:226400 epidermodysplasia verruciformis, susceptibility to, 1 skos:exactMatch MONDO:0100045 semapv:UnspecifiedMatching -OMIM:226440 epidermolysis bullosa, late-onset localized junctional, with mental retardation skos:exactMatch MONDO:0009177 semapv:UnspecifiedMatching +OMIM:226440 epidermolysis bullosa, late-onset localized junctional, with impaired intellectual development skos:exactMatch MONDO:0009177 semapv:UnspecifiedMatching OMIM:226500 epidermolysis bullosa dystrophica neurotrophica skos:exactMatch MONDO:0009178 semapv:UnspecifiedMatching OMIM:226600 epidermolysis bullosa dystrophica, autosomal recessive skos:exactMatch MONDO:0009179 semapv:UnspecifiedMatching OMIM:226650 epidermolysis bullosa, junctional 1a, intermediate skos:exactMatch MONDO:0009180 semapv:UnspecifiedMatching @@ -21583,7 +21605,7 @@ OMIM:226730 epidermolysis bullosa, junctional 5b, with pyloric atresia skos:exac OMIM:226730 epidermolysis bullosa, junctional 5b, with pyloric atresia skos:exactMatch UMLS:C1856934 semapv:UnspecifiedMatching OMIM:226735 epidermolysis bullosa with diaphragmatic hernia skos:exactMatch MONDO:0009184 semapv:UnspecifiedMatching OMIM:226750 kohlschutter-tonz syndrome skos:exactMatch MONDO:0009185 semapv:UnspecifiedMatching -OMIM:226800 epilepsy, photogenic, with spastic diplegia and mental retardation skos:exactMatch MONDO:0009186 semapv:UnspecifiedMatching +OMIM:226800 epilepsy, photogenic, with spastic diplegia and impaired intellectual development skos:exactMatch MONDO:0009186 semapv:UnspecifiedMatching OMIM:226810 epilepsy with bilateral occipital calcifications skos:exactMatch MONDO:0009187 semapv:UnspecifiedMatching OMIM:226850 epilepsy-telangiectasia skos:exactMatch MONDO:0009188 semapv:UnspecifiedMatching OMIM:226900 epiphyseal dysplasia, multiple, 4 skos:exactMatch MONDO:0009189 semapv:UnspecifiedMatching @@ -21602,7 +21624,7 @@ OMIM:227150 ethanolaminosis skos:exactMatch MONDO:0009199 semapv:UnspecifiedMat OMIM:227210 eyebrows, duplication of, with stretchable skin and syndactyly skos:exactMatch MONDO:0009200 semapv:UnspecifiedMatching OMIM:227220 skin/hair/eye pigmentation, variation in, 1 skos:exactMatch MONDO:0044255 semapv:UnspecifiedMatching OMIM:227240 skin/hair/eye pigmentation, variation in, 5 skos:exactMatch MONDO:0044256 semapv:UnspecifiedMatching -OMIM:227250 facial abnormalities, kyphoscoliosis, and mental retardation skos:exactMatch MONDO:0009201 semapv:UnspecifiedMatching +OMIM:227250 facial abnormalities, kyphoscoliosis, and impaired intellectual development skos:exactMatch MONDO:0009201 semapv:UnspecifiedMatching OMIM:227255 facial dysmorphism with multiple malformations skos:exactMatch MONDO:0009202 semapv:UnspecifiedMatching OMIM:227260 focal facial dermal dysplasia 3, setleis type skos:exactMatch MONDO:0009203 semapv:UnspecifiedMatching OMIM:227270 faciocardiomelic dysplasia, lethal skos:exactMatch MONDO:0009204 semapv:UnspecifiedMatching @@ -21798,7 +21820,7 @@ OMIM:233805 growth factors, combined defect of skos:exactMatch MONDO:0009312 se OMIM:233810 growth retardation, small and puffy hands and feet, and eczema skos:exactMatch MONDO:0009313 semapv:UnspecifiedMatching OMIM:233910 hyperphenylalaninemia, bh4-deficient, B skos:exactMatch MONDO:0100186 semapv:UnspecifiedMatching OMIM:234000 factor 12 deficiency skos:exactMatch MONDO:0009315 semapv:UnspecifiedMatching -OMIM:234030 hair defect with photosensitivity and mental retardation skos:exactMatch MONDO:0022316 semapv:UnspecifiedMatching +OMIM:234030 hair defect with photosensitivity and impaired intellectual development skos:exactMatch MONDO:0022316 semapv:UnspecifiedMatching OMIM:234050 trichothiodystrophy 4, nonphotosensitive skos:exactMatch MONDO:0021013 semapv:UnspecifiedMatching OMIM:234100 hallermann-streiff syndrome skos:exactMatch MONDO:0009318 semapv:UnspecifiedMatching OMIM:234200 neurodegeneration with brain iron accumulation 1 skos:exactMatch MONDO:0009319 semapv:UnspecifiedMatching @@ -21965,7 +21987,7 @@ OMIM:241530 hypophosphatemic rickets with hypercalciuria, hereditary skos:exactM OMIM:241540 hypopituitarism, congenital, with central diabetes insipidus skos:exactMatch MONDO:0009432 semapv:UnspecifiedMatching OMIM:241550 hypoplastic left heart syndrome 1 skos:exactMatch MONDO:0009433 semapv:UnspecifiedMatching OMIM:241600 immunodeficiency 43 skos:exactMatch MONDO:0009434 semapv:UnspecifiedMatching -OMIM:241760 hypospadias-mental retardation syndrome skos:exactMatch MONDO:0009435 semapv:UnspecifiedMatching +OMIM:241760 hypospadias-impaired intellectual development syndrome skos:exactMatch MONDO:0009435 semapv:UnspecifiedMatching OMIM:241800 pallister-hall-like syndrome skos:exactMatch MONDO:0009436 semapv:UnspecifiedMatching OMIM:241800 pallister-hall-like syndrome skos:exactMatch Orphanet:2113 semapv:UnspecifiedMatching OMIM:241800 pallister-hall-like syndrome skos:exactMatch UMLS:C5435677 semapv:UnspecifiedMatching @@ -21978,9 +22000,9 @@ OMIM:242150 keratitis-ichthyosis-deafness syndrome, autosomal recessive skos:exa OMIM:242300 ichthyosis, congenital, autosomal recessive 1 skos:exactMatch MONDO:0009441 semapv:UnspecifiedMatching OMIM:242400 ichthyosis congenita with biliary atresia skos:exactMatch MONDO:0009442 semapv:UnspecifiedMatching OMIM:242500 ichthyosis, congenital, autosomal recessive 4b skos:exactMatch MONDO:0009443 semapv:UnspecifiedMatching -OMIM:242510 ichthyosis with alopecia, eclabium, ectropion, and mental retardation skos:exactMatch MONDO:0009444 semapv:UnspecifiedMatching +OMIM:242510 ichthyosis with alopecia, eclabium, ectropion, and impaired intellectual development skos:exactMatch MONDO:0009444 semapv:UnspecifiedMatching OMIM:242520 ichthyosis, hepatosplenomegaly, and cerebellar degeneration skos:exactMatch MONDO:0009445 semapv:UnspecifiedMatching -OMIM:242530 ichthyosis, mental retardation, dwarfism, and renal impairment skos:exactMatch MONDO:0009446 semapv:UnspecifiedMatching +OMIM:242530 ichthyosis, impaired intellectual development, dwarfism, and renal impairment skos:exactMatch MONDO:0009446 semapv:UnspecifiedMatching OMIM:242550 ichthyosis, split hairs, and amino aciduria skos:exactMatch MONDO:0009447 semapv:UnspecifiedMatching OMIM:242600 iminoglycinuria skos:exactMatch MONDO:0009448 semapv:UnspecifiedMatching OMIM:242670 ciliary dyskinesia with defective radial spokes skos:exactMatch MONDO:0009449 semapv:UnspecifiedMatching @@ -21998,7 +22020,7 @@ OMIM:242880 immunoerythromyeloid hypoplasia skos:exactMatch MONDO:0009456 semap OMIM:242890 immunoglobulin d level 1n plasma, low skos:exactMatch MONDO:0009457 semapv:UnspecifiedMatching OMIM:242900 schimke immunoosseous dysplasia skos:exactMatch MONDO:0009458 semapv:UnspecifiedMatching OMIM:243000 indifference to pain, congenital, autosomal recessive skos:exactMatch MONDO:0009459 semapv:UnspecifiedMatching -OMIM:243050 indolylacroyl glycinuria with mental retardation skos:exactMatch MONDO:0009460 semapv:UnspecifiedMatching +OMIM:243050 indolylacroyl glycinuria with impaired intellectual development skos:exactMatch MONDO:0009460 semapv:UnspecifiedMatching OMIM:243060 spermatogenic failure 5 skos:exactMatch MONDO:0009461 semapv:UnspecifiedMatching OMIM:243080 inosine phosphorylase deficiency, immune defect due to skos:exactMatch MONDO:0009462 semapv:UnspecifiedMatching OMIM:243100 internal carotid arteries, hypoplasia of skos:exactMatch MONDO:0009463 semapv:UnspecifiedMatching @@ -22082,13 +22104,13 @@ OMIM:246300 leprosy, susceptibility to, 3 skos:exactMatch MONDO:0009518 semapv: OMIM:246400 letterer-siwe disease skos:exactMatch MONDO:0009519 semapv:UnspecifiedMatching OMIM:246450 3-hydroxy-3-methylglutaryl-coa lyase deficiency skos:exactMatch MONDO:0009520 semapv:UnspecifiedMatching OMIM:246470 leukemia, acute myelocytic, with polyposis coli and colon cancer skos:exactMatch MONDO:0009521 semapv:UnspecifiedMatching -OMIM:246500 leukomelanoderma, infantilism, mental retardation, hypodontia, hypotrichosis skos:exactMatch MONDO:0009522 semapv:UnspecifiedMatching +OMIM:246500 leukomelanoderma, infantilism, impaired intellectual development, hypodontia, hypotrichosis skos:exactMatch MONDO:0009522 semapv:UnspecifiedMatching OMIM:246530 LTC4S skos:exactMatch UMLS:C1416932 semapv:UnspecifiedMatching OMIM:246530 LTC4S skos:exactMatch hgnc.symbol:6719 semapv:UnspecifiedMatching OMIM:246530 LTC4S skos:exactMatch hgnc.symbol:LTC4S semapv:UnspecifiedMatching OMIM:246530 LTC4S skos:exactMatch ncbigene:4056 semapv:UnspecifiedMatching OMIM:246550 lichtenstein syndrome skos:exactMatch MONDO:0009523 semapv:UnspecifiedMatching -OMIM:246555 limb defects, distal transverse, with mental retardation and spasticity skos:exactMatch MONDO:0009524 semapv:UnspecifiedMatching +OMIM:246555 limb defects, distal transverse, with impaired intellectual development and spasticity skos:exactMatch MONDO:0009524 semapv:UnspecifiedMatching OMIM:246560 split-hand/foot malformation 3 skos:exactMatch MONDO:0009525 semapv:UnspecifiedMatching OMIM:246570 fibular aplasia, tibial campomelia, and oligosyndactyly syndrome skos:exactMatch MONDO:0009526 semapv:UnspecifiedMatching OMIM:246600 PNLIP skos:exactMatch hgnc.symbol:9155 semapv:UnspecifiedMatching @@ -22136,7 +22158,7 @@ OMIM:248360 malonyl-coa decarboxylase deficiency skos:exactMatch Orphanet:943 s OMIM:248360 malonyl-coa decarboxylase deficiency skos:exactMatch UMLS:C0342793 semapv:UnspecifiedMatching OMIM:248370 mandibuloacral dysplasia with type a lipodystrophy skos:exactMatch MONDO:0009557 semapv:UnspecifiedMatching OMIM:248390 treacher collins syndrome 3 skos:exactMatch MONDO:0009558 semapv:UnspecifiedMatching -OMIM:248400 mandibulofacial dysostosis with mental retardation skos:exactMatch MONDO:0009559 semapv:UnspecifiedMatching +OMIM:248400 mandibulofacial dysostosis with impaired intellectual development skos:exactMatch MONDO:0009559 semapv:UnspecifiedMatching OMIM:248450 manitoba oculotrichoanal syndrome skos:exactMatch MONDO:0009560 semapv:UnspecifiedMatching OMIM:248500 mannosidosis, alpha b, lysosomal skos:exactMatch MONDO:0009561 semapv:UnspecifiedMatching OMIM:248500 mannosidosis, alpha b, lysosomal skos:exactMatch Orphanet:309282 semapv:UnspecifiedMatching @@ -22153,7 +22175,7 @@ OMIM:248611 BCKDHB skos:exactMatch hgnc.symbol:BCKDHB semapv:UnspecifiedMatchin OMIM:248611 BCKDHB skos:exactMatch ncbigene:594 semapv:UnspecifiedMatching OMIM:248700 marden-walker syndrome skos:exactMatch MONDO:0009564 semapv:UnspecifiedMatching OMIM:248760 marfanoid habitus with microcephaly and glomerulonephritis skos:exactMatch MONDO:0009565 semapv:UnspecifiedMatching -OMIM:248770 marfanoid mental retardation syndrome, autosomal skos:exactMatch MONDO:0009566 semapv:UnspecifiedMatching +OMIM:248770 marfanoid impaired intellectual developmental syndrome, autosomal skos:exactMatch MONDO:0009566 semapv:UnspecifiedMatching OMIM:248800 marinesco-sjogren syndrome skos:exactMatch MONDO:0009567 semapv:UnspecifiedMatching OMIM:248800 marinesco-sjogren syndrome skos:exactMatch Orphanet:559 semapv:UnspecifiedMatching OMIM:248800 marinesco-sjogren syndrome skos:exactMatch UMLS:C0024814 semapv:UnspecifiedMatching @@ -22182,10 +22204,10 @@ OMIM:249310 neuhauser syndrome skos:exactMatch MONDO:0009577 semapv:Unspecified OMIM:249400 melanosis, neurocutaneous skos:exactMatch MONDO:0009578 semapv:UnspecifiedMatching OMIM:249420 frank-ter haar syndrome skos:exactMatch MONDO:0009579 semapv:UnspecifiedMatching OMIM:249500 intellectual developmental disorder, autosomal recessive 1 skos:exactMatch MONDO:0009580 semapv:UnspecifiedMatching -OMIM:249599 mental retardation syndrome, belgian type skos:exactMatch MONDO:0009581 semapv:UnspecifiedMatching +OMIM:249599 intellectual developmental disorder, belgian type skos:exactMatch MONDO:0009581 semapv:UnspecifiedMatching OMIM:249600 mental retardation syndrome, mietens-weber type skos:exactMatch MONDO:0009582 semapv:UnspecifiedMatching OMIM:249620 ohdo syndrome skos:exactMatch MONDO:0009583 semapv:UnspecifiedMatching -OMIM:249630 mental retardation, buenos aires type skos:exactMatch MONDO:0009584 semapv:UnspecifiedMatching +OMIM:249630 mutchinick syndrome skos:exactMatch MONDO:0009584 semapv:UnspecifiedMatching OMIM:249650 mercaptolactate-cysteine disulfiduria skos:exactMatch MONDO:0009585 semapv:UnspecifiedMatching OMIM:249660 skos:exactMatch MONDO:0009586 semapv:UnspecifiedMatching OMIM:249670 mesoaxial hexadactyly and cardiac malformation skos:exactMatch MONDO:0009587 semapv:UnspecifiedMatching @@ -22276,8 +22298,8 @@ OMIM:252011 mitochondrial complex 2 deficiency, nuclear type 1 skos:exactMatch M OMIM:252011 mitochondrial complex 2 deficiency, nuclear type 1 skos:exactMatch Orphanet:3208 semapv:UnspecifiedMatching OMIM:252011 mitochondrial complex 2 deficiency, nuclear type 1 skos:exactMatch UMLS:C1855008 semapv:UnspecifiedMatching OMIM:252100 orofaciodigital syndrome 2 skos:exactMatch MONDO:0009642 semapv:UnspecifiedMatching -OMIM:252150 molybdenum cofactor deficiency, complementation group a skos:exactMatch MONDO:0009643 semapv:UnspecifiedMatching -OMIM:252160 molybdenum cofactor deficiency, complementation group B skos:exactMatch MONDO:0009644 semapv:UnspecifiedMatching +OMIM:252150 molybdenum cofactor deficiency, type a skos:exactMatch MONDO:0009643 semapv:UnspecifiedMatching +OMIM:252160 molybdenum cofactor deficiency, type B skos:exactMatch MONDO:0009644 semapv:UnspecifiedMatching OMIM:252250 monocyte chemotactic disorder skos:exactMatch MONDO:0009645 semapv:UnspecifiedMatching OMIM:252270 monosomy 7 myelodysplasia and leukemia syndrome 1 skos:exactMatch MONDO:0009646 semapv:UnspecifiedMatching OMIM:252270 monosomy 7 myelodysplasia and leukemia syndrome 1 skos:exactMatch Orphanet:495930 semapv:UnspecifiedMatching @@ -22343,7 +22365,7 @@ OMIM:253280 muscular dystrophy-dystroglycanopathy (congenital with brain and eye OMIM:253290 multiple pterygium syndrome, lethal type skos:exactMatch MONDO:0009668 semapv:UnspecifiedMatching OMIM:253300 spinal muscular atrophy, type 1 skos:exactMatch MONDO:0009669 semapv:UnspecifiedMatching OMIM:253310 lethal congenital contracture syndrome 1 skos:exactMatch MONDO:0009670 semapv:UnspecifiedMatching -OMIM:253320 multicore myopathy with mental retardation, short stature, and hypogonadotropic hypogonadism skos:exactMatch MONDO:0009671 semapv:UnspecifiedMatching +OMIM:253320 chudley syndrome skos:exactMatch MONDO:0009671 semapv:UnspecifiedMatching OMIM:253400 spinal muscular atrophy, type 3 skos:exactMatch MONDO:0009672 semapv:UnspecifiedMatching OMIM:253550 spinal muscular atrophy, type 2 skos:exactMatch MONDO:0009673 semapv:UnspecifiedMatching OMIM:253590 muscular dystrophy, adult-onset, with leukoencephalopathy skos:exactMatch MONDO:0009674 semapv:UnspecifiedMatching @@ -22409,7 +22431,7 @@ OMIM:255320 congenital myopathy 1b, autosomal recessive skos:exactMatch UMLS:C18 OMIM:255500 myopia 18, autosomal recessive skos:exactMatch MONDO:0009713 semapv:UnspecifiedMatching OMIM:255600 myosclerosis, autosomal recessive skos:exactMatch MONDO:0009714 semapv:UnspecifiedMatching OMIM:255700 myotonia congenita, autosomal recessive skos:exactMatch MONDO:0009715 semapv:UnspecifiedMatching -OMIM:255710 myotonia with skeletal abnormalities and mental retardation skos:exactMatch MONDO:0009716 semapv:UnspecifiedMatching +OMIM:255710 myotonia with skeletal abnormalities and impaired intellectual development skos:exactMatch MONDO:0009716 semapv:UnspecifiedMatching OMIM:255800 schwartz-jampel syndrome, type 1 skos:exactMatch MONDO:0100435 semapv:UnspecifiedMatching OMIM:255900 myxedema skos:exactMatch MONDO:0009718 semapv:UnspecifiedMatching OMIM:255960 myxoma, intracardiac skos:exactMatch MONDO:0009719 semapv:UnspecifiedMatching @@ -22417,7 +22439,7 @@ OMIM:255990 nathalie syndrome skos:exactMatch MONDO:0009721 semapv:UnspecifiedM OMIM:255995 congenital myopathy 13 skos:exactMatch MONDO:0009722 semapv:UnspecifiedMatching OMIM:255995 congenital myopathy 13 skos:exactMatch Orphanet:168572 semapv:UnspecifiedMatching OMIM:255995 congenital myopathy 13 skos:exactMatch UMLS:C1850625 semapv:UnspecifiedMatching -OMIM:256000 leigh syndrome skos:exactMatch MONDO:0009723 semapv:UnspecifiedMatching +OMIM:256000 leigh syndrome, nuclear skos:exactMatch MONDO:0009723 semapv:UnspecifiedMatching OMIM:256020 focal segmental glomerulosclerosis 10 skos:exactMatch MONDO:0009724 semapv:UnspecifiedMatching OMIM:256020 focal segmental glomerulosclerosis 10 skos:exactMatch Orphanet:2613 semapv:UnspecifiedMatching OMIM:256020 focal segmental glomerulosclerosis 10 skos:exactMatch UMLS:C0403548 semapv:UnspecifiedMatching @@ -22678,7 +22700,7 @@ OMIM:264090 wiedemann-rautenstrauch syndrome skos:exactMatch Orphanet:3455 sema OMIM:264090 wiedemann-rautenstrauch syndrome skos:exactMatch UMLS:C0406586 semapv:UnspecifiedMatching OMIM:264110 prolactin deficiency, isolated skos:exactMatch MONDO:0009911 semapv:UnspecifiedMatching OMIM:264120 prolactin deficiency with obesity and enlarged testes skos:exactMatch MONDO:0009912 semapv:UnspecifiedMatching -OMIM:264140 prune belly syndrome with pulmonic stenosis, mental retardation, and deafness skos:exactMatch MONDO:0009913 semapv:UnspecifiedMatching +OMIM:264140 prune belly syndrome with pulmonic stenosis, impaired intellectual development, and deafness skos:exactMatch MONDO:0009913 semapv:UnspecifiedMatching OMIM:264180 pseudodiastrophic dysplasia skos:exactMatch MONDO:0009914 semapv:UnspecifiedMatching OMIM:264180 pseudodiastrophic dysplasia skos:exactMatch Orphanet:85174 semapv:UnspecifiedMatching OMIM:264180 pseudodiastrophic dysplasia skos:exactMatch UMLS:C0432206 semapv:UnspecifiedMatching @@ -22780,7 +22802,7 @@ OMIM:268000 retinitis pigmentosa skos:exactMatch MONDO:0019200 semapv:Unspecifi OMIM:268000 retinitis pigmentosa skos:exactMatch Orphanet:791 semapv:UnspecifiedMatching OMIM:268000 retinitis pigmentosa skos:exactMatch UMLS:C0035334 semapv:UnspecifiedMatching OMIM:268010 retinitis pigmentosa inversa with deafness skos:exactMatch MONDO:0009982 semapv:UnspecifiedMatching -OMIM:268020 retinitis pigmentosa, deafness, mental retardation, and hypogonadism skos:exactMatch MONDO:0009983 semapv:UnspecifiedMatching +OMIM:268020 retinitis pigmentosa, deafness, impaired intellectual development, and hypogonadism skos:exactMatch MONDO:0009983 semapv:UnspecifiedMatching OMIM:268025 retinitis pigmentosa, late-adult onset skos:exactMatch MONDO:0009984 semapv:UnspecifiedMatching OMIM:268040 retinohepatoendocrinologic syndrome skos:exactMatch MONDO:0009985 semapv:UnspecifiedMatching OMIM:268040 retinohepatoendocrinologic syndrome skos:exactMatch Orphanet:3087 semapv:UnspecifiedMatching @@ -22854,7 +22876,7 @@ OMIM:270420 diarrhea 3, secretory sodium, congenital, with or without other cong OMIM:270425 sodium-potassium-atpase activity of red cell skos:exactMatch MONDO:0010037 semapv:UnspecifiedMatching OMIM:270450 insulin-like growth factor i, resistance to skos:exactMatch MONDO:0010038 semapv:UnspecifiedMatching OMIM:270460 sonoda syndrome skos:exactMatch MONDO:0010039 semapv:UnspecifiedMatching -OMIM:270500 ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and mental retardation skos:exactMatch MONDO:0010040 semapv:UnspecifiedMatching +OMIM:270500 ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and impaired intellectual development skos:exactMatch MONDO:0010040 semapv:UnspecifiedMatching OMIM:270550 spastic ataxia, charlevoix-saguenay type skos:exactMatch MONDO:0010041 semapv:UnspecifiedMatching OMIM:270600 spastic diplegia and impaired intellectual development skos:exactMatch MONDO:0010042 semapv:UnspecifiedMatching OMIM:270685 spastic paraplegia 17, autosomal dominant skos:exactMatch MONDO:0010043 semapv:UnspecifiedMatching @@ -22867,13 +22889,13 @@ OMIM:270800 spastic paraplegia 5a, autosomal recessive skos:exactMatch MONDO:001 OMIM:270800 spastic paraplegia 5a, autosomal recessive skos:exactMatch Orphanet:100986 semapv:UnspecifiedMatching OMIM:270800 spastic paraplegia 5a, autosomal recessive skos:exactMatch UMLS:C1849115 semapv:UnspecifiedMatching OMIM:270805 spastic paraplegia with myoclonic epilepsy skos:exactMatch MONDO:0010048 semapv:UnspecifiedMatching -OMIM:270850 spastic paresis, glaucoma, and mental retardation skos:exactMatch MONDO:0010049 semapv:UnspecifiedMatching +OMIM:270850 spastic paresis, glaucoma, and impaired intellectual development skos:exactMatch MONDO:0010049 semapv:UnspecifiedMatching OMIM:270900 spastic pseudosclerosis skos:exactMatch MONDO:0010050 semapv:UnspecifiedMatching -OMIM:270950 spastic quadriplegia, retinitis pigmentosa, and mental retardation skos:exactMatch MONDO:0010051 semapv:UnspecifiedMatching +OMIM:270950 spastic quadriplegia, retinitis pigmentosa, and impaired intellectual development skos:exactMatch MONDO:0010051 semapv:UnspecifiedMatching OMIM:270960 spermatogenic failure 4 skos:exactMatch MONDO:0010052 semapv:UnspecifiedMatching OMIM:270970 spherocytosis, type 3 skos:exactMatch MONDO:0010053 semapv:UnspecifiedMatching -OMIM:271109 spinal muscular atrophy with mental retardation skos:exactMatch MONDO:0010054 semapv:UnspecifiedMatching -OMIM:271110 spinal muscular atrophy with microcephaly and mental subnormality skos:exactMatch MONDO:0010055 semapv:UnspecifiedMatching +OMIM:271109 spinal muscular atrophy with impaired intellectual development skos:exactMatch MONDO:0010054 semapv:UnspecifiedMatching +OMIM:271110 spinal muscular atrophy with microcephaly and impaired intellectual development skos:exactMatch MONDO:0010055 semapv:UnspecifiedMatching OMIM:271150 spinal muscular atrophy, type 4 skos:exactMatch MONDO:0010056 semapv:UnspecifiedMatching OMIM:271200 spinal muscular atrophy, ryukyuan type skos:exactMatch MONDO:0010057 semapv:UnspecifiedMatching OMIM:271220 spinal muscular atrophy, scapuloperoneal skos:exactMatch MONDO:0010058 semapv:UnspecifiedMatching @@ -22891,7 +22913,7 @@ OMIM:271510 spondyloepimetaphyseal dysplasia, sponastrime type skos:exactMatch U OMIM:271520 spondylocostal dysostosis with anal atresia and urogenital anomalies skos:exactMatch MONDO:0010069 semapv:UnspecifiedMatching OMIM:271530 brachyolmia type 1, hobaek type skos:exactMatch MONDO:0010070 semapv:UnspecifiedMatching OMIM:271600 spondyloepiphyseal dysplasia tarda, autosomal recessive skos:exactMatch MONDO:0010072 semapv:UnspecifiedMatching -OMIM:271620 spondyloepiphyseal dysplasia tarda with mental retardation skos:exactMatch MONDO:0010073 semapv:UnspecifiedMatching +OMIM:271620 spondyloepiphyseal dysplasia tarda with impaired intellectual development skos:exactMatch MONDO:0010073 semapv:UnspecifiedMatching OMIM:271630 brachyolmia type 1, toledo type skos:exactMatch MONDO:0010074 semapv:UnspecifiedMatching OMIM:271640 spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures skos:exactMatch MONDO:0010075 semapv:UnspecifiedMatching OMIM:271640 spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures skos:exactMatch Orphanet:93359 semapv:UnspecifiedMatching @@ -23042,7 +23064,7 @@ OMIM:276710 tyrosinemia, type 3 skos:exactMatch Orphanet:69723 semapv:Unspecifi OMIM:276710 tyrosinemia, type 3 skos:exactMatch UMLS:C0268623 semapv:UnspecifiedMatching OMIM:276800 tyrosinosis skos:exactMatch MONDO:0010163 semapv:UnspecifiedMatching OMIM:276820 ulna and fibula, absence of, with severe limb deficiency skos:exactMatch MONDO:0010164 semapv:UnspecifiedMatching -OMIM:276821 ulnar hypoplasia with mental retardation skos:exactMatch MONDO:0010165 semapv:UnspecifiedMatching +OMIM:276821 ulnar hypoplasia with impaired intellectual development skos:exactMatch MONDO:0010165 semapv:UnspecifiedMatching OMIM:276822 ulnar agenesis and endocardial fibroelastosis skos:exactMatch MONDO:0010166 semapv:UnspecifiedMatching OMIM:276880 urocanase deficiency skos:exactMatch MONDO:0010167 semapv:UnspecifiedMatching OMIM:276900 usher syndrome, type 1 skos:exactMatch MONDO:0700087 semapv:UnspecifiedMatching @@ -23080,7 +23102,7 @@ OMIM:277410 methylmalonic aciduria and homocystinuria, cbld type skos:exactMatch OMIM:277440 vitamin d-dependent rickets, type 2a skos:exactMatch MONDO:0010186 semapv:UnspecifiedMatching OMIM:277450 vitamin k-dependent clotting factors, combined deficiency of, 1 skos:exactMatch MONDO:0010187 semapv:UnspecifiedMatching OMIM:277460 ataxia with vitamin e deficiency skos:exactMatch MONDO:0010188 semapv:UnspecifiedMatching -OMIM:277465 vitiligo, progressive, with mental retardation and urethral duplication skos:exactMatch MONDO:0010189 semapv:UnspecifiedMatching +OMIM:277465 vitiligo, progressive, with impaired intellectual development and urethral duplication skos:exactMatch MONDO:0010189 semapv:UnspecifiedMatching OMIM:277470 pontocerebellar hypoplasia, type 2a skos:exactMatch MONDO:0010190 semapv:UnspecifiedMatching OMIM:277480 von willebrand disease, type 3 skos:exactMatch MONDO:0010191 semapv:UnspecifiedMatching OMIM:277580 waardenburg syndrome, type 4a skos:exactMatch MONDO:0010192 semapv:UnspecifiedMatching @@ -23098,7 +23120,7 @@ OMIM:277900 wilson disease skos:exactMatch UMLS:C0019202 semapv:UnspecifiedMatc OMIM:277950 winchester syndrome skos:exactMatch MONDO:0010201 semapv:UnspecifiedMatching OMIM:277950 winchester syndrome skos:exactMatch Orphanet:371428 semapv:UnspecifiedMatching OMIM:277950 winchester syndrome skos:exactMatch UMLS:C0432289 semapv:UnspecifiedMatching -OMIM:277990 wolff mental retardation syndrome skos:exactMatch MONDO:0010203 semapv:UnspecifiedMatching +OMIM:277990 wolff syndrome skos:exactMatch MONDO:0010203 semapv:UnspecifiedMatching OMIM:278000 cholesteryl ester storage disease skos:exactMatch MONDO:0019149 semapv:UnspecifiedMatching OMIM:278150 hypotrichosis 8 skos:exactMatch MONDO:0010206 semapv:UnspecifiedMatching OMIM:278200 woolly hair, hypotrichosis, everted lower lip, and outstanding ears skos:exactMatch MONDO:0010207 semapv:UnspecifiedMatching @@ -23306,7 +23328,7 @@ OMIM:300061 ZMYM3 skos:exactMatch hgnc.symbol:13054 semapv:UnspecifiedMatching OMIM:300061 ZMYM3 skos:exactMatch hgnc.symbol:ZMYM3 semapv:UnspecifiedMatching OMIM:300061 ZMYM3 skos:exactMatch ncbigene:9203 semapv:UnspecifiedMatching OMIM:300062 intellectual developmental disorder, X-linked 14 skos:exactMatch MONDO:0010236 semapv:UnspecifiedMatching -OMIM:300064 mental retardation, x-linked, with craniofacial dysmorphism skos:exactMatch MONDO:0010237 semapv:UnspecifiedMatching +OMIM:300064 hyde-forster syndrome skos:exactMatch MONDO:0010237 semapv:UnspecifiedMatching OMIM:300065 CENPI skos:exactMatch hgnc.symbol:3968 semapv:UnspecifiedMatching OMIM:300065 CENPI skos:exactMatch hgnc.symbol:CENPI semapv:UnspecifiedMatching OMIM:300065 CENPI skos:exactMatch ncbigene:2491 semapv:UnspecifiedMatching @@ -25148,7 +25170,6 @@ OMIM:300776 ALG13 skos:exactMatch ncbigene:79868 semapv:UnspecifiedMatching OMIM:300777 TMLHE skos:exactMatch hgnc.symbol:18308 semapv:UnspecifiedMatching OMIM:300777 TMLHE skos:exactMatch hgnc.symbol:TMLHE semapv:UnspecifiedMatching OMIM:300777 TMLHE skos:exactMatch ncbigene:55217 semapv:UnspecifiedMatching -OMIM:300778 skos:exactMatch MONDO:0010425 semapv:UnspecifiedMatching OMIM:300778 skos:exactMatch Orphanet:98955 semapv:UnspecifiedMatching OMIM:300778 skos:exactMatch UMLS:C2749050 semapv:UnspecifiedMatching OMIM:300779 corneal dystrophy, endothelial, X-linked skos:exactMatch MONDO:0010426 semapv:UnspecifiedMatching @@ -25908,6 +25929,7 @@ OMIM:301116 intellectual developmental disorder, X-linked 113 skos:exactMatch MO OMIM:301117 CXORF38 skos:exactMatch hgnc.symbol:28589 semapv:UnspecifiedMatching OMIM:301117 CXORF38 skos:exactMatch hgnc.symbol:CXorf38 semapv:UnspecifiedMatching OMIM:301117 CXORF38 skos:exactMatch ncbigene:159013 semapv:UnspecifiedMatching +OMIM:301118 intellectual developmental disorder, x-linked, syndromic 37 skos:exactMatch MONDO:0958322 semapv:UnspecifiedMatching OMIM:301200 amelogenesis imperfecta, type 1e skos:exactMatch MONDO:0010521 semapv:UnspecifiedMatching OMIM:301201 amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 2 skos:exactMatch MONDO:0010522 semapv:UnspecifiedMatching OMIM:301220 pigmentary disorder, reticulate, with systemic manifestations, X-linked skos:exactMatch MONDO:0010523 semapv:UnspecifiedMatching @@ -25999,7 +26021,7 @@ OMIM:304100 corpus callosum, partial agenesis of, X-linked skos:exactMatch MONDO OMIM:304110 craniofrontonasal syndrome skos:exactMatch MONDO:0010570 semapv:UnspecifiedMatching OMIM:304120 otopalatodigital syndrome, type 2 skos:exactMatch MONDO:0010571 semapv:UnspecifiedMatching OMIM:304150 occipital horn syndrome skos:exactMatch MONDO:0010572 semapv:UnspecifiedMatching -OMIM:304200 cutis verticis gyrata, thyroid aplasia, and mental retardation skos:exactMatch MONDO:0010573 semapv:UnspecifiedMatching +OMIM:304200 cutis verticis gyrata, thyroid aplasia, and impaired intellectual development skos:exactMatch MONDO:0010573 semapv:UnspecifiedMatching OMIM:304300 cyanide, inability to smell skos:exactMatch MONDO:0044262 semapv:UnspecifiedMatching OMIM:304340 pettigrew syndrome skos:exactMatch MONDO:0010574 semapv:UnspecifiedMatching OMIM:304350 deafness-hypogonadism syndrome skos:exactMatch MONDO:0010575 semapv:UnspecifiedMatching @@ -26097,7 +26119,7 @@ OMIM:307010 hydrocephalus with cerebellar agenesis skos:exactMatch MONDO:0010612 OMIM:307030 glycerol kinase deficiency skos:exactMatch MONDO:0010613 semapv:UnspecifiedMatching OMIM:307150 hypertrichosis, congenital generalized, 2 skos:exactMatch MONDO:0010614 semapv:UnspecifiedMatching OMIM:307200 isolated growth hormone deficiency, type iii, with agammaglobulinemia skos:exactMatch MONDO:0010615 semapv:UnspecifiedMatching -OMIM:307500 hypogonadism, male, with mental retardation and skeletal anomalies skos:exactMatch MONDO:0010617 semapv:UnspecifiedMatching +OMIM:307500 hypogonadism, male, with impaired intellectual development and skeletal anomalies skos:exactMatch MONDO:0010617 semapv:UnspecifiedMatching OMIM:307700 hypoparathyroidism, X-linked skos:exactMatch MONDO:0010618 semapv:UnspecifiedMatching OMIM:307800 hypophosphatemic rickets, X-linked dominant skos:exactMatch MONDO:0010619 semapv:UnspecifiedMatching OMIM:307830 hypouricemia, familial renal, due to tubular hypersecretion skos:exactMatch MONDO:0010620 semapv:UnspecifiedMatching @@ -26203,7 +26225,7 @@ OMIM:309350 melnick-needles syndrome skos:exactMatch MONDO:0010650 semapv:Unspe OMIM:309400 menkes disease skos:exactMatch MONDO:0010651 semapv:UnspecifiedMatching OMIM:309400 menkes disease skos:exactMatch Orphanet:565 semapv:UnspecifiedMatching OMIM:309400 menkes disease skos:exactMatch UMLS:C0022716 semapv:UnspecifiedMatching -OMIM:309480 mental retardation and psoriasis skos:exactMatch MONDO:0010652 semapv:UnspecifiedMatching +OMIM:309480 impaired intellectual development and psoriasis skos:exactMatch MONDO:0010652 semapv:UnspecifiedMatching OMIM:309500 renpenning syndrome 1 skos:exactMatch MONDO:0010653 semapv:UnspecifiedMatching OMIM:309510 partington syndrome skos:exactMatch MONDO:0010654 semapv:UnspecifiedMatching OMIM:309510 partington syndrome skos:exactMatch Orphanet:94083 semapv:UnspecifiedMatching @@ -26220,7 +26242,7 @@ OMIM:309550 FMR1 skos:exactMatch hgnc.symbol:3775 semapv:UnspecifiedMatching OMIM:309550 FMR1 skos:exactMatch hgnc.symbol:FMR1 semapv:UnspecifiedMatching OMIM:309550 FMR1 skos:exactMatch ncbigene:2332 semapv:UnspecifiedMatching OMIM:309555 intellectual developmental disorder, x-linked, syndromic, gustavson type skos:exactMatch MONDO:0010661 semapv:UnspecifiedMatching -OMIM:309560 mental retardation with spastic paraplegia and palmoplantar hyperkeratosis skos:exactMatch MONDO:0010662 semapv:UnspecifiedMatching +OMIM:309560 impaired intellectual development with spastic paraplegia and palmoplantar hyperkeratosis skos:exactMatch MONDO:0010662 semapv:UnspecifiedMatching OMIM:309580 intellectual disability-hypotonic facies syndrome, x-linked, 1 skos:exactMatch MONDO:0010663 semapv:UnspecifiedMatching OMIM:309583 intellectual developmental disorder, x-linked, syndromic, snyder-robinson type skos:exactMatch MONDO:0010664 semapv:UnspecifiedMatching OMIM:309585 intellectual developmental disorder, x-linked, syndromic, wilson-turner type skos:exactMatch MONDO:0010665 semapv:UnspecifiedMatching @@ -26232,7 +26254,7 @@ OMIM:309590 intellectual developmental disorder, x-linked, syndromic, turner typ OMIM:309590 intellectual developmental disorder, x-linked, syndromic, turner type skos:exactMatch UMLS:C2678046 semapv:UnspecifiedMatching OMIM:309605 skos:exactMatch MONDO:0010666 semapv:UnspecifiedMatching OMIM:309610 prieto syndrome skos:exactMatch MONDO:0010667 semapv:UnspecifiedMatching -OMIM:309620 mental retardation, skeletal dysplasia, and abducens palsy skos:exactMatch MONDO:0010668 semapv:UnspecifiedMatching +OMIM:309620 christian syndrome skos:exactMatch MONDO:0010668 semapv:UnspecifiedMatching OMIM:309630 metacarpal 4-5 fusion skos:exactMatch MONDO:0010669 semapv:UnspecifiedMatching OMIM:309640 mental retardation with spastic paraplegia skos:exactMatch MONDO:0010670 semapv:UnspecifiedMatching OMIM:309800 microphthalmia, syndromic 1 skos:exactMatch MONDO:0010671 semapv:UnspecifiedMatching @@ -26398,7 +26420,7 @@ OMIM:312820 SSX1 skos:exactMatch hgnc.symbol:11335 semapv:UnspecifiedMatching OMIM:312820 SSX1 skos:exactMatch hgnc.symbol:SSX1 semapv:UnspecifiedMatching OMIM:312820 SSX1 skos:exactMatch ncbigene:6756 semapv:UnspecifiedMatching OMIM:312830 scarf syndrome skos:exactMatch MONDO:0010728 semapv:UnspecifiedMatching -OMIM:312840 schimke X-linked mental retardation syndrome skos:exactMatch MONDO:0010729 semapv:UnspecifiedMatching +OMIM:312840 schimke syndrome skos:exactMatch MONDO:0010729 semapv:UnspecifiedMatching OMIM:312861 HTR2C skos:exactMatch hgnc.symbol:5295 semapv:UnspecifiedMatching OMIM:312861 HTR2C skos:exactMatch hgnc.symbol:HTR2C semapv:UnspecifiedMatching OMIM:312861 HTR2C skos:exactMatch ncbigene:3358 semapv:UnspecifiedMatching @@ -27121,7 +27143,7 @@ OMIM:600119 SGCA skos:exactMatch hgnc.symbol:10805 semapv:UnspecifiedMatching OMIM:600119 SGCA skos:exactMatch hgnc.symbol:SGCA semapv:UnspecifiedMatching OMIM:600119 SGCA skos:exactMatch ncbigene:6442 semapv:UnspecifiedMatching OMIM:600121 rhizomelic chondrodysplasia punctata, type 3 skos:exactMatch MONDO:0010823 semapv:UnspecifiedMatching -OMIM:600122 male pseudohermaphroditism/mental retardation syndrome, verloes type skos:exactMatch MONDO:0010824 semapv:UnspecifiedMatching +OMIM:600122 verloes syndrome skos:exactMatch MONDO:0010824 semapv:UnspecifiedMatching OMIM:600123 atrioventricular septal defect with blepharophimosis and anal and radial defects skos:exactMatch MONDO:0010825 semapv:UnspecifiedMatching OMIM:600123 atrioventricular septal defect with blepharophimosis and anal and radial defects skos:exactMatch Orphanet:1352 semapv:UnspecifiedMatching OMIM:600123 atrioventricular septal defect with blepharophimosis and anal and radial defects skos:exactMatch UMLS:C1838606 semapv:UnspecifiedMatching @@ -27220,7 +27242,7 @@ OMIM:600157 AP1B1 skos:exactMatch UMLS:C1412434 semapv:UnspecifiedMatching OMIM:600157 AP1B1 skos:exactMatch hgnc.symbol:554 semapv:UnspecifiedMatching OMIM:600157 AP1B1 skos:exactMatch hgnc.symbol:AP1B1 semapv:UnspecifiedMatching OMIM:600157 AP1B1 skos:exactMatch ncbigene:162 semapv:UnspecifiedMatching -OMIM:600159 pterygium colli and mental retardation with facial and digital anomalies skos:exactMatch MONDO:0010835 semapv:UnspecifiedMatching +OMIM:600159 pterygium colli and impaired intellectual development with facial and digital anomalies skos:exactMatch MONDO:0010835 semapv:UnspecifiedMatching OMIM:600160 CDKN2A skos:exactMatch hgnc.symbol:1787 semapv:UnspecifiedMatching OMIM:600160 CDKN2A skos:exactMatch hgnc.symbol:CDKN2A semapv:UnspecifiedMatching OMIM:600160 CDKN2A skos:exactMatch ncbigene:1029 semapv:UnspecifiedMatching @@ -29186,7 +29208,7 @@ OMIM:600903 wiskott-aldrich syndrome, autosomal dominant skos:exactMatch MONDO:0 OMIM:600904 ASTN1 skos:exactMatch hgnc.symbol:773 semapv:UnspecifiedMatching OMIM:600904 ASTN1 skos:exactMatch hgnc.symbol:ASTN1 semapv:UnspecifiedMatching OMIM:600904 ASTN1 skos:exactMatch ncbigene:460 semapv:UnspecifiedMatching -OMIM:600906 ectodermal dysplasia with mental retardation and syndactyly skos:exactMatch MONDO:0010955 semapv:UnspecifiedMatching +OMIM:600906 ectodermal dysplasia with impaired intellectual development and syndactyly skos:exactMatch MONDO:0010955 semapv:UnspecifiedMatching OMIM:600907 enamel hypoplasia, cataracts, and aqueductal stenosis skos:exactMatch MONDO:0010956 semapv:UnspecifiedMatching OMIM:600909 LSS skos:exactMatch UMLS:C1416926 semapv:UnspecifiedMatching OMIM:600909 LSS skos:exactMatch UMLS:C4225300 semapv:UnspecifiedMatching @@ -29550,7 +29572,7 @@ OMIM:601037 HNRNPF skos:exactMatch ncbigene:3185 semapv:UnspecifiedMatching OMIM:601038 DIO3 skos:exactMatch hgnc.symbol:2885 semapv:UnspecifiedMatching OMIM:601038 DIO3 skos:exactMatch hgnc.symbol:DIO3 semapv:UnspecifiedMatching OMIM:601038 DIO3 skos:exactMatch ncbigene:1735 semapv:UnspecifiedMatching -OMIM:601039 ichthyosis-mental retardation syndrome with large keratohyalin granules 1n the skin skos:exactMatch MONDO:0010982 semapv:UnspecifiedMatching +OMIM:601039 ichthyosis-impaired intellectual developmental syndrome with large keratohyalin granules 1n the skin skos:exactMatch MONDO:0010982 semapv:UnspecifiedMatching OMIM:601040 SCARB1 skos:exactMatch hgnc.symbol:1664 semapv:UnspecifiedMatching OMIM:601040 SCARB1 skos:exactMatch hgnc.symbol:SCARB1 semapv:UnspecifiedMatching OMIM:601040 SCARB1 skos:exactMatch ncbigene:949 semapv:UnspecifiedMatching @@ -30010,7 +30032,7 @@ OMIM:601215 ATR skos:exactMatch hgnc.symbol:882 semapv:UnspecifiedMatching OMIM:601215 ATR skos:exactMatch hgnc.symbol:ATR semapv:UnspecifiedMatching OMIM:601215 ATR skos:exactMatch ncbigene:545 semapv:UnspecifiedMatching OMIM:601216 dental anomalies and short stature skos:exactMatch MONDO:0011018 semapv:UnspecifiedMatching -OMIM:601217 alopecia-mental retardation syndrome with convulsions and hypergonadotropic hypogonadism skos:exactMatch MONDO:0011019 semapv:UnspecifiedMatching +OMIM:601217 alopecia-impaired intellectual developmental syndrome with convulsions and hypergonadotropic hypogonadism skos:exactMatch MONDO:0011019 semapv:UnspecifiedMatching OMIM:601218 ADARB1 skos:exactMatch UMLS:C1412216 semapv:UnspecifiedMatching OMIM:601218 ADARB1 skos:exactMatch UMLS:C5394312 semapv:UnspecifiedMatching OMIM:601218 ADARB1 skos:exactMatch hgnc.symbol:226 semapv:UnspecifiedMatching @@ -30342,7 +30364,7 @@ OMIM:601348 ectrodactyly of lower limbs, congenital heart defect, and micrognath OMIM:601349 microphthalmia, syndromic 8 skos:exactMatch MONDO:0011045 semapv:UnspecifiedMatching OMIM:601350 short stature syndrome, brussels type skos:exactMatch MONDO:0011046 semapv:UnspecifiedMatching OMIM:601351 growth retardation, deafness, femoral epiphyseal dysplasia, and lacrimal duct obstruction skos:exactMatch MONDO:0011047 semapv:UnspecifiedMatching -OMIM:601352 mental retardation, microcephaly, epilepsy, and coarse face skos:exactMatch MONDO:0011048 semapv:UnspecifiedMatching +OMIM:601352 impaired intellectual development, microcephaly, epilepsy, and coarse face skos:exactMatch MONDO:0011048 semapv:UnspecifiedMatching OMIM:601353 brachycephaly, deafness, cataract, microstomia, and impaired intellectual development skos:exactMatch MONDO:0011049 semapv:UnspecifiedMatching OMIM:601355 microcephaly, congenital heart disease, unilateral renal agenesis, and hyposegmented lungs skos:exactMatch MONDO:0011050 semapv:UnspecifiedMatching OMIM:601356 lethal short-limb skeletal dysplasia, al gazali type skos:exactMatch MONDO:0011051 semapv:UnspecifiedMatching @@ -31599,7 +31621,7 @@ OMIM:601791 PEX14 skos:exactMatch ncbigene:5195 semapv:UnspecifiedMatching OMIM:601792 PPP1R2 skos:exactMatch hgnc.symbol:9288 semapv:UnspecifiedMatching OMIM:601792 PPP1R2 skos:exactMatch hgnc.symbol:PPP1R2 semapv:UnspecifiedMatching OMIM:601792 PPP1R2 skos:exactMatch ncbigene:5504 semapv:UnspecifiedMatching -OMIM:601794 coloboma-obesity-hypogenitalism-mental retardation syndrome skos:exactMatch MONDO:0011145 semapv:UnspecifiedMatching +OMIM:601794 coloboma-obesity-hypogenitalism-impaired intellectual development syndrome skos:exactMatch MONDO:0011145 semapv:UnspecifiedMatching OMIM:601795 MAPK3 skos:exactMatch UMLS:C1366765 semapv:UnspecifiedMatching OMIM:601795 MAPK3 skos:exactMatch hgnc.symbol:6877 semapv:UnspecifiedMatching OMIM:601795 MAPK3 skos:exactMatch hgnc.symbol:MAPK3 semapv:UnspecifiedMatching @@ -33703,7 +33725,7 @@ OMIM:602552 NUP88 skos:exactMatch hgnc.symbol:NUP88 semapv:UnspecifiedMatching OMIM:602552 NUP88 skos:exactMatch ncbigene:4927 semapv:UnspecifiedMatching OMIM:602553 anal atresia, hypospadias, and penoscrotal inversion skos:exactMatch MONDO:0011248 semapv:UnspecifiedMatching OMIM:602554 torsion dystonia with onset 1n infancy skos:exactMatch MONDO:0011249 semapv:UnspecifiedMatching -OMIM:602555 microcephaly, macrotia, and mental retardation skos:exactMatch MONDO:0011250 semapv:UnspecifiedMatching +OMIM:602555 microcephaly, macrotia, and impaired intellectual development skos:exactMatch MONDO:0011250 semapv:UnspecifiedMatching OMIM:602556 facial dysmorphism, cleft palate, hearing loss, and camptodactyly skos:exactMatch MONDO:0011251 semapv:UnspecifiedMatching OMIM:602557 spondyloepimetaphyseal dysplasia, shohat type skos:exactMatch MONDO:0011252 semapv:UnspecifiedMatching OMIM:602557 spondyloepimetaphyseal dysplasia, shohat type skos:exactMatch Orphanet:93352 semapv:UnspecifiedMatching @@ -33718,7 +33740,7 @@ OMIM:602563 NKX6-1 skos:exactMatch UMLS:C1417738 semapv:UnspecifiedMatching OMIM:602563 NKX6-1 skos:exactMatch hgnc.symbol:7839 semapv:UnspecifiedMatching OMIM:602563 NKX6-1 skos:exactMatch hgnc.symbol:NKX6-1 semapv:UnspecifiedMatching OMIM:602563 NKX6-1 skos:exactMatch ncbigene:4825 semapv:UnspecifiedMatching -OMIM:602564 emphysema, congenital, with deafness, penoscrotal web, and mental retardation skos:exactMatch MONDO:0011256 semapv:UnspecifiedMatching +OMIM:602564 emphysema, congenital, with deafness, penoscrotal web, and intellectual developmental disorder skos:exactMatch MONDO:0011256 semapv:UnspecifiedMatching OMIM:602565 CCL25 skos:exactMatch hgnc.symbol:10624 semapv:UnspecifiedMatching OMIM:602565 CCL25 skos:exactMatch hgnc.symbol:CCL25 semapv:UnspecifiedMatching OMIM:602565 CCL25 skos:exactMatch ncbigene:6370 semapv:UnspecifiedMatching @@ -33843,7 +33865,7 @@ OMIM:602609 PIK3C3 skos:exactMatch ncbigene:5289 semapv:UnspecifiedMatching OMIM:602610 PIK3R4 skos:exactMatch hgnc.symbol:8982 semapv:UnspecifiedMatching OMIM:602610 PIK3R4 skos:exactMatch hgnc.symbol:PIK3R4 semapv:UnspecifiedMatching OMIM:602610 PIK3R4 skos:exactMatch ncbigene:30849 semapv:UnspecifiedMatching -OMIM:602611 spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and mental retardation skos:exactMatch MONDO:0011261 semapv:UnspecifiedMatching +OMIM:602611 spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and impaired intellectual development skos:exactMatch MONDO:0011261 semapv:UnspecifiedMatching OMIM:602612 camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye skos:exactMatch MONDO:0011262 semapv:UnspecifiedMatching OMIM:602613 skeletal dysplasia and progressive central nervous system degeneration, lethal skos:exactMatch MONDO:0011263 semapv:UnspecifiedMatching OMIM:602614 MAP3K7 skos:exactMatch hgnc.symbol:6859 semapv:UnspecifiedMatching @@ -34064,7 +34086,7 @@ OMIM:602683 ADGRB2 skos:exactMatch ncbigene:576 semapv:UnspecifiedMatching OMIM:602684 ADGRB3 skos:exactMatch hgnc.symbol:945 semapv:UnspecifiedMatching OMIM:602684 ADGRB3 skos:exactMatch hgnc.symbol:ADGRB3 semapv:UnspecifiedMatching OMIM:602684 ADGRB3 skos:exactMatch ncbigene:577 semapv:UnspecifiedMatching -OMIM:602685 mental retardation, severe, with spasticity and pigmentary tapetoretinal degeneration skos:exactMatch MONDO:0011267 semapv:UnspecifiedMatching +OMIM:602685 intellectual developmental disorder with spasticity and pigmentary tapetoretinal degeneration skos:exactMatch MONDO:0011267 semapv:UnspecifiedMatching OMIM:602686 MAD1L1 skos:exactMatch hgnc.symbol:6762 semapv:UnspecifiedMatching OMIM:602686 MAD1L1 skos:exactMatch hgnc.symbol:MAD1L1 semapv:UnspecifiedMatching OMIM:602686 MAD1L1 skos:exactMatch ncbigene:8379 semapv:UnspecifiedMatching @@ -35433,7 +35455,7 @@ OMIM:603131 PMPCB skos:exactMatch ncbigene:9512 semapv:UnspecifiedMatching OMIM:603132 ZNF189 skos:exactMatch hgnc.symbol:12980 semapv:UnspecifiedMatching OMIM:603132 ZNF189 skos:exactMatch hgnc.symbol:ZNF189 semapv:UnspecifiedMatching OMIM:603132 ZNF189 skos:exactMatch ncbigene:7743 semapv:UnspecifiedMatching -OMIM:603133 dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and mental retardation skos:exactMatch MONDO:0011290 semapv:UnspecifiedMatching +OMIM:603133 dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and impaired intellectual development skos:exactMatch MONDO:0011290 semapv:UnspecifiedMatching OMIM:603134 CUL1 skos:exactMatch hgnc.symbol:2551 semapv:UnspecifiedMatching OMIM:603134 CUL1 skos:exactMatch hgnc.symbol:CUL1 semapv:UnspecifiedMatching OMIM:603134 CUL1 skos:exactMatch ncbigene:8454 semapv:UnspecifiedMatching @@ -36334,7 +36356,7 @@ OMIM:603436 ZNF205 skos:exactMatch ncbigene:7755 semapv:UnspecifiedMatching OMIM:603437 YBX3 skos:exactMatch hgnc.symbol:2428 semapv:UnspecifiedMatching OMIM:603437 YBX3 skos:exactMatch hgnc.symbol:YBX3 semapv:UnspecifiedMatching OMIM:603437 YBX3 skos:exactMatch ncbigene:8531 semapv:UnspecifiedMatching -OMIM:603438 radioulnar synostosis with microcephaly, short stature, scoliosis, and mental retardation skos:exactMatch MONDO:0011320 semapv:UnspecifiedMatching +OMIM:603438 tsukahara syndrome skos:exactMatch MONDO:0011320 semapv:UnspecifiedMatching OMIM:603439 expansile bone lesions skos:exactMatch MONDO:0011321 semapv:UnspecifiedMatching OMIM:603440 CDK17 skos:exactMatch hgnc.symbol:8750 semapv:UnspecifiedMatching OMIM:603440 CDK17 skos:exactMatch hgnc.symbol:CDK17 semapv:UnspecifiedMatching @@ -36701,7 +36723,7 @@ OMIM:603570 VNN1 skos:exactMatch ncbigene:8876 semapv:UnspecifiedMatching OMIM:603571 VNN2 skos:exactMatch hgnc.symbol:12706 semapv:UnspecifiedMatching OMIM:603571 VNN2 skos:exactMatch hgnc.symbol:VNN2 semapv:UnspecifiedMatching OMIM:603571 VNN2 skos:exactMatch ncbigene:8875 semapv:UnspecifiedMatching -OMIM:603572 microcephaly, facial abnormalities, micromelia, and mental retardation skos:exactMatch MONDO:0011341 semapv:UnspecifiedMatching +OMIM:603572 microcephaly, facial abnormalities, micromelia, and impaired intellectual development skos:exactMatch MONDO:0011341 semapv:UnspecifiedMatching OMIM:603573 MBD3 skos:exactMatch hgnc.symbol:6918 semapv:UnspecifiedMatching OMIM:603573 MBD3 skos:exactMatch hgnc.symbol:MBD3 semapv:UnspecifiedMatching OMIM:603573 MBD3 skos:exactMatch ncbigene:53615 semapv:UnspecifiedMatching @@ -37884,7 +37906,7 @@ OMIM:603984 ZNF737 skos:exactMatch hgnc.symbol:ZNF737 semapv:UnspecifiedMatchin OMIM:603984 ZNF737 skos:exactMatch ncbigene:100129842 semapv:UnspecifiedMatching OMIM:603985 zinc finger protein 103 skos:exactMatch UMLS:C1858873 semapv:UnspecifiedMatching OMIM:603987 zinc finger protein 105 skos:exactMatch UMLS:C1858872 semapv:UnspecifiedMatching -OMIM:603988 zinc finger protein 106 skos:exactMatch UMLS:C1858871 semapv:UnspecifiedMatching +OMIM:603988 ZNF106 skos:exactMatch UMLS:C1858871 semapv:UnspecifiedMatching OMIM:603989 ZNF107 skos:exactMatch hgnc.symbol:12887 semapv:UnspecifiedMatching OMIM:603989 ZNF107 skos:exactMatch hgnc.symbol:ZNF107 semapv:UnspecifiedMatching OMIM:603989 ZNF107 skos:exactMatch ncbigene:51427 semapv:UnspecifiedMatching @@ -38757,7 +38779,7 @@ OMIM:604313 GALK1 skos:exactMatch hgnc.symbol:4118 semapv:UnspecifiedMatching OMIM:604313 GALK1 skos:exactMatch hgnc.symbol:GALK1 semapv:UnspecifiedMatching OMIM:604313 GALK1 skos:exactMatch ncbigene:2584 semapv:UnspecifiedMatching OMIM:604314 blepharophimosis with facial and genital anomalies and impaired intellectual development skos:exactMatch MONDO:0011432 semapv:UnspecifiedMatching -OMIM:604315 anemia, congenital hypoplastic, with multiple congenital anomalies/mental retardation syndrome skos:exactMatch MONDO:0011433 semapv:UnspecifiedMatching +OMIM:604315 anemia, congenital hypoplastic, with multiple congenital anomalies/impaired intellectual development syndrome skos:exactMatch MONDO:0011433 semapv:UnspecifiedMatching OMIM:604316 psoriasis 5, susceptibility to skos:exactMatch MONDO:0011434 semapv:UnspecifiedMatching OMIM:604317 microcephaly 2, primary, autosomal recessive, with or without cortical malformations skos:exactMatch MONDO:0011435 semapv:UnspecifiedMatching OMIM:604318 GTF2IRD1 skos:exactMatch hgnc.symbol:4661 semapv:UnspecifiedMatching @@ -41888,7 +41910,7 @@ OMIM:605398 CXCL16 skos:exactMatch ncbigene:58191 semapv:UnspecifiedMatching OMIM:605399 NID2 skos:exactMatch hgnc.symbol:13389 semapv:UnspecifiedMatching OMIM:605399 NID2 skos:exactMatch hgnc.symbol:NID2 semapv:UnspecifiedMatching OMIM:605399 NID2 skos:exactMatch ncbigene:22795 semapv:UnspecifiedMatching -OMIM:605400 fibromatosis, gingival, with hypertrichosis and mental retardation skos:exactMatch MONDO:0011550 semapv:UnspecifiedMatching +OMIM:605400 fibromatosis, gingival, with hypertrichosis and impaired intellectual development skos:exactMatch MONDO:0011550 semapv:UnspecifiedMatching OMIM:605401 IQGAP2 skos:exactMatch hgnc.symbol:6111 semapv:UnspecifiedMatching OMIM:605401 IQGAP2 skos:exactMatch hgnc.symbol:IQGAP2 semapv:UnspecifiedMatching OMIM:605401 IQGAP2 skos:exactMatch ncbigene:10788 semapv:UnspecifiedMatching @@ -44344,8 +44366,8 @@ OMIM:606240 thyroid cancer, nonmedullary, 3 skos:exactMatch MONDO:0011653 semap OMIM:606241 DICER1 skos:exactMatch hgnc.symbol:17098 semapv:UnspecifiedMatching OMIM:606241 DICER1 skos:exactMatch hgnc.symbol:DICER1 semapv:UnspecifiedMatching OMIM:606241 DICER1 skos:exactMatch ncbigene:23405 semapv:UnspecifiedMatching -OMIM:606242 mental retardation, microcephaly, growth retardation, joint contractures, and facial dysmorphism skos:exactMatch MONDO:0011654 semapv:UnspecifiedMatching -OMIM:606242 mental retardation, microcephaly, growth retardation, joint contractures, and facial dysmorphism skos:exactMatch UMLS:C1853480 semapv:UnspecifiedMatching +OMIM:606242 kondoh syndrome skos:exactMatch MONDO:0011654 semapv:UnspecifiedMatching +OMIM:606242 kondoh syndrome skos:exactMatch UMLS:C1853480 semapv:UnspecifiedMatching OMIM:606243 alveolar soft part sarcoma skos:exactMatch MONDO:0011655 semapv:UnspecifiedMatching OMIM:606244 STAM2 skos:exactMatch hgnc.symbol:11358 semapv:UnspecifiedMatching OMIM:606244 STAM2 skos:exactMatch hgnc.symbol:STAM2 semapv:UnspecifiedMatching @@ -46093,7 +46115,7 @@ OMIM:606849 UBL5 skos:exactMatch ncbigene:59286 semapv:UnspecifiedMatching OMIM:606850 MIPOL1 skos:exactMatch hgnc.symbol:21460 semapv:UnspecifiedMatching OMIM:606850 MIPOL1 skos:exactMatch hgnc.symbol:MIPOL1 semapv:UnspecifiedMatching OMIM:606850 MIPOL1 skos:exactMatch ncbigene:145282 semapv:UnspecifiedMatching -OMIM:606851 cree mental retardation syndrome skos:exactMatch MONDO:0011736 semapv:UnspecifiedMatching +OMIM:606851 cree impaired intellectual development syndrome skos:exactMatch MONDO:0011736 semapv:UnspecifiedMatching OMIM:606852 parkinson disease 10 skos:exactMatch MONDO:0011737 semapv:UnspecifiedMatching OMIM:606853 ATP6V1G2 skos:exactMatch hgnc.symbol:862 semapv:UnspecifiedMatching OMIM:606853 ATP6V1G2 skos:exactMatch hgnc.symbol:ATP6V1G2 semapv:UnspecifiedMatching @@ -48128,7 +48150,7 @@ OMIM:607563 SLC17A6 skos:exactMatch ncbigene:57084 semapv:UnspecifiedMatching OMIM:607564 TRIM6 skos:exactMatch hgnc.symbol:16277 semapv:UnspecifiedMatching OMIM:607564 TRIM6 skos:exactMatch hgnc.symbol:TRIM6 semapv:UnspecifiedMatching OMIM:607564 TRIM6 skos:exactMatch ncbigene:117854 semapv:UnspecifiedMatching -OMIM:607565 spastic paraplegia, ataxia, and mental retardation skos:exactMatch MONDO:0011858 semapv:UnspecifiedMatching +OMIM:607565 spastic paraplegia, ataxia, and impaired intellectual development skos:exactMatch MONDO:0011858 semapv:UnspecifiedMatching OMIM:607566 EPM2A skos:exactMatch hgnc.symbol:3413 semapv:UnspecifiedMatching OMIM:607566 EPM2A skos:exactMatch hgnc.symbol:EPM2A semapv:UnspecifiedMatching OMIM:607566 EPM2A skos:exactMatch ncbigene:7957 semapv:UnspecifiedMatching @@ -49211,7 +49233,7 @@ OMIM:607946 ADIPOR2 skos:exactMatch ncbigene:79602 semapv:UnspecifiedMatching OMIM:607947 KCNRG skos:exactMatch hgnc.symbol:18893 semapv:UnspecifiedMatching OMIM:607947 KCNRG skos:exactMatch hgnc.symbol:KCNRG semapv:UnspecifiedMatching OMIM:607947 KCNRG skos:exactMatch ncbigene:283518 semapv:UnspecifiedMatching -OMIM:607948 mycobacterium tuberculosis, susceptibility to skos:exactMatch MONDO:0011940 semapv:UnspecifiedMatching +OMIM:607948 mycobacterium tuberculosis, susceptibility to skos:exactMatch MONDO:0000070 semapv:UnspecifiedMatching OMIM:607949 mycobacterium tuberculosis, susceptibility to, 1 skos:exactMatch MONDO:0011941 semapv:UnspecifiedMatching OMIM:607950 testis-specific protease 50 skos:exactMatch hgnc.symbol:17910 semapv:UnspecifiedMatching OMIM:607950 testis-specific protease 50 skos:exactMatch hgnc.symbol:PRSS50 semapv:UnspecifiedMatching @@ -49824,7 +49846,7 @@ OMIM:608152 PTGES2 skos:exactMatch ncbigene:80142 semapv:UnspecifiedMatching OMIM:608153 PPP1R14A skos:exactMatch hgnc.symbol:14871 semapv:UnspecifiedMatching OMIM:608153 PPP1R14A skos:exactMatch hgnc.symbol:PPP1R14A semapv:UnspecifiedMatching OMIM:608153 PPP1R14A skos:exactMatch ncbigene:94274 semapv:UnspecifiedMatching -OMIM:608154 lipodystrophy, generalized, with mental retardation, deafness, short stature, and slender bones skos:exactMatch MONDO:0011976 semapv:UnspecifiedMatching +OMIM:608154 lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones skos:exactMatch MONDO:0011976 semapv:UnspecifiedMatching OMIM:608155 SYNPO skos:exactMatch hgnc.symbol:30672 semapv:UnspecifiedMatching OMIM:608155 SYNPO skos:exactMatch hgnc.symbol:SYNPO semapv:UnspecifiedMatching OMIM:608155 SYNPO skos:exactMatch ncbigene:11346 semapv:UnspecifiedMatching @@ -50193,7 +50215,7 @@ OMIM:608276 SLC22A16 skos:exactMatch ncbigene:85413 semapv:UnspecifiedMatching OMIM:608277 CHST15 skos:exactMatch hgnc.symbol:18137 semapv:UnspecifiedMatching OMIM:608277 CHST15 skos:exactMatch hgnc.symbol:CHST15 semapv:UnspecifiedMatching OMIM:608277 CHST15 skos:exactMatch ncbigene:51363 semapv:UnspecifiedMatching -OMIM:608278 growth failure, microcephaly, mental retardation, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy skos:exactMatch MONDO:0012005 semapv:UnspecifiedMatching +OMIM:608278 growth failure, microcephaly, impaired intellectual development, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy skos:exactMatch MONDO:0012005 semapv:UnspecifiedMatching OMIM:608279 craniosynostosis with ocular abnormalities and hallucal defects skos:exactMatch MONDO:0012006 semapv:UnspecifiedMatching OMIM:608280 GAS5 skos:exactMatch hgnc.symbol:16355 semapv:UnspecifiedMatching OMIM:608280 GAS5 skos:exactMatch hgnc.symbol:GAS5 semapv:UnspecifiedMatching @@ -52231,7 +52253,7 @@ OMIM:609035 RAPH1 skos:exactMatch ncbigene:65059 semapv:UnspecifiedMatching OMIM:609036 APBB1IP skos:exactMatch hgnc.symbol:17379 semapv:UnspecifiedMatching OMIM:609036 APBB1IP skos:exactMatch hgnc.symbol:APBB1IP semapv:UnspecifiedMatching OMIM:609036 APBB1IP skos:exactMatch ncbigene:54518 semapv:UnspecifiedMatching -OMIM:609037 mental retardation with optic atrophy, facial dysmorphism, microcephaly, and short stature skos:exactMatch MONDO:0012178 semapv:UnspecifiedMatching +OMIM:609037 intellectual developmental disorder with optic atrophy, facial dysmorphism, microcephaly, and short stature skos:exactMatch MONDO:0012178 semapv:UnspecifiedMatching OMIM:609038 RND1 skos:exactMatch hgnc.symbol:18314 semapv:UnspecifiedMatching OMIM:609038 RND1 skos:exactMatch hgnc.symbol:RND1 semapv:UnspecifiedMatching OMIM:609038 RND1 skos:exactMatch ncbigene:27289 semapv:UnspecifiedMatching @@ -53303,7 +53325,7 @@ OMIM:609436 FGF21 skos:exactMatch ncbigene:26291 semapv:UnspecifiedMatching OMIM:609437 STK40 skos:exactMatch hgnc.symbol:21373 semapv:UnspecifiedMatching OMIM:609437 STK40 skos:exactMatch hgnc.symbol:STK40 semapv:UnspecifiedMatching OMIM:609437 STK40 skos:exactMatch ncbigene:83931 semapv:UnspecifiedMatching -OMIM:609438 mental retardation, keratoconus, febrile seizures, and sinoatrial block skos:exactMatch MONDO:0012272 semapv:UnspecifiedMatching +OMIM:609438 intellectual developmental disorder with keratoconus, febrile seizures, and sinoatrial block skos:exactMatch MONDO:0012272 semapv:UnspecifiedMatching OMIM:609439 deafness, autosomal recessive 48 skos:exactMatch MONDO:0012273 semapv:UnspecifiedMatching OMIM:609440 UTP11L skos:exactMatch hgnc.symbol:24329 semapv:UnspecifiedMatching OMIM:609440 UTP11L skos:exactMatch hgnc.symbol:UTP11 semapv:UnspecifiedMatching @@ -62566,7 +62588,7 @@ OMIM:612945 RAB4B skos:exactMatch hgnc.symbol:RAB4B semapv:UnspecifiedMatching OMIM:612945 RAB4B skos:exactMatch ncbigene:53916 semapv:UnspecifiedMatching OMIM:612946 hadziselimovic syndrome skos:exactMatch MONDO:0013053 semapv:UnspecifiedMatching OMIM:612947 microcephaly, growth retardation, cataract, hearing loss, and unusual appearance skos:exactMatch MONDO:0013054 semapv:UnspecifiedMatching -OMIM:612948 stargardt macular degeneration, absent or hypoplastic corpus callosum, mental retardation, and dysmorphic facial features skos:exactMatch MONDO:0013055 semapv:UnspecifiedMatching +OMIM:612948 stargardt macular degeneration, absent or hypoplastic corpus callosum, impaired intellectual development, and dysmorphic facial features skos:exactMatch MONDO:0013055 semapv:UnspecifiedMatching OMIM:612949 developmental and epileptic encephalopathy 39 with leukodystrophy skos:exactMatch MONDO:0013056 semapv:UnspecifiedMatching OMIM:612949 developmental and epileptic encephalopathy 39 with leukodystrophy skos:exactMatch Orphanet:353217 semapv:UnspecifiedMatching OMIM:612949 developmental and epileptic encephalopathy 39 with leukodystrophy skos:exactMatch UMLS:C2751855 semapv:UnspecifiedMatching @@ -64170,7 +64192,7 @@ OMIM:613624 ZNF592 skos:exactMatch hgnc.symbol:28986 semapv:UnspecifiedMatching OMIM:613624 ZNF592 skos:exactMatch hgnc.symbol:ZNF592 semapv:UnspecifiedMatching OMIM:613624 ZNF592 skos:exactMatch ncbigene:9640 semapv:UnspecifiedMatching OMIM:613625 factor 5 and factor viii, combined deficiency of, 2 skos:exactMatch MONDO:0013331 semapv:UnspecifiedMatching -OMIM:613627 brachydactyly, type a1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation skos:exactMatch MONDO:0013332 semapv:UnspecifiedMatching +OMIM:613627 tsukahara syndrome skos:exactMatch MONDO:0013332 semapv:UnspecifiedMatching OMIM:613628 odontoid hypoplasia skos:exactMatch MONDO:0013333 semapv:UnspecifiedMatching OMIM:613629 PIEZO2 skos:exactMatch hgnc.symbol:26270 semapv:UnspecifiedMatching OMIM:613629 PIEZO2 skos:exactMatch hgnc.symbol:PIEZO2 semapv:UnspecifiedMatching @@ -66443,7 +66465,7 @@ OMIM:614682 AGXT2L1 skos:exactMatch ncbigene:64850 semapv:UnspecifiedMatching OMIM:614683 PHYKPL skos:exactMatch hgnc.symbol:28249 semapv:UnspecifiedMatching OMIM:614683 PHYKPL skos:exactMatch hgnc.symbol:PHYKPL semapv:UnspecifiedMatching OMIM:614683 PHYKPL skos:exactMatch ncbigene:85007 semapv:UnspecifiedMatching -OMIM:614684 hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, mental retardation, and recurrent inflammatory episodes skos:exactMatch MONDO:0013856 semapv:UnspecifiedMatching +OMIM:614684 hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes skos:exactMatch MONDO:0013856 semapv:UnspecifiedMatching OMIM:614685 ZNF597 skos:exactMatch hgnc.symbol:26573 semapv:UnspecifiedMatching OMIM:614685 ZNF597 skos:exactMatch hgnc.symbol:ZNF597 semapv:UnspecifiedMatching OMIM:614685 ZNF597 skos:exactMatch ncbigene:146434 semapv:UnspecifiedMatching @@ -68291,7 +68313,7 @@ OMIM:615499 PDP2 skos:exactMatch ncbigene:57546 semapv:UnspecifiedMatching OMIM:615500 ciliary dyskinesia, primary, 26 skos:exactMatch MONDO:0014211 semapv:UnspecifiedMatching OMIM:615500 ciliary dyskinesia, primary, 26 skos:exactMatch Orphanet:244 semapv:UnspecifiedMatching OMIM:615500 ciliary dyskinesia, primary, 26 skos:exactMatch UMLS:C3809684 semapv:UnspecifiedMatching -OMIM:615501 molybdenum cofactor deficiency, complementation group c skos:exactMatch MONDO:0014212 semapv:UnspecifiedMatching +OMIM:615501 molybdenum cofactor deficiency, type c skos:exactMatch MONDO:0014212 semapv:UnspecifiedMatching OMIM:615502 intellectual developmental disorder, autosomal dominant 21 skos:exactMatch MONDO:0014213 semapv:UnspecifiedMatching OMIM:615503 short-rib thoracic dysplasia 8 with or without polydactyly skos:exactMatch MONDO:0014214 semapv:UnspecifiedMatching OMIM:615504 ciliary dyskinesia, primary, 27 skos:exactMatch MONDO:0014215 semapv:UnspecifiedMatching @@ -68961,7 +68983,7 @@ OMIM:615787 NADK2 skos:exactMatch ncbigene:133686 semapv:UnspecifiedMatching OMIM:615788 N4BP2L2 skos:exactMatch hgnc.symbol:26916 semapv:UnspecifiedMatching OMIM:615788 N4BP2L2 skos:exactMatch hgnc.symbol:N4BP2L2 semapv:UnspecifiedMatching OMIM:615788 N4BP2L2 skos:exactMatch ncbigene:10443 semapv:UnspecifiedMatching -OMIM:615789 short stature with microcephaly and distinctive facies skos:exactMatch MONDO:0014347 semapv:UnspecifiedMatching +OMIM:615789 rothmund-thomson syndrome, type 3 skos:exactMatch MONDO:0014347 semapv:UnspecifiedMatching OMIM:615790 AHDC1 skos:exactMatch UMLS:C1826617 semapv:UnspecifiedMatching OMIM:615790 AHDC1 skos:exactMatch UMLS:C4014419 semapv:UnspecifiedMatching OMIM:615790 AHDC1 skos:exactMatch hgnc.symbol:25230 semapv:UnspecifiedMatching @@ -77791,7 +77813,7 @@ OMIM:619537 ANGEL1 skos:exactMatch hgnc.symbol:19961 semapv:UnspecifiedMatching OMIM:619537 ANGEL1 skos:exactMatch hgnc.symbol:ANGEL1 semapv:UnspecifiedMatching OMIM:619537 ANGEL1 skos:exactMatch ncbigene:23357 semapv:UnspecifiedMatching OMIM:619538 cerebral cavernous malformations 4 skos:exactMatch MONDO:0859192 semapv:UnspecifiedMatching -OMIM:619539 neuroocular syndrome skos:exactMatch MONDO:0859193 semapv:UnspecifiedMatching +OMIM:619539 neuroocular syndrome 1 skos:exactMatch MONDO:0859193 semapv:UnspecifiedMatching OMIM:619540 PPP1R3E skos:exactMatch hgnc.symbol:14943 semapv:UnspecifiedMatching OMIM:619540 PPP1R3E skos:exactMatch hgnc.symbol:PPP1R3E semapv:UnspecifiedMatching OMIM:619540 PPP1R3E skos:exactMatch ncbigene:90673 semapv:UnspecifiedMatching @@ -80221,6 +80243,7 @@ OMIM:620743 SDE2 skos:exactMatch ncbigene:163859 semapv:UnspecifiedMatching OMIM:620744 spermatogenic failure 90 skos:exactMatch MONDO:0958242 semapv:UnspecifiedMatching OMIM:620745 deafness, autosomal recessive 123 skos:exactMatch MONDO:0958277 semapv:UnspecifiedMatching OMIM:620746 neurodevelopmental disorder with hypotonia and characteristic brain abnormalities skos:exactMatch MONDO:0958278 semapv:UnspecifiedMatching +OMIM:620747 neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities skos:exactMatch MONDO:0958323 semapv:UnspecifiedMatching OMIM:620748 megalencephaly-polydactyly syndrome skos:exactMatch MONDO:0958279 semapv:UnspecifiedMatching OMIM:620749 ZNF438 skos:exactMatch hgnc.symbol:21029 semapv:UnspecifiedMatching OMIM:620749 ZNF438 skos:exactMatch hgnc.symbol:ZNF438 semapv:UnspecifiedMatching @@ -80240,9 +80263,11 @@ OMIM:620753 CCDC90B skos:exactMatch ncbigene:60492 semapv:UnspecifiedMatching OMIM:620754 PRELID3B skos:exactMatch hgnc.symbol:15892 semapv:UnspecifiedMatching OMIM:620754 PRELID3B skos:exactMatch hgnc.symbol:PRELID3B semapv:UnspecifiedMatching OMIM:620754 PRELID3B skos:exactMatch ncbigene:51012 semapv:UnspecifiedMatching +OMIM:620755 generalized epilepsy with febrile seizures plus, type 12 skos:exactMatch MONDO:0958324 semapv:UnspecifiedMatching OMIM:620756 ECHDC3 skos:exactMatch hgnc.symbol:23489 semapv:UnspecifiedMatching OMIM:620756 ECHDC3 skos:exactMatch hgnc.symbol:ECHDC3 semapv:UnspecifiedMatching OMIM:620756 ECHDC3 skos:exactMatch ncbigene:79746 semapv:UnspecifiedMatching +OMIM:620757 thrombocytopenia 12 with or without myopathy skos:exactMatch MONDO:0958325 semapv:UnspecifiedMatching OMIM:620758 TIMM23B skos:exactMatch hgnc.symbol:23581 semapv:UnspecifiedMatching OMIM:620758 TIMM23B skos:exactMatch hgnc.symbol:TIMM23B semapv:UnspecifiedMatching OMIM:620758 TIMM23B skos:exactMatch ncbigene:100652748 semapv:UnspecifiedMatching @@ -80253,6 +80278,8 @@ OMIM:620760 MLDHR skos:exactMatch ncbigene:133834869 semapv:UnspecifiedMatching OMIM:620761 C9ORF85 skos:exactMatch hgnc.symbol:28784 semapv:UnspecifiedMatching OMIM:620761 C9ORF85 skos:exactMatch hgnc.symbol:C9orf85 semapv:UnspecifiedMatching OMIM:620761 C9ORF85 skos:exactMatch ncbigene:138241 semapv:UnspecifiedMatching +OMIM:620762 macular dystrophy with or without cone dysfunction skos:exactMatch MONDO:0958326 semapv:UnspecifiedMatching +OMIM:620763 corneal dystrophy, lisch epithelial skos:exactMatch MONDO:0010425 semapv:UnspecifiedMatching OMIM:620764 MISFA skos:exactMatch hgnc.symbol:MISFA semapv:UnspecifiedMatching OMIM:620764 MISFA skos:exactMatch ncbigene:100506540 semapv:UnspecifiedMatching OMIM:620765 MTFR1L skos:exactMatch hgnc.symbol:28836 semapv:UnspecifiedMatching @@ -80261,6 +80288,7 @@ OMIM:620765 MTFR1L skos:exactMatch ncbigene:56181 semapv:UnspecifiedMatching OMIM:620766 FMC1 skos:exactMatch hgnc.symbol:26946 semapv:UnspecifiedMatching OMIM:620766 FMC1 skos:exactMatch hgnc.symbol:FMC1 semapv:UnspecifiedMatching OMIM:620766 FMC1 skos:exactMatch ncbigene:154791 semapv:UnspecifiedMatching +OMIM:620767 seckel syndrome 11 skos:exactMatch MONDO:0958328 semapv:UnspecifiedMatching OMIM:620768 RBFA skos:exactMatch hgnc.symbol:26120 semapv:UnspecifiedMatching OMIM:620768 RBFA skos:exactMatch hgnc.symbol:RBFA semapv:UnspecifiedMatching OMIM:620768 RBFA skos:exactMatch ncbigene:79863 semapv:UnspecifiedMatching @@ -80270,15 +80298,26 @@ OMIM:620769 HTD2 skos:exactMatch ncbigene:109703458 semapv:UnspecifiedMatching OMIM:620770 MTLN skos:exactMatch hgnc.symbol:27339 semapv:UnspecifiedMatching OMIM:620770 MTLN skos:exactMatch hgnc.symbol:MTLN semapv:UnspecifiedMatching OMIM:620770 MTLN skos:exactMatch ncbigene:205251 semapv:UnspecifiedMatching +OMIM:620771 jeffries-lakhani neurodevelopmental syndrome skos:exactMatch MONDO:0958329 semapv:UnspecifiedMatching +OMIM:620772 developmental and epileptic encephalopathy 113 skos:exactMatch MONDO:0958330 semapv:UnspecifiedMatching OMIM:620773 PROSER1 skos:exactMatch hgnc.symbol:20291 semapv:UnspecifiedMatching OMIM:620773 PROSER1 skos:exactMatch hgnc.symbol:PROSER1 semapv:UnspecifiedMatching OMIM:620773 PROSER1 skos:exactMatch ncbigene:80209 semapv:UnspecifiedMatching +OMIM:620774 developmental and epileptic encephalopathy 114 skos:exactMatch MONDO:0958331 semapv:UnspecifiedMatching +OMIM:620775 neuromuscular disorder, congenital, with dysmorphic facies skos:exactMatch MONDO:0958332 semapv:UnspecifiedMatching +OMIM:620776 thrombocytopenia 13, syndromic skos:exactMatch MONDO:0958333 semapv:UnspecifiedMatching +OMIM:620777 pulmonary hypertension, primary, 6 skos:exactMatch MONDO:0958334 semapv:UnspecifiedMatching OMIM:620778 KIR3DS1 skos:exactMatch hgnc.symbol:6340 semapv:UnspecifiedMatching OMIM:620778 KIR3DS1 skos:exactMatch hgnc.symbol:KIR3DS1 semapv:UnspecifiedMatching OMIM:620778 KIR3DS1 skos:exactMatch ncbigene:3813 semapv:UnspecifiedMatching +OMIM:620779 intellectual developmental disorder, autosomal recessive 82 skos:exactMatch MONDO:0968944 semapv:UnspecifiedMatching +OMIM:620780 cutis laxa, autosomal recessive, type 1d skos:exactMatch MONDO:0958335 semapv:UnspecifiedMatching OMIM:620781 TMEM208 skos:exactMatch hgnc.symbol:25015 semapv:UnspecifiedMatching OMIM:620781 TMEM208 skos:exactMatch hgnc.symbol:TMEM208 semapv:UnspecifiedMatching OMIM:620781 TMEM208 skos:exactMatch ncbigene:29100 semapv:UnspecifiedMatching +OMIM:620782 neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder skos:exactMatch MONDO:0968945 semapv:UnspecifiedMatching +OMIM:620783 developmental and epileptic encephalopathy 115 skos:exactMatch MONDO:0968946 semapv:UnspecifiedMatching +OMIM:620784 neurodevelopmental disorder plus optic atrophy skos:exactMatch MONDO:0968947 semapv:UnspecifiedMatching OMIM:620787 TCAIM skos:exactMatch hgnc.symbol:25241 semapv:UnspecifiedMatching OMIM:620787 TCAIM skos:exactMatch hgnc.symbol:TCAIM semapv:UnspecifiedMatching OMIM:620787 TCAIM skos:exactMatch ncbigene:285343 semapv:UnspecifiedMatching @@ -80291,6 +80330,66 @@ OMIM:620791 CEP76 skos:exactMatch ncbigene:79959 semapv:UnspecifiedMatching OMIM:620797 DNLZ skos:exactMatch hgnc.symbol:33879 semapv:UnspecifiedMatching OMIM:620797 DNLZ skos:exactMatch hgnc.symbol:DNLZ semapv:UnspecifiedMatching OMIM:620797 DNLZ skos:exactMatch ncbigene:728489 semapv:UnspecifiedMatching +OMIM:620798 FRYL skos:exactMatch hgnc.symbol:29127 semapv:UnspecifiedMatching +OMIM:620798 FRYL skos:exactMatch hgnc.symbol:FRYL semapv:UnspecifiedMatching +OMIM:620798 FRYL skos:exactMatch ncbigene:285527 semapv:UnspecifiedMatching +OMIM:620799 LINC00941 skos:exactMatch hgnc.symbol:48635 semapv:UnspecifiedMatching +OMIM:620799 LINC00941 skos:exactMatch hgnc.symbol:LINC00941 semapv:UnspecifiedMatching +OMIM:620799 LINC00941 skos:exactMatch ncbigene:100287314 semapv:UnspecifiedMatching +OMIM:620800 SAMD13 skos:exactMatch hgnc.symbol:24582 semapv:UnspecifiedMatching +OMIM:620800 SAMD13 skos:exactMatch hgnc.symbol:SAMD13 semapv:UnspecifiedMatching +OMIM:620800 SAMD13 skos:exactMatch ncbigene:148418 semapv:UnspecifiedMatching +OMIM:620801 GK5 skos:exactMatch hgnc.symbol:28635 semapv:UnspecifiedMatching +OMIM:620801 GK5 skos:exactMatch hgnc.symbol:GK5 semapv:UnspecifiedMatching +OMIM:620801 GK5 skos:exactMatch ncbigene:256356 semapv:UnspecifiedMatching +OMIM:620802 WDSUB1 skos:exactMatch hgnc.symbol:26697 semapv:UnspecifiedMatching +OMIM:620802 WDSUB1 skos:exactMatch hgnc.symbol:WDSUB1 semapv:UnspecifiedMatching +OMIM:620802 WDSUB1 skos:exactMatch ncbigene:151525 semapv:UnspecifiedMatching +OMIM:620803 HIGD1C skos:exactMatch hgnc.symbol:28044 semapv:UnspecifiedMatching +OMIM:620803 HIGD1C skos:exactMatch hgnc.symbol:HIGD1C semapv:UnspecifiedMatching +OMIM:620803 HIGD1C skos:exactMatch ncbigene:613227 semapv:UnspecifiedMatching +OMIM:620804 MOB3C skos:exactMatch hgnc.symbol:29800 semapv:UnspecifiedMatching +OMIM:620804 MOB3C skos:exactMatch hgnc.symbol:MOB3C semapv:UnspecifiedMatching +OMIM:620804 MOB3C skos:exactMatch ncbigene:148932 semapv:UnspecifiedMatching +OMIM:620805 ISOC1 skos:exactMatch hgnc.symbol:24254 semapv:UnspecifiedMatching +OMIM:620805 ISOC1 skos:exactMatch hgnc.symbol:ISOC1 semapv:UnspecifiedMatching +OMIM:620805 ISOC1 skos:exactMatch ncbigene:51015 semapv:UnspecifiedMatching +OMIM:620808 SNHG17 skos:exactMatch hgnc.symbol:48600 semapv:UnspecifiedMatching +OMIM:620808 SNHG17 skos:exactMatch hgnc.symbol:SNHG17 semapv:UnspecifiedMatching +OMIM:620808 SNHG17 skos:exactMatch ncbigene:388796 semapv:UnspecifiedMatching +OMIM:620809 ASCL5 skos:exactMatch hgnc.symbol:33169 semapv:UnspecifiedMatching +OMIM:620809 ASCL5 skos:exactMatch hgnc.symbol:ASCL5 semapv:UnspecifiedMatching +OMIM:620809 ASCL5 skos:exactMatch ncbigene:647219 semapv:UnspecifiedMatching +OMIM:620810 SNORD94 skos:exactMatch hgnc.symbol:32756 semapv:UnspecifiedMatching +OMIM:620810 SNORD94 skos:exactMatch hgnc.symbol:SNORD94 semapv:UnspecifiedMatching +OMIM:620810 SNORD94 skos:exactMatch ncbigene:692225 semapv:UnspecifiedMatching +OMIM:620811 SCARNA1 skos:exactMatch hgnc.symbol:32555 semapv:UnspecifiedMatching +OMIM:620811 SCARNA1 skos:exactMatch hgnc.symbol:SCARNA1 semapv:UnspecifiedMatching +OMIM:620811 SCARNA1 skos:exactMatch ncbigene:677774 semapv:UnspecifiedMatching +OMIM:620812 CLDN25 skos:exactMatch hgnc.symbol:37218 semapv:UnspecifiedMatching +OMIM:620812 CLDN25 skos:exactMatch hgnc.symbol:CLDN25 semapv:UnspecifiedMatching +OMIM:620812 CLDN25 skos:exactMatch ncbigene:644672 semapv:UnspecifiedMatching +OMIM:620821 ITPRIPL1 skos:exactMatch hgnc.symbol:29371 semapv:UnspecifiedMatching +OMIM:620821 ITPRIPL1 skos:exactMatch hgnc.symbol:ITPRIPL1 semapv:UnspecifiedMatching +OMIM:620821 ITPRIPL1 skos:exactMatch ncbigene:150771 semapv:UnspecifiedMatching +OMIM:620822 RNU4-1 skos:exactMatch hgnc.symbol:10192 semapv:UnspecifiedMatching +OMIM:620822 RNU4-1 skos:exactMatch hgnc.symbol:RNU4-1 semapv:UnspecifiedMatching +OMIM:620822 RNU4-1 skos:exactMatch ncbigene:26835 semapv:UnspecifiedMatching +OMIM:620823 RNU4-2 skos:exactMatch hgnc.symbol:10193 semapv:UnspecifiedMatching +OMIM:620823 RNU4-2 skos:exactMatch hgnc.symbol:RNU4-2 semapv:UnspecifiedMatching +OMIM:620823 RNU4-2 skos:exactMatch ncbigene:26834 semapv:UnspecifiedMatching +OMIM:620824 GLTPD2 skos:exactMatch hgnc.symbol:33756 semapv:UnspecifiedMatching +OMIM:620824 GLTPD2 skos:exactMatch hgnc.symbol:GLTPD2 semapv:UnspecifiedMatching +OMIM:620824 GLTPD2 skos:exactMatch ncbigene:388323 semapv:UnspecifiedMatching +OMIM:620826 WDR54 skos:exactMatch hgnc.symbol:25770 semapv:UnspecifiedMatching +OMIM:620826 WDR54 skos:exactMatch hgnc.symbol:WDR54 semapv:UnspecifiedMatching +OMIM:620826 WDR54 skos:exactMatch ncbigene:84058 semapv:UnspecifiedMatching +OMIM:620827 ZNF229 skos:exactMatch hgnc.symbol:13022 semapv:UnspecifiedMatching +OMIM:620827 ZNF229 skos:exactMatch hgnc.symbol:ZNF229 semapv:UnspecifiedMatching +OMIM:620827 ZNF229 skos:exactMatch ncbigene:7772 semapv:UnspecifiedMatching +OMIM:620828 OR9I1 skos:exactMatch hgnc.symbol:14718 semapv:UnspecifiedMatching +OMIM:620828 OR9I1 skos:exactMatch hgnc.symbol:OR9I1 semapv:UnspecifiedMatching +OMIM:620828 OR9I1 skos:exactMatch ncbigene:219954 semapv:UnspecifiedMatching omim.ps:100070 Aortic aneurysm, familial abdominal skos:exactMatch MONDO:0007031 semapv:UnspecifiedMatching omim.ps:100300 Adams-Oliver syndrome skos:exactMatch MONDO:0007034 semapv:UnspecifiedMatching omim.ps:101800 Acrodysostosis skos:exactMatch MONDO:0019797 semapv:UnspecifiedMatching @@ -80321,8 +80420,9 @@ omim.ps:109400 Basal cell nevus syndrome skos:exactMatch MONDO:0007187 semapv:U omim.ps:109720 Biliary cirrhosis, primary skos:exactMatch MONDO:0005388 semapv:UnspecifiedMatching omim.ps:109730 Aortic valve disease skos:exactMatch MONDO:0007194 semapv:UnspecifiedMatching omim.ps:112240 Cole-Carpenter syndrome skos:exactMatch MONDO:0016085 semapv:UnspecifiedMatching +omim.ps:113650 Branchiootorenal syndrome skos:exactMatch MONDO:0007029 semapv:UnspecifiedMatching omim.ps:113700 Breasts and/or nipples, aplasia or hypoplasia of skos:exactMatch MONDO:0015855 semapv:UnspecifiedMatching -omim.ps:113800 Epidermolytic hyperkeratosis skos:exactMatch MONDO:0957316 semapv:UnspecifiedMatching +omim.ps:113800 Epidermolytic hyperkeratosis skos:exactMatch MONDO:0007239 semapv:UnspecifiedMatching omim.ps:113900 Progressive familial heart block skos:exactMatch MONDO:0019490 semapv:UnspecifiedMatching omim.ps:114580 Familial candidiasis skos:exactMatch MONDO:0015279 semapv:UnspecifiedMatching omim.ps:115150 Cardiofaciocutaneous syndrome skos:exactMatch MONDO:0015280 semapv:UnspecifiedMatching @@ -80390,6 +80490,7 @@ omim.ps:142690 Acne inversa skos:exactMatch MONDO:0024516 semapv:UnspecifiedMat omim.ps:142700 Developmental dysplasia of the hip skos:exactMatch MONDO:0000158 semapv:UnspecifiedMatching omim.ps:143880 Hypercalcemia, infantile skos:exactMatch MONDO:0000212 semapv:UnspecifiedMatching omim.ps:143890 Hypercholesterolemia, familial skos:exactMatch MONDO:0005439 semapv:UnspecifiedMatching +omim.ps:144200 Palmoplantar keratoderma, epidermolytic skos:exactMatch MONDO:0968949 semapv:UnspecifiedMatching omim.ps:145000 Hyperparathyroidism skos:exactMatch MONDO:0016166 semapv:UnspecifiedMatching omim.ps:145260 Pseudohypoaldosteronism, type II skos:exactMatch MONDO:0019162 semapv:UnspecifiedMatching omim.ps:145420 Teebi hypertelorism syndrome skos:exactMatch MONDO:0030639 semapv:UnspecifiedMatching @@ -80547,6 +80648,7 @@ omim.ps:215500 Choroidal dystrophy, central areolar skos:exactMatch MONDO:000898 omim.ps:218330 Cranioectodermal dysplasia skos:exactMatch MONDO:0009032 semapv:UnspecifiedMatching omim.ps:219000 Fraser syndrome skos:exactMatch MONDO:0009046 semapv:UnspecifiedMatching omim.ps:220110 Mitochondrial complex IV deficiency, nuclear-type skos:exactMatch MONDO:0033885 semapv:UnspecifiedMatching +omim.ps:220150 Hypouricemia, renal skos:exactMatch MONDO:0968951 semapv:UnspecifiedMatching omim.ps:220210 Ritscher-Schinzel syndrome skos:exactMatch MONDO:0019078 semapv:UnspecifiedMatching omim.ps:220290 Deafness, autosomal recessive skos:exactMatch MONDO:0019588 semapv:UnspecifiedMatching omim.ps:220400 Jervell and Lange-Nielsen syndrome skos:exactMatch MONDO:0002441 semapv:UnspecifiedMatching @@ -80634,6 +80736,7 @@ omim.ps:257920 3MC syndrome skos:exactMatch MONDO:0017398 semapv:UnspecifiedMat omim.ps:258150 Spermatogenic failure skos:exactMatch MONDO:0004983 semapv:UnspecifiedMatching omim.ps:258315 Omodysplasia skos:exactMatch MONDO:0017136 semapv:UnspecifiedMatching omim.ps:259100 Hypertropic osteoarthropathy, primary skos:exactMatch MONDO:0016620 semapv:UnspecifiedMatching +omim.ps:259450 Bruck syndrome skos:exactMatch MONDO:0017195 semapv:UnspecifiedMatching omim.ps:259700 Osteopetrosis, autosomal recessive skos:exactMatch MONDO:0019026 semapv:UnspecifiedMatching omim.ps:259900 Hyperoxaluria, primary skos:exactMatch MONDO:0002474 semapv:UnspecifiedMatching omim.ps:260370 Pancreatic agenesis skos:exactMatch MONDO:0009832 semapv:UnspecifiedMatching @@ -80735,6 +80838,7 @@ omim.ps:601678 Bartter syndrome skos:exactMatch MONDO:0015231 semapv:Unspecifie omim.ps:601764 Seizures, benign familial infantile skos:exactMatch MONDO:0017615 semapv:UnspecifiedMatching omim.ps:602014 Hypomagnesemia skos:exactMatch MONDO:0018100 semapv:UnspecifiedMatching omim.ps:602483 Auriculocondylar syndrome skos:exactMatch MONDO:0000107 semapv:UnspecifiedMatching +omim.ps:602588 Branchiootic syndrome skos:exactMatch MONDO:0018878 semapv:UnspecifiedMatching omim.ps:602875 Acromesomelic dysplasia skos:exactMatch MONDO:0019696 semapv:UnspecifiedMatching omim.ps:603041 Mitochondrial DNA depletion syndrome skos:exactMatch MONDO:0018158 semapv:UnspecifiedMatching omim.ps:603075 Macular degeneration, age-related skos:exactMatch MONDO:0005150 semapv:UnspecifiedMatching diff --git a/src/ontology/external/nord.robot.owl b/src/ontology/external/nord.robot.owl index d02d1884..82ef8c6f 100644 --- a/src/ontology/external/nord.robot.owl +++ b/src/ontology/external/nord.robot.owl @@ -8,7 +8,7 @@ xmlns:rdfs="http://www.w3.org/2000/01/rdf-schema#" xmlns:oboInOwl="http://www.geneontology.org/formats/oboInOwl#"> - + @@ -1043,6 +1043,20 @@ + + + + + + + + + + MONDO:NORD + + + + @@ -1326,6 +1340,13 @@ Pinta + + + + + MONDO:NORD + NORD:1580 + @@ -1339,13 +1360,6 @@ NORD:1580 http://purl.obolibrary.org/obo/mondo#NORD_LABEL - - - - - MONDO:NORD - NORD:1580 - @@ -2411,6 +2425,20 @@ + + + + + + + + + + MONDO:NORD + + + + @@ -5710,6 +5738,20 @@ + + + + + + + + + + MONDO:NORD + + + + @@ -9072,6 +9114,20 @@ + + + + + + + + + + MONDO:NORD + + + + @@ -12955,12 +13011,6 @@ Keratosis Follicularis - - - - NORD:1329 - MONDO:NORD - @@ -12975,6 +13025,12 @@ MONDO:NORD NORD:1329 + + + + NORD:1329 + MONDO:NORD + @@ -13098,6 +13154,20 @@ + + + + + + + + + + MONDO:NORD + + + + @@ -32506,6 +32576,20 @@ + + + + + + + + + + MONDO:NORD + + + + @@ -74144,6 +74228,20 @@ + + + + + + + + + + MONDO:NORD + + + + @@ -85116,6 +85214,20 @@ + + + + + + + + + + MONDO:NORD + + + + @@ -101428,20 +101540,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -101828,20 +101926,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -102046,20 +102130,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -103092,20 +103162,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -103850,20 +103906,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -103920,20 +103962,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -105672,20 +105700,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -110072,20 +110086,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -111718,20 +111718,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -113352,20 +113338,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -113380,20 +113352,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -113890,20 +113848,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -114376,34 +114320,6 @@ - - - - - - - - - - MONDO:NORD - - - - - - - - - - - - - - MONDO:NORD - - - - @@ -115738,20 +115654,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -117402,20 +117304,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -119332,20 +119220,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -122764,20 +122638,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -123522,20 +123382,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -127860,34 +127706,6 @@ - - - - - - - - - - MONDO:NORD - - - - - - - - - - - - - - MONDO:NORD - - - - @@ -130996,20 +130814,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -131132,34 +130936,6 @@ - - - - - - - - - - MONDO:NORD - - - - - - - - - - - - - - MONDO:NORD - - - - @@ -131174,20 +130950,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -131230,20 +130992,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -131258,20 +131006,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -131286,20 +131020,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -131792,20 +131512,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -136092,20 +135798,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -137232,20 +136924,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -141646,20 +141324,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -143418,6 +143082,27 @@ + + + + MN1 C-Terminal Truncation Syndrome + + + + + + MN1 C-Terminal Truncation Syndrome + http://purl.obolibrary.org/obo/mondo#NORD_LABEL + + + + + + MONDO:NORD + + + + @@ -143518,6 +143203,20 @@ + + + + + + + + + + MONDO:NORD + + + + @@ -144906,20 +144605,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -145707,13 +145392,29 @@ + NORD:2036 + PIK3CA-Related Overgrowth Spectrum + + + + NORD:2036 + MONDO:NORD + + + + + PIK3CA-Related Overgrowth Spectrum + NORD:2036 + http://purl.obolibrary.org/obo/mondo#NORD_LABEL + MONDO:NORD + NORD:2036 @@ -146880,20 +146581,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -147468,20 +147155,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -148046,6 +147719,20 @@ + + + + + + + + + + MONDO:NORD + + + + @@ -148620,20 +148307,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -149446,20 +149119,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -150248,20 +149907,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -150514,20 +150159,6 @@ - - - - - - - - - - MONDO:NORD - - - - @@ -154012,6 +153643,20 @@ + + + + + + + + + + MONDO:NORD + + + + @@ -154098,28 +153743,6 @@ - - - - NORD:850 - - - - - - NORD:850 - MONDO:NORD - - - - - - MONDO:NORD - NORD:850 - - - - diff --git a/src/ontology/external/nord.robot.tsv b/src/ontology/external/nord.robot.tsv index 2b524ce8..70977bdf 100644 --- a/src/ontology/external/nord.robot.tsv +++ b/src/ontology/external/nord.robot.tsv @@ -1,12 +1,15 @@ mondo_id report_ref report_ref_source preferred_name preferred_name_source synonym_type subset subset_source subset_source2 ID A oboInOwl:hasDbXref >A oboInOwl:source A oboInOwl:hasExactSynonym >A oboInOwl:hasDbXref >A oboInOwl:hasSynonymType AI oboInOwl:inSubset >A oboInOwl:source >A oboInOwl:source +MONDO:0014017 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0032908 MN1 C-Terminal Truncation Syndrome http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0032922 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:8000024 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:8000015 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:8000018 NORD:850 MONDO:NORD NORD:850 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:850 MONDO:NORD MONDO:8000012 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:8000011 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:8000008 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:8000006 NORD:1849 MONDO:NORD WHIM Syndrome NORD:1849 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:1849 MONDO:NORD +MONDO:0859573 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0859154 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0850115 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0850108 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -162,7 +165,6 @@ MONDO:0100211 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0100195 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0100194 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0100188 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0100189 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0100186 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0100165 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0100164 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -245,7 +247,6 @@ MONDO:0054838 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0054842 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0054843 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0054837 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0054836 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0054835 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0054832 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0054833 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -265,7 +266,6 @@ MONDO:0054782 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0054771 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0054776 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0054764 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0054770 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0054761 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0054763 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0054748 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -319,7 +319,6 @@ MONDO:0044777 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0044778 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0044776 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0044749 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0044747 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0044742 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0044739 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0044740 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -379,7 +378,6 @@ MONDO:0044624 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0044621 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0044619 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0044617 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0044618 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0044355 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0044406 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0044350 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -457,7 +455,6 @@ MONDO:0036483 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0036218 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0036212 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0036217 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0036192 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0036193 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0036045 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0036189 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -499,7 +496,6 @@ MONDO:0035707 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0035696 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0035706 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0035694 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0035684 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0035685 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0035679 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0035670 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -584,7 +580,6 @@ MONDO:0035237 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0035235 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0035220 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0035173 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0035162 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0035160 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0035153 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0035159 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -614,14 +609,12 @@ MONDO:0034823 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0034676 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0034820 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0034216 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0034217 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0034204 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0034212 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0034189 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0034150 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0034186 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0034146 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0034147 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0034145 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0034142 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0034143 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -641,7 +634,6 @@ MONDO:0033968 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0033969 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0033954 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0033948 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0033947 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0033946 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0033938 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0033926 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -872,7 +864,6 @@ MONDO:0032526 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0032564 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0032485 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0031520 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0031615 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0031481 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0031446 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0031421 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -1184,7 +1175,6 @@ MONDO:0024277 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0024265 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0024266 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0024264 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0024252 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0023868 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0023820 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0023833 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -1248,7 +1238,6 @@ MONDO:0022559 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0022519 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0022454 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0022424 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0022399 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0022394 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0022349 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0022357 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -1262,7 +1251,6 @@ MONDO:0021964 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0021994 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0021957 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0021944 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0021927 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0021907 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0021879 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0021824 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -1405,7 +1393,6 @@ MONDO:0020543 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0020540 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020541 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020538 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0020537 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020533 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020535 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020532 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -1422,7 +1409,6 @@ MONDO:0020509 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0020508 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020507 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020505 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0020506 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020501 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020502 NORD:1873 MONDO:NORD NORD:1873 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:1873 MONDO:NORD MONDO:0020500 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -1520,7 +1506,6 @@ MONDO:0020396 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0020393 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020394 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020391 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0020392 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020389 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020390 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020388 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -1534,7 +1519,6 @@ MONDO:0020379 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0020376 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020377 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020374 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0020375 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020372 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020373 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020370 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -1558,9 +1542,6 @@ MONDO:0020349 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0020347 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020348 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020344 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0020345 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0020346 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0020342 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020340 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020341 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020338 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -1594,19 +1575,12 @@ MONDO:0020298 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0020291 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020289 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020290 NORD:821 MONDO:NORD Atrioventricular Septal Defect NORD:821 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:821 MONDO:NORD -MONDO:0020287 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020288 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0020285 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020286 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0020256 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0020245 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020213 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020214 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020212 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0020194 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020161 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0020146 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0020144 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020135 NORD:1596 MONDO:NORD NORD:1596 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:1596 MONDO:NORD MONDO:0020115 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020112 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -1614,7 +1588,6 @@ MONDO:0020110 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0020108 NORD:774 MONDO:NORD Anemia, Hemolytic, Acquired Autoimmune NORD:774 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:774 MONDO:NORD MONDO:0020102 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020099 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0020093 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020088 NORD:1131 MONDO:NORD NORD:1131 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:1131 MONDO:NORD MONDO:0020082 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0020081 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -1789,7 +1762,6 @@ MONDO:0019764 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0019761 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019762 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019759 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0019758 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019756 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019757 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019753 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -1817,8 +1789,6 @@ MONDO:0019701 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0019698 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019695 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019696 NORD:724 MONDO:NORD NORD:724 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:724 MONDO:NORD -MONDO:0019693 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0019689 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019682 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019685 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019680 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -1881,7 +1851,6 @@ MONDO:0019606 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0019607 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019605 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019600 NORD:1870 MONDO:NORD NORD:1870 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:1870 MONDO:NORD -MONDO:0019597 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019591 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019588 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019587 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -1947,7 +1916,6 @@ MONDO:0019514 NORD:879 MONDO:NORD Budd Chiari Syndrome NORD:879 http://purl.obol MONDO:0019509 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019507 NORD:765 MONDO:NORD NORD:765 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:765 MONDO:NORD MONDO:0019508 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0019505 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019504 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019502 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019500 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -1959,7 +1927,6 @@ MONDO:0019490 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0019488 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019489 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019487 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0019486 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019484 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019485 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019482 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -2105,7 +2072,6 @@ MONDO:0019308 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0019307 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019306 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019287 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0019286 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019283 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019276 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019267 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -2150,7 +2116,6 @@ MONDO:0019181 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0019179 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019180 NORD:1229 MONDO:NORD NORD:1229 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:1229 MONDO:NORD MONDO:0019177 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0019176 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019173 NORD:1644 MONDO:NORD NORD:1644 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:1644 MONDO:NORD MONDO:0019171 NORD:1675 MONDO:NORD Long QT Syndrome NORD:1675 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:1675 MONDO:NORD MONDO:0019170 NORD:1588 MONDO:NORD NORD:1588 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:1588 MONDO:NORD @@ -2171,7 +2136,6 @@ MONDO:0019153 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0019151 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019152 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019149 NORD:929 MONDO:NORD NORD:929 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:929 MONDO:NORD -MONDO:0019150 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019148 NORD:1862 MONDO:NORD NORD:1862 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:1862 MONDO:NORD MONDO:0019145 NORD:1899 MONDO:NORD Protein C Deficiency NORD:1899 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:1899 MONDO:NORD MONDO:0019144 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -2179,14 +2143,12 @@ MONDO:0019142 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0019143 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019141 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019140 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0019138 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019137 NORD:1511 MONDO:NORD Non-24-Hour Sleep-Wake Disorder NORD:1511 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:1511 MONDO:NORD MONDO:0019136 NORD:1946 MONDO:NORD Mucormycosis NORD:1946 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:1946 MONDO:NORD MONDO:0019134 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019131 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019130 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019127 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0019126 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019124 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0019125 NORD:1655 MONDO:NORD NORD:1655 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:1655 MONDO:NORD MONDO:0019122 NORD:728 MONDO:NORD Acute Eosinophilic Pneumonia NORD:728 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:728 MONDO:NORD @@ -2349,7 +2311,6 @@ MONDO:0018893 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0018891 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018892 NORD:1863 MONDO:NORD NORD:1863 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:1863 MONDO:NORD MONDO:0018890 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0018888 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018889 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018885 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018884 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -2410,7 +2371,6 @@ MONDO:0018818 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0018815 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018813 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018811 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0018812 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018809 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018810 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018807 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -2444,7 +2404,6 @@ MONDO:0018762 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0018760 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018759 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018757 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0018758 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018755 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018756 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018752 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -2474,7 +2433,6 @@ MONDO:0018710 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0018711 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018709 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018705 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0018706 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018703 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018702 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018698 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -2571,11 +2529,8 @@ MONDO:0018583 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0018585 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018582 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018581 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0018580 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018576 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018577 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0018574 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0018575 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018572 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018573 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018570 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -2590,7 +2545,6 @@ MONDO:0018554 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0018551 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018552 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018548 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0018550 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018547 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018546 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018544 NORD:736 MONDO:NORD X-Linked Adrenoleukodystrophy NORD:736 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:736 MONDO:NORD @@ -2602,7 +2556,6 @@ MONDO:0018537 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0018536 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018534 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018535 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0018532 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018533 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018528 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018525 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -2679,8 +2632,6 @@ MONDO:0018419 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0018416 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018417 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018408 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0018393 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0018394 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018384 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018382 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018380 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -2710,10 +2661,8 @@ MONDO:0018343 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0018344 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018341 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018342 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0018340 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018339 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018338 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0018337 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018333 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018334 NORD:1242 MONDO:NORD Hiccups, Chronic NORD:1242 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:1242 MONDO:NORD MONDO:0018330 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -2747,8 +2696,6 @@ MONDO:0018298 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0018280 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018281 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018278 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0018279 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0018277 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018274 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018273 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018271 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -2786,7 +2733,6 @@ MONDO:0018226 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0018224 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018225 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018223 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0018222 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018218 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018221 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018216 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -2840,7 +2786,6 @@ MONDO:0018146 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0018147 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018145 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018143 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0018144 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018141 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018142 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018136 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -2858,9 +2803,6 @@ MONDO:0018123 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0018124 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018116 NORD:1170 MONDO:NORD NORD:1170 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:1170 MONDO:NORD MONDO:0018115 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0018114 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0018112 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0018113 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018109 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018108 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0018106 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -2960,12 +2902,9 @@ MONDO:0017972 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0017973 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017968 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017967 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0017966 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017958 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0017955 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017953 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017951 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0017950 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017949 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017947 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017948 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -2989,7 +2928,6 @@ MONDO:0017927 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0017924 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017925 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017923 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0017922 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017921 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017919 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017920 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -3056,7 +2994,6 @@ MONDO:0017833 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0017830 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017831 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017829 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0017828 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017826 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017827 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017824 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -3139,9 +3076,7 @@ MONDO:0017691 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0017685 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017683 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017677 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0017681 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017675 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0017673 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017659 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017649 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017648 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -3150,7 +3085,6 @@ MONDO:0017640 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0017638 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017636 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017630 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0017629 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017627 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017628 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017625 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -3246,7 +3180,6 @@ MONDO:0017461 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0017455 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017453 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017446 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0017447 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017444 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017445 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017442 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -3260,7 +3193,6 @@ MONDO:0017435 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0017436 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017426 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017423 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0017420 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017419 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017418 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017417 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -3315,7 +3247,6 @@ MONDO:0017339 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0017340 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017337 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017335 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0017336 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017332 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017334 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017330 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -3344,7 +3275,6 @@ MONDO:0017295 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0017291 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017292 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017289 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0017288 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017285 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017286 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017284 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -3371,14 +3301,11 @@ MONDO:0017246 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0017244 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017245 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017243 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0017240 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0017241 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017239 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017237 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017238 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017235 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017233 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0017234 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017231 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017232 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017229 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -3394,7 +3321,6 @@ MONDO:0017221 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0017219 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017220 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017217 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0017218 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017216 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017214 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017215 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -3430,7 +3356,6 @@ MONDO:0017176 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0017177 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017174 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017175 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0017173 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017171 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017172 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017169 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -3503,22 +3428,18 @@ MONDO:0017062 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0017063 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017060 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017061 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0017059 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017056 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0017057 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017055 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017053 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017054 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017051 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017052 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017050 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0017049 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017048 NORD:1628 MONDO:NORD NORD:1628 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:1628 MONDO:NORD MONDO:0017046 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017043 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017042 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017039 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0017036 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017018 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017013 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0017010 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -3546,7 +3467,6 @@ MONDO:0016975 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0016971 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0016930 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0016929 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0016899 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0016888 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0016865 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0016863 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -3630,7 +3550,6 @@ MONDO:0016748 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0016746 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0016747 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0016745 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0016744 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0016742 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0016740 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0016739 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -3643,7 +3562,6 @@ MONDO:0016731 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0016729 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0016727 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0016724 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD -MONDO:0016725 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0016723 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0016722 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0016718 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -4622,6 +4540,7 @@ MONDO:0014985 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0014981 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0014977 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0014976 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0014973 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0014975 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0014972 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0014969 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -8185,6 +8104,7 @@ MONDO:0009617 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0009615 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0009614 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0009613 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0009612 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0009611 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0009610 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0009609 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -9388,6 +9308,7 @@ MONDO:0007445 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0007442 NORD:1043 MONDO:NORD Dentinogenesis Imperfecta Type III NORD:1043 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:1043 MONDO:NORD MONDO:0007443 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0007441 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0007437 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0007436 NORD:1041 MONDO:NORD NORD:1041 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:1041 MONDO:NORD MONDO:0007435 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0007434 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -9639,6 +9560,7 @@ MONDO:0006806 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0006794 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0006792 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0006789 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0006760 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0006746 NORD:1092 MONDO:NORD NORD:1092 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:1092 MONDO:NORD MONDO:0006745 NORD:1086 MONDO:NORD Empty Sella Syndrome NORD:1086 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:1086 MONDO:NORD MONDO:0006664 NORD:820 MONDO:NORD Atrial Septal Defects NORD:820 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:820 MONDO:NORD @@ -9846,6 +9768,7 @@ MONDO:0005055 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0005045 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0005040 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0005035 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0005034 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0005033 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0005029 NORD:1110 MONDO:NORD NORD:1110 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:1110 MONDO:NORD MONDO:0005028 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -10068,6 +9991,7 @@ MONDO:0002083 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0002073 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0002048 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0002034 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0002012 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0001995 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0001994 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0001977 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -10157,6 +10081,7 @@ MONDO:0000736 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0000754 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0000734 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0000732 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0000733 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0000722 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0000700 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0000659 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD @@ -10219,6 +10144,56 @@ MONDO:0000044 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.ob MONDO:0000045 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0000023 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0000015 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0100189 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0043230 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0035162 NORD:2036 MONDO:NORD PIK3CA-Related Overgrowth Spectrum NORD:2036 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare NORD:2036 MONDO:NORD +MONDO:0035160 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0034217 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0034147 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0022399 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0020537 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0020506 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0020392 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0020375 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0020346 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0020345 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0020286 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0020256 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0019758 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0019597 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0019505 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0019486 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0019150 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0019138 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0019126 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0018916 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0018812 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0018758 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0018580 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0018575 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0018574 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0018532 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0018340 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0018222 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0018144 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0018114 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0018112 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0017955 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0017950 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0017922 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0017828 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0017681 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0017673 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0017629 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0017447 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0017336 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0017288 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0017241 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0017218 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0017057 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0017049 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0016744 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD +MONDO:0016725 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0016647 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0016599 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD MONDO:0016579 http://purl.obolibrary.org/obo/mondo#NORD_LABEL http://purl.obolibrary.org/obo/mondo#nord_rare MONDO:NORD diff --git a/src/ontology/imports/omo_import.owl b/src/ontology/imports/omo_import.owl index 6f0a0df2..b7bf5540 100644 --- a/src/ontology/imports/omo_import.owl +++ b/src/ontology/imports/omo_import.owl @@ -7,9 +7,9 @@ Prefix(rdfs:=) Ontology( - + Annotation( ) -Annotation(owl:versionInfo "2024-05-01") +Annotation(owl:versionInfo "2024-05-23") Declaration(Class()) Declaration(Class()) diff --git a/src/ontology/imports/ro_import.owl b/src/ontology/imports/ro_import.owl index 40a5d310..21643b93 100644 --- a/src/ontology/imports/ro_import.owl +++ b/src/ontology/imports/ro_import.owl @@ -7,9 +7,9 @@ Prefix(rdfs:=) Ontology( - -Annotation( ) -Annotation(owl:versionInfo "2024-05-01") + +Annotation( ) +Annotation(owl:versionInfo "2024-05-23") Declaration(Class()) Declaration(Class()) @@ -440,7 +440,6 @@ AnnotationAssertion( ) AnnotationAssertion( ) AnnotationAssertion(rdfs:label "part of"@en) -AnnotationAssertion(rdfs:label "part of") AnnotationAssertion(rdfs:seeAlso ) AnnotationAssertion(rdfs:seeAlso ) AnnotationAssertion(rdfs:seeAlso "https://wiki.geneontology.org/Part_of"^^xsd:anyURI) @@ -467,7 +466,6 @@ AnnotationAssertion( ) AnnotationAssertion( ) AnnotationAssertion(rdfs:label "has part"@en) -AnnotationAssertion(rdfs:label "has part") SubObjectPropertyOf( ) TransitiveObjectProperty() @@ -523,8 +521,6 @@ AnnotationAssertion( "is bearer of"@en) AnnotationAssertion( ) AnnotationAssertion(rdfs:label "has characteristic"@en) -AnnotationAssertion(rdfs:label "has characteristic") -AnnotationAssertion(rdfs:seeAlso "https://github.com/oborel/obo-relations/pull/284") InverseFunctionalObjectProperty() ObjectPropertyRange( ) @@ -552,9 +548,7 @@ AnnotationAssertion( "has_participant"@en) AnnotationAssertion( "http://www.obofoundry.org/ro/#OBO_REL:has_participant") AnnotationAssertion(rdfs:label "has participant"@en) -AnnotationAssertion(rdfs:label "has participant") ObjectPropertyDomain( ) -ObjectPropertyDomain( ) ObjectPropertyRange( ) # Object Property: (function of) @@ -1024,7 +1018,6 @@ AnnotationAssertion( ) AnnotationAssertion( ) AnnotationAssertion(rdfs:label "enabled by"@en) -AnnotationAssertion(rdfs:label "enabled by") AnnotationAssertion(rdfs:seeAlso "https://wiki.geneontology.org/Enabled_by"^^xsd:anyURI) SubObjectPropertyOf( ) SubObjectPropertyOf( ) @@ -1755,10 +1748,10 @@ AnnotationAssertion(rdfs:seeAlso "ht AnnotationAssertion( "A diagnostic testing device utilizes a specimen.") AnnotationAssertion( "X device utilizes material Y means X and Y are material entities, and X is capable of some process P that has input Y.") -AnnotationAssertion( ) -AnnotationAssertion( ) AnnotationAssertion( "A diagnostic testing device utilizes a specimen means that the diagnostic testing device is capable of an assay, and this assay a specimen as its input.") AnnotationAssertion( "See github ticket https://github.com/oborel/obo-relations/issues/497") +AnnotationAssertion( ) +AnnotationAssertion( ) AnnotationAssertion( "2021-11-08T12:00:00Z"^^xsd:dateTime) AnnotationAssertion( "utilizes") AnnotationAssertion(rdfs:label "device utilizes material"@en) @@ -1823,7 +1816,6 @@ AnnotationAssertion( "An occurrent that has temporal proper parts and for some time t, p s-depends_on some material entity at t."@en) AnnotationAssertion(rdfs:label "process"@en) SubClassOf( ) -SubClassOf( ObjectAllValuesFrom( )) # Class: (disposition) @@ -1856,7 +1848,6 @@ AnnotationAssertion(rdfs:seeAlso "h AnnotationAssertion(rdfs:seeAlso "https://github.com/oborel/obo-relations/pull/284") SubClassOf( ) SubClassOf( ObjectAllValuesFrom( )) -SubClassOf( ObjectAllValuesFrom( )) DisjointClasses( ) # Class: (role) @@ -1960,7 +1951,6 @@ AnnotationAssertion(rdfs:comment "No AnnotationAssertion(rdfs:label "biological process"@en) AnnotationAssertion(rdfs:label "biological_process") SubClassOf( ) -SubClassOf( ObjectSomeValuesFrom( )) # Class: (kinase activity) @@ -2359,17 +2349,17 @@ DLSafeRule(Body(ObjectPropertyAtom( V DLSafeRule(Annotation(rdfs:comment "If a molecular function (X) has a regulatory subfunction, then any gene product which is an input to that subfunction has an activity that directly_regulates X. Note: this is intended for cases where the regaultory subfunction is protein binding, so it could be tightened with an additional clause to specify this.") Annotation(rdfs:label "inferring direct reg edge from input to regulatory subfunction") Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) DLSafeRule(Annotation(rdfs:label "inferring direct neg reg edge from input to regulatory subfunction") Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) DLSafeRule(Annotation(rdfs:label "inferring direct positive reg edge from input to regulatory subfunction") Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) -DLSafeRule(Annotation(rdfs:label "effector input is compound function input") Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) -DLSafeRule(Annotation(rdfs:label "Input of effector is input of its parent MF") Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) -DLSafeRule(Annotation(rdfs:comment "if effector directly regulates X, its parent MF directly regulates X") Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) -DLSafeRule(Annotation(rdfs:comment "if effector directly positively regulates X, its parent MF directly positively regulates X") Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) -DLSafeRule(Annotation(rdfs:label "if effector directly negatively regulates X, its parent MF directly negatively regulates X") Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) -DLSafeRule(Annotation(rdfs:label "'causally downstream of' and 'overlaps' should be disjoint properties (a SWRL rule is required because these are non-simple properties).") Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ClassAtom(owl:Nothing Variable()) ClassAtom(owl:Nothing Variable()))) -DLSafeRule(Annotation(rdfs:label "'causally upstream of' and 'overlaps' should be disjoint properties (a SWRL rule is required because these are non-simple properties).") Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ClassAtom(owl:Nothing Variable()) ClassAtom(owl:Nothing Variable()))) -DLSafeRule(Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) -DLSafeRule(Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) -DLSafeRule(Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) -DLSafeRule(Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) -DLSafeRule(Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) -DLSafeRule(Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) +DLSafeRule(Annotation(rdfs:label "effector input is compound function input") Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) +DLSafeRule(Annotation(rdfs:label "Input of effector is input of its parent MF") Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) +DLSafeRule(Annotation(rdfs:comment "if effector directly regulates X, its parent MF directly regulates X") Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) +DLSafeRule(Annotation(rdfs:comment "if effector directly positively regulates X, its parent MF directly positively regulates X") Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) +DLSafeRule(Annotation(rdfs:label "if effector directly negatively regulates X, its parent MF directly negatively regulates X") Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) +DLSafeRule(Annotation(rdfs:label "'causally downstream of' and 'overlaps' should be disjoint properties (a SWRL rule is required because these are non-simple properties).") Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ClassAtom(owl:Nothing Variable()) ClassAtom(owl:Nothing Variable()))) +DLSafeRule(Annotation(rdfs:label "'causally upstream of' and 'overlaps' should be disjoint properties (a SWRL rule is required because these are non-simple properties).") Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ClassAtom(owl:Nothing Variable()) ClassAtom(owl:Nothing Variable()))) +DLSafeRule(Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) +DLSafeRule(Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) +DLSafeRule(Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) +DLSafeRule(Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) +DLSafeRule(Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) +DLSafeRule(Body(ObjectPropertyAtom( Variable() Variable()) ObjectPropertyAtom( Variable() Variable()))Head(ObjectPropertyAtom( Variable() Variable()))) ) \ No newline at end of file diff --git a/src/ontology/lexmatch/README.md b/src/ontology/lexmatch/README.md index fecb53ff..8c22674d 100644 --- a/src/ontology/lexmatch/README.md +++ b/src/ontology/lexmatch/README.md @@ -3,8 +3,8 @@ * mondo-only: Positive mappings in MONDO not caught by the lexical mapping pipeline * split-mapping-set: Unmapped mappings broken down by predicate_id ## Summary of mappings: - * Number of mappings in [`unmapped_doid_lex`](unmapped_doid_lex.tsv): 45 - * Number of mappings in [`unmapped_doid_lex_exact`](unmapped_doid_lex.tsv): 14 + * Number of mappings in [`unmapped_doid_lex`](unmapped_doid_lex.tsv): 5 + * Number of mappings in [`unmapped_doid_lex_exact`](unmapped_doid_lex.tsv): 2 * Number of mappings in [`unmapped_doid_mondo`](mondo-only/unmapped_doid_mondo.tsv): 34 * Number of mappings in [`unmapped_doid_mondo_exact`](mondo-only/unmapped_doid_mondo.tsv): 34 * Number of mappings in [`unmapped_icd10cm_lex`](unmapped_icd10cm_lex.tsv): 1956 @@ -12,46 +12,44 @@ * Number of mappings in [`unmapped_icd10cm_mondo`](mondo-only/unmapped_icd10cm_mondo.tsv): 3 * Number of mappings in [`unmapped_icd10cm_mondo_exact`](mondo-only/unmapped_icd10cm_mondo.tsv): 3 * Number of mappings in [`unmapped_icd10who_lex`](unmapped_icd10who_lex.tsv): 1224 - * Number of mappings in [`unmapped_icd10who_lex_exact`](unmapped_icd10who_lex.tsv): 481 + * Number of mappings in [`unmapped_icd10who_lex_exact`](unmapped_icd10who_lex.tsv): 482 * Number of mappings in [`unmapped_icd10who_mondo`](mondo-only/unmapped_icd10who_mondo.tsv): 2 * Number of mappings in [`unmapped_icd10who_mondo_exact`](mondo-only/unmapped_icd10who_mondo.tsv): 2 * Number of mappings in [`unmapped_icd11foundation_lex`](unmapped_icd11foundation_lex.tsv): 9765 * Number of mappings in [`unmapped_icd11foundation_lex_exact`](unmapped_icd11foundation_lex.tsv): 6086 * Number of mappings in [`unmapped_icd11foundation_mondo`](mondo-only/unmapped_icd11foundation_mondo.tsv): 1 * Number of mappings in [`unmapped_icd11foundation_mondo_exact`](mondo-only/unmapped_icd11foundation_mondo.tsv): 1 - * Number of mappings in [`unmapped_ncit_lex`](unmapped_ncit_lex.tsv): 99 - * Number of mappings in [`unmapped_ncit_lex_exact`](unmapped_ncit_lex.tsv): 42 - * Number of mappings in [`unmapped_ncit_mondo`](mondo-only/unmapped_ncit_mondo.tsv): 25 - * Number of mappings in [`unmapped_ncit_mondo_exact`](mondo-only/unmapped_ncit_mondo.tsv): 22 - * Number of mappings in [`unmapped_omim_lex`](unmapped_omim_lex.tsv): 3 + * Number of mappings in [`unmapped_ncit_lex`](unmapped_ncit_lex.tsv): 113 + * Number of mappings in [`unmapped_ncit_lex_exact`](unmapped_ncit_lex.tsv): 45 + * Number of mappings in [`unmapped_ncit_mondo`](mondo-only/unmapped_ncit_mondo.tsv): 34 + * Number of mappings in [`unmapped_ncit_mondo_exact`](mondo-only/unmapped_ncit_mondo.tsv): 26 + * Number of mappings in [`unmapped_omim_lex`](unmapped_omim_lex.tsv): 2 * Number of mappings in [`unmapped_omim_lex_exact`](unmapped_omim_lex.tsv): 1 - * Number of mappings in [`unmapped_omim_mondo`](mondo-only/unmapped_omim_mondo.tsv): 117 - * Number of mappings in [`unmapped_omim_mondo_exact`](mondo-only/unmapped_omim_mondo.tsv): 117 + * Number of mappings in [`unmapped_omim_mondo`](mondo-only/unmapped_omim_mondo.tsv): 118 + * Number of mappings in [`unmapped_omim_mondo_exact`](mondo-only/unmapped_omim_mondo.tsv): 118 * Number of mappings in [`unmapped_ordo_lex`](unmapped_ordo_lex.tsv): 1 * Number of mappings in [`unmapped_ordo_lex_exact`](unmapped_ordo_lex.tsv): 1 - * Number of mappings in [`unmapped_ordo_mondo`](mondo-only/unmapped_ordo_mondo.tsv): 882 - * Number of mappings in [`unmapped_ordo_mondo_exact`](mondo-only/unmapped_ordo_mondo.tsv): 882 + * Number of mappings in [`unmapped_ordo_mondo`](mondo-only/unmapped_ordo_mondo.tsv): 881 + * Number of mappings in [`unmapped_ordo_mondo_exact`](mondo-only/unmapped_ordo_mondo.tsv): 881 ## mondo_XXXXmatch_ontology - * Number of mappings in [`mondo_closematch_orphanet`](split-mapping-set/mondo_closematch_orphanet.tsv): 3 - * Number of mappings in [`mondo_exactmatch_orphanet`](split-mapping-set/mondo_exactmatch_orphanet.tsv): 881 - * Number of mappings in [`mondo_closematch_icd10who`](split-mapping-set/mondo_closematch_icd10who.tsv): 147 - * Number of mappings in [`mondo_broadmatch_icd10who`](split-mapping-set/mondo_broadmatch_icd10who.tsv): 30 - * Number of mappings in [`mondo_narrowmatch_icd10who`](split-mapping-set/mondo_narrowmatch_icd10who.tsv): 25 - * Number of mappings in [`mondo_exactmatch_icd10who`](split-mapping-set/mondo_exactmatch_icd10who.tsv): 1224 - * Number of mappings in [`mondo_closematch_doid`](split-mapping-set/mondo_closematch_doid.tsv): 212 - * Number of mappings in [`mondo_narrowmatch_doid`](split-mapping-set/mondo_narrowmatch_doid.tsv): 1 - * Number of mappings in [`mondo_exactmatch_doid`](split-mapping-set/mondo_exactmatch_doid.tsv): 77 - * Number of mappings in [`mondo_closematch_icd11.foundation`](split-mapping-set/mondo_closematch_icd11.foundation.tsv): 3152 + * Number of mappings in [`mondo_exactmatch_omimps`](split-mapping-set/mondo_exactmatch_omimps.tsv): 5 + * Number of mappings in [`mondo_closematch_ncit`](split-mapping-set/mondo_closematch_ncit.tsv): 75 + * Number of mappings in [`mondo_broadmatch_ncit`](split-mapping-set/mondo_broadmatch_ncit.tsv): 10 + * Number of mappings in [`mondo_exactmatch_ncit`](split-mapping-set/mondo_exactmatch_ncit.tsv): 145 + * Number of mappings in [`mondo_closematch_icd11.foundation`](split-mapping-set/mondo_closematch_icd11.foundation.tsv): 3155 * Number of mappings in [`mondo_broadmatch_icd11.foundation`](split-mapping-set/mondo_broadmatch_icd11.foundation.tsv): 199 * Number of mappings in [`mondo_exactmatch_icd11.foundation`](split-mapping-set/mondo_exactmatch_icd11.foundation.tsv): 9764 - * Number of mappings in [`mondo_closematch_ncit`](split-mapping-set/mondo_closematch_ncit.tsv): 72 - * Number of mappings in [`mondo_broadmatch_ncit`](split-mapping-set/mondo_broadmatch_ncit.tsv): 10 - * Number of mappings in [`mondo_exactmatch_ncit`](split-mapping-set/mondo_exactmatch_ncit.tsv): 122 - * Number of mappings in [`mondo_exactmatch_omim`](split-mapping-set/mondo_exactmatch_omim.tsv): 112 - * Number of mappings in [`mondo_closematch_icd10cm`](split-mapping-set/mondo_closematch_icd10cm.tsv): 5994 + * Number of mappings in [`mondo_closematch_doid`](split-mapping-set/mondo_closematch_doid.tsv): 23 + * Number of mappings in [`mondo_exactmatch_doid`](split-mapping-set/mondo_exactmatch_doid.tsv): 37 + * Number of mappings in [`mondo_narrowmatch_doid`](split-mapping-set/mondo_narrowmatch_doid.tsv): 1 + * Number of mappings in [`mondo_exactmatch_omim`](split-mapping-set/mondo_exactmatch_omim.tsv): 113 + * Number of mappings in [`mondo_closematch_icd10cm`](split-mapping-set/mondo_closematch_icd10cm.tsv): 5995 * Number of mappings in [`mondo_broadmatch_icd10cm`](split-mapping-set/mondo_broadmatch_icd10cm.tsv): 69 - * Number of mappings in [`mondo_narrowmatch_icd10cm`](split-mapping-set/mondo_narrowmatch_icd10cm.tsv): 58 * Number of mappings in [`mondo_exactmatch_icd10cm`](split-mapping-set/mondo_exactmatch_icd10cm.tsv): 1957 - * Number of mappings in [`mondo_closematch_omimps`](split-mapping-set/mondo_closematch_omimps.tsv): 4 - * Number of mappings in [`mondo_broadmatch_omimps`](split-mapping-set/mondo_broadmatch_omimps.tsv): 1 - * Number of mappings in [`mondo_exactmatch_omimps`](split-mapping-set/mondo_exactmatch_omimps.tsv): 6 + * Number of mappings in [`mondo_narrowmatch_icd10cm`](split-mapping-set/mondo_narrowmatch_icd10cm.tsv): 58 + * Number of mappings in [`mondo_closematch_icd10who`](split-mapping-set/mondo_closematch_icd10who.tsv): 147 + * Number of mappings in [`mondo_broadmatch_icd10who`](split-mapping-set/mondo_broadmatch_icd10who.tsv): 30 + * Number of mappings in [`mondo_exactmatch_icd10who`](split-mapping-set/mondo_exactmatch_icd10who.tsv): 1224 + * Number of mappings in [`mondo_narrowmatch_icd10who`](split-mapping-set/mondo_narrowmatch_icd10who.tsv): 25 + * Number of mappings in [`mondo_closematch_orphanet`](split-mapping-set/mondo_closematch_orphanet.tsv): 3 + * Number of mappings in [`mondo_exactmatch_orphanet`](split-mapping-set/mondo_exactmatch_orphanet.tsv): 880 diff --git a/src/ontology/lexmatch/all_exact.robot.tsv b/src/ontology/lexmatch/all_exact.robot.tsv index b0e7b838..103b5e2a 100644 --- a/src/ontology/lexmatch/all_exact.robot.tsv +++ b/src/ontology/lexmatch/all_exact.robot.tsv @@ -1,7 +1,6 @@ subject_id predicate_id object_id subject_label object_label mapping_justification mapping_tool confidence subject_match_field object_match_field match_string ID >A oboInOwl:source A oboInOwl:hasDbXref -MONDO:0015991 MONDO:equivalentTo OMIMPS:215700 citrullinemia Citrullinemia semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label citrullinemia -MONDO:0018875 MONDO:equivalentTo OMIMPS:151623 Li-Fraumeni syndrome Li-Fraumeni syndrome semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label li-fraumeni syndrome +MONDO:0859193 MONDO:equivalentTo OMIMPS:619539 neuroocular syndrome Neuroocular syndrome semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label neuroocular syndrome MONDO:0000022 MONDO:equivalentTo ICD10CM:N39.44 nocturnal enuresis Nocturnal enuresis semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label nocturnal enuresis MONDO:0000190 MONDO:equivalentTo ICD10CM:I49.01 ventricular fibrillation Ventricular fibrillation semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label ventricular fibrillation MONDO:0000397 MONDO:equivalentTo ICD10CM:G80.4 ataxic cerebral palsy Ataxic cerebral palsy semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label ataxic cerebral palsy @@ -4084,12 +4083,14 @@ MONDO:0958096 MONDO:equivalentTo icd11.foundation:824243127 monomorphic epitheli MONDO:0968955 MONDO:equivalentTo icd11.foundation:1793262466 hypocalcified amelogenesis imperfecta Hypocalcified amelogenesis imperfecta semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label hypocalcified amelogenesis imperfecta MONDO:1010000 MONDO:equivalentTo icd11.foundation:1571230529 pythiosis Pythiosis semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label pythiosis MONDO:8000010 MONDO:equivalentTo icd11.foundation:1173370808 antiphospholipid syndrome Antiphospholipid syndrome semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label antiphospholipid syndrome +MONDO:0003222 MONDO:equivalentTo NCIT:C4661 central nervous system melanocytic neoplasm Central Nervous System Melanocytic Neoplasm semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label central nervous system melanocytic neoplasm MONDO:0004520 MONDO:equivalentTo NCIT:C192096 intratubular embryonal carcinoma Intratubular Embryonal Carcinoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label intratubular embryonal carcinoma MONDO:0015301 MONDO:equivalentTo NCIT:C199391 primary cutaneous amyloidosis Primary Cutaneous Amyloidosis semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label primary cutaneous amyloidosis +MONDO:0015391 MONDO:equivalentTo NCIT:C202982 nasopharyngeal teratoma Nasopharyngeal Teratoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label nasopharyngeal teratoma MONDO:0017289 MONDO:equivalentTo NCIT:C190105 fetal lung interstitial tumor Fetal Lung Interstitial Tumor semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label fetal lung interstitial tumor MONDO:0019500 MONDO:equivalentTo NCIT:C189045 extragonadal teratoma Extragonadal Teratoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label extragonadal teratoma +MONDO:0019964 MONDO:equivalentTo NCIT:C6430 thymic neuroendocrine tumor Thymic Neuroendocrine Tumor semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label thymic neuroendocrine tumor MONDO:0044037 MONDO:equivalentTo NCIT:C74524 livedo reticularis Livedo Reticularis semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label livedo reticularis -MONDO:0850110 MONDO:equivalentTo NCIT:C48613 melanoma in congenital melanocytic nevus Melanoma in Congenital Melanocytic Nevus semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label melanoma in congenital melanocytic nevus MONDO:0850112 MONDO:equivalentTo NCIT:C139012 breast implant-associated anaplastic large cell lymphoma Breast Implant-Associated Anaplastic Large Cell Lymphoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label breast implant-associated anaplastic large cell lymphoma MONDO:0850154 MONDO:equivalentTo NCIT:C4824 tongue carcinoma Tongue Carcinoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label tongue carcinoma MONDO:0850267 MONDO:equivalentTo NCIT:C7972 childhood acute megakaryoblastic leukemia Childhood Acute Megakaryoblastic Leukemia semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label childhood acute megakaryoblastic leukemia @@ -4141,37 +4142,18 @@ MONDO:0958161 MONDO:equivalentTo NCIT:C199260 B acute lymphoblastic leukemia wit MONDO:0958162 MONDO:equivalentTo NCIT:C199232 B acute lymphoblastic leukemia with DUX4 rearrangement B Acute Lymphoblastic Leukemia with DUX4 Rearrangement semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label b acute lymphoblastic leukemia with dux4 rearrangement MONDO:0958164 MONDO:equivalentTo NCIT:C177898 poorly differentiated chordoma Poorly Differentiated Chordoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label poorly differentiated chordoma MONDO:0958165 MONDO:equivalentTo NCIT:C154496 anaplastic sarcoma of the kidney Anaplastic Sarcoma of the Kidney semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label anaplastic sarcoma of the kidney +MONDO:0958295 MONDO:equivalentTo NCIT:C178468 BCOR ITD sarcoma BCOR ITD Sarcoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label bcor itd sarcoma +MONDO:0958296 MONDO:equivalentTo NCIT:C178466 BCOR-CCNB3 sarcoma BCOR-CCNB3 Sarcoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label bcor-ccnb3 sarcoma +MONDO:0958297 MONDO:equivalentTo NCIT:C189007 childhood sarcoma with BCOR genetic alterations Childhood Sarcoma with BCOR Genetic Alterations semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label childhood sarcoma with bcor genetic alterations +MONDO:0958298 MONDO:equivalentTo NCIT:C189003 childhood round cell sarcoma with EWSR1-non-ETS fusion Childhood Round Cell Sarcoma with EWSR1-non-ETS Fusion semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label childhood round cell sarcoma with ewsr1-non-ets fusion +MONDO:0958299 MONDO:equivalentTo NCIT:C178460 round cell sarcoma with EWSR1-NFATC2 gene fusion Round Cell Sarcoma with EWSR1-NFATC2 Gene Fusion semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label round cell sarcoma with ewsr1-nfatc2 gene fusion +MONDO:0958300 MONDO:equivalentTo NCIT:C178461 round cell sarcoma with EWSR1-PATZ1 gene fusion Round Cell Sarcoma with EWSR1-PATZ1 Gene Fusion semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label round cell sarcoma with ewsr1-patz1 gene fusion +MONDO:0958301 MONDO:equivalentTo NCIT:C178462 round cell sarcoma with FUS-NFATC2 gene fusion Round Cell Sarcoma with FUS-NFATC2 Gene Fusion semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label round cell sarcoma with fus-nfatc2 gene fusion +MONDO:0958302 MONDO:equivalentTo NCIT:C37210 TFEB-rearranged renal cell carcinoma TFEB-Rearranged Renal Cell Carcinoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label tfeb-rearranged renal cell carcinoma +MONDO:0958303 MONDO:equivalentTo NCIT:C189242 childhood renal cell carcinoma with MiT translocations Childhood Renal Cell Carcinoma with MiT Translocations semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label childhood renal cell carcinoma with mit translocations +MONDO:0005641 MONDO:equivalentTo DOID:2934 aleutian mink disease aleutian mink disease semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label aleutian mink disease +MONDO:0005676 MONDO:equivalentTo DOID:5154 borna disease borna disease semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label borna disease MONDO:0007744 MONDO:equivalentTo DOID:0111368 cholesterol-ester transfer protein deficiency cholesterol-ester transfer protein deficiency semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label cholesterol-ester transfer protein deficiency -MONDO:0009619 MONDO:equivalentTo DOID:0081432 microcephaly-micromelia syndrome microcephaly-micromelia syndrome semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:251230 -MONDO:0009681 MONDO:equivalentTo DOID:0060946 Ullrich congenital muscular dystrophy 1A Ullrich congenital muscular dystrophy 1A semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:254090 -MONDO:0011610 MONDO:equivalentTo DOID:0081446 dimethylglycine dehydrogenase deficiency dimethylglycine dehydrogenase deficiency semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:605850 -MONDO:0013931 MONDO:equivalentTo DOID:0081433 peroxisome biogenesis disorder 4B Peroxisome biogenesis disorder 4B semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:614863 -MONDO:0013933 MONDO:equivalentTo DOID:0081434 peroxisome biogenesis disorder 5B Peroxisome biogenesis disorder 5B semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:614867 -MONDO:0013937 MONDO:equivalentTo DOID:0081435 peroxisome biogenesis disorder 6B Peroxisome biogenesis disorder 6B semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:614871 -MONDO:0013939 MONDO:equivalentTo DOID:0081436 peroxisome biogenesis disorder 7B Peroxisome biogenesis disorder 7B semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:614873 -MONDO:0013943 MONDO:equivalentTo DOID:0081437 peroxisome biogenesis disorder 8B Peroxisome biogenesis disorder 8B semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:614877 -MONDO:0013945 MONDO:equivalentTo DOID:0081438 peroxisome biogenesis disorder 9B Peroxisome biogenesis disorder 9B semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:614879 -MONDO:0013950 MONDO:equivalentTo DOID:0081439 peroxisome biogenesis disorder 11B Peroxisome biogenesis disorder 11B semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:614885 -MONDO:0014654 MONDO:equivalentTo DOID:0060944 Ullrich congenital muscular dystrophy 2 Ullrich congenital muscular dystrophy 2 semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:616470 -MONDO:0014669 MONDO:equivalentTo DOID:0081447 cone-rod dystrophy 21 cone-rod dystrophy 21 semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:616502 -MONDO:0015004 MONDO:equivalentTo DOID:0060936 dystonia 28, childhood-onset dystonia 28, childhood-onset semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:617284 -MONDO:0018540 MONDO:equivalentTo DOID:0081451 PFAPA syndrome PFAPA syndrome semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label pfapa syndrome -MONDO:0025691 MONDO:equivalentTo DOID:0060937 dystonia 30 dystonia 30 semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:619291 -MONDO:0030440 MONDO:equivalentTo DOID:0081448 cone-rod dystrophy 22 cone-rod dystrophy 22 semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:619531 -MONDO:0030455 MONDO:equivalentTo DOID:0060938 dystonia 31 dystonia 31 semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:619565 -MONDO:0030486 MONDO:equivalentTo DOID:0060939 dystonia 32 dystonia 32 semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:619637 -MONDO:0030513 MONDO:equivalentTo DOID:0060940 dystonia 33 dystonia 33 semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:619687 -MONDO:0030608 MONDO:equivalentTo DOID:0060941 interstitial lung disease 1 interstitial lung disease 1 semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:619611 -MONDO:0030958 MONDO:equivalentTo DOID:0060955 dystonia 35, childhood-onset dystonia 35, childhood-onset semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:619921 -MONDO:0054549 MONDO:equivalentTo DOID:0081440 peroxisome biogenesis disorder 10B Peroxisome biogenesis disorder 10B semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:617370 -MONDO:0060533 MONDO:equivalentTo DOID:0081431 microcephaly, short stature, and limb abnormalities microcephaly, short stature, and limb abnormalities semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:617604 -MONDO:0859139 MONDO:equivalentTo DOID:0081442 blepharophimosis-impaired intellectual development syndrome blepharophimosis-impaired intellectual development syndrome semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:619293 -MONDO:0859377 MONDO:equivalentTo DOID:0081444 neurodevelopmental disorder with poor growth and behavioral abnormalities neurodevelopmental disorder with poor growth and behavioral abnormalities semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:620242 -MONDO:0957240 MONDO:equivalentTo DOID:0081449 cone-rod dystrophy 24 cone-rod dystrophy 24 semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:620342 -MONDO:0957539 MONDO:equivalentTo DOID:0060966 dystonia 22, juvenile-onset dystonia 22, juvenile-onset semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:620453 -MONDO:0957542 MONDO:equivalentTo DOID:0060967 dystonia 22, adult-onset dystonia 22, adult-onset semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:620456 -MONDO:0958235 MONDO:equivalentTo DOID:0060942 Ullrich congenital muscular dystrophy 1B Ullrich congenital muscular dystrophy 1B semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:620727 -MONDO:0958236 MONDO:equivalentTo DOID:0060943 Ullrich congenital muscular dystrophy 1C Ullrich congenital muscular dystrophy 1C semapv:LexicalMatching oaklib 0.9411764705882352 skos:exactMatch skos:exactMatch omim:620728 MONDO:0000088 MONDO:equivalentTo ICD10WHO:E30.1 precocious puberty Precocious puberty semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label precocious puberty MONDO:0000245 MONDO:equivalentTo ICD10WHO:B35.5 tinea imbricata Tinea imbricata semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label tinea imbricata MONDO:0000367 MONDO:equivalentTo ICD10WHO:B68 taeniasis Taeniasis semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label taeniasis @@ -4833,7 +4815,6 @@ MONDO:0020356 MONDO:equivalentTo ICD10WHO:Q13.0 coloboma of iris Coloboma of iri MONDO:0020366 MONDO:equivalentTo ICD10WHO:Q15.0 congenital glaucoma Congenital glaucoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label congenital glaucoma MONDO:0020398 MONDO:equivalentTo ICD10WHO:Q23.2 congenital mitral stenosis Congenital mitral stenosis semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label congenital mitral stenosis MONDO:0020502 MONDO:equivalentTo ICD10WHO:A95 yellow fever Yellow fever semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label yellow fever -MONDO:0020548 MONDO:equivalentTo ICD10WHO:H13.3 ocular pemphigoid Ocular pemphigoid semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label ocular pemphigoid MONDO:0020568 MONDO:equivalentTo ICD10WHO:B87.0 cutaneous myiasis Cutaneous myiasis semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label cutaneous myiasis MONDO:0020599 MONDO:equivalentTo ICD10WHO:D68.4 acquired coagulation factor deficiency Acquired coagulation factor deficiency semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label acquired coagulation factor deficiency MONDO:0020600 MONDO:equivalentTo ICD10WHO:J02 acute pharyngitis Acute pharyngitis semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label acute pharyngitis diff --git a/src/ontology/lexmatch/mondo-only/unmapped_ncit_mondo.tsv b/src/ontology/lexmatch/mondo-only/unmapped_ncit_mondo.tsv index d6a1fb35..1de0cd54 100644 --- a/src/ontology/lexmatch/mondo-only/unmapped_ncit_mondo.tsv +++ b/src/ontology/lexmatch/mondo-only/unmapped_ncit_mondo.tsv @@ -2,7 +2,9 @@ subject_id subject_label object_id predicate_id object_label mapping_justificati ID A oboInOwl:hasDbXref >A oboInOwl:source MONDO:0000651 obsolete thoracic disorder NCIT:C35742 MONDO:equivalentTo Thoracic Disorder semapv:UnspecifiedMatching MONDO:0002063 obsolete breast papillomatosis NCIT:C6977 MONDO:equivalentTo Breast Papillomatosis semapv:UnspecifiedMatching +MONDO:0002938 metatypical basal cell carcinoma NCIT:C66903 MONDO:equivalentTo Skin Metatypical Carcinoma semapv:UnspecifiedMatching MONDO:0003043 obsolete extraskeletal mesenchymal chondrosarcoma NCIT:C27481 MONDO:equivalentTo Mesenchymal Extraskeletal Chondrosarcoma semapv:UnspecifiedMatching +MONDO:0003450 eccrine papillary adenoma NCIT:C4173 MONDO:equivalentTo Papillary Eccrine Adenoma semapv:UnspecifiedMatching MONDO:0003998 obsolete vaginal tubular adenoma NCIT:C40257 MONDO:equivalentTo Vaginal Tubular Adenoma semapv:UnspecifiedMatching MONDO:0004204 squamous cell skin papilloma NCIT:C4462 MONDO:equivalentTo Skin Squamous Papilloma semapv:UnspecifiedMatching MONDO:0004419 lymphoma-like variant infiltrating bladder urothelial carcinoma NCIT:C39822 MONDO:equivalentTo Infiltrating Bladder Urothelial Carcinoma, Lymphoma-Like Variant semapv:UnspecifiedMatching @@ -10,6 +12,8 @@ MONDO:0004819 indolent plasma cell myeloma NCIT:C7150 MONDO:equivalentTo Indolen MONDO:0005362 erectile dysfunction NCIT:C34801 MONDO:equivalentTo Male Erectile Disorder semapv:UnspecifiedMatching MONDO:0006315 obsolete neoplastic medium-sized B-lymphocyte with basophilic cytoplasm NCIT:C37005 MONDO:equivalentTo Neoplastic Medium-Sized B-Lymphocyte with Basophilic Cytoplasm semapv:UnspecifiedMatching MONDO:0006475 obsolete unclassified renal cell carcinoma NCIT:C27892 MONDO:equivalentTo Unclassified Renal Cell Carcinoma semapv:UnspecifiedMatching +MONDO:0013171 purine nucleoside phosphorylase deficiency NCIT:C3963 MONDO:equivalentTo Purine-Nucleoside Phosphorylase Deficiency semapv:UnspecifiedMatching +MONDO:0016747 primary melanoma of the central nervous system NCIT:C5505 MONDO:equivalentTo Central Nervous System Melanoma semapv:UnspecifiedMatching MONDO:0017308 obsolete Marfan syndrome type 2 NCIT:C75007 MONDO:equivalentTo Marfan Syndrome Type II semapv:UnspecifiedMatching MONDO:0020078 obsolete acute myeloid leukemia with recurrent genetic anomaly NCIT:C7175 MONDO:equivalentTo Acute Myeloid Leukemia with Recurrent Genetic Abnormalities semapv:UnspecifiedMatching MONDO:0020591 obsolete disorder of peritoneum NCIT:C26848 MONDO:equivalentTo Peritoneal Disorder semapv:UnspecifiedMatching diff --git a/src/ontology/lexmatch/mondo-only/unmapped_ncit_mondo_exact.tsv b/src/ontology/lexmatch/mondo-only/unmapped_ncit_mondo_exact.tsv index 1c4e2abb..d01d35d3 100644 --- a/src/ontology/lexmatch/mondo-only/unmapped_ncit_mondo_exact.tsv +++ b/src/ontology/lexmatch/mondo-only/unmapped_ncit_mondo_exact.tsv @@ -1,5 +1,10 @@ subject_id subject_label object_id predicate_id object_label mapping_justification mapping_tool confidence subject_match_field object_match_field match_string ID A oboInOwl:hasDbXref >A oboInOwl:source +MONDO:0003222 central nervous system melanocytic neoplasm NCIT:C5504 MONDO:equivalentTo Central Nervous System Melanocytic Neoplasm semapv:UnspecifiedMatching +MONDO:0004141 melanomatosis NCIT:C9499 MONDO:equivalentTo Melanomatosis semapv:UnspecifiedMatching MONDO:0005065 mesothelioma NCIT:C3234 MONDO:equivalentTo Mesothelioma semapv:UnspecifiedMatching +MONDO:0005104 aJCC grade 1 sarcoma NCIT:C9419 MONDO:equivalentTo AJCC Grade 1 Sarcoma semapv:UnspecifiedMatching +MONDO:0005369 carcinoid tumor NCIT:C2915 MONDO:equivalentTo Carcinoid Tumor semapv:UnspecifiedMatching MONDO:0015040 myelodysplastic syndrome with excess blasts-1 NCIT:C7167 MONDO:equivalentTo Myelodysplastic Syndrome with Excess Blasts-1 semapv:UnspecifiedMatching +MONDO:0015540 hemophagocytic syndrome NCIT:C35439 MONDO:equivalentTo Hemophagocytic Syndrome semapv:UnspecifiedMatching MONDO:0020805 benign basal cell neoplasm NCIT:C4743 MONDO:equivalentTo Benign Basal Cell Neoplasm semapv:UnspecifiedMatching diff --git a/src/ontology/lexmatch/mondo-only/unmapped_omim_mondo.tsv b/src/ontology/lexmatch/mondo-only/unmapped_omim_mondo.tsv index ff214c42..97b85d61 100644 --- a/src/ontology/lexmatch/mondo-only/unmapped_omim_mondo.tsv +++ b/src/ontology/lexmatch/mondo-only/unmapped_omim_mondo.tsv @@ -22,6 +22,7 @@ MONDO:0008204 obsolete patella aplasia, coxa vara, and tarsal synostosis OMIM:16 MONDO:0008415 obsolete Scholte syndrome OMIM:181515 MONDO:equivalentTo semapv:UnspecifiedMatching MONDO:0008548 obsolete theophylline Biotransformation OMIM:187650 MONDO:equivalentTo theophylline biotransformation semapv:UnspecifiedMatching MONDO:0008625 obsolete urate-binding globulin, decrease 1N OMIM:191530 MONDO:equivalentTo urate-binding globulin, decrease 1n semapv:UnspecifiedMatching +MONDO:0008873 microcephalic osteodysplastic primordial dwarfism, type 3 OMIM:210730 MONDO:equivalentTo semapv:UnspecifiedMatching MONDO:0009535 obsolete lymphedema, congenital recessive OMIM:247440 MONDO:equivalentTo semapv:UnspecifiedMatching MONDO:0009553 obsolete Plasmodium falciparum blood infection level OMIM:248310 MONDO:equivalentTo plasmodium falciparum blood infection level semapv:UnspecifiedMatching MONDO:0009586 mesangial sclerosis, diffuse renal, with ocular abnormalities OMIM:249660 MONDO:equivalentTo semapv:UnspecifiedMatching diff --git a/src/ontology/lexmatch/mondo-only/unmapped_ordo_mondo.tsv b/src/ontology/lexmatch/mondo-only/unmapped_ordo_mondo.tsv index e8902f35..64e78790 100644 --- a/src/ontology/lexmatch/mondo-only/unmapped_ordo_mondo.tsv +++ b/src/ontology/lexmatch/mondo-only/unmapped_ordo_mondo.tsv @@ -503,8 +503,8 @@ MONDO:0018775 obsolete axonal hereditary motor and sensory neuropathy Orphanet:4 MONDO:0018779 obsolete hypercontractile muscle stiffness syndrome Orphanet:476403 MONDO:equivalentTo Hypercontractile muscle stiffness syndrome semapv:UnspecifiedMatching MONDO:0018787 obsolete genetic cerebral small vessel disease Orphanet:477754 MONDO:equivalentTo Genetic cerebral small vessel disease semapv:UnspecifiedMatching MONDO:0018788 obsolete COL4A1 or COL4A2-related cerebral small vessel disease Orphanet:477759 MONDO:equivalentTo COL4A1 or COL4A2-related cerebral small vessel disease semapv:UnspecifiedMatching -MONDO:0018789 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with ischemic tendancy Orphanet:477762 MONDO:equivalentTo COL4A1 or COL4A2-related cerebral small vessel disease with ischemic tendancy semapv:UnspecifiedMatching -MONDO:0018790 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendancy Orphanet:477765 MONDO:equivalentTo COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendancy semapv:UnspecifiedMatching +MONDO:0018789 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with ischemic tendency Orphanet:477762 MONDO:equivalentTo COL4A1 or COL4A2-related cerebral small vessel disease with ischemic tendancy semapv:UnspecifiedMatching +MONDO:0018790 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendency Orphanet:477765 MONDO:equivalentTo COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendancy semapv:UnspecifiedMatching MONDO:0018791 obsolete Moyomoya angiopathy Orphanet:477768 MONDO:equivalentTo Moyamoya angiopathy semapv:UnspecifiedMatching MONDO:0018792 obsolete Moyamoya syndrome Orphanet:477771 MONDO:equivalentTo Rare disorder with a moyamoya angiopathy semapv:UnspecifiedMatching MONDO:0018796 obsolete isolated constitutional thrombocytopenia Orphanet:477797 MONDO:equivalentTo Isolated constitutional thrombocytopenia semapv:UnspecifiedMatching @@ -620,7 +620,6 @@ MONDO:0020027 obsolete rare allergic disease Orphanet:98050 MONDO:equivalentTo R MONDO:0020028 obsolete rare allergic respiratory disease Orphanet:98052 MONDO:equivalentTo Rare allergic respiratory disease semapv:UnspecifiedMatching MONDO:0020029 obsolete rare genetic cardiac disease Orphanet:98054 MONDO:equivalentTo Rare genetic cardiac disease semapv:UnspecifiedMatching MONDO:0020030 obsolete rare genetic renal disease Orphanet:98056 MONDO:equivalentTo Rare genetic renal disease semapv:UnspecifiedMatching -MONDO:0020031 obsolete rare tumor Orphanet:98057 MONDO:equivalentTo Rare tumor semapv:UnspecifiedMatching MONDO:0020032 obsolete rare urinary tract tumor Orphanet:98058 MONDO:equivalentTo Rare urinary tract tumor semapv:UnspecifiedMatching MONDO:0020033 obsolete rare digestive tumor Orphanet:98059 MONDO:equivalentTo Rare digestive tumor semapv:UnspecifiedMatching MONDO:0020034 obsolete rare respiratory tract neoplasm Orphanet:98060 MONDO:equivalentTo Rare respiratory tumor semapv:UnspecifiedMatching diff --git a/src/ontology/lexmatch/split-mapping-set/mondo_broadmatch_omimps.tsv b/src/ontology/lexmatch/split-mapping-set/mondo_broadmatch_omimps.tsv deleted file mode 100644 index 4682eabe..00000000 --- a/src/ontology/lexmatch/split-mapping-set/mondo_broadmatch_omimps.tsv +++ /dev/null @@ -1,2 +0,0 @@ -subject_id subject_label predicate_id object_id object_label mapping_justification mapping_tool confidence subject_match_field object_match_field match_string comment -MONDO:0008988 citrullinemia type I skos:broadMatch OMIMPS:215700 Citrullinemia semapv:LexicalMatching oaklib 0.8 oio:hasBroadSynonym rdfs:label citrullinemia LEXMATCH diff --git a/src/ontology/lexmatch/split-mapping-set/mondo_closematch_doid.tsv b/src/ontology/lexmatch/split-mapping-set/mondo_closematch_doid.tsv index b3a89f4a..9b0cd8d7 100644 --- a/src/ontology/lexmatch/split-mapping-set/mondo_closematch_doid.tsv +++ b/src/ontology/lexmatch/split-mapping-set/mondo_closematch_doid.tsv @@ -1,213 +1,24 @@ subject_id subject_label predicate_id object_id object_label mapping_justification mapping_tool confidence subject_match_field object_match_field match_string comment +MONDO:0005641 aleutian mink disease skos:closeMatch DOID:2934 aleutian mink disease semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref mesh:d000453 LEXMATCH +MONDO:0005641 aleutian mink disease skos:closeMatch DOID:2934 aleutian mink disease semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch mesh:d000453 LEXMATCH +MONDO:0005641 aleutian mink disease skos:closeMatch DOID:2934 aleutian mink disease semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym oio:hasExactSynonym aleutian disease LEXMATCH +MONDO:0005641 aleutian mink disease skos:closeMatch DOID:2934 aleutian mink disease semapv:LexicalMatching oaklib 0.5 skos:relatedMatch oio:hasDbXref mesh:d000453 LEXMATCH +MONDO:0005641 aleutian mink disease skos:closeMatch DOID:2934 aleutian mink disease semapv:LexicalMatching oaklib 0.5 skos:relatedMatch skos:exactMatch mesh:d000453 LEXMATCH +MONDO:0005676 borna disease skos:closeMatch DOID:5154 borna disease semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref mesh:d001890 LEXMATCH +MONDO:0005676 borna disease skos:closeMatch DOID:5154 borna disease semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch mesh:d001890 LEXMATCH +MONDO:0005676 borna disease skos:closeMatch DOID:5154 borna disease semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym oio:hasExactSynonym enzootic encephalomyelitis LEXMATCH +MONDO:0005676 borna disease skos:closeMatch DOID:5154 borna disease semapv:LexicalMatching oaklib 0.5 skos:relatedMatch oio:hasDbXref mesh:d001890 LEXMATCH +MONDO:0005676 borna disease skos:closeMatch DOID:5154 borna disease semapv:LexicalMatching oaklib 0.5 skos:relatedMatch skos:exactMatch mesh:d001890 LEXMATCH MONDO:0006702 chronic inflammatory demyelinating polyradiculoneuropathy skos:closeMatch DOID:2536 chronic inflammatory demyelinating polyneuritis semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref icd10cm:g61.81 LEXMATCH MONDO:0006702 chronic inflammatory demyelinating polyradiculoneuropathy skos:closeMatch DOID:2536 chronic inflammatory demyelinating polyneuritis semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref mesh:d020277 LEXMATCH MONDO:0006702 chronic inflammatory demyelinating polyradiculoneuropathy skos:closeMatch DOID:2536 chronic inflammatory demyelinating polyneuritis semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label chronic inflammatory demyelinating polyneuritis LEXMATCH MONDO:0006702 chronic inflammatory demyelinating polyradiculoneuropathy skos:closeMatch DOID:2536 chronic inflammatory demyelinating polyneuritis semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref icd10cm:g61.81 LEXMATCH MONDO:0006702 chronic inflammatory demyelinating polyradiculoneuropathy skos:closeMatch DOID:2536 chronic inflammatory demyelinating polyneuritis semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref mesh:d020277 LEXMATCH -MONDO:0007495 dystonia 5 skos:closeMatch DOID:0060963 dystonia, DOPA-responsive semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:128230 LEXMATCH -MONDO:0007495 dystonia 5 skos:closeMatch DOID:0060963 dystonia, DOPA-responsive semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:128230 LEXMATCH -MONDO:0007495 dystonia 5 skos:closeMatch DOID:0060963 dystonia, DOPA-responsive semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym oio:hasExactSynonym dopa-responsive dystonia, autosomal dominant LEXMATCH -MONDO:0007495 dystonia 5 skos:closeMatch DOID:0060963 dystonia, DOPA-responsive semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym oio:hasExactSynonym dystonia, dopa-responsive, autosomal dominant LEXMATCH -MONDO:0007495 dystonia 5 skos:closeMatch DOID:0060963 dystonia, DOPA-responsive semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym oio:hasExactSynonym dystonia, progressive, with diurnal variation LEXMATCH -MONDO:0007495 dystonia 5 skos:closeMatch DOID:0060963 dystonia, DOPA-responsive semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym oio:hasExactSynonym dystonia-parkinsonism with diurnal fluctuation LEXMATCH -MONDO:0007495 dystonia 5 skos:closeMatch DOID:0060963 dystonia, DOPA-responsive semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label dystonia, dopa-responsive LEXMATCH -MONDO:0007495 dystonia 5 skos:closeMatch DOID:0060963 dystonia, DOPA-responsive semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:128230 LEXMATCH -MONDO:0007495 dystonia 5 skos:closeMatch DOID:0060963 dystonia, DOPA-responsive semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:128230 LEXMATCH -MONDO:0007495 dystonia 5 skos:closeMatch DOID:0060963 dystonia, DOPA-responsive semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:128230 LEXMATCH -MONDO:0009619 microcephaly-micromelia syndrome skos:closeMatch DOID:0081432 microcephaly-micromelia syndrome semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:251230 LEXMATCH -MONDO:0009619 microcephaly-micromelia syndrome skos:closeMatch DOID:0081432 microcephaly-micromelia syndrome semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:251230 LEXMATCH -MONDO:0009619 microcephaly-micromelia syndrome skos:closeMatch DOID:0081432 microcephaly-micromelia syndrome semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:251230 LEXMATCH -MONDO:0009619 microcephaly-micromelia syndrome skos:closeMatch DOID:0081432 microcephaly-micromelia syndrome semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:251230 LEXMATCH -MONDO:0009619 microcephaly-micromelia syndrome skos:closeMatch DOID:0081432 microcephaly-micromelia syndrome semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:251230 LEXMATCH -MONDO:0009681 Ullrich congenital muscular dystrophy 1A skos:closeMatch DOID:0060946 Ullrich congenital muscular dystrophy 1A semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:254090 LEXMATCH -MONDO:0009681 Ullrich congenital muscular dystrophy 1A skos:closeMatch DOID:0060946 Ullrich congenital muscular dystrophy 1A semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:254090 LEXMATCH -MONDO:0009681 Ullrich congenital muscular dystrophy 1A skos:closeMatch DOID:0060946 Ullrich congenital muscular dystrophy 1A semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:254090 LEXMATCH -MONDO:0009681 Ullrich congenital muscular dystrophy 1A skos:closeMatch DOID:0060946 Ullrich congenital muscular dystrophy 1A semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:254090 LEXMATCH -MONDO:0009681 Ullrich congenital muscular dystrophy 1A skos:closeMatch DOID:0060946 Ullrich congenital muscular dystrophy 1A semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:254090 LEXMATCH -MONDO:0009849 hyperimmunoglobulinemia D with periodic fever skos:closeMatch DOID:0081450 hyperimmunoglobulinemia D periodic fever syndrome semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref gard:2788 LEXMATCH -MONDO:0009849 hyperimmunoglobulinemia D with periodic fever skos:closeMatch DOID:0081450 hyperimmunoglobulinemia D periodic fever syndrome semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:260920 LEXMATCH -MONDO:0009849 hyperimmunoglobulinemia D with periodic fever skos:closeMatch DOID:0081450 hyperimmunoglobulinemia D periodic fever syndrome semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:260920 LEXMATCH -MONDO:0009849 hyperimmunoglobulinemia D with periodic fever skos:closeMatch DOID:0081450 hyperimmunoglobulinemia D periodic fever syndrome semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:260920 LEXMATCH -MONDO:0009849 hyperimmunoglobulinemia D with periodic fever skos:closeMatch DOID:0081450 hyperimmunoglobulinemia D periodic fever syndrome semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:260920 LEXMATCH -MONDO:0009849 hyperimmunoglobulinemia D with periodic fever skos:closeMatch DOID:0081450 hyperimmunoglobulinemia D periodic fever syndrome semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:260920 LEXMATCH -MONDO:0011053 intellectual disability-sparse hair-brachydactyly syndrome skos:closeMatch DOID:0081441 Nicolaides-Baraitser syndrome semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref gard:270 LEXMATCH -MONDO:0011053 intellectual disability-sparse hair-brachydactyly syndrome skos:closeMatch DOID:0081441 Nicolaides-Baraitser syndrome semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:601358 LEXMATCH -MONDO:0011053 intellectual disability-sparse hair-brachydactyly syndrome skos:closeMatch DOID:0081441 Nicolaides-Baraitser syndrome semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:601358 LEXMATCH -MONDO:0011053 intellectual disability-sparse hair-brachydactyly syndrome skos:closeMatch DOID:0081441 Nicolaides-Baraitser syndrome semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label nicolaides-baraitser syndrome LEXMATCH -MONDO:0011053 intellectual disability-sparse hair-brachydactyly syndrome skos:closeMatch DOID:0081441 Nicolaides-Baraitser syndrome semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:601358 LEXMATCH -MONDO:0011053 intellectual disability-sparse hair-brachydactyly syndrome skos:closeMatch DOID:0081441 Nicolaides-Baraitser syndrome semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:601358 LEXMATCH -MONDO:0011053 intellectual disability-sparse hair-brachydactyly syndrome skos:closeMatch DOID:0081441 Nicolaides-Baraitser syndrome semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:601358 LEXMATCH -MONDO:0011382 sickle cell anemia skos:closeMatch DOID:0081445 sickle cell disease semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:603903 LEXMATCH -MONDO:0011382 sickle cell anemia skos:closeMatch DOID:0081445 sickle cell disease semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:603903 LEXMATCH -MONDO:0011382 sickle cell anemia skos:closeMatch DOID:0081445 sickle cell disease semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:603903 LEXMATCH -MONDO:0011382 sickle cell anemia skos:closeMatch DOID:0081445 sickle cell disease semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:603903 LEXMATCH -MONDO:0011382 sickle cell anemia skos:closeMatch DOID:0081445 sickle cell disease semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:603903 LEXMATCH -MONDO:0011610 dimethylglycine dehydrogenase deficiency skos:closeMatch DOID:0081446 dimethylglycine dehydrogenase deficiency semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:605850 LEXMATCH -MONDO:0011610 dimethylglycine dehydrogenase deficiency skos:closeMatch DOID:0081446 dimethylglycine dehydrogenase deficiency semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:605850 LEXMATCH -MONDO:0011610 dimethylglycine dehydrogenase deficiency skos:closeMatch DOID:0081446 dimethylglycine dehydrogenase deficiency semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:605850 LEXMATCH -MONDO:0011610 dimethylglycine dehydrogenase deficiency skos:closeMatch DOID:0081446 dimethylglycine dehydrogenase deficiency semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:605850 LEXMATCH -MONDO:0011610 dimethylglycine dehydrogenase deficiency skos:closeMatch DOID:0081446 dimethylglycine dehydrogenase deficiency semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:605850 LEXMATCH -MONDO:0013931 peroxisome biogenesis disorder 4B skos:closeMatch DOID:0081433 Peroxisome biogenesis disorder 4B semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:614863 LEXMATCH -MONDO:0013931 peroxisome biogenesis disorder 4B skos:closeMatch DOID:0081433 Peroxisome biogenesis disorder 4B semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:614863 LEXMATCH -MONDO:0013931 peroxisome biogenesis disorder 4B skos:closeMatch DOID:0081433 Peroxisome biogenesis disorder 4B semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:614863 LEXMATCH -MONDO:0013931 peroxisome biogenesis disorder 4B skos:closeMatch DOID:0081433 Peroxisome biogenesis disorder 4B semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:614863 LEXMATCH -MONDO:0013931 peroxisome biogenesis disorder 4B skos:closeMatch DOID:0081433 Peroxisome biogenesis disorder 4B semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:614863 LEXMATCH -MONDO:0013933 peroxisome biogenesis disorder 5B skos:closeMatch DOID:0081434 Peroxisome biogenesis disorder 5B semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:614867 LEXMATCH -MONDO:0013933 peroxisome biogenesis disorder 5B skos:closeMatch DOID:0081434 Peroxisome biogenesis disorder 5B semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:614867 LEXMATCH -MONDO:0013933 peroxisome biogenesis disorder 5B skos:closeMatch DOID:0081434 Peroxisome biogenesis disorder 5B semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:614867 LEXMATCH -MONDO:0013933 peroxisome biogenesis disorder 5B skos:closeMatch DOID:0081434 Peroxisome biogenesis disorder 5B semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:614867 LEXMATCH -MONDO:0013933 peroxisome biogenesis disorder 5B skos:closeMatch DOID:0081434 Peroxisome biogenesis disorder 5B semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:614867 LEXMATCH -MONDO:0013937 peroxisome biogenesis disorder 6B skos:closeMatch DOID:0081435 Peroxisome biogenesis disorder 6B semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:614871 LEXMATCH -MONDO:0013937 peroxisome biogenesis disorder 6B skos:closeMatch DOID:0081435 Peroxisome biogenesis disorder 6B semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:614871 LEXMATCH -MONDO:0013937 peroxisome biogenesis disorder 6B skos:closeMatch DOID:0081435 Peroxisome biogenesis disorder 6B semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:614871 LEXMATCH -MONDO:0013937 peroxisome biogenesis disorder 6B skos:closeMatch DOID:0081435 Peroxisome biogenesis disorder 6B semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:614871 LEXMATCH -MONDO:0013937 peroxisome biogenesis disorder 6B skos:closeMatch DOID:0081435 Peroxisome biogenesis disorder 6B semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:614871 LEXMATCH -MONDO:0013939 peroxisome biogenesis disorder 7B skos:closeMatch DOID:0081436 Peroxisome biogenesis disorder 7B semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:614873 LEXMATCH -MONDO:0013939 peroxisome biogenesis disorder 7B skos:closeMatch DOID:0081436 Peroxisome biogenesis disorder 7B semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:614873 LEXMATCH -MONDO:0013939 peroxisome biogenesis disorder 7B skos:closeMatch DOID:0081436 Peroxisome biogenesis disorder 7B semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:614873 LEXMATCH -MONDO:0013939 peroxisome biogenesis disorder 7B skos:closeMatch DOID:0081436 Peroxisome biogenesis disorder 7B semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:614873 LEXMATCH -MONDO:0013939 peroxisome biogenesis disorder 7B skos:closeMatch DOID:0081436 Peroxisome biogenesis disorder 7B semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:614873 LEXMATCH -MONDO:0013943 peroxisome biogenesis disorder 8B skos:closeMatch DOID:0081437 Peroxisome biogenesis disorder 8B semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:614877 LEXMATCH -MONDO:0013943 peroxisome biogenesis disorder 8B skos:closeMatch DOID:0081437 Peroxisome biogenesis disorder 8B semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:614877 LEXMATCH -MONDO:0013943 peroxisome biogenesis disorder 8B skos:closeMatch DOID:0081437 Peroxisome biogenesis disorder 8B semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:614877 LEXMATCH -MONDO:0013943 peroxisome biogenesis disorder 8B skos:closeMatch DOID:0081437 Peroxisome biogenesis disorder 8B semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:614877 LEXMATCH -MONDO:0013943 peroxisome biogenesis disorder 8B skos:closeMatch DOID:0081437 Peroxisome biogenesis disorder 8B semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:614877 LEXMATCH -MONDO:0013945 peroxisome biogenesis disorder 9B skos:closeMatch DOID:0081438 Peroxisome biogenesis disorder 9B semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:614879 LEXMATCH -MONDO:0013945 peroxisome biogenesis disorder 9B skos:closeMatch DOID:0081438 Peroxisome biogenesis disorder 9B semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:614879 LEXMATCH -MONDO:0013945 peroxisome biogenesis disorder 9B skos:closeMatch DOID:0081438 Peroxisome biogenesis disorder 9B semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:614879 LEXMATCH -MONDO:0013945 peroxisome biogenesis disorder 9B skos:closeMatch DOID:0081438 Peroxisome biogenesis disorder 9B semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:614879 LEXMATCH -MONDO:0013945 peroxisome biogenesis disorder 9B skos:closeMatch DOID:0081438 Peroxisome biogenesis disorder 9B semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:614879 LEXMATCH -MONDO:0013950 peroxisome biogenesis disorder 11B skos:closeMatch DOID:0081439 Peroxisome biogenesis disorder 11B semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:614885 LEXMATCH -MONDO:0013950 peroxisome biogenesis disorder 11B skos:closeMatch DOID:0081439 Peroxisome biogenesis disorder 11B semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:614885 LEXMATCH -MONDO:0013950 peroxisome biogenesis disorder 11B skos:closeMatch DOID:0081439 Peroxisome biogenesis disorder 11B semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:614885 LEXMATCH -MONDO:0013950 peroxisome biogenesis disorder 11B skos:closeMatch DOID:0081439 Peroxisome biogenesis disorder 11B semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:614885 LEXMATCH -MONDO:0013950 peroxisome biogenesis disorder 11B skos:closeMatch DOID:0081439 Peroxisome biogenesis disorder 11B semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:614885 LEXMATCH -MONDO:0014654 Ullrich congenital muscular dystrophy 2 skos:closeMatch DOID:0060944 Ullrich congenital muscular dystrophy 2 semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:616470 LEXMATCH -MONDO:0014654 Ullrich congenital muscular dystrophy 2 skos:closeMatch DOID:0060944 Ullrich congenital muscular dystrophy 2 semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:616470 LEXMATCH -MONDO:0014654 Ullrich congenital muscular dystrophy 2 skos:closeMatch DOID:0060944 Ullrich congenital muscular dystrophy 2 semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:616470 LEXMATCH -MONDO:0014654 Ullrich congenital muscular dystrophy 2 skos:closeMatch DOID:0060944 Ullrich congenital muscular dystrophy 2 semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:616470 LEXMATCH -MONDO:0014654 Ullrich congenital muscular dystrophy 2 skos:closeMatch DOID:0060944 Ullrich congenital muscular dystrophy 2 semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:616470 LEXMATCH -MONDO:0014669 cone-rod dystrophy 21 skos:closeMatch DOID:0081447 cone-rod dystrophy 21 semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:616502 LEXMATCH -MONDO:0014669 cone-rod dystrophy 21 skos:closeMatch DOID:0081447 cone-rod dystrophy 21 semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:616502 LEXMATCH -MONDO:0014669 cone-rod dystrophy 21 skos:closeMatch DOID:0081447 cone-rod dystrophy 21 semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:616502 LEXMATCH -MONDO:0014669 cone-rod dystrophy 21 skos:closeMatch DOID:0081447 cone-rod dystrophy 21 semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:616502 LEXMATCH -MONDO:0014669 cone-rod dystrophy 21 skos:closeMatch DOID:0081447 cone-rod dystrophy 21 semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:616502 LEXMATCH -MONDO:0015004 dystonia 28, childhood-onset skos:closeMatch DOID:0060936 dystonia 28, childhood-onset semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:617284 LEXMATCH -MONDO:0015004 dystonia 28, childhood-onset skos:closeMatch DOID:0060936 dystonia 28, childhood-onset semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref umls:c4310633 LEXMATCH -MONDO:0015004 dystonia 28, childhood-onset skos:closeMatch DOID:0060936 dystonia 28, childhood-onset semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:617284 LEXMATCH -MONDO:0015004 dystonia 28, childhood-onset skos:closeMatch DOID:0060936 dystonia 28, childhood-onset semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:617284 LEXMATCH -MONDO:0015004 dystonia 28, childhood-onset skos:closeMatch DOID:0060936 dystonia 28, childhood-onset semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref umls:c4310633 LEXMATCH -MONDO:0015004 dystonia 28, childhood-onset skos:closeMatch DOID:0060936 dystonia 28, childhood-onset semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:617284 LEXMATCH -MONDO:0015004 dystonia 28, childhood-onset skos:closeMatch DOID:0060936 dystonia 28, childhood-onset semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:617284 LEXMATCH -MONDO:0018540 PFAPA syndrome skos:closeMatch DOID:0081451 PFAPA syndrome semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref gard:5657 LEXMATCH -MONDO:0019507 amelogenesis imperfecta skos:closeMatch DOID:0060945 amelogenesis imperfecta type 1K semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref gard:5791 LEXMATCH -MONDO:0025691 dystonia 30 skos:closeMatch DOID:0060937 dystonia 30 semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:619291 LEXMATCH -MONDO:0025691 dystonia 30 skos:closeMatch DOID:0060937 dystonia 30 semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:619291 LEXMATCH -MONDO:0025691 dystonia 30 skos:closeMatch DOID:0060937 dystonia 30 semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:619291 LEXMATCH -MONDO:0025691 dystonia 30 skos:closeMatch DOID:0060937 dystonia 30 semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:619291 LEXMATCH -MONDO:0025691 dystonia 30 skos:closeMatch DOID:0060937 dystonia 30 semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:619291 LEXMATCH -MONDO:0030440 cone-rod dystrophy 22 skos:closeMatch DOID:0081448 cone-rod dystrophy 22 semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:619531 LEXMATCH -MONDO:0030440 cone-rod dystrophy 22 skos:closeMatch DOID:0081448 cone-rod dystrophy 22 semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:619531 LEXMATCH -MONDO:0030440 cone-rod dystrophy 22 skos:closeMatch DOID:0081448 cone-rod dystrophy 22 semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:619531 LEXMATCH -MONDO:0030440 cone-rod dystrophy 22 skos:closeMatch DOID:0081448 cone-rod dystrophy 22 semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:619531 LEXMATCH -MONDO:0030440 cone-rod dystrophy 22 skos:closeMatch DOID:0081448 cone-rod dystrophy 22 semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:619531 LEXMATCH -MONDO:0030455 dystonia 31 skos:closeMatch DOID:0060938 dystonia 31 semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:619565 LEXMATCH -MONDO:0030455 dystonia 31 skos:closeMatch DOID:0060938 dystonia 31 semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:619565 LEXMATCH -MONDO:0030455 dystonia 31 skos:closeMatch DOID:0060938 dystonia 31 semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:619565 LEXMATCH -MONDO:0030455 dystonia 31 skos:closeMatch DOID:0060938 dystonia 31 semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:619565 LEXMATCH -MONDO:0030455 dystonia 31 skos:closeMatch DOID:0060938 dystonia 31 semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:619565 LEXMATCH -MONDO:0030486 dystonia 32 skos:closeMatch DOID:0060939 dystonia 32 semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:619637 LEXMATCH -MONDO:0030486 dystonia 32 skos:closeMatch DOID:0060939 dystonia 32 semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:619637 LEXMATCH -MONDO:0030486 dystonia 32 skos:closeMatch DOID:0060939 dystonia 32 semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:619637 LEXMATCH -MONDO:0030486 dystonia 32 skos:closeMatch DOID:0060939 dystonia 32 semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:619637 LEXMATCH -MONDO:0030486 dystonia 32 skos:closeMatch DOID:0060939 dystonia 32 semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:619637 LEXMATCH -MONDO:0030513 dystonia 33 skos:closeMatch DOID:0060940 dystonia 33 semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:619687 LEXMATCH -MONDO:0030513 dystonia 33 skos:closeMatch DOID:0060940 dystonia 33 semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:619687 LEXMATCH -MONDO:0030513 dystonia 33 skos:closeMatch DOID:0060940 dystonia 33 semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:619687 LEXMATCH -MONDO:0030513 dystonia 33 skos:closeMatch DOID:0060940 dystonia 33 semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:619687 LEXMATCH -MONDO:0030513 dystonia 33 skos:closeMatch DOID:0060940 dystonia 33 semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:619687 LEXMATCH -MONDO:0030538 dystonia 34, myoclonic skos:closeMatch DOID:0060957 myoclonic dystonia 34 semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:619724 LEXMATCH -MONDO:0030538 dystonia 34, myoclonic skos:closeMatch DOID:0060957 myoclonic dystonia 34 semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:619724 LEXMATCH -MONDO:0030538 dystonia 34, myoclonic skos:closeMatch DOID:0060957 myoclonic dystonia 34 semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:619724 LEXMATCH -MONDO:0030538 dystonia 34, myoclonic skos:closeMatch DOID:0060957 myoclonic dystonia 34 semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:619724 LEXMATCH -MONDO:0030538 dystonia 34, myoclonic skos:closeMatch DOID:0060957 myoclonic dystonia 34 semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:619724 LEXMATCH -MONDO:0030608 interstitial lung disease 1 skos:closeMatch DOID:0060941 interstitial lung disease 1 semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:619611 LEXMATCH -MONDO:0030608 interstitial lung disease 1 skos:closeMatch DOID:0060941 interstitial lung disease 1 semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:619611 LEXMATCH -MONDO:0030608 interstitial lung disease 1 skos:closeMatch DOID:0060941 interstitial lung disease 1 semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:619611 LEXMATCH -MONDO:0030608 interstitial lung disease 1 skos:closeMatch DOID:0060941 interstitial lung disease 1 semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:619611 LEXMATCH -MONDO:0030608 interstitial lung disease 1 skos:closeMatch DOID:0060941 interstitial lung disease 1 semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:619611 LEXMATCH -MONDO:0030958 dystonia 35, childhood-onset skos:closeMatch DOID:0060955 dystonia 35, childhood-onset semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:619921 LEXMATCH -MONDO:0030958 dystonia 35, childhood-onset skos:closeMatch DOID:0060955 dystonia 35, childhood-onset semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:619921 LEXMATCH -MONDO:0030958 dystonia 35, childhood-onset skos:closeMatch DOID:0060955 dystonia 35, childhood-onset semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:619921 LEXMATCH -MONDO:0030958 dystonia 35, childhood-onset skos:closeMatch DOID:0060955 dystonia 35, childhood-onset semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:619921 LEXMATCH -MONDO:0030958 dystonia 35, childhood-onset skos:closeMatch DOID:0060955 dystonia 35, childhood-onset semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:619921 LEXMATCH -MONDO:0031084 amelogenesis imperfecta, IIa 1K skos:closeMatch DOID:0060945 amelogenesis imperfecta type 1K semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:620104 LEXMATCH -MONDO:0031084 amelogenesis imperfecta, IIa 1K skos:closeMatch DOID:0060945 amelogenesis imperfecta type 1K semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:620104 LEXMATCH -MONDO:0031084 amelogenesis imperfecta, IIa 1K skos:closeMatch DOID:0060945 amelogenesis imperfecta type 1K semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:620104 LEXMATCH -MONDO:0031084 amelogenesis imperfecta, IIa 1K skos:closeMatch DOID:0060945 amelogenesis imperfecta type 1K semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:620104 LEXMATCH -MONDO:0031084 amelogenesis imperfecta, IIa 1K skos:closeMatch DOID:0060945 amelogenesis imperfecta type 1K semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:620104 LEXMATCH -MONDO:0032790 neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities skos:closeMatch DOID:0081443 Stolerman neurodevelopmental syndrome semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:618505 LEXMATCH -MONDO:0032790 neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities skos:closeMatch DOID:0081443 Stolerman neurodevelopmental syndrome semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:618505 LEXMATCH -MONDO:0032790 neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities skos:closeMatch DOID:0081443 Stolerman neurodevelopmental syndrome semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:618505 LEXMATCH -MONDO:0032790 neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities skos:closeMatch DOID:0081443 Stolerman neurodevelopmental syndrome semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:618505 LEXMATCH -MONDO:0032790 neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities skos:closeMatch DOID:0081443 Stolerman neurodevelopmental syndrome semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:618505 LEXMATCH -MONDO:0032849 neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies skos:closeMatch DOID:0070539 Halperin-Birk syndrome semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:618651 LEXMATCH -MONDO:0032849 neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies skos:closeMatch DOID:0070539 Halperin-Birk syndrome semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:618651 LEXMATCH -MONDO:0032849 neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies skos:closeMatch DOID:0070539 Halperin-Birk syndrome semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym oio:hasExactSynonym neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies LEXMATCH -MONDO:0032849 neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies skos:closeMatch DOID:0070539 Halperin-Birk syndrome semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:618651 LEXMATCH -MONDO:0032849 neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies skos:closeMatch DOID:0070539 Halperin-Birk syndrome semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:618651 LEXMATCH -MONDO:0032849 neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies skos:closeMatch DOID:0070539 Halperin-Birk syndrome semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:618651 LEXMATCH -MONDO:0054549 peroxisome biogenesis disorder 10B skos:closeMatch DOID:0081440 Peroxisome biogenesis disorder 10B semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:617370 LEXMATCH -MONDO:0054549 peroxisome biogenesis disorder 10B skos:closeMatch DOID:0081440 Peroxisome biogenesis disorder 10B semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:617370 LEXMATCH -MONDO:0054549 peroxisome biogenesis disorder 10B skos:closeMatch DOID:0081440 Peroxisome biogenesis disorder 10B semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:617370 LEXMATCH -MONDO:0054549 peroxisome biogenesis disorder 10B skos:closeMatch DOID:0081440 Peroxisome biogenesis disorder 10B semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:617370 LEXMATCH -MONDO:0054549 peroxisome biogenesis disorder 10B skos:closeMatch DOID:0081440 Peroxisome biogenesis disorder 10B semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:617370 LEXMATCH -MONDO:0060533 microcephaly, short stature, and limb abnormalities skos:closeMatch DOID:0081431 microcephaly, short stature, and limb abnormalities semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:617604 LEXMATCH -MONDO:0060533 microcephaly, short stature, and limb abnormalities skos:closeMatch DOID:0081431 microcephaly, short stature, and limb abnormalities semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:617604 LEXMATCH -MONDO:0060533 microcephaly, short stature, and limb abnormalities skos:closeMatch DOID:0081431 microcephaly, short stature, and limb abnormalities semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:617604 LEXMATCH -MONDO:0060533 microcephaly, short stature, and limb abnormalities skos:closeMatch DOID:0081431 microcephaly, short stature, and limb abnormalities semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:617604 LEXMATCH -MONDO:0060533 microcephaly, short stature, and limb abnormalities skos:closeMatch DOID:0081431 microcephaly, short stature, and limb abnormalities semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:617604 LEXMATCH -MONDO:0800029 interstitial lung disease 2 skos:closeMatch DOID:0060941 interstitial lung disease 1 semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref gard:8609 LEXMATCH -MONDO:0859139 blepharophimosis-impaired intellectual development syndrome skos:closeMatch DOID:0081442 blepharophimosis-impaired intellectual development syndrome semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:619293 LEXMATCH -MONDO:0859139 blepharophimosis-impaired intellectual development syndrome skos:closeMatch DOID:0081442 blepharophimosis-impaired intellectual development syndrome semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:619293 LEXMATCH -MONDO:0859139 blepharophimosis-impaired intellectual development syndrome skos:closeMatch DOID:0081442 blepharophimosis-impaired intellectual development syndrome semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:619293 LEXMATCH -MONDO:0859139 blepharophimosis-impaired intellectual development syndrome skos:closeMatch DOID:0081442 blepharophimosis-impaired intellectual development syndrome semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:619293 LEXMATCH -MONDO:0859139 blepharophimosis-impaired intellectual development syndrome skos:closeMatch DOID:0081442 blepharophimosis-impaired intellectual development syndrome semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:619293 LEXMATCH -MONDO:0859377 neurodevelopmental disorder with poor growth and behavioral abnormalities skos:closeMatch DOID:0081444 neurodevelopmental disorder with poor growth and behavioral abnormalities semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:620242 LEXMATCH -MONDO:0859377 neurodevelopmental disorder with poor growth and behavioral abnormalities skos:closeMatch DOID:0081444 neurodevelopmental disorder with poor growth and behavioral abnormalities semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:620242 LEXMATCH -MONDO:0859377 neurodevelopmental disorder with poor growth and behavioral abnormalities skos:closeMatch DOID:0081444 neurodevelopmental disorder with poor growth and behavioral abnormalities semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:620242 LEXMATCH -MONDO:0859377 neurodevelopmental disorder with poor growth and behavioral abnormalities skos:closeMatch DOID:0081444 neurodevelopmental disorder with poor growth and behavioral abnormalities semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:620242 LEXMATCH -MONDO:0859377 neurodevelopmental disorder with poor growth and behavioral abnormalities skos:closeMatch DOID:0081444 neurodevelopmental disorder with poor growth and behavioral abnormalities semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:620242 LEXMATCH -MONDO:0957240 cone-rod dystrophy 24 skos:closeMatch DOID:0081449 cone-rod dystrophy 24 semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:620342 LEXMATCH -MONDO:0957240 cone-rod dystrophy 24 skos:closeMatch DOID:0081449 cone-rod dystrophy 24 semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:620342 LEXMATCH -MONDO:0957240 cone-rod dystrophy 24 skos:closeMatch DOID:0081449 cone-rod dystrophy 24 semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:620342 LEXMATCH -MONDO:0957240 cone-rod dystrophy 24 skos:closeMatch DOID:0081449 cone-rod dystrophy 24 semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:620342 LEXMATCH -MONDO:0957240 cone-rod dystrophy 24 skos:closeMatch DOID:0081449 cone-rod dystrophy 24 semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:620342 LEXMATCH -MONDO:0957385 dystonia 37, early-onset, with striatal lesions skos:closeMatch DOID:0060956 dystonia 37, early-onset with striatal lesions semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:620427 LEXMATCH -MONDO:0957385 dystonia 37, early-onset, with striatal lesions skos:closeMatch DOID:0060956 dystonia 37, early-onset with striatal lesions semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:620427 LEXMATCH -MONDO:0957385 dystonia 37, early-onset, with striatal lesions skos:closeMatch DOID:0060956 dystonia 37, early-onset with striatal lesions semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:620427 LEXMATCH -MONDO:0957385 dystonia 37, early-onset, with striatal lesions skos:closeMatch DOID:0060956 dystonia 37, early-onset with striatal lesions semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:620427 LEXMATCH -MONDO:0957385 dystonia 37, early-onset, with striatal lesions skos:closeMatch DOID:0060956 dystonia 37, early-onset with striatal lesions semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:620427 LEXMATCH -MONDO:0957539 dystonia 22, juvenile-onset skos:closeMatch DOID:0060966 dystonia 22, juvenile-onset semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:620453 LEXMATCH -MONDO:0957539 dystonia 22, juvenile-onset skos:closeMatch DOID:0060966 dystonia 22, juvenile-onset semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:620453 LEXMATCH -MONDO:0957539 dystonia 22, juvenile-onset skos:closeMatch DOID:0060966 dystonia 22, juvenile-onset semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:620453 LEXMATCH -MONDO:0957539 dystonia 22, juvenile-onset skos:closeMatch DOID:0060966 dystonia 22, juvenile-onset semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:620453 LEXMATCH -MONDO:0957539 dystonia 22, juvenile-onset skos:closeMatch DOID:0060966 dystonia 22, juvenile-onset semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:620453 LEXMATCH -MONDO:0957542 dystonia 22, adult-onset skos:closeMatch DOID:0060967 dystonia 22, adult-onset semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:620456 LEXMATCH -MONDO:0957542 dystonia 22, adult-onset skos:closeMatch DOID:0060967 dystonia 22, adult-onset semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:620456 LEXMATCH -MONDO:0957542 dystonia 22, adult-onset skos:closeMatch DOID:0060967 dystonia 22, adult-onset semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:620456 LEXMATCH -MONDO:0957542 dystonia 22, adult-onset skos:closeMatch DOID:0060967 dystonia 22, adult-onset semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:620456 LEXMATCH -MONDO:0957542 dystonia 22, adult-onset skos:closeMatch DOID:0060967 dystonia 22, adult-onset semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:620456 LEXMATCH -MONDO:0958235 Ullrich congenital muscular dystrophy 1B skos:closeMatch DOID:0060942 Ullrich congenital muscular dystrophy 1B semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:620727 LEXMATCH -MONDO:0958235 Ullrich congenital muscular dystrophy 1B skos:closeMatch DOID:0060942 Ullrich congenital muscular dystrophy 1B semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:620727 LEXMATCH -MONDO:0958235 Ullrich congenital muscular dystrophy 1B skos:closeMatch DOID:0060942 Ullrich congenital muscular dystrophy 1B semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:620727 LEXMATCH -MONDO:0958235 Ullrich congenital muscular dystrophy 1B skos:closeMatch DOID:0060942 Ullrich congenital muscular dystrophy 1B semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:620727 LEXMATCH -MONDO:0958235 Ullrich congenital muscular dystrophy 1B skos:closeMatch DOID:0060942 Ullrich congenital muscular dystrophy 1B semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:620727 LEXMATCH -MONDO:0958236 Ullrich congenital muscular dystrophy 1C skos:closeMatch DOID:0060943 Ullrich congenital muscular dystrophy 1C semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:620728 LEXMATCH -MONDO:0958236 Ullrich congenital muscular dystrophy 1C skos:closeMatch DOID:0060943 Ullrich congenital muscular dystrophy 1C semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:620728 LEXMATCH -MONDO:0958236 Ullrich congenital muscular dystrophy 1C skos:closeMatch DOID:0060943 Ullrich congenital muscular dystrophy 1C semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:620728 LEXMATCH -MONDO:0958236 Ullrich congenital muscular dystrophy 1C skos:closeMatch DOID:0060943 Ullrich congenital muscular dystrophy 1C semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:620728 LEXMATCH -MONDO:0958236 Ullrich congenital muscular dystrophy 1C skos:closeMatch DOID:0060943 Ullrich congenital muscular dystrophy 1C semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE skos:exactMatch omim:620728 LEXMATCH -MONDO:0968944 intellectual developmental disorder, autosomal recessive 82 skos:closeMatch DOID:0060947 autosomal recessive intellectual developmental disorder 82 semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:620779 LEXMATCH -MONDO:0968944 intellectual developmental disorder, autosomal recessive 82 skos:closeMatch DOID:0060947 autosomal recessive intellectual developmental disorder 82 semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch omim:620779 LEXMATCH -MONDO:0968944 intellectual developmental disorder, autosomal recessive 82 skos:closeMatch DOID:0060947 autosomal recessive intellectual developmental disorder 82 semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:620779 LEXMATCH +MONDO:0957421 borna virus encephalitis skos:closeMatch DOID:5154 borna disease semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref mesh:d001890 LEXMATCH +MONDO:0957421 borna virus encephalitis skos:closeMatch DOID:5154 borna disease semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch mesh:d001890 LEXMATCH +MONDO:0957421 borna virus encephalitis skos:closeMatch DOID:5154 borna disease semapv:LexicalMatching oaklib 0.5 skos:relatedMatch oio:hasDbXref mesh:d001890 LEXMATCH +MONDO:0957421 borna virus encephalitis skos:closeMatch DOID:5154 borna disease semapv:LexicalMatching oaklib 0.5 skos:relatedMatch skos:exactMatch mesh:d001890 LEXMATCH +MONDO:1010029 aleutian mink disease, human skos:closeMatch DOID:2934 aleutian mink disease semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref mesh:d000453 LEXMATCH +MONDO:1010029 aleutian mink disease, human skos:closeMatch DOID:2934 aleutian mink disease semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch mesh:d000453 LEXMATCH +MONDO:1010029 aleutian mink disease, human skos:closeMatch DOID:2934 aleutian mink disease semapv:LexicalMatching oaklib 0.5 skos:relatedMatch oio:hasDbXref mesh:d000453 LEXMATCH +MONDO:1010029 aleutian mink disease, human skos:closeMatch DOID:2934 aleutian mink disease semapv:LexicalMatching oaklib 0.5 skos:relatedMatch skos:exactMatch mesh:d000453 LEXMATCH diff --git a/src/ontology/lexmatch/split-mapping-set/mondo_closematch_icd10cm.tsv b/src/ontology/lexmatch/split-mapping-set/mondo_closematch_icd10cm.tsv index f30fa5e0..8b22f56e 100644 --- a/src/ontology/lexmatch/split-mapping-set/mondo_closematch_icd10cm.tsv +++ b/src/ontology/lexmatch/split-mapping-set/mondo_closematch_icd10cm.tsv @@ -4103,8 +4103,8 @@ MONDO:0012354 platelet-type bleeding disorder 8 skos:closeMatch ICD10CM:D69.8 Ot MONDO:0012354 platelet-type bleeding disorder 8 skos:closeMatch ICD10CM:D69.8 Other specified hemorrhagic conditions semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref-INVERSE doid:0060692 LEXMATCH MONDO:0012355 autosomal recessive nonsyndromic hearing loss 28 skos:closeMatch ICD10CM:H90.3 Sensorineural hearing loss, bilateral semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref-INVERSE doid:0110486 LEXMATCH MONDO:0012355 autosomal recessive nonsyndromic hearing loss 28 skos:closeMatch ICD10CM:H90.3 Sensorineural hearing loss, bilateral semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref-INVERSE doid:0110486 LEXMATCH -MONDO:0012360 congenital nongoitrous hypothryoidism 3 skos:closeMatch ICD10CM:E03.1 Congenital hypothyroidism without goiter semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref-INVERSE doid:0070127 LEXMATCH -MONDO:0012360 congenital nongoitrous hypothryoidism 3 skos:closeMatch ICD10CM:E03.1 Congenital hypothyroidism without goiter semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref-INVERSE doid:0070127 LEXMATCH +MONDO:0012360 congenital nongoitrous hypothyroidism 3 skos:closeMatch ICD10CM:E03.1 Congenital hypothyroidism without goiter semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref-INVERSE doid:0070127 LEXMATCH +MONDO:0012360 congenital nongoitrous hypothyroidism 3 skos:closeMatch ICD10CM:E03.1 Congenital hypothyroidism without goiter semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref-INVERSE doid:0070127 LEXMATCH MONDO:0012363 retinitis pigmentosa 32 skos:closeMatch ICD10CM:H35.5 Hereditary retinal dystrophy semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref-INVERSE doid:0110355 LEXMATCH MONDO:0012363 retinitis pigmentosa 32 skos:closeMatch ICD10CM:H35.5 Hereditary retinal dystrophy semapv:LexicalMatching oaklib 0.5 rdf:ID oio:hasDbXref-INVERSE mondo:0012363 LEXMATCH MONDO:0012363 retinitis pigmentosa 32 skos:closeMatch ICD10CM:H35.5 Hereditary retinal dystrophy semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref-INVERSE doid:0110355 LEXMATCH @@ -4689,8 +4689,8 @@ MONDO:0013754 cutis laxa, autosomal recessive, type 1B skos:closeMatch ICD10CM:Q MONDO:0013754 cutis laxa, autosomal recessive, type 1B skos:closeMatch ICD10CM:Q82.8 Other specified congenital malformations of skin semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref-INVERSE doid:0070133 LEXMATCH MONDO:0013755 PYCR1-related de Barsy syndrome skos:closeMatch ICD10CM:Q82.8 Other specified congenital malformations of skin semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref-INVERSE doid:0070138 LEXMATCH MONDO:0013755 PYCR1-related de Barsy syndrome skos:closeMatch ICD10CM:Q82.8 Other specified congenital malformations of skin semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref-INVERSE doid:0070138 LEXMATCH -MONDO:0013757 congenital nongoitrous hypothryoidism 6 skos:closeMatch ICD10CM:E03.1 Congenital hypothyroidism without goiter semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref-INVERSE doid:0070128 LEXMATCH -MONDO:0013757 congenital nongoitrous hypothryoidism 6 skos:closeMatch ICD10CM:E03.1 Congenital hypothyroidism without goiter semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref-INVERSE doid:0070128 LEXMATCH +MONDO:0013757 congenital nongoitrous hypothyroidism 6 skos:closeMatch ICD10CM:E03.1 Congenital hypothyroidism without goiter semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref-INVERSE doid:0070128 LEXMATCH +MONDO:0013757 congenital nongoitrous hypothyroidism 6 skos:closeMatch ICD10CM:E03.1 Congenital hypothyroidism without goiter semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref-INVERSE doid:0070128 LEXMATCH MONDO:0013758 Charcot-Marie-Tooth disease dominant intermediate E skos:closeMatch ICD10CM:G60.0 Hereditary motor and sensory neuropathy semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref-INVERSE doid:0110205 LEXMATCH MONDO:0013758 Charcot-Marie-Tooth disease dominant intermediate E skos:closeMatch ICD10CM:G60.0 Hereditary motor and sensory neuropathy semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref-INVERSE doid:0110205 LEXMATCH MONDO:0013766 familial cold autoinflammatory syndrome 3 skos:closeMatch ICD10CM:L50.2 Urticaria due to cold and heat semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref-INVERSE doid:0090064 LEXMATCH @@ -5219,6 +5219,7 @@ MONDO:0016502 Hermansky-Pudlak syndrome without pulmonary fibrosis skos:closeMat MONDO:0016567 locked-in syndrome skos:closeMatch ICD10CM:G83.5 Locked-in state semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref-INVERSE doid:12697 LEXMATCH MONDO:0016567 locked-in syndrome skos:closeMatch ICD10CM:G83.5 Locked-in state semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref-INVERSE doid:12697 LEXMATCH MONDO:0016581 conotruncal heart malformations skos:closeMatch ICD10CM:Q20.0 Common arterial trunk semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym oio:hasExactSynonym persistent truncus arteriosus LEXMATCH +MONDO:0016586 systemic mastocytosis skos:closeMatch ICD10CM:C96.21 Aggressive systemic mastocytosis semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label aggressive systemic mastocytosis LEXMATCH MONDO:0016586 systemic mastocytosis skos:closeMatch ICD10CM:D47.02 Systemic mastocytosis semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref-INVERSE doid:349 LEXMATCH MONDO:0016586 systemic mastocytosis skos:closeMatch ICD10CM:D47.02 Systemic mastocytosis semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref-INVERSE doid:349 LEXMATCH MONDO:0016595 inhalational anthrax skos:closeMatch ICD10CM:A22.1 Pulmonary anthrax semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym oio:hasExactSynonym inhalation anthrax LEXMATCH diff --git a/src/ontology/lexmatch/split-mapping-set/mondo_closematch_icd11.foundation.tsv b/src/ontology/lexmatch/split-mapping-set/mondo_closematch_icd11.foundation.tsv index 4bb46596..356bc796 100644 --- a/src/ontology/lexmatch/split-mapping-set/mondo_closematch_icd11.foundation.tsv +++ b/src/ontology/lexmatch/split-mapping-set/mondo_closematch_icd11.foundation.tsv @@ -285,6 +285,7 @@ MONDO:0004646 decubitus ulcer skos:closeMatch icd11.foundation:455330172 Pressur MONDO:0004651 smallpox skos:closeMatch icd11.foundation:2054716425 Smallpox semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym oio:hasExactSynonym variola LEXMATCH MONDO:0004653 atypical chronic myeloid leukemia, BCR-ABL1 negative skos:closeMatch icd11.foundation:331838766 Atypical chronic myeloid leukaemia, BCR-ABL1-negative semapv:LexicalMatching oaklib 0.5 rdf:ID oio:hasDbXref-INVERSE mondo:0004653 LEXMATCH MONDO:0004664 helminthiasis skos:closeMatch icd11.foundation:863306856 Other and unspecified infestation by parasitic worms semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym oio:hasExactSynonym worm infection LEXMATCH +MONDO:0004665 nodular sclerosis classical Hodgkin lymphoma skos:closeMatch icd11.foundation:1995941600 Nodular sclerosis classical Hodgkin lymphoma semapv:LexicalMatching oaklib 0.5 rdf:ID oio:hasDbXref-INVERSE mondo:0004665 LEXMATCH MONDO:0004678 dermatophytosis skos:closeMatch icd11.foundation:1802307036 Dermatophytosis semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym oio:hasExactSynonym ringworm LEXMATCH MONDO:0004684 plantar fibromatosis skos:closeMatch icd11.foundation:409482033 Plantar fascial fibromatosis semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label plantar fascial fibromatosis LEXMATCH MONDO:0004691 autosomal dominant polycystic kidney disease skos:closeMatch icd11.foundation:91220434 Autosomal dominant polycystic kidney disease semapv:LexicalMatching oaklib 0.5 rdf:ID oio:hasDbXref-INVERSE mondo:0004691 LEXMATCH @@ -293,6 +294,7 @@ MONDO:0004693 squamous carcinoma in situ skos:closeMatch icd11.foundation:759415 MONDO:0004712 herpes simplex dermatitis skos:closeMatch icd11.foundation:340796263 Eczema herpeticum semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label eczema herpeticum LEXMATCH MONDO:0004731 central sleep apnea syndrome skos:closeMatch icd11.foundation:1750742010 Congenital central alveolar sleep-related hypoventilation semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym oio:hasExactSynonym ondine syndrome LEXMATCH MONDO:0004737 homocystinuria skos:closeMatch icd11.foundation:1480749127 Classical homocystinuria semapv:LexicalMatching oaklib 0.5 oio:hasNarrowSynonym oio:hasExactSynonym cystathionine synthase deficiency LEXMATCH +MONDO:0004745 priapism skos:closeMatch icd11.foundation:842663091 Low-flow priapism semapv:LexicalMatching oaklib 0.5 oio:hasNarrowSynonym rdfs:label low-flow priapism LEXMATCH MONDO:0004757 chronic ethmoidal sinusitis skos:closeMatch icd11.foundation:1076459084 Chronic ethmoidal sinusitis semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym oio:hasExactSynonym chronic ethmoiditis LEXMATCH MONDO:0004784 allergic asthma skos:closeMatch icd11.foundation:1011332383 Allergic atopic asthma semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym oio:hasExactSynonym atopic asthma LEXMATCH MONDO:0004796 infectious meningitis skos:closeMatch icd11.foundation:1479386045 Meningitis (nearest) (TM2) semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym oio:hasExactSynonym meningitis LEXMATCH @@ -800,6 +802,7 @@ MONDO:0008097 linear nevus sebaceous syndrome skos:closeMatch icd11.foundation:1 MONDO:0008101 familial supernumerary nipples skos:closeMatch icd11.foundation:1458532658 Supernumerary breasts semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym oio:hasExactSynonym polymastia LEXMATCH MONDO:0008104 Noonan syndrome 1 skos:closeMatch icd11.foundation:1044395354 Noonan syndrome semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label noonan syndrome LEXMATCH MONDO:0008108 oculocerebrocutaneous syndrome skos:closeMatch icd11.foundation:417997287 Oculo-cerebro-cutaneous syndrome semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label oculo-cerebro-cutaneous syndrome LEXMATCH +MONDO:0008109 ocular cicatricial pemphigoid skos:closeMatch icd11.foundation:953963439 Mucous membrane pemphigoid with ocular involvement semapv:LexicalMatching oaklib 0.5 rdf:ID oio:hasDbXref-INVERSE mondo:0008109 LEXMATCH MONDO:0008136 isolated optic nerve hypoplasia skos:closeMatch icd11.foundation:609162974 Isolated optic nerve hypoplasia semapv:LexicalMatching oaklib 0.5 rdf:ID oio:hasDbXref-INVERSE mondo:0008136 LEXMATCH MONDO:0008145 Ollier disease skos:closeMatch icd11.foundation:1341485804 Enchondromatosis semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym oio:hasExactSynonym multiple enchondromatosis LEXMATCH MONDO:0008145 Ollier disease skos:closeMatch icd11.foundation:1341485804 Enchondromatosis semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label enchondromatosis LEXMATCH @@ -1920,6 +1923,8 @@ MONDO:0016581 conotruncal heart malformations skos:closeMatch icd11.foundation:1 MONDO:0016581 conotruncal heart malformations skos:closeMatch icd11.foundation:1832500366 Common arterial trunk semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym oio:hasExactSynonym persistent truncus arteriosus LEXMATCH MONDO:0016581 conotruncal heart malformations skos:closeMatch icd11.foundation:1832500366 Common arterial trunk semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym oio:hasExactSynonym truncus arteriosus communis LEXMATCH MONDO:0016586 systemic mastocytosis skos:closeMatch icd11.foundation:1144812971 Systemic mastocytosis semapv:LexicalMatching oaklib 0.5 rdf:ID oio:hasDbXref-INVERSE mondo:0016586 LEXMATCH +MONDO:0016586 systemic mastocytosis skos:closeMatch icd11.foundation:377330181 Aggressive systemic mastocytosis semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label aggressive systemic mastocytosis LEXMATCH +MONDO:0016586 systemic mastocytosis skos:closeMatch icd11.foundation:870477963 Aggressive systemic mastocytosis semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label aggressive systemic mastocytosis LEXMATCH MONDO:0016593 acquired ataxia skos:closeMatch icd11.foundation:71197968 Acquired ataxia semapv:LexicalMatching oaklib 0.5 rdf:ID oio:hasDbXref-INVERSE mondo:0016593 LEXMATCH MONDO:0016595 inhalational anthrax skos:closeMatch icd11.foundation:534877374 Pulmonary anthrax semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym oio:hasExactSynonym inhalation anthrax LEXMATCH MONDO:0016608 megalencephaly skos:closeMatch icd11.foundation:368780653 Megalencephaly semapv:LexicalMatching oaklib 0.5 rdf:ID oio:hasDbXref-INVERSE mondo:0016608 LEXMATCH @@ -2667,7 +2672,6 @@ MONDO:0020316 acute myeloid leukemia with abnormal bone marrow eosinophils inv(1 MONDO:0020323 primary mediastinal large B-cell lymphoma skos:closeMatch icd11.foundation:950282079 Primary mediastinal large B-cell lymphoma semapv:LexicalMatching oaklib 0.5 rdf:ID oio:hasDbXref-INVERSE mondo:0020323 LEXMATCH MONDO:0020324 intravascular large B-cell lymphoma skos:closeMatch icd11.foundation:952730197 Intravascular large B-cell lymphoma semapv:LexicalMatching oaklib 0.5 rdf:ID oio:hasDbXref-INVERSE mondo:0020324 LEXMATCH MONDO:0020326 lymphomatoid papulosis skos:closeMatch icd11.foundation:1791207220 Lymphomatoid papulosis semapv:LexicalMatching oaklib 0.5 rdf:ID oio:hasDbXref-INVERSE mondo:0020326 LEXMATCH -MONDO:0020327 classic Hodgkin lymphoma, nodular sclerosis type skos:closeMatch icd11.foundation:1995941600 Nodular sclerosis classical Hodgkin lymphoma semapv:LexicalMatching oaklib 0.5 rdf:ID oio:hasDbXref-INVERSE mondo:0020327 LEXMATCH MONDO:0020334 mast cell leukemia skos:closeMatch icd11.foundation:1359806843 Mast cell leukaemia semapv:LexicalMatching oaklib 0.5 rdf:ID oio:hasDbXref-INVERSE mondo:0020334 LEXMATCH MONDO:0020338 adult pure red cell aplasia skos:closeMatch icd11.foundation:45753120 Acquired pure red cell aplasia semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label acquired pure red cell aplasia LEXMATCH MONDO:0020338 adult pure red cell aplasia skos:closeMatch icd11.foundation:45753120 Acquired pure red cell aplasia semapv:LexicalMatching oaklib 0.5 rdf:ID oio:hasDbXref-INVERSE mondo:0020338 LEXMATCH @@ -2717,7 +2721,6 @@ MONDO:0020544 streptococcal toxic-shock syndrome skos:closeMatch icd11.foundatio MONDO:0020545 staphylococcal toxic-shock syndrome skos:closeMatch icd11.foundation:788554020 Staphylococcal toxic shock syndrome semapv:LexicalMatching oaklib 0.5 rdf:ID oio:hasDbXref-INVERSE mondo:0020545 LEXMATCH MONDO:0020546 acute graft versus host disease skos:closeMatch icd11.foundation:83784921 Acute graft-versus-host disease semapv:LexicalMatching oaklib 0.5 rdf:ID oio:hasDbXref-INVERSE mondo:0020546 LEXMATCH MONDO:0020547 chronic graft versus host disease skos:closeMatch icd11.foundation:621183043 Chronic graft-versus-host disease semapv:LexicalMatching oaklib 0.5 rdf:ID oio:hasDbXref-INVERSE mondo:0020547 LEXMATCH -MONDO:0020548 ocular pemphigoid skos:closeMatch icd11.foundation:953963439 Mucous membrane pemphigoid with ocular involvement semapv:LexicalMatching oaklib 0.5 rdf:ID oio:hasDbXref-INVERSE mondo:0020548 LEXMATCH MONDO:0020553 secondary pulmonary hemosiderosis skos:closeMatch icd11.foundation:878618614 Secondary pulmonary haemosiderosis semapv:LexicalMatching oaklib 0.5 rdf:ID oio:hasDbXref-INVERSE mondo:0020553 LEXMATCH MONDO:0020567 apnea of prematurity skos:closeMatch icd11.foundation:894774581 Primary central sleep apnoea of prematurity semapv:LexicalMatching oaklib 0.5 rdf:ID oio:hasDbXref-INVERSE mondo:0020567 LEXMATCH MONDO:0020568 cutaneous myiasis skos:closeMatch icd11.foundation:1342682193 Cutaneous myiasis semapv:LexicalMatching oaklib 0.5 rdf:ID oio:hasDbXref-INVERSE mondo:0020568 LEXMATCH diff --git a/src/ontology/lexmatch/split-mapping-set/mondo_closematch_ncit.tsv b/src/ontology/lexmatch/split-mapping-set/mondo_closematch_ncit.tsv index 31b6738c..e6535a6b 100644 --- a/src/ontology/lexmatch/split-mapping-set/mondo_closematch_ncit.tsv +++ b/src/ontology/lexmatch/split-mapping-set/mondo_closematch_ncit.tsv @@ -20,7 +20,8 @@ MONDO:0003523 gastrin-producing neuroendocrine tumor skos:closeMatch NCIT:C65188 MONDO:0003544 spinal cord cancer skos:closeMatch NCIT:C168693 Spinal Neoplasm semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label spinal neoplasm LEXMATCH MONDO:0003611 uterine ligament papillary cystadenoma associated with von Hippel-Lindau disease skos:closeMatch NCIT:C155952 Uterine Ligament Papillary Cystadenoma semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label uterine ligament papillary cystadenoma LEXMATCH MONDO:0003766 thalamic cancer skos:closeMatch NCIT:C6221 Thalamic Neoplasm semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label thalamic neoplasm LEXMATCH -MONDO:0004063 intermediate cell type iris melanoma skos:closeMatch NCIT:C174506 Iris Mixed Cell Melanoma semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label iris mixed cell melanoma LEXMATCH +MONDO:0003865 acral lentiginous melanoma skos:closeMatch NCIT:C204883 Acral Melanoma semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label acral melanoma LEXMATCH +MONDO:0003865 acral lentiginous melanoma skos:closeMatch NCIT:C204887 Subungual Melanoma semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label subungual melanoma LEXMATCH MONDO:0004245 ependymal tumor of brain skos:closeMatch NCIT:C156462 Brain Ependymoma semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label brain ependymoma LEXMATCH MONDO:0004631 tongue cancer skos:closeMatch NCIT:C4824 Tongue Carcinoma semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label tongue carcinoma LEXMATCH MONDO:0004948 B-cell chronic lymphocytic leukemia skos:closeMatch NCIT:C7540 Small Lymphocytic Lymphoma semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label small lymphocytic lymphoma LEXMATCH @@ -43,6 +44,8 @@ MONDO:0006292 malignant mesothelioma skos:closeMatch NCIT:C8420 Diffuse Malignan MONDO:0006312 myofibroma skos:closeMatch NCIT:C27498 Infantile Hemangiopericytoma semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label infantile hemangiopericytoma LEXMATCH MONDO:0006405 salivary gland small cell carcinoma skos:closeMatch NCIT:C173653 Salivary Gland Neuroendocrine Carcinoma semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label salivary gland neuroendocrine carcinoma LEXMATCH MONDO:0006717 cutaneous fibrous histiocytoma skos:closeMatch NCIT:C170736 Pleomorphic Fibroma semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label pleomorphic fibroma LEXMATCH +MONDO:0006738 eccrine acrospiroma skos:closeMatch NCIT:C205539 Solid Cystic Hidradenoma semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label solid cystic hidradenoma LEXMATCH +MONDO:0006787 hidrocystoma skos:closeMatch NCIT:C205459 Apocrine Cystadenoma semapv:LexicalMatching oaklib 0.5 oio:hasNarrowSynonym rdfs:label apocrine cystadenoma LEXMATCH MONDO:0007564 pilomatrixoma skos:closeMatch NCIT:C27520 Benign Hair Follicle Neoplasm semapv:LexicalMatching oaklib 0.5 oio:hasNarrowSynonym rdfs:label benign hair follicle neoplasm LEXMATCH MONDO:0007585 exostoses, multiple, type 1 skos:closeMatch NCIT:C53457 Multiple Osteochondromas semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label multiple osteochondromas LEXMATCH MONDO:0007896 acute monocytic leukemia skos:closeMatch NCIT:C7171 Acute Monoblastic Leukemia semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label acute monoblastic leukemia LEXMATCH diff --git a/src/ontology/lexmatch/split-mapping-set/mondo_closematch_omimps.tsv b/src/ontology/lexmatch/split-mapping-set/mondo_closematch_omimps.tsv deleted file mode 100644 index 4901dc4a..00000000 --- a/src/ontology/lexmatch/split-mapping-set/mondo_closematch_omimps.tsv +++ /dev/null @@ -1,5 +0,0 @@ -subject_id subject_label predicate_id object_id object_label mapping_justification mapping_tool confidence subject_match_field object_match_field match_string comment -MONDO:0018875 Li-Fraumeni syndrome skos:closeMatch OMIMPS:151623 Li-Fraumeni syndrome semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref-INVERSE doid:3012 LEXMATCH -MONDO:0018875 Li-Fraumeni syndrome skos:closeMatch OMIMPS:151623 Li-Fraumeni syndrome semapv:LexicalMatching oaklib 0.5 oio:hasDbXref skos:exactMatch-INVERSE doid:3012 LEXMATCH -MONDO:0018875 Li-Fraumeni syndrome skos:closeMatch OMIMPS:151623 Li-Fraumeni syndrome semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref-INVERSE doid:3012 LEXMATCH -MONDO:0018875 Li-Fraumeni syndrome skos:closeMatch OMIMPS:151623 Li-Fraumeni syndrome semapv:LexicalMatching oaklib 0.5 skos:exactMatch skos:exactMatch-INVERSE doid:3012 LEXMATCH diff --git a/src/ontology/lexmatch/split-mapping-set/mondo_closematch_orphanet.tsv b/src/ontology/lexmatch/split-mapping-set/mondo_closematch_orphanet.tsv index 0ae58a69..e987a6fc 100644 --- a/src/ontology/lexmatch/split-mapping-set/mondo_closematch_orphanet.tsv +++ b/src/ontology/lexmatch/split-mapping-set/mondo_closematch_orphanet.tsv @@ -1,4 +1,4 @@ subject_id subject_label predicate_id object_id object_label mapping_justification mapping_tool confidence subject_match_field object_match_field match_string comment -MONDO:0008302 centra precocious puberty 1 skos:closeMatch Orphanet:650097 Genetic central precocious puberty in male semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:176400 LEXMATCH -MONDO:0008302 centra precocious puberty 1 skos:closeMatch Orphanet:650097 Genetic central precocious puberty in male semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:176400 LEXMATCH -MONDO:0008302 centra precocious puberty 1 skos:closeMatch Orphanet:650097 Genetic central precocious puberty in male semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:176400 LEXMATCH +MONDO:0008302 central precocious puberty 1 skos:closeMatch Orphanet:650097 Genetic central precocious puberty in male semapv:LexicalMatching oaklib 0.5 oio:hasDbXref oio:hasDbXref omim:176400 LEXMATCH +MONDO:0008302 central precocious puberty 1 skos:closeMatch Orphanet:650097 Genetic central precocious puberty in male semapv:LexicalMatching oaklib 0.5 skos:exactMatch oio:hasDbXref omim:176400 LEXMATCH +MONDO:0008302 central precocious puberty 1 skos:closeMatch Orphanet:650097 Genetic central precocious puberty in male semapv:LexicalMatching oaklib 0.5 skos:exactMatch-INVERSE oio:hasDbXref omim:176400 LEXMATCH diff --git a/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_doid.tsv b/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_doid.tsv index 3df8b33c..834c1099 100644 --- a/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_doid.tsv +++ b/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_doid.tsv @@ -22,57 +22,17 @@ MONDO:0004268 obsolete subareolar duct papillomatosis skos:exactMatch DOID:7533 MONDO:0004391 obsolete adult extraosseous chondrosarcoma skos:exactMatch DOID:7902 adult extraskeletal myxoid chondrosarcoma semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0004398 mediastinal schwannoma skos:exactMatch DOID:7922 obsolete benign mediastinal neurilemmoma semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0005128 obsolete sensory system disease skos:exactMatch DOID:0050155 sensory system disease semapv:UnspecifiedMatching MONDO_MAPPINGS +MONDO:0005641 aleutian mink disease skos:exactMatch DOID:2934 aleutian mink disease semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label aleutian mink disease LEXMATCH +MONDO:0005676 borna disease skos:exactMatch DOID:5154 borna disease semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label borna disease LEXMATCH MONDO:0005862 obsolete multiple chemical sensitivity skos:exactMatch DOID:4661 multiple chemical sensitivity semapv:UnspecifiedMatching MONDO_MAPPINGS -MONDO:0007495 dystonia 5 skos:exactMatch DOID:0060963 dystonia, DOPA-responsive semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:128230 LEXMATCH MONDO:0007744 cholesterol-ester transfer protein deficiency skos:exactMatch DOID:0111368 cholesterol-ester transfer protein deficiency semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label cholesterol-ester transfer protein deficiency LEXMATCH -MONDO:0009619 microcephaly-micromelia syndrome skos:exactMatch DOID:0081432 microcephaly-micromelia syndrome semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:251230 LEXMATCH MONDO:0009669 spinal muscular atrophy, type 1 skos:exactMatch DOID:0060160 childhood spinal muscular atrophy semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym oio:hasExactSynonym survival motor neuron spinal muscular atrophy LEXMATCH -MONDO:0009681 Ullrich congenital muscular dystrophy 1A skos:exactMatch DOID:0060946 Ullrich congenital muscular dystrophy 1A semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:254090 LEXMATCH -MONDO:0009849 hyperimmunoglobulinemia D with periodic fever skos:exactMatch DOID:0081450 hyperimmunoglobulinemia D periodic fever syndrome semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:260920 LEXMATCH -MONDO:0011053 intellectual disability-sparse hair-brachydactyly syndrome skos:exactMatch DOID:0081441 Nicolaides-Baraitser syndrome semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:601358 LEXMATCH -MONDO:0011382 sickle cell anemia skos:exactMatch DOID:0081445 sickle cell disease semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:603903 LEXMATCH -MONDO:0011610 dimethylglycine dehydrogenase deficiency skos:exactMatch DOID:0081446 dimethylglycine dehydrogenase deficiency semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:605850 LEXMATCH MONDO:0012144 Waardenburg syndrome type 2D skos:exactMatch DOID:0110952 obsolete Waardenburg syndrome type 2D semapv:UnspecifiedMatching MONDO_MAPPINGS -MONDO:0013931 peroxisome biogenesis disorder 4B skos:exactMatch DOID:0081433 Peroxisome biogenesis disorder 4B semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:614863 LEXMATCH -MONDO:0013933 peroxisome biogenesis disorder 5B skos:exactMatch DOID:0081434 Peroxisome biogenesis disorder 5B semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:614867 LEXMATCH -MONDO:0013937 peroxisome biogenesis disorder 6B skos:exactMatch DOID:0081435 Peroxisome biogenesis disorder 6B semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:614871 LEXMATCH -MONDO:0013939 peroxisome biogenesis disorder 7B skos:exactMatch DOID:0081436 Peroxisome biogenesis disorder 7B semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:614873 LEXMATCH -MONDO:0013943 peroxisome biogenesis disorder 8B skos:exactMatch DOID:0081437 Peroxisome biogenesis disorder 8B semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:614877 LEXMATCH -MONDO:0013945 peroxisome biogenesis disorder 9B skos:exactMatch DOID:0081438 Peroxisome biogenesis disorder 9B semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:614879 LEXMATCH -MONDO:0013950 peroxisome biogenesis disorder 11B skos:exactMatch DOID:0081439 Peroxisome biogenesis disorder 11B semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:614885 LEXMATCH -MONDO:0014654 Ullrich congenital muscular dystrophy 2 skos:exactMatch DOID:0060944 Ullrich congenital muscular dystrophy 2 semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:616470 LEXMATCH -MONDO:0014669 cone-rod dystrophy 21 skos:exactMatch DOID:0081447 cone-rod dystrophy 21 semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:616502 LEXMATCH -MONDO:0015004 dystonia 28, childhood-onset skos:exactMatch DOID:0060936 dystonia 28, childhood-onset semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:617284 LEXMATCH MONDO:0017841 obsolete autoimmune disease with skin involvement skos:exactMatch DOID:0060039 autoimmune disease of skin and connective tissue semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0018251 obsolete glycogen storage disease due to phosphorylase kinase deficiency skos:exactMatch DOID:0050594 glycogen storage disease IX semapv:UnspecifiedMatching MONDO_MAPPINGS -MONDO:0018540 PFAPA syndrome skos:exactMatch DOID:0081451 PFAPA syndrome semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label pfapa syndrome LEXMATCH MONDO:0021199 obsolete disease by anatomical system skos:exactMatch DOID:7 disease of anatomical entity semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0021668 obsolete disorder involving pain skos:exactMatch DOID:0060164 pain disorder semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0024657 obsolete macrocystic neurilemmoma skos:exactMatch DOID:3203 macrocystic neurilemmoma semapv:UnspecifiedMatching MONDO_MAPPINGS -MONDO:0025691 dystonia 30 skos:exactMatch DOID:0060937 dystonia 30 semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:619291 LEXMATCH -MONDO:0030440 cone-rod dystrophy 22 skos:exactMatch DOID:0081448 cone-rod dystrophy 22 semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:619531 LEXMATCH -MONDO:0030455 dystonia 31 skos:exactMatch DOID:0060938 dystonia 31 semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:619565 LEXMATCH -MONDO:0030486 dystonia 32 skos:exactMatch DOID:0060939 dystonia 32 semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:619637 LEXMATCH -MONDO:0030513 dystonia 33 skos:exactMatch DOID:0060940 dystonia 33 semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:619687 LEXMATCH -MONDO:0030538 dystonia 34, myoclonic skos:exactMatch DOID:0060957 myoclonic dystonia 34 semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:619724 LEXMATCH -MONDO:0030608 interstitial lung disease 1 skos:exactMatch DOID:0060941 interstitial lung disease 1 semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:619611 LEXMATCH -MONDO:0030958 dystonia 35, childhood-onset skos:exactMatch DOID:0060955 dystonia 35, childhood-onset semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:619921 LEXMATCH -MONDO:0031084 amelogenesis imperfecta, IIa 1K skos:exactMatch DOID:0060945 amelogenesis imperfecta type 1K semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:620104 LEXMATCH -MONDO:0032790 neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities skos:exactMatch DOID:0081443 Stolerman neurodevelopmental syndrome semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:618505 LEXMATCH -MONDO:0032849 neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies skos:exactMatch DOID:0070539 Halperin-Birk syndrome semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:618651 LEXMATCH -MONDO:0035534 DONSON-related microcephaly-short stature-limb abnormalities spectrum skos:exactMatch DOID:0081431 microcephaly, short stature, and limb abnormalities semapv:LexicalMatching oaklib 0.8 rdfs:label oio:hasExactSynonym donson-related microcephaly-short stature-limb abnormalities spectrum LEXMATCH -MONDO:0054549 peroxisome biogenesis disorder 10B skos:exactMatch DOID:0081440 Peroxisome biogenesis disorder 10B semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:617370 LEXMATCH -MONDO:0060533 microcephaly, short stature, and limb abnormalities skos:exactMatch DOID:0081431 microcephaly, short stature, and limb abnormalities semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:617604 LEXMATCH MONDO:0100140 obsolete mild COVID-19 infection skos:exactMatch DOID:0081014 non-severe COVID-19 semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0100142 obsolete severe COVID-19 infection skos:exactMatch DOID:0081013 severe COVID-19 semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0100143 obsolete critical COVID-19 infection skos:exactMatch DOID:0081012 critical COVID-19 semapv:UnspecifiedMatching MONDO_MAPPINGS -MONDO:0800029 interstitial lung disease 2 skos:exactMatch DOID:0060941 interstitial lung disease 1 semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym oio:hasExactSynonym idiopathic pulmonary fibrosis LEXMATCH -MONDO:0859139 blepharophimosis-impaired intellectual development syndrome skos:exactMatch DOID:0081442 blepharophimosis-impaired intellectual development syndrome semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:619293 LEXMATCH -MONDO:0859377 neurodevelopmental disorder with poor growth and behavioral abnormalities skos:exactMatch DOID:0081444 neurodevelopmental disorder with poor growth and behavioral abnormalities semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:620242 LEXMATCH -MONDO:0957240 cone-rod dystrophy 24 skos:exactMatch DOID:0081449 cone-rod dystrophy 24 semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:620342 LEXMATCH -MONDO:0957385 dystonia 37, early-onset, with striatal lesions skos:exactMatch DOID:0060956 dystonia 37, early-onset with striatal lesions semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:620427 LEXMATCH -MONDO:0957539 dystonia 22, juvenile-onset skos:exactMatch DOID:0060966 dystonia 22, juvenile-onset semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:620453 LEXMATCH -MONDO:0957542 dystonia 22, adult-onset skos:exactMatch DOID:0060967 dystonia 22, adult-onset semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:620456 LEXMATCH -MONDO:0958235 Ullrich congenital muscular dystrophy 1B skos:exactMatch DOID:0060942 Ullrich congenital muscular dystrophy 1B semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:620727 LEXMATCH -MONDO:0958236 Ullrich congenital muscular dystrophy 1C skos:exactMatch DOID:0060943 Ullrich congenital muscular dystrophy 1C semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:620728 LEXMATCH -MONDO:0968944 intellectual developmental disorder, autosomal recessive 82 skos:exactMatch DOID:0060947 autosomal recessive intellectual developmental disorder 82 semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:620779 LEXMATCH diff --git a/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_icd10who.tsv b/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_icd10who.tsv index 20d05467..fa9f055c 100644 --- a/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_icd10who.tsv +++ b/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_icd10who.tsv @@ -764,6 +764,7 @@ MONDO:0007955 Meckel diverticulum skos:exactMatch ICD10WHO:Q43.0 Meckel divertic MONDO:0008007 tooth ankylosis skos:exactMatch ICD10WHO:K03.5 Ankylosis of teeth semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label ankylosis of teeth LEXMATCH MONDO:0008015 motion sickness skos:exactMatch ICD10WHO:T75.3 Motion sickness semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label motion sickness LEXMATCH MONDO:0008054 juvenile dermatomyositis skos:exactMatch ICD10WHO:M33.0 Juvenile dermatomyositis semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label juvenile dermatomyositis LEXMATCH +MONDO:0008109 ocular cicatricial pemphigoid skos:exactMatch ICD10WHO:H13.3 Ocular pemphigoid semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label ocular pemphigoid LEXMATCH MONDO:0008114 obsessive-compulsive disorder skos:exactMatch ICD10WHO:F42 Obsessive-compulsive disorder semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label obsessive-compulsive disorder LEXMATCH MONDO:0008159 postmenopausal osteoporosis skos:exactMatch ICD10WHO:M81.0 Postmenopausal osteoporosis semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label postmenopausal osteoporosis LEXMATCH MONDO:0008170 ovarian cancer skos:exactMatch ICD10WHO:C56 Malignant neoplasm of ovary semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label malignant neoplasm of ovary LEXMATCH @@ -1101,7 +1102,6 @@ MONDO:0020502 yellow fever skos:exactMatch ICD10WHO:A95 Yellow fever semapv:Lexi MONDO:0020502 yellow fever skos:exactMatch ICD10WHO:A95.0 Sylvatic yellow fever semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label sylvatic yellow fever LEXMATCH MONDO:0020502 yellow fever skos:exactMatch ICD10WHO:A95.1 Urban yellow fever semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label urban yellow fever LEXMATCH MONDO:0020528 ACTH-dependent Cushing syndrome skos:exactMatch ICD10WHO:E24.0 Pituitary-dependent Cushing disease semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label pituitary-dependent cushing disease LEXMATCH -MONDO:0020548 ocular pemphigoid skos:exactMatch ICD10WHO:H13.3 Ocular pemphigoid semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label ocular pemphigoid LEXMATCH MONDO:0020568 cutaneous myiasis skos:exactMatch ICD10WHO:B87.0 Cutaneous myiasis semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label cutaneous myiasis LEXMATCH MONDO:0020599 acquired coagulation factor deficiency skos:exactMatch ICD10WHO:D68.4 Acquired coagulation factor deficiency semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label acquired coagulation factor deficiency LEXMATCH MONDO:0020600 acute pharyngitis skos:exactMatch ICD10WHO:J02 Acute pharyngitis semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label acute pharyngitis LEXMATCH diff --git a/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_icd11.foundation.tsv b/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_icd11.foundation.tsv index 2ca3aaec..267df1b1 100644 --- a/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_icd11.foundation.tsv +++ b/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_icd11.foundation.tsv @@ -4315,6 +4315,7 @@ MONDO:0008108 oculocerebrocutaneous syndrome skos:exactMatch icd11.foundation:41 MONDO:0008108 oculocerebrocutaneous syndrome skos:exactMatch icd11.foundation:417997287 Oculo-cerebro-cutaneous syndrome semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym oio:hasExactSynonym leichtman-wood-rohn syndrome LEXMATCH MONDO:0008108 oculocerebrocutaneous syndrome skos:exactMatch icd11.foundation:417997287 Oculo-cerebro-cutaneous syndrome semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym oio:hasExactSynonym orbital cyst with cerebral and focal dermal malformations LEXMATCH MONDO:0008109 ocular cicatricial pemphigoid skos:exactMatch icd11.foundation:953963439 Mucous membrane pemphigoid with ocular involvement semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym oio:hasExactSynonym ocular cicatricial pemphigoid LEXMATCH +MONDO:0008109 ocular cicatricial pemphigoid skos:exactMatch icd11.foundation:953963439 Mucous membrane pemphigoid with ocular involvement semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym oio:hasExactSynonym ocular pemphigoid LEXMATCH MONDO:0008109 ocular cicatricial pemphigoid skos:exactMatch icd11.foundation:953963439 Mucous membrane pemphigoid with ocular involvement semapv:LexicalMatching oaklib 0.8 rdfs:label oio:hasExactSynonym ocular cicatricial pemphigoid LEXMATCH MONDO:0008111 oculodentodigital dysplasia skos:exactMatch icd11.foundation:1440334374 Oculo-dento-digital dysplasia semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label oculo-dento-digital dysplasia LEXMATCH MONDO:0008114 obsessive-compulsive disorder skos:exactMatch icd11.foundation:1582741816 Obsessive-compulsive disorder semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label obsessive-compulsive disorder LEXMATCH @@ -8781,7 +8782,6 @@ MONDO:0020533 streptobacillary rat-bite fever skos:exactMatch icd11.foundation:6 MONDO:0020535 house allergic alveolitis skos:exactMatch icd11.foundation:1985023223 House allergic alveolitis semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label house allergic alveolitis LEXMATCH MONDO:0020540 ovarian gynandroblastoma skos:exactMatch icd11.foundation:278327610 Gynandroblastoma of ovary semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label gynandroblastoma of ovary LEXMATCH MONDO:0020542 malignant Sertoli-Leydig cell tumor of ovary skos:exactMatch icd11.foundation:1092610858 Ovarian malignant Sertoli-Leydig cell tumour semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label ovarian malignant sertoli-leydig cell tumour LEXMATCH -MONDO:0020548 ocular pemphigoid skos:exactMatch icd11.foundation:953963439 Mucous membrane pemphigoid with ocular involvement semapv:LexicalMatching oaklib 0.8 rdfs:label oio:hasExactSynonym ocular pemphigoid LEXMATCH MONDO:0020549 invasive hydatidiform mole skos:exactMatch icd11.foundation:1784853924 Chorioadenoma destruens semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label chorioadenoma destruens LEXMATCH MONDO:0020549 invasive hydatidiform mole skos:exactMatch icd11.foundation:1940625642 Invasive hydatidiform mole semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label invasive hydatidiform mole LEXMATCH MONDO:0020549 invasive hydatidiform mole skos:exactMatch icd11.foundation:8044628 Invasive mole semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym oio:hasExactSynonym invasive hydatidiform mole LEXMATCH diff --git a/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_ncit.tsv b/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_ncit.tsv index 4c4bc291..ffe960ab 100644 --- a/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_ncit.tsv +++ b/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_ncit.tsv @@ -1,6 +1,7 @@ subject_id subject_label predicate_id object_id object_label mapping_justification mapping_tool confidence subject_match_field object_match_field match_string comment MONDO:0000376 respiratory system cancer skos:exactMatch NCIT:C4571 Malignant Respiratory System Neoplasm semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label malignant respiratory system neoplasm LEXMATCH MONDO:0000651 obsolete thoracic disorder skos:exactMatch NCIT:C35742 Thoracic Disorder semapv:UnspecifiedMatching MONDO_MAPPINGS +MONDO:0000930 nodular malignant melanoma skos:exactMatch NCIT:C205125 Nodular Melanoma semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label nodular melanoma LEXMATCH MONDO:0001580 lacrimal duct cancer skos:exactMatch NCIT:C175319 Malignant Lacrimal Drainage System Neoplasm semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label malignant lacrimal drainage system neoplasm LEXMATCH MONDO:0002038 head and neck carcinoma skos:exactMatch NCIT:C6077 Neck Carcinoma semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label neck carcinoma LEXMATCH MONDO:0002063 obsolete breast papillomatosis skos:exactMatch NCIT:C6977 Breast Papillomatosis semapv:UnspecifiedMatching MONDO_MAPPINGS @@ -12,12 +13,17 @@ MONDO:0002691 liver cancer skos:exactMatch NCIT:C190593 Malignant Liver Neoplasm MONDO:0002877 cervical carcinosarcoma skos:exactMatch NCIT:C40226 Cervical Mixed Epithelial and Mesenchymal Neoplasm semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label cervical mixed epithelial and mesenchymal neoplasm LEXMATCH MONDO:0002928 carcinosarcoma skos:exactMatch NCIT:C3730 Mixed Mesodermal (Mullerian) Tumor semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label mixed mesodermal (mullerian) tumor LEXMATCH MONDO:0002928 carcinosarcoma skos:exactMatch NCIT:C8975 Malignant Mixed Mesodermal (Mullerian) Tumor semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label malignant mixed mesodermal (mullerian) tumor LEXMATCH +MONDO:0002938 metatypical basal cell carcinoma skos:exactMatch NCIT:C66903 Skin Metatypical Carcinoma semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0003043 obsolete extraskeletal mesenchymal chondrosarcoma skos:exactMatch NCIT:C27481 Mesenchymal Extraskeletal Chondrosarcoma semapv:UnspecifiedMatching MONDO_MAPPINGS +MONDO:0003222 central nervous system melanocytic neoplasm skos:exactMatch NCIT:C4661 Central Nervous System Melanocytic Neoplasm semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label central nervous system melanocytic neoplasm LEXMATCH +MONDO:0003222 central nervous system melanocytic neoplasm skos:exactMatch NCIT:C5504 Central Nervous System Melanocytic Neoplasm semapv:UnspecifiedMatching MONDO_MAPPINGS +MONDO:0003450 eccrine papillary adenoma skos:exactMatch NCIT:C4173 Papillary Eccrine Adenoma semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0003531 papillary eccrine carcinoma skos:exactMatch NCIT:C27527 Tubular Apocrine Adenoma semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label tubular apocrine adenoma LEXMATCH MONDO:0003649 esophageal neuroendocrine tumor skos:exactMatch NCIT:C5821 Esophageal Neuroendocrine Neoplasm semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label esophageal neuroendocrine neoplasm LEXMATCH MONDO:0003822 non-invasive bladder papillary urothelial neoplasm skos:exactMatch NCIT:C191672 Papillary Urothelial Neoplasm of Low Malignant Potential semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label papillary urothelial neoplasm of low malignant potential LEXMATCH MONDO:0003998 obsolete vaginal tubular adenoma skos:exactMatch NCIT:C40257 Vaginal Tubular Adenoma semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0004075 infiltrating lipoma skos:exactMatch NCIT:C7450 Intramuscular Lipoma semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label intramuscular lipoma LEXMATCH +MONDO:0004141 melanomatosis skos:exactMatch NCIT:C9499 Melanomatosis semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0004180 benign urinary system neoplasm skos:exactMatch NCIT:C192667 Benign Urinary Tract Neoplasm semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label benign urinary tract neoplasm LEXMATCH MONDO:0004204 squamous cell skin papilloma skos:exactMatch NCIT:C4462 Skin Squamous Papilloma semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0004419 lymphoma-like variant infiltrating bladder urothelial carcinoma skos:exactMatch NCIT:C39822 Infiltrating Bladder Urothelial Carcinoma, Lymphoma-Like Variant semapv:UnspecifiedMatching MONDO_MAPPINGS @@ -28,7 +34,10 @@ MONDO:0004819 indolent plasma cell myeloma skos:exactMatch NCIT:C7150 Indolent M MONDO:0004957 mucinous adenocarcinoma skos:exactMatch NCIT:C27379 Mucin-Producing Adenocarcinoma semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label mucin-producing adenocarcinoma LEXMATCH MONDO:0005004 clear cell adenocarcinoma skos:exactMatch NCIT:C4156 Water-Clear Cell Adenocarcinoma semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label water-clear cell adenocarcinoma LEXMATCH MONDO:0005065 mesothelioma skos:exactMatch NCIT:C3234 Mesothelioma semapv:UnspecifiedMatching MONDO_MAPPINGS +MONDO:0005104 aJCC grade 1 sarcoma skos:exactMatch NCIT:C9419 AJCC Grade 1 Sarcoma semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0005362 erectile dysfunction skos:exactMatch NCIT:C34801 Male Erectile Disorder semapv:UnspecifiedMatching MONDO_MAPPINGS +MONDO:0005369 carcinoid tumor skos:exactMatch NCIT:C203250 Neuroendocrine Tumor G1 semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label neuroendocrine tumor g1 LEXMATCH +MONDO:0005369 carcinoid tumor skos:exactMatch NCIT:C2915 Carcinoid Tumor semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0006295 malignant urinary system neoplasm skos:exactMatch NCIT:C192668 Malignant Urinary Tract Neoplasm semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label malignant urinary tract neoplasm LEXMATCH MONDO:0006315 obsolete neoplastic medium-sized B-lymphocyte with basophilic cytoplasm skos:exactMatch NCIT:C37005 Neoplastic Medium-Sized B-Lymphocyte with Basophilic Cytoplasm semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0006329 olfactory neuroblastoma skos:exactMatch NCIT:C6016 Paranasal Sinus Olfactory Neuroblastoma semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label paranasal sinus olfactory neuroblastoma LEXMATCH @@ -36,11 +45,16 @@ MONDO:0006363 peritoneal multicystic mesothelioma skos:exactMatch NCIT:C3765 Mul MONDO:0006451 thymic carcinoma skos:exactMatch NCIT:C7612 Malignant Thymoma semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label malignant thymoma LEXMATCH MONDO:0006475 obsolete unclassified renal cell carcinoma skos:exactMatch NCIT:C27892 Unclassified Renal Cell Carcinoma semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0006717 cutaneous fibrous histiocytoma skos:exactMatch NCIT:C8402 Fibrohistiocytic Neoplasm semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label fibrohistiocytic neoplasm LEXMATCH +MONDO:0006738 eccrine acrospiroma skos:exactMatch NCIT:C205462 Eccrine Poroma semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label eccrine poroma LEXMATCH MONDO:0009933 congenital pulmonary lymphangiectasia skos:exactMatch NCIT:C45630 Diffuse Pulmonary Lymphangiomatosis semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label diffuse pulmonary lymphangiomatosis LEXMATCH +MONDO:0013171 purine nucleoside phosphorylase deficiency skos:exactMatch NCIT:C3963 Purine-Nucleoside Phosphorylase Deficiency semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0015040 myelodysplastic syndrome with excess blasts-1 skos:exactMatch NCIT:C7167 Myelodysplastic Syndrome with Excess Blasts-1 semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0015301 primary cutaneous amyloidosis skos:exactMatch NCIT:C199391 Primary Cutaneous Amyloidosis semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label primary cutaneous amyloidosis LEXMATCH +MONDO:0015391 nasopharyngeal teratoma skos:exactMatch NCIT:C202982 Nasopharyngeal Teratoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label nasopharyngeal teratoma LEXMATCH +MONDO:0015540 hemophagocytic syndrome skos:exactMatch NCIT:C35439 Hemophagocytic Syndrome semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0015686 primary peritoneal carcinoma skos:exactMatch NCIT:C4182 Serous Surface Papillary Carcinoma semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label serous surface papillary carcinoma LEXMATCH MONDO:0016715 ependymoblastoma skos:exactMatch NCIT:C186534 Embryonal Tumor with Multilayered Rosettes semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label embryonal tumor with multilayered rosettes LEXMATCH +MONDO:0016747 primary melanoma of the central nervous system skos:exactMatch NCIT:C5505 Central Nervous System Melanoma semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0016824 infantile myofibromatosis skos:exactMatch NCIT:C27498 Infantile Hemangiopericytoma semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label infantile hemangiopericytoma LEXMATCH MONDO:0017289 fetal lung interstitial tumor skos:exactMatch NCIT:C190105 Fetal Lung Interstitial Tumor semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label fetal lung interstitial tumor LEXMATCH MONDO:0017308 obsolete Marfan syndrome type 2 skos:exactMatch NCIT:C75007 Marfan Syndrome Type II semapv:UnspecifiedMatching MONDO_MAPPINGS @@ -54,6 +68,7 @@ MONDO:0019468 T-cell prolymphocytic leukemia skos:exactMatch NCIT:C70649 T-Cell MONDO:0019473 enteropathy-associated T-cell lymphoma skos:exactMatch NCIT:C150495 Intestinal T-Cell Lymphoma semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label intestinal t-cell lymphoma LEXMATCH MONDO:0019496 neuroendocrine neoplasm skos:exactMatch NCIT:C188218 Neuroendocrine Tumor semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label neuroendocrine tumor LEXMATCH MONDO:0019500 extragonadal teratoma skos:exactMatch NCIT:C189045 Extragonadal Teratoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label extragonadal teratoma LEXMATCH +MONDO:0019964 thymic neuroendocrine tumor skos:exactMatch NCIT:C6430 Thymic Neuroendocrine Tumor semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label thymic neuroendocrine tumor LEXMATCH MONDO:0020078 obsolete acute myeloid leukemia with recurrent genetic anomaly skos:exactMatch NCIT:C7175 Acute Myeloid Leukemia with Recurrent Genetic Abnormalities semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0020541 maligant granulosa cell tumor of ovary skos:exactMatch NCIT:C7288 Adult Ovarian Granulosa Cell Tumor semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label adult ovarian granulosa cell tumor LEXMATCH MONDO:0020591 obsolete disorder of peritoneum skos:exactMatch NCIT:C26848 Peritoneal Disorder semapv:UnspecifiedMatching MONDO_MAPPINGS @@ -69,7 +84,6 @@ MONDO:0043881 obsolete acute eosinophilic leukemia skos:exactMatch NCIT:C26813 A MONDO:0044037 livedo reticularis skos:exactMatch NCIT:C74524 Livedo Reticularis semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label livedo reticularis LEXMATCH MONDO:0700092 neurodevelopmental disorder skos:exactMatch NCIT:C1535926 semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0700219 neoplastic meningitis skos:exactMatch NCIT:C27383 Meningeal Carcinomatosis semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label meningeal carcinomatosis LEXMATCH -MONDO:0850110 melanoma in congenital melanocytic nevus skos:exactMatch NCIT:C48613 Melanoma in Congenital Melanocytic Nevus semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label melanoma in congenital melanocytic nevus LEXMATCH MONDO:0850112 breast implant-associated anaplastic large cell lymphoma skos:exactMatch NCIT:C139012 Breast Implant-Associated Anaplastic Large Cell Lymphoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label breast implant-associated anaplastic large cell lymphoma LEXMATCH MONDO:0850154 tongue carcinoma skos:exactMatch NCIT:C4824 Tongue Carcinoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label tongue carcinoma LEXMATCH MONDO:0850267 childhood acute megakaryoblastic leukemia skos:exactMatch NCIT:C7972 Childhood Acute Megakaryoblastic Leukemia semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label childhood acute megakaryoblastic leukemia LEXMATCH @@ -121,3 +135,12 @@ MONDO:0958161 B acute lymphoblastic leukemia with PAX5 P80R mutation skos:exactM MONDO:0958162 B acute lymphoblastic leukemia with DUX4 rearrangement skos:exactMatch NCIT:C199232 B Acute Lymphoblastic Leukemia with DUX4 Rearrangement semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label b acute lymphoblastic leukemia with dux4 rearrangement LEXMATCH MONDO:0958164 poorly differentiated chordoma skos:exactMatch NCIT:C177898 Poorly Differentiated Chordoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label poorly differentiated chordoma LEXMATCH MONDO:0958165 anaplastic sarcoma of the kidney skos:exactMatch NCIT:C154496 Anaplastic Sarcoma of the Kidney semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label anaplastic sarcoma of the kidney LEXMATCH +MONDO:0958295 BCOR ITD sarcoma skos:exactMatch NCIT:C178468 BCOR ITD Sarcoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label bcor itd sarcoma LEXMATCH +MONDO:0958296 BCOR-CCNB3 sarcoma skos:exactMatch NCIT:C178466 BCOR-CCNB3 Sarcoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label bcor-ccnb3 sarcoma LEXMATCH +MONDO:0958297 childhood sarcoma with BCOR genetic alterations skos:exactMatch NCIT:C189007 Childhood Sarcoma with BCOR Genetic Alterations semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label childhood sarcoma with bcor genetic alterations LEXMATCH +MONDO:0958298 childhood round cell sarcoma with EWSR1-non-ETS fusion skos:exactMatch NCIT:C189003 Childhood Round Cell Sarcoma with EWSR1-non-ETS Fusion semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label childhood round cell sarcoma with ewsr1-non-ets fusion LEXMATCH +MONDO:0958299 round cell sarcoma with EWSR1-NFATC2 gene fusion skos:exactMatch NCIT:C178460 Round Cell Sarcoma with EWSR1-NFATC2 Gene Fusion semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label round cell sarcoma with ewsr1-nfatc2 gene fusion LEXMATCH +MONDO:0958300 round cell sarcoma with EWSR1-PATZ1 gene fusion skos:exactMatch NCIT:C178461 Round Cell Sarcoma with EWSR1-PATZ1 Gene Fusion semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label round cell sarcoma with ewsr1-patz1 gene fusion LEXMATCH +MONDO:0958301 round cell sarcoma with FUS-NFATC2 gene fusion skos:exactMatch NCIT:C178462 Round Cell Sarcoma with FUS-NFATC2 Gene Fusion semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label round cell sarcoma with fus-nfatc2 gene fusion LEXMATCH +MONDO:0958302 TFEB-rearranged renal cell carcinoma skos:exactMatch NCIT:C37210 TFEB-Rearranged Renal Cell Carcinoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label tfeb-rearranged renal cell carcinoma LEXMATCH +MONDO:0958303 childhood renal cell carcinoma with MiT translocations skos:exactMatch NCIT:C189242 Childhood Renal Cell Carcinoma with MiT Translocations semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label childhood renal cell carcinoma with mit translocations LEXMATCH diff --git a/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_omim.tsv b/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_omim.tsv index 175bb3b6..89c83b5d 100644 --- a/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_omim.tsv +++ b/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_omim.tsv @@ -19,6 +19,7 @@ MONDO:0008204 obsolete patella aplasia, coxa vara, and tarsal synostosis skos:ex MONDO:0008415 obsolete Scholte syndrome skos:exactMatch OMIM:181515 semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0008548 obsolete theophylline Biotransformation skos:exactMatch OMIM:187650 theophylline biotransformation semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0008625 obsolete urate-binding globulin, decrease 1N skos:exactMatch OMIM:191530 urate-binding globulin, decrease 1n semapv:UnspecifiedMatching MONDO_MAPPINGS +MONDO:0008873 microcephalic osteodysplastic primordial dwarfism, type 3 skos:exactMatch OMIM:210730 semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0009535 obsolete lymphedema, congenital recessive skos:exactMatch OMIM:247440 semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0009553 obsolete Plasmodium falciparum blood infection level skos:exactMatch OMIM:248310 plasmodium falciparum blood infection level semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0009586 mesangial sclerosis, diffuse renal, with ocular abnormalities skos:exactMatch OMIM:249660 semapv:UnspecifiedMatching MONDO_MAPPINGS diff --git a/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_omimps.tsv b/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_omimps.tsv index c13538e6..105c656c 100644 --- a/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_omimps.tsv +++ b/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_omimps.tsv @@ -1,7 +1,6 @@ subject_id subject_label predicate_id object_id object_label mapping_justification mapping_tool confidence subject_match_field object_match_field match_string comment MONDO:0000049 obsolete invasive pneumococcal disease, recurrent isolated skos:exactMatch OMIMPS:610799 semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0000218 obsolete preimplantation embryonic lethality skos:exactMatch OMIMPS:616814 semapv:UnspecifiedMatching MONDO_MAPPINGS -MONDO:0015991 citrullinemia skos:exactMatch OMIMPS:215700 Citrullinemia semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label citrullinemia LEXMATCH -MONDO:0018875 Li-Fraumeni syndrome skos:exactMatch OMIMPS:151623 Li-Fraumeni syndrome semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label li-fraumeni syndrome LEXMATCH MONDO:0033196 obsolete skin/hair/eye pigmentation, variation in skos:exactMatch OMIMPS:227220 Skin/hair/eye pigmentation, variation in semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0044278 obsolete short sleeper skos:exactMatch OMIMPS:612975 Short sleep, familial natural semapv:UnspecifiedMatching MONDO_MAPPINGS +MONDO:0859193 neuroocular syndrome skos:exactMatch OMIMPS:619539 Neuroocular syndrome semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label neuroocular syndrome LEXMATCH diff --git a/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_orphanet.tsv b/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_orphanet.tsv index ae92ed2c..5795f009 100644 --- a/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_orphanet.tsv +++ b/src/ontology/lexmatch/split-mapping-set/mondo_exactmatch_orphanet.tsv @@ -502,8 +502,8 @@ MONDO:0018775 obsolete axonal hereditary motor and sensory neuropathy skos:exact MONDO:0018779 obsolete hypercontractile muscle stiffness syndrome skos:exactMatch Orphanet:476403 Hypercontractile muscle stiffness syndrome semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0018787 obsolete genetic cerebral small vessel disease skos:exactMatch Orphanet:477754 Genetic cerebral small vessel disease semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0018788 obsolete COL4A1 or COL4A2-related cerebral small vessel disease skos:exactMatch Orphanet:477759 COL4A1 or COL4A2-related cerebral small vessel disease semapv:UnspecifiedMatching MONDO_MAPPINGS -MONDO:0018789 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with ischemic tendancy skos:exactMatch Orphanet:477762 COL4A1 or COL4A2-related cerebral small vessel disease with ischemic tendancy semapv:UnspecifiedMatching MONDO_MAPPINGS -MONDO:0018790 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendancy skos:exactMatch Orphanet:477765 COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendancy semapv:UnspecifiedMatching MONDO_MAPPINGS +MONDO:0018789 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with ischemic tendency skos:exactMatch Orphanet:477762 COL4A1 or COL4A2-related cerebral small vessel disease with ischemic tendancy semapv:UnspecifiedMatching MONDO_MAPPINGS +MONDO:0018790 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendency skos:exactMatch Orphanet:477765 COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendancy semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0018791 obsolete Moyomoya angiopathy skos:exactMatch Orphanet:477768 Moyamoya angiopathy semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0018792 obsolete Moyamoya syndrome skos:exactMatch Orphanet:477771 Rare disorder with a moyamoya angiopathy semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0018796 obsolete isolated constitutional thrombocytopenia skos:exactMatch Orphanet:477797 Isolated constitutional thrombocytopenia semapv:UnspecifiedMatching MONDO_MAPPINGS @@ -619,7 +619,6 @@ MONDO:0020027 obsolete rare allergic disease skos:exactMatch Orphanet:98050 Rare MONDO:0020028 obsolete rare allergic respiratory disease skos:exactMatch Orphanet:98052 Rare allergic respiratory disease semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0020029 obsolete rare genetic cardiac disease skos:exactMatch Orphanet:98054 Rare genetic cardiac disease semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0020030 obsolete rare genetic renal disease skos:exactMatch Orphanet:98056 Rare genetic renal disease semapv:UnspecifiedMatching MONDO_MAPPINGS -MONDO:0020031 obsolete rare tumor skos:exactMatch Orphanet:98057 Rare tumor semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0020032 obsolete rare urinary tract tumor skos:exactMatch Orphanet:98058 Rare urinary tract tumor semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0020033 obsolete rare digestive tumor skos:exactMatch Orphanet:98059 Rare digestive tumor semapv:UnspecifiedMatching MONDO_MAPPINGS MONDO:0020034 obsolete rare respiratory tract neoplasm skos:exactMatch Orphanet:98060 Rare respiratory tumor semapv:UnspecifiedMatching MONDO_MAPPINGS diff --git a/src/ontology/lexmatch/unmapped_doid_lex.tsv b/src/ontology/lexmatch/unmapped_doid_lex.tsv index f046e0ee..8673660b 100644 --- a/src/ontology/lexmatch/unmapped_doid_lex.tsv +++ b/src/ontology/lexmatch/unmapped_doid_lex.tsv @@ -1,15 +1,3 @@ subject_id subject_label object_id predicate_id object_label mapping_justification mapping_tool confidence subject_match_field object_match_field match_string ID A oboInOwl:hasDbXref >A oboInOwl:source -MONDO:0007495 dystonia 5 DOID:0060963 MONDO:equivalentTo dystonia, DOPA-responsive semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:128230 MONDO:0009669 spinal muscular atrophy, type 1 DOID:0060160 MONDO:equivalentTo childhood spinal muscular atrophy semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym oio:hasExactSynonym survival motor neuron spinal muscular atrophy -MONDO:0009849 hyperimmunoglobulinemia D with periodic fever DOID:0081450 MONDO:equivalentTo hyperimmunoglobulinemia D periodic fever syndrome semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:260920 -MONDO:0011053 intellectual disability-sparse hair-brachydactyly syndrome DOID:0081441 MONDO:equivalentTo Nicolaides-Baraitser syndrome semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:601358 -MONDO:0011382 sickle cell anemia DOID:0081445 MONDO:equivalentTo sickle cell disease semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:603903 -MONDO:0030538 dystonia 34, myoclonic DOID:0060957 MONDO:equivalentTo myoclonic dystonia 34 semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:619724 -MONDO:0031084 amelogenesis imperfecta, IIa 1K DOID:0060945 MONDO:equivalentTo amelogenesis imperfecta type 1K semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:620104 -MONDO:0032790 neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities DOID:0081443 MONDO:equivalentTo Stolerman neurodevelopmental syndrome semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:618505 -MONDO:0032849 neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies DOID:0070539 MONDO:equivalentTo Halperin-Birk syndrome semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:618651 -MONDO:0035534 DONSON-related microcephaly-short stature-limb abnormalities spectrum DOID:0081431 MONDO:equivalentTo microcephaly, short stature, and limb abnormalities semapv:LexicalMatching oaklib 0.8 rdfs:label oio:hasExactSynonym donson-related microcephaly-short stature-limb abnormalities spectrum -MONDO:0800029 interstitial lung disease 2 DOID:0060941 MONDO:equivalentTo interstitial lung disease 1 semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym oio:hasExactSynonym idiopathic pulmonary fibrosis -MONDO:0957385 dystonia 37, early-onset, with striatal lesions DOID:0060956 MONDO:equivalentTo dystonia 37, early-onset with striatal lesions semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:620427 -MONDO:0968944 intellectual developmental disorder, autosomal recessive 82 DOID:0060947 MONDO:equivalentTo autosomal recessive intellectual developmental disorder 82 semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:620779 diff --git a/src/ontology/lexmatch/unmapped_doid_lex_exact.tsv b/src/ontology/lexmatch/unmapped_doid_lex_exact.tsv index 887df763..bab9455e 100644 --- a/src/ontology/lexmatch/unmapped_doid_lex_exact.tsv +++ b/src/ontology/lexmatch/unmapped_doid_lex_exact.tsv @@ -1,33 +1,5 @@ subject_id subject_label object_id predicate_id object_label mapping_justification mapping_tool confidence subject_match_field object_match_field match_string ID A oboInOwl:hasDbXref >A oboInOwl:source +MONDO:0005641 aleutian mink disease DOID:2934 MONDO:equivalentTo aleutian mink disease semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label aleutian mink disease +MONDO:0005676 borna disease DOID:5154 MONDO:equivalentTo borna disease semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label borna disease MONDO:0007744 cholesterol-ester transfer protein deficiency DOID:0111368 MONDO:equivalentTo cholesterol-ester transfer protein deficiency semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label cholesterol-ester transfer protein deficiency -MONDO:0009619 microcephaly-micromelia syndrome DOID:0081432 MONDO:equivalentTo microcephaly-micromelia syndrome semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:251230 -MONDO:0009681 Ullrich congenital muscular dystrophy 1A DOID:0060946 MONDO:equivalentTo Ullrich congenital muscular dystrophy 1A semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:254090 -MONDO:0011610 dimethylglycine dehydrogenase deficiency DOID:0081446 MONDO:equivalentTo dimethylglycine dehydrogenase deficiency semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:605850 -MONDO:0013931 peroxisome biogenesis disorder 4B DOID:0081433 MONDO:equivalentTo Peroxisome biogenesis disorder 4B semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:614863 -MONDO:0013933 peroxisome biogenesis disorder 5B DOID:0081434 MONDO:equivalentTo Peroxisome biogenesis disorder 5B semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:614867 -MONDO:0013937 peroxisome biogenesis disorder 6B DOID:0081435 MONDO:equivalentTo Peroxisome biogenesis disorder 6B semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:614871 -MONDO:0013939 peroxisome biogenesis disorder 7B DOID:0081436 MONDO:equivalentTo Peroxisome biogenesis disorder 7B semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:614873 -MONDO:0013943 peroxisome biogenesis disorder 8B DOID:0081437 MONDO:equivalentTo Peroxisome biogenesis disorder 8B semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:614877 -MONDO:0013945 peroxisome biogenesis disorder 9B DOID:0081438 MONDO:equivalentTo Peroxisome biogenesis disorder 9B semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:614879 -MONDO:0013950 peroxisome biogenesis disorder 11B DOID:0081439 MONDO:equivalentTo Peroxisome biogenesis disorder 11B semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:614885 -MONDO:0014654 Ullrich congenital muscular dystrophy 2 DOID:0060944 MONDO:equivalentTo Ullrich congenital muscular dystrophy 2 semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:616470 -MONDO:0014669 cone-rod dystrophy 21 DOID:0081447 MONDO:equivalentTo cone-rod dystrophy 21 semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:616502 -MONDO:0015004 dystonia 28, childhood-onset DOID:0060936 MONDO:equivalentTo dystonia 28, childhood-onset semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:617284 -MONDO:0018540 PFAPA syndrome DOID:0081451 MONDO:equivalentTo PFAPA syndrome semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label pfapa syndrome -MONDO:0025691 dystonia 30 DOID:0060937 MONDO:equivalentTo dystonia 30 semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:619291 -MONDO:0030440 cone-rod dystrophy 22 DOID:0081448 MONDO:equivalentTo cone-rod dystrophy 22 semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:619531 -MONDO:0030455 dystonia 31 DOID:0060938 MONDO:equivalentTo dystonia 31 semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:619565 -MONDO:0030486 dystonia 32 DOID:0060939 MONDO:equivalentTo dystonia 32 semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:619637 -MONDO:0030513 dystonia 33 DOID:0060940 MONDO:equivalentTo dystonia 33 semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:619687 -MONDO:0030608 interstitial lung disease 1 DOID:0060941 MONDO:equivalentTo interstitial lung disease 1 semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:619611 -MONDO:0030958 dystonia 35, childhood-onset DOID:0060955 MONDO:equivalentTo dystonia 35, childhood-onset semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:619921 -MONDO:0054549 peroxisome biogenesis disorder 10B DOID:0081440 MONDO:equivalentTo Peroxisome biogenesis disorder 10B semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:617370 -MONDO:0060533 microcephaly, short stature, and limb abnormalities DOID:0081431 MONDO:equivalentTo microcephaly, short stature, and limb abnormalities semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:617604 -MONDO:0859139 blepharophimosis-impaired intellectual development syndrome DOID:0081442 MONDO:equivalentTo blepharophimosis-impaired intellectual development syndrome semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:619293 -MONDO:0859377 neurodevelopmental disorder with poor growth and behavioral abnormalities DOID:0081444 MONDO:equivalentTo neurodevelopmental disorder with poor growth and behavioral abnormalities semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:620242 -MONDO:0957240 cone-rod dystrophy 24 DOID:0081449 MONDO:equivalentTo cone-rod dystrophy 24 semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:620342 -MONDO:0957539 dystonia 22, juvenile-onset DOID:0060966 MONDO:equivalentTo dystonia 22, juvenile-onset semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:620453 -MONDO:0957542 dystonia 22, adult-onset DOID:0060967 MONDO:equivalentTo dystonia 22, adult-onset semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:620456 -MONDO:0958235 Ullrich congenital muscular dystrophy 1B DOID:0060942 MONDO:equivalentTo Ullrich congenital muscular dystrophy 1B semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:620727 -MONDO:0958236 Ullrich congenital muscular dystrophy 1C DOID:0060943 MONDO:equivalentTo Ullrich congenital muscular dystrophy 1C semapv:LexicalMatching oaklib 0.9411764705882353 skos:exactMatch skos:exactMatch omim:620728 diff --git a/src/ontology/lexmatch/unmapped_icd10who_lex.tsv b/src/ontology/lexmatch/unmapped_icd10who_lex.tsv index 20fc5452..39853c30 100644 --- a/src/ontology/lexmatch/unmapped_icd10who_lex.tsv +++ b/src/ontology/lexmatch/unmapped_icd10who_lex.tsv @@ -296,6 +296,7 @@ MONDO:0007885 Legg-Calve-Perthes disease ICD10WHO:M91 MONDO:equivalentTo Juvenil MONDO:0007885 Legg-Calve-Perthes disease ICD10WHO:M91.2 MONDO:equivalentTo Coxa plana semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label coxa plana MONDO:0007885 Legg-Calve-Perthes disease ICD10WHO:M91.3 MONDO:equivalentTo Pseudocoxalgia semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label pseudocoxalgia MONDO:0008007 tooth ankylosis ICD10WHO:K03.5 MONDO:equivalentTo Ankylosis of teeth semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label ankylosis of teeth +MONDO:0008109 ocular cicatricial pemphigoid ICD10WHO:H13.3 MONDO:equivalentTo Ocular pemphigoid semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label ocular pemphigoid MONDO:0008170 ovarian cancer ICD10WHO:C56 MONDO:equivalentTo Malignant neoplasm of ovary semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label malignant neoplasm of ovary MONDO:0008171 nephrolithiasis ICD10WHO:N20 MONDO:equivalentTo Calculus of kidney and ureter semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label calculus of kidney and ureter MONDO:0008231 Peyronie disease ICD10WHO:N48.6 MONDO:equivalentTo Induratio penis plastica semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label induratio penis plastica diff --git a/src/ontology/lexmatch/unmapped_icd10who_lex_exact.tsv b/src/ontology/lexmatch/unmapped_icd10who_lex_exact.tsv index 8142b3e5..1cd4d177 100644 --- a/src/ontology/lexmatch/unmapped_icd10who_lex_exact.tsv +++ b/src/ontology/lexmatch/unmapped_icd10who_lex_exact.tsv @@ -661,7 +661,6 @@ MONDO:0020356 coloboma of iris ICD10WHO:Q13.0 MONDO:equivalentTo Coloboma of iri MONDO:0020366 congenital glaucoma ICD10WHO:Q15.0 MONDO:equivalentTo Congenital glaucoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label congenital glaucoma MONDO:0020398 congenital mitral stenosis ICD10WHO:Q23.2 MONDO:equivalentTo Congenital mitral stenosis semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label congenital mitral stenosis MONDO:0020502 yellow fever ICD10WHO:A95 MONDO:equivalentTo Yellow fever semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label yellow fever -MONDO:0020548 ocular pemphigoid ICD10WHO:H13.3 MONDO:equivalentTo Ocular pemphigoid semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label ocular pemphigoid MONDO:0020568 cutaneous myiasis ICD10WHO:B87.0 MONDO:equivalentTo Cutaneous myiasis semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label cutaneous myiasis MONDO:0020599 acquired coagulation factor deficiency ICD10WHO:D68.4 MONDO:equivalentTo Acquired coagulation factor deficiency semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label acquired coagulation factor deficiency MONDO:0020600 acute pharyngitis ICD10WHO:J02 MONDO:equivalentTo Acute pharyngitis semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label acute pharyngitis diff --git a/src/ontology/lexmatch/unmapped_icd11foundation_lex.tsv b/src/ontology/lexmatch/unmapped_icd11foundation_lex.tsv index 3622824e..cf08d64c 100644 --- a/src/ontology/lexmatch/unmapped_icd11foundation_lex.tsv +++ b/src/ontology/lexmatch/unmapped_icd11foundation_lex.tsv @@ -3100,6 +3100,7 @@ MONDO:0008108 oculocerebrocutaneous syndrome icd11.foundation:417997287 MONDO:eq MONDO:0008108 oculocerebrocutaneous syndrome icd11.foundation:417997287 MONDO:equivalentTo Oculo-cerebro-cutaneous syndrome semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym oio:hasExactSynonym leichtman-wood-rohn syndrome MONDO:0008108 oculocerebrocutaneous syndrome icd11.foundation:417997287 MONDO:equivalentTo Oculo-cerebro-cutaneous syndrome semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym oio:hasExactSynonym orbital cyst with cerebral and focal dermal malformations MONDO:0008109 ocular cicatricial pemphigoid icd11.foundation:953963439 MONDO:equivalentTo Mucous membrane pemphigoid with ocular involvement semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym oio:hasExactSynonym ocular cicatricial pemphigoid +MONDO:0008109 ocular cicatricial pemphigoid icd11.foundation:953963439 MONDO:equivalentTo Mucous membrane pemphigoid with ocular involvement semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym oio:hasExactSynonym ocular pemphigoid MONDO:0008109 ocular cicatricial pemphigoid icd11.foundation:953963439 MONDO:equivalentTo Mucous membrane pemphigoid with ocular involvement semapv:LexicalMatching oaklib 0.8 rdfs:label oio:hasExactSynonym ocular cicatricial pemphigoid MONDO:0008111 oculodentodigital dysplasia icd11.foundation:1440334374 MONDO:equivalentTo Oculo-dento-digital dysplasia semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label oculo-dento-digital dysplasia MONDO:0008134 autosomal dominant optic atrophy, classic form icd11.foundation:1745857753 MONDO:equivalentTo Childhood-onset autosomal dominant optic atrophy semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym oio:hasExactSynonym autosomal dominant optic atrophy, kjer type @@ -5480,7 +5481,6 @@ MONDO:0020533 streptobacillary rat-bite fever icd11.foundation:614000128 MONDO:e MONDO:0020533 streptobacillary rat-bite fever icd11.foundation:614000128 MONDO:equivalentTo Streptobacillosis semapv:LexicalMatching oaklib 0.8 rdfs:label oio:hasExactSynonym streptobacillary rat-bite fever MONDO:0020540 ovarian gynandroblastoma icd11.foundation:278327610 MONDO:equivalentTo Gynandroblastoma of ovary semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label gynandroblastoma of ovary MONDO:0020542 malignant Sertoli-Leydig cell tumor of ovary icd11.foundation:1092610858 MONDO:equivalentTo Ovarian malignant Sertoli-Leydig cell tumour semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label ovarian malignant sertoli-leydig cell tumour -MONDO:0020548 ocular pemphigoid icd11.foundation:953963439 MONDO:equivalentTo Mucous membrane pemphigoid with ocular involvement semapv:LexicalMatching oaklib 0.8 rdfs:label oio:hasExactSynonym ocular pemphigoid MONDO:0020549 invasive hydatidiform mole icd11.foundation:1784853924 MONDO:equivalentTo Chorioadenoma destruens semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label chorioadenoma destruens MONDO:0020549 invasive hydatidiform mole icd11.foundation:8044628 MONDO:equivalentTo Invasive mole semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym oio:hasExactSynonym invasive hydatidiform mole MONDO:0020549 invasive hydatidiform mole icd11.foundation:8044628 MONDO:equivalentTo Invasive mole semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label invasive mole diff --git a/src/ontology/lexmatch/unmapped_ncit_lex.tsv b/src/ontology/lexmatch/unmapped_ncit_lex.tsv index 02dc78cc..1e319f5a 100644 --- a/src/ontology/lexmatch/unmapped_ncit_lex.tsv +++ b/src/ontology/lexmatch/unmapped_ncit_lex.tsv @@ -1,6 +1,7 @@ subject_id subject_label object_id predicate_id object_label mapping_justification mapping_tool confidence subject_match_field object_match_field match_string ID A oboInOwl:hasDbXref >A oboInOwl:source MONDO:0000376 respiratory system cancer NCIT:C4571 MONDO:equivalentTo Malignant Respiratory System Neoplasm semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label malignant respiratory system neoplasm +MONDO:0000930 nodular malignant melanoma NCIT:C205125 MONDO:equivalentTo Nodular Melanoma semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label nodular melanoma MONDO:0001580 lacrimal duct cancer NCIT:C175319 MONDO:equivalentTo Malignant Lacrimal Drainage System Neoplasm semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label malignant lacrimal drainage system neoplasm MONDO:0002038 head and neck carcinoma NCIT:C6077 MONDO:equivalentTo Neck Carcinoma semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label neck carcinoma MONDO:0002073 malignant pineal area germ cell neoplasm NCIT:C4659 MONDO:equivalentTo Pineal Region Germ Cell Tumor semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label pineal region germ cell tumor @@ -20,11 +21,13 @@ MONDO:0004526 mixed endometrial stromal and smooth muscle tumor NCIT:C40179 MOND MONDO:0004724 submandibular gland cancer NCIT:C3526 MONDO:equivalentTo Malignant Submandibular Gland Neoplasm semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label malignant submandibular gland neoplasm MONDO:0004957 mucinous adenocarcinoma NCIT:C27379 MONDO:equivalentTo Mucin-Producing Adenocarcinoma semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label mucin-producing adenocarcinoma MONDO:0005004 clear cell adenocarcinoma NCIT:C4156 MONDO:equivalentTo Water-Clear Cell Adenocarcinoma semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label water-clear cell adenocarcinoma +MONDO:0005369 carcinoid tumor NCIT:C203250 MONDO:equivalentTo Neuroendocrine Tumor G1 semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label neuroendocrine tumor g1 MONDO:0006295 malignant urinary system neoplasm NCIT:C192668 MONDO:equivalentTo Malignant Urinary Tract Neoplasm semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label malignant urinary tract neoplasm MONDO:0006329 olfactory neuroblastoma NCIT:C6016 MONDO:equivalentTo Paranasal Sinus Olfactory Neuroblastoma semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label paranasal sinus olfactory neuroblastoma MONDO:0006363 peritoneal multicystic mesothelioma NCIT:C3765 MONDO:equivalentTo Multicystic Mesothelioma semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label multicystic mesothelioma MONDO:0006451 thymic carcinoma NCIT:C7612 MONDO:equivalentTo Malignant Thymoma semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label malignant thymoma MONDO:0006717 cutaneous fibrous histiocytoma NCIT:C8402 MONDO:equivalentTo Fibrohistiocytic Neoplasm semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label fibrohistiocytic neoplasm +MONDO:0006738 eccrine acrospiroma NCIT:C205462 MONDO:equivalentTo Eccrine Poroma semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label eccrine poroma MONDO:0009933 congenital pulmonary lymphangiectasia NCIT:C45630 MONDO:equivalentTo Diffuse Pulmonary Lymphangiomatosis semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label diffuse pulmonary lymphangiomatosis MONDO:0015686 primary peritoneal carcinoma NCIT:C4182 MONDO:equivalentTo Serous Surface Papillary Carcinoma semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label serous surface papillary carcinoma MONDO:0016715 ependymoblastoma NCIT:C186534 MONDO:equivalentTo Embryonal Tumor with Multilayered Rosettes semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label embryonal tumor with multilayered rosettes diff --git a/src/ontology/lexmatch/unmapped_ncit_lex_exact.tsv b/src/ontology/lexmatch/unmapped_ncit_lex_exact.tsv index 59c4b9a1..6460ee36 100644 --- a/src/ontology/lexmatch/unmapped_ncit_lex_exact.tsv +++ b/src/ontology/lexmatch/unmapped_ncit_lex_exact.tsv @@ -1,11 +1,13 @@ subject_id subject_label object_id predicate_id object_label mapping_justification mapping_tool confidence subject_match_field object_match_field match_string ID A oboInOwl:hasDbXref >A oboInOwl:source +MONDO:0003222 central nervous system melanocytic neoplasm NCIT:C4661 MONDO:equivalentTo Central Nervous System Melanocytic Neoplasm semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label central nervous system melanocytic neoplasm MONDO:0004520 intratubular embryonal carcinoma NCIT:C192096 MONDO:equivalentTo Intratubular Embryonal Carcinoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label intratubular embryonal carcinoma MONDO:0015301 primary cutaneous amyloidosis NCIT:C199391 MONDO:equivalentTo Primary Cutaneous Amyloidosis semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label primary cutaneous amyloidosis +MONDO:0015391 nasopharyngeal teratoma NCIT:C202982 MONDO:equivalentTo Nasopharyngeal Teratoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label nasopharyngeal teratoma MONDO:0017289 fetal lung interstitial tumor NCIT:C190105 MONDO:equivalentTo Fetal Lung Interstitial Tumor semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label fetal lung interstitial tumor MONDO:0019500 extragonadal teratoma NCIT:C189045 MONDO:equivalentTo Extragonadal Teratoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label extragonadal teratoma +MONDO:0019964 thymic neuroendocrine tumor NCIT:C6430 MONDO:equivalentTo Thymic Neuroendocrine Tumor semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label thymic neuroendocrine tumor MONDO:0044037 livedo reticularis NCIT:C74524 MONDO:equivalentTo Livedo Reticularis semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label livedo reticularis -MONDO:0850110 melanoma in congenital melanocytic nevus NCIT:C48613 MONDO:equivalentTo Melanoma in Congenital Melanocytic Nevus semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label melanoma in congenital melanocytic nevus MONDO:0850112 breast implant-associated anaplastic large cell lymphoma NCIT:C139012 MONDO:equivalentTo Breast Implant-Associated Anaplastic Large Cell Lymphoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label breast implant-associated anaplastic large cell lymphoma MONDO:0850154 tongue carcinoma NCIT:C4824 MONDO:equivalentTo Tongue Carcinoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label tongue carcinoma MONDO:0850267 childhood acute megakaryoblastic leukemia NCIT:C7972 MONDO:equivalentTo Childhood Acute Megakaryoblastic Leukemia semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label childhood acute megakaryoblastic leukemia @@ -57,3 +59,12 @@ MONDO:0958161 B acute lymphoblastic leukemia with PAX5 P80R mutation NCIT:C19926 MONDO:0958162 B acute lymphoblastic leukemia with DUX4 rearrangement NCIT:C199232 MONDO:equivalentTo B Acute Lymphoblastic Leukemia with DUX4 Rearrangement semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label b acute lymphoblastic leukemia with dux4 rearrangement MONDO:0958164 poorly differentiated chordoma NCIT:C177898 MONDO:equivalentTo Poorly Differentiated Chordoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label poorly differentiated chordoma MONDO:0958165 anaplastic sarcoma of the kidney NCIT:C154496 MONDO:equivalentTo Anaplastic Sarcoma of the Kidney semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label anaplastic sarcoma of the kidney +MONDO:0958295 BCOR ITD sarcoma NCIT:C178468 MONDO:equivalentTo BCOR ITD Sarcoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label bcor itd sarcoma +MONDO:0958296 BCOR-CCNB3 sarcoma NCIT:C178466 MONDO:equivalentTo BCOR-CCNB3 Sarcoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label bcor-ccnb3 sarcoma +MONDO:0958297 childhood sarcoma with BCOR genetic alterations NCIT:C189007 MONDO:equivalentTo Childhood Sarcoma with BCOR Genetic Alterations semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label childhood sarcoma with bcor genetic alterations +MONDO:0958298 childhood round cell sarcoma with EWSR1-non-ETS fusion NCIT:C189003 MONDO:equivalentTo Childhood Round Cell Sarcoma with EWSR1-non-ETS Fusion semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label childhood round cell sarcoma with ewsr1-non-ets fusion +MONDO:0958299 round cell sarcoma with EWSR1-NFATC2 gene fusion NCIT:C178460 MONDO:equivalentTo Round Cell Sarcoma with EWSR1-NFATC2 Gene Fusion semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label round cell sarcoma with ewsr1-nfatc2 gene fusion +MONDO:0958300 round cell sarcoma with EWSR1-PATZ1 gene fusion NCIT:C178461 MONDO:equivalentTo Round Cell Sarcoma with EWSR1-PATZ1 Gene Fusion semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label round cell sarcoma with ewsr1-patz1 gene fusion +MONDO:0958301 round cell sarcoma with FUS-NFATC2 gene fusion NCIT:C178462 MONDO:equivalentTo Round Cell Sarcoma with FUS-NFATC2 Gene Fusion semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label round cell sarcoma with fus-nfatc2 gene fusion +MONDO:0958302 TFEB-rearranged renal cell carcinoma NCIT:C37210 MONDO:equivalentTo TFEB-Rearranged Renal Cell Carcinoma semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label tfeb-rearranged renal cell carcinoma +MONDO:0958303 childhood renal cell carcinoma with MiT translocations NCIT:C189242 MONDO:equivalentTo Childhood Renal Cell Carcinoma with MiT Translocations semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label childhood renal cell carcinoma with mit translocations diff --git a/src/ontology/lexmatch/unmapped_omim_lex_exact.tsv b/src/ontology/lexmatch/unmapped_omim_lex_exact.tsv index b83c417f..3fd9064f 100644 --- a/src/ontology/lexmatch/unmapped_omim_lex_exact.tsv +++ b/src/ontology/lexmatch/unmapped_omim_lex_exact.tsv @@ -1,4 +1,3 @@ subject_id subject_label object_id predicate_id object_label mapping_justification mapping_tool confidence subject_match_field object_match_field match_string ID A oboInOwl:hasDbXref >A oboInOwl:source -MONDO:0015991 citrullinemia OMIMPS:215700 MONDO:equivalentTo Citrullinemia semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label citrullinemia -MONDO:0018875 Li-Fraumeni syndrome OMIMPS:151623 MONDO:equivalentTo Li-Fraumeni syndrome semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label li-fraumeni syndrome +MONDO:0859193 neuroocular syndrome OMIMPS:619539 MONDO:equivalentTo Neuroocular syndrome semapv:LexicalMatching oaklib 0.8497788951776651 rdfs:label rdfs:label neuroocular syndrome diff --git a/src/ontology/metadata/doid-metrics.json b/src/ontology/metadata/doid-metrics.json index 8e024eaa..8a9b7509 100644 --- a/src/ontology/metadata/doid-metrics.json +++ b/src/ontology/metadata/doid-metrics.json @@ -4,8 +4,8 @@ "abox_axiom_count_incl": 0, "annotation_property_count": 27, "annotation_property_count_incl": 27, - "axiom_count": 115964, - "axiom_count_incl": 115964, + "axiom_count": 115971, + "axiom_count_incl": 115971, "class_count": 13099, "class_count_incl": 13099, "dataproperty_count": 0, @@ -26,7 +26,7 @@ "obj_property_count_incl": 2, "ontology_anno_count": 11, "ontology_iri": "http://purl.obolibrary.org/obo/mondo/sources/doid.owl", - "ontology_version_iri": "http://purl.obolibrary.org/obo/mondo/sources/2024-05-01/doid.owl", + "ontology_version_iri": "http://purl.obolibrary.org/obo/mondo/sources/2024-05-23/doid.owl", "owl2": true, "owl2_dl": true, "owl2_el": true, @@ -67,14 +67,14 @@ "valid_imports": [], "valid_imports_incl": [], "axiom_type_count": { - "AnnotationAssertion": 86726, + "AnnotationAssertion": 86733, "SubAnnotationPropertyOf": 1, "DisjointClasses": 26, "Declaration": 13127, "SubClassOf": 16084 }, "axiom_type_count_incl": { - "AnnotationAssertion": 86726, + "AnnotationAssertion": 86733, "SubAnnotationPropertyOf": 1, "DisjointClasses": 26, "Declaration": 13127, @@ -111,7 +111,7 @@ "dc": "http://purl.org/dc/terms/" }, "namespace_axiom_count": { - "oboInOwl": 57633, + "oboInOwl": 57634, "owl": 2484, "DOID": 43932, "HP": 118, @@ -125,7 +125,7 @@ "SYMP": 306, "dc11": 2, "rdf": 61, - "IAO": 2205, + "IAO": 2211, "CHEBI": 90, "UBERON": 394, "SO": 17, @@ -134,7 +134,7 @@ "dc": 1 }, "namespace_axiom_count_incl": { - "oboInOwl": 57633, + "oboInOwl": 57634, "owl": 2484, "DOID": 43932, "HP": 118, @@ -148,7 +148,7 @@ "SYMP": 306, "dc11": 2, "rdf": 61, - "IAO": 2205, + "IAO": 2211, "CHEBI": 90, "UBERON": 394, "SO": 17, diff --git a/src/ontology/metadata/gard-metrics.json b/src/ontology/metadata/gard-metrics.json index 9e6c51c2..b1422d95 100644 --- a/src/ontology/metadata/gard-metrics.json +++ b/src/ontology/metadata/gard-metrics.json @@ -26,7 +26,7 @@ "obj_property_count_incl": 0, "ontology_anno_count": 1, "ontology_iri": "http://purl.obolibrary.org/obo/mondo/sources/gard.owl", - "ontology_version_iri": "http://purl.obolibrary.org/obo/mondo/sources/2024-05-01/gard.owl", + "ontology_version_iri": "http://purl.obolibrary.org/obo/mondo/sources/2024-05-23/gard.owl", "owl2": true, "owl2_dl": true, "owl2_el": true, diff --git a/src/ontology/metadata/icd10cm-metrics.json b/src/ontology/metadata/icd10cm-metrics.json index 7592d6af..06b353ad 100644 --- a/src/ontology/metadata/icd10cm-metrics.json +++ b/src/ontology/metadata/icd10cm-metrics.json @@ -26,7 +26,7 @@ "obj_property_count_incl": 0, "ontology_anno_count": 4, "ontology_iri": "http://purl.obolibrary.org/obo/mondo/sources/icd10cm.owl", - "ontology_version_iri": "http://purl.obolibrary.org/obo/mondo/sources/2024-05-01/icd10cm.owl", + "ontology_version_iri": "http://purl.obolibrary.org/obo/mondo/sources/2024-05-23/icd10cm.owl", "owl2": true, "owl2_dl": true, "owl2_el": true, diff --git a/src/ontology/metadata/icd10who-metrics.json b/src/ontology/metadata/icd10who-metrics.json index 7469f026..0270cac4 100644 --- a/src/ontology/metadata/icd10who-metrics.json +++ b/src/ontology/metadata/icd10who-metrics.json @@ -26,7 +26,7 @@ "obj_property_count_incl": 0, "ontology_anno_count": 4, "ontology_iri": "http://purl.obolibrary.org/obo/mondo/sources/icd10who.owl", - "ontology_version_iri": "http://purl.obolibrary.org/obo/mondo/sources/2024-05-01/icd10who.owl", + "ontology_version_iri": "http://purl.obolibrary.org/obo/mondo/sources/2024-05-23/icd10who.owl", "owl2": true, "owl2_dl": true, "owl2_el": true, diff --git a/src/ontology/metadata/icd11foundation-metrics.json b/src/ontology/metadata/icd11foundation-metrics.json index 9f1db3b9..f84aad12 100644 --- a/src/ontology/metadata/icd11foundation-metrics.json +++ b/src/ontology/metadata/icd11foundation-metrics.json @@ -26,7 +26,7 @@ "obj_property_count_incl": 0, "ontology_anno_count": 5, "ontology_iri": "http://purl.obolibrary.org/obo/mondo/sources/icd11foundation.owl", - "ontology_version_iri": "http://purl.obolibrary.org/obo/mondo/sources/2024-05-01/icd11foundation.owl", + "ontology_version_iri": "http://purl.obolibrary.org/obo/mondo/sources/2024-05-23/icd11foundation.owl", "owl2": true, "owl2_dl": true, "owl2_el": true, diff --git a/src/ontology/metadata/ncit-metrics.json b/src/ontology/metadata/ncit-metrics.json index 8ec6a7be..f8e814bb 100644 --- a/src/ontology/metadata/ncit-metrics.json +++ b/src/ontology/metadata/ncit-metrics.json @@ -4,10 +4,10 @@ "abox_axiom_count_incl": 0, "annotation_property_count": 12, "annotation_property_count_incl": 12, - "axiom_count": 612685, - "axiom_count_incl": 612685, - "class_count": 15628, - "class_count_incl": 15628, + "axiom_count": 623834, + "axiom_count_incl": 623834, + "class_count": 15971, + "class_count_incl": 15971, "dataproperty_count": 0, "dataproperty_count_incl": 0, "datatypes_count": 24, @@ -20,13 +20,13 @@ "expressivity_incl": "CINT", "individual_count": 0, "individual_count_incl": 0, - "logical_axiom_count": 32780, - "logical_axiom_count_incl": 32780, + "logical_axiom_count": 33655, + "logical_axiom_count_incl": 33655, "obj_property_count": 0, "obj_property_count_incl": 0, "ontology_anno_count": 7, "ontology_iri": "http://purl.obolibrary.org/obo/mondo/sources/ncit.owl", - "ontology_version_iri": "http://purl.obolibrary.org/obo/mondo/sources/2024-05-01/ncit.owl", + "ontology_version_iri": "http://purl.obolibrary.org/obo/mondo/sources/2024-05-23/ncit.owl", "owl2": true, "owl2_dl": true, "owl2_el": false, @@ -37,13 +37,13 @@ "rdfs": false, "rule_count": 0, "rule_count_incl": 0, - "signature_entity_count": 15664, - "signature_entity_count_incl": 15664, + "signature_entity_count": 16007, + "signature_entity_count_incl": 16007, "syntax": "RDF/XML Syntax", - "tbox_axiom_count": 32780, - "tbox_axiom_count_incl": 32780, - "tboxrbox_axiom_count": 32780, - "tboxrbox_axiom_count_incl": 32780, + "tbox_axiom_count": 33655, + "tbox_axiom_count_incl": 33655, + "tboxrbox_axiom_count": 33655, + "tboxrbox_axiom_count_incl": 33655, "axiom_types": [ "AnnotationAssertion", "EquivalentClasses", @@ -69,28 +69,28 @@ "valid_imports": [], "valid_imports_incl": [], "axiom_type_count": { - "AnnotationAssertion": 564246, - "EquivalentClasses": 6027, + "AnnotationAssertion": 574177, + "EquivalentClasses": 6260, "DatatypeDefinition": 19, "AnnotationPropertyRangeOf": 1, - "Declaration": 15658, - "SubClassOf": 26734 + "Declaration": 16001, + "SubClassOf": 27376 }, "axiom_type_count_incl": { - "AnnotationAssertion": 564246, - "EquivalentClasses": 6027, + "AnnotationAssertion": 574177, + "EquivalentClasses": 6260, "DatatypeDefinition": 19, "AnnotationPropertyRangeOf": 1, - "Declaration": 15658, - "SubClassOf": 26734 + "Declaration": 16001, + "SubClassOf": 27376 }, "class_expression_count": { - "Class": 88896, - "ObjectIntersectionOf": 6027 + "Class": 91288, + "ObjectIntersectionOf": 6260 }, "class_expression_count_incl": { - "Class": 88896, - "ObjectIntersectionOf": 6027 + "Class": 91288, + "ObjectIntersectionOf": 6260 }, "curie_map": { "NCIT": "http://purl.obolibrary.org/obo/NCIT_", @@ -104,27 +104,27 @@ }, "namespace_axiom_count": { "prefix_unknown": 1, - "NCIT": 88937, - "oboInOwl": 371929, - "owl": 5166, + "NCIT": 91329, + "oboInOwl": 377852, + "owl": 5221, "rdf": 19, "IAO": 1, - "rdfs": 187155, + "rdfs": 191108, "dc": 3 }, "namespace_axiom_count_incl": { "prefix_unknown": 1, - "NCIT": 88937, - "oboInOwl": 371929, - "owl": 5166, + "NCIT": 91329, + "oboInOwl": 377852, + "owl": 5221, "rdf": 19, "IAO": 1, - "rdfs": 187155, + "rdfs": 191108, "dc": 3 }, "namespace_entity_count": { "prefix_unknown": 1, - "NCIT": 15650, + "NCIT": 15993, "oboInOwl": 3, "owl": 2, "rdf": 1, @@ -135,7 +135,7 @@ }, "namespace_entity_count_incl": { "prefix_unknown": 1, - "NCIT": 15650, + "NCIT": 15993, "oboInOwl": 3, "owl": 2, "rdf": 1, diff --git a/src/ontology/metadata/omim-metrics.json b/src/ontology/metadata/omim-metrics.json index aa5828d9..d21b7706 100644 --- a/src/ontology/metadata/omim-metrics.json +++ b/src/ontology/metadata/omim-metrics.json @@ -4,10 +4,10 @@ "abox_axiom_count_incl": 0, "annotation_property_count": 18, "annotation_property_count_incl": 18, - "axiom_count": 345588, - "axiom_count_incl": 345588, - "class_count": 19482, - "class_count_incl": 19482, + "axiom_count": 345890, + "axiom_count_incl": 345890, + "class_count": 19488, + "class_count_incl": 19488, "dataproperty_count": 0, "dataproperty_count_incl": 0, "datatypes_count": 2, @@ -20,13 +20,13 @@ "expressivity_incl": "E", "individual_count": 0, "individual_count_incl": 0, - "logical_axiom_count": 22689, - "logical_axiom_count_incl": 22689, + "logical_axiom_count": 22703, + "logical_axiom_count_incl": 22703, "obj_property_count": 7, "obj_property_count_incl": 7, "ontology_anno_count": 1, "ontology_iri": "http://purl.obolibrary.org/obo/mondo/sources/omim.owl", - "ontology_version_iri": "http://purl.obolibrary.org/obo/mondo/sources/2024-05-01/omim.owl", + "ontology_version_iri": "http://purl.obolibrary.org/obo/mondo/sources/2024-05-23/omim.owl", "owl2": true, "owl2_dl": true, "owl2_el": true, @@ -37,13 +37,13 @@ "rdfs": false, "rule_count": 0, "rule_count_incl": 0, - "signature_entity_count": 19509, - "signature_entity_count_incl": 19509, + "signature_entity_count": 19515, + "signature_entity_count_incl": 19515, "syntax": "RDF/XML Syntax", - "tbox_axiom_count": 22689, - "tbox_axiom_count_incl": 22689, - "tboxrbox_axiom_count": 22689, - "tboxrbox_axiom_count_incl": 22689, + "tbox_axiom_count": 22703, + "tbox_axiom_count_incl": 22703, + "tboxrbox_axiom_count": 22703, + "tboxrbox_axiom_count_incl": 22703, "axiom_types": [ "AnnotationAssertion", "SubAnnotationPropertyOf", @@ -65,24 +65,24 @@ "valid_imports": [], "valid_imports_incl": [], "axiom_type_count": { - "AnnotationAssertion": 303395, + "AnnotationAssertion": 303677, "SubAnnotationPropertyOf": 1, - "Declaration": 19503, - "SubClassOf": 22689 + "Declaration": 19509, + "SubClassOf": 22703 }, "axiom_type_count_incl": { - "AnnotationAssertion": 303395, + "AnnotationAssertion": 303677, "SubAnnotationPropertyOf": 1, - "Declaration": 19503, - "SubClassOf": 22689 + "Declaration": 19509, + "SubClassOf": 22703 }, "class_expression_count": { - "Class": 64850, - "ObjectSomeValuesFrom": 17792 + "Class": 64884, + "ObjectSomeValuesFrom": 17798 }, "class_expression_count_incl": { - "Class": 64850, - "ObjectSomeValuesFrom": 17792 + "Class": 64884, + "ObjectSomeValuesFrom": 17798 }, "curie_map": { "oboInOwl": "http://www.geneontology.org/formats/oboInOwl#", @@ -99,35 +99,35 @@ "obo": "http://purl.obolibrary.org/obo/" }, "namespace_axiom_count": { - "prefix_unknown": 87651, - "oboInOwl": 91485, - "MONDO": 19018, - "rdf": 20948, - "owl": 1362, - "IAO": 55204, - "skos": 80849, - "rdfs": 39991, - "biolink": 36809, - "CHR": 7578, - "RO": 17799, + "prefix_unknown": 87727, + "oboInOwl": 91607, + "MONDO": 19033, + "rdf": 20975, + "owl": 1363, + "IAO": 55205, + "skos": 80953, + "rdfs": 40015, + "biolink": 36834, + "CHR": 7579, + "RO": 17805, "obo": 2 }, "namespace_axiom_count_incl": { - "prefix_unknown": 87651, - "oboInOwl": 91485, - "MONDO": 19018, - "rdf": 20948, - "owl": 1362, - "IAO": 55204, - "skos": 80849, - "rdfs": 39991, - "biolink": 36809, - "CHR": 7578, - "RO": 17799, + "prefix_unknown": 87727, + "oboInOwl": 91607, + "MONDO": 19033, + "rdf": 20975, + "owl": 1363, + "IAO": 55205, + "skos": 80953, + "rdfs": 40015, + "biolink": 36834, + "CHR": 7579, + "RO": 17805, "obo": 2 }, "namespace_entity_count": { - "prefix_unknown": 18036, + "prefix_unknown": 18042, "oboInOwl": 4, "owl": 2, "xsd": 1, @@ -142,7 +142,7 @@ "obo": 1 }, "namespace_entity_count_incl": { - "prefix_unknown": 18036, + "prefix_unknown": 18042, "oboInOwl": 4, "owl": 2, "xsd": 1, diff --git a/src/ontology/metadata/ordo-metrics.json b/src/ontology/metadata/ordo-metrics.json index b0850886..2a496bd3 100644 --- a/src/ontology/metadata/ordo-metrics.json +++ b/src/ontology/metadata/ordo-metrics.json @@ -26,7 +26,7 @@ "obj_property_count_incl": 4, "ontology_anno_count": 12, "ontology_iri": "http://purl.obolibrary.org/obo/mondo/sources/ordo.owl", - "ontology_version_iri": "http://purl.obolibrary.org/obo/mondo/sources/2024-05-01/ordo.owl", + "ontology_version_iri": "http://purl.obolibrary.org/obo/mondo/sources/2024-05-23/ordo.owl", "owl2": true, "owl2_dl": true, "owl2_el": true, diff --git a/src/ontology/reports/component_signature-doid.tsv b/src/ontology/reports/component_signature-doid.tsv index 994e2d77..ed610bf7 100644 --- a/src/ontology/reports/component_signature-doid.tsv +++ b/src/ontology/reports/component_signature-doid.tsv @@ -11856,6 +11856,196 @@ + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + @@ -12178,196 +12368,6 @@ - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - diff --git a/src/ontology/reports/component_signature-ncit.tsv b/src/ontology/reports/component_signature-ncit.tsv index 76eb1c1b..03f711a1 100644 --- a/src/ontology/reports/component_signature-ncit.tsv +++ b/src/ontology/reports/component_signature-ncit.tsv @@ -350,8 +350,6 @@ - - @@ -2372,7 +2370,6 @@ - @@ -2674,7 +2671,6 @@ - @@ -3238,7 +3234,6 @@ - @@ -3357,7 +3352,6 @@ - @@ -4014,7 +4008,6 @@ - @@ -4067,6 +4060,7 @@ + @@ -4763,7 +4757,6 @@ - @@ -4996,7 +4989,6 @@ - @@ -5978,6 +5970,375 @@ + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + @@ -7501,7 +7862,6 @@ - @@ -7586,7 +7946,6 @@ - @@ -8164,7 +8523,6 @@ - @@ -9228,7 +9586,6 @@ - @@ -9419,7 +9776,6 @@ - @@ -9497,7 +9853,6 @@ - @@ -10702,8 +11057,6 @@ - - @@ -11099,7 +11452,6 @@ - @@ -12107,7 +12459,6 @@ - @@ -12441,7 +12792,6 @@ - @@ -12720,7 +13070,6 @@ - @@ -12792,7 +13141,6 @@ - @@ -13978,6 +14326,7 @@ + @@ -14081,7 +14430,6 @@ - @@ -15242,12 +15590,8 @@ - - - - @@ -15320,7 +15664,6 @@ - diff --git a/src/ontology/reports/component_signature-omim.tsv b/src/ontology/reports/component_signature-omim.tsv index ab308e93..30bd3280 100644 --- a/src/ontology/reports/component_signature-omim.tsv +++ b/src/ontology/reports/component_signature-omim.tsv @@ -4085,6 +4085,7 @@ + @@ -7438,6 +7439,7 @@ + @@ -9469,7 +9471,6 @@ - @@ -14035,6 +14036,7 @@ + @@ -17846,6 +17848,9 @@ + + + @@ -18419,6 +18424,7 @@ + diff --git a/src/ontology/reports/doid.subclass.added-obsolete.robot.tsv b/src/ontology/reports/doid.subclass.added-obsolete.robot.tsv index 6f6cb3c5..b2a76bb7 100644 --- a/src/ontology/reports/doid.subclass.added-obsolete.robot.tsv +++ b/src/ontology/reports/doid.subclass.added-obsolete.robot.tsv @@ -144,7 +144,6 @@ MONDO:0004268 obsolete subareolar duct papillomatosis MONDO:0002482 DOID:7533 DO MONDO:0004335 digestive system disorder MONDO:0021199 DOID:77 DOID:7 obsolete disease by anatomical system MONDO:0004391 obsolete adult extraosseous chondrosarcoma MONDO:0003044 DOID:7902 DOID:4549 obsolete extraosseous chondrosarcoma MONDO:0004392 intracranial extraskeletal myxoid chondrosarcoma MONDO:0003044 DOID:7903 DOID:4549 obsolete extraosseous chondrosarcoma -MONDO:0004527 congenital granular cell tumor MONDO:0000839 DOID:8303 DOID:0080015 obsolete congenital abnormality MONDO:0004557 congenital fibrosarcoma MONDO:0000839 DOID:8418 DOID:0080015 obsolete congenital abnormality MONDO:0004626 obsolete Hodgkin's paragranuloma MONDO:0004952 DOID:8642 DOID:8567 Hodgkins lymphoma MONDO:0004632 obsolete Hodgkin's granuloma MONDO:0004952 DOID:8651 DOID:8567 Hodgkins lymphoma @@ -266,6 +265,7 @@ MONDO:0011107 congenital hypotrichosis with juvenile macular dystrophy MONDO:000 MONDO:0011132 T-cell immunodeficiency, congenital alopecia, and nail dystrophy MONDO:0000839 DOID:0060769 DOID:0080015 obsolete congenital abnormality MONDO:0011325 Fanconi anemia complementation group F MONDO:0000275 DOID:0111088 DOID:0050177 obsolete monogenic disease MONDO:0011331 congenital chylothorax MONDO:0000839 DOID:0060646 DOID:0080015 obsolete congenital abnormality +MONDO:0011382 sickle cell anemia MONDO:0003804 DOID:0081445 DOID:620 obsolete blood protein disease MONDO:0011385 intervertebral disk degenerative disorder MONDO:0000834 DOID:90 DOID:0080007 obsolete bone deterioration disease MONDO:0011400 dilated cardiomyopathy 1G MONDO:0000275 DOID:0110430 DOID:0050177 obsolete monogenic disease MONDO:0011415 Leber congenital amaurosis 3 MONDO:0000275 DOID:0110331 DOID:0050177 obsolete monogenic disease @@ -328,7 +328,7 @@ MONDO:0013198 dilated cardiomyopathy 1EE MONDO:0000275 DOID:0110453 DOID:0050177 MONDO:0013211 dilated cardiomyopathy 1FF MONDO:0000275 DOID:0110459 DOID:0050177 obsolete monogenic disease MONDO:0013287 agammaglobulinemia 2, autosomal recessive MONDO:0000275 DOID:0060024 DOID:0050177 obsolete monogenic disease MONDO:0013339 dilated cardiomyopathy 1GG MONDO:0000275 DOID:0110435 DOID:0050177 obsolete monogenic disease -MONDO:0013400 Congenital adrenal insuffiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency MONDO:0000839 DOID:0050546 DOID:0080015 obsolete congenital abnormality +MONDO:0013400 Congenital adrenal insufficiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency MONDO:0000839 DOID:0050546 DOID:0080015 obsolete congenital abnormality MONDO:0013449 Leber congenital amaurosis 7 MONDO:0000275 DOID:0110333 DOID:0050177 obsolete monogenic disease MONDO:0013506 schizophrenia 16 MONDO:0000275 DOID:0070092 DOID:0050177 obsolete monogenic disease MONDO:0013515 osteogenesis imperfecta type 6 MONDO:0000275 DOID:0110350 DOID:0050177 obsolete monogenic disease @@ -355,6 +355,7 @@ MONDO:0015280 cardiofaciocutaneous syndrome MONDO:0000275 DOID:0060233 DOID:0050 MONDO:0015286 congenital disorder of glycosylation MONDO:0000839 DOID:5212 DOID:0080015 obsolete congenital abnormality MONDO:0015404 rapidly involuting congenital hemangioma MONDO:0000839 DOID:0080895 DOID:0080015 obsolete congenital abnormality MONDO:0015528 congenital epulis MONDO:0000839 DOID:7280 DOID:0080015 obsolete congenital abnormality +MONDO:0015528 congenital epulis MONDO:0000839 DOID:8303 DOID:0080015 obsolete congenital abnormality MONDO:0015627 multiple epiphyseal dysplasia due to collagen 9 anomaly MONDO:0000275 DOID:0070305 DOID:0050177 obsolete monogenic disease MONDO:0015722 congenital vitamin K-dependent coagulation factors deficiency MONDO:0000275 DOID:0112172 DOID:0050177 obsolete monogenic disease MONDO:0015993 cone-rod dystrophy MONDO:0000275 DOID:0050572 DOID:0050177 obsolete monogenic disease diff --git a/src/ontology/reports/doid.subclass.added.robot.tsv b/src/ontology/reports/doid.subclass.added.robot.tsv index c4439170..24ae501a 100644 --- a/src/ontology/reports/doid.subclass.added.robot.tsv +++ b/src/ontology/reports/doid.subclass.added.robot.tsv @@ -539,11 +539,11 @@ MONDO:0004432 mature pericardial teratoma MONDO:0000629 DOID:8012 DOID:0060091 c MONDO:0004440 pineal region meningioma MONDO:0003249 DOID:8031 DOID:5032 pineal gland cancer MONDO:0004466 neuronitis MONDO:0002602 DOID:8117 DOID:331 central nervous system disorder MONDO:0004482 fibroosseous pseudotumor of the digits MONDO:0000631 DOID:8153 DOID:0060094 bone benign neoplasm +MONDO:0004491 uterine corpus choriocarcinoma MONDO:0004491 DOID:8187 DOID:8188 uterine corpus choriocarcinoma MONDO:0004492 mediastinitis MONDO:0003900 DOID:819 DOID:65 connective tissue disorder MONDO:0004496 myocarditis MONDO:0002824 DOID:820 DOID:3978 extrinsic cardiomyopathy MONDO:0004518 anterior urethra cancer MONDO:0004203 DOID:8272 DOID:738 female urethral cancer MONDO:0004526 mixed endometrial stromal and smooth muscle tumor MONDO:0006003 DOID:8302 DOID:9460 uterine corpus cancer -MONDO:0004527 congenital granular cell tumor MONDO:0002616 DOID:8303 DOID:3350 mesenchymal cell neoplasm MONDO:0004528 lymph node palisaded myofibroblastoma MONDO:0021443 DOID:8304 DOID:0080617 benign neoplasm of lymph node MONDO:0004529 non-ossifying fibromyxoid tumor MONDO:0002616 DOID:8305 DOID:3350 mesenchymal cell neoplasm MONDO:0004533 perineural angioma MONDO:0000628 DOID:8331 DOID:0060090 central nervous system organ benign neoplasm @@ -955,7 +955,9 @@ MONDO:0007473 Duane retraction syndrome MONDO:0003432 DOID:12557 DOID:540 strabi MONDO:0007485 dyskeratosis congenita, autosomal dominant 1 MONDO:0000426 DOID:0070014 DOID:0050736 autosomal dominant disease MONDO:0007492 early-onset generalized limb-onset dystonia MONDO:0000426 DOID:0060730 DOID:0050736 autosomal dominant disease MONDO:0007493 torsion dystonia 4 MONDO:0000426 DOID:0090041 DOID:0050736 autosomal dominant disease +MONDO:0007495 dystonia 5 MONDO:0000426 DOID:0060963 DOID:0050736 autosomal dominant disease MONDO:0007495 dystonia 5 MONDO:0000426 DOID:0090043 DOID:0050736 autosomal dominant disease +MONDO:0007495 dystonia 5 MONDO:0006025 DOID:0060963 DOID:0050737 autosomal recessive disease MONDO:0007495 dystonia 5 MONDO:0006025 DOID:0090043 DOID:0050737 autosomal recessive disease MONDO:0007496 dystonia 12 MONDO:0000426 DOID:0090056 DOID:0050736 autosomal dominant disease MONDO:0007507 absence of fingerprints-congenital milia syndrome MONDO:0019287 DOID:0080725 DOID:2121 ectodermal dysplasia syndrome @@ -1156,7 +1158,7 @@ MONDO:0008287 Greig cephalopolysyndactyly syndrome MONDO:0019796 DOID:14761 DOID MONDO:0008289 brain small vessel disease 1 with or without ocular anomalies MONDO:0000426 DOID:0090125 DOID:0050736 autosomal dominant disease MONDO:0008292 punctate palmoplantar keratoderma type 2 MONDO:0000426 DOID:0080213 DOID:0050736 autosomal dominant disease MONDO:0008301 Guttmacher syndrome MONDO:0000426 DOID:0111544 DOID:0050736 autosomal dominant disease -MONDO:0008302 centra precocious puberty 1 MONDO:0000426 DOID:0112310 DOID:0050736 autosomal dominant disease +MONDO:0008302 central precocious puberty 1 MONDO:0000426 DOID:0112310 DOID:0050736 autosomal dominant disease MONDO:0008303 familial male-limited precocious puberty MONDO:0000426 DOID:0111545 DOID:0050736 autosomal dominant disease MONDO:0008305 Currarino triad MONDO:0000426 DOID:0111546 DOID:0050736 autosomal dominant disease MONDO:0008306 ABri amyloidosis MONDO:0000426 DOID:0070029 DOID:0050736 autosomal dominant disease @@ -1511,6 +1513,7 @@ MONDO:0009605 methemoglobinemia type 4 MONDO:0002145 DOID:0112316 DOID:1923 diso MONDO:0009605 methemoglobinemia type 4 MONDO:0006025 DOID:0112316 DOID:0050737 autosomal recessive disease MONDO:0009609 methylcobalamin deficiency type cblG MONDO:0002012 DOID:0050733 DOID:14749 methylmalonic acidemia MONDO:0009610 3-methylglutaconic aciduria type 1 MONDO:0006025 DOID:0110002 DOID:0050737 autosomal recessive disease +MONDO:0009619 microcephaly-micromelia syndrome MONDO:0002254 DOID:0081432 DOID:225 syndromic disease MONDO:0009623 Nijmegen breakage syndrome MONDO:0002254 DOID:7400 DOID:225 syndromic disease MONDO:0009624 microcephaly and chorioretinopathy 1 MONDO:0006025 DOID:0080105 DOID:0050737 autosomal recessive disease MONDO:0009626 pseudo-TORCH syndrome MONDO:0002254 DOID:0050656 DOID:225 syndromic disease @@ -1574,6 +1577,7 @@ MONDO:0009841 PEHO syndrome MONDO:0005560 DOID:0080539 DOID:936 brain disorder MONDO:0009843 hypomyelinating leukodystrophy 3 MONDO:0006025 DOID:0060790 DOID:0050737 autosomal recessive disease MONDO:0009846 pentosuria MONDO:0004736 DOID:0111258 DOID:9252 inborn disorder of amino acid metabolism MONDO:0009846 pentosuria MONDO:0006025 DOID:0111258 DOID:0050737 autosomal recessive disease +MONDO:0009849 hyperimmunoglobulinemia D with periodic fever MONDO:0002468 DOID:0081450 DOID:2959 hyperimmunoglobulin syndrome MONDO:0009862 dihydropteridine reductase deficiency MONDO:0850519 DOID:0081130 DOID:0081132 tetrahydrobiopterin (BH4)-deficient hyperphenylalaninemia MONDO:0009863 BH4-deficient hyperphenylalaninemia A MONDO:0850519 DOID:0090106 DOID:0081132 tetrahydrobiopterin (BH4)-deficient hyperphenylalaninemia MONDO:0009872 Bjornstad syndrome MONDO:0002254 DOID:0050677 DOID:225 syndromic disease @@ -1996,6 +2000,7 @@ MONDO:0011033 type 1 diabetes mellitus 13 MONDO:0005147 DOID:0110752 DOID:9744 t MONDO:0011037 renal dysplasia, cystic, susceptibility to MONDO:0000426 DOID:0111682 DOID:0050736 autosomal dominant disease MONDO:0011037 renal dysplasia, cystic, susceptibility to MONDO:0002473 DOID:0111682 DOID:2975 cystic kidney disease MONDO:0011045 MMEP syndrome MONDO:0000429 DOID:0111803 DOID:0050739 autosomal genetic disease +MONDO:0011053 intellectual disability-sparse hair-brachydactyly syndrome MONDO:0000426 DOID:0081441 DOID:0050736 autosomal dominant disease MONDO:0011066 Charcot-Marie-Tooth disease type 4B1 MONDO:0006025 DOID:0110191 DOID:0050737 autosomal recessive disease MONDO:0011068 type 1 diabetes mellitus 12 MONDO:0005147 DOID:0110751 DOID:9744 type 1 diabetes mellitus MONDO:0011075 retinitis pigmentosa 18 MONDO:0000426 DOID:0110356 DOID:0050736 autosomal dominant disease @@ -2089,6 +2094,7 @@ MONDO:0011374 hypercholesterolemia, familial, 4 MONDO:0005439 DOID:0090105 DOID: MONDO:0011377 long QT syndrome 3 MONDO:0000426 DOID:0110646 DOID:0050736 autosomal dominant disease MONDO:0011381 dominant beta-thalassemia MONDO:0000426 DOID:0080770 DOID:0050736 autosomal dominant disease MONDO:0011382 sickle cell anemia MONDO:0002280 DOID:10923 DOID:2355 anemia +MONDO:0011382 sickle cell anemia MONDO:0011382 DOID:10923 DOID:0081445 sickle cell anemia MONDO:0011383 autoimmune lymphoproliferative syndrome type 2A MONDO:0000426 DOID:0110115 DOID:0050736 autosomal dominant disease MONDO:0011387 psoriasis 4, susceptibility to MONDO:0005083 DOID:0111280 DOID:8893 psoriasis MONDO:0011390 focal segmental glomerulosclerosis 2 MONDO:0000426 DOID:0111129 DOID:0050736 autosomal dominant disease @@ -2161,6 +2167,8 @@ MONDO:0011601 neonatal intrahepatic cholestasis due to citrin deficiency MONDO:0 MONDO:0011603 GNE myopathy MONDO:0006025 DOID:0080718 DOID:0050737 autosomal recessive disease MONDO:0011608 dermatitis, atopic, 5 MONDO:0004980 DOID:0110101 DOID:3310 atopic eczema MONDO:0011609 dermatitis, atopic, 6 MONDO:0004980 DOID:0110102 DOID:3310 atopic eczema +MONDO:0011610 dimethylglycine dehydrogenase deficiency MONDO:0004736 DOID:0081446 DOID:9252 inborn disorder of amino acid metabolism +MONDO:0011610 dimethylglycine dehydrogenase deficiency MONDO:0006025 DOID:0081446 DOID:0050737 autosomal recessive disease MONDO:0011613 autosomal recessive early-onset Parkinson disease 6 MONDO:0006025 DOID:0060369 DOID:0050737 autosomal recessive disease MONDO:0011614 3-hydroxy-3-methylglutaryl-CoA synthase deficiency MONDO:0006025 DOID:0081168 DOID:0050737 autosomal recessive disease MONDO:0011629 MOGS-congenital disorder of glycosylation MONDO:0006025 DOID:0070254 DOID:0050737 autosomal recessive disease @@ -2328,7 +2336,7 @@ MONDO:0012336 cataract 22 multiple types MONDO:0006025 DOID:0110268 DOID:0050737 MONDO:0012338 epilepsy, idiopathic generalized, susceptibility to, 4 MONDO:0005579 DOID:0111319 DOID:1827 epilepsy, idiopathic generalized MONDO:0012353 erythrocytosis, familial, 3 MONDO:0000426 DOID:0080338 DOID:0050736 autosomal dominant disease MONDO:0012354 platelet-type bleeding disorder 8 MONDO:0006025 DOID:0060692 DOID:0050737 autosomal recessive disease -MONDO:0012360 congenital nongoitrous hypothryoidism 3 MONDO:0000426 DOID:0070127 DOID:0050736 autosomal dominant disease +MONDO:0012360 congenital nongoitrous hypothyroidism 3 MONDO:0000426 DOID:0070127 DOID:0050736 autosomal dominant disease MONDO:0012371 Noonan syndrome 3 MONDO:0000426 DOID:0060581 DOID:0050736 autosomal dominant disease MONDO:0012381 hyperinsulinism due to INSR deficiency MONDO:0000426 DOID:0070220 DOID:0050736 autosomal dominant disease MONDO:0012382 hyperinsulinemic hypoglycemia, familial, 4 MONDO:0006025 DOID:0070215 DOID:0050737 autosomal recessive disease @@ -2649,8 +2657,8 @@ MONDO:0013395 retinitis pigmentosa 4 MONDO:0000426 DOID:0110372 DOID:0050736 aut MONDO:0013395 retinitis pigmentosa 4 MONDO:0006025 DOID:0110372 DOID:0050737 autosomal recessive disease MONDO:0013396 chromosome 1p32-p31 deletion syndrome MONDO:0000426 DOID:0060409 DOID:0050736 autosomal dominant disease MONDO:0013396 chromosome 1p32-p31 deletion syndrome MONDO:0002254 DOID:0060409 DOID:225 syndromic disease -MONDO:0013400 Congenital adrenal insuffiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency MONDO:0000426 DOID:0050546 DOID:0050736 autosomal dominant disease -MONDO:0013400 Congenital adrenal insuffiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency MONDO:0006025 DOID:0050546 DOID:0050737 autosomal recessive disease +MONDO:0013400 Congenital adrenal insufficiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency MONDO:0000426 DOID:0050546 DOID:0050736 autosomal dominant disease +MONDO:0013400 Congenital adrenal insufficiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency MONDO:0006025 DOID:0050546 DOID:0050737 autosomal recessive disease MONDO:0013401 hereditary spastic paraplegia 51 MONDO:0006025 DOID:0110803 DOID:0050737 autosomal recessive disease MONDO:0013402 retinitis pigmentosa 27 MONDO:0000426 DOID:0110397 DOID:0050736 autosomal dominant disease MONDO:0013409 age related macular degeneration 5 MONDO:0005150 DOID:0110028 DOID:10871 age-related macular degeneration @@ -2661,7 +2669,6 @@ MONDO:0013413 retinitis pigmentosa 45 MONDO:0006025 DOID:0110402 DOID:0050737 au MONDO:0013415 chromosome 17p13.1 deletion syndrome MONDO:0000426 DOID:0060402 DOID:0050736 autosomal dominant disease MONDO:0013424 3p- syndrome MONDO:0000426 DOID:0060417 DOID:0050736 autosomal dominant disease MONDO:0013427 immunodeficiency 31B MONDO:0003778 DOID:0111944 DOID:612 inborn error of immunity -MONDO:0013427 immunodeficiency 31B MONDO:0006025 DOID:0111944 DOID:0050737 autosomal recessive disease MONDO:0013429 retinitis pigmentosa 40 MONDO:0006025 DOID:0110375 DOID:0050737 autosomal recessive disease MONDO:0013438 pontocerebellar hypoplasia type 2D MONDO:0006025 DOID:0060270 DOID:0050737 autosomal recessive disease MONDO:0013441 asphyxiating thoracic dystrophy 4 MONDO:0006025 DOID:0110088 DOID:0050737 autosomal recessive disease @@ -2763,7 +2770,7 @@ MONDO:0013744 cataract 37 MONDO:0000426 DOID:0110252 DOID:0050736 autosomal domi MONDO:0013750 atrial septal defect 8 MONDO:0000426 DOID:0110113 DOID:0050736 autosomal dominant disease MONDO:0013753 Charcot-Marie-Tooth disease axonal type 2P MONDO:0000426 DOID:0110169 DOID:0050736 autosomal dominant disease MONDO:0013753 Charcot-Marie-Tooth disease axonal type 2P MONDO:0006025 DOID:0110169 DOID:0050737 autosomal recessive disease -MONDO:0013757 congenital nongoitrous hypothryoidism 6 MONDO:0000426 DOID:0070128 DOID:0050736 autosomal dominant disease +MONDO:0013757 congenital nongoitrous hypothyroidism 6 MONDO:0000426 DOID:0070128 DOID:0050736 autosomal dominant disease MONDO:0013766 familial cold autoinflammatory syndrome 3 MONDO:0000426 DOID:0090064 DOID:0050736 autosomal dominant disease MONDO:0013767 autoimmune lymphoproliferative syndrome type 4 MONDO:0000426 DOID:0110117 DOID:0050736 autosomal dominant disease MONDO:0013770 atrial septal defect 9 MONDO:0000426 DOID:0110114 DOID:0050736 autosomal dominant disease @@ -2793,7 +2800,7 @@ MONDO:0013859 cataract 38 MONDO:0006025 DOID:0110245 DOID:0050737 autosomal rece MONDO:0013864 Cornelia de Lange syndrome 4 MONDO:0000426 DOID:0080508 DOID:0050736 autosomal dominant disease MONDO:0013865 mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency MONDO:0006025 DOID:0111480 DOID:0050737 autosomal recessive disease MONDO:0013866 neuronal ceroid lipofuscinosis 11 MONDO:0006025 DOID:0110732 DOID:0050737 autosomal recessive disease -MONDO:0013867 brown-Vialetto-van Laere syndrome 2 MONDO:0006025 DOID:0080786 DOID:0050737 autosomal recessive disease +MONDO:0013867 Brown-Vialetto-van Laere syndrome 2 MONDO:0006025 DOID:0080786 DOID:0050737 autosomal recessive disease MONDO:0013869 adenine phosphoribosyltransferase deficiency MONDO:0006025 DOID:0060350 DOID:0050737 autosomal recessive disease MONDO:0013870 TMEM165-congenital disorder of glycosylation MONDO:0006025 DOID:0070263 DOID:0050737 autosomal recessive disease MONDO:0013875 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome MONDO:0006025 DOID:0110001 DOID:0050737 autosomal recessive disease @@ -2817,6 +2824,7 @@ MONDO:0013919 epilepsy, idiopathic generalized, susceptibility to, 12 MONDO:0005 MONDO:0013924 osteogenesis imperfecta type 13 MONDO:0006025 DOID:0110342 DOID:0050737 autosomal recessive disease MONDO:0013926 hypogonadotropic hypogonadism 14 with or without anosmia MONDO:0000426 DOID:0090087 DOID:0050736 autosomal dominant disease MONDO:0013928 dystonia 23 MONDO:0000426 DOID:0090051 DOID:0050736 autosomal dominant disease +MONDO:0013931 peroxisome biogenesis disorder 4B MONDO:0000426 DOID:0081433 DOID:0050736 autosomal dominant disease MONDO:0013946 hypogonadotropic hypogonadism 15 with or without anosmia MONDO:0000426 DOID:0090075 DOID:0050736 autosomal dominant disease MONDO:0013953 immunodeficiency 28 MONDO:0006025 DOID:0111995 DOID:0050737 autosomal recessive disease MONDO:0013954 Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency MONDO:0003778 DOID:0111950 DOID:612 inborn error of immunity @@ -3171,6 +3179,7 @@ MONDO:0014665 Charcot-Marie-Tooth disease axonal type 2V MONDO:0000426 DOID:0110 MONDO:0014666 hypomyelinating leukodystrophy 11 MONDO:0006025 DOID:0060792 DOID:0050737 autosomal recessive disease MONDO:0014667 cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3 MONDO:0006025 DOID:0080359 DOID:0050737 autosomal recessive disease MONDO:0014668 cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4 MONDO:0006025 DOID:0080360 DOID:0050737 autosomal recessive disease +MONDO:0014669 cone-rod dystrophy 21 MONDO:0006025 DOID:0081447 DOID:0050737 autosomal recessive disease MONDO:0014672 osteogenesis imperfecta type 17 MONDO:0006025 DOID:0110338 DOID:0050737 autosomal recessive disease MONDO:0014673 cataract 44 MONDO:0006025 DOID:0110267 DOID:0050737 autosomal recessive disease MONDO:0014676 Emery-Dreifuss muscular dystrophy 3, autosomal recessive MONDO:0006025 DOID:0070248 DOID:0050737 autosomal recessive disease @@ -3298,6 +3307,7 @@ MONDO:0014993 myofibrillar myopathy 8 MONDO:0006025 DOID:0080308 DOID:0050737 au MONDO:0015000 developmental and epileptic encephalopathy, 48 MONDO:0006025 DOID:0080448 DOID:0050737 autosomal recessive disease MONDO:0015002 developmental and epileptic encephalopathy, 49 MONDO:0006025 DOID:0080441 DOID:0050737 autosomal recessive disease MONDO:0015003 dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities MONDO:0006025 DOID:0081419 DOID:0050737 autosomal recessive disease +MONDO:0015004 dystonia 28, childhood-onset MONDO:0000426 DOID:0060936 DOID:0050736 autosomal dominant disease MONDO:0015008 amelogenesis imperfecta, type 1J MONDO:0006025 DOID:0080953 DOID:0050737 autosomal recessive disease MONDO:0015011 optic atrophy 11 MONDO:0006025 DOID:0111436 DOID:0050737 autosomal recessive disease MONDO:0015013 retinitis pigmentosa 77 MONDO:0006025 DOID:0080350 DOID:0050737 autosomal recessive disease @@ -3338,6 +3348,7 @@ MONDO:0015517 common variable immunodeficiency MONDO:0007179 DOID:12177 DOID:417 MONDO:0015523 epithelioid hemangioendothelioma MONDO:0000898 DOID:0080190 DOID:0080189 malignant hemangioma MONDO:0015526 cold-induced sweating syndrome MONDO:0002254 DOID:0060294 DOID:225 syndromic disease MONDO:0015526 cold-induced sweating syndrome MONDO:0006025 DOID:0060294 DOID:0050737 autosomal recessive disease +MONDO:0015528 congenital epulis MONDO:0002616 DOID:8303 DOID:3350 mesenchymal cell neoplasm MONDO:0015588 limbic encephalitis MONDO:0000568 DOID:0080741 DOID:0060004 autoimmune disorder of central nervous system MONDO:0015601 X-linked intellectual disability, van Esch type MONDO:0020605 DOID:0111840 DOID:0080012 X-linked recessive disease MONDO:0015609 advanced sleep phase syndrome MONDO:0000426 DOID:0050628 DOID:0050736 autosomal dominant disease @@ -3414,6 +3425,7 @@ MONDO:0017282 alveolar echinococcosis MONDO:0005275 DOID:12148 DOID:850 lung dis MONDO:0017282 alveolar echinococcosis MONDO:0005560 DOID:12148 DOID:936 brain disorder MONDO:0017304 ocular albinism MONDO:0005328 DOID:0050633 DOID:5614 eye disorder MONDO:0017312 Perrault syndrome MONDO:0002254 DOID:0050857 DOID:225 syndromic disease +MONDO:0017347 plasmablastic lymphoma MONDO:0968974 DOID:0080779 DOID:0081452 large B-cell lymphoma MONDO:0017373 poliomyelitis MONDO:0003620 DOID:4953 DOID:574 peripheral nervous system disorder MONDO:0017376 reactive arthritis MONDO:0000589 DOID:6196 DOID:0060032 autoimmune disorder of musculoskeletal system MONDO:0017398 3MC syndrome MONDO:0002254 DOID:0060225 DOID:225 syndromic disease @@ -3464,6 +3476,7 @@ MONDO:0018472 familial isolated trichomegaly MONDO:0006025 DOID:0111566 DOID:005 MONDO:0018484 semicircular canal dehiscence syndrome MONDO:0002467 DOID:0080193 DOID:2952 inner ear disorder MONDO:0018493 malignant hyperthermia of anesthesia MONDO:0000426 DOID:8545 DOID:0050736 autosomal dominant disease MONDO:0018493 malignant hyperthermia of anesthesia MONDO:0003939 DOID:8545 DOID:66 muscle tissue disorder +MONDO:0018540 PFAPA syndrome MONDO:0007179 DOID:0081451 DOID:417 autoimmune disease MONDO:0018543 autosomal dominant hypocalcemia MONDO:0004689 DOID:0090109 DOID:896 inborn metal metabolism disorder MONDO:0018544 adrenoleukodystrophy MONDO:0020605 DOID:10588 DOID:0080012 X-linked recessive disease MONDO:0018556 Lambert-Eaton myasthenic syndrome MONDO:0000589 DOID:0050214 DOID:0060032 autoimmune disorder of musculoskeletal system @@ -3501,6 +3514,7 @@ MONDO:0018855 keratosis pilaris atrophicans MONDO:0019269 DOID:0080751 DOID:1697 MONDO:0018870 arterial calcification of infancy MONDO:0000473 DOID:0050644 DOID:0050828 arterial disorder MONDO:0018875 Li-Fraumeni syndrome MONDO:0018875 DOID:0111503 DOID:3012 Li-Fraumeni syndrome MONDO:0018881 myelodysplastic syndrome MONDO:0005374 DOID:0050908 DOID:4960 bone marrow neoplasm +MONDO:0018905 diffuse large B-cell lymphoma MONDO:0968974 DOID:0050745 DOID:0081452 large B-cell lymphoma MONDO:0018910 oculocutaneous albinism MONDO:0002254 DOID:0050632 DOID:225 syndromic disease MONDO:0018910 oculocutaneous albinism MONDO:0006025 DOID:0050632 DOID:0050737 autosomal recessive disease MONDO:0018911 maturity-onset diabetes of the young MONDO:0000426 DOID:0050524 DOID:0050736 autosomal dominant disease @@ -3597,6 +3611,8 @@ MONDO:0020291 hypoplastic right heart syndrome MONDO:0005453 DOID:0070315 DOID:1 MONDO:0020300 autosomal dominant nocturnal frontal lobe epilepsy MONDO:0000426 DOID:0060681 DOID:0050736 autosomal dominant disease MONDO:0020310 familial focal epilepsy with variable foci MONDO:0000426 DOID:0081420 DOID:0050736 autosomal dominant disease MONDO:0020322 acute biphenotypic leukemia MONDO:0015760 DOID:9953 DOID:0081312 T-cell non-Hodgkin lymphoma +MONDO:0020323 primary mediastinal large B-cell lymphoma MONDO:0968974 DOID:0080210 DOID:0081452 large B-cell lymphoma +MONDO:0020324 intravascular large B-cell lymphoma MONDO:0968974 DOID:0081311 DOID:0081452 large B-cell lymphoma MONDO:0020367 juvenile open angle glaucoma MONDO:0000426 DOID:1068 DOID:0050736 autosomal dominant disease MONDO:0020370 Cogan-Reese syndrome MONDO:0005328 DOID:0060217 DOID:5614 eye disorder MONDO:0020478 Leber plus disease MONDO:0002254 DOID:0111754 DOID:225 syndromic disease @@ -3705,6 +3721,7 @@ MONDO:0024889 benign mesonephroma MONDO:0004972 DOID:2616 DOID:657 adenoma MONDO:0024892 soft tissue amyloid neoplasm MONDO:0002616 DOID:6755 DOID:3350 mesenchymal cell neoplasm MONDO:0025353 developmental and epileptic encephalopathy, 90 MONDO:0000425 DOID:0070381 DOID:0050735 X-linked disease MONDO:0025354 spermatogenic failure, X-linked, 3 MONDO:0020605 DOID:0112274 DOID:0080012 X-linked recessive disease +MONDO:0025691 dystonia 30 MONDO:0000426 DOID:0060937 DOID:0050736 autosomal dominant disease MONDO:0025701 leukodystrophy, hypomyelinating, 22 MONDO:0000426 DOID:0070402 DOID:0050736 autosomal dominant disease MONDO:0026720 mitochondrial complex 1 deficiency, nuclear type 12 MONDO:0020605 DOID:0112099 DOID:0080012 X-linked recessive disease MONDO:0026721 mitochondrial complex 1 deficiency, nuclear type 30 MONDO:0020605 DOID:0112098 DOID:0080012 X-linked recessive disease @@ -3779,25 +3796,34 @@ MONDO:0030378 combined oxidative phosphorylation deficiency 53 MONDO:0006025 DOI MONDO:0030430 spermatogenic failure 56 MONDO:0006025 DOID:0112336 DOID:0050737 autosomal recessive disease MONDO:0030438 pontocerebellar hypoplasia, type 16 MONDO:0006025 DOID:0112333 DOID:0050737 autosomal recessive disease MONDO:0030439 spermatogenic failure 57 MONDO:0006025 DOID:0112338 DOID:0050737 autosomal recessive disease +MONDO:0030440 cone-rod dystrophy 22 MONDO:0006025 DOID:0081448 DOID:0050737 autosomal recessive disease MONDO:0030453 developmental and epileptic encephalopathy 97 MONDO:0000426 DOID:0070383 DOID:0050736 autosomal dominant disease +MONDO:0030455 dystonia 31 MONDO:0006025 DOID:0060938 DOID:0050737 autosomal recessive disease MONDO:0030463 spermatogenic failure 58 MONDO:0006025 DOID:0112352 DOID:0050737 autosomal recessive disease MONDO:0030472 developmental and epileptic encephalopathy 98 MONDO:0000426 DOID:0070384 DOID:0050736 autosomal dominant disease MONDO:0030473 developmental and epileptic encephalopathy 99 MONDO:0000426 DOID:0070385 DOID:0050736 autosomal dominant disease MONDO:0030482 spastic paraplegia 84, autosomal recessive MONDO:0006025 DOID:0112347 DOID:0050737 autosomal recessive disease +MONDO:0030486 dystonia 32 MONDO:0006025 DOID:0060939 DOID:0050737 autosomal recessive disease MONDO:0030492 spermatogenic failure 59 MONDO:0006025 DOID:0112357 DOID:0050737 autosomal recessive disease MONDO:0030493 spermatogenic failure 60 MONDO:0006025 DOID:0112355 DOID:0050737 autosomal recessive disease MONDO:0030507 spermatogenic failure 61 MONDO:0006025 DOID:0112350 DOID:0050737 autosomal recessive disease MONDO:0030508 spermatogenic failure 62 MONDO:0006025 DOID:0112351 DOID:0050737 autosomal recessive disease MONDO:0030512 spastic paraplegia 85, autosomal recessive MONDO:0006025 DOID:0112345 DOID:0050737 autosomal recessive disease +MONDO:0030513 dystonia 33 MONDO:0000426 DOID:0060940 DOID:0050736 autosomal dominant disease +MONDO:0030513 dystonia 33 MONDO:0006025 DOID:0060940 DOID:0050737 autosomal recessive disease MONDO:0030514 leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy MONDO:0006025 DOID:0070397 DOID:0050737 autosomal recessive disease MONDO:0030515 spermatogenic failure 63 MONDO:0006025 DOID:0112356 DOID:0050737 autosomal recessive disease MONDO:0030519 agammaglobulinemia 9, autosomal recessive MONDO:0006025 DOID:0081141 DOID:0050737 autosomal recessive disease MONDO:0030522 spermatogenic failure 64 MONDO:0006025 DOID:0112353 DOID:0050737 autosomal recessive disease MONDO:0030529 agammaglobulinemia 10, autosomal dominant MONDO:0000426 DOID:0081142 DOID:0050736 autosomal dominant disease MONDO:0030531 spermatogenic failure 65 MONDO:0006025 DOID:0112354 DOID:0050737 autosomal recessive disease +MONDO:0030538 dystonia 34, myoclonic MONDO:0000426 DOID:0060957 DOID:0050736 autosomal dominant disease MONDO:0030543 combined oxidative phosphorylation deficiency 54 MONDO:0006025 DOID:0070427 DOID:0050737 autosomal recessive disease MONDO:0030553 acromesomelic dysplasia 4 MONDO:0006025 DOID:0081238 DOID:0050737 autosomal recessive disease MONDO:0030604 cystic partially differentiated nephroblastoma MONDO:0850150 DOID:7571 DOID:0080616 kidney cortex disease +MONDO:0030608 interstitial lung disease 1 MONDO:0000426 DOID:0060941 DOID:0050736 autosomal dominant disease +MONDO:0030608 interstitial lung disease 1 MONDO:0006025 DOID:0060941 DOID:0050737 autosomal recessive disease +MONDO:0030608 interstitial lung disease 1 MONDO:0015925 DOID:0060941 DOID:3082 interstitial lung disease MONDO:0030639 Teebi hypertelorism syndrome MONDO:0002254 DOID:0081073 DOID:225 syndromic disease MONDO:0030673 spastic paraplegia 86, autosomal recessive MONDO:0006025 DOID:0112342 DOID:0050737 autosomal recessive disease MONDO:0030680 cardiomyopathy, dilated, 2F MONDO:0006025 DOID:0081162 DOID:0050737 autosomal recessive disease @@ -3831,6 +3857,7 @@ MONDO:0030939 premature ovarian failure 18 MONDO:0006025 DOID:0112269 DOID:00507 MONDO:0030953 short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2 MONDO:0002254 DOID:0112358 DOID:225 syndromic disease MONDO:0030953 short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2 MONDO:0006025 DOID:0112358 DOID:0050737 autosomal recessive disease MONDO:0030957 developmental and epileptic encephalopathy 103 MONDO:0000426 DOID:0070389 DOID:0050736 autosomal dominant disease +MONDO:0030958 dystonia 35, childhood-onset MONDO:0006025 DOID:0060955 DOID:0050737 autosomal recessive disease MONDO:0030962 nephrotic syndrome, type 23 MONDO:0006025 DOID:0112266 DOID:0050737 autosomal recessive disease MONDO:0030981 immunodeficiency 79 MONDO:0001222 DOID:0112277 DOID:11200 congenital T-cell immunodeficiency MONDO:0030981 immunodeficiency 79 MONDO:0006025 DOID:0112277 DOID:0050737 autosomal recessive disease @@ -3941,6 +3968,7 @@ MONDO:0032782 immunodeficiency 63 with lymphoproliferation and autoimmunity MOND MONDO:0032783 aortic valve disease 3 MONDO:0000426 DOID:0080977 DOID:0050736 autosomal dominant disease MONDO:0032786 Noonan syndrome 11 MONDO:0000426 DOID:0112169 DOID:0050736 autosomal dominant disease MONDO:0032787 holoprosencephaly 12 with or without pancreatic agenesis MONDO:0000426 DOID:0081398 DOID:0050736 autosomal dominant disease +MONDO:0032790 neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities MONDO:0002254 DOID:0081443 DOID:225 syndromic disease MONDO:0032796 hyper-IgE recurrent infection syndrome 4, autosomal recessive MONDO:0006025 DOID:0080596 DOID:0050737 autosomal recessive disease MONDO:0032797 myopathy, congenital, with tremor MONDO:0000426 DOID:0081348 DOID:0050736 autosomal dominant disease MONDO:0032799 mitochondrial DNA depletion syndrome 16 (hepatic type) MONDO:0006025 DOID:0070446 DOID:0050737 autosomal recessive disease @@ -3966,6 +3994,8 @@ MONDO:0032845 spermatogenic failure 39 MONDO:0006025 DOID:0111926 DOID:0050737 a MONDO:0032846 osteogenesis imperfecta, type 20 MONDO:0006025 DOID:0111849 DOID:0050737 autosomal recessive disease MONDO:0032848 immunodeficiency 65, susceptibility to viral infections MONDO:0003778 DOID:0111978 DOID:612 inborn error of immunity MONDO:0032848 immunodeficiency 65, susceptibility to viral infections MONDO:0006025 DOID:0111978 DOID:0050737 autosomal recessive disease +MONDO:0032849 neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies MONDO:0002254 DOID:0070539 DOID:225 syndromic disease +MONDO:0032849 neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies MONDO:0006025 DOID:0070539 DOID:0050737 autosomal recessive disease MONDO:0032850 neurooculocardiogenitourinary syndrome MONDO:0000426 DOID:0111675 DOID:0050736 autosomal dominant disease MONDO:0032850 neurooculocardiogenitourinary syndrome MONDO:0002254 DOID:0111675 DOID:225 syndromic disease MONDO:0032852 myopathy, congenital, with structured cores and z-line abnormalities MONDO:0000426 DOID:0081342 DOID:0050736 autosomal dominant disease @@ -4206,6 +4236,8 @@ MONDO:0060455 X-linked congenital hemolytic anemia MONDO:0020605 DOID:0111846 DO MONDO:0060489 46,XX sex reversal 4 MONDO:0000426 DOID:0111764 DOID:0050736 autosomal dominant disease MONDO:0060491 neurodevelopmental disorder with involuntary movements MONDO:0000426 DOID:0112276 DOID:0050736 autosomal dominant disease MONDO:0060491 neurodevelopmental disorder with involuntary movements MONDO:0005395 DOID:0112276 DOID:480 movement disorder +MONDO:0060533 microcephaly, short stature, and limb abnormalities MONDO:0005516 DOID:0081431 DOID:2256 osteochondrodysplasia +MONDO:0060533 microcephaly, short stature, and limb abnormalities MONDO:0006025 DOID:0081431 DOID:0050737 autosomal recessive disease MONDO:0060549 congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay MONDO:0000426 DOID:0112359 DOID:0050736 autosomal dominant disease MONDO:0060549 congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay MONDO:0002254 DOID:0112359 DOID:225 syndromic disease MONDO:0060583 platelet abnormalities with eosinophilia and immune-mediated inflammatory disease MONDO:0006025 DOID:0112004 DOID:0050737 autosomal recessive disease @@ -4295,6 +4327,9 @@ MONDO:0850130 gastroesophageal adenocarcinoma MONDO:0850129 DOID:0080375 DOID:00 MONDO:0850149 nephroma MONDO:0850150 DOID:0080615 DOID:0080616 kidney cortex disease MONDO:0850284 extrinsic asthma MONDO:0005271 DOID:0080811 DOID:1205 allergic disease MONDO:0850302 intracranial meningioma MONDO:0001657 DOID:0060106 DOID:1319 brain cancer +MONDO:0850426 high-grade B-cell lymphoma double-hit/triple-hit MONDO:0968974 DOID:0081004 DOID:0081452 large B-cell lymphoma +MONDO:0859139 blepharophimosis-impaired intellectual development syndrome MONDO:0000426 DOID:0081442 DOID:0050736 autosomal dominant disease +MONDO:0859139 blepharophimosis-impaired intellectual development syndrome MONDO:0002254 DOID:0081442 DOID:225 syndromic disease MONDO:0859152 neurodevelopmental disorder with cerebellar atrophy and motor dysfunction MONDO:0019502 DOID:0070443 DOID:0060308 autosomal recessive non-syndromic intellectual disability MONDO:0859160 mitochondrial complex IV deficiency, nuclear type 22 MONDO:0006025 DOID:0070507 DOID:0050737 autosomal recessive disease MONDO:0859160 mitochondrial complex IV deficiency, nuclear type 22 MONDO:0957524 DOID:0070507 DOID:0081377 COX deficiency, benign infantile mitochondrial myopathy @@ -4334,6 +4369,7 @@ MONDO:0859337 combined oxidative phosphorylation deficiency 57 MONDO:0006025 DOI MONDO:0859355 inflammatory poikiloderma with hair abnormalities and acral keratoses MONDO:0006025 DOID:0070510 DOID:0050737 autosomal recessive disease MONDO:0859362 hyperinsulinemic hypoglycemia, familial, 8 MONDO:0006025 DOID:0081328 DOID:0050737 autosomal recessive disease MONDO:0859363 spastic paraplegia 79A, autosomal dominant, with ataxia MONDO:0000426 DOID:0070455 DOID:0050736 autosomal dominant disease +MONDO:0859377 neurodevelopmental disorder with poor growth and behavioral abnormalities MONDO:0019502 DOID:0081444 DOID:0060308 autosomal recessive non-syndromic intellectual disability MONDO:0859378 leukodystrophy, hypomyelinating, 25 MONDO:0000426 DOID:0070401 DOID:0050736 autosomal dominant disease MONDO:0859514 congenital myopathy 18 MONDO:0000426 DOID:0081350 DOID:0050736 autosomal dominant disease MONDO:0859514 congenital myopathy 18 MONDO:0006025 DOID:0081350 DOID:0050737 autosomal recessive disease @@ -4347,6 +4383,7 @@ MONDO:0859529 amyotrophic lateral sclerosis 27, juvenile MONDO:0000426 DOID:0081 MONDO:0957215 congenital myopathy 20 MONDO:0006025 DOID:0081352 DOID:0050737 autosomal recessive disease MONDO:0957221 spastic paraplegia 70, autosomal recessive MONDO:0006025 DOID:0070454 DOID:0050737 autosomal recessive disease MONDO:0957224 congenital myopathy 21 with early respiratory failure MONDO:0006025 DOID:0081353 DOID:0050737 autosomal recessive disease +MONDO:0957240 cone-rod dystrophy 24 MONDO:0000426 DOID:0081449 DOID:0050736 autosomal dominant disease MONDO:0957247 congenital myopathy 22A, classic MONDO:0006025 DOID:0081354 DOID:0050737 autosomal recessive disease MONDO:0957248 developmental and epileptic encephalopathy 31B MONDO:0006025 DOID:0070376 DOID:0050737 autosomal recessive disease MONDO:0957254 mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A MONDO:0000426 DOID:0070461 DOID:0050736 autosomal dominant disease @@ -4359,11 +4396,14 @@ MONDO:0957308 spastic paraplegia 90A, autosomal dominant MONDO:0000426 DOID:0070 MONDO:0957309 spastic paraplegia 90B, autosomal recessive MONDO:0000426 DOID:0070460 DOID:0050736 autosomal dominant disease MONDO:0957317 hematuria, benign familial MONDO:0000426 DOID:0111365 DOID:0050736 autosomal dominant disease MONDO:0957317 hematuria, benign familial MONDO:0002118 DOID:0111365 DOID:18 urinary system disorder +MONDO:0957385 dystonia 37, early-onset, with striatal lesions MONDO:0006025 DOID:0060956 DOID:0050737 autosomal recessive disease MONDO:0957386 neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities MONDO:0019502 DOID:0081387 DOID:0060308 autosomal recessive non-syndromic intellectual disability MONDO:0957497 disabling pansclerotic morphea of childhood MONDO:0019562 DOID:0081373 DOID:8472 localized scleroderma MONDO:0957538 amyotrophic lateral sclerosis 28 MONDO:0000426 DOID:0081382 DOID:0050736 autosomal dominant disease +MONDO:0957539 dystonia 22, juvenile-onset MONDO:0006025 DOID:0060966 DOID:0050737 autosomal recessive disease MONDO:0957541 neurodevelopmental disorder with hypotonia and speech delay, with or without seizures MONDO:0000429 DOID:0070512 DOID:0050739 autosomal genetic disease MONDO:0957541 neurodevelopmental disorder with hypotonia and speech delay, with or without seizures MONDO:0002254 DOID:0070512 DOID:225 syndromic disease +MONDO:0957542 dystonia 22, adult-onset MONDO:0006025 DOID:0060967 DOID:0050737 autosomal recessive disease MONDO:0957576 parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development MONDO:0006025 DOID:0070486 DOID:0050737 autosomal recessive disease MONDO:0957576 parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development MONDO:0017279 DOID:0070486 DOID:0060894 young-onset Parkinson disease MONDO:0957583 neurodevelopmental disorder with dysmorphic facies and behavioral abnormalities MONDO:0015802 DOID:0070513 DOID:0060307 autosomal dominant non-syndromic intellectual disability diff --git a/src/ontology/reports/doid.subclass.confirmed.robot.tsv b/src/ontology/reports/doid.subclass.confirmed.robot.tsv index 13c9af6a..4dcdd8d2 100644 --- a/src/ontology/reports/doid.subclass.confirmed.robot.tsv +++ b/src/ontology/reports/doid.subclass.confirmed.robot.tsv @@ -2255,7 +2255,6 @@ MONDO:0003626 uterine ligament serous adenocarcinoma MONDO:0002741 DOID:5747 DOI MONDO:0003627 rheumatic pulmonary valve disease MONDO:0000603 DOID:5748 DOID:0060051 autoimmune disorder of cardiovascular system MONDO:0003627 rheumatic pulmonary valve disease MONDO:0003628 DOID:5748 DOID:5749 pulmonary valve disorder MONDO:0003628 pulmonary valve disorder MONDO:0002869 DOID:5749 DOID:4079 heart valve disorder -MONDO:0003629 uterine corpus serous adenocarcinoma MONDO:0006003 DOID:5750 DOID:9460 uterine corpus cancer MONDO:0003630 pancreatic serous cystadenocarcinoma MONDO:0002867 DOID:5751 DOID:4073 pancreatic cystadenocarcinoma MONDO:0003631 cervical serous adenocarcinoma MONDO:0005153 DOID:5752 DOID:3702 cervical adenocarcinoma MONDO:0003632 endocervicitis MONDO:0002345 DOID:5757 DOID:2568 cervicitis @@ -2903,9 +2902,7 @@ MONDO:0004487 endometrial type cervical adenomyoma MONDO:0003238 DOID:8178 DOID: MONDO:0004488 cervical atypical polypoid adenomyoma MONDO:0003238 DOID:8179 DOID:4995 cervical adenomyoma MONDO:0004489 fallopian tube gestational choriocarcinoma MONDO:0006206 DOID:8186 DOID:1963 fallopian tube carcinoma MONDO:0004489 fallopian tube gestational choriocarcinoma MONDO:0020550 DOID:8186 DOID:2025 gestational choriocarcinoma -MONDO:0004490 gestational uterine corpus choriocarcinoma MONDO:0004491 DOID:8187 DOID:8188 uterine corpus choriocarcinoma -MONDO:0004490 gestational uterine corpus choriocarcinoma MONDO:0020550 DOID:8187 DOID:2025 gestational choriocarcinoma -MONDO:0004491 uterine corpus choriocarcinoma MONDO:0005207 DOID:8188 DOID:3594 choriocarcinoma +MONDO:0004491 uterine corpus choriocarcinoma MONDO:0020550 DOID:8187 DOID:2025 gestational choriocarcinoma MONDO:0004493 testicular yolk sac tumor, papillary pattern MONDO:0003402 DOID:8193 DOID:5344 testicular yolk sac tumor MONDO:0004494 testicular yolk sac tumor, hepatoid pattern MONDO:0003402 DOID:8195 DOID:5344 testicular yolk sac tumor MONDO:0004495 myotonic cataract MONDO:0005129 DOID:82 DOID:83 cataract @@ -3761,6 +3758,7 @@ MONDO:0006181 digestive system carcinoma MONDO:0002516 DOID:0050922 DOID:3119 di MONDO:0006181 digestive system carcinoma MONDO:0004993 DOID:0050922 DOID:305 carcinoma MONDO:0006183 disseminated peritoneal leiomyomatosis MONDO:0000650 DOID:5728 DOID:0060117 peritoneal benign neoplasm MONDO:0006191 endometrial clear cell adenocarcinoma MONDO:0005461 DOID:5299 DOID:2870 endometrium adenocarcinoma +MONDO:0006196 endometrial serous adenocarcinoma MONDO:0006003 DOID:5750 DOID:9460 uterine corpus cancer MONDO:0006198 endometrial squamous cell carcinoma MONDO:0002447 DOID:5533 DOID:2871 endometrial carcinoma MONDO:0006198 endometrial squamous cell carcinoma MONDO:0005096 DOID:5533 DOID:1749 squamous cell carcinoma MONDO:0006200 epithelioid cell uveal melanoma MONDO:0002973 DOID:7040 DOID:4360 epithelioid cell melanoma @@ -4472,7 +4470,7 @@ MONDO:0008297 variegate porphyria MONDO:0002520 DOID:4346 DOID:3133 hepatic porp MONDO:0008300 Prader-Willi syndrome MONDO:0002254 DOID:11983 DOID:225 syndromic disease MONDO:0008300 Prader-Willi syndrome MONDO:0019040 DOID:11983 DOID:0080014 chromosomal disorder MONDO:0008301 Guttmacher syndrome MONDO:0002254 DOID:0111544 DOID:225 syndromic disease -MONDO:0008302 centra precocious puberty 1 MONDO:0019165 DOID:0112310 DOID:0112308 central precocious puberty +MONDO:0008302 central precocious puberty 1 MONDO:0019165 DOID:0112310 DOID:0112308 central precocious puberty MONDO:0008305 Currarino triad MONDO:0002254 DOID:0111546 DOID:225 syndromic disease MONDO:0008306 ABri amyloidosis MONDO:0005620 DOID:0070029 DOID:9246 cerebral amyloid angiopathy MONDO:0008315 prostate cancer MONDO:0005836 DOID:10283 DOID:3856 male reproductive organ cancer @@ -4829,6 +4827,7 @@ MONDO:0009670 lethal congenital contracture syndrome 1 MONDO:0017436 DOID:006055 MONDO:0009675 autosomal recessive limb-girdle muscular dystrophy type 2A MONDO:0015152 DOID:0110275 DOID:0110274 autosomal recessive limb-girdle muscular dystrophy MONDO:0009676 autosomal recessive limb-girdle muscular dystrophy type 2B MONDO:0015152 DOID:0110276 DOID:0110274 autosomal recessive limb-girdle muscular dystrophy MONDO:0009677 autosomal recessive limb-girdle muscular dystrophy type 2C MONDO:0015152 DOID:0110277 DOID:0110274 autosomal recessive limb-girdle muscular dystrophy +MONDO:0009681 Ullrich congenital muscular dystrophy 1A MONDO:0000355 DOID:0060946 DOID:0050558 Ullrich congenital muscular dystrophy MONDO:0009683 autosomal recessive limb-girdle muscular dystrophy type 2H MONDO:0015152 DOID:0110282 DOID:0110274 autosomal recessive limb-girdle muscular dystrophy MONDO:0009685 Miyoshi myopathy MONDO:0018949 DOID:0070198 DOID:11720 distal myopathy MONDO:0009689 congenital myasthenic syndrome 6 MONDO:0018940 DOID:0110671 DOID:3635 congenital myasthenic syndrome @@ -6055,7 +6054,7 @@ MONDO:0013388 developmental and epileptic encephalopathy, 11 MONDO:0100062 DOID: MONDO:0013390 autosomal recessive limb-girdle muscular dystrophy type 2Q MONDO:0015152 DOID:0110285 DOID:0110274 autosomal recessive limb-girdle muscular dystrophy MONDO:0013392 autosomal recessive spinocerebellar ataxia 10 MONDO:0015244 DOID:0050999 DOID:0050950 autosomal recessive cerebellar ataxia MONDO:0013395 retinitis pigmentosa 4 MONDO:0019200 DOID:0110372 DOID:10584 retinitis pigmentosa -MONDO:0013400 Congenital adrenal insuffiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency MONDO:0005495 DOID:0050546 DOID:9553 adrenal gland disorder +MONDO:0013400 Congenital adrenal insufficiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency MONDO:0005495 DOID:0050546 DOID:9553 adrenal gland disorder MONDO:0013401 hereditary spastic paraplegia 51 MONDO:0019064 DOID:0110803 DOID:2476 hereditary spastic paraplegia MONDO:0013402 retinitis pigmentosa 27 MONDO:0019200 DOID:0110397 DOID:10584 retinitis pigmentosa MONDO:0013404 hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase MONDO:0000351 DOID:0111039 DOID:0050544 disorder of methionine catabolism @@ -6070,6 +6069,7 @@ MONDO:0013416 age related macular degeneration 8 MONDO:0005150 DOID:0110020 DOID MONDO:0013420 age related macular degeneration 12 MONDO:0005150 DOID:0110024 DOID:10871 age-related macular degeneration MONDO:0013425 retinitis pigmentosa 20 MONDO:0019200 DOID:0110353 DOID:10584 retinitis pigmentosa MONDO:0013426 aneurysm-osteoarthritis syndrome MONDO:0018954 DOID:0070237 DOID:0050466 Loeys-Dietz syndrome +MONDO:0013427 immunodeficiency 31B MONDO:0006025 DOID:0111944 DOID:0050737 autosomal recessive disease MONDO:0013428 Meier-Gorlin syndrome 2 MONDO:0016817 DOID:0080513 DOID:0060306 Meier-Gorlin syndrome MONDO:0013429 retinitis pigmentosa 40 MONDO:0019200 DOID:0110375 DOID:10584 retinitis pigmentosa MONDO:0013430 Meier-Gorlin syndrome 3 MONDO:0016817 DOID:0080514 DOID:0060306 Meier-Gorlin syndrome @@ -6255,7 +6255,7 @@ MONDO:0013862 immunodeficiency, common variable, 7 MONDO:0015517 DOID:0081150 DO MONDO:0013863 combined immunodeficiency due to LRBA deficiency MONDO:0015517 DOID:0081151 DOID:12177 common variable immunodeficiency MONDO:0013864 Cornelia de Lange syndrome 4 MONDO:0016033 DOID:0080508 DOID:11725 Cornelia de Lange syndrome MONDO:0013865 mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency MONDO:0000732 DOID:0111480 DOID:0060286 combined oxidative phosphorylation deficiency -MONDO:0013867 brown-Vialetto-van Laere syndrome 2 MONDO:0008891 DOID:0080786 DOID:0050694 riboflavin transporter deficiency +MONDO:0013867 Brown-Vialetto-van Laere syndrome 2 MONDO:0008891 DOID:0080786 DOID:0050694 riboflavin transporter deficiency MONDO:0013870 TMEM165-congenital disorder of glycosylation MONDO:0005501 DOID:0070263 DOID:0050571 congenital disorder of glycosylation type II MONDO:0013871 Seckel syndrome 6 MONDO:0019342 DOID:0070006 DOID:0050569 Seckel syndrome MONDO:0013873 IMAGe syndrome MONDO:0002254 DOID:0050885 DOID:225 syndromic disease @@ -6564,6 +6564,7 @@ MONDO:0014650 familial temporal lobe epilepsy 8 MONDO:0005115 DOID:0060754 DOID: MONDO:0014651 acrofacial dysostosis Cincinnati type MONDO:0018237 DOID:0060353 DOID:0060379 acrofacial dysostosis MONDO:0014652 exudative vitreoretinopathy 6 MONDO:0019516 DOID:0111410 DOID:0050535 exudative vitreoretinopathy MONDO:0014653 retinitis pigmentosa 72 MONDO:0019200 DOID:0110395 DOID:10584 retinitis pigmentosa +MONDO:0014654 Ullrich congenital muscular dystrophy 2 MONDO:0000355 DOID:0060944 DOID:0050558 Ullrich congenital muscular dystrophy MONDO:0014657 primary ciliary dyskinesia 32 MONDO:0016575 DOID:0110603 DOID:9562 primary ciliary dyskinesia MONDO:0014658 severe achondroplasia-developmental delay-acanthosis nigricans syndrome MONDO:0000426 DOID:0111158 DOID:0050736 autosomal dominant disease MONDO:0014660 microcephaly 15, primary, autosomal recessive MONDO:0016660 DOID:0070277 DOID:0070296 autosomal recessive primary microcephaly @@ -6573,6 +6574,7 @@ MONDO:0014665 Charcot-Marie-Tooth disease axonal type 2V MONDO:0018993 DOID:0110 MONDO:0014666 hypomyelinating leukodystrophy 11 MONDO:0019046 DOID:0060792 DOID:0060786 leukodystrophy MONDO:0014667 cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3 MONDO:0015487 DOID:0080359 DOID:0050713 fatal infantile encephalocardiomyopathy MONDO:0014668 cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4 MONDO:0015487 DOID:0080360 DOID:0050713 fatal infantile encephalocardiomyopathy +MONDO:0014669 cone-rod dystrophy 21 MONDO:0015993 DOID:0081447 DOID:0050572 cone-rod dystrophy MONDO:0014674 maturity-onset diabetes of the young type 14 MONDO:0018911 DOID:0111111 DOID:0050524 maturity-onset diabetes of the young MONDO:0014675 autosomal recessive nonsyndromic hearing loss 104 MONDO:0019588 DOID:0110465 DOID:0050565 hearing loss, autosomal recessive MONDO:0014676 Emery-Dreifuss muscular dystrophy 3, autosomal recessive MONDO:0016830 DOID:0070248 DOID:11726 Emery-Dreifuss muscular dystrophy @@ -7399,6 +7401,7 @@ MONDO:0030378 combined oxidative phosphorylation deficiency 53 MONDO:0000732 DOI MONDO:0030430 spermatogenic failure 56 MONDO:0004983 DOID:0112336 DOID:0111910 spermatogenic failure MONDO:0030438 pontocerebellar hypoplasia, type 16 MONDO:0020135 DOID:0112333 DOID:0060264 pontocerebellar hypoplasia MONDO:0030439 spermatogenic failure 57 MONDO:0004983 DOID:0112338 DOID:0111910 spermatogenic failure +MONDO:0030440 cone-rod dystrophy 22 MONDO:0015993 DOID:0081448 DOID:0050572 cone-rod dystrophy MONDO:0030453 developmental and epileptic encephalopathy 97 MONDO:0100062 DOID:0070383 DOID:0112202 developmental and epileptic encephalopathy MONDO:0030463 spermatogenic failure 58 MONDO:0004983 DOID:0112352 DOID:0111910 spermatogenic failure MONDO:0030472 developmental and epileptic encephalopathy 98 MONDO:0100062 DOID:0070384 DOID:0112202 developmental and epileptic encephalopathy @@ -7471,6 +7474,7 @@ MONDO:0031028 developmental and epileptic encephalopathy 105 with hypopituitaris MONDO:0031031 intellectual developmental disorder, autosomal recessive 77 MONDO:0019502 DOID:0081236 DOID:0060308 autosomal recessive non-syndromic intellectual disability MONDO:0031052 developmental and epileptic encephalopathy 106 MONDO:0100062 DOID:0070392 DOID:0112202 developmental and epileptic encephalopathy MONDO:0031055 developmental and epileptic encephalopathy 107 MONDO:0100062 DOID:0070393 DOID:0112202 developmental and epileptic encephalopathy +MONDO:0031084 amelogenesis imperfecta, IIa 1K MONDO:0019507 DOID:0060945 DOID:2187 amelogenesis imperfecta MONDO:0031329 craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome MONDO:0002254 DOID:0081072 DOID:225 syndromic disease MONDO:0032526 spinocerebellar ataxia 48 MONDO:0020380 DOID:0111746 DOID:1441 autosomal dominant cerebellar ataxia MONDO:0032577 retinitis pigmentosa 83 MONDO:0019200 DOID:0112140 DOID:10584 retinitis pigmentosa @@ -8059,6 +8063,7 @@ MONDO:0957203 intellectual developmental disorder, X-linked 111 MONDO:0019181 DO MONDO:0957215 congenital myopathy 20 MONDO:0019952 DOID:0081352 DOID:0081337 congenital myopathy MONDO:0957221 spastic paraplegia 70, autosomal recessive MONDO:0019064 DOID:0070454 DOID:2476 hereditary spastic paraplegia MONDO:0957224 congenital myopathy 21 with early respiratory failure MONDO:0019952 DOID:0081353 DOID:0081337 congenital myopathy +MONDO:0957240 cone-rod dystrophy 24 MONDO:0015993 DOID:0081449 DOID:0050572 cone-rod dystrophy MONDO:0957247 congenital myopathy 22A, classic MONDO:0019952 DOID:0081354 DOID:0081337 congenital myopathy MONDO:0957248 developmental and epileptic encephalopathy 31B MONDO:0100062 DOID:0070376 DOID:0112202 developmental and epileptic encephalopathy MONDO:0957255 mitochondrial complex V (ATP synthase) deficiency, nuclear type 7 MONDO:0014471 DOID:0070464 DOID:0111143 mitochondrial proton-transporting ATP synthase complex deficiency @@ -8091,6 +8096,19 @@ MONDO:0958180 prolonged electroretinal response suppression 1 MONDO:0012033 DOID MONDO:0958184 epidermolytic hyperkeratosis 2 MONDO:0007239 DOID:0081359 DOID:4603 epidermolytic ichthyosis MONDO:0958189 basal cell nevus syndrome 2 MONDO:0007187 DOID:0070366 DOID:2512 nevoid basal cell carcinoma syndrome MONDO:0958190 prolonged electroretinal response suppression 2 MONDO:0012033 DOID:0070364 DOID:0050335 bradyopsia +MONDO:0958235 Ullrich congenital muscular dystrophy 1B MONDO:0000355 DOID:0060942 DOID:0050558 Ullrich congenital muscular dystrophy +MONDO:0958236 Ullrich congenital muscular dystrophy 1C MONDO:0000355 DOID:0060943 DOID:0050558 Ullrich congenital muscular dystrophy +MONDO:0958295 BCOR ITD sarcoma MONDO:0958159 DOID:0081403 DOID:0081402 sarcoma with BCOR genetic alterations +MONDO:0958296 BCOR-CCNB3 sarcoma MONDO:0958159 DOID:0081404 DOID:0081402 sarcoma with BCOR genetic alterations +MONDO:0958297 childhood sarcoma with BCOR genetic alterations MONDO:0958159 DOID:0081405 DOID:0081402 sarcoma with BCOR genetic alterations +MONDO:0958298 childhood round cell sarcoma with EWSR1-non-ETS fusion MONDO:0958160 DOID:0081407 DOID:0081406 round cell sarcoma with EWSR1-non-ETS fusion +MONDO:0958299 round cell sarcoma with EWSR1-NFATC2 gene fusion MONDO:0958160 DOID:0081408 DOID:0081406 round cell sarcoma with EWSR1-non-ETS fusion +MONDO:0958300 round cell sarcoma with EWSR1-PATZ1 gene fusion MONDO:0958160 DOID:0081409 DOID:0081406 round cell sarcoma with EWSR1-non-ETS fusion +MONDO:0958301 round cell sarcoma with FUS-NFATC2 gene fusion MONDO:0958160 DOID:0081410 DOID:0081406 round cell sarcoma with EWSR1-non-ETS fusion +MONDO:0958302 TFEB-rearranged renal cell carcinoma MONDO:0017886 DOID:0081414 DOID:0081413 MIT family translocation renal cell carcinoma +MONDO:0958303 childhood renal cell carcinoma with MiT translocations MONDO:0017886 DOID:0081416 DOID:0081413 MIT family translocation renal cell carcinoma +MONDO:0968944 intellectual developmental disorder, autosomal recessive 82 MONDO:0019502 DOID:0060947 DOID:0060308 autosomal recessive non-syndromic intellectual disability +MONDO:0968974 large B-cell lymphoma MONDO:0004095 DOID:0081452 DOID:707 B-cell neoplasm MONDO:8000011 visceral neuropathy, familial, 1, autosomal recessive MONDO:0000858 DOID:0080679 DOID:0080072 neuronal intestinal dysplasia MONDO:8000018 benign paroxysmal positional vertigo MONDO:0004900 DOID:13941 DOID:9847 peripheral vertigo MONDO:8000024 autoimmune lymphoproliferative syndrome, type III caused by mutation in PRKCD MONDO:0017979 DOID:0110119 DOID:6688 autoimmune lymphoproliferative syndrome diff --git a/src/ontology/reports/doid_mapping_status.tsv b/src/ontology/reports/doid_mapping_status.tsv index 0aa92e9c..8d63b74f 100644 --- a/src/ontology/reports/doid_mapping_status.tsv +++ b/src/ontology/reports/doid_mapping_status.tsv @@ -1,59 +1,11 @@ subject_id subject_label is_mapped is_excluded is_deprecated DOID:0060160 childhood spinal muscular atrophy False False False DOID:0060333 mitochondrial complex V (ATP synthase) deficiency nuclear type 4 False False False -DOID:0060936 dystonia 28, childhood-onset False False False -DOID:0060937 dystonia 30 False False False -DOID:0060938 dystonia 31 False False False -DOID:0060939 dystonia 32 False False False -DOID:0060940 dystonia 33 False False False -DOID:0060941 interstitial lung disease 1 False False False -DOID:0060942 Ullrich congenital muscular dystrophy 1B False False False -DOID:0060943 Ullrich congenital muscular dystrophy 1C False False False -DOID:0060944 Ullrich congenital muscular dystrophy 2 False False False -DOID:0060945 amelogenesis imperfecta type 1K False False False -DOID:0060946 Ullrich congenital muscular dystrophy 1A False False False -DOID:0060947 autosomal recessive intellectual developmental disorder 82 False False False -DOID:0060955 dystonia 35, childhood-onset False False False -DOID:0060956 dystonia 37, early-onset with striatal lesions False False False -DOID:0060957 myoclonic dystonia 34 False False False -DOID:0060963 dystonia, DOPA-responsive False False False -DOID:0060966 dystonia 22, juvenile-onset False False False -DOID:0060967 dystonia 22, adult-onset False False False -DOID:0070539 Halperin-Birk syndrome False False False -DOID:0081403 BCOR ITD sarcoma False False False -DOID:0081404 BCOR-CCNB3 sarcoma False False False -DOID:0081405 childhood sarcoma with BCOR genetic alterations False False False -DOID:0081407 childhood round cell sarcoma with EWSR1-non-ETS fusion False False False -DOID:0081408 round cell sarcoma with EWSR1-NFATC2 gene fusion False False False -DOID:0081409 round cell sarcoma with EWSR1-PATZ1 gene fusion False False False -DOID:0081410 round cell sarcoma with FUS-NFATC2 gene fusion False False False -DOID:0081414 TFEB-rearranged renal cell carcinoma False False False -DOID:0081416 childhood renal cell carcinoma with MiT translocations False False False -DOID:0081431 microcephaly, short stature, and limb abnormalities False False False -DOID:0081432 microcephaly-micromelia syndrome False False False -DOID:0081433 Peroxisome biogenesis disorder 4B False False False -DOID:0081434 Peroxisome biogenesis disorder 5B False False False -DOID:0081435 Peroxisome biogenesis disorder 6B False False False -DOID:0081436 Peroxisome biogenesis disorder 7B False False False -DOID:0081437 Peroxisome biogenesis disorder 8B False False False -DOID:0081438 Peroxisome biogenesis disorder 9B False False False -DOID:0081439 Peroxisome biogenesis disorder 11B False False False -DOID:0081440 Peroxisome biogenesis disorder 10B False False False -DOID:0081441 Nicolaides-Baraitser syndrome False False False -DOID:0081442 blepharophimosis-impaired intellectual development syndrome False False False -DOID:0081443 Stolerman neurodevelopmental syndrome False False False -DOID:0081444 neurodevelopmental disorder with poor growth and behavioral abnormalities False False False -DOID:0081445 sickle cell disease False False False -DOID:0081446 dimethylglycine dehydrogenase deficiency False False False -DOID:0081447 cone-rod dystrophy 21 False False False -DOID:0081448 cone-rod dystrophy 22 False False False -DOID:0081449 cone-rod dystrophy 24 False False False -DOID:0081450 hyperimmunoglobulinemia D periodic fever syndrome False False False -DOID:0081451 PFAPA syndrome False False False -DOID:0081452 large B-cell lymphoma False False False DOID:0111368 cholesterol-ester transfer protein deficiency False False False DOID:2536 chronic inflammatory demyelinating polyneuritis False False False +DOID:2934 aleutian mink disease False False False DOID:4668 congenital kyphosis False False False +DOID:5154 borna disease False False False DOID:9373 postural kyphosis False False False DOID:2214 obsolete inherited blood coagulation disease False False True DOID:0040003 benzylpenicillin allergy False True False @@ -4075,6 +4027,24 @@ DOID:0060932 developmental dysplasia of the hip 2 True False False DOID:0060933 developmental delay, dysmorphic facies, and brain anomalies True False False DOID:0060934 neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy True False False DOID:0060935 infantile hypotonia with psychomotor retardation and characteristic facies-3 True False False +DOID:0060936 dystonia 28, childhood-onset True False False +DOID:0060937 dystonia 30 True False False +DOID:0060938 dystonia 31 True False False +DOID:0060939 dystonia 32 True False False +DOID:0060940 dystonia 33 True False False +DOID:0060941 interstitial lung disease 1 True False False +DOID:0060942 Ullrich congenital muscular dystrophy 1B True False False +DOID:0060943 Ullrich congenital muscular dystrophy 1C True False False +DOID:0060944 Ullrich congenital muscular dystrophy 2 True False False +DOID:0060945 amelogenesis imperfecta type 1K True False False +DOID:0060946 Ullrich congenital muscular dystrophy 1A True False False +DOID:0060947 autosomal recessive intellectual developmental disorder 82 True False False +DOID:0060955 dystonia 35, childhood-onset True False False +DOID:0060956 dystonia 37, early-onset with striatal lesions True False False +DOID:0060957 myoclonic dystonia 34 True False False +DOID:0060963 dystonia, DOPA-responsive True False False +DOID:0060966 dystonia 22, juvenile-onset True False False +DOID:0060967 dystonia 22, adult-onset True False False DOID:0070000 3-methylglutaconic aciduria type 8 True False False DOID:0070002 3-methylglutaconic aciduria type 9 True False False DOID:0070003 blastoma True False False @@ -4596,6 +4566,7 @@ DOID:0070535 arrhythmogenic biventricular cardiomyopathy True False False DOID:0070536 neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures True False False DOID:0070537 spastic tetraplegia, thin corpus callosum, and progressive microcephaly True False False DOID:0070538 syndromic X-linked intellectual developmental disorder bain type True False False +DOID:0070539 Halperin-Birk syndrome True False False DOID:0080000 muscular disease True False False DOID:0080001 bone disease True False False DOID:0080005 bone remodeling disease True False False @@ -5911,11 +5882,20 @@ DOID:0081399 autosomal dominant distal hereditary motor neuronopathy 10 True Fal DOID:0081400 autosomal dominant distal hereditary motor neuronopathy 11 True False False DOID:0081401 autosomal dominant distal hereditary motor neuronopathy 13 True False False DOID:0081402 sarcoma with BCOR genetic alterations True False False +DOID:0081403 BCOR ITD sarcoma True False False +DOID:0081404 BCOR-CCNB3 sarcoma True False False +DOID:0081405 childhood sarcoma with BCOR genetic alterations True False False DOID:0081406 round cell sarcoma with EWSR1-non-ETS fusion True False False +DOID:0081407 childhood round cell sarcoma with EWSR1-non-ETS fusion True False False +DOID:0081408 round cell sarcoma with EWSR1-NFATC2 gene fusion True False False +DOID:0081409 round cell sarcoma with EWSR1-PATZ1 gene fusion True False False +DOID:0081410 round cell sarcoma with FUS-NFATC2 gene fusion True False False DOID:0081411 B acute lymphoblastic leukemia with PAX5 P80R mutation True False False DOID:0081412 B acute lymphoblastic leukemia with DUX4 rearrangement True False False DOID:0081413 renal cell carcinoma with MiT translocations True False False +DOID:0081414 TFEB-rearranged renal cell carcinoma True False False DOID:0081415 TFE3-rearranged renal cell carcinoma True False False +DOID:0081416 childhood renal cell carcinoma with MiT translocations True False False DOID:0081417 poorly differentiated chordoma True False False DOID:0081418 anaplastic sarcoma of the kidney True False False DOID:0081419 childhood-onset dystonia with optic atrophy and basal ganglia abnormalities True False False @@ -5930,6 +5910,28 @@ DOID:0081427 autosomal recessive distal hereditary motor neuronopathy 8 True Fal DOID:0081428 autosomal recessive distal hereditary motor neuronopathy 9 True False False DOID:0081429 autosomal recessive distal hereditary motor neuronopathy 10 True False False DOID:0081430 intellectual developmental disorder with autistic features and language delay, with or without seizures True False False +DOID:0081431 microcephaly, short stature, and limb abnormalities True False False +DOID:0081432 microcephaly-micromelia syndrome True False False +DOID:0081433 Peroxisome biogenesis disorder 4B True False False +DOID:0081434 Peroxisome biogenesis disorder 5B True False False +DOID:0081435 Peroxisome biogenesis disorder 6B True False False +DOID:0081436 Peroxisome biogenesis disorder 7B True False False +DOID:0081437 Peroxisome biogenesis disorder 8B True False False +DOID:0081438 Peroxisome biogenesis disorder 9B True False False +DOID:0081439 Peroxisome biogenesis disorder 11B True False False +DOID:0081440 Peroxisome biogenesis disorder 10B True False False +DOID:0081441 Nicolaides-Baraitser syndrome True False False +DOID:0081442 blepharophimosis-impaired intellectual development syndrome True False False +DOID:0081443 Stolerman neurodevelopmental syndrome True False False +DOID:0081444 neurodevelopmental disorder with poor growth and behavioral abnormalities True False False +DOID:0081445 sickle cell disease True False False +DOID:0081446 dimethylglycine dehydrogenase deficiency True False False +DOID:0081447 cone-rod dystrophy 21 True False False +DOID:0081448 cone-rod dystrophy 22 True False False +DOID:0081449 cone-rod dystrophy 24 True False False +DOID:0081450 hyperimmunoglobulinemia D periodic fever syndrome True False False +DOID:0081451 PFAPA syndrome True False False +DOID:0081452 large B-cell lymphoma True False False DOID:0090001 Fraser syndrome True False False DOID:0090002 Tietz syndrome True False False DOID:0090003 agenesis of the corpus callosum with peripheral neuropathy True False False @@ -10726,7 +10728,6 @@ DOID:2921 glomerulonephritis True False False DOID:2926 Klippel-Trenaunay syndrome True False False DOID:2929 Newcastle disease True False False DOID:293 lacrimal gland carcinoma True False False -DOID:2934 aleutian mink disease True False False DOID:2935 Chediak-Higashi syndrome True False False DOID:2938 Epstein-Barr virus infectious disease True False False DOID:294 lacrimal gland cancer True False False @@ -11934,7 +11935,6 @@ DOID:5150 neurofibroma of gallbladder True False False DOID:5151 plexiform neurofibroma True False False DOID:5152 cellular neurofibroma True False False DOID:5153 atypical neurofibroma True False False -DOID:5154 borna disease True False False DOID:5155 multiple mucosal neuroma True False False DOID:5157 benign pleural mesothelioma True False False DOID:5158 pleural cancer True False False diff --git a/src/ontology/reports/doid_unmapped_terms.tsv b/src/ontology/reports/doid_unmapped_terms.tsv index e4b530c4..8fef67d4 100644 --- a/src/ontology/reports/doid_unmapped_terms.tsv +++ b/src/ontology/reports/doid_unmapped_terms.tsv @@ -1,57 +1,9 @@ subject_id subject_label -DOID:0081403 BCOR ITD sarcoma -DOID:0081404 BCOR-CCNB3 sarcoma -DOID:0070539 Halperin-Birk syndrome -DOID:0081441 Nicolaides-Baraitser syndrome -DOID:0081451 PFAPA syndrome -DOID:0081440 Peroxisome biogenesis disorder 10B -DOID:0081439 Peroxisome biogenesis disorder 11B -DOID:0081433 Peroxisome biogenesis disorder 4B -DOID:0081434 Peroxisome biogenesis disorder 5B -DOID:0081435 Peroxisome biogenesis disorder 6B -DOID:0081436 Peroxisome biogenesis disorder 7B -DOID:0081437 Peroxisome biogenesis disorder 8B -DOID:0081438 Peroxisome biogenesis disorder 9B -DOID:0081443 Stolerman neurodevelopmental syndrome -DOID:0081414 TFEB-rearranged renal cell carcinoma -DOID:0060946 Ullrich congenital muscular dystrophy 1A -DOID:0060942 Ullrich congenital muscular dystrophy 1B -DOID:0060943 Ullrich congenital muscular dystrophy 1C -DOID:0060944 Ullrich congenital muscular dystrophy 2 -DOID:0060945 amelogenesis imperfecta type 1K -DOID:0060947 autosomal recessive intellectual developmental disorder 82 -DOID:0081442 blepharophimosis-impaired intellectual development syndrome -DOID:0081416 childhood renal cell carcinoma with MiT translocations -DOID:0081407 childhood round cell sarcoma with EWSR1-non-ETS fusion -DOID:0081405 childhood sarcoma with BCOR genetic alterations +DOID:2934 aleutian mink disease +DOID:5154 borna disease DOID:0060160 childhood spinal muscular atrophy DOID:0111368 cholesterol-ester transfer protein deficiency DOID:2536 chronic inflammatory demyelinating polyneuritis -DOID:0081447 cone-rod dystrophy 21 -DOID:0081448 cone-rod dystrophy 22 -DOID:0081449 cone-rod dystrophy 24 DOID:4668 congenital kyphosis -DOID:0081446 dimethylglycine dehydrogenase deficiency -DOID:0060967 dystonia 22, adult-onset -DOID:0060966 dystonia 22, juvenile-onset -DOID:0060936 dystonia 28, childhood-onset -DOID:0060937 dystonia 30 -DOID:0060938 dystonia 31 -DOID:0060939 dystonia 32 -DOID:0060940 dystonia 33 -DOID:0060955 dystonia 35, childhood-onset -DOID:0060956 dystonia 37, early-onset with striatal lesions -DOID:0060963 dystonia, DOPA-responsive -DOID:0081450 hyperimmunoglobulinemia D periodic fever syndrome -DOID:0060941 interstitial lung disease 1 -DOID:0081452 large B-cell lymphoma -DOID:0081431 microcephaly, short stature, and limb abnormalities -DOID:0081432 microcephaly-micromelia syndrome DOID:0060333 mitochondrial complex V (ATP synthase) deficiency nuclear type 4 -DOID:0060957 myoclonic dystonia 34 -DOID:0081444 neurodevelopmental disorder with poor growth and behavioral abnormalities DOID:9373 postural kyphosis -DOID:0081408 round cell sarcoma with EWSR1-NFATC2 gene fusion -DOID:0081409 round cell sarcoma with EWSR1-PATZ1 gene fusion -DOID:0081410 round cell sarcoma with FUS-NFATC2 gene fusion -DOID:0081445 sickle cell disease diff --git a/src/ontology/reports/mirror_signature-doid.tsv b/src/ontology/reports/mirror_signature-doid.tsv index ed44cd65..806f3c5b 100644 --- a/src/ontology/reports/mirror_signature-doid.tsv +++ b/src/ontology/reports/mirror_signature-doid.tsv @@ -15250,6 +15250,207 @@ + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + @@ -16423,207 +16624,6 @@ - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - diff --git a/src/ontology/reports/mirror_signature-mondo.tsv b/src/ontology/reports/mirror_signature-mondo.tsv index 337437ef..b0f7c77c 100644 --- a/src/ontology/reports/mirror_signature-mondo.tsv +++ b/src/ontology/reports/mirror_signature-mondo.tsv @@ -1114,6 +1114,7 @@ + @@ -3837,7 +3838,6 @@ - @@ -4849,6 +4849,7 @@ + @@ -4916,6 +4917,11 @@ + + + + + @@ -6551,6 +6557,7 @@ + @@ -8517,6 +8524,7 @@ + @@ -9843,6 +9851,7 @@ + @@ -10468,6 +10477,7 @@ + @@ -11054,6 +11064,8 @@ + + @@ -11215,6 +11227,7 @@ + @@ -42232,6 +42245,9 @@ + + + @@ -42827,6 +42843,7 @@ + @@ -42836,6 +42853,7 @@ + @@ -42849,6 +42867,7 @@ + @@ -43702,6 +43721,15 @@ + + + + + + + + + @@ -43739,6 +43767,19 @@ + + + + + + + + + + + + + @@ -43768,6 +43809,7 @@ + @@ -44772,6 +44814,7 @@ + @@ -45690,6 +45733,8 @@ + + @@ -45723,6 +45768,7 @@ + diff --git a/src/ontology/reports/mirror_signature-ncit.tsv b/src/ontology/reports/mirror_signature-ncit.tsv index 7e817d78..db7395ae 100644 --- a/src/ontology/reports/mirror_signature-ncit.tsv +++ b/src/ontology/reports/mirror_signature-ncit.tsv @@ -24043,8 +24043,6 @@ http://purl.obolibrary.org/obo/NCIT_C121917 http://purl.obolibrary.org/obo/NCIT_C121918 http://purl.obolibrary.org/obo/NCIT_C121919 http://purl.obolibrary.org/obo/NCIT_C12192 -http://purl.obolibrary.org/obo/NCIT_C121923 -http://purl.obolibrary.org/obo/NCIT_C121924 http://purl.obolibrary.org/obo/NCIT_C121925 http://purl.obolibrary.org/obo/NCIT_C121926 http://purl.obolibrary.org/obo/NCIT_C121927 @@ -25039,7 +25037,6 @@ http://purl.obolibrary.org/obo/NCIT_C122828 http://purl.obolibrary.org/obo/NCIT_C122829 http://purl.obolibrary.org/obo/NCIT_C122830 http://purl.obolibrary.org/obo/NCIT_C122831 -http://purl.obolibrary.org/obo/NCIT_C122832 http://purl.obolibrary.org/obo/NCIT_C122833 http://purl.obolibrary.org/obo/NCIT_C122834 http://purl.obolibrary.org/obo/NCIT_C122835 @@ -49864,7 +49861,6 @@ http://purl.obolibrary.org/obo/NCIT_C147308 http://purl.obolibrary.org/obo/NCIT_C147309 http://purl.obolibrary.org/obo/NCIT_C147310 http://purl.obolibrary.org/obo/NCIT_C147311 -http://purl.obolibrary.org/obo/NCIT_C147312 http://purl.obolibrary.org/obo/NCIT_C147313 http://purl.obolibrary.org/obo/NCIT_C147314 http://purl.obolibrary.org/obo/NCIT_C147315 @@ -54790,7 +54786,6 @@ http://purl.obolibrary.org/obo/NCIT_C153313 http://purl.obolibrary.org/obo/NCIT_C153314 http://purl.obolibrary.org/obo/NCIT_C153315 http://purl.obolibrary.org/obo/NCIT_C153316 -http://purl.obolibrary.org/obo/NCIT_C153317 http://purl.obolibrary.org/obo/NCIT_C153319 http://purl.obolibrary.org/obo/NCIT_C15332 http://purl.obolibrary.org/obo/NCIT_C153320 @@ -55509,7 +55504,6 @@ http://purl.obolibrary.org/obo/NCIT_C154136 http://purl.obolibrary.org/obo/NCIT_C154137 http://purl.obolibrary.org/obo/NCIT_C154138 http://purl.obolibrary.org/obo/NCIT_C154139 -http://purl.obolibrary.org/obo/NCIT_C15414 http://purl.obolibrary.org/obo/NCIT_C154140 http://purl.obolibrary.org/obo/NCIT_C154141 http://purl.obolibrary.org/obo/NCIT_C154142 @@ -57352,7 +57346,6 @@ http://purl.obolibrary.org/obo/NCIT_C156049 http://purl.obolibrary.org/obo/NCIT_C15605 http://purl.obolibrary.org/obo/NCIT_C156050 http://purl.obolibrary.org/obo/NCIT_C156051 -http://purl.obolibrary.org/obo/NCIT_C156052 http://purl.obolibrary.org/obo/NCIT_C156053 http://purl.obolibrary.org/obo/NCIT_C156054 http://purl.obolibrary.org/obo/NCIT_C156055 @@ -57818,7 +57811,6 @@ http://purl.obolibrary.org/obo/NCIT_C156483 http://purl.obolibrary.org/obo/NCIT_C156484 http://purl.obolibrary.org/obo/NCIT_C156485 http://purl.obolibrary.org/obo/NCIT_C156486 -http://purl.obolibrary.org/obo/NCIT_C156487 http://purl.obolibrary.org/obo/NCIT_C156488 http://purl.obolibrary.org/obo/NCIT_C156489 http://purl.obolibrary.org/obo/NCIT_C15649 @@ -60644,7 +60636,6 @@ http://purl.obolibrary.org/obo/NCIT_C159252 http://purl.obolibrary.org/obo/NCIT_C159253 http://purl.obolibrary.org/obo/NCIT_C159254 http://purl.obolibrary.org/obo/NCIT_C159255 -http://purl.obolibrary.org/obo/NCIT_C159256 http://purl.obolibrary.org/obo/NCIT_C159257 http://purl.obolibrary.org/obo/NCIT_C159258 http://purl.obolibrary.org/obo/NCIT_C159259 @@ -64280,7 +64271,6 @@ http://purl.obolibrary.org/obo/NCIT_C162844 http://purl.obolibrary.org/obo/NCIT_C162845 http://purl.obolibrary.org/obo/NCIT_C162846 http://purl.obolibrary.org/obo/NCIT_C162847 -http://purl.obolibrary.org/obo/NCIT_C162848 http://purl.obolibrary.org/obo/NCIT_C162849 http://purl.obolibrary.org/obo/NCIT_C16285 http://purl.obolibrary.org/obo/NCIT_C162850 @@ -66862,7 +66852,6 @@ http://purl.obolibrary.org/obo/NCIT_C165519 http://purl.obolibrary.org/obo/NCIT_C16552 http://purl.obolibrary.org/obo/NCIT_C165520 http://purl.obolibrary.org/obo/NCIT_C165521 -http://purl.obolibrary.org/obo/NCIT_C165522 http://purl.obolibrary.org/obo/NCIT_C165523 http://purl.obolibrary.org/obo/NCIT_C165525 http://purl.obolibrary.org/obo/NCIT_C165526 @@ -72054,7 +72043,6 @@ http://purl.obolibrary.org/obo/NCIT_C171536 http://purl.obolibrary.org/obo/NCIT_C171537 http://purl.obolibrary.org/obo/NCIT_C171538 http://purl.obolibrary.org/obo/NCIT_C171539 -http://purl.obolibrary.org/obo/NCIT_C17154 http://purl.obolibrary.org/obo/NCIT_C171540 http://purl.obolibrary.org/obo/NCIT_C171541 http://purl.obolibrary.org/obo/NCIT_C171542 @@ -73383,7 +73371,6 @@ http://purl.obolibrary.org/obo/NCIT_C172805 http://purl.obolibrary.org/obo/NCIT_C172806 http://purl.obolibrary.org/obo/NCIT_C172807 http://purl.obolibrary.org/obo/NCIT_C172808 -http://purl.obolibrary.org/obo/NCIT_C172809 http://purl.obolibrary.org/obo/NCIT_C17281 http://purl.obolibrary.org/obo/NCIT_C172810 http://purl.obolibrary.org/obo/NCIT_C172811 @@ -74110,7 +74097,6 @@ http://purl.obolibrary.org/obo/NCIT_C17353 http://purl.obolibrary.org/obo/NCIT_C173530 http://purl.obolibrary.org/obo/NCIT_C173531 http://purl.obolibrary.org/obo/NCIT_C173535 -http://purl.obolibrary.org/obo/NCIT_C173536 http://purl.obolibrary.org/obo/NCIT_C173537 http://purl.obolibrary.org/obo/NCIT_C173538 http://purl.obolibrary.org/obo/NCIT_C173539 @@ -74161,7 +74147,6 @@ http://purl.obolibrary.org/obo/NCIT_C173581 http://purl.obolibrary.org/obo/NCIT_C173582 http://purl.obolibrary.org/obo/NCIT_C173583 http://purl.obolibrary.org/obo/NCIT_C173584 -http://purl.obolibrary.org/obo/NCIT_C173585 http://purl.obolibrary.org/obo/NCIT_C173586 http://purl.obolibrary.org/obo/NCIT_C173587 http://purl.obolibrary.org/obo/NCIT_C173588 @@ -76607,7 +76592,6 @@ http://purl.obolibrary.org/obo/NCIT_C175852 http://purl.obolibrary.org/obo/NCIT_C175853 http://purl.obolibrary.org/obo/NCIT_C175854 http://purl.obolibrary.org/obo/NCIT_C175855 -http://purl.obolibrary.org/obo/NCIT_C175856 http://purl.obolibrary.org/obo/NCIT_C175857 http://purl.obolibrary.org/obo/NCIT_C175858 http://purl.obolibrary.org/obo/NCIT_C175859 @@ -77447,7 +77431,6 @@ http://purl.obolibrary.org/obo/NCIT_C176619 http://purl.obolibrary.org/obo/NCIT_C17662 http://purl.obolibrary.org/obo/NCIT_C176620 http://purl.obolibrary.org/obo/NCIT_C176621 -http://purl.obolibrary.org/obo/NCIT_C176622 http://purl.obolibrary.org/obo/NCIT_C176623 http://purl.obolibrary.org/obo/NCIT_C176624 http://purl.obolibrary.org/obo/NCIT_C176625 @@ -88692,7 +88675,6 @@ http://purl.obolibrary.org/obo/NCIT_C187030 http://purl.obolibrary.org/obo/NCIT_C187031 http://purl.obolibrary.org/obo/NCIT_C187032 http://purl.obolibrary.org/obo/NCIT_C187033 -http://purl.obolibrary.org/obo/NCIT_C187034 http://purl.obolibrary.org/obo/NCIT_C187035 http://purl.obolibrary.org/obo/NCIT_C187036 http://purl.obolibrary.org/obo/NCIT_C187037 @@ -89010,7 +88992,6 @@ http://purl.obolibrary.org/obo/NCIT_C187324 http://purl.obolibrary.org/obo/NCIT_C187325 http://purl.obolibrary.org/obo/NCIT_C187326 http://purl.obolibrary.org/obo/NCIT_C187327 -http://purl.obolibrary.org/obo/NCIT_C187328 http://purl.obolibrary.org/obo/NCIT_C187329 http://purl.obolibrary.org/obo/NCIT_C18733 http://purl.obolibrary.org/obo/NCIT_C187330 @@ -91816,7 +91797,6 @@ http://purl.obolibrary.org/obo/NCIT_C189902 http://purl.obolibrary.org/obo/NCIT_C189903 http://purl.obolibrary.org/obo/NCIT_C189904 http://purl.obolibrary.org/obo/NCIT_C189905 -http://purl.obolibrary.org/obo/NCIT_C189906 http://purl.obolibrary.org/obo/NCIT_C189907 http://purl.obolibrary.org/obo/NCIT_C189908 http://purl.obolibrary.org/obo/NCIT_C189909 @@ -93820,7 +93800,6 @@ http://purl.obolibrary.org/obo/NCIT_C191756 http://purl.obolibrary.org/obo/NCIT_C191757 http://purl.obolibrary.org/obo/NCIT_C191758 http://purl.obolibrary.org/obo/NCIT_C191759 -http://purl.obolibrary.org/obo/NCIT_C191760 http://purl.obolibrary.org/obo/NCIT_C191761 http://purl.obolibrary.org/obo/NCIT_C191762 http://purl.obolibrary.org/obo/NCIT_C191763 @@ -100498,7 +100477,6 @@ http://purl.obolibrary.org/obo/NCIT_C198025 http://purl.obolibrary.org/obo/NCIT_C198026 http://purl.obolibrary.org/obo/NCIT_C198027 http://purl.obolibrary.org/obo/NCIT_C198028 -http://purl.obolibrary.org/obo/NCIT_C198029 http://purl.obolibrary.org/obo/NCIT_C19803 http://purl.obolibrary.org/obo/NCIT_C198030 http://purl.obolibrary.org/obo/NCIT_C198031 @@ -103222,7 +103200,6 @@ http://purl.obolibrary.org/obo/NCIT_C20052 http://purl.obolibrary.org/obo/NCIT_C200520 http://purl.obolibrary.org/obo/NCIT_C200521 http://purl.obolibrary.org/obo/NCIT_C200522 -http://purl.obolibrary.org/obo/NCIT_C200523 http://purl.obolibrary.org/obo/NCIT_C200524 http://purl.obolibrary.org/obo/NCIT_C200525 http://purl.obolibrary.org/obo/NCIT_C200526 @@ -104345,441 +104322,4390 @@ http://purl.obolibrary.org/obo/NCIT_C201554 http://purl.obolibrary.org/obo/NCIT_C201555 http://purl.obolibrary.org/obo/NCIT_C201556 http://purl.obolibrary.org/obo/NCIT_C201557 +http://purl.obolibrary.org/obo/NCIT_C201558 +http://purl.obolibrary.org/obo/NCIT_C201559 http://purl.obolibrary.org/obo/NCIT_C20156 +http://purl.obolibrary.org/obo/NCIT_C201560 +http://purl.obolibrary.org/obo/NCIT_C201561 +http://purl.obolibrary.org/obo/NCIT_C201562 +http://purl.obolibrary.org/obo/NCIT_C201563 +http://purl.obolibrary.org/obo/NCIT_C201564 +http://purl.obolibrary.org/obo/NCIT_C201565 +http://purl.obolibrary.org/obo/NCIT_C201566 +http://purl.obolibrary.org/obo/NCIT_C201567 +http://purl.obolibrary.org/obo/NCIT_C201568 +http://purl.obolibrary.org/obo/NCIT_C201569 http://purl.obolibrary.org/obo/NCIT_C20157 +http://purl.obolibrary.org/obo/NCIT_C201570 +http://purl.obolibrary.org/obo/NCIT_C201571 +http://purl.obolibrary.org/obo/NCIT_C201572 +http://purl.obolibrary.org/obo/NCIT_C201573 +http://purl.obolibrary.org/obo/NCIT_C201574 +http://purl.obolibrary.org/obo/NCIT_C201576 +http://purl.obolibrary.org/obo/NCIT_C201577 +http://purl.obolibrary.org/obo/NCIT_C201578 +http://purl.obolibrary.org/obo/NCIT_C201579 http://purl.obolibrary.org/obo/NCIT_C20158 +http://purl.obolibrary.org/obo/NCIT_C201580 +http://purl.obolibrary.org/obo/NCIT_C201581 +http://purl.obolibrary.org/obo/NCIT_C201582 +http://purl.obolibrary.org/obo/NCIT_C201583 +http://purl.obolibrary.org/obo/NCIT_C201584 +http://purl.obolibrary.org/obo/NCIT_C201585 +http://purl.obolibrary.org/obo/NCIT_C201586 +http://purl.obolibrary.org/obo/NCIT_C201587 +http://purl.obolibrary.org/obo/NCIT_C201588 +http://purl.obolibrary.org/obo/NCIT_C201589 http://purl.obolibrary.org/obo/NCIT_C20159 +http://purl.obolibrary.org/obo/NCIT_C201590 +http://purl.obolibrary.org/obo/NCIT_C201591 +http://purl.obolibrary.org/obo/NCIT_C201592 +http://purl.obolibrary.org/obo/NCIT_C201593 +http://purl.obolibrary.org/obo/NCIT_C201594 +http://purl.obolibrary.org/obo/NCIT_C201595 +http://purl.obolibrary.org/obo/NCIT_C201596 +http://purl.obolibrary.org/obo/NCIT_C201597 +http://purl.obolibrary.org/obo/NCIT_C201598 +http://purl.obolibrary.org/obo/NCIT_C201599 http://purl.obolibrary.org/obo/NCIT_C2016 http://purl.obolibrary.org/obo/NCIT_C20160 +http://purl.obolibrary.org/obo/NCIT_C201600 +http://purl.obolibrary.org/obo/NCIT_C201601 +http://purl.obolibrary.org/obo/NCIT_C201602 +http://purl.obolibrary.org/obo/NCIT_C201603 +http://purl.obolibrary.org/obo/NCIT_C201604 +http://purl.obolibrary.org/obo/NCIT_C201605 +http://purl.obolibrary.org/obo/NCIT_C201606 +http://purl.obolibrary.org/obo/NCIT_C201607 +http://purl.obolibrary.org/obo/NCIT_C201608 +http://purl.obolibrary.org/obo/NCIT_C201609 http://purl.obolibrary.org/obo/NCIT_C20161 +http://purl.obolibrary.org/obo/NCIT_C201610 +http://purl.obolibrary.org/obo/NCIT_C201611 +http://purl.obolibrary.org/obo/NCIT_C201612 +http://purl.obolibrary.org/obo/NCIT_C201613 +http://purl.obolibrary.org/obo/NCIT_C201614 +http://purl.obolibrary.org/obo/NCIT_C201615 +http://purl.obolibrary.org/obo/NCIT_C201616 +http://purl.obolibrary.org/obo/NCIT_C201617 +http://purl.obolibrary.org/obo/NCIT_C201618 +http://purl.obolibrary.org/obo/NCIT_C201619 http://purl.obolibrary.org/obo/NCIT_C20162 +http://purl.obolibrary.org/obo/NCIT_C201621 +http://purl.obolibrary.org/obo/NCIT_C201622 +http://purl.obolibrary.org/obo/NCIT_C201623 +http://purl.obolibrary.org/obo/NCIT_C201624 +http://purl.obolibrary.org/obo/NCIT_C201625 +http://purl.obolibrary.org/obo/NCIT_C201626 +http://purl.obolibrary.org/obo/NCIT_C201627 +http://purl.obolibrary.org/obo/NCIT_C201628 +http://purl.obolibrary.org/obo/NCIT_C201629 http://purl.obolibrary.org/obo/NCIT_C20163 +http://purl.obolibrary.org/obo/NCIT_C201630 +http://purl.obolibrary.org/obo/NCIT_C201631 +http://purl.obolibrary.org/obo/NCIT_C201632 +http://purl.obolibrary.org/obo/NCIT_C201633 +http://purl.obolibrary.org/obo/NCIT_C201634 +http://purl.obolibrary.org/obo/NCIT_C201635 +http://purl.obolibrary.org/obo/NCIT_C201636 +http://purl.obolibrary.org/obo/NCIT_C201637 +http://purl.obolibrary.org/obo/NCIT_C201638 +http://purl.obolibrary.org/obo/NCIT_C201639 http://purl.obolibrary.org/obo/NCIT_C20164 +http://purl.obolibrary.org/obo/NCIT_C201640 +http://purl.obolibrary.org/obo/NCIT_C201641 +http://purl.obolibrary.org/obo/NCIT_C201642 +http://purl.obolibrary.org/obo/NCIT_C201643 +http://purl.obolibrary.org/obo/NCIT_C201644 +http://purl.obolibrary.org/obo/NCIT_C201645 +http://purl.obolibrary.org/obo/NCIT_C201646 +http://purl.obolibrary.org/obo/NCIT_C201647 +http://purl.obolibrary.org/obo/NCIT_C201648 +http://purl.obolibrary.org/obo/NCIT_C201649 http://purl.obolibrary.org/obo/NCIT_C20165 +http://purl.obolibrary.org/obo/NCIT_C201650 +http://purl.obolibrary.org/obo/NCIT_C201651 +http://purl.obolibrary.org/obo/NCIT_C201652 +http://purl.obolibrary.org/obo/NCIT_C201653 +http://purl.obolibrary.org/obo/NCIT_C201654 +http://purl.obolibrary.org/obo/NCIT_C201655 +http://purl.obolibrary.org/obo/NCIT_C201656 +http://purl.obolibrary.org/obo/NCIT_C201657 +http://purl.obolibrary.org/obo/NCIT_C201658 +http://purl.obolibrary.org/obo/NCIT_C201659 http://purl.obolibrary.org/obo/NCIT_C20166 +http://purl.obolibrary.org/obo/NCIT_C201660 +http://purl.obolibrary.org/obo/NCIT_C201661 +http://purl.obolibrary.org/obo/NCIT_C201662 +http://purl.obolibrary.org/obo/NCIT_C201663 +http://purl.obolibrary.org/obo/NCIT_C201664 +http://purl.obolibrary.org/obo/NCIT_C201665 +http://purl.obolibrary.org/obo/NCIT_C201666 +http://purl.obolibrary.org/obo/NCIT_C201667 +http://purl.obolibrary.org/obo/NCIT_C201668 +http://purl.obolibrary.org/obo/NCIT_C201669 http://purl.obolibrary.org/obo/NCIT_C20167 +http://purl.obolibrary.org/obo/NCIT_C201670 +http://purl.obolibrary.org/obo/NCIT_C201671 +http://purl.obolibrary.org/obo/NCIT_C201672 +http://purl.obolibrary.org/obo/NCIT_C201673 +http://purl.obolibrary.org/obo/NCIT_C201674 +http://purl.obolibrary.org/obo/NCIT_C201675 +http://purl.obolibrary.org/obo/NCIT_C201676 +http://purl.obolibrary.org/obo/NCIT_C201677 +http://purl.obolibrary.org/obo/NCIT_C201678 +http://purl.obolibrary.org/obo/NCIT_C201679 http://purl.obolibrary.org/obo/NCIT_C20168 +http://purl.obolibrary.org/obo/NCIT_C201680 +http://purl.obolibrary.org/obo/NCIT_C201681 +http://purl.obolibrary.org/obo/NCIT_C201682 +http://purl.obolibrary.org/obo/NCIT_C201683 +http://purl.obolibrary.org/obo/NCIT_C201684 +http://purl.obolibrary.org/obo/NCIT_C201685 +http://purl.obolibrary.org/obo/NCIT_C201686 +http://purl.obolibrary.org/obo/NCIT_C201687 +http://purl.obolibrary.org/obo/NCIT_C201688 +http://purl.obolibrary.org/obo/NCIT_C201689 http://purl.obolibrary.org/obo/NCIT_C20169 +http://purl.obolibrary.org/obo/NCIT_C201690 +http://purl.obolibrary.org/obo/NCIT_C201691 +http://purl.obolibrary.org/obo/NCIT_C201692 +http://purl.obolibrary.org/obo/NCIT_C201693 +http://purl.obolibrary.org/obo/NCIT_C201694 +http://purl.obolibrary.org/obo/NCIT_C201695 +http://purl.obolibrary.org/obo/NCIT_C201696 +http://purl.obolibrary.org/obo/NCIT_C201697 +http://purl.obolibrary.org/obo/NCIT_C201698 +http://purl.obolibrary.org/obo/NCIT_C201699 http://purl.obolibrary.org/obo/NCIT_C2017 http://purl.obolibrary.org/obo/NCIT_C20170 +http://purl.obolibrary.org/obo/NCIT_C201700 +http://purl.obolibrary.org/obo/NCIT_C201701 +http://purl.obolibrary.org/obo/NCIT_C201702 +http://purl.obolibrary.org/obo/NCIT_C201703 +http://purl.obolibrary.org/obo/NCIT_C201704 +http://purl.obolibrary.org/obo/NCIT_C201705 +http://purl.obolibrary.org/obo/NCIT_C201706 +http://purl.obolibrary.org/obo/NCIT_C201707 +http://purl.obolibrary.org/obo/NCIT_C201708 +http://purl.obolibrary.org/obo/NCIT_C201709 http://purl.obolibrary.org/obo/NCIT_C20171 +http://purl.obolibrary.org/obo/NCIT_C201710 +http://purl.obolibrary.org/obo/NCIT_C201711 +http://purl.obolibrary.org/obo/NCIT_C201712 +http://purl.obolibrary.org/obo/NCIT_C201713 +http://purl.obolibrary.org/obo/NCIT_C201714 +http://purl.obolibrary.org/obo/NCIT_C201715 +http://purl.obolibrary.org/obo/NCIT_C201716 +http://purl.obolibrary.org/obo/NCIT_C201717 +http://purl.obolibrary.org/obo/NCIT_C201718 +http://purl.obolibrary.org/obo/NCIT_C201719 http://purl.obolibrary.org/obo/NCIT_C20172 +http://purl.obolibrary.org/obo/NCIT_C201720 +http://purl.obolibrary.org/obo/NCIT_C201721 +http://purl.obolibrary.org/obo/NCIT_C201722 +http://purl.obolibrary.org/obo/NCIT_C201723 +http://purl.obolibrary.org/obo/NCIT_C201724 +http://purl.obolibrary.org/obo/NCIT_C201725 +http://purl.obolibrary.org/obo/NCIT_C201726 +http://purl.obolibrary.org/obo/NCIT_C201727 +http://purl.obolibrary.org/obo/NCIT_C201728 +http://purl.obolibrary.org/obo/NCIT_C201729 http://purl.obolibrary.org/obo/NCIT_C20173 +http://purl.obolibrary.org/obo/NCIT_C201730 +http://purl.obolibrary.org/obo/NCIT_C201731 +http://purl.obolibrary.org/obo/NCIT_C201732 +http://purl.obolibrary.org/obo/NCIT_C201733 +http://purl.obolibrary.org/obo/NCIT_C201734 +http://purl.obolibrary.org/obo/NCIT_C201735 +http://purl.obolibrary.org/obo/NCIT_C201736 +http://purl.obolibrary.org/obo/NCIT_C201737 +http://purl.obolibrary.org/obo/NCIT_C201738 +http://purl.obolibrary.org/obo/NCIT_C201739 http://purl.obolibrary.org/obo/NCIT_C20174 +http://purl.obolibrary.org/obo/NCIT_C201740 +http://purl.obolibrary.org/obo/NCIT_C201741 +http://purl.obolibrary.org/obo/NCIT_C201742 +http://purl.obolibrary.org/obo/NCIT_C201743 +http://purl.obolibrary.org/obo/NCIT_C201744 +http://purl.obolibrary.org/obo/NCIT_C201745 +http://purl.obolibrary.org/obo/NCIT_C201746 +http://purl.obolibrary.org/obo/NCIT_C201747 +http://purl.obolibrary.org/obo/NCIT_C201748 +http://purl.obolibrary.org/obo/NCIT_C201749 http://purl.obolibrary.org/obo/NCIT_C20175 +http://purl.obolibrary.org/obo/NCIT_C201750 +http://purl.obolibrary.org/obo/NCIT_C201751 +http://purl.obolibrary.org/obo/NCIT_C201752 +http://purl.obolibrary.org/obo/NCIT_C201753 +http://purl.obolibrary.org/obo/NCIT_C201754 +http://purl.obolibrary.org/obo/NCIT_C201755 +http://purl.obolibrary.org/obo/NCIT_C201756 +http://purl.obolibrary.org/obo/NCIT_C201757 +http://purl.obolibrary.org/obo/NCIT_C201758 +http://purl.obolibrary.org/obo/NCIT_C201759 http://purl.obolibrary.org/obo/NCIT_C20176 +http://purl.obolibrary.org/obo/NCIT_C201760 +http://purl.obolibrary.org/obo/NCIT_C201761 +http://purl.obolibrary.org/obo/NCIT_C201762 +http://purl.obolibrary.org/obo/NCIT_C201763 +http://purl.obolibrary.org/obo/NCIT_C201764 +http://purl.obolibrary.org/obo/NCIT_C201765 +http://purl.obolibrary.org/obo/NCIT_C201769 http://purl.obolibrary.org/obo/NCIT_C20177 +http://purl.obolibrary.org/obo/NCIT_C201770 +http://purl.obolibrary.org/obo/NCIT_C201771 +http://purl.obolibrary.org/obo/NCIT_C201772 +http://purl.obolibrary.org/obo/NCIT_C201773 +http://purl.obolibrary.org/obo/NCIT_C201774 +http://purl.obolibrary.org/obo/NCIT_C201775 +http://purl.obolibrary.org/obo/NCIT_C201776 +http://purl.obolibrary.org/obo/NCIT_C201777 +http://purl.obolibrary.org/obo/NCIT_C201778 +http://purl.obolibrary.org/obo/NCIT_C201779 http://purl.obolibrary.org/obo/NCIT_C20178 +http://purl.obolibrary.org/obo/NCIT_C201780 +http://purl.obolibrary.org/obo/NCIT_C201781 +http://purl.obolibrary.org/obo/NCIT_C201782 +http://purl.obolibrary.org/obo/NCIT_C201783 +http://purl.obolibrary.org/obo/NCIT_C201784 +http://purl.obolibrary.org/obo/NCIT_C201785 +http://purl.obolibrary.org/obo/NCIT_C201786 +http://purl.obolibrary.org/obo/NCIT_C201787 +http://purl.obolibrary.org/obo/NCIT_C201788 +http://purl.obolibrary.org/obo/NCIT_C201789 http://purl.obolibrary.org/obo/NCIT_C20179 +http://purl.obolibrary.org/obo/NCIT_C201790 +http://purl.obolibrary.org/obo/NCIT_C201791 +http://purl.obolibrary.org/obo/NCIT_C201792 +http://purl.obolibrary.org/obo/NCIT_C201793 +http://purl.obolibrary.org/obo/NCIT_C201794 +http://purl.obolibrary.org/obo/NCIT_C201795 +http://purl.obolibrary.org/obo/NCIT_C201796 +http://purl.obolibrary.org/obo/NCIT_C201797 +http://purl.obolibrary.org/obo/NCIT_C201798 +http://purl.obolibrary.org/obo/NCIT_C201799 http://purl.obolibrary.org/obo/NCIT_C2018 http://purl.obolibrary.org/obo/NCIT_C20180 +http://purl.obolibrary.org/obo/NCIT_C201800 +http://purl.obolibrary.org/obo/NCIT_C201801 +http://purl.obolibrary.org/obo/NCIT_C201802 +http://purl.obolibrary.org/obo/NCIT_C201803 +http://purl.obolibrary.org/obo/NCIT_C201804 +http://purl.obolibrary.org/obo/NCIT_C201805 +http://purl.obolibrary.org/obo/NCIT_C201806 +http://purl.obolibrary.org/obo/NCIT_C201807 +http://purl.obolibrary.org/obo/NCIT_C201808 +http://purl.obolibrary.org/obo/NCIT_C201809 http://purl.obolibrary.org/obo/NCIT_C20181 +http://purl.obolibrary.org/obo/NCIT_C201810 +http://purl.obolibrary.org/obo/NCIT_C201811 +http://purl.obolibrary.org/obo/NCIT_C201812 +http://purl.obolibrary.org/obo/NCIT_C201813 +http://purl.obolibrary.org/obo/NCIT_C201814 +http://purl.obolibrary.org/obo/NCIT_C201815 +http://purl.obolibrary.org/obo/NCIT_C201816 +http://purl.obolibrary.org/obo/NCIT_C201817 +http://purl.obolibrary.org/obo/NCIT_C201818 +http://purl.obolibrary.org/obo/NCIT_C201819 http://purl.obolibrary.org/obo/NCIT_C20182 +http://purl.obolibrary.org/obo/NCIT_C201820 +http://purl.obolibrary.org/obo/NCIT_C201821 +http://purl.obolibrary.org/obo/NCIT_C201822 +http://purl.obolibrary.org/obo/NCIT_C201823 +http://purl.obolibrary.org/obo/NCIT_C201824 +http://purl.obolibrary.org/obo/NCIT_C201825 +http://purl.obolibrary.org/obo/NCIT_C201826 +http://purl.obolibrary.org/obo/NCIT_C201827 +http://purl.obolibrary.org/obo/NCIT_C201828 +http://purl.obolibrary.org/obo/NCIT_C201829 http://purl.obolibrary.org/obo/NCIT_C20183 +http://purl.obolibrary.org/obo/NCIT_C201830 +http://purl.obolibrary.org/obo/NCIT_C201831 +http://purl.obolibrary.org/obo/NCIT_C201832 +http://purl.obolibrary.org/obo/NCIT_C201833 +http://purl.obolibrary.org/obo/NCIT_C201834 +http://purl.obolibrary.org/obo/NCIT_C201835 +http://purl.obolibrary.org/obo/NCIT_C201836 +http://purl.obolibrary.org/obo/NCIT_C201837 +http://purl.obolibrary.org/obo/NCIT_C201838 +http://purl.obolibrary.org/obo/NCIT_C201839 http://purl.obolibrary.org/obo/NCIT_C20184 +http://purl.obolibrary.org/obo/NCIT_C201840 +http://purl.obolibrary.org/obo/NCIT_C201841 +http://purl.obolibrary.org/obo/NCIT_C201842 +http://purl.obolibrary.org/obo/NCIT_C201843 +http://purl.obolibrary.org/obo/NCIT_C201844 +http://purl.obolibrary.org/obo/NCIT_C201845 +http://purl.obolibrary.org/obo/NCIT_C201846 +http://purl.obolibrary.org/obo/NCIT_C201847 +http://purl.obolibrary.org/obo/NCIT_C201848 +http://purl.obolibrary.org/obo/NCIT_C201849 http://purl.obolibrary.org/obo/NCIT_C20185 +http://purl.obolibrary.org/obo/NCIT_C201850 +http://purl.obolibrary.org/obo/NCIT_C201851 +http://purl.obolibrary.org/obo/NCIT_C201852 +http://purl.obolibrary.org/obo/NCIT_C201853 +http://purl.obolibrary.org/obo/NCIT_C201854 +http://purl.obolibrary.org/obo/NCIT_C201855 +http://purl.obolibrary.org/obo/NCIT_C201856 +http://purl.obolibrary.org/obo/NCIT_C201857 +http://purl.obolibrary.org/obo/NCIT_C201858 +http://purl.obolibrary.org/obo/NCIT_C201859 http://purl.obolibrary.org/obo/NCIT_C20186 +http://purl.obolibrary.org/obo/NCIT_C201860 +http://purl.obolibrary.org/obo/NCIT_C201861 +http://purl.obolibrary.org/obo/NCIT_C201862 +http://purl.obolibrary.org/obo/NCIT_C201863 +http://purl.obolibrary.org/obo/NCIT_C201864 +http://purl.obolibrary.org/obo/NCIT_C201865 +http://purl.obolibrary.org/obo/NCIT_C201866 +http://purl.obolibrary.org/obo/NCIT_C201867 +http://purl.obolibrary.org/obo/NCIT_C201868 +http://purl.obolibrary.org/obo/NCIT_C201869 http://purl.obolibrary.org/obo/NCIT_C20187 +http://purl.obolibrary.org/obo/NCIT_C201870 +http://purl.obolibrary.org/obo/NCIT_C201871 +http://purl.obolibrary.org/obo/NCIT_C201872 +http://purl.obolibrary.org/obo/NCIT_C201873 +http://purl.obolibrary.org/obo/NCIT_C201874 +http://purl.obolibrary.org/obo/NCIT_C201875 +http://purl.obolibrary.org/obo/NCIT_C201876 +http://purl.obolibrary.org/obo/NCIT_C201877 +http://purl.obolibrary.org/obo/NCIT_C201878 +http://purl.obolibrary.org/obo/NCIT_C201879 http://purl.obolibrary.org/obo/NCIT_C20188 +http://purl.obolibrary.org/obo/NCIT_C201880 +http://purl.obolibrary.org/obo/NCIT_C201881 +http://purl.obolibrary.org/obo/NCIT_C201882 +http://purl.obolibrary.org/obo/NCIT_C201883 +http://purl.obolibrary.org/obo/NCIT_C201884 +http://purl.obolibrary.org/obo/NCIT_C201885 +http://purl.obolibrary.org/obo/NCIT_C201886 +http://purl.obolibrary.org/obo/NCIT_C201887 +http://purl.obolibrary.org/obo/NCIT_C201889 http://purl.obolibrary.org/obo/NCIT_C20189 +http://purl.obolibrary.org/obo/NCIT_C201890 +http://purl.obolibrary.org/obo/NCIT_C201891 +http://purl.obolibrary.org/obo/NCIT_C201892 +http://purl.obolibrary.org/obo/NCIT_C201893 +http://purl.obolibrary.org/obo/NCIT_C201894 +http://purl.obolibrary.org/obo/NCIT_C201895 +http://purl.obolibrary.org/obo/NCIT_C201896 +http://purl.obolibrary.org/obo/NCIT_C201897 +http://purl.obolibrary.org/obo/NCIT_C201898 +http://purl.obolibrary.org/obo/NCIT_C201899 http://purl.obolibrary.org/obo/NCIT_C2019 http://purl.obolibrary.org/obo/NCIT_C20190 +http://purl.obolibrary.org/obo/NCIT_C201900 +http://purl.obolibrary.org/obo/NCIT_C201901 +http://purl.obolibrary.org/obo/NCIT_C201902 +http://purl.obolibrary.org/obo/NCIT_C201903 +http://purl.obolibrary.org/obo/NCIT_C201904 +http://purl.obolibrary.org/obo/NCIT_C201905 +http://purl.obolibrary.org/obo/NCIT_C201906 +http://purl.obolibrary.org/obo/NCIT_C201907 +http://purl.obolibrary.org/obo/NCIT_C201908 +http://purl.obolibrary.org/obo/NCIT_C201909 http://purl.obolibrary.org/obo/NCIT_C20191 +http://purl.obolibrary.org/obo/NCIT_C201910 +http://purl.obolibrary.org/obo/NCIT_C201911 +http://purl.obolibrary.org/obo/NCIT_C201912 +http://purl.obolibrary.org/obo/NCIT_C201913 +http://purl.obolibrary.org/obo/NCIT_C201914 +http://purl.obolibrary.org/obo/NCIT_C201915 +http://purl.obolibrary.org/obo/NCIT_C201916 +http://purl.obolibrary.org/obo/NCIT_C201917 +http://purl.obolibrary.org/obo/NCIT_C201918 +http://purl.obolibrary.org/obo/NCIT_C201919 +http://purl.obolibrary.org/obo/NCIT_C201920 +http://purl.obolibrary.org/obo/NCIT_C201921 +http://purl.obolibrary.org/obo/NCIT_C201922 +http://purl.obolibrary.org/obo/NCIT_C201923 +http://purl.obolibrary.org/obo/NCIT_C201924 +http://purl.obolibrary.org/obo/NCIT_C201925 +http://purl.obolibrary.org/obo/NCIT_C201926 +http://purl.obolibrary.org/obo/NCIT_C201927 +http://purl.obolibrary.org/obo/NCIT_C201928 +http://purl.obolibrary.org/obo/NCIT_C201929 http://purl.obolibrary.org/obo/NCIT_C20193 +http://purl.obolibrary.org/obo/NCIT_C201930 +http://purl.obolibrary.org/obo/NCIT_C201931 +http://purl.obolibrary.org/obo/NCIT_C201932 +http://purl.obolibrary.org/obo/NCIT_C201933 +http://purl.obolibrary.org/obo/NCIT_C201934 +http://purl.obolibrary.org/obo/NCIT_C201935 +http://purl.obolibrary.org/obo/NCIT_C201936 +http://purl.obolibrary.org/obo/NCIT_C201937 +http://purl.obolibrary.org/obo/NCIT_C201938 +http://purl.obolibrary.org/obo/NCIT_C201939 http://purl.obolibrary.org/obo/NCIT_C20194 +http://purl.obolibrary.org/obo/NCIT_C201940 +http://purl.obolibrary.org/obo/NCIT_C201941 +http://purl.obolibrary.org/obo/NCIT_C201942 +http://purl.obolibrary.org/obo/NCIT_C201943 +http://purl.obolibrary.org/obo/NCIT_C201944 +http://purl.obolibrary.org/obo/NCIT_C201945 +http://purl.obolibrary.org/obo/NCIT_C201946 +http://purl.obolibrary.org/obo/NCIT_C201947 +http://purl.obolibrary.org/obo/NCIT_C201948 +http://purl.obolibrary.org/obo/NCIT_C201949 http://purl.obolibrary.org/obo/NCIT_C20195 +http://purl.obolibrary.org/obo/NCIT_C201950 +http://purl.obolibrary.org/obo/NCIT_C201951 +http://purl.obolibrary.org/obo/NCIT_C201952 +http://purl.obolibrary.org/obo/NCIT_C201953 +http://purl.obolibrary.org/obo/NCIT_C201954 +http://purl.obolibrary.org/obo/NCIT_C201955 +http://purl.obolibrary.org/obo/NCIT_C201956 +http://purl.obolibrary.org/obo/NCIT_C201957 +http://purl.obolibrary.org/obo/NCIT_C201958 +http://purl.obolibrary.org/obo/NCIT_C201959 +http://purl.obolibrary.org/obo/NCIT_C201960 +http://purl.obolibrary.org/obo/NCIT_C201961 +http://purl.obolibrary.org/obo/NCIT_C201962 +http://purl.obolibrary.org/obo/NCIT_C201963 +http://purl.obolibrary.org/obo/NCIT_C201964 +http://purl.obolibrary.org/obo/NCIT_C201965 +http://purl.obolibrary.org/obo/NCIT_C201966 +http://purl.obolibrary.org/obo/NCIT_C201967 +http://purl.obolibrary.org/obo/NCIT_C201968 +http://purl.obolibrary.org/obo/NCIT_C201969 http://purl.obolibrary.org/obo/NCIT_C20197 +http://purl.obolibrary.org/obo/NCIT_C201972 +http://purl.obolibrary.org/obo/NCIT_C201973 +http://purl.obolibrary.org/obo/NCIT_C201974 +http://purl.obolibrary.org/obo/NCIT_C201975 +http://purl.obolibrary.org/obo/NCIT_C201976 +http://purl.obolibrary.org/obo/NCIT_C201977 +http://purl.obolibrary.org/obo/NCIT_C201978 +http://purl.obolibrary.org/obo/NCIT_C201979 http://purl.obolibrary.org/obo/NCIT_C20198 +http://purl.obolibrary.org/obo/NCIT_C201980 +http://purl.obolibrary.org/obo/NCIT_C201981 +http://purl.obolibrary.org/obo/NCIT_C201982 +http://purl.obolibrary.org/obo/NCIT_C201983 +http://purl.obolibrary.org/obo/NCIT_C201984 +http://purl.obolibrary.org/obo/NCIT_C201985 +http://purl.obolibrary.org/obo/NCIT_C201986 +http://purl.obolibrary.org/obo/NCIT_C201987 +http://purl.obolibrary.org/obo/NCIT_C201988 +http://purl.obolibrary.org/obo/NCIT_C201989 http://purl.obolibrary.org/obo/NCIT_C20199 +http://purl.obolibrary.org/obo/NCIT_C201990 +http://purl.obolibrary.org/obo/NCIT_C201991 +http://purl.obolibrary.org/obo/NCIT_C201992 +http://purl.obolibrary.org/obo/NCIT_C201993 +http://purl.obolibrary.org/obo/NCIT_C201994 +http://purl.obolibrary.org/obo/NCIT_C201995 +http://purl.obolibrary.org/obo/NCIT_C201996 +http://purl.obolibrary.org/obo/NCIT_C201997 +http://purl.obolibrary.org/obo/NCIT_C201998 +http://purl.obolibrary.org/obo/NCIT_C201999 http://purl.obolibrary.org/obo/NCIT_C202 http://purl.obolibrary.org/obo/NCIT_C2020 http://purl.obolibrary.org/obo/NCIT_C20200 +http://purl.obolibrary.org/obo/NCIT_C202000 +http://purl.obolibrary.org/obo/NCIT_C202001 +http://purl.obolibrary.org/obo/NCIT_C202002 +http://purl.obolibrary.org/obo/NCIT_C202003 +http://purl.obolibrary.org/obo/NCIT_C202004 +http://purl.obolibrary.org/obo/NCIT_C202005 +http://purl.obolibrary.org/obo/NCIT_C202006 +http://purl.obolibrary.org/obo/NCIT_C202007 +http://purl.obolibrary.org/obo/NCIT_C202008 +http://purl.obolibrary.org/obo/NCIT_C202009 http://purl.obolibrary.org/obo/NCIT_C20201 +http://purl.obolibrary.org/obo/NCIT_C202010 +http://purl.obolibrary.org/obo/NCIT_C202011 +http://purl.obolibrary.org/obo/NCIT_C202012 +http://purl.obolibrary.org/obo/NCIT_C202013 +http://purl.obolibrary.org/obo/NCIT_C202014 +http://purl.obolibrary.org/obo/NCIT_C202015 +http://purl.obolibrary.org/obo/NCIT_C202016 +http://purl.obolibrary.org/obo/NCIT_C202017 +http://purl.obolibrary.org/obo/NCIT_C202018 +http://purl.obolibrary.org/obo/NCIT_C202019 http://purl.obolibrary.org/obo/NCIT_C20202 +http://purl.obolibrary.org/obo/NCIT_C202020 +http://purl.obolibrary.org/obo/NCIT_C202021 +http://purl.obolibrary.org/obo/NCIT_C202022 +http://purl.obolibrary.org/obo/NCIT_C202023 +http://purl.obolibrary.org/obo/NCIT_C202024 +http://purl.obolibrary.org/obo/NCIT_C202026 +http://purl.obolibrary.org/obo/NCIT_C202027 +http://purl.obolibrary.org/obo/NCIT_C202028 +http://purl.obolibrary.org/obo/NCIT_C202029 http://purl.obolibrary.org/obo/NCIT_C20203 +http://purl.obolibrary.org/obo/NCIT_C202030 +http://purl.obolibrary.org/obo/NCIT_C202031 +http://purl.obolibrary.org/obo/NCIT_C202032 +http://purl.obolibrary.org/obo/NCIT_C202033 +http://purl.obolibrary.org/obo/NCIT_C202034 +http://purl.obolibrary.org/obo/NCIT_C202035 +http://purl.obolibrary.org/obo/NCIT_C202036 +http://purl.obolibrary.org/obo/NCIT_C202037 +http://purl.obolibrary.org/obo/NCIT_C202038 +http://purl.obolibrary.org/obo/NCIT_C202039 http://purl.obolibrary.org/obo/NCIT_C20204 +http://purl.obolibrary.org/obo/NCIT_C202040 +http://purl.obolibrary.org/obo/NCIT_C202041 +http://purl.obolibrary.org/obo/NCIT_C202042 +http://purl.obolibrary.org/obo/NCIT_C202043 +http://purl.obolibrary.org/obo/NCIT_C202044 +http://purl.obolibrary.org/obo/NCIT_C202045 +http://purl.obolibrary.org/obo/NCIT_C202046 +http://purl.obolibrary.org/obo/NCIT_C202047 +http://purl.obolibrary.org/obo/NCIT_C202048 +http://purl.obolibrary.org/obo/NCIT_C202049 http://purl.obolibrary.org/obo/NCIT_C20205 +http://purl.obolibrary.org/obo/NCIT_C202050 +http://purl.obolibrary.org/obo/NCIT_C202051 +http://purl.obolibrary.org/obo/NCIT_C202052 +http://purl.obolibrary.org/obo/NCIT_C202053 +http://purl.obolibrary.org/obo/NCIT_C202054 +http://purl.obolibrary.org/obo/NCIT_C202055 +http://purl.obolibrary.org/obo/NCIT_C202056 +http://purl.obolibrary.org/obo/NCIT_C202057 +http://purl.obolibrary.org/obo/NCIT_C202058 +http://purl.obolibrary.org/obo/NCIT_C202059 http://purl.obolibrary.org/obo/NCIT_C20206 +http://purl.obolibrary.org/obo/NCIT_C202060 +http://purl.obolibrary.org/obo/NCIT_C202061 +http://purl.obolibrary.org/obo/NCIT_C202062 +http://purl.obolibrary.org/obo/NCIT_C202063 +http://purl.obolibrary.org/obo/NCIT_C202064 +http://purl.obolibrary.org/obo/NCIT_C202065 +http://purl.obolibrary.org/obo/NCIT_C202066 +http://purl.obolibrary.org/obo/NCIT_C202067 +http://purl.obolibrary.org/obo/NCIT_C202068 +http://purl.obolibrary.org/obo/NCIT_C202069 http://purl.obolibrary.org/obo/NCIT_C20207 +http://purl.obolibrary.org/obo/NCIT_C202070 +http://purl.obolibrary.org/obo/NCIT_C202071 +http://purl.obolibrary.org/obo/NCIT_C202072 +http://purl.obolibrary.org/obo/NCIT_C202073 +http://purl.obolibrary.org/obo/NCIT_C202074 +http://purl.obolibrary.org/obo/NCIT_C202075 +http://purl.obolibrary.org/obo/NCIT_C202076 +http://purl.obolibrary.org/obo/NCIT_C202077 +http://purl.obolibrary.org/obo/NCIT_C202078 +http://purl.obolibrary.org/obo/NCIT_C202079 http://purl.obolibrary.org/obo/NCIT_C20208 +http://purl.obolibrary.org/obo/NCIT_C202080 +http://purl.obolibrary.org/obo/NCIT_C202081 +http://purl.obolibrary.org/obo/NCIT_C202082 +http://purl.obolibrary.org/obo/NCIT_C202083 +http://purl.obolibrary.org/obo/NCIT_C202084 +http://purl.obolibrary.org/obo/NCIT_C202085 +http://purl.obolibrary.org/obo/NCIT_C202086 +http://purl.obolibrary.org/obo/NCIT_C202087 +http://purl.obolibrary.org/obo/NCIT_C202088 +http://purl.obolibrary.org/obo/NCIT_C202089 http://purl.obolibrary.org/obo/NCIT_C20209 +http://purl.obolibrary.org/obo/NCIT_C202090 +http://purl.obolibrary.org/obo/NCIT_C202091 +http://purl.obolibrary.org/obo/NCIT_C202092 +http://purl.obolibrary.org/obo/NCIT_C202093 +http://purl.obolibrary.org/obo/NCIT_C202094 +http://purl.obolibrary.org/obo/NCIT_C202095 +http://purl.obolibrary.org/obo/NCIT_C202096 +http://purl.obolibrary.org/obo/NCIT_C202097 +http://purl.obolibrary.org/obo/NCIT_C202098 +http://purl.obolibrary.org/obo/NCIT_C202099 http://purl.obolibrary.org/obo/NCIT_C2021 http://purl.obolibrary.org/obo/NCIT_C20210 +http://purl.obolibrary.org/obo/NCIT_C202100 +http://purl.obolibrary.org/obo/NCIT_C202101 +http://purl.obolibrary.org/obo/NCIT_C202102 +http://purl.obolibrary.org/obo/NCIT_C202103 +http://purl.obolibrary.org/obo/NCIT_C202104 +http://purl.obolibrary.org/obo/NCIT_C202105 +http://purl.obolibrary.org/obo/NCIT_C202106 +http://purl.obolibrary.org/obo/NCIT_C202107 +http://purl.obolibrary.org/obo/NCIT_C202108 +http://purl.obolibrary.org/obo/NCIT_C202109 http://purl.obolibrary.org/obo/NCIT_C20211 +http://purl.obolibrary.org/obo/NCIT_C202110 +http://purl.obolibrary.org/obo/NCIT_C202111 +http://purl.obolibrary.org/obo/NCIT_C202112 +http://purl.obolibrary.org/obo/NCIT_C202113 +http://purl.obolibrary.org/obo/NCIT_C202114 +http://purl.obolibrary.org/obo/NCIT_C202115 +http://purl.obolibrary.org/obo/NCIT_C202116 +http://purl.obolibrary.org/obo/NCIT_C202117 +http://purl.obolibrary.org/obo/NCIT_C202118 +http://purl.obolibrary.org/obo/NCIT_C202119 http://purl.obolibrary.org/obo/NCIT_C20212 +http://purl.obolibrary.org/obo/NCIT_C202121 +http://purl.obolibrary.org/obo/NCIT_C202122 +http://purl.obolibrary.org/obo/NCIT_C202123 +http://purl.obolibrary.org/obo/NCIT_C202124 +http://purl.obolibrary.org/obo/NCIT_C202125 +http://purl.obolibrary.org/obo/NCIT_C202126 +http://purl.obolibrary.org/obo/NCIT_C202128 +http://purl.obolibrary.org/obo/NCIT_C202129 http://purl.obolibrary.org/obo/NCIT_C20213 +http://purl.obolibrary.org/obo/NCIT_C202130 +http://purl.obolibrary.org/obo/NCIT_C202131 +http://purl.obolibrary.org/obo/NCIT_C202132 +http://purl.obolibrary.org/obo/NCIT_C202133 +http://purl.obolibrary.org/obo/NCIT_C202134 +http://purl.obolibrary.org/obo/NCIT_C202135 +http://purl.obolibrary.org/obo/NCIT_C202136 +http://purl.obolibrary.org/obo/NCIT_C202137 +http://purl.obolibrary.org/obo/NCIT_C202138 +http://purl.obolibrary.org/obo/NCIT_C202139 http://purl.obolibrary.org/obo/NCIT_C20214 +http://purl.obolibrary.org/obo/NCIT_C202140 +http://purl.obolibrary.org/obo/NCIT_C202141 +http://purl.obolibrary.org/obo/NCIT_C202142 +http://purl.obolibrary.org/obo/NCIT_C202143 +http://purl.obolibrary.org/obo/NCIT_C202144 +http://purl.obolibrary.org/obo/NCIT_C202145 +http://purl.obolibrary.org/obo/NCIT_C202146 +http://purl.obolibrary.org/obo/NCIT_C202147 +http://purl.obolibrary.org/obo/NCIT_C202148 +http://purl.obolibrary.org/obo/NCIT_C202149 http://purl.obolibrary.org/obo/NCIT_C20215 +http://purl.obolibrary.org/obo/NCIT_C202150 +http://purl.obolibrary.org/obo/NCIT_C202151 +http://purl.obolibrary.org/obo/NCIT_C202152 +http://purl.obolibrary.org/obo/NCIT_C202153 +http://purl.obolibrary.org/obo/NCIT_C202154 +http://purl.obolibrary.org/obo/NCIT_C202155 +http://purl.obolibrary.org/obo/NCIT_C202156 +http://purl.obolibrary.org/obo/NCIT_C202157 +http://purl.obolibrary.org/obo/NCIT_C202158 +http://purl.obolibrary.org/obo/NCIT_C202159 http://purl.obolibrary.org/obo/NCIT_C20216 +http://purl.obolibrary.org/obo/NCIT_C202160 +http://purl.obolibrary.org/obo/NCIT_C202161 http://purl.obolibrary.org/obo/NCIT_C20217 http://purl.obolibrary.org/obo/NCIT_C20218 http://purl.obolibrary.org/obo/NCIT_C20219 http://purl.obolibrary.org/obo/NCIT_C20220 +http://purl.obolibrary.org/obo/NCIT_C202205 +http://purl.obolibrary.org/obo/NCIT_C202206 +http://purl.obolibrary.org/obo/NCIT_C202207 +http://purl.obolibrary.org/obo/NCIT_C202208 +http://purl.obolibrary.org/obo/NCIT_C202209 http://purl.obolibrary.org/obo/NCIT_C20221 +http://purl.obolibrary.org/obo/NCIT_C202210 +http://purl.obolibrary.org/obo/NCIT_C202211 +http://purl.obolibrary.org/obo/NCIT_C202212 +http://purl.obolibrary.org/obo/NCIT_C202213 +http://purl.obolibrary.org/obo/NCIT_C202214 +http://purl.obolibrary.org/obo/NCIT_C202215 +http://purl.obolibrary.org/obo/NCIT_C202216 +http://purl.obolibrary.org/obo/NCIT_C202217 +http://purl.obolibrary.org/obo/NCIT_C202218 +http://purl.obolibrary.org/obo/NCIT_C202219 http://purl.obolibrary.org/obo/NCIT_C20222 +http://purl.obolibrary.org/obo/NCIT_C202220 +http://purl.obolibrary.org/obo/NCIT_C202221 +http://purl.obolibrary.org/obo/NCIT_C202222 +http://purl.obolibrary.org/obo/NCIT_C202223 +http://purl.obolibrary.org/obo/NCIT_C202224 +http://purl.obolibrary.org/obo/NCIT_C202225 +http://purl.obolibrary.org/obo/NCIT_C202226 +http://purl.obolibrary.org/obo/NCIT_C202227 +http://purl.obolibrary.org/obo/NCIT_C202228 +http://purl.obolibrary.org/obo/NCIT_C202229 http://purl.obolibrary.org/obo/NCIT_C20223 +http://purl.obolibrary.org/obo/NCIT_C202230 +http://purl.obolibrary.org/obo/NCIT_C202231 +http://purl.obolibrary.org/obo/NCIT_C202232 +http://purl.obolibrary.org/obo/NCIT_C202233 +http://purl.obolibrary.org/obo/NCIT_C202234 +http://purl.obolibrary.org/obo/NCIT_C202235 +http://purl.obolibrary.org/obo/NCIT_C202236 +http://purl.obolibrary.org/obo/NCIT_C202237 +http://purl.obolibrary.org/obo/NCIT_C202238 +http://purl.obolibrary.org/obo/NCIT_C202239 http://purl.obolibrary.org/obo/NCIT_C20224 +http://purl.obolibrary.org/obo/NCIT_C202240 +http://purl.obolibrary.org/obo/NCIT_C202241 +http://purl.obolibrary.org/obo/NCIT_C202242 +http://purl.obolibrary.org/obo/NCIT_C202243 +http://purl.obolibrary.org/obo/NCIT_C202244 +http://purl.obolibrary.org/obo/NCIT_C202245 +http://purl.obolibrary.org/obo/NCIT_C202246 +http://purl.obolibrary.org/obo/NCIT_C202247 +http://purl.obolibrary.org/obo/NCIT_C202248 +http://purl.obolibrary.org/obo/NCIT_C202249 http://purl.obolibrary.org/obo/NCIT_C20225 +http://purl.obolibrary.org/obo/NCIT_C202250 +http://purl.obolibrary.org/obo/NCIT_C202251 +http://purl.obolibrary.org/obo/NCIT_C202252 +http://purl.obolibrary.org/obo/NCIT_C202253 +http://purl.obolibrary.org/obo/NCIT_C202254 +http://purl.obolibrary.org/obo/NCIT_C202255 +http://purl.obolibrary.org/obo/NCIT_C202256 +http://purl.obolibrary.org/obo/NCIT_C202257 +http://purl.obolibrary.org/obo/NCIT_C202258 +http://purl.obolibrary.org/obo/NCIT_C202259 http://purl.obolibrary.org/obo/NCIT_C20226 +http://purl.obolibrary.org/obo/NCIT_C202260 +http://purl.obolibrary.org/obo/NCIT_C202261 +http://purl.obolibrary.org/obo/NCIT_C202262 +http://purl.obolibrary.org/obo/NCIT_C202263 +http://purl.obolibrary.org/obo/NCIT_C202264 +http://purl.obolibrary.org/obo/NCIT_C202265 +http://purl.obolibrary.org/obo/NCIT_C202266 +http://purl.obolibrary.org/obo/NCIT_C202267 +http://purl.obolibrary.org/obo/NCIT_C202268 +http://purl.obolibrary.org/obo/NCIT_C202269 http://purl.obolibrary.org/obo/NCIT_C20227 +http://purl.obolibrary.org/obo/NCIT_C202270 +http://purl.obolibrary.org/obo/NCIT_C202271 +http://purl.obolibrary.org/obo/NCIT_C202272 +http://purl.obolibrary.org/obo/NCIT_C202273 +http://purl.obolibrary.org/obo/NCIT_C202274 +http://purl.obolibrary.org/obo/NCIT_C202275 +http://purl.obolibrary.org/obo/NCIT_C202276 +http://purl.obolibrary.org/obo/NCIT_C202277 +http://purl.obolibrary.org/obo/NCIT_C202278 +http://purl.obolibrary.org/obo/NCIT_C202279 http://purl.obolibrary.org/obo/NCIT_C20228 +http://purl.obolibrary.org/obo/NCIT_C202280 +http://purl.obolibrary.org/obo/NCIT_C202281 +http://purl.obolibrary.org/obo/NCIT_C202282 +http://purl.obolibrary.org/obo/NCIT_C202283 +http://purl.obolibrary.org/obo/NCIT_C202284 +http://purl.obolibrary.org/obo/NCIT_C202285 +http://purl.obolibrary.org/obo/NCIT_C202286 +http://purl.obolibrary.org/obo/NCIT_C202287 +http://purl.obolibrary.org/obo/NCIT_C202288 +http://purl.obolibrary.org/obo/NCIT_C202289 http://purl.obolibrary.org/obo/NCIT_C20229 +http://purl.obolibrary.org/obo/NCIT_C202290 +http://purl.obolibrary.org/obo/NCIT_C202291 +http://purl.obolibrary.org/obo/NCIT_C202292 +http://purl.obolibrary.org/obo/NCIT_C202293 +http://purl.obolibrary.org/obo/NCIT_C202294 +http://purl.obolibrary.org/obo/NCIT_C202295 +http://purl.obolibrary.org/obo/NCIT_C202296 +http://purl.obolibrary.org/obo/NCIT_C202297 +http://purl.obolibrary.org/obo/NCIT_C202298 +http://purl.obolibrary.org/obo/NCIT_C202299 http://purl.obolibrary.org/obo/NCIT_C2023 http://purl.obolibrary.org/obo/NCIT_C20230 +http://purl.obolibrary.org/obo/NCIT_C202300 +http://purl.obolibrary.org/obo/NCIT_C202301 +http://purl.obolibrary.org/obo/NCIT_C202302 +http://purl.obolibrary.org/obo/NCIT_C202303 +http://purl.obolibrary.org/obo/NCIT_C202304 +http://purl.obolibrary.org/obo/NCIT_C202305 +http://purl.obolibrary.org/obo/NCIT_C202306 +http://purl.obolibrary.org/obo/NCIT_C202307 +http://purl.obolibrary.org/obo/NCIT_C202308 +http://purl.obolibrary.org/obo/NCIT_C202309 http://purl.obolibrary.org/obo/NCIT_C20231 +http://purl.obolibrary.org/obo/NCIT_C202310 +http://purl.obolibrary.org/obo/NCIT_C202311 +http://purl.obolibrary.org/obo/NCIT_C202312 +http://purl.obolibrary.org/obo/NCIT_C202313 +http://purl.obolibrary.org/obo/NCIT_C202314 +http://purl.obolibrary.org/obo/NCIT_C202315 +http://purl.obolibrary.org/obo/NCIT_C202316 +http://purl.obolibrary.org/obo/NCIT_C202317 +http://purl.obolibrary.org/obo/NCIT_C202318 +http://purl.obolibrary.org/obo/NCIT_C202319 http://purl.obolibrary.org/obo/NCIT_C20232 +http://purl.obolibrary.org/obo/NCIT_C202320 +http://purl.obolibrary.org/obo/NCIT_C202321 +http://purl.obolibrary.org/obo/NCIT_C202322 +http://purl.obolibrary.org/obo/NCIT_C202323 +http://purl.obolibrary.org/obo/NCIT_C202324 +http://purl.obolibrary.org/obo/NCIT_C202325 +http://purl.obolibrary.org/obo/NCIT_C202326 +http://purl.obolibrary.org/obo/NCIT_C202327 +http://purl.obolibrary.org/obo/NCIT_C202329 http://purl.obolibrary.org/obo/NCIT_C20233 +http://purl.obolibrary.org/obo/NCIT_C202330 +http://purl.obolibrary.org/obo/NCIT_C202331 +http://purl.obolibrary.org/obo/NCIT_C202332 +http://purl.obolibrary.org/obo/NCIT_C202333 +http://purl.obolibrary.org/obo/NCIT_C202334 +http://purl.obolibrary.org/obo/NCIT_C202336 +http://purl.obolibrary.org/obo/NCIT_C202337 +http://purl.obolibrary.org/obo/NCIT_C202338 +http://purl.obolibrary.org/obo/NCIT_C202339 http://purl.obolibrary.org/obo/NCIT_C20234 +http://purl.obolibrary.org/obo/NCIT_C202340 +http://purl.obolibrary.org/obo/NCIT_C202341 +http://purl.obolibrary.org/obo/NCIT_C202342 +http://purl.obolibrary.org/obo/NCIT_C202343 +http://purl.obolibrary.org/obo/NCIT_C202344 +http://purl.obolibrary.org/obo/NCIT_C202345 +http://purl.obolibrary.org/obo/NCIT_C202346 +http://purl.obolibrary.org/obo/NCIT_C202347 +http://purl.obolibrary.org/obo/NCIT_C202348 +http://purl.obolibrary.org/obo/NCIT_C202349 http://purl.obolibrary.org/obo/NCIT_C20235 +http://purl.obolibrary.org/obo/NCIT_C202350 +http://purl.obolibrary.org/obo/NCIT_C202351 +http://purl.obolibrary.org/obo/NCIT_C202352 +http://purl.obolibrary.org/obo/NCIT_C202353 +http://purl.obolibrary.org/obo/NCIT_C202354 +http://purl.obolibrary.org/obo/NCIT_C202355 +http://purl.obolibrary.org/obo/NCIT_C202356 +http://purl.obolibrary.org/obo/NCIT_C202357 +http://purl.obolibrary.org/obo/NCIT_C202358 +http://purl.obolibrary.org/obo/NCIT_C202359 http://purl.obolibrary.org/obo/NCIT_C20236 +http://purl.obolibrary.org/obo/NCIT_C202360 +http://purl.obolibrary.org/obo/NCIT_C202361 +http://purl.obolibrary.org/obo/NCIT_C202362 +http://purl.obolibrary.org/obo/NCIT_C202363 +http://purl.obolibrary.org/obo/NCIT_C202364 +http://purl.obolibrary.org/obo/NCIT_C202366 +http://purl.obolibrary.org/obo/NCIT_C202367 +http://purl.obolibrary.org/obo/NCIT_C202368 +http://purl.obolibrary.org/obo/NCIT_C202369 http://purl.obolibrary.org/obo/NCIT_C20237 +http://purl.obolibrary.org/obo/NCIT_C202370 +http://purl.obolibrary.org/obo/NCIT_C202371 +http://purl.obolibrary.org/obo/NCIT_C202372 +http://purl.obolibrary.org/obo/NCIT_C202373 +http://purl.obolibrary.org/obo/NCIT_C202374 +http://purl.obolibrary.org/obo/NCIT_C202375 +http://purl.obolibrary.org/obo/NCIT_C202376 +http://purl.obolibrary.org/obo/NCIT_C202377 +http://purl.obolibrary.org/obo/NCIT_C202378 +http://purl.obolibrary.org/obo/NCIT_C202379 http://purl.obolibrary.org/obo/NCIT_C20238 +http://purl.obolibrary.org/obo/NCIT_C202380 +http://purl.obolibrary.org/obo/NCIT_C202381 +http://purl.obolibrary.org/obo/NCIT_C202382 +http://purl.obolibrary.org/obo/NCIT_C202383 +http://purl.obolibrary.org/obo/NCIT_C202384 +http://purl.obolibrary.org/obo/NCIT_C202385 +http://purl.obolibrary.org/obo/NCIT_C202386 +http://purl.obolibrary.org/obo/NCIT_C202387 +http://purl.obolibrary.org/obo/NCIT_C202388 +http://purl.obolibrary.org/obo/NCIT_C202389 http://purl.obolibrary.org/obo/NCIT_C20239 +http://purl.obolibrary.org/obo/NCIT_C202390 +http://purl.obolibrary.org/obo/NCIT_C202391 +http://purl.obolibrary.org/obo/NCIT_C202392 +http://purl.obolibrary.org/obo/NCIT_C202393 +http://purl.obolibrary.org/obo/NCIT_C202394 +http://purl.obolibrary.org/obo/NCIT_C202395 +http://purl.obolibrary.org/obo/NCIT_C202396 +http://purl.obolibrary.org/obo/NCIT_C202397 +http://purl.obolibrary.org/obo/NCIT_C202398 +http://purl.obolibrary.org/obo/NCIT_C202399 http://purl.obolibrary.org/obo/NCIT_C2024 http://purl.obolibrary.org/obo/NCIT_C20240 +http://purl.obolibrary.org/obo/NCIT_C202400 +http://purl.obolibrary.org/obo/NCIT_C202401 +http://purl.obolibrary.org/obo/NCIT_C202402 +http://purl.obolibrary.org/obo/NCIT_C202403 +http://purl.obolibrary.org/obo/NCIT_C202404 +http://purl.obolibrary.org/obo/NCIT_C202405 +http://purl.obolibrary.org/obo/NCIT_C202406 +http://purl.obolibrary.org/obo/NCIT_C202407 +http://purl.obolibrary.org/obo/NCIT_C202408 +http://purl.obolibrary.org/obo/NCIT_C202409 http://purl.obolibrary.org/obo/NCIT_C20241 +http://purl.obolibrary.org/obo/NCIT_C202410 +http://purl.obolibrary.org/obo/NCIT_C202411 +http://purl.obolibrary.org/obo/NCIT_C202412 +http://purl.obolibrary.org/obo/NCIT_C202413 +http://purl.obolibrary.org/obo/NCIT_C202414 +http://purl.obolibrary.org/obo/NCIT_C202415 +http://purl.obolibrary.org/obo/NCIT_C202416 +http://purl.obolibrary.org/obo/NCIT_C202417 +http://purl.obolibrary.org/obo/NCIT_C202418 +http://purl.obolibrary.org/obo/NCIT_C202419 http://purl.obolibrary.org/obo/NCIT_C20242 +http://purl.obolibrary.org/obo/NCIT_C202420 +http://purl.obolibrary.org/obo/NCIT_C202421 +http://purl.obolibrary.org/obo/NCIT_C202422 +http://purl.obolibrary.org/obo/NCIT_C202423 +http://purl.obolibrary.org/obo/NCIT_C202424 +http://purl.obolibrary.org/obo/NCIT_C202425 +http://purl.obolibrary.org/obo/NCIT_C202426 +http://purl.obolibrary.org/obo/NCIT_C202427 +http://purl.obolibrary.org/obo/NCIT_C202428 +http://purl.obolibrary.org/obo/NCIT_C202429 http://purl.obolibrary.org/obo/NCIT_C20243 +http://purl.obolibrary.org/obo/NCIT_C202430 +http://purl.obolibrary.org/obo/NCIT_C202431 +http://purl.obolibrary.org/obo/NCIT_C202432 +http://purl.obolibrary.org/obo/NCIT_C202433 +http://purl.obolibrary.org/obo/NCIT_C202434 +http://purl.obolibrary.org/obo/NCIT_C202435 +http://purl.obolibrary.org/obo/NCIT_C202436 +http://purl.obolibrary.org/obo/NCIT_C202437 +http://purl.obolibrary.org/obo/NCIT_C202438 +http://purl.obolibrary.org/obo/NCIT_C202439 http://purl.obolibrary.org/obo/NCIT_C20244 +http://purl.obolibrary.org/obo/NCIT_C202440 +http://purl.obolibrary.org/obo/NCIT_C202441 +http://purl.obolibrary.org/obo/NCIT_C202442 +http://purl.obolibrary.org/obo/NCIT_C202443 +http://purl.obolibrary.org/obo/NCIT_C202444 +http://purl.obolibrary.org/obo/NCIT_C202445 +http://purl.obolibrary.org/obo/NCIT_C202446 +http://purl.obolibrary.org/obo/NCIT_C202447 +http://purl.obolibrary.org/obo/NCIT_C202448 +http://purl.obolibrary.org/obo/NCIT_C202449 http://purl.obolibrary.org/obo/NCIT_C20245 +http://purl.obolibrary.org/obo/NCIT_C202450 +http://purl.obolibrary.org/obo/NCIT_C202451 +http://purl.obolibrary.org/obo/NCIT_C202452 +http://purl.obolibrary.org/obo/NCIT_C202453 +http://purl.obolibrary.org/obo/NCIT_C202454 +http://purl.obolibrary.org/obo/NCIT_C202455 +http://purl.obolibrary.org/obo/NCIT_C202456 +http://purl.obolibrary.org/obo/NCIT_C202457 +http://purl.obolibrary.org/obo/NCIT_C202458 +http://purl.obolibrary.org/obo/NCIT_C202459 http://purl.obolibrary.org/obo/NCIT_C20246 +http://purl.obolibrary.org/obo/NCIT_C202460 +http://purl.obolibrary.org/obo/NCIT_C202461 +http://purl.obolibrary.org/obo/NCIT_C202462 +http://purl.obolibrary.org/obo/NCIT_C202463 +http://purl.obolibrary.org/obo/NCIT_C202464 +http://purl.obolibrary.org/obo/NCIT_C202465 +http://purl.obolibrary.org/obo/NCIT_C202466 +http://purl.obolibrary.org/obo/NCIT_C202467 +http://purl.obolibrary.org/obo/NCIT_C202468 +http://purl.obolibrary.org/obo/NCIT_C202469 http://purl.obolibrary.org/obo/NCIT_C20247 +http://purl.obolibrary.org/obo/NCIT_C202470 +http://purl.obolibrary.org/obo/NCIT_C202471 +http://purl.obolibrary.org/obo/NCIT_C202472 +http://purl.obolibrary.org/obo/NCIT_C202473 +http://purl.obolibrary.org/obo/NCIT_C202474 +http://purl.obolibrary.org/obo/NCIT_C202475 +http://purl.obolibrary.org/obo/NCIT_C202476 +http://purl.obolibrary.org/obo/NCIT_C202477 +http://purl.obolibrary.org/obo/NCIT_C202478 +http://purl.obolibrary.org/obo/NCIT_C202479 http://purl.obolibrary.org/obo/NCIT_C20248 +http://purl.obolibrary.org/obo/NCIT_C202480 +http://purl.obolibrary.org/obo/NCIT_C202481 +http://purl.obolibrary.org/obo/NCIT_C202482 +http://purl.obolibrary.org/obo/NCIT_C202483 +http://purl.obolibrary.org/obo/NCIT_C202484 +http://purl.obolibrary.org/obo/NCIT_C202485 +http://purl.obolibrary.org/obo/NCIT_C202486 +http://purl.obolibrary.org/obo/NCIT_C202487 +http://purl.obolibrary.org/obo/NCIT_C202488 +http://purl.obolibrary.org/obo/NCIT_C202489 http://purl.obolibrary.org/obo/NCIT_C20249 +http://purl.obolibrary.org/obo/NCIT_C202490 +http://purl.obolibrary.org/obo/NCIT_C202491 +http://purl.obolibrary.org/obo/NCIT_C202492 +http://purl.obolibrary.org/obo/NCIT_C202493 +http://purl.obolibrary.org/obo/NCIT_C202494 +http://purl.obolibrary.org/obo/NCIT_C202495 +http://purl.obolibrary.org/obo/NCIT_C202496 +http://purl.obolibrary.org/obo/NCIT_C202497 +http://purl.obolibrary.org/obo/NCIT_C202498 +http://purl.obolibrary.org/obo/NCIT_C202499 http://purl.obolibrary.org/obo/NCIT_C2025 http://purl.obolibrary.org/obo/NCIT_C20250 +http://purl.obolibrary.org/obo/NCIT_C202500 +http://purl.obolibrary.org/obo/NCIT_C202501 +http://purl.obolibrary.org/obo/NCIT_C202502 +http://purl.obolibrary.org/obo/NCIT_C202503 +http://purl.obolibrary.org/obo/NCIT_C202504 +http://purl.obolibrary.org/obo/NCIT_C202505 +http://purl.obolibrary.org/obo/NCIT_C202506 +http://purl.obolibrary.org/obo/NCIT_C202507 +http://purl.obolibrary.org/obo/NCIT_C202508 +http://purl.obolibrary.org/obo/NCIT_C202509 http://purl.obolibrary.org/obo/NCIT_C20251 +http://purl.obolibrary.org/obo/NCIT_C202510 +http://purl.obolibrary.org/obo/NCIT_C202511 +http://purl.obolibrary.org/obo/NCIT_C202512 +http://purl.obolibrary.org/obo/NCIT_C202513 +http://purl.obolibrary.org/obo/NCIT_C202514 +http://purl.obolibrary.org/obo/NCIT_C202515 +http://purl.obolibrary.org/obo/NCIT_C202516 +http://purl.obolibrary.org/obo/NCIT_C202517 +http://purl.obolibrary.org/obo/NCIT_C202518 +http://purl.obolibrary.org/obo/NCIT_C202519 http://purl.obolibrary.org/obo/NCIT_C20252 +http://purl.obolibrary.org/obo/NCIT_C202520 +http://purl.obolibrary.org/obo/NCIT_C202521 +http://purl.obolibrary.org/obo/NCIT_C202522 +http://purl.obolibrary.org/obo/NCIT_C202523 +http://purl.obolibrary.org/obo/NCIT_C202524 +http://purl.obolibrary.org/obo/NCIT_C202525 +http://purl.obolibrary.org/obo/NCIT_C202526 +http://purl.obolibrary.org/obo/NCIT_C202527 +http://purl.obolibrary.org/obo/NCIT_C202528 +http://purl.obolibrary.org/obo/NCIT_C202529 http://purl.obolibrary.org/obo/NCIT_C20253 +http://purl.obolibrary.org/obo/NCIT_C202530 +http://purl.obolibrary.org/obo/NCIT_C202531 +http://purl.obolibrary.org/obo/NCIT_C202532 +http://purl.obolibrary.org/obo/NCIT_C202533 +http://purl.obolibrary.org/obo/NCIT_C202534 +http://purl.obolibrary.org/obo/NCIT_C202535 +http://purl.obolibrary.org/obo/NCIT_C202536 +http://purl.obolibrary.org/obo/NCIT_C202537 +http://purl.obolibrary.org/obo/NCIT_C202538 +http://purl.obolibrary.org/obo/NCIT_C202539 http://purl.obolibrary.org/obo/NCIT_C20254 +http://purl.obolibrary.org/obo/NCIT_C202540 +http://purl.obolibrary.org/obo/NCIT_C202541 +http://purl.obolibrary.org/obo/NCIT_C202542 +http://purl.obolibrary.org/obo/NCIT_C202543 +http://purl.obolibrary.org/obo/NCIT_C202544 +http://purl.obolibrary.org/obo/NCIT_C202545 +http://purl.obolibrary.org/obo/NCIT_C202546 +http://purl.obolibrary.org/obo/NCIT_C202547 +http://purl.obolibrary.org/obo/NCIT_C202548 +http://purl.obolibrary.org/obo/NCIT_C202549 http://purl.obolibrary.org/obo/NCIT_C20255 +http://purl.obolibrary.org/obo/NCIT_C202550 +http://purl.obolibrary.org/obo/NCIT_C202551 +http://purl.obolibrary.org/obo/NCIT_C202552 +http://purl.obolibrary.org/obo/NCIT_C202553 +http://purl.obolibrary.org/obo/NCIT_C202554 +http://purl.obolibrary.org/obo/NCIT_C202555 +http://purl.obolibrary.org/obo/NCIT_C202556 +http://purl.obolibrary.org/obo/NCIT_C202557 +http://purl.obolibrary.org/obo/NCIT_C202558 +http://purl.obolibrary.org/obo/NCIT_C202559 http://purl.obolibrary.org/obo/NCIT_C20256 +http://purl.obolibrary.org/obo/NCIT_C202560 +http://purl.obolibrary.org/obo/NCIT_C202561 +http://purl.obolibrary.org/obo/NCIT_C202562 +http://purl.obolibrary.org/obo/NCIT_C202563 +http://purl.obolibrary.org/obo/NCIT_C202564 +http://purl.obolibrary.org/obo/NCIT_C202565 +http://purl.obolibrary.org/obo/NCIT_C202566 +http://purl.obolibrary.org/obo/NCIT_C202567 +http://purl.obolibrary.org/obo/NCIT_C202568 +http://purl.obolibrary.org/obo/NCIT_C202569 http://purl.obolibrary.org/obo/NCIT_C20257 +http://purl.obolibrary.org/obo/NCIT_C202570 +http://purl.obolibrary.org/obo/NCIT_C202571 +http://purl.obolibrary.org/obo/NCIT_C202572 +http://purl.obolibrary.org/obo/NCIT_C202573 +http://purl.obolibrary.org/obo/NCIT_C202574 +http://purl.obolibrary.org/obo/NCIT_C202575 +http://purl.obolibrary.org/obo/NCIT_C202576 +http://purl.obolibrary.org/obo/NCIT_C202577 +http://purl.obolibrary.org/obo/NCIT_C202578 +http://purl.obolibrary.org/obo/NCIT_C202579 http://purl.obolibrary.org/obo/NCIT_C20258 +http://purl.obolibrary.org/obo/NCIT_C202580 +http://purl.obolibrary.org/obo/NCIT_C202581 +http://purl.obolibrary.org/obo/NCIT_C202582 +http://purl.obolibrary.org/obo/NCIT_C202583 +http://purl.obolibrary.org/obo/NCIT_C202584 +http://purl.obolibrary.org/obo/NCIT_C202585 +http://purl.obolibrary.org/obo/NCIT_C202586 +http://purl.obolibrary.org/obo/NCIT_C202587 +http://purl.obolibrary.org/obo/NCIT_C202588 +http://purl.obolibrary.org/obo/NCIT_C202589 http://purl.obolibrary.org/obo/NCIT_C20259 +http://purl.obolibrary.org/obo/NCIT_C202590 +http://purl.obolibrary.org/obo/NCIT_C202591 +http://purl.obolibrary.org/obo/NCIT_C202592 +http://purl.obolibrary.org/obo/NCIT_C202593 +http://purl.obolibrary.org/obo/NCIT_C202594 +http://purl.obolibrary.org/obo/NCIT_C202595 +http://purl.obolibrary.org/obo/NCIT_C202596 +http://purl.obolibrary.org/obo/NCIT_C202597 +http://purl.obolibrary.org/obo/NCIT_C202598 +http://purl.obolibrary.org/obo/NCIT_C202599 http://purl.obolibrary.org/obo/NCIT_C2026 http://purl.obolibrary.org/obo/NCIT_C20260 +http://purl.obolibrary.org/obo/NCIT_C202600 +http://purl.obolibrary.org/obo/NCIT_C202601 +http://purl.obolibrary.org/obo/NCIT_C202602 +http://purl.obolibrary.org/obo/NCIT_C202603 +http://purl.obolibrary.org/obo/NCIT_C202604 +http://purl.obolibrary.org/obo/NCIT_C202605 +http://purl.obolibrary.org/obo/NCIT_C202606 +http://purl.obolibrary.org/obo/NCIT_C202607 +http://purl.obolibrary.org/obo/NCIT_C202608 +http://purl.obolibrary.org/obo/NCIT_C202609 http://purl.obolibrary.org/obo/NCIT_C20261 +http://purl.obolibrary.org/obo/NCIT_C202610 +http://purl.obolibrary.org/obo/NCIT_C202611 +http://purl.obolibrary.org/obo/NCIT_C202612 +http://purl.obolibrary.org/obo/NCIT_C202613 +http://purl.obolibrary.org/obo/NCIT_C202614 +http://purl.obolibrary.org/obo/NCIT_C202615 +http://purl.obolibrary.org/obo/NCIT_C202616 +http://purl.obolibrary.org/obo/NCIT_C202617 +http://purl.obolibrary.org/obo/NCIT_C202618 +http://purl.obolibrary.org/obo/NCIT_C202619 http://purl.obolibrary.org/obo/NCIT_C20262 +http://purl.obolibrary.org/obo/NCIT_C202620 +http://purl.obolibrary.org/obo/NCIT_C202621 +http://purl.obolibrary.org/obo/NCIT_C202622 +http://purl.obolibrary.org/obo/NCIT_C202623 +http://purl.obolibrary.org/obo/NCIT_C202624 +http://purl.obolibrary.org/obo/NCIT_C202625 +http://purl.obolibrary.org/obo/NCIT_C202626 +http://purl.obolibrary.org/obo/NCIT_C202627 +http://purl.obolibrary.org/obo/NCIT_C202628 +http://purl.obolibrary.org/obo/NCIT_C202629 http://purl.obolibrary.org/obo/NCIT_C20263 +http://purl.obolibrary.org/obo/NCIT_C202630 +http://purl.obolibrary.org/obo/NCIT_C202631 +http://purl.obolibrary.org/obo/NCIT_C202632 +http://purl.obolibrary.org/obo/NCIT_C202633 +http://purl.obolibrary.org/obo/NCIT_C202634 +http://purl.obolibrary.org/obo/NCIT_C202635 +http://purl.obolibrary.org/obo/NCIT_C202636 +http://purl.obolibrary.org/obo/NCIT_C202637 +http://purl.obolibrary.org/obo/NCIT_C202638 +http://purl.obolibrary.org/obo/NCIT_C202639 http://purl.obolibrary.org/obo/NCIT_C20264 +http://purl.obolibrary.org/obo/NCIT_C202640 +http://purl.obolibrary.org/obo/NCIT_C202641 +http://purl.obolibrary.org/obo/NCIT_C202642 +http://purl.obolibrary.org/obo/NCIT_C202643 +http://purl.obolibrary.org/obo/NCIT_C202644 +http://purl.obolibrary.org/obo/NCIT_C202645 +http://purl.obolibrary.org/obo/NCIT_C202646 +http://purl.obolibrary.org/obo/NCIT_C202647 +http://purl.obolibrary.org/obo/NCIT_C202648 +http://purl.obolibrary.org/obo/NCIT_C202649 http://purl.obolibrary.org/obo/NCIT_C20265 +http://purl.obolibrary.org/obo/NCIT_C202650 +http://purl.obolibrary.org/obo/NCIT_C202651 +http://purl.obolibrary.org/obo/NCIT_C202652 +http://purl.obolibrary.org/obo/NCIT_C202653 +http://purl.obolibrary.org/obo/NCIT_C202654 +http://purl.obolibrary.org/obo/NCIT_C202655 +http://purl.obolibrary.org/obo/NCIT_C202656 +http://purl.obolibrary.org/obo/NCIT_C202657 +http://purl.obolibrary.org/obo/NCIT_C202658 +http://purl.obolibrary.org/obo/NCIT_C202659 http://purl.obolibrary.org/obo/NCIT_C20266 +http://purl.obolibrary.org/obo/NCIT_C202660 +http://purl.obolibrary.org/obo/NCIT_C202663 +http://purl.obolibrary.org/obo/NCIT_C202664 +http://purl.obolibrary.org/obo/NCIT_C202665 +http://purl.obolibrary.org/obo/NCIT_C202666 +http://purl.obolibrary.org/obo/NCIT_C202667 +http://purl.obolibrary.org/obo/NCIT_C202668 +http://purl.obolibrary.org/obo/NCIT_C202669 http://purl.obolibrary.org/obo/NCIT_C20267 +http://purl.obolibrary.org/obo/NCIT_C202670 +http://purl.obolibrary.org/obo/NCIT_C202671 +http://purl.obolibrary.org/obo/NCIT_C202672 +http://purl.obolibrary.org/obo/NCIT_C202673 +http://purl.obolibrary.org/obo/NCIT_C202674 +http://purl.obolibrary.org/obo/NCIT_C202675 +http://purl.obolibrary.org/obo/NCIT_C202676 +http://purl.obolibrary.org/obo/NCIT_C202677 +http://purl.obolibrary.org/obo/NCIT_C202678 +http://purl.obolibrary.org/obo/NCIT_C202679 http://purl.obolibrary.org/obo/NCIT_C20268 +http://purl.obolibrary.org/obo/NCIT_C202680 +http://purl.obolibrary.org/obo/NCIT_C202681 +http://purl.obolibrary.org/obo/NCIT_C202682 +http://purl.obolibrary.org/obo/NCIT_C202683 +http://purl.obolibrary.org/obo/NCIT_C202685 +http://purl.obolibrary.org/obo/NCIT_C202686 +http://purl.obolibrary.org/obo/NCIT_C202687 +http://purl.obolibrary.org/obo/NCIT_C202688 +http://purl.obolibrary.org/obo/NCIT_C202689 http://purl.obolibrary.org/obo/NCIT_C20269 +http://purl.obolibrary.org/obo/NCIT_C202690 +http://purl.obolibrary.org/obo/NCIT_C202691 +http://purl.obolibrary.org/obo/NCIT_C202692 +http://purl.obolibrary.org/obo/NCIT_C202693 +http://purl.obolibrary.org/obo/NCIT_C202694 +http://purl.obolibrary.org/obo/NCIT_C202695 +http://purl.obolibrary.org/obo/NCIT_C202696 +http://purl.obolibrary.org/obo/NCIT_C202697 +http://purl.obolibrary.org/obo/NCIT_C202698 +http://purl.obolibrary.org/obo/NCIT_C202699 http://purl.obolibrary.org/obo/NCIT_C2027 http://purl.obolibrary.org/obo/NCIT_C20270 +http://purl.obolibrary.org/obo/NCIT_C202700 +http://purl.obolibrary.org/obo/NCIT_C202701 +http://purl.obolibrary.org/obo/NCIT_C202702 +http://purl.obolibrary.org/obo/NCIT_C202703 +http://purl.obolibrary.org/obo/NCIT_C202704 +http://purl.obolibrary.org/obo/NCIT_C202705 +http://purl.obolibrary.org/obo/NCIT_C202706 +http://purl.obolibrary.org/obo/NCIT_C202707 +http://purl.obolibrary.org/obo/NCIT_C202708 +http://purl.obolibrary.org/obo/NCIT_C202709 http://purl.obolibrary.org/obo/NCIT_C20271 +http://purl.obolibrary.org/obo/NCIT_C202710 +http://purl.obolibrary.org/obo/NCIT_C202711 +http://purl.obolibrary.org/obo/NCIT_C202712 +http://purl.obolibrary.org/obo/NCIT_C202713 +http://purl.obolibrary.org/obo/NCIT_C202714 +http://purl.obolibrary.org/obo/NCIT_C202715 +http://purl.obolibrary.org/obo/NCIT_C202716 +http://purl.obolibrary.org/obo/NCIT_C202717 +http://purl.obolibrary.org/obo/NCIT_C202718 +http://purl.obolibrary.org/obo/NCIT_C202719 http://purl.obolibrary.org/obo/NCIT_C20272 +http://purl.obolibrary.org/obo/NCIT_C202720 +http://purl.obolibrary.org/obo/NCIT_C202721 +http://purl.obolibrary.org/obo/NCIT_C202722 +http://purl.obolibrary.org/obo/NCIT_C202723 +http://purl.obolibrary.org/obo/NCIT_C202724 +http://purl.obolibrary.org/obo/NCIT_C202725 +http://purl.obolibrary.org/obo/NCIT_C202726 +http://purl.obolibrary.org/obo/NCIT_C202727 +http://purl.obolibrary.org/obo/NCIT_C202728 +http://purl.obolibrary.org/obo/NCIT_C202729 http://purl.obolibrary.org/obo/NCIT_C20273 +http://purl.obolibrary.org/obo/NCIT_C202730 +http://purl.obolibrary.org/obo/NCIT_C202731 +http://purl.obolibrary.org/obo/NCIT_C202732 +http://purl.obolibrary.org/obo/NCIT_C202733 +http://purl.obolibrary.org/obo/NCIT_C202734 +http://purl.obolibrary.org/obo/NCIT_C202735 +http://purl.obolibrary.org/obo/NCIT_C202736 +http://purl.obolibrary.org/obo/NCIT_C202737 +http://purl.obolibrary.org/obo/NCIT_C202738 +http://purl.obolibrary.org/obo/NCIT_C202739 http://purl.obolibrary.org/obo/NCIT_C20274 +http://purl.obolibrary.org/obo/NCIT_C202740 +http://purl.obolibrary.org/obo/NCIT_C202741 +http://purl.obolibrary.org/obo/NCIT_C202742 +http://purl.obolibrary.org/obo/NCIT_C202743 +http://purl.obolibrary.org/obo/NCIT_C202744 +http://purl.obolibrary.org/obo/NCIT_C202745 +http://purl.obolibrary.org/obo/NCIT_C202746 +http://purl.obolibrary.org/obo/NCIT_C202747 +http://purl.obolibrary.org/obo/NCIT_C202748 +http://purl.obolibrary.org/obo/NCIT_C202749 http://purl.obolibrary.org/obo/NCIT_C20275 +http://purl.obolibrary.org/obo/NCIT_C202750 +http://purl.obolibrary.org/obo/NCIT_C202751 +http://purl.obolibrary.org/obo/NCIT_C202752 +http://purl.obolibrary.org/obo/NCIT_C202753 +http://purl.obolibrary.org/obo/NCIT_C202754 +http://purl.obolibrary.org/obo/NCIT_C202755 +http://purl.obolibrary.org/obo/NCIT_C202756 +http://purl.obolibrary.org/obo/NCIT_C202757 +http://purl.obolibrary.org/obo/NCIT_C202758 +http://purl.obolibrary.org/obo/NCIT_C202759 http://purl.obolibrary.org/obo/NCIT_C20276 +http://purl.obolibrary.org/obo/NCIT_C202760 +http://purl.obolibrary.org/obo/NCIT_C202761 +http://purl.obolibrary.org/obo/NCIT_C202762 +http://purl.obolibrary.org/obo/NCIT_C202763 +http://purl.obolibrary.org/obo/NCIT_C202764 +http://purl.obolibrary.org/obo/NCIT_C202765 +http://purl.obolibrary.org/obo/NCIT_C202766 +http://purl.obolibrary.org/obo/NCIT_C202767 +http://purl.obolibrary.org/obo/NCIT_C202768 +http://purl.obolibrary.org/obo/NCIT_C202769 http://purl.obolibrary.org/obo/NCIT_C20277 +http://purl.obolibrary.org/obo/NCIT_C202770 +http://purl.obolibrary.org/obo/NCIT_C202771 +http://purl.obolibrary.org/obo/NCIT_C202772 +http://purl.obolibrary.org/obo/NCIT_C202773 +http://purl.obolibrary.org/obo/NCIT_C202774 +http://purl.obolibrary.org/obo/NCIT_C202777 +http://purl.obolibrary.org/obo/NCIT_C202778 +http://purl.obolibrary.org/obo/NCIT_C202779 http://purl.obolibrary.org/obo/NCIT_C20278 +http://purl.obolibrary.org/obo/NCIT_C202780 +http://purl.obolibrary.org/obo/NCIT_C202781 +http://purl.obolibrary.org/obo/NCIT_C202782 +http://purl.obolibrary.org/obo/NCIT_C202783 +http://purl.obolibrary.org/obo/NCIT_C202784 +http://purl.obolibrary.org/obo/NCIT_C202785 +http://purl.obolibrary.org/obo/NCIT_C202786 +http://purl.obolibrary.org/obo/NCIT_C202787 +http://purl.obolibrary.org/obo/NCIT_C202788 +http://purl.obolibrary.org/obo/NCIT_C202789 http://purl.obolibrary.org/obo/NCIT_C20279 +http://purl.obolibrary.org/obo/NCIT_C202790 +http://purl.obolibrary.org/obo/NCIT_C202791 +http://purl.obolibrary.org/obo/NCIT_C202792 +http://purl.obolibrary.org/obo/NCIT_C202793 +http://purl.obolibrary.org/obo/NCIT_C202794 +http://purl.obolibrary.org/obo/NCIT_C202795 +http://purl.obolibrary.org/obo/NCIT_C202796 +http://purl.obolibrary.org/obo/NCIT_C202797 +http://purl.obolibrary.org/obo/NCIT_C202798 +http://purl.obolibrary.org/obo/NCIT_C202799 http://purl.obolibrary.org/obo/NCIT_C2028 http://purl.obolibrary.org/obo/NCIT_C20280 +http://purl.obolibrary.org/obo/NCIT_C202800 +http://purl.obolibrary.org/obo/NCIT_C202801 +http://purl.obolibrary.org/obo/NCIT_C202802 +http://purl.obolibrary.org/obo/NCIT_C202803 +http://purl.obolibrary.org/obo/NCIT_C202804 +http://purl.obolibrary.org/obo/NCIT_C202805 +http://purl.obolibrary.org/obo/NCIT_C202806 +http://purl.obolibrary.org/obo/NCIT_C202807 +http://purl.obolibrary.org/obo/NCIT_C202808 +http://purl.obolibrary.org/obo/NCIT_C202809 http://purl.obolibrary.org/obo/NCIT_C20281 +http://purl.obolibrary.org/obo/NCIT_C202810 +http://purl.obolibrary.org/obo/NCIT_C202811 +http://purl.obolibrary.org/obo/NCIT_C202812 +http://purl.obolibrary.org/obo/NCIT_C202813 +http://purl.obolibrary.org/obo/NCIT_C202814 +http://purl.obolibrary.org/obo/NCIT_C202815 +http://purl.obolibrary.org/obo/NCIT_C202816 +http://purl.obolibrary.org/obo/NCIT_C202817 +http://purl.obolibrary.org/obo/NCIT_C202818 +http://purl.obolibrary.org/obo/NCIT_C202819 http://purl.obolibrary.org/obo/NCIT_C20282 +http://purl.obolibrary.org/obo/NCIT_C202820 +http://purl.obolibrary.org/obo/NCIT_C202821 +http://purl.obolibrary.org/obo/NCIT_C202822 +http://purl.obolibrary.org/obo/NCIT_C202823 +http://purl.obolibrary.org/obo/NCIT_C202824 +http://purl.obolibrary.org/obo/NCIT_C202825 +http://purl.obolibrary.org/obo/NCIT_C202826 +http://purl.obolibrary.org/obo/NCIT_C202827 +http://purl.obolibrary.org/obo/NCIT_C202828 +http://purl.obolibrary.org/obo/NCIT_C202829 http://purl.obolibrary.org/obo/NCIT_C20283 +http://purl.obolibrary.org/obo/NCIT_C202830 +http://purl.obolibrary.org/obo/NCIT_C202831 +http://purl.obolibrary.org/obo/NCIT_C202832 +http://purl.obolibrary.org/obo/NCIT_C202833 +http://purl.obolibrary.org/obo/NCIT_C202834 +http://purl.obolibrary.org/obo/NCIT_C202835 +http://purl.obolibrary.org/obo/NCIT_C202836 +http://purl.obolibrary.org/obo/NCIT_C202837 +http://purl.obolibrary.org/obo/NCIT_C202838 +http://purl.obolibrary.org/obo/NCIT_C202839 http://purl.obolibrary.org/obo/NCIT_C20284 +http://purl.obolibrary.org/obo/NCIT_C202840 +http://purl.obolibrary.org/obo/NCIT_C202841 +http://purl.obolibrary.org/obo/NCIT_C202842 +http://purl.obolibrary.org/obo/NCIT_C202843 +http://purl.obolibrary.org/obo/NCIT_C202844 +http://purl.obolibrary.org/obo/NCIT_C202845 +http://purl.obolibrary.org/obo/NCIT_C202846 +http://purl.obolibrary.org/obo/NCIT_C202847 +http://purl.obolibrary.org/obo/NCIT_C202848 +http://purl.obolibrary.org/obo/NCIT_C202849 http://purl.obolibrary.org/obo/NCIT_C20285 +http://purl.obolibrary.org/obo/NCIT_C202850 +http://purl.obolibrary.org/obo/NCIT_C202851 +http://purl.obolibrary.org/obo/NCIT_C202852 +http://purl.obolibrary.org/obo/NCIT_C202853 +http://purl.obolibrary.org/obo/NCIT_C202854 +http://purl.obolibrary.org/obo/NCIT_C202855 +http://purl.obolibrary.org/obo/NCIT_C202857 +http://purl.obolibrary.org/obo/NCIT_C202858 +http://purl.obolibrary.org/obo/NCIT_C202859 http://purl.obolibrary.org/obo/NCIT_C20286 +http://purl.obolibrary.org/obo/NCIT_C202860 +http://purl.obolibrary.org/obo/NCIT_C202861 +http://purl.obolibrary.org/obo/NCIT_C202862 +http://purl.obolibrary.org/obo/NCIT_C202863 +http://purl.obolibrary.org/obo/NCIT_C202864 +http://purl.obolibrary.org/obo/NCIT_C202865 +http://purl.obolibrary.org/obo/NCIT_C202866 +http://purl.obolibrary.org/obo/NCIT_C202867 +http://purl.obolibrary.org/obo/NCIT_C202868 +http://purl.obolibrary.org/obo/NCIT_C202869 http://purl.obolibrary.org/obo/NCIT_C20287 +http://purl.obolibrary.org/obo/NCIT_C202870 +http://purl.obolibrary.org/obo/NCIT_C202871 +http://purl.obolibrary.org/obo/NCIT_C202872 +http://purl.obolibrary.org/obo/NCIT_C202873 +http://purl.obolibrary.org/obo/NCIT_C202874 +http://purl.obolibrary.org/obo/NCIT_C202875 +http://purl.obolibrary.org/obo/NCIT_C202876 +http://purl.obolibrary.org/obo/NCIT_C202877 +http://purl.obolibrary.org/obo/NCIT_C202878 +http://purl.obolibrary.org/obo/NCIT_C202879 http://purl.obolibrary.org/obo/NCIT_C20288 +http://purl.obolibrary.org/obo/NCIT_C202880 +http://purl.obolibrary.org/obo/NCIT_C202881 +http://purl.obolibrary.org/obo/NCIT_C202882 +http://purl.obolibrary.org/obo/NCIT_C202883 +http://purl.obolibrary.org/obo/NCIT_C202884 +http://purl.obolibrary.org/obo/NCIT_C202885 +http://purl.obolibrary.org/obo/NCIT_C202886 +http://purl.obolibrary.org/obo/NCIT_C202887 +http://purl.obolibrary.org/obo/NCIT_C202888 +http://purl.obolibrary.org/obo/NCIT_C202889 http://purl.obolibrary.org/obo/NCIT_C20289 +http://purl.obolibrary.org/obo/NCIT_C202890 +http://purl.obolibrary.org/obo/NCIT_C202891 +http://purl.obolibrary.org/obo/NCIT_C202892 +http://purl.obolibrary.org/obo/NCIT_C202893 +http://purl.obolibrary.org/obo/NCIT_C202894 +http://purl.obolibrary.org/obo/NCIT_C202895 +http://purl.obolibrary.org/obo/NCIT_C202896 +http://purl.obolibrary.org/obo/NCIT_C202897 +http://purl.obolibrary.org/obo/NCIT_C202898 +http://purl.obolibrary.org/obo/NCIT_C202899 http://purl.obolibrary.org/obo/NCIT_C2029 http://purl.obolibrary.org/obo/NCIT_C20290 +http://purl.obolibrary.org/obo/NCIT_C202900 +http://purl.obolibrary.org/obo/NCIT_C202901 +http://purl.obolibrary.org/obo/NCIT_C202902 +http://purl.obolibrary.org/obo/NCIT_C202903 +http://purl.obolibrary.org/obo/NCIT_C202904 +http://purl.obolibrary.org/obo/NCIT_C202905 +http://purl.obolibrary.org/obo/NCIT_C202906 +http://purl.obolibrary.org/obo/NCIT_C202907 +http://purl.obolibrary.org/obo/NCIT_C202908 +http://purl.obolibrary.org/obo/NCIT_C202909 http://purl.obolibrary.org/obo/NCIT_C20291 +http://purl.obolibrary.org/obo/NCIT_C202910 +http://purl.obolibrary.org/obo/NCIT_C202911 +http://purl.obolibrary.org/obo/NCIT_C202912 +http://purl.obolibrary.org/obo/NCIT_C202913 +http://purl.obolibrary.org/obo/NCIT_C202914 +http://purl.obolibrary.org/obo/NCIT_C202915 +http://purl.obolibrary.org/obo/NCIT_C202916 +http://purl.obolibrary.org/obo/NCIT_C202917 +http://purl.obolibrary.org/obo/NCIT_C202918 +http://purl.obolibrary.org/obo/NCIT_C202919 http://purl.obolibrary.org/obo/NCIT_C20292 +http://purl.obolibrary.org/obo/NCIT_C202920 +http://purl.obolibrary.org/obo/NCIT_C202921 +http://purl.obolibrary.org/obo/NCIT_C202922 +http://purl.obolibrary.org/obo/NCIT_C202923 +http://purl.obolibrary.org/obo/NCIT_C202924 +http://purl.obolibrary.org/obo/NCIT_C202925 +http://purl.obolibrary.org/obo/NCIT_C202926 +http://purl.obolibrary.org/obo/NCIT_C202927 +http://purl.obolibrary.org/obo/NCIT_C202928 +http://purl.obolibrary.org/obo/NCIT_C202929 http://purl.obolibrary.org/obo/NCIT_C20293 +http://purl.obolibrary.org/obo/NCIT_C202930 +http://purl.obolibrary.org/obo/NCIT_C202931 +http://purl.obolibrary.org/obo/NCIT_C202933 +http://purl.obolibrary.org/obo/NCIT_C202934 +http://purl.obolibrary.org/obo/NCIT_C202935 +http://purl.obolibrary.org/obo/NCIT_C202936 +http://purl.obolibrary.org/obo/NCIT_C202937 +http://purl.obolibrary.org/obo/NCIT_C202938 +http://purl.obolibrary.org/obo/NCIT_C202939 http://purl.obolibrary.org/obo/NCIT_C20294 +http://purl.obolibrary.org/obo/NCIT_C202940 +http://purl.obolibrary.org/obo/NCIT_C202941 +http://purl.obolibrary.org/obo/NCIT_C202942 +http://purl.obolibrary.org/obo/NCIT_C202943 +http://purl.obolibrary.org/obo/NCIT_C202944 +http://purl.obolibrary.org/obo/NCIT_C202945 +http://purl.obolibrary.org/obo/NCIT_C202946 +http://purl.obolibrary.org/obo/NCIT_C202947 +http://purl.obolibrary.org/obo/NCIT_C202948 +http://purl.obolibrary.org/obo/NCIT_C202949 http://purl.obolibrary.org/obo/NCIT_C20295 +http://purl.obolibrary.org/obo/NCIT_C202950 +http://purl.obolibrary.org/obo/NCIT_C202951 +http://purl.obolibrary.org/obo/NCIT_C202952 +http://purl.obolibrary.org/obo/NCIT_C202953 +http://purl.obolibrary.org/obo/NCIT_C202954 +http://purl.obolibrary.org/obo/NCIT_C202955 +http://purl.obolibrary.org/obo/NCIT_C202956 +http://purl.obolibrary.org/obo/NCIT_C202957 +http://purl.obolibrary.org/obo/NCIT_C202959 http://purl.obolibrary.org/obo/NCIT_C20296 +http://purl.obolibrary.org/obo/NCIT_C202960 +http://purl.obolibrary.org/obo/NCIT_C202961 +http://purl.obolibrary.org/obo/NCIT_C202962 +http://purl.obolibrary.org/obo/NCIT_C202963 +http://purl.obolibrary.org/obo/NCIT_C202964 +http://purl.obolibrary.org/obo/NCIT_C202965 +http://purl.obolibrary.org/obo/NCIT_C202966 +http://purl.obolibrary.org/obo/NCIT_C202967 +http://purl.obolibrary.org/obo/NCIT_C202968 +http://purl.obolibrary.org/obo/NCIT_C202969 http://purl.obolibrary.org/obo/NCIT_C20297 +http://purl.obolibrary.org/obo/NCIT_C202970 +http://purl.obolibrary.org/obo/NCIT_C202971 +http://purl.obolibrary.org/obo/NCIT_C202972 +http://purl.obolibrary.org/obo/NCIT_C202973 +http://purl.obolibrary.org/obo/NCIT_C202974 +http://purl.obolibrary.org/obo/NCIT_C202975 +http://purl.obolibrary.org/obo/NCIT_C202976 +http://purl.obolibrary.org/obo/NCIT_C202977 +http://purl.obolibrary.org/obo/NCIT_C202978 +http://purl.obolibrary.org/obo/NCIT_C202979 http://purl.obolibrary.org/obo/NCIT_C20298 +http://purl.obolibrary.org/obo/NCIT_C202980 +http://purl.obolibrary.org/obo/NCIT_C202981 +http://purl.obolibrary.org/obo/NCIT_C202982 +http://purl.obolibrary.org/obo/NCIT_C202983 +http://purl.obolibrary.org/obo/NCIT_C202984 +http://purl.obolibrary.org/obo/NCIT_C202985 +http://purl.obolibrary.org/obo/NCIT_C202986 +http://purl.obolibrary.org/obo/NCIT_C202987 +http://purl.obolibrary.org/obo/NCIT_C202988 +http://purl.obolibrary.org/obo/NCIT_C202989 http://purl.obolibrary.org/obo/NCIT_C20299 +http://purl.obolibrary.org/obo/NCIT_C202990 +http://purl.obolibrary.org/obo/NCIT_C202991 +http://purl.obolibrary.org/obo/NCIT_C202992 +http://purl.obolibrary.org/obo/NCIT_C202993 +http://purl.obolibrary.org/obo/NCIT_C202994 +http://purl.obolibrary.org/obo/NCIT_C202995 +http://purl.obolibrary.org/obo/NCIT_C202996 +http://purl.obolibrary.org/obo/NCIT_C202997 +http://purl.obolibrary.org/obo/NCIT_C202999 http://purl.obolibrary.org/obo/NCIT_C203 http://purl.obolibrary.org/obo/NCIT_C2030 http://purl.obolibrary.org/obo/NCIT_C20300 +http://purl.obolibrary.org/obo/NCIT_C203000 +http://purl.obolibrary.org/obo/NCIT_C203001 +http://purl.obolibrary.org/obo/NCIT_C203002 +http://purl.obolibrary.org/obo/NCIT_C203003 +http://purl.obolibrary.org/obo/NCIT_C203004 +http://purl.obolibrary.org/obo/NCIT_C203005 +http://purl.obolibrary.org/obo/NCIT_C203006 +http://purl.obolibrary.org/obo/NCIT_C203007 +http://purl.obolibrary.org/obo/NCIT_C203008 +http://purl.obolibrary.org/obo/NCIT_C203009 http://purl.obolibrary.org/obo/NCIT_C20301 +http://purl.obolibrary.org/obo/NCIT_C203010 +http://purl.obolibrary.org/obo/NCIT_C203011 +http://purl.obolibrary.org/obo/NCIT_C203012 +http://purl.obolibrary.org/obo/NCIT_C203013 +http://purl.obolibrary.org/obo/NCIT_C203014 +http://purl.obolibrary.org/obo/NCIT_C203015 +http://purl.obolibrary.org/obo/NCIT_C203016 +http://purl.obolibrary.org/obo/NCIT_C203017 +http://purl.obolibrary.org/obo/NCIT_C203018 +http://purl.obolibrary.org/obo/NCIT_C203019 http://purl.obolibrary.org/obo/NCIT_C20302 +http://purl.obolibrary.org/obo/NCIT_C203020 +http://purl.obolibrary.org/obo/NCIT_C203021 +http://purl.obolibrary.org/obo/NCIT_C203022 +http://purl.obolibrary.org/obo/NCIT_C203023 +http://purl.obolibrary.org/obo/NCIT_C203024 +http://purl.obolibrary.org/obo/NCIT_C203025 +http://purl.obolibrary.org/obo/NCIT_C203026 +http://purl.obolibrary.org/obo/NCIT_C203027 +http://purl.obolibrary.org/obo/NCIT_C203028 +http://purl.obolibrary.org/obo/NCIT_C203029 http://purl.obolibrary.org/obo/NCIT_C20303 +http://purl.obolibrary.org/obo/NCIT_C203030 +http://purl.obolibrary.org/obo/NCIT_C203031 +http://purl.obolibrary.org/obo/NCIT_C203032 +http://purl.obolibrary.org/obo/NCIT_C203033 +http://purl.obolibrary.org/obo/NCIT_C203034 +http://purl.obolibrary.org/obo/NCIT_C203035 +http://purl.obolibrary.org/obo/NCIT_C203036 +http://purl.obolibrary.org/obo/NCIT_C203037 +http://purl.obolibrary.org/obo/NCIT_C203038 +http://purl.obolibrary.org/obo/NCIT_C203039 http://purl.obolibrary.org/obo/NCIT_C20304 +http://purl.obolibrary.org/obo/NCIT_C203040 +http://purl.obolibrary.org/obo/NCIT_C203041 +http://purl.obolibrary.org/obo/NCIT_C203042 +http://purl.obolibrary.org/obo/NCIT_C203043 +http://purl.obolibrary.org/obo/NCIT_C203044 +http://purl.obolibrary.org/obo/NCIT_C203045 +http://purl.obolibrary.org/obo/NCIT_C203046 +http://purl.obolibrary.org/obo/NCIT_C203047 +http://purl.obolibrary.org/obo/NCIT_C203048 +http://purl.obolibrary.org/obo/NCIT_C203049 http://purl.obolibrary.org/obo/NCIT_C20305 +http://purl.obolibrary.org/obo/NCIT_C203050 +http://purl.obolibrary.org/obo/NCIT_C203051 +http://purl.obolibrary.org/obo/NCIT_C203052 +http://purl.obolibrary.org/obo/NCIT_C203053 +http://purl.obolibrary.org/obo/NCIT_C203054 +http://purl.obolibrary.org/obo/NCIT_C203055 +http://purl.obolibrary.org/obo/NCIT_C203056 +http://purl.obolibrary.org/obo/NCIT_C203057 +http://purl.obolibrary.org/obo/NCIT_C203058 +http://purl.obolibrary.org/obo/NCIT_C203059 http://purl.obolibrary.org/obo/NCIT_C20306 +http://purl.obolibrary.org/obo/NCIT_C203060 +http://purl.obolibrary.org/obo/NCIT_C203061 +http://purl.obolibrary.org/obo/NCIT_C203062 +http://purl.obolibrary.org/obo/NCIT_C203063 +http://purl.obolibrary.org/obo/NCIT_C203064 +http://purl.obolibrary.org/obo/NCIT_C203065 +http://purl.obolibrary.org/obo/NCIT_C203066 +http://purl.obolibrary.org/obo/NCIT_C203067 +http://purl.obolibrary.org/obo/NCIT_C203068 +http://purl.obolibrary.org/obo/NCIT_C203069 http://purl.obolibrary.org/obo/NCIT_C20307 +http://purl.obolibrary.org/obo/NCIT_C203070 +http://purl.obolibrary.org/obo/NCIT_C203071 +http://purl.obolibrary.org/obo/NCIT_C203072 +http://purl.obolibrary.org/obo/NCIT_C203073 +http://purl.obolibrary.org/obo/NCIT_C203074 +http://purl.obolibrary.org/obo/NCIT_C203075 +http://purl.obolibrary.org/obo/NCIT_C203076 +http://purl.obolibrary.org/obo/NCIT_C203077 +http://purl.obolibrary.org/obo/NCIT_C203078 +http://purl.obolibrary.org/obo/NCIT_C203079 http://purl.obolibrary.org/obo/NCIT_C20308 +http://purl.obolibrary.org/obo/NCIT_C203080 +http://purl.obolibrary.org/obo/NCIT_C203081 +http://purl.obolibrary.org/obo/NCIT_C203082 +http://purl.obolibrary.org/obo/NCIT_C203083 +http://purl.obolibrary.org/obo/NCIT_C203084 +http://purl.obolibrary.org/obo/NCIT_C203085 +http://purl.obolibrary.org/obo/NCIT_C203086 +http://purl.obolibrary.org/obo/NCIT_C203087 +http://purl.obolibrary.org/obo/NCIT_C203088 +http://purl.obolibrary.org/obo/NCIT_C203089 http://purl.obolibrary.org/obo/NCIT_C20309 +http://purl.obolibrary.org/obo/NCIT_C203090 +http://purl.obolibrary.org/obo/NCIT_C203091 +http://purl.obolibrary.org/obo/NCIT_C203092 +http://purl.obolibrary.org/obo/NCIT_C203093 +http://purl.obolibrary.org/obo/NCIT_C203094 +http://purl.obolibrary.org/obo/NCIT_C203095 +http://purl.obolibrary.org/obo/NCIT_C203096 +http://purl.obolibrary.org/obo/NCIT_C203097 +http://purl.obolibrary.org/obo/NCIT_C203098 +http://purl.obolibrary.org/obo/NCIT_C203099 http://purl.obolibrary.org/obo/NCIT_C2031 http://purl.obolibrary.org/obo/NCIT_C20310 +http://purl.obolibrary.org/obo/NCIT_C203100 +http://purl.obolibrary.org/obo/NCIT_C203101 +http://purl.obolibrary.org/obo/NCIT_C203102 +http://purl.obolibrary.org/obo/NCIT_C203103 +http://purl.obolibrary.org/obo/NCIT_C203104 +http://purl.obolibrary.org/obo/NCIT_C203105 +http://purl.obolibrary.org/obo/NCIT_C203106 +http://purl.obolibrary.org/obo/NCIT_C203107 +http://purl.obolibrary.org/obo/NCIT_C203108 +http://purl.obolibrary.org/obo/NCIT_C203109 http://purl.obolibrary.org/obo/NCIT_C20311 +http://purl.obolibrary.org/obo/NCIT_C203110 +http://purl.obolibrary.org/obo/NCIT_C203111 +http://purl.obolibrary.org/obo/NCIT_C203112 +http://purl.obolibrary.org/obo/NCIT_C203113 +http://purl.obolibrary.org/obo/NCIT_C203114 +http://purl.obolibrary.org/obo/NCIT_C203115 +http://purl.obolibrary.org/obo/NCIT_C203116 +http://purl.obolibrary.org/obo/NCIT_C203117 +http://purl.obolibrary.org/obo/NCIT_C203118 +http://purl.obolibrary.org/obo/NCIT_C203119 http://purl.obolibrary.org/obo/NCIT_C20312 +http://purl.obolibrary.org/obo/NCIT_C203120 +http://purl.obolibrary.org/obo/NCIT_C203121 +http://purl.obolibrary.org/obo/NCIT_C203122 +http://purl.obolibrary.org/obo/NCIT_C203123 +http://purl.obolibrary.org/obo/NCIT_C203124 +http://purl.obolibrary.org/obo/NCIT_C203125 +http://purl.obolibrary.org/obo/NCIT_C203126 +http://purl.obolibrary.org/obo/NCIT_C203127 +http://purl.obolibrary.org/obo/NCIT_C203128 +http://purl.obolibrary.org/obo/NCIT_C203129 http://purl.obolibrary.org/obo/NCIT_C20313 +http://purl.obolibrary.org/obo/NCIT_C203130 +http://purl.obolibrary.org/obo/NCIT_C203131 +http://purl.obolibrary.org/obo/NCIT_C203132 +http://purl.obolibrary.org/obo/NCIT_C203133 +http://purl.obolibrary.org/obo/NCIT_C203134 +http://purl.obolibrary.org/obo/NCIT_C203135 +http://purl.obolibrary.org/obo/NCIT_C203136 +http://purl.obolibrary.org/obo/NCIT_C203137 +http://purl.obolibrary.org/obo/NCIT_C203138 +http://purl.obolibrary.org/obo/NCIT_C203139 http://purl.obolibrary.org/obo/NCIT_C20314 +http://purl.obolibrary.org/obo/NCIT_C203140 +http://purl.obolibrary.org/obo/NCIT_C203141 +http://purl.obolibrary.org/obo/NCIT_C203142 +http://purl.obolibrary.org/obo/NCIT_C203143 +http://purl.obolibrary.org/obo/NCIT_C203144 +http://purl.obolibrary.org/obo/NCIT_C203145 +http://purl.obolibrary.org/obo/NCIT_C203146 +http://purl.obolibrary.org/obo/NCIT_C203147 +http://purl.obolibrary.org/obo/NCIT_C203148 +http://purl.obolibrary.org/obo/NCIT_C203149 http://purl.obolibrary.org/obo/NCIT_C20315 +http://purl.obolibrary.org/obo/NCIT_C203150 +http://purl.obolibrary.org/obo/NCIT_C203151 +http://purl.obolibrary.org/obo/NCIT_C203152 +http://purl.obolibrary.org/obo/NCIT_C203153 +http://purl.obolibrary.org/obo/NCIT_C203154 +http://purl.obolibrary.org/obo/NCIT_C203155 +http://purl.obolibrary.org/obo/NCIT_C203156 +http://purl.obolibrary.org/obo/NCIT_C203157 +http://purl.obolibrary.org/obo/NCIT_C203158 +http://purl.obolibrary.org/obo/NCIT_C203159 http://purl.obolibrary.org/obo/NCIT_C20316 +http://purl.obolibrary.org/obo/NCIT_C203160 +http://purl.obolibrary.org/obo/NCIT_C203161 +http://purl.obolibrary.org/obo/NCIT_C203162 +http://purl.obolibrary.org/obo/NCIT_C203163 +http://purl.obolibrary.org/obo/NCIT_C203164 +http://purl.obolibrary.org/obo/NCIT_C203165 +http://purl.obolibrary.org/obo/NCIT_C203166 +http://purl.obolibrary.org/obo/NCIT_C203167 +http://purl.obolibrary.org/obo/NCIT_C203168 +http://purl.obolibrary.org/obo/NCIT_C203169 http://purl.obolibrary.org/obo/NCIT_C20317 +http://purl.obolibrary.org/obo/NCIT_C203170 +http://purl.obolibrary.org/obo/NCIT_C203171 +http://purl.obolibrary.org/obo/NCIT_C203172 +http://purl.obolibrary.org/obo/NCIT_C203173 +http://purl.obolibrary.org/obo/NCIT_C203174 +http://purl.obolibrary.org/obo/NCIT_C203175 +http://purl.obolibrary.org/obo/NCIT_C203176 +http://purl.obolibrary.org/obo/NCIT_C203177 +http://purl.obolibrary.org/obo/NCIT_C203178 +http://purl.obolibrary.org/obo/NCIT_C203179 http://purl.obolibrary.org/obo/NCIT_C20318 +http://purl.obolibrary.org/obo/NCIT_C203180 +http://purl.obolibrary.org/obo/NCIT_C203181 +http://purl.obolibrary.org/obo/NCIT_C203182 +http://purl.obolibrary.org/obo/NCIT_C203183 +http://purl.obolibrary.org/obo/NCIT_C203184 +http://purl.obolibrary.org/obo/NCIT_C203185 +http://purl.obolibrary.org/obo/NCIT_C203186 +http://purl.obolibrary.org/obo/NCIT_C203187 +http://purl.obolibrary.org/obo/NCIT_C203188 +http://purl.obolibrary.org/obo/NCIT_C203189 http://purl.obolibrary.org/obo/NCIT_C20319 +http://purl.obolibrary.org/obo/NCIT_C203190 +http://purl.obolibrary.org/obo/NCIT_C203191 +http://purl.obolibrary.org/obo/NCIT_C203192 +http://purl.obolibrary.org/obo/NCIT_C203193 +http://purl.obolibrary.org/obo/NCIT_C203194 +http://purl.obolibrary.org/obo/NCIT_C203195 +http://purl.obolibrary.org/obo/NCIT_C203196 +http://purl.obolibrary.org/obo/NCIT_C203197 +http://purl.obolibrary.org/obo/NCIT_C203198 +http://purl.obolibrary.org/obo/NCIT_C203199 http://purl.obolibrary.org/obo/NCIT_C2032 http://purl.obolibrary.org/obo/NCIT_C20320 +http://purl.obolibrary.org/obo/NCIT_C203200 +http://purl.obolibrary.org/obo/NCIT_C203201 +http://purl.obolibrary.org/obo/NCIT_C203202 +http://purl.obolibrary.org/obo/NCIT_C203203 +http://purl.obolibrary.org/obo/NCIT_C203204 +http://purl.obolibrary.org/obo/NCIT_C203205 +http://purl.obolibrary.org/obo/NCIT_C203206 +http://purl.obolibrary.org/obo/NCIT_C203207 +http://purl.obolibrary.org/obo/NCIT_C203208 +http://purl.obolibrary.org/obo/NCIT_C203209 +http://purl.obolibrary.org/obo/NCIT_C203210 +http://purl.obolibrary.org/obo/NCIT_C203211 +http://purl.obolibrary.org/obo/NCIT_C203212 +http://purl.obolibrary.org/obo/NCIT_C203213 +http://purl.obolibrary.org/obo/NCIT_C203214 +http://purl.obolibrary.org/obo/NCIT_C203215 +http://purl.obolibrary.org/obo/NCIT_C203216 +http://purl.obolibrary.org/obo/NCIT_C203217 +http://purl.obolibrary.org/obo/NCIT_C203218 +http://purl.obolibrary.org/obo/NCIT_C203219 http://purl.obolibrary.org/obo/NCIT_C20322 +http://purl.obolibrary.org/obo/NCIT_C203220 +http://purl.obolibrary.org/obo/NCIT_C203221 +http://purl.obolibrary.org/obo/NCIT_C203222 +http://purl.obolibrary.org/obo/NCIT_C203223 +http://purl.obolibrary.org/obo/NCIT_C203224 +http://purl.obolibrary.org/obo/NCIT_C203225 +http://purl.obolibrary.org/obo/NCIT_C203226 +http://purl.obolibrary.org/obo/NCIT_C203227 +http://purl.obolibrary.org/obo/NCIT_C203228 +http://purl.obolibrary.org/obo/NCIT_C203229 http://purl.obolibrary.org/obo/NCIT_C20323 +http://purl.obolibrary.org/obo/NCIT_C203230 +http://purl.obolibrary.org/obo/NCIT_C203231 +http://purl.obolibrary.org/obo/NCIT_C203232 +http://purl.obolibrary.org/obo/NCIT_C203233 +http://purl.obolibrary.org/obo/NCIT_C203234 +http://purl.obolibrary.org/obo/NCIT_C203235 +http://purl.obolibrary.org/obo/NCIT_C203236 +http://purl.obolibrary.org/obo/NCIT_C203237 +http://purl.obolibrary.org/obo/NCIT_C203238 +http://purl.obolibrary.org/obo/NCIT_C203239 http://purl.obolibrary.org/obo/NCIT_C20324 +http://purl.obolibrary.org/obo/NCIT_C203240 +http://purl.obolibrary.org/obo/NCIT_C203241 +http://purl.obolibrary.org/obo/NCIT_C203242 +http://purl.obolibrary.org/obo/NCIT_C203243 +http://purl.obolibrary.org/obo/NCIT_C203244 +http://purl.obolibrary.org/obo/NCIT_C203245 +http://purl.obolibrary.org/obo/NCIT_C203246 +http://purl.obolibrary.org/obo/NCIT_C203247 +http://purl.obolibrary.org/obo/NCIT_C203248 +http://purl.obolibrary.org/obo/NCIT_C203249 http://purl.obolibrary.org/obo/NCIT_C20325 +http://purl.obolibrary.org/obo/NCIT_C203250 +http://purl.obolibrary.org/obo/NCIT_C203251 +http://purl.obolibrary.org/obo/NCIT_C203252 +http://purl.obolibrary.org/obo/NCIT_C203253 +http://purl.obolibrary.org/obo/NCIT_C203254 +http://purl.obolibrary.org/obo/NCIT_C203255 +http://purl.obolibrary.org/obo/NCIT_C203256 +http://purl.obolibrary.org/obo/NCIT_C203257 +http://purl.obolibrary.org/obo/NCIT_C203258 +http://purl.obolibrary.org/obo/NCIT_C203259 http://purl.obolibrary.org/obo/NCIT_C20326 +http://purl.obolibrary.org/obo/NCIT_C203260 +http://purl.obolibrary.org/obo/NCIT_C203261 +http://purl.obolibrary.org/obo/NCIT_C203262 +http://purl.obolibrary.org/obo/NCIT_C203263 +http://purl.obolibrary.org/obo/NCIT_C203264 +http://purl.obolibrary.org/obo/NCIT_C203265 +http://purl.obolibrary.org/obo/NCIT_C203266 +http://purl.obolibrary.org/obo/NCIT_C203267 +http://purl.obolibrary.org/obo/NCIT_C203268 +http://purl.obolibrary.org/obo/NCIT_C203269 http://purl.obolibrary.org/obo/NCIT_C20327 +http://purl.obolibrary.org/obo/NCIT_C203270 +http://purl.obolibrary.org/obo/NCIT_C203271 +http://purl.obolibrary.org/obo/NCIT_C203272 +http://purl.obolibrary.org/obo/NCIT_C203273 +http://purl.obolibrary.org/obo/NCIT_C203274 +http://purl.obolibrary.org/obo/NCIT_C203275 +http://purl.obolibrary.org/obo/NCIT_C203276 +http://purl.obolibrary.org/obo/NCIT_C203277 +http://purl.obolibrary.org/obo/NCIT_C203278 +http://purl.obolibrary.org/obo/NCIT_C203279 http://purl.obolibrary.org/obo/NCIT_C20328 +http://purl.obolibrary.org/obo/NCIT_C203280 +http://purl.obolibrary.org/obo/NCIT_C203281 +http://purl.obolibrary.org/obo/NCIT_C203282 +http://purl.obolibrary.org/obo/NCIT_C203283 +http://purl.obolibrary.org/obo/NCIT_C203284 +http://purl.obolibrary.org/obo/NCIT_C203285 +http://purl.obolibrary.org/obo/NCIT_C203286 +http://purl.obolibrary.org/obo/NCIT_C203287 +http://purl.obolibrary.org/obo/NCIT_C203288 +http://purl.obolibrary.org/obo/NCIT_C203289 http://purl.obolibrary.org/obo/NCIT_C20329 +http://purl.obolibrary.org/obo/NCIT_C203290 +http://purl.obolibrary.org/obo/NCIT_C203291 +http://purl.obolibrary.org/obo/NCIT_C203292 +http://purl.obolibrary.org/obo/NCIT_C203293 +http://purl.obolibrary.org/obo/NCIT_C203294 +http://purl.obolibrary.org/obo/NCIT_C203295 +http://purl.obolibrary.org/obo/NCIT_C203296 +http://purl.obolibrary.org/obo/NCIT_C203297 +http://purl.obolibrary.org/obo/NCIT_C203298 +http://purl.obolibrary.org/obo/NCIT_C203299 http://purl.obolibrary.org/obo/NCIT_C2033 http://purl.obolibrary.org/obo/NCIT_C20330 +http://purl.obolibrary.org/obo/NCIT_C203300 +http://purl.obolibrary.org/obo/NCIT_C203301 +http://purl.obolibrary.org/obo/NCIT_C203302 +http://purl.obolibrary.org/obo/NCIT_C203303 +http://purl.obolibrary.org/obo/NCIT_C203304 +http://purl.obolibrary.org/obo/NCIT_C203305 +http://purl.obolibrary.org/obo/NCIT_C203306 +http://purl.obolibrary.org/obo/NCIT_C203308 +http://purl.obolibrary.org/obo/NCIT_C203309 http://purl.obolibrary.org/obo/NCIT_C20331 +http://purl.obolibrary.org/obo/NCIT_C203310 +http://purl.obolibrary.org/obo/NCIT_C203311 +http://purl.obolibrary.org/obo/NCIT_C203312 +http://purl.obolibrary.org/obo/NCIT_C203313 +http://purl.obolibrary.org/obo/NCIT_C203314 +http://purl.obolibrary.org/obo/NCIT_C203315 +http://purl.obolibrary.org/obo/NCIT_C203316 +http://purl.obolibrary.org/obo/NCIT_C203317 +http://purl.obolibrary.org/obo/NCIT_C203318 +http://purl.obolibrary.org/obo/NCIT_C203319 http://purl.obolibrary.org/obo/NCIT_C20332 +http://purl.obolibrary.org/obo/NCIT_C203320 +http://purl.obolibrary.org/obo/NCIT_C203321 +http://purl.obolibrary.org/obo/NCIT_C203322 +http://purl.obolibrary.org/obo/NCIT_C203323 +http://purl.obolibrary.org/obo/NCIT_C203324 +http://purl.obolibrary.org/obo/NCIT_C203325 +http://purl.obolibrary.org/obo/NCIT_C203326 +http://purl.obolibrary.org/obo/NCIT_C203327 +http://purl.obolibrary.org/obo/NCIT_C203328 +http://purl.obolibrary.org/obo/NCIT_C203329 http://purl.obolibrary.org/obo/NCIT_C20333 +http://purl.obolibrary.org/obo/NCIT_C203330 +http://purl.obolibrary.org/obo/NCIT_C203331 +http://purl.obolibrary.org/obo/NCIT_C203332 +http://purl.obolibrary.org/obo/NCIT_C203333 +http://purl.obolibrary.org/obo/NCIT_C203334 +http://purl.obolibrary.org/obo/NCIT_C203335 +http://purl.obolibrary.org/obo/NCIT_C203336 +http://purl.obolibrary.org/obo/NCIT_C203337 +http://purl.obolibrary.org/obo/NCIT_C203338 +http://purl.obolibrary.org/obo/NCIT_C203339 http://purl.obolibrary.org/obo/NCIT_C20334 +http://purl.obolibrary.org/obo/NCIT_C203340 +http://purl.obolibrary.org/obo/NCIT_C203341 +http://purl.obolibrary.org/obo/NCIT_C203342 +http://purl.obolibrary.org/obo/NCIT_C203344 +http://purl.obolibrary.org/obo/NCIT_C203345 +http://purl.obolibrary.org/obo/NCIT_C203346 +http://purl.obolibrary.org/obo/NCIT_C203347 +http://purl.obolibrary.org/obo/NCIT_C203348 +http://purl.obolibrary.org/obo/NCIT_C203349 http://purl.obolibrary.org/obo/NCIT_C20335 +http://purl.obolibrary.org/obo/NCIT_C203350 +http://purl.obolibrary.org/obo/NCIT_C203351 +http://purl.obolibrary.org/obo/NCIT_C203352 +http://purl.obolibrary.org/obo/NCIT_C203353 +http://purl.obolibrary.org/obo/NCIT_C203354 +http://purl.obolibrary.org/obo/NCIT_C203355 +http://purl.obolibrary.org/obo/NCIT_C203356 +http://purl.obolibrary.org/obo/NCIT_C203357 +http://purl.obolibrary.org/obo/NCIT_C203358 +http://purl.obolibrary.org/obo/NCIT_C203359 http://purl.obolibrary.org/obo/NCIT_C20336 +http://purl.obolibrary.org/obo/NCIT_C203360 +http://purl.obolibrary.org/obo/NCIT_C203361 +http://purl.obolibrary.org/obo/NCIT_C203362 +http://purl.obolibrary.org/obo/NCIT_C203363 +http://purl.obolibrary.org/obo/NCIT_C203364 +http://purl.obolibrary.org/obo/NCIT_C203365 +http://purl.obolibrary.org/obo/NCIT_C203366 +http://purl.obolibrary.org/obo/NCIT_C203367 +http://purl.obolibrary.org/obo/NCIT_C203368 +http://purl.obolibrary.org/obo/NCIT_C203369 http://purl.obolibrary.org/obo/NCIT_C20337 +http://purl.obolibrary.org/obo/NCIT_C203370 +http://purl.obolibrary.org/obo/NCIT_C203371 +http://purl.obolibrary.org/obo/NCIT_C203372 +http://purl.obolibrary.org/obo/NCIT_C203373 +http://purl.obolibrary.org/obo/NCIT_C203374 +http://purl.obolibrary.org/obo/NCIT_C203375 +http://purl.obolibrary.org/obo/NCIT_C203376 +http://purl.obolibrary.org/obo/NCIT_C203377 +http://purl.obolibrary.org/obo/NCIT_C203378 +http://purl.obolibrary.org/obo/NCIT_C203379 http://purl.obolibrary.org/obo/NCIT_C20338 +http://purl.obolibrary.org/obo/NCIT_C203380 +http://purl.obolibrary.org/obo/NCIT_C203381 +http://purl.obolibrary.org/obo/NCIT_C203382 +http://purl.obolibrary.org/obo/NCIT_C203383 +http://purl.obolibrary.org/obo/NCIT_C203384 +http://purl.obolibrary.org/obo/NCIT_C203385 +http://purl.obolibrary.org/obo/NCIT_C203386 +http://purl.obolibrary.org/obo/NCIT_C203387 +http://purl.obolibrary.org/obo/NCIT_C203388 +http://purl.obolibrary.org/obo/NCIT_C203389 http://purl.obolibrary.org/obo/NCIT_C20339 +http://purl.obolibrary.org/obo/NCIT_C203390 +http://purl.obolibrary.org/obo/NCIT_C203391 +http://purl.obolibrary.org/obo/NCIT_C203392 +http://purl.obolibrary.org/obo/NCIT_C203393 +http://purl.obolibrary.org/obo/NCIT_C203394 +http://purl.obolibrary.org/obo/NCIT_C203395 +http://purl.obolibrary.org/obo/NCIT_C203396 +http://purl.obolibrary.org/obo/NCIT_C203397 +http://purl.obolibrary.org/obo/NCIT_C203398 +http://purl.obolibrary.org/obo/NCIT_C203399 http://purl.obolibrary.org/obo/NCIT_C2034 http://purl.obolibrary.org/obo/NCIT_C20340 +http://purl.obolibrary.org/obo/NCIT_C203400 +http://purl.obolibrary.org/obo/NCIT_C203401 +http://purl.obolibrary.org/obo/NCIT_C203402 +http://purl.obolibrary.org/obo/NCIT_C203403 +http://purl.obolibrary.org/obo/NCIT_C203404 +http://purl.obolibrary.org/obo/NCIT_C203405 +http://purl.obolibrary.org/obo/NCIT_C203406 +http://purl.obolibrary.org/obo/NCIT_C203407 +http://purl.obolibrary.org/obo/NCIT_C203409 http://purl.obolibrary.org/obo/NCIT_C20341 +http://purl.obolibrary.org/obo/NCIT_C203410 +http://purl.obolibrary.org/obo/NCIT_C203411 +http://purl.obolibrary.org/obo/NCIT_C203412 +http://purl.obolibrary.org/obo/NCIT_C203413 +http://purl.obolibrary.org/obo/NCIT_C203414 +http://purl.obolibrary.org/obo/NCIT_C203415 +http://purl.obolibrary.org/obo/NCIT_C203416 +http://purl.obolibrary.org/obo/NCIT_C203417 +http://purl.obolibrary.org/obo/NCIT_C203418 +http://purl.obolibrary.org/obo/NCIT_C203419 http://purl.obolibrary.org/obo/NCIT_C20342 +http://purl.obolibrary.org/obo/NCIT_C203420 +http://purl.obolibrary.org/obo/NCIT_C203421 +http://purl.obolibrary.org/obo/NCIT_C203422 +http://purl.obolibrary.org/obo/NCIT_C203423 +http://purl.obolibrary.org/obo/NCIT_C203424 +http://purl.obolibrary.org/obo/NCIT_C203425 +http://purl.obolibrary.org/obo/NCIT_C203426 +http://purl.obolibrary.org/obo/NCIT_C203427 +http://purl.obolibrary.org/obo/NCIT_C203428 +http://purl.obolibrary.org/obo/NCIT_C203429 http://purl.obolibrary.org/obo/NCIT_C20343 +http://purl.obolibrary.org/obo/NCIT_C203431 +http://purl.obolibrary.org/obo/NCIT_C203432 +http://purl.obolibrary.org/obo/NCIT_C203433 +http://purl.obolibrary.org/obo/NCIT_C203434 +http://purl.obolibrary.org/obo/NCIT_C203435 +http://purl.obolibrary.org/obo/NCIT_C203436 +http://purl.obolibrary.org/obo/NCIT_C203437 +http://purl.obolibrary.org/obo/NCIT_C203438 +http://purl.obolibrary.org/obo/NCIT_C203439 http://purl.obolibrary.org/obo/NCIT_C20344 +http://purl.obolibrary.org/obo/NCIT_C203441 +http://purl.obolibrary.org/obo/NCIT_C203442 +http://purl.obolibrary.org/obo/NCIT_C203443 +http://purl.obolibrary.org/obo/NCIT_C203444 +http://purl.obolibrary.org/obo/NCIT_C203445 +http://purl.obolibrary.org/obo/NCIT_C203446 +http://purl.obolibrary.org/obo/NCIT_C203447 +http://purl.obolibrary.org/obo/NCIT_C203448 +http://purl.obolibrary.org/obo/NCIT_C203449 http://purl.obolibrary.org/obo/NCIT_C20345 +http://purl.obolibrary.org/obo/NCIT_C203450 +http://purl.obolibrary.org/obo/NCIT_C203451 +http://purl.obolibrary.org/obo/NCIT_C203452 +http://purl.obolibrary.org/obo/NCIT_C203453 +http://purl.obolibrary.org/obo/NCIT_C203454 +http://purl.obolibrary.org/obo/NCIT_C203455 +http://purl.obolibrary.org/obo/NCIT_C203456 +http://purl.obolibrary.org/obo/NCIT_C203457 +http://purl.obolibrary.org/obo/NCIT_C203458 +http://purl.obolibrary.org/obo/NCIT_C203459 http://purl.obolibrary.org/obo/NCIT_C20346 +http://purl.obolibrary.org/obo/NCIT_C203460 +http://purl.obolibrary.org/obo/NCIT_C203461 +http://purl.obolibrary.org/obo/NCIT_C203462 +http://purl.obolibrary.org/obo/NCIT_C203463 +http://purl.obolibrary.org/obo/NCIT_C203464 +http://purl.obolibrary.org/obo/NCIT_C203465 +http://purl.obolibrary.org/obo/NCIT_C203466 +http://purl.obolibrary.org/obo/NCIT_C203467 +http://purl.obolibrary.org/obo/NCIT_C203468 +http://purl.obolibrary.org/obo/NCIT_C203469 http://purl.obolibrary.org/obo/NCIT_C20347 +http://purl.obolibrary.org/obo/NCIT_C203470 +http://purl.obolibrary.org/obo/NCIT_C203471 +http://purl.obolibrary.org/obo/NCIT_C203472 +http://purl.obolibrary.org/obo/NCIT_C203473 +http://purl.obolibrary.org/obo/NCIT_C203474 +http://purl.obolibrary.org/obo/NCIT_C203475 +http://purl.obolibrary.org/obo/NCIT_C203476 +http://purl.obolibrary.org/obo/NCIT_C203477 +http://purl.obolibrary.org/obo/NCIT_C203478 +http://purl.obolibrary.org/obo/NCIT_C203479 http://purl.obolibrary.org/obo/NCIT_C20348 +http://purl.obolibrary.org/obo/NCIT_C203480 +http://purl.obolibrary.org/obo/NCIT_C203481 +http://purl.obolibrary.org/obo/NCIT_C203482 +http://purl.obolibrary.org/obo/NCIT_C203483 +http://purl.obolibrary.org/obo/NCIT_C203484 +http://purl.obolibrary.org/obo/NCIT_C203485 +http://purl.obolibrary.org/obo/NCIT_C203486 +http://purl.obolibrary.org/obo/NCIT_C203487 +http://purl.obolibrary.org/obo/NCIT_C203488 +http://purl.obolibrary.org/obo/NCIT_C203489 http://purl.obolibrary.org/obo/NCIT_C20349 +http://purl.obolibrary.org/obo/NCIT_C203490 +http://purl.obolibrary.org/obo/NCIT_C203491 +http://purl.obolibrary.org/obo/NCIT_C203492 +http://purl.obolibrary.org/obo/NCIT_C203493 +http://purl.obolibrary.org/obo/NCIT_C203494 +http://purl.obolibrary.org/obo/NCIT_C203495 +http://purl.obolibrary.org/obo/NCIT_C203496 +http://purl.obolibrary.org/obo/NCIT_C203497 +http://purl.obolibrary.org/obo/NCIT_C203498 +http://purl.obolibrary.org/obo/NCIT_C203499 http://purl.obolibrary.org/obo/NCIT_C2035 http://purl.obolibrary.org/obo/NCIT_C20350 +http://purl.obolibrary.org/obo/NCIT_C203500 +http://purl.obolibrary.org/obo/NCIT_C203501 +http://purl.obolibrary.org/obo/NCIT_C203502 +http://purl.obolibrary.org/obo/NCIT_C203503 +http://purl.obolibrary.org/obo/NCIT_C203504 +http://purl.obolibrary.org/obo/NCIT_C203505 +http://purl.obolibrary.org/obo/NCIT_C203506 +http://purl.obolibrary.org/obo/NCIT_C203507 +http://purl.obolibrary.org/obo/NCIT_C203508 +http://purl.obolibrary.org/obo/NCIT_C203509 +http://purl.obolibrary.org/obo/NCIT_C203510 +http://purl.obolibrary.org/obo/NCIT_C203511 +http://purl.obolibrary.org/obo/NCIT_C203512 +http://purl.obolibrary.org/obo/NCIT_C203513 +http://purl.obolibrary.org/obo/NCIT_C203514 +http://purl.obolibrary.org/obo/NCIT_C203515 +http://purl.obolibrary.org/obo/NCIT_C203516 +http://purl.obolibrary.org/obo/NCIT_C203517 +http://purl.obolibrary.org/obo/NCIT_C203518 +http://purl.obolibrary.org/obo/NCIT_C203519 http://purl.obolibrary.org/obo/NCIT_C20352 +http://purl.obolibrary.org/obo/NCIT_C203520 +http://purl.obolibrary.org/obo/NCIT_C203521 +http://purl.obolibrary.org/obo/NCIT_C203522 +http://purl.obolibrary.org/obo/NCIT_C203523 +http://purl.obolibrary.org/obo/NCIT_C203524 +http://purl.obolibrary.org/obo/NCIT_C203525 +http://purl.obolibrary.org/obo/NCIT_C203526 +http://purl.obolibrary.org/obo/NCIT_C203527 +http://purl.obolibrary.org/obo/NCIT_C203528 +http://purl.obolibrary.org/obo/NCIT_C203529 http://purl.obolibrary.org/obo/NCIT_C20353 +http://purl.obolibrary.org/obo/NCIT_C203530 +http://purl.obolibrary.org/obo/NCIT_C203531 +http://purl.obolibrary.org/obo/NCIT_C203532 +http://purl.obolibrary.org/obo/NCIT_C203533 +http://purl.obolibrary.org/obo/NCIT_C203534 +http://purl.obolibrary.org/obo/NCIT_C203535 +http://purl.obolibrary.org/obo/NCIT_C203536 +http://purl.obolibrary.org/obo/NCIT_C203537 +http://purl.obolibrary.org/obo/NCIT_C203538 +http://purl.obolibrary.org/obo/NCIT_C203539 http://purl.obolibrary.org/obo/NCIT_C20354 +http://purl.obolibrary.org/obo/NCIT_C203540 +http://purl.obolibrary.org/obo/NCIT_C203541 +http://purl.obolibrary.org/obo/NCIT_C203542 +http://purl.obolibrary.org/obo/NCIT_C203543 +http://purl.obolibrary.org/obo/NCIT_C203544 +http://purl.obolibrary.org/obo/NCIT_C203545 +http://purl.obolibrary.org/obo/NCIT_C203546 http://purl.obolibrary.org/obo/NCIT_C20355 +http://purl.obolibrary.org/obo/NCIT_C203557 +http://purl.obolibrary.org/obo/NCIT_C203558 +http://purl.obolibrary.org/obo/NCIT_C203559 http://purl.obolibrary.org/obo/NCIT_C20356 +http://purl.obolibrary.org/obo/NCIT_C203560 +http://purl.obolibrary.org/obo/NCIT_C203561 +http://purl.obolibrary.org/obo/NCIT_C203562 +http://purl.obolibrary.org/obo/NCIT_C203563 +http://purl.obolibrary.org/obo/NCIT_C203564 +http://purl.obolibrary.org/obo/NCIT_C203565 +http://purl.obolibrary.org/obo/NCIT_C203566 +http://purl.obolibrary.org/obo/NCIT_C203567 +http://purl.obolibrary.org/obo/NCIT_C203568 +http://purl.obolibrary.org/obo/NCIT_C203569 http://purl.obolibrary.org/obo/NCIT_C20357 +http://purl.obolibrary.org/obo/NCIT_C203570 +http://purl.obolibrary.org/obo/NCIT_C203571 +http://purl.obolibrary.org/obo/NCIT_C203572 +http://purl.obolibrary.org/obo/NCIT_C203573 +http://purl.obolibrary.org/obo/NCIT_C203574 +http://purl.obolibrary.org/obo/NCIT_C203575 +http://purl.obolibrary.org/obo/NCIT_C203576 +http://purl.obolibrary.org/obo/NCIT_C203577 +http://purl.obolibrary.org/obo/NCIT_C203578 +http://purl.obolibrary.org/obo/NCIT_C203579 http://purl.obolibrary.org/obo/NCIT_C20358 +http://purl.obolibrary.org/obo/NCIT_C203580 +http://purl.obolibrary.org/obo/NCIT_C203581 +http://purl.obolibrary.org/obo/NCIT_C203582 +http://purl.obolibrary.org/obo/NCIT_C203583 +http://purl.obolibrary.org/obo/NCIT_C203584 +http://purl.obolibrary.org/obo/NCIT_C203585 +http://purl.obolibrary.org/obo/NCIT_C203586 +http://purl.obolibrary.org/obo/NCIT_C203587 +http://purl.obolibrary.org/obo/NCIT_C203588 +http://purl.obolibrary.org/obo/NCIT_C203589 http://purl.obolibrary.org/obo/NCIT_C20359 +http://purl.obolibrary.org/obo/NCIT_C203590 +http://purl.obolibrary.org/obo/NCIT_C203591 +http://purl.obolibrary.org/obo/NCIT_C203592 +http://purl.obolibrary.org/obo/NCIT_C203593 +http://purl.obolibrary.org/obo/NCIT_C203594 +http://purl.obolibrary.org/obo/NCIT_C203595 +http://purl.obolibrary.org/obo/NCIT_C203596 +http://purl.obolibrary.org/obo/NCIT_C203597 +http://purl.obolibrary.org/obo/NCIT_C203598 +http://purl.obolibrary.org/obo/NCIT_C203599 http://purl.obolibrary.org/obo/NCIT_C2036 http://purl.obolibrary.org/obo/NCIT_C20360 +http://purl.obolibrary.org/obo/NCIT_C203600 +http://purl.obolibrary.org/obo/NCIT_C203602 +http://purl.obolibrary.org/obo/NCIT_C203603 +http://purl.obolibrary.org/obo/NCIT_C203604 +http://purl.obolibrary.org/obo/NCIT_C203605 +http://purl.obolibrary.org/obo/NCIT_C203606 +http://purl.obolibrary.org/obo/NCIT_C203607 +http://purl.obolibrary.org/obo/NCIT_C203608 +http://purl.obolibrary.org/obo/NCIT_C203609 http://purl.obolibrary.org/obo/NCIT_C20361 +http://purl.obolibrary.org/obo/NCIT_C203610 +http://purl.obolibrary.org/obo/NCIT_C203611 +http://purl.obolibrary.org/obo/NCIT_C203612 +http://purl.obolibrary.org/obo/NCIT_C203613 +http://purl.obolibrary.org/obo/NCIT_C203614 +http://purl.obolibrary.org/obo/NCIT_C203615 +http://purl.obolibrary.org/obo/NCIT_C203616 +http://purl.obolibrary.org/obo/NCIT_C203617 +http://purl.obolibrary.org/obo/NCIT_C203618 +http://purl.obolibrary.org/obo/NCIT_C203619 http://purl.obolibrary.org/obo/NCIT_C20362 +http://purl.obolibrary.org/obo/NCIT_C203620 +http://purl.obolibrary.org/obo/NCIT_C203621 +http://purl.obolibrary.org/obo/NCIT_C203622 +http://purl.obolibrary.org/obo/NCIT_C203623 +http://purl.obolibrary.org/obo/NCIT_C203624 +http://purl.obolibrary.org/obo/NCIT_C203625 +http://purl.obolibrary.org/obo/NCIT_C203626 +http://purl.obolibrary.org/obo/NCIT_C203627 +http://purl.obolibrary.org/obo/NCIT_C203628 +http://purl.obolibrary.org/obo/NCIT_C203629 http://purl.obolibrary.org/obo/NCIT_C20363 +http://purl.obolibrary.org/obo/NCIT_C203630 +http://purl.obolibrary.org/obo/NCIT_C203631 +http://purl.obolibrary.org/obo/NCIT_C203632 +http://purl.obolibrary.org/obo/NCIT_C203633 +http://purl.obolibrary.org/obo/NCIT_C203634 +http://purl.obolibrary.org/obo/NCIT_C203635 +http://purl.obolibrary.org/obo/NCIT_C203636 +http://purl.obolibrary.org/obo/NCIT_C203637 +http://purl.obolibrary.org/obo/NCIT_C203638 +http://purl.obolibrary.org/obo/NCIT_C203639 http://purl.obolibrary.org/obo/NCIT_C20364 +http://purl.obolibrary.org/obo/NCIT_C203640 +http://purl.obolibrary.org/obo/NCIT_C203641 +http://purl.obolibrary.org/obo/NCIT_C203642 +http://purl.obolibrary.org/obo/NCIT_C203643 +http://purl.obolibrary.org/obo/NCIT_C203644 +http://purl.obolibrary.org/obo/NCIT_C203645 +http://purl.obolibrary.org/obo/NCIT_C203646 +http://purl.obolibrary.org/obo/NCIT_C203647 +http://purl.obolibrary.org/obo/NCIT_C203648 +http://purl.obolibrary.org/obo/NCIT_C203649 http://purl.obolibrary.org/obo/NCIT_C20365 +http://purl.obolibrary.org/obo/NCIT_C203650 +http://purl.obolibrary.org/obo/NCIT_C203651 +http://purl.obolibrary.org/obo/NCIT_C203652 +http://purl.obolibrary.org/obo/NCIT_C203653 +http://purl.obolibrary.org/obo/NCIT_C203654 +http://purl.obolibrary.org/obo/NCIT_C203655 +http://purl.obolibrary.org/obo/NCIT_C203656 +http://purl.obolibrary.org/obo/NCIT_C203657 +http://purl.obolibrary.org/obo/NCIT_C203658 +http://purl.obolibrary.org/obo/NCIT_C203660 +http://purl.obolibrary.org/obo/NCIT_C203661 +http://purl.obolibrary.org/obo/NCIT_C203662 +http://purl.obolibrary.org/obo/NCIT_C203663 +http://purl.obolibrary.org/obo/NCIT_C203664 +http://purl.obolibrary.org/obo/NCIT_C203665 +http://purl.obolibrary.org/obo/NCIT_C203666 +http://purl.obolibrary.org/obo/NCIT_C203667 +http://purl.obolibrary.org/obo/NCIT_C203668 +http://purl.obolibrary.org/obo/NCIT_C203669 http://purl.obolibrary.org/obo/NCIT_C20367 +http://purl.obolibrary.org/obo/NCIT_C203670 +http://purl.obolibrary.org/obo/NCIT_C203671 +http://purl.obolibrary.org/obo/NCIT_C203672 +http://purl.obolibrary.org/obo/NCIT_C203673 +http://purl.obolibrary.org/obo/NCIT_C203674 +http://purl.obolibrary.org/obo/NCIT_C203675 +http://purl.obolibrary.org/obo/NCIT_C203676 +http://purl.obolibrary.org/obo/NCIT_C203677 +http://purl.obolibrary.org/obo/NCIT_C203678 +http://purl.obolibrary.org/obo/NCIT_C203679 http://purl.obolibrary.org/obo/NCIT_C20368 +http://purl.obolibrary.org/obo/NCIT_C203680 +http://purl.obolibrary.org/obo/NCIT_C203681 +http://purl.obolibrary.org/obo/NCIT_C203682 +http://purl.obolibrary.org/obo/NCIT_C203683 +http://purl.obolibrary.org/obo/NCIT_C203684 +http://purl.obolibrary.org/obo/NCIT_C203685 +http://purl.obolibrary.org/obo/NCIT_C203686 +http://purl.obolibrary.org/obo/NCIT_C203687 +http://purl.obolibrary.org/obo/NCIT_C203688 +http://purl.obolibrary.org/obo/NCIT_C203689 http://purl.obolibrary.org/obo/NCIT_C20369 +http://purl.obolibrary.org/obo/NCIT_C203690 +http://purl.obolibrary.org/obo/NCIT_C203691 +http://purl.obolibrary.org/obo/NCIT_C203692 +http://purl.obolibrary.org/obo/NCIT_C203693 +http://purl.obolibrary.org/obo/NCIT_C203694 +http://purl.obolibrary.org/obo/NCIT_C203695 +http://purl.obolibrary.org/obo/NCIT_C203696 +http://purl.obolibrary.org/obo/NCIT_C203697 +http://purl.obolibrary.org/obo/NCIT_C203698 +http://purl.obolibrary.org/obo/NCIT_C203699 http://purl.obolibrary.org/obo/NCIT_C2037 http://purl.obolibrary.org/obo/NCIT_C20370 +http://purl.obolibrary.org/obo/NCIT_C203700 +http://purl.obolibrary.org/obo/NCIT_C203701 +http://purl.obolibrary.org/obo/NCIT_C203702 +http://purl.obolibrary.org/obo/NCIT_C203703 +http://purl.obolibrary.org/obo/NCIT_C203704 +http://purl.obolibrary.org/obo/NCIT_C203705 +http://purl.obolibrary.org/obo/NCIT_C203706 +http://purl.obolibrary.org/obo/NCIT_C203707 +http://purl.obolibrary.org/obo/NCIT_C203708 +http://purl.obolibrary.org/obo/NCIT_C203709 http://purl.obolibrary.org/obo/NCIT_C20371 +http://purl.obolibrary.org/obo/NCIT_C203710 +http://purl.obolibrary.org/obo/NCIT_C203711 +http://purl.obolibrary.org/obo/NCIT_C203712 +http://purl.obolibrary.org/obo/NCIT_C203713 +http://purl.obolibrary.org/obo/NCIT_C203714 +http://purl.obolibrary.org/obo/NCIT_C203715 +http://purl.obolibrary.org/obo/NCIT_C203716 +http://purl.obolibrary.org/obo/NCIT_C203717 +http://purl.obolibrary.org/obo/NCIT_C203718 +http://purl.obolibrary.org/obo/NCIT_C203719 http://purl.obolibrary.org/obo/NCIT_C20372 +http://purl.obolibrary.org/obo/NCIT_C203720 +http://purl.obolibrary.org/obo/NCIT_C203721 +http://purl.obolibrary.org/obo/NCIT_C203722 +http://purl.obolibrary.org/obo/NCIT_C203723 +http://purl.obolibrary.org/obo/NCIT_C203724 +http://purl.obolibrary.org/obo/NCIT_C203725 +http://purl.obolibrary.org/obo/NCIT_C203726 +http://purl.obolibrary.org/obo/NCIT_C203727 +http://purl.obolibrary.org/obo/NCIT_C203728 +http://purl.obolibrary.org/obo/NCIT_C203729 http://purl.obolibrary.org/obo/NCIT_C20373 +http://purl.obolibrary.org/obo/NCIT_C203730 +http://purl.obolibrary.org/obo/NCIT_C203731 +http://purl.obolibrary.org/obo/NCIT_C203732 +http://purl.obolibrary.org/obo/NCIT_C203733 +http://purl.obolibrary.org/obo/NCIT_C203734 +http://purl.obolibrary.org/obo/NCIT_C203735 +http://purl.obolibrary.org/obo/NCIT_C203736 +http://purl.obolibrary.org/obo/NCIT_C203737 +http://purl.obolibrary.org/obo/NCIT_C203738 +http://purl.obolibrary.org/obo/NCIT_C203739 http://purl.obolibrary.org/obo/NCIT_C20374 +http://purl.obolibrary.org/obo/NCIT_C203740 +http://purl.obolibrary.org/obo/NCIT_C203741 +http://purl.obolibrary.org/obo/NCIT_C203742 +http://purl.obolibrary.org/obo/NCIT_C203743 +http://purl.obolibrary.org/obo/NCIT_C203744 +http://purl.obolibrary.org/obo/NCIT_C203745 +http://purl.obolibrary.org/obo/NCIT_C203746 +http://purl.obolibrary.org/obo/NCIT_C203747 +http://purl.obolibrary.org/obo/NCIT_C203748 +http://purl.obolibrary.org/obo/NCIT_C203749 http://purl.obolibrary.org/obo/NCIT_C20375 +http://purl.obolibrary.org/obo/NCIT_C203750 +http://purl.obolibrary.org/obo/NCIT_C203751 +http://purl.obolibrary.org/obo/NCIT_C203752 +http://purl.obolibrary.org/obo/NCIT_C203753 +http://purl.obolibrary.org/obo/NCIT_C203754 +http://purl.obolibrary.org/obo/NCIT_C203755 +http://purl.obolibrary.org/obo/NCIT_C203756 +http://purl.obolibrary.org/obo/NCIT_C203757 +http://purl.obolibrary.org/obo/NCIT_C203758 +http://purl.obolibrary.org/obo/NCIT_C203759 http://purl.obolibrary.org/obo/NCIT_C20376 +http://purl.obolibrary.org/obo/NCIT_C203760 +http://purl.obolibrary.org/obo/NCIT_C203761 +http://purl.obolibrary.org/obo/NCIT_C203762 +http://purl.obolibrary.org/obo/NCIT_C203763 +http://purl.obolibrary.org/obo/NCIT_C203764 +http://purl.obolibrary.org/obo/NCIT_C203765 +http://purl.obolibrary.org/obo/NCIT_C203766 +http://purl.obolibrary.org/obo/NCIT_C203767 +http://purl.obolibrary.org/obo/NCIT_C203768 +http://purl.obolibrary.org/obo/NCIT_C203769 http://purl.obolibrary.org/obo/NCIT_C20377 +http://purl.obolibrary.org/obo/NCIT_C203770 +http://purl.obolibrary.org/obo/NCIT_C203771 +http://purl.obolibrary.org/obo/NCIT_C203772 +http://purl.obolibrary.org/obo/NCIT_C203773 +http://purl.obolibrary.org/obo/NCIT_C203774 +http://purl.obolibrary.org/obo/NCIT_C203775 +http://purl.obolibrary.org/obo/NCIT_C203776 +http://purl.obolibrary.org/obo/NCIT_C203777 +http://purl.obolibrary.org/obo/NCIT_C203778 +http://purl.obolibrary.org/obo/NCIT_C203779 http://purl.obolibrary.org/obo/NCIT_C20378 +http://purl.obolibrary.org/obo/NCIT_C203780 +http://purl.obolibrary.org/obo/NCIT_C203781 +http://purl.obolibrary.org/obo/NCIT_C203782 +http://purl.obolibrary.org/obo/NCIT_C203783 +http://purl.obolibrary.org/obo/NCIT_C203784 +http://purl.obolibrary.org/obo/NCIT_C203785 +http://purl.obolibrary.org/obo/NCIT_C203786 +http://purl.obolibrary.org/obo/NCIT_C203787 +http://purl.obolibrary.org/obo/NCIT_C203788 +http://purl.obolibrary.org/obo/NCIT_C203789 http://purl.obolibrary.org/obo/NCIT_C20379 +http://purl.obolibrary.org/obo/NCIT_C203790 +http://purl.obolibrary.org/obo/NCIT_C203791 +http://purl.obolibrary.org/obo/NCIT_C203792 +http://purl.obolibrary.org/obo/NCIT_C203793 +http://purl.obolibrary.org/obo/NCIT_C203794 +http://purl.obolibrary.org/obo/NCIT_C203795 +http://purl.obolibrary.org/obo/NCIT_C203796 +http://purl.obolibrary.org/obo/NCIT_C203797 +http://purl.obolibrary.org/obo/NCIT_C203798 +http://purl.obolibrary.org/obo/NCIT_C203799 http://purl.obolibrary.org/obo/NCIT_C2038 http://purl.obolibrary.org/obo/NCIT_C20380 +http://purl.obolibrary.org/obo/NCIT_C203800 +http://purl.obolibrary.org/obo/NCIT_C203801 +http://purl.obolibrary.org/obo/NCIT_C203802 +http://purl.obolibrary.org/obo/NCIT_C203803 +http://purl.obolibrary.org/obo/NCIT_C203804 +http://purl.obolibrary.org/obo/NCIT_C203805 +http://purl.obolibrary.org/obo/NCIT_C203806 +http://purl.obolibrary.org/obo/NCIT_C203807 +http://purl.obolibrary.org/obo/NCIT_C203808 +http://purl.obolibrary.org/obo/NCIT_C203809 http://purl.obolibrary.org/obo/NCIT_C20381 +http://purl.obolibrary.org/obo/NCIT_C203810 +http://purl.obolibrary.org/obo/NCIT_C203811 +http://purl.obolibrary.org/obo/NCIT_C203812 +http://purl.obolibrary.org/obo/NCIT_C203813 +http://purl.obolibrary.org/obo/NCIT_C203814 +http://purl.obolibrary.org/obo/NCIT_C203815 +http://purl.obolibrary.org/obo/NCIT_C203816 +http://purl.obolibrary.org/obo/NCIT_C203817 +http://purl.obolibrary.org/obo/NCIT_C203818 +http://purl.obolibrary.org/obo/NCIT_C203819 http://purl.obolibrary.org/obo/NCIT_C20382 +http://purl.obolibrary.org/obo/NCIT_C203820 +http://purl.obolibrary.org/obo/NCIT_C203821 +http://purl.obolibrary.org/obo/NCIT_C203822 +http://purl.obolibrary.org/obo/NCIT_C203823 +http://purl.obolibrary.org/obo/NCIT_C203824 +http://purl.obolibrary.org/obo/NCIT_C203825 +http://purl.obolibrary.org/obo/NCIT_C203826 +http://purl.obolibrary.org/obo/NCIT_C203827 +http://purl.obolibrary.org/obo/NCIT_C203828 +http://purl.obolibrary.org/obo/NCIT_C203829 http://purl.obolibrary.org/obo/NCIT_C20383 +http://purl.obolibrary.org/obo/NCIT_C203830 +http://purl.obolibrary.org/obo/NCIT_C203831 +http://purl.obolibrary.org/obo/NCIT_C203832 +http://purl.obolibrary.org/obo/NCIT_C203833 +http://purl.obolibrary.org/obo/NCIT_C203834 +http://purl.obolibrary.org/obo/NCIT_C203835 +http://purl.obolibrary.org/obo/NCIT_C203836 +http://purl.obolibrary.org/obo/NCIT_C203837 +http://purl.obolibrary.org/obo/NCIT_C203838 +http://purl.obolibrary.org/obo/NCIT_C203839 http://purl.obolibrary.org/obo/NCIT_C20384 +http://purl.obolibrary.org/obo/NCIT_C203840 +http://purl.obolibrary.org/obo/NCIT_C203841 +http://purl.obolibrary.org/obo/NCIT_C203842 +http://purl.obolibrary.org/obo/NCIT_C203843 +http://purl.obolibrary.org/obo/NCIT_C203844 +http://purl.obolibrary.org/obo/NCIT_C203845 +http://purl.obolibrary.org/obo/NCIT_C203846 +http://purl.obolibrary.org/obo/NCIT_C203847 +http://purl.obolibrary.org/obo/NCIT_C203848 +http://purl.obolibrary.org/obo/NCIT_C203849 http://purl.obolibrary.org/obo/NCIT_C20385 +http://purl.obolibrary.org/obo/NCIT_C203850 +http://purl.obolibrary.org/obo/NCIT_C203852 +http://purl.obolibrary.org/obo/NCIT_C203853 +http://purl.obolibrary.org/obo/NCIT_C203854 +http://purl.obolibrary.org/obo/NCIT_C203855 +http://purl.obolibrary.org/obo/NCIT_C203856 +http://purl.obolibrary.org/obo/NCIT_C203857 +http://purl.obolibrary.org/obo/NCIT_C203858 +http://purl.obolibrary.org/obo/NCIT_C203859 http://purl.obolibrary.org/obo/NCIT_C20386 +http://purl.obolibrary.org/obo/NCIT_C203860 +http://purl.obolibrary.org/obo/NCIT_C203861 +http://purl.obolibrary.org/obo/NCIT_C203862 +http://purl.obolibrary.org/obo/NCIT_C203863 +http://purl.obolibrary.org/obo/NCIT_C203864 +http://purl.obolibrary.org/obo/NCIT_C203865 +http://purl.obolibrary.org/obo/NCIT_C203866 +http://purl.obolibrary.org/obo/NCIT_C203867 +http://purl.obolibrary.org/obo/NCIT_C203868 +http://purl.obolibrary.org/obo/NCIT_C203869 http://purl.obolibrary.org/obo/NCIT_C20387 +http://purl.obolibrary.org/obo/NCIT_C203870 +http://purl.obolibrary.org/obo/NCIT_C203871 +http://purl.obolibrary.org/obo/NCIT_C203872 +http://purl.obolibrary.org/obo/NCIT_C203873 +http://purl.obolibrary.org/obo/NCIT_C203874 +http://purl.obolibrary.org/obo/NCIT_C203875 +http://purl.obolibrary.org/obo/NCIT_C203876 +http://purl.obolibrary.org/obo/NCIT_C203877 +http://purl.obolibrary.org/obo/NCIT_C203878 +http://purl.obolibrary.org/obo/NCIT_C203879 http://purl.obolibrary.org/obo/NCIT_C20388 +http://purl.obolibrary.org/obo/NCIT_C203880 +http://purl.obolibrary.org/obo/NCIT_C203881 +http://purl.obolibrary.org/obo/NCIT_C203882 +http://purl.obolibrary.org/obo/NCIT_C203883 +http://purl.obolibrary.org/obo/NCIT_C203884 +http://purl.obolibrary.org/obo/NCIT_C203885 +http://purl.obolibrary.org/obo/NCIT_C203886 +http://purl.obolibrary.org/obo/NCIT_C203887 +http://purl.obolibrary.org/obo/NCIT_C203888 +http://purl.obolibrary.org/obo/NCIT_C203889 http://purl.obolibrary.org/obo/NCIT_C20389 +http://purl.obolibrary.org/obo/NCIT_C203890 +http://purl.obolibrary.org/obo/NCIT_C203891 +http://purl.obolibrary.org/obo/NCIT_C203892 +http://purl.obolibrary.org/obo/NCIT_C203893 +http://purl.obolibrary.org/obo/NCIT_C203894 +http://purl.obolibrary.org/obo/NCIT_C203895 +http://purl.obolibrary.org/obo/NCIT_C203896 +http://purl.obolibrary.org/obo/NCIT_C203897 +http://purl.obolibrary.org/obo/NCIT_C203898 +http://purl.obolibrary.org/obo/NCIT_C203899 http://purl.obolibrary.org/obo/NCIT_C2039 http://purl.obolibrary.org/obo/NCIT_C20390 +http://purl.obolibrary.org/obo/NCIT_C203900 +http://purl.obolibrary.org/obo/NCIT_C203901 +http://purl.obolibrary.org/obo/NCIT_C203902 +http://purl.obolibrary.org/obo/NCIT_C203903 +http://purl.obolibrary.org/obo/NCIT_C203904 +http://purl.obolibrary.org/obo/NCIT_C203905 +http://purl.obolibrary.org/obo/NCIT_C203906 +http://purl.obolibrary.org/obo/NCIT_C203907 +http://purl.obolibrary.org/obo/NCIT_C203908 +http://purl.obolibrary.org/obo/NCIT_C203909 http://purl.obolibrary.org/obo/NCIT_C20391 +http://purl.obolibrary.org/obo/NCIT_C203910 +http://purl.obolibrary.org/obo/NCIT_C203911 +http://purl.obolibrary.org/obo/NCIT_C203912 +http://purl.obolibrary.org/obo/NCIT_C203913 +http://purl.obolibrary.org/obo/NCIT_C203914 +http://purl.obolibrary.org/obo/NCIT_C203915 +http://purl.obolibrary.org/obo/NCIT_C203916 +http://purl.obolibrary.org/obo/NCIT_C203917 +http://purl.obolibrary.org/obo/NCIT_C203918 +http://purl.obolibrary.org/obo/NCIT_C203919 http://purl.obolibrary.org/obo/NCIT_C20392 +http://purl.obolibrary.org/obo/NCIT_C203920 +http://purl.obolibrary.org/obo/NCIT_C203921 +http://purl.obolibrary.org/obo/NCIT_C203922 +http://purl.obolibrary.org/obo/NCIT_C203923 +http://purl.obolibrary.org/obo/NCIT_C203924 +http://purl.obolibrary.org/obo/NCIT_C203925 +http://purl.obolibrary.org/obo/NCIT_C203926 +http://purl.obolibrary.org/obo/NCIT_C203927 +http://purl.obolibrary.org/obo/NCIT_C203928 +http://purl.obolibrary.org/obo/NCIT_C203929 http://purl.obolibrary.org/obo/NCIT_C20393 +http://purl.obolibrary.org/obo/NCIT_C203930 +http://purl.obolibrary.org/obo/NCIT_C203931 +http://purl.obolibrary.org/obo/NCIT_C203932 +http://purl.obolibrary.org/obo/NCIT_C203933 +http://purl.obolibrary.org/obo/NCIT_C203934 +http://purl.obolibrary.org/obo/NCIT_C203935 +http://purl.obolibrary.org/obo/NCIT_C203936 +http://purl.obolibrary.org/obo/NCIT_C203937 +http://purl.obolibrary.org/obo/NCIT_C203938 +http://purl.obolibrary.org/obo/NCIT_C203939 http://purl.obolibrary.org/obo/NCIT_C20394 +http://purl.obolibrary.org/obo/NCIT_C203940 +http://purl.obolibrary.org/obo/NCIT_C203941 +http://purl.obolibrary.org/obo/NCIT_C203942 +http://purl.obolibrary.org/obo/NCIT_C203943 +http://purl.obolibrary.org/obo/NCIT_C203944 +http://purl.obolibrary.org/obo/NCIT_C203945 +http://purl.obolibrary.org/obo/NCIT_C203946 +http://purl.obolibrary.org/obo/NCIT_C203947 +http://purl.obolibrary.org/obo/NCIT_C203948 +http://purl.obolibrary.org/obo/NCIT_C203949 http://purl.obolibrary.org/obo/NCIT_C20395 +http://purl.obolibrary.org/obo/NCIT_C203950 +http://purl.obolibrary.org/obo/NCIT_C203951 +http://purl.obolibrary.org/obo/NCIT_C203952 +http://purl.obolibrary.org/obo/NCIT_C203953 +http://purl.obolibrary.org/obo/NCIT_C203954 +http://purl.obolibrary.org/obo/NCIT_C203955 +http://purl.obolibrary.org/obo/NCIT_C203956 +http://purl.obolibrary.org/obo/NCIT_C203957 +http://purl.obolibrary.org/obo/NCIT_C203958 +http://purl.obolibrary.org/obo/NCIT_C203959 http://purl.obolibrary.org/obo/NCIT_C20396 +http://purl.obolibrary.org/obo/NCIT_C203960 +http://purl.obolibrary.org/obo/NCIT_C203961 +http://purl.obolibrary.org/obo/NCIT_C203962 +http://purl.obolibrary.org/obo/NCIT_C203963 +http://purl.obolibrary.org/obo/NCIT_C203964 +http://purl.obolibrary.org/obo/NCIT_C203965 +http://purl.obolibrary.org/obo/NCIT_C203966 +http://purl.obolibrary.org/obo/NCIT_C203967 +http://purl.obolibrary.org/obo/NCIT_C203968 +http://purl.obolibrary.org/obo/NCIT_C203969 http://purl.obolibrary.org/obo/NCIT_C20397 +http://purl.obolibrary.org/obo/NCIT_C203970 +http://purl.obolibrary.org/obo/NCIT_C203971 +http://purl.obolibrary.org/obo/NCIT_C203972 +http://purl.obolibrary.org/obo/NCIT_C203973 +http://purl.obolibrary.org/obo/NCIT_C203974 +http://purl.obolibrary.org/obo/NCIT_C203975 +http://purl.obolibrary.org/obo/NCIT_C203976 +http://purl.obolibrary.org/obo/NCIT_C203977 +http://purl.obolibrary.org/obo/NCIT_C203978 +http://purl.obolibrary.org/obo/NCIT_C203979 http://purl.obolibrary.org/obo/NCIT_C20398 +http://purl.obolibrary.org/obo/NCIT_C203980 +http://purl.obolibrary.org/obo/NCIT_C203981 +http://purl.obolibrary.org/obo/NCIT_C203982 +http://purl.obolibrary.org/obo/NCIT_C203983 +http://purl.obolibrary.org/obo/NCIT_C203984 +http://purl.obolibrary.org/obo/NCIT_C203985 +http://purl.obolibrary.org/obo/NCIT_C203986 +http://purl.obolibrary.org/obo/NCIT_C203987 +http://purl.obolibrary.org/obo/NCIT_C203988 +http://purl.obolibrary.org/obo/NCIT_C203989 http://purl.obolibrary.org/obo/NCIT_C20399 +http://purl.obolibrary.org/obo/NCIT_C203990 +http://purl.obolibrary.org/obo/NCIT_C203991 +http://purl.obolibrary.org/obo/NCIT_C203992 +http://purl.obolibrary.org/obo/NCIT_C203993 +http://purl.obolibrary.org/obo/NCIT_C203994 +http://purl.obolibrary.org/obo/NCIT_C203995 +http://purl.obolibrary.org/obo/NCIT_C203996 +http://purl.obolibrary.org/obo/NCIT_C203997 +http://purl.obolibrary.org/obo/NCIT_C203998 +http://purl.obolibrary.org/obo/NCIT_C203999 http://purl.obolibrary.org/obo/NCIT_C204 http://purl.obolibrary.org/obo/NCIT_C2040 +http://purl.obolibrary.org/obo/NCIT_C204000 +http://purl.obolibrary.org/obo/NCIT_C204001 +http://purl.obolibrary.org/obo/NCIT_C204002 +http://purl.obolibrary.org/obo/NCIT_C204003 +http://purl.obolibrary.org/obo/NCIT_C204004 +http://purl.obolibrary.org/obo/NCIT_C204005 +http://purl.obolibrary.org/obo/NCIT_C204006 +http://purl.obolibrary.org/obo/NCIT_C204007 +http://purl.obolibrary.org/obo/NCIT_C204008 +http://purl.obolibrary.org/obo/NCIT_C204009 http://purl.obolibrary.org/obo/NCIT_C20401 +http://purl.obolibrary.org/obo/NCIT_C204010 +http://purl.obolibrary.org/obo/NCIT_C204011 +http://purl.obolibrary.org/obo/NCIT_C204012 +http://purl.obolibrary.org/obo/NCIT_C204013 +http://purl.obolibrary.org/obo/NCIT_C204014 +http://purl.obolibrary.org/obo/NCIT_C204015 +http://purl.obolibrary.org/obo/NCIT_C204016 +http://purl.obolibrary.org/obo/NCIT_C204017 +http://purl.obolibrary.org/obo/NCIT_C204018 +http://purl.obolibrary.org/obo/NCIT_C204019 http://purl.obolibrary.org/obo/NCIT_C20402 +http://purl.obolibrary.org/obo/NCIT_C204020 +http://purl.obolibrary.org/obo/NCIT_C204021 +http://purl.obolibrary.org/obo/NCIT_C204022 +http://purl.obolibrary.org/obo/NCIT_C204023 +http://purl.obolibrary.org/obo/NCIT_C204024 +http://purl.obolibrary.org/obo/NCIT_C204025 +http://purl.obolibrary.org/obo/NCIT_C204026 +http://purl.obolibrary.org/obo/NCIT_C204027 +http://purl.obolibrary.org/obo/NCIT_C204028 +http://purl.obolibrary.org/obo/NCIT_C204029 http://purl.obolibrary.org/obo/NCIT_C20403 +http://purl.obolibrary.org/obo/NCIT_C204030 +http://purl.obolibrary.org/obo/NCIT_C204031 +http://purl.obolibrary.org/obo/NCIT_C204032 +http://purl.obolibrary.org/obo/NCIT_C204033 +http://purl.obolibrary.org/obo/NCIT_C204034 +http://purl.obolibrary.org/obo/NCIT_C204035 +http://purl.obolibrary.org/obo/NCIT_C204036 +http://purl.obolibrary.org/obo/NCIT_C204037 +http://purl.obolibrary.org/obo/NCIT_C204038 +http://purl.obolibrary.org/obo/NCIT_C204039 http://purl.obolibrary.org/obo/NCIT_C20404 +http://purl.obolibrary.org/obo/NCIT_C204040 +http://purl.obolibrary.org/obo/NCIT_C204041 +http://purl.obolibrary.org/obo/NCIT_C204042 +http://purl.obolibrary.org/obo/NCIT_C204043 +http://purl.obolibrary.org/obo/NCIT_C204044 +http://purl.obolibrary.org/obo/NCIT_C204045 +http://purl.obolibrary.org/obo/NCIT_C204046 +http://purl.obolibrary.org/obo/NCIT_C204047 +http://purl.obolibrary.org/obo/NCIT_C204048 +http://purl.obolibrary.org/obo/NCIT_C204049 http://purl.obolibrary.org/obo/NCIT_C20405 +http://purl.obolibrary.org/obo/NCIT_C204050 +http://purl.obolibrary.org/obo/NCIT_C204051 +http://purl.obolibrary.org/obo/NCIT_C204052 +http://purl.obolibrary.org/obo/NCIT_C204053 +http://purl.obolibrary.org/obo/NCIT_C204054 +http://purl.obolibrary.org/obo/NCIT_C204055 +http://purl.obolibrary.org/obo/NCIT_C204056 +http://purl.obolibrary.org/obo/NCIT_C204057 +http://purl.obolibrary.org/obo/NCIT_C204058 +http://purl.obolibrary.org/obo/NCIT_C204059 http://purl.obolibrary.org/obo/NCIT_C20406 +http://purl.obolibrary.org/obo/NCIT_C204060 +http://purl.obolibrary.org/obo/NCIT_C204061 +http://purl.obolibrary.org/obo/NCIT_C204062 +http://purl.obolibrary.org/obo/NCIT_C204063 +http://purl.obolibrary.org/obo/NCIT_C204064 +http://purl.obolibrary.org/obo/NCIT_C204065 +http://purl.obolibrary.org/obo/NCIT_C204066 +http://purl.obolibrary.org/obo/NCIT_C204067 +http://purl.obolibrary.org/obo/NCIT_C204068 +http://purl.obolibrary.org/obo/NCIT_C204069 http://purl.obolibrary.org/obo/NCIT_C20407 +http://purl.obolibrary.org/obo/NCIT_C204070 +http://purl.obolibrary.org/obo/NCIT_C204071 +http://purl.obolibrary.org/obo/NCIT_C204072 +http://purl.obolibrary.org/obo/NCIT_C204073 +http://purl.obolibrary.org/obo/NCIT_C204074 +http://purl.obolibrary.org/obo/NCIT_C204075 +http://purl.obolibrary.org/obo/NCIT_C204076 +http://purl.obolibrary.org/obo/NCIT_C204077 +http://purl.obolibrary.org/obo/NCIT_C204078 +http://purl.obolibrary.org/obo/NCIT_C204079 http://purl.obolibrary.org/obo/NCIT_C20408 +http://purl.obolibrary.org/obo/NCIT_C204080 +http://purl.obolibrary.org/obo/NCIT_C204081 +http://purl.obolibrary.org/obo/NCIT_C204082 +http://purl.obolibrary.org/obo/NCIT_C204083 +http://purl.obolibrary.org/obo/NCIT_C204084 +http://purl.obolibrary.org/obo/NCIT_C204085 +http://purl.obolibrary.org/obo/NCIT_C204086 +http://purl.obolibrary.org/obo/NCIT_C204087 +http://purl.obolibrary.org/obo/NCIT_C204088 +http://purl.obolibrary.org/obo/NCIT_C204089 http://purl.obolibrary.org/obo/NCIT_C20409 +http://purl.obolibrary.org/obo/NCIT_C204090 +http://purl.obolibrary.org/obo/NCIT_C204091 +http://purl.obolibrary.org/obo/NCIT_C204092 +http://purl.obolibrary.org/obo/NCIT_C204093 +http://purl.obolibrary.org/obo/NCIT_C204094 +http://purl.obolibrary.org/obo/NCIT_C204095 +http://purl.obolibrary.org/obo/NCIT_C204096 +http://purl.obolibrary.org/obo/NCIT_C204097 +http://purl.obolibrary.org/obo/NCIT_C204098 +http://purl.obolibrary.org/obo/NCIT_C204099 http://purl.obolibrary.org/obo/NCIT_C2041 http://purl.obolibrary.org/obo/NCIT_C20410 +http://purl.obolibrary.org/obo/NCIT_C204100 +http://purl.obolibrary.org/obo/NCIT_C204101 +http://purl.obolibrary.org/obo/NCIT_C204102 +http://purl.obolibrary.org/obo/NCIT_C204103 +http://purl.obolibrary.org/obo/NCIT_C204104 +http://purl.obolibrary.org/obo/NCIT_C204105 +http://purl.obolibrary.org/obo/NCIT_C204106 +http://purl.obolibrary.org/obo/NCIT_C204107 +http://purl.obolibrary.org/obo/NCIT_C204108 +http://purl.obolibrary.org/obo/NCIT_C204109 http://purl.obolibrary.org/obo/NCIT_C20411 +http://purl.obolibrary.org/obo/NCIT_C204110 +http://purl.obolibrary.org/obo/NCIT_C204111 +http://purl.obolibrary.org/obo/NCIT_C204112 +http://purl.obolibrary.org/obo/NCIT_C204113 +http://purl.obolibrary.org/obo/NCIT_C204114 +http://purl.obolibrary.org/obo/NCIT_C204115 +http://purl.obolibrary.org/obo/NCIT_C204116 +http://purl.obolibrary.org/obo/NCIT_C204117 +http://purl.obolibrary.org/obo/NCIT_C204118 +http://purl.obolibrary.org/obo/NCIT_C204119 http://purl.obolibrary.org/obo/NCIT_C20412 +http://purl.obolibrary.org/obo/NCIT_C204120 +http://purl.obolibrary.org/obo/NCIT_C204121 +http://purl.obolibrary.org/obo/NCIT_C204122 +http://purl.obolibrary.org/obo/NCIT_C204123 +http://purl.obolibrary.org/obo/NCIT_C204124 +http://purl.obolibrary.org/obo/NCIT_C204125 +http://purl.obolibrary.org/obo/NCIT_C204126 +http://purl.obolibrary.org/obo/NCIT_C204127 +http://purl.obolibrary.org/obo/NCIT_C204128 +http://purl.obolibrary.org/obo/NCIT_C204129 http://purl.obolibrary.org/obo/NCIT_C20413 +http://purl.obolibrary.org/obo/NCIT_C204131 +http://purl.obolibrary.org/obo/NCIT_C204132 +http://purl.obolibrary.org/obo/NCIT_C204133 +http://purl.obolibrary.org/obo/NCIT_C204134 +http://purl.obolibrary.org/obo/NCIT_C204135 +http://purl.obolibrary.org/obo/NCIT_C204136 +http://purl.obolibrary.org/obo/NCIT_C204137 +http://purl.obolibrary.org/obo/NCIT_C204138 +http://purl.obolibrary.org/obo/NCIT_C204139 http://purl.obolibrary.org/obo/NCIT_C20414 +http://purl.obolibrary.org/obo/NCIT_C204140 +http://purl.obolibrary.org/obo/NCIT_C204141 +http://purl.obolibrary.org/obo/NCIT_C204142 +http://purl.obolibrary.org/obo/NCIT_C204143 +http://purl.obolibrary.org/obo/NCIT_C204144 +http://purl.obolibrary.org/obo/NCIT_C204145 +http://purl.obolibrary.org/obo/NCIT_C204146 +http://purl.obolibrary.org/obo/NCIT_C204147 +http://purl.obolibrary.org/obo/NCIT_C204148 +http://purl.obolibrary.org/obo/NCIT_C204149 http://purl.obolibrary.org/obo/NCIT_C20415 +http://purl.obolibrary.org/obo/NCIT_C204150 +http://purl.obolibrary.org/obo/NCIT_C204151 +http://purl.obolibrary.org/obo/NCIT_C204152 +http://purl.obolibrary.org/obo/NCIT_C204153 +http://purl.obolibrary.org/obo/NCIT_C204154 +http://purl.obolibrary.org/obo/NCIT_C204155 +http://purl.obolibrary.org/obo/NCIT_C204156 +http://purl.obolibrary.org/obo/NCIT_C204157 +http://purl.obolibrary.org/obo/NCIT_C204158 +http://purl.obolibrary.org/obo/NCIT_C204159 http://purl.obolibrary.org/obo/NCIT_C20416 +http://purl.obolibrary.org/obo/NCIT_C204160 +http://purl.obolibrary.org/obo/NCIT_C204161 +http://purl.obolibrary.org/obo/NCIT_C204162 +http://purl.obolibrary.org/obo/NCIT_C204163 +http://purl.obolibrary.org/obo/NCIT_C204164 +http://purl.obolibrary.org/obo/NCIT_C204165 +http://purl.obolibrary.org/obo/NCIT_C204166 +http://purl.obolibrary.org/obo/NCIT_C204167 +http://purl.obolibrary.org/obo/NCIT_C204168 +http://purl.obolibrary.org/obo/NCIT_C204169 http://purl.obolibrary.org/obo/NCIT_C20417 +http://purl.obolibrary.org/obo/NCIT_C204170 +http://purl.obolibrary.org/obo/NCIT_C204171 +http://purl.obolibrary.org/obo/NCIT_C204172 +http://purl.obolibrary.org/obo/NCIT_C204173 +http://purl.obolibrary.org/obo/NCIT_C204174 +http://purl.obolibrary.org/obo/NCIT_C204175 +http://purl.obolibrary.org/obo/NCIT_C204176 +http://purl.obolibrary.org/obo/NCIT_C204177 +http://purl.obolibrary.org/obo/NCIT_C204178 +http://purl.obolibrary.org/obo/NCIT_C204179 http://purl.obolibrary.org/obo/NCIT_C20418 +http://purl.obolibrary.org/obo/NCIT_C204180 +http://purl.obolibrary.org/obo/NCIT_C204181 +http://purl.obolibrary.org/obo/NCIT_C204182 +http://purl.obolibrary.org/obo/NCIT_C204183 +http://purl.obolibrary.org/obo/NCIT_C204184 +http://purl.obolibrary.org/obo/NCIT_C204185 +http://purl.obolibrary.org/obo/NCIT_C204186 +http://purl.obolibrary.org/obo/NCIT_C204187 +http://purl.obolibrary.org/obo/NCIT_C204188 +http://purl.obolibrary.org/obo/NCIT_C204189 http://purl.obolibrary.org/obo/NCIT_C20419 +http://purl.obolibrary.org/obo/NCIT_C204190 +http://purl.obolibrary.org/obo/NCIT_C204191 +http://purl.obolibrary.org/obo/NCIT_C204192 +http://purl.obolibrary.org/obo/NCIT_C204193 +http://purl.obolibrary.org/obo/NCIT_C204194 +http://purl.obolibrary.org/obo/NCIT_C204195 +http://purl.obolibrary.org/obo/NCIT_C204196 +http://purl.obolibrary.org/obo/NCIT_C204197 +http://purl.obolibrary.org/obo/NCIT_C204198 +http://purl.obolibrary.org/obo/NCIT_C204199 http://purl.obolibrary.org/obo/NCIT_C2042 http://purl.obolibrary.org/obo/NCIT_C20420 +http://purl.obolibrary.org/obo/NCIT_C204200 +http://purl.obolibrary.org/obo/NCIT_C204201 +http://purl.obolibrary.org/obo/NCIT_C204202 +http://purl.obolibrary.org/obo/NCIT_C204204 +http://purl.obolibrary.org/obo/NCIT_C204205 +http://purl.obolibrary.org/obo/NCIT_C204206 +http://purl.obolibrary.org/obo/NCIT_C204207 +http://purl.obolibrary.org/obo/NCIT_C204208 +http://purl.obolibrary.org/obo/NCIT_C204209 http://purl.obolibrary.org/obo/NCIT_C20421 +http://purl.obolibrary.org/obo/NCIT_C204210 +http://purl.obolibrary.org/obo/NCIT_C204211 +http://purl.obolibrary.org/obo/NCIT_C204212 +http://purl.obolibrary.org/obo/NCIT_C204213 +http://purl.obolibrary.org/obo/NCIT_C204214 +http://purl.obolibrary.org/obo/NCIT_C204215 +http://purl.obolibrary.org/obo/NCIT_C204216 +http://purl.obolibrary.org/obo/NCIT_C204217 +http://purl.obolibrary.org/obo/NCIT_C204218 +http://purl.obolibrary.org/obo/NCIT_C204219 http://purl.obolibrary.org/obo/NCIT_C20422 +http://purl.obolibrary.org/obo/NCIT_C204220 +http://purl.obolibrary.org/obo/NCIT_C204221 +http://purl.obolibrary.org/obo/NCIT_C204222 +http://purl.obolibrary.org/obo/NCIT_C204223 +http://purl.obolibrary.org/obo/NCIT_C204224 +http://purl.obolibrary.org/obo/NCIT_C204225 +http://purl.obolibrary.org/obo/NCIT_C204226 +http://purl.obolibrary.org/obo/NCIT_C204227 +http://purl.obolibrary.org/obo/NCIT_C204228 +http://purl.obolibrary.org/obo/NCIT_C204229 http://purl.obolibrary.org/obo/NCIT_C20423 +http://purl.obolibrary.org/obo/NCIT_C204230 +http://purl.obolibrary.org/obo/NCIT_C204231 +http://purl.obolibrary.org/obo/NCIT_C204232 +http://purl.obolibrary.org/obo/NCIT_C204233 +http://purl.obolibrary.org/obo/NCIT_C204234 +http://purl.obolibrary.org/obo/NCIT_C204235 +http://purl.obolibrary.org/obo/NCIT_C204236 +http://purl.obolibrary.org/obo/NCIT_C204237 +http://purl.obolibrary.org/obo/NCIT_C204238 +http://purl.obolibrary.org/obo/NCIT_C204239 http://purl.obolibrary.org/obo/NCIT_C20424 +http://purl.obolibrary.org/obo/NCIT_C204240 +http://purl.obolibrary.org/obo/NCIT_C204241 +http://purl.obolibrary.org/obo/NCIT_C204242 +http://purl.obolibrary.org/obo/NCIT_C204243 +http://purl.obolibrary.org/obo/NCIT_C204244 +http://purl.obolibrary.org/obo/NCIT_C204245 +http://purl.obolibrary.org/obo/NCIT_C204246 +http://purl.obolibrary.org/obo/NCIT_C204247 +http://purl.obolibrary.org/obo/NCIT_C204248 +http://purl.obolibrary.org/obo/NCIT_C204249 http://purl.obolibrary.org/obo/NCIT_C20425 +http://purl.obolibrary.org/obo/NCIT_C204250 +http://purl.obolibrary.org/obo/NCIT_C204251 +http://purl.obolibrary.org/obo/NCIT_C204252 +http://purl.obolibrary.org/obo/NCIT_C204253 +http://purl.obolibrary.org/obo/NCIT_C204254 +http://purl.obolibrary.org/obo/NCIT_C204255 +http://purl.obolibrary.org/obo/NCIT_C204256 +http://purl.obolibrary.org/obo/NCIT_C204257 +http://purl.obolibrary.org/obo/NCIT_C204258 +http://purl.obolibrary.org/obo/NCIT_C204259 http://purl.obolibrary.org/obo/NCIT_C20426 +http://purl.obolibrary.org/obo/NCIT_C204260 +http://purl.obolibrary.org/obo/NCIT_C204261 +http://purl.obolibrary.org/obo/NCIT_C204262 +http://purl.obolibrary.org/obo/NCIT_C204263 +http://purl.obolibrary.org/obo/NCIT_C204264 +http://purl.obolibrary.org/obo/NCIT_C204265 +http://purl.obolibrary.org/obo/NCIT_C204266 +http://purl.obolibrary.org/obo/NCIT_C204267 +http://purl.obolibrary.org/obo/NCIT_C204268 +http://purl.obolibrary.org/obo/NCIT_C204269 http://purl.obolibrary.org/obo/NCIT_C20427 +http://purl.obolibrary.org/obo/NCIT_C204270 +http://purl.obolibrary.org/obo/NCIT_C204271 +http://purl.obolibrary.org/obo/NCIT_C204272 +http://purl.obolibrary.org/obo/NCIT_C204273 +http://purl.obolibrary.org/obo/NCIT_C204274 +http://purl.obolibrary.org/obo/NCIT_C204275 +http://purl.obolibrary.org/obo/NCIT_C204276 +http://purl.obolibrary.org/obo/NCIT_C204277 +http://purl.obolibrary.org/obo/NCIT_C204278 +http://purl.obolibrary.org/obo/NCIT_C204279 http://purl.obolibrary.org/obo/NCIT_C20428 +http://purl.obolibrary.org/obo/NCIT_C204280 +http://purl.obolibrary.org/obo/NCIT_C204281 +http://purl.obolibrary.org/obo/NCIT_C204282 +http://purl.obolibrary.org/obo/NCIT_C204283 +http://purl.obolibrary.org/obo/NCIT_C204284 +http://purl.obolibrary.org/obo/NCIT_C204285 +http://purl.obolibrary.org/obo/NCIT_C204286 +http://purl.obolibrary.org/obo/NCIT_C204287 +http://purl.obolibrary.org/obo/NCIT_C204288 +http://purl.obolibrary.org/obo/NCIT_C204289 http://purl.obolibrary.org/obo/NCIT_C20429 +http://purl.obolibrary.org/obo/NCIT_C204290 +http://purl.obolibrary.org/obo/NCIT_C204291 +http://purl.obolibrary.org/obo/NCIT_C204292 +http://purl.obolibrary.org/obo/NCIT_C204293 +http://purl.obolibrary.org/obo/NCIT_C204294 +http://purl.obolibrary.org/obo/NCIT_C204295 +http://purl.obolibrary.org/obo/NCIT_C204296 +http://purl.obolibrary.org/obo/NCIT_C204297 +http://purl.obolibrary.org/obo/NCIT_C204298 +http://purl.obolibrary.org/obo/NCIT_C204299 http://purl.obolibrary.org/obo/NCIT_C2043 http://purl.obolibrary.org/obo/NCIT_C20430 +http://purl.obolibrary.org/obo/NCIT_C204300 +http://purl.obolibrary.org/obo/NCIT_C204301 +http://purl.obolibrary.org/obo/NCIT_C204302 +http://purl.obolibrary.org/obo/NCIT_C204303 +http://purl.obolibrary.org/obo/NCIT_C204304 +http://purl.obolibrary.org/obo/NCIT_C204305 +http://purl.obolibrary.org/obo/NCIT_C204306 +http://purl.obolibrary.org/obo/NCIT_C204307 +http://purl.obolibrary.org/obo/NCIT_C204308 +http://purl.obolibrary.org/obo/NCIT_C204309 http://purl.obolibrary.org/obo/NCIT_C20431 +http://purl.obolibrary.org/obo/NCIT_C204310 +http://purl.obolibrary.org/obo/NCIT_C204311 +http://purl.obolibrary.org/obo/NCIT_C204312 +http://purl.obolibrary.org/obo/NCIT_C204313 +http://purl.obolibrary.org/obo/NCIT_C204314 +http://purl.obolibrary.org/obo/NCIT_C204315 +http://purl.obolibrary.org/obo/NCIT_C204316 +http://purl.obolibrary.org/obo/NCIT_C204317 +http://purl.obolibrary.org/obo/NCIT_C204318 +http://purl.obolibrary.org/obo/NCIT_C204319 http://purl.obolibrary.org/obo/NCIT_C20432 +http://purl.obolibrary.org/obo/NCIT_C204320 +http://purl.obolibrary.org/obo/NCIT_C204321 +http://purl.obolibrary.org/obo/NCIT_C204322 +http://purl.obolibrary.org/obo/NCIT_C204323 +http://purl.obolibrary.org/obo/NCIT_C204324 +http://purl.obolibrary.org/obo/NCIT_C204325 +http://purl.obolibrary.org/obo/NCIT_C204326 +http://purl.obolibrary.org/obo/NCIT_C204327 +http://purl.obolibrary.org/obo/NCIT_C204328 +http://purl.obolibrary.org/obo/NCIT_C204329 http://purl.obolibrary.org/obo/NCIT_C20433 +http://purl.obolibrary.org/obo/NCIT_C204330 +http://purl.obolibrary.org/obo/NCIT_C204331 +http://purl.obolibrary.org/obo/NCIT_C204332 +http://purl.obolibrary.org/obo/NCIT_C204333 +http://purl.obolibrary.org/obo/NCIT_C204334 +http://purl.obolibrary.org/obo/NCIT_C204335 +http://purl.obolibrary.org/obo/NCIT_C204336 +http://purl.obolibrary.org/obo/NCIT_C204337 +http://purl.obolibrary.org/obo/NCIT_C204338 +http://purl.obolibrary.org/obo/NCIT_C204339 http://purl.obolibrary.org/obo/NCIT_C20434 +http://purl.obolibrary.org/obo/NCIT_C204340 +http://purl.obolibrary.org/obo/NCIT_C204341 +http://purl.obolibrary.org/obo/NCIT_C204342 +http://purl.obolibrary.org/obo/NCIT_C204343 +http://purl.obolibrary.org/obo/NCIT_C204344 +http://purl.obolibrary.org/obo/NCIT_C204345 +http://purl.obolibrary.org/obo/NCIT_C204346 +http://purl.obolibrary.org/obo/NCIT_C204347 +http://purl.obolibrary.org/obo/NCIT_C204348 +http://purl.obolibrary.org/obo/NCIT_C204349 http://purl.obolibrary.org/obo/NCIT_C20435 +http://purl.obolibrary.org/obo/NCIT_C204350 +http://purl.obolibrary.org/obo/NCIT_C204351 +http://purl.obolibrary.org/obo/NCIT_C204352 +http://purl.obolibrary.org/obo/NCIT_C204353 +http://purl.obolibrary.org/obo/NCIT_C204354 +http://purl.obolibrary.org/obo/NCIT_C204355 +http://purl.obolibrary.org/obo/NCIT_C204356 +http://purl.obolibrary.org/obo/NCIT_C204357 +http://purl.obolibrary.org/obo/NCIT_C204358 +http://purl.obolibrary.org/obo/NCIT_C204359 http://purl.obolibrary.org/obo/NCIT_C20436 +http://purl.obolibrary.org/obo/NCIT_C204360 +http://purl.obolibrary.org/obo/NCIT_C204361 +http://purl.obolibrary.org/obo/NCIT_C204362 +http://purl.obolibrary.org/obo/NCIT_C204363 +http://purl.obolibrary.org/obo/NCIT_C204364 +http://purl.obolibrary.org/obo/NCIT_C204365 +http://purl.obolibrary.org/obo/NCIT_C204366 +http://purl.obolibrary.org/obo/NCIT_C204367 +http://purl.obolibrary.org/obo/NCIT_C204368 +http://purl.obolibrary.org/obo/NCIT_C204369 http://purl.obolibrary.org/obo/NCIT_C20437 +http://purl.obolibrary.org/obo/NCIT_C204370 +http://purl.obolibrary.org/obo/NCIT_C204371 +http://purl.obolibrary.org/obo/NCIT_C204372 +http://purl.obolibrary.org/obo/NCIT_C204373 +http://purl.obolibrary.org/obo/NCIT_C204374 +http://purl.obolibrary.org/obo/NCIT_C204375 +http://purl.obolibrary.org/obo/NCIT_C204376 +http://purl.obolibrary.org/obo/NCIT_C204377 +http://purl.obolibrary.org/obo/NCIT_C204378 +http://purl.obolibrary.org/obo/NCIT_C204379 +http://purl.obolibrary.org/obo/NCIT_C204380 +http://purl.obolibrary.org/obo/NCIT_C204381 +http://purl.obolibrary.org/obo/NCIT_C204382 +http://purl.obolibrary.org/obo/NCIT_C204383 +http://purl.obolibrary.org/obo/NCIT_C204384 +http://purl.obolibrary.org/obo/NCIT_C204385 +http://purl.obolibrary.org/obo/NCIT_C204386 +http://purl.obolibrary.org/obo/NCIT_C204387 +http://purl.obolibrary.org/obo/NCIT_C204388 +http://purl.obolibrary.org/obo/NCIT_C204389 http://purl.obolibrary.org/obo/NCIT_C20439 +http://purl.obolibrary.org/obo/NCIT_C204390 +http://purl.obolibrary.org/obo/NCIT_C204391 +http://purl.obolibrary.org/obo/NCIT_C204392 +http://purl.obolibrary.org/obo/NCIT_C204393 +http://purl.obolibrary.org/obo/NCIT_C204394 +http://purl.obolibrary.org/obo/NCIT_C204395 +http://purl.obolibrary.org/obo/NCIT_C204396 +http://purl.obolibrary.org/obo/NCIT_C204397 +http://purl.obolibrary.org/obo/NCIT_C204398 +http://purl.obolibrary.org/obo/NCIT_C204399 http://purl.obolibrary.org/obo/NCIT_C2044 http://purl.obolibrary.org/obo/NCIT_C20440 +http://purl.obolibrary.org/obo/NCIT_C204400 +http://purl.obolibrary.org/obo/NCIT_C204401 +http://purl.obolibrary.org/obo/NCIT_C204402 +http://purl.obolibrary.org/obo/NCIT_C204403 +http://purl.obolibrary.org/obo/NCIT_C204404 +http://purl.obolibrary.org/obo/NCIT_C204405 +http://purl.obolibrary.org/obo/NCIT_C204406 +http://purl.obolibrary.org/obo/NCIT_C204407 +http://purl.obolibrary.org/obo/NCIT_C204408 +http://purl.obolibrary.org/obo/NCIT_C204409 http://purl.obolibrary.org/obo/NCIT_C20441 +http://purl.obolibrary.org/obo/NCIT_C204410 +http://purl.obolibrary.org/obo/NCIT_C204411 +http://purl.obolibrary.org/obo/NCIT_C204412 +http://purl.obolibrary.org/obo/NCIT_C204413 +http://purl.obolibrary.org/obo/NCIT_C204414 +http://purl.obolibrary.org/obo/NCIT_C204415 +http://purl.obolibrary.org/obo/NCIT_C204416 +http://purl.obolibrary.org/obo/NCIT_C204417 +http://purl.obolibrary.org/obo/NCIT_C204418 +http://purl.obolibrary.org/obo/NCIT_C204419 http://purl.obolibrary.org/obo/NCIT_C20442 +http://purl.obolibrary.org/obo/NCIT_C204420 +http://purl.obolibrary.org/obo/NCIT_C204421 +http://purl.obolibrary.org/obo/NCIT_C204422 +http://purl.obolibrary.org/obo/NCIT_C204423 +http://purl.obolibrary.org/obo/NCIT_C204424 +http://purl.obolibrary.org/obo/NCIT_C204425 +http://purl.obolibrary.org/obo/NCIT_C204426 +http://purl.obolibrary.org/obo/NCIT_C204427 +http://purl.obolibrary.org/obo/NCIT_C204428 +http://purl.obolibrary.org/obo/NCIT_C204429 +http://purl.obolibrary.org/obo/NCIT_C204430 +http://purl.obolibrary.org/obo/NCIT_C204431 +http://purl.obolibrary.org/obo/NCIT_C204432 +http://purl.obolibrary.org/obo/NCIT_C204433 +http://purl.obolibrary.org/obo/NCIT_C204434 +http://purl.obolibrary.org/obo/NCIT_C204435 +http://purl.obolibrary.org/obo/NCIT_C204436 +http://purl.obolibrary.org/obo/NCIT_C204437 +http://purl.obolibrary.org/obo/NCIT_C204438 +http://purl.obolibrary.org/obo/NCIT_C204439 http://purl.obolibrary.org/obo/NCIT_C20444 +http://purl.obolibrary.org/obo/NCIT_C204440 +http://purl.obolibrary.org/obo/NCIT_C204441 +http://purl.obolibrary.org/obo/NCIT_C204442 +http://purl.obolibrary.org/obo/NCIT_C204443 +http://purl.obolibrary.org/obo/NCIT_C204444 +http://purl.obolibrary.org/obo/NCIT_C204445 +http://purl.obolibrary.org/obo/NCIT_C204446 +http://purl.obolibrary.org/obo/NCIT_C204447 +http://purl.obolibrary.org/obo/NCIT_C204448 +http://purl.obolibrary.org/obo/NCIT_C204449 http://purl.obolibrary.org/obo/NCIT_C20445 +http://purl.obolibrary.org/obo/NCIT_C204450 +http://purl.obolibrary.org/obo/NCIT_C204451 +http://purl.obolibrary.org/obo/NCIT_C204452 +http://purl.obolibrary.org/obo/NCIT_C204453 +http://purl.obolibrary.org/obo/NCIT_C204454 +http://purl.obolibrary.org/obo/NCIT_C204455 +http://purl.obolibrary.org/obo/NCIT_C204456 +http://purl.obolibrary.org/obo/NCIT_C204457 +http://purl.obolibrary.org/obo/NCIT_C204458 +http://purl.obolibrary.org/obo/NCIT_C204459 http://purl.obolibrary.org/obo/NCIT_C20446 +http://purl.obolibrary.org/obo/NCIT_C204460 +http://purl.obolibrary.org/obo/NCIT_C204461 +http://purl.obolibrary.org/obo/NCIT_C204462 +http://purl.obolibrary.org/obo/NCIT_C204463 +http://purl.obolibrary.org/obo/NCIT_C204464 +http://purl.obolibrary.org/obo/NCIT_C204465 +http://purl.obolibrary.org/obo/NCIT_C204466 +http://purl.obolibrary.org/obo/NCIT_C204467 +http://purl.obolibrary.org/obo/NCIT_C204468 +http://purl.obolibrary.org/obo/NCIT_C204469 http://purl.obolibrary.org/obo/NCIT_C20447 +http://purl.obolibrary.org/obo/NCIT_C204470 +http://purl.obolibrary.org/obo/NCIT_C204471 +http://purl.obolibrary.org/obo/NCIT_C204472 +http://purl.obolibrary.org/obo/NCIT_C204473 +http://purl.obolibrary.org/obo/NCIT_C204474 +http://purl.obolibrary.org/obo/NCIT_C204476 +http://purl.obolibrary.org/obo/NCIT_C204477 +http://purl.obolibrary.org/obo/NCIT_C204478 +http://purl.obolibrary.org/obo/NCIT_C204479 http://purl.obolibrary.org/obo/NCIT_C20448 +http://purl.obolibrary.org/obo/NCIT_C204480 +http://purl.obolibrary.org/obo/NCIT_C204481 +http://purl.obolibrary.org/obo/NCIT_C204482 +http://purl.obolibrary.org/obo/NCIT_C204483 +http://purl.obolibrary.org/obo/NCIT_C204484 +http://purl.obolibrary.org/obo/NCIT_C204485 +http://purl.obolibrary.org/obo/NCIT_C204486 +http://purl.obolibrary.org/obo/NCIT_C204487 +http://purl.obolibrary.org/obo/NCIT_C204488 +http://purl.obolibrary.org/obo/NCIT_C204489 http://purl.obolibrary.org/obo/NCIT_C20449 +http://purl.obolibrary.org/obo/NCIT_C204490 +http://purl.obolibrary.org/obo/NCIT_C204491 +http://purl.obolibrary.org/obo/NCIT_C204492 +http://purl.obolibrary.org/obo/NCIT_C204493 +http://purl.obolibrary.org/obo/NCIT_C204494 +http://purl.obolibrary.org/obo/NCIT_C204495 +http://purl.obolibrary.org/obo/NCIT_C204496 +http://purl.obolibrary.org/obo/NCIT_C204497 +http://purl.obolibrary.org/obo/NCIT_C204498 +http://purl.obolibrary.org/obo/NCIT_C204499 http://purl.obolibrary.org/obo/NCIT_C2045 http://purl.obolibrary.org/obo/NCIT_C20450 +http://purl.obolibrary.org/obo/NCIT_C204500 +http://purl.obolibrary.org/obo/NCIT_C204501 +http://purl.obolibrary.org/obo/NCIT_C204502 +http://purl.obolibrary.org/obo/NCIT_C204503 +http://purl.obolibrary.org/obo/NCIT_C204505 +http://purl.obolibrary.org/obo/NCIT_C204506 +http://purl.obolibrary.org/obo/NCIT_C204507 +http://purl.obolibrary.org/obo/NCIT_C204508 +http://purl.obolibrary.org/obo/NCIT_C204509 http://purl.obolibrary.org/obo/NCIT_C20451 +http://purl.obolibrary.org/obo/NCIT_C204510 +http://purl.obolibrary.org/obo/NCIT_C204511 +http://purl.obolibrary.org/obo/NCIT_C204512 +http://purl.obolibrary.org/obo/NCIT_C204513 +http://purl.obolibrary.org/obo/NCIT_C204514 +http://purl.obolibrary.org/obo/NCIT_C204515 +http://purl.obolibrary.org/obo/NCIT_C204516 +http://purl.obolibrary.org/obo/NCIT_C204517 +http://purl.obolibrary.org/obo/NCIT_C204518 +http://purl.obolibrary.org/obo/NCIT_C204519 http://purl.obolibrary.org/obo/NCIT_C20452 +http://purl.obolibrary.org/obo/NCIT_C204520 +http://purl.obolibrary.org/obo/NCIT_C204521 +http://purl.obolibrary.org/obo/NCIT_C204522 +http://purl.obolibrary.org/obo/NCIT_C204523 +http://purl.obolibrary.org/obo/NCIT_C204524 +http://purl.obolibrary.org/obo/NCIT_C204525 +http://purl.obolibrary.org/obo/NCIT_C204526 +http://purl.obolibrary.org/obo/NCIT_C204527 +http://purl.obolibrary.org/obo/NCIT_C204528 +http://purl.obolibrary.org/obo/NCIT_C204529 http://purl.obolibrary.org/obo/NCIT_C20453 +http://purl.obolibrary.org/obo/NCIT_C204530 +http://purl.obolibrary.org/obo/NCIT_C204531 +http://purl.obolibrary.org/obo/NCIT_C204532 +http://purl.obolibrary.org/obo/NCIT_C204533 +http://purl.obolibrary.org/obo/NCIT_C204534 +http://purl.obolibrary.org/obo/NCIT_C204535 +http://purl.obolibrary.org/obo/NCIT_C204536 +http://purl.obolibrary.org/obo/NCIT_C204537 +http://purl.obolibrary.org/obo/NCIT_C204538 +http://purl.obolibrary.org/obo/NCIT_C204539 http://purl.obolibrary.org/obo/NCIT_C20454 +http://purl.obolibrary.org/obo/NCIT_C204540 +http://purl.obolibrary.org/obo/NCIT_C204541 +http://purl.obolibrary.org/obo/NCIT_C204542 +http://purl.obolibrary.org/obo/NCIT_C204543 +http://purl.obolibrary.org/obo/NCIT_C204544 +http://purl.obolibrary.org/obo/NCIT_C204545 +http://purl.obolibrary.org/obo/NCIT_C204546 +http://purl.obolibrary.org/obo/NCIT_C204547 +http://purl.obolibrary.org/obo/NCIT_C204548 +http://purl.obolibrary.org/obo/NCIT_C204549 http://purl.obolibrary.org/obo/NCIT_C20455 +http://purl.obolibrary.org/obo/NCIT_C204550 +http://purl.obolibrary.org/obo/NCIT_C204551 +http://purl.obolibrary.org/obo/NCIT_C204552 +http://purl.obolibrary.org/obo/NCIT_C204553 +http://purl.obolibrary.org/obo/NCIT_C204554 +http://purl.obolibrary.org/obo/NCIT_C204555 +http://purl.obolibrary.org/obo/NCIT_C204556 +http://purl.obolibrary.org/obo/NCIT_C204557 +http://purl.obolibrary.org/obo/NCIT_C204558 +http://purl.obolibrary.org/obo/NCIT_C204559 http://purl.obolibrary.org/obo/NCIT_C20456 +http://purl.obolibrary.org/obo/NCIT_C204560 +http://purl.obolibrary.org/obo/NCIT_C204561 +http://purl.obolibrary.org/obo/NCIT_C204562 +http://purl.obolibrary.org/obo/NCIT_C204563 +http://purl.obolibrary.org/obo/NCIT_C204564 +http://purl.obolibrary.org/obo/NCIT_C204565 +http://purl.obolibrary.org/obo/NCIT_C204566 +http://purl.obolibrary.org/obo/NCIT_C204567 +http://purl.obolibrary.org/obo/NCIT_C204568 +http://purl.obolibrary.org/obo/NCIT_C204569 http://purl.obolibrary.org/obo/NCIT_C20457 +http://purl.obolibrary.org/obo/NCIT_C204570 +http://purl.obolibrary.org/obo/NCIT_C204571 +http://purl.obolibrary.org/obo/NCIT_C204572 +http://purl.obolibrary.org/obo/NCIT_C204574 +http://purl.obolibrary.org/obo/NCIT_C204576 +http://purl.obolibrary.org/obo/NCIT_C204577 +http://purl.obolibrary.org/obo/NCIT_C204578 +http://purl.obolibrary.org/obo/NCIT_C204579 http://purl.obolibrary.org/obo/NCIT_C20458 +http://purl.obolibrary.org/obo/NCIT_C204580 +http://purl.obolibrary.org/obo/NCIT_C204581 +http://purl.obolibrary.org/obo/NCIT_C204582 +http://purl.obolibrary.org/obo/NCIT_C204583 +http://purl.obolibrary.org/obo/NCIT_C204584 +http://purl.obolibrary.org/obo/NCIT_C204585 +http://purl.obolibrary.org/obo/NCIT_C204586 +http://purl.obolibrary.org/obo/NCIT_C204587 +http://purl.obolibrary.org/obo/NCIT_C204588 +http://purl.obolibrary.org/obo/NCIT_C204589 http://purl.obolibrary.org/obo/NCIT_C20459 +http://purl.obolibrary.org/obo/NCIT_C204590 +http://purl.obolibrary.org/obo/NCIT_C204591 +http://purl.obolibrary.org/obo/NCIT_C204592 +http://purl.obolibrary.org/obo/NCIT_C204593 +http://purl.obolibrary.org/obo/NCIT_C204594 +http://purl.obolibrary.org/obo/NCIT_C204595 +http://purl.obolibrary.org/obo/NCIT_C204596 +http://purl.obolibrary.org/obo/NCIT_C204597 +http://purl.obolibrary.org/obo/NCIT_C204598 +http://purl.obolibrary.org/obo/NCIT_C204599 http://purl.obolibrary.org/obo/NCIT_C20460 +http://purl.obolibrary.org/obo/NCIT_C204600 +http://purl.obolibrary.org/obo/NCIT_C204601 +http://purl.obolibrary.org/obo/NCIT_C204602 +http://purl.obolibrary.org/obo/NCIT_C204603 +http://purl.obolibrary.org/obo/NCIT_C204604 +http://purl.obolibrary.org/obo/NCIT_C204605 +http://purl.obolibrary.org/obo/NCIT_C204606 +http://purl.obolibrary.org/obo/NCIT_C204607 +http://purl.obolibrary.org/obo/NCIT_C204608 +http://purl.obolibrary.org/obo/NCIT_C204609 http://purl.obolibrary.org/obo/NCIT_C20461 +http://purl.obolibrary.org/obo/NCIT_C204610 +http://purl.obolibrary.org/obo/NCIT_C204611 +http://purl.obolibrary.org/obo/NCIT_C204612 +http://purl.obolibrary.org/obo/NCIT_C204613 +http://purl.obolibrary.org/obo/NCIT_C204614 +http://purl.obolibrary.org/obo/NCIT_C204615 +http://purl.obolibrary.org/obo/NCIT_C204616 +http://purl.obolibrary.org/obo/NCIT_C204617 +http://purl.obolibrary.org/obo/NCIT_C204618 +http://purl.obolibrary.org/obo/NCIT_C204619 http://purl.obolibrary.org/obo/NCIT_C20462 +http://purl.obolibrary.org/obo/NCIT_C204620 +http://purl.obolibrary.org/obo/NCIT_C204621 +http://purl.obolibrary.org/obo/NCIT_C204622 +http://purl.obolibrary.org/obo/NCIT_C204623 +http://purl.obolibrary.org/obo/NCIT_C204624 +http://purl.obolibrary.org/obo/NCIT_C204625 +http://purl.obolibrary.org/obo/NCIT_C204626 +http://purl.obolibrary.org/obo/NCIT_C204627 +http://purl.obolibrary.org/obo/NCIT_C204628 +http://purl.obolibrary.org/obo/NCIT_C204629 http://purl.obolibrary.org/obo/NCIT_C20463 +http://purl.obolibrary.org/obo/NCIT_C204630 +http://purl.obolibrary.org/obo/NCIT_C204631 +http://purl.obolibrary.org/obo/NCIT_C204632 +http://purl.obolibrary.org/obo/NCIT_C204633 +http://purl.obolibrary.org/obo/NCIT_C204634 +http://purl.obolibrary.org/obo/NCIT_C204635 +http://purl.obolibrary.org/obo/NCIT_C204636 +http://purl.obolibrary.org/obo/NCIT_C204637 +http://purl.obolibrary.org/obo/NCIT_C204638 +http://purl.obolibrary.org/obo/NCIT_C204639 http://purl.obolibrary.org/obo/NCIT_C20464 +http://purl.obolibrary.org/obo/NCIT_C204640 +http://purl.obolibrary.org/obo/NCIT_C204641 +http://purl.obolibrary.org/obo/NCIT_C204642 +http://purl.obolibrary.org/obo/NCIT_C204643 +http://purl.obolibrary.org/obo/NCIT_C204644 +http://purl.obolibrary.org/obo/NCIT_C204645 +http://purl.obolibrary.org/obo/NCIT_C204646 +http://purl.obolibrary.org/obo/NCIT_C204647 +http://purl.obolibrary.org/obo/NCIT_C204648 +http://purl.obolibrary.org/obo/NCIT_C204649 http://purl.obolibrary.org/obo/NCIT_C20465 +http://purl.obolibrary.org/obo/NCIT_C204650 +http://purl.obolibrary.org/obo/NCIT_C204651 +http://purl.obolibrary.org/obo/NCIT_C204652 +http://purl.obolibrary.org/obo/NCIT_C204653 +http://purl.obolibrary.org/obo/NCIT_C204654 +http://purl.obolibrary.org/obo/NCIT_C204655 +http://purl.obolibrary.org/obo/NCIT_C204656 +http://purl.obolibrary.org/obo/NCIT_C204657 +http://purl.obolibrary.org/obo/NCIT_C204658 +http://purl.obolibrary.org/obo/NCIT_C204659 http://purl.obolibrary.org/obo/NCIT_C20466 +http://purl.obolibrary.org/obo/NCIT_C204660 +http://purl.obolibrary.org/obo/NCIT_C204661 +http://purl.obolibrary.org/obo/NCIT_C204662 +http://purl.obolibrary.org/obo/NCIT_C204663 +http://purl.obolibrary.org/obo/NCIT_C204664 +http://purl.obolibrary.org/obo/NCIT_C204665 +http://purl.obolibrary.org/obo/NCIT_C204666 +http://purl.obolibrary.org/obo/NCIT_C204667 +http://purl.obolibrary.org/obo/NCIT_C204668 +http://purl.obolibrary.org/obo/NCIT_C204669 http://purl.obolibrary.org/obo/NCIT_C20467 +http://purl.obolibrary.org/obo/NCIT_C204670 +http://purl.obolibrary.org/obo/NCIT_C204671 +http://purl.obolibrary.org/obo/NCIT_C204672 +http://purl.obolibrary.org/obo/NCIT_C204673 +http://purl.obolibrary.org/obo/NCIT_C204674 +http://purl.obolibrary.org/obo/NCIT_C204675 +http://purl.obolibrary.org/obo/NCIT_C204676 +http://purl.obolibrary.org/obo/NCIT_C204677 +http://purl.obolibrary.org/obo/NCIT_C204678 +http://purl.obolibrary.org/obo/NCIT_C204679 http://purl.obolibrary.org/obo/NCIT_C20468 +http://purl.obolibrary.org/obo/NCIT_C204680 +http://purl.obolibrary.org/obo/NCIT_C204681 +http://purl.obolibrary.org/obo/NCIT_C204682 +http://purl.obolibrary.org/obo/NCIT_C204683 +http://purl.obolibrary.org/obo/NCIT_C204684 +http://purl.obolibrary.org/obo/NCIT_C204685 +http://purl.obolibrary.org/obo/NCIT_C204686 +http://purl.obolibrary.org/obo/NCIT_C204687 +http://purl.obolibrary.org/obo/NCIT_C204688 +http://purl.obolibrary.org/obo/NCIT_C204689 http://purl.obolibrary.org/obo/NCIT_C20469 +http://purl.obolibrary.org/obo/NCIT_C204690 +http://purl.obolibrary.org/obo/NCIT_C204691 +http://purl.obolibrary.org/obo/NCIT_C204692 +http://purl.obolibrary.org/obo/NCIT_C204693 +http://purl.obolibrary.org/obo/NCIT_C204694 +http://purl.obolibrary.org/obo/NCIT_C204695 +http://purl.obolibrary.org/obo/NCIT_C204696 +http://purl.obolibrary.org/obo/NCIT_C204697 +http://purl.obolibrary.org/obo/NCIT_C204698 +http://purl.obolibrary.org/obo/NCIT_C204699 http://purl.obolibrary.org/obo/NCIT_C2047 http://purl.obolibrary.org/obo/NCIT_C20470 +http://purl.obolibrary.org/obo/NCIT_C204700 +http://purl.obolibrary.org/obo/NCIT_C204701 +http://purl.obolibrary.org/obo/NCIT_C204702 +http://purl.obolibrary.org/obo/NCIT_C204703 +http://purl.obolibrary.org/obo/NCIT_C204704 +http://purl.obolibrary.org/obo/NCIT_C204705 +http://purl.obolibrary.org/obo/NCIT_C204706 +http://purl.obolibrary.org/obo/NCIT_C204707 +http://purl.obolibrary.org/obo/NCIT_C204708 +http://purl.obolibrary.org/obo/NCIT_C204709 http://purl.obolibrary.org/obo/NCIT_C20471 +http://purl.obolibrary.org/obo/NCIT_C204710 +http://purl.obolibrary.org/obo/NCIT_C204711 +http://purl.obolibrary.org/obo/NCIT_C204712 +http://purl.obolibrary.org/obo/NCIT_C204713 +http://purl.obolibrary.org/obo/NCIT_C204714 +http://purl.obolibrary.org/obo/NCIT_C204715 +http://purl.obolibrary.org/obo/NCIT_C204716 +http://purl.obolibrary.org/obo/NCIT_C204717 +http://purl.obolibrary.org/obo/NCIT_C204718 +http://purl.obolibrary.org/obo/NCIT_C204719 +http://purl.obolibrary.org/obo/NCIT_C204720 +http://purl.obolibrary.org/obo/NCIT_C204721 +http://purl.obolibrary.org/obo/NCIT_C204722 +http://purl.obolibrary.org/obo/NCIT_C204723 +http://purl.obolibrary.org/obo/NCIT_C204724 +http://purl.obolibrary.org/obo/NCIT_C204725 +http://purl.obolibrary.org/obo/NCIT_C204726 +http://purl.obolibrary.org/obo/NCIT_C204727 +http://purl.obolibrary.org/obo/NCIT_C204728 +http://purl.obolibrary.org/obo/NCIT_C204729 http://purl.obolibrary.org/obo/NCIT_C20473 +http://purl.obolibrary.org/obo/NCIT_C204730 +http://purl.obolibrary.org/obo/NCIT_C204731 +http://purl.obolibrary.org/obo/NCIT_C204732 +http://purl.obolibrary.org/obo/NCIT_C204733 +http://purl.obolibrary.org/obo/NCIT_C204734 +http://purl.obolibrary.org/obo/NCIT_C204735 +http://purl.obolibrary.org/obo/NCIT_C204736 +http://purl.obolibrary.org/obo/NCIT_C204737 +http://purl.obolibrary.org/obo/NCIT_C204738 +http://purl.obolibrary.org/obo/NCIT_C204739 http://purl.obolibrary.org/obo/NCIT_C20474 +http://purl.obolibrary.org/obo/NCIT_C204740 +http://purl.obolibrary.org/obo/NCIT_C204741 +http://purl.obolibrary.org/obo/NCIT_C204742 +http://purl.obolibrary.org/obo/NCIT_C204743 +http://purl.obolibrary.org/obo/NCIT_C204744 +http://purl.obolibrary.org/obo/NCIT_C204745 +http://purl.obolibrary.org/obo/NCIT_C204746 +http://purl.obolibrary.org/obo/NCIT_C204747 +http://purl.obolibrary.org/obo/NCIT_C204748 +http://purl.obolibrary.org/obo/NCIT_C204749 http://purl.obolibrary.org/obo/NCIT_C20475 +http://purl.obolibrary.org/obo/NCIT_C204750 +http://purl.obolibrary.org/obo/NCIT_C204751 +http://purl.obolibrary.org/obo/NCIT_C204752 +http://purl.obolibrary.org/obo/NCIT_C204753 +http://purl.obolibrary.org/obo/NCIT_C204754 +http://purl.obolibrary.org/obo/NCIT_C204755 +http://purl.obolibrary.org/obo/NCIT_C204756 +http://purl.obolibrary.org/obo/NCIT_C204757 +http://purl.obolibrary.org/obo/NCIT_C204758 +http://purl.obolibrary.org/obo/NCIT_C204759 http://purl.obolibrary.org/obo/NCIT_C20476 +http://purl.obolibrary.org/obo/NCIT_C204760 +http://purl.obolibrary.org/obo/NCIT_C204761 +http://purl.obolibrary.org/obo/NCIT_C204762 +http://purl.obolibrary.org/obo/NCIT_C204763 +http://purl.obolibrary.org/obo/NCIT_C204764 +http://purl.obolibrary.org/obo/NCIT_C204765 +http://purl.obolibrary.org/obo/NCIT_C204766 +http://purl.obolibrary.org/obo/NCIT_C204767 +http://purl.obolibrary.org/obo/NCIT_C204768 +http://purl.obolibrary.org/obo/NCIT_C204769 http://purl.obolibrary.org/obo/NCIT_C20477 +http://purl.obolibrary.org/obo/NCIT_C204770 +http://purl.obolibrary.org/obo/NCIT_C204771 +http://purl.obolibrary.org/obo/NCIT_C204772 +http://purl.obolibrary.org/obo/NCIT_C204773 +http://purl.obolibrary.org/obo/NCIT_C204774 +http://purl.obolibrary.org/obo/NCIT_C204775 +http://purl.obolibrary.org/obo/NCIT_C204776 +http://purl.obolibrary.org/obo/NCIT_C204777 +http://purl.obolibrary.org/obo/NCIT_C204778 +http://purl.obolibrary.org/obo/NCIT_C204779 http://purl.obolibrary.org/obo/NCIT_C20478 +http://purl.obolibrary.org/obo/NCIT_C204780 +http://purl.obolibrary.org/obo/NCIT_C204781 +http://purl.obolibrary.org/obo/NCIT_C204782 +http://purl.obolibrary.org/obo/NCIT_C204783 +http://purl.obolibrary.org/obo/NCIT_C204784 +http://purl.obolibrary.org/obo/NCIT_C204785 +http://purl.obolibrary.org/obo/NCIT_C204787 +http://purl.obolibrary.org/obo/NCIT_C204788 +http://purl.obolibrary.org/obo/NCIT_C204789 http://purl.obolibrary.org/obo/NCIT_C20479 +http://purl.obolibrary.org/obo/NCIT_C204790 +http://purl.obolibrary.org/obo/NCIT_C204791 +http://purl.obolibrary.org/obo/NCIT_C204792 +http://purl.obolibrary.org/obo/NCIT_C204793 +http://purl.obolibrary.org/obo/NCIT_C204794 +http://purl.obolibrary.org/obo/NCIT_C204795 +http://purl.obolibrary.org/obo/NCIT_C204796 +http://purl.obolibrary.org/obo/NCIT_C204797 +http://purl.obolibrary.org/obo/NCIT_C204798 +http://purl.obolibrary.org/obo/NCIT_C204799 http://purl.obolibrary.org/obo/NCIT_C2048 http://purl.obolibrary.org/obo/NCIT_C20480 +http://purl.obolibrary.org/obo/NCIT_C204800 +http://purl.obolibrary.org/obo/NCIT_C204801 +http://purl.obolibrary.org/obo/NCIT_C204802 +http://purl.obolibrary.org/obo/NCIT_C204803 +http://purl.obolibrary.org/obo/NCIT_C204804 +http://purl.obolibrary.org/obo/NCIT_C204805 +http://purl.obolibrary.org/obo/NCIT_C204806 +http://purl.obolibrary.org/obo/NCIT_C204807 +http://purl.obolibrary.org/obo/NCIT_C204808 +http://purl.obolibrary.org/obo/NCIT_C204809 http://purl.obolibrary.org/obo/NCIT_C20481 +http://purl.obolibrary.org/obo/NCIT_C204810 +http://purl.obolibrary.org/obo/NCIT_C204811 +http://purl.obolibrary.org/obo/NCIT_C204812 +http://purl.obolibrary.org/obo/NCIT_C204813 +http://purl.obolibrary.org/obo/NCIT_C204814 +http://purl.obolibrary.org/obo/NCIT_C204815 +http://purl.obolibrary.org/obo/NCIT_C204816 +http://purl.obolibrary.org/obo/NCIT_C204817 +http://purl.obolibrary.org/obo/NCIT_C204818 +http://purl.obolibrary.org/obo/NCIT_C204819 +http://purl.obolibrary.org/obo/NCIT_C204820 +http://purl.obolibrary.org/obo/NCIT_C204821 +http://purl.obolibrary.org/obo/NCIT_C204822 +http://purl.obolibrary.org/obo/NCIT_C204823 +http://purl.obolibrary.org/obo/NCIT_C204824 +http://purl.obolibrary.org/obo/NCIT_C204825 +http://purl.obolibrary.org/obo/NCIT_C204826 +http://purl.obolibrary.org/obo/NCIT_C204827 +http://purl.obolibrary.org/obo/NCIT_C204828 +http://purl.obolibrary.org/obo/NCIT_C204829 http://purl.obolibrary.org/obo/NCIT_C20483 +http://purl.obolibrary.org/obo/NCIT_C204830 +http://purl.obolibrary.org/obo/NCIT_C204831 +http://purl.obolibrary.org/obo/NCIT_C204832 +http://purl.obolibrary.org/obo/NCIT_C204833 +http://purl.obolibrary.org/obo/NCIT_C204834 +http://purl.obolibrary.org/obo/NCIT_C204835 +http://purl.obolibrary.org/obo/NCIT_C204836 +http://purl.obolibrary.org/obo/NCIT_C204837 +http://purl.obolibrary.org/obo/NCIT_C204838 +http://purl.obolibrary.org/obo/NCIT_C204839 http://purl.obolibrary.org/obo/NCIT_C20484 +http://purl.obolibrary.org/obo/NCIT_C204840 +http://purl.obolibrary.org/obo/NCIT_C204841 +http://purl.obolibrary.org/obo/NCIT_C204842 +http://purl.obolibrary.org/obo/NCIT_C204843 +http://purl.obolibrary.org/obo/NCIT_C204844 +http://purl.obolibrary.org/obo/NCIT_C204845 +http://purl.obolibrary.org/obo/NCIT_C204846 +http://purl.obolibrary.org/obo/NCIT_C204847 +http://purl.obolibrary.org/obo/NCIT_C204848 +http://purl.obolibrary.org/obo/NCIT_C204849 http://purl.obolibrary.org/obo/NCIT_C20485 +http://purl.obolibrary.org/obo/NCIT_C204850 +http://purl.obolibrary.org/obo/NCIT_C204851 +http://purl.obolibrary.org/obo/NCIT_C204852 +http://purl.obolibrary.org/obo/NCIT_C204853 +http://purl.obolibrary.org/obo/NCIT_C204854 +http://purl.obolibrary.org/obo/NCIT_C204855 +http://purl.obolibrary.org/obo/NCIT_C204856 +http://purl.obolibrary.org/obo/NCIT_C204857 +http://purl.obolibrary.org/obo/NCIT_C204858 +http://purl.obolibrary.org/obo/NCIT_C204859 http://purl.obolibrary.org/obo/NCIT_C20486 +http://purl.obolibrary.org/obo/NCIT_C204860 +http://purl.obolibrary.org/obo/NCIT_C204861 +http://purl.obolibrary.org/obo/NCIT_C204862 +http://purl.obolibrary.org/obo/NCIT_C204863 +http://purl.obolibrary.org/obo/NCIT_C204864 +http://purl.obolibrary.org/obo/NCIT_C204865 +http://purl.obolibrary.org/obo/NCIT_C204866 +http://purl.obolibrary.org/obo/NCIT_C204867 +http://purl.obolibrary.org/obo/NCIT_C204868 +http://purl.obolibrary.org/obo/NCIT_C204869 http://purl.obolibrary.org/obo/NCIT_C20487 +http://purl.obolibrary.org/obo/NCIT_C204870 +http://purl.obolibrary.org/obo/NCIT_C204871 +http://purl.obolibrary.org/obo/NCIT_C204872 +http://purl.obolibrary.org/obo/NCIT_C204873 +http://purl.obolibrary.org/obo/NCIT_C204874 +http://purl.obolibrary.org/obo/NCIT_C204875 +http://purl.obolibrary.org/obo/NCIT_C204876 +http://purl.obolibrary.org/obo/NCIT_C204877 +http://purl.obolibrary.org/obo/NCIT_C204878 +http://purl.obolibrary.org/obo/NCIT_C204879 http://purl.obolibrary.org/obo/NCIT_C20488 +http://purl.obolibrary.org/obo/NCIT_C204880 +http://purl.obolibrary.org/obo/NCIT_C204881 +http://purl.obolibrary.org/obo/NCIT_C204882 +http://purl.obolibrary.org/obo/NCIT_C204883 +http://purl.obolibrary.org/obo/NCIT_C204884 +http://purl.obolibrary.org/obo/NCIT_C204885 +http://purl.obolibrary.org/obo/NCIT_C204886 +http://purl.obolibrary.org/obo/NCIT_C204887 +http://purl.obolibrary.org/obo/NCIT_C204888 +http://purl.obolibrary.org/obo/NCIT_C204889 http://purl.obolibrary.org/obo/NCIT_C20489 +http://purl.obolibrary.org/obo/NCIT_C204890 +http://purl.obolibrary.org/obo/NCIT_C204891 +http://purl.obolibrary.org/obo/NCIT_C204892 +http://purl.obolibrary.org/obo/NCIT_C204893 +http://purl.obolibrary.org/obo/NCIT_C204894 +http://purl.obolibrary.org/obo/NCIT_C204895 +http://purl.obolibrary.org/obo/NCIT_C204896 +http://purl.obolibrary.org/obo/NCIT_C204897 +http://purl.obolibrary.org/obo/NCIT_C204898 +http://purl.obolibrary.org/obo/NCIT_C204899 http://purl.obolibrary.org/obo/NCIT_C2049 http://purl.obolibrary.org/obo/NCIT_C20490 +http://purl.obolibrary.org/obo/NCIT_C204900 +http://purl.obolibrary.org/obo/NCIT_C204901 +http://purl.obolibrary.org/obo/NCIT_C204902 +http://purl.obolibrary.org/obo/NCIT_C204903 +http://purl.obolibrary.org/obo/NCIT_C204904 +http://purl.obolibrary.org/obo/NCIT_C204905 +http://purl.obolibrary.org/obo/NCIT_C204906 +http://purl.obolibrary.org/obo/NCIT_C204907 +http://purl.obolibrary.org/obo/NCIT_C204908 +http://purl.obolibrary.org/obo/NCIT_C204909 http://purl.obolibrary.org/obo/NCIT_C20491 +http://purl.obolibrary.org/obo/NCIT_C204910 +http://purl.obolibrary.org/obo/NCIT_C204911 +http://purl.obolibrary.org/obo/NCIT_C204912 +http://purl.obolibrary.org/obo/NCIT_C204913 +http://purl.obolibrary.org/obo/NCIT_C204914 +http://purl.obolibrary.org/obo/NCIT_C204915 +http://purl.obolibrary.org/obo/NCIT_C204916 +http://purl.obolibrary.org/obo/NCIT_C204917 +http://purl.obolibrary.org/obo/NCIT_C204918 +http://purl.obolibrary.org/obo/NCIT_C204919 http://purl.obolibrary.org/obo/NCIT_C20492 +http://purl.obolibrary.org/obo/NCIT_C204920 +http://purl.obolibrary.org/obo/NCIT_C204921 +http://purl.obolibrary.org/obo/NCIT_C204922 +http://purl.obolibrary.org/obo/NCIT_C204923 +http://purl.obolibrary.org/obo/NCIT_C204924 +http://purl.obolibrary.org/obo/NCIT_C204925 +http://purl.obolibrary.org/obo/NCIT_C204926 +http://purl.obolibrary.org/obo/NCIT_C204927 +http://purl.obolibrary.org/obo/NCIT_C204928 +http://purl.obolibrary.org/obo/NCIT_C204929 http://purl.obolibrary.org/obo/NCIT_C20493 +http://purl.obolibrary.org/obo/NCIT_C204930 +http://purl.obolibrary.org/obo/NCIT_C204931 +http://purl.obolibrary.org/obo/NCIT_C204932 +http://purl.obolibrary.org/obo/NCIT_C204933 +http://purl.obolibrary.org/obo/NCIT_C204934 +http://purl.obolibrary.org/obo/NCIT_C204935 +http://purl.obolibrary.org/obo/NCIT_C204936 +http://purl.obolibrary.org/obo/NCIT_C204937 +http://purl.obolibrary.org/obo/NCIT_C204938 +http://purl.obolibrary.org/obo/NCIT_C204939 http://purl.obolibrary.org/obo/NCIT_C20494 +http://purl.obolibrary.org/obo/NCIT_C204940 +http://purl.obolibrary.org/obo/NCIT_C204941 +http://purl.obolibrary.org/obo/NCIT_C204942 +http://purl.obolibrary.org/obo/NCIT_C204943 +http://purl.obolibrary.org/obo/NCIT_C204944 +http://purl.obolibrary.org/obo/NCIT_C204945 +http://purl.obolibrary.org/obo/NCIT_C204946 +http://purl.obolibrary.org/obo/NCIT_C204947 +http://purl.obolibrary.org/obo/NCIT_C204948 +http://purl.obolibrary.org/obo/NCIT_C204949 http://purl.obolibrary.org/obo/NCIT_C20495 +http://purl.obolibrary.org/obo/NCIT_C204950 +http://purl.obolibrary.org/obo/NCIT_C204951 +http://purl.obolibrary.org/obo/NCIT_C204952 +http://purl.obolibrary.org/obo/NCIT_C204953 +http://purl.obolibrary.org/obo/NCIT_C204954 +http://purl.obolibrary.org/obo/NCIT_C204955 +http://purl.obolibrary.org/obo/NCIT_C204956 +http://purl.obolibrary.org/obo/NCIT_C204957 +http://purl.obolibrary.org/obo/NCIT_C204958 +http://purl.obolibrary.org/obo/NCIT_C204959 http://purl.obolibrary.org/obo/NCIT_C20496 +http://purl.obolibrary.org/obo/NCIT_C204960 +http://purl.obolibrary.org/obo/NCIT_C204961 +http://purl.obolibrary.org/obo/NCIT_C204962 +http://purl.obolibrary.org/obo/NCIT_C204963 +http://purl.obolibrary.org/obo/NCIT_C204964 +http://purl.obolibrary.org/obo/NCIT_C204965 +http://purl.obolibrary.org/obo/NCIT_C204966 +http://purl.obolibrary.org/obo/NCIT_C204967 +http://purl.obolibrary.org/obo/NCIT_C204968 +http://purl.obolibrary.org/obo/NCIT_C204969 http://purl.obolibrary.org/obo/NCIT_C20497 +http://purl.obolibrary.org/obo/NCIT_C204970 +http://purl.obolibrary.org/obo/NCIT_C204971 +http://purl.obolibrary.org/obo/NCIT_C204972 +http://purl.obolibrary.org/obo/NCIT_C204973 +http://purl.obolibrary.org/obo/NCIT_C204974 +http://purl.obolibrary.org/obo/NCIT_C204975 +http://purl.obolibrary.org/obo/NCIT_C204976 +http://purl.obolibrary.org/obo/NCIT_C204977 +http://purl.obolibrary.org/obo/NCIT_C204978 +http://purl.obolibrary.org/obo/NCIT_C204979 http://purl.obolibrary.org/obo/NCIT_C20498 +http://purl.obolibrary.org/obo/NCIT_C204980 +http://purl.obolibrary.org/obo/NCIT_C204981 +http://purl.obolibrary.org/obo/NCIT_C204982 +http://purl.obolibrary.org/obo/NCIT_C204983 +http://purl.obolibrary.org/obo/NCIT_C204984 +http://purl.obolibrary.org/obo/NCIT_C204985 +http://purl.obolibrary.org/obo/NCIT_C204986 +http://purl.obolibrary.org/obo/NCIT_C204987 +http://purl.obolibrary.org/obo/NCIT_C204988 +http://purl.obolibrary.org/obo/NCIT_C204989 http://purl.obolibrary.org/obo/NCIT_C20499 +http://purl.obolibrary.org/obo/NCIT_C204990 +http://purl.obolibrary.org/obo/NCIT_C204991 +http://purl.obolibrary.org/obo/NCIT_C204992 +http://purl.obolibrary.org/obo/NCIT_C204993 +http://purl.obolibrary.org/obo/NCIT_C204994 +http://purl.obolibrary.org/obo/NCIT_C204995 +http://purl.obolibrary.org/obo/NCIT_C204996 +http://purl.obolibrary.org/obo/NCIT_C204997 +http://purl.obolibrary.org/obo/NCIT_C204998 +http://purl.obolibrary.org/obo/NCIT_C204999 http://purl.obolibrary.org/obo/NCIT_C205 http://purl.obolibrary.org/obo/NCIT_C2050 http://purl.obolibrary.org/obo/NCIT_C20500 +http://purl.obolibrary.org/obo/NCIT_C205000 +http://purl.obolibrary.org/obo/NCIT_C205001 +http://purl.obolibrary.org/obo/NCIT_C205002 +http://purl.obolibrary.org/obo/NCIT_C205003 +http://purl.obolibrary.org/obo/NCIT_C205004 +http://purl.obolibrary.org/obo/NCIT_C205005 +http://purl.obolibrary.org/obo/NCIT_C205006 +http://purl.obolibrary.org/obo/NCIT_C205007 +http://purl.obolibrary.org/obo/NCIT_C205008 +http://purl.obolibrary.org/obo/NCIT_C205009 http://purl.obolibrary.org/obo/NCIT_C20501 +http://purl.obolibrary.org/obo/NCIT_C205010 +http://purl.obolibrary.org/obo/NCIT_C205011 +http://purl.obolibrary.org/obo/NCIT_C205012 +http://purl.obolibrary.org/obo/NCIT_C205013 +http://purl.obolibrary.org/obo/NCIT_C205014 +http://purl.obolibrary.org/obo/NCIT_C205015 +http://purl.obolibrary.org/obo/NCIT_C205016 +http://purl.obolibrary.org/obo/NCIT_C205017 +http://purl.obolibrary.org/obo/NCIT_C205018 +http://purl.obolibrary.org/obo/NCIT_C205019 http://purl.obolibrary.org/obo/NCIT_C20502 +http://purl.obolibrary.org/obo/NCIT_C205020 +http://purl.obolibrary.org/obo/NCIT_C205021 +http://purl.obolibrary.org/obo/NCIT_C205022 +http://purl.obolibrary.org/obo/NCIT_C205023 +http://purl.obolibrary.org/obo/NCIT_C205024 +http://purl.obolibrary.org/obo/NCIT_C205025 +http://purl.obolibrary.org/obo/NCIT_C205026 +http://purl.obolibrary.org/obo/NCIT_C205027 +http://purl.obolibrary.org/obo/NCIT_C205028 +http://purl.obolibrary.org/obo/NCIT_C205029 http://purl.obolibrary.org/obo/NCIT_C20503 +http://purl.obolibrary.org/obo/NCIT_C205030 +http://purl.obolibrary.org/obo/NCIT_C205031 +http://purl.obolibrary.org/obo/NCIT_C205032 +http://purl.obolibrary.org/obo/NCIT_C205033 +http://purl.obolibrary.org/obo/NCIT_C205034 +http://purl.obolibrary.org/obo/NCIT_C205035 +http://purl.obolibrary.org/obo/NCIT_C205036 +http://purl.obolibrary.org/obo/NCIT_C205037 +http://purl.obolibrary.org/obo/NCIT_C205038 +http://purl.obolibrary.org/obo/NCIT_C205039 http://purl.obolibrary.org/obo/NCIT_C20504 +http://purl.obolibrary.org/obo/NCIT_C205040 +http://purl.obolibrary.org/obo/NCIT_C205041 +http://purl.obolibrary.org/obo/NCIT_C205042 +http://purl.obolibrary.org/obo/NCIT_C205043 +http://purl.obolibrary.org/obo/NCIT_C205044 +http://purl.obolibrary.org/obo/NCIT_C205045 +http://purl.obolibrary.org/obo/NCIT_C205047 +http://purl.obolibrary.org/obo/NCIT_C205048 +http://purl.obolibrary.org/obo/NCIT_C205049 http://purl.obolibrary.org/obo/NCIT_C20505 +http://purl.obolibrary.org/obo/NCIT_C205050 +http://purl.obolibrary.org/obo/NCIT_C205051 +http://purl.obolibrary.org/obo/NCIT_C205052 +http://purl.obolibrary.org/obo/NCIT_C205053 +http://purl.obolibrary.org/obo/NCIT_C205054 +http://purl.obolibrary.org/obo/NCIT_C205055 +http://purl.obolibrary.org/obo/NCIT_C205056 +http://purl.obolibrary.org/obo/NCIT_C205057 +http://purl.obolibrary.org/obo/NCIT_C205058 +http://purl.obolibrary.org/obo/NCIT_C205059 http://purl.obolibrary.org/obo/NCIT_C20506 +http://purl.obolibrary.org/obo/NCIT_C205060 +http://purl.obolibrary.org/obo/NCIT_C205061 +http://purl.obolibrary.org/obo/NCIT_C205062 +http://purl.obolibrary.org/obo/NCIT_C205063 +http://purl.obolibrary.org/obo/NCIT_C205064 +http://purl.obolibrary.org/obo/NCIT_C205065 +http://purl.obolibrary.org/obo/NCIT_C205066 +http://purl.obolibrary.org/obo/NCIT_C205067 +http://purl.obolibrary.org/obo/NCIT_C205068 +http://purl.obolibrary.org/obo/NCIT_C205069 http://purl.obolibrary.org/obo/NCIT_C20507 +http://purl.obolibrary.org/obo/NCIT_C205070 +http://purl.obolibrary.org/obo/NCIT_C205071 +http://purl.obolibrary.org/obo/NCIT_C205072 +http://purl.obolibrary.org/obo/NCIT_C205073 +http://purl.obolibrary.org/obo/NCIT_C205074 +http://purl.obolibrary.org/obo/NCIT_C205075 +http://purl.obolibrary.org/obo/NCIT_C205076 +http://purl.obolibrary.org/obo/NCIT_C205077 +http://purl.obolibrary.org/obo/NCIT_C205078 +http://purl.obolibrary.org/obo/NCIT_C205079 http://purl.obolibrary.org/obo/NCIT_C20508 +http://purl.obolibrary.org/obo/NCIT_C205080 +http://purl.obolibrary.org/obo/NCIT_C205081 +http://purl.obolibrary.org/obo/NCIT_C205082 +http://purl.obolibrary.org/obo/NCIT_C205083 +http://purl.obolibrary.org/obo/NCIT_C205084 +http://purl.obolibrary.org/obo/NCIT_C205085 +http://purl.obolibrary.org/obo/NCIT_C205086 +http://purl.obolibrary.org/obo/NCIT_C205087 +http://purl.obolibrary.org/obo/NCIT_C205088 +http://purl.obolibrary.org/obo/NCIT_C205089 http://purl.obolibrary.org/obo/NCIT_C20509 +http://purl.obolibrary.org/obo/NCIT_C205090 +http://purl.obolibrary.org/obo/NCIT_C205091 +http://purl.obolibrary.org/obo/NCIT_C205092 +http://purl.obolibrary.org/obo/NCIT_C205093 +http://purl.obolibrary.org/obo/NCIT_C205094 +http://purl.obolibrary.org/obo/NCIT_C205095 +http://purl.obolibrary.org/obo/NCIT_C205096 +http://purl.obolibrary.org/obo/NCIT_C205097 +http://purl.obolibrary.org/obo/NCIT_C205098 +http://purl.obolibrary.org/obo/NCIT_C205099 http://purl.obolibrary.org/obo/NCIT_C2051 http://purl.obolibrary.org/obo/NCIT_C20510 +http://purl.obolibrary.org/obo/NCIT_C205100 +http://purl.obolibrary.org/obo/NCIT_C205101 +http://purl.obolibrary.org/obo/NCIT_C205102 +http://purl.obolibrary.org/obo/NCIT_C205103 +http://purl.obolibrary.org/obo/NCIT_C205104 +http://purl.obolibrary.org/obo/NCIT_C205105 +http://purl.obolibrary.org/obo/NCIT_C205106 +http://purl.obolibrary.org/obo/NCIT_C205107 +http://purl.obolibrary.org/obo/NCIT_C205108 +http://purl.obolibrary.org/obo/NCIT_C205109 http://purl.obolibrary.org/obo/NCIT_C20511 +http://purl.obolibrary.org/obo/NCIT_C205110 +http://purl.obolibrary.org/obo/NCIT_C205111 +http://purl.obolibrary.org/obo/NCIT_C205112 +http://purl.obolibrary.org/obo/NCIT_C205113 +http://purl.obolibrary.org/obo/NCIT_C205114 +http://purl.obolibrary.org/obo/NCIT_C205115 +http://purl.obolibrary.org/obo/NCIT_C205116 +http://purl.obolibrary.org/obo/NCIT_C205117 +http://purl.obolibrary.org/obo/NCIT_C205118 +http://purl.obolibrary.org/obo/NCIT_C205119 http://purl.obolibrary.org/obo/NCIT_C20512 +http://purl.obolibrary.org/obo/NCIT_C205120 +http://purl.obolibrary.org/obo/NCIT_C205121 +http://purl.obolibrary.org/obo/NCIT_C205122 +http://purl.obolibrary.org/obo/NCIT_C205123 +http://purl.obolibrary.org/obo/NCIT_C205124 +http://purl.obolibrary.org/obo/NCIT_C205125 +http://purl.obolibrary.org/obo/NCIT_C205126 +http://purl.obolibrary.org/obo/NCIT_C205127 +http://purl.obolibrary.org/obo/NCIT_C205128 +http://purl.obolibrary.org/obo/NCIT_C205129 http://purl.obolibrary.org/obo/NCIT_C20513 +http://purl.obolibrary.org/obo/NCIT_C205130 +http://purl.obolibrary.org/obo/NCIT_C205131 +http://purl.obolibrary.org/obo/NCIT_C205132 +http://purl.obolibrary.org/obo/NCIT_C205133 +http://purl.obolibrary.org/obo/NCIT_C205134 +http://purl.obolibrary.org/obo/NCIT_C205137 +http://purl.obolibrary.org/obo/NCIT_C205138 +http://purl.obolibrary.org/obo/NCIT_C205139 http://purl.obolibrary.org/obo/NCIT_C20514 +http://purl.obolibrary.org/obo/NCIT_C205140 +http://purl.obolibrary.org/obo/NCIT_C205141 +http://purl.obolibrary.org/obo/NCIT_C205142 +http://purl.obolibrary.org/obo/NCIT_C205143 +http://purl.obolibrary.org/obo/NCIT_C205144 +http://purl.obolibrary.org/obo/NCIT_C205145 +http://purl.obolibrary.org/obo/NCIT_C205146 +http://purl.obolibrary.org/obo/NCIT_C205147 +http://purl.obolibrary.org/obo/NCIT_C205148 +http://purl.obolibrary.org/obo/NCIT_C205149 http://purl.obolibrary.org/obo/NCIT_C20515 +http://purl.obolibrary.org/obo/NCIT_C205150 +http://purl.obolibrary.org/obo/NCIT_C205151 +http://purl.obolibrary.org/obo/NCIT_C205152 +http://purl.obolibrary.org/obo/NCIT_C205153 +http://purl.obolibrary.org/obo/NCIT_C205154 +http://purl.obolibrary.org/obo/NCIT_C205155 +http://purl.obolibrary.org/obo/NCIT_C205156 +http://purl.obolibrary.org/obo/NCIT_C205157 +http://purl.obolibrary.org/obo/NCIT_C205158 +http://purl.obolibrary.org/obo/NCIT_C205159 +http://purl.obolibrary.org/obo/NCIT_C205160 +http://purl.obolibrary.org/obo/NCIT_C205161 +http://purl.obolibrary.org/obo/NCIT_C205162 +http://purl.obolibrary.org/obo/NCIT_C205163 +http://purl.obolibrary.org/obo/NCIT_C205164 +http://purl.obolibrary.org/obo/NCIT_C205165 +http://purl.obolibrary.org/obo/NCIT_C205166 +http://purl.obolibrary.org/obo/NCIT_C205167 +http://purl.obolibrary.org/obo/NCIT_C205168 +http://purl.obolibrary.org/obo/NCIT_C205169 http://purl.obolibrary.org/obo/NCIT_C20517 +http://purl.obolibrary.org/obo/NCIT_C205170 +http://purl.obolibrary.org/obo/NCIT_C205171 +http://purl.obolibrary.org/obo/NCIT_C205172 +http://purl.obolibrary.org/obo/NCIT_C205173 +http://purl.obolibrary.org/obo/NCIT_C205174 +http://purl.obolibrary.org/obo/NCIT_C205175 +http://purl.obolibrary.org/obo/NCIT_C205176 +http://purl.obolibrary.org/obo/NCIT_C205177 +http://purl.obolibrary.org/obo/NCIT_C205178 +http://purl.obolibrary.org/obo/NCIT_C205179 http://purl.obolibrary.org/obo/NCIT_C20518 +http://purl.obolibrary.org/obo/NCIT_C205180 +http://purl.obolibrary.org/obo/NCIT_C205181 +http://purl.obolibrary.org/obo/NCIT_C205182 +http://purl.obolibrary.org/obo/NCIT_C205183 +http://purl.obolibrary.org/obo/NCIT_C205184 +http://purl.obolibrary.org/obo/NCIT_C205185 +http://purl.obolibrary.org/obo/NCIT_C205186 +http://purl.obolibrary.org/obo/NCIT_C205187 +http://purl.obolibrary.org/obo/NCIT_C205188 +http://purl.obolibrary.org/obo/NCIT_C205189 http://purl.obolibrary.org/obo/NCIT_C20519 +http://purl.obolibrary.org/obo/NCIT_C205190 +http://purl.obolibrary.org/obo/NCIT_C205191 +http://purl.obolibrary.org/obo/NCIT_C205192 +http://purl.obolibrary.org/obo/NCIT_C205193 +http://purl.obolibrary.org/obo/NCIT_C205194 +http://purl.obolibrary.org/obo/NCIT_C205195 +http://purl.obolibrary.org/obo/NCIT_C205196 +http://purl.obolibrary.org/obo/NCIT_C205197 +http://purl.obolibrary.org/obo/NCIT_C205198 +http://purl.obolibrary.org/obo/NCIT_C205199 http://purl.obolibrary.org/obo/NCIT_C2052 http://purl.obolibrary.org/obo/NCIT_C20520 +http://purl.obolibrary.org/obo/NCIT_C205200 +http://purl.obolibrary.org/obo/NCIT_C205201 +http://purl.obolibrary.org/obo/NCIT_C205202 +http://purl.obolibrary.org/obo/NCIT_C205203 +http://purl.obolibrary.org/obo/NCIT_C205204 +http://purl.obolibrary.org/obo/NCIT_C205205 +http://purl.obolibrary.org/obo/NCIT_C205206 +http://purl.obolibrary.org/obo/NCIT_C205207 +http://purl.obolibrary.org/obo/NCIT_C205208 +http://purl.obolibrary.org/obo/NCIT_C205209 http://purl.obolibrary.org/obo/NCIT_C20521 +http://purl.obolibrary.org/obo/NCIT_C205210 +http://purl.obolibrary.org/obo/NCIT_C205211 +http://purl.obolibrary.org/obo/NCIT_C205212 +http://purl.obolibrary.org/obo/NCIT_C205213 +http://purl.obolibrary.org/obo/NCIT_C205214 +http://purl.obolibrary.org/obo/NCIT_C205215 +http://purl.obolibrary.org/obo/NCIT_C205216 +http://purl.obolibrary.org/obo/NCIT_C205217 +http://purl.obolibrary.org/obo/NCIT_C205218 +http://purl.obolibrary.org/obo/NCIT_C205219 http://purl.obolibrary.org/obo/NCIT_C20522 +http://purl.obolibrary.org/obo/NCIT_C205220 +http://purl.obolibrary.org/obo/NCIT_C205221 +http://purl.obolibrary.org/obo/NCIT_C205222 +http://purl.obolibrary.org/obo/NCIT_C205223 +http://purl.obolibrary.org/obo/NCIT_C205224 +http://purl.obolibrary.org/obo/NCIT_C205225 +http://purl.obolibrary.org/obo/NCIT_C205226 +http://purl.obolibrary.org/obo/NCIT_C205227 +http://purl.obolibrary.org/obo/NCIT_C205228 +http://purl.obolibrary.org/obo/NCIT_C205229 +http://purl.obolibrary.org/obo/NCIT_C205230 +http://purl.obolibrary.org/obo/NCIT_C205231 +http://purl.obolibrary.org/obo/NCIT_C205232 +http://purl.obolibrary.org/obo/NCIT_C205233 +http://purl.obolibrary.org/obo/NCIT_C205234 +http://purl.obolibrary.org/obo/NCIT_C205235 +http://purl.obolibrary.org/obo/NCIT_C205236 +http://purl.obolibrary.org/obo/NCIT_C205237 +http://purl.obolibrary.org/obo/NCIT_C205238 +http://purl.obolibrary.org/obo/NCIT_C205239 http://purl.obolibrary.org/obo/NCIT_C20524 +http://purl.obolibrary.org/obo/NCIT_C205240 +http://purl.obolibrary.org/obo/NCIT_C205241 +http://purl.obolibrary.org/obo/NCIT_C205242 +http://purl.obolibrary.org/obo/NCIT_C205243 +http://purl.obolibrary.org/obo/NCIT_C205244 +http://purl.obolibrary.org/obo/NCIT_C205245 +http://purl.obolibrary.org/obo/NCIT_C205246 +http://purl.obolibrary.org/obo/NCIT_C205247 +http://purl.obolibrary.org/obo/NCIT_C205248 +http://purl.obolibrary.org/obo/NCIT_C205249 http://purl.obolibrary.org/obo/NCIT_C20525 +http://purl.obolibrary.org/obo/NCIT_C205250 +http://purl.obolibrary.org/obo/NCIT_C205251 +http://purl.obolibrary.org/obo/NCIT_C205252 +http://purl.obolibrary.org/obo/NCIT_C205253 +http://purl.obolibrary.org/obo/NCIT_C205254 +http://purl.obolibrary.org/obo/NCIT_C205255 +http://purl.obolibrary.org/obo/NCIT_C205256 +http://purl.obolibrary.org/obo/NCIT_C205257 +http://purl.obolibrary.org/obo/NCIT_C205258 +http://purl.obolibrary.org/obo/NCIT_C205259 http://purl.obolibrary.org/obo/NCIT_C20526 +http://purl.obolibrary.org/obo/NCIT_C205260 +http://purl.obolibrary.org/obo/NCIT_C205261 +http://purl.obolibrary.org/obo/NCIT_C205262 +http://purl.obolibrary.org/obo/NCIT_C205263 +http://purl.obolibrary.org/obo/NCIT_C205264 +http://purl.obolibrary.org/obo/NCIT_C205265 +http://purl.obolibrary.org/obo/NCIT_C205266 +http://purl.obolibrary.org/obo/NCIT_C205267 +http://purl.obolibrary.org/obo/NCIT_C205268 +http://purl.obolibrary.org/obo/NCIT_C205269 http://purl.obolibrary.org/obo/NCIT_C20527 +http://purl.obolibrary.org/obo/NCIT_C205270 +http://purl.obolibrary.org/obo/NCIT_C205271 +http://purl.obolibrary.org/obo/NCIT_C205272 +http://purl.obolibrary.org/obo/NCIT_C205273 +http://purl.obolibrary.org/obo/NCIT_C205274 +http://purl.obolibrary.org/obo/NCIT_C205275 +http://purl.obolibrary.org/obo/NCIT_C205276 +http://purl.obolibrary.org/obo/NCIT_C205277 +http://purl.obolibrary.org/obo/NCIT_C205278 +http://purl.obolibrary.org/obo/NCIT_C205279 http://purl.obolibrary.org/obo/NCIT_C20528 +http://purl.obolibrary.org/obo/NCIT_C205280 +http://purl.obolibrary.org/obo/NCIT_C205281 +http://purl.obolibrary.org/obo/NCIT_C205282 +http://purl.obolibrary.org/obo/NCIT_C205283 +http://purl.obolibrary.org/obo/NCIT_C205284 +http://purl.obolibrary.org/obo/NCIT_C205285 +http://purl.obolibrary.org/obo/NCIT_C205286 +http://purl.obolibrary.org/obo/NCIT_C205287 +http://purl.obolibrary.org/obo/NCIT_C205288 +http://purl.obolibrary.org/obo/NCIT_C205289 http://purl.obolibrary.org/obo/NCIT_C20529 +http://purl.obolibrary.org/obo/NCIT_C205290 +http://purl.obolibrary.org/obo/NCIT_C205291 +http://purl.obolibrary.org/obo/NCIT_C205292 +http://purl.obolibrary.org/obo/NCIT_C205293 +http://purl.obolibrary.org/obo/NCIT_C205294 +http://purl.obolibrary.org/obo/NCIT_C205295 +http://purl.obolibrary.org/obo/NCIT_C205296 +http://purl.obolibrary.org/obo/NCIT_C205297 +http://purl.obolibrary.org/obo/NCIT_C205298 +http://purl.obolibrary.org/obo/NCIT_C205299 http://purl.obolibrary.org/obo/NCIT_C2053 http://purl.obolibrary.org/obo/NCIT_C20530 +http://purl.obolibrary.org/obo/NCIT_C205300 +http://purl.obolibrary.org/obo/NCIT_C205301 +http://purl.obolibrary.org/obo/NCIT_C205302 +http://purl.obolibrary.org/obo/NCIT_C205303 +http://purl.obolibrary.org/obo/NCIT_C205304 +http://purl.obolibrary.org/obo/NCIT_C205305 +http://purl.obolibrary.org/obo/NCIT_C205307 +http://purl.obolibrary.org/obo/NCIT_C205308 +http://purl.obolibrary.org/obo/NCIT_C205309 http://purl.obolibrary.org/obo/NCIT_C20531 +http://purl.obolibrary.org/obo/NCIT_C205310 +http://purl.obolibrary.org/obo/NCIT_C205311 +http://purl.obolibrary.org/obo/NCIT_C205312 +http://purl.obolibrary.org/obo/NCIT_C205313 +http://purl.obolibrary.org/obo/NCIT_C205314 +http://purl.obolibrary.org/obo/NCIT_C205315 +http://purl.obolibrary.org/obo/NCIT_C205316 +http://purl.obolibrary.org/obo/NCIT_C205318 +http://purl.obolibrary.org/obo/NCIT_C205319 http://purl.obolibrary.org/obo/NCIT_C20532 +http://purl.obolibrary.org/obo/NCIT_C205320 +http://purl.obolibrary.org/obo/NCIT_C205321 +http://purl.obolibrary.org/obo/NCIT_C205322 +http://purl.obolibrary.org/obo/NCIT_C205323 +http://purl.obolibrary.org/obo/NCIT_C205324 +http://purl.obolibrary.org/obo/NCIT_C205325 +http://purl.obolibrary.org/obo/NCIT_C205326 +http://purl.obolibrary.org/obo/NCIT_C205327 +http://purl.obolibrary.org/obo/NCIT_C205328 http://purl.obolibrary.org/obo/NCIT_C20533 +http://purl.obolibrary.org/obo/NCIT_C205330 +http://purl.obolibrary.org/obo/NCIT_C205331 +http://purl.obolibrary.org/obo/NCIT_C205332 +http://purl.obolibrary.org/obo/NCIT_C205333 +http://purl.obolibrary.org/obo/NCIT_C205334 +http://purl.obolibrary.org/obo/NCIT_C205335 +http://purl.obolibrary.org/obo/NCIT_C205336 +http://purl.obolibrary.org/obo/NCIT_C205337 +http://purl.obolibrary.org/obo/NCIT_C205338 +http://purl.obolibrary.org/obo/NCIT_C205339 http://purl.obolibrary.org/obo/NCIT_C20534 +http://purl.obolibrary.org/obo/NCIT_C205340 +http://purl.obolibrary.org/obo/NCIT_C205341 +http://purl.obolibrary.org/obo/NCIT_C205342 +http://purl.obolibrary.org/obo/NCIT_C205343 +http://purl.obolibrary.org/obo/NCIT_C205344 +http://purl.obolibrary.org/obo/NCIT_C205345 +http://purl.obolibrary.org/obo/NCIT_C205346 +http://purl.obolibrary.org/obo/NCIT_C205347 +http://purl.obolibrary.org/obo/NCIT_C205348 +http://purl.obolibrary.org/obo/NCIT_C205349 http://purl.obolibrary.org/obo/NCIT_C20535 +http://purl.obolibrary.org/obo/NCIT_C205350 +http://purl.obolibrary.org/obo/NCIT_C205351 +http://purl.obolibrary.org/obo/NCIT_C205352 +http://purl.obolibrary.org/obo/NCIT_C205353 +http://purl.obolibrary.org/obo/NCIT_C205354 +http://purl.obolibrary.org/obo/NCIT_C205355 +http://purl.obolibrary.org/obo/NCIT_C205356 +http://purl.obolibrary.org/obo/NCIT_C205357 +http://purl.obolibrary.org/obo/NCIT_C205358 +http://purl.obolibrary.org/obo/NCIT_C205359 http://purl.obolibrary.org/obo/NCIT_C20536 +http://purl.obolibrary.org/obo/NCIT_C205360 +http://purl.obolibrary.org/obo/NCIT_C205361 +http://purl.obolibrary.org/obo/NCIT_C205362 +http://purl.obolibrary.org/obo/NCIT_C205363 +http://purl.obolibrary.org/obo/NCIT_C205364 +http://purl.obolibrary.org/obo/NCIT_C205365 +http://purl.obolibrary.org/obo/NCIT_C205366 +http://purl.obolibrary.org/obo/NCIT_C205367 +http://purl.obolibrary.org/obo/NCIT_C205368 +http://purl.obolibrary.org/obo/NCIT_C205369 http://purl.obolibrary.org/obo/NCIT_C20537 +http://purl.obolibrary.org/obo/NCIT_C205371 +http://purl.obolibrary.org/obo/NCIT_C205372 +http://purl.obolibrary.org/obo/NCIT_C205373 +http://purl.obolibrary.org/obo/NCIT_C205374 +http://purl.obolibrary.org/obo/NCIT_C205375 +http://purl.obolibrary.org/obo/NCIT_C205376 +http://purl.obolibrary.org/obo/NCIT_C205377 +http://purl.obolibrary.org/obo/NCIT_C205378 +http://purl.obolibrary.org/obo/NCIT_C205379 http://purl.obolibrary.org/obo/NCIT_C20538 +http://purl.obolibrary.org/obo/NCIT_C205380 +http://purl.obolibrary.org/obo/NCIT_C205381 +http://purl.obolibrary.org/obo/NCIT_C205382 +http://purl.obolibrary.org/obo/NCIT_C205383 +http://purl.obolibrary.org/obo/NCIT_C205384 +http://purl.obolibrary.org/obo/NCIT_C205385 +http://purl.obolibrary.org/obo/NCIT_C205386 +http://purl.obolibrary.org/obo/NCIT_C205387 +http://purl.obolibrary.org/obo/NCIT_C205388 +http://purl.obolibrary.org/obo/NCIT_C205389 http://purl.obolibrary.org/obo/NCIT_C20539 +http://purl.obolibrary.org/obo/NCIT_C205390 +http://purl.obolibrary.org/obo/NCIT_C205391 +http://purl.obolibrary.org/obo/NCIT_C205392 +http://purl.obolibrary.org/obo/NCIT_C205393 +http://purl.obolibrary.org/obo/NCIT_C205394 +http://purl.obolibrary.org/obo/NCIT_C205395 +http://purl.obolibrary.org/obo/NCIT_C205396 +http://purl.obolibrary.org/obo/NCIT_C205397 +http://purl.obolibrary.org/obo/NCIT_C205398 +http://purl.obolibrary.org/obo/NCIT_C205399 http://purl.obolibrary.org/obo/NCIT_C2054 http://purl.obolibrary.org/obo/NCIT_C20540 +http://purl.obolibrary.org/obo/NCIT_C205400 +http://purl.obolibrary.org/obo/NCIT_C205401 +http://purl.obolibrary.org/obo/NCIT_C205402 +http://purl.obolibrary.org/obo/NCIT_C205403 +http://purl.obolibrary.org/obo/NCIT_C205404 +http://purl.obolibrary.org/obo/NCIT_C205405 +http://purl.obolibrary.org/obo/NCIT_C205406 +http://purl.obolibrary.org/obo/NCIT_C205407 +http://purl.obolibrary.org/obo/NCIT_C205408 http://purl.obolibrary.org/obo/NCIT_C20541 +http://purl.obolibrary.org/obo/NCIT_C205410 +http://purl.obolibrary.org/obo/NCIT_C205411 +http://purl.obolibrary.org/obo/NCIT_C205412 +http://purl.obolibrary.org/obo/NCIT_C205413 +http://purl.obolibrary.org/obo/NCIT_C205414 +http://purl.obolibrary.org/obo/NCIT_C205415 +http://purl.obolibrary.org/obo/NCIT_C205416 +http://purl.obolibrary.org/obo/NCIT_C205417 +http://purl.obolibrary.org/obo/NCIT_C205418 +http://purl.obolibrary.org/obo/NCIT_C205419 http://purl.obolibrary.org/obo/NCIT_C20542 +http://purl.obolibrary.org/obo/NCIT_C205420 +http://purl.obolibrary.org/obo/NCIT_C205421 +http://purl.obolibrary.org/obo/NCIT_C205422 +http://purl.obolibrary.org/obo/NCIT_C205423 +http://purl.obolibrary.org/obo/NCIT_C205424 +http://purl.obolibrary.org/obo/NCIT_C205425 +http://purl.obolibrary.org/obo/NCIT_C205426 +http://purl.obolibrary.org/obo/NCIT_C205427 +http://purl.obolibrary.org/obo/NCIT_C205428 +http://purl.obolibrary.org/obo/NCIT_C205429 http://purl.obolibrary.org/obo/NCIT_C20543 +http://purl.obolibrary.org/obo/NCIT_C205430 +http://purl.obolibrary.org/obo/NCIT_C205431 +http://purl.obolibrary.org/obo/NCIT_C205432 +http://purl.obolibrary.org/obo/NCIT_C205433 +http://purl.obolibrary.org/obo/NCIT_C205434 +http://purl.obolibrary.org/obo/NCIT_C205435 +http://purl.obolibrary.org/obo/NCIT_C205436 +http://purl.obolibrary.org/obo/NCIT_C205437 +http://purl.obolibrary.org/obo/NCIT_C205438 +http://purl.obolibrary.org/obo/NCIT_C205439 http://purl.obolibrary.org/obo/NCIT_C20544 +http://purl.obolibrary.org/obo/NCIT_C205440 +http://purl.obolibrary.org/obo/NCIT_C205441 +http://purl.obolibrary.org/obo/NCIT_C205442 +http://purl.obolibrary.org/obo/NCIT_C205443 +http://purl.obolibrary.org/obo/NCIT_C205444 +http://purl.obolibrary.org/obo/NCIT_C205445 +http://purl.obolibrary.org/obo/NCIT_C205446 +http://purl.obolibrary.org/obo/NCIT_C205447 +http://purl.obolibrary.org/obo/NCIT_C205448 +http://purl.obolibrary.org/obo/NCIT_C205449 http://purl.obolibrary.org/obo/NCIT_C20545 +http://purl.obolibrary.org/obo/NCIT_C205450 +http://purl.obolibrary.org/obo/NCIT_C205451 +http://purl.obolibrary.org/obo/NCIT_C205452 +http://purl.obolibrary.org/obo/NCIT_C205453 +http://purl.obolibrary.org/obo/NCIT_C205454 +http://purl.obolibrary.org/obo/NCIT_C205455 +http://purl.obolibrary.org/obo/NCIT_C205456 +http://purl.obolibrary.org/obo/NCIT_C205457 +http://purl.obolibrary.org/obo/NCIT_C205458 +http://purl.obolibrary.org/obo/NCIT_C205459 +http://purl.obolibrary.org/obo/NCIT_C205460 +http://purl.obolibrary.org/obo/NCIT_C205461 +http://purl.obolibrary.org/obo/NCIT_C205462 +http://purl.obolibrary.org/obo/NCIT_C205463 +http://purl.obolibrary.org/obo/NCIT_C205464 +http://purl.obolibrary.org/obo/NCIT_C205465 +http://purl.obolibrary.org/obo/NCIT_C205466 +http://purl.obolibrary.org/obo/NCIT_C205467 +http://purl.obolibrary.org/obo/NCIT_C205468 +http://purl.obolibrary.org/obo/NCIT_C205469 http://purl.obolibrary.org/obo/NCIT_C20547 +http://purl.obolibrary.org/obo/NCIT_C205470 +http://purl.obolibrary.org/obo/NCIT_C205471 +http://purl.obolibrary.org/obo/NCIT_C205472 +http://purl.obolibrary.org/obo/NCIT_C205473 +http://purl.obolibrary.org/obo/NCIT_C205474 +http://purl.obolibrary.org/obo/NCIT_C205475 +http://purl.obolibrary.org/obo/NCIT_C205476 +http://purl.obolibrary.org/obo/NCIT_C205477 +http://purl.obolibrary.org/obo/NCIT_C205478 +http://purl.obolibrary.org/obo/NCIT_C205479 http://purl.obolibrary.org/obo/NCIT_C20548 +http://purl.obolibrary.org/obo/NCIT_C205480 +http://purl.obolibrary.org/obo/NCIT_C205481 +http://purl.obolibrary.org/obo/NCIT_C205482 +http://purl.obolibrary.org/obo/NCIT_C205483 +http://purl.obolibrary.org/obo/NCIT_C205484 +http://purl.obolibrary.org/obo/NCIT_C205485 +http://purl.obolibrary.org/obo/NCIT_C205486 +http://purl.obolibrary.org/obo/NCIT_C205487 +http://purl.obolibrary.org/obo/NCIT_C205488 +http://purl.obolibrary.org/obo/NCIT_C205489 http://purl.obolibrary.org/obo/NCIT_C20549 +http://purl.obolibrary.org/obo/NCIT_C205490 +http://purl.obolibrary.org/obo/NCIT_C205491 +http://purl.obolibrary.org/obo/NCIT_C205492 +http://purl.obolibrary.org/obo/NCIT_C205493 +http://purl.obolibrary.org/obo/NCIT_C205494 +http://purl.obolibrary.org/obo/NCIT_C205495 +http://purl.obolibrary.org/obo/NCIT_C205496 +http://purl.obolibrary.org/obo/NCIT_C205497 +http://purl.obolibrary.org/obo/NCIT_C205498 +http://purl.obolibrary.org/obo/NCIT_C205499 http://purl.obolibrary.org/obo/NCIT_C2055 http://purl.obolibrary.org/obo/NCIT_C20550 +http://purl.obolibrary.org/obo/NCIT_C205500 +http://purl.obolibrary.org/obo/NCIT_C205501 +http://purl.obolibrary.org/obo/NCIT_C205502 +http://purl.obolibrary.org/obo/NCIT_C205503 +http://purl.obolibrary.org/obo/NCIT_C205504 +http://purl.obolibrary.org/obo/NCIT_C205505 +http://purl.obolibrary.org/obo/NCIT_C205506 +http://purl.obolibrary.org/obo/NCIT_C205507 +http://purl.obolibrary.org/obo/NCIT_C205508 +http://purl.obolibrary.org/obo/NCIT_C205509 http://purl.obolibrary.org/obo/NCIT_C20551 +http://purl.obolibrary.org/obo/NCIT_C205510 +http://purl.obolibrary.org/obo/NCIT_C205511 +http://purl.obolibrary.org/obo/NCIT_C205512 +http://purl.obolibrary.org/obo/NCIT_C205513 +http://purl.obolibrary.org/obo/NCIT_C205514 +http://purl.obolibrary.org/obo/NCIT_C205515 +http://purl.obolibrary.org/obo/NCIT_C205516 +http://purl.obolibrary.org/obo/NCIT_C205517 +http://purl.obolibrary.org/obo/NCIT_C205518 +http://purl.obolibrary.org/obo/NCIT_C205519 http://purl.obolibrary.org/obo/NCIT_C20552 +http://purl.obolibrary.org/obo/NCIT_C205520 +http://purl.obolibrary.org/obo/NCIT_C205521 +http://purl.obolibrary.org/obo/NCIT_C205522 +http://purl.obolibrary.org/obo/NCIT_C205523 +http://purl.obolibrary.org/obo/NCIT_C205524 +http://purl.obolibrary.org/obo/NCIT_C205525 +http://purl.obolibrary.org/obo/NCIT_C205526 +http://purl.obolibrary.org/obo/NCIT_C205527 +http://purl.obolibrary.org/obo/NCIT_C205528 +http://purl.obolibrary.org/obo/NCIT_C205529 http://purl.obolibrary.org/obo/NCIT_C20553 +http://purl.obolibrary.org/obo/NCIT_C205530 +http://purl.obolibrary.org/obo/NCIT_C205531 +http://purl.obolibrary.org/obo/NCIT_C205532 +http://purl.obolibrary.org/obo/NCIT_C205533 +http://purl.obolibrary.org/obo/NCIT_C205534 +http://purl.obolibrary.org/obo/NCIT_C205535 +http://purl.obolibrary.org/obo/NCIT_C205536 +http://purl.obolibrary.org/obo/NCIT_C205537 +http://purl.obolibrary.org/obo/NCIT_C205538 +http://purl.obolibrary.org/obo/NCIT_C205539 http://purl.obolibrary.org/obo/NCIT_C20554 +http://purl.obolibrary.org/obo/NCIT_C205540 +http://purl.obolibrary.org/obo/NCIT_C205541 +http://purl.obolibrary.org/obo/NCIT_C205542 +http://purl.obolibrary.org/obo/NCIT_C205543 +http://purl.obolibrary.org/obo/NCIT_C205544 +http://purl.obolibrary.org/obo/NCIT_C205545 +http://purl.obolibrary.org/obo/NCIT_C205546 +http://purl.obolibrary.org/obo/NCIT_C205547 +http://purl.obolibrary.org/obo/NCIT_C205548 +http://purl.obolibrary.org/obo/NCIT_C205549 http://purl.obolibrary.org/obo/NCIT_C20555 +http://purl.obolibrary.org/obo/NCIT_C205550 +http://purl.obolibrary.org/obo/NCIT_C205551 +http://purl.obolibrary.org/obo/NCIT_C205552 +http://purl.obolibrary.org/obo/NCIT_C205553 +http://purl.obolibrary.org/obo/NCIT_C205554 +http://purl.obolibrary.org/obo/NCIT_C205555 +http://purl.obolibrary.org/obo/NCIT_C205556 +http://purl.obolibrary.org/obo/NCIT_C205557 +http://purl.obolibrary.org/obo/NCIT_C205558 +http://purl.obolibrary.org/obo/NCIT_C205559 http://purl.obolibrary.org/obo/NCIT_C20556 +http://purl.obolibrary.org/obo/NCIT_C205560 +http://purl.obolibrary.org/obo/NCIT_C205561 +http://purl.obolibrary.org/obo/NCIT_C205562 +http://purl.obolibrary.org/obo/NCIT_C205563 +http://purl.obolibrary.org/obo/NCIT_C205564 +http://purl.obolibrary.org/obo/NCIT_C205565 +http://purl.obolibrary.org/obo/NCIT_C205566 +http://purl.obolibrary.org/obo/NCIT_C205567 +http://purl.obolibrary.org/obo/NCIT_C205568 +http://purl.obolibrary.org/obo/NCIT_C205569 http://purl.obolibrary.org/obo/NCIT_C20557 +http://purl.obolibrary.org/obo/NCIT_C205570 +http://purl.obolibrary.org/obo/NCIT_C205571 +http://purl.obolibrary.org/obo/NCIT_C205572 +http://purl.obolibrary.org/obo/NCIT_C205573 +http://purl.obolibrary.org/obo/NCIT_C205574 +http://purl.obolibrary.org/obo/NCIT_C205575 +http://purl.obolibrary.org/obo/NCIT_C205576 +http://purl.obolibrary.org/obo/NCIT_C205577 +http://purl.obolibrary.org/obo/NCIT_C205578 +http://purl.obolibrary.org/obo/NCIT_C205579 http://purl.obolibrary.org/obo/NCIT_C20558 +http://purl.obolibrary.org/obo/NCIT_C205580 +http://purl.obolibrary.org/obo/NCIT_C205581 +http://purl.obolibrary.org/obo/NCIT_C205582 +http://purl.obolibrary.org/obo/NCIT_C205583 +http://purl.obolibrary.org/obo/NCIT_C205584 +http://purl.obolibrary.org/obo/NCIT_C205585 +http://purl.obolibrary.org/obo/NCIT_C205586 +http://purl.obolibrary.org/obo/NCIT_C205587 +http://purl.obolibrary.org/obo/NCIT_C205588 +http://purl.obolibrary.org/obo/NCIT_C205589 http://purl.obolibrary.org/obo/NCIT_C20559 +http://purl.obolibrary.org/obo/NCIT_C205590 +http://purl.obolibrary.org/obo/NCIT_C205591 +http://purl.obolibrary.org/obo/NCIT_C205592 +http://purl.obolibrary.org/obo/NCIT_C205593 +http://purl.obolibrary.org/obo/NCIT_C205594 +http://purl.obolibrary.org/obo/NCIT_C205595 +http://purl.obolibrary.org/obo/NCIT_C205596 +http://purl.obolibrary.org/obo/NCIT_C205597 +http://purl.obolibrary.org/obo/NCIT_C205598 +http://purl.obolibrary.org/obo/NCIT_C205599 http://purl.obolibrary.org/obo/NCIT_C2056 http://purl.obolibrary.org/obo/NCIT_C20560 +http://purl.obolibrary.org/obo/NCIT_C205600 +http://purl.obolibrary.org/obo/NCIT_C205601 +http://purl.obolibrary.org/obo/NCIT_C205602 +http://purl.obolibrary.org/obo/NCIT_C205603 +http://purl.obolibrary.org/obo/NCIT_C205605 +http://purl.obolibrary.org/obo/NCIT_C205606 http://purl.obolibrary.org/obo/NCIT_C20561 http://purl.obolibrary.org/obo/NCIT_C20562 http://purl.obolibrary.org/obo/NCIT_C20563 @@ -111165,7 +115091,6 @@ http://purl.obolibrary.org/obo/NCIT_C27889 http://purl.obolibrary.org/obo/NCIT_C2789 http://purl.obolibrary.org/obo/NCIT_C27890 http://purl.obolibrary.org/obo/NCIT_C27891 -http://purl.obolibrary.org/obo/NCIT_C27892 http://purl.obolibrary.org/obo/NCIT_C27893 http://purl.obolibrary.org/obo/NCIT_C27894 http://purl.obolibrary.org/obo/NCIT_C27896 @@ -112325,7 +116250,6 @@ http://purl.obolibrary.org/obo/NCIT_C29146 http://purl.obolibrary.org/obo/NCIT_C29147 http://purl.obolibrary.org/obo/NCIT_C29148 http://purl.obolibrary.org/obo/NCIT_C29149 -http://purl.obolibrary.org/obo/NCIT_C2915 http://purl.obolibrary.org/obo/NCIT_C29150 http://purl.obolibrary.org/obo/NCIT_C29151 http://purl.obolibrary.org/obo/NCIT_C29152 @@ -117067,7 +120991,6 @@ http://purl.obolibrary.org/obo/NCIT_C35435 http://purl.obolibrary.org/obo/NCIT_C35436 http://purl.obolibrary.org/obo/NCIT_C35437 http://purl.obolibrary.org/obo/NCIT_C35438 -http://purl.obolibrary.org/obo/NCIT_C35439 http://purl.obolibrary.org/obo/NCIT_C3544 http://purl.obolibrary.org/obo/NCIT_C35440 http://purl.obolibrary.org/obo/NCIT_C35441 @@ -117696,7 +121619,6 @@ http://purl.obolibrary.org/obo/NCIT_C36030 http://purl.obolibrary.org/obo/NCIT_C36031 http://purl.obolibrary.org/obo/NCIT_C36032 http://purl.obolibrary.org/obo/NCIT_C36033 -http://purl.obolibrary.org/obo/NCIT_C36034 http://purl.obolibrary.org/obo/NCIT_C36035 http://purl.obolibrary.org/obo/NCIT_C36036 http://purl.obolibrary.org/obo/NCIT_C36037 @@ -121459,7 +125381,6 @@ http://purl.obolibrary.org/obo/NCIT_C39626 http://purl.obolibrary.org/obo/NCIT_C39627 http://purl.obolibrary.org/obo/NCIT_C39628 http://purl.obolibrary.org/obo/NCIT_C39629 -http://purl.obolibrary.org/obo/NCIT_C3963 http://purl.obolibrary.org/obo/NCIT_C39630 http://purl.obolibrary.org/obo/NCIT_C39631 http://purl.obolibrary.org/obo/NCIT_C39632 @@ -123351,7 +127272,6 @@ http://purl.obolibrary.org/obo/NCIT_C41726 http://purl.obolibrary.org/obo/NCIT_C41727 http://purl.obolibrary.org/obo/NCIT_C41728 http://purl.obolibrary.org/obo/NCIT_C41729 -http://purl.obolibrary.org/obo/NCIT_C4173 http://purl.obolibrary.org/obo/NCIT_C41730 http://purl.obolibrary.org/obo/NCIT_C41731 http://purl.obolibrary.org/obo/NCIT_C41732 @@ -124756,7 +128676,6 @@ http://purl.obolibrary.org/obo/NCIT_C43245 http://purl.obolibrary.org/obo/NCIT_C43246 http://purl.obolibrary.org/obo/NCIT_C43247 http://purl.obolibrary.org/obo/NCIT_C43248 -http://purl.obolibrary.org/obo/NCIT_C43249 http://purl.obolibrary.org/obo/NCIT_C4325 http://purl.obolibrary.org/obo/NCIT_C43251 http://purl.obolibrary.org/obo/NCIT_C43253 @@ -130427,7 +134346,6 @@ http://purl.obolibrary.org/obo/NCIT_C50033 http://purl.obolibrary.org/obo/NCIT_C50034 http://purl.obolibrary.org/obo/NCIT_C50035 http://purl.obolibrary.org/obo/NCIT_C50036 -http://purl.obolibrary.org/obo/NCIT_C50037 http://purl.obolibrary.org/obo/NCIT_C50038 http://purl.obolibrary.org/obo/NCIT_C50039 http://purl.obolibrary.org/obo/NCIT_C5004 @@ -132494,7 +136412,6 @@ http://purl.obolibrary.org/obo/NCIT_C51979 http://purl.obolibrary.org/obo/NCIT_C5198 http://purl.obolibrary.org/obo/NCIT_C51980 http://purl.obolibrary.org/obo/NCIT_C51981 -http://purl.obolibrary.org/obo/NCIT_C51982 http://purl.obolibrary.org/obo/NCIT_C51985 http://purl.obolibrary.org/obo/NCIT_C51986 http://purl.obolibrary.org/obo/NCIT_C51987 @@ -134773,7 +138690,6 @@ http://purl.obolibrary.org/obo/NCIT_C54142 http://purl.obolibrary.org/obo/NCIT_C54144 http://purl.obolibrary.org/obo/NCIT_C54145 http://purl.obolibrary.org/obo/NCIT_C54146 -http://purl.obolibrary.org/obo/NCIT_C54147 http://purl.obolibrary.org/obo/NCIT_C54148 http://purl.obolibrary.org/obo/NCIT_C54149 http://purl.obolibrary.org/obo/NCIT_C5415 @@ -135658,7 +139574,6 @@ http://purl.obolibrary.org/obo/NCIT_C55036 http://purl.obolibrary.org/obo/NCIT_C55037 http://purl.obolibrary.org/obo/NCIT_C55038 http://purl.obolibrary.org/obo/NCIT_C55039 -http://purl.obolibrary.org/obo/NCIT_C5504 http://purl.obolibrary.org/obo/NCIT_C55040 http://purl.obolibrary.org/obo/NCIT_C55041 http://purl.obolibrary.org/obo/NCIT_C55042 @@ -135669,7 +139584,6 @@ http://purl.obolibrary.org/obo/NCIT_C55046 http://purl.obolibrary.org/obo/NCIT_C55047 http://purl.obolibrary.org/obo/NCIT_C55048 http://purl.obolibrary.org/obo/NCIT_C55049 -http://purl.obolibrary.org/obo/NCIT_C5505 http://purl.obolibrary.org/obo/NCIT_C55050 http://purl.obolibrary.org/obo/NCIT_C55051 http://purl.obolibrary.org/obo/NCIT_C55052 @@ -142614,10 +146528,8 @@ http://purl.obolibrary.org/obo/NCIT_C61395 http://purl.obolibrary.org/obo/NCIT_C61396 http://purl.obolibrary.org/obo/NCIT_C61397 http://purl.obolibrary.org/obo/NCIT_C61398 -http://purl.obolibrary.org/obo/NCIT_C61399 http://purl.obolibrary.org/obo/NCIT_C614 http://purl.obolibrary.org/obo/NCIT_C6140 -http://purl.obolibrary.org/obo/NCIT_C61400 http://purl.obolibrary.org/obo/NCIT_C61401 http://purl.obolibrary.org/obo/NCIT_C61402 http://purl.obolibrary.org/obo/NCIT_C61403 @@ -144767,7 +148679,6 @@ http://purl.obolibrary.org/obo/NCIT_C63465 http://purl.obolibrary.org/obo/NCIT_C63466 http://purl.obolibrary.org/obo/NCIT_C63467 http://purl.obolibrary.org/obo/NCIT_C63468 -http://purl.obolibrary.org/obo/NCIT_C63469 http://purl.obolibrary.org/obo/NCIT_C6347 http://purl.obolibrary.org/obo/NCIT_C63470 http://purl.obolibrary.org/obo/NCIT_C63471 @@ -145521,7 +149432,6 @@ http://purl.obolibrary.org/obo/NCIT_C64187 http://purl.obolibrary.org/obo/NCIT_C64188 http://purl.obolibrary.org/obo/NCIT_C64189 http://purl.obolibrary.org/obo/NCIT_C6419 -http://purl.obolibrary.org/obo/NCIT_C64190 http://purl.obolibrary.org/obo/NCIT_C64191 http://purl.obolibrary.org/obo/NCIT_C64192 http://purl.obolibrary.org/obo/NCIT_C64193 @@ -145650,7 +149560,6 @@ http://purl.obolibrary.org/obo/NCIT_C64306 http://purl.obolibrary.org/obo/NCIT_C64307 http://purl.obolibrary.org/obo/NCIT_C64308 http://purl.obolibrary.org/obo/NCIT_C64309 -http://purl.obolibrary.org/obo/NCIT_C6431 http://purl.obolibrary.org/obo/NCIT_C64310 http://purl.obolibrary.org/obo/NCIT_C64311 http://purl.obolibrary.org/obo/NCIT_C64312 @@ -148435,7 +152344,6 @@ http://purl.obolibrary.org/obo/NCIT_C669 http://purl.obolibrary.org/obo/NCIT_C6690 http://purl.obolibrary.org/obo/NCIT_C66900 http://purl.obolibrary.org/obo/NCIT_C66902 -http://purl.obolibrary.org/obo/NCIT_C66903 http://purl.obolibrary.org/obo/NCIT_C66904 http://purl.obolibrary.org/obo/NCIT_C66905 http://purl.obolibrary.org/obo/NCIT_C66907 @@ -148762,7 +152670,6 @@ http://purl.obolibrary.org/obo/NCIT_C67226 http://purl.obolibrary.org/obo/NCIT_C67227 http://purl.obolibrary.org/obo/NCIT_C67229 http://purl.obolibrary.org/obo/NCIT_C6723 -http://purl.obolibrary.org/obo/NCIT_C67231 http://purl.obolibrary.org/obo/NCIT_C67232 http://purl.obolibrary.org/obo/NCIT_C67233 http://purl.obolibrary.org/obo/NCIT_C67234 @@ -150469,7 +154376,6 @@ http://purl.obolibrary.org/obo/NCIT_C70446 http://purl.obolibrary.org/obo/NCIT_C70447 http://purl.obolibrary.org/obo/NCIT_C70448 http://purl.obolibrary.org/obo/NCIT_C70449 -http://purl.obolibrary.org/obo/NCIT_C7045 http://purl.obolibrary.org/obo/NCIT_C70450 http://purl.obolibrary.org/obo/NCIT_C70451 http://purl.obolibrary.org/obo/NCIT_C70452 @@ -157638,7 +161544,6 @@ http://purl.obolibrary.org/obo/NCIT_C77182 http://purl.obolibrary.org/obo/NCIT_C77183 http://purl.obolibrary.org/obo/NCIT_C77184 http://purl.obolibrary.org/obo/NCIT_C77185 -http://purl.obolibrary.org/obo/NCIT_C77186 http://purl.obolibrary.org/obo/NCIT_C77187 http://purl.obolibrary.org/obo/NCIT_C77188 http://purl.obolibrary.org/obo/NCIT_C77189 @@ -165857,7 +169762,6 @@ http://purl.obolibrary.org/obo/NCIT_C85116 http://purl.obolibrary.org/obo/NCIT_C85117 http://purl.obolibrary.org/obo/NCIT_C85118 http://purl.obolibrary.org/obo/NCIT_C85119 -http://purl.obolibrary.org/obo/NCIT_C8512 http://purl.obolibrary.org/obo/NCIT_C85120 http://purl.obolibrary.org/obo/NCIT_C85121 http://purl.obolibrary.org/obo/NCIT_C85122 @@ -173477,7 +177381,6 @@ http://purl.obolibrary.org/obo/NCIT_C92201 http://purl.obolibrary.org/obo/NCIT_C92202 http://purl.obolibrary.org/obo/NCIT_C92203 http://purl.obolibrary.org/obo/NCIT_C92205 -http://purl.obolibrary.org/obo/NCIT_C92206 http://purl.obolibrary.org/obo/NCIT_C92207 http://purl.obolibrary.org/obo/NCIT_C92208 http://purl.obolibrary.org/obo/NCIT_C92209 @@ -175608,7 +179511,6 @@ http://purl.obolibrary.org/obo/NCIT_C94156 http://purl.obolibrary.org/obo/NCIT_C94157 http://purl.obolibrary.org/obo/NCIT_C94158 http://purl.obolibrary.org/obo/NCIT_C94159 -http://purl.obolibrary.org/obo/NCIT_C9416 http://purl.obolibrary.org/obo/NCIT_C94160 http://purl.obolibrary.org/obo/NCIT_C94161 http://purl.obolibrary.org/obo/NCIT_C94162 @@ -175641,7 +179543,6 @@ http://purl.obolibrary.org/obo/NCIT_C94186 http://purl.obolibrary.org/obo/NCIT_C94187 http://purl.obolibrary.org/obo/NCIT_C94188 http://purl.obolibrary.org/obo/NCIT_C94189 -http://purl.obolibrary.org/obo/NCIT_C9419 http://purl.obolibrary.org/obo/NCIT_C94190 http://purl.obolibrary.org/obo/NCIT_C94191 http://purl.obolibrary.org/obo/NCIT_C94192 @@ -175653,7 +179554,6 @@ http://purl.obolibrary.org/obo/NCIT_C94197 http://purl.obolibrary.org/obo/NCIT_C94198 http://purl.obolibrary.org/obo/NCIT_C94199 http://purl.obolibrary.org/obo/NCIT_C942 -http://purl.obolibrary.org/obo/NCIT_C9420 http://purl.obolibrary.org/obo/NCIT_C94200 http://purl.obolibrary.org/obo/NCIT_C94201 http://purl.obolibrary.org/obo/NCIT_C94202 @@ -175663,7 +179563,6 @@ http://purl.obolibrary.org/obo/NCIT_C94206 http://purl.obolibrary.org/obo/NCIT_C94207 http://purl.obolibrary.org/obo/NCIT_C94208 http://purl.obolibrary.org/obo/NCIT_C94209 -http://purl.obolibrary.org/obo/NCIT_C9421 http://purl.obolibrary.org/obo/NCIT_C94211 http://purl.obolibrary.org/obo/NCIT_C94212 http://purl.obolibrary.org/obo/NCIT_C94213 @@ -176493,7 +180392,6 @@ http://purl.obolibrary.org/obo/NCIT_C94986 http://purl.obolibrary.org/obo/NCIT_C94987 http://purl.obolibrary.org/obo/NCIT_C94988 http://purl.obolibrary.org/obo/NCIT_C94989 -http://purl.obolibrary.org/obo/NCIT_C9499 http://purl.obolibrary.org/obo/NCIT_C94990 http://purl.obolibrary.org/obo/NCIT_C94991 http://purl.obolibrary.org/obo/NCIT_C94992 diff --git a/src/ontology/reports/mirror_signature-omim.tsv b/src/ontology/reports/mirror_signature-omim.tsv index 7bf8d95c..620f77fa 100644 --- a/src/ontology/reports/mirror_signature-omim.tsv +++ b/src/ontology/reports/mirror_signature-omim.tsv @@ -9316,6 +9316,7 @@ + @@ -30173,6 +30174,24 @@ + + + + + + + + + + + + + + + + + + @@ -30746,6 +30765,7 @@ + diff --git a/src/ontology/reports/ncit.subclass.added-obsolete.robot.tsv b/src/ontology/reports/ncit.subclass.added-obsolete.robot.tsv index 6abd33eb..8beb245a 100644 --- a/src/ontology/reports/ncit.subclass.added-obsolete.robot.tsv +++ b/src/ontology/reports/ncit.subclass.added-obsolete.robot.tsv @@ -1,7 +1,6 @@ subject_mondo_id subject_mondo_label object_mondo_id subject_source_id object_source_id object_mondo_label ID AI obo:mondo#excluded_subClassOf >A oboInOwl:source MONDO:0005586 head and neck neoplasm MONDO:0021059 NCIT:C3077 NCIT:C27571 obsolete head or neck disorder/disorder -MONDO:0006475 obsolete unclassified renal cell carcinoma MONDO:0005549 NCIT:C27892 NCIT:C9385 renal cell adenocarcinoma MONDO:0006901 peritoneal neoplasm MONDO:0020591 NCIT:C3322 NCIT:C26848 obsolete disorder of peritoneum MONDO:0012883 acute promyelocytic leukemia MONDO:0020078 NCIT:C3182 NCIT:C7175 obsolete acute myeloid leukemia with recurrent genetic anomaly MONDO:0017894 acute myeloid leukemia with CEBPA somatic mutations MONDO:0020078 NCIT:C82433 NCIT:C7175 obsolete acute myeloid leukemia with recurrent genetic anomaly @@ -10,7 +9,6 @@ MONDO:0021350 neoplasm of thorax MONDO:0000651 NCIT:C3406 NCIT:C35742 obsolete t MONDO:0021386 neoplasm of mediastinum MONDO:0043707 NCIT:C3221 NCIT:C26826 obsolete mediastinal disorder MONDO:0024645 retroperitoneal neoplasm MONDO:0020595 NCIT:C3357 NCIT:C27667 obsolete disorder of retroperitoneum MONDO:0036491 obsolete rare childhood malignant neoplasm MONDO:0006517 NCIT:C114451 NCIT:C4005 childhood malignant neoplasm -MONDO:0036491 obsolete rare childhood malignant neoplasm MONDO:0021200 NCIT:C114451 NCIT:C4873 obsolete rare disease MONDO:0042494 childhood malignant melanoma MONDO:0036491 NCIT:C131506 NCIT:C114451 obsolete rare childhood malignant neoplasm MONDO:0044923 acute myeloid leukemia with mutated NPM1 MONDO:0020078 NCIT:C82431 NCIT:C7175 obsolete acute myeloid leukemia with recurrent genetic anomaly MONDO:0100375 acute myeloid leukemia, t(15;17)(q24;q21) MONDO:0020078 NCIT:C36055 NCIT:C7175 obsolete acute myeloid leukemia with recurrent genetic anomaly diff --git a/src/ontology/reports/ncit.subclass.added.robot.tsv b/src/ontology/reports/ncit.subclass.added.robot.tsv index d6488635..8bf18fce 100644 --- a/src/ontology/reports/ncit.subclass.added.robot.tsv +++ b/src/ontology/reports/ncit.subclass.added.robot.tsv @@ -31,6 +31,7 @@ MONDO:0001652 scrotum melanoma MONDO:0021112 NCIT:C7361 NCIT:C3560 scrotum cance MONDO:0001748 maxillary sinus carcinoma MONDO:0001748 NCIT:C9332 NCIT:C3540 maxillary sinus carcinoma MONDO:0001778 dermoid cyst of skin MONDO:0021440 NCIT:C4632 NCIT:C2896 benign neoplasm of skin MONDO:0001789 neurofibroma of spinal cord MONDO:0021506 NCIT:C5145 NCIT:C3627 benign neoplasm of spinal cord +MONDO:0001893 spinal cord melanoma MONDO:0003761 NCIT:C5158 NCIT:C5317 leptomeningeal melanoma MONDO:0001975 cavernous hemangioma of orbit MONDO:0001974 NCIT:C4546 NCIT:C6245 hemangioma of orbit MONDO:0001977 ureteral lymphoma MONDO:0017207 NCIT:C6175 NCIT:C7185 primary organ-specific lymphoma MONDO:0002064 breast angiomatosis MONDO:0000620 NCIT:C40381 NCIT:C4505 breast benign neoplasm @@ -63,7 +64,6 @@ MONDO:0002447 endometrial carcinoma MONDO:0006003 NCIT:C7558 NCIT:C61574 uterine MONDO:0002472 carcinoma ex pleomorphic adenoma MONDO:0024878 NCIT:C4397 NCIT:C36310 secondary carcinoma MONDO:0002478 mixed germ cell-sex cord-stromal tumor MONDO:0006054 NCIT:C5241 NCIT:C3674 reproductive system neoplasm MONDO:0002527 keratoacanthoma MONDO:0002529 NCIT:C3146 NCIT:C4819 skin squamous cell carcinoma -MONDO:0002544 brain oligodendroglioma MONDO:0021632 NCIT:C9377 NCIT:C170814 primary brain neoplasm MONDO:0002546 schwannoma MONDO:0000648 NCIT:C3269 NCIT:C4789 nervous system benign neoplasm MONDO:0002551 c-P angle neurinoma MONDO:0002546 NCIT:C5413 NCIT:C3269 schwannoma MONDO:0002553 cerebellopontine angle tumor MONDO:0021632 NCIT:C5414 NCIT:C170814 primary brain neoplasm @@ -90,6 +90,7 @@ MONDO:0002809 pancreatic cystadenoma MONDO:0036976 NCIT:C4374 NCIT:C4092 benign MONDO:0002810 pancreatic serous cystic neoplasm MONDO:0037256 NCIT:C41248 NCIT:C7074 serous neoplasm MONDO:0002834 primary prostate urothelial carcinoma MONDO:0040679 NCIT:C39898 NCIT:C4030 urothelial carcinoma MONDO:0002848 skeletal muscle neoplasm MONDO:0021545 NCIT:C6514 NCIT:C4063 myomatous neoplasm +MONDO:0002855 ectomesenchymoma MONDO:0018078 NCIT:C4716 NCIT:C9306 soft tissue sarcoma MONDO:0002868 bile duct mucinous cystic neoplasm with an associated invasive carcinoma MONDO:0003193 NCIT:C4130 NCIT:C27813 bile duct adenocarcinoma MONDO:0002872 trophoblastic neoplasm MONDO:0005626 NCIT:C3422 NCIT:C3709 epithelial neoplasm MONDO:0002878 uterine corpus adenosarcoma MONDO:0005210 NCIT:C6336 NCIT:C6339 uterine corpus sarcoma @@ -190,7 +191,6 @@ MONDO:0004158 pancreatic mucinous-cystic neoplasm with an associated invasive ca MONDO:0004164 lymphoepithelioma-like acinar prostate adenocarcinoma MONDO:0003572 NCIT:C39885 NCIT:C4107 nasopharyngeal type undifferentiated carcinoma MONDO:0004217 childhood brain germinoma MONDO:0004218 NCIT:C6207 NCIT:C5795 childhood germ cell brain tumor MONDO:0004218 childhood germ cell brain tumor MONDO:0021632 NCIT:C5795 NCIT:C170814 primary brain neoplasm -MONDO:0004223 polyp of middle ear MONDO:0021482 NCIT:C6933 NCIT:C4602 benign neoplasm of middle ear MONDO:0004225 monoclonal gammopathy of uncertain significance MONDO:0004949 NCIT:C3996 NCIT:C27910 neoplasm of mature B-cells MONDO:0004230 adenomatoid tumor MONDO:0005165 NCIT:C3762 NCIT:C3677 benign neoplasm MONDO:0004238 petrous apex meningioma MONDO:0002998 NCIT:C5271 NCIT:C5272 skull base meningioma @@ -213,9 +213,7 @@ MONDO:0004447 pituitary stalk meningioma MONDO:0004312 NCIT:C5311 NCIT:C6776 sup MONDO:0004467 mature gastric teratoma MONDO:0021449 NCIT:C5260 NCIT:C3599 benign neoplasm of stomach MONDO:0004473 epiglottis cancer MONDO:0004473 NCIT:C35697 NCIT:C4836 epiglottis cancer MONDO:0004488 cervical atypical polypoid adenomyoma MONDO:0003236 NCIT:C40234 NCIT:C6895 atypical polypoid adenomyoma -MONDO:0004491 uterine corpus choriocarcinoma MONDO:0020550 NCIT:C27246 NCIT:C4646 gestational choriocarcinoma MONDO:0004500 lung superior sulcus carcinoma MONDO:0002806 NCIT:C7779 NCIT:C35875 bronchogenic carcinoma -MONDO:0004512 meningeal melanomatosis MONDO:0003761 NCIT:C6891 NCIT:C5317 leptomeningeal melanoma MONDO:0004550 malignant cornea melanoma MONDO:0006320 NCIT:C4553 NCIT:C8711 non-cutaneous melanoma MONDO:0004560 follicular infundibulum tumor MONDO:0002093 NCIT:C4469 NCIT:C7419 acanthoma MONDO:0004561 retinal melanoma MONDO:0006320 NCIT:C8601 NCIT:C8711 non-cutaneous melanoma @@ -224,7 +222,6 @@ MONDO:0004699 gastrointestinal lymphoma MONDO:0017207 NCIT:C38162 NCIT:C7185 pri MONDO:0004752 neurofibroma of the heart MONDO:0021450 NCIT:C5359 NCIT:C3605 benign neoplasm of heart MONDO:0004756 nasal cavity neoplasm MONDO:0056820 NCIT:C4413 NCIT:C7336 nasal cavity and paranasal sinus neoplasm MONDO:0004837 neurofibroma of the esophagus MONDO:0021459 NCIT:C5704 NCIT:C3598 benign neoplasm of esophagus -MONDO:0004942 orbit lymphoma MONDO:0017207 NCIT:C6244 NCIT:C7185 primary organ-specific lymphoma MONDO:0004943 orbit sarcoma MONDO:0018078 NCIT:C6095 NCIT:C9306 soft tissue sarcoma MONDO:0004948 B-cell chronic lymphocytic leukemia MONDO:0003864 NCIT:C3163 NCIT:C27911 chronic lymphocytic leukemia/small lymphocytic lymphoma MONDO:0004963 T-cell acute lymphoblastic leukemia MONDO:0003537 NCIT:C3183 NCIT:C8694 precursor T-lymphoblastic lymphoma/leukemia @@ -282,7 +279,6 @@ MONDO:0006283 lymphoepithelioma-like lung carcinoma MONDO:0003572 NCIT:C45519 NC MONDO:0006317 neurothekeoma MONDO:0000648 NCIT:C7018 NCIT:C4789 nervous system benign neoplasm MONDO:0006368 phosphaturic mesenchymal tumor MONDO:0002616 NCIT:C67237 NCIT:C7059 mesenchymal cell neoplasm MONDO:0006377 pleural biphasic mesothelioma MONDO:0005112 NCIT:C45665 NCIT:C7376 malignant pleural mesothelioma -MONDO:0006385 primary intraosseous squamous cell carcinoma MONDO:0004958 NCIT:C54295 NCIT:C4833 oral cavity squamous cell carcinoma MONDO:0006388 prolactin-producing pituitary gland carcinoma MONDO:0010911 NCIT:C5962 NCIT:C3342 prolactin-producing pituitary gland adenoma MONDO:0006411 sinonasal undifferentiated carcinoma MONDO:0056819 NCIT:C54294 NCIT:C54293 nasal cavity and paranasal sinus carcinoma MONDO:0006412 sinus histiocytosis with massive lymphadenopathy MONDO:0006247 NCIT:C36075 NCIT:C9294 histiocytic and dendritic cell neoplasm @@ -295,15 +291,15 @@ MONDO:0006474 transitional cell carcinoma MONDO:0037254 NCIT:C2930 NCIT:C6783 tr MONDO:0006486 uveal melanoma MONDO:0006320 NCIT:C7712 NCIT:C8711 non-cutaneous melanoma MONDO:0006489 vaginal melanoma MONDO:0001402 NCIT:C27394 NCIT:C7410 vaginal cancer MONDO:0006490 vaginal squamous cell carcinoma MONDO:0006490 NCIT:C7736 NCIT:C180915 vaginal squamous cell carcinoma +MONDO:0006579 melanoacanthoma MONDO:0002093 NCIT:C27548 NCIT:C7419 acanthoma MONDO:0006622 vulvar seborrheic keratosis MONDO:0000643 NCIT:C6375 NCIT:C3611 vulvar benign neoplasm MONDO:0006745 endometrioid stromal sarcoma MONDO:0037742 NCIT:C8973 NCIT:C8384 endometrioid stromal and related neoplasms MONDO:0006745 endometrioid stromal sarcoma MONDO:0044337 NCIT:C8973 NCIT:C6926 stromal sarcoma MONDO:0006778 halo nevus MONDO:0044794 NCIT:C7602 NCIT:C7571 benign melanocytic skin nevus MONDO:0006813 intradermal nevus MONDO:0044794 NCIT:C3804 NCIT:C7571 benign melanocytic skin nevus +MONDO:0006905 pigmented spindle cell nevus MONDO:0044796 NCIT:C4751 NCIT:C66758 spindle cell nevus MONDO:0006998 tonsil cancer MONDO:0005515 NCIT:C7404 NCIT:C9314 oral cavity cancer MONDO:0007203 blue rubber bleb nevus MONDO:0018715 NCIT:C4486 NCIT:C3841 congenital hemangioma -MONDO:0007565 familial cylindromatosis MONDO:0021812 NCIT:C43352 NCIT:C27094 adnexal spiradenoma/cylindroma of a sweat gland -MONDO:0007667 subependymoma MONDO:0021632 NCIT:C3795 NCIT:C170814 primary brain neoplasm MONDO:0007672 glomuvenous malformation MONDO:0002299 NCIT:C5350 NCIT:C4222 glomangioma MONDO:0007708 Kasabach-Merritt syndrome MONDO:0024461 NCIT:C3821 NCIT:C27503 angiomatosis MONDO:0007888 hereditary leiomyomatosis and renal cell cancer MONDO:0003008 NCIT:C51302 NCIT:C39789 hereditary renal cell carcinoma @@ -326,13 +322,15 @@ MONDO:0011908 juvenile myelomonocytic leukemia MONDO:0006517 NCIT:C9233 NCIT:C40 MONDO:0011927 tufted angioma MONDO:0002407 NCIT:C4487 NCIT:C7457 capillary hemangioma MONDO:0015074 thyroid tumor MONDO:0021351 NCIT:C3414 NCIT:C3260 neoplasm of neck MONDO:0015447 differentiated thyroid carcinoma MONDO:0024622 NCIT:C7153 NCIT:C27380 thyroid gland adenocarcinoma -MONDO:0015534 juvenile xanthogranuloma MONDO:0021440 NCIT:C3451 NCIT:C2896 benign neoplasm of skin +MONDO:0015534 juvenile xanthogranuloma MONDO:0006247 NCIT:C3451 NCIT:C9294 histiocytic and dendritic cell neoplasm MONDO:0015688 myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2 MONDO:0004992 NCIT:C84270 NCIT:C9305 cancer MONDO:0015760 T-cell non-Hodgkin lymphoma MONDO:0024615 NCIT:C3466 NCIT:C27908 T-cell and NK-cell neoplasm MONDO:0015864 mixed germ cell tumor MONDO:0021043 NCIT:C4290 NCIT:C6930 mixed neoplasm MONDO:0016682 giant cell glioblastoma MONDO:0002402 NCIT:C4325 NCIT:C4090 malignant giant cell tumor MONDO:0016683 gliomatosis cerebri MONDO:0021632 NCIT:C4318 NCIT:C170814 primary brain neoplasm MONDO:0016684 anaplastic astrocytoma MONDO:0021640 NCIT:C9477 NCIT:C127816 grade III glioma +MONDO:0016690 pleomorphic xanthoastrocytoma MONDO:0021639 NCIT:C4323 NCIT:C132505 grade II glioma +MONDO:0016693 subependymal giant cell astrocytoma MONDO:0021631 NCIT:C3696 NCIT:C60780 brain astrocytoma MONDO:0016706 chordoid glioma of the third ventricle MONDO:0021632 NCIT:C5592 NCIT:C170814 primary brain neoplasm MONDO:0016717 choroid plexus neoplasm MONDO:0002682 NCIT:C3473 NCIT:C2937 cerebral ventricle cancer MONDO:0016717 choroid plexus neoplasm MONDO:0005626 NCIT:C3473 NCIT:C3709 epithelial neoplasm @@ -383,7 +381,6 @@ MONDO:0020325 anaplastic large cell lymphoma MONDO:0020633 NCIT:C3720 NCIT:C3602 MONDO:0020334 mast cell leukemia MONDO:0004643 NCIT:C3169 NCIT:C3172 myeloid leukemia MONDO:0020511 precursor B-cell acute lymphoblastic leukemia MONDO:0004947 NCIT:C8644 NCIT:C8936 B-cell acute lymphoblastic leukemia MONDO:0020634 grade III meningioma MONDO:0021322 NCIT:C38938 NCIT:C4628 malignant tumor of meninges -MONDO:0020646 ocular adnexal lymphoma MONDO:0004034 NCIT:C88145 NCIT:C35690 eye lymphoma MONDO:0021039 extraskeletal Ewing sarcoma/peripheral primitive neuroectodermal tumor MONDO:0024637 NCIT:C27293 NCIT:C4867 malignant soft tissue neoplasm MONDO:0021065 pleural neoplasm MONDO:0021350 NCIT:C3332 NCIT:C3406 neoplasm of thorax MONDO:0021071 laryngeal neoplasm MONDO:0021351 NCIT:C3156 NCIT:C3260 neoplasm of neck diff --git a/src/ontology/reports/ncit.subclass.confirmed.robot.tsv b/src/ontology/reports/ncit.subclass.confirmed.robot.tsv index c871fb18..96b77c1b 100644 --- a/src/ontology/reports/ncit.subclass.confirmed.robot.tsv +++ b/src/ontology/reports/ncit.subclass.confirmed.robot.tsv @@ -82,7 +82,6 @@ MONDO:0000928 eyelid melanoma MONDO:0021313 NCIT:C4358 NCIT:C6786 eyelid cancer MONDO:0000929 balloon cell malignant melanoma MONDO:0005012 NCIT:C4227 NCIT:C3510 cutaneous melanoma MONDO:0000930 nodular malignant melanoma MONDO:0005012 NCIT:C4225 NCIT:C3510 cutaneous melanoma MONDO:0000933 subglottis neoplasm MONDO:0021071 NCIT:C4426 NCIT:C3156 laryngeal neoplasm -MONDO:0000934 laryngeal leiomyoma MONDO:0001572 NCIT:C6027 NCIT:C3157 leiomyoma MONDO:0000935 larynx squamous papilloma MONDO:0001825 NCIT:C7742 NCIT:C3712 squamous papilloma MONDO:0000935 larynx squamous papilloma MONDO:0002354 NCIT:C7742 NCIT:C3601 benign laryngeal neoplasm MONDO:0000951 thymus lymphoma MONDO:0002586 NCIT:C6451 NCIT:C4962 thymus cancer @@ -102,7 +101,6 @@ MONDO:0000970 breast lipoma MONDO:0000620 NCIT:C4647 NCIT:C4505 breast benign ne MONDO:0000970 breast lipoma MONDO:0005106 NCIT:C4647 NCIT:C3192 lipoma MONDO:0000971 chest wall lipoma MONDO:0005106 NCIT:C6719 NCIT:C3192 lipoma MONDO:0000971 chest wall lipoma MONDO:0021529 NCIT:C6719 NCIT:C8529 benign neoplasm of chest wall -MONDO:0000973 external ear lipoma MONDO:0005106 NCIT:C4618 NCIT:C3192 lipoma MONDO:0000974 axillary lipoma MONDO:0005106 NCIT:C35419 NCIT:C3192 lipoma MONDO:0000974 axillary lipoma MONDO:0036781 NCIT:C35419 NCIT:C35750 benign axillary neoplasm MONDO:0000975 lipoma of spermatic cord MONDO:0000976 NCIT:C3606 NCIT:C6384 paratesticular lipoma @@ -262,15 +260,12 @@ MONDO:0001888 anus lymphoma MONDO:0001879 NCIT:C5601 NCIT:C7379 anus cancer MONDO:0001892 spinal cord lymphoma MONDO:0002571 NCIT:C5157 NCIT:C9301 primary central nervous system lymphoma MONDO:0001892 spinal cord lymphoma MONDO:0003544 NCIT:C5157 NCIT:C3572 spinal cord cancer MONDO:0001893 spinal cord melanoma MONDO:0003544 NCIT:C5158 NCIT:C3572 spinal cord cancer -MONDO:0001893 spinal cord melanoma MONDO:0016747 NCIT:C5158 NCIT:C5505 primary melanoma of the central nervous system MONDO:0001894 spinal cord sarcoma MONDO:0002217 NCIT:C5152 NCIT:C5153 central nervous system sarcoma MONDO:0001894 spinal cord sarcoma MONDO:0003544 NCIT:C5152 NCIT:C3572 spinal cord cancer MONDO:0001939 skin epithelioid hemangioma MONDO:0003110 NCIT:C7393 NCIT:C4905 skin hemangioma MONDO:0001939 skin epithelioid hemangioma MONDO:0021169 NCIT:C7393 NCIT:C4298 epithelioid hemangioma -MONDO:0001974 hemangioma of orbit MONDO:0006500 NCIT:C6245 NCIT:C3085 hemangioma MONDO:0001975 cavernous hemangioma of orbit MONDO:0003155 NCIT:C4546 NCIT:C3086 cavernous hemangioma MONDO:0001977 ureteral lymphoma MONDO:0008627 NCIT:C6175 NCIT:C7543 ureter cancer -MONDO:0001978 regional ureteric cancer MONDO:0006481 NCIT:C9356 NCIT:C8993 ureter carcinoma MONDO:0001990 malignant cardiac peripheral nerve sheath neoplasm MONDO:0003354 NCIT:C5367 NCIT:C7723 heart sarcoma MONDO:0001990 malignant cardiac peripheral nerve sheath neoplasm MONDO:0017827 NCIT:C5367 NCIT:C3798 malignant peripheral nerve sheath tumor MONDO:0001991 malignant cardiac germ cell tumor MONDO:0001340 NCIT:C5371 NCIT:C3548 heart cancer @@ -588,7 +583,6 @@ MONDO:0002578 botryoid rhabdomyosarcoma MONDO:0009993 NCIT:C9150 NCIT:C8971 embr MONDO:0002579 orbit embryonal rhabdomyosarcoma MONDO:0002580 NCIT:C6246 NCIT:C4543 orbit rhabdomyosarcoma MONDO:0002579 orbit embryonal rhabdomyosarcoma MONDO:0009993 NCIT:C6246 NCIT:C8971 embryonal rhabdomyosarcoma MONDO:0002580 orbit rhabdomyosarcoma MONDO:0004943 NCIT:C4543 NCIT:C6095 orbit sarcoma -MONDO:0002580 orbit rhabdomyosarcoma MONDO:0005212 NCIT:C4543 NCIT:C3359 rhabdomyosarcoma MONDO:0002583 mucinous ovarian cystadenoma MONDO:0005183 NCIT:C4512 NCIT:C4060 ovarian cystadenoma MONDO:0002583 mucinous ovarian cystadenoma MONDO:0006859 NCIT:C4512 NCIT:C2973 mucinous cystadenoma MONDO:0002586 thymus cancer MONDO:0005197 NCIT:C4962 NCIT:C3412 thymus neoplasm @@ -851,22 +845,18 @@ MONDO:0002930 kidney sarcoma MONDO:0018078 NCIT:C4525 NCIT:C9306 soft tissue sar MONDO:0002934 intravascular angioleiomyoma MONDO:0006646 NCIT:C5355 NCIT:C3747 angioleiomyoma MONDO:0002935 penis basal cell carcinoma MONDO:0005341 NCIT:C39961 NCIT:C2921 skin basal cell carcinoma MONDO:0002936 scrotum basal cell carcinoma MONDO:0005341 NCIT:C6386 NCIT:C2921 skin basal cell carcinoma -MONDO:0002938 metatypical basal cell carcinoma MONDO:0005341 NCIT:C66903 NCIT:C2921 skin basal cell carcinoma -MONDO:0002939 skin pigmented basal cell carcinoma MONDO:0005341 NCIT:C9359 NCIT:C2921 skin basal cell carcinoma MONDO:0002940 anal margin basal cell carcinoma MONDO:0005341 NCIT:C7473 NCIT:C2921 skin basal cell carcinoma MONDO:0002941 anal margin carcinoma MONDO:0002656 NCIT:C7472 NCIT:C4914 skin carcinoma MONDO:0002941 anal margin carcinoma MONDO:0003199 NCIT:C7472 NCIT:C9291 anal carcinoma MONDO:0002943 external ear basal cell carcinoma MONDO:0005341 NCIT:C6082 NCIT:C2921 skin basal cell carcinoma MONDO:0002944 external ear carcinoma MONDO:0003574 NCIT:C6081 NCIT:C4653 external ear cancer MONDO:0002945 micronodular basal cell carcinoma MONDO:0005341 NCIT:C27541 NCIT:C2921 skin basal cell carcinoma -MONDO:0002947 adamantinoid basal cell epithelioma MONDO:0005341 NCIT:C7585 NCIT:C2921 skin basal cell carcinoma MONDO:0002948 skin fibroepithelial basal cell carcinoma MONDO:0005341 NCIT:C4109 NCIT:C2921 skin basal cell carcinoma MONDO:0002949 morpheaform basal cell carcinoma MONDO:0005341 NCIT:C27182 NCIT:C2921 skin basal cell carcinoma MONDO:0002950 skin clear cell basal cell carcinoma MONDO:0005341 NCIT:C27536 NCIT:C2921 skin basal cell carcinoma MONDO:0002951 skin adenoid basal cell carcinoma MONDO:0005341 NCIT:C27535 NCIT:C2921 skin basal cell carcinoma MONDO:0002953 skin infiltrative basal cell carcinoma MONDO:0005341 NCIT:C27539 NCIT:C2921 skin basal cell carcinoma MONDO:0002955 vulva basal cell carcinoma MONDO:0005341 NCIT:C6381 NCIT:C2921 skin basal cell carcinoma -MONDO:0002956 skin cystic basal cell carcinoma MONDO:0005341 NCIT:C27537 NCIT:C2921 skin basal cell carcinoma MONDO:0002957 sarcomatoid basal cell carcinoma MONDO:0005341 NCIT:C38111 NCIT:C2921 skin basal cell carcinoma MONDO:0002958 signet ring basal cell carcinoma MONDO:0005341 NCIT:C38110 NCIT:C2921 skin basal cell carcinoma MONDO:0002961 large cell acanthoma MONDO:0002093 NCIT:C27518 NCIT:C7419 acanthoma @@ -902,7 +892,6 @@ MONDO:0003001 seminoma MONDO:0020580 NCIT:C9309 NCIT:C121618 germinomatous germ MONDO:0003003 cervical alveolar soft part sarcoma MONDO:0011655 NCIT:C40225 NCIT:C3750 alveolar soft part sarcoma MONDO:0003007 childhood kidney cell carcinoma MONDO:0005549 NCIT:C6568 NCIT:C9385 renal cell adenocarcinoma MONDO:0003008 hereditary renal cell carcinoma MONDO:0005549 NCIT:C39789 NCIT:C9385 renal cell adenocarcinoma -MONDO:0003012 sarcomatoid renal cell carcinoma MONDO:0005549 NCIT:C27893 NCIT:C9385 renal cell adenocarcinoma MONDO:0003012 sarcomatoid renal cell carcinoma MONDO:0006406 NCIT:C27893 NCIT:C27004 sarcomatoid carcinoma MONDO:0003021 central nervous system angiosarcoma MONDO:0002217 NCIT:C5450 NCIT:C5153 central nervous system sarcoma MONDO:0003022 pediatric angiosarcoma MONDO:0016982 NCIT:C9174 NCIT:C3088 angiosarcoma @@ -965,7 +954,6 @@ MONDO:0003112 malignant gastric germ cell tumor MONDO:0001056 NCIT:C5486 NCIT:C9 MONDO:0003112 malignant gastric germ cell tumor MONDO:0003113 NCIT:C5486 NCIT:C8881 extragonadal germ cell cancer MONDO:0003113 extragonadal germ cell cancer MONDO:0006290 NCIT:C8881 NCIT:C4925 malignant germ cell tumor MONDO:0003113 extragonadal germ cell cancer MONDO:0018201 NCIT:C8881 NCIT:C3918 extragonadal germ cell tumor -MONDO:0003115 subglottic hemangioma MONDO:0006500 NCIT:C6026 NCIT:C3085 hemangioma MONDO:0003115 subglottic hemangioma MONDO:0021530 NCIT:C6026 NCIT:C4427 benign neoplasm of subglottis MONDO:0003118 testicular Brenner tumor MONDO:0024235 NCIT:C39953 NCIT:C39954 Brenner tumor MONDO:0003120 mixed testicular germ cell cancer MONDO:0003510 NCIT:C6347 NCIT:C9063 malignant testicular germ cell tumor @@ -993,8 +981,6 @@ MONDO:0003164 cauda equina neoplasm MONDO:0003103 NCIT:C5479 NCIT:C5119 nerve ro MONDO:0003165 cerebellar astrocytoma MONDO:0002913 NCIT:C9475 NCIT:C2935 cerebellar neoplasm MONDO:0003165 cerebellar astrocytoma MONDO:0021631 NCIT:C9475 NCIT:C60780 brain astrocytoma MONDO:0003168 cerebellar pilocytic astrocytoma MONDO:0003165 NCIT:C6809 NCIT:C9475 cerebellar astrocytoma -MONDO:0003168 cerebellar pilocytic astrocytoma MONDO:0016691 NCIT:C6809 NCIT:C4047 pilocytic astrocytoma -MONDO:0003168 cerebellar pilocytic astrocytoma MONDO:0021499 NCIT:C6809 NCIT:C4955 benign neoplasm of cerebellum MONDO:0003169 diencephalic astrocytomas MONDO:0021631 NCIT:C5128 NCIT:C60780 brain astrocytoma MONDO:0003170 gliofibroma MONDO:0021636 NCIT:C5419 NCIT:C6958 astrocytic tumor MONDO:0003172 glomeruloid hemangioma MONDO:0006500 NCIT:C27505 NCIT:C3085 hemangioma @@ -1044,9 +1030,7 @@ MONDO:0003216 ureter adenocarcinoma MONDO:0006481 NCIT:C6155 NCIT:C8993 ureter c MONDO:0003218 adenocarcinoma in situ MONDO:0004647 NCIT:C4123 NCIT:C2917 in situ carcinoma MONDO:0003218 adenocarcinoma in situ MONDO:0004970 NCIT:C4123 NCIT:C2852 adenocarcinoma MONDO:0003219 gastroesophageal junction adenocarcinoma MONDO:0004970 NCIT:C9296 NCIT:C2852 adenocarcinoma -MONDO:0003219 gastroesophageal junction adenocarcinoma MONDO:0006181 NCIT:C9296 NCIT:C96963 digestive system carcinoma MONDO:0003220 gallbladder carcinoma MONDO:0005411 NCIT:C3844 NCIT:C7481 gallbladder cancer -MONDO:0003222 central nervous system melanocytic neoplasm MONDO:0021143 NCIT:C5504 NCIT:C7058 melanocytic neoplasm MONDO:0003234 optic nerve astrocytoma MONDO:0003235 NCIT:C6769 NCIT:C4537 optic nerve glioma MONDO:0003234 optic nerve astrocytoma MONDO:0024649 NCIT:C6769 NCIT:C7533 optic tract astrocytoma MONDO:0003235 optic nerve glioma MONDO:0002640 NCIT:C4537 NCIT:C4801 optic nerve neoplasm @@ -1168,7 +1152,6 @@ MONDO:0003372 vulvar leiomyosarcoma MONDO:0005058 NCIT:C40318 NCIT:C3158 leiomyo MONDO:0003372 vulvar leiomyosarcoma MONDO:0005214 NCIT:C40318 NCIT:C40317 vulva sarcoma MONDO:0003373 kidney leiomyosarcoma MONDO:0002930 NCIT:C6183 NCIT:C4525 kidney sarcoma MONDO:0003373 kidney leiomyosarcoma MONDO:0005058 NCIT:C6183 NCIT:C3158 leiomyosarcoma -MONDO:0003374 laryngeal leiomyosarcoma MONDO:0005058 NCIT:C6022 NCIT:C3158 leiomyosarcoma MONDO:0003376 mediastinum leiomyosarcoma MONDO:0002852 NCIT:C6619 NCIT:C6606 mediastinum sarcoma MONDO:0003376 mediastinum leiomyosarcoma MONDO:0005058 NCIT:C6619 NCIT:C3158 leiomyosarcoma MONDO:0003377 extrahepatic bile duct leiomyosarcoma MONDO:0024658 NCIT:C5848 NCIT:C5029 extrahepatic bile duct sarcoma @@ -1219,9 +1202,6 @@ MONDO:0003421 mixed cell adenoma MONDO:0021043 NCIT:C4157 NCIT:C6930 mixed neopl MONDO:0003422 lung adenoma MONDO:0002732 NCIT:C4455 NCIT:C4454 lung benign neoplasm MONDO:0003422 lung adenoma MONDO:0004972 NCIT:C4455 NCIT:C2855 adenoma MONDO:0003422 lung adenoma MONDO:0036976 NCIT:C4455 NCIT:C4092 benign epithelial neoplasm -MONDO:0003423 middle ear adenoma MONDO:0004972 NCIT:C6834 NCIT:C2855 adenoma -MONDO:0003423 middle ear adenoma MONDO:0021482 NCIT:C6834 NCIT:C4602 benign neoplasm of middle ear -MONDO:0003423 middle ear adenoma MONDO:0036976 NCIT:C6834 NCIT:C4092 benign epithelial neoplasm MONDO:0003424 oncocytic adenoma MONDO:0004972 NCIT:C3759 NCIT:C2855 adenoma MONDO:0003424 oncocytic adenoma MONDO:0010795 NCIT:C3759 NCIT:C7072 oncocytic neoplasm MONDO:0003426 clear cell adenoma MONDO:0004972 NCIT:C4151 NCIT:C2855 adenoma @@ -1342,7 +1322,6 @@ MONDO:0003585 adult liposarcoma MONDO:0005060 NCIT:C7811 NCIT:C3194 liposarcoma MONDO:0003586 esophagus liposarcoma MONDO:0001204 NCIT:C5705 NCIT:C5341 esophagus sarcoma MONDO:0003586 esophagus liposarcoma MONDO:0005060 NCIT:C5705 NCIT:C3194 liposarcoma MONDO:0003587 pediatric liposarcoma MONDO:0005060 NCIT:C8091 NCIT:C3194 liposarcoma -MONDO:0003588 larynx liposarcoma MONDO:0005060 NCIT:C6021 NCIT:C3194 liposarcoma MONDO:0003589 liposarcoma of the ovary MONDO:0002225 NCIT:C6419 NCIT:C8267 ovarian sarcoma MONDO:0003589 liposarcoma of the ovary MONDO:0005060 NCIT:C6419 NCIT:C3194 liposarcoma MONDO:0003591 kidney liposarcoma MONDO:0002930 NCIT:C6185 NCIT:C4525 kidney sarcoma @@ -1481,7 +1460,6 @@ MONDO:0003759 childhood ovarian yolk sac tumor MONDO:0003400 NCIT:C6551 NCIT:C27 MONDO:0003759 childhood ovarian yolk sac tumor MONDO:0006344 NCIT:C6551 NCIT:C8107 ovarian yolk sac tumor MONDO:0003760 pediatric ovarian germ cell tumor MONDO:0011366 NCIT:C8588 NCIT:C3873 ovarian germ cell tumor MONDO:0003761 leptomeningeal melanoma MONDO:0003762 NCIT:C5317 NCIT:C8506 malignant leptomeningeal tumor -MONDO:0003761 leptomeningeal melanoma MONDO:0016747 NCIT:C5317 NCIT:C5505 primary melanoma of the central nervous system MONDO:0003762 malignant leptomeningeal tumor MONDO:0021322 NCIT:C8506 NCIT:C4628 malignant tumor of meninges MONDO:0003764 pediatric leptomeningeal melanoma MONDO:0003761 NCIT:C5318 NCIT:C5317 leptomeningeal melanoma MONDO:0003765 adult leptomeningeal melanoma MONDO:0003761 NCIT:C5319 NCIT:C5317 leptomeningeal melanoma @@ -1676,8 +1654,6 @@ MONDO:0003972 gastric body carcinoma MONDO:0004950 NCIT:C8399 NCIT:C4911 gastric MONDO:0003973 tubular variant testicular seminoma MONDO:0003669 NCIT:C40959 NCIT:C7328 testicular seminoma MONDO:0003975 Littre gland carcinoma MONDO:0004197 NCIT:C39865 NCIT:C39867 male urethral cancer MONDO:0003976 malignant type AB thymoma MONDO:0016975 NCIT:C6886 NCIT:C6885 thymoma type AB -MONDO:0003978 colon small cell neuroendocrine carcinoma MONDO:0002032 NCIT:C6761 NCIT:C4910 colon carcinoma -MONDO:0003978 colon small cell neuroendocrine carcinoma MONDO:0002882 NCIT:C6761 NCIT:C5697 colon neuroendocrine neoplasm MONDO:0003979 intrahepatic bile duct cystadenoma MONDO:0003420 NCIT:C96835 NCIT:C4129 bile duct cystadenoma MONDO:0003980 schwannoma of jugular foramen MONDO:0004820 NCIT:C5323 NCIT:C41430 peripheral nerve schwannoma MONDO:0003982 bilateral breast carcinoma MONDO:0004989 NCIT:C8287 NCIT:C4872 breast carcinoma @@ -1825,7 +1801,6 @@ MONDO:0004131 anal verrucous carcinoma MONDO:0006082 NCIT:C7470 NCIT:C9161 anal MONDO:0004132 anal canal squamous cell carcinoma MONDO:0006082 NCIT:C7469 NCIT:C9161 anal squamous cell carcinoma MONDO:0004132 anal canal squamous cell carcinoma MONDO:0007108 NCIT:C7469 NCIT:C7489 anal canal carcinoma MONDO:0004136 ovarian endometrioid cystadenoma MONDO:0005183 NCIT:C40075 NCIT:C4060 ovarian cystadenoma -MONDO:0004141 melanomatosis MONDO:0005105 NCIT:C9499 NCIT:C3224 melanoma MONDO:0004142 lung combined large cell neuroendocrine carcinoma MONDO:0003960 NCIT:C7267 NCIT:C5672 pulmonary large cell neuroendocrine carcinoma MONDO:0004142 lung combined large cell neuroendocrine carcinoma MONDO:0006167 NCIT:C7267 NCIT:C7591 combined lung carcinoma MONDO:0004148 gallbladder papillary neoplasm with an associated invasive carcinoma MONDO:0002518 NCIT:C5743 NCIT:C7130 gallbladder papillary neoplasm @@ -1852,7 +1827,6 @@ MONDO:0004178 testicular yolk sac tumor, endodermal sinus pattern MONDO:0003402 MONDO:0004180 benign urinary system neoplasm MONDO:0021066 NCIT:C4893 NCIT:C3431 urinary system neoplasm MONDO:0004185 ovarian serous cystadenofibroma MONDO:0003464 NCIT:C40032 NCIT:C8985 cystadenofibroma MONDO:0004185 ovarian serous cystadenofibroma MONDO:0006340 NCIT:C40032 NCIT:C40031 ovarian serous adenofibroma -MONDO:0004186 cranial nodular fasciitis MONDO:0004187 NCIT:C27248 NCIT:C3827 nodular fasciitis MONDO:0004188 iris spindle cell melanoma MONDO:0003744 NCIT:C6098 NCIT:C7986 spindle cell intraocular melanoma MONDO:0004188 iris spindle cell melanoma MONDO:0004064 NCIT:C6098 NCIT:C9088 iris melanoma MONDO:0004192 urethra cancer MONDO:0021239 NCIT:C7507 NCIT:C3428 urethra neoplasm @@ -2122,6 +2096,7 @@ MONDO:0004487 endometrial type cervical adenomyoma MONDO:0003238 NCIT:C40233 NCI MONDO:0004488 cervical atypical polypoid adenomyoma MONDO:0003238 NCIT:C40234 NCIT:C40231 cervical adenomyoma MONDO:0004489 fallopian tube gestational choriocarcinoma MONDO:0006206 NCIT:C6278 NCIT:C3867 fallopian tube carcinoma MONDO:0004489 fallopian tube gestational choriocarcinoma MONDO:0020550 NCIT:C6278 NCIT:C4646 gestational choriocarcinoma +MONDO:0004491 uterine corpus choriocarcinoma MONDO:0020550 NCIT:C27246 NCIT:C4646 gestational choriocarcinoma MONDO:0004493 testicular yolk sac tumor, papillary pattern MONDO:0003402 NCIT:C39928 NCIT:C8000 testicular yolk sac tumor MONDO:0004494 testicular yolk sac tumor, hepatoid pattern MONDO:0003402 NCIT:C39931 NCIT:C8000 testicular yolk sac tumor MONDO:0004498 sacral spinal canal and spinal cord meningioma MONDO:0001279 NCIT:C5299 NCIT:C5134 intraspinal meningioma @@ -2138,7 +2113,6 @@ MONDO:0004507 atypical breast papilloma MONDO:0021097 NCIT:C36089 NCIT:C3863 int MONDO:0004509 intrahepatic biliary papillomatosis MONDO:0003455 NCIT:C7125 NCIT:C6881 bile duct papillary neoplasm MONDO:0004510 inflammatory liposarcoma MONDO:0006097 NCIT:C6508 NCIT:C6505 atypical lipomatous tumor MONDO:0004511 lower clivus meningioma MONDO:0003908 NCIT:C5288 NCIT:C5289 clivus meningioma -MONDO:0004512 meningeal melanomatosis MONDO:0004141 NCIT:C6891 NCIT:C9499 melanomatosis MONDO:0004513 adult pleomorphic rhabdomyosarcoma MONDO:0017386 NCIT:C27369 NCIT:C4258 pleomorphic rhabdomyosarcoma MONDO:0004516 bulbomembranous urethral cancer MONDO:0004197 NCIT:C39869 NCIT:C39867 male urethral cancer MONDO:0004518 anterior urethra cancer MONDO:0004192 NCIT:C7641 NCIT:C7507 urethra cancer @@ -2473,7 +2447,6 @@ MONDO:0005966 spleen cancer MONDO:0036696 NCIT:C3539 NCIT:C3383 spleen neoplasm MONDO:0006006 verrucous carcinoma MONDO:0002979 NCIT:C3781 NCIT:C4102 papillary squamous carcinoma MONDO:0006028 cecum adenocarcinoma MONDO:0002271 NCIT:C5543 NCIT:C4349 colon adenocarcinoma MONDO:0006028 cecum adenocarcinoma MONDO:0006029 NCIT:C5543 NCIT:C3491 cecum carcinoma -MONDO:0006029 cecum carcinoma MONDO:0002032 NCIT:C3491 NCIT:C4910 colon carcinoma MONDO:0006029 cecum carcinoma MONDO:0002033 NCIT:C3491 NCIT:C9329 cecum cancer MONDO:0006034 gastric adenosquamous carcinoma MONDO:0006074 NCIT:C5474 NCIT:C3727 adenosquamous carcinoma MONDO:0006035 gastric tubular adenocarcinoma MONDO:0005606 NCIT:C5473 NCIT:C65192 tubular adenocarcinoma @@ -2510,7 +2483,6 @@ MONDO:0006091 appendix neuroendocrine tumor G1 MONDO:0015066 NCIT:C4138 NCIT:C96 MONDO:0006092 appendix villous adenoma MONDO:0006088 NCIT:C5512 NCIT:C43550 appendix adenoma MONDO:0006093 ascending colon neuroendocrine tumor G1 MONDO:0006155 NCIT:C6427 NCIT:C5497 colon neuroendocrine tumor G1 MONDO:0006094 Askin tumor MONDO:0018271 NCIT:C7542 NCIT:C9341 peripheral primitive neuroectodermal tumor -MONDO:0006095 atypical carcinoid tumor MONDO:0005369 NCIT:C72074 NCIT:C2915 carcinoid tumor MONDO:0006098 atypical lobular breast hyperplasia MONDO:0002486 NCIT:C4730 NCIT:C27939 lobular neoplasia MONDO:0006102 basaloid carcinoma MONDO:0004993 NCIT:C4121 NCIT:C2916 carcinoma MONDO:0006103 benign adrenal gland pheochromocytoma MONDO:0004974 NCIT:C48305 NCIT:C3326 adrenal gland pheochromocytoma @@ -2527,7 +2499,6 @@ MONDO:0006115 blast phase chronic myelogenous leukemia, BCR-ABL1 positive MONDO: MONDO:0006117 breast diffuse large B-cell lymphoma MONDO:0018905 NCIT:C40375 NCIT:C8851 diffuse large B-cell lymphoma MONDO:0006119 breast mucosa-associated lymphoid tissue lymphoma MONDO:0007650 NCIT:C35688 NCIT:C3898 MALT lymphoma MONDO:0006123 cardiac rhabdomyoma MONDO:0036688 NCIT:C6739 NCIT:C3358 rhabdomyoma -MONDO:0006126 cecum neuroendocrine tumor G1 MONDO:0005694 NCIT:C5501 NCIT:C4433 cecal neoplasm MONDO:0006126 cecum neuroendocrine tumor G1 MONDO:0006155 NCIT:C5501 NCIT:C5497 colon neuroendocrine tumor G1 MONDO:0006128 central nervous system anaplastic large cell lymphoma MONDO:0020325 NCIT:C5322 NCIT:C3720 anaplastic large cell lymphoma MONDO:0006130 central nervous system neoplasm MONDO:0002602 NCIT:C9293 NCIT:C2934 central nervous system disorder @@ -2554,10 +2525,8 @@ MONDO:0006163 colorectal serrated adenocarcinoma MONDO:0005008 NCIT:C96485 NCIT: MONDO:0006164 colorectal sessile serrated adenoma/polyp MONDO:0005484 NCIT:C83176 NCIT:C5673 colorectal adenoma MONDO:0006165 colorectal squamous cell carcinoma MONDO:0005096 NCIT:C43588 NCIT:C2929 squamous cell carcinoma MONDO:0006165 colorectal squamous cell carcinoma MONDO:0024331 NCIT:C43588 NCIT:C2955 colorectal carcinoma -MONDO:0006172 conjunctival nevus MONDO:0005073 NCIT:C4551 NCIT:C7570 melanocytic nevus MONDO:0006172 conjunctival nevus MONDO:0006105 NCIT:C4551 NCIT:C3622 benign conjunctival neoplasm MONDO:0006174 cortisol-producing adrenal cortex adenoma MONDO:0003924 NCIT:C48449 NCIT:C9003 adrenal cortex adenoma -MONDO:0006179 desmoplastic ameloblastoma MONDO:0017795 NCIT:C39758 NCIT:C4313 ameloblastoma MONDO:0006180 digestive system adenoma MONDO:0004972 NCIT:C36207 NCIT:C2855 adenoma MONDO:0006181 digestive system carcinoma MONDO:0002516 NCIT:C96963 NCIT:C4890 digestive system cancer MONDO:0006181 digestive system carcinoma MONDO:0004993 NCIT:C96963 NCIT:C2916 carcinoma @@ -2783,9 +2752,7 @@ MONDO:0006455 thymic undifferentiated carcinoma MONDO:0006451 NCIT:C35718 NCIT:C MONDO:0006456 thymoma MONDO:0018079 NCIT:C3411 NCIT:C6450 thymic epithelial neoplasm MONDO:0006458 thymoma type B3 MONDO:0016974 NCIT:C7997 NCIT:C7114 thymoma type B MONDO:0006459 thymoma type B1 MONDO:0016974 NCIT:C6887 NCIT:C7114 thymoma type B -MONDO:0006462 thyroid gland diffuse large B-cell lymphoma MONDO:0018905 NCIT:C6046 NCIT:C8851 diffuse large B-cell lymphoma MONDO:0006463 thyroid gland mucoepidermoid carcinoma MONDO:0003036 NCIT:C38762 NCIT:C3772 mucoepidermoid carcinoma -MONDO:0006464 thyroid gland mucosa-associated lymphoid tissue lymphoma MONDO:0007650 NCIT:C7601 NCIT:C3898 MALT lymphoma MONDO:0006466 thyroid gland spindle cell tumor with thymus-like differentiation MONDO:0015075 NCIT:C46105 NCIT:C4815 thyroid gland carcinoma MONDO:0006468 thyroid gland undifferentiated (anaplastic) carcinoma MONDO:0005232 NCIT:C3878 NCIT:C3780 large cell carcinoma MONDO:0006468 thyroid gland undifferentiated (anaplastic) carcinoma MONDO:0005617 NCIT:C3878 NCIT:C3692 undifferentiated carcinoma @@ -2829,7 +2796,6 @@ MONDO:0006557 hemangioma of subcutaneous tissue MONDO:0006500 NCIT:C8540 NCIT:C3 MONDO:0006563 inverted follicular keratosis MONDO:0008420 NCIT:C9007 NCIT:C9006 seborrheic keratosis MONDO:0006574 lipomatosis MONDO:0044983 NCIT:C3193 NCIT:C4502 benign lipomatous neoplasm MONDO:0006578 mediastinal lipomatosis MONDO:0006574 NCIT:C27488 NCIT:C3193 lipomatosis -MONDO:0006579 melanoacanthoma MONDO:0008420 NCIT:C27548 NCIT:C9006 seborrheic keratosis MONDO:0006593 pelvic lipomatosis MONDO:0006574 NCIT:C27486 NCIT:C3193 lipomatosis MONDO:0006612 steroid lipomatosis MONDO:0006574 NCIT:C27487 NCIT:C3193 lipomatosis MONDO:0006621 vulvar inverted follicular keratosis MONDO:0006563 NCIT:C40291 NCIT:C9007 inverted follicular keratosis @@ -3078,8 +3044,6 @@ MONDO:0016740 choriocarcinoma of the central nervous system MONDO:0003578 NCIT:C MONDO:0016740 choriocarcinoma of the central nervous system MONDO:0005207 NCIT:C7012 NCIT:C2948 choriocarcinoma MONDO:0016740 choriocarcinoma of the central nervous system MONDO:0020574 NCIT:C7012 NCIT:C100093 central nervous system nongerminomatous germ cell tumor MONDO:0016743 tumor of meninges MONDO:0006130 NCIT:C3229 NCIT:C9293 central nervous system neoplasm -MONDO:0016747 primary melanoma of the central nervous system MONDO:0003222 NCIT:C5505 NCIT:C5504 central nervous system melanocytic neoplasm -MONDO:0016747 primary melanoma of the central nervous system MONDO:0006320 NCIT:C5505 NCIT:C8711 non-cutaneous melanoma MONDO:0016755 neurofibroma MONDO:0002547 NCIT:C3272 NCIT:C4972 nerve sheath neoplasm MONDO:0016787 epithelioid trophoblastic tumor MONDO:0018944 NCIT:C6900 NCIT:C4699 gestational trophoblastic neoplasm MONDO:0016824 infantile myofibromatosis MONDO:0003342 NCIT:C3742 NCIT:C6529 benign perivascular tumor @@ -3120,10 +3084,7 @@ MONDO:0017827 malignant peripheral nerve sheath tumor MONDO:0021089 NCIT:C3798 N MONDO:0017858 acute erythroid leukemia MONDO:0015667 NCIT:C8923 NCIT:C27753 acute myeloid leukemia by FAB classification MONDO:0017858 acute erythroid leukemia MONDO:0020703 NCIT:C8923 NCIT:C7064 erythroid neoplasm MONDO:0017884 papillary renal cell carcinoma MONDO:0002512 NCIT:C6975 NCIT:C2853 papillary adenocarcinoma -MONDO:0017884 papillary renal cell carcinoma MONDO:0005549 NCIT:C6975 NCIT:C9385 renal cell adenocarcinoma -MONDO:0017885 chromophobe renal cell carcinoma MONDO:0005549 NCIT:C4146 NCIT:C9385 renal cell adenocarcinoma MONDO:0017887 renal cell carcinoma associated with neuroblastoma MONDO:0005549 NCIT:C100051 NCIT:C9385 renal cell adenocarcinoma -MONDO:0017890 tubulocystic renal cell carcinoma MONDO:0005549 NCIT:C126303 NCIT:C9385 renal cell adenocarcinoma MONDO:0017895 familial papillary or follicular thyroid carcinoma MONDO:0015447 NCIT:C118829 NCIT:C7153 differentiated thyroid carcinoma MONDO:0018031 granulomatous slack skin disease MONDO:0045071 NCIT:C35464 NCIT:C39644 mycosis fungoides variant MONDO:0018055 pediatric hepatocellular carcinoma MONDO:0007256 NCIT:C7955 NCIT:C3099 hepatocellular carcinoma @@ -3201,12 +3162,9 @@ MONDO:0019023 cutaneous mastocytosis MONDO:0007950 NCIT:C7137 NCIT:C84269 mastoc MONDO:0019025 extracutaneous mastocytoma MONDO:0003079 NCIT:C7136 NCIT:C9303 mastocytoma MONDO:0019035 pancreatoblastoma MONDO:0002116 NCIT:C4265 NCIT:C7430 malignant exocrine pancreas neoplasm MONDO:0019077 warty dyskeratoma MONDO:0002093 NCIT:C4087 NCIT:C7419 acanthoma -MONDO:0019086 carcinoma of esophagus MONDO:0006181 NCIT:C3513 NCIT:C96963 digestive system carcinoma MONDO:0019086 carcinoma of esophagus MONDO:0007576 NCIT:C3513 NCIT:C7478 esophageal cancer MONDO:0019134 central neurocytoma MONDO:0002682 NCIT:C3791 NCIT:C2937 cerebral ventricle cancer MONDO:0019134 central neurocytoma MONDO:0016729 NCIT:C3791 NCIT:C4747 mixed neuronal-glial tumor -MONDO:0019210 cutaneous neuroendocrine carcinoma MONDO:0002656 NCIT:C9231 NCIT:C4914 skin carcinoma -MONDO:0019210 cutaneous neuroendocrine carcinoma MONDO:0003363 NCIT:C9231 NCIT:C4574 malignant dermis tumor MONDO:0019328 macrocystic lymphatic malformation MONDO:0002013 NCIT:C53316 NCIT:C8965 lymphangioma MONDO:0019373 desmoplastic small round cell tumor MONDO:0006974 NCIT:C8300 NCIT:C3746 small cell sarcoma MONDO:0019373 desmoplastic small round cell tumor MONDO:0018078 NCIT:C8300 NCIT:C9306 soft tissue sarcoma @@ -3237,7 +3195,6 @@ MONDO:0019803 angioma serpiginosum MONDO:0003110 NCIT:C3926 NCIT:C4905 skin hema MONDO:0019954 pancreatic neuroendocrine tumor MONDO:0000386 NCIT:C27720 NCIT:C95404 digestive system neuroendocrine tumor, grade 1/2 MONDO:0019954 pancreatic neuroendocrine tumor MONDO:0005815 NCIT:C27720 NCIT:C27031 pancreatic neuroendocrine neoplasm MONDO:0019962 thyroid lymphoma MONDO:0002108 NCIT:C5265 NCIT:C7510 thyroid cancer -MONDO:0019962 thyroid lymphoma MONDO:0017207 NCIT:C5265 NCIT:C7185 primary organ-specific lymphoma MONDO:0020076 myeloproliferative neoplasm MONDO:0005170 NCIT:C4345 NCIT:C9290 myeloid neoplasm MONDO:0020076 myeloproliferative neoplasm MONDO:0021138 NCIT:C4345 NCIT:C35501 bone marrow cancer MONDO:0020204 conjunctival tumor MONDO:0006170 NCIT:C2961 NCIT:C27605 conjunctival disorder @@ -3278,11 +3235,9 @@ MONDO:0020633 anaplastic cancer MONDO:0004992 NCIT:C36025 NCIT:C9305 cancer MONDO:0020634 grade III meningioma MONDO:0016642 NCIT:C38938 NCIT:C3230 meningioma MONDO:0020635 anaplastic meningioma MONDO:0020633 NCIT:C4051 NCIT:C36025 anaplastic cancer MONDO:0020635 anaplastic meningioma MONDO:0020634 NCIT:C4051 NCIT:C38938 grade III meningioma -MONDO:0020638 superficial spreading melanoma MONDO:0005012 NCIT:C9152 NCIT:C3510 cutaneous melanoma MONDO:0020641 respiratory tract neoplasm MONDO:0005087 NCIT:C3355 NCIT:C26871 respiratory system disorder MONDO:0020644 lung non-Hodgkin lymphoma MONDO:0003987 NCIT:C5684 NCIT:C4794 lung lymphoma MONDO:0020644 lung non-Hodgkin lymphoma MONDO:0018908 NCIT:C5684 NCIT:C3211 non-Hodgkin lymphoma -MONDO:0020646 ocular adnexal lymphoma MONDO:0018908 NCIT:C88145 NCIT:C3211 non-Hodgkin lymphoma MONDO:0020649 warty carcinoma of the penis MONDO:0020656 NCIT:C6981 NCIT:C27682 human papillomavirus-related penile squamous cell carcinoma MONDO:0020653 vaginal adenocarcinoma MONDO:0001704 NCIT:C7981 NCIT:C40250 vaginal glandular neoplasm MONDO:0020653 vaginal adenocarcinoma MONDO:0004970 NCIT:C7981 NCIT:C2852 adenocarcinoma @@ -3664,7 +3619,6 @@ MONDO:0021538 verrucous carcinoma of oral cavity MONDO:0004958 NCIT:C8174 NCIT:C MONDO:0021538 verrucous carcinoma of oral cavity MONDO:0006006 NCIT:C8174 NCIT:C3781 verrucous carcinoma MONDO:0021542 hemangioma of choroid MONDO:0006500 NCIT:C4562 NCIT:C3085 hemangioma MONDO:0021542 hemangioma of choroid MONDO:0021487 NCIT:C4562 NCIT:C3625 benign neoplasm of choroid -MONDO:0021543 hemangioma of gingiva MONDO:0006500 NCIT:C4831 NCIT:C3085 hemangioma MONDO:0021543 hemangioma of gingiva MONDO:0021491 NCIT:C4831 NCIT:C4598 benign neoplasm of gum MONDO:0021545 myomatous neoplasm MONDO:0002616 NCIT:C4063 NCIT:C7059 mesenchymal cell neoplasm MONDO:0021576 fallopian tube endometrioid tumor MONDO:0021092 NCIT:C40111 NCIT:C3032 fallopian tube neoplasm @@ -3701,7 +3655,6 @@ MONDO:0021663 sarcomatoid squamous cell carcinoma MONDO:0006406 NCIT:C27084 NCIT MONDO:0021812 adnexal spiradenoma/cylindroma of a sweat gland MONDO:0021489 NCIT:C27094 NCIT:C4879 benign neoplasm of sweat gland MONDO:0021879 small cell variant anaplastic large cell lymphoma MONDO:0020325 NCIT:C7208 NCIT:C3720 anaplastic large cell lymphoma MONDO:0022578 childhood bladder carcinoma MONDO:0004986 NCIT:C118816 NCIT:C4912 urinary bladder carcinoma -MONDO:0022642 childhood carcinoid tumor MONDO:0005369 NCIT:C118810 NCIT:C2915 carcinoid tumor MONDO:0022963 desmoplastic infantile astrocytoma MONDO:0016729 NCIT:C9476 NCIT:C4747 mixed neuronal-glial tumor MONDO:0022965 desmoplastic infantile ganglioglioma MONDO:0016729 NCIT:C4738 NCIT:C4747 mixed neuronal-glial tumor MONDO:0023122 familial prostate carcinoma MONDO:0005159 NCIT:C103817 NCIT:C4863 prostate carcinoma @@ -3965,6 +3918,7 @@ MONDO:0045052 benign osteogenic neoplasm MONDO:0045053 NCIT:C6602 NCIT:C6603 ost MONDO:0045053 osteogenic neoplasm MONDO:0002616 NCIT:C6603 NCIT:C7059 mesenchymal cell neoplasm MONDO:0045055 glycogen-rich carcinoma MONDO:0004993 NCIT:C4153 NCIT:C2916 carcinoma MONDO:0045056 grade II meningioma MONDO:0016642 NCIT:C38937 NCIT:C3230 meningioma +MONDO:0045060 intraductal cribriform breast adenocarcinoma MONDO:0005023 NCIT:C5138 NCIT:C2924 ductal breast carcinoma in situ MONDO:0045063 major salivary gland adenoid cystic carcinoma MONDO:0003175 NCIT:C5905 NCIT:C8026 salivary gland adenoid cystic carcinoma MONDO:0045063 major salivary gland adenoid cystic carcinoma MONDO:0006284 NCIT:C5905 NCIT:C5907 major salivary gland carcinoma MONDO:0045068 minor salivary gland adenoid cystic carcinoma MONDO:0003175 NCIT:C5936 NCIT:C8026 salivary gland adenoid cystic carcinoma diff --git a/src/ontology/reports/ncit_excluded_terms_in_mondo_xrefs.tsv b/src/ontology/reports/ncit_excluded_terms_in_mondo_xrefs.tsv index b7456968..ae4f932f 100644 --- a/src/ontology/reports/ncit_excluded_terms_in_mondo_xrefs.tsv +++ b/src/ontology/reports/ncit_excluded_terms_in_mondo_xrefs.tsv @@ -223,6 +223,7 @@ NCIT:C98583 Type 1 Thanatophoric Dysplasia True False True True NCIT:C2986 Type 1 Diabetes Mellitus True False True True NCIT:C113824 Twin-Twin Transfusion Syndrome True False True True NCIT:C26900 Turner Syndrome True False True True +NCIT:C43352 Turban Tumor Syndrome True False True True NCIT:C119051 Tumor Necrosis Factor Receptor 1-Associated Periodic Syndrome True False True True NCIT:C3425 Tumor Lysis Syndrome True False True True NCIT:C85208 Tularemia True False True True @@ -303,6 +304,7 @@ NCIT:C98585 Total Anomalous Pulmonary Venous Return True False True True NCIT:C156361 Torsion Dystonia 6 True False True True NCIT:C40553 Tooth and Nail Syndrome True False True True NCIT:C116006 Tonsillitis True False True True +NCIT:C3022 Tonic-Clonic Epilepsy True False True True NCIT:C85193 Tolosa-Hunt Syndrome True False True True NCIT:C112181 Tinea Infection True False True True NCIT:C34579 Tick-Borne Viral Encephalitis True False True True @@ -717,7 +719,6 @@ NCIT:C34966 Pyloric Stenosis True False True True NCIT:C34965 Pyelonephritis True False True True NCIT:C34964 Pyelitis True False True True NCIT:C131187 Pycnodysostosis True False True True -NCIT:C3963 Purine-Nucleoside Phosphorylase Deficiency True False True True NCIT:C176817 Purine Nucleoside Phosphorylase Deficiency True False True True NCIT:C34974 Pure Red Cell Aplasia True False True True NCIT:C85039 Pulmonary Veno-Occlusive Disease True False True True @@ -1015,7 +1016,7 @@ NCIT:C61233 Paroxysmal Nocturnal Hemoglobinuria True False True True NCIT:C125385 Paroxysmal Extreme Pain Disorder True False True True NCIT:C114281 Parotitis True False True True NCIT:C79702 Paronychia True False True True -NCIT:C26845 Parkinson's Disease True False True True +NCIT:C26845 Parkinson Disease True False True True NCIT:C54102 Parinaud Syndrome True False True True NCIT:C131575 Parietal Lobe Ependymal Tumor True False True True NCIT:C34897 Paratyphoid Fever True False True True @@ -1381,7 +1382,6 @@ NCIT:C35548 Monoclonal Gammopathy True False True True NCIT:C131839 Monocarboxylate Transporter 1 Hyperinsulinism True False True True NCIT:C128421 Monkeypox True False True True NCIT:C84894 Monilethrix True False True True -NCIT:C3945 Mongolian Spot True False True True NCIT:C35770 Monckeberg Arteriosclerosis True False True True NCIT:C84893 Mobius Syndrome True False True True NCIT:C118846 Miyoshi Muscular Dystrophy 1 True False True True @@ -1413,6 +1413,7 @@ NCIT:C117004 Migraine Without Aura True False True True NCIT:C117005 Migraine With Aura True False True True NCIT:C89715 Migraine True False True True NCIT:C128424 Middle East Respiratory Syndrome True False True True +NCIT:C6933 Middle Ear Polyp True False True True NCIT:C3654 Middle Ear Cholesteatoma True False True True NCIT:C84891 Microsporidiosis True False True True NCIT:C70549 Microscopic Polyarteritis True False True True @@ -2003,7 +2004,6 @@ NCIT:C27039 Hemophilic Arthritis True False True True NCIT:C26721 Hemophilia B True False True True NCIT:C27146 Hemophilia A True False True True NCIT:C3093 Hemophilia True False True True -NCIT:C35439 Hemophagocytic Syndrome True False True True NCIT:C34792 Hemophagocytic Lymphohistiocytosis True False True True NCIT:C75545 Hemolytic Uremic Syndrome True False True True NCIT:C101304 Hemolytic Disease of the Newborn True False True True @@ -2065,7 +2065,6 @@ NCIT:C3065 Granuloma Inguinale True False True True NCIT:C3470 Granuloma Annulare True False True True NCIT:C2863 Granulocytopenia True False True True NCIT:C34651 Granular Corneal Dystrophy True False True True -NCIT:C3022 Grand Mal Epilepsy True False True True NCIT:C3063 Graft Versus Host Disease True False True True NCIT:C28082 Grade 4 True False True True NCIT:C28079 Grade 3 True False True True @@ -2285,6 +2284,7 @@ NCIT:C35706 Exudative Glomerulonephritis True False True True NCIT:C34369 Extrinsic Allergic Alveolitis True False True True NCIT:C7760 Extratemporal Epilepsy True False True True NCIT:C97069 Extrahepatic Biliary Atresia True False True True +NCIT:C4366 External Ear Polyp True False True True NCIT:C128417 Extensively Drug-Resistant Tuberculosis True False True True NCIT:C92562 Expressive Language Disorder True False True True NCIT:C3029 Exostosis True False True True @@ -2300,7 +2300,7 @@ NCIT:C26950 Esophageal Ulcer True False True True NCIT:C3953 Esophageal Leukoplakia True False True True NCIT:C87072 Esophageal Atresia True False True True NCIT:C101039 Escobar Syndrome True False True True -NCIT:C34594 Escherichia Coli Infection True False True True +NCIT:C34594 Escherichia coli Infection True False True True NCIT:C84698 Erythropoietic Protoporphyria True False True True NCIT:C84697 Erythropoietic Porphyria True False True True NCIT:C3025 Erythroplakia True False True True @@ -2687,10 +2687,10 @@ NCIT:C98876 Congenital Hydrocephalus True False True True NCIT:C97071 Congenital Hepatic Fibrosis True False True True NCIT:C104003 Congenital Hematological Disorder True False True True NCIT:C95834 Congenital Heart Disease True False True True +NCIT:C4675 Congenital Granular Cell Epulis True False True True NCIT:C50648 Congenital Glaucoma True False True True NCIT:C120046 Congenital Fiber-Type Disproportion True False True True NCIT:C27049 Congenital Eyelid Ptosis True False True True -NCIT:C4675 Congenital Epulis True False True True NCIT:C34566 Congenital Ectopic Lens True False True True NCIT:C84646 Congenital Dyserythropoietic Anemia True False True True NCIT:C126874 Congenital Disorder of Glycosylation Type Ij True False True True @@ -2702,6 +2702,7 @@ NCIT:C126869 Congenital Disorder of Glycosylation Type Ic True False True True NCIT:C126868 Congenital Disorder of Glycosylation Type Ia True False True True NCIT:C126746 Congenital Disorder of Deglycosylation True False True True NCIT:C98893 Congenital Diaphragmatic Hernia True False True True +NCIT:C3945 Congenital Dermal Melanocytosis True False True True NCIT:C122427 Congenital Cytomegaloviral Infection True False True True NCIT:C98892 Congenital Cystic Adenomatoid Malformation of the Lung True False True True NCIT:C129865 Congenital Contractural Arachnodactyly True False True True diff --git a/src/ontology/reports/ncit_excluded_terms_in_mondo_xrefs_summary.tsv b/src/ontology/reports/ncit_excluded_terms_in_mondo_xrefs_summary.tsv index 10053bbc..6943bf7b 100644 --- a/src/ontology/reports/ncit_excluded_terms_in_mondo_xrefs_summary.tsv +++ b/src/ontology/reports/ncit_excluded_terms_in_mondo_xrefs_summary.tsv @@ -1,2 +1,2 @@ n_in1_notIn2_in3 pct_in1_notIn2_in3__over_in1 -3478 0.0191 +3479 0.0187 diff --git a/src/ontology/reports/ncit_exclusion_reasons.robot.template.tsv b/src/ontology/reports/ncit_exclusion_reasons.robot.template.tsv index c0b60baf..1e5f9b42 100644 --- a/src/ontology/reports/ncit_exclusion_reasons.robot.template.tsv +++ b/src/ontology/reports/ncit_exclusion_reasons.robot.template.tsv @@ -24648,7 +24648,6 @@ NCIT:C122828 MONDO:excludeNonDisease NCIT:C122829 MONDO:excludeNonDisease NCIT:C122830 MONDO:excludeNonDisease NCIT:C122831 MONDO:excludeNonDisease -NCIT:C122832 MONDO:excludeNonDisease NCIT:C122833 MONDO:excludeNonDisease NCIT:C122834 MONDO:excludeNonDisease NCIT:C122835 MONDO:excludeNonDisease @@ -47774,7 +47773,6 @@ NCIT:C147308 MONDO:excludeNonDisease NCIT:C147309 MONDO:excludeNonDisease NCIT:C147310 MONDO:excludeNonDisease NCIT:C147311 MONDO:excludeNonDisease -NCIT:C147312 MONDO:excludeNonDisease NCIT:C147313 MONDO:excludeNonDisease NCIT:C147314 MONDO:excludeNonDisease NCIT:C147315 MONDO:excludeNonDisease @@ -53065,7 +53063,6 @@ NCIT:C154136 MONDO:excludeNonDisease NCIT:C154137 MONDO:excludeNonDisease NCIT:C154138 MONDO:excludeNonDisease NCIT:C154139 MONDO:excludeNonDisease -NCIT:C15414 MONDO:excludeNonDisease NCIT:C154140 MONDO:excludeNonDisease NCIT:C154141 MONDO:excludeNonDisease NCIT:C154142 MONDO:excludeNonDisease @@ -54787,7 +54784,6 @@ NCIT:C156048 MONDO:excludeNonDisease NCIT:C156049 MONDO:excludeNonDisease NCIT:C15605 MONDO:excludeNonDisease NCIT:C156051 MONDO:excludeNonDisease -NCIT:C156052 MONDO:excludeNonDisease NCIT:C156053 MONDO:excludeNonDisease NCIT:C156054 MONDO:excludeNonDisease NCIT:C156055 MONDO:excludeNonDisease @@ -57734,7 +57730,6 @@ NCIT:C15925 MONDO:excludeNonDisease NCIT:C159253 MONDO:excludeNonDisease NCIT:C159254 MONDO:excludeNonDisease NCIT:C159255 MONDO:excludeNonDisease -NCIT:C159256 MONDO:excludeNonDisease NCIT:C159257 MONDO:excludeNonDisease NCIT:C159258 MONDO:excludeNonDisease NCIT:C159259 MONDO:excludeNonDisease @@ -68315,7 +68310,6 @@ NCIT:C171536 MONDO:excludeNonDisease NCIT:C171537 MONDO:excludeNonDisease NCIT:C171538 MONDO:excludeNonDisease NCIT:C171539 MONDO:excludeNonDisease -NCIT:C17154 MONDO:excludeNonDisease NCIT:C171540 MONDO:excludeNonDisease NCIT:C171541 MONDO:excludeNonDisease NCIT:C171542 MONDO:excludeNonDisease @@ -69513,7 +69507,6 @@ NCIT:C172801 MONDO:excludeNonDisease NCIT:C172802 MONDO:excludeNonDisease NCIT:C172805 MONDO:excludeNonDisease NCIT:C172807 MONDO:excludeNonDisease -NCIT:C172809 MONDO:excludeNonDisease NCIT:C17281 MONDO:excludeNonDisease NCIT:C172816 MONDO:excludeNonDisease NCIT:C172817 MONDO:excludeNonDisease @@ -70111,7 +70104,6 @@ NCIT:C173527 MONDO:excludeNonDisease NCIT:C173528 MONDO:excludeNonDisease NCIT:C17353 MONDO:excludeNonDisease NCIT:C173535 MONDO:excludeNonDisease -NCIT:C173536 MONDO:excludeNonDisease NCIT:C173537 MONDO:excludeNonDisease NCIT:C173538 MONDO:excludeNonDisease NCIT:C173539 MONDO:excludeNonDisease @@ -70316,7 +70308,6 @@ NCIT:C173791 MONDO:excludeNonDisease NCIT:C173792 MONDO:excludeNonDisease NCIT:C173794 MONDO:excludeNonDisease NCIT:C173796 MONDO:excludeNonDisease -NCIT:C173798 MONDO:excludeNonDisease NCIT:C17380 MONDO:excludeNonDisease NCIT:C173800 MONDO:excludeNonDisease NCIT:C173801 MONDO:excludeNonDisease @@ -72337,7 +72328,6 @@ NCIT:C175852 MONDO:excludeNonDisease NCIT:C175853 MONDO:excludeNonDisease NCIT:C175854 MONDO:excludeNonDisease NCIT:C175855 MONDO:excludeNonDisease -NCIT:C175856 MONDO:excludeNonDisease NCIT:C175857 MONDO:excludeNonDisease NCIT:C175858 MONDO:excludeNonDisease NCIT:C175859 MONDO:excludeNonDisease @@ -73143,7 +73133,6 @@ NCIT:C176619 MONDO:excludeNonDisease NCIT:C17662 MONDO:excludeNonDisease NCIT:C176620 MONDO:excludeNonDisease NCIT:C176621 MONDO:excludeNonDisease -NCIT:C176622 MONDO:excludeNonDisease NCIT:C176623 MONDO:excludeNonDisease NCIT:C176624 MONDO:excludeNonDisease NCIT:C176625 MONDO:excludeNonDisease @@ -78810,6 +78799,7 @@ NCIT:C182353 MONDO:excludeNonDisease NCIT:C182354 MONDO:excludeNonDisease NCIT:C182355 MONDO:excludeNonDisease NCIT:C182356 MONDO:excludeNonDisease +NCIT:C182357 MONDO:excludeNonDisease NCIT:C182358 MONDO:excludeNonDisease NCIT:C182359 MONDO:excludeNonDisease NCIT:C182360 MONDO:excludeNonDisease @@ -83741,7 +83731,6 @@ NCIT:C187030 MONDO:excludeNonDisease NCIT:C187031 MONDO:excludeNonDisease NCIT:C187032 MONDO:excludeNonDisease NCIT:C187033 MONDO:excludeNonDisease -NCIT:C187034 MONDO:excludeNonDisease NCIT:C187035 MONDO:excludeNonDisease NCIT:C187036 MONDO:excludeNonDisease NCIT:C187037 MONDO:excludeNonDisease @@ -86577,7 +86566,6 @@ NCIT:C189902 MONDO:excludeNonDisease NCIT:C189903 MONDO:excludeNonDisease NCIT:C189904 MONDO:excludeNonDisease NCIT:C189905 MONDO:excludeNonDisease -NCIT:C189906 MONDO:excludeNonDisease NCIT:C189907 MONDO:excludeNonDisease NCIT:C189908 MONDO:excludeNonDisease NCIT:C189909 MONDO:excludeNonDisease @@ -88385,7 +88373,6 @@ NCIT:C191756 MONDO:excludeNonDisease NCIT:C191757 MONDO:excludeNonDisease NCIT:C191758 MONDO:excludeNonDisease NCIT:C191759 MONDO:excludeNonDisease -NCIT:C191760 MONDO:excludeNonDisease NCIT:C191761 MONDO:excludeNonDisease NCIT:C191762 MONDO:excludeNonDisease NCIT:C191765 MONDO:excludeNonDisease @@ -94925,7 +94912,6 @@ NCIT:C198024 MONDO:excludeNonDisease NCIT:C198025 MONDO:excludeNonDisease NCIT:C198026 MONDO:excludeNonDisease NCIT:C198028 MONDO:excludeNonDisease -NCIT:C198029 MONDO:excludeNonDisease NCIT:C19803 MONDO:excludeNonDisease NCIT:C198033 MONDO:excludeNonDisease NCIT:C198037 MONDO:excludeNonDisease @@ -97288,7 +97274,6 @@ NCIT:C200519 MONDO:excludeNonDisease NCIT:C20052 MONDO:excludeNonDisease NCIT:C200521 MONDO:excludeNonDisease NCIT:C200522 MONDO:excludeNonDisease -NCIT:C200523 MONDO:excludeNonDisease NCIT:C200525 MONDO:excludeNonDisease NCIT:C200526 MONDO:excludeNonDisease NCIT:C200527 MONDO:excludeNonDisease @@ -98375,441 +98360,4021 @@ NCIT:C201554 MONDO:excludeNonDisease NCIT:C201555 MONDO:excludeNonDisease NCIT:C201556 MONDO:excludeNonDisease NCIT:C201557 MONDO:excludeNonDisease +NCIT:C201558 MONDO:excludeNonDisease +NCIT:C201559 MONDO:excludeNonDisease NCIT:C20156 MONDO:excludeNonDisease +NCIT:C201560 MONDO:excludeNonDisease +NCIT:C201561 MONDO:excludeNonDisease +NCIT:C201562 MONDO:excludeNonDisease +NCIT:C201563 MONDO:excludeNonDisease +NCIT:C201564 MONDO:excludeNonDisease +NCIT:C201565 MONDO:excludeNonDisease +NCIT:C201566 MONDO:excludeNonDisease +NCIT:C201567 MONDO:excludeNonDisease +NCIT:C201568 MONDO:excludeNonDisease +NCIT:C201569 MONDO:excludeNonDisease NCIT:C20157 MONDO:excludeNonDisease +NCIT:C201570 MONDO:excludeNonDisease +NCIT:C201571 MONDO:excludeNonDisease +NCIT:C201572 MONDO:excludeNonDisease +NCIT:C201573 MONDO:excludeNonDisease +NCIT:C201574 MONDO:excludeNonDisease +NCIT:C201576 MONDO:excludeNonDisease +NCIT:C201577 MONDO:excludeNonDisease +NCIT:C201578 MONDO:excludeNonDisease +NCIT:C201579 MONDO:excludeNonDisease NCIT:C20158 MONDO:excludeNonDisease +NCIT:C201580 MONDO:excludeNonDisease +NCIT:C201581 MONDO:excludeNonDisease +NCIT:C201582 MONDO:excludeNonDisease +NCIT:C201583 MONDO:excludeNonDisease +NCIT:C201584 MONDO:excludeNonDisease +NCIT:C201585 MONDO:excludeNonDisease +NCIT:C201586 MONDO:excludeNonDisease +NCIT:C201587 MONDO:excludeNonDisease +NCIT:C201588 MONDO:excludeNonDisease +NCIT:C201589 MONDO:excludeNonDisease NCIT:C20159 MONDO:excludeNonDisease +NCIT:C201590 MONDO:excludeNonDisease +NCIT:C201591 MONDO:excludeNonDisease +NCIT:C201592 MONDO:excludeNonDisease +NCIT:C201593 MONDO:excludeNonDisease +NCIT:C201594 MONDO:excludeNonDisease +NCIT:C201595 MONDO:excludeNonDisease +NCIT:C201596 MONDO:excludeNonDisease +NCIT:C201597 MONDO:excludeNonDisease +NCIT:C201598 MONDO:excludeNonDisease +NCIT:C201599 MONDO:excludeNonDisease NCIT:C2016 MONDO:excludeNonDisease NCIT:C20160 MONDO:excludeNonDisease +NCIT:C201600 MONDO:excludeNonDisease +NCIT:C201601 MONDO:excludeNonDisease +NCIT:C201602 MONDO:excludeNonDisease +NCIT:C201603 MONDO:excludeNonDisease +NCIT:C201604 MONDO:excludeNonDisease +NCIT:C201605 MONDO:excludeNonDisease +NCIT:C201606 MONDO:excludeNonDisease +NCIT:C201607 MONDO:excludeNonDisease +NCIT:C201608 MONDO:excludeNonDisease +NCIT:C201609 MONDO:excludeNonDisease NCIT:C20161 MONDO:excludeNonDisease +NCIT:C201610 MONDO:excludeNonDisease +NCIT:C201611 MONDO:excludeNonDisease +NCIT:C201612 MONDO:excludeNonDisease +NCIT:C201613 MONDO:excludeNonDisease +NCIT:C201614 MONDO:excludeNonDisease +NCIT:C201615 MONDO:excludeNonDisease +NCIT:C201616 MONDO:excludeNonDisease +NCIT:C201617 MONDO:excludeNonDisease +NCIT:C201618 MONDO:excludeNonDisease +NCIT:C201619 MONDO:excludeNonDisease NCIT:C20162 MONDO:excludeNonDisease +NCIT:C201621 MONDO:excludeNonDisease +NCIT:C201622 MONDO:excludeNonDisease +NCIT:C201623 MONDO:excludeNonDisease +NCIT:C201624 MONDO:excludeNonDisease +NCIT:C201625 MONDO:excludeNonDisease +NCIT:C201626 MONDO:excludeNonDisease +NCIT:C201627 MONDO:excludeNonDisease +NCIT:C201628 MONDO:excludeNonDisease +NCIT:C201629 MONDO:excludeNonDisease NCIT:C20163 MONDO:excludeNonDisease +NCIT:C201630 MONDO:excludeNonDisease +NCIT:C201631 MONDO:excludeNonDisease +NCIT:C201632 MONDO:excludeNonDisease +NCIT:C201633 MONDO:excludeNonDisease +NCIT:C201638 MONDO:excludeNonDisease +NCIT:C201639 MONDO:excludeNonDisease NCIT:C20164 MONDO:excludeNonDisease +NCIT:C201640 MONDO:excludeNonDisease +NCIT:C201641 MONDO:excludeNonDisease +NCIT:C201642 MONDO:excludeNonDisease +NCIT:C201643 MONDO:excludeNonDisease +NCIT:C201644 MONDO:excludeNonDisease +NCIT:C201645 MONDO:excludeNonDisease +NCIT:C201646 MONDO:excludeNonDisease +NCIT:C201647 MONDO:excludeNonDisease +NCIT:C201648 MONDO:excludeNonDisease +NCIT:C201649 MONDO:excludeNonDisease NCIT:C20165 MONDO:excludeNonDisease +NCIT:C201650 MONDO:excludeNonDisease +NCIT:C201651 MONDO:excludeNonDisease +NCIT:C201652 MONDO:excludeNonDisease +NCIT:C201653 MONDO:excludeNonDisease +NCIT:C201654 MONDO:excludeNonDisease +NCIT:C201655 MONDO:excludeNonDisease +NCIT:C201656 MONDO:excludeNonDisease +NCIT:C201657 MONDO:excludeNonDisease +NCIT:C201658 MONDO:excludeNonDisease +NCIT:C201659 MONDO:excludeNonDisease NCIT:C20166 MONDO:excludeNonDisease +NCIT:C201660 MONDO:excludeNonDisease +NCIT:C201661 MONDO:excludeNonDisease +NCIT:C201662 MONDO:excludeNonDisease +NCIT:C201663 MONDO:excludeNonDisease +NCIT:C201664 MONDO:excludeNonDisease +NCIT:C201665 MONDO:excludeNonDisease +NCIT:C201666 MONDO:excludeNonDisease +NCIT:C201667 MONDO:excludeNonDisease +NCIT:C201668 MONDO:excludeNonDisease +NCIT:C201669 MONDO:excludeNonDisease NCIT:C20167 MONDO:excludeNonDisease +NCIT:C201670 MONDO:excludeNonDisease +NCIT:C201671 MONDO:excludeNonDisease +NCIT:C201672 MONDO:excludeNonDisease +NCIT:C201673 MONDO:excludeNonDisease +NCIT:C201674 MONDO:excludeNonDisease +NCIT:C201675 MONDO:excludeNonDisease +NCIT:C201676 MONDO:excludeNonDisease +NCIT:C201677 MONDO:excludeNonDisease +NCIT:C201678 MONDO:excludeNonDisease +NCIT:C201679 MONDO:excludeNonDisease NCIT:C20168 MONDO:excludeNonDisease +NCIT:C201680 MONDO:excludeNonDisease +NCIT:C201681 MONDO:excludeNonDisease +NCIT:C201682 MONDO:excludeNonDisease +NCIT:C201683 MONDO:excludeNonDisease +NCIT:C201684 MONDO:excludeNonDisease +NCIT:C201685 MONDO:excludeNonDisease +NCIT:C201686 MONDO:excludeNonDisease +NCIT:C201687 MONDO:excludeNonDisease +NCIT:C201688 MONDO:excludeNonDisease +NCIT:C201689 MONDO:excludeNonDisease NCIT:C20169 MONDO:excludeNonDisease +NCIT:C201690 MONDO:excludeNonDisease +NCIT:C201691 MONDO:excludeNonDisease +NCIT:C201692 MONDO:excludeNonDisease +NCIT:C201693 MONDO:excludeNonDisease +NCIT:C201694 MONDO:excludeNonDisease +NCIT:C201695 MONDO:excludeNonDisease +NCIT:C201696 MONDO:excludeNonDisease +NCIT:C201697 MONDO:excludeNonDisease +NCIT:C201698 MONDO:excludeNonDisease +NCIT:C201699 MONDO:excludeNonDisease NCIT:C2017 MONDO:excludeNonDisease NCIT:C20170 MONDO:excludeNonDisease +NCIT:C201700 MONDO:excludeNonDisease +NCIT:C201701 MONDO:excludeNonDisease +NCIT:C201702 MONDO:excludeNonDisease +NCIT:C201703 MONDO:excludeNonDisease +NCIT:C201704 MONDO:excludeNonDisease +NCIT:C201705 MONDO:excludeNonDisease +NCIT:C201706 MONDO:excludeNonDisease +NCIT:C201707 MONDO:excludeNonDisease +NCIT:C201708 MONDO:excludeNonDisease +NCIT:C201709 MONDO:excludeNonDisease NCIT:C20171 MONDO:excludeNonDisease +NCIT:C201710 MONDO:excludeNonDisease +NCIT:C201711 MONDO:excludeNonDisease +NCIT:C201712 MONDO:excludeNonDisease +NCIT:C201713 MONDO:excludeNonDisease +NCIT:C201714 MONDO:excludeNonDisease +NCIT:C201715 MONDO:excludeNonDisease +NCIT:C201716 MONDO:excludeNonDisease +NCIT:C201717 MONDO:excludeNonDisease +NCIT:C201718 MONDO:excludeNonDisease +NCIT:C201719 MONDO:excludeNonDisease NCIT:C20172 MONDO:excludeNonDisease +NCIT:C201720 MONDO:excludeNonDisease +NCIT:C201721 MONDO:excludeNonDisease +NCIT:C201722 MONDO:excludeNonDisease +NCIT:C201723 MONDO:excludeNonDisease +NCIT:C201724 MONDO:excludeNonDisease +NCIT:C201725 MONDO:excludeNonDisease +NCIT:C201726 MONDO:excludeNonDisease +NCIT:C201727 MONDO:excludeNonDisease +NCIT:C201728 MONDO:excludeNonDisease +NCIT:C201729 MONDO:excludeNonDisease NCIT:C20173 MONDO:excludeNonDisease +NCIT:C201730 MONDO:excludeNonDisease +NCIT:C201731 MONDO:excludeNonDisease +NCIT:C201732 MONDO:excludeNonDisease +NCIT:C201733 MONDO:excludeNonDisease +NCIT:C201734 MONDO:excludeNonDisease +NCIT:C201735 MONDO:excludeNonDisease +NCIT:C201736 MONDO:excludeNonDisease +NCIT:C201737 MONDO:excludeNonDisease +NCIT:C201738 MONDO:excludeNonDisease +NCIT:C201739 MONDO:excludeNonDisease NCIT:C20174 MONDO:excludeNonDisease +NCIT:C201740 MONDO:excludeNonDisease +NCIT:C201741 MONDO:excludeNonDisease +NCIT:C201744 MONDO:excludeNonDisease +NCIT:C201745 MONDO:excludeNonDisease NCIT:C20175 MONDO:excludeNonDisease +NCIT:C201750 MONDO:excludeNonDisease +NCIT:C201751 MONDO:excludeNonDisease +NCIT:C201752 MONDO:excludeNonDisease +NCIT:C201753 MONDO:excludeNonDisease +NCIT:C201754 MONDO:excludeNonDisease +NCIT:C201755 MONDO:excludeNonDisease +NCIT:C201756 MONDO:excludeNonDisease +NCIT:C201757 MONDO:excludeNonDisease +NCIT:C201758 MONDO:excludeNonDisease +NCIT:C201759 MONDO:excludeNonDisease NCIT:C20176 MONDO:excludeNonDisease +NCIT:C201760 MONDO:excludeNonDisease +NCIT:C201761 MONDO:excludeNonDisease +NCIT:C201762 MONDO:excludeNonDisease +NCIT:C201763 MONDO:excludeNonDisease +NCIT:C201765 MONDO:excludeNonDisease +NCIT:C201769 MONDO:excludeNonDisease NCIT:C20177 MONDO:excludeNonDisease +NCIT:C201771 MONDO:excludeNonDisease +NCIT:C201773 MONDO:excludeNonDisease +NCIT:C201774 MONDO:excludeNonDisease +NCIT:C201775 MONDO:excludeNonDisease +NCIT:C201776 MONDO:excludeNonDisease +NCIT:C201777 MONDO:excludeNonDisease +NCIT:C201778 MONDO:excludeNonDisease +NCIT:C201779 MONDO:excludeNonDisease NCIT:C20178 MONDO:excludeNonDisease +NCIT:C201780 MONDO:excludeNonDisease +NCIT:C201782 MONDO:excludeNonDisease +NCIT:C201783 MONDO:excludeNonDisease +NCIT:C201784 MONDO:excludeNonDisease +NCIT:C201785 MONDO:excludeNonDisease +NCIT:C201787 MONDO:excludeNonDisease +NCIT:C201788 MONDO:excludeNonDisease +NCIT:C201789 MONDO:excludeNonDisease NCIT:C20179 MONDO:excludeNonDisease +NCIT:C201790 MONDO:excludeNonDisease +NCIT:C201791 MONDO:excludeNonDisease +NCIT:C201792 MONDO:excludeNonDisease +NCIT:C201793 MONDO:excludeNonDisease +NCIT:C201794 MONDO:excludeNonDisease +NCIT:C201795 MONDO:excludeNonDisease +NCIT:C201796 MONDO:excludeNonDisease +NCIT:C201797 MONDO:excludeNonDisease +NCIT:C201798 MONDO:excludeNonDisease +NCIT:C201799 MONDO:excludeNonDisease NCIT:C2018 MONDO:excludeNonDisease NCIT:C20180 MONDO:excludeNonDisease +NCIT:C201800 MONDO:excludeNonDisease +NCIT:C201801 MONDO:excludeNonDisease +NCIT:C201802 MONDO:excludeNonDisease +NCIT:C201803 MONDO:excludeNonDisease +NCIT:C201804 MONDO:excludeNonDisease +NCIT:C201805 MONDO:excludeNonDisease +NCIT:C201806 MONDO:excludeNonDisease +NCIT:C201807 MONDO:excludeNonDisease +NCIT:C201808 MONDO:excludeNonDisease +NCIT:C201809 MONDO:excludeNonDisease NCIT:C20181 MONDO:excludeNonDisease +NCIT:C201810 MONDO:excludeNonDisease +NCIT:C201811 MONDO:excludeNonDisease +NCIT:C201812 MONDO:excludeNonDisease +NCIT:C201813 MONDO:excludeNonDisease +NCIT:C201814 MONDO:excludeNonDisease +NCIT:C201815 MONDO:excludeNonDisease +NCIT:C201816 MONDO:excludeNonDisease +NCIT:C201817 MONDO:excludeNonDisease +NCIT:C201818 MONDO:excludeNonDisease +NCIT:C201819 MONDO:excludeNonDisease NCIT:C20182 MONDO:excludeNonDisease +NCIT:C201820 MONDO:excludeNonDisease +NCIT:C201822 MONDO:excludeNonDisease +NCIT:C201824 MONDO:excludeNonDisease +NCIT:C201825 MONDO:excludeNonDisease +NCIT:C201826 MONDO:excludeNonDisease +NCIT:C201827 MONDO:excludeNonDisease +NCIT:C201828 MONDO:excludeNonDisease +NCIT:C201829 MONDO:excludeNonDisease NCIT:C20183 MONDO:excludeNonDisease +NCIT:C201830 MONDO:excludeNonDisease +NCIT:C201831 MONDO:excludeNonDisease +NCIT:C201833 MONDO:excludeNonDisease +NCIT:C201834 MONDO:excludeNonDisease +NCIT:C201835 MONDO:excludeNonDisease +NCIT:C201836 MONDO:excludeNonDisease NCIT:C20184 MONDO:excludeNonDisease +NCIT:C201840 MONDO:excludeNonDisease +NCIT:C201841 MONDO:excludeNonDisease +NCIT:C201842 MONDO:excludeNonDisease +NCIT:C201843 MONDO:excludeNonDisease +NCIT:C201844 MONDO:excludeNonDisease +NCIT:C201845 MONDO:excludeNonDisease +NCIT:C201846 MONDO:excludeNonDisease +NCIT:C201847 MONDO:excludeNonDisease +NCIT:C201848 MONDO:excludeNonDisease NCIT:C20185 MONDO:excludeNonDisease +NCIT:C201850 MONDO:excludeNonDisease +NCIT:C201851 MONDO:excludeNonDisease +NCIT:C201852 MONDO:excludeNonDisease +NCIT:C201853 MONDO:excludeNonDisease +NCIT:C201854 MONDO:excludeNonDisease +NCIT:C201855 MONDO:excludeNonDisease +NCIT:C201856 MONDO:excludeNonDisease +NCIT:C201857 MONDO:excludeNonDisease +NCIT:C201858 MONDO:excludeNonDisease +NCIT:C201859 MONDO:excludeNonDisease NCIT:C20186 MONDO:excludeNonDisease +NCIT:C201860 MONDO:excludeNonDisease +NCIT:C201861 MONDO:excludeNonDisease +NCIT:C201862 MONDO:excludeNonDisease +NCIT:C201863 MONDO:excludeNonDisease +NCIT:C201864 MONDO:excludeNonDisease +NCIT:C201865 MONDO:excludeNonDisease +NCIT:C201866 MONDO:excludeNonDisease +NCIT:C201867 MONDO:excludeNonDisease +NCIT:C201868 MONDO:excludeNonDisease +NCIT:C201869 MONDO:excludeNonDisease NCIT:C20187 MONDO:excludeNonDisease +NCIT:C201870 MONDO:excludeNonDisease +NCIT:C201871 MONDO:excludeNonDisease +NCIT:C201872 MONDO:excludeNonDisease +NCIT:C201873 MONDO:excludeNonDisease +NCIT:C201874 MONDO:excludeNonDisease +NCIT:C201875 MONDO:excludeNonDisease +NCIT:C201876 MONDO:excludeNonDisease +NCIT:C201877 MONDO:excludeNonDisease +NCIT:C201879 MONDO:excludeNonDisease NCIT:C20188 MONDO:excludeNonDisease +NCIT:C201881 MONDO:excludeNonDisease +NCIT:C201882 MONDO:excludeNonDisease +NCIT:C201883 MONDO:excludeNonDisease +NCIT:C201884 MONDO:excludeNonDisease +NCIT:C201885 MONDO:excludeNonDisease +NCIT:C201886 MONDO:excludeNonDisease +NCIT:C201887 MONDO:excludeNonDisease +NCIT:C201889 MONDO:excludeNonDisease NCIT:C20189 MONDO:excludeNonDisease +NCIT:C201890 MONDO:excludeNonDisease +NCIT:C201891 MONDO:excludeNonDisease +NCIT:C201892 MONDO:excludeNonDisease +NCIT:C201893 MONDO:excludeNonDisease +NCIT:C201894 MONDO:excludeNonDisease +NCIT:C201895 MONDO:excludeNonDisease +NCIT:C201896 MONDO:excludeNonDisease +NCIT:C201897 MONDO:excludeNonDisease +NCIT:C201898 MONDO:excludeNonDisease +NCIT:C201899 MONDO:excludeNonDisease NCIT:C2019 MONDO:excludeNonDisease NCIT:C20190 MONDO:excludeNonDisease +NCIT:C201901 MONDO:excludeNonDisease +NCIT:C201902 MONDO:excludeNonDisease +NCIT:C201903 MONDO:excludeNonDisease +NCIT:C201908 MONDO:excludeNonDisease +NCIT:C201909 MONDO:excludeNonDisease NCIT:C20191 MONDO:excludeNonDisease +NCIT:C201910 MONDO:excludeNonDisease +NCIT:C201911 MONDO:excludeNonDisease +NCIT:C201912 MONDO:excludeNonDisease +NCIT:C201913 MONDO:excludeNonDisease +NCIT:C201914 MONDO:excludeNonDisease +NCIT:C201915 MONDO:excludeNonDisease +NCIT:C201916 MONDO:excludeNonDisease +NCIT:C201917 MONDO:excludeNonDisease +NCIT:C201918 MONDO:excludeNonDisease +NCIT:C201919 MONDO:excludeNonDisease +NCIT:C201920 MONDO:excludeNonDisease +NCIT:C201921 MONDO:excludeNonDisease +NCIT:C201922 MONDO:excludeNonDisease +NCIT:C201923 MONDO:excludeNonDisease +NCIT:C201924 MONDO:excludeNonDisease +NCIT:C201925 MONDO:excludeNonDisease +NCIT:C201926 MONDO:excludeNonDisease +NCIT:C201927 MONDO:excludeNonDisease +NCIT:C201928 MONDO:excludeNonDisease +NCIT:C201929 MONDO:excludeNonDisease NCIT:C20193 MONDO:excludeNonDisease +NCIT:C201930 MONDO:excludeNonDisease +NCIT:C201931 MONDO:excludeNonDisease +NCIT:C201932 MONDO:excludeNonDisease +NCIT:C201933 MONDO:excludeNonDisease +NCIT:C201934 MONDO:excludeNonDisease +NCIT:C201935 MONDO:excludeNonDisease +NCIT:C201936 MONDO:excludeNonDisease +NCIT:C201937 MONDO:excludeNonDisease +NCIT:C201938 MONDO:excludeNonDisease +NCIT:C201939 MONDO:excludeNonDisease NCIT:C20194 MONDO:excludeNonDisease +NCIT:C201940 MONDO:excludeNonDisease +NCIT:C201941 MONDO:excludeNonDisease +NCIT:C201942 MONDO:excludeNonDisease +NCIT:C201943 MONDO:excludeNonDisease +NCIT:C201944 MONDO:excludeNonDisease +NCIT:C201945 MONDO:excludeNonDisease +NCIT:C201946 MONDO:excludeNonDisease +NCIT:C201947 MONDO:excludeNonDisease +NCIT:C201948 MONDO:excludeNonDisease +NCIT:C201949 MONDO:excludeNonDisease NCIT:C20195 MONDO:excludeNonDisease +NCIT:C201950 MONDO:excludeNonDisease +NCIT:C201954 MONDO:excludeNonDisease +NCIT:C201955 MONDO:excludeNonDisease +NCIT:C201956 MONDO:excludeNonDisease +NCIT:C201957 MONDO:excludeNonDisease +NCIT:C201958 MONDO:excludeNonDisease +NCIT:C201959 MONDO:excludeNonDisease +NCIT:C201962 MONDO:excludeNonDisease +NCIT:C201963 MONDO:excludeNonDisease +NCIT:C201964 MONDO:excludeNonDisease +NCIT:C201965 MONDO:excludeNonDisease NCIT:C20197 MONDO:excludeNonDisease +NCIT:C201972 MONDO:excludeNonDisease +NCIT:C201974 MONDO:excludeNonDisease +NCIT:C201979 MONDO:excludeNonDisease NCIT:C20198 MONDO:excludeNonDisease +NCIT:C201980 MONDO:excludeNonDisease +NCIT:C201981 MONDO:excludeNonDisease +NCIT:C201982 MONDO:excludeNonDisease +NCIT:C201983 MONDO:excludeNonDisease +NCIT:C201984 MONDO:excludeNonDisease +NCIT:C201985 MONDO:excludeNonDisease +NCIT:C201986 MONDO:excludeNonDisease +NCIT:C201987 MONDO:excludeNonDisease +NCIT:C201988 MONDO:excludeNonDisease +NCIT:C201989 MONDO:excludeNonDisease NCIT:C20199 MONDO:excludeNonDisease +NCIT:C201990 MONDO:excludeNonDisease +NCIT:C201991 MONDO:excludeNonDisease +NCIT:C201992 MONDO:excludeNonDisease +NCIT:C201993 MONDO:excludeNonDisease +NCIT:C201994 MONDO:excludeNonDisease +NCIT:C201995 MONDO:excludeNonDisease +NCIT:C201996 MONDO:excludeNonDisease +NCIT:C201997 MONDO:excludeNonDisease +NCIT:C201998 MONDO:excludeNonDisease +NCIT:C201999 MONDO:excludeNonDisease NCIT:C202 MONDO:excludeNonDisease NCIT:C2020 MONDO:excludeNonDisease NCIT:C20200 MONDO:excludeNonDisease +NCIT:C202000 MONDO:excludeNonDisease +NCIT:C202001 MONDO:excludeNonDisease +NCIT:C202002 MONDO:excludeNonDisease +NCIT:C202003 MONDO:excludeNonDisease +NCIT:C202004 MONDO:excludeNonDisease +NCIT:C202005 MONDO:excludeNonDisease +NCIT:C202006 MONDO:excludeNonDisease +NCIT:C202007 MONDO:excludeNonDisease +NCIT:C202008 MONDO:excludeNonDisease +NCIT:C202009 MONDO:excludeNonDisease NCIT:C20201 MONDO:excludeNonDisease +NCIT:C202011 MONDO:excludeNonDisease +NCIT:C202012 MONDO:excludeNonDisease +NCIT:C202013 MONDO:excludeNonDisease +NCIT:C202014 MONDO:excludeNonDisease +NCIT:C202015 MONDO:excludeNonDisease +NCIT:C202016 MONDO:excludeNonDisease +NCIT:C202017 MONDO:excludeNonDisease +NCIT:C202018 MONDO:excludeNonDisease +NCIT:C202019 MONDO:excludeNonDisease NCIT:C20202 MONDO:excludeNonDisease +NCIT:C202020 MONDO:excludeNonDisease +NCIT:C202021 MONDO:excludeNonDisease +NCIT:C202022 MONDO:excludeNonDisease +NCIT:C202023 MONDO:excludeNonDisease +NCIT:C202024 MONDO:excludeNonDisease +NCIT:C202026 MONDO:excludeNonDisease +NCIT:C202027 MONDO:excludeNonDisease +NCIT:C202028 MONDO:excludeNonDisease +NCIT:C202029 MONDO:excludeNonDisease NCIT:C20203 MONDO:excludeNonDisease +NCIT:C202030 MONDO:excludeNonDisease +NCIT:C202031 MONDO:excludeNonDisease +NCIT:C202032 MONDO:excludeNonDisease +NCIT:C202033 MONDO:excludeNonDisease +NCIT:C202034 MONDO:excludeNonDisease +NCIT:C202035 MONDO:excludeNonDisease +NCIT:C202036 MONDO:excludeNonDisease +NCIT:C202037 MONDO:excludeNonDisease +NCIT:C202038 MONDO:excludeNonDisease +NCIT:C202039 MONDO:excludeNonDisease NCIT:C20204 MONDO:excludeNonDisease +NCIT:C202040 MONDO:excludeNonDisease +NCIT:C202041 MONDO:excludeNonDisease +NCIT:C202042 MONDO:excludeNonDisease +NCIT:C202043 MONDO:excludeNonDisease +NCIT:C202044 MONDO:excludeNonDisease +NCIT:C202045 MONDO:excludeNonDisease +NCIT:C202046 MONDO:excludeNonDisease +NCIT:C202047 MONDO:excludeNonDisease +NCIT:C202048 MONDO:excludeNonDisease +NCIT:C202049 MONDO:excludeNonDisease NCIT:C20205 MONDO:excludeNonDisease +NCIT:C202050 MONDO:excludeNonDisease +NCIT:C202051 MONDO:excludeNonDisease +NCIT:C202052 MONDO:excludeNonDisease +NCIT:C202053 MONDO:excludeNonDisease +NCIT:C202054 MONDO:excludeNonDisease +NCIT:C202055 MONDO:excludeNonDisease +NCIT:C202056 MONDO:excludeNonDisease NCIT:C20206 MONDO:excludeNonDisease +NCIT:C202060 MONDO:excludeNonDisease +NCIT:C202062 MONDO:excludeNonDisease +NCIT:C202063 MONDO:excludeNonDisease +NCIT:C202064 MONDO:excludeNonDisease +NCIT:C202065 MONDO:excludeNonDisease +NCIT:C202066 MONDO:excludeNonDisease +NCIT:C202067 MONDO:excludeNonDisease +NCIT:C202068 MONDO:excludeNonDisease +NCIT:C202069 MONDO:excludeNonDisease NCIT:C20207 MONDO:excludeNonDisease +NCIT:C202070 MONDO:excludeNonDisease +NCIT:C202071 MONDO:excludeNonDisease +NCIT:C202072 MONDO:excludeNonDisease +NCIT:C202073 MONDO:excludeNonDisease +NCIT:C202074 MONDO:excludeNonDisease +NCIT:C202075 MONDO:excludeNonDisease +NCIT:C202076 MONDO:excludeNonDisease NCIT:C20208 MONDO:excludeNonDisease +NCIT:C202082 MONDO:excludeNonDisease +NCIT:C202083 MONDO:excludeNonDisease +NCIT:C202084 MONDO:excludeNonDisease +NCIT:C202085 MONDO:excludeNonDisease +NCIT:C202086 MONDO:excludeNonDisease +NCIT:C202087 MONDO:excludeNonDisease +NCIT:C202088 MONDO:excludeNonDisease +NCIT:C202089 MONDO:excludeNonDisease NCIT:C20209 MONDO:excludeNonDisease +NCIT:C202090 MONDO:excludeNonDisease +NCIT:C202091 MONDO:excludeNonDisease +NCIT:C202092 MONDO:excludeNonDisease +NCIT:C202093 MONDO:excludeNonDisease +NCIT:C202094 MONDO:excludeNonDisease +NCIT:C202095 MONDO:excludeNonDisease +NCIT:C202096 MONDO:excludeNonDisease +NCIT:C202097 MONDO:excludeNonDisease +NCIT:C202098 MONDO:excludeNonDisease +NCIT:C202099 MONDO:excludeNonDisease NCIT:C2021 MONDO:excludeNonDisease NCIT:C20210 MONDO:excludeNonDisease +NCIT:C202100 MONDO:excludeNonDisease +NCIT:C202101 MONDO:excludeNonDisease +NCIT:C202102 MONDO:excludeNonDisease +NCIT:C202103 MONDO:excludeNonDisease +NCIT:C202104 MONDO:excludeNonDisease +NCIT:C202105 MONDO:excludeNonDisease +NCIT:C202106 MONDO:excludeNonDisease +NCIT:C202107 MONDO:excludeNonDisease +NCIT:C202108 MONDO:excludeNonDisease +NCIT:C202109 MONDO:excludeNonDisease NCIT:C20211 MONDO:excludeNonDisease +NCIT:C202110 MONDO:excludeNonDisease +NCIT:C202111 MONDO:excludeNonDisease +NCIT:C202112 MONDO:excludeNonDisease +NCIT:C202113 MONDO:excludeNonDisease +NCIT:C202114 MONDO:excludeNonDisease +NCIT:C202115 MONDO:excludeNonDisease +NCIT:C202116 MONDO:excludeNonDisease +NCIT:C202117 MONDO:excludeNonDisease +NCIT:C202118 MONDO:excludeNonDisease +NCIT:C202119 MONDO:excludeNonDisease NCIT:C20212 MONDO:excludeNonDisease +NCIT:C202121 MONDO:excludeNonDisease +NCIT:C202122 MONDO:excludeNonDisease +NCIT:C202123 MONDO:excludeNonDisease +NCIT:C202124 MONDO:excludeNonDisease +NCIT:C202125 MONDO:excludeNonDisease +NCIT:C202126 MONDO:excludeNonDisease +NCIT:C202129 MONDO:excludeNonDisease NCIT:C20213 MONDO:excludeNonDisease +NCIT:C202134 MONDO:excludeNonDisease +NCIT:C202135 MONDO:excludeNonDisease +NCIT:C202136 MONDO:excludeNonDisease +NCIT:C202137 MONDO:excludeNonDisease +NCIT:C202138 MONDO:excludeNonDisease +NCIT:C202139 MONDO:excludeNonDisease NCIT:C20214 MONDO:excludeNonDisease +NCIT:C202140 MONDO:excludeNonDisease +NCIT:C202141 MONDO:excludeNonDisease +NCIT:C202142 MONDO:excludeNonDisease +NCIT:C202143 MONDO:excludeNonDisease +NCIT:C202144 MONDO:excludeNonDisease +NCIT:C202145 MONDO:excludeNonDisease +NCIT:C202146 MONDO:excludeNonDisease +NCIT:C202147 MONDO:excludeNonDisease +NCIT:C202148 MONDO:excludeNonDisease +NCIT:C202149 MONDO:excludeNonDisease NCIT:C20215 MONDO:excludeNonDisease +NCIT:C202150 MONDO:excludeNonDisease +NCIT:C202151 MONDO:excludeNonDisease +NCIT:C202152 MONDO:excludeNonDisease +NCIT:C202153 MONDO:excludeNonDisease +NCIT:C202154 MONDO:excludeNonDisease +NCIT:C202155 MONDO:excludeNonDisease +NCIT:C202156 MONDO:excludeNonDisease +NCIT:C202157 MONDO:excludeNonDisease +NCIT:C202158 MONDO:excludeNonDisease +NCIT:C202159 MONDO:excludeNonDisease NCIT:C20216 MONDO:excludeNonDisease +NCIT:C202160 MONDO:excludeNonDisease +NCIT:C202161 MONDO:excludeNonDisease NCIT:C20217 MONDO:excludeNonDisease NCIT:C20218 MONDO:excludeNonDisease NCIT:C20219 MONDO:excludeNonDisease NCIT:C20220 MONDO:excludeNonDisease +NCIT:C202206 MONDO:excludeNonDisease +NCIT:C202207 MONDO:excludeNonDisease +NCIT:C202208 MONDO:excludeNonDisease NCIT:C20221 MONDO:excludeNonDisease +NCIT:C202210 MONDO:excludeNonDisease +NCIT:C202211 MONDO:excludeNonDisease +NCIT:C202212 MONDO:excludeNonDisease +NCIT:C202213 MONDO:excludeNonDisease +NCIT:C202214 MONDO:excludeNonDisease +NCIT:C202215 MONDO:excludeNonDisease +NCIT:C202216 MONDO:excludeNonDisease +NCIT:C202217 MONDO:excludeNonDisease +NCIT:C202218 MONDO:excludeNonDisease +NCIT:C202219 MONDO:excludeNonDisease NCIT:C20222 MONDO:excludeNonDisease +NCIT:C202220 MONDO:excludeNonDisease +NCIT:C202221 MONDO:excludeNonDisease +NCIT:C202222 MONDO:excludeNonDisease +NCIT:C202223 MONDO:excludeNonDisease +NCIT:C202224 MONDO:excludeNonDisease +NCIT:C202225 MONDO:excludeNonDisease +NCIT:C202226 MONDO:excludeNonDisease +NCIT:C202227 MONDO:excludeNonDisease +NCIT:C202228 MONDO:excludeNonDisease +NCIT:C202229 MONDO:excludeNonDisease NCIT:C20223 MONDO:excludeNonDisease +NCIT:C202230 MONDO:excludeNonDisease +NCIT:C202231 MONDO:excludeNonDisease +NCIT:C202232 MONDO:excludeNonDisease +NCIT:C202233 MONDO:excludeNonDisease +NCIT:C202234 MONDO:excludeNonDisease +NCIT:C202235 MONDO:excludeNonDisease +NCIT:C202236 MONDO:excludeNonDisease +NCIT:C202237 MONDO:excludeNonDisease +NCIT:C202238 MONDO:excludeNonDisease +NCIT:C202239 MONDO:excludeNonDisease NCIT:C20224 MONDO:excludeNonDisease +NCIT:C202240 MONDO:excludeNonDisease +NCIT:C202241 MONDO:excludeNonDisease +NCIT:C202242 MONDO:excludeNonDisease +NCIT:C202243 MONDO:excludeNonDisease +NCIT:C202244 MONDO:excludeNonDisease +NCIT:C202245 MONDO:excludeNonDisease +NCIT:C202246 MONDO:excludeNonDisease +NCIT:C202247 MONDO:excludeNonDisease +NCIT:C202248 MONDO:excludeNonDisease +NCIT:C202249 MONDO:excludeNonDisease NCIT:C20225 MONDO:excludeNonDisease +NCIT:C202250 MONDO:excludeNonDisease +NCIT:C202251 MONDO:excludeNonDisease +NCIT:C202255 MONDO:excludeNonDisease +NCIT:C202259 MONDO:excludeNonDisease NCIT:C20226 MONDO:excludeNonDisease +NCIT:C202266 MONDO:excludeNonDisease +NCIT:C202267 MONDO:excludeNonDisease +NCIT:C202268 MONDO:excludeNonDisease +NCIT:C202269 MONDO:excludeNonDisease NCIT:C20227 MONDO:excludeNonDisease +NCIT:C202270 MONDO:excludeNonDisease +NCIT:C202271 MONDO:excludeNonDisease +NCIT:C202272 MONDO:excludeNonDisease +NCIT:C202273 MONDO:excludeNonDisease +NCIT:C202274 MONDO:excludeNonDisease +NCIT:C202275 MONDO:excludeNonDisease +NCIT:C202276 MONDO:excludeNonDisease +NCIT:C202277 MONDO:excludeNonDisease +NCIT:C202278 MONDO:excludeNonDisease +NCIT:C202279 MONDO:excludeNonDisease NCIT:C20228 MONDO:excludeNonDisease +NCIT:C202280 MONDO:excludeNonDisease +NCIT:C202281 MONDO:excludeNonDisease +NCIT:C202282 MONDO:excludeNonDisease +NCIT:C202283 MONDO:excludeNonDisease +NCIT:C202284 MONDO:excludeNonDisease +NCIT:C202285 MONDO:excludeNonDisease +NCIT:C202286 MONDO:excludeNonDisease +NCIT:C202287 MONDO:excludeNonDisease +NCIT:C202288 MONDO:excludeNonDisease +NCIT:C202289 MONDO:excludeNonDisease NCIT:C20229 MONDO:excludeNonDisease +NCIT:C202290 MONDO:excludeNonDisease +NCIT:C202291 MONDO:excludeNonDisease +NCIT:C202292 MONDO:excludeNonDisease +NCIT:C202293 MONDO:excludeNonDisease +NCIT:C202294 MONDO:excludeNonDisease +NCIT:C202295 MONDO:excludeNonDisease +NCIT:C202296 MONDO:excludeNonDisease +NCIT:C202297 MONDO:excludeNonDisease NCIT:C2023 MONDO:excludeNonDisease NCIT:C20230 MONDO:excludeNonDisease +NCIT:C202300 MONDO:excludeNonDisease +NCIT:C202301 MONDO:excludeNonDisease +NCIT:C202302 MONDO:excludeNonDisease +NCIT:C202303 MONDO:excludeNonDisease +NCIT:C202304 MONDO:excludeNonDisease +NCIT:C202305 MONDO:excludeNonDisease +NCIT:C202306 MONDO:excludeNonDisease +NCIT:C202307 MONDO:excludeNonDisease +NCIT:C202308 MONDO:excludeNonDisease +NCIT:C202309 MONDO:excludeNonDisease NCIT:C20231 MONDO:excludeNonDisease +NCIT:C202310 MONDO:excludeNonDisease +NCIT:C202311 MONDO:excludeNonDisease +NCIT:C202312 MONDO:excludeNonDisease +NCIT:C202313 MONDO:excludeNonDisease +NCIT:C202314 MONDO:excludeNonDisease +NCIT:C202315 MONDO:excludeNonDisease +NCIT:C202316 MONDO:excludeNonDisease +NCIT:C202317 MONDO:excludeNonDisease +NCIT:C202318 MONDO:excludeNonDisease +NCIT:C202319 MONDO:excludeNonDisease NCIT:C20232 MONDO:excludeNonDisease +NCIT:C202320 MONDO:excludeNonDisease +NCIT:C202321 MONDO:excludeNonDisease +NCIT:C202322 MONDO:excludeNonDisease +NCIT:C202323 MONDO:excludeNonDisease +NCIT:C202324 MONDO:excludeNonDisease +NCIT:C202325 MONDO:excludeNonDisease +NCIT:C202326 MONDO:excludeNonDisease +NCIT:C202327 MONDO:excludeNonDisease +NCIT:C202329 MONDO:excludeNonDisease NCIT:C20233 MONDO:excludeNonDisease +NCIT:C202330 MONDO:excludeNonDisease +NCIT:C202331 MONDO:excludeNonDisease +NCIT:C202332 MONDO:excludeNonDisease +NCIT:C202333 MONDO:excludeNonDisease +NCIT:C202334 MONDO:excludeNonDisease +NCIT:C202336 MONDO:excludeNonDisease +NCIT:C202337 MONDO:excludeNonDisease +NCIT:C202338 MONDO:excludeNonDisease +NCIT:C202339 MONDO:excludeNonDisease NCIT:C20234 MONDO:excludeNonDisease +NCIT:C202340 MONDO:excludeNonDisease +NCIT:C202341 MONDO:excludeNonDisease +NCIT:C202342 MONDO:excludeNonDisease +NCIT:C202343 MONDO:excludeNonDisease +NCIT:C202344 MONDO:excludeNonDisease +NCIT:C202345 MONDO:excludeNonDisease +NCIT:C202346 MONDO:excludeNonDisease +NCIT:C202347 MONDO:excludeNonDisease +NCIT:C202348 MONDO:excludeNonDisease +NCIT:C202349 MONDO:excludeNonDisease NCIT:C20235 MONDO:excludeNonDisease +NCIT:C202350 MONDO:excludeNonDisease +NCIT:C202351 MONDO:excludeNonDisease +NCIT:C202352 MONDO:excludeNonDisease +NCIT:C202353 MONDO:excludeNonDisease +NCIT:C202354 MONDO:excludeNonDisease +NCIT:C202355 MONDO:excludeNonDisease +NCIT:C202356 MONDO:excludeNonDisease +NCIT:C202357 MONDO:excludeNonDisease +NCIT:C202358 MONDO:excludeNonDisease +NCIT:C202359 MONDO:excludeNonDisease NCIT:C20236 MONDO:excludeNonDisease +NCIT:C202360 MONDO:excludeNonDisease +NCIT:C202361 MONDO:excludeNonDisease +NCIT:C202362 MONDO:excludeNonDisease +NCIT:C202363 MONDO:excludeNonDisease +NCIT:C202364 MONDO:excludeNonDisease +NCIT:C202366 MONDO:excludeNonDisease +NCIT:C202367 MONDO:excludeNonDisease +NCIT:C202368 MONDO:excludeNonDisease +NCIT:C202369 MONDO:excludeNonDisease NCIT:C20237 MONDO:excludeNonDisease +NCIT:C202370 MONDO:excludeNonDisease +NCIT:C202371 MONDO:excludeNonDisease +NCIT:C202372 MONDO:excludeNonDisease +NCIT:C202373 MONDO:excludeNonDisease +NCIT:C202374 MONDO:excludeNonDisease +NCIT:C202375 MONDO:excludeNonDisease +NCIT:C202376 MONDO:excludeNonDisease +NCIT:C202377 MONDO:excludeNonDisease +NCIT:C202378 MONDO:excludeNonDisease +NCIT:C202379 MONDO:excludeNonDisease NCIT:C20238 MONDO:excludeNonDisease +NCIT:C202380 MONDO:excludeNonDisease +NCIT:C202381 MONDO:excludeNonDisease +NCIT:C202382 MONDO:excludeNonDisease +NCIT:C202383 MONDO:excludeNonDisease +NCIT:C202384 MONDO:excludeNonDisease +NCIT:C202385 MONDO:excludeNonDisease +NCIT:C202386 MONDO:excludeNonDisease +NCIT:C202387 MONDO:excludeNonDisease +NCIT:C202388 MONDO:excludeNonDisease +NCIT:C202389 MONDO:excludeNonDisease NCIT:C20239 MONDO:excludeNonDisease +NCIT:C202390 MONDO:excludeNonDisease +NCIT:C202391 MONDO:excludeNonDisease +NCIT:C202392 MONDO:excludeNonDisease +NCIT:C202393 MONDO:excludeNonDisease +NCIT:C202394 MONDO:excludeNonDisease +NCIT:C202395 MONDO:excludeNonDisease +NCIT:C202396 MONDO:excludeNonDisease +NCIT:C202397 MONDO:excludeNonDisease +NCIT:C202398 MONDO:excludeNonDisease +NCIT:C202399 MONDO:excludeNonDisease NCIT:C2024 MONDO:excludeNonDisease NCIT:C20240 MONDO:excludeNonDisease +NCIT:C202400 MONDO:excludeNonDisease +NCIT:C202401 MONDO:excludeNonDisease +NCIT:C202402 MONDO:excludeNonDisease +NCIT:C202403 MONDO:excludeNonDisease +NCIT:C202404 MONDO:excludeNonDisease +NCIT:C202405 MONDO:excludeNonDisease +NCIT:C202406 MONDO:excludeNonDisease +NCIT:C202407 MONDO:excludeNonDisease +NCIT:C202408 MONDO:excludeNonDisease +NCIT:C202409 MONDO:excludeNonDisease NCIT:C20241 MONDO:excludeNonDisease +NCIT:C202410 MONDO:excludeNonDisease +NCIT:C202411 MONDO:excludeNonDisease +NCIT:C202412 MONDO:excludeNonDisease +NCIT:C202413 MONDO:excludeNonDisease +NCIT:C202414 MONDO:excludeNonDisease +NCIT:C202415 MONDO:excludeNonDisease +NCIT:C202416 MONDO:excludeNonDisease +NCIT:C202417 MONDO:excludeNonDisease +NCIT:C202418 MONDO:excludeNonDisease +NCIT:C202419 MONDO:excludeNonDisease NCIT:C20242 MONDO:excludeNonDisease +NCIT:C202420 MONDO:excludeNonDisease +NCIT:C202421 MONDO:excludeNonDisease +NCIT:C202422 MONDO:excludeNonDisease +NCIT:C202423 MONDO:excludeNonDisease +NCIT:C202424 MONDO:excludeNonDisease +NCIT:C202425 MONDO:excludeNonDisease +NCIT:C202426 MONDO:excludeNonDisease +NCIT:C202427 MONDO:excludeNonDisease +NCIT:C202428 MONDO:excludeNonDisease +NCIT:C202429 MONDO:excludeNonDisease NCIT:C20243 MONDO:excludeNonDisease +NCIT:C202430 MONDO:excludeNonDisease +NCIT:C202431 MONDO:excludeNonDisease +NCIT:C202432 MONDO:excludeNonDisease +NCIT:C202433 MONDO:excludeNonDisease +NCIT:C202434 MONDO:excludeNonDisease +NCIT:C202435 MONDO:excludeNonDisease +NCIT:C202436 MONDO:excludeNonDisease +NCIT:C202437 MONDO:excludeNonDisease +NCIT:C202438 MONDO:excludeNonDisease +NCIT:C202439 MONDO:excludeNonDisease NCIT:C20244 MONDO:excludeNonDisease +NCIT:C202440 MONDO:excludeNonDisease +NCIT:C202441 MONDO:excludeNonDisease +NCIT:C202442 MONDO:excludeNonDisease +NCIT:C202443 MONDO:excludeNonDisease +NCIT:C202444 MONDO:excludeNonDisease +NCIT:C202445 MONDO:excludeNonDisease +NCIT:C202446 MONDO:excludeNonDisease +NCIT:C202447 MONDO:excludeNonDisease +NCIT:C202448 MONDO:excludeNonDisease +NCIT:C202449 MONDO:excludeNonDisease NCIT:C20245 MONDO:excludeNonDisease +NCIT:C202450 MONDO:excludeNonDisease +NCIT:C202451 MONDO:excludeNonDisease +NCIT:C202452 MONDO:excludeNonDisease +NCIT:C202453 MONDO:excludeNonDisease +NCIT:C202454 MONDO:excludeNonDisease +NCIT:C202455 MONDO:excludeNonDisease +NCIT:C202456 MONDO:excludeNonDisease +NCIT:C202457 MONDO:excludeNonDisease +NCIT:C202458 MONDO:excludeNonDisease +NCIT:C202459 MONDO:excludeNonDisease NCIT:C20246 MONDO:excludeNonDisease +NCIT:C202460 MONDO:excludeNonDisease +NCIT:C202461 MONDO:excludeNonDisease +NCIT:C202462 MONDO:excludeNonDisease +NCIT:C202463 MONDO:excludeNonDisease +NCIT:C202464 MONDO:excludeNonDisease +NCIT:C202465 MONDO:excludeNonDisease +NCIT:C202466 MONDO:excludeNonDisease +NCIT:C202467 MONDO:excludeNonDisease +NCIT:C202468 MONDO:excludeNonDisease +NCIT:C202469 MONDO:excludeNonDisease NCIT:C20247 MONDO:excludeNonDisease +NCIT:C202470 MONDO:excludeNonDisease +NCIT:C202471 MONDO:excludeNonDisease +NCIT:C202472 MONDO:excludeNonDisease +NCIT:C202473 MONDO:excludeNonDisease +NCIT:C202474 MONDO:excludeNonDisease +NCIT:C202475 MONDO:excludeNonDisease +NCIT:C202476 MONDO:excludeNonDisease +NCIT:C202477 MONDO:excludeNonDisease +NCIT:C202478 MONDO:excludeNonDisease +NCIT:C202479 MONDO:excludeNonDisease NCIT:C20248 MONDO:excludeNonDisease +NCIT:C202480 MONDO:excludeNonDisease +NCIT:C202481 MONDO:excludeNonDisease +NCIT:C202482 MONDO:excludeNonDisease +NCIT:C202483 MONDO:excludeNonDisease +NCIT:C202484 MONDO:excludeNonDisease +NCIT:C202485 MONDO:excludeNonDisease +NCIT:C202486 MONDO:excludeNonDisease +NCIT:C202487 MONDO:excludeNonDisease +NCIT:C202488 MONDO:excludeNonDisease +NCIT:C202489 MONDO:excludeNonDisease NCIT:C20249 MONDO:excludeNonDisease +NCIT:C202490 MONDO:excludeNonDisease +NCIT:C202491 MONDO:excludeNonDisease +NCIT:C202492 MONDO:excludeNonDisease +NCIT:C202493 MONDO:excludeNonDisease +NCIT:C202494 MONDO:excludeNonDisease +NCIT:C202495 MONDO:excludeNonDisease +NCIT:C202496 MONDO:excludeNonDisease +NCIT:C202498 MONDO:excludeNonDisease +NCIT:C202499 MONDO:excludeNonDisease NCIT:C2025 MONDO:excludeNonDisease NCIT:C20250 MONDO:excludeNonDisease +NCIT:C202501 MONDO:excludeNonDisease +NCIT:C202502 MONDO:excludeNonDisease +NCIT:C202503 MONDO:excludeNonDisease +NCIT:C202504 MONDO:excludeNonDisease +NCIT:C202505 MONDO:excludeNonDisease +NCIT:C202506 MONDO:excludeNonDisease +NCIT:C202507 MONDO:excludeNonDisease +NCIT:C202508 MONDO:excludeNonDisease +NCIT:C202509 MONDO:excludeNonDisease NCIT:C20251 MONDO:excludeNonDisease +NCIT:C202510 MONDO:excludeNonDisease +NCIT:C202511 MONDO:excludeNonDisease +NCIT:C202512 MONDO:excludeNonDisease +NCIT:C202513 MONDO:excludeNonDisease +NCIT:C202514 MONDO:excludeNonDisease +NCIT:C202515 MONDO:excludeNonDisease +NCIT:C202516 MONDO:excludeNonDisease +NCIT:C202517 MONDO:excludeNonDisease +NCIT:C202518 MONDO:excludeNonDisease +NCIT:C202519 MONDO:excludeNonDisease NCIT:C20252 MONDO:excludeNonDisease +NCIT:C202520 MONDO:excludeNonDisease +NCIT:C202521 MONDO:excludeNonDisease +NCIT:C202522 MONDO:excludeNonDisease +NCIT:C202523 MONDO:excludeNonDisease +NCIT:C202524 MONDO:excludeNonDisease +NCIT:C202525 MONDO:excludeNonDisease +NCIT:C202526 MONDO:excludeNonDisease +NCIT:C202527 MONDO:excludeNonDisease +NCIT:C202528 MONDO:excludeNonDisease +NCIT:C202529 MONDO:excludeNonDisease NCIT:C20253 MONDO:excludeNonDisease +NCIT:C202530 MONDO:excludeNonDisease +NCIT:C202531 MONDO:excludeNonDisease +NCIT:C202532 MONDO:excludeNonDisease +NCIT:C202533 MONDO:excludeNonDisease +NCIT:C202534 MONDO:excludeNonDisease +NCIT:C202535 MONDO:excludeNonDisease +NCIT:C202536 MONDO:excludeNonDisease +NCIT:C202537 MONDO:excludeNonDisease +NCIT:C202538 MONDO:excludeNonDisease +NCIT:C202539 MONDO:excludeNonDisease NCIT:C20254 MONDO:excludeNonDisease +NCIT:C202540 MONDO:excludeNonDisease +NCIT:C202541 MONDO:excludeNonDisease +NCIT:C202542 MONDO:excludeNonDisease +NCIT:C202543 MONDO:excludeNonDisease +NCIT:C202544 MONDO:excludeNonDisease +NCIT:C202545 MONDO:excludeNonDisease +NCIT:C202546 MONDO:excludeNonDisease +NCIT:C202547 MONDO:excludeNonDisease +NCIT:C202548 MONDO:excludeNonDisease +NCIT:C202549 MONDO:excludeNonDisease NCIT:C20255 MONDO:excludeNonDisease +NCIT:C202550 MONDO:excludeNonDisease +NCIT:C202551 MONDO:excludeNonDisease +NCIT:C202552 MONDO:excludeNonDisease +NCIT:C202553 MONDO:excludeNonDisease +NCIT:C202554 MONDO:excludeNonDisease +NCIT:C202555 MONDO:excludeNonDisease +NCIT:C202556 MONDO:excludeNonDisease +NCIT:C202557 MONDO:excludeNonDisease +NCIT:C202558 MONDO:excludeNonDisease +NCIT:C202559 MONDO:excludeNonDisease NCIT:C20256 MONDO:excludeNonDisease +NCIT:C202560 MONDO:excludeNonDisease +NCIT:C202561 MONDO:excludeNonDisease +NCIT:C202562 MONDO:excludeNonDisease +NCIT:C202563 MONDO:excludeNonDisease +NCIT:C202564 MONDO:excludeNonDisease +NCIT:C202565 MONDO:excludeNonDisease +NCIT:C202566 MONDO:excludeNonDisease +NCIT:C202567 MONDO:excludeNonDisease +NCIT:C202568 MONDO:excludeNonDisease +NCIT:C202569 MONDO:excludeNonDisease NCIT:C20257 MONDO:excludeNonDisease +NCIT:C202570 MONDO:excludeNonDisease +NCIT:C202571 MONDO:excludeNonDisease +NCIT:C202572 MONDO:excludeNonDisease +NCIT:C202573 MONDO:excludeNonDisease +NCIT:C202575 MONDO:excludeNonDisease +NCIT:C202576 MONDO:excludeNonDisease +NCIT:C202577 MONDO:excludeNonDisease +NCIT:C202578 MONDO:excludeNonDisease +NCIT:C202579 MONDO:excludeNonDisease NCIT:C20258 MONDO:excludeNonDisease +NCIT:C202580 MONDO:excludeNonDisease +NCIT:C202581 MONDO:excludeNonDisease +NCIT:C202586 MONDO:excludeNonDisease +NCIT:C202587 MONDO:excludeNonDisease +NCIT:C202588 MONDO:excludeNonDisease +NCIT:C202589 MONDO:excludeNonDisease NCIT:C20259 MONDO:excludeNonDisease +NCIT:C202590 MONDO:excludeNonDisease +NCIT:C202591 MONDO:excludeNonDisease +NCIT:C202592 MONDO:excludeNonDisease +NCIT:C202593 MONDO:excludeNonDisease +NCIT:C202595 MONDO:excludeNonDisease +NCIT:C202596 MONDO:excludeNonDisease +NCIT:C202597 MONDO:excludeNonDisease +NCIT:C202598 MONDO:excludeNonDisease +NCIT:C202599 MONDO:excludeNonDisease NCIT:C2026 MONDO:excludeNonDisease NCIT:C20260 MONDO:excludeNonDisease +NCIT:C202600 MONDO:excludeNonDisease +NCIT:C202601 MONDO:excludeNonDisease +NCIT:C202602 MONDO:excludeNonDisease +NCIT:C202603 MONDO:excludeNonDisease +NCIT:C202604 MONDO:excludeNonDisease +NCIT:C202605 MONDO:excludeNonDisease +NCIT:C202606 MONDO:excludeNonDisease +NCIT:C202607 MONDO:excludeNonDisease +NCIT:C202608 MONDO:excludeNonDisease NCIT:C20261 MONDO:excludeNonDisease +NCIT:C202610 MONDO:excludeNonDisease +NCIT:C202612 MONDO:excludeNonDisease +NCIT:C202614 MONDO:excludeNonDisease +NCIT:C202615 MONDO:excludeNonDisease +NCIT:C202616 MONDO:excludeNonDisease +NCIT:C202617 MONDO:excludeNonDisease +NCIT:C202618 MONDO:excludeNonDisease +NCIT:C202619 MONDO:excludeNonDisease NCIT:C20262 MONDO:excludeNonDisease +NCIT:C202626 MONDO:excludeNonDisease +NCIT:C202627 MONDO:excludeNonDisease +NCIT:C202628 MONDO:excludeNonDisease +NCIT:C202629 MONDO:excludeNonDisease NCIT:C20263 MONDO:excludeNonDisease +NCIT:C202630 MONDO:excludeNonDisease +NCIT:C202631 MONDO:excludeNonDisease +NCIT:C202632 MONDO:excludeNonDisease +NCIT:C202636 MONDO:excludeNonDisease +NCIT:C202637 MONDO:excludeNonDisease +NCIT:C202638 MONDO:excludeNonDisease +NCIT:C202639 MONDO:excludeNonDisease NCIT:C20264 MONDO:excludeNonDisease +NCIT:C202640 MONDO:excludeNonDisease +NCIT:C202641 MONDO:excludeNonDisease +NCIT:C202642 MONDO:excludeNonDisease +NCIT:C202643 MONDO:excludeNonDisease +NCIT:C202644 MONDO:excludeNonDisease +NCIT:C202645 MONDO:excludeNonDisease +NCIT:C202648 MONDO:excludeNonDisease +NCIT:C202649 MONDO:excludeNonDisease NCIT:C20265 MONDO:excludeNonDisease +NCIT:C202650 MONDO:excludeNonDisease +NCIT:C202651 MONDO:excludeNonDisease +NCIT:C202653 MONDO:excludeNonDisease +NCIT:C202657 MONDO:excludeNonDisease +NCIT:C202658 MONDO:excludeNonDisease +NCIT:C202659 MONDO:excludeNonDisease NCIT:C20266 MONDO:excludeNonDisease +NCIT:C202660 MONDO:excludeNonDisease +NCIT:C202663 MONDO:excludeNonDisease +NCIT:C202664 MONDO:excludeNonDisease +NCIT:C202665 MONDO:excludeNonDisease +NCIT:C202666 MONDO:excludeNonDisease +NCIT:C202667 MONDO:excludeNonDisease +NCIT:C202668 MONDO:excludeNonDisease +NCIT:C202669 MONDO:excludeNonDisease NCIT:C20267 MONDO:excludeNonDisease +NCIT:C202670 MONDO:excludeNonDisease +NCIT:C202671 MONDO:excludeNonDisease +NCIT:C202672 MONDO:excludeNonDisease +NCIT:C202673 MONDO:excludeNonDisease +NCIT:C202674 MONDO:excludeNonDisease +NCIT:C202675 MONDO:excludeNonDisease +NCIT:C202676 MONDO:excludeNonDisease +NCIT:C202677 MONDO:excludeNonDisease +NCIT:C202678 MONDO:excludeNonDisease +NCIT:C202679 MONDO:excludeNonDisease NCIT:C20268 MONDO:excludeNonDisease +NCIT:C202680 MONDO:excludeNonDisease +NCIT:C202681 MONDO:excludeNonDisease +NCIT:C202682 MONDO:excludeNonDisease +NCIT:C202683 MONDO:excludeNonDisease +NCIT:C202685 MONDO:excludeNonDisease +NCIT:C202686 MONDO:excludeNonDisease +NCIT:C202687 MONDO:excludeNonDisease +NCIT:C202688 MONDO:excludeNonDisease +NCIT:C202689 MONDO:excludeNonDisease NCIT:C20269 MONDO:excludeNonDisease +NCIT:C202690 MONDO:excludeNonDisease +NCIT:C202691 MONDO:excludeNonDisease +NCIT:C202692 MONDO:excludeNonDisease +NCIT:C202693 MONDO:excludeNonDisease +NCIT:C202694 MONDO:excludeNonDisease +NCIT:C202695 MONDO:excludeNonDisease +NCIT:C202696 MONDO:excludeNonDisease +NCIT:C202697 MONDO:excludeNonDisease +NCIT:C202698 MONDO:excludeNonDisease +NCIT:C202699 MONDO:excludeNonDisease NCIT:C2027 MONDO:excludeNonDisease NCIT:C20270 MONDO:excludeNonDisease +NCIT:C202700 MONDO:excludeNonDisease +NCIT:C202701 MONDO:excludeNonDisease +NCIT:C202702 MONDO:excludeNonDisease +NCIT:C202703 MONDO:excludeNonDisease +NCIT:C202704 MONDO:excludeNonDisease +NCIT:C202705 MONDO:excludeNonDisease +NCIT:C202706 MONDO:excludeNonDisease +NCIT:C202707 MONDO:excludeNonDisease +NCIT:C202708 MONDO:excludeNonDisease +NCIT:C202709 MONDO:excludeNonDisease NCIT:C20271 MONDO:excludeNonDisease +NCIT:C202710 MONDO:excludeNonDisease +NCIT:C202712 MONDO:excludeNonDisease +NCIT:C202713 MONDO:excludeNonDisease +NCIT:C202714 MONDO:excludeNonDisease +NCIT:C202715 MONDO:excludeNonDisease +NCIT:C202716 MONDO:excludeNonDisease +NCIT:C202717 MONDO:excludeNonDisease +NCIT:C202718 MONDO:excludeNonDisease +NCIT:C202719 MONDO:excludeNonDisease NCIT:C20272 MONDO:excludeNonDisease +NCIT:C202720 MONDO:excludeNonDisease +NCIT:C202721 MONDO:excludeNonDisease +NCIT:C202722 MONDO:excludeNonDisease +NCIT:C202723 MONDO:excludeNonDisease +NCIT:C202724 MONDO:excludeNonDisease +NCIT:C202725 MONDO:excludeNonDisease +NCIT:C202726 MONDO:excludeNonDisease +NCIT:C202727 MONDO:excludeNonDisease +NCIT:C202728 MONDO:excludeNonDisease +NCIT:C202729 MONDO:excludeNonDisease NCIT:C20273 MONDO:excludeNonDisease +NCIT:C202730 MONDO:excludeNonDisease +NCIT:C202731 MONDO:excludeNonDisease +NCIT:C202732 MONDO:excludeNonDisease +NCIT:C202733 MONDO:excludeNonDisease +NCIT:C202734 MONDO:excludeNonDisease +NCIT:C202735 MONDO:excludeNonDisease +NCIT:C202736 MONDO:excludeNonDisease +NCIT:C202737 MONDO:excludeNonDisease +NCIT:C202738 MONDO:excludeNonDisease +NCIT:C202739 MONDO:excludeNonDisease NCIT:C20274 MONDO:excludeNonDisease +NCIT:C202740 MONDO:excludeNonDisease +NCIT:C202741 MONDO:excludeNonDisease +NCIT:C202742 MONDO:excludeNonDisease +NCIT:C202743 MONDO:excludeNonDisease +NCIT:C202744 MONDO:excludeNonDisease +NCIT:C202745 MONDO:excludeNonDisease +NCIT:C202746 MONDO:excludeNonDisease +NCIT:C202747 MONDO:excludeNonDisease +NCIT:C202748 MONDO:excludeNonDisease +NCIT:C202749 MONDO:excludeNonDisease NCIT:C20275 MONDO:excludeNonDisease +NCIT:C202750 MONDO:excludeNonDisease +NCIT:C202751 MONDO:excludeNonDisease +NCIT:C202752 MONDO:excludeNonDisease +NCIT:C202753 MONDO:excludeNonDisease +NCIT:C202754 MONDO:excludeNonDisease +NCIT:C202755 MONDO:excludeNonDisease +NCIT:C202756 MONDO:excludeNonDisease +NCIT:C202757 MONDO:excludeNonDisease +NCIT:C202758 MONDO:excludeNonDisease +NCIT:C202759 MONDO:excludeNonDisease NCIT:C20276 MONDO:excludeNonDisease +NCIT:C202760 MONDO:excludeNonDisease +NCIT:C202761 MONDO:excludeNonDisease +NCIT:C202762 MONDO:excludeNonDisease +NCIT:C202763 MONDO:excludeNonDisease +NCIT:C202764 MONDO:excludeNonDisease +NCIT:C202765 MONDO:excludeNonDisease +NCIT:C202766 MONDO:excludeNonDisease +NCIT:C202767 MONDO:excludeNonDisease +NCIT:C202768 MONDO:excludeNonDisease +NCIT:C202769 MONDO:excludeNonDisease NCIT:C20277 MONDO:excludeNonDisease +NCIT:C202770 MONDO:excludeNonDisease +NCIT:C202771 MONDO:excludeNonDisease +NCIT:C202772 MONDO:excludeNonDisease +NCIT:C202773 MONDO:excludeNonDisease +NCIT:C202774 MONDO:excludeNonDisease +NCIT:C202777 MONDO:excludeNonDisease +NCIT:C202778 MONDO:excludeNonDisease +NCIT:C202779 MONDO:excludeNonDisease NCIT:C20278 MONDO:excludeNonDisease +NCIT:C202780 MONDO:excludeNonDisease +NCIT:C202781 MONDO:excludeNonDisease +NCIT:C202782 MONDO:excludeNonDisease +NCIT:C202783 MONDO:excludeNonDisease +NCIT:C202784 MONDO:excludeNonDisease +NCIT:C202785 MONDO:excludeNonDisease +NCIT:C202786 MONDO:excludeNonDisease +NCIT:C202787 MONDO:excludeNonDisease +NCIT:C202788 MONDO:excludeNonDisease +NCIT:C202789 MONDO:excludeNonDisease NCIT:C20279 MONDO:excludeNonDisease +NCIT:C202790 MONDO:excludeNonDisease +NCIT:C202791 MONDO:excludeNonDisease +NCIT:C202792 MONDO:excludeNonDisease +NCIT:C202793 MONDO:excludeNonDisease +NCIT:C202794 MONDO:excludeNonDisease +NCIT:C202795 MONDO:excludeNonDisease +NCIT:C202796 MONDO:excludeNonDisease +NCIT:C202797 MONDO:excludeNonDisease +NCIT:C202798 MONDO:excludeNonDisease +NCIT:C202799 MONDO:excludeNonDisease NCIT:C2028 MONDO:excludeNonDisease NCIT:C20280 MONDO:excludeNonDisease +NCIT:C202800 MONDO:excludeNonDisease +NCIT:C202801 MONDO:excludeNonDisease +NCIT:C202802 MONDO:excludeNonDisease +NCIT:C202803 MONDO:excludeNonDisease +NCIT:C202804 MONDO:excludeNonDisease +NCIT:C202805 MONDO:excludeNonDisease +NCIT:C202806 MONDO:excludeNonDisease +NCIT:C202807 MONDO:excludeNonDisease +NCIT:C202808 MONDO:excludeNonDisease +NCIT:C202809 MONDO:excludeNonDisease NCIT:C20281 MONDO:excludeNonDisease +NCIT:C202810 MONDO:excludeNonDisease +NCIT:C202811 MONDO:excludeNonDisease +NCIT:C202812 MONDO:excludeNonDisease +NCIT:C202813 MONDO:excludeNonDisease +NCIT:C202814 MONDO:excludeNonDisease +NCIT:C202815 MONDO:excludeNonDisease +NCIT:C202816 MONDO:excludeNonDisease +NCIT:C202817 MONDO:excludeNonDisease +NCIT:C202818 MONDO:excludeNonDisease +NCIT:C202819 MONDO:excludeNonDisease NCIT:C20282 MONDO:excludeNonDisease +NCIT:C202820 MONDO:excludeNonDisease +NCIT:C202821 MONDO:excludeNonDisease +NCIT:C202822 MONDO:excludeNonDisease +NCIT:C202823 MONDO:excludeNonDisease +NCIT:C202824 MONDO:excludeNonDisease +NCIT:C202825 MONDO:excludeNonDisease +NCIT:C202826 MONDO:excludeNonDisease +NCIT:C202827 MONDO:excludeNonDisease +NCIT:C202828 MONDO:excludeNonDisease +NCIT:C202829 MONDO:excludeNonDisease NCIT:C20283 MONDO:excludeNonDisease +NCIT:C202830 MONDO:excludeNonDisease +NCIT:C202831 MONDO:excludeNonDisease +NCIT:C202832 MONDO:excludeNonDisease +NCIT:C202833 MONDO:excludeNonDisease +NCIT:C202834 MONDO:excludeNonDisease +NCIT:C202835 MONDO:excludeNonDisease +NCIT:C202836 MONDO:excludeNonDisease +NCIT:C202837 MONDO:excludeNonDisease +NCIT:C202838 MONDO:excludeNonDisease +NCIT:C202839 MONDO:excludeNonDisease NCIT:C20284 MONDO:excludeNonDisease +NCIT:C202840 MONDO:excludeNonDisease +NCIT:C202841 MONDO:excludeNonDisease +NCIT:C202842 MONDO:excludeNonDisease +NCIT:C202843 MONDO:excludeNonDisease +NCIT:C202844 MONDO:excludeNonDisease +NCIT:C202845 MONDO:excludeNonDisease +NCIT:C202846 MONDO:excludeNonDisease +NCIT:C202847 MONDO:excludeNonDisease +NCIT:C202848 MONDO:excludeNonDisease NCIT:C20285 MONDO:excludeNonDisease +NCIT:C202850 MONDO:excludeNonDisease +NCIT:C202854 MONDO:excludeNonDisease +NCIT:C202855 MONDO:excludeNonDisease +NCIT:C202857 MONDO:excludeNonDisease NCIT:C20286 MONDO:excludeNonDisease +NCIT:C202862 MONDO:excludeNonDisease +NCIT:C202863 MONDO:excludeNonDisease +NCIT:C202864 MONDO:excludeNonDisease +NCIT:C202865 MONDO:excludeNonDisease +NCIT:C202866 MONDO:excludeNonDisease +NCIT:C202867 MONDO:excludeNonDisease +NCIT:C202868 MONDO:excludeNonDisease +NCIT:C202869 MONDO:excludeNonDisease NCIT:C20287 MONDO:excludeNonDisease +NCIT:C202870 MONDO:excludeNonDisease +NCIT:C202871 MONDO:excludeNonDisease +NCIT:C202872 MONDO:excludeNonDisease +NCIT:C202873 MONDO:excludeNonDisease +NCIT:C202874 MONDO:excludeNonDisease +NCIT:C202875 MONDO:excludeNonDisease NCIT:C20288 MONDO:excludeNonDisease +NCIT:C202885 MONDO:excludeNonDisease +NCIT:C202886 MONDO:excludeNonDisease +NCIT:C202887 MONDO:excludeNonDisease +NCIT:C202888 MONDO:excludeNonDisease +NCIT:C202889 MONDO:excludeNonDisease NCIT:C20289 MONDO:excludeNonDisease +NCIT:C202890 MONDO:excludeNonDisease +NCIT:C202891 MONDO:excludeNonDisease +NCIT:C202892 MONDO:excludeNonDisease +NCIT:C202893 MONDO:excludeNonDisease +NCIT:C202895 MONDO:excludeNonDisease NCIT:C2029 MONDO:excludeNonDisease NCIT:C20290 MONDO:excludeNonDisease +NCIT:C202900 MONDO:excludeNonDisease +NCIT:C202902 MONDO:excludeNonDisease +NCIT:C202903 MONDO:excludeNonDisease +NCIT:C202905 MONDO:excludeNonDisease +NCIT:C202906 MONDO:excludeNonDisease +NCIT:C202907 MONDO:excludeNonDisease +NCIT:C202908 MONDO:excludeNonDisease +NCIT:C202909 MONDO:excludeNonDisease NCIT:C20291 MONDO:excludeNonDisease +NCIT:C202910 MONDO:excludeNonDisease +NCIT:C202911 MONDO:excludeNonDisease +NCIT:C202912 MONDO:excludeNonDisease +NCIT:C202913 MONDO:excludeNonDisease +NCIT:C202915 MONDO:excludeNonDisease +NCIT:C202916 MONDO:excludeNonDisease +NCIT:C202917 MONDO:excludeNonDisease +NCIT:C202918 MONDO:excludeNonDisease +NCIT:C202919 MONDO:excludeNonDisease NCIT:C20292 MONDO:excludeNonDisease +NCIT:C202920 MONDO:excludeNonDisease +NCIT:C202928 MONDO:excludeNonDisease NCIT:C20293 MONDO:excludeNonDisease +NCIT:C202931 MONDO:excludeNonDisease +NCIT:C202933 MONDO:excludeNonDisease +NCIT:C202934 MONDO:excludeNonDisease +NCIT:C202937 MONDO:excludeNonDisease +NCIT:C202938 MONDO:excludeNonDisease +NCIT:C202939 MONDO:excludeNonDisease NCIT:C20294 MONDO:excludeNonDisease +NCIT:C202940 MONDO:excludeNonDisease +NCIT:C202941 MONDO:excludeNonDisease +NCIT:C202942 MONDO:excludeNonDisease +NCIT:C202943 MONDO:excludeNonDisease +NCIT:C202944 MONDO:excludeNonDisease +NCIT:C202945 MONDO:excludeNonDisease +NCIT:C202946 MONDO:excludeNonDisease +NCIT:C202947 MONDO:excludeNonDisease +NCIT:C202948 MONDO:excludeNonDisease +NCIT:C202949 MONDO:excludeNonDisease NCIT:C20295 MONDO:excludeNonDisease +NCIT:C202950 MONDO:excludeNonDisease +NCIT:C202951 MONDO:excludeNonDisease +NCIT:C202956 MONDO:excludeNonDisease +NCIT:C202957 MONDO:excludeNonDisease +NCIT:C202959 MONDO:excludeNonDisease NCIT:C20296 MONDO:excludeNonDisease +NCIT:C202960 MONDO:excludeNonDisease +NCIT:C202961 MONDO:excludeNonDisease +NCIT:C202962 MONDO:excludeNonDisease +NCIT:C202963 MONDO:excludeNonDisease +NCIT:C202964 MONDO:excludeNonDisease +NCIT:C202965 MONDO:excludeNonDisease +NCIT:C202968 MONDO:excludeNonDisease +NCIT:C202969 MONDO:excludeNonDisease NCIT:C20297 MONDO:excludeNonDisease +NCIT:C202970 MONDO:excludeNonDisease +NCIT:C202974 MONDO:excludeNonDisease +NCIT:C202976 MONDO:excludeNonDisease NCIT:C20298 MONDO:excludeNonDisease +NCIT:C202988 MONDO:excludeNonDisease NCIT:C20299 MONDO:excludeNonDisease +NCIT:C202999 MONDO:excludeNonDisease NCIT:C203 MONDO:excludeNonDisease NCIT:C2030 MONDO:excludeNonDisease NCIT:C20300 MONDO:excludeNonDisease +NCIT:C203000 MONDO:excludeNonDisease +NCIT:C203001 MONDO:excludeNonDisease +NCIT:C203003 MONDO:excludeNonDisease NCIT:C20301 MONDO:excludeNonDisease +NCIT:C203019 MONDO:excludeNonDisease NCIT:C20302 MONDO:excludeNonDisease +NCIT:C203020 MONDO:excludeNonDisease +NCIT:C203021 MONDO:excludeNonDisease +NCIT:C203022 MONDO:excludeNonDisease +NCIT:C203023 MONDO:excludeNonDisease +NCIT:C203024 MONDO:excludeNonDisease +NCIT:C203025 MONDO:excludeNonDisease +NCIT:C203026 MONDO:excludeNonDisease +NCIT:C203027 MONDO:excludeNonDisease +NCIT:C203028 MONDO:excludeNonDisease +NCIT:C203029 MONDO:excludeNonDisease NCIT:C20303 MONDO:excludeNonDisease +NCIT:C203030 MONDO:excludeNonDisease +NCIT:C203031 MONDO:excludeNonDisease +NCIT:C203032 MONDO:excludeNonDisease +NCIT:C203033 MONDO:excludeNonDisease +NCIT:C203034 MONDO:excludeNonDisease +NCIT:C203035 MONDO:excludeNonDisease +NCIT:C203036 MONDO:excludeNonDisease +NCIT:C203037 MONDO:excludeNonDisease +NCIT:C203038 MONDO:excludeNonDisease +NCIT:C203039 MONDO:excludeNonDisease NCIT:C20304 MONDO:excludeNonDisease +NCIT:C203040 MONDO:excludeNonDisease +NCIT:C203041 MONDO:excludeNonDisease +NCIT:C203042 MONDO:excludeNonDisease +NCIT:C203043 MONDO:excludeNonDisease +NCIT:C203044 MONDO:excludeNonDisease +NCIT:C203045 MONDO:excludeNonDisease +NCIT:C203046 MONDO:excludeNonDisease +NCIT:C203047 MONDO:excludeNonDisease +NCIT:C203048 MONDO:excludeNonDisease +NCIT:C203049 MONDO:excludeNonDisease NCIT:C20305 MONDO:excludeNonDisease +NCIT:C203050 MONDO:excludeNonDisease +NCIT:C203051 MONDO:excludeNonDisease +NCIT:C203052 MONDO:excludeNonDisease +NCIT:C203053 MONDO:excludeNonDisease +NCIT:C203054 MONDO:excludeNonDisease +NCIT:C203055 MONDO:excludeNonDisease +NCIT:C203056 MONDO:excludeNonDisease +NCIT:C203057 MONDO:excludeNonDisease +NCIT:C203058 MONDO:excludeNonDisease +NCIT:C203059 MONDO:excludeNonDisease NCIT:C20306 MONDO:excludeNonDisease +NCIT:C203060 MONDO:excludeNonDisease +NCIT:C203061 MONDO:excludeNonDisease +NCIT:C203062 MONDO:excludeNonDisease +NCIT:C203063 MONDO:excludeNonDisease +NCIT:C203064 MONDO:excludeNonDisease +NCIT:C203065 MONDO:excludeNonDisease +NCIT:C203066 MONDO:excludeNonDisease +NCIT:C203067 MONDO:excludeNonDisease +NCIT:C203068 MONDO:excludeNonDisease +NCIT:C203069 MONDO:excludeNonDisease NCIT:C20307 MONDO:excludeNonDisease +NCIT:C203070 MONDO:excludeNonDisease +NCIT:C203071 MONDO:excludeNonDisease +NCIT:C203072 MONDO:excludeNonDisease +NCIT:C203073 MONDO:excludeNonDisease +NCIT:C203074 MONDO:excludeNonDisease +NCIT:C203075 MONDO:excludeNonDisease +NCIT:C203076 MONDO:excludeNonDisease +NCIT:C203077 MONDO:excludeNonDisease +NCIT:C203078 MONDO:excludeNonDisease +NCIT:C203079 MONDO:excludeNonDisease NCIT:C20308 MONDO:excludeNonDisease +NCIT:C203080 MONDO:excludeNonDisease +NCIT:C203081 MONDO:excludeNonDisease +NCIT:C203082 MONDO:excludeNonDisease +NCIT:C203083 MONDO:excludeNonDisease +NCIT:C203084 MONDO:excludeNonDisease +NCIT:C203085 MONDO:excludeNonDisease +NCIT:C203086 MONDO:excludeNonDisease +NCIT:C203087 MONDO:excludeNonDisease +NCIT:C203088 MONDO:excludeNonDisease +NCIT:C203089 MONDO:excludeNonDisease NCIT:C20309 MONDO:excludeNonDisease +NCIT:C203090 MONDO:excludeNonDisease +NCIT:C203091 MONDO:excludeNonDisease +NCIT:C203092 MONDO:excludeNonDisease +NCIT:C203093 MONDO:excludeNonDisease +NCIT:C203094 MONDO:excludeNonDisease +NCIT:C203095 MONDO:excludeNonDisease +NCIT:C203096 MONDO:excludeNonDisease +NCIT:C203097 MONDO:excludeNonDisease +NCIT:C203098 MONDO:excludeNonDisease +NCIT:C203099 MONDO:excludeNonDisease NCIT:C2031 MONDO:excludeNonDisease NCIT:C20310 MONDO:excludeNonDisease +NCIT:C203100 MONDO:excludeNonDisease +NCIT:C203101 MONDO:excludeNonDisease +NCIT:C203102 MONDO:excludeNonDisease +NCIT:C203103 MONDO:excludeNonDisease +NCIT:C203104 MONDO:excludeNonDisease +NCIT:C203105 MONDO:excludeNonDisease +NCIT:C203106 MONDO:excludeNonDisease +NCIT:C203107 MONDO:excludeNonDisease +NCIT:C203108 MONDO:excludeNonDisease +NCIT:C203109 MONDO:excludeNonDisease NCIT:C20311 MONDO:excludeNonDisease +NCIT:C203110 MONDO:excludeNonDisease +NCIT:C203111 MONDO:excludeNonDisease +NCIT:C203112 MONDO:excludeNonDisease +NCIT:C203113 MONDO:excludeNonDisease +NCIT:C203114 MONDO:excludeNonDisease +NCIT:C203115 MONDO:excludeNonDisease +NCIT:C203116 MONDO:excludeNonDisease +NCIT:C203117 MONDO:excludeNonDisease +NCIT:C203118 MONDO:excludeNonDisease +NCIT:C203119 MONDO:excludeNonDisease NCIT:C20312 MONDO:excludeNonDisease +NCIT:C203120 MONDO:excludeNonDisease +NCIT:C203121 MONDO:excludeNonDisease +NCIT:C203122 MONDO:excludeNonDisease +NCIT:C203123 MONDO:excludeNonDisease +NCIT:C203124 MONDO:excludeNonDisease +NCIT:C203125 MONDO:excludeNonDisease +NCIT:C203126 MONDO:excludeNonDisease +NCIT:C203127 MONDO:excludeNonDisease +NCIT:C203128 MONDO:excludeNonDisease +NCIT:C203129 MONDO:excludeNonDisease NCIT:C20313 MONDO:excludeNonDisease +NCIT:C203130 MONDO:excludeNonDisease +NCIT:C203131 MONDO:excludeNonDisease +NCIT:C203132 MONDO:excludeNonDisease +NCIT:C203133 MONDO:excludeNonDisease +NCIT:C203134 MONDO:excludeNonDisease +NCIT:C203135 MONDO:excludeNonDisease +NCIT:C203136 MONDO:excludeNonDisease +NCIT:C203137 MONDO:excludeNonDisease +NCIT:C203138 MONDO:excludeNonDisease +NCIT:C203139 MONDO:excludeNonDisease NCIT:C20314 MONDO:excludeNonDisease +NCIT:C203140 MONDO:excludeNonDisease +NCIT:C203141 MONDO:excludeNonDisease +NCIT:C203142 MONDO:excludeNonDisease +NCIT:C203143 MONDO:excludeNonDisease +NCIT:C203144 MONDO:excludeNonDisease +NCIT:C203145 MONDO:excludeNonDisease +NCIT:C203146 MONDO:excludeNonDisease +NCIT:C203147 MONDO:excludeNonDisease +NCIT:C203148 MONDO:excludeNonDisease +NCIT:C203149 MONDO:excludeNonDisease NCIT:C20315 MONDO:excludeNonDisease +NCIT:C203150 MONDO:excludeNonDisease +NCIT:C203151 MONDO:excludeNonDisease +NCIT:C203152 MONDO:excludeNonDisease +NCIT:C203153 MONDO:excludeNonDisease +NCIT:C203154 MONDO:excludeNonDisease +NCIT:C203155 MONDO:excludeNonDisease +NCIT:C203156 MONDO:excludeNonDisease +NCIT:C203157 MONDO:excludeNonDisease +NCIT:C203158 MONDO:excludeNonDisease +NCIT:C203159 MONDO:excludeNonDisease NCIT:C20316 MONDO:excludeNonDisease +NCIT:C203160 MONDO:excludeNonDisease +NCIT:C203161 MONDO:excludeNonDisease +NCIT:C203162 MONDO:excludeNonDisease +NCIT:C203163 MONDO:excludeNonDisease +NCIT:C203164 MONDO:excludeNonDisease +NCIT:C203165 MONDO:excludeNonDisease +NCIT:C203166 MONDO:excludeNonDisease +NCIT:C203167 MONDO:excludeNonDisease +NCIT:C203168 MONDO:excludeNonDisease +NCIT:C203169 MONDO:excludeNonDisease NCIT:C20317 MONDO:excludeNonDisease +NCIT:C203170 MONDO:excludeNonDisease +NCIT:C203171 MONDO:excludeNonDisease +NCIT:C203172 MONDO:excludeNonDisease +NCIT:C203173 MONDO:excludeNonDisease +NCIT:C203174 MONDO:excludeNonDisease +NCIT:C203175 MONDO:excludeNonDisease +NCIT:C203176 MONDO:excludeNonDisease +NCIT:C203177 MONDO:excludeNonDisease +NCIT:C203178 MONDO:excludeNonDisease +NCIT:C203179 MONDO:excludeNonDisease NCIT:C20318 MONDO:excludeNonDisease +NCIT:C203180 MONDO:excludeNonDisease +NCIT:C203181 MONDO:excludeNonDisease +NCIT:C203182 MONDO:excludeNonDisease +NCIT:C203183 MONDO:excludeNonDisease +NCIT:C203184 MONDO:excludeNonDisease +NCIT:C203185 MONDO:excludeNonDisease +NCIT:C203186 MONDO:excludeNonDisease +NCIT:C203187 MONDO:excludeNonDisease +NCIT:C203188 MONDO:excludeNonDisease +NCIT:C203189 MONDO:excludeNonDisease NCIT:C20319 MONDO:excludeNonDisease +NCIT:C203190 MONDO:excludeNonDisease +NCIT:C203191 MONDO:excludeNonDisease +NCIT:C203192 MONDO:excludeNonDisease +NCIT:C203193 MONDO:excludeNonDisease +NCIT:C203194 MONDO:excludeNonDisease +NCIT:C203195 MONDO:excludeNonDisease +NCIT:C203196 MONDO:excludeNonDisease +NCIT:C203197 MONDO:excludeNonDisease +NCIT:C203198 MONDO:excludeNonDisease +NCIT:C203199 MONDO:excludeNonDisease NCIT:C2032 MONDO:excludeNonDisease NCIT:C20320 MONDO:excludeNonDisease +NCIT:C203200 MONDO:excludeNonDisease +NCIT:C203201 MONDO:excludeNonDisease +NCIT:C203202 MONDO:excludeNonDisease +NCIT:C203203 MONDO:excludeNonDisease +NCIT:C203204 MONDO:excludeNonDisease +NCIT:C203205 MONDO:excludeNonDisease +NCIT:C203206 MONDO:excludeNonDisease +NCIT:C203207 MONDO:excludeNonDisease +NCIT:C203208 MONDO:excludeNonDisease +NCIT:C203209 MONDO:excludeNonDisease +NCIT:C203210 MONDO:excludeNonDisease +NCIT:C203211 MONDO:excludeNonDisease +NCIT:C203212 MONDO:excludeNonDisease +NCIT:C203213 MONDO:excludeNonDisease +NCIT:C203214 MONDO:excludeNonDisease +NCIT:C203215 MONDO:excludeNonDisease +NCIT:C203216 MONDO:excludeNonDisease +NCIT:C203217 MONDO:excludeNonDisease +NCIT:C203218 MONDO:excludeNonDisease +NCIT:C203219 MONDO:excludeNonDisease NCIT:C20322 MONDO:excludeNonDisease +NCIT:C203220 MONDO:excludeNonDisease +NCIT:C203221 MONDO:excludeNonDisease +NCIT:C203222 MONDO:excludeNonDisease +NCIT:C203223 MONDO:excludeNonDisease +NCIT:C203224 MONDO:excludeNonDisease +NCIT:C203225 MONDO:excludeNonDisease +NCIT:C203226 MONDO:excludeNonDisease +NCIT:C203227 MONDO:excludeNonDisease +NCIT:C203228 MONDO:excludeNonDisease +NCIT:C203229 MONDO:excludeNonDisease NCIT:C20323 MONDO:excludeNonDisease +NCIT:C203230 MONDO:excludeNonDisease +NCIT:C203231 MONDO:excludeNonDisease +NCIT:C203232 MONDO:excludeNonDisease +NCIT:C203233 MONDO:excludeNonDisease +NCIT:C203234 MONDO:excludeNonDisease +NCIT:C203235 MONDO:excludeNonDisease +NCIT:C203236 MONDO:excludeNonDisease +NCIT:C203237 MONDO:excludeNonDisease +NCIT:C203238 MONDO:excludeNonDisease +NCIT:C203239 MONDO:excludeNonDisease NCIT:C20324 MONDO:excludeNonDisease +NCIT:C203240 MONDO:excludeNonDisease +NCIT:C203241 MONDO:excludeNonDisease +NCIT:C203242 MONDO:excludeNonDisease +NCIT:C203243 MONDO:excludeNonDisease +NCIT:C203244 MONDO:excludeNonDisease +NCIT:C203245 MONDO:excludeNonDisease +NCIT:C203246 MONDO:excludeNonDisease +NCIT:C203247 MONDO:excludeNonDisease +NCIT:C203248 MONDO:excludeNonDisease +NCIT:C203249 MONDO:excludeNonDisease NCIT:C20325 MONDO:excludeNonDisease +NCIT:C203254 MONDO:excludeNonDisease +NCIT:C203255 MONDO:excludeNonDisease +NCIT:C203256 MONDO:excludeNonDisease +NCIT:C203257 MONDO:excludeNonDisease NCIT:C20326 MONDO:excludeNonDisease +NCIT:C203261 MONDO:excludeNonDisease +NCIT:C203264 MONDO:excludeNonDisease +NCIT:C203268 MONDO:excludeNonDisease NCIT:C20327 MONDO:excludeNonDisease +NCIT:C203275 MONDO:excludeNonDisease +NCIT:C203276 MONDO:excludeNonDisease +NCIT:C203277 MONDO:excludeNonDisease +NCIT:C203278 MONDO:excludeNonDisease +NCIT:C203279 MONDO:excludeNonDisease NCIT:C20328 MONDO:excludeNonDisease +NCIT:C203280 MONDO:excludeNonDisease +NCIT:C203281 MONDO:excludeNonDisease +NCIT:C203287 MONDO:excludeNonDisease +NCIT:C203288 MONDO:excludeNonDisease +NCIT:C203289 MONDO:excludeNonDisease NCIT:C20329 MONDO:excludeNonDisease +NCIT:C203290 MONDO:excludeNonDisease +NCIT:C203291 MONDO:excludeNonDisease +NCIT:C203292 MONDO:excludeNonDisease +NCIT:C203293 MONDO:excludeNonDisease +NCIT:C203294 MONDO:excludeNonDisease +NCIT:C203295 MONDO:excludeNonDisease +NCIT:C203296 MONDO:excludeNonDisease +NCIT:C203297 MONDO:excludeNonDisease +NCIT:C203298 MONDO:excludeNonDisease +NCIT:C203299 MONDO:excludeNonDisease NCIT:C2033 MONDO:excludeNonDisease NCIT:C20330 MONDO:excludeNonDisease +NCIT:C203300 MONDO:excludeNonDisease +NCIT:C203301 MONDO:excludeNonDisease +NCIT:C203303 MONDO:excludeNonDisease +NCIT:C203304 MONDO:excludeNonDisease +NCIT:C203305 MONDO:excludeNonDisease +NCIT:C203306 MONDO:excludeNonDisease NCIT:C20331 MONDO:excludeNonDisease +NCIT:C203317 MONDO:excludeNonDisease +NCIT:C203318 MONDO:excludeNonDisease +NCIT:C203319 MONDO:excludeNonDisease NCIT:C20332 MONDO:excludeNonDisease +NCIT:C203320 MONDO:excludeNonDisease +NCIT:C203321 MONDO:excludeNonDisease +NCIT:C203322 MONDO:excludeNonDisease +NCIT:C203323 MONDO:excludeNonDisease +NCIT:C203324 MONDO:excludeNonDisease +NCIT:C203325 MONDO:excludeNonDisease +NCIT:C203326 MONDO:excludeNonDisease +NCIT:C203327 MONDO:excludeNonDisease +NCIT:C203328 MONDO:excludeNonDisease +NCIT:C203329 MONDO:excludeNonDisease NCIT:C20333 MONDO:excludeNonDisease +NCIT:C203330 MONDO:excludeNonDisease +NCIT:C203332 MONDO:excludeNonDisease +NCIT:C203333 MONDO:excludeNonDisease +NCIT:C203334 MONDO:excludeNonDisease +NCIT:C203335 MONDO:excludeNonDisease +NCIT:C203336 MONDO:excludeNonDisease +NCIT:C203337 MONDO:excludeNonDisease +NCIT:C203338 MONDO:excludeNonDisease NCIT:C20334 MONDO:excludeNonDisease +NCIT:C203340 MONDO:excludeNonDisease +NCIT:C203345 MONDO:excludeNonDisease +NCIT:C203346 MONDO:excludeNonDisease +NCIT:C203347 MONDO:excludeNonDisease +NCIT:C203348 MONDO:excludeNonDisease +NCIT:C203349 MONDO:excludeNonDisease NCIT:C20335 MONDO:excludeNonDisease +NCIT:C203350 MONDO:excludeNonDisease +NCIT:C203351 MONDO:excludeNonDisease +NCIT:C203352 MONDO:excludeNonDisease +NCIT:C203353 MONDO:excludeNonDisease +NCIT:C203354 MONDO:excludeNonDisease +NCIT:C203355 MONDO:excludeNonDisease +NCIT:C203356 MONDO:excludeNonDisease +NCIT:C203357 MONDO:excludeNonDisease +NCIT:C203358 MONDO:excludeNonDisease +NCIT:C203359 MONDO:excludeNonDisease NCIT:C20336 MONDO:excludeNonDisease +NCIT:C203360 MONDO:excludeNonDisease +NCIT:C203361 MONDO:excludeNonDisease +NCIT:C203363 MONDO:excludeNonDisease +NCIT:C203364 MONDO:excludeNonDisease +NCIT:C203365 MONDO:excludeNonDisease +NCIT:C203366 MONDO:excludeNonDisease +NCIT:C203367 MONDO:excludeNonDisease +NCIT:C203368 MONDO:excludeNonDisease NCIT:C20337 MONDO:excludeNonDisease +NCIT:C203371 MONDO:excludeNonDisease +NCIT:C203372 MONDO:excludeNonDisease +NCIT:C203373 MONDO:excludeNonDisease +NCIT:C203377 MONDO:excludeNonDisease +NCIT:C203378 MONDO:excludeNonDisease +NCIT:C203379 MONDO:excludeNonDisease NCIT:C20338 MONDO:excludeNonDisease +NCIT:C203382 MONDO:excludeNonDisease +NCIT:C203383 MONDO:excludeNonDisease NCIT:C20339 MONDO:excludeNonDisease +NCIT:C203396 MONDO:excludeNonDisease +NCIT:C203397 MONDO:excludeNonDisease +NCIT:C203398 MONDO:excludeNonDisease +NCIT:C203399 MONDO:excludeNonDisease NCIT:C2034 MONDO:excludeNonDisease NCIT:C20340 MONDO:excludeNonDisease +NCIT:C203400 MONDO:excludeNonDisease +NCIT:C203401 MONDO:excludeNonDisease +NCIT:C203402 MONDO:excludeNonDisease +NCIT:C203403 MONDO:excludeNonDisease +NCIT:C203404 MONDO:excludeNonDisease +NCIT:C203405 MONDO:excludeNonDisease NCIT:C20341 MONDO:excludeNonDisease +NCIT:C203414 MONDO:excludeNonDisease +NCIT:C203416 MONDO:excludeNonDisease +NCIT:C203417 MONDO:excludeNonDisease +NCIT:C203418 MONDO:excludeNonDisease +NCIT:C203419 MONDO:excludeNonDisease NCIT:C20342 MONDO:excludeNonDisease +NCIT:C203420 MONDO:excludeNonDisease +NCIT:C203421 MONDO:excludeNonDisease +NCIT:C203423 MONDO:excludeNonDisease +NCIT:C203424 MONDO:excludeNonDisease +NCIT:C203425 MONDO:excludeNonDisease +NCIT:C203427 MONDO:excludeNonDisease +NCIT:C203429 MONDO:excludeNonDisease NCIT:C20343 MONDO:excludeNonDisease +NCIT:C203436 MONDO:excludeNonDisease +NCIT:C203438 MONDO:excludeNonDisease +NCIT:C203439 MONDO:excludeNonDisease NCIT:C20344 MONDO:excludeNonDisease +NCIT:C203441 MONDO:excludeNonDisease +NCIT:C203442 MONDO:excludeNonDisease +NCIT:C203445 MONDO:excludeNonDisease +NCIT:C203446 MONDO:excludeNonDisease +NCIT:C203447 MONDO:excludeNonDisease +NCIT:C203448 MONDO:excludeNonDisease +NCIT:C203449 MONDO:excludeNonDisease NCIT:C20345 MONDO:excludeNonDisease +NCIT:C203450 MONDO:excludeNonDisease +NCIT:C203451 MONDO:excludeNonDisease +NCIT:C203452 MONDO:excludeNonDisease +NCIT:C203453 MONDO:excludeNonDisease +NCIT:C203454 MONDO:excludeNonDisease +NCIT:C203455 MONDO:excludeNonDisease +NCIT:C203456 MONDO:excludeNonDisease +NCIT:C203457 MONDO:excludeNonDisease +NCIT:C203458 MONDO:excludeNonDisease +NCIT:C203459 MONDO:excludeNonDisease NCIT:C20346 MONDO:excludeNonDisease +NCIT:C203460 MONDO:excludeNonDisease +NCIT:C203461 MONDO:excludeNonDisease +NCIT:C203462 MONDO:excludeNonDisease +NCIT:C203463 MONDO:excludeNonDisease +NCIT:C203464 MONDO:excludeNonDisease +NCIT:C203465 MONDO:excludeNonDisease +NCIT:C203466 MONDO:excludeNonDisease +NCIT:C203467 MONDO:excludeNonDisease +NCIT:C203468 MONDO:excludeNonDisease NCIT:C20347 MONDO:excludeNonDisease +NCIT:C203470 MONDO:excludeNonDisease +NCIT:C203471 MONDO:excludeNonDisease +NCIT:C203472 MONDO:excludeNonDisease +NCIT:C203473 MONDO:excludeNonDisease +NCIT:C203474 MONDO:excludeNonDisease +NCIT:C203475 MONDO:excludeNonDisease +NCIT:C203476 MONDO:excludeNonDisease +NCIT:C203477 MONDO:excludeNonDisease +NCIT:C203478 MONDO:excludeNonDisease +NCIT:C203479 MONDO:excludeNonDisease NCIT:C20348 MONDO:excludeNonDisease +NCIT:C203480 MONDO:excludeNonDisease +NCIT:C203481 MONDO:excludeNonDisease +NCIT:C203482 MONDO:excludeNonDisease +NCIT:C203483 MONDO:excludeNonDisease +NCIT:C203484 MONDO:excludeNonDisease +NCIT:C203485 MONDO:excludeNonDisease +NCIT:C203486 MONDO:excludeNonDisease +NCIT:C203487 MONDO:excludeNonDisease +NCIT:C203488 MONDO:excludeNonDisease +NCIT:C203489 MONDO:excludeNonDisease NCIT:C20349 MONDO:excludeNonDisease +NCIT:C203490 MONDO:excludeNonDisease +NCIT:C203491 MONDO:excludeNonDisease +NCIT:C203492 MONDO:excludeNonDisease +NCIT:C203493 MONDO:excludeNonDisease +NCIT:C203494 MONDO:excludeNonDisease +NCIT:C203495 MONDO:excludeNonDisease +NCIT:C203496 MONDO:excludeNonDisease +NCIT:C203497 MONDO:excludeNonDisease +NCIT:C203498 MONDO:excludeNonDisease +NCIT:C203499 MONDO:excludeNonDisease NCIT:C2035 MONDO:excludeNonDisease NCIT:C20350 MONDO:excludeNonDisease +NCIT:C203500 MONDO:excludeNonDisease +NCIT:C203501 MONDO:excludeNonDisease +NCIT:C203502 MONDO:excludeNonDisease +NCIT:C203503 MONDO:excludeNonDisease +NCIT:C203504 MONDO:excludeNonDisease +NCIT:C203505 MONDO:excludeNonDisease +NCIT:C203506 MONDO:excludeNonDisease +NCIT:C203507 MONDO:excludeNonDisease +NCIT:C203508 MONDO:excludeNonDisease +NCIT:C203509 MONDO:excludeNonDisease +NCIT:C203510 MONDO:excludeNonDisease +NCIT:C203512 MONDO:excludeNonDisease +NCIT:C203514 MONDO:excludeNonDisease +NCIT:C203516 MONDO:excludeNonDisease +NCIT:C203517 MONDO:excludeNonDisease +NCIT:C203518 MONDO:excludeNonDisease +NCIT:C203519 MONDO:excludeNonDisease NCIT:C20352 MONDO:excludeNonDisease +NCIT:C203520 MONDO:excludeNonDisease +NCIT:C203521 MONDO:excludeNonDisease +NCIT:C203522 MONDO:excludeNonDisease +NCIT:C203524 MONDO:excludeNonDisease +NCIT:C203525 MONDO:excludeNonDisease +NCIT:C203527 MONDO:excludeNonDisease +NCIT:C203528 MONDO:excludeNonDisease +NCIT:C203529 MONDO:excludeNonDisease NCIT:C20353 MONDO:excludeNonDisease +NCIT:C203530 MONDO:excludeNonDisease +NCIT:C203531 MONDO:excludeNonDisease +NCIT:C203532 MONDO:excludeNonDisease +NCIT:C203533 MONDO:excludeNonDisease +NCIT:C203534 MONDO:excludeNonDisease +NCIT:C203535 MONDO:excludeNonDisease +NCIT:C203536 MONDO:excludeNonDisease +NCIT:C203537 MONDO:excludeNonDisease +NCIT:C203538 MONDO:excludeNonDisease +NCIT:C203539 MONDO:excludeNonDisease NCIT:C20354 MONDO:excludeNonDisease +NCIT:C203540 MONDO:excludeNonDisease +NCIT:C203541 MONDO:excludeNonDisease +NCIT:C203542 MONDO:excludeNonDisease +NCIT:C203543 MONDO:excludeNonDisease +NCIT:C203544 MONDO:excludeNonDisease +NCIT:C203545 MONDO:excludeNonDisease +NCIT:C203546 MONDO:excludeNonDisease NCIT:C20355 MONDO:excludeNonDisease +NCIT:C203557 MONDO:excludeNonDisease +NCIT:C203558 MONDO:excludeNonDisease +NCIT:C203559 MONDO:excludeNonDisease NCIT:C20356 MONDO:excludeNonDisease +NCIT:C203560 MONDO:excludeNonDisease +NCIT:C203561 MONDO:excludeNonDisease +NCIT:C203562 MONDO:excludeNonDisease +NCIT:C203563 MONDO:excludeNonDisease +NCIT:C203564 MONDO:excludeNonDisease +NCIT:C203565 MONDO:excludeNonDisease +NCIT:C203566 MONDO:excludeNonDisease +NCIT:C203567 MONDO:excludeNonDisease +NCIT:C203568 MONDO:excludeNonDisease +NCIT:C203569 MONDO:excludeNonDisease NCIT:C20357 MONDO:excludeNonDisease +NCIT:C203570 MONDO:excludeNonDisease +NCIT:C203571 MONDO:excludeNonDisease +NCIT:C203572 MONDO:excludeNonDisease +NCIT:C203573 MONDO:excludeNonDisease +NCIT:C203574 MONDO:excludeNonDisease +NCIT:C203575 MONDO:excludeNonDisease +NCIT:C203576 MONDO:excludeNonDisease +NCIT:C203577 MONDO:excludeNonDisease +NCIT:C203578 MONDO:excludeNonDisease +NCIT:C203579 MONDO:excludeNonDisease NCIT:C20358 MONDO:excludeNonDisease +NCIT:C203580 MONDO:excludeNonDisease +NCIT:C203581 MONDO:excludeNonDisease +NCIT:C203582 MONDO:excludeNonDisease +NCIT:C203584 MONDO:excludeNonDisease +NCIT:C203585 MONDO:excludeNonDisease +NCIT:C203586 MONDO:excludeNonDisease +NCIT:C203587 MONDO:excludeNonDisease +NCIT:C203588 MONDO:excludeNonDisease +NCIT:C203589 MONDO:excludeNonDisease NCIT:C20359 MONDO:excludeNonDisease +NCIT:C203590 MONDO:excludeNonDisease +NCIT:C203591 MONDO:excludeNonDisease +NCIT:C203592 MONDO:excludeNonDisease +NCIT:C203593 MONDO:excludeNonDisease +NCIT:C203594 MONDO:excludeNonDisease +NCIT:C203595 MONDO:excludeNonDisease +NCIT:C203596 MONDO:excludeNonDisease +NCIT:C203597 MONDO:excludeNonDisease +NCIT:C203598 MONDO:excludeNonDisease +NCIT:C203599 MONDO:excludeNonDisease NCIT:C2036 MONDO:excludeNonDisease NCIT:C20360 MONDO:excludeNonDisease +NCIT:C203600 MONDO:excludeNonDisease +NCIT:C203602 MONDO:excludeNonDisease +NCIT:C203603 MONDO:excludeNonDisease +NCIT:C203604 MONDO:excludeNonDisease +NCIT:C203605 MONDO:excludeNonDisease +NCIT:C203606 MONDO:excludeNonDisease +NCIT:C203607 MONDO:excludeNonDisease +NCIT:C203608 MONDO:excludeNonDisease +NCIT:C203609 MONDO:excludeNonDisease NCIT:C20361 MONDO:excludeNonDisease +NCIT:C203610 MONDO:excludeNonDisease +NCIT:C203611 MONDO:excludeNonDisease +NCIT:C203612 MONDO:excludeNonDisease +NCIT:C203613 MONDO:excludeNonDisease +NCIT:C203614 MONDO:excludeNonDisease +NCIT:C203615 MONDO:excludeNonDisease +NCIT:C203616 MONDO:excludeNonDisease +NCIT:C203617 MONDO:excludeNonDisease NCIT:C20362 MONDO:excludeNonDisease +NCIT:C203620 MONDO:excludeNonDisease +NCIT:C203621 MONDO:excludeNonDisease +NCIT:C203622 MONDO:excludeNonDisease +NCIT:C203623 MONDO:excludeNonDisease +NCIT:C203624 MONDO:excludeNonDisease +NCIT:C203625 MONDO:excludeNonDisease +NCIT:C203626 MONDO:excludeNonDisease +NCIT:C203627 MONDO:excludeNonDisease +NCIT:C203628 MONDO:excludeNonDisease +NCIT:C203629 MONDO:excludeNonDisease NCIT:C20363 MONDO:excludeNonDisease +NCIT:C203630 MONDO:excludeNonDisease +NCIT:C203631 MONDO:excludeNonDisease +NCIT:C203632 MONDO:excludeNonDisease +NCIT:C203633 MONDO:excludeNonDisease +NCIT:C203634 MONDO:excludeNonDisease +NCIT:C203635 MONDO:excludeNonDisease +NCIT:C203636 MONDO:excludeNonDisease +NCIT:C203637 MONDO:excludeNonDisease +NCIT:C203638 MONDO:excludeNonDisease +NCIT:C203639 MONDO:excludeNonDisease NCIT:C20364 MONDO:excludeNonDisease +NCIT:C203640 MONDO:excludeNonDisease +NCIT:C203641 MONDO:excludeNonDisease +NCIT:C203642 MONDO:excludeNonDisease +NCIT:C203643 MONDO:excludeNonDisease +NCIT:C203644 MONDO:excludeNonDisease +NCIT:C203645 MONDO:excludeNonDisease +NCIT:C203646 MONDO:excludeNonDisease +NCIT:C203647 MONDO:excludeNonDisease +NCIT:C203648 MONDO:excludeNonDisease +NCIT:C203649 MONDO:excludeNonDisease NCIT:C20365 MONDO:excludeNonDisease +NCIT:C203650 MONDO:excludeNonDisease +NCIT:C203651 MONDO:excludeNonDisease +NCIT:C203652 MONDO:excludeNonDisease +NCIT:C203653 MONDO:excludeNonDisease +NCIT:C203654 MONDO:excludeNonDisease +NCIT:C203655 MONDO:excludeNonDisease +NCIT:C203656 MONDO:excludeNonDisease +NCIT:C203657 MONDO:excludeNonDisease +NCIT:C203658 MONDO:excludeNonDisease +NCIT:C203660 MONDO:excludeNonDisease +NCIT:C203661 MONDO:excludeNonDisease +NCIT:C203662 MONDO:excludeNonDisease +NCIT:C203663 MONDO:excludeNonDisease +NCIT:C203664 MONDO:excludeNonDisease +NCIT:C203665 MONDO:excludeNonDisease +NCIT:C203666 MONDO:excludeNonDisease +NCIT:C203668 MONDO:excludeNonDisease NCIT:C20367 MONDO:excludeNonDisease +NCIT:C203670 MONDO:excludeNonDisease +NCIT:C203671 MONDO:excludeNonDisease +NCIT:C203672 MONDO:excludeNonDisease +NCIT:C203674 MONDO:excludeNonDisease +NCIT:C203676 MONDO:excludeNonDisease +NCIT:C203677 MONDO:excludeNonDisease +NCIT:C203678 MONDO:excludeNonDisease +NCIT:C203679 MONDO:excludeNonDisease NCIT:C20368 MONDO:excludeNonDisease +NCIT:C203680 MONDO:excludeNonDisease +NCIT:C203681 MONDO:excludeNonDisease +NCIT:C203682 MONDO:excludeNonDisease +NCIT:C203683 MONDO:excludeNonDisease +NCIT:C203684 MONDO:excludeNonDisease +NCIT:C203685 MONDO:excludeNonDisease +NCIT:C203686 MONDO:excludeNonDisease +NCIT:C203687 MONDO:excludeNonDisease +NCIT:C203688 MONDO:excludeNonDisease +NCIT:C203689 MONDO:excludeNonDisease NCIT:C20369 MONDO:excludeNonDisease +NCIT:C203690 MONDO:excludeNonDisease +NCIT:C203691 MONDO:excludeNonDisease +NCIT:C203692 MONDO:excludeNonDisease +NCIT:C203693 MONDO:excludeNonDisease +NCIT:C203694 MONDO:excludeNonDisease +NCIT:C203695 MONDO:excludeNonDisease +NCIT:C203696 MONDO:excludeNonDisease +NCIT:C203697 MONDO:excludeNonDisease +NCIT:C203698 MONDO:excludeNonDisease +NCIT:C203699 MONDO:excludeNonDisease NCIT:C2037 MONDO:excludeNonDisease NCIT:C20370 MONDO:excludeNonDisease +NCIT:C203701 MONDO:excludeNonDisease +NCIT:C203702 MONDO:excludeNonDisease +NCIT:C203703 MONDO:excludeNonDisease +NCIT:C203704 MONDO:excludeNonDisease +NCIT:C203705 MONDO:excludeNonDisease +NCIT:C203706 MONDO:excludeNonDisease +NCIT:C203707 MONDO:excludeNonDisease +NCIT:C203708 MONDO:excludeNonDisease +NCIT:C203709 MONDO:excludeNonDisease NCIT:C20371 MONDO:excludeNonDisease +NCIT:C203710 MONDO:excludeNonDisease +NCIT:C203711 MONDO:excludeNonDisease +NCIT:C203712 MONDO:excludeNonDisease +NCIT:C203713 MONDO:excludeNonDisease +NCIT:C203714 MONDO:excludeNonDisease +NCIT:C203715 MONDO:excludeNonDisease +NCIT:C203716 MONDO:excludeNonDisease +NCIT:C203717 MONDO:excludeNonDisease +NCIT:C203718 MONDO:excludeNonDisease +NCIT:C203719 MONDO:excludeNonDisease NCIT:C20372 MONDO:excludeNonDisease +NCIT:C203720 MONDO:excludeNonDisease +NCIT:C203721 MONDO:excludeNonDisease +NCIT:C203722 MONDO:excludeNonDisease +NCIT:C203723 MONDO:excludeNonDisease +NCIT:C203724 MONDO:excludeNonDisease +NCIT:C203725 MONDO:excludeNonDisease +NCIT:C203726 MONDO:excludeNonDisease +NCIT:C203727 MONDO:excludeNonDisease +NCIT:C203728 MONDO:excludeNonDisease +NCIT:C203729 MONDO:excludeNonDisease NCIT:C20373 MONDO:excludeNonDisease +NCIT:C203730 MONDO:excludeNonDisease +NCIT:C203731 MONDO:excludeNonDisease +NCIT:C203732 MONDO:excludeNonDisease +NCIT:C203733 MONDO:excludeNonDisease +NCIT:C203734 MONDO:excludeNonDisease +NCIT:C203735 MONDO:excludeNonDisease +NCIT:C203736 MONDO:excludeNonDisease +NCIT:C203737 MONDO:excludeNonDisease +NCIT:C203738 MONDO:excludeNonDisease +NCIT:C203739 MONDO:excludeNonDisease NCIT:C20374 MONDO:excludeNonDisease +NCIT:C203740 MONDO:excludeNonDisease +NCIT:C203741 MONDO:excludeNonDisease +NCIT:C203742 MONDO:excludeNonDisease +NCIT:C203743 MONDO:excludeNonDisease +NCIT:C203744 MONDO:excludeNonDisease +NCIT:C203745 MONDO:excludeNonDisease +NCIT:C203746 MONDO:excludeNonDisease +NCIT:C203747 MONDO:excludeNonDisease +NCIT:C203748 MONDO:excludeNonDisease +NCIT:C203749 MONDO:excludeNonDisease NCIT:C20375 MONDO:excludeNonDisease +NCIT:C203750 MONDO:excludeNonDisease +NCIT:C203751 MONDO:excludeNonDisease +NCIT:C203752 MONDO:excludeNonDisease +NCIT:C203753 MONDO:excludeNonDisease +NCIT:C203754 MONDO:excludeNonDisease +NCIT:C203755 MONDO:excludeNonDisease +NCIT:C203756 MONDO:excludeNonDisease +NCIT:C203757 MONDO:excludeNonDisease +NCIT:C203758 MONDO:excludeNonDisease +NCIT:C203759 MONDO:excludeNonDisease NCIT:C20376 MONDO:excludeNonDisease +NCIT:C203760 MONDO:excludeNonDisease +NCIT:C203761 MONDO:excludeNonDisease +NCIT:C203762 MONDO:excludeNonDisease +NCIT:C203763 MONDO:excludeNonDisease +NCIT:C203764 MONDO:excludeNonDisease +NCIT:C203765 MONDO:excludeNonDisease +NCIT:C203766 MONDO:excludeNonDisease +NCIT:C203767 MONDO:excludeNonDisease +NCIT:C203768 MONDO:excludeNonDisease +NCIT:C203769 MONDO:excludeNonDisease NCIT:C20377 MONDO:excludeNonDisease +NCIT:C203770 MONDO:excludeNonDisease +NCIT:C203771 MONDO:excludeNonDisease +NCIT:C203772 MONDO:excludeNonDisease +NCIT:C203773 MONDO:excludeNonDisease +NCIT:C203774 MONDO:excludeNonDisease +NCIT:C203775 MONDO:excludeNonDisease +NCIT:C203776 MONDO:excludeNonDisease +NCIT:C203777 MONDO:excludeNonDisease +NCIT:C203778 MONDO:excludeNonDisease +NCIT:C203779 MONDO:excludeNonDisease NCIT:C20378 MONDO:excludeNonDisease +NCIT:C203780 MONDO:excludeNonDisease +NCIT:C203781 MONDO:excludeNonDisease +NCIT:C203782 MONDO:excludeNonDisease +NCIT:C203783 MONDO:excludeNonDisease +NCIT:C203784 MONDO:excludeNonDisease +NCIT:C203785 MONDO:excludeNonDisease +NCIT:C203786 MONDO:excludeNonDisease +NCIT:C203787 MONDO:excludeNonDisease +NCIT:C203788 MONDO:excludeNonDisease +NCIT:C203789 MONDO:excludeNonDisease NCIT:C20379 MONDO:excludeNonDisease +NCIT:C203790 MONDO:excludeNonDisease +NCIT:C203791 MONDO:excludeNonDisease +NCIT:C203792 MONDO:excludeNonDisease +NCIT:C203793 MONDO:excludeNonDisease +NCIT:C203794 MONDO:excludeNonDisease +NCIT:C203796 MONDO:excludeNonDisease +NCIT:C203797 MONDO:excludeNonDisease +NCIT:C203798 MONDO:excludeNonDisease +NCIT:C203799 MONDO:excludeNonDisease NCIT:C2038 MONDO:excludeNonDisease NCIT:C20380 MONDO:excludeNonDisease +NCIT:C203800 MONDO:excludeNonDisease +NCIT:C203801 MONDO:excludeNonDisease +NCIT:C203802 MONDO:excludeNonDisease +NCIT:C203803 MONDO:excludeNonDisease +NCIT:C203804 MONDO:excludeNonDisease +NCIT:C203805 MONDO:excludeNonDisease +NCIT:C203806 MONDO:excludeNonDisease +NCIT:C203807 MONDO:excludeNonDisease +NCIT:C203808 MONDO:excludeNonDisease +NCIT:C203809 MONDO:excludeNonDisease NCIT:C20381 MONDO:excludeNonDisease +NCIT:C203810 MONDO:excludeNonDisease +NCIT:C203811 MONDO:excludeNonDisease +NCIT:C203812 MONDO:excludeNonDisease +NCIT:C203813 MONDO:excludeNonDisease +NCIT:C203814 MONDO:excludeNonDisease +NCIT:C203816 MONDO:excludeNonDisease +NCIT:C203817 MONDO:excludeNonDisease +NCIT:C203818 MONDO:excludeNonDisease +NCIT:C203819 MONDO:excludeNonDisease NCIT:C20382 MONDO:excludeNonDisease +NCIT:C203820 MONDO:excludeNonDisease +NCIT:C203821 MONDO:excludeNonDisease +NCIT:C203822 MONDO:excludeNonDisease +NCIT:C203823 MONDO:excludeNonDisease +NCIT:C203824 MONDO:excludeNonDisease +NCIT:C203825 MONDO:excludeNonDisease +NCIT:C203826 MONDO:excludeNonDisease +NCIT:C203827 MONDO:excludeNonDisease +NCIT:C203828 MONDO:excludeNonDisease +NCIT:C203829 MONDO:excludeNonDisease NCIT:C20383 MONDO:excludeNonDisease +NCIT:C203830 MONDO:excludeNonDisease +NCIT:C203831 MONDO:excludeNonDisease +NCIT:C203832 MONDO:excludeNonDisease +NCIT:C203833 MONDO:excludeNonDisease +NCIT:C203834 MONDO:excludeNonDisease +NCIT:C203835 MONDO:excludeNonDisease +NCIT:C203836 MONDO:excludeNonDisease +NCIT:C203837 MONDO:excludeNonDisease +NCIT:C203838 MONDO:excludeNonDisease +NCIT:C203839 MONDO:excludeNonDisease NCIT:C20384 MONDO:excludeNonDisease +NCIT:C203840 MONDO:excludeNonDisease +NCIT:C203841 MONDO:excludeNonDisease +NCIT:C203842 MONDO:excludeNonDisease +NCIT:C203843 MONDO:excludeNonDisease +NCIT:C203844 MONDO:excludeNonDisease +NCIT:C203845 MONDO:excludeNonDisease +NCIT:C203846 MONDO:excludeNonDisease +NCIT:C203847 MONDO:excludeNonDisease +NCIT:C203848 MONDO:excludeNonDisease +NCIT:C203849 MONDO:excludeNonDisease NCIT:C20385 MONDO:excludeNonDisease +NCIT:C203850 MONDO:excludeNonDisease +NCIT:C203852 MONDO:excludeNonDisease +NCIT:C203853 MONDO:excludeNonDisease +NCIT:C203854 MONDO:excludeNonDisease +NCIT:C203855 MONDO:excludeNonDisease +NCIT:C203856 MONDO:excludeNonDisease +NCIT:C203857 MONDO:excludeNonDisease +NCIT:C203858 MONDO:excludeNonDisease +NCIT:C203859 MONDO:excludeNonDisease NCIT:C20386 MONDO:excludeNonDisease +NCIT:C203860 MONDO:excludeNonDisease +NCIT:C203861 MONDO:excludeNonDisease +NCIT:C203862 MONDO:excludeNonDisease +NCIT:C203863 MONDO:excludeNonDisease +NCIT:C203864 MONDO:excludeNonDisease +NCIT:C203865 MONDO:excludeNonDisease +NCIT:C203866 MONDO:excludeNonDisease +NCIT:C203867 MONDO:excludeNonDisease +NCIT:C203868 MONDO:excludeNonDisease +NCIT:C203869 MONDO:excludeNonDisease NCIT:C20387 MONDO:excludeNonDisease +NCIT:C203870 MONDO:excludeNonDisease +NCIT:C203871 MONDO:excludeNonDisease +NCIT:C203872 MONDO:excludeNonDisease +NCIT:C203873 MONDO:excludeNonDisease +NCIT:C203874 MONDO:excludeNonDisease +NCIT:C203875 MONDO:excludeNonDisease +NCIT:C203876 MONDO:excludeNonDisease +NCIT:C203877 MONDO:excludeNonDisease +NCIT:C203878 MONDO:excludeNonDisease +NCIT:C203879 MONDO:excludeNonDisease NCIT:C20388 MONDO:excludeNonDisease +NCIT:C203880 MONDO:excludeNonDisease +NCIT:C203881 MONDO:excludeNonDisease +NCIT:C203882 MONDO:excludeNonDisease +NCIT:C203883 MONDO:excludeNonDisease +NCIT:C203884 MONDO:excludeNonDisease +NCIT:C203885 MONDO:excludeNonDisease +NCIT:C203886 MONDO:excludeNonDisease +NCIT:C203887 MONDO:excludeNonDisease +NCIT:C203888 MONDO:excludeNonDisease +NCIT:C203889 MONDO:excludeNonDisease NCIT:C20389 MONDO:excludeNonDisease +NCIT:C203890 MONDO:excludeNonDisease +NCIT:C203891 MONDO:excludeNonDisease +NCIT:C203892 MONDO:excludeNonDisease +NCIT:C203893 MONDO:excludeNonDisease +NCIT:C203894 MONDO:excludeNonDisease +NCIT:C203895 MONDO:excludeNonDisease +NCIT:C203896 MONDO:excludeNonDisease +NCIT:C203897 MONDO:excludeNonDisease +NCIT:C203898 MONDO:excludeNonDisease +NCIT:C203899 MONDO:excludeNonDisease NCIT:C2039 MONDO:excludeNonDisease NCIT:C20390 MONDO:excludeNonDisease +NCIT:C203900 MONDO:excludeNonDisease +NCIT:C203901 MONDO:excludeNonDisease +NCIT:C203902 MONDO:excludeNonDisease +NCIT:C203903 MONDO:excludeNonDisease +NCIT:C203905 MONDO:excludeNonDisease +NCIT:C203906 MONDO:excludeNonDisease +NCIT:C203907 MONDO:excludeNonDisease +NCIT:C203908 MONDO:excludeNonDisease +NCIT:C203909 MONDO:excludeNonDisease NCIT:C20391 MONDO:excludeNonDisease +NCIT:C203910 MONDO:excludeNonDisease +NCIT:C203911 MONDO:excludeNonDisease +NCIT:C203912 MONDO:excludeNonDisease +NCIT:C203913 MONDO:excludeNonDisease +NCIT:C203914 MONDO:excludeNonDisease +NCIT:C203915 MONDO:excludeNonDisease +NCIT:C203916 MONDO:excludeNonDisease +NCIT:C203917 MONDO:excludeNonDisease +NCIT:C203918 MONDO:excludeNonDisease +NCIT:C203919 MONDO:excludeNonDisease NCIT:C20392 MONDO:excludeNonDisease +NCIT:C203920 MONDO:excludeNonDisease +NCIT:C203921 MONDO:excludeNonDisease +NCIT:C203922 MONDO:excludeNonDisease +NCIT:C203923 MONDO:excludeNonDisease +NCIT:C203924 MONDO:excludeNonDisease +NCIT:C203925 MONDO:excludeNonDisease +NCIT:C203926 MONDO:excludeNonDisease +NCIT:C203927 MONDO:excludeNonDisease +NCIT:C203928 MONDO:excludeNonDisease +NCIT:C203929 MONDO:excludeNonDisease NCIT:C20393 MONDO:excludeNonDisease +NCIT:C203930 MONDO:excludeNonDisease +NCIT:C203931 MONDO:excludeNonDisease +NCIT:C203932 MONDO:excludeNonDisease +NCIT:C203933 MONDO:excludeNonDisease +NCIT:C203934 MONDO:excludeNonDisease +NCIT:C203935 MONDO:excludeNonDisease +NCIT:C203936 MONDO:excludeNonDisease +NCIT:C203937 MONDO:excludeNonDisease +NCIT:C203938 MONDO:excludeNonDisease +NCIT:C203939 MONDO:excludeNonDisease NCIT:C20394 MONDO:excludeNonDisease +NCIT:C203940 MONDO:excludeNonDisease +NCIT:C203941 MONDO:excludeNonDisease +NCIT:C203942 MONDO:excludeNonDisease +NCIT:C203943 MONDO:excludeNonDisease +NCIT:C203944 MONDO:excludeNonDisease +NCIT:C203945 MONDO:excludeNonDisease +NCIT:C203947 MONDO:excludeNonDisease NCIT:C20395 MONDO:excludeNonDisease +NCIT:C203950 MONDO:excludeNonDisease +NCIT:C203951 MONDO:excludeNonDisease +NCIT:C203952 MONDO:excludeNonDisease +NCIT:C203953 MONDO:excludeNonDisease +NCIT:C203954 MONDO:excludeNonDisease +NCIT:C203955 MONDO:excludeNonDisease +NCIT:C203956 MONDO:excludeNonDisease +NCIT:C203957 MONDO:excludeNonDisease +NCIT:C203958 MONDO:excludeNonDisease +NCIT:C203959 MONDO:excludeNonDisease NCIT:C20396 MONDO:excludeNonDisease +NCIT:C203960 MONDO:excludeNonDisease +NCIT:C203961 MONDO:excludeNonDisease +NCIT:C203962 MONDO:excludeNonDisease +NCIT:C203963 MONDO:excludeNonDisease +NCIT:C203964 MONDO:excludeNonDisease +NCIT:C203965 MONDO:excludeNonDisease +NCIT:C203966 MONDO:excludeNonDisease +NCIT:C203967 MONDO:excludeNonDisease NCIT:C20397 MONDO:excludeNonDisease +NCIT:C203970 MONDO:excludeNonDisease +NCIT:C203971 MONDO:excludeNonDisease +NCIT:C203972 MONDO:excludeNonDisease +NCIT:C203973 MONDO:excludeNonDisease +NCIT:C203974 MONDO:excludeNonDisease +NCIT:C203975 MONDO:excludeNonDisease +NCIT:C203976 MONDO:excludeNonDisease +NCIT:C203977 MONDO:excludeNonDisease +NCIT:C203978 MONDO:excludeNonDisease +NCIT:C203979 MONDO:excludeNonDisease NCIT:C20398 MONDO:excludeNonDisease +NCIT:C203980 MONDO:excludeNonDisease +NCIT:C203981 MONDO:excludeNonDisease +NCIT:C203982 MONDO:excludeNonDisease +NCIT:C203983 MONDO:excludeNonDisease +NCIT:C203984 MONDO:excludeNonDisease +NCIT:C203985 MONDO:excludeNonDisease +NCIT:C203986 MONDO:excludeNonDisease +NCIT:C203987 MONDO:excludeNonDisease +NCIT:C203988 MONDO:excludeNonDisease +NCIT:C203989 MONDO:excludeNonDisease NCIT:C20399 MONDO:excludeNonDisease +NCIT:C203990 MONDO:excludeNonDisease +NCIT:C203991 MONDO:excludeNonDisease +NCIT:C203992 MONDO:excludeNonDisease +NCIT:C203993 MONDO:excludeNonDisease +NCIT:C203994 MONDO:excludeNonDisease +NCIT:C203995 MONDO:excludeNonDisease +NCIT:C203996 MONDO:excludeNonDisease +NCIT:C203997 MONDO:excludeNonDisease +NCIT:C203998 MONDO:excludeNonDisease +NCIT:C203999 MONDO:excludeNonDisease NCIT:C204 MONDO:excludeNonDisease NCIT:C2040 MONDO:excludeNonDisease +NCIT:C204000 MONDO:excludeNonDisease +NCIT:C204001 MONDO:excludeNonDisease +NCIT:C204002 MONDO:excludeNonDisease +NCIT:C204003 MONDO:excludeNonDisease +NCIT:C204004 MONDO:excludeNonDisease +NCIT:C204005 MONDO:excludeNonDisease +NCIT:C204006 MONDO:excludeNonDisease +NCIT:C204007 MONDO:excludeNonDisease +NCIT:C204008 MONDO:excludeNonDisease +NCIT:C204009 MONDO:excludeNonDisease NCIT:C20401 MONDO:excludeNonDisease +NCIT:C204010 MONDO:excludeNonDisease +NCIT:C204011 MONDO:excludeNonDisease +NCIT:C204012 MONDO:excludeNonDisease +NCIT:C204013 MONDO:excludeNonDisease +NCIT:C204014 MONDO:excludeNonDisease +NCIT:C204015 MONDO:excludeNonDisease +NCIT:C204016 MONDO:excludeNonDisease +NCIT:C204017 MONDO:excludeNonDisease +NCIT:C204018 MONDO:excludeNonDisease +NCIT:C204019 MONDO:excludeNonDisease NCIT:C20402 MONDO:excludeNonDisease +NCIT:C204020 MONDO:excludeNonDisease +NCIT:C204021 MONDO:excludeNonDisease +NCIT:C204022 MONDO:excludeNonDisease +NCIT:C204023 MONDO:excludeNonDisease +NCIT:C204024 MONDO:excludeNonDisease +NCIT:C204025 MONDO:excludeNonDisease +NCIT:C204026 MONDO:excludeNonDisease +NCIT:C204027 MONDO:excludeNonDisease +NCIT:C204028 MONDO:excludeNonDisease +NCIT:C204029 MONDO:excludeNonDisease NCIT:C20403 MONDO:excludeNonDisease +NCIT:C204030 MONDO:excludeNonDisease +NCIT:C204031 MONDO:excludeNonDisease +NCIT:C204032 MONDO:excludeNonDisease +NCIT:C204033 MONDO:excludeNonDisease +NCIT:C204034 MONDO:excludeNonDisease +NCIT:C204039 MONDO:excludeNonDisease NCIT:C20404 MONDO:excludeNonDisease +NCIT:C204040 MONDO:excludeNonDisease +NCIT:C204041 MONDO:excludeNonDisease +NCIT:C204042 MONDO:excludeNonDisease +NCIT:C204043 MONDO:excludeNonDisease +NCIT:C204044 MONDO:excludeNonDisease +NCIT:C204045 MONDO:excludeNonDisease +NCIT:C204046 MONDO:excludeNonDisease +NCIT:C204047 MONDO:excludeNonDisease +NCIT:C204048 MONDO:excludeNonDisease +NCIT:C204049 MONDO:excludeNonDisease NCIT:C20405 MONDO:excludeNonDisease +NCIT:C204050 MONDO:excludeNonDisease +NCIT:C204051 MONDO:excludeNonDisease +NCIT:C204052 MONDO:excludeNonDisease +NCIT:C204053 MONDO:excludeNonDisease +NCIT:C204054 MONDO:excludeNonDisease +NCIT:C204055 MONDO:excludeNonDisease +NCIT:C204056 MONDO:excludeNonDisease +NCIT:C204057 MONDO:excludeNonDisease +NCIT:C204058 MONDO:excludeNonDisease +NCIT:C204059 MONDO:excludeNonDisease NCIT:C20406 MONDO:excludeNonDisease +NCIT:C204060 MONDO:excludeNonDisease +NCIT:C204061 MONDO:excludeNonDisease +NCIT:C204062 MONDO:excludeNonDisease +NCIT:C204063 MONDO:excludeNonDisease +NCIT:C204064 MONDO:excludeNonDisease +NCIT:C204065 MONDO:excludeNonDisease +NCIT:C204066 MONDO:excludeNonDisease +NCIT:C204067 MONDO:excludeNonDisease +NCIT:C204068 MONDO:excludeNonDisease +NCIT:C204069 MONDO:excludeNonDisease NCIT:C20407 MONDO:excludeNonDisease +NCIT:C204070 MONDO:excludeNonDisease +NCIT:C204071 MONDO:excludeNonDisease +NCIT:C204072 MONDO:excludeNonDisease +NCIT:C204073 MONDO:excludeNonDisease +NCIT:C204074 MONDO:excludeNonDisease +NCIT:C204075 MONDO:excludeNonDisease +NCIT:C204076 MONDO:excludeNonDisease +NCIT:C204077 MONDO:excludeNonDisease +NCIT:C204078 MONDO:excludeNonDisease +NCIT:C204079 MONDO:excludeNonDisease NCIT:C20408 MONDO:excludeNonDisease +NCIT:C204080 MONDO:excludeNonDisease +NCIT:C204081 MONDO:excludeNonDisease +NCIT:C204082 MONDO:excludeNonDisease +NCIT:C204083 MONDO:excludeNonDisease +NCIT:C204084 MONDO:excludeNonDisease +NCIT:C204085 MONDO:excludeNonDisease +NCIT:C204086 MONDO:excludeNonDisease +NCIT:C204087 MONDO:excludeNonDisease +NCIT:C204088 MONDO:excludeNonDisease +NCIT:C204089 MONDO:excludeNonDisease NCIT:C20409 MONDO:excludeNonDisease +NCIT:C204090 MONDO:excludeNonDisease +NCIT:C204091 MONDO:excludeNonDisease +NCIT:C204092 MONDO:excludeNonDisease +NCIT:C204093 MONDO:excludeNonDisease +NCIT:C204094 MONDO:excludeNonDisease +NCIT:C204095 MONDO:excludeNonDisease +NCIT:C204096 MONDO:excludeNonDisease +NCIT:C204097 MONDO:excludeNonDisease +NCIT:C204098 MONDO:excludeNonDisease +NCIT:C204099 MONDO:excludeNonDisease NCIT:C2041 MONDO:excludeNonDisease NCIT:C20410 MONDO:excludeNonDisease +NCIT:C204100 MONDO:excludeNonDisease +NCIT:C204101 MONDO:excludeNonDisease +NCIT:C204102 MONDO:excludeNonDisease +NCIT:C204103 MONDO:excludeNonDisease +NCIT:C204104 MONDO:excludeNonDisease +NCIT:C204105 MONDO:excludeNonDisease +NCIT:C204106 MONDO:excludeNonDisease +NCIT:C204107 MONDO:excludeNonDisease +NCIT:C204108 MONDO:excludeNonDisease +NCIT:C204109 MONDO:excludeNonDisease NCIT:C20411 MONDO:excludeNonDisease +NCIT:C204110 MONDO:excludeNonDisease +NCIT:C204111 MONDO:excludeNonDisease +NCIT:C204112 MONDO:excludeNonDisease +NCIT:C204113 MONDO:excludeNonDisease +NCIT:C204114 MONDO:excludeNonDisease +NCIT:C204115 MONDO:excludeNonDisease +NCIT:C204116 MONDO:excludeNonDisease +NCIT:C204117 MONDO:excludeNonDisease +NCIT:C204118 MONDO:excludeNonDisease +NCIT:C204119 MONDO:excludeNonDisease NCIT:C20412 MONDO:excludeNonDisease +NCIT:C204120 MONDO:excludeNonDisease +NCIT:C204121 MONDO:excludeNonDisease +NCIT:C204122 MONDO:excludeNonDisease +NCIT:C204123 MONDO:excludeNonDisease +NCIT:C204125 MONDO:excludeNonDisease +NCIT:C204127 MONDO:excludeNonDisease +NCIT:C204128 MONDO:excludeNonDisease +NCIT:C204129 MONDO:excludeNonDisease NCIT:C20413 MONDO:excludeNonDisease +NCIT:C204131 MONDO:excludeNonDisease +NCIT:C204132 MONDO:excludeNonDisease +NCIT:C204133 MONDO:excludeNonDisease +NCIT:C204134 MONDO:excludeNonDisease +NCIT:C204135 MONDO:excludeNonDisease +NCIT:C204136 MONDO:excludeNonDisease +NCIT:C204137 MONDO:excludeNonDisease +NCIT:C204138 MONDO:excludeNonDisease +NCIT:C204139 MONDO:excludeNonDisease NCIT:C20414 MONDO:excludeNonDisease +NCIT:C204140 MONDO:excludeNonDisease +NCIT:C204141 MONDO:excludeNonDisease +NCIT:C204142 MONDO:excludeNonDisease +NCIT:C204143 MONDO:excludeNonDisease +NCIT:C204144 MONDO:excludeNonDisease +NCIT:C204145 MONDO:excludeNonDisease +NCIT:C204146 MONDO:excludeNonDisease +NCIT:C204147 MONDO:excludeNonDisease +NCIT:C204148 MONDO:excludeNonDisease +NCIT:C204149 MONDO:excludeNonDisease NCIT:C20415 MONDO:excludeNonDisease +NCIT:C204150 MONDO:excludeNonDisease +NCIT:C204151 MONDO:excludeNonDisease +NCIT:C204152 MONDO:excludeNonDisease +NCIT:C204153 MONDO:excludeNonDisease +NCIT:C204154 MONDO:excludeNonDisease +NCIT:C204155 MONDO:excludeNonDisease +NCIT:C204156 MONDO:excludeNonDisease +NCIT:C204157 MONDO:excludeNonDisease +NCIT:C204158 MONDO:excludeNonDisease +NCIT:C204159 MONDO:excludeNonDisease NCIT:C20416 MONDO:excludeNonDisease +NCIT:C204160 MONDO:excludeNonDisease +NCIT:C204161 MONDO:excludeNonDisease +NCIT:C204162 MONDO:excludeNonDisease +NCIT:C204163 MONDO:excludeNonDisease +NCIT:C204164 MONDO:excludeNonDisease +NCIT:C204165 MONDO:excludeNonDisease +NCIT:C204166 MONDO:excludeNonDisease +NCIT:C204167 MONDO:excludeNonDisease +NCIT:C204168 MONDO:excludeNonDisease +NCIT:C204169 MONDO:excludeNonDisease NCIT:C20417 MONDO:excludeNonDisease +NCIT:C204170 MONDO:excludeNonDisease +NCIT:C204171 MONDO:excludeNonDisease +NCIT:C204172 MONDO:excludeNonDisease +NCIT:C204173 MONDO:excludeNonDisease +NCIT:C204174 MONDO:excludeNonDisease +NCIT:C204175 MONDO:excludeNonDisease +NCIT:C204176 MONDO:excludeNonDisease +NCIT:C204177 MONDO:excludeNonDisease +NCIT:C204178 MONDO:excludeNonDisease +NCIT:C204179 MONDO:excludeNonDisease NCIT:C20418 MONDO:excludeNonDisease +NCIT:C204180 MONDO:excludeNonDisease +NCIT:C204181 MONDO:excludeNonDisease +NCIT:C204182 MONDO:excludeNonDisease +NCIT:C204183 MONDO:excludeNonDisease +NCIT:C204184 MONDO:excludeNonDisease +NCIT:C204185 MONDO:excludeNonDisease +NCIT:C204186 MONDO:excludeNonDisease +NCIT:C204187 MONDO:excludeNonDisease +NCIT:C204188 MONDO:excludeNonDisease +NCIT:C204189 MONDO:excludeNonDisease NCIT:C20419 MONDO:excludeNonDisease +NCIT:C204190 MONDO:excludeNonDisease +NCIT:C204191 MONDO:excludeNonDisease +NCIT:C204192 MONDO:excludeNonDisease +NCIT:C204193 MONDO:excludeNonDisease +NCIT:C204194 MONDO:excludeNonDisease +NCIT:C204195 MONDO:excludeNonDisease +NCIT:C204196 MONDO:excludeNonDisease +NCIT:C204197 MONDO:excludeNonDisease +NCIT:C204198 MONDO:excludeNonDisease +NCIT:C204199 MONDO:excludeNonDisease NCIT:C2042 MONDO:excludeNonDisease NCIT:C20420 MONDO:excludeNonDisease +NCIT:C204200 MONDO:excludeNonDisease +NCIT:C204201 MONDO:excludeNonDisease +NCIT:C204202 MONDO:excludeNonDisease +NCIT:C204204 MONDO:excludeNonDisease +NCIT:C204205 MONDO:excludeNonDisease +NCIT:C204206 MONDO:excludeNonDisease +NCIT:C204207 MONDO:excludeNonDisease +NCIT:C204208 MONDO:excludeNonDisease +NCIT:C204209 MONDO:excludeNonDisease NCIT:C20421 MONDO:excludeNonDisease +NCIT:C204210 MONDO:excludeNonDisease +NCIT:C204211 MONDO:excludeNonDisease +NCIT:C204212 MONDO:excludeNonDisease +NCIT:C204213 MONDO:excludeNonDisease +NCIT:C204214 MONDO:excludeNonDisease +NCIT:C204215 MONDO:excludeNonDisease +NCIT:C204216 MONDO:excludeNonDisease +NCIT:C204217 MONDO:excludeNonDisease +NCIT:C204218 MONDO:excludeNonDisease +NCIT:C204219 MONDO:excludeNonDisease NCIT:C20422 MONDO:excludeNonDisease +NCIT:C204220 MONDO:excludeNonDisease +NCIT:C204221 MONDO:excludeNonDisease +NCIT:C204222 MONDO:excludeNonDisease +NCIT:C204223 MONDO:excludeNonDisease +NCIT:C204224 MONDO:excludeNonDisease +NCIT:C204225 MONDO:excludeNonDisease +NCIT:C204226 MONDO:excludeNonDisease +NCIT:C204227 MONDO:excludeNonDisease +NCIT:C204228 MONDO:excludeNonDisease +NCIT:C204229 MONDO:excludeNonDisease NCIT:C20423 MONDO:excludeNonDisease +NCIT:C204230 MONDO:excludeNonDisease +NCIT:C204231 MONDO:excludeNonDisease +NCIT:C204232 MONDO:excludeNonDisease +NCIT:C204233 MONDO:excludeNonDisease +NCIT:C204234 MONDO:excludeNonDisease +NCIT:C204235 MONDO:excludeNonDisease +NCIT:C204236 MONDO:excludeNonDisease +NCIT:C204237 MONDO:excludeNonDisease +NCIT:C204238 MONDO:excludeNonDisease +NCIT:C204239 MONDO:excludeNonDisease NCIT:C20424 MONDO:excludeNonDisease +NCIT:C204240 MONDO:excludeNonDisease +NCIT:C204241 MONDO:excludeNonDisease +NCIT:C204242 MONDO:excludeNonDisease +NCIT:C204243 MONDO:excludeNonDisease +NCIT:C204244 MONDO:excludeNonDisease +NCIT:C204245 MONDO:excludeNonDisease +NCIT:C204246 MONDO:excludeNonDisease +NCIT:C204247 MONDO:excludeNonDisease +NCIT:C204248 MONDO:excludeNonDisease +NCIT:C204249 MONDO:excludeNonDisease NCIT:C20425 MONDO:excludeNonDisease +NCIT:C204250 MONDO:excludeNonDisease +NCIT:C204251 MONDO:excludeNonDisease +NCIT:C204252 MONDO:excludeNonDisease +NCIT:C204253 MONDO:excludeNonDisease +NCIT:C204254 MONDO:excludeNonDisease +NCIT:C204255 MONDO:excludeNonDisease +NCIT:C204256 MONDO:excludeNonDisease +NCIT:C204257 MONDO:excludeNonDisease +NCIT:C204258 MONDO:excludeNonDisease +NCIT:C204259 MONDO:excludeNonDisease NCIT:C20426 MONDO:excludeNonDisease +NCIT:C204260 MONDO:excludeNonDisease +NCIT:C204261 MONDO:excludeNonDisease +NCIT:C204262 MONDO:excludeNonDisease +NCIT:C204263 MONDO:excludeNonDisease +NCIT:C204264 MONDO:excludeNonDisease +NCIT:C204265 MONDO:excludeNonDisease +NCIT:C204266 MONDO:excludeNonDisease +NCIT:C204267 MONDO:excludeNonDisease +NCIT:C204268 MONDO:excludeNonDisease +NCIT:C204269 MONDO:excludeNonDisease NCIT:C20427 MONDO:excludeNonDisease +NCIT:C204270 MONDO:excludeNonDisease +NCIT:C204271 MONDO:excludeNonDisease +NCIT:C204272 MONDO:excludeNonDisease +NCIT:C204273 MONDO:excludeNonDisease +NCIT:C204274 MONDO:excludeNonDisease +NCIT:C204275 MONDO:excludeNonDisease +NCIT:C204276 MONDO:excludeNonDisease +NCIT:C204277 MONDO:excludeNonDisease +NCIT:C204278 MONDO:excludeNonDisease +NCIT:C204279 MONDO:excludeNonDisease NCIT:C20428 MONDO:excludeNonDisease +NCIT:C204280 MONDO:excludeNonDisease +NCIT:C204281 MONDO:excludeNonDisease +NCIT:C204282 MONDO:excludeNonDisease +NCIT:C204283 MONDO:excludeNonDisease +NCIT:C204284 MONDO:excludeNonDisease +NCIT:C204285 MONDO:excludeNonDisease +NCIT:C204286 MONDO:excludeNonDisease +NCIT:C204287 MONDO:excludeNonDisease +NCIT:C204288 MONDO:excludeNonDisease +NCIT:C204289 MONDO:excludeNonDisease NCIT:C20429 MONDO:excludeNonDisease +NCIT:C204290 MONDO:excludeNonDisease +NCIT:C204291 MONDO:excludeNonDisease +NCIT:C204292 MONDO:excludeNonDisease +NCIT:C204293 MONDO:excludeNonDisease +NCIT:C204294 MONDO:excludeNonDisease +NCIT:C204295 MONDO:excludeNonDisease +NCIT:C204296 MONDO:excludeNonDisease +NCIT:C204297 MONDO:excludeNonDisease +NCIT:C204298 MONDO:excludeNonDisease +NCIT:C204299 MONDO:excludeNonDisease NCIT:C2043 MONDO:excludeNonDisease NCIT:C20430 MONDO:excludeNonDisease +NCIT:C204300 MONDO:excludeNonDisease +NCIT:C204301 MONDO:excludeNonDisease +NCIT:C204302 MONDO:excludeNonDisease +NCIT:C204303 MONDO:excludeNonDisease +NCIT:C204304 MONDO:excludeNonDisease +NCIT:C204305 MONDO:excludeNonDisease +NCIT:C204306 MONDO:excludeNonDisease +NCIT:C204307 MONDO:excludeNonDisease +NCIT:C204308 MONDO:excludeNonDisease +NCIT:C204309 MONDO:excludeNonDisease NCIT:C20431 MONDO:excludeNonDisease +NCIT:C204310 MONDO:excludeNonDisease +NCIT:C204311 MONDO:excludeNonDisease +NCIT:C204312 MONDO:excludeNonDisease +NCIT:C204313 MONDO:excludeNonDisease +NCIT:C204314 MONDO:excludeNonDisease +NCIT:C204315 MONDO:excludeNonDisease +NCIT:C204316 MONDO:excludeNonDisease +NCIT:C204317 MONDO:excludeNonDisease +NCIT:C204318 MONDO:excludeNonDisease +NCIT:C204319 MONDO:excludeNonDisease NCIT:C20432 MONDO:excludeNonDisease +NCIT:C204320 MONDO:excludeNonDisease +NCIT:C204321 MONDO:excludeNonDisease +NCIT:C204322 MONDO:excludeNonDisease +NCIT:C204323 MONDO:excludeNonDisease +NCIT:C204324 MONDO:excludeNonDisease +NCIT:C204325 MONDO:excludeNonDisease +NCIT:C204326 MONDO:excludeNonDisease +NCIT:C204327 MONDO:excludeNonDisease +NCIT:C204328 MONDO:excludeNonDisease +NCIT:C204329 MONDO:excludeNonDisease NCIT:C20433 MONDO:excludeNonDisease +NCIT:C204330 MONDO:excludeNonDisease +NCIT:C204331 MONDO:excludeNonDisease +NCIT:C204332 MONDO:excludeNonDisease +NCIT:C204333 MONDO:excludeNonDisease +NCIT:C204334 MONDO:excludeNonDisease +NCIT:C204335 MONDO:excludeNonDisease +NCIT:C204336 MONDO:excludeNonDisease +NCIT:C204337 MONDO:excludeNonDisease +NCIT:C204338 MONDO:excludeNonDisease +NCIT:C204339 MONDO:excludeNonDisease NCIT:C20434 MONDO:excludeNonDisease +NCIT:C204340 MONDO:excludeNonDisease +NCIT:C204341 MONDO:excludeNonDisease +NCIT:C204342 MONDO:excludeNonDisease +NCIT:C204343 MONDO:excludeNonDisease +NCIT:C204344 MONDO:excludeNonDisease +NCIT:C204345 MONDO:excludeNonDisease +NCIT:C204346 MONDO:excludeNonDisease +NCIT:C204347 MONDO:excludeNonDisease +NCIT:C204348 MONDO:excludeNonDisease +NCIT:C204349 MONDO:excludeNonDisease NCIT:C20435 MONDO:excludeNonDisease +NCIT:C204350 MONDO:excludeNonDisease +NCIT:C204351 MONDO:excludeNonDisease +NCIT:C204352 MONDO:excludeNonDisease +NCIT:C204353 MONDO:excludeNonDisease +NCIT:C204354 MONDO:excludeNonDisease +NCIT:C204356 MONDO:excludeNonDisease +NCIT:C204357 MONDO:excludeNonDisease +NCIT:C204358 MONDO:excludeNonDisease +NCIT:C204359 MONDO:excludeNonDisease NCIT:C20436 MONDO:excludeNonDisease +NCIT:C204360 MONDO:excludeNonDisease +NCIT:C204361 MONDO:excludeNonDisease +NCIT:C204362 MONDO:excludeNonDisease +NCIT:C204363 MONDO:excludeNonDisease +NCIT:C204364 MONDO:excludeNonDisease +NCIT:C204365 MONDO:excludeNonDisease +NCIT:C204366 MONDO:excludeNonDisease +NCIT:C204367 MONDO:excludeNonDisease +NCIT:C204368 MONDO:excludeNonDisease +NCIT:C204369 MONDO:excludeNonDisease NCIT:C20437 MONDO:excludeNonDisease +NCIT:C204370 MONDO:excludeNonDisease +NCIT:C204371 MONDO:excludeNonDisease +NCIT:C204372 MONDO:excludeNonDisease +NCIT:C204373 MONDO:excludeNonDisease +NCIT:C204374 MONDO:excludeNonDisease +NCIT:C204375 MONDO:excludeNonDisease +NCIT:C204376 MONDO:excludeNonDisease +NCIT:C204377 MONDO:excludeNonDisease +NCIT:C204378 MONDO:excludeNonDisease +NCIT:C204379 MONDO:excludeNonDisease +NCIT:C204380 MONDO:excludeNonDisease +NCIT:C204381 MONDO:excludeNonDisease +NCIT:C204382 MONDO:excludeNonDisease +NCIT:C204384 MONDO:excludeNonDisease +NCIT:C204386 MONDO:excludeNonDisease +NCIT:C204387 MONDO:excludeNonDisease +NCIT:C204388 MONDO:excludeNonDisease +NCIT:C204389 MONDO:excludeNonDisease NCIT:C20439 MONDO:excludeNonDisease +NCIT:C204390 MONDO:excludeNonDisease +NCIT:C204391 MONDO:excludeNonDisease +NCIT:C204392 MONDO:excludeNonDisease +NCIT:C204393 MONDO:excludeNonDisease +NCIT:C204394 MONDO:excludeNonDisease +NCIT:C204395 MONDO:excludeNonDisease +NCIT:C204396 MONDO:excludeNonDisease +NCIT:C204397 MONDO:excludeNonDisease +NCIT:C204398 MONDO:excludeNonDisease +NCIT:C204399 MONDO:excludeNonDisease NCIT:C2044 MONDO:excludeNonDisease NCIT:C20440 MONDO:excludeNonDisease +NCIT:C204400 MONDO:excludeNonDisease +NCIT:C204401 MONDO:excludeNonDisease +NCIT:C204402 MONDO:excludeNonDisease +NCIT:C204403 MONDO:excludeNonDisease +NCIT:C204404 MONDO:excludeNonDisease +NCIT:C204405 MONDO:excludeNonDisease +NCIT:C204406 MONDO:excludeNonDisease +NCIT:C204407 MONDO:excludeNonDisease +NCIT:C204408 MONDO:excludeNonDisease +NCIT:C204409 MONDO:excludeNonDisease NCIT:C20441 MONDO:excludeNonDisease +NCIT:C204410 MONDO:excludeNonDisease +NCIT:C204411 MONDO:excludeNonDisease +NCIT:C204412 MONDO:excludeNonDisease +NCIT:C204413 MONDO:excludeNonDisease +NCIT:C204414 MONDO:excludeNonDisease +NCIT:C204415 MONDO:excludeNonDisease +NCIT:C204416 MONDO:excludeNonDisease +NCIT:C204417 MONDO:excludeNonDisease +NCIT:C204418 MONDO:excludeNonDisease +NCIT:C204419 MONDO:excludeNonDisease NCIT:C20442 MONDO:excludeNonDisease +NCIT:C204420 MONDO:excludeNonDisease +NCIT:C204421 MONDO:excludeNonDisease +NCIT:C204422 MONDO:excludeNonDisease +NCIT:C204423 MONDO:excludeNonDisease +NCIT:C204424 MONDO:excludeNonDisease +NCIT:C204425 MONDO:excludeNonDisease +NCIT:C204426 MONDO:excludeNonDisease +NCIT:C204427 MONDO:excludeNonDisease +NCIT:C204428 MONDO:excludeNonDisease +NCIT:C204429 MONDO:excludeNonDisease +NCIT:C204430 MONDO:excludeNonDisease +NCIT:C204431 MONDO:excludeNonDisease +NCIT:C204432 MONDO:excludeNonDisease +NCIT:C204433 MONDO:excludeNonDisease +NCIT:C204434 MONDO:excludeNonDisease +NCIT:C204435 MONDO:excludeNonDisease +NCIT:C204436 MONDO:excludeNonDisease +NCIT:C204438 MONDO:excludeNonDisease +NCIT:C204439 MONDO:excludeNonDisease NCIT:C20444 MONDO:excludeNonDisease +NCIT:C204440 MONDO:excludeNonDisease +NCIT:C204441 MONDO:excludeNonDisease +NCIT:C204442 MONDO:excludeNonDisease +NCIT:C204443 MONDO:excludeNonDisease +NCIT:C204444 MONDO:excludeNonDisease +NCIT:C204445 MONDO:excludeNonDisease +NCIT:C204446 MONDO:excludeNonDisease +NCIT:C204447 MONDO:excludeNonDisease +NCIT:C204448 MONDO:excludeNonDisease +NCIT:C204449 MONDO:excludeNonDisease NCIT:C20445 MONDO:excludeNonDisease +NCIT:C204450 MONDO:excludeNonDisease +NCIT:C204451 MONDO:excludeNonDisease +NCIT:C204452 MONDO:excludeNonDisease +NCIT:C204453 MONDO:excludeNonDisease +NCIT:C204454 MONDO:excludeNonDisease +NCIT:C204455 MONDO:excludeNonDisease +NCIT:C204456 MONDO:excludeNonDisease +NCIT:C204457 MONDO:excludeNonDisease +NCIT:C204458 MONDO:excludeNonDisease +NCIT:C204459 MONDO:excludeNonDisease NCIT:C20446 MONDO:excludeNonDisease +NCIT:C204460 MONDO:excludeNonDisease +NCIT:C204461 MONDO:excludeNonDisease +NCIT:C204462 MONDO:excludeNonDisease +NCIT:C204463 MONDO:excludeNonDisease +NCIT:C204464 MONDO:excludeNonDisease +NCIT:C204465 MONDO:excludeNonDisease +NCIT:C204466 MONDO:excludeNonDisease +NCIT:C204467 MONDO:excludeNonDisease +NCIT:C204468 MONDO:excludeNonDisease +NCIT:C204469 MONDO:excludeNonDisease NCIT:C20447 MONDO:excludeNonDisease +NCIT:C204470 MONDO:excludeNonDisease +NCIT:C204471 MONDO:excludeNonDisease +NCIT:C204472 MONDO:excludeNonDisease +NCIT:C204473 MONDO:excludeNonDisease +NCIT:C204474 MONDO:excludeNonDisease +NCIT:C204476 MONDO:excludeNonDisease +NCIT:C204477 MONDO:excludeNonDisease +NCIT:C204478 MONDO:excludeNonDisease +NCIT:C204479 MONDO:excludeNonDisease NCIT:C20448 MONDO:excludeNonDisease +NCIT:C204480 MONDO:excludeNonDisease +NCIT:C204481 MONDO:excludeNonDisease +NCIT:C204483 MONDO:excludeNonDisease +NCIT:C204484 MONDO:excludeNonDisease +NCIT:C204485 MONDO:excludeNonDisease +NCIT:C204486 MONDO:excludeNonDisease +NCIT:C204487 MONDO:excludeNonDisease +NCIT:C204488 MONDO:excludeNonDisease +NCIT:C204489 MONDO:excludeNonDisease NCIT:C20449 MONDO:excludeNonDisease +NCIT:C204490 MONDO:excludeNonDisease +NCIT:C204491 MONDO:excludeNonDisease +NCIT:C204492 MONDO:excludeNonDisease +NCIT:C204493 MONDO:excludeNonDisease +NCIT:C204494 MONDO:excludeNonDisease +NCIT:C204495 MONDO:excludeNonDisease +NCIT:C204496 MONDO:excludeNonDisease +NCIT:C204497 MONDO:excludeNonDisease +NCIT:C204498 MONDO:excludeNonDisease +NCIT:C204499 MONDO:excludeNonDisease NCIT:C2045 MONDO:excludeNonDisease NCIT:C20450 MONDO:excludeNonDisease +NCIT:C204500 MONDO:excludeNonDisease +NCIT:C204501 MONDO:excludeNonDisease +NCIT:C204502 MONDO:excludeNonDisease +NCIT:C204503 MONDO:excludeNonDisease +NCIT:C204505 MONDO:excludeNonDisease +NCIT:C204506 MONDO:excludeNonDisease +NCIT:C204507 MONDO:excludeNonDisease +NCIT:C204508 MONDO:excludeNonDisease +NCIT:C204509 MONDO:excludeNonDisease NCIT:C20451 MONDO:excludeNonDisease +NCIT:C204510 MONDO:excludeNonDisease +NCIT:C204511 MONDO:excludeNonDisease +NCIT:C204512 MONDO:excludeNonDisease +NCIT:C204513 MONDO:excludeNonDisease +NCIT:C204515 MONDO:excludeNonDisease +NCIT:C204517 MONDO:excludeNonDisease +NCIT:C204518 MONDO:excludeNonDisease +NCIT:C204519 MONDO:excludeNonDisease NCIT:C20452 MONDO:excludeNonDisease +NCIT:C204520 MONDO:excludeNonDisease +NCIT:C204521 MONDO:excludeNonDisease +NCIT:C204522 MONDO:excludeNonDisease +NCIT:C204523 MONDO:excludeNonDisease +NCIT:C204524 MONDO:excludeNonDisease +NCIT:C204525 MONDO:excludeNonDisease +NCIT:C204526 MONDO:excludeNonDisease +NCIT:C204527 MONDO:excludeNonDisease +NCIT:C204528 MONDO:excludeNonDisease +NCIT:C204529 MONDO:excludeNonDisease NCIT:C20453 MONDO:excludeNonDisease +NCIT:C204530 MONDO:excludeNonDisease +NCIT:C204531 MONDO:excludeNonDisease +NCIT:C204532 MONDO:excludeNonDisease +NCIT:C204533 MONDO:excludeNonDisease +NCIT:C204534 MONDO:excludeNonDisease +NCIT:C204535 MONDO:excludeNonDisease +NCIT:C204536 MONDO:excludeNonDisease +NCIT:C204537 MONDO:excludeNonDisease +NCIT:C204538 MONDO:excludeNonDisease +NCIT:C204539 MONDO:excludeNonDisease NCIT:C20454 MONDO:excludeNonDisease +NCIT:C204540 MONDO:excludeNonDisease +NCIT:C204541 MONDO:excludeNonDisease +NCIT:C204542 MONDO:excludeNonDisease +NCIT:C204543 MONDO:excludeNonDisease +NCIT:C204544 MONDO:excludeNonDisease +NCIT:C204545 MONDO:excludeNonDisease +NCIT:C204546 MONDO:excludeNonDisease +NCIT:C204547 MONDO:excludeNonDisease +NCIT:C204548 MONDO:excludeNonDisease +NCIT:C204549 MONDO:excludeNonDisease NCIT:C20455 MONDO:excludeNonDisease +NCIT:C204550 MONDO:excludeNonDisease +NCIT:C204551 MONDO:excludeNonDisease +NCIT:C204552 MONDO:excludeNonDisease +NCIT:C204553 MONDO:excludeNonDisease +NCIT:C204554 MONDO:excludeNonDisease +NCIT:C204555 MONDO:excludeNonDisease +NCIT:C204556 MONDO:excludeNonDisease +NCIT:C204557 MONDO:excludeNonDisease +NCIT:C204558 MONDO:excludeNonDisease +NCIT:C204559 MONDO:excludeNonDisease NCIT:C20456 MONDO:excludeNonDisease +NCIT:C204560 MONDO:excludeNonDisease +NCIT:C204561 MONDO:excludeNonDisease +NCIT:C204562 MONDO:excludeNonDisease +NCIT:C204563 MONDO:excludeNonDisease +NCIT:C204564 MONDO:excludeNonDisease +NCIT:C204565 MONDO:excludeNonDisease +NCIT:C204566 MONDO:excludeNonDisease +NCIT:C204567 MONDO:excludeNonDisease +NCIT:C204568 MONDO:excludeNonDisease +NCIT:C204569 MONDO:excludeNonDisease NCIT:C20457 MONDO:excludeNonDisease +NCIT:C204570 MONDO:excludeNonDisease +NCIT:C204571 MONDO:excludeNonDisease +NCIT:C204572 MONDO:excludeNonDisease +NCIT:C204576 MONDO:excludeNonDisease +NCIT:C204577 MONDO:excludeNonDisease +NCIT:C204578 MONDO:excludeNonDisease +NCIT:C204579 MONDO:excludeNonDisease NCIT:C20458 MONDO:excludeNonDisease +NCIT:C204580 MONDO:excludeNonDisease +NCIT:C204581 MONDO:excludeNonDisease +NCIT:C204582 MONDO:excludeNonDisease +NCIT:C204583 MONDO:excludeNonDisease +NCIT:C204584 MONDO:excludeNonDisease +NCIT:C204585 MONDO:excludeNonDisease +NCIT:C204586 MONDO:excludeNonDisease +NCIT:C204587 MONDO:excludeNonDisease +NCIT:C204588 MONDO:excludeNonDisease +NCIT:C204589 MONDO:excludeNonDisease NCIT:C20459 MONDO:excludeNonDisease +NCIT:C204590 MONDO:excludeNonDisease +NCIT:C204591 MONDO:excludeNonDisease +NCIT:C204592 MONDO:excludeNonDisease +NCIT:C204593 MONDO:excludeNonDisease +NCIT:C204594 MONDO:excludeNonDisease +NCIT:C204595 MONDO:excludeNonDisease +NCIT:C204596 MONDO:excludeNonDisease +NCIT:C204597 MONDO:excludeNonDisease +NCIT:C204598 MONDO:excludeNonDisease +NCIT:C204599 MONDO:excludeNonDisease NCIT:C20460 MONDO:excludeNonDisease +NCIT:C204600 MONDO:excludeNonDisease +NCIT:C204601 MONDO:excludeNonDisease +NCIT:C204602 MONDO:excludeNonDisease +NCIT:C204603 MONDO:excludeNonDisease +NCIT:C204604 MONDO:excludeNonDisease +NCIT:C204605 MONDO:excludeNonDisease +NCIT:C204606 MONDO:excludeNonDisease +NCIT:C204607 MONDO:excludeNonDisease +NCIT:C204608 MONDO:excludeNonDisease +NCIT:C204609 MONDO:excludeNonDisease NCIT:C20461 MONDO:excludeNonDisease +NCIT:C204610 MONDO:excludeNonDisease +NCIT:C204611 MONDO:excludeNonDisease +NCIT:C204612 MONDO:excludeNonDisease +NCIT:C204613 MONDO:excludeNonDisease +NCIT:C204614 MONDO:excludeNonDisease +NCIT:C204615 MONDO:excludeNonDisease +NCIT:C204616 MONDO:excludeNonDisease +NCIT:C204617 MONDO:excludeNonDisease +NCIT:C204618 MONDO:excludeNonDisease +NCIT:C204619 MONDO:excludeNonDisease NCIT:C20462 MONDO:excludeNonDisease +NCIT:C204620 MONDO:excludeNonDisease +NCIT:C204621 MONDO:excludeNonDisease +NCIT:C204622 MONDO:excludeNonDisease +NCIT:C204623 MONDO:excludeNonDisease +NCIT:C204624 MONDO:excludeNonDisease +NCIT:C204625 MONDO:excludeNonDisease +NCIT:C204626 MONDO:excludeNonDisease +NCIT:C204627 MONDO:excludeNonDisease +NCIT:C204628 MONDO:excludeNonDisease +NCIT:C204629 MONDO:excludeNonDisease NCIT:C20463 MONDO:excludeNonDisease +NCIT:C204630 MONDO:excludeNonDisease +NCIT:C204631 MONDO:excludeNonDisease +NCIT:C204632 MONDO:excludeNonDisease +NCIT:C204633 MONDO:excludeNonDisease +NCIT:C204634 MONDO:excludeNonDisease +NCIT:C204635 MONDO:excludeNonDisease +NCIT:C204636 MONDO:excludeNonDisease +NCIT:C204637 MONDO:excludeNonDisease +NCIT:C204638 MONDO:excludeNonDisease +NCIT:C204639 MONDO:excludeNonDisease NCIT:C20464 MONDO:excludeNonDisease +NCIT:C204640 MONDO:excludeNonDisease +NCIT:C204641 MONDO:excludeNonDisease +NCIT:C204642 MONDO:excludeNonDisease +NCIT:C204643 MONDO:excludeNonDisease +NCIT:C204644 MONDO:excludeNonDisease +NCIT:C204645 MONDO:excludeNonDisease +NCIT:C204646 MONDO:excludeNonDisease +NCIT:C204647 MONDO:excludeNonDisease +NCIT:C204648 MONDO:excludeNonDisease +NCIT:C204649 MONDO:excludeNonDisease NCIT:C20465 MONDO:excludeNonDisease +NCIT:C204650 MONDO:excludeNonDisease +NCIT:C204651 MONDO:excludeNonDisease +NCIT:C204652 MONDO:excludeNonDisease +NCIT:C204653 MONDO:excludeNonDisease +NCIT:C204654 MONDO:excludeNonDisease +NCIT:C204655 MONDO:excludeNonDisease +NCIT:C204656 MONDO:excludeNonDisease +NCIT:C204657 MONDO:excludeNonDisease +NCIT:C204658 MONDO:excludeNonDisease +NCIT:C204659 MONDO:excludeNonDisease NCIT:C20466 MONDO:excludeNonDisease +NCIT:C204660 MONDO:excludeNonDisease +NCIT:C204661 MONDO:excludeNonDisease +NCIT:C204662 MONDO:excludeNonDisease +NCIT:C204663 MONDO:excludeNonDisease +NCIT:C204664 MONDO:excludeNonDisease +NCIT:C204665 MONDO:excludeNonDisease +NCIT:C204666 MONDO:excludeNonDisease +NCIT:C204667 MONDO:excludeNonDisease +NCIT:C204668 MONDO:excludeNonDisease +NCIT:C204669 MONDO:excludeNonDisease NCIT:C20467 MONDO:excludeNonDisease +NCIT:C204670 MONDO:excludeNonDisease +NCIT:C204671 MONDO:excludeNonDisease +NCIT:C204672 MONDO:excludeNonDisease +NCIT:C204673 MONDO:excludeNonDisease +NCIT:C204674 MONDO:excludeNonDisease +NCIT:C204675 MONDO:excludeNonDisease +NCIT:C204676 MONDO:excludeNonDisease +NCIT:C204677 MONDO:excludeNonDisease +NCIT:C204678 MONDO:excludeNonDisease +NCIT:C204679 MONDO:excludeNonDisease NCIT:C20468 MONDO:excludeNonDisease +NCIT:C204680 MONDO:excludeNonDisease +NCIT:C204681 MONDO:excludeNonDisease +NCIT:C204682 MONDO:excludeNonDisease +NCIT:C204683 MONDO:excludeNonDisease +NCIT:C204684 MONDO:excludeNonDisease +NCIT:C204685 MONDO:excludeNonDisease +NCIT:C204686 MONDO:excludeNonDisease +NCIT:C204687 MONDO:excludeNonDisease +NCIT:C204688 MONDO:excludeNonDisease +NCIT:C204689 MONDO:excludeNonDisease NCIT:C20469 MONDO:excludeNonDisease +NCIT:C204690 MONDO:excludeNonDisease +NCIT:C204691 MONDO:excludeNonDisease +NCIT:C204692 MONDO:excludeNonDisease +NCIT:C204693 MONDO:excludeNonDisease +NCIT:C204694 MONDO:excludeNonDisease +NCIT:C204695 MONDO:excludeNonDisease +NCIT:C204696 MONDO:excludeNonDisease +NCIT:C204697 MONDO:excludeNonDisease +NCIT:C204698 MONDO:excludeNonDisease +NCIT:C204699 MONDO:excludeNonDisease NCIT:C2047 MONDO:excludeNonDisease NCIT:C20470 MONDO:excludeNonDisease +NCIT:C204700 MONDO:excludeNonDisease +NCIT:C204701 MONDO:excludeNonDisease +NCIT:C204702 MONDO:excludeNonDisease +NCIT:C204703 MONDO:excludeNonDisease +NCIT:C204704 MONDO:excludeNonDisease +NCIT:C204705 MONDO:excludeNonDisease +NCIT:C204706 MONDO:excludeNonDisease +NCIT:C204707 MONDO:excludeNonDisease +NCIT:C204708 MONDO:excludeNonDisease +NCIT:C204709 MONDO:excludeNonDisease NCIT:C20471 MONDO:excludeNonDisease +NCIT:C204710 MONDO:excludeNonDisease +NCIT:C204711 MONDO:excludeNonDisease +NCIT:C204712 MONDO:excludeNonDisease +NCIT:C204713 MONDO:excludeNonDisease +NCIT:C204714 MONDO:excludeNonDisease +NCIT:C204715 MONDO:excludeNonDisease +NCIT:C204716 MONDO:excludeNonDisease +NCIT:C204717 MONDO:excludeNonDisease +NCIT:C204718 MONDO:excludeNonDisease +NCIT:C204719 MONDO:excludeNonDisease +NCIT:C204720 MONDO:excludeNonDisease +NCIT:C204721 MONDO:excludeNonDisease +NCIT:C204722 MONDO:excludeNonDisease +NCIT:C204723 MONDO:excludeNonDisease +NCIT:C204724 MONDO:excludeNonDisease +NCIT:C204725 MONDO:excludeNonDisease +NCIT:C204726 MONDO:excludeNonDisease +NCIT:C204727 MONDO:excludeNonDisease +NCIT:C204728 MONDO:excludeNonDisease +NCIT:C204729 MONDO:excludeNonDisease NCIT:C20473 MONDO:excludeNonDisease +NCIT:C204730 MONDO:excludeNonDisease +NCIT:C204731 MONDO:excludeNonDisease +NCIT:C204732 MONDO:excludeNonDisease +NCIT:C204733 MONDO:excludeNonDisease +NCIT:C204734 MONDO:excludeNonDisease +NCIT:C204735 MONDO:excludeNonDisease +NCIT:C204736 MONDO:excludeNonDisease +NCIT:C204737 MONDO:excludeNonDisease +NCIT:C204738 MONDO:excludeNonDisease NCIT:C20474 MONDO:excludeNonDisease +NCIT:C204742 MONDO:excludeNonDisease +NCIT:C204743 MONDO:excludeNonDisease +NCIT:C204744 MONDO:excludeNonDisease +NCIT:C204745 MONDO:excludeNonDisease +NCIT:C204746 MONDO:excludeNonDisease +NCIT:C204747 MONDO:excludeNonDisease +NCIT:C204748 MONDO:excludeNonDisease +NCIT:C204749 MONDO:excludeNonDisease NCIT:C20475 MONDO:excludeNonDisease +NCIT:C204750 MONDO:excludeNonDisease +NCIT:C204751 MONDO:excludeNonDisease +NCIT:C204752 MONDO:excludeNonDisease +NCIT:C204753 MONDO:excludeNonDisease +NCIT:C204754 MONDO:excludeNonDisease +NCIT:C204757 MONDO:excludeNonDisease +NCIT:C204758 MONDO:excludeNonDisease +NCIT:C204759 MONDO:excludeNonDisease NCIT:C20476 MONDO:excludeNonDisease +NCIT:C204760 MONDO:excludeNonDisease +NCIT:C204761 MONDO:excludeNonDisease +NCIT:C204762 MONDO:excludeNonDisease +NCIT:C204763 MONDO:excludeNonDisease +NCIT:C204764 MONDO:excludeNonDisease +NCIT:C204765 MONDO:excludeNonDisease +NCIT:C204766 MONDO:excludeNonDisease +NCIT:C204767 MONDO:excludeNonDisease +NCIT:C204768 MONDO:excludeNonDisease +NCIT:C204769 MONDO:excludeNonDisease NCIT:C20477 MONDO:excludeNonDisease +NCIT:C204770 MONDO:excludeNonDisease +NCIT:C204771 MONDO:excludeNonDisease +NCIT:C204772 MONDO:excludeNonDisease +NCIT:C204773 MONDO:excludeNonDisease +NCIT:C204774 MONDO:excludeNonDisease +NCIT:C204775 MONDO:excludeNonDisease +NCIT:C204776 MONDO:excludeNonDisease +NCIT:C204777 MONDO:excludeNonDisease +NCIT:C204778 MONDO:excludeNonDisease +NCIT:C204779 MONDO:excludeNonDisease NCIT:C20478 MONDO:excludeNonDisease +NCIT:C204780 MONDO:excludeNonDisease +NCIT:C204781 MONDO:excludeNonDisease +NCIT:C204782 MONDO:excludeNonDisease +NCIT:C204783 MONDO:excludeNonDisease +NCIT:C204784 MONDO:excludeNonDisease +NCIT:C204785 MONDO:excludeNonDisease NCIT:C20479 MONDO:excludeNonDisease +NCIT:C204791 MONDO:excludeNonDisease +NCIT:C204792 MONDO:excludeNonDisease +NCIT:C204793 MONDO:excludeNonDisease +NCIT:C204794 MONDO:excludeNonDisease +NCIT:C204795 MONDO:excludeNonDisease +NCIT:C204796 MONDO:excludeNonDisease +NCIT:C204797 MONDO:excludeNonDisease +NCIT:C204798 MONDO:excludeNonDisease +NCIT:C204799 MONDO:excludeNonDisease NCIT:C2048 MONDO:excludeNonDisease NCIT:C20480 MONDO:excludeNonDisease +NCIT:C204800 MONDO:excludeNonDisease +NCIT:C204801 MONDO:excludeNonDisease +NCIT:C204802 MONDO:excludeNonDisease +NCIT:C204803 MONDO:excludeNonDisease +NCIT:C204804 MONDO:excludeNonDisease +NCIT:C204805 MONDO:excludeNonDisease +NCIT:C204806 MONDO:excludeNonDisease +NCIT:C204807 MONDO:excludeNonDisease +NCIT:C204808 MONDO:excludeNonDisease +NCIT:C204809 MONDO:excludeNonDisease NCIT:C20481 MONDO:excludeNonDisease +NCIT:C204810 MONDO:excludeNonDisease +NCIT:C204811 MONDO:excludeNonDisease +NCIT:C204812 MONDO:excludeNonDisease +NCIT:C204813 MONDO:excludeNonDisease +NCIT:C204814 MONDO:excludeNonDisease +NCIT:C204815 MONDO:excludeNonDisease +NCIT:C204816 MONDO:excludeNonDisease +NCIT:C204817 MONDO:excludeNonDisease +NCIT:C204818 MONDO:excludeNonDisease +NCIT:C204819 MONDO:excludeNonDisease +NCIT:C204820 MONDO:excludeNonDisease +NCIT:C204821 MONDO:excludeNonDisease +NCIT:C204822 MONDO:excludeNonDisease +NCIT:C204823 MONDO:excludeNonDisease +NCIT:C204824 MONDO:excludeNonDisease +NCIT:C204825 MONDO:excludeNonDisease +NCIT:C204826 MONDO:excludeNonDisease +NCIT:C204827 MONDO:excludeNonDisease +NCIT:C204828 MONDO:excludeNonDisease +NCIT:C204829 MONDO:excludeNonDisease NCIT:C20483 MONDO:excludeNonDisease +NCIT:C204830 MONDO:excludeNonDisease +NCIT:C204831 MONDO:excludeNonDisease +NCIT:C204832 MONDO:excludeNonDisease +NCIT:C204833 MONDO:excludeNonDisease +NCIT:C204834 MONDO:excludeNonDisease +NCIT:C204835 MONDO:excludeNonDisease +NCIT:C204836 MONDO:excludeNonDisease +NCIT:C204837 MONDO:excludeNonDisease +NCIT:C204838 MONDO:excludeNonDisease +NCIT:C204839 MONDO:excludeNonDisease NCIT:C20484 MONDO:excludeNonDisease +NCIT:C204841 MONDO:excludeNonDisease +NCIT:C204842 MONDO:excludeNonDisease +NCIT:C204844 MONDO:excludeNonDisease +NCIT:C204845 MONDO:excludeNonDisease +NCIT:C204846 MONDO:excludeNonDisease +NCIT:C204847 MONDO:excludeNonDisease +NCIT:C204848 MONDO:excludeNonDisease +NCIT:C204849 MONDO:excludeNonDisease NCIT:C20485 MONDO:excludeNonDisease +NCIT:C204850 MONDO:excludeNonDisease +NCIT:C204851 MONDO:excludeNonDisease +NCIT:C204852 MONDO:excludeNonDisease +NCIT:C204853 MONDO:excludeNonDisease +NCIT:C204854 MONDO:excludeNonDisease +NCIT:C204855 MONDO:excludeNonDisease +NCIT:C204856 MONDO:excludeNonDisease +NCIT:C204857 MONDO:excludeNonDisease +NCIT:C204858 MONDO:excludeNonDisease +NCIT:C204859 MONDO:excludeNonDisease NCIT:C20486 MONDO:excludeNonDisease +NCIT:C204860 MONDO:excludeNonDisease +NCIT:C204861 MONDO:excludeNonDisease +NCIT:C204862 MONDO:excludeNonDisease +NCIT:C204863 MONDO:excludeNonDisease +NCIT:C204869 MONDO:excludeNonDisease NCIT:C20487 MONDO:excludeNonDisease +NCIT:C204870 MONDO:excludeNonDisease +NCIT:C204871 MONDO:excludeNonDisease +NCIT:C204872 MONDO:excludeNonDisease +NCIT:C204873 MONDO:excludeNonDisease +NCIT:C204874 MONDO:excludeNonDisease +NCIT:C204875 MONDO:excludeNonDisease +NCIT:C204876 MONDO:excludeNonDisease +NCIT:C204877 MONDO:excludeNonDisease +NCIT:C204878 MONDO:excludeNonDisease +NCIT:C204879 MONDO:excludeNonDisease NCIT:C20488 MONDO:excludeNonDisease +NCIT:C204880 MONDO:excludeNonDisease +NCIT:C204881 MONDO:excludeNonDisease +NCIT:C204882 MONDO:excludeNonDisease +NCIT:C204884 MONDO:excludeNonDisease +NCIT:C204885 MONDO:excludeNonDisease +NCIT:C204886 MONDO:excludeNonDisease NCIT:C20489 MONDO:excludeNonDisease +NCIT:C204890 MONDO:excludeNonDisease +NCIT:C204891 MONDO:excludeNonDisease +NCIT:C204892 MONDO:excludeNonDisease +NCIT:C204893 MONDO:excludeNonDisease +NCIT:C204894 MONDO:excludeNonDisease +NCIT:C204895 MONDO:excludeNonDisease +NCIT:C204896 MONDO:excludeNonDisease +NCIT:C204897 MONDO:excludeNonDisease +NCIT:C204898 MONDO:excludeNonDisease +NCIT:C204899 MONDO:excludeNonDisease NCIT:C2049 MONDO:excludeNonDisease NCIT:C20490 MONDO:excludeNonDisease +NCIT:C204900 MONDO:excludeNonDisease +NCIT:C204901 MONDO:excludeNonDisease +NCIT:C204902 MONDO:excludeNonDisease +NCIT:C204903 MONDO:excludeNonDisease +NCIT:C204904 MONDO:excludeNonDisease +NCIT:C204905 MONDO:excludeNonDisease +NCIT:C204906 MONDO:excludeNonDisease +NCIT:C204908 MONDO:excludeNonDisease +NCIT:C204909 MONDO:excludeNonDisease NCIT:C20491 MONDO:excludeNonDisease +NCIT:C204912 MONDO:excludeNonDisease +NCIT:C204913 MONDO:excludeNonDisease +NCIT:C204914 MONDO:excludeNonDisease +NCIT:C204915 MONDO:excludeNonDisease +NCIT:C204916 MONDO:excludeNonDisease +NCIT:C204917 MONDO:excludeNonDisease +NCIT:C204918 MONDO:excludeNonDisease +NCIT:C204919 MONDO:excludeNonDisease NCIT:C20492 MONDO:excludeNonDisease +NCIT:C204920 MONDO:excludeNonDisease +NCIT:C204921 MONDO:excludeNonDisease +NCIT:C204922 MONDO:excludeNonDisease +NCIT:C204923 MONDO:excludeNonDisease +NCIT:C204924 MONDO:excludeNonDisease +NCIT:C204925 MONDO:excludeNonDisease +NCIT:C204926 MONDO:excludeNonDisease +NCIT:C204927 MONDO:excludeNonDisease +NCIT:C204928 MONDO:excludeNonDisease +NCIT:C204929 MONDO:excludeNonDisease NCIT:C20493 MONDO:excludeNonDisease +NCIT:C204930 MONDO:excludeNonDisease +NCIT:C204931 MONDO:excludeNonDisease +NCIT:C204932 MONDO:excludeNonDisease +NCIT:C204933 MONDO:excludeNonDisease +NCIT:C204934 MONDO:excludeNonDisease +NCIT:C204935 MONDO:excludeNonDisease +NCIT:C204936 MONDO:excludeNonDisease +NCIT:C204937 MONDO:excludeNonDisease +NCIT:C204938 MONDO:excludeNonDisease +NCIT:C204939 MONDO:excludeNonDisease NCIT:C20494 MONDO:excludeNonDisease +NCIT:C204940 MONDO:excludeNonDisease +NCIT:C204941 MONDO:excludeNonDisease +NCIT:C204942 MONDO:excludeNonDisease +NCIT:C204943 MONDO:excludeNonDisease +NCIT:C204944 MONDO:excludeNonDisease +NCIT:C204945 MONDO:excludeNonDisease +NCIT:C204946 MONDO:excludeNonDisease +NCIT:C204947 MONDO:excludeNonDisease +NCIT:C204948 MONDO:excludeNonDisease +NCIT:C204949 MONDO:excludeNonDisease NCIT:C20495 MONDO:excludeNonDisease +NCIT:C204950 MONDO:excludeNonDisease +NCIT:C204951 MONDO:excludeNonDisease +NCIT:C204952 MONDO:excludeNonDisease +NCIT:C204953 MONDO:excludeNonDisease +NCIT:C204954 MONDO:excludeNonDisease +NCIT:C204955 MONDO:excludeNonDisease +NCIT:C204956 MONDO:excludeNonDisease +NCIT:C204957 MONDO:excludeNonDisease +NCIT:C204958 MONDO:excludeNonDisease +NCIT:C204959 MONDO:excludeNonDisease NCIT:C20496 MONDO:excludeNonDisease +NCIT:C204960 MONDO:excludeNonDisease +NCIT:C204961 MONDO:excludeNonDisease +NCIT:C204962 MONDO:excludeNonDisease +NCIT:C204963 MONDO:excludeNonDisease +NCIT:C204964 MONDO:excludeNonDisease +NCIT:C204965 MONDO:excludeNonDisease +NCIT:C204966 MONDO:excludeNonDisease +NCIT:C204967 MONDO:excludeNonDisease +NCIT:C204968 MONDO:excludeNonDisease +NCIT:C204969 MONDO:excludeNonDisease NCIT:C20497 MONDO:excludeNonDisease +NCIT:C204970 MONDO:excludeNonDisease +NCIT:C204971 MONDO:excludeNonDisease +NCIT:C204972 MONDO:excludeNonDisease +NCIT:C204973 MONDO:excludeNonDisease +NCIT:C204974 MONDO:excludeNonDisease +NCIT:C204975 MONDO:excludeNonDisease NCIT:C20498 MONDO:excludeNonDisease +NCIT:C204983 MONDO:excludeNonDisease +NCIT:C204989 MONDO:excludeNonDisease NCIT:C20499 MONDO:excludeNonDisease +NCIT:C204990 MONDO:excludeNonDisease +NCIT:C204992 MONDO:excludeNonDisease +NCIT:C204993 MONDO:excludeNonDisease +NCIT:C204994 MONDO:excludeNonDisease +NCIT:C204995 MONDO:excludeNonDisease +NCIT:C204996 MONDO:excludeNonDisease +NCIT:C204997 MONDO:excludeNonDisease +NCIT:C204998 MONDO:excludeNonDisease +NCIT:C204999 MONDO:excludeNonDisease NCIT:C205 MONDO:excludeNonDisease NCIT:C2050 MONDO:excludeNonDisease NCIT:C20500 MONDO:excludeNonDisease +NCIT:C205000 MONDO:excludeNonDisease +NCIT:C205001 MONDO:excludeNonDisease +NCIT:C205002 MONDO:excludeNonDisease +NCIT:C205003 MONDO:excludeNonDisease +NCIT:C205004 MONDO:excludeNonDisease +NCIT:C205005 MONDO:excludeNonDisease +NCIT:C205006 MONDO:excludeNonDisease +NCIT:C205007 MONDO:excludeNonDisease +NCIT:C205008 MONDO:excludeNonDisease +NCIT:C205009 MONDO:excludeNonDisease NCIT:C20501 MONDO:excludeNonDisease +NCIT:C205010 MONDO:excludeNonDisease +NCIT:C205011 MONDO:excludeNonDisease +NCIT:C205012 MONDO:excludeNonDisease +NCIT:C205013 MONDO:excludeNonDisease +NCIT:C205014 MONDO:excludeNonDisease +NCIT:C205015 MONDO:excludeNonDisease +NCIT:C205016 MONDO:excludeNonDisease +NCIT:C205017 MONDO:excludeNonDisease +NCIT:C205018 MONDO:excludeNonDisease +NCIT:C205019 MONDO:excludeNonDisease NCIT:C20502 MONDO:excludeNonDisease +NCIT:C205020 MONDO:excludeNonDisease +NCIT:C205021 MONDO:excludeNonDisease +NCIT:C205022 MONDO:excludeNonDisease +NCIT:C205023 MONDO:excludeNonDisease +NCIT:C205024 MONDO:excludeNonDisease +NCIT:C205025 MONDO:excludeNonDisease +NCIT:C205026 MONDO:excludeNonDisease +NCIT:C205027 MONDO:excludeNonDisease +NCIT:C205028 MONDO:excludeNonDisease +NCIT:C205029 MONDO:excludeNonDisease NCIT:C20503 MONDO:excludeNonDisease +NCIT:C205030 MONDO:excludeNonDisease +NCIT:C205031 MONDO:excludeNonDisease +NCIT:C205032 MONDO:excludeNonDisease +NCIT:C205033 MONDO:excludeNonDisease +NCIT:C205034 MONDO:excludeNonDisease +NCIT:C205035 MONDO:excludeNonDisease +NCIT:C205036 MONDO:excludeNonDisease +NCIT:C205037 MONDO:excludeNonDisease +NCIT:C205038 MONDO:excludeNonDisease +NCIT:C205039 MONDO:excludeNonDisease NCIT:C20504 MONDO:excludeNonDisease +NCIT:C205040 MONDO:excludeNonDisease +NCIT:C205041 MONDO:excludeNonDisease +NCIT:C205042 MONDO:excludeNonDisease +NCIT:C205043 MONDO:excludeNonDisease +NCIT:C205044 MONDO:excludeNonDisease +NCIT:C205045 MONDO:excludeNonDisease +NCIT:C205047 MONDO:excludeNonDisease +NCIT:C205048 MONDO:excludeNonDisease +NCIT:C205049 MONDO:excludeNonDisease NCIT:C20505 MONDO:excludeNonDisease +NCIT:C205050 MONDO:excludeNonDisease +NCIT:C205051 MONDO:excludeNonDisease +NCIT:C205052 MONDO:excludeNonDisease +NCIT:C205053 MONDO:excludeNonDisease +NCIT:C205054 MONDO:excludeNonDisease +NCIT:C205055 MONDO:excludeNonDisease +NCIT:C205056 MONDO:excludeNonDisease +NCIT:C205058 MONDO:excludeNonDisease +NCIT:C205059 MONDO:excludeNonDisease NCIT:C20506 MONDO:excludeNonDisease +NCIT:C205060 MONDO:excludeNonDisease +NCIT:C205061 MONDO:excludeNonDisease +NCIT:C205062 MONDO:excludeNonDisease +NCIT:C205063 MONDO:excludeNonDisease +NCIT:C205064 MONDO:excludeNonDisease +NCIT:C205065 MONDO:excludeNonDisease +NCIT:C205066 MONDO:excludeNonDisease +NCIT:C205067 MONDO:excludeNonDisease +NCIT:C205068 MONDO:excludeNonDisease NCIT:C20507 MONDO:excludeNonDisease +NCIT:C205070 MONDO:excludeNonDisease +NCIT:C205071 MONDO:excludeNonDisease +NCIT:C205072 MONDO:excludeNonDisease +NCIT:C205073 MONDO:excludeNonDisease +NCIT:C205074 MONDO:excludeNonDisease +NCIT:C205075 MONDO:excludeNonDisease +NCIT:C205076 MONDO:excludeNonDisease +NCIT:C205077 MONDO:excludeNonDisease +NCIT:C205078 MONDO:excludeNonDisease +NCIT:C205079 MONDO:excludeNonDisease NCIT:C20508 MONDO:excludeNonDisease +NCIT:C205080 MONDO:excludeNonDisease +NCIT:C205081 MONDO:excludeNonDisease +NCIT:C205082 MONDO:excludeNonDisease +NCIT:C205083 MONDO:excludeNonDisease +NCIT:C205084 MONDO:excludeNonDisease +NCIT:C205085 MONDO:excludeNonDisease +NCIT:C205086 MONDO:excludeNonDisease +NCIT:C205087 MONDO:excludeNonDisease +NCIT:C205088 MONDO:excludeNonDisease +NCIT:C205089 MONDO:excludeNonDisease NCIT:C20509 MONDO:excludeNonDisease +NCIT:C205090 MONDO:excludeNonDisease +NCIT:C205091 MONDO:excludeNonDisease +NCIT:C205092 MONDO:excludeNonDisease +NCIT:C205093 MONDO:excludeNonDisease +NCIT:C205094 MONDO:excludeNonDisease +NCIT:C205095 MONDO:excludeNonDisease +NCIT:C205096 MONDO:excludeNonDisease +NCIT:C205097 MONDO:excludeNonDisease +NCIT:C205098 MONDO:excludeNonDisease +NCIT:C205099 MONDO:excludeNonDisease NCIT:C2051 MONDO:excludeNonDisease NCIT:C20510 MONDO:excludeNonDisease +NCIT:C205100 MONDO:excludeNonDisease +NCIT:C205101 MONDO:excludeNonDisease +NCIT:C205102 MONDO:excludeNonDisease +NCIT:C205103 MONDO:excludeNonDisease +NCIT:C205104 MONDO:excludeNonDisease +NCIT:C205105 MONDO:excludeNonDisease +NCIT:C205106 MONDO:excludeNonDisease +NCIT:C205107 MONDO:excludeNonDisease +NCIT:C205108 MONDO:excludeNonDisease +NCIT:C205109 MONDO:excludeNonDisease NCIT:C20511 MONDO:excludeNonDisease +NCIT:C205110 MONDO:excludeNonDisease +NCIT:C205111 MONDO:excludeNonDisease +NCIT:C205112 MONDO:excludeNonDisease +NCIT:C205113 MONDO:excludeNonDisease +NCIT:C205114 MONDO:excludeNonDisease +NCIT:C205115 MONDO:excludeNonDisease +NCIT:C205116 MONDO:excludeNonDisease +NCIT:C205117 MONDO:excludeNonDisease +NCIT:C205118 MONDO:excludeNonDisease +NCIT:C205119 MONDO:excludeNonDisease NCIT:C20512 MONDO:excludeNonDisease +NCIT:C205120 MONDO:excludeNonDisease +NCIT:C205121 MONDO:excludeNonDisease +NCIT:C205122 MONDO:excludeNonDisease +NCIT:C205123 MONDO:excludeNonDisease +NCIT:C205124 MONDO:excludeNonDisease +NCIT:C205126 MONDO:excludeNonDisease +NCIT:C205128 MONDO:excludeNonDisease NCIT:C20513 MONDO:excludeNonDisease +NCIT:C205133 MONDO:excludeNonDisease +NCIT:C205134 MONDO:excludeNonDisease +NCIT:C205137 MONDO:excludeNonDisease +NCIT:C205138 MONDO:excludeNonDisease +NCIT:C205139 MONDO:excludeNonDisease NCIT:C20514 MONDO:excludeNonDisease +NCIT:C205140 MONDO:excludeNonDisease +NCIT:C205141 MONDO:excludeNonDisease +NCIT:C205142 MONDO:excludeNonDisease +NCIT:C205143 MONDO:excludeNonDisease +NCIT:C205144 MONDO:excludeNonDisease +NCIT:C205145 MONDO:excludeNonDisease +NCIT:C205146 MONDO:excludeNonDisease +NCIT:C205147 MONDO:excludeNonDisease +NCIT:C205148 MONDO:excludeNonDisease +NCIT:C205149 MONDO:excludeNonDisease NCIT:C20515 MONDO:excludeNonDisease +NCIT:C205150 MONDO:excludeNonDisease +NCIT:C205151 MONDO:excludeNonDisease +NCIT:C205152 MONDO:excludeNonDisease +NCIT:C205153 MONDO:excludeNonDisease +NCIT:C205154 MONDO:excludeNonDisease +NCIT:C205155 MONDO:excludeNonDisease +NCIT:C205156 MONDO:excludeNonDisease +NCIT:C205157 MONDO:excludeNonDisease +NCIT:C205158 MONDO:excludeNonDisease +NCIT:C205159 MONDO:excludeNonDisease +NCIT:C205160 MONDO:excludeNonDisease +NCIT:C205161 MONDO:excludeNonDisease +NCIT:C205162 MONDO:excludeNonDisease +NCIT:C205163 MONDO:excludeNonDisease +NCIT:C205164 MONDO:excludeNonDisease +NCIT:C205165 MONDO:excludeNonDisease +NCIT:C205166 MONDO:excludeNonDisease +NCIT:C205167 MONDO:excludeNonDisease +NCIT:C205168 MONDO:excludeNonDisease +NCIT:C205169 MONDO:excludeNonDisease NCIT:C20517 MONDO:excludeNonDisease +NCIT:C205170 MONDO:excludeNonDisease +NCIT:C205171 MONDO:excludeNonDisease +NCIT:C205172 MONDO:excludeNonDisease +NCIT:C205173 MONDO:excludeNonDisease +NCIT:C205174 MONDO:excludeNonDisease +NCIT:C205175 MONDO:excludeNonDisease +NCIT:C205176 MONDO:excludeNonDisease +NCIT:C205177 MONDO:excludeNonDisease +NCIT:C205178 MONDO:excludeNonDisease +NCIT:C205179 MONDO:excludeNonDisease NCIT:C20518 MONDO:excludeNonDisease +NCIT:C205180 MONDO:excludeNonDisease +NCIT:C205181 MONDO:excludeNonDisease +NCIT:C205182 MONDO:excludeNonDisease +NCIT:C205183 MONDO:excludeNonDisease +NCIT:C205184 MONDO:excludeNonDisease +NCIT:C205185 MONDO:excludeNonDisease +NCIT:C205186 MONDO:excludeNonDisease +NCIT:C205189 MONDO:excludeNonDisease NCIT:C20519 MONDO:excludeNonDisease +NCIT:C205190 MONDO:excludeNonDisease +NCIT:C205191 MONDO:excludeNonDisease +NCIT:C205192 MONDO:excludeNonDisease +NCIT:C205193 MONDO:excludeNonDisease +NCIT:C205194 MONDO:excludeNonDisease +NCIT:C205195 MONDO:excludeNonDisease +NCIT:C205196 MONDO:excludeNonDisease +NCIT:C205197 MONDO:excludeNonDisease +NCIT:C205198 MONDO:excludeNonDisease +NCIT:C205199 MONDO:excludeNonDisease NCIT:C2052 MONDO:excludeNonDisease NCIT:C20520 MONDO:excludeNonDisease +NCIT:C205200 MONDO:excludeNonDisease +NCIT:C205201 MONDO:excludeNonDisease +NCIT:C205202 MONDO:excludeNonDisease +NCIT:C205203 MONDO:excludeNonDisease +NCIT:C205204 MONDO:excludeNonDisease +NCIT:C205205 MONDO:excludeNonDisease +NCIT:C205206 MONDO:excludeNonDisease +NCIT:C205207 MONDO:excludeNonDisease +NCIT:C205208 MONDO:excludeNonDisease +NCIT:C205209 MONDO:excludeNonDisease NCIT:C20521 MONDO:excludeNonDisease +NCIT:C205210 MONDO:excludeNonDisease +NCIT:C205211 MONDO:excludeNonDisease +NCIT:C205212 MONDO:excludeNonDisease +NCIT:C205213 MONDO:excludeNonDisease +NCIT:C205214 MONDO:excludeNonDisease +NCIT:C205215 MONDO:excludeNonDisease +NCIT:C205216 MONDO:excludeNonDisease +NCIT:C205217 MONDO:excludeNonDisease +NCIT:C205218 MONDO:excludeNonDisease +NCIT:C205219 MONDO:excludeNonDisease NCIT:C20522 MONDO:excludeNonDisease +NCIT:C205220 MONDO:excludeNonDisease +NCIT:C205221 MONDO:excludeNonDisease +NCIT:C205222 MONDO:excludeNonDisease +NCIT:C205223 MONDO:excludeNonDisease +NCIT:C205224 MONDO:excludeNonDisease +NCIT:C205225 MONDO:excludeNonDisease +NCIT:C205227 MONDO:excludeNonDisease +NCIT:C205228 MONDO:excludeNonDisease +NCIT:C205229 MONDO:excludeNonDisease +NCIT:C205230 MONDO:excludeNonDisease +NCIT:C205231 MONDO:excludeNonDisease +NCIT:C205232 MONDO:excludeNonDisease +NCIT:C205233 MONDO:excludeNonDisease +NCIT:C205234 MONDO:excludeNonDisease +NCIT:C205235 MONDO:excludeNonDisease +NCIT:C205236 MONDO:excludeNonDisease +NCIT:C205237 MONDO:excludeNonDisease +NCIT:C205239 MONDO:excludeNonDisease NCIT:C20524 MONDO:excludeNonDisease +NCIT:C205240 MONDO:excludeNonDisease +NCIT:C205241 MONDO:excludeNonDisease +NCIT:C205242 MONDO:excludeNonDisease +NCIT:C205243 MONDO:excludeNonDisease +NCIT:C205244 MONDO:excludeNonDisease +NCIT:C205245 MONDO:excludeNonDisease +NCIT:C205246 MONDO:excludeNonDisease +NCIT:C205247 MONDO:excludeNonDisease +NCIT:C205248 MONDO:excludeNonDisease +NCIT:C205249 MONDO:excludeNonDisease NCIT:C20525 MONDO:excludeNonDisease +NCIT:C205250 MONDO:excludeNonDisease +NCIT:C205251 MONDO:excludeNonDisease +NCIT:C205252 MONDO:excludeNonDisease +NCIT:C205253 MONDO:excludeNonDisease +NCIT:C205254 MONDO:excludeNonDisease +NCIT:C205255 MONDO:excludeNonDisease +NCIT:C205256 MONDO:excludeNonDisease +NCIT:C205257 MONDO:excludeNonDisease +NCIT:C205258 MONDO:excludeNonDisease +NCIT:C205259 MONDO:excludeNonDisease NCIT:C20526 MONDO:excludeNonDisease +NCIT:C205260 MONDO:excludeNonDisease +NCIT:C205261 MONDO:excludeNonDisease +NCIT:C205262 MONDO:excludeNonDisease +NCIT:C205263 MONDO:excludeNonDisease +NCIT:C205264 MONDO:excludeNonDisease +NCIT:C205265 MONDO:excludeNonDisease +NCIT:C205266 MONDO:excludeNonDisease +NCIT:C205267 MONDO:excludeNonDisease +NCIT:C205268 MONDO:excludeNonDisease +NCIT:C205269 MONDO:excludeNonDisease NCIT:C20527 MONDO:excludeNonDisease +NCIT:C205270 MONDO:excludeNonDisease +NCIT:C205271 MONDO:excludeNonDisease +NCIT:C205272 MONDO:excludeNonDisease +NCIT:C205273 MONDO:excludeNonDisease +NCIT:C205274 MONDO:excludeNonDisease +NCIT:C205275 MONDO:excludeNonDisease +NCIT:C205276 MONDO:excludeNonDisease +NCIT:C205277 MONDO:excludeNonDisease +NCIT:C205278 MONDO:excludeNonDisease +NCIT:C205279 MONDO:excludeNonDisease NCIT:C20528 MONDO:excludeNonDisease +NCIT:C205280 MONDO:excludeNonDisease +NCIT:C205281 MONDO:excludeNonDisease +NCIT:C205282 MONDO:excludeNonDisease +NCIT:C205283 MONDO:excludeNonDisease +NCIT:C205284 MONDO:excludeNonDisease +NCIT:C205285 MONDO:excludeNonDisease +NCIT:C205288 MONDO:excludeNonDisease NCIT:C20529 MONDO:excludeNonDisease +NCIT:C205291 MONDO:excludeNonDisease +NCIT:C205292 MONDO:excludeNonDisease +NCIT:C205293 MONDO:excludeNonDisease +NCIT:C205294 MONDO:excludeNonDisease +NCIT:C205296 MONDO:excludeNonDisease +NCIT:C205297 MONDO:excludeNonDisease +NCIT:C205299 MONDO:excludeNonDisease NCIT:C2053 MONDO:excludeNonDisease NCIT:C20530 MONDO:excludeNonDisease +NCIT:C205300 MONDO:excludeNonDisease +NCIT:C205302 MONDO:excludeNonDisease +NCIT:C205304 MONDO:excludeNonDisease +NCIT:C205305 MONDO:excludeNonDisease NCIT:C20531 MONDO:excludeNonDisease +NCIT:C205312 MONDO:excludeNonDisease +NCIT:C205315 MONDO:excludeNonDisease +NCIT:C205316 MONDO:excludeNonDisease +NCIT:C205318 MONDO:excludeNonDisease +NCIT:C205319 MONDO:excludeNonDisease NCIT:C20532 MONDO:excludeNonDisease +NCIT:C205320 MONDO:excludeNonDisease +NCIT:C205321 MONDO:excludeNonDisease +NCIT:C205322 MONDO:excludeNonDisease +NCIT:C205323 MONDO:excludeNonDisease +NCIT:C205324 MONDO:excludeNonDisease +NCIT:C205325 MONDO:excludeNonDisease +NCIT:C205326 MONDO:excludeNonDisease +NCIT:C205327 MONDO:excludeNonDisease +NCIT:C205328 MONDO:excludeNonDisease NCIT:C20533 MONDO:excludeNonDisease +NCIT:C205330 MONDO:excludeNonDisease +NCIT:C205331 MONDO:excludeNonDisease +NCIT:C205332 MONDO:excludeNonDisease +NCIT:C205333 MONDO:excludeNonDisease +NCIT:C205334 MONDO:excludeNonDisease +NCIT:C205335 MONDO:excludeNonDisease +NCIT:C205336 MONDO:excludeNonDisease +NCIT:C205337 MONDO:excludeNonDisease +NCIT:C205338 MONDO:excludeNonDisease +NCIT:C205339 MONDO:excludeNonDisease NCIT:C20534 MONDO:excludeNonDisease +NCIT:C205340 MONDO:excludeNonDisease +NCIT:C205341 MONDO:excludeNonDisease +NCIT:C205342 MONDO:excludeNonDisease +NCIT:C205343 MONDO:excludeNonDisease +NCIT:C205344 MONDO:excludeNonDisease +NCIT:C205345 MONDO:excludeNonDisease +NCIT:C205346 MONDO:excludeNonDisease +NCIT:C205347 MONDO:excludeNonDisease +NCIT:C205348 MONDO:excludeNonDisease +NCIT:C205349 MONDO:excludeNonDisease NCIT:C20535 MONDO:excludeNonDisease +NCIT:C205350 MONDO:excludeNonDisease +NCIT:C205351 MONDO:excludeNonDisease +NCIT:C205352 MONDO:excludeNonDisease +NCIT:C205353 MONDO:excludeNonDisease +NCIT:C205354 MONDO:excludeNonDisease +NCIT:C205355 MONDO:excludeNonDisease +NCIT:C205356 MONDO:excludeNonDisease +NCIT:C205358 MONDO:excludeNonDisease +NCIT:C205359 MONDO:excludeNonDisease NCIT:C20536 MONDO:excludeNonDisease +NCIT:C205360 MONDO:excludeNonDisease +NCIT:C205362 MONDO:excludeNonDisease +NCIT:C205363 MONDO:excludeNonDisease +NCIT:C205364 MONDO:excludeNonDisease +NCIT:C205365 MONDO:excludeNonDisease +NCIT:C205366 MONDO:excludeNonDisease +NCIT:C205367 MONDO:excludeNonDisease +NCIT:C205368 MONDO:excludeNonDisease +NCIT:C205369 MONDO:excludeNonDisease NCIT:C20537 MONDO:excludeNonDisease +NCIT:C205372 MONDO:excludeNonDisease +NCIT:C205373 MONDO:excludeNonDisease +NCIT:C205374 MONDO:excludeNonDisease +NCIT:C205375 MONDO:excludeNonDisease +NCIT:C205376 MONDO:excludeNonDisease +NCIT:C205377 MONDO:excludeNonDisease +NCIT:C205378 MONDO:excludeNonDisease +NCIT:C205379 MONDO:excludeNonDisease NCIT:C20538 MONDO:excludeNonDisease +NCIT:C205380 MONDO:excludeNonDisease +NCIT:C205381 MONDO:excludeNonDisease +NCIT:C205382 MONDO:excludeNonDisease +NCIT:C205383 MONDO:excludeNonDisease +NCIT:C205384 MONDO:excludeNonDisease +NCIT:C205385 MONDO:excludeNonDisease +NCIT:C205386 MONDO:excludeNonDisease +NCIT:C205387 MONDO:excludeNonDisease +NCIT:C205388 MONDO:excludeNonDisease +NCIT:C205389 MONDO:excludeNonDisease NCIT:C20539 MONDO:excludeNonDisease +NCIT:C205390 MONDO:excludeNonDisease +NCIT:C205391 MONDO:excludeNonDisease +NCIT:C205392 MONDO:excludeNonDisease +NCIT:C205393 MONDO:excludeNonDisease +NCIT:C205394 MONDO:excludeNonDisease +NCIT:C205395 MONDO:excludeNonDisease +NCIT:C205396 MONDO:excludeNonDisease +NCIT:C205397 MONDO:excludeNonDisease +NCIT:C205398 MONDO:excludeNonDisease +NCIT:C205399 MONDO:excludeNonDisease NCIT:C2054 MONDO:excludeNonDisease NCIT:C20540 MONDO:excludeNonDisease +NCIT:C205400 MONDO:excludeNonDisease +NCIT:C205401 MONDO:excludeNonDisease +NCIT:C205402 MONDO:excludeNonDisease +NCIT:C205403 MONDO:excludeNonDisease +NCIT:C205404 MONDO:excludeNonDisease +NCIT:C205405 MONDO:excludeNonDisease +NCIT:C205406 MONDO:excludeNonDisease +NCIT:C205407 MONDO:excludeNonDisease +NCIT:C205408 MONDO:excludeNonDisease NCIT:C20541 MONDO:excludeNonDisease +NCIT:C205410 MONDO:excludeNonDisease +NCIT:C205411 MONDO:excludeNonDisease +NCIT:C205412 MONDO:excludeNonDisease +NCIT:C205413 MONDO:excludeNonDisease +NCIT:C205414 MONDO:excludeNonDisease +NCIT:C205415 MONDO:excludeNonDisease +NCIT:C205416 MONDO:excludeNonDisease +NCIT:C205417 MONDO:excludeNonDisease +NCIT:C205418 MONDO:excludeNonDisease +NCIT:C205419 MONDO:excludeNonDisease NCIT:C20542 MONDO:excludeNonDisease +NCIT:C205420 MONDO:excludeNonDisease +NCIT:C205421 MONDO:excludeNonDisease +NCIT:C205422 MONDO:excludeNonDisease +NCIT:C205423 MONDO:excludeNonDisease +NCIT:C205424 MONDO:excludeNonDisease +NCIT:C205425 MONDO:excludeNonDisease +NCIT:C205426 MONDO:excludeNonDisease +NCIT:C205427 MONDO:excludeNonDisease +NCIT:C205428 MONDO:excludeNonDisease +NCIT:C205429 MONDO:excludeNonDisease NCIT:C20543 MONDO:excludeNonDisease +NCIT:C205430 MONDO:excludeNonDisease +NCIT:C205431 MONDO:excludeNonDisease +NCIT:C205432 MONDO:excludeNonDisease +NCIT:C205433 MONDO:excludeNonDisease +NCIT:C205434 MONDO:excludeNonDisease +NCIT:C205435 MONDO:excludeNonDisease +NCIT:C205436 MONDO:excludeNonDisease +NCIT:C205437 MONDO:excludeNonDisease +NCIT:C205438 MONDO:excludeNonDisease +NCIT:C205439 MONDO:excludeNonDisease NCIT:C20544 MONDO:excludeNonDisease +NCIT:C205440 MONDO:excludeNonDisease +NCIT:C205441 MONDO:excludeNonDisease +NCIT:C205442 MONDO:excludeNonDisease +NCIT:C205443 MONDO:excludeNonDisease +NCIT:C205444 MONDO:excludeNonDisease +NCIT:C205445 MONDO:excludeNonDisease +NCIT:C205446 MONDO:excludeNonDisease +NCIT:C205447 MONDO:excludeNonDisease +NCIT:C205448 MONDO:excludeNonDisease +NCIT:C205449 MONDO:excludeNonDisease NCIT:C20545 MONDO:excludeNonDisease +NCIT:C205450 MONDO:excludeNonDisease +NCIT:C205451 MONDO:excludeNonDisease +NCIT:C205452 MONDO:excludeNonDisease +NCIT:C205453 MONDO:excludeNonDisease +NCIT:C205454 MONDO:excludeNonDisease +NCIT:C205455 MONDO:excludeNonDisease +NCIT:C205456 MONDO:excludeNonDisease +NCIT:C205457 MONDO:excludeNonDisease +NCIT:C205458 MONDO:excludeNonDisease +NCIT:C205460 MONDO:excludeNonDisease +NCIT:C205461 MONDO:excludeNonDisease +NCIT:C205464 MONDO:excludeNonDisease +NCIT:C205465 MONDO:excludeNonDisease +NCIT:C205466 MONDO:excludeNonDisease +NCIT:C205467 MONDO:excludeNonDisease +NCIT:C205468 MONDO:excludeNonDisease +NCIT:C205469 MONDO:excludeNonDisease NCIT:C20547 MONDO:excludeNonDisease +NCIT:C205470 MONDO:excludeNonDisease +NCIT:C205471 MONDO:excludeNonDisease +NCIT:C205472 MONDO:excludeNonDisease +NCIT:C205473 MONDO:excludeNonDisease +NCIT:C205474 MONDO:excludeNonDisease +NCIT:C205477 MONDO:excludeNonDisease +NCIT:C205478 MONDO:excludeNonDisease +NCIT:C205479 MONDO:excludeNonDisease NCIT:C20548 MONDO:excludeNonDisease +NCIT:C205480 MONDO:excludeNonDisease +NCIT:C205481 MONDO:excludeNonDisease +NCIT:C205482 MONDO:excludeNonDisease +NCIT:C205483 MONDO:excludeNonDisease +NCIT:C205484 MONDO:excludeNonDisease +NCIT:C205485 MONDO:excludeNonDisease +NCIT:C205486 MONDO:excludeNonDisease +NCIT:C205487 MONDO:excludeNonDisease +NCIT:C205488 MONDO:excludeNonDisease +NCIT:C205489 MONDO:excludeNonDisease NCIT:C20549 MONDO:excludeNonDisease +NCIT:C205490 MONDO:excludeNonDisease +NCIT:C205491 MONDO:excludeNonDisease +NCIT:C205492 MONDO:excludeNonDisease +NCIT:C205493 MONDO:excludeNonDisease +NCIT:C205494 MONDO:excludeNonDisease +NCIT:C205495 MONDO:excludeNonDisease +NCIT:C205496 MONDO:excludeNonDisease +NCIT:C205497 MONDO:excludeNonDisease +NCIT:C205498 MONDO:excludeNonDisease +NCIT:C205499 MONDO:excludeNonDisease NCIT:C2055 MONDO:excludeNonDisease NCIT:C20550 MONDO:excludeNonDisease +NCIT:C205500 MONDO:excludeNonDisease +NCIT:C205501 MONDO:excludeNonDisease +NCIT:C205502 MONDO:excludeNonDisease +NCIT:C205503 MONDO:excludeNonDisease +NCIT:C205504 MONDO:excludeNonDisease +NCIT:C205505 MONDO:excludeNonDisease +NCIT:C205506 MONDO:excludeNonDisease +NCIT:C205507 MONDO:excludeNonDisease +NCIT:C205508 MONDO:excludeNonDisease +NCIT:C205509 MONDO:excludeNonDisease NCIT:C20551 MONDO:excludeNonDisease +NCIT:C205510 MONDO:excludeNonDisease +NCIT:C205511 MONDO:excludeNonDisease +NCIT:C205512 MONDO:excludeNonDisease +NCIT:C205513 MONDO:excludeNonDisease +NCIT:C205514 MONDO:excludeNonDisease +NCIT:C205515 MONDO:excludeNonDisease +NCIT:C205516 MONDO:excludeNonDisease +NCIT:C205517 MONDO:excludeNonDisease +NCIT:C205518 MONDO:excludeNonDisease +NCIT:C205519 MONDO:excludeNonDisease NCIT:C20552 MONDO:excludeNonDisease +NCIT:C205520 MONDO:excludeNonDisease +NCIT:C205521 MONDO:excludeNonDisease +NCIT:C205522 MONDO:excludeNonDisease +NCIT:C205523 MONDO:excludeNonDisease +NCIT:C205524 MONDO:excludeNonDisease +NCIT:C205525 MONDO:excludeNonDisease +NCIT:C205526 MONDO:excludeNonDisease +NCIT:C205527 MONDO:excludeNonDisease +NCIT:C205528 MONDO:excludeNonDisease +NCIT:C205529 MONDO:excludeNonDisease NCIT:C20553 MONDO:excludeNonDisease +NCIT:C205530 MONDO:excludeNonDisease +NCIT:C205531 MONDO:excludeNonDisease +NCIT:C205532 MONDO:excludeNonDisease +NCIT:C205533 MONDO:excludeNonDisease +NCIT:C205534 MONDO:excludeNonDisease +NCIT:C205535 MONDO:excludeNonDisease +NCIT:C205536 MONDO:excludeNonDisease +NCIT:C205537 MONDO:excludeNonDisease +NCIT:C205538 MONDO:excludeNonDisease NCIT:C20554 MONDO:excludeNonDisease +NCIT:C205540 MONDO:excludeNonDisease +NCIT:C205541 MONDO:excludeNonDisease +NCIT:C205542 MONDO:excludeNonDisease +NCIT:C205543 MONDO:excludeNonDisease +NCIT:C205544 MONDO:excludeNonDisease +NCIT:C205545 MONDO:excludeNonDisease +NCIT:C205546 MONDO:excludeNonDisease +NCIT:C205547 MONDO:excludeNonDisease +NCIT:C205548 MONDO:excludeNonDisease +NCIT:C205549 MONDO:excludeNonDisease NCIT:C20555 MONDO:excludeNonDisease +NCIT:C205550 MONDO:excludeNonDisease +NCIT:C205552 MONDO:excludeNonDisease +NCIT:C205553 MONDO:excludeNonDisease +NCIT:C205554 MONDO:excludeNonDisease +NCIT:C205555 MONDO:excludeNonDisease +NCIT:C205556 MONDO:excludeNonDisease +NCIT:C205557 MONDO:excludeNonDisease +NCIT:C205558 MONDO:excludeNonDisease +NCIT:C205559 MONDO:excludeNonDisease NCIT:C20556 MONDO:excludeNonDisease +NCIT:C205560 MONDO:excludeNonDisease +NCIT:C205561 MONDO:excludeNonDisease +NCIT:C205562 MONDO:excludeNonDisease +NCIT:C205563 MONDO:excludeNonDisease +NCIT:C205564 MONDO:excludeNonDisease +NCIT:C205565 MONDO:excludeNonDisease +NCIT:C205566 MONDO:excludeNonDisease +NCIT:C205567 MONDO:excludeNonDisease +NCIT:C205568 MONDO:excludeNonDisease +NCIT:C205569 MONDO:excludeNonDisease NCIT:C20557 MONDO:excludeNonDisease +NCIT:C205570 MONDO:excludeNonDisease +NCIT:C205571 MONDO:excludeNonDisease +NCIT:C205572 MONDO:excludeNonDisease +NCIT:C205573 MONDO:excludeNonDisease +NCIT:C205574 MONDO:excludeNonDisease +NCIT:C205575 MONDO:excludeNonDisease +NCIT:C205576 MONDO:excludeNonDisease +NCIT:C205577 MONDO:excludeNonDisease +NCIT:C205578 MONDO:excludeNonDisease +NCIT:C205579 MONDO:excludeNonDisease NCIT:C20558 MONDO:excludeNonDisease +NCIT:C205580 MONDO:excludeNonDisease +NCIT:C205581 MONDO:excludeNonDisease +NCIT:C205582 MONDO:excludeNonDisease +NCIT:C205583 MONDO:excludeNonDisease +NCIT:C205584 MONDO:excludeNonDisease +NCIT:C205585 MONDO:excludeNonDisease +NCIT:C205586 MONDO:excludeNonDisease +NCIT:C205587 MONDO:excludeNonDisease +NCIT:C205588 MONDO:excludeNonDisease +NCIT:C205589 MONDO:excludeNonDisease NCIT:C20559 MONDO:excludeNonDisease +NCIT:C205590 MONDO:excludeNonDisease +NCIT:C205591 MONDO:excludeNonDisease +NCIT:C205592 MONDO:excludeNonDisease +NCIT:C205593 MONDO:excludeNonDisease +NCIT:C205594 MONDO:excludeNonDisease +NCIT:C205595 MONDO:excludeNonDisease +NCIT:C205596 MONDO:excludeNonDisease +NCIT:C205597 MONDO:excludeNonDisease +NCIT:C205598 MONDO:excludeNonDisease +NCIT:C205599 MONDO:excludeNonDisease NCIT:C2056 MONDO:excludeNonDisease NCIT:C20560 MONDO:excludeNonDisease +NCIT:C205600 MONDO:excludeNonDisease +NCIT:C205601 MONDO:excludeNonDisease +NCIT:C205602 MONDO:excludeNonDisease +NCIT:C205603 MONDO:excludeNonDisease +NCIT:C205605 MONDO:excludeNonDisease +NCIT:C205606 MONDO:excludeNonDisease NCIT:C20561 MONDO:excludeNonDisease NCIT:C20562 MONDO:excludeNonDisease NCIT:C20563 MONDO:excludeNonDisease @@ -109068,7 +112633,6 @@ NCIT:C35435 MONDO:excludeNonDisease NCIT:C35436 MONDO:excludeNonDisease NCIT:C35437 MONDO:excludeNonDisease NCIT:C35438 MONDO:excludeNonDisease -NCIT:C35439 MONDO:excludeNonDisease NCIT:C35440 MONDO:excludeNonDisease NCIT:C35441 MONDO:excludeNonDisease NCIT:C35443 MONDO:excludeNonDisease @@ -112907,7 +116471,6 @@ NCIT:C39626 MONDO:excludeNonDisease NCIT:C39627 MONDO:excludeNonDisease NCIT:C39628 MONDO:excludeNonDisease NCIT:C39629 MONDO:excludeNonDisease -NCIT:C3963 MONDO:excludeNonDisease NCIT:C39630 MONDO:excludeNonDisease NCIT:C39631 MONDO:excludeNonDisease NCIT:C39632 MONDO:excludeNonDisease @@ -115389,7 +118952,6 @@ NCIT:C43245 MONDO:excludeNonDisease NCIT:C43246 MONDO:excludeNonDisease NCIT:C43247 MONDO:excludeNonDisease NCIT:C43248 MONDO:excludeNonDisease -NCIT:C43249 MONDO:excludeNonDisease NCIT:C43251 MONDO:excludeNonDisease NCIT:C43253 MONDO:excludeNonDisease NCIT:C43255 MONDO:excludeNonDisease @@ -115445,6 +119007,7 @@ NCIT:C43320 MONDO:excludeNonDisease NCIT:C43337 MONDO:excludeNonDisease NCIT:C43338 MONDO:excludeNonDisease NCIT:C43339 MONDO:excludeNonDisease +NCIT:C43352 MONDO:excludeNonDisease NCIT:C43358 MONDO:excludeNonDisease NCIT:C43359 MONDO:excludeNonDisease NCIT:C43360 MONDO:excludeNonDisease @@ -115673,6 +119236,7 @@ NCIT:C43647 MONDO:excludeNonDisease NCIT:C43648 MONDO:excludeNonDisease NCIT:C43649 MONDO:excludeNonDisease NCIT:C43650 MONDO:excludeNonDisease +NCIT:C4366 MONDO:excludeNonDisease NCIT:C4367 MONDO:excludeNonDisease NCIT:C43670 MONDO:excludeNonDisease NCIT:C43671 MONDO:excludeNonDisease @@ -120230,7 +123794,6 @@ NCIT:C50033 MONDO:excludeNonDisease NCIT:C50034 MONDO:excludeNonDisease NCIT:C50035 MONDO:excludeNonDisease NCIT:C50036 MONDO:excludeNonDisease -NCIT:C50037 MONDO:excludeNonDisease NCIT:C50038 MONDO:excludeNonDisease NCIT:C50039 MONDO:excludeNonDisease NCIT:C50040 MONDO:excludeNonDisease @@ -122142,7 +125705,6 @@ NCIT:C51979 MONDO:excludeNonDisease NCIT:C5198 MONDO:excludeNonDisease NCIT:C51980 MONDO:excludeNonDisease NCIT:C51981 MONDO:excludeNonDisease -NCIT:C51982 MONDO:excludeNonDisease NCIT:C51985 MONDO:excludeNonDisease NCIT:C51986 MONDO:excludeNonDisease NCIT:C51987 MONDO:excludeNonDisease @@ -124200,7 +127762,6 @@ NCIT:C54142 MONDO:excludeNonDisease NCIT:C54144 MONDO:excludeNonDisease NCIT:C54145 MONDO:excludeNonDisease NCIT:C54146 MONDO:excludeNonDisease -NCIT:C54147 MONDO:excludeNonDisease NCIT:C54148 MONDO:excludeNonDisease NCIT:C54149 MONDO:excludeNonDisease NCIT:C5415 MONDO:excludeNonDisease @@ -129698,6 +133259,7 @@ NCIT:C59706 MONDO:excludeNonDisease NCIT:C59707 MONDO:excludeNonDisease NCIT:C59708 MONDO:excludeNonDisease NCIT:C59709 MONDO:excludeNonDisease +NCIT:C5971 MONDO:excludeNonDisease NCIT:C59710 MONDO:excludeNonDisease NCIT:C59711 MONDO:excludeNonDisease NCIT:C59712 MONDO:excludeNonDisease @@ -131122,9 +134684,7 @@ NCIT:C61395 MONDO:excludeNonDisease NCIT:C61396 MONDO:excludeNonDisease NCIT:C61397 MONDO:excludeNonDisease NCIT:C61398 MONDO:excludeNonDisease -NCIT:C61399 MONDO:excludeNonDisease NCIT:C614 MONDO:excludeNonDisease -NCIT:C61400 MONDO:excludeNonDisease NCIT:C61401 MONDO:excludeNonDisease NCIT:C61402 MONDO:excludeNonDisease NCIT:C61403 MONDO:excludeNonDisease @@ -133078,7 +136638,6 @@ NCIT:C63465 MONDO:excludeNonDisease NCIT:C63466 MONDO:excludeNonDisease NCIT:C63467 MONDO:excludeNonDisease NCIT:C63468 MONDO:excludeNonDisease -NCIT:C63469 MONDO:excludeNonDisease NCIT:C63470 MONDO:excludeNonDisease NCIT:C63471 MONDO:excludeNonDisease NCIT:C63472 MONDO:excludeNonDisease @@ -133482,7 +137041,6 @@ NCIT:C64186 MONDO:excludeNonDisease NCIT:C64187 MONDO:excludeNonDisease NCIT:C64188 MONDO:excludeNonDisease NCIT:C64189 MONDO:excludeNonDisease -NCIT:C64190 MONDO:excludeNonDisease NCIT:C64191 MONDO:excludeNonDisease NCIT:C64192 MONDO:excludeNonDisease NCIT:C64193 MONDO:excludeNonDisease @@ -136284,7 +139842,6 @@ NCIT:C67220 MONDO:excludeNonDisease NCIT:C67226 MONDO:excludeNonDisease NCIT:C67227 MONDO:excludeNonDisease NCIT:C67229 MONDO:excludeNonDisease -NCIT:C67231 MONDO:excludeNonDisease NCIT:C67232 MONDO:excludeNonDisease NCIT:C67233 MONDO:excludeNonDisease NCIT:C67234 MONDO:excludeNonDisease @@ -137611,6 +141168,7 @@ NCIT:C69317 MONDO:excludeNonDisease NCIT:C69318 MONDO:excludeNonDisease NCIT:C69319 MONDO:excludeNonDisease NCIT:C69320 MONDO:excludeNonDisease +NCIT:C6933 MONDO:excludeNonDisease NCIT:C694 MONDO:excludeNonDisease NCIT:C6940 MONDO:excludeNonDisease NCIT:C69402 MONDO:excludeNonDisease @@ -144281,7 +147839,6 @@ NCIT:C77182 MONDO:excludeNonDisease NCIT:C77183 MONDO:excludeNonDisease NCIT:C77184 MONDO:excludeNonDisease NCIT:C77185 MONDO:excludeNonDisease -NCIT:C77186 MONDO:excludeNonDisease NCIT:C77187 MONDO:excludeNonDisease NCIT:C77188 MONDO:excludeNonDisease NCIT:C77189 MONDO:excludeNonDisease @@ -150382,7 +153939,6 @@ NCIT:C83716 MONDO:excludeNonDisease NCIT:C83717 MONDO:excludeNonDisease NCIT:C83718 MONDO:excludeNonDisease NCIT:C83719 MONDO:excludeNonDisease -NCIT:C8372 MONDO:excludeNonDisease NCIT:C83720 MONDO:excludeNonDisease NCIT:C83721 MONDO:excludeNonDisease NCIT:C83722 MONDO:excludeNonDisease @@ -158419,7 +161975,6 @@ NCIT:C92201 MONDO:excludeNonDisease NCIT:C92202 MONDO:excludeNonDisease NCIT:C92203 MONDO:excludeNonDisease NCIT:C92205 MONDO:excludeNonDisease -NCIT:C92206 MONDO:excludeNonDisease NCIT:C92207 MONDO:excludeNonDisease NCIT:C92208 MONDO:excludeNonDisease NCIT:C92209 MONDO:excludeNonDisease diff --git a/src/ontology/reports/ncit_mapped_deprecated_terms.robot.template.tsv b/src/ontology/reports/ncit_mapped_deprecated_terms.robot.template.tsv index bc7b6e42..67bdd3f4 100644 --- a/src/ontology/reports/ncit_mapped_deprecated_terms.robot.template.tsv +++ b/src/ontology/reports/ncit_mapped_deprecated_terms.robot.template.tsv @@ -1,13 +1,23 @@ mondo_id source_id source ID A oboInOwl:hasDbXref >A oboInOwl:source MONDO:0002063 NCIT:C6977 MONDO:equivalentObsolete +MONDO:0002938 NCIT:C66903 MONDO:equivalentObsolete +MONDO:0003222 NCIT:C5504 MONDO:equivalentObsolete +MONDO:0003450 NCIT:C4173 MONDO:equivalentObsolete MONDO:0003998 NCIT:C40257 MONDO:equivalentObsolete +MONDO:0004141 NCIT:C9499 MONDO:equivalentObsolete MONDO:0004204 NCIT:C4462 MONDO:equivalentObsolete MONDO:0004419 NCIT:C39822 MONDO:equivalentObsolete MONDO:0004819 NCIT:C7150 MONDO:equivalentObsolete MONDO:0005065 NCIT:C3234 MONDO:equivalentObsolete +MONDO:0005104 NCIT:C9419 MONDO:equivalentObsolete MONDO:0005362 NCIT:C34801 MONDO:equivalentObsolete +MONDO:0005369 NCIT:C2915 MONDO:equivalentObsolete +MONDO:0006475 NCIT:C27892 MONDO:equivalentObsolete +MONDO:0013171 NCIT:C3963 MONDO:equivalentObsolete MONDO:0015040 NCIT:C7167 MONDO:equivalentObsolete +MONDO:0015540 NCIT:C35439 MONDO:equivalentObsolete +MONDO:0016747 NCIT:C5505 MONDO:equivalentObsolete MONDO:0017308 NCIT:C75007 MONDO:equivalentObsolete MONDO:0020804 NCIT:C7586 MONDO:equivalentObsolete MONDO:0020805 NCIT:C4743 MONDO:equivalentObsolete diff --git a/src/ontology/reports/ncit_mapping_status.tsv b/src/ontology/reports/ncit_mapping_status.tsv index 6221e6e0..c18be74b 100644 --- a/src/ontology/reports/ncit_mapping_status.tsv +++ b/src/ontology/reports/ncit_mapping_status.tsv @@ -1,5 +1,5 @@ subject_id subject_label is_mapped is_excluded is_deprecated -NCIT:C100054 Conjunctival Melanocytic Intraepithelial Neoplasia False False False +NCIT:C100054 Conjunctival Melanocytic Intraepithelial Lesion False False False NCIT:C101539 Stage I Differentiated Thyroid Gland Carcinoma Under 45 Years AJCC v7 False False False NCIT:C101540 Stage I Differentiated Thyroid Gland Carcinoma 45 Years and Older AJCC v7 False False False NCIT:C101541 Stage II Differentiated Thyroid Gland Carcinoma Under 45 Years AJCC v7 False False False @@ -182,7 +182,7 @@ NCIT:C115212 Familial Waldenstrom Macroglobulinemia False False False NCIT:C115225 Hereditary Neuroblastoma False False False NCIT:C115245 Metastatic Digestive System Neuroendocrine Tumor G1 False False False NCIT:C115250 Adult Mixed Glioma False False False -NCIT:C115253 Adult Primary Meningeal Melanocytic Neoplasm False False False +NCIT:C115253 Adult Central Nervous System Melanocytic Neoplasm False False False NCIT:C115263 Adult Myxopapillary Ependymoma False False False NCIT:C115292 Localized Childhood Soft Tissue Sarcoma False False False NCIT:C115327 Adult Pineal Gland Astrocytoma False False False @@ -311,8 +311,6 @@ NCIT:C121871 Chondrosarcoma, Grade 3 False False False NCIT:C121881 Secondary Central Chondrosarcoma False False False NCIT:C121882 Secondary Peripheral Chondrosarcoma False False False NCIT:C121901 Benign Notochordal Cell Tumor False False False -NCIT:C121923 Ivory Exostosis False False False -NCIT:C121924 Enostosis False False False NCIT:C121925 Intermediate Osteogenic Neoplasm False False False NCIT:C121926 Intermediate Bone Neoplasm False False False NCIT:C121929 Non-Ossifying Fibroma False False False @@ -433,7 +431,7 @@ NCIT:C126479 Broad Ligament Serous Adenocarcinoma False False False NCIT:C126480 Low Grade Broad Ligament Serous Adenocarcinoma False False False NCIT:C126598 Thyroid Gland Noninvasive Follicular Neoplasm with Papillary-Like Nuclear Features False False False NCIT:C126750 Oropharyngeal Poorly Differentiated Carcinoma False False False -NCIT:C126751 Oropharyngeal Basaloid Carcinoma False False False +NCIT:C126751 Oropharyngeal Basaloid Squamous Cell Carcinoma False False False NCIT:C126769 Endometrial Dedifferentiated Carcinoma False False False NCIT:C126772 Endometrial Large Cell Neuroendocrine Carcinoma False False False NCIT:C126773 Uterine Corpus Neuroendocrine Tumor G1 False False False @@ -488,7 +486,7 @@ NCIT:C128142 Vulvar Squamous Intraepithelial Lesion, HPV-Associated False False NCIT:C128162 Vulvar Adenocarcinoma of Mammary Gland Type False False False NCIT:C128164 Vulvar Adenocarcinoma of Sweat Gland Origin False False False NCIT:C128165 Malignant Vulvar Phyllodes Tumor False False False -NCIT:C128166 Vulvar Adenocarcinoma, Intestinal-Type False False False +NCIT:C128166 Vulvar Mucinous Adenocarcinoma, Intestinal-Type False False False NCIT:C128167 Vulvar Keratoacanthoma False False False NCIT:C128171 Colon Adenoma with Severe Dysplasia False False False NCIT:C128240 Vulvar Hidradenoma Papilliferum False False False @@ -771,9 +769,9 @@ NCIT:C133460 Postneoadjuvant Therapy Stage IVA Esophageal Squamous Cell Carcinom NCIT:C133461 Postneoadjuvant Therapy Stage IVB Esophageal Squamous Cell Carcinoma AJCC v8 False False False NCIT:C133494 Large B-Cell Lymphoma with IRF4 Rearrangement False False False NCIT:C133499 Recurrent Atypical Teratoid/Rhabdoid Tumor False False False -NCIT:C133501 Breast Carcinoma Metastatic in the Central Nervous System False False False -NCIT:C133503 Lung Carcinoma Metastatic in the Central Nervous System False False False -NCIT:C133504 Melanoma Metastatic in the Central Nervous System False False False +NCIT:C133501 Metastatic Breast Carcinoma in the Central Nervous System False False False +NCIT:C133503 Metastatic Lung Carcinoma in the Central Nervous System False False False +NCIT:C133504 Metastatic Melanoma in the Central Nervous System False False False NCIT:C133519 Pathologic Stage 0 Esophageal Squamous Cell Carcinoma AJCC v8 False False False NCIT:C133521 Pathologic Stage I Esophageal Squamous Cell Carcinoma AJCC v8 False False False NCIT:C133525 Pathologic Stage IA Esophageal Squamous Cell Carcinoma AJCC v8 False False False @@ -1301,27 +1299,27 @@ NCIT:C136816 Stage III Retroperitoneal Sarcoma AJCC v8 False False False NCIT:C136817 Stage IIIA Retroperitoneal Sarcoma AJCC v8 False False False NCIT:C136818 Stage IIIB Retroperitoneal Sarcoma AJCC v8 False False False NCIT:C136819 Stage IV Retroperitoneal Sarcoma AJCC v8 False False False -NCIT:C136825 Atypical Spitz Nevus False False False -NCIT:C136869 Merkel Cell Carcinoma by AJCC v7 Stage False False False -NCIT:C136870 Merkel Cell Carcinoma by AJCC v8 Stage False False False -NCIT:C136871 Merkel Cell Carcinoma by AJCC v8 Clinical Stage False False False -NCIT:C136872 Clinical Stage 0 Merkel Cell Carcinoma AJCC v8 False False False -NCIT:C136873 Clinical Stage I Merkel Cell Carcinoma AJCC v8 False False False -NCIT:C136874 Clinical Stage II Merkel Cell Carcinoma AJCC v8 False False False -NCIT:C136875 Clinical Stage IIA Merkel Cell Carcinoma AJCC v8 False False False -NCIT:C136876 Clinical Stage IIB Merkel Cell Carcinoma AJCC v8 False False False -NCIT:C136877 Clinical Stage III Merkel Cell Carcinoma AJCC v8 False False False -NCIT:C136878 Clinical Stage IV Merkel Cell Carcinoma AJCC v8 False False False -NCIT:C136880 Merkel Cell Carcinoma by AJCC v8 Pathologic Stage False False False -NCIT:C136881 Pathologic Stage 0 Merkel Cell Carcinoma AJCC v8 False False False -NCIT:C136882 Pathologic Stage I Merkel Cell Carcinoma AJCC v8 False False False -NCIT:C136883 Pathologic Stage II Merkel Cell Carcinoma AJCC v8 False False False -NCIT:C136884 Pathologic Stage IIA Merkel Cell Carcinoma AJCC v8 False False False -NCIT:C136885 Pathologic Stage IIB Merkel Cell Carcinoma AJCC v8 False False False -NCIT:C136886 Pathologic Stage III Merkel Cell Carcinoma AJCC v8 False False False -NCIT:C136887 Pathologic Stage IIIA Merkel Cell Carcinoma AJCC v8 False False False -NCIT:C136888 Pathologic Stage IIIB Merkel Cell Carcinoma AJCC v8 False False False -NCIT:C136889 Pathologic Stage IV Merkel Cell Carcinoma AJCC v8 False False False +NCIT:C136825 Spitz Melanocytoma False False False +NCIT:C136869 Cutaneous Merkel Cell Carcinoma by AJCC v7 Stage False False False +NCIT:C136870 Cutaneous Merkel Cell Carcinoma by AJCC v8 Stage False False False +NCIT:C136871 Cutaneous Merkel Cell Carcinoma by AJCC v8 Clinical Stage False False False +NCIT:C136872 Clinical Stage 0 Cutaneous Merkel Cell Carcinoma AJCC v8 False False False +NCIT:C136873 Clinical Stage I Cutaneous Merkel Cell Carcinoma AJCC v8 False False False +NCIT:C136874 Clinical Stage II Cutaneous Merkel Cell Carcinoma AJCC v8 False False False +NCIT:C136875 Clinical Stage IIA Cutaneous Merkel Cell Carcinoma AJCC v8 False False False +NCIT:C136876 Clinical Stage IIB Cutaneous Merkel Cell Carcinoma AJCC v8 False False False +NCIT:C136877 Clinical Stage III Cutaneous Merkel Cell Carcinoma AJCC v8 False False False +NCIT:C136878 Clinical Stage IV Cutaneous Merkel Cell Carcinoma AJCC v8 False False False +NCIT:C136880 Cutaneous Merkel Cell Carcinoma by AJCC v8 Pathologic Stage False False False +NCIT:C136881 Pathologic Stage 0 Cutaneous Merkel Cell Carcinoma AJCC v8 False False False +NCIT:C136882 Pathologic Stage I Cutaneous Merkel Cell Carcinoma AJCC v8 False False False +NCIT:C136883 Pathologic Stage II Cutaneous Merkel Cell Carcinoma AJCC v8 False False False +NCIT:C136884 Pathologic Stage IIA Cutaneous Merkel Cell Carcinoma AJCC v8 False False False +NCIT:C136885 Pathologic Stage IIB Cutaneous Merkel Cell Carcinoma AJCC v8 False False False +NCIT:C136886 Pathologic Stage III Cutaneous Merkel Cell Carcinoma AJCC v8 False False False +NCIT:C136887 Pathologic Stage IIIA Cutaneous Merkel Cell Carcinoma AJCC v8 False False False +NCIT:C136888 Pathologic Stage IIIB Cutaneous Merkel Cell Carcinoma AJCC v8 False False False +NCIT:C136889 Pathologic Stage IV Cutaneous Merkel Cell Carcinoma AJCC v8 False False False NCIT:C136971 Recurrent Lymphocyte-Rich Classic Hodgkin Lymphoma False False False NCIT:C136972 Intermediate Atypical Prostate Carcinoma False False False NCIT:C136977 Rainbow Trout Mesothelioma False False False @@ -2214,14 +2212,13 @@ NCIT:C153206 Locally Advanced Lung Carcinoma False False False NCIT:C153213 Locally Advanced Head and Neck Carcinoma False False False NCIT:C153224 Colorectal Carcinoma Metastatic in the Lung False False False NCIT:C153226 Breast Carcinoma Metastatic in the Spine False False False -NCIT:C153227 Breast Carcinoma Metastatic in the Lymph Nodes False False False +NCIT:C153227 Metastatic Breast Carcinoma in the Lymph Nodes False False False NCIT:C153238 Metastatic Breast Carcinoma False False False NCIT:C153278 Locally Advanced Unresectable Malignant Neoplasm False False False NCIT:C153279 Metastatic Unresectable Malignant Neoplasm False False False NCIT:C153286 Refractory Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor False False False NCIT:C153315 Metastatic Unresectable Carcinoma False False False NCIT:C153316 Metastatic Unresectable Gastric Adenocarcinoma False False False -NCIT:C153317 Advanced Unresectable Gastric Adenocarcinoma False False False NCIT:C153319 Metastatic Gastric Adenocarcinoma False False False NCIT:C153320 Metastatic Gastric Carcinoma False False False NCIT:C153323 Metastatic Chordoma False False False @@ -2360,7 +2357,7 @@ NCIT:C155791 Malignant Skull Base Neoplasm False False False NCIT:C155792 Benign Skull Neoplasm False False False NCIT:C155793 Benign Skull Base Neoplasm False False False NCIT:C155796 Pituitary Gland Non-Hodgkin Lymphoma False False False -NCIT:C155797 Primary Pituitary Gland Diffuse Large B-Cell Lymphoma False False False +NCIT:C155797 Pituitary Gland Diffuse Large B-Cell Lymphoma False False False NCIT:C155801 Sellar Germ Cell Tumor False False False NCIT:C155802 Sellar Germinoma False False False NCIT:C155803 Suprasellar Germinoma False False False @@ -2521,7 +2518,6 @@ NCIT:C156483 Benign Genitourinary System Neoplasm False False False NCIT:C156484 Malignant Genitourinary System Neoplasm False False False NCIT:C156485 Metastatic Neuroendocrine Neoplasm False False False NCIT:C156486 Advanced Neuroendocrine Neoplasm False False False -NCIT:C156487 Advanced Carcinoid Tumor False False False NCIT:C156488 Metastatic Pancreatic Neuroendocrine Tumor False False False NCIT:C156489 Advanced Pancreatic Neuroendocrine Tumor False False False NCIT:C156492 Metastatic Digestive System Neuroendocrine Neoplasm False False False @@ -2949,7 +2945,7 @@ NCIT:C162453 Refractory High Grade B-Cell Lymphoma with MYC, BCL2, and BCL6 Rear NCIT:C162460 Thymic Neuroendocrine Neoplasm False False False NCIT:C162461 Metastatic Thymic Neuroendocrine Neoplasm False False False NCIT:C162466 Intratubular Large Cell Hyalinizing Sertoli Cell Neoplasia False False False -NCIT:C162467 Primary Diffuse Large B-Cell Lymphoma of the Testis False False False +NCIT:C162467 Testicular Diffuse Large B-Cell Lymphoma False False False NCIT:C162468 Testicular Nasal Type Extranodal NK/T-Cell Lymphoma False False False NCIT:C162469 Testicular Myeloid Sarcoma False False False NCIT:C162470 Testicular Plasmacytoma False False False @@ -3067,7 +3063,6 @@ NCIT:C162826 Benign Retropharyngeal Neoplasm False False False NCIT:C162828 Malignant Retropharyngeal Neoplasm False False False NCIT:C162833 Unresectable Oropharyngeal Squamous Cell Carcinoma False False False NCIT:C162845 Unresectable Malignant Digestive System Neoplasm False False False -NCIT:C162848 Digital Papillary Adenoma False False False NCIT:C162876 Metastatic Paranasal Sinus Squamous Cell Carcinoma False False False NCIT:C162881 Locally Advanced Oropharyngeal Squamous Cell Carcinoma False False False NCIT:C162882 Metastatic Sinonasal Squamous Cell Carcinoma False False False @@ -3122,7 +3117,7 @@ NCIT:C164246 Advanced Malignant PEComa False False False NCIT:C164247 Locally Advanced Unresectable Malignant PEComa False False False NCIT:C164248 Warty Carcinoma False False False NCIT:C164249 Differentiated Intraepithelial Neoplasia False False False -NCIT:C164250 Human Papillomavirus-Negative Squamous Cell Carcinoma False False False +NCIT:C164250 Human Papillomavirus-Independent Squamous Cell Carcinoma False False False NCIT:C164251 Sinonasal Exophytic Papilloma False False False NCIT:C164252 Invasive Sarcomatoid Urothelial Carcinoma False False False NCIT:C164253 Gastrointestinal Tract Adenoma, Intestinal-Type False False False @@ -3133,7 +3128,7 @@ NCIT:C164313 NF1-Associated Malignant Peripheral Nerve Sheath Tumor False False NCIT:C164314 Sporadic Malignant Peripheral Nerve Sheath Tumor False False False NCIT:C164316 Radiation-Induced Malignant Peripheral Nerve Sheath Tumor False False False NCIT:C16444 Cloudman S91 Malignant Melanoma False False False -NCIT:C165171 Unresectable Liver and Intrahepatic Bile Duct Carcinoma False False False +NCIT:C165171 Unresectable Liver Carcinoma False False False NCIT:C165172 Unresectable Ampulla of Vater Carcinoma False False False NCIT:C165173 Unresectable Periampullary Adenocarcinoma False False False NCIT:C165174 Unresectable Head and Neck Carcinoma False False False @@ -3159,7 +3154,7 @@ NCIT:C165288 Refractory Endometrial Transitional Cell Carcinoma False False Fals NCIT:C165289 Refractory Endometrial Adenocarcinoma False False False NCIT:C165290 Refractory Endometrial Mucinous Adenocarcinoma False False False NCIT:C165291 Recurrent Endometrial Mucinous Adenocarcinoma False False False -NCIT:C165293 Resectable Liver and Intrahepatic Bile Duct Carcinoma False False False +NCIT:C165293 Resectable Liver Carcinoma False False False NCIT:C165298 Refractory Endometrial Undifferentiated Carcinoma False False False NCIT:C165299 Advanced Gastric Carcinoma False False False NCIT:C165300 Advanced Merkel Cell Carcinoma False False False @@ -3176,7 +3171,7 @@ NCIT:C165456 Unresectable Pancreatic Neuroendocrine Neoplasm False False False NCIT:C165458 Advanced Ovarian Carcinoma False False False NCIT:C165465 Skin Verrucous Carcinoma False False False NCIT:C165466 Skin Squamous Cell Carcinoma with Osteoclast-Like Giant Cells False False False -NCIT:C165467 Skin Lymphoepithelioma-Like Carcinoma False False False +NCIT:C165467 Skin Lymphoepithelial Carcinoma False False False NCIT:C165468 Skin Squamous Cell Carcinoma with Sarcomatoid Differentiation False False False NCIT:C165472 Locally Advanced Oral Cavity Squamous Cell Carcinoma False False False NCIT:C165473 Locally Advanced Laryngeal Squamous Cell Carcinoma False False False @@ -3185,8 +3180,7 @@ NCIT:C165485 Lichen Planus-Like Keratosis False False False NCIT:C165491 Unresectable Triple-Negative Breast Carcinoma False False False NCIT:C165497 Spitz Melanoma False False False NCIT:C165498 Pigmented Epithelioid Melanocytoma False False False -NCIT:C165522 BAP1-Inactivated Skin Melanocytic Neoplasm False False False -NCIT:C165523 Combined BAP1-Inactivated Nevus False False False +NCIT:C165523 Combined BAP1-Inactivated Melanocytoma False False False NCIT:C165525 BAP1-Inactivated Melanocytoma False False False NCIT:C165529 Combined Nevus False False False NCIT:C165535 Unresectable Acral Lentiginous Melanoma False False False @@ -3577,8 +3571,8 @@ NCIT:C171576 Aggressive Variant Prostate Carcinoma False False False NCIT:C171579 Advanced Chromophobe Renal Cell Carcinoma False False False NCIT:C171580 Metastatic Chromophobe Renal Cell Carcinoma False False False NCIT:C171581 Advanced Sarcomatoid Renal Cell Carcinoma False False False -NCIT:C171582 Advanced Unclassified Renal Cell Carcinoma False False False -NCIT:C171583 Metastatic Unclassified Renal Cell Carcinoma False False False +NCIT:C171582 Advanced Renal Cell Carcinoma, Not Otherwise Specified False False False +NCIT:C171583 Metastatic Renal Cell Carcinoma, Not Otherwise Specified False False False NCIT:C171585 Unresectable Colorectal Adenocarcinoma False False False NCIT:C171604 Refractory Esophageal Carcinoma False False False NCIT:C171605 Refractory Squamous Cell Carcinoma False False False @@ -3598,7 +3592,7 @@ NCIT:C172183 Progesterone Receptor-Positive Malignant Neoplasm False False False NCIT:C172206 Sinusoidal Hemangioma False False False NCIT:C172218 Locally Advanced Papillary Renal Cell Carcinoma False False False NCIT:C172219 Locally Advanced Sarcomatoid Renal Cell Carcinoma False False False -NCIT:C172222 Locally Advanced Unclassified Renal Cell Carcinoma False False False +NCIT:C172222 Locally Advanced Renal Cell Carcinoma, Not Otherwise Specified False False False NCIT:C172227 Locally Advanced Esophageal Adenocarcinoma False False False NCIT:C172234 Metastatic Ovarian Undifferentiated Carcinoma False False False NCIT:C172235 Unresectable Ovarian Undifferentiated Carcinoma False False False @@ -3725,8 +3719,8 @@ NCIT:C172955 Digestive System Kaposi Sarcoma False False False NCIT:C172980 Gastrointestinal Clear Cell Sarcoma/Malignant Gastrointestinal Neuroectodermal Tumor False False False NCIT:C173046 Refractory Indolent Non-Hodgkin Lymphoma False False False NCIT:C173077 Sinonasal Keratinizing Squamous Cell Carcinoma False False False -NCIT:C173078 Sinonasal Human Papillomavirus-Related Carcinoma with Adenoid Cystic-Like Features False False False -NCIT:C173079 Sinonasal Spindle Cell Squamous Cell Carcinoma False False False +NCIT:C173078 Sinonasal Human Papillomavirus-Related Multiphenotypic Carcinoma False False False +NCIT:C173079 Sinonasal Spindle Cell Squamous Carcinoma False False False NCIT:C173080 Sinonasal Lymphoepithelial Carcinoma False False False NCIT:C173087 Head and Neck NUT Carcinoma False False False NCIT:C173088 Sinonasal NUT Carcinoma False False False @@ -3768,7 +3762,7 @@ NCIT:C173171 Sinonasal Non-Hodgkin Lymphoma False False False NCIT:C173172 Sinonasal Extranodal NK/T-Cell Lymphoma False False False NCIT:C173173 Nasal Cavity Extranodal NK/T-Cell Lymphoma False False False NCIT:C173174 Sinonasal Olfactory Neuroblastoma False False False -NCIT:C173175 Sinonasal Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor False False False +NCIT:C173175 Sinonasal Ewing Sarcoma False False False NCIT:C173176 Malignant Sinonasal Soft Tissue Neoplasm False False False NCIT:C173324 Microsatellite Stable Colorectal Carcinoma False False False NCIT:C173328 Refractory Non-Cutaneous Melanoma False False False @@ -3790,7 +3784,7 @@ NCIT:C173356 Pharyngeal Hodgkin Lymphoma False False False NCIT:C173357 Nasopharyngeal Lymphoma False False False NCIT:C173359 Nasopharyngeal Non-Hodgkin Lymphoma False False False NCIT:C173361 Nasopharyngeal Hodgkin Lymphoma False False False -NCIT:C173385 Neuroendocrine Carcinoma, Excluding Head and Neck False False False +NCIT:C173385 Cutaneous Merkel Cell Carcinoma False False False NCIT:C173387 Head and Neck Neuroendocrine Tumor False False False NCIT:C173388 Head and Neck Neuroendocrine Tumor G2 False False False NCIT:C173390 Laryngeal Neuroendocrine Carcinoma False False False @@ -3809,7 +3803,7 @@ NCIT:C173408 Laryngeal Soft Tissue Sarcoma False False False NCIT:C173409 Recurrent Mature T-Cell and NK-Cell Neoplasm False False False NCIT:C173411 Refractory Mature T-Cell and NK-Cell Neoplasm False False False NCIT:C173412 Laryngeal Pleomorphic Adenoma False False False -NCIT:C173414 Oropharyngeal Human Papillomavirus-Negative Squamous Cell Carcinoma False False False +NCIT:C173414 Oropharyngeal Human Papillomavirus-Independent Squamous Cell Carcinoma False False False NCIT:C173475 Oral Verruca Vulgaris False False False NCIT:C173476 Oral Squamous Papilloma False False False NCIT:C173477 Oral Cavity Kaposi Sarcoma False False False @@ -3833,7 +3827,6 @@ NCIT:C173577 Oropharyngeal Lymphoma False False False NCIT:C173578 Oropharyngeal Hodgkin Lymphoma False False False NCIT:C173579 Oropharyngeal Non-Hodgkin Lymphoma False False False NCIT:C173580 Head and Neck Follicular Dendritic Cell Sarcoma False False False -NCIT:C173585 Neck Carcinoma of Unknown Primary False False False NCIT:C173586 Extracutaneous Merkel Cell Carcinoma False False False NCIT:C173587 Head and Neck Merkel Cell Carcinoma False False False NCIT:C173588 Head and Neck Heterotopia-Associated Carcinoma False False False @@ -3881,8 +3874,9 @@ NCIT:C173733 Sclerosing Odontogenic Carcinoma False False False NCIT:C173735 Odontogenic Carcinosarcoma False False False NCIT:C173738 Odontogenic Sarcoma False False False NCIT:C173739 Ameloblastic Fibrodentinosarcoma False False False -NCIT:C173740 Ameloblastic Fibroodontosarcoma False False False +NCIT:C173740 Ameloblastic Fibro-Odontosarcoma False False False NCIT:C173797 Tonsillar Disorder False False False +NCIT:C173798 Non-Neoplastic Tonsillar Disorder False False False NCIT:C173799 Appendix Disorder False False False NCIT:C173807 Tongue Adenosquamous Carcinoma False False False NCIT:C173808 Retroperitoneal Undifferentiated Pleomorphic Sarcoma False False False @@ -3943,7 +3937,7 @@ NCIT:C174403 Conjunctival Carcinoma False False False NCIT:C174404 Conjunctival Sebaceous Carcinoma False False False NCIT:C174416 Conjunctival Junctional Nevus False False False NCIT:C174418 Conjunctival Compound Nevus False False False -NCIT:C174426 Conjunctival Subepithelial Nevus False False False +NCIT:C174426 Conjunctival Subepithelial (Stromal) Nevus False False False NCIT:C174443 Locally Advanced Adrenal Cortical Carcinoma False False False NCIT:C174448 Inflamed Juvenile Conjunctival Nevus False False False NCIT:C174452 Conjunctival Blue Nevus False False False @@ -3957,7 +3951,7 @@ NCIT:C174501 Choroid Nevus False False False NCIT:C174502 Uveal Nevus False False False NCIT:C174503 Uveal Melanocytoma False False False NCIT:C174505 Locally Advanced Cervical Squamous Cell Carcinoma False False False -NCIT:C174506 Iris Mixed Cell Melanoma False False False +NCIT:C174506 Iris Mixed Epithelioid and Spindle Cell Melanoma False False False NCIT:C174507 Metastatic Malignant Neoplasm in the Uvea False False False NCIT:C174508 Refractory Vulvar Carcinoma False False False NCIT:C174509 Refractory Vaginal Carcinoma False False False @@ -4130,8 +4124,8 @@ NCIT:C176680 Recurrent Breast Implant-Associated Anaplastic Large Cell Lymphoma NCIT:C176681 Refractory Breast Implant-Associated Anaplastic Large Cell Lymphoma False False False NCIT:C176682 Locally Recurrent Head and Neck Squamous Cell Carcinoma False False False NCIT:C176697 Rectal Large Cell Neuroendocrine Carcinoma False False False -NCIT:C176705 Functioning Lung Carcinoid Tumor False False False -NCIT:C176706 Non-Functioning Lung Carcinoid Tumor False False False +NCIT:C176705 Functioning Lung Neuroendocrine Tumor False False False +NCIT:C176706 Non-Functioning Lung Neuroendocrine Tumor False False False NCIT:C176711 Recurrent Lung Neuroendocrine Neoplasm False False False NCIT:C176715 Locally Advanced Lung Neuroendocrine Neoplasm False False False NCIT:C176727 Advanced Lung Adenocarcinoma False False False @@ -4164,10 +4158,10 @@ NCIT:C177000 Refractory Sezary Syndrome False False False NCIT:C177149 Refractory Male Reproductive System Carcinoma False False False NCIT:C177150 Refractory Penile Carcinoma False False False NCIT:C177151 Refractory Rectal Squamous Cell Carcinoma False False False -NCIT:C177153 Metastatic Nasopharyngeal Nonkeratinizing Carcinoma False False False -NCIT:C177243 Metastatic Lung Carcinoid Tumor False False False -NCIT:C177245 Advanced Lung Carcinoid Tumor False False False -NCIT:C177246 Unresectable Lung Carcinoid Tumor False False False +NCIT:C177153 Metastatic Nasopharyngeal Non-Keratinizing Carcinoma False False False +NCIT:C177243 Metastatic Lung Neuroendocrine Tumor False False False +NCIT:C177245 Advanced Lung Neuroendocrine Tumor False False False +NCIT:C177246 Unresectable Lung Neuroendocrine Tumor False False False NCIT:C177278 EWSR1-SMAD3-Positive Fibroblastic Tumor False False False NCIT:C177323 Angiofibroma of Soft Tissue False False False NCIT:C177324 Superficial CD34-Positive Fibroblastic Tumor False False False @@ -4301,7 +4295,7 @@ NCIT:C179182 Locally Recurrent Uterine Corpus Leiomyosarcoma False False False NCIT:C179203 Recurrent Primary Myelofibrosis False False False NCIT:C179204 Recurrent Acute Bilineal Leukemia False False False NCIT:C179205 Refractory Acute Bilineal Leukemia False False False -NCIT:C179206 Melanoma Metastatic in the Brain False False False +NCIT:C179206 Metastatic Melanoma in the Brain False False False NCIT:C179207 Refractory Ovarian Squamous Cell Carcinoma False False False NCIT:C179208 Ovarian Signet Ring Cell Carcinoma False False False NCIT:C179209 Refractory Lung Adenocarcinoma False False False @@ -4393,7 +4387,7 @@ NCIT:C180404 Refractory Thyroid Gland Medullary Carcinoma False False False NCIT:C180406 Unresectable Colon Carcinoma False False False NCIT:C180407 Tectal Glioma False False False NCIT:C180408 Recurrent Tectal Glioma False False False -NCIT:C180510 Low Grade Endometrial Endometrioid Adenocarcinoma False False False +NCIT:C180510 Endometrial Low Grade Endometrioid Adenocarcinoma False False False NCIT:C180512 POLE-Ultramutated Endometrial Endometrioid Adenocarcinoma False False False NCIT:C180514 Mismatch Repair-Deficient Endometrial Endometrioid Adenocarcinoma False False False NCIT:C180515 p53-Mutant Endometrial Endometrioid Adenocarcinoma False False False @@ -4566,7 +4560,6 @@ NCIT:C182111 Metastatic Penile Squamous Cell Carcinoma False False False NCIT:C182127 Metastatic Conjunctival Melanoma False False False NCIT:C182151 Diffuse Midline Glioma False False False NCIT:C182235 Second Primary Tumor False False False -NCIT:C182357 Diffusion Restriction False False False NCIT:C182436 Diffuse Non-Pontine Midline Glioma False False False NCIT:C183045 Bronchiolar Adenoma/Ciliated Muconodular Papillary Tumor False False False NCIT:C183109 Invasive Lung Non-Mucinous Adenocarcinoma False False False @@ -4760,7 +4753,7 @@ NCIT:C186730 Cytogenetically Normal Acute Myeloid Leukemia Post Cytotoxic Therap NCIT:C186731 Oral Melanocytic Nevus False False False NCIT:C186732 Aggressive Systemic Mastocytosis with an Associated Germ Cell Tumor False False False NCIT:C186735 Systemic Mastocytosis with an Associated Germ Cell Tumor False False False -NCIT:C187051 Human Papillomavirus-Related Head and Neck Squamous Cell Carcinoma of Unknown Primary False False False +NCIT:C187051 Human Papillomavirus-Related Neck Squamous Cell Carcinoma of Unknown Primary False False False NCIT:C187056 Childhood Acute Leukemia False False False NCIT:C187086 Pituitary Neuroendocrine Tumor of PIT1-Lineage False False False NCIT:C187087 Pituitary Neuroendocrine Tumor of TPIT-Lineage False False False @@ -4783,8 +4776,8 @@ NCIT:C187197 Refractory Childhood Lymphoma False False False NCIT:C187207 Childhood Malignant Brain Neoplasm False False False NCIT:C187210 Advanced Childhood Malignant Solid Neoplasm False False False NCIT:C187211 Metastatic Childhood Malignant Neoplasm in the Brain False False False -NCIT:C187212 Metastatic Childhood Malignant Brain Neoplasm False False False -NCIT:C187213 Advanced Childhood Malignant Brain Neoplasm False False False +NCIT:C187212 Metastatic Childhood Primary Malignant Brain Neoplasm False False False +NCIT:C187213 Advanced Childhood Primary Malignant Brain Neoplasm False False False NCIT:C187214 Refractory Childhood Central Nervous System Neoplasm False False False NCIT:C187215 Refractory Childhood Brain Neoplasm False False False NCIT:C187234 Metastatic Ovarian Serous Cystadenocarcinoma False False False @@ -4797,7 +4790,6 @@ NCIT:C187261 Thyroid Gland Follicular Adenoma with Papillary Architecture False NCIT:C187273 Low Risk Thyroid Gland Neoplasm False False False NCIT:C187284 Thyroid Gland Tumor of Uncertain Malignant Potential False False False NCIT:C187316 Advanced Malignant Testicular Germ Cell Tumor False False False -NCIT:C187328 Locally Advanced Carcinoid Tumor False False False NCIT:C187332 Locally Advanced Digestive System Neuroendocrine Tumor G1 False False False NCIT:C187341 Locally Advanced Digestive System Neuroendocrine Tumor G2 False False False NCIT:C187345 Unresectable Digestive System Neuroendocrine Tumor G2 False False False @@ -4821,7 +4813,7 @@ NCIT:C187449 Refractory Childhood Acute Myeloid Leukemia False False False NCIT:C187450 Oligometastatic Pancreatic Ductal Adenocarcinoma False False False NCIT:C187643 Thyroid Gland Follicular Carcinoma, Signet Ring Cell Variant False False False NCIT:C187644 Classic Thyroid Gland Papillary Carcinoma False False False -NCIT:C187645 Follicular-Derived Thyroid Gland Carcinoma, High Grade False False False +NCIT:C187645 High Grade Follicular Cell-Derived Non-Anaplastic Thyroid Gland Carcinoma False False False NCIT:C187648 Differentiated High Grade Thyroid Gland Carcinoma False False False NCIT:C187985 Mouse Mantle Cell Lymphoma False False False NCIT:C187992 Thyroid Gland Mixed Medullary and Follicular Carcinoma False False False @@ -4878,7 +4870,7 @@ NCIT:C188207 Metastatic Uterine Corpus Leiomyosarcoma False False False NCIT:C188208 Locally Advanced Uterine Corpus Leiomyosarcoma False False False NCIT:C188209 Unresectable Uterine Corpus Leiomyosarcoma False False False NCIT:C188213 Schwannoma of the Seventh Cranial Nerve False False False -NCIT:C188217 Pancreatic Mixed Ductal-Neuroendocrine Neoplasm False False False +NCIT:C188217 Pancreatic Mixed Ductal Adenocarcinoma-Neuroendocrine Neoplasm False False False NCIT:C188218 Neuroendocrine Tumor False False False NCIT:C188221 Cervical Neuroendocrine Tumor False False False NCIT:C188222 Head and Neck Neuroendocrine Neoplasm False False False @@ -5093,7 +5085,7 @@ NCIT:C190123 Childhood Skin Neoplasm False False False NCIT:C190125 Childhood Malignant Skin Neoplasm False False False NCIT:C190137 Advanced Ocular Melanoma False False False NCIT:C190138 Locally Advanced Unresectable Uveal Melanoma False False False -NCIT:C190149 Human Papillomavirus-Negative Head and Neck Squamous Cell Carcinoma of Unknown Primary False False False +NCIT:C190149 Human Papillomavirus-Negative Neck Squamous Cell Carcinoma of Unknown Primary False False False NCIT:C190150 Childhood Laryngeal Squamous Papilloma False False False NCIT:C190152 Childhood Odontogenic Neoplasm False False False NCIT:C190154 Childhood Ameloblastoma False False False @@ -5138,7 +5130,7 @@ NCIT:C190402 EBV-Related T/NK-Cell Lymphoproliferative Disorder False False Fals NCIT:C190413 Locally Advanced Colorectal Adenocarcinoma False False False NCIT:C190415 Locally Advanced Colon Adenocarcinoma False False False NCIT:C190505 Unresectable Papillary Renal Cell Carcinoma False False False -NCIT:C190508 Unresectable Unclassified Renal Cell Carcinoma False False False +NCIT:C190508 Unresectable Renal Cell Carcinoma, Not Otherwise Specified False False False NCIT:C190573 Childhood Benign Neoplasm False False False NCIT:C190574 Childhood Benign Breast Neoplasm False False False NCIT:C190575 Childhood Malignant Breast Neoplasm False False False @@ -5620,14 +5612,14 @@ NCIT:C199148 FIGO Grade 2 Endometrioid Adenocarcinoma False False False NCIT:C199149 High Grade Endometrioid Adenocarcinoma False False False NCIT:C199150 Recurrent Low Grade Endometrioid Adenocarcinoma False False False NCIT:C199152 Recurrent High Grade Endometrioid Adenocarcinoma False False False -NCIT:C199153 Recurrent Low Grade Endometrial Endometrioid Adenocarcinoma False False False -NCIT:C199156 Recurrent High Grade Endometrial Endometrioid Adenocarcinoma False False False -NCIT:C199159 Low Grade Ovarian Endometrioid Adenocarcinoma False False False +NCIT:C199153 Recurrent Endometrial Low Grade Endometrioid Adenocarcinoma False False False +NCIT:C199156 Recurrent Endometrial High Grade Endometrioid Adenocarcinoma False False False +NCIT:C199159 Ovarian Low Grade Endometrioid Adenocarcinoma False False False NCIT:C199160 FIGO Grade 1 Ovarian Endometrioid Adenocarcinoma False False False NCIT:C199162 FIGO Grade 2 Ovarian Endometrioid Adenocarcinoma False False False -NCIT:C199166 High Grade Ovarian Endometrioid Adenocarcinoma False False False -NCIT:C199167 Recurrent Low Grade Ovarian Endometrioid Adenocarcinoma False False False -NCIT:C199168 Recurrent High Grade Ovarian Endometrioid Adenocarcinoma False False False +NCIT:C199166 Ovarian High Grade Endometrioid Adenocarcinoma False False False +NCIT:C199167 Recurrent Ovarian Low Grade Endometrioid Adenocarcinoma False False False +NCIT:C199168 Recurrent Ovarian High Grade Endometrioid Adenocarcinoma False False False NCIT:C199170 Early T Precursor Lymphoblastic Leukemia/Lymphoma False False False NCIT:C199171 Early T Precursor Acute Lymphoblastic Leukemia with BCL11B Rearrangement False False False NCIT:C199172 Early T Precursor Acute Lymphoblastic Leukemia, Not Otherwise Specified False False False @@ -5777,6 +5769,375 @@ NCIT:C201129 Angiofibroma of Nose False False False NCIT:C201135 Goblet Cell Adenocarcinoma False False False NCIT:C201136 Solid Pseudopapillary Neoplasm False False False NCIT:C201196 Metastatic Pancreatic Acinar Cell Carcinoma False False False +NCIT:C201634 SWI/SNF Complex-Deficient Sinonasal Carcinoma False False False +NCIT:C201635 SMARCB1-Deficient Sinonasal Carcinoma False False False +NCIT:C201636 SMARCB1-Deficient Sinonasal Adenocarcinoma False False False +NCIT:C201637 SMARCA4 -Deficient Sinonasal Carcinoma False False False +NCIT:C201742 Tracheal Verrucous Carcinoma False False False +NCIT:C201743 Hypopharyngeal Verrucous Carcinoma False False False +NCIT:C201746 Hypopharyngeal Basaloid Squamous Cell Carcinoma False False False +NCIT:C201747 Tracheal Basaloid Squamous Cell Carcinoma False False False +NCIT:C201748 Hypopharyngeal Papillary Squamous Cell Carcinoma False False False +NCIT:C201749 Hypopharyngeal Spindle Cell Squamous Carcinoma False False False +NCIT:C201764 Salivary Gland Intercalated Duct Adenoma False False False +NCIT:C201770 Parotid Gland Keratocystoma False False False +NCIT:C201772 Salivary Gland Microsecretory Adenocarcinoma False False False +NCIT:C201781 Salivary Gland Polymorphous Adenocarcinoma, Conventional Subtype False False False +NCIT:C201786 Salivary Gland Polymorphous Adenocarcinoma, Cribriform Subtype False False False +NCIT:C201821 Hyalinizing Clear Cell Carcinoma False False False +NCIT:C201823 Salivary Gland Hyalinizing Clear Cell Carcinoma False False False +NCIT:C201832 Minor Salivary Gland Sclerosing Microcystic Adenocarcinoma False False False +NCIT:C201837 Unresectable Penile Carcinoma False False False +NCIT:C201838 Unresectable Penile Squamous Cell Carcinoma False False False +NCIT:C201839 Oncocytic Variant of Chromophobe Renal Cell Carcinoma False False False +NCIT:C201849 Localized Prostate Adenocarcinoma False False False +NCIT:C201878 Tongue Verrucous Carcinoma False False False +NCIT:C201880 Tongue Ectomesenchymal Chondromyxoid Tumor False False False +NCIT:C201900 Palatine Tonsil Hamartomatous Polyp False False False +NCIT:C201904 Oropharyngeal Keratinizing Squamous Cell Carcinoma False False False +NCIT:C201905 Oropharyngeal Human Papillomavirus-Independent Keratinizing Squamous Cell Carcinoma False False False +NCIT:C201906 Oropharyngeal Human Papillomavirus-Related Keratinizing Squamous Cell Carcinoma False False False +NCIT:C201907 Oropharyngeal Human Papillomavirus-Related Non-Keratinizing Squamous Cell Carcinoma False False False +NCIT:C201951 Locally Advanced Extraskeletal Myxoid Chondrosarcoma False False False +NCIT:C201952 Resectable Soft Tissue Sarcoma of the Trunk and Extremities False False False +NCIT:C201953 Unresectable Chromophobe Renal Cell Carcinoma False False False +NCIT:C201960 Transformed Chronic Lymphocytic Leukemia to Hodgkin Lymphoma False False False +NCIT:C201961 Transformed Small Lymphocytic Lymphoma to Hodgkin Lymphoma False False False +NCIT:C201966 Pineoblastoma Molecular Subtypes False False False +NCIT:C201967 Pineoblastoma miRNA Processing Altered 1 False False False +NCIT:C201968 Pineoblastoma miRNA Processing Altered 2 False False False +NCIT:C201969 Pineoblastoma, RB1-Altered False False False +NCIT:C201973 Pineoblastoma, MYC/FOXR2-Activated False False False +NCIT:C201975 Brain Pilocytic Astrocytoma False False False +NCIT:C201976 Spinal Cord Pilocytic Astrocytoma False False False +NCIT:C201977 Brain Low Grade Glioma False False False +NCIT:C201978 Pulmonary Mucinous Cystic Tumor of Borderline Malignancy False False False +NCIT:C202010 Embryonal Tumor with Multilayered Rosettes of the Fourth Ventricle False False False +NCIT:C202057 Clear Cell Calcifying Epithelial Odontogenic Tumor False False False +NCIT:C202058 Cystic/Microcystic Calcifying Epithelial Odontogenic Tumor False False False +NCIT:C202059 Non-Calcifying/Langerhans Cell-Rich Calcifying Epithelial Odontogenic Tumor False False False +NCIT:C202061 Adenoid Ameloblastoma False False False +NCIT:C202077 Central Odontogenic Fibroma False False False +NCIT:C202078 Odontogenic Fibroma, Amyloid Subtype False False False +NCIT:C202079 Odontogenic Fibroma, Granular Cell Subtype False False False +NCIT:C202080 Odontogenic Fibroma, Ossifying Subtype False False False +NCIT:C202081 Hybrid Odontogenic Fibroma with Central Giant Cell Granuloma False False False +NCIT:C202128 Transformed EGFR-Positive Lung Adenocarcinoma to Squamous Cell Carcinoma False False False +NCIT:C202130 EGFR-Positive Lung Adenocarcinoma False False False +NCIT:C202131 EGFR-Positive Lung Non-Small Cell Carcinoma False False False +NCIT:C202132 Transformed EGFR-Positive Lung Non-Small Cell Carcinoma to Small Cell Carcinoma False False False +NCIT:C202133 Transformed EGFR-Positive Lung Adenocarcinoma to Small Cell Carcinoma False False False +NCIT:C202205 Juvenile Trabecular Ossifying Fibroma False False False +NCIT:C202209 Psammomatoid Ossifying Fibroma False False False +NCIT:C202252 Surface Osteoma False False False +NCIT:C202253 Central Osteoma False False False +NCIT:C202254 Jaw Osteoma False False False +NCIT:C202256 Jaw Osteoblastoma False False False +NCIT:C202257 Jaw Chondromyxoid Fibroma False False False +NCIT:C202258 Jaw Desmoplastic Fibroma False False False +NCIT:C202260 Maxillofacial Osteochondroma False False False +NCIT:C202261 Jaw Osteosarcoma False False False +NCIT:C202262 Malignant Maxillofacial Neoplasm False False False +NCIT:C202263 Rhabdomyosarcoma with TFCP2 Rearrangement False False False +NCIT:C202264 Maxillofacial Rhabdomyosarcoma with TFCP2 Rearrangement False False False +NCIT:C202265 Jaw Rhabdomyosarcoma with TFCP2 Rearrangement False False False +NCIT:C202298 Childhood Malignant Glioma False False False +NCIT:C202299 Childhood Low Grade Glioma False False False +NCIT:C202497 Non-Clear Cell Renal Cell Carcinoma False False False +NCIT:C202500 Locally Advanced Unresectable Digestive System Adenocarcinoma False False False +NCIT:C202574 Ear Osteoma False False False +NCIT:C202582 Middle Ear Papilloma False False False +NCIT:C202583 Middle Ear Inverted Sinonasal-Type Papilloma False False False +NCIT:C202584 Middle Ear Exophytic Sinonasal-Type Papilloma False False False +NCIT:C202585 Middle Ear Oncocytic Sinonasal-Type Papilloma False False False +NCIT:C202594 External Auditory Canal Squamous Cell Carcinoma False False False +NCIT:C202609 Buccal Mucosa Lipoma False False False +NCIT:C202611 Head and Neck Liposarcoma False False False +NCIT:C202613 Head and Neck Nodular Fasciitis False False False +NCIT:C202620 Orbit Solitary Fibrous Tumor False False False +NCIT:C202621 Tongue Low Grade Myofibroblastic Sarcoma False False False +NCIT:C202622 Gingival Low Grade Myofibroblastic Sarcoma False False False +NCIT:C202623 Head and Neck Soft Tissue Neoplasm False False False +NCIT:C202624 Benign Head and Neck Soft Tissue Neoplasm False False False +NCIT:C202625 Malignant Head and Neck Soft Tissue Neoplasm False False False +NCIT:C202633 Proximal Colon Carcinoma False False False +NCIT:C202634 Distal Colon Carcinoma False False False +NCIT:C202635 Head and Neck Inflammatory Myofibroblastic Tumor False False False +NCIT:C202646 Head and Neck Lipoma False False False +NCIT:C202647 Head and Neck Hemangioma False False False +NCIT:C202652 Head and Neck Epithelioid Hemangioma False False False +NCIT:C202654 Head and Neck Lymphangioma False False False +NCIT:C202655 Head and Neck Epithelioid Hemangioendothelioma False False False +NCIT:C202656 Head and Neck Angiosarcoma False False False +NCIT:C202711 Head and Neck Leiomyoma False False False +NCIT:C202849 Head and Neck EBV-Associated Smooth Muscle Tumor False False False +NCIT:C202851 Smooth Muscle Tumor of Uncertain Malignant Potential False False False +NCIT:C202852 Sinonasal Smooth Muscle Tumor of Uncertain Malignant Potential False False False +NCIT:C202853 Head and Neck Leiomyosarcoma False False False +NCIT:C202858 Head and Neck Rhabdomyoma False False False +NCIT:C202859 Head and Neck Rhabdomyosarcoma False False False +NCIT:C202860 Oral Cavity Neurofibroma False False False +NCIT:C202861 Tongue Neurofibroma False False False +NCIT:C202876 Oral Cavity Schwannoma False False False +NCIT:C202877 Tongue Schwannoma False False False +NCIT:C202878 Head and Neck Malignant Peripheral Nerve Sheath Tumor False False False +NCIT:C202879 Head and Neck Phosphaturic Mesenchymal Tumor False False False +NCIT:C202880 Appendicular Skeleton Phosphaturic Mesenchymal Tumor False False False +NCIT:C202881 Head and Neck Extraskeletal Myxoid Chondrosarcoma False False False +NCIT:C202882 Orbit Extraskeletal Myxoid Chondrosarcoma False False False +NCIT:C202883 Poorly Differentiated Synovial Sarcoma False False False +NCIT:C202884 Head and Neck Synovial Sarcoma False False False +NCIT:C202894 Advanced Prostate Small Cell Neuroendocrine Carcinoma False False False +NCIT:C202896 GLI1-Altered Soft Tissue Tumor False False False +NCIT:C202897 Head and Neck GLI1-Altered Soft Tissue Tumor False False False +NCIT:C202898 Tongue GLI1-Altered Soft Tissue Tumor False False False +NCIT:C202899 Refractory Non-Muscle Invasive Bladder Carcinoma False False False +NCIT:C202901 Head and Neck Undifferentiated Pleomorphic Sarcoma False False False +NCIT:C202904 Head and Neck Ewing Sarcoma False False False +NCIT:C202914 Head and Neck Myeloid Sarcoma False False False +NCIT:C202921 Head and Neck Lymphoma False False False +NCIT:C202922 Head and Neck Hodgkin Lymphoma False False False +NCIT:C202923 Head and Neck Non-Hodgkin Lymphoma False False False +NCIT:C202924 Head and Neck Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue False False False +NCIT:C202925 Head and Neck Mantle Cell Lymphoma False False False +NCIT:C202926 Head and Neck Follicular Lymphoma False False False +NCIT:C202927 Head and Neck Pediatric-Type Follicular Lymphoma False False False +NCIT:C202929 Head and Neck Large B-Cell Lymphoma with IRF4 Rearrangement False False False +NCIT:C202930 Head and Neck Diffuse Large B-Cell Lymphoma False False False +NCIT:C202935 Head and Neck Burkitt Lymphoma False False False +NCIT:C202936 Head and Neck Plasmablastic Lymphoma False False False +NCIT:C202952 Primary CD30-Positive T-Cell Lymphoproliferative Disorder False False False +NCIT:C202953 Primary Head and Neck Mucosal CD30-Positive T-Cell Lymphoproliferative Disorder False False False +NCIT:C202954 Head and Neck Hematopoietic and Lymphoid Cell Neoplasm False False False +NCIT:C202955 Primary Oral Cavity CD30-Positive T-Cell Lymphoproliferative Disorder False False False +NCIT:C202966 Cutaneous Juvenile Xanthogranuloma False False False +NCIT:C202967 Head and Neck Juvenile Xanthogranuloma False False False +NCIT:C202971 Head and Neck Rosai-Dorfman-Destombes Disease False False False +NCIT:C202972 Head and Neck Erdheim-Chester Disease False False False +NCIT:C202973 Head and Neck Plasmacytoma False False False +NCIT:C202975 Head and Neck Dermoid Cyst False False False +NCIT:C202977 Head and Neck Germ Cell Tumor False False False +NCIT:C202978 Sinonasal Germ Cell Tumor False False False +NCIT:C202979 Nasopharyngeal Germ Cell Tumor False False False +NCIT:C202980 Head and Neck Teratoma False False False +NCIT:C202981 Sinonasal Teratoma False False False +NCIT:C202982 Nasopharyngeal Teratoma False False False +NCIT:C202983 Malignant Head and Neck Germ Cell Tumor False False False +NCIT:C202984 Malignant Sinonasal Germ Cell Tumor False False False +NCIT:C202985 Malignant Nasopharyngeal Germ Cell Tumor False False False +NCIT:C202986 Recurrent HHV8-Positive Diffuse Large B-Cell Lymphoma, Not Otherwise Specified False False False +NCIT:C202987 Refractory HHV8-Positive Diffuse Large B-Cell Lymphoma, Not Otherwise Specified False False False +NCIT:C202989 Refractory Lymphomatoid Granulomatosis False False False +NCIT:C202990 Sinonasal Neuroendocrine Neoplasm False False False +NCIT:C202991 Sinonasal Neuroendocrine Tumor False False False +NCIT:C202992 Nasal Cavity Neuroendocrine Neoplasm False False False +NCIT:C202993 Paranasal Sinus Neuroendocrine Neoplasm False False False +NCIT:C202994 Nasal Cavity Neuroendocrine Tumor False False False +NCIT:C202995 Paranasal Sinus Neuroendocrine Tumor False False False +NCIT:C202996 Nasal Cavity Neuroendocrine Carcinoma False False False +NCIT:C202997 Paranasal Sinus Neuroendocrine Carcinoma False False False +NCIT:C203002 Nasal Cavity Small Cell Neuroendocrine Carcinoma False False False +NCIT:C203004 Paranasal Sinus Small Cell Neuroendocrine Carcinoma False False False +NCIT:C203005 Nasal Cavity Large Cell Neuroendocrine Carcinoma False False False +NCIT:C203006 Paranasal Sinus Large Cell Neuroendocrine Carcinoma False False False +NCIT:C203007 Sinonasal Neuroendocrine Tumor G1 False False False +NCIT:C203008 Nasal Cavity Neuroendocrine Tumor G1 False False False +NCIT:C203009 Paranasal Sinus Neuroendocrine Tumor G1 False False False +NCIT:C203010 Sinonasal Neuroendocrine Tumor G2 False False False +NCIT:C203011 Nasal Cavity Neuroendocrine Tumor G2 False False False +NCIT:C203012 Paranasal Sinus Neuroendocrine Tumor G2 False False False +NCIT:C203013 Nasopharyngeal Neuroendocrine Carcinoma False False False +NCIT:C203014 Nasopharyngeal Small Cell Neuroendocrine Carcinoma False False False +NCIT:C203015 Nasopharyngeal Large Cell Neuroendocrine Carcinoma False False False +NCIT:C203016 Oropharyngeal Neuroendocrine Carcinoma False False False +NCIT:C203017 Oropharyngeal Small Cell Neuroendocrine Carcinoma False False False +NCIT:C203018 Oropharyngeal Large Cell Neuroendocrine Carcinoma False False False +NCIT:C203250 Neuroendocrine Tumor G1 False False False +NCIT:C203251 Neuroendocrine Tumor G3 False False False +NCIT:C203252 Advanced Digestive System Neuroendocrine Tumor G3 False False False +NCIT:C203253 Advanced Digestive System Neuroendocrine Carcinoma False False False +NCIT:C203258 Foregut Neuroendocrine Tumor G1 False False False +NCIT:C203259 Foregut Neuroendocrine Tumor G2 False False False +NCIT:C203260 Foregut Neuroendocrine Tumor G3 False False False +NCIT:C203262 Hindgut Neuroendocrine Tumor G1 False False False +NCIT:C203263 Unresectable Diffuse Midline Glioma False False False +NCIT:C203265 Hindgut Neuroendocrine Tumor G2 False False False +NCIT:C203266 Hindgut Neuroendocrine Tumor G3 False False False +NCIT:C203267 Recurrent Diffuse Midline Glioma False False False +NCIT:C203269 Unresectable Astrocytoma, IDH-Mutant False False False +NCIT:C203270 Unresectable Oligodendroglioma, IDH-Mutant and 1p/19q-Codeleted False False False +NCIT:C203271 Unresectable Diffuse Midline Glioma, H3 K27M-Mutant False False False +NCIT:C203272 Unresectable Diffuse Hemispheric Glioma, H3 G34-Mutant False False False +NCIT:C203273 Recurrent Diffuse Hemispheric Glioma, H3 G34-Mutant False False False +NCIT:C203274 Recurrent Astrocytic Tumor False False False +NCIT:C203282 Unresectable Astrocytic Tumor False False False +NCIT:C203283 Unresectable Pilocytic Astrocytoma False False False +NCIT:C203284 Unresectable Oligodendroglioma False False False +NCIT:C203285 Recurrent Diffuse Glioma False False False +NCIT:C203286 Unresectable Diffuse Glioma False False False +NCIT:C203302 Recurrent Glioneuronal and Neuronal Tumors False False False +NCIT:C203308 Unresectable Glioneuronal and Neuronal Tumors False False False +NCIT:C203309 Unresectable Primary Central Nervous System Neoplasm False False False +NCIT:C203310 Unresectable Primary Malignant Central Nervous System Neoplasm False False False +NCIT:C203311 Advanced Fallopian Tube High Grade Serous Adenocarcinoma False False False +NCIT:C203312 Advanced Primary Peritoneal High Grade Serous Adenocarcinoma False False False +NCIT:C203313 Metastatic Platinum-Resistant Fallopian Tube Carcinoma False False False +NCIT:C203314 Metastatic Platinum-Resistant Primary Peritoneal Carcinoma False False False +NCIT:C203315 Unresectable Platinum-Resistant Fallopian Tube Carcinoma False False False +NCIT:C203316 Unresectable Platinum-Resistant Primary Peritoneal Carcinoma False False False +NCIT:C203331 Unresectable Breast Adenocarcinoma False False False +NCIT:C203339 Recurrent Breast Ductal Carcinoma In Situ False False False +NCIT:C203341 Recurrent Breast Medullary Carcinoma False False False +NCIT:C203342 Recurrent Breast Mucinous Carcinoma False False False +NCIT:C203344 Recurrent Breast Papillary Carcinoma False False False +NCIT:C203362 Recurrent Breast Tubular Carcinoma False False False +NCIT:C203369 Refractory WHO Grade 4 Glioma False False False +NCIT:C203370 Salivary Gland High Grade Adenocarcinoma, Not Otherwise Specified False False False +NCIT:C203374 Salivary Gland Low Grade Adenocarcinoma, Not Otherwise Specified False False False +NCIT:C203375 Salivary Gland Intermediate Grade Adenocarcinoma, Not Otherwise Specified False False False +NCIT:C203376 Salivary Gland Intestinal-Type Adenocarcinoma False False False +NCIT:C203380 Metastatic Salivary Gland Secretory Carcinoma False False False +NCIT:C203381 Recurrent Salivary Gland Mucoepidermoid Carcinoma False False False +NCIT:C203384 Colon Neuroendocrine Carcinoma False False False +NCIT:C203385 Rectal Neuroendocrine Carcinoma False False False +NCIT:C203386 Cecum Neuroendocrine Tumor False False False +NCIT:C203387 Ascending Colon Neuroendocrine Tumor False False False +NCIT:C203388 Descending Colon Neuroendocrine Tumor False False False +NCIT:C203389 Sigmoid Colon Neuroendocrine Tumor False False False +NCIT:C203390 Transverse Colon Neuroendocrine Tumor False False False +NCIT:C203391 Ascending Colon Neuroendocrine Tumor G2 False False False +NCIT:C203392 Cecum Neuroendocrine Tumor G2 False False False +NCIT:C203393 Descending Colon Neuroendocrine Tumor G2 False False False +NCIT:C203394 Sigmoid Colon Neuroendocrine Tumor G2 False False False +NCIT:C203395 Transverse Colon Neuroendocrine Tumor G2 False False False +NCIT:C203406 Metastatic Bladder Adenocarcinoma False False False +NCIT:C203407 Locally Advanced Bladder Adenocarcinoma False False False +NCIT:C203409 Unresectable Bladder Adenocarcinoma False False False +NCIT:C203410 Locally Advanced Bladder Squamous Cell Carcinoma False False False +NCIT:C203411 Unresectable Bladder Squamous Cell Carcinoma False False False +NCIT:C203412 Locally Advanced Kidney Medullary Carcinoma False False False +NCIT:C203413 Locally Advanced Penile Squamous Cell Carcinoma False False False +NCIT:C203415 Locally Advanced Bladder Small Cell Neuroendocrine Carcinoma False False False +NCIT:C203422 Histiocytic Disorder False False False +NCIT:C203426 T Acute Lymphoblastic Leukemia, HOXA Dysregulated False False False +NCIT:C203428 T Acute Lymphoblastic Leukemia with SPI1 Rearrangement False False False +NCIT:C203431 T Acute Lymphoblastic Leukemia with TLX1 Rearrangement False False False +NCIT:C203432 T Acute Lymphoblastic Leukemia with TLX3 Rearrangement False False False +NCIT:C203433 T Acute Lymphoblastic Leukemia with TAL1 Rearrangement False False False +NCIT:C203434 T Acute Lymphoblastic Leukemia with LMO1 Rearrangement False False False +NCIT:C203435 T Acute Lymphoblastic Leukemia with LMO2 Rearrangement False False False +NCIT:C203437 Acute Leukemia of Ambiguous Lineage with BCL11B Rearrangement False False False +NCIT:C203443 Myelodysplastic Chronic Myelomonocytic Leukemia False False False +NCIT:C203444 Myeloproliferative Chronic Myelomonocytic Leukemia False False False +NCIT:C203469 T Acute Lymphoblastic Leukemia with Recurrent Genetic Abnormalities False False False +NCIT:C203511 Metastatic Olfactory Neuroblastoma False False False +NCIT:C203513 Locally Advanced Olfactory Neuroblastoma False False False +NCIT:C203515 Locally Advanced Sinonasal Carcinoma False False False +NCIT:C203523 Refractory Juvenile Myelomonocytic Leukemia False False False +NCIT:C203526 Locally Advanced Neuroblastoma False False False +NCIT:C203583 Sarcoma GX False False False +NCIT:C203618 Locally Advanced Appendix Adenocarcinoma False False False +NCIT:C203619 Unresectable Appendix Adenocarcinoma False False False +NCIT:C203667 Recurrent Primary Cutaneous Diffuse Large B-Cell Lymphoma False False False +NCIT:C203669 Refractory Primary Cutaneous Diffuse Large B-Cell Lymphoma False False False +NCIT:C203673 Esophageal and Gastroesophageal Junction Carcinoma False False False +NCIT:C203675 Gastroesophageal Junction Carcinoma False False False +NCIT:C203700 Unresectable HER2-Low Breast Carcinoma False False False +NCIT:C203795 Pancreatic Mixed Ductal Adenocarcinoma-Neuroendocrine Tumor False False False +NCIT:C203815 Recurrent Bladder Non-Invasive Papillary Urothelial Carcinoma, Low Grade False False False +NCIT:C203904 Chronic Phase Chronic Myeloid Leukemia, Philadelphia Chromosome Positive, BCR-ABL1 Positive False False False +NCIT:C203946 Low Grade Mucinous Carcinoma Peritonei False False False +NCIT:C203948 High Grade Mucinous Carcinoma Peritonei False False False +NCIT:C203949 High Grade Mucinous Carcinoma Peritonei with Signet Ring Cells False False False +NCIT:C203968 Verruca Palmaris False False False +NCIT:C203969 Verruca Plana False False False +NCIT:C204035 Advanced Pancreatic Adenosquamous Carcinoma False False False +NCIT:C204036 Advanced Digestive System Neuroendocrine Tumor False False False +NCIT:C204037 Metastatic Digestive System Neuroendocrine Tumor False False False +NCIT:C204038 Locally Advanced Digestive System Neuroendocrine Tumor False False False +NCIT:C204124 Recurrent B-Cell Malignant Neoplasm False False False +NCIT:C204126 Refractory B-Cell Malignant Neoplasm False False False +NCIT:C204355 Skin Nodulocystic Basal Cell Carcinoma False False False +NCIT:C204383 Merkel Cell Polyoma Virus-Positive Merkel Cell Carcinoma False False False +NCIT:C204385 Merkel Cell Polyoma Virus-Negative Merkel Cell Carcinoma False False False +NCIT:C204437 Locally Advanced HER2-Low Breast Carcinoma False False False +NCIT:C204482 Lentiginous Melanocytic Nevus False False False +NCIT:C204514 WNT-Activated Deep Penetrating/Plexiform Melanocytoma (Nevus) False False False +NCIT:C204516 Plexiform Spindle Cell Melanocytoma False False False +NCIT:C204574 PRKAR1A-Inactivated Pigmented Epithelioid Melanocytoma False False False +NCIT:C204739 MITF Pathway-Activated Melanocytic Tumor False False False +NCIT:C204740 Clear Cell Tumor with Melanocytic Differentiation and ACTIN-MITF Translocation False False False +NCIT:C204741 Clear Cell Tumor with Melanocytic Differentiation and MITF-CREM Translocation False False False +NCIT:C204755 Clear Cell Tumor with Melanocytic Differentiation and ACTB-MITF Translocation False False False +NCIT:C204756 Clear Cell Tumor with Melanocytic Differentiation and ACTG1-MITF Translocation False False False +NCIT:C204787 Compound Spitz Nevus False False False +NCIT:C204788 Junctional Spitz Nevus False False False +NCIT:C204789 Dermal Spitz Nevus False False False +NCIT:C204790 Spitz Tumor False False False +NCIT:C204840 Melanoma in Intermittently Sun-Exposed Skin False False False +NCIT:C204843 Low-CSD Melanoma, Superficial Spreading Melanoma Subtype False False False +NCIT:C204864 Melanoma in Chronically Sun-Exposed Skin False False False +NCIT:C204865 Metastatic Platinum-Refractory Ovarian Carcinoma False False False +NCIT:C204866 Advanced Platinum-Refractory Ovarian Carcinoma False False False +NCIT:C204867 Unresectable Platinum-Refractory Ovarian Carcinoma False False False +NCIT:C204868 Locally Advanced Platinum-Refractory Ovarian Carcinoma False False False +NCIT:C204883 Acral Melanoma False False False +NCIT:C204887 Subungual Melanoma False False False +NCIT:C204888 Volar Melanoma False False False +NCIT:C204889 Nail Apparatus Melanoma False False False +NCIT:C204907 Mucosal Nevus False False False +NCIT:C204910 Dendritic Blue Nevus False False False +NCIT:C204911 Sclerosing Blue Nevus False False False +NCIT:C204976 Intermediate Congenital Melanocytic Nevus False False False +NCIT:C204977 Conjunctival Melanocytic Neoplasm False False False +NCIT:C204978 Conjunctival Balloon Cell Nevus False False False +NCIT:C204979 Low Grade Conjunctival Melanocytic Intraepithelial Lesion False False False +NCIT:C204980 High Grade Conjunctival Melanocytic Intraepithelial Lesion False False False +NCIT:C204981 Conjunctival Melanoma In Situ False False False +NCIT:C204982 Platinum-Resistant Fallopian Tube High Grade Serous Adenocarcinoma False False False +NCIT:C204984 Recurrent Platinum-Resistant Fallopian Tube High Grade Serous Adenocarcinoma False False False +NCIT:C204985 Platinum-Resistant Primary Peritoneal High Grade Serous Adenocarcinoma False False False +NCIT:C204986 Recurrent Platinum-Resistant Primary Peritoneal High Grade Serous Adenocarcinoma False False False +NCIT:C204987 Platinum-Refractory Ovarian High Grade Serous Adenocarcinoma False False False +NCIT:C204988 Platinum-Refractory Fallopian Tube High Grade Serous Adenocarcinoma False False False +NCIT:C204991 Platinum-Refractory Primary Peritoneal High Grade Serous Adenocarcinoma False False False +NCIT:C205057 Uveal Melanocytic Neoplasm False False False +NCIT:C205069 Diffuse Meningeal Melanocytic Neoplasm False False False +NCIT:C205125 Nodular Melanoma False False False +NCIT:C205127 De Novo Nodular Melanoma False False False +NCIT:C205129 Dermal Melanoma False False False +NCIT:C205130 Metastatic Melanoma in the Skin False False False +NCIT:C205131 Metastatic Melanoma in the Lymph Nodes False False False +NCIT:C205132 Metastatic Melanoma in the Viscera False False False +NCIT:C205187 Platinum-Sensitive Endometrial Carcinoma False False False +NCIT:C205188 Recurrent Platinum-Sensitive Endometrial Carcinoma False False False +NCIT:C205226 Locally Advanced Unresectable Pancreatic Ductal Adenocarcinoma False False False +NCIT:C205238 Recurrent Castration-Sensitive Prostate Carcinoma False False False +NCIT:C205286 Early Stage Bladder Urothelial Carcinoma False False False +NCIT:C205287 Early Stage Cervical Carcinoma False False False +NCIT:C205289 Early Stage Clear Cell Renal Cell Carcinoma False False False +NCIT:C205290 Early Stage Colorectal Carcinoma False False False +NCIT:C205295 Early Stage Endometrial Carcinoma False False False +NCIT:C205298 Early Stage Esophageal Carcinoma False False False +NCIT:C205301 Early Stage Hepatocellular Carcinoma False False False +NCIT:C205303 Early Stage Lung Non-Small Cell Carcinoma False False False +NCIT:C205307 Early Stage Malignant Skin Neoplasm False False False +NCIT:C205308 Resectable Cervical Carcinoma False False False +NCIT:C205309 Resectable Clear Cell Renal Cell Carcinoma False False False +NCIT:C205310 Resectable Endometrial Carcinoma False False False +NCIT:C205311 Resectable Esophageal Carcinoma False False False +NCIT:C205313 Resectable Malignant Solid Neoplasm False False False +NCIT:C205314 Resectable Triple-Negative Breast Carcinoma False False False +NCIT:C205357 Primary Cutaneous NUT Adnexal Carcinoma False False False +NCIT:C205361 Localized Renal Cell Carcinoma False False False +NCIT:C205371 Trichogerminoma False False False +NCIT:C205459 Apocrine Cystadenoma False False False +NCIT:C205462 Eccrine Poroma False False False +NCIT:C205463 Apocrine Poroma False False False +NCIT:C205475 Hidroacanthoma Simplex False False False +NCIT:C205476 Poroid Hidradenoma False False False +NCIT:C205539 Solid Cystic Hidradenoma False False False +NCIT:C205551 Skin Syncytial Myoepithelioma False False False NCIT:C21600 Mouse Neuroglia Neoplasm False False False NCIT:C21601 Mouse Lobular Neoplasm False False False NCIT:C21602 Mouse Lymphoma False False False @@ -6926,7 +7287,7 @@ NCIT:C27520 Benign Hair Follicle Neoplasm False False False NCIT:C27521 Classic Type Trichilemmoma False False False NCIT:C27522 Desmoplastic Trichilemmoma False False False NCIT:C27523 Classic Type Trichoepithelioma False False False -NCIT:C27524 Desmoplastic Trichoepithelioma False False False +NCIT:C27524 Columnar Trichoblastoma False False False NCIT:C27526 Follicular Myxoma False False False NCIT:C27527 Tubular Apocrine Adenoma False False False NCIT:C27529 Malignant Skin Vascular Neoplasm False False False @@ -7146,7 +7507,7 @@ NCIT:C3162 B-Cell Leukemia False False False NCIT:C3165 CALLA Positive Lymphoblastic Leukemia False False False NCIT:C3173 Accelerated Phase Chronic Myeloid Leukemia, BCR-ABL1 Positive False False False NCIT:C3175 Chronic Phase Chronic Myeloid Leukemia, BCR-ABL1 Positive False False False -NCIT:C3176 Myeloid Leukemia, Philadelphia- Negative False False False +NCIT:C3176 Myeloid Leukemia, Philadelphia-Negative False False False NCIT:C3202 Ovarian Stromal Luteoma False False False NCIT:C3210 Mixed Cell Lymphoma False False False NCIT:C3263 Neoplasm by Site False False False @@ -7254,7 +7615,7 @@ NCIT:C3578 Metastatic Malignant Neoplasm in the Mediastinum False False False NCIT:C3579 Metastatic Malignant Neoplasm in the Pleura False False False NCIT:C3580 Metastatic Malignant Neoplasm in the Bone False False False NCIT:C3581 Ann Arbor Stage III Nodular Sclerosis Classic Hodgkin Lymphoma False False False -NCIT:C35814 Hematopoietic and Lymphoid System Disorder False False False +NCIT:C35814 Hematopoietic and Lymphatic System Disorder False False False NCIT:C35816 Monoblastic Sarcoma False False False NCIT:C35817 Blastic Granulocytic Sarcoma False False False NCIT:C35818 Immature Granulocytic Sarcoma False False False @@ -7284,7 +7645,6 @@ NCIT:C36030 Osteolytic Neoplasm False False False NCIT:C36031 Papillary Neoplasm False False False NCIT:C36032 Premalignant Neoplasm False False False NCIT:C36033 Tubular Neoplasm False False False -NCIT:C36034 Villous Neoplasm False False False NCIT:C36035 Encapsulated Neoplasm False False False NCIT:C36036 Non-Encapsulated Neoplasm False False False NCIT:C36037 Localized Neoplasm False False False @@ -7335,13 +7695,13 @@ NCIT:C36272 Chronic Lymphocytic Leukemia with Plasmacytoid Differentiation False NCIT:C36273 Small Lymphocytic Lymphoma with Plasmacytoid Differentiation False False False NCIT:C36276 Polyclonal Polymorphic Post-Transplant Lymphoproliferative Disorder False False False NCIT:C36277 Monoclonal Polymorphic Post-Transplant Lymphoproliferative Disorder False False False -NCIT:C36300 Breast Carcinoma Metastatic in the Lung False False False -NCIT:C36301 Breast Carcinoma Metastatic in the Brain False False False -NCIT:C36302 Breast Carcinoma Metastatic in the Liver False False False -NCIT:C36303 Breast Carcinoma Metastatic in the Bone False False False -NCIT:C36304 Lung Carcinoma Metastatic in the Brain False False False -NCIT:C36305 Lung Carcinoma Metastatic in the Bone False False False -NCIT:C36306 Lung Carcinoma Metastatic in the Liver False False False +NCIT:C36300 Metastatic Breast Carcinoma in the Lung False False False +NCIT:C36301 Metastatic Breast Carcinoma in the Brain False False False +NCIT:C36302 Metastatic Breast Carcinoma in the Liver False False False +NCIT:C36303 Metastatic Breast Carcinoma in the Bone False False False +NCIT:C36304 Metastatic Lung Carcinoma in the Brain False False False +NCIT:C36305 Metastatic Lung Carcinoma in the Bone False False False +NCIT:C36306 Metastatic Lung Carcinoma in the Liver False False False NCIT:C36307 Prostate Carcinoma Metastatic in the Lung False False False NCIT:C36308 Prostate Carcinoma Metastatic in the Bone False False False NCIT:C36309 Colon Carcinoma Metastatic in the Liver False False False @@ -7371,7 +7731,7 @@ NCIT:C37258 Paraganglioma-Like Dermal Melanocytic Tumor False False False NCIT:C37264 Benign Kidney Mixed Epithelial and Stromal Tumor False False False NCIT:C37268 Atypical Small Acinar Proliferation of the Prostate Gland False False False NCIT:C37272 Vulvar Intraepithelial Neoplasia, HPV-Independent False False False -NCIT:C37290 Head and Neck Basaloid Carcinoma False False False +NCIT:C37290 Head and Neck Basaloid Squamous Cell Carcinoma False False False NCIT:C3730 Mixed Mesodermal (Mullerian) Tumor False False False NCIT:C3738 Osteoclastic Giant Cell-Rich Tumor of Bone False False False NCIT:C3740 Desmoplastic Fibroma False False False @@ -7441,7 +7801,7 @@ NCIT:C39749 Type II Endometrial Adenocarcinoma False False False NCIT:C39750 Glioblastoma, IDH-Wildtype False False False NCIT:C39751 Secondary Glioblastoma False False False NCIT:C39754 Acanthomatous Ameloblastoma False False False -NCIT:C39755 Solid/Multicystic Ameloblastoma False False False +NCIT:C39755 Conventional Ameloblastoma False False False NCIT:C39756 Unicystic Ameloblastoma False False False NCIT:C39757 Basal Cell Ameloblastoma False False False NCIT:C39790 Renal Cell Carcinoma with Constitutional Chromosome 3 Translocations False False False @@ -7563,7 +7923,7 @@ NCIT:C40140 Borderline Uterine Ligament Neoplasm False False False NCIT:C40145 Type I Endometrial Adenocarcinoma False False False NCIT:C40146 FIGO Grade 1 Endometrial Endometrioid Adenocarcinoma False False False NCIT:C40147 FIGO Grade 2 Endometrial Endometrioid Adenocarcinoma False False False -NCIT:C40148 High Grade Endometrial Endometrioid Adenocarcinoma False False False +NCIT:C40148 Endometrial High Grade Endometrioid Adenocarcinoma False False False NCIT:C40149 FIGO Grade 1 Endometrial Mucinous Adenocarcinoma False False False NCIT:C4015 Metastatic Malignant Neoplasm in the Central Nervous System False False False NCIT:C40150 FIGO Grade 2 Endometrial Mucinous Adenocarcinoma False False False @@ -7595,7 +7955,7 @@ NCIT:C40228 Malignant Mixed Epithelial and Mesenchymal Neoplasm of the Cervix Fa NCIT:C40240 Cervical Blue Nevus False False False NCIT:C40243 Vaginal Keratinizing Squamous Cell Carcinoma False False False NCIT:C40244 Vaginal Non-Keratinizing Squamous Cell Carcinoma False False False -NCIT:C40245 Vaginal Basaloid Carcinoma False False False +NCIT:C40245 Vaginal Basaloid Squamous Cell Carcinoma False False False NCIT:C40248 Vaginal Warty Carcinoma False False False NCIT:C40251 Vaginal Endometrioid Adenocarcinoma False False False NCIT:C40252 Vaginal Mucinous Adenocarcinoma False False False @@ -7731,7 +8091,7 @@ NCIT:C4232 Melanoma in Junctional Nevus False False False NCIT:C4235 Melanoma Arising in Giant Congenital Nevus False False False NCIT:C4238 Type A Spindle Cell Melanoma False False False NCIT:C4239 Type B Spindle Cell Melanoma False False False -NCIT:C4240 Melanoma Arising from Blue Nevus False False False +NCIT:C4240 Melanoma Arising in Blue Nevus False False False NCIT:C4241 Cellular Blue Nevus False False False NCIT:C4246 Atypical Fibroxanthoma False False False NCIT:C4249 Fibrolipoma False False False @@ -7758,13 +8118,13 @@ NCIT:C43223 Myeloid Leukemia Associated with Down Syndrome False False False NCIT:C43277 Pure Cutaneous Mastocytosis False False False NCIT:C43310 Malignant Hair Follicle Neoplasm False False False NCIT:C43311 Germinative Follicular Epithelium Neoplasm False False False -NCIT:C43312 Mixed Epithelial and Mesenchymal Hair Follicle Neoplasm False False False +NCIT:C43312 Adamantinoid Trichoblastoma False False False NCIT:C43313 Pilar-Associated Mesenchyme Neoplasm False False False NCIT:C43315 Benign Outer Hair Sheath and Infundibulum Neoplasm False False False NCIT:C43316 Malignant Outer Hair Sheath and Infundibulum Neoplasm False False False NCIT:C43319 Benign Germinative Follicular Epithelium Neoplasm False False False NCIT:C43321 Malignant Germinative Follicular Epithelium Neoplasm False False False -NCIT:C43322 Benign Mixed Epithelial and Mesenchymal Hair Follicle Neoplasm False False False +NCIT:C43322 Cribriform Trichoblastoma False False False NCIT:C43323 Benign Pilar-Associated Mesenchyme Neoplasm False False False NCIT:C43324 Outer Hair Sheath and Infundibulum Neoplasm False False False NCIT:C43325 Trichoadenoma False False False @@ -7784,7 +8144,7 @@ NCIT:C43346 Ductal Eccrine Carcinoma with Spindle Cell Elements False False Fals NCIT:C43347 Squamoid Eccrine Ductal Carcinoma False False False NCIT:C43349 Ductal Eccrine Carcinoma with Abundant Fibromyxoid Stroma False False False NCIT:C43351 Sporadic Cylindroma False False False -NCIT:C43353 Classical Poroma False False False +NCIT:C43353 Classic Poroma False False False NCIT:C43354 Porocarcinoma In Situ False False False NCIT:C43355 Syringoacanthoma False False False NCIT:C43372 Lentigo Maligna False False False @@ -7909,8 +8269,8 @@ NCIT:C45516 Lung Clear Cell Adenocarcinoma False False False NCIT:C45541 Lung Spindle Cell Carcinoma False False False NCIT:C45542 Lung Pleomorphic Carcinoma False False False NCIT:C45543 Lung Carcinosarcoma False False False -NCIT:C45550 Lung Typical Carcinoid Tumor False False False -NCIT:C45551 Lung Atypical Carcinoid Tumor False False False +NCIT:C45550 Lung Neuroendocrine Tumor G1 False False False +NCIT:C45551 Lung Neuroendocrine Tumor G2 False False False NCIT:C4556 Iris Nevus False False False NCIT:C45567 Low Grade Lung Neuroendocrine Neoplasm False False False NCIT:C45568 Intermediate Grade Lung Neuroendocrine Neoplasm False False False @@ -7950,8 +8310,8 @@ NCIT:C45708 Microscopic Thymoma False False False NCIT:C45709 Sclerosing Thymoma False False False NCIT:C4571 Malignant Respiratory System Neoplasm False False False NCIT:C45710 Thymus Lipofibroadenoma False False False -NCIT:C45719 Thymic Atypical Carcinoid Tumor False False False -NCIT:C45720 Thymic Typical Carcinoid Tumor False False False +NCIT:C45719 Thymic Neuroendocrine Tumor G2 False False False +NCIT:C45720 Thymic Neuroendocrine Tumor G1 False False False NCIT:C45722 Combined Thymic Epithelial Neoplasm False False False NCIT:C4573 Malignant Skin Appendage Neoplasm False False False NCIT:C45732 Mediastinal Germ Cell Tumor with Somatic-Type Malignancy False False False @@ -8036,7 +8396,7 @@ NCIT:C4649 Palate Squamous Cell Carcinoma False False False NCIT:C4650 Parotid Gland Pleomorphic Adenoma False False False NCIT:C4656 Intracranial Meningioma False False False NCIT:C4659 Pineal Region Germ Cell Tumor False False False -NCIT:C4661 Primary Meningeal Melanocytic Neoplasm False False False +NCIT:C4661 Central Nervous System Melanocytic Neoplasm False False False NCIT:C4700 Giant Cell Fibroblastoma False False False NCIT:C4711 Borderline Cystadenoma False False False NCIT:C4712 Adenocarcinoma with Metaplasia False False False @@ -8084,7 +8444,7 @@ NCIT:C4846 Pancreatic Intraepithelial Neoplasia-2 False False False NCIT:C48596 Invasive Prostate Carcinoma False False False NCIT:C48607 Invasive Cutaneous Melanoma False False False NCIT:C48612 Minimal Deviation Melanoma False False False -NCIT:C48613 Melanoma in Congenital Melanocytic Nevus False False False +NCIT:C48613 Melanoma Arising in Congenital Melanocytic Nevus False False False NCIT:C48614 Desmoplastic Neurotropic Melanoma False False False NCIT:C48622 Mucosal Lentiginous Melanoma False False False NCIT:C4881 Metastatic Malignant Neoplasm in the Spine False False False @@ -8234,8 +8594,8 @@ NCIT:C5149 Supratentorial Glioblastoma False False False NCIT:C5150 Cerebellar Glioblastoma False False False NCIT:C5151 Cerebral Glioblastoma False False False NCIT:C5163 Breast Adenocarcinoma with Squamous Metaplasia False False False -NCIT:C5167 High Grade Breast Mucoepidermoid Carcinoma False False False -NCIT:C5168 Low Grade Breast Mucoepidermoid Carcinoma False False False +NCIT:C5167 Breast High Grade Mucoepidermoid Carcinoma False False False +NCIT:C5168 Breast Low Grade Mucoepidermoid Carcinoma False False False NCIT:C5170 Breast Neuroendocrine Tumor G1 False False False NCIT:C5171 Metastatic Breast Neuroendocrine Tumor G1 False False False NCIT:C5176 Metastatic Breast Signet Ring Cell Carcinoma False False False @@ -8256,7 +8616,7 @@ NCIT:C5222 Stage IC Ovarian Cancer AJCC v6 and v7 False False False NCIT:C5223 Stage IIA Ovarian Cancer AJCC V6 and v7 False False False NCIT:C5224 Stage IIB Ovarian Cancer AJCC v6 and v7 False False False NCIT:C5225 Stage IIC Ovarian Cancer AJCC v6 and v7 False False False -NCIT:C5229 Ovarian Carcinoid Tumor False False False +NCIT:C5229 Ovarian Neuroendocrine Tumor False False False NCIT:C5231 Ovarian Leydig Cell Tumor False False False NCIT:C5233 Ovarian Fibrosarcoma False False False NCIT:C5244 Ovarian Soft Tissue Neoplasm False False False @@ -8297,7 +8657,7 @@ NCIT:C5357 Benign Cardiac Germ Cell Tumor False False False NCIT:C5358 Cardiac Schwannoma False False False NCIT:C53589 Cellular Myxoma False False False NCIT:C53594 Pleomorphic Hyalinizing Angiectatic Tumor of Soft Parts False False False -NCIT:C53595 Ectopic Hamartomatous Thymoma False False False +NCIT:C53595 Branchioma False False False NCIT:C5362 Cardiac Epithelioid Hemangioendothelioma False False False NCIT:C5363 Cardiac Kaposi Sarcoma False False False NCIT:C5369 Secondary Heart Lymphoma False False False @@ -8348,14 +8708,14 @@ NCIT:C54298 Ameloblastic Carcinoma-Secondary Type (Dedifferentiated), Intraosseo NCIT:C54299 Ameloblastic Carcinoma-Secondary Type (Dedifferentiated), Peripheral False False False NCIT:C5430 Intracranial Germinoma False False False NCIT:C54300 Clear Cell Odontogenic Carcinoma False False False -NCIT:C54303 Primary Intraosseous Squamous Cell Carcinoma Derived From Keratocystic Odontogenic Tumor False False False +NCIT:C54303 Primary Intraosseous Carcinoma, Not Otherwise Specified, Derived from Odontogenic Keratocyst False False False NCIT:C5431 Lipomatosis of Nerve False False False NCIT:C54317 Odontoameloblastoma False False False NCIT:C54319 Calcifying Cystic Odontogenic Tumor False False False NCIT:C54323 Dentinogenic Ghost Cell Tumor False False False -NCIT:C54334 Laryngeal Basaloid Carcinoma False False False +NCIT:C54334 Laryngeal Basaloid Squamous Cell Carcinoma False False False NCIT:C54335 Laryngeal Papillary Squamous Cell Carcinoma False False False -NCIT:C54336 Laryngeal Squamous Cell Carcinoma, Spindle Cell Variant False False False +NCIT:C54336 Laryngeal Spindle Cell Squamous Carcinoma False False False NCIT:C54337 Laryngeal Acantholytic Squamous Cell Carcinoma False False False NCIT:C54338 Laryngeal Adenosquamous Carcinoma False False False NCIT:C54339 Laryngeal Undifferentiated Carcinoma False False False @@ -8364,10 +8724,10 @@ NCIT:C54342 Laryngeal Giant Cell Carcinoma False False False NCIT:C54345 Sinonasal Oncocytic Papilloma False False False NCIT:C54347 Nasal Cavity Exophytic Papilloma False False False NCIT:C5435 Kadish Stage C Olfactory Neuroblastoma False False False -NCIT:C54360 Nasopharyngeal Basaloid Carcinoma False False False +NCIT:C54360 Nasopharyngeal Basaloid Squamous Cell Carcinoma False False False NCIT:C54389 Nasopharyngeal Differentiated Carcinoma False False False NCIT:C5439 Drop Metastasis in the Spinal Cord False False False -NCIT:C54400 Nasopharyngeal Papillary Adenocarcinoma False False False +NCIT:C54400 Nasopharyngeal Low Grade Papillary Adenocarcinoma False False False NCIT:C5442 Intracranial Melanoma False False False NCIT:C5444 Intracranial Lipoma False False False NCIT:C5446 Meningeal Gliomatosis False False False @@ -8596,7 +8956,6 @@ NCIT:C5958 Sublingual Gland Adenocarcinoma False False False NCIT:C5959 Minor Salivary Gland Squamous Cell Carcinoma False False False NCIT:C5960 Childhood Supratentorial Neoplasm False False False NCIT:C5966 Anaplastic Brain Stem Astrocytoma False False False -NCIT:C5971 Ear Polyp False False False NCIT:C5976 Minor Salivary Gland Carcinoma ex Pleomorphic Adenoma False False False NCIT:C5977 Submandibular Gland Carcinoma ex Pleomorphic Adenoma False False False NCIT:C5978 Salivary Gland Myoepithelioma False False False @@ -8980,7 +9339,7 @@ NCIT:C6219 Childhood Benign Cerebral Neoplasm False False False NCIT:C62191 Salivary Gland Clear Cell Carcinoma False False False NCIT:C62192 Salivary Gland Intraductal Carcinoma False False False NCIT:C62193 Salivary Gland Mucinous Adenocarcinoma False False False -NCIT:C62194 Salivary Gland Oncocytic Carcinoma False False False +NCIT:C62194 Salivary Gland Oncocytic Adenocarcinoma False False False NCIT:C62196 Salivary Gland Adenocarcinoma, Not Otherwise Specified False False False NCIT:C6221 Thalamic Neoplasm False False False NCIT:C62210 Breast Tubular Adenoma False False False @@ -9388,9 +9747,9 @@ NCIT:C64166 Squamous Cell Papilloma of the Rat Tongue False False False NCIT:C64167 Squamous Cell Carcinoma of the Rat Tongue False False False NCIT:C6417 Recurrent Adrenal Cortical Carcinoma False False False NCIT:C64178 Teratoma of the Rat Ovary False False False -NCIT:C6421 Foregut Neuroendocrine Tumor G1 False False False +NCIT:C6421 Foregut Neuroendocrine Tumor False False False NCIT:C6422 Midgut Neuroendocrine Tumor G1 False False False -NCIT:C6423 Hindgut Neuroendocrine Tumor G1 False False False +NCIT:C6423 Hindgut Neuroendocrine Tumor False False False NCIT:C6424 Meckel Diverticulum Neuroendocrine Tumor G1 False False False NCIT:C6425 Duodenal Neuroendocrine Tumor G1 False False False NCIT:C6426 Transverse Colon Neuroendocrine Tumor G1 False False False @@ -9424,7 +9783,7 @@ NCIT:C64296 Mucus Cell Hyperplasia of the Rat Bronchiole False False False NCIT:C64297 Mucus Cell Hyperplasia of the Rat Bronchus False False False NCIT:C64298 Mucus Cell Hyperplasia of the Rat Larynx False False False NCIT:C64299 Mucus Cell Hyperplasia of the Rat Trachea False False False -NCIT:C6430 Thymic Carcinoid Tumor False False False +NCIT:C6430 Thymic Neuroendocrine Tumor False False False NCIT:C64300 Sebaceous Cell Hyperplasia of the Rat Zymbal Gland False False False NCIT:C64301 Squamous Cell Hyperplasia of the Rat Clitoral Gland False False False NCIT:C64302 Squamous Cell Hyperplasia of the Rat Esophagus False False False @@ -9435,7 +9794,6 @@ NCIT:C64306 Squamous Cell Hyperplasia of the Rat Preputial Gland False False Fal NCIT:C64307 Squamous Cell Hyperplasia of the Rat Skin Subcutaneous Tissue False False False NCIT:C64308 Squamous Cell Hyperplasia of the Rat Tongue False False False NCIT:C64309 Squamous Cell Hyperplasia of the Rat Vagina False False False -NCIT:C6431 Metastatic Carcinoid Tumor False False False NCIT:C64310 Squamous Cell Hyperplasia of the Rat Zymbal Gland False False False NCIT:C64311 Squamous Cell Metaplasia of the Rat Bronchiole False False False NCIT:C64312 Squamous Cell Metaplasia of the Rat Bronchus False False False @@ -9592,7 +9950,7 @@ NCIT:C6675 Stage IB Lung Small Cell Carcinoma AJCC v7 False False False NCIT:C66750 Adult Granulosa Cell Tumor False False False NCIT:C66751 Granulosa Cell-Theca Cell Tumor False False False NCIT:C66752 Clear Cell Neoplasm False False False -NCIT:C66753 Malignant Melanoma in Precancerous Melanosis False False False +NCIT:C66753 Melanoma in Precancerous Melanosis False False False NCIT:C66754 Small Congenital Melanocytic Nevus False False False NCIT:C66755 Proliferative Nodules in Congenital Melanocytic Nevus False False False NCIT:C66759 Giant Cell Sarcoma False False False @@ -9782,7 +10140,7 @@ NCIT:C68703 Adult Supratentorial Embryonal Tumor, Not Otherwise Specified False NCIT:C6871 Sinonasal Inverted Papilloma False False False NCIT:C6873 Stage IV Anal Canal Cancer AJCC v6 and v7 False False False NCIT:C6877 Grade III Glandular Intraepithelial Neoplasia False False False -NCIT:C6878 Pancreatic Mixed Acinar-Neuroendocrine Carcinoma False False False +NCIT:C6878 Pancreatic Mixed Acinar Carcinoma-Neuroendocrine Carcinoma False False False NCIT:C6883 Pancreatic Mucinous-Cystic Neoplasm with Intermediate Grade Dysplasia False False False NCIT:C68837 Favorable Non-Hodgkin Lymphoma False False False NCIT:C68838 Unfavorable Non-Hodgkin Lymphoma False False False @@ -9824,7 +10182,6 @@ NCIT:C7037 Gastric Tubulovillous Adenoma False False False NCIT:C7038 Gastric Villous Adenoma False False False NCIT:C7041 Colon Tubular Adenoma False False False NCIT:C7042 Colon Ganglioneuroma False False False -NCIT:C7045 Malignant Intracranial Neoplasm by Morphology False False False NCIT:C7046 Urinary System Paraganglioma False False False NCIT:C7048 Supratentorial Meningioma False False False NCIT:C7051 Meningioma by Site False False False @@ -9929,7 +10286,7 @@ NCIT:C7197 Type A Lymphomatoid Papulosis False False False NCIT:C7198 Type B Lymphomatoid Papulosis False False False NCIT:C7199 Type C Lymphomatoid Papulosis False False False NCIT:C7200 Anaplastic Large Cell Lymphoma, Lymphomatoid Papulosis-Like Histology False False False -NCIT:C7201 Infrequent Neoplasm False False False +NCIT:C7201 Rare Neoplasm False False False NCIT:C7204 T-Zone Variant Peripheral T-Cell Lymphoma False False False NCIT:C7205 Lymphoepithelioid Variant Peripheral T-Cell Lymphoma, Not Otherwise Specified False False False NCIT:C7206 Common Variant Anaplastic Large Cell Lymphoma False False False @@ -10023,7 +10380,7 @@ NCIT:C7351 Grade II Squamous Intraepithelial Neoplasia False False False NCIT:C7360 Grade II Prostatic Intraepithelial Neoplasia False False False NCIT:C7371 Accessory Urethral Gland Adenocarcinoma False False False NCIT:C7372 Cerebellar Glioneuronal and Neuronal Tumors False False False -NCIT:C7373 Nasopharyngeal Nonkeratinizing Carcinoma False False False +NCIT:C7373 Nasopharyngeal Non-Keratinizing Carcinoma False False False NCIT:C7381 Invasive Follicular Variant Thyroid Gland Papillary Carcinoma False False False NCIT:C7389 Benign Vascular Neoplasm False False False NCIT:C7390 Malignant Vascular Neoplasm False False False @@ -10066,8 +10423,8 @@ NCIT:C7493 Ameloblastic Carcinoma-Primary Type False False False NCIT:C7496 Ameloblastic Carcinoma-Secondary Type (Dedifferentiated) False False False NCIT:C7497 Ameloblastic Carcinoma Derived From Odontogenic Cyst False False False NCIT:C7498 Keratinizing Primary Intraosseous Squamous Cell Carcinoma-Solid Type False False False -NCIT:C7499 Non-Keratinizing Primary Intraosseous Squamous Cell Carcinoma -Solid Type False False False -NCIT:C7500 Primary Intraosseous Squamous Cell Carcinoma Derived From Odontogenic Cyst False False False +NCIT:C7499 Non-Keratinizing Primary Intraosseous Squamous Cell Carcinoma-Solid Type False False False +NCIT:C7500 Primary Intraosseous Carcinoma, Not Otherwise Specified, Derived from Odontogenic Cyst False False False NCIT:C7501 Odontogenic Myxoma False False False NCIT:C7503 Borderline Phyllodes Tumor False False False NCIT:C7508 Recurrent Urethral Carcinoma False False False @@ -10101,7 +10458,7 @@ NCIT:C7556 Stage A Prostate Cancer False False False NCIT:C7559 Atypical Adenoma False False False NCIT:C7565 Eccrine Hidrocystoma False False False NCIT:C7573 Metastatic Malignant Neoplasm in the Urethra False False False -NCIT:C7576 Deep Penetrating Nevus False False False +NCIT:C7576 Deep Penetrating Melanocytoma False False False NCIT:C7577 Recurrent Nevus False False False NCIT:C7578 Nevus of Female Genitalia False False False NCIT:C7580 Skin Appendage Adenoma False False False @@ -10127,7 +10484,7 @@ NCIT:C7628 Refractory Neoplasm False False False NCIT:C7630 Intermediate Lipomatous Neoplasm False False False NCIT:C76326 Metastatic Breast Ductal Carcinoma False False False NCIT:C76328 Metastatic Breast Lobular Carcinoma False False False -NCIT:C7639 Regional Malignant Urethral Neoplasm False False False +NCIT:C7639 Locally Advanced Urethral Carcinoma False False False NCIT:C7642 Epipodophyllotoxin-Related Myelodysplastic Syndrome False False False NCIT:C7643 Alkylating Agent-Related Myelodysplastic Syndrome False False False NCIT:C7645 Breast Intracystic Papillary Carcinoma False False False @@ -10359,12 +10716,12 @@ NCIT:C8001 Testicular Mixed Embryonal Carcinoma and Yolk Sac Tumor False False F NCIT:C8002 Testicular Mixed Yolk Sac Tumor and Teratoma False False False NCIT:C8003 Testicular Mixed Yolk Sac Tumor and Teratoma with Seminoma False False False NCIT:C8006 Pancreatic Somatostatin-Producing Neuroendocrine Tumor False False False -NCIT:C8012 Low Grade Salivary Gland Carcinoma False False False +NCIT:C8012 Salivary Gland Low Grade Carcinoma False False False NCIT:C8014 Lip Basal Cell Carcinoma False False False -NCIT:C8015 Low Grade Salivary Gland Mucoepidermoid Carcinoma False False False -NCIT:C8017 Intermediate Grade Salivary Gland Mucoepidermoid Carcinoma False False False -NCIT:C8018 High Grade Salivary Gland Carcinoma False False False -NCIT:C8019 High Grade Salivary Gland Mucoepidermoid Carcinoma False False False +NCIT:C8015 Salivary Gland Low Grade Mucoepidermoid Carcinoma False False False +NCIT:C8017 Salivary Gland Intermediate Grade Mucoepidermoid Carcinoma False False False +NCIT:C8018 Salivary Gland High Grade Carcinoma False False False +NCIT:C8019 Salivary Gland High Grade Mucoepidermoid Carcinoma False False False NCIT:C8021 Salivary Gland Adenocarcinoma False False False NCIT:C8022 Salivary Gland Poorly Differentiated Squamous Cell Carcinoma False False False NCIT:C8024 Salivary Gland Undifferentiated Carcinoma False False False @@ -10372,7 +10729,7 @@ NCIT:C8025 Malignant Mixed Tumor of the Salivary Gland False False False NCIT:C80280 Diffuse Large B-Cell Lymphoma, Not Otherwise Specified False False False NCIT:C80289 Diffuse Large B-Cell Lymphoma Associated with Chronic Inflammation False False False NCIT:C8029 Progressive Hairy Cell Leukemia Initial Treatment False False False -NCIT:C80290 Plasmablastic Lymphoma of the Oral Mucosa False False False +NCIT:C80290 Oral Cavity Plasmablastic Lymphoma False False False NCIT:C80291 High Grade B-Cell Lymphoma, Not Otherwise Specified False False False NCIT:C80297 Pediatric-Type Follicular Lymphoma False False False NCIT:C80298 Intestinal Follicular Lymphoma False False False @@ -10632,6 +10989,7 @@ NCIT:C8336 High Grade Squamous Intraepithelial Neoplasia False False False NCIT:C8355 Atypical Hyperplasia False False False NCIT:C8367 Low Grade Intraepithelial Neoplasia False False False NCIT:C8368 Grade II Intraepithelial Neoplasia False False False +NCIT:C8372 Hamartomatous Polyp False False False NCIT:C8373 Lymphangiomatosis False False False NCIT:C8376 Adenocarcinoma In Situ in Villous Adenoma False False False NCIT:C8387 Childhood Cerebral Diffuse Astrocytoma False False False @@ -10691,7 +11049,6 @@ NCIT:C8504 Indolent Non-Hodgkin Lymphoma False False False NCIT:C8505 Invasive Malignant Neoplasm False False False NCIT:C8509 Primary Neoplasm False False False NCIT:C8511 Refractory Carcinoma False False False -NCIT:C8512 Malignant Neoplasm with Regional Lymph Node Involvement False False False NCIT:C8513 Stage I Colorectal Cancer AJCC v6 and v7 False False False NCIT:C8514 Stage II Colorectal Cancer AJCC v6 False False False NCIT:C8515 Stage III Colorectal Cancer AJCC v6 False False False @@ -10745,19 +11102,19 @@ NCIT:C8584 Stage IIC Soft Tissue Sarcoma False False False NCIT:C8585 Stage III Soft Tissue Sarcoma AJCC v7 False False False NCIT:C8586 Stage IV Soft Tissue Sarcoma AJCC v7 False False False NCIT:C8587 Precancerous Polyp False False False -NCIT:C85887 Stage 0 Merkel Cell Carcinoma AJCC v7 False False False -NCIT:C85889 Stage I Merkel Cell Carcinoma AJCC v7 False False False -NCIT:C85890 Stage IA Merkel Cell Carcinoma AJCC v7 False False False -NCIT:C85892 Stage IB Merkel Cell Carcinoma AJCC v7 False False False -NCIT:C85893 Stage II Merkel Cell Carcinoma AJCC v7 False False False -NCIT:C85894 Stage IIA Merkel Cell Carcinoma AJCC v7 False False False -NCIT:C85895 Stage IIB Merkel Cell Carcinoma AJCC v7 False False False -NCIT:C85896 Stage IIC Merkel Cell Carcinoma AJCC v7 False False False -NCIT:C85897 Stage III Merkel Cell Carcinoma AJCC v7 False False False -NCIT:C85898 Stage IIIA Merkel Cell Carcinoma AJCC v7 False False False -NCIT:C85899 Stage IIIB Merkel Cell Carcinoma AJCC v7 False False False +NCIT:C85887 Stage 0 Cutaneous Merkel Cell Carcinoma AJCC v7 False False False +NCIT:C85889 Stage I Cutaneous Merkel Cell Carcinoma AJCC v7 False False False +NCIT:C85890 Stage IA Cutaneous Merkel Cell Carcinoma AJCC v7 False False False +NCIT:C85892 Stage IB Cutaneous Merkel Cell Carcinoma AJCC v7 False False False +NCIT:C85893 Stage II Cutaneous Merkel Cell Carcinoma AJCC v7 False False False +NCIT:C85894 Stage IIA Cutaneous Merkel Cell Carcinoma AJCC v7 False False False +NCIT:C85895 Stage IIB Cutaneous Merkel Cell Carcinoma AJCC v7 False False False +NCIT:C85896 Stage IIC Cutaneous Merkel Cell Carcinoma AJCC v7 False False False +NCIT:C85897 Stage III Cutaneous Merkel Cell Carcinoma AJCC v7 False False False +NCIT:C85898 Stage IIIA Cutaneous Merkel Cell Carcinoma AJCC v7 False False False +NCIT:C85899 Stage IIIB Cutaneous Merkel Cell Carcinoma AJCC v7 False False False NCIT:C8590 Lymphocyte Predominant Type Hodgkin's Disease False False False -NCIT:C85900 Stage IV Merkel Cell Carcinoma AJCC v7 False False False +NCIT:C85900 Stage IV Cutaneous Merkel Cell Carcinoma AJCC v7 False False False NCIT:C8594 Leukemic Phase of Lymphoma False False False NCIT:C8595 Postcricoid Carcinoma False False False NCIT:C8597 Retro-Orbital Neoplasm False False False @@ -10855,7 +11212,7 @@ NCIT:C8701 Refractory Non-Hodgkin Lymphoma False False False NCIT:C8702 Recurrent Transformed Non-Hodgkin Lymphoma False False False NCIT:C8703 Advanced Pericardial Malignant Mesothelioma False False False NCIT:C8705 Recurrent Peritoneal Malignant Mesothelioma False False False -NCIT:C87055 Oropharyngeal Human Papillomavirus-Positive Squamous Cell Carcinoma False False False +NCIT:C87055 Oropharyngeal Human Papillomavirus-Related Squamous Cell Carcinoma False False False NCIT:C8706 Advanced Pleural Malignant Mesothelioma False False False NCIT:C8707 Recurrent Pleural Malignant Mesothelioma False False False NCIT:C8708 Metastatic Angiosarcoma False False False @@ -10879,7 +11236,7 @@ NCIT:C87156 Stage III Gestational Trophoblastic Tumor AJCC v7 False False False NCIT:C87157 Stage IIIA Gestational Trophoblastic Tumor AJCC v7 False False False NCIT:C87158 Stage IIIB Gestational Trophoblastic Tumor AJCC v7 False False False NCIT:C87159 Stage IV Gestational Trophoblastic Tumor AJCC v7 False False False -NCIT:C8716 Regional Malignant Ureter Neoplasm False False False +NCIT:C8716 Advanced Ureter Carcinoma False False False NCIT:C87160 Stage IVA Gestational Trophoblastic Tumor AJCC v7 False False False NCIT:C87161 Stage IVB Gestational Trophoblastic Tumor AJCC v7 False False False NCIT:C87178 Stage I Bone Cancer AJCC v7 False False False @@ -11337,7 +11694,7 @@ NCIT:C89999 Stage IV Colon Cancer AJCC v7 False False False NCIT:C90016 Stage IV Rectal Cancer AJCC v7 False False False NCIT:C90019 Stage IV Rectosigmoid Cancer AJCC v7 False False False NCIT:C9004 Benign Adrenal Cortical Neoplasm False False False -NCIT:C9016 AIDS-Related Plasmablastic Lymphoma of the Oral Mucosa False False False +NCIT:C9016 AIDS-Related Oral Cavity Plasmablastic Lymphoma False False False NCIT:C9017 AIDS-Related Primary Effusion Lymphoma False False False NCIT:C90180 Stage III Hepatocellular Carcinoma AJCC v7 False False False NCIT:C90181 Stage IV Hepatocellular Carcinoma AJCC v7 False False False @@ -11347,12 +11704,12 @@ NCIT:C90217 Stage II Gallbladder Cancer AJCC v7 False False False NCIT:C90218 Stage III Gallbladder Cancer AJCC v7 False False False NCIT:C90219 Stage IV Gallbladder Cancer AJCC v7 False False False NCIT:C9023 Sarcoma by FNCLCC Grade False False False -NCIT:C9024 FNCLCC Sarcoma Grade 1 False False False +NCIT:C9024 Sarcoma G1 False False False NCIT:C9025 Well Differentiated Fibrosarcoma False False False NCIT:C9026 Low Grade Malignant Peripheral Nerve Sheath Tumor False False False NCIT:C9027 Atypical Cartilaginous Tumor/Chondrosarcoma, Grade 1 False False False -NCIT:C9028 FNCLCC Sarcoma Grade 2 False False False -NCIT:C9029 FNCLCC Sarcoma Grade 3 False False False +NCIT:C9028 Sarcoma G2 False False False +NCIT:C9029 Sarcoma G3 False False False NCIT:C9030 High Grade Malignant Peripheral Nerve Sheath Tumor False False False NCIT:C9031 Poorly Differentiated Angiosarcoma False False False NCIT:C9032 Ann Arbor Stage I Adult Hodgkin Lymphoma False False False @@ -11487,7 +11844,7 @@ NCIT:C9165 Childhood Acute Eosinophilic Leukemia False False False NCIT:C9169 Gallbladder Adenocarcinoma with Squamous Metaplasia False False False NCIT:C9172 Testicular Mixed Embryonal Carcinoma and Yolk Sac Tumor with Seminoma False False False NCIT:C9173 Testicular Mixed Choriocarcinoma and Seminoma False False False -NCIT:C91741 Middle Ear Carcinoma In Situ False False False +NCIT:C91741 External Auditory Canal Squamous Cell Carcinoma In Situ False False False NCIT:C9176 Non-Metastatic Gestational Trophoblastic Tumor False False False NCIT:C9177 Good Prognosis Metastatic Gestational Trophoblastic Tumor False False False NCIT:C9178 Poor Prognosis Metastatic Gestational Trophoblastic Tumor False False False @@ -11622,11 +11979,8 @@ NCIT:C9412 Angiosarcoma NCI Grade 3 False False False NCIT:C9413 Kaposi Sarcoma NCI Grade 2 False False False NCIT:C9414 Kaposi Sarcoma NCI Grade 3 False False False NCIT:C9415 Sarcoma NCI Grade 3 False False False -NCIT:C9416 Sarcoma by AJCC Grade False False False NCIT:C9417 Low Grade Sarcoma False False False NCIT:C9418 High Grade Sarcoma False False False -NCIT:C9420 AJCC Grade 2 Sarcoma False False False -NCIT:C9421 AJCC Grade 3 Sarcoma False False False NCIT:C9422 AJCC Grade 4 Sarcoma False False False NCIT:C9431 Childhood Hematopoietic and Lymphoid Cell Neoplasm False False False NCIT:C9446 Grade 1 Colorectal Adenocarcinoma False False False @@ -11693,7 +12047,7 @@ NCIT:C95429 Pancreatic Intraepithelial Neoplasia-1A False False False NCIT:C95430 Pancreatic Intraepithelial Neoplasia-1B False False False NCIT:C95432 High Grade Pancreatic Intraepithelial Neoplasia False False False NCIT:C95458 Pancreatic Mixed Acinar-Ductal Carcinoma False False False -NCIT:C95460 Pancreatic Mixed Acinar-Ductal Neuroendocrine Carcinoma False False False +NCIT:C95460 Pancreatic Mixed Ductal Adenocarcinoma-Acinar Carcinoma-Neuroendocrine Carcinoma False False False NCIT:C95465 Pancreatic Hepatoid Adenocarcinoma False False False NCIT:C95466 Pancreatic Medullary Carcinoma False False False NCIT:C95470 Pancreatic Serous Adenoma False False False @@ -11928,7 +12282,7 @@ NCIT:C97053 Invasive Breast Lobular Carcinoma, Tubulolobular Variant False False NCIT:C97057 Condyloma Acuminatum with Dysplasia False False False NCIT:C97058 Mixed Congenital Mesoblastic Nephroma False False False NCIT:C97076 Giant Cell Angioblastoma False False False -NCIT:C97135 Sclerosing Polycystic Adenosis False False False +NCIT:C97135 Sclerosing Polycystic Adenoma False False False NCIT:C97310 Myelodysplastic Syndrome with Somatic Mutation False False False NCIT:C97965 Breast Solid Neuroendocrine Carcinoma False False False NCIT:C98996 Neonatal Disorder False False False @@ -12175,6 +12529,8 @@ NCIT:C121535 Gamma-Secretase Inhibitor LY3039478 False False True NCIT:C121545 Fluorescent Protease-activated Peptide AVB-620 False False True NCIT:C121649 Vofatamab False False True NCIT:C121702 Fatigue on Average False False True +NCIT:C121923 Ivory Exostosis False False True +NCIT:C121924 Enostosis False False True NCIT:C12216 Fluorouracil-Uracil/Leucovorin Calcium False False True NCIT:C12217 GW776/5-Fluorouracil Combination Tablet False False True NCIT:C122345 Feel Worried False False True @@ -12183,6 +12539,7 @@ NCIT:C12241 Branchial Cleft False False True NCIT:C12247 Postcricoid Region False False True NCIT:C12248 Hypopharyngeal Aspect of the Aryepiglottic Fold False False True NCIT:C12283 Lung and Bronchus False False True +NCIT:C122832 Vepoloxamer False False True NCIT:C122874 Pan-IDH Mutant Inhibitor AG-881 False False True NCIT:C12289 Bone of Skull and Face and Associated Joints False False True NCIT:C12293 Skin of Other and Unspecified Parts of Face False False True @@ -12871,6 +13228,7 @@ NCIT:C14728 HTH Mouse False False True NCIT:C14729 H2 Recombinant from (c57BL X BALB/c)F1 False False True NCIT:C14730 HTG/GoSfSn Mouse False False True NCIT:C14731 8 Way Cross, 1966, G Schlager, Kansas U False False True +NCIT:C147312 Blasts to Nucleated Cells Ratio Measurement False False True NCIT:C14732 BPH/2Slg Mouse False False True NCIT:C14733 BPL/1 Mouse False False True NCIT:C14734 BPN/3 Mouse False False True @@ -13310,6 +13668,7 @@ NCIT:C15319 Research False False True NCIT:C153211 Anti-HER2/Anti-HER3 Bispecific Monoclonal Antibody MCLA-128 False False True NCIT:C153234 Elevated PSA False False True NCIT:C153311 Horse Anti-thymocyte Globulin False False True +NCIT:C153317 Advanced Unresectable Gastric Adenocarcinoma False False True NCIT:C153381 MVA-HPV16E6/E7-IL2 Vaccine TG4001 False False True NCIT:C153565 Prefer to Make Decision About Which Treatment I Will Receive False False True NCIT:C153613 Recurrent Fallopian Tube Serous Adenocarcinoma False False True @@ -13319,6 +13678,7 @@ NCIT:C153817 Recurrent Malignant Ovarian Transitional Cell Tumor False False Tru NCIT:C15405 Prevention False False True NCIT:C15408 Transfusion False False True NCIT:C15410 Biological Response Modifier Therapy False False True +NCIT:C15414 ADCC Assay False False True NCIT:C15427 Lymph Node Dissection False False True NCIT:C154334 Methylated MGMT Gene Promoter False False True NCIT:C154553 SLCT Inhibitor GNS561 False False True @@ -13331,9 +13691,11 @@ NCIT:C155798 Chimeric Antigen Receptor T-cell Therapy False False True NCIT:C155886 Ciclopirox Prodrug CPX-POM False False True NCIT:C15592 Incomplete Freund's Adjuvant/MART-1 False False True NCIT:C156033 Rothmund Thomson Syndrome False False True +NCIT:C156052 BCMA x CD3 T-cell Engaging Antibody CC-93269 False False True NCIT:C156154 Recombinant Ornithodoros moubata Saliva-derived Small Protein Complement C5 Inhibitor False False True NCIT:C156415 MDM2 Inhibitor KRT-232 False False True NCIT:C156459 Extrapulmonary SC carcinoma False False True +NCIT:C156487 Advanced Carcinoid Tumor False False True NCIT:C156508 Monoclonal Protein Spike to Total Protein Ratio Measurement False False True NCIT:C156654 Development International Birth Date False False True NCIT:C156655 Electronic Document Room False False True @@ -13530,6 +13892,7 @@ NCIT:C159139 GDC Wilms Tumor Histologic Subtype Terminology False False True NCIT:C159140 GDC Zygosity Terminology False False True NCIT:C159171 Someone There to Confide in or Talk About Yourself or Your Problems False False True NCIT:C15924 Definitive Radiation Therapy False False True +NCIT:C159256 Specimen Source Site False False True NCIT:C159559 Haemophilia Quality of Life Questionnaire for Adults False False True NCIT:C159609 Anti-CEACAM6 Antibody BAY1834942 False False True NCIT:C15965 Nutrition, Other False False True @@ -13568,6 +13931,7 @@ NCIT:C162536 Non-Human Papillomavirus-Related Penile Intraepithelial Neoplasia F NCIT:C162638 Non-Metastatic Prostate Carcinoma False False True NCIT:C16266 Adolescents False False True NCIT:C16283 Native American False False True +NCIT:C162848 Digital Papillary Adenoma False False True NCIT:C162880 5-HT4 Agonist TAK-954 False False True NCIT:C162997 WHO Follicular Lymphoma Histologic Grading System False False True NCIT:C162998 WHO Follicular Lymphoma Histologic Grade 1 False False True @@ -13596,6 +13960,7 @@ NCIT:C16471 Costs False False True NCIT:C165257 Test_New_Concept False False True NCIT:C165259 Docetaxel Formulation CKD-810 False False True NCIT:C16545 Endoscope False False True +NCIT:C165522 BAP1-Inactivated Skin Melanocytic Tumor False False True NCIT:C165976 Neutrophil-Activating Peptide 2 Measurement False False True NCIT:C16609 Regulation of Gene Expression False False True NCIT:C166252 Actual Dose of Medication False False True @@ -13700,6 +14065,7 @@ NCIT:C171332 GDC Margins Involved Site Terminology False False True NCIT:C171333 GDC Hysterectomy Margins Involved Terminology False False True NCIT:C17150 SOS Function False False True NCIT:C171500 Bilevel Positive Airway Pressure Ventilation False False True +NCIT:C17154 Surgical Specialty False False True NCIT:C17168 Stent False False True NCIT:C171855 Codeine Anhydrous False False True NCIT:C171886 Flortanidazole F-18 False False True @@ -13713,6 +14079,7 @@ NCIT:C172294 GDC Tissue Collection Type Terminology False False True NCIT:C17261 Diagnostic Radiology False False True NCIT:C172612 Recombinant Human Interleukin-22 IgG4-Fc Fusion Protein UTTR1147A False False True NCIT:C17265 Serbia and Montenegro False False True +NCIT:C172809 Tyrosine Kinase Inhibitor TL-895 False False True NCIT:C173006 Feel Left Out False False True NCIT:C173009 Feel Isolated From Others False False True NCIT:C17308 CD18 Antigen False False True @@ -13724,7 +14091,9 @@ NCIT:C173521 CNS Status/Disease Status False False True NCIT:C173529 Inotropic Agent False False True NCIT:C173532 High-Risk Ganglioneuroblastoma False False True NCIT:C173533 Advanced Leukemia False False True +NCIT:C173536 Bcl-2 Inhibitor LP-108 False False True NCIT:C173567 Gadolinium-based Contrast Agent BAY1747846 False False True +NCIT:C173585 Neck Carcinoma of Unknown Primary False False True NCIT:C17364 Wilms' Tumor Gene False False True NCIT:C173646 GDC Columnar Mucosa Present Terminology False False True NCIT:C173647 GDC Alcohol Type Terminology False False True @@ -13757,6 +14126,7 @@ NCIT:C17535 RGD Receptor False False True NCIT:C175441 Anti-RANKL Monoclonal Antibody JMT103 False False True NCIT:C175708 Hyperlipoproteinemia, Type I False False True NCIT:C175801 Inupadenant False False True +NCIT:C175856 Sulanemadlin False False True NCIT:C17591 GRB2 Protein False False True NCIT:C176015 Immunodeficiency 14 False False True NCIT:C17625 Pump False False True @@ -13764,6 +14134,7 @@ NCIT:C176290 Every Two Days False False True NCIT:C17645 Radionuclide Scanning False False True NCIT:C17652 Gerontology False False True NCIT:C176587 TP53-Associated Li-Fraumeni Syndrome False False True +NCIT:C176622 Gastrointestinal Defects And Immunodeficiency Syndrome False False True NCIT:C176707 Physical Examination Finding False False True NCIT:C176761 Thyroid Peroxidase Antibody Measurement False False True NCIT:C176788 PQ/CMC Application Submission Type Terminology False False True @@ -13840,9 +14211,11 @@ NCIT:C18688 Cell Biology, Other False False True NCIT:C18693 Chemistry, Other False False True NCIT:C18699 Clinical Dental Sciences, Other False False True NCIT:C18703 Clinical Nursing Care, Other False False True +NCIT:C187034 ALK Inhibitor SY-3505 False False True NCIT:C18704 Clinical Nursing Sciences, Other False False True NCIT:C18716 Computer Sciences, Other False False True NCIT:C18719 Conjugated Carrier False False True +NCIT:C187328 Locally Advanced Carcinoid Tumor False False True NCIT:C18767 Environmental Health Sciences, Other False False True NCIT:C187711 Class-switched Memory B-Lymphocyte Subpopulation to Class-switched Memory B-Lymphocyte Ratio Measurement False False True NCIT:C18779 Experimental Models, Other False False True @@ -13863,6 +14236,7 @@ NCIT:C18910 Oncogene E1A/E1B False False True NCIT:C18911 Oncology, Other False False True NCIT:C1896 Monoclonal Antibody, for Clinical Diagnosis False False True NCIT:C189890 Ocifisertib Fumarate False False True +NCIT:C189906 HER2 Inhibitor BI 1810631 False False True NCIT:C18999 Reproduction, Other False False True NCIT:C19013 Retinoid Receptor False False True NCIT:C19039 Special Interest Category (Clinical Trials Code) False False True @@ -13881,6 +14255,7 @@ NCIT:C19159 Special Equipment False False True NCIT:C19162 Thrusts I II III IV VI False False True NCIT:C19174 Lower GI Series False False True NCIT:C19176 Radioactive False False True +NCIT:C191760 Cyclophosphamide/Doxorubicin/Vincristine Regimen False False True NCIT:C192094 Retired Concept 2022 False False True NCIT:C1921 Prothymosin L False False True NCIT:C19218 NCI Board of Scientific Advisors False False True @@ -13928,6 +14303,7 @@ NCIT:C19724 Children's Cancer Group False False True NCIT:C19742 Gamma Particle False False True NCIT:C197965 Schizotypal Disorder False False True NCIT:C197982 Swyer-James-MacLeod Syndrome False False True +NCIT:C198029 BV-AVD Regimen False False True NCIT:C19806 Model Genes and Proteins False False True NCIT:C19822 Allelotyping False False True NCIT:C198469 Administration Method of Administration False False True @@ -13943,6 +14319,7 @@ NCIT:C19985 Diagnostics Validation Network False False True NCIT:C19995 Attributes of Chemicals False False True NCIT:C20025 14.3.3 Sigma Gene False False True NCIT:C2004 SGN-15 False False True +NCIT:C200523 Extended Release Chewable Tablet False False True NCIT:C2008 MDX-447 False False True NCIT:C20101 Proto-Oncogene, Signaling Factor False False True NCIT:C2011 MDX-4 False False True @@ -13953,10 +14330,14 @@ NCIT:C201506 Concomitant/Prior Medications End Relative to Reference Time Point NCIT:C201508 Substance Use End Relative to Reference Time Point False False True NCIT:C20192 Miscellaneous Occupation False False True NCIT:C20196 Cancer Center False False True +NCIT:C202120 Pachydermoperiostosis False False True NCIT:C2022 Gonadotropin-Releasing Hormone Analogue False False True +NCIT:C202932 Anti-GPC3 CAR T-lymphocytes AZD5851 False False True NCIT:C20321 hCdt1 False False True +NCIT:C203440 Retired Concept 2023 False False True NCIT:C20351 MAGE Family A Gene False False True NCIT:C20366 Diaphranography False False True +NCIT:C204203 Intracorpus Cavernosum Route of Administration False False True NCIT:C20438 Granulocyte Colony-Stimulating Factor False False True NCIT:C20443 Neurotrophin False False True NCIT:C2046 TNP-40 False False True @@ -15881,6 +16262,7 @@ NCIT:C35864 Extra-Adrenal Pheochromocytoma False False True NCIT:C35865 Malignant Extra-Adrenal Pheochromocytoma False False True NCIT:C35878 Monoclonal Paraproteinemia False False True NCIT:C35934 Locally Metastatic Malignant Neoplasm False False True +NCIT:C36034 Villous Neoplasm False False True NCIT:C36093 Endometrial Mucinous Adenocarcinoma False False True NCIT:C36259 Acute Promyelocytic Leukemia with t(15;17)(q22;q12); PML/RARA False False True NCIT:C36275 Splenic Marginal Zone Lymphoma without Villous Lymphocytes False False True @@ -16086,6 +16468,7 @@ NCIT:C4312 Malignant Ameloblastoma False False True NCIT:C43219 Multipotent Bone Marrow Stem Cell with Wide Myeloid Potential False False True NCIT:C43229 Primitive Bone Marrow Myeloid Stem Cell False False True NCIT:C43235 Not Reported False False True +NCIT:C43249 Mature Tissue Histiocyte False False True NCIT:C43252 Antigen Processing Cell False False True NCIT:C43262 Exophthalmos False False True NCIT:C43284 Systemic Mastocytosis False False True @@ -16316,6 +16699,7 @@ NCIT:C49690 Phase III/IV Trial False False True NCIT:C4971 Malignant Squamous Cell Neoplasm False False True NCIT:C49889 Cooling Module Device Component False False True NCIT:C49891 Line Cord Device Component False False True +NCIT:C50037 Logic Board Device False False True NCIT:C50090 Other Device Component False False True NCIT:C50318 Injector System Device Component False False True NCIT:C50340 Alarm System Device Component False False True @@ -16357,6 +16741,7 @@ NCIT:C5179 Primary Squamous Cell Breast Carcinoma False False True NCIT:C51942 Papanicolaou Test False False True NCIT:C51970 Virtual Colonoscopy False False True NCIT:C51971 Antisense Therapy False False True +NCIT:C51982 Implantation False False True NCIT:C51983 Nutritional Supplementation False False True NCIT:C51990 Whole-Body Irradiation False False True NCIT:C52028 EEF1B1 wt Allele False False True @@ -16417,6 +16802,7 @@ NCIT:C53631 Laryngopharynx False False True NCIT:C54064 Continue False False True NCIT:C54067 Health Professional False False True NCIT:C5410 Primary Intraocular Lymphoma False False True +NCIT:C54147 Correctional Institute False False True NCIT:C54349 Preexisting Condition False False True NCIT:C54375 BCPR wt Allele False False True NCIT:C54377 BRCA3 wt Allele False False True @@ -16452,6 +16838,8 @@ NCIT:C6090 Lacrimal Gland Malignant Mixed Tumor False False True NCIT:C61129 Cryoablation False False True NCIT:C61266 A-Glucuronidase Deficiency False False True NCIT:C61364 Homeopathy False False True +NCIT:C61399 Radiation Underexposure False False True +NCIT:C61400 Radiation Overexposure False False True NCIT:C61411 Cancer Disease Progression False False True NCIT:C61496 MKC-1 False False True NCIT:C61560 Delivery False False True @@ -16519,6 +16907,7 @@ NCIT:C63450 CHOP Regimen False False True NCIT:C63451 CHOPE Regimen False False True NCIT:C63452 R-CHOP Regimen False False True NCIT:C63456 ICE Regimen False False True +NCIT:C63469 CDE Regimen False False True NCIT:C63494 Hematopoietic Stem Cell Mobilization False False True NCIT:C63538 Dextropropoxyphene Hydrochloride False False True NCIT:C6354 Classic Seminoma False False True @@ -16537,7 +16926,9 @@ NCIT:C63912 Pars Intermedia Adenoma of the Rat Pituitary Gland False False True NCIT:C64024 Adenoma of the Rat Rete Testis False False True NCIT:C64116 Lipoma of the Rat Kidney False False True NCIT:C64117 Liposarcoma of the Rat Kidney False False True +NCIT:C64190 CISCA Regimen False False True NCIT:C6420 Aortic Paraganglioma False False True +NCIT:C6431 Metastatic Carcinoid Tumor False False True NCIT:C64622 As Needed False False True NCIT:C64663 Send False False True NCIT:C64664 Not More Than False False True @@ -16578,6 +16969,7 @@ NCIT:C66993 Wound False False True NCIT:C67203 Vinorelbine-Gemcitabine Regimen False False True NCIT:C67207 ADE Regimen False False True NCIT:C67225 Stereotactic Radiation Therapy False False True +NCIT:C67231 VAdriaC Regimen False False True NCIT:C67294 NWTS Regimen 1 False False True NCIT:C67362 Fundamental Constant False False True NCIT:C67370 Labial Mucosa False False True @@ -16655,6 +17047,7 @@ NCIT:C7005 Hemangiopericytoma of the Central Nervous System False False True NCIT:C7031 Appendix Mixed Carcinoid-Adenocarcinoma False False True NCIT:C7040 Central Nervous System Neoplasms by Morphology False False True NCIT:C7044 Intracranial Central Nervous System Neoplasms by Morphology False False True +NCIT:C7045 Malignant Intracranial Neoplasm by Morphology False False True NCIT:C7047 Functioning Pituitary Gland Neoplasm False False True NCIT:C7050 Meningioma by Morphology False False True NCIT:C70536 50 Percent Tissue Culture Infective Dose False False True @@ -16791,6 +17184,7 @@ NCIT:C76872 Ethohexadiol False False True NCIT:C76914 Azaribine False False True NCIT:C76918 Ropidoxuridine False False True NCIT:C7701 Reactive Lymphocyte Count False False True +NCIT:C77186 Ajellomyces capsulatus False False True NCIT:C7722 Cardiac Fibroma False False True NCIT:C77385 Follicle Stimulating Hormone Beta Polypeptide False False True NCIT:C77388 4-Iodo-3-Nitrobenzamide False False True @@ -16904,6 +17298,7 @@ NCIT:C84876 Nutritional Supplement Drink False False True NCIT:C84936 Noma False False True NCIT:C84960 Ornithine Transcarbamylase Deficiency False False True NCIT:C85066 Shy-Drager Syndrome False False True +NCIT:C8512 Malignant Neoplasm with Regional Lymph Node Involvement False False True NCIT:C85322 Pollen Pollen False False True NCIT:C85461 Iodine I 123 Iodobenzamide False False True NCIT:C85518 In-Ovo Route of Administration False False True @@ -16993,6 +17388,7 @@ NCIT:C91386 Anti-PGF Monoclonal Antibody RO5323441 False False True NCIT:C91714 Immunotherapeutic GSK1572932A False False True NCIT:C9201 Angioimmunoblastic Lymphadenopathy with Dysproteinemia False False True NCIT:C92204 Modified Rankin Scale False False True +NCIT:C92206 Short Limb Dwarfism-Saddle Nose-Spinal Alterations-Metaphyseal Striation Syndrome False False True NCIT:C92223 Iodine I-123 False False True NCIT:C92230 Early R Wave Progression False False True NCIT:C92449 Childhood Abuse and Neglect False False True @@ -17020,7 +17416,10 @@ NCIT:C93329 Conformation-sensitive Gel Electrophoresis False False True NCIT:C93350 Hyperthermia Therapy False False True NCIT:C9342 Spindle Cell Intraocular Melanoma False False True NCIT:C9373 Adult Brain Medulloblastoma False False True +NCIT:C9416 Sarcoma by AJCC Grade False False True +NCIT:C9420 AJCC Grade 2 Sarcoma False False True NCIT:C94204 Data and Safety Monitoring Board False False True +NCIT:C9421 AJCC Grade 3 Sarcoma False False True NCIT:C94210 Fibromun False False True NCIT:C9424 Combined Small and Large Cell Lung Carcinoma False False True NCIT:C94371 Instillation False False True @@ -18542,7 +18941,7 @@ NCIT:C101339 Venous Thrombosis Related to Vascular Access Complication False Tru NCIT:C10134 Mechlorethamine/Methotrexate/Prednisone/Procarbazine/Vincristine False True False NCIT:C101340 ARVCF Gene False True False NCIT:C101341 ARVCF wt Allele False True False -NCIT:C101342 Armadillo Repeat Protein Deleted In Velo-Cardio-Facial Syndrome False True False +NCIT:C101342 Splicing Regulator ARVCF False True False NCIT:C101343 CRY1 Gene False True False NCIT:C101344 CRY1 wt Allele False True False NCIT:C101345 Cryptochrome-1 False True False @@ -18625,9 +19024,9 @@ NCIT:C101415 Single-Stranded DNA Cytosine Deaminase False True False NCIT:C101416 LIN28B Gene False True False NCIT:C101417 LIN28B wt Allele False True False NCIT:C101418 Protein Lin-28 Homolog B False True False -NCIT:C101419 DDX58 Gene False True False +NCIT:C101419 RIGI Gene False True False NCIT:C10142 Asparaginase/Cyclophosphamide/Cytarabine/Mercaptopurine/Methotrexate/Vincristine False True False -NCIT:C101420 DDX58 wt Allele False True False +NCIT:C101420 RIGI wt Allele False True False NCIT:C101421 Antiviral Innate Immune Response Receptor RIG-I False True False NCIT:C101422 POSTN Gene False True False NCIT:C101423 POSTN wt Allele False True False @@ -21317,7 +21716,7 @@ NCIT:C103874 SDHA wt Allele False True False NCIT:C103875 Succinate Dehydrogenase [Ubiquinone] Flavoprotein Subunit, Mitochondrial False True False NCIT:C103876 ABCA5 Gene False True False NCIT:C103877 ABCA5 wt Allele False True False -NCIT:C103878 ATP-Binding Cassette Sub-Family A Member 5 False True False +NCIT:C103878 Cholesterol Transporter ABCA5 False True False NCIT:C103879 ABCC4 Gene False True False NCIT:C10388 BCG/Mitomycin False True False NCIT:C103880 ABCC4 wt Allele False True False @@ -21904,9 +22303,9 @@ NCIT:C104418 Transcription Factor GATA-6 False True False NCIT:C104419 Autologous GM-CSF-secreting Lethally Irradiated Leukemia Cell Vaccine False True False NCIT:C10442 Cyclophosphamide/Doxorubicin/Etoposide/Prednisolone/Vincristine False True False NCIT:C104420 Zirconium Zr 89 DFO-MSTP2109A False True False -NCIT:C104421 GBA Gene False True False -NCIT:C104422 GBA wt Allele False True False -NCIT:C104423 Glucosylceramidase False True False +NCIT:C104421 GBA1 Gene False True False +NCIT:C104422 GBA1 wt Allele False True False +NCIT:C104423 Lysosomal Acid Glucosylceramidase False True False NCIT:C104424 GBA2 Gene False True False NCIT:C104425 GBA2 wt Allele False True False NCIT:C104426 Non-Lysosomal Glucosylceramidase False True False @@ -24409,7 +24808,7 @@ NCIT:C106696 Columbia-Suicide Severity Rating Scale Baseline/Screening Version Q NCIT:C106697 Geriatric Depression Scale Questionnaire False True False NCIT:C106698 Geriatric Depression Scale Short Form Questionnaire False True False NCIT:C106699 Health Assessment Questionnaire Disability Index With Pain Visual Analog Scale Questionnaire False True False -NCIT:C1067 Dexamethasone Acetate False True False +NCIT:C1067 Dexamethasone Acetate, Unspecified False True False NCIT:C10670 Eflornithine/Piroxicam False True False NCIT:C106700 Modified Medical Research Council Dyspnea Scale Questionnaire False True False NCIT:C106701 BDI - Functional Impairment False True False @@ -31484,7 +31883,7 @@ NCIT:C113163 Oplunofusp False True False NCIT:C113164 Tisotumab Vedotin False True False NCIT:C113165 HSD11B1 Gene False True False NCIT:C113166 HSD11B1 wt Allele False True False -NCIT:C113167 Corticosteroid 11-Beta-Dehydrogenase Isozyme 1 False True False +NCIT:C113167 11-Beta-Hydroxysteroid Dehydrogenase 1 False True False NCIT:C113168 Hyperprolactinemia False True False NCIT:C11317 Gemcitabine/Irinotecan False True False NCIT:C113173 Cerdulatinib False True False @@ -37165,10 +37564,10 @@ NCIT:C118665 Have Trouble Finding Right Words to Express Myself False True False NCIT:C118666 Have Used Wrong Word When Referring to an Object False True False NCIT:C118667 Have Trouble Saying What I Mean in Conversation False True False NCIT:C118668 Polyethylene Glycol Hydrogel False True False -NCIT:C118669 MDM2/MDMX Inhibitor ALRN-6924 False True False +NCIT:C118669 Sulanemadlin False True False NCIT:C11867 Interleukin-2/MAGE-12 Peptide Vaccine/Montanide ISA-51 False True False NCIT:C118670 Rhenium Re 188 BMEDA-labeled Liposomes False True False -NCIT:C118671 Avitinib Maleate False True False +NCIT:C118671 Abivertinib Maleate Anhydrous False True False NCIT:C118672 Tasurgratinib False True False NCIT:C118673 Opioid Agonist GIC-1002 False True False NCIT:C118674 Trastuzumab Duocarmazine False True False @@ -38144,12 +38543,12 @@ NCIT:C119689 CLOCK Gene False True False NCIT:C11969 GPI-0100/MUC-2-Globo H-KLH Conjugate Vaccine False True False NCIT:C119690 CLOCK wt Allele False True False NCIT:C119691 Circadian Locomoter Output Cycles Protein Kaput False True False -NCIT:C119692 ARNTL Gene False True False -NCIT:C119693 ARNTL wt Allele False True False -NCIT:C119694 Aryl Hydrocarbon Receptor Nuclear Translocator-Like Protein 1 False True False -NCIT:C119695 ARNTL2 Gene False True False -NCIT:C119696 ARNTL2 wt Allele False True False -NCIT:C119697 Aryl Hydrocarbon Receptor Nuclear Translocator-Like Protein 2 False True False +NCIT:C119692 BMAL1 Gene False True False +NCIT:C119693 BMAL1 wt Allele False True False +NCIT:C119694 Basic Helix-Loop-Helix ARNT-Like Protein 1 False True False +NCIT:C119695 BMAL2 Gene False True False +NCIT:C119696 BMAL2 wt Allele False True False +NCIT:C119697 Basic Helix-Loop-Helix ARNT-Like Protein 2 False True False NCIT:C119698 Have Swelling in Stomach Area False True False NCIT:C119699 Have Cramps in Stomach Area False True False NCIT:C1197 Pirarubicin False True False @@ -38803,7 +39202,7 @@ NCIT:C120308 Transdermal 17beta-Estradiol Gel BHR-200 False True False NCIT:C120309 Axicabtagene Ciloleucel False True False NCIT:C12031 EGFR Antisense DNA/Sargramostim False True False NCIT:C120310 CYP17 Lyase Inhibitor ASN001 False True False -NCIT:C120311 meta-Fluorine F 18 Fluorobenzylguanidine False True False +NCIT:C120311 Florbenguane F18 False True False NCIT:C120312 HDAC Inhibitor MPT0E028 False True False NCIT:C120313 S-equol False True False NCIT:C120314 Compound Kushen Injection False True False @@ -38858,7 +39257,7 @@ NCIT:C120358 Digit Span Backward Subtest (WISC-V) False True False NCIT:C120359 Digit Span Sequencing Subtest (WISC-V) False True False NCIT:C12036 Calcium Citrate/Cholecalciferol/Zoledronate False True False NCIT:C120360 Coding Subtest (WISC-V) False True False -NCIT:C120361 Vocabulary Subtest (WISC-V) False True False +NCIT:C120361 Vocabulary Subtest (WISC-V Subtest) False True False NCIT:C120362 Symbol Search Subtest (WISC-V) False True False NCIT:C120363 Coding Subtest (WAIS-IV) False True False NCIT:C120364 Block Design Subtest (WAIS-IV) False True False @@ -40397,7 +40796,7 @@ NCIT:C121841 Approved for Non-Human Use Product False True False NCIT:C121843 De Novo Classification Request False True False NCIT:C121847 NCPDP Dose Unit of Measure Terminology False True False NCIT:C121848 Autologous NSCLC Peptide-specific Dendritic Cell Vaccine False True False -NCIT:C121849 BET Inhibitor BMS-986158 False True False +NCIT:C121849 Ezobresib False True False NCIT:C12185 BMS-275291/Zoledronate False True False NCIT:C121850 Cetuximab Sarotalocan Sodium False True False NCIT:C121851 Cocoa Extract False True False @@ -40564,7 +40963,7 @@ NCIT:C122028 Rating of Perceived Exertion False True False NCIT:C122029 Warm-Up False True False NCIT:C12203 Cyclophosphamide/Dexamethasone/Doxorubicin/Rituximab/Vincristine False True False NCIT:C122030 Priming Exercise False True False -NCIT:C122031 Seated Row False True False +NCIT:C122031 Seated Rowing False True False NCIT:C122032 Chest Press False True False NCIT:C122033 Leg Press False True False NCIT:C122034 One Repetition Maximum False True False @@ -41385,7 +41784,6 @@ NCIT:C122828 Cyclin-Dependent Kinase 4 Inhibitor D False True False NCIT:C122829 WDFY2 Gene False True False NCIT:C122830 WDFY2 wt Allele False True False NCIT:C122831 WD Repeat and FYVE Domain-Containing Protein 2 False True False -NCIT:C122832 Vepoloxamer False True False NCIT:C122833 Anti-CD37 Monoclonal Antibody BI 836826 False True False NCIT:C122834 Selective Estrogen Receptor Degrader AZD9496 False True False NCIT:C122835 Inosine 5'-monophosphate Dehydrogenase Inhibitor FF-10501-01 False True False @@ -42678,7 +43076,7 @@ NCIT:C124113 BABAM1 wt Allele False True False NCIT:C124114 BRISC and BRCA1-A Complex Member 1 False True False NCIT:C124115 SLC3A2 Gene False True False NCIT:C124116 SLC3A2 wt Allele False True False -NCIT:C124117 4F2 Cell-Surface Antigen Heavy Chain False True False +NCIT:C124117 Amino Acid Transporter Heavy Chain SLC3A2 False True False NCIT:C124118 HOXC9 Gene False True False NCIT:C124119 HOXC9 wt Allele False True False NCIT:C12412 Testis False True False @@ -42796,7 +43194,7 @@ NCIT:C124222 Immunoglobulin Heavy Chain Diversity and Joining Region Gene Rearra NCIT:C124224 Pigmentary Change in Skin False True False NCIT:C124225 Cobomarsen False True False NCIT:C124226 Uzansertib False True False -NCIT:C124227 Anti-IL-8 Monoclonal Antibody BMS-986253 False True False +NCIT:C124227 Adakitug False True False NCIT:C124228 High Occupancy Target Region False True False NCIT:C124229 Bintrafusp Alfa False True False NCIT:C12423 Nasopharynx False True False @@ -43397,7 +43795,7 @@ NCIT:C124790 Oral Mucositis WHO Grade IV False True False NCIT:C124791 Antipneumocystis Agent False True False NCIT:C124792 Amphotericin Product False True False NCIT:C124793 SMO Gene Mutation False True False -NCIT:C124794 Extended Release Chewable Tablet False True False +NCIT:C124794 Extended Release Chewable Tablet Dosage Form False True False NCIT:C124795 Autologous CD19CAR-CD28-CD3zeta-EGFRt-expressing Tn/mem-enriched T-lymphocytes False True False NCIT:C124796 Darovasertib False True False NCIT:C124797 Carbon C 14 Lenvatinib Mesylate False True False @@ -44949,7 +45347,7 @@ NCIT:C126268 Over Ninety Activity Hours False True False NCIT:C126269 Iodine I 131 SGMIB-Anti-HER2 CAM-H2 False True False NCIT:C12627 Myelinated Nerve Fiber False True False NCIT:C126270 Autologous HBV-specific TCR-redirected T-Lymphocytes False True False -NCIT:C126271 PI3K p110beta/delta Inhibitor KA2237 False True False +NCIT:C126271 PI3K p110beta/delta Inhibitor CVL237 False True False NCIT:C126272 Fluorescence Imaging Agent EMI-137 False True False NCIT:C126274 Fuzuloparib False True False NCIT:C126275 Anti-LAMP1 Antibody-drug Conjugate SAR428926 False True False @@ -48346,7 +48744,7 @@ NCIT:C129706 IL2RA Positive False True False NCIT:C129708 Feel Self-Conscious About Letting Partner See My Breasts False True False NCIT:C129709 Liquid Component Present False True False NCIT:C12971 Breast False True False -NCIT:C129710 BTK Inhibitor M7583 False True False +NCIT:C129710 BTK Inhibitor TL-895 False True False NCIT:C129711 Botanical Agent LEAC-102 False True False NCIT:C129712 Etelcalcetide False True False NCIT:C129713 Gallium Ga 68 P15-041 False True False @@ -50795,7 +51193,7 @@ NCIT:C132153 WARS2 wt Allele False True False NCIT:C132154 Tryptophan-tRNA Ligase, Mitochondrial False True False NCIT:C132155 VSIG10L Gene False True False NCIT:C132156 VSIG10L wt Allele False True False -NCIT:C132157 V-Set and Immunoglobulin-Domain Containing Protein 10-Like False True False +NCIT:C132157 V-Set and Immunoglobulin Domain-Containing Protein 10-Like False True False NCIT:C132158 PCAT1 Gene False True False NCIT:C132159 PCAT1 wt Allele False True False NCIT:C13216 Human Chromosome 20 False True False @@ -51349,7 +51747,7 @@ NCIT:C132673 Unknown Primary Tumor pN3 TNM Finding v8 False True False NCIT:C132674 Unknown Primary Tumor pN3a TNM Finding v8 False True False NCIT:C132675 Unknown Primary Tumor pN3b TNM Finding v8 False True False NCIT:C13268 Nucleosome False True False -NCIT:C132681 Anti-CD40/Anti-TAA Bispecific Monoclonal Antibody ABBV-428 False True False +NCIT:C132681 Anti-CD40/Anti-mesothelin Bispecific Antibody ABBV-428 False True False NCIT:C132682 Lidocaine Hydrochloride Ophthalmic Gel False True False NCIT:C132683 Anti-LeY-CAR-transduced Autologous T-Lymphocytes False True False NCIT:C132684 H3.3K27M-specific Peptide Vaccine False True False @@ -52394,15 +52792,15 @@ NCIT:C13394 Myelogenous False True False NCIT:C133940 Temperature 40 (+/-) 2 Degrees C and Relative Humidity Not More Than 25% False True False NCIT:C13395 t(8;21)(q22;q22) False True False NCIT:C13396 Allogeneic Lymphocyte False True False -NCIT:C133961 Deliverable Volume/Fill Volume False True False +NCIT:C133961 Deliverable Volume/Fill Volume Test False True False NCIT:C133964 Heavy Metals/Elemental Impurities Analysis False True False NCIT:C13397 B-DNA False True False -NCIT:C133974 Crystallinity False True False -NCIT:C133975 Tablet Friability False True False -NCIT:C133979 Viscosity/Rheological Properties False True False +NCIT:C133974 Crystallinity Analysis False True False +NCIT:C133975 Tablet Friability Determination False True False +NCIT:C133979 Viscosity/Rheological Property Analysis False True False NCIT:C13398 Embryonic Fluid False True False NCIT:C133983 Pyrogenicity/Endotoxin Assessment False True False -NCIT:C133985 Redispersibility False True False +NCIT:C133985 Redispersibility Measurement False True False NCIT:C13399 All Sites False True False NCIT:C133990 Commercial Batch False True False NCIT:C133991 Development Batch False True False @@ -52415,7 +52813,7 @@ NCIT:C133997 Macromolecular CIF False True False NCIT:C133998 Does Not Conform False True False NCIT:C133999 Inverted False True False NCIT:C1340 Valrubicin False True False -NCIT:C13400 Anatomic Sites, Other False True False +NCIT:C13400 Other Anatomic Site False True False NCIT:C134000 Organic Impurity False True False NCIT:C134001 Inorganic Impurity False True False NCIT:C134002 Residual Solvent Test False True False @@ -52499,8 +52897,8 @@ NCIT:C13411 Unspecified Anatomic Sites False True False NCIT:C134110 Appendiceal Carcinoma pN2 TNM Finding v8 False True False NCIT:C134112 Sub-Visible Particulates False True False NCIT:C134113 Syringe Functionality Testing False True False -NCIT:C134114 Total Organic Carbon False True False -NCIT:C134115 Uniformity of Dosage Units False True False +NCIT:C134114 Total Organic Carbon Measurement False True False +NCIT:C134115 Uniformity of Dosage Units Analysis False True False NCIT:C134116 Water Content Determination False True False NCIT:C13412 V3 Loop False True False NCIT:C13413 Whole Organism False True False @@ -52563,28 +52961,28 @@ NCIT:C134246 System Suitability False True False NCIT:C134248 Analytical Procedure Quantitation Limit False True False NCIT:C134249 Container Closure Integrity Testing False True False NCIT:C13425 DNA Binding Domain False True False -NCIT:C134250 Content Uniformity False True False -NCIT:C134252 Pharmaceutical Disintegration False True False -NCIT:C134253 Pharmaceutical Dissolution False True False -NCIT:C134254 Impurities/Degradation Products/Related Substances Assessment False True False -NCIT:C134255 Loss on Drying False True False -NCIT:C134256 Microbial Limit False True False -NCIT:C134257 Particle Size Distribution False True False +NCIT:C134250 Content Uniformity Test False True False +NCIT:C134252 Pharmaceutical Disintegration Test False True False +NCIT:C134253 Pharmaceutical Dissolution Test False True False +NCIT:C134254 Impurities/Degradation Products/Related Substances Test False True False +NCIT:C134255 Loss on Drying Measurement False True False +NCIT:C134256 Microbial Limit Determination False True False +NCIT:C134257 Particle Size Distribution Analysis False True False NCIT:C134259 Physicochemical Property Analysis False True False NCIT:C13426 Protein Binding Domain False True False -NCIT:C134260 Powder Bulk Density False True False -NCIT:C134261 Clarity of Solution False True False -NCIT:C134262 Color of Solution False True False -NCIT:C134263 Conductivity False True False -NCIT:C134264 Hardness False True False -NCIT:C134265 Tablet Properties False True False -NCIT:C134266 Tap Density False True False -NCIT:C134267 Plume Geometry False True False +NCIT:C134260 Powder Bulk Density Measurement False True False +NCIT:C134261 Clarity of Solution Measurement False True False +NCIT:C134262 Color of Solution Measurement False True False +NCIT:C134263 Conductivity Measurement False True False +NCIT:C134264 Hardness Measurement False True False +NCIT:C134265 Tablet Property Analysis False True False +NCIT:C134266 Tap Density Determination False True False +NCIT:C134267 Plume Geometry Test False True False NCIT:C134269 Polymorphic Form Determination False True False NCIT:C13427 Zinc-Binding, DNA-Binding Motif False True False NCIT:C134270 Potency Assay False True False -NCIT:C134272 Reconstitution Time False True False -NCIT:C134276 Residue on Ignition False True False +NCIT:C134272 Reconstitution Time Measurement False True False +NCIT:C134276 Residue on Ignition Measurement False True False NCIT:C134277 Spray Pattern Assessment False True False NCIT:C134278 Sterility Test False True False NCIT:C134279 Sub-Visible Particle False True False @@ -54920,7 +55318,7 @@ NCIT:C137818 Androgen Receptor Antagonist TAS3681 False True False NCIT:C137819 Allogeneic CD19-specific Universal CAR19-expressing T-lymphocytes False True False NCIT:C13782 14q11.2 False True False NCIT:C137820 Anti-TIM3 Monoclonal Antibody LY3321367 False True False -NCIT:C137821 Antibody-drug Conjugate MEDI7247 False True False +NCIT:C137821 Anti-ASCT2 Antibody-drug Conjugate MEDI7247 False True False NCIT:C137822 Zirconium Zr 89 Crefmirlimab Berdoxam False True False NCIT:C137823 Personalized Live-attenuated Double-deleted Listeria monocytogenes False True False NCIT:C137824 Leronlimab False True False @@ -54950,7 +55348,7 @@ NCIT:C137847 Current Difficulty Learning New Tasks or Instructions False True Fa NCIT:C137848 Central Lumpectomy with Resection of the Nipple-Areolar Complex False True False NCIT:C137849 Biopsy of Nipple and Areola False True False NCIT:C13785 1p22 False True False -NCIT:C137850 Full-thickness Skin Biopsy of Nipple and Areola False True False +NCIT:C137850 Full-Thickness Skin Biopsy of Nipple and Areola False True False NCIT:C137851 Core Biopsy of Breast False True False NCIT:C137852 Palpation Finding False True False NCIT:C137853 Largest Dimension of Residual Neoplasm False True False @@ -56166,10 +56564,10 @@ NCIT:C138987 Nottingham Grade 1 False True False NCIT:C138988 Nottingham Grade 2 False True False NCIT:C138989 Nottingham Grade 3 False True False NCIT:C13899 1q32.2 False True False -NCIT:C138990 Product Description/Appearance False True False +NCIT:C138990 Product Description/Appearance Assessment False True False NCIT:C138991 Flumbatinib False True False NCIT:C138992 Homogeneity Assessment False True False -NCIT:C138993 Material Identification False True False +NCIT:C138993 Material Identification Test False True False NCIT:C138994 Copanlisib Hydrochloride False True False NCIT:C138995 Capmatinib Hydrochloride False True False NCIT:C138996 Icotinib False True False @@ -63985,7 +64383,6 @@ NCIT:C147308 Beta-2 Glycoprotein 1 IgA Antibody Measurement False True False NCIT:C147309 Base Deficit False True False NCIT:C147310 Borrelia burgdorferi IgG and IgM Antibody Measurement False True False NCIT:C147311 Basophilic Erythroblast Count False True False -NCIT:C147312 Blasts to Nucleated Cells Ratio Measurement False True False NCIT:C147313 Complement C1 Esterase Inhibitor Measurement False True False NCIT:C147314 Calcium Corrected for Total Protein Measurement False True False NCIT:C147315 Chemokine (C-C Motif) Ligand 21 Measurement False True False @@ -66212,7 +66609,7 @@ NCIT:C150378 Autologous Anti-CD19 CAR TCR-zeta/4-1BB-transduced T Lymphocytes Bi NCIT:C150379 Candida albicans Antigen Injection False True False NCIT:C150380 East Indian Sandalwood Oil Cream False True False NCIT:C150381 CMV/EBV/ADV/BKV-specific Cytotoxic T Lymphocytes False True False -NCIT:C150382 Autologous Anti-Claudin18.2-transduced T Lymphocytes CT041 False True False +NCIT:C150382 Satricabtagene Autoleucel False True False NCIT:C150383 FGFR1/2/3 Inhibitor HMPL-453 False True False NCIT:C150384 Vandetanib-eluting Radiopaque Bead BTG-002814 False True False NCIT:C150385 Ecological Momentary Assessment False True False @@ -66365,7 +66762,7 @@ NCIT:C150583 FANCA Biallelic Inactivation False True False NCIT:C150584 ATM Monoallelic Inactivation False True False NCIT:C150585 TAM/c-Met Inhibitor RXDX-106 False True False NCIT:C150586 CAR T-Cells AMG 119 False True False -NCIT:C150587 Complete Remission with Incomplete Hematological Recovery False True False +NCIT:C150587 Complete Remission in Leukemia with Incomplete Hematologic Recovery False True False NCIT:C150590 Serclutamab Talirine False True False NCIT:C150596 Hepatic Steatosis False True False NCIT:C150599 MECOM Positive False True False @@ -68560,9 +68957,9 @@ NCIT:C153271 RSPO Gene Fusion Positive False True False NCIT:C153272 TFE3 Gene Translocation False True False NCIT:C153273 TFEB Gene Translocation False True False NCIT:C153274 DNMT3 Family False True False -NCIT:C153275 TDGF1 Gene False True False -NCIT:C153276 TDGF1 wt Allele False True False -NCIT:C153277 Teratocarcinoma-Derived Growth Factor 1 False True False +NCIT:C153275 CRIPTO Gene False True False +NCIT:C153276 CRIPTO wt Allele False True False +NCIT:C153277 Protein Cripto False True False NCIT:C15328 Splenectomy False True False NCIT:C153280 FCN2 Gene False True False NCIT:C153281 FCN2 wt Allele False True False @@ -68635,7 +69032,7 @@ NCIT:C153369 Global Registration Identifier for Donors False True False NCIT:C15337 Thoracotomy False True False NCIT:C153370 Metastatic Soft Tissue Sarcoma, Excluding Liposarcoma False True False NCIT:C153371 Locally Advanced Soft Tissue Sarcoma, Excluding Liposarcoma False True False -NCIT:C153372 Oxidative Phosphorylation Inhibitor IM156 False True False +NCIT:C153372 Lixumistat Acetate False True False NCIT:C153373 Elagolix False True False NCIT:C153374 Helicobacter pylori Therapeutic Vaccine IMX101 False True False NCIT:C153375 Nidanilimab False True False @@ -68876,7 +69273,7 @@ NCIT:C153627 Suspension for Injection in Multidose Container Dosage Form False T NCIT:C15364 Managed Care False True False NCIT:C15365 Outcomes Research False True False NCIT:C15366 Platelet Transfusion False True False -NCIT:C15367 Risk Assessment False True False +NCIT:C15367 Health Risk Assessment False True False NCIT:C15369 Allogeneic Bone Marrow Transplantation False True False NCIT:C1537 Bruceanol F False True False NCIT:C15370 Steroid Therapy False True False @@ -69237,7 +69634,6 @@ NCIT:C154136 Bone Marrow Stromal Antigen 2 False True False NCIT:C154137 BST2 Positive False True False NCIT:C154138 Type-Specific HPV Antibody False True False NCIT:C154139 CCND1/IGHG1 Fusion Negative False True False -NCIT:C15414 ADCC Assay False True False NCIT:C154140 Myeloblasts 5 Percent or Less of Bone Marrow Nucleated Cells False True False NCIT:C154141 Sukuma Language False True False NCIT:C154142 Sundanese Language False True False @@ -69477,7 +69873,7 @@ NCIT:C154418 Month Imputed False True False NCIT:C154419 Genderqueer False True False NCIT:C15442 Interleukin-2/Zidovudine False True False NCIT:C154420 Other Gender False True False -NCIT:C154421 Transgender False True False +NCIT:C154421 Transgender Identity False True False NCIT:C154422 Insurance Claim False True False NCIT:C154423 Unable to Classify False True False NCIT:C154424 Adult Foster Home False True False @@ -70870,7 +71266,7 @@ NCIT:C155964 Submucosal 2 Invasion False True False NCIT:C155965 Submucosal 3 Invasion False True False NCIT:C155966 Survey of Autonomic Symptoms False True False NCIT:C155967 Alsevalimab False True False -NCIT:C155968 Carbon C 14-TAK-659 False True False +NCIT:C155968 Carbon C 14 Mivavotinib Citrate False True False NCIT:C155969 Total Tumor mRNA-pulsed Tumor-specific Ex vivo-expanded Autologous Lymphocyte Transfer Cells False True False NCIT:C15597 Incomplete Freund's Adjuvant/Interleukin-12/MART-1 Antigen False True False NCIT:C155970 Anti-CD33/CD3 Bispecific Antibody GEM 333 False True False @@ -70942,7 +71338,6 @@ NCIT:C156048 Inactivating SETD2 Gene Mutation False True False NCIT:C156049 TP53 Negative False True False NCIT:C15605 Nutrition, Trace Elements False True False NCIT:C156051 MTAP Negative False True False -NCIT:C156052 BCMA x CD3 T-cell Engaging Antibody CC-93269 False True False NCIT:C156053 Cabazitaxel/Prednisone Regimen False True False NCIT:C156054 Human Papillomavirus-63 False True False NCIT:C156055 Human Papillomavirus-70 False True False @@ -71516,7 +71911,7 @@ NCIT:C156698 Rhenium Re-188 Etidronate False True False NCIT:C1567 Strontium Sr-89 False True False NCIT:C15670 Thermal Ablation Therapy False True False NCIT:C156700 Gumarontinib False True False -NCIT:C156701 Porcupine Inhibitor RXC004 False True False +NCIT:C156701 Zamaporvint False True False NCIT:C156702 Para-toluenesulfonamide False True False NCIT:C156703 Fine Motor Skills False True False NCIT:C156705 Runimotamab False True False @@ -71549,7 +71944,7 @@ NCIT:C156740 Murizatoclax False True False NCIT:C156741 Manelimab False True False NCIT:C156742 Carbon C 11-osimertinib False True False NCIT:C156743 EZH2 Inhibitor PF-06821497 False True False -NCIT:C156744 CYP11A1 inhibitor ODM-208 False True False +NCIT:C156744 Opevesostat False True False NCIT:C156747 AssureMDx False True False NCIT:C156748 Millimeter-Wave Holographic Imaging False True False NCIT:C156749 Melanoma Risk Factor False True False @@ -73298,7 +73693,7 @@ NCIT:C15853 Repository Operation, Serum False True False NCIT:C158530 Reticulon-4 Receptor-Like 1 False True False NCIT:C158531 Immunodeficiency with Hyper-IgM, X-Linked, Type 1 False True False NCIT:C158532 PD-L1 Inhibitor INCB086550 False True False -NCIT:C158533 Autologous CAR-mbIL15-Safety Switch T-cells PRGN-3005 False True False +NCIT:C158533 Autologous Anti-MUC16 CAR-mbIL15-Safety Switch T-cells PRGN-3005 False True False NCIT:C158534 RUNDC1 Gene False True False NCIT:C158535 RUNDC1 wt Allele False True False NCIT:C158536 RUN Domain-Containing Protein 1 False True False @@ -73867,7 +74262,6 @@ NCIT:C15925 Nutrition, Alcohol False True False NCIT:C159253 Specify If Other Studies False True False NCIT:C159254 Palms of Hands and Soles of Feet False True False NCIT:C159255 Specify Other KIT Mutation False True False -NCIT:C159256 Specimen Source Site False True False NCIT:C159257 Was Interferon Gamma Treatment Administered Prior to Specimen Resection False True False NCIT:C159258 Was Interferon Gamma Treatment Administered 90 Days Prior to Specimen Resection False True False NCIT:C159259 SNCB Gene False True False @@ -75537,7 +75931,7 @@ NCIT:C160843 Interferon Gamma Treatment was not Administered 90 Days Prior to Sp NCIT:C160844 Interferon Gamma Treatment Administration 90 Days Prior to Specimen Resection Unknown False True False NCIT:C160845 Are Sarcomatoid Features Present False True False NCIT:C160846 Sarcomatoid Features Absent False True False -NCIT:C160847 Autologous CAR-mbIL15-Safety Switch T-cells PRGN-3006 False True False +NCIT:C160847 Autologous Anti-CD33 CAR-mbIL15-Safety Switch T-cells PRGN-3006 False True False NCIT:C160849 Predominantly Fatty Breast False True False NCIT:C16085 Basic Cancer Research False True False NCIT:C160850 Breast Scattered Fibroglandular Densities False True False @@ -75623,8 +76017,8 @@ NCIT:C160937 Beta-lactamase Negative Bacteria Measurement False True False NCIT:C160938 Latex Safety Information False True False NCIT:C160939 Implantable Device Status False True False NCIT:C16094 Cardiac Function Study False True False -NCIT:C160940 Gender Fluid False True False -NCIT:C160941 Gender Variant False True False +NCIT:C160940 Gender Fluid Identity False True False +NCIT:C160941 Non-Binary Gender False True False NCIT:C160942 Reduced Device Function False True False NCIT:C160943 Device Status False True False NCIT:C160944 Reported in Error False True False @@ -76041,7 +76435,7 @@ NCIT:C161595 Encorafenib-Binimetinib-Cetuximab Regimen False True False NCIT:C161596 Encorafenib-Binimetinib-Panitumumab Regimen False True False NCIT:C161597 Zeluvalimab False True False NCIT:C161598 Zanzalintinib False True False -NCIT:C161599 Antibody-drug Conjugate ABBV-011 False True False +NCIT:C161599 Anti-SEZ6 Antibody-drug Conjugate ABBV-011 False True False NCIT:C1616 Lavendustin B False True False NCIT:C16160 Genetic Population Study False True False NCIT:C161600 Bio-enhanced Curcumin Extract Formulation False True False @@ -76469,7 +76863,7 @@ NCIT:C162007 Functional Tests Group Identifier False True False NCIT:C162008 Meal Data Group Identifier False True False NCIT:C162009 Musculoskeletal Findings, Connective and Soft Tissue Findings Group Identifier False True False NCIT:C16201 Hematopoietic Stem Cell Research False True False -NCIT:C162010 ITK Inhibitor CPI-818 False True False +NCIT:C162010 Soquelitinib False True False NCIT:C162011 Nervous System Findings Group Identifier False True False NCIT:C162012 Ophthalmic Examinations Group Identifier False True False NCIT:C162013 Procedure Agents Group Identifier False True False @@ -76937,7 +77331,7 @@ NCIT:C162530 cobas MPX Test False True False NCIT:C162532 Tinengotinib False True False NCIT:C162533 Src Kinase Inhibitor AP 23846 False True False NCIT:C162534 Abdominal Surgery Patient False True False -NCIT:C162535 IAP Inhibitor APG-1387 False True False +NCIT:C162535 Dasminapant False True False NCIT:C162537 Lorukafusp alfa False True False NCIT:C16254 Estradiol 17-Beta-Dehydrogenase 2 False True False NCIT:C162540 Aranose False True False @@ -77049,7 +77443,7 @@ NCIT:C162682 IPSS-R Risk Category Intermediate False True False NCIT:C162683 IPSS-R Risk Category High False True False NCIT:C162684 IPSS-R Risk Category Very High False True False NCIT:C162685 Low Nicotine Content Cigarette False True False -NCIT:C162686 Virus-Associated Hemophagocytic Syndrome False True False +NCIT:C162686 Virus-Related Hemophagocytic Lymphohistiocytosis False True False NCIT:C162687 Severe Chronic Active EBV Infection False True False NCIT:C16269 Aging False True False NCIT:C162690 Slide ID Examined by Pathologist False True False @@ -77311,11 +77705,11 @@ NCIT:C162978 H2BC18 Gene False True False NCIT:C162979 H2BC18 wt Allele False True False NCIT:C16298 Antibody-Dependent Cellular Cytotoxicity False True False NCIT:C162980 Histone H2B Type 2-F False True False -NCIT:C162981 H2AW Gene False True False -NCIT:C162982 H2AW wt Allele False True False +NCIT:C162981 H2AC25 Gene False True False +NCIT:C162982 H2AC25 wt Allele False True False NCIT:C162984 Histone H2A Type 3 False True False -NCIT:C162985 H2BU1 Gene False True False -NCIT:C162986 H2BU1 wt Allele False True False +NCIT:C162985 H2BC26 Gene False True False +NCIT:C162986 H2BC26 wt Allele False True False NCIT:C162987 Histone H2B Type 3-B False True False NCIT:C162989 INC Demographic and Maternal Terminology False True False NCIT:C16299 Negative Regulation of Coagulation False True False @@ -78048,7 +78442,7 @@ NCIT:C163984 Montreal Cognitive Assessment, Version 8.3 False True False NCIT:C163985 Avotaciclib False True False NCIT:C163986 Hybrid Selected Genomic Library False True False NCIT:C163987 Affinity Enriched Genomic Library False True False -NCIT:C163988 Poly-T Enriched Genomic Library False True False +NCIT:C163988 Poly-A Enriched Genomic Library False True False NCIT:C163989 Randomly Selected Genomic Library False True False NCIT:C16399 Cell Differentiation Process False True False NCIT:C163990 rRNA Depleted Genomic Library False True False @@ -78906,7 +79300,7 @@ NCIT:C164811 Genetic Reference Sequence Identifier False True False NCIT:C164812 Genetic Reference Value False True False NCIT:C164813 Genetic Variation Identifier False True False NCIT:C164814 Genome Assembly Source False True False -NCIT:C164815 Genome Assembly Version False True False +NCIT:C164815 Reference Genome Assembly Version False True False NCIT:C164816 Government Funding Category Code False True False NCIT:C164817 Government Funding NCI Program Code False True False NCIT:C164818 Healthcare Provider Role Code False True False @@ -80482,7 +80876,7 @@ NCIT:C166402 Uniformly-labeled [13C]fructose False True False NCIT:C166403 Cemiplimab Regimen False True False NCIT:C166407 Cyclin Gene Mutation False True False NCIT:C166408 Chromosome Arm 19q Loss of Heterozygosity False True False -NCIT:C166409 Anti-TROP2 Antibody-drug Conjugate SKB264 False True False +NCIT:C166409 Sacituzumab Tirumotecan False True False NCIT:C16641 Glutathione S-Transferase False True False NCIT:C166410 KRAS G12C Inhibitor LY3499446 False True False NCIT:C166411 NCSTN Gene Mutation False True False @@ -81287,7 +81681,7 @@ NCIT:C167153 PA2G4 wt Allele False True False NCIT:C167154 Proliferation-Associated Protein 2G4 False True False NCIT:C167155 Blasts 2 Percent or More of Bone Marrow Nucleated Cells False True False NCIT:C167156 Quemliclustat False True False -NCIT:C167157 KRASG12C Inhibitor JNJ-74699157 False True False +NCIT:C167157 KRAS G12C Inhibitor JNJ-74699157 False True False NCIT:C167158 FLT3 NM_004119.2:c.2039C>T False True False NCIT:C167159 FLT3 NP_004110.2:p.A690V False True False NCIT:C16716 Idiotype False True False @@ -81339,7 +81733,7 @@ NCIT:C167206 Dalutrafusp Alfa False True False NCIT:C167207 Partially Engineered T-regulatory Cell Donor Graft TRGFT-201 False True False NCIT:C167208 Autologous Peripheral Blood Lymphocytes from Ibrutinib-treated Chronic Lymphocytic Leukemia Patients IOV-2001 False True False NCIT:C167209 Measurable Lesion False True False -NCIT:C167210 RET/SRC Inhibitor TPX-0046 False True False +NCIT:C167210 Enbezotinib False True False NCIT:C167211 Gastrectomy Patient False True False NCIT:C167212 Phytate Persodium False True False NCIT:C167213 Robotic Bariatric Sleeve Gastrectomy False True False @@ -82191,7 +82585,7 @@ NCIT:C168577 Marrow Fibrosis Grade 1 False True False NCIT:C168578 Marrow Fibrosis Grade 2 False True False NCIT:C168579 Marrow Fibrosis Grade 3 False True False NCIT:C16858 Polarization Microscopy False True False -NCIT:C168580 Bispecific Antibody AMG 509 False True False +NCIT:C168580 Xaluritamig False True False NCIT:C168581 Liver Fibrosis False True False NCIT:C168582 Steroid Resistant Acute Graft Versus Host Disease False True False NCIT:C168586 Asparagine Synthetase Deficiency False True False @@ -82210,7 +82604,7 @@ NCIT:C1686 ZD2767 False True False NCIT:C16860 Epoxide Hydrolase 1 False True False NCIT:C168600 Anti-PD-1/CD47 Infusion Protein HX009 False True False NCIT:C168601 Senaparib False True False -NCIT:C168603 Anti-LAG-3 Monoclonal Antibody IBI-110 False True False +NCIT:C168603 Negalstobart False True False NCIT:C168604 Tecaginlimab False True False NCIT:C168605 Recombinant Human Papillomavirus 11-valent Vaccine False True False NCIT:C168606 Selective Estrogen Receptor Degrader LX-039 False True False @@ -82228,7 +82622,7 @@ NCIT:C168619 IDH2 inhibitor False True False NCIT:C16862 Microwave Radiation False True False NCIT:C168622 PQ/CMC Strength Operator Terminology False True False NCIT:C168623 Specify Other Adverse Event False True False -NCIT:C168624 PQ/CMC Sponsor Identifier Type Terminology False True False +NCIT:C168624 PQ/CMC Organization-Site Identifier Type Terminology False True False NCIT:C168625 Best Overall Response Registered from Start of Therapy to a Time Point of Interest False True False NCIT:C168626 Best Secondary Endpoint Response Registered from Start of Therapy to a Time Point of Interest False True False NCIT:C168627 PQ/CMC Strength Type Terminology False True False @@ -82406,7 +82800,7 @@ NCIT:C168840 Chemotherapy Course 5 False True False NCIT:C168841 Chemotherapy Course 6 False True False NCIT:C168842 European Society for Blood and Marrow Transplantation False True False NCIT:C168843 Age in Days at Enrollment False True False -NCIT:C168844 Age in Days at Last Known Survival False True False +NCIT:C168844 Age in Days at Last Known Survival Status False True False NCIT:C168845 Age in Days at Vitals False True False NCIT:C168846 Age in Days at Blood Analysis False True False NCIT:C168847 Age in Days at Lumbar Puncture False True False @@ -83426,7 +83820,7 @@ NCIT:C170394 VOLULORIDE False True False NCIT:C170395 Ziresovir False True False NCIT:C170396 Ziritaxestat False True False NCIT:C170397 Formal Search False True False -NCIT:C170398 Preliminary Search False True False +NCIT:C170398 Preliminary Donor Registry Search False True False NCIT:C170399 Blasts 6 Percent or More of Bone Marrow Nucleated Cells False True False NCIT:C1704 Nelarabine False True False NCIT:C17040 Public Health Nursing False True False @@ -83877,7 +84271,7 @@ NCIT:C170897 Primary Medical Oncologist False True False NCIT:C170898 Primary Referring Physician False True False NCIT:C170899 Autologous Blinatumomab-expanded T-Cells False True False NCIT:C1709 Particulate False True False -NCIT:C17090 Research Support False True False +NCIT:C17090 Research Funding False True False NCIT:C170900 PD-L1 Inhibitor GS-4224 False True False NCIT:C170903 Anti-CD19 iCAR NK Cells False True False NCIT:C170904 Anti-CD19/CD22 CAR NK Cells False True False @@ -84068,7 +84462,7 @@ NCIT:C171166 EchoMark False True False NCIT:C171167 Autologous Anti-CD123 CAR-T Cells False True False NCIT:C17117 Saudi Arabia False True False NCIT:C171172 Tracheoscopy False True False -NCIT:C171173 Xisomab 3G3 False True False +NCIT:C171173 Gruticibart False True False NCIT:C171174 Cannabis Use Disorder False True False NCIT:C171175 Delins Mutation False True False NCIT:C171176 Nucleic Acid Aliquot False True False @@ -84178,7 +84572,7 @@ NCIT:C171273 Gene Symbol of Target in Immunohistochemistry Assay False True Fals NCIT:C171274 Median Absolute Percentage Deviation False True False NCIT:C171275 Copy Number Median Absolute Percentage Deviation False True False NCIT:C171276 MD5 Checksum False True False -NCIT:C171277 Nucleic Acid Concentration False True False +NCIT:C171277 Nucleic Acid Concentration Measurement False True False NCIT:C171278 Nucleic Acid Sample Type Indicator False True False NCIT:C171279 Aliquot Volume False True False NCIT:C17128 Sex Hormone-Binding Globulin False True False @@ -84257,7 +84651,7 @@ NCIT:C171367 NEWS2 - NEWS Total False True False NCIT:C171368 NEWS2 - Monitoring Frequency False True False NCIT:C171369 NEWS2 - Escalation of Care False True False NCIT:C17137 Skin Test False True False -NCIT:C171370 Copper Cu 67 Tyr3-octreotate False True False +NCIT:C171370 Copper Cu 67 Ucasareotide Dasaroxetan False True False NCIT:C171371 Genetically Modified Interleukin-12 Transgene-encoding Bifidobacterium longum False True False NCIT:C171372 IRDye800-labeled Heterodimeric Peptide KSP-QRH 919288G False True False NCIT:C171374 Cationic Peptide Cream Cypep-1 False True False @@ -84325,7 +84719,7 @@ NCIT:C171431 Cetuximab/Docetaxel Regimen False True False NCIT:C171432 Eligibility for Post-Operative Systemic Therapy False True False NCIT:C171433 Treatment Performed at Study Site Indicator False True False NCIT:C171434 Treatment Performed in Measurable Residual Disease Indicator False True False -NCIT:C171435 Sample Anatomic Site False True False +NCIT:C171435 Specimen Anatomic Site False True False NCIT:C171436 Sample Pathology Indicator False True False NCIT:C171437 ICDC Summarized Sample Type Indicator False True False NCIT:C171438 Tumor Sample Origin Indicator False True False @@ -84395,7 +84789,6 @@ NCIT:C171536 Telemedicine Visit False True False NCIT:C171537 Telephone Call False True False NCIT:C171538 Endogenous Cushing Syndrome False True False NCIT:C171539 Recurrent Endogenous Cushing Syndrome False True False -NCIT:C17154 Surgical Specialty False True False NCIT:C171540 Oncolytic Herpes Simplex Virus-1 ONCR-177 False True False NCIT:C171541 Exlinkibart False True False NCIT:C171542 Food Insecurity False True False @@ -85210,7 +85603,7 @@ NCIT:C172386 Autologous Nectin-4/FAP-targeted CAR-T Cells False True False NCIT:C172387 Autologous CD19/PD-1 Bispecific CAR-T Cells False True False NCIT:C172388 Trastuzumab Imbotolimod False True False NCIT:C172389 Metastatic Site Code False True False -NCIT:C17239 Veterans Administration False True False +NCIT:C17239 Department of Veterans Affairs False True False NCIT:C172390 CDK7 Inhibitor SY-5609 False True False NCIT:C172391 Anti-integrin Beta-6/MMAE Antibody-drug Conjugate SGN-B6A False True False NCIT:C172394 Boditrectinib False True False @@ -85498,7 +85891,7 @@ NCIT:C172697 Age in Days at Start of Transfusion Procedure False True False NCIT:C172698 Age in Days at Start of Total Dose Calculation False True False NCIT:C1727 Perifosine False True False NCIT:C17270 Phosphatidylinositol-4,5-Bisphosphate 3-Kinase False True False -NCIT:C172708 Allogeneic Anti-CD19 CAR T-cells ALLO-501A False True False +NCIT:C172708 Cemacabtagene Ansegedleucel False True False NCIT:C17271 Amino Acid Transporter False True False NCIT:C172711 Abrupt Nuclear Anaplasia False True False NCIT:C172715 Focus of Carcinoma Cells Measuring Equal to or Less Than 2 cm Present False True False @@ -85582,7 +85975,6 @@ NCIT:C172801 Translational Motion Component False True False NCIT:C172802 Posoleucel False True False NCIT:C172805 ERK1/2 Inhibitor HH2710 False True False NCIT:C172807 X-Linked Protoporphyria False True False -NCIT:C172809 Tyrosine Kinase Inhibitor TL-895 False True False NCIT:C17281 Tumor Necrosis Factor Receptor Superfamily Member 5 False True False NCIT:C172816 HIV-1 Protease Inhibitor ASC09/Ritonavir False True False NCIT:C172817 Anti-CD7 CAR T-cells False True False @@ -85661,7 +86053,7 @@ NCIT:C172896 Worry that Breast Cancer Recurrence Would Interfere with Physical A NCIT:C172897 Worry that Breast Cancer Recurrence Would Threaten my Life False True False NCIT:C172898 Worry that Breast Cancer Recurrence Would Harm Self-Confidence False True False NCIT:C172899 Worry that Breast Cancer Recurrence Would be More Serious than First Diagnosis False True False -NCIT:C1729 CT2584 HMS False True False +NCIT:C1729 CT2584 False True False NCIT:C17290 Dihydropyrimidine Dehydrogenase [NADP(+)] False True False NCIT:C172900 Worry that Breast Cancer Recurrence Would Cause Financial Problems False True False NCIT:C172901 Worry that Breast Cancer Recurrence Would Interfere with Sense of Sexuality False True False @@ -85689,7 +86081,7 @@ NCIT:C172920 Thought Likert Scale False True False NCIT:C172921 Upset Likert Scale False True False NCIT:C172922 Worry Likert Scale False True False NCIT:C172923 Fear Likert Scale False True False -NCIT:C172924 Anti-Ribonucleoprotein Antibody ATRC-101 False True False +NCIT:C172924 Alextatug False True False NCIT:C172925 Gastro-resistant Oral Suspension Dosage Form False True False NCIT:C172926 Prolonged-release Oral Suspension Dosage Form False True False NCIT:C172927 Right Ventricular Assist Device Insertion False True False @@ -85885,7 +86277,7 @@ NCIT:C173158 Disease Free False True False NCIT:C173159 Extremity Question False True False NCIT:C17316 DBL Oncoprotein False True False NCIT:C173160 Feelings Question False True False -NCIT:C173165 EGFR/TGFb Fusion Monoclonal Antibody BCA101 False True False +NCIT:C173165 Ficerafusp Alfa False True False NCIT:C173167 Sinonasal Chondromesenchymal Hamartoma False True False NCIT:C173168 Ketogenic Diet False True False NCIT:C17317 Regulatory Protein E2, Human Papillomavirus Type 16 False True False @@ -86039,7 +86431,7 @@ NCIT:C173370 TGF-beta Receptor 1 Kinase Inhibitor SH3051 False True False NCIT:C173371 Interleukin-12-Fc Fusion Protein DF6002 False True False NCIT:C173372 Gallium Ga 68-labeled DX600 False True False NCIT:C173373 Ruthenium-based Small Molecule Therapeutic BOLD-100 False True False -NCIT:C173374 Androgen Receptor Inhibitor EPI-7386 False True False +NCIT:C173374 Masofaniten False True False NCIT:C173377 Dazostinag Disodium False True False NCIT:C173378 Autologous Anti-ICAM-1-CAR-CD28-4-1BB-CD3zeta-expressing T-cells AIC100 False True False NCIT:C17338 Tenascin False True False @@ -86167,7 +86559,6 @@ NCIT:C173527 Environmental Agent False True False NCIT:C173528 Indwelling Central Venous Catheter False True False NCIT:C17353 Fluorescence Activated Cell Sorting False True False NCIT:C173535 Heat-treated bacterium Mycobacterium obuense IMM-101 False True False -NCIT:C173536 Bcl-2 Inhibitor LP-108 False True False NCIT:C173537 Absolute Reticulocyte Count False True False NCIT:C173538 Gallium Ga 68-DOTA-FAPI-04 False True False NCIT:C173539 Tobemstomig False True False @@ -86371,7 +86762,6 @@ NCIT:C173791 Breast Question False True False NCIT:C173792 Satisfaction Question False True False NCIT:C173794 Non-Neoplastic Tongue Disorder False True False NCIT:C173796 Non-Neoplastic Gingival Disorder False True False -NCIT:C173798 Non-Neoplastic Tonsillar Disorder False True False NCIT:C17380 NF-kB False True False NCIT:C173800 Non-Neoplastic Appendix Disorder False True False NCIT:C173801 C3 Complement Inhibitor AMY-101 False True False @@ -86599,7 +86989,7 @@ NCIT:C174057 Anti-CD38 Antibody-drug Conjugate STI-6129 False True False NCIT:C174058 Unobtainable False True False NCIT:C174059 Anti-interleukin-2 Receptor Subunit Gamma Monoclonal Antibody REGN7257 False True False NCIT:C17406 Endoglin False True False -NCIT:C174060 Tankyrase Inhibitor STP1002 False True False +NCIT:C174060 Basroparib False True False NCIT:C174061 Rett Syndrome Severity Scale Clinical Classification False True False NCIT:C174062 Short Form 8 Health Survey Standard, US Version 1.0 Questionnaire False True False NCIT:C174063 Short Form 8 Health Survey Acute, US Version 1.0 Questionnaire False True False @@ -86714,7 +87104,7 @@ NCIT:C174164 Perceived Compatibility with Current Clinical Practice False True F NCIT:C174165 Biallelic MUTYH Gene Mutation False True False NCIT:C174166 ERCC Family Gene False True False NCIT:C174168 ERCC Family Gene Mutation False True False -NCIT:C174169 C/EBP Beta Antagonist ST101 False True False +NCIT:C174169 Lucicebtide False True False NCIT:C17417 RNA Helicase False True False NCIT:C174170 FEN1 Gene Mutation False True False NCIT:C174171 SIRPa-4-1BBL Fusion Protein DSP107 False True False @@ -87015,7 +87405,7 @@ NCIT:C174464 DUX4L10 Gene False True False NCIT:C174465 t(2;16)(q35;p11) False True False NCIT:C174466 FUS/FEV Fusion Gene False True False NCIT:C174467 FUS/FEV Fusion Protein False True False -NCIT:C174469 Copper Cu 64-MeCOSar-Tyr3-octreotate False True False +NCIT:C174469 Copper Cu 64 Ucasareotide Dasaroxetan False True False NCIT:C174470 KLF17 Gene False True False NCIT:C174471 KLF17 wt Allele False True False NCIT:C174472 Krueppel-Like Factor 17 False True False @@ -87818,7 +88208,7 @@ NCIT:C175247 Supplemental Data File False True False NCIT:C175249 Diseased False True False NCIT:C17525 Prostate-Specific Antigen False True False NCIT:C175250 Biospecimen Collection Chronology False True False -NCIT:C175251 CDK2 Inhibitor PF-07104091 False True False +NCIT:C175251 Tagtociclib False True False NCIT:C175252 Arm or Leg Response Group Answer False True False NCIT:C175253 Percent of Time Answer False True False NCIT:C175254 Pain Score Answer False True False @@ -88033,7 +88423,7 @@ NCIT:C175509 Deupirfenidone False True False NCIT:C17551 Advocacy False True False NCIT:C175510 TAEK-VAC-HerBy Vaccine False True False NCIT:C175511 Autologous Anti-PSMA CAR-T Cells P-PSMA-101 False True False -NCIT:C175512 SRPK1/ABCG2 Inhibitor SCO-101 False True False +NCIT:C175512 Emidurdar False True False NCIT:C175513 Eliapixant False True False NCIT:C175514 Quercetin/Saw Palmetto/Cranberry/Bromelain/Papain/Zinc Supplement False True False NCIT:C175517 ICDC Value Terminology False True False @@ -88054,7 +88444,7 @@ NCIT:C17553 Clinical Ethics False True False NCIT:C175530 Rose Geranium in Sesame Oil Nasal Spray False True False NCIT:C175531 Subject Identifier Source False True False NCIT:C175532 Parent Biospecimen False True False -NCIT:C175534 Autologous CD19 CAR-expressing T-cells YTB323 False True False +NCIT:C175534 Rapcabtagene Autoleucel False True False NCIT:C175535 Transdermal Gel in Sachet Dosage Form False True False NCIT:C175536 pNGVL4a-CRT-E6E7L2 DNA Vaccine False True False NCIT:C175537 AuroLase Therapy False True False @@ -88062,7 +88452,7 @@ NCIT:C175538 TruSight Oncology 500 Assay False True False NCIT:C17554 Transcriptional Activation False True False NCIT:C175540 Daiichi Sankyo False True False NCIT:C175541 Iovance Biotherapeutics False True False -NCIT:C175542 IDH1 Mutant Inhibitor LY3410738 False True False +NCIT:C175542 Crelosidenib False True False NCIT:C175543 Axl/Mer Inhibitor PF-07265807 False True False NCIT:C175544 CIBMTR Center Support False True False NCIT:C175545 Ticket Assignment False True False @@ -88100,7 +88490,7 @@ NCIT:C175577 Traditional Chinese False True False NCIT:C175578 Autologous Alpha-PNE Switchable CAR-T Cells CLBR001 False True False NCIT:C175579 CD19-specific Adapter Molecule SWI019 False True False NCIT:C17558 Echo-Planar Imaging False True False -NCIT:C175580 pan-NOTCH Protein-Protein Interaction Inhibitor CB-103 False True False +NCIT:C175580 Limantrafin False True False NCIT:C175582 t(11;17) False True False NCIT:C175583 t(8;16) False True False NCIT:C175584 t(1;22) False True False @@ -88380,7 +88770,6 @@ NCIT:C175852 Rezvilutamide False True False NCIT:C175853 Rintodestrant False True False NCIT:C175854 Simpinicline Citrate False True False NCIT:C175855 Sivopixant False True False -NCIT:C175856 Sulanemadlin False True False NCIT:C175857 Suntinorexton False True False NCIT:C175858 Tarlatamab False True False NCIT:C175859 Telazorlimab False True False @@ -88472,7 +88861,7 @@ NCIT:C175941 Cotsiranib False True False NCIT:C175942 Hsp90 Inhibitor MPT0B640 False True False NCIT:C175943 Welgenaleucel False True False NCIT:C175944 Ponsegromab False True False -NCIT:C175945 PD-1-targeted IL-2 Variant Antibody Fusion Protein RO7284755 False True False +NCIT:C175945 Eciskafusp Alfa False True False NCIT:C175946 Gallium Ga 68-WL12 False True False NCIT:C175947 DLL3/CD3e Tri-specific T-cell Activating Construct HPN328 False True False NCIT:C175948 Fluorine F 18-WL12 False True False @@ -89131,7 +89520,7 @@ NCIT:C176567 RFX5 wt Allele False True False NCIT:C176568 Autologous Anti-CD22 CAR-expressing T-cells SCRI-CAR22v2 False True False NCIT:C176569 DNA-Binding Protein RFX5 False True False NCIT:C17657 Molecular Epidemiology False True False -NCIT:C176570 Synthetic MVA-based SARS-CoV-2 Vaccine COH04S1 False True False +NCIT:C176570 Synthetic MVA-based SARS-CoV-2 Vaccine GEO-CM04S1 False True False NCIT:C176571 RFXANK Gene False True False NCIT:C176572 RFXANK wt Allele False True False NCIT:C176573 Autologous Tolerogenic Proinsulin Peptide-loaded Dendritic Cells PIpepTolDC False True False @@ -89182,7 +89571,6 @@ NCIT:C176618 ZNF341 Gene False True False NCIT:C17662 Antigen Processing False True False NCIT:C176620 ZNF341 wt Allele False True False NCIT:C176621 Zinc Finger Protein 341 False True False -NCIT:C176622 Gastrointestinal Defects And Immunodeficiency Syndrome False True False NCIT:C176623 iPSC-derived CD16/IL-15RF-expressing CD38-eliminated NK Cells FT538 False True False NCIT:C176625 Anti-DR5 Agonistic Monoclonal Antibody IGM-8444 False True False NCIT:C176626 Focused Ultrasound Mesencephalotomy False True False @@ -89262,7 +89650,7 @@ NCIT:C176699 Moderate Grade Fever False True False NCIT:C1767 Chaparrin False True False NCIT:C17670 Cytoplasmic Receptor False True False NCIT:C176700 Phosphorus-32 Beta Radiation False True False -NCIT:C176703 PIK3R1-Associated Immunodeficiency False True False +NCIT:C176703 Activated PI3K Delta Syndrome 2 False True False NCIT:C176704 YARSopathy False True False NCIT:C176708 Imaging Finding False True False NCIT:C176709 Breast Finding False True False @@ -89363,12 +89751,12 @@ NCIT:C176802 Amendment to Investigational New Drug False True False NCIT:C176803 Amendment to Master Drug File False True False NCIT:C176804 Severe Combined Immunodeficiency, Autosomal Recessive, T-Cell Negative, B Cell-Positive, NK Cell-Positive False True False NCIT:C176805 Interferon Gamma Receptor 2 Deficiency False True False -NCIT:C176807 Severe Combined Immunodeficiency, Autosomal Recessive, T-Cell Negative, B-Cell Positive, NK-Cell Negative False True False +NCIT:C176807 JAK3-deficient Severe Combined Immunodeficiency False True False NCIT:C176808 LCK-Associated Immunodeficiency False True False NCIT:C176809 Immunodeficiency, Common Variable, 8, with Autoimmunity False True False NCIT:C17681 Metalloproteinase Inhibitor 3 False True False NCIT:C176810 Microbiological Property False True False -NCIT:C176811 Physico-Chemical Properties False True False +NCIT:C176811 Physicochemical Properties False True False NCIT:C176812 Process Related Impurity False True False NCIT:C176813 Product Related Impurity False True False NCIT:C176815 Residual Solvent False True False @@ -89385,10 +89773,10 @@ NCIT:C176828 Medical Expenditure Panel Survey False True False NCIT:C176829 Self-Administered Comorbidity Questionnaire False True False NCIT:C17683 Core-Binding Factor False True False NCIT:C176830 Fear of Cancer Recurrence Questionnaire False True False -NCIT:C176831 CDK2/4/6 Inhibitor NUV-422 False True False +NCIT:C176831 Inixaciclib False True False NCIT:C176832 Financial Hardship False True False NCIT:C176833 Patient-Centered Communication in Cancer Care-Long Form False True False -NCIT:C176834 CD38-targeting Antibody Recruiting Molecule KP1237 False True False +NCIT:C176834 Noraramtide False True False NCIT:C176835 CAHPS Cancer Care Survey False True False NCIT:C176836 EORTC Quality of Life Questionnaire-Core 30 False True False NCIT:C176837 Functional Assessment of Chronic Illness Therapy-Spiritual Well-Being 12 Item Scale False True False @@ -89406,7 +89794,7 @@ NCIT:C176847 Pneumatic Compression Therapy False True False NCIT:C176848 Pneumatic Compression Therapy with Reminders False True False NCIT:C176849 Healthcare Utilization False True False NCIT:C17685 Receptor Tyrosine-Protein Kinase ErbB-4 False True False -NCIT:C176850 Allogeneic Anti-CD19 1XX-CAR T-cells FT819 False True False +NCIT:C176850 iPSC-derived Allogeneic Anti-CD19 1XX-CAR T-cells FT819 False True False NCIT:C176851 CXCR2 Agonist MGTA-145 False True False NCIT:C176852 Gallium Ga 68-DOTA-5G False True False NCIT:C176853 Lutetium Lu 177-DOTA-ABM-5G False True False @@ -89584,7 +89972,7 @@ NCIT:C177107 PPP1CB wt Allele False True False NCIT:C177108 Serine/Threonine-Protein Phosphatase PP1-Beta Catalytic Subunit False True False NCIT:C177109 None of These Describe Me False True False NCIT:C17711 Prokaryotic Cell Component False True False -NCIT:C177110 Anti-C5aR1 Monoclonal Antibody TJ210 False True False +NCIT:C177110 Izastobart False True False NCIT:C177111 Anti-MUC1/EGFR Bispecific Antibody Drug Conjugate M1231 False True False NCIT:C177112 OCA5 Gene False True False NCIT:C177113 More than 1 Mitosis per 50 HPF and Less than 3 Mitoses per 10 HPF False True False @@ -90793,7 +91181,7 @@ NCIT:C17828 Biological Process False True False NCIT:C178280 Pradusinstobart False True False NCIT:C178281 Polzastobart False True False NCIT:C178282 Anti-FOXP3 Antisense Oligonucleotide AZD8701 False True False -NCIT:C178284 Anti-EGFR/CD28 Bispecific Antibody REGN7075 False True False +NCIT:C178284 Dalmitamig False True False NCIT:C178285 PIK3CA-Related Overgrowth Spectrum False True False NCIT:C178286 Anaplasia Indicator False True False NCIT:C178287 Anaplasia Descriptor False True False @@ -90808,7 +91196,7 @@ NCIT:C178294 Acute Radiation Skin Toxicity False True False NCIT:C178295 HMGA1 Gene Product False True False NCIT:C178296 Douglas Bag Method False True False NCIT:C178297 Partially HLA-matched AdV/CMV/EBV/BKV-specific Allogeneic T-lymphocytes False True False -NCIT:C178298 Autologous Anti-HER2 TAC T Cells TAC01-HER2 False True False +NCIT:C178298 Fencabtagene Autoleucel False True False NCIT:C178299 HER2 Inhibitor ZN-A-1041 False True False NCIT:C1783 Piposulfan False True False NCIT:C17830 Gynecologic Oncologist False True False @@ -90833,7 +91221,7 @@ NCIT:C178316 Autologous PD-1 Nanobody-expressing Anti-MSLN CAR T-cells False Tru NCIT:C178317 Personalized Neoantigen Plasmid DNA Melanoma Vaccine EVX-02 False True False NCIT:C178318 Gunagratinib False True False NCIT:C178319 Ribocytokine IL-2 BNT151 False True False -NCIT:C17832 Internist False True False +NCIT:C17832 Internal Medicine Physician False True False NCIT:C178320 Anti-PD-1 Monoclonal Antibody TY101 False True False NCIT:C178321 Anti-RANKL Monoclonal Antibody HS-20090 False True False NCIT:C178322 IRDye800CW-Nimotuzumab False True False @@ -90864,7 +91252,7 @@ NCIT:C178344 Urtica dioica Extract False True False NCIT:C178345 Anti-PD-1 Monoclonal Antibody MW11 False True False NCIT:C178346 Gallium Ga 68 AIP-301 False True False NCIT:C178347 Anti-CD40 Agonist Antibody YH003 False True False -NCIT:C178349 Kinase Inhibitor UCT-01-097 False True False +NCIT:C178349 ERK1/2 Inhibitor UCT-01-097 False True False NCIT:C17835 Eye Surgeon False True False NCIT:C178350 Help Question False True False NCIT:C178351 PHF1 Gene Rearrangement False True False @@ -90905,7 +91293,7 @@ NCIT:C178391 Genetic Predisposition to Neoplasm False True False NCIT:C178392 Genetic Predisposition to Non-Syndromic Wilms Tumor False True False NCIT:C178395 Secondhand Smoke Exposure Answer False True False NCIT:C178396 Izalontamab False True False -NCIT:C178397 Nectin-4-targeting Bicyclic Peptide/MMAE BT8009 False True False +NCIT:C178397 Zelenectide Pevedotin False True False NCIT:C178398 Retlirafusp Alfa False True False NCIT:C178399 Cancer Cell Metabolism Modulator OMT-111 False True False NCIT:C1784 Oregovomab False True False @@ -90918,7 +91306,7 @@ NCIT:C178404 Honey-based Nutritional Supplement False True False NCIT:C178405 Anti-PD-1 Monoclonal Antibody GNR-051 False True False NCIT:C178406 Anti-mucin-1/PE Immunoconjugate BM7PE False True False NCIT:C178407 Anti-VISTA Monoclonal Antibody W0180 False True False -NCIT:C178408 Anti-CD22/CD3 Bispecific Antibody JNJ-75348780 False True False +NCIT:C178408 Rezetamig False True False NCIT:C178409 Autologous Anti-PD-L1-armored Anti-CD22 CAR T Cells False True False NCIT:C178410 Anti-PSMA Antibody-drug Conjugate ARX517 False True False NCIT:C178411 Amyotrophic Lateral Sclerosis 23 False True False @@ -90956,7 +91344,7 @@ NCIT:C178445 Autologous MG7-pulsed Dendritic Cell Vaccine False True False NCIT:C178446 Anti-EGFR/c-Met Bispecific Antibody CKD-702 False True False NCIT:C178447 Autologous Neoantigen-specific T-lymphocytes GEN-011 False True False NCIT:C178448 Emfizatamab False True False -NCIT:C178449 Anti-PD-1/CTLA-4 Bispecific Antibody SI-B003 False True False +NCIT:C178449 Danvilostomig False True False NCIT:C17845 Hematologist/Oncologist, Pediatric False True False NCIT:C178450 Memorial Sloan-Kettering Cancer Center/Motzer Score for Metastatic Renal Cell Carcinoma False True False NCIT:C178451 Fermented Soybean Extract MS-20 False True False @@ -91057,7 +91445,7 @@ NCIT:C178573 NP40 Lysis Buffer False True False NCIT:C178574 SUMO-Activating Enzyme False True False NCIT:C178575 BCMA-specific Universal CAR-expressing T-lymphocytes LCAR-BCX False True False NCIT:C178576 Anti-TROP2 Monoclonal Antibody-Tub196 Conjugate JS108 False True False -NCIT:C178577 Anti-CD19/CD3 Bispecific Antibody TNB-486 False True False +NCIT:C178577 Anti-CD19/CD3 Bispecific Antibody AZD0486 False True False NCIT:C178578 TRK Inhibitor VC004 False True False NCIT:C178579 SLC6A19 Gene False True False NCIT:C17858 Pediatric Neurologic Oncology False True False @@ -91612,7 +92000,7 @@ NCIT:C179198 Electronically Activated Recording False True False NCIT:C179199 Omacetaxine False True False NCIT:C1792 Recombinant Human 6Ckine False True False NCIT:C17920 CD166 Antigen False True False -NCIT:C179200 CDK7 Inhibitor XL102 False True False +NCIT:C179200 Tacaciclib False True False NCIT:C179201 Fluorine F 18 FTC-146 False True False NCIT:C179202 Mitotic Rate Less than One per Square Millimeter False True False NCIT:C17921 Guanine Nucleotide Exchange Factor VAV2 False True False @@ -91721,7 +92109,7 @@ NCIT:C179317 Decreased CYBB Expression False True False NCIT:C179318 Low Glutathione Level False True False NCIT:C179319 Mesonephric Differentiation False True False NCIT:C17932 Angiogenic Process False True False -NCIT:C179323 PKMYT1 Inhibitor RP-6306 False True False +NCIT:C179323 Lunresertib False True False NCIT:C179324 GSK3B Gene Mutation False True False NCIT:C179325 Activating GSK3B Gene Mutation False True False NCIT:C179326 Technetium Tc-99m-MIRC208 False True False @@ -92014,7 +92402,7 @@ NCIT:C179623 Oncolytic Vaccinia Virus Expressing Anti-CTLA-4 Antibody and GM-CSF NCIT:C179624 Oncolytic Herpes Simplex Virus-1 Expressing Anti-CTLA-4 Antibody/CD40L/4-1BBL RP3 False True False NCIT:C179625 Dresbuxelimab False True False NCIT:C179626 Anti-CCR7 Monoclonal Antibody CAP-100 False True False -NCIT:C179627 Pan-TRK Inhibitor ICP-723 False True False +NCIT:C179627 Zurletrectinib False True False NCIT:C179628 BET Inhibitor JAB-8263 False True False NCIT:C179629 A2AR Antagonist EXS21546 False True False NCIT:C17963 BCL2 Gene False True False @@ -92080,7 +92468,7 @@ NCIT:C17969 X-Ray Repair Cross-Complementing Protein 5 False True False NCIT:C179690 IL17RC wt Allele False True False NCIT:C179691 Interleukin-17 Receptor C False True False NCIT:C179692 FR Alpha/TRPV6 Bispecific Ligand Drug Conjugate CBP-1008 False True False -NCIT:C179693 Menin Inhibitor DS-1594b False True False +NCIT:C179693 Emilumenib Succinate False True False NCIT:C179694 MALT1 Inhibitor MPT-0118 False True False NCIT:C179695 Specimen Appearance Assessment False True False NCIT:C179696 KPNA2 Gene False True False @@ -92111,7 +92499,7 @@ NCIT:C179718 SGTA Gene False True False NCIT:C179719 Resiquimod Hydrogel-based Sustained-release formulation False True False NCIT:C179720 SGTA wt Allele False True False NCIT:C179722 Leuprolide Acetate Sustained-release Microspheres PT105 False True False -NCIT:C179723 PTPN2 Inhibitor ABBV-CLS-484 False True False +NCIT:C179723 Osunprotafib False True False NCIT:C179724 Overlapping Lesion False True False NCIT:C179725 Varnimcabtagene Autoleucel False True False NCIT:C179726 Small Glutamine-Rich Tetratricopeptide Repeat-Containing Protein Alpha False True False @@ -92229,7 +92617,7 @@ NCIT:C179828 Round Window Niche False True False NCIT:C179829 Secondary Tympanic Membrane False True False NCIT:C17983 Guanine Nucleotide-Binding Protein G(s) Subunit Alpha Isoforms XLas False True False NCIT:C179830 Experimental Organism Jejunoileum False True False -NCIT:C179831 Anti-EGFR/c-Met Bispecific Antibody MCLA-129 False True False +NCIT:C179831 Pamvatamig False True False NCIT:C179832 TMPRSS4 Gene False True False NCIT:C179833 TMPRSS4 wt Allele False True False NCIT:C179834 Transmembrane Protease Serine 4 False True False @@ -92754,8 +93142,8 @@ NCIT:C180324 GISAID Accession ID False True False NCIT:C180325 SARS Coronavirus 2 P.3 False True False NCIT:C180326 Lartesertib False True False NCIT:C180327 Pansexuality False True False -NCIT:C180328 Gender Questioning False True False -NCIT:C180329 Agender False True False +NCIT:C180328 Gender Questioning Identity False True False +NCIT:C180329 Agender Identity False True False NCIT:C18033 Zinc Finger and BTB Domain-Containing Protein 48 False True False NCIT:C180330 Vesicopexy False True False NCIT:C180331 ULK1/2 Inhibitor DCC-3116 False True False @@ -92832,7 +93220,7 @@ NCIT:C18041 Thymosin Beta-15A False True False NCIT:C180410 Autologous Anti-ILT3 CAR-T Cells False True False NCIT:C180411 Bcl-2 Inhibitor ABBV-623 False True False NCIT:C180412 BTK Inhibitor ABBV-992 False True False -NCIT:C180413 Anti-Claudin18.2 ADC CMG901 False True False +NCIT:C180413 Anti-Claudin18.2 ADC AZD0901 False True False NCIT:C180414 Zaidi Recurrence Risk Score False True False NCIT:C180415 Zaidi Recurrence Risk Score Less than 6 False True False NCIT:C180416 Zaidi Recurrence Risk Score Greater than or Equal to 6 False True False @@ -92934,7 +93322,7 @@ NCIT:C180501 PAX2 Gene Mutation False True False NCIT:C180502 Inactivating PAX2 Gene Mutation False True False NCIT:C180503 Myc Inhibitor OMO-103 False True False NCIT:C180504 Cimderlirsen Sodium False True False -NCIT:C180505 Anti-CD38 Monoclonal Antibody CM313 False True False +NCIT:C180505 Lumrotatug False True False NCIT:C180506 TGF-beta2 Antisense Oligonucleotide TASO-001 False True False NCIT:C180507 Keynatinib False True False NCIT:C180508 Docetaxel Depot Formulation NZ-DTX False True False @@ -92957,7 +93345,7 @@ NCIT:C180529 Autologous Anti-MART-1 F5 TCR Tumor Infiltrating Lymphocytes False NCIT:C180531 Inezetamab False True False NCIT:C180533 Empagliflozin/Linagliptin False True False NCIT:C180534 Chondrus crispus False True False -NCIT:C180535 Alflutinib False True False +NCIT:C180535 Firmonertinib False True False NCIT:C180538 HMGA1 Gene Rearrangement False True False NCIT:C180539 HMGA2 Gene Rearrangement False True False NCIT:C18054 Neurogenic Locus Notch Homolog Protein 4 False True False @@ -93052,7 +93440,7 @@ NCIT:C18063 Gray False True False NCIT:C180630 Mother Smoked Cigarettes While Pregnant with You False True False NCIT:C180631 Telework False True False NCIT:C180632 Lifestyle Counseling False True False -NCIT:C180636 Allogeneic Multi-virus-specific T-cells ALVR106 False True False +NCIT:C180636 Spunoleucel False True False NCIT:C180637 Deleted in Esophageal Cancer 1 Long Non-Coding RNA False True False NCIT:C180638 Atidarsagene Autotemcel False True False NCIT:C180639 Belcesiran False True False @@ -93087,7 +93475,7 @@ NCIT:C180664 Vanglusagene Ensiparvovec False True False NCIT:C180665 Zalunfiban False True False NCIT:C180666 Palliative Chemotherapy False True False NCIT:C180667 Hiking False True False -NCIT:C180668 EGFR Mutant-selective Inhibitor BLU-945 False True False +NCIT:C180668 Tigozertinib False True False NCIT:C180669 Enzyme Substrate False True False NCIT:C18067 Inner City False True False NCIT:C180671 Esomeprazole Topical Cream False True False @@ -93289,7 +93677,7 @@ NCIT:C180853 FILIP1L Gene False True False NCIT:C180854 FILIP1L wt Allele False True False NCIT:C180855 Filamin A-Interacting Protein 1-Like False True False NCIT:C180856 Topical Keratinocyte Growth Factor Hair Serum False True False -NCIT:C180857 Pan-TRK Inhibitor PBI-200 False True False +NCIT:C180857 Paltimatrectinib False True False NCIT:C180858 Stratified Columnar Tumor Cells with Intracytoplasmic Mucin Vacuoles Present False True False NCIT:C18086 Data Management False True False NCIT:C180862 Digital Cognitive Behavioral Stress Management False True False @@ -93303,7 +93691,7 @@ NCIT:C180873 Cryoprecipitated Plasma False True False NCIT:C18088 Developmental Neurobiology False True False NCIT:C180882 Presymptomatic False True False NCIT:C180883 Actigraphy False True False -NCIT:C180884 Anti-claudin18.2/Anti-4-1BB Bispecific Antibody TJ-CD4B False True False +NCIT:C180884 Givastomig False True False NCIT:C180886 International Diffuse Intrinsic Pontine Glioma Registry Case Report Form Questionnaire False True False NCIT:C180889 Anti-CD226 Agonist Antibody LY3435151 False True False NCIT:C18089 Environmental Engineering False True False @@ -93314,7 +93702,7 @@ NCIT:C1809 Samarium Sm-153 False True False NCIT:C18090 FOS Family Protein False True False NCIT:C180900 Cervical Cancer pT1b3 TNM Finding v9 False True False NCIT:C180901 AJCC v9 Stage False True False -NCIT:C180902 EGFR-targeting Agent ABBV-637 False True False +NCIT:C180902 Anti-EGFR Antibody-drug Conjugate ABBV-637 False True False NCIT:C180903 Herb False True False NCIT:C180904 Anti-ILT2/Anti-ILT4 Monoclonal Antibody NGM707 False True False NCIT:C180905 Traditional Medicine False True False @@ -93429,7 +93817,7 @@ NCIT:C181021 TGF-beta Receptor 1 Inhibitor GFH018 False True False NCIT:C181022 Anti-LAG-3/Anti-PD-L1 Bispecific Antibody IBI323 False True False NCIT:C181023 On Protocol Therapy False True False NCIT:C181024 Anti-CD7 CAR T Cells SenL-T7 False True False -NCIT:C181025 Antibody-drug Conjugate SHR-A1904 False True False +NCIT:C181025 Anti-Claudin 18.2 Antibody-drug Conjugate SHR-A1904 False True False NCIT:C181026 Flexible Heteroarotinoid Sulfur Heteroarotinoid A2 False True False NCIT:C181027 Anti-PD-1/TGF-beta RII Bifunctional Fusion Protein JS201 False True False NCIT:C18103 Protein Synthesis False True False @@ -93501,7 +93889,7 @@ NCIT:C181100 METTL14 wt Allele False True False NCIT:C181101 PSPN Gene False True False NCIT:C181102 PSPN wt Allele False True False NCIT:C181103 Persephin False True False -NCIT:C181104 Bispecific Antibody JNJ-70218902 False True False +NCIT:C181104 Anti-TMEFF2/Anti-CD3 Bispecific Antibody JNJ-70218902 False True False NCIT:C181105 PAIP1 Gene False True False NCIT:C181106 PAIP1 wt Allele False True False NCIT:C181107 Polyadenylate-Binding Protein-Interacting Protein 1 False True False @@ -94081,7 +94469,7 @@ NCIT:C181673 MLST8 Gene False True False NCIT:C181674 MLST8 wt Allele False True False NCIT:C181675 Target of Rapamycin Complex Subunit LST8 False True False NCIT:C181676 Anti-BCMA/Anti-CD3 Bispecific Antibody WVT078 False True False -NCIT:C181677 Engineered Interleukin-18 Variant ST-067 False True False +NCIT:C181677 Vevoctadekin False True False NCIT:C181678 PLEKHA2 Gene False True False NCIT:C181679 PLEKHA2 wt Allele False True False NCIT:C18168 DNA-Binding Protein Inhibitor ID-2 False True False @@ -94162,7 +94550,7 @@ NCIT:C181748 PD-L1 Inhibitor ABSK043 False True False NCIT:C181749 Locally-acting Temozolomide Formulation SI-053 False True False NCIT:C18175 Neuregulin-2 False True False NCIT:C181750 Allogeneic Human T Cell Progenitors SMART 101 False True False -NCIT:C181751 KRAS-G12C Inhibitor LY3537982 False True False +NCIT:C181751 KRAS G12C Inhibitor LY3537982 False True False NCIT:C181752 Anti-CAIX CAR T Cells False True False NCIT:C181753 Adenosine A2A Receptor Antagonist TT-10 False True False NCIT:C181755 Anti-ALK-1 Monoclonal Antibody GT90001 False True False @@ -94319,7 +94707,7 @@ NCIT:C1819 Hydrocortisone Sodium Succinate False True False NCIT:C18190 Histopathologic Examination False True False NCIT:C181900 AdC68 Expressing PSA/PSMA/PSCA Vaccine PF-06755992 False True False NCIT:C181901 PSA/PSMA/PSCA-encoding DNA Plasmid Vaccine PF-06755990 False True False -NCIT:C181904 KRAS G12C Inhibitor JAB-21822 False True False +NCIT:C181904 Glecirasib False True False NCIT:C181908 Second Usual Pace Walk Time False True False NCIT:C181909 Cervical Florid Reactive Lymphoid Hyperplasia False True False NCIT:C18191 Computer Analysis False True False @@ -94414,7 +94802,7 @@ NCIT:C182006 Myelin-binding Imaging Agent False True False NCIT:C182007 Menin Inhibitor DSP-5336 False True False NCIT:C182008 Bcl-2 Inhibitor TQB3909 False True False NCIT:C182009 Enlonstobart False True False -NCIT:C182010 Anti-CD73 Monoclonal Antibody INCA00186 False True False +NCIT:C182010 Uprevstobart False True False NCIT:C182011 ATM Kinase/DNA-PK Inhibitor XRD-0394 False True False NCIT:C182012 Anti-IGF1R Monoclonal Antibody False True False NCIT:C182013 Immersion Medium False True False @@ -94773,6 +95161,7 @@ NCIT:C182353 Duration of Symptoms Prior to Diagnosis False True False NCIT:C182354 Distant Metastasis to False True False NCIT:C182355 Distant Disease Type False True False NCIT:C182356 Diffusion Sequence False True False +NCIT:C182357 Diffusion Restriction False True False NCIT:C182358 Diffuse Hemispheric False True False NCIT:C182359 Difficulty in School False True False NCIT:C182360 Did Radiation Treatment Require Sedation False True False @@ -95628,7 +96017,7 @@ NCIT:C183148 Reflectance Confocal Microscopy False True False NCIT:C183149 Intra-oral Reflectance Confocal Microscopy False True False NCIT:C18315 Transrectal Ultrasound False True False NCIT:C183150 Non-focal False True False -NCIT:C183151 Androgen Receptor Degrader ARV-766 False True False +NCIT:C183151 Luxdegalutamide False True False NCIT:C183153 Mucosal-Dominant Pemphigus Vulgaris False True False NCIT:C183154 DUT Gene False True False NCIT:C183155 DUT wt Allele False True False @@ -96881,7 +97270,7 @@ NCIT:C184303 No Attempt to Orgasm or Climax False True False NCIT:C184304 No Orgasm or Climax False True False NCIT:C184305 Endocannabinoid False True False NCIT:C184306 Phytocannabinoid False True False -NCIT:C184307 Anti-TIGIT Monoclonal Antibody AK127 False True False +NCIT:C184307 Lancastotug False True False NCIT:C184308 Lutetium Lu 177 AB-3PRGD2 False True False NCIT:C184309 Anti-BCMA CAR-NK Cells False True False NCIT:C18431 Oncogene, Transcription Factor False True False @@ -97762,7 +98151,7 @@ NCIT:C185123 Equecabtagene Autoleucel False True False NCIT:C185124 ER Alpha-targeting Chimeric Protein Degrader AC682 False True False NCIT:C185125 CBL-B Inhibitor NX-1607 False True False NCIT:C185126 Autologous WT1-directed CRISPR/Cas9-engineered TCR-T Cells NTLA-5001 False True False -NCIT:C185127 Anti-plectin Monoclonal Antibody ZB131 False True False +NCIT:C185127 Ibentatug False True False NCIT:C185128 Anti-B7-H4/Anti-CD3 Bispecific Antibody PF-07260437 False True False NCIT:C185129 Antibody STING Drug Conjugate TAK-500 False True False NCIT:C18513 Nuclear Grade False True False @@ -97912,7 +98301,7 @@ NCIT:C185284 VEGFR3 Inhibitor EVT801 False True False NCIT:C185285 Anti-PD-L1/Anti-LAG-3 Bispecific Antibody ABL501 False True False NCIT:C185286 Pegylated CD25/CD122-selective Interleukin-2 Mutein STK-012 False True False NCIT:C185287 Myc Inhibitor WBC100 False True False -NCIT:C185288 Kras G12C Inhibitor MK-1084 False True False +NCIT:C185288 KRAS G12C Inhibitor MK-1084 False True False NCIT:C185289 CBL-B Inhibitor-treated Autologous Tumor-infiltrating Lymphocytes DeTIL-0255 False True False NCIT:C18529 GLI Family Gene False True False NCIT:C185290 TransCon IL-2 Beta/Gamma False True False @@ -97952,7 +98341,7 @@ NCIT:C185326 Central Imaging Review False True False NCIT:C185327 Staging Laparotomy False True False NCIT:C185328 Stability Study Batch False True False NCIT:C185329 Angle-Resolved Low-Coherence Interferometry False True False -NCIT:C18533 Abelson Tyrosine-Protein Kinase 2 False True False +NCIT:C18533 Tyrosine-Protein Kinase ABL2 False True False NCIT:C185330 UNG Gene Product False True False NCIT:C185331 Uracil-DNA Glycosylase Isoform 1 False True False NCIT:C185332 4 Degrees Celsius False True False @@ -98053,10 +98442,10 @@ NCIT:C185424 KALRN wt Allele False True False NCIT:C185425 Anti-PD-1/TGFbRII Fusion Protein LBL-015 False True False NCIT:C185426 Anti-PD-L1/TGFbetaRII Fusion Protein BJ-005 False True False NCIT:C185427 Kalirin False True False -NCIT:C185428 Kinase Inhibitor UCT-03-008 False True False +NCIT:C185428 CDK4/6 Inhibitor UCT-03-008 False True False NCIT:C185429 Autologous Interleukin-15-armored Anti-glypican-3 CAR-iC9-expressing T-lymphocytes False True False NCIT:C18543 YES1 Gene False True False -NCIT:C185430 Antibody-drug Conjugate TORL-1-23 False True False +NCIT:C185430 Anti-CLDN6 Antibody-drug Conjugate TORL-1-23 False True False NCIT:C185431 Liver Cancer Neoantigens-sensitized Autoimmune Cells IPM001 False True False NCIT:C185432 Sexually Active False True False NCIT:C185433 Sexual Relations False True False @@ -98325,11 +98714,11 @@ NCIT:C185683 Glutamate Decarboxylase 2 False True False NCIT:C185684 Suspected Germ Cell Failure False True False NCIT:C185685 Confirmed Germ Cell Failure False True False NCIT:C185686 Late Effects Details False True False -NCIT:C185687 SLC9A3R1 Gene False True False +NCIT:C185687 NHERF1 Gene False True False NCIT:C185688 Gastrointestinal Adhesion False True False NCIT:C185689 Renal Tubule Damage False True False NCIT:C18569 FGF2 Gene False True False -NCIT:C185690 SLC9A3R1 wt Allele False True False +NCIT:C185690 NHERF1 wt Allele False True False NCIT:C185691 CTCAE Version False True False NCIT:C185692 Na(+)/H(+) Exchange Regulatory Cofactor NHE-RF1 False True False NCIT:C185693 Toxicity Details False True False @@ -98516,7 +98905,7 @@ NCIT:C185860 Collagenase Clostridium histolyticum EN3835 False True False NCIT:C185861 Anti-Claudin-18.2 Monoclonal Antibody NBL-015 False True False NCIT:C185862 Flonoltinib Maleate False True False NCIT:C185863 EGFR Mutant-selective Inhibitor BLU-701 False True False -NCIT:C185864 Menin Inhibitor BMF-219 False True False +NCIT:C185864 Icovamenib False True False NCIT:C185865 Anti-DLL4/Anti-VEGF-A Bispecific Antibody CTX-009 False True False NCIT:C185866 1.5 Tesla Magnetic Resonance Imaging False True False NCIT:C185867 Fu Zheng Jie Du Hua Yu False True False @@ -99048,11 +99437,11 @@ NCIT:C186365 European Association of Urology Non-muscle-invasive Bladder Cancer NCIT:C186366 Anti-CD20/anti-CD3 Bispecific Antibody CM355 False True False NCIT:C186367 Autologous Anti-CD79a/anti-CD20 CAR T-cells bbT369 False True False NCIT:C186368 Anti-PD-L1 Antibody-drug Conjugate SGN-PDL1V False True False -NCIT:C186369 MEK Inhibitor NFX-179 False True False +NCIT:C186369 Nedometinib False True False NCIT:C18637 Auditory Psychophysics False True False NCIT:C186370 Anti-CD73 Monoclonal Antibody JAB-BX102 False True False NCIT:C186371 Allogeneic Virus-specific T-lymphocytes R-MVST False True False -NCIT:C186372 Anti-CTLA-4 Monoclonal Antibody BA3071 False True False +NCIT:C186372 Evalstotug False True False NCIT:C186373 Selective Estrogen Receptor Degrader AND019 False True False NCIT:C186374 Anti-CCR8 Monoclonal Antibody LM-108 False True False NCIT:C186375 Blasts Less than 0.01 Percent of Bone Marrow Nucleated Cells False True False @@ -99188,7 +99577,7 @@ NCIT:C186507 Enasidenib Regimen False True False NCIT:C186508 Entrectinib Regimen False True False NCIT:C186509 Tivozanib Regimen False True False NCIT:C186510 Dostarlimab Regimen False True False -NCIT:C186512 Monoclonal Antibody TORL-2-307-MAB False True False +NCIT:C186512 Anti-Claudin18.2 Monoclonal Antibody TORL-2-307-MAB False True False NCIT:C186513 Trametinib Regimen False True False NCIT:C186514 Recombinant Human Hyaluronidase/Trastuzumab Regimen False True False NCIT:C186515 Bevacizumab/Tipiracil/Trifluridine Regimen False True False @@ -99293,7 +99682,7 @@ NCIT:C186654 CD73 Inhibitor ATG-037 False True False NCIT:C186655 Allogeneic CD16-expressing Natural Killer Cells CYNK-101 False True False NCIT:C186656 Tubulin Polymerization Inhibitor AB8939 False True False NCIT:C186657 Gallium Ga 68-DOTA-siglec-9 False True False -NCIT:C186659 EP4 Antagonist CR6086 False True False +NCIT:C186659 Vorbipiprant False True False NCIT:C18666 Cancer Biology False True False NCIT:C186661 Anti-PD-1/Anti-TGF-beta Bifunctional Fusion Protein TQB2868 False True False NCIT:C186664 Cytotoxic Chemotherapeutic Agent False True False @@ -99694,7 +100083,6 @@ NCIT:C187030 CSF1R Inhibitor HMPL-653 False True False NCIT:C187031 Thiostrepton False True False NCIT:C187032 HER2 Inhibitor SPH5030 False True False NCIT:C187033 Akt-1 Antisense Oligonucleotide WGI-0301 False True False -NCIT:C187034 ALK Inhibitor SY-3505 False True False NCIT:C187035 Oncolytic HSV-1 Expressing IL-12 and IL-15/IL-15-receptor Alpha VG2025 False True False NCIT:C187036 Umbilical Cord Blood-derived MAK Immune Cells False True False NCIT:C187037 RET Inhibitor LOXO-260 False True False @@ -99789,7 +100177,7 @@ NCIT:C187127 ENPP1 Inhibitor RBS2418 False True False NCIT:C187128 Anti-LAIR1 Monoclonal Antibody NGM438 False True False NCIT:C187129 Anti-CD19/Anti-CD20/Anti-CD22 CAR-T Cells LCAR-AIO False True False NCIT:C18713 Combinatorial Synthesis of Biomolecules False True False -NCIT:C187130 Allogeneic Nicotinamide-expanded Natural Killer Cells GDA-201 False True False +NCIT:C187130 Nadravaleucel False True False NCIT:C187131 P30-linked EphA2/CMV pp65/Survivin Peptide Vaccine P30-EPS False True False NCIT:C187132 Black Seed Oil Extract Supplement False True False NCIT:C187133 Dacomitinib Regimen False True False @@ -100993,7 +101381,7 @@ NCIT:C18836 High-LET Radiation False True False NCIT:C188360 Anti-CD38/Anti-CD47 Bispecific Antibody ISB 1442 False True False NCIT:C188361 Anti-CD47 Monoclonal Antibody HMPL-A83 False True False NCIT:C188362 Selective Estrogen Receptor Covalent Antagonist TQB3915 False True False -NCIT:C188363 Antibody-drug Conjugate DB-1305 False True False +NCIT:C188363 Anti-TROP-2 Antibody-drug Conjugate DB-1305 False True False NCIT:C188364 STAT3 Degrader KT-333 False True False NCIT:C188365 Adenovirus 5 CEA/MUC1/Brachyury Vaccine Tri-Ad5 False True False NCIT:C188367 Persistent Locoregional Disease False True False @@ -101248,7 +101636,7 @@ NCIT:C188604 Bidridistrogene Xeboparvovec False True False NCIT:C188605 Firzotemcel False True False NCIT:C188606 Rimtoregtide False True False NCIT:C188607 Golocdacimab False True False -NCIT:C188608 Rhenium (186re) Obisbemeda False True False +NCIT:C188608 Rhenium Re 186 Obisbemeda False True False NCIT:C188609 Ruzotolimod False True False NCIT:C18861 Lipid Biochemistry False True False NCIT:C188610 Evazarsen False True False @@ -101435,9 +101823,9 @@ NCIT:C188785 EZH2 NP_004447.2:p.Y646S False True False NCIT:C188786 EZH2 NM_004456.5:c.1937A>G False True False NCIT:C188787 EZH2 NP_004447.2:p.Y646C False True False NCIT:C18879 Minority Health and Assistance, Targeted False True False -NCIT:C188792 T-cell-redirecting Antibody JNJ-80948543 False True False +NCIT:C188792 Anti-CD79b/CD20/CD3 Trispecific Antibody JNJ-80948543 False True False NCIT:C188793 Oncolytic RNA Virus IVX037 False True False -NCIT:C188794 Antibody-drug Conjugate YL201 False True False +NCIT:C188794 Anti-B7-H3 Antibody-drug Conjugate YL201 False True False NCIT:C188795 GnRH Antagonist SHR7280 False True False NCIT:C188796 HCFC1 Gene False True False NCIT:C188797 HCFC1 wt Allele False True False @@ -101630,7 +102018,7 @@ NCIT:C18904 Nutrition: Training Dollars False True False NCIT:C189040 Gleason Score 5+3=8 False True False NCIT:C189041 Gleason Score 9-10 False True False NCIT:C189044 Gozetotide False True False -NCIT:C189047 FGFR4 Inhibitor ABSK-011 False True False +NCIT:C189047 Irpagratinib False True False NCIT:C189048 PSMA-targeting T-cell Redirecting Agent JNJ-80038114 False True False NCIT:C189049 Anti-CD38-CAR-TCRz/4-1BB-expressing T-lymphocytes False True False NCIT:C18905 Occupational Carcinogenesis False True False @@ -102525,7 +102913,6 @@ NCIT:C189902 24 Hour Release Patch Dosage Form False True False NCIT:C189903 72 Hour Release Patch Dosage Form False True False NCIT:C189904 Weekly Release Patch Dosage Form False True False NCIT:C189905 Non-synonymous ERBB2 Gene Mutation False True False -NCIT:C189906 HER2 Inhibitor BI 1810631 False True False NCIT:C189907 NRG1 Gene Rearrangement False True False NCIT:C189908 Extended Release Lotion Dosage Form False True False NCIT:C189909 First Subject Visit Date False True False @@ -102717,10 +103104,10 @@ NCIT:C190118 Anti-Claudin18.2/Anti-CD47 Bispecific Antibody PT886 False True Fal NCIT:C19012 Resource Sharing False True False NCIT:C190120 Aurora A Kinase Inhibitor JAB-2485 False True False NCIT:C190122 Cisplatin Micelle Formulation HA132 False True False -NCIT:C190124 Anti-PD-L1/4-1BB Bispecific Antibody ATG-101 False True False +NCIT:C190124 Xirestomig False True False NCIT:C190126 BET/CBP/p300 Inhibitor EP31670 False True False NCIT:C190127 Acetylglucosaminyltransferase V Inhibitor PhOx430 False True False -NCIT:C190128 Tyrosine Kinase Inhibitor IDRX-42 False True False +NCIT:C190128 KIT-mutant Inhibitor IDRX-42 False True False NCIT:C190129 OAS3 Gene False True False NCIT:C190130 OAS3 wt Allele False True False NCIT:C190131 2'-5'-Oligoadenylate Synthase 3 False True False @@ -102770,7 +103157,7 @@ NCIT:C190181 Mass Spectrometry Markup Language False True False NCIT:C190182 Markup Language False True False NCIT:C190183 NIfTI Format False True False NCIT:C190184 Python Script Format False True False -NCIT:C190185 Anti-BTN1A1 Monoclonal Antibody hSTC810 False True False +NCIT:C190185 Nelmastobart False True False NCIT:C190186 R Format False True False NCIT:C190187 R Markdown Format False True False NCIT:C190188 Sequence Record Format False True False @@ -103249,7 +103636,7 @@ NCIT:C190674 ADNP wt Allele False True False NCIT:C190675 Activity-Dependent Neuroprotector Homeobox Protein False True False NCIT:C190682 Fibroblast Activation Protein Alpha-activated Doxorubicin Prodrug AVA6000 False True False NCIT:C190683 Darunavir/Ritonavir False True False -NCIT:C190684 Pan-FGFR Inhibitor KIN-3248 False True False +NCIT:C190684 Resigratinib False True False NCIT:C190686 Anti-folate Receptor Alpha Antibody-drug Conjugate AMT-151 False True False NCIT:C190687 Anti-Claudin 18.2 Antibody-drug Conjugate JS107 False True False NCIT:C190688 Anti-CD39 Monoclonal Antibody JS019 False True False @@ -104333,7 +104720,6 @@ NCIT:C191756 Anti-ALPP/ALPPL2/MMAE ADC SGN-ALPV False True False NCIT:C191757 Anti-CLDN18.2 Monoclonal Antibody ZL-1211 False True False NCIT:C191758 Doxorubicin/Ifosfamide/Vincristine Regimen False True False NCIT:C191759 Butyrate Level Finding False True False -NCIT:C191760 Cyclophosphamide/Doxorubicin/Vincristine Regimen False True False NCIT:C191761 R-CEOP Regimen False True False NCIT:C191762 Autologous Tumor Infiltrating Lymphocytes TBio-4101 False True False NCIT:C191765 Autosomal Dominant Lower Extremity-Predominant Spinal Muscular Atrophy-1 False True False @@ -104661,7 +105047,7 @@ NCIT:C192098 Microcephaly-Capillary Malformation Syndrome False True False NCIT:C19210 Office of Science Planning and Analysis False True False NCIT:C192101 Weight-based Dose False True False NCIT:C192102 Fixed Dose False True False -NCIT:C192103 Selective Estrogen Receptor Degrader SCO-120 False True False +NCIT:C192103 Bexirestrant False True False NCIT:C192104 4-Dimensional Magnetic Resonance Imaging False True False NCIT:C192108 Risk Assessment for Hereditary Cancer False True False NCIT:C192109 Medical Product Dispensation- or Prescription-Related Activity False True False @@ -110873,7 +111259,6 @@ NCIT:C198024 Toronto Classification v2 Stage, Tier 2 False True False NCIT:C198025 Children's Oncology Group (COG)/National Wilms Tumor Study Group (NWTSG) Stage False True False NCIT:C198026 International Society of Pediatric Oncology (SIOP) Stage False True False NCIT:C198028 R-ABVD Regimen False True False -NCIT:C198029 BV-AVD Regimen False True False NCIT:C19803 SWI2/SNF2 False True False NCIT:C198033 Leukemic Infiltration of Central Nervous System False True False NCIT:C198037 Blasts Present in Cerebrospinal Fluid without Clinical Signs of Central Nervous System Involvement False True False @@ -111745,7 +112130,7 @@ NCIT:C199041 Emzeltrectinib False True False NCIT:C199042 Enlicitide Chloride False True False NCIT:C199043 Ersodetug False True False NCIT:C199044 Esonadogene Imvoparvovec False True False -NCIT:C199045 Etimumotide False True False +NCIT:C199045 Etimupepimut False True False NCIT:C199046 Evruleucel False True False NCIT:C199047 Fazamorexant False True False NCIT:C199048 Faznolutamide False True False @@ -111781,7 +112166,7 @@ NCIT:C199074 Navacaprant False True False NCIT:C199075 Neracorvir False True False NCIT:C199076 Nevadistinel False True False NCIT:C199077 Nimucitinib False True False -NCIT:C199078 Nisotirotide False True False +NCIT:C199078 Nisotirostide False True False NCIT:C199079 Nizubaglustat False True False NCIT:C19908 Quadruple Phase Spiral CT False True False NCIT:C199080 Oberotatug Ravtansine False True False @@ -111969,7 +112354,7 @@ NCIT:C199283 BRAF V600E Degrader CFT1946 False True False NCIT:C199285 Autologous Anti-GPC3-CAR T-lymphocytes Ori-C101 False True False NCIT:C199286 Allogeneic Anti-CD19 T-cells ThisCART19A False True False NCIT:C199287 Lead Pb 203 VMT-a-NET False True False -NCIT:C199288 Trispecific Antibody JNJ-79635322 False True False +NCIT:C199288 Anti-BCMA/GPRC5D/CD3 Trispecific Antibody JNJ-79635322 False True False NCIT:C199289 Anti-DLL3/Anti-CD47 Bispecific Antibody PT217 False True False NCIT:C19929 FGFR1 Gene False True False NCIT:C199290 Autologous Tumor Infiltrating Lymphocytes C-TIL051 False True False @@ -112292,7 +112677,7 @@ NCIT:C199608 CA3 Gene False True False NCIT:C199609 CA3 wt Allele False True False NCIT:C19961 In Vivo Cellular and Molecular Imaging Centers False True False NCIT:C199610 Carbonic Anhydrase 3 False True False -NCIT:C199611 Anti-CD161 Monoclonal Antibody IMT-009 False True False +NCIT:C199611 Rezorstobart False True False NCIT:C199612 Iduronicrin Genleukocel-T False True False NCIT:C199613 Modified Vaccinia Virus Ankara Expressing Flt3L/OX40L MQ710 False True False NCIT:C199614 Methyl Bacteriopurpurinimide False True False @@ -112774,7 +113159,7 @@ NCIT:C20007 Physician Scientist Award (Program) (PSA) False True False NCIT:C200070 Anti-CD19/CD3 T-cell Engaging Bispecific Antibody CLN-978 False True False NCIT:C200071 Autologous TP53 R175H Mutant-specific HLA-A*02:01-restricted TCR Gene Engineered T-lymphocytes NT-175 False True False NCIT:C200072 Allogeneic Hypoimmune Anti-CD19 CAR T-cells SC291 False True False -NCIT:C200075 Anti-SARS-CoV-2 Monoclonal Antibody AZD3152 False True False +NCIT:C200075 Sipavibart False True False NCIT:C200076 Anti-SARS-CoV-2 Monoclonal Antibodies AZD5156 False True False NCIT:C200077 GATA3 Overexpression Positive False True False NCIT:C200078 TBX21 Overexpression Positive False True False @@ -113236,7 +113621,6 @@ NCIT:C200519 Powder for Gastro-Resistant Oral Suspension False True False NCIT:C20052 Papillomavirus Protein E4 False True False NCIT:C200521 Granules for Gastro-Resistant Oral Suspension False True False NCIT:C200522 Powder for Prolonged-Release Oral Suspension False True False -NCIT:C200523 Extended Release Chewable Tablet False True False NCIT:C200525 Anti-4-1BB/5T4 Bispecific Antibody ALG.APV-527 False True False NCIT:C200526 Beehive Powder Dosage Form False True False NCIT:C200527 Anti-Notch1 Monoclonal Antibody False True False @@ -114323,441 +114707,4021 @@ NCIT:C201554 Therapeutic Hematopoietic Stem Cells False True False NCIT:C201555 Hematocrit Less than 45 Percent False True False NCIT:C201556 Therapeutic Mesenchymal Stem Cells False True False NCIT:C201557 Therapeutic Peripheral Blood Stem Cells False True False +NCIT:C201558 iPSC-derived MSCs CYP-001 False True False +NCIT:C201559 Anoscopy False True False NCIT:C20156 Radiation-Induced Recombination False True False +NCIT:C201560 Manufactures Cosmetic Products False True False +NCIT:C201561 Platelet Count Less Than 150x10^9/L False True False +NCIT:C201562 Platelet Count Greater Than or Equal to 150x10^9/L False True False +NCIT:C201563 Yttrium-90 Brachytherapy False True False +NCIT:C201564 Not Significant False True False +NCIT:C201565 Distribute Cosmetics False True False +NCIT:C201566 12-Lipoxygenase Inhibitor VLX-1005 False True False +NCIT:C201567 Gastrointestinal Thrombotic Microangiopathy False True False +NCIT:C201568 Engineered Toxin Body Targeting CTLA-4 MT-8421 False True False +NCIT:C201569 Hydrogel-based Resiquimod STM-416 False True False NCIT:C20157 Non-Human Gene False True False +NCIT:C201570 F11 Gene False True False +NCIT:C201571 F11 wt Allele False True False +NCIT:C201572 Coagulation Factor XI False True False +NCIT:C201573 FCN3 Gene False True False +NCIT:C201574 FCN3 wt Allele False True False +NCIT:C201576 Ficolin-3 False True False +NCIT:C201577 Farnesyl Transferase Inhibitor KO-2806 False True False +NCIT:C201578 Steroid Resistant Chronic Graft Versus Host Disease False True False +NCIT:C201579 Wildtype Staining Pattern False True False NCIT:C20158 Non-Human Protein False True False +NCIT:C201580 Aberrant Staining Pattern False True False +NCIT:C201581 Nuclear Staining Pattern False True False +NCIT:C201582 Cytoplasmic Staining False True False +NCIT:C201583 Null Staining Pattern False True False +NCIT:C201584 IL-2/IL-12-based Fusion Protein CLN-617 False True False +NCIT:C201585 Deafness, Autosomal Dominant 58 False True False +NCIT:C201586 Deafness, Autosomal Recessive 12 False True False +NCIT:C201587 Hypomyelinating Leukodystrophy-22 False True False +NCIT:C201588 Visceral Myopathy 1 False True False +NCIT:C201589 Li-Campeau Syndrome False True False NCIT:C20159 Drosophila Protein False True False +NCIT:C201590 Developmental and Epileptic Encephalopathy 9 False True False +NCIT:C201591 Arterial Calcification due to Deficiency of CD73 False True False +NCIT:C201592 Focal Cortical Dysplasia False True False +NCIT:C201593 Focal Cortical Dysplasia Type 2 False True False +NCIT:C201594 Knobloch Syndrome 1 False True False +NCIT:C201595 Sifrim-Hitz-Weiss Syndrome False True False +NCIT:C201596 Dystonia 11, Myoclonic False True False +NCIT:C201597 Osteootohepatoenteric Syndrome False True False +NCIT:C201598 Anti-DLL4 Monoclonal Antibody False True False +NCIT:C201599 HemOnc Terminology False True False NCIT:C2016 VGEF Mixed-Backbone Antisense Oligonucleotide GEM 220 False True False NCIT:C20160 NCI Center for Cancer Research False True False +NCIT:C201600 HemOnc Agent Terminology False True False +NCIT:C201601 HemOnc Regimen Terminology False True False +NCIT:C201602 Age at Adverse Event Resolution False True False +NCIT:C201603 Age at Cycle End False True False +NCIT:C201604 Age at Cycle Start False True False +NCIT:C201605 Age at Cytology Test False True False +NCIT:C201606 Age at End of Concomitant Medication Administration False True False +NCIT:C201607 Age at End of Treatment Course False True False +NCIT:C201608 Age at Function Test False True False +NCIT:C201609 Age at Histology Assessment False True False NCIT:C20161 Component of the National Cancer Institute False True False +NCIT:C201610 Age at Imaging False True False +NCIT:C201611 Age at Immunohistochemistry False True False +NCIT:C201612 Age at Last Known Survival False True False +NCIT:C201613 Age at Measurable Residual Disease Assessment False True False +NCIT:C201614 Age at Onset Adverse Event False True False +NCIT:C201615 Age at Procedure False True False +NCIT:C201616 Age at End of Radiation Therapy False True False +NCIT:C201617 Age at Radiation Therapy Course Start False True False +NCIT:C201618 Age at Response Assessment False True False +NCIT:C201619 Age at Secondary Malignancy Neoplasm False True False NCIT:C20162 Component of the Division of Cancer Biology False True False +NCIT:C201621 Age at Staging Assessment False True False +NCIT:C201622 Age at Start of Cellular Immunotherapy False True False +NCIT:C201623 Age at Start of Concomitant Medication Administration False True False +NCIT:C201624 SWI/SNF Complex Deficiency False True False +NCIT:C201625 Age at Start of Transfusion Procedure False True False +NCIT:C201626 Focal Cortical Dysplasia Type 1 False True False +NCIT:C201627 Focal Cortical Dysplasia Type 3 False True False +NCIT:C201628 Age at Start of Treatment Course False True False +NCIT:C201629 Age at Stem Cell Transplant False True False NCIT:C20163 Component of the Division of Cancer Epidemiology and Genetics False True False +NCIT:C201630 Age at Time of Laboratory Test False True False +NCIT:C201631 Age at Treatment Assignment False True False +NCIT:C201632 Age at Tumor Assessment False True False +NCIT:C201633 Age at Vitals False True False +NCIT:C201638 Age at Surgery False True False +NCIT:C201639 Age at Last Known Disease Status False True False NCIT:C20164 Component of the Division of Cancer Prevention False True False +NCIT:C201640 GCH1 Gene False True False +NCIT:C201641 GCH1 wt Allele False True False +NCIT:C201642 GTP Cyclohydrolase 1 False True False +NCIT:C201643 GCK Gene False True False +NCIT:C201644 GCK wt Allele False True False +NCIT:C201645 Hexokinase-4 False True False +NCIT:C201646 Anti-PD-L2 Monoclonal Antibody False True False +NCIT:C201647 ATM Inhibitor SYH2051 False True False +NCIT:C201648 Autologous Tumor Cells/Bacillus Calmette-Guerin/Formalin-based Vaccine False True False +NCIT:C201649 RBCs-Anti-PD1 Antibody Conjugate WTX212 False True False NCIT:C20165 Component of the Division of Cancer Treatment and Diagnosis False True False +NCIT:C201650 Anti-PD-1 siRNA PH-762 False True False +NCIT:C201651 Anti-CD20/CD3 Bispecific Antibody EX103 False True False +NCIT:C201652 Bispecific Antibody QLF3108 False True False +NCIT:C201653 Anti-PD-1/Anti-VEGF Bispecific Antibody JS207 False True False +NCIT:C201654 Allogeneic Anti-B7-H3 CAR Gamma Delta T-cells QH104 False True False +NCIT:C201655 Anti-CD24 Monoclonal Antibody ATG-031 False True False +NCIT:C201656 Anti-CD19/Anti-CD3/Anti-CD28 Trispecific Antibody CC312 False True False +NCIT:C201657 GFPT1 Gene False True False +NCIT:C201658 GFPT1 wt Allele False True False +NCIT:C201659 Glutamine-Fructose-6-Phosphate Aminotransferase [Isomerizing] 1 False True False NCIT:C20166 Component of the Division of Extramural Activities False True False +NCIT:C201660 GIPC1 Gene False True False +NCIT:C201661 GIPC1 wt Allele False True False +NCIT:C201662 PDZ Domain-Containing Protein GIPC1 False True False +NCIT:C201663 t(2;4)(q36.1;q31.1) False True False +NCIT:C201664 PAX3/MAML3 Fusion Gene False True False +NCIT:C201665 PAX3/MAML3 Fusion Protein False True False +NCIT:C201666 ATM Kinase Inhibitor False True False +NCIT:C201667 GJB1 Gene False True False +NCIT:C201668 GJB1 wt Allele False True False +NCIT:C201669 Gap Junction Beta-1 Protein False True False NCIT:C20167 Component of the Intramural Research Program False True False +NCIT:C201670 GJB3 Gene False True False +NCIT:C201671 GJB3 wt Allele False True False +NCIT:C201672 Gap Junction Beta-3 Protein False True False +NCIT:C201673 GJB4 Gene False True False +NCIT:C201674 GJB4 wt Allele False True False +NCIT:C201675 Gap Junction Beta-4 Protein False True False +NCIT:C201676 TRPM4 Gene False True False +NCIT:C201677 TRPM4 wt Allele False True False +NCIT:C201678 Transient Receptor Potential Cation Channel Subfamily M Member 4 False True False +NCIT:C201679 Anti-DLK-1 Antibody-drug Conjugate ADCT-701 False True False NCIT:C20168 Component of NCI Governance False True False +NCIT:C201680 GLUD1 Gene False True False +NCIT:C201681 Fibroblast-activation Protein Inhibitor False True False +NCIT:C201682 GLUD1 wt Allele False True False +NCIT:C201683 Glutamate Dehydrogenase 1, Mitochondrial False True False +NCIT:C201684 GLYCTK Gene False True False +NCIT:C201685 GLYCTK wt Allele False True False +NCIT:C201686 Glycerate Kinase False True False +NCIT:C201687 Autologous Anti-L1CAM-CAR-EGFRt-expressing T-cells False True False +NCIT:C201688 siRNA Therapeutic Agent False True False +NCIT:C201689 Kidney Fibrosis False True False NCIT:C20169 Component of the Office of the Director False True False +NCIT:C201690 EGFR/HER2 Mutant-selective Inhibitor STX-721 False True False +NCIT:C201691 EGFR Signaling Pathway Alteration Positive False True False +NCIT:C201692 GM2A Gene False True False +NCIT:C201693 GM2A wt Allele False True False +NCIT:C201694 Ganglioside GM2 Activator False True False +NCIT:C201695 GNB5 Gene False True False +NCIT:C201696 GNB5 wt Allele False True False +NCIT:C201697 Guanine Nucleotide-Binding Protein Subunit Beta-5 False True False +NCIT:C201698 GNE Gene False True False +NCIT:C201699 GNE wt Allele False True False NCIT:C2017 Steroidal Aromatase Inhibitor False True False NCIT:C20170 Component of the Division of Cancer Control and Population Sciences False True False +NCIT:C201700 Bifunctional UDP-N-Acetylglucosamine 2-Epimerase/N-Acetylmannosamine Kinase False True False +NCIT:C201701 GNPTG Gene False True False +NCIT:C201702 GNPTG wt Allele False True False +NCIT:C201703 N-Acetylglucosamine-1-Phosphotransferase Subunit Gamma False True False +NCIT:C201704 GPR143 Gene False True False +NCIT:C201705 GPR143 wt Allele False True False +NCIT:C201706 G-Protein Coupled Receptor 143 False True False +NCIT:C201707 HADH Gene False True False +NCIT:C201708 HADH wt Allele False True False +NCIT:C201709 Hydroxyacyl-Coenzyme A Dehydrogenase, Mitochondrial False True False NCIT:C20171 Component of the Center for Cancer Research False True False +NCIT:C201710 HADHA Gene False True False +NCIT:C201711 HADHA wt Allele False True False +NCIT:C201712 Trifunctional Enzyme Subunit Alpha, Mitochondrial False True False +NCIT:C201713 RXR-alpha Variant-targeting Agent NM6603 False True False +NCIT:C201714 PPP2R1A Gene Mutation False True False +NCIT:C201715 PPP2R1A Gene Mutation Negative False True False +NCIT:C201716 HADHB Gene False True False +NCIT:C201717 HADHB wt Allele False True False +NCIT:C201718 Trifunctional Enzyme Subunit Beta, Mitochondrial False True False +NCIT:C201719 Inactivating STAG2 Gene Mutation False True False NCIT:C20172 Component of the National Institutes of Health False True False +NCIT:C201720 HPV-Reactive T-Cell Finding False True False +NCIT:C201721 Allogeneic Anti-NY-ESO-1-TCR-IL-15-transduced Cord Blood-derived Natural Killer Cells False True False +NCIT:C201722 Short Chain Fatty Acid Measurement False True False +NCIT:C201723 Prostate Cryotherapy False True False +NCIT:C201724 Urethroplasty False True False +NCIT:C201725 Photovaporization of the Prostate False True False +NCIT:C201726 Bladder Neck Surgery False True False +NCIT:C201727 Urethral Sling Implantation False True False +NCIT:C201728 Artificial Urinary Sphincter Implantation False True False +NCIT:C201729 Penile Prosthesis Implantation False True False NCIT:C20173 Tetracycline Control False True False +NCIT:C201730 Urethral Stricture Surgery False True False +NCIT:C201731 HEXA Gene False True False +NCIT:C201732 HEXA wt Allele False True False +NCIT:C201733 Beta-Hexosaminidase Subunit Alpha False True False +NCIT:C201734 HEXB Gene False True False +NCIT:C201735 HEXB wt Allele False True False +NCIT:C201736 Beta-Hexosaminidase Subunit Beta False True False +NCIT:C201737 HK1 Gene False True False +NCIT:C201738 HK1 wt Allele False True False +NCIT:C201739 Hexokinase-1 False True False NCIT:C20174 NRG1 Gene False True False +NCIT:C201740 Hypopharyngeal Epithelial Dysplasia False True False +NCIT:C201741 HNF4A Gene False True False +NCIT:C201744 HNF4A wt Allele False True False +NCIT:C201745 Hepatocyte Nuclear Factor 4-Alpha False True False NCIT:C20175 Myelography False True False +NCIT:C201750 DNA Polymerase Theta Inhibitor ART6043 False True False +NCIT:C201751 HPS1 Gene False True False +NCIT:C201752 HPS1 wt Allele False True False +NCIT:C201753 BLOC-3 Complex Member HPS1 False True False +NCIT:C201754 Drug Enforcement Administration Number False True False +NCIT:C201755 Anti-claudin-1 Monoclonal Antibody ALE.C04 False True False +NCIT:C201756 HPS6 Gene False True False +NCIT:C201757 HPS6 wt Allele False True False +NCIT:C201758 BLOC-2 Complex Member HPS6 False True False +NCIT:C201759 AP3B1 Gene False True False NCIT:C20176 Nephrotomography False True False +NCIT:C201760 AP3B1 wt Allele False True False +NCIT:C201761 AP-3 Complex Subunit Beta-1 False True False +NCIT:C201762 HSD11B2 Gene False True False +NCIT:C201763 HSD11B2 wt Allele False True False +NCIT:C201765 11-Beta-Hydroxysteroid Dehydrogenase Type 2 False True False +NCIT:C201769 SPL Small Business False True False NCIT:C20177 Intravenous Pyelography False True False +NCIT:C201771 t(6;9)(q22-23;p23-24) False True False +NCIT:C201773 CD19-expressing Oncolytic Virus CF33 False True False +NCIT:C201774 CLDN1 Gene False True False +NCIT:C201775 CLDN1 wt Allele False True False +NCIT:C201776 Claudin-1 False True False +NCIT:C201777 MEF2C/SS18 Fusion Gene False True False +NCIT:C201778 CLDN7 Gene False True False +NCIT:C201779 CLDN7 wt Allele False True False NCIT:C20178 Mammogram False True False +NCIT:C201780 Claudin-7 False True False +NCIT:C201782 PRKD1 Gene Mutation False True False +NCIT:C201783 PRKD1 Gene Rearrangement False True False +NCIT:C201784 PRKD2 Gene Rearrangement False True False +NCIT:C201785 PRKD3 Gene Rearrangement False True False +NCIT:C201787 Childhood Cancer Data Initiative False True False +NCIT:C201788 mzIdentML False True False +NCIT:C201789 mtx False True False NCIT:C20179 Toxicogenomics False True False +NCIT:C201790 dbGaP Consent Group False True False +NCIT:C201791 Allogeneic CD19/CD20-specific CAR-T Cells P-CD19CD20-ALLO1 False True False +NCIT:C201792 HYAL1 Gene False True False +NCIT:C201793 HYAL1 wt Allele False True False +NCIT:C201794 Hyaluronidase-1 False True False +NCIT:C201795 IL36RN Gene False True False +NCIT:C201796 Heterogeneous Morphology False True False +NCIT:C201797 Heterogeneous Breast Morphology False True False +NCIT:C201798 IL36RN wt Allele False True False +NCIT:C201799 Predominantly Fibroglandular Tissue False True False NCIT:C2018 Non-Steroidal Aromatase Inhibitor False True False NCIT:C20180 Cell Cycle Phase False True False +NCIT:C201800 Predominantly Fibroglandular Breast Tissue False True False +NCIT:C201801 Interleukin-36 Receptor Antagonist Protein False True False +NCIT:C201802 INF2 Gene False True False +NCIT:C201803 INF2 wt Allele False True False +NCIT:C201804 Inverted Formin-2 False True False +NCIT:C201805 IPO8 Gene False True False +NCIT:C201806 IPO8 wt Allele False True False +NCIT:C201807 Importin-8 False True False +NCIT:C201808 KIF18A Inhibitor False True False +NCIT:C201809 Phosphorylated Histone H3 Positive False True False NCIT:C20181 Conceptual Entity False True False +NCIT:C201810 4-Beta-Hydroxycholesterol to Total Cholesterol Ratio Measurement False True False +NCIT:C201811 Autologous Anti-CLDN18.2 TAC T-cells TAC01-CLDN18.2 False True False +NCIT:C201812 CD8 Positive Memory T-Lymphocyte False True False +NCIT:C201813 Transcription Factor Protein SON-DP False True False +NCIT:C201814 ITGA1 Gene False True False +NCIT:C201815 Apoaequorin/Vitamin D Supplement False True False +NCIT:C201816 ITGA1 wt Allele False True False +NCIT:C201817 Integrin Alpha-1 False True False +NCIT:C201818 Anti-C5 Monoclonal Antibody False True False +NCIT:C201819 ITGA3 Gene False True False NCIT:C20182 Population Process False True False +NCIT:C201820 ITGA3 wt Allele False True False +NCIT:C201822 Integrin Alpha-3 False True False +NCIT:C201824 Anti-RANKL Monoclonal Antibody False True False +NCIT:C201825 CASR Gene False True False +NCIT:C201826 Anti-CD123/Kinesin Spindle Protein Inhibitor Antibody-drug Conjugate VIP943 False True False +NCIT:C201827 Anti-LIV-1 Antibody-drug Conjugate BRY812 False True False +NCIT:C201828 KRAS G12D Inhibitor RMC-9805 False True False +NCIT:C201829 Monoclonal Antibody GIM-122 False True False NCIT:C20183 Telomere Reverse Transcriptase False True False +NCIT:C201830 Technetium Tc 99m-CN7DG False True False +NCIT:C201831 CASR wt Allele False True False +NCIT:C201833 Extracellular Calcium-Sensing Receptor False True False +NCIT:C201834 ITM2B Gene False True False +NCIT:C201835 ITM2B wt Allele False True False +NCIT:C201836 Integral Membrane Protein 2B False True False NCIT:C20184 Protein Complex Subunit False True False +NCIT:C201840 ITPA Gene False True False +NCIT:C201841 Gallium Ga 68 R8760 False True False +NCIT:C201842 ITPA wt Allele False True False +NCIT:C201843 Inosine Triphosphate Pyrophosphatase False True False +NCIT:C201844 Immune Effector Cell Associated Neurotoxicity Syndrome Grade 5 False True False +NCIT:C201845 Necrotizing Sialometaplasia False True False +NCIT:C201846 Oral Melanoacanthoma False True False +NCIT:C201847 Human Papillomavirus-Related Oral Epithelial Dysplasia False True False +NCIT:C201848 GPRC5D-targeting Agent False True False NCIT:C20185 Gene Transfer False True False +NCIT:C201850 Myeloperoxidase-DNA Complex False True False +NCIT:C201851 t(X;18) False True False +NCIT:C201852 t(X;18)(p11.2-q11.2) False True False +NCIT:C201853 KRAS G12C Inhibitor False True False +NCIT:C201854 Spatially-fractionated Radiation Therapy False True False +NCIT:C201855 GRPR-targeting Radioconjugate False True False +NCIT:C201856 JPH2 Gene False True False +NCIT:C201857 JPH2 wt Allele False True False +NCIT:C201858 JPH2 Gene Product False True False +NCIT:C201859 Junctophilin-2 False True False NCIT:C20186 Nuclear Factor-I False True False +NCIT:C201860 Junctophilin-2 N-Terminal Fragment False True False +NCIT:C201861 PD-L1 Tumor Proportion Score 1-49 False True False +NCIT:C201862 GALNS Gene False True False +NCIT:C201863 GALNS wt Allele False True False +NCIT:C201864 N-Acetylgalactosamine-6-Sulfatase False True False +NCIT:C201865 DDX5 Degrader FL118 False True False +NCIT:C201866 Cornell Assessment of Pediatric Delirium False True False +NCIT:C201867 ASTCT Consensus Grading System for Cytokine Release Syndrome False True False +NCIT:C201868 Bortezomib/Daratumumab and Hyaluronidase/Dexamethasone Regimen False True False +NCIT:C201869 SARS Coronavirus 2 XBB.1.16.15 False True False NCIT:C20187 Cancer Science False True False +NCIT:C201870 SARS Coronavirus 2 HK.3 False True False +NCIT:C201871 SARS Coronavirus 2 HF.1 False True False +NCIT:C201872 SARS Coronavirus 2 GK.1.1 False True False +NCIT:C201873 SARS Coronavirus 2 GK.2 False True False +NCIT:C201874 SARS Coronavirus 2 DV.7 False True False +NCIT:C201875 Data Collection End Date False True False +NCIT:C201876 Reason for End of Data Collection False True False +NCIT:C201877 CD247 Gene Product False True False +NCIT:C201879 Daratumumab and Hyaluronidase/Dexamethasone/Lenalidomide Regimen False True False NCIT:C20188 Social Circumstances False True False +NCIT:C201881 Inpatient Hospital False True False +NCIT:C201882 Outpatient Hospital False True False +NCIT:C201883 Cyclophosphamide/Fludarabine/Rituximab and Hyaluronidase Regimen False True False +NCIT:C201884 Birthing Center False True False +NCIT:C201885 Independent Clinic False True False +NCIT:C201886 Residential Substance Abuse Treatment Facility False True False +NCIT:C201887 Mass Immunization Center False True False +NCIT:C201889 Comprehensive Outpatient Rehabilitation Facility False True False NCIT:C20189 Property or Attribute False True False +NCIT:C201890 Rural Health Clinic False True False +NCIT:C201891 Observation Room False True False +NCIT:C201892 Hospital Birthing Center False True False +NCIT:C201893 Radiation Therapy Center False True False +NCIT:C201894 Home Health Agency False True False +NCIT:C201895 Rehabilitation Agency False True False +NCIT:C201896 Emergency Medical Services False True False +NCIT:C201897 Military Field Hospital False True False +NCIT:C201898 Hospital Ship False True False +NCIT:C201899 Adult Care Home False True False NCIT:C2019 Dihydropyrimidine Dehydrogenase Inhibitor False True False NCIT:C20190 Chemical Agents False True False +NCIT:C201901 American Sign Language False True False +NCIT:C201902 Montenegrin Language False True False +NCIT:C201903 HGF Gene Amplification False True False +NCIT:C201908 RREB1/MRTFB Fusion Gene False True False +NCIT:C201909 RREB1/MRTFB Fusion Protein False True False NCIT:C20191 Cell-Matrix Adhesion Process False True False +NCIT:C201910 Oral Azacitidine Regimen False True False +NCIT:C201911 Daratumumab and Hyaluronidase/Dexamethasone/Pomalidomide Regimen False True False +NCIT:C201912 Bilateral Hip Replacement False True False +NCIT:C201913 Age at Exposure False True False +NCIT:C201914 AXL Inhibitor NTQ2494 False True False +NCIT:C201915 Oncolytic Virus M1-c6v1 False True False +NCIT:C201916 Anti-dectin-2 Agonist Monoclonal Antibody BDC-3042 False True False +NCIT:C201917 Autologous Anti-CDH17 CAR-T Cells CHM-2101 False True False +NCIT:C201918 HLA-G Positive Cells Present False True False +NCIT:C201919 Red-light Photodynamic Therapy False True False +NCIT:C201920 Anti-nectin-4 Antibody-drug Conjugate ADRX-0706 False True False +NCIT:C201921 Age at Molecular Analysis False True False +NCIT:C201922 Surgical Implantation False True False +NCIT:C201923 Humanization False True False +NCIT:C201924 Cytogenomic False True False +NCIT:C201925 Metagenomic False True False +NCIT:C201926 Metatranscriptomic False True False +NCIT:C201927 Tissue Dissociation Method False True False +NCIT:C201928 End Bias False True False +NCIT:C201929 Oligo-dT Primer False True False NCIT:C20193 Genetic Drift False True False +NCIT:C201930 Random Primer False True False +NCIT:C201931 RNA Spike-In Standard False True False +NCIT:C201932 Unique Molecular Identifier False True False +NCIT:C201933 Chimeric Antigen Receptor Natural Killer Cells False True False +NCIT:C201934 Yeast-derived Beta-glucan Supplement False True False +NCIT:C201935 Robotic Water Ablation Therapy False True False +NCIT:C201936 Cisplatin/Gemcitabine/Toripalimab Regimen False True False +NCIT:C201937 MET NP_000236.2:p.D1228X False True False +NCIT:C201938 MET NP_000236.2:p.Y1230X False True False +NCIT:C201939 Required Intervention to Prevent Permanent Impairment/Damage False True False NCIT:C20194 Regulatory Gene False True False +NCIT:C201940 Aminoacyl-tRNA Ligase Family False True False +NCIT:C201941 DPP6 Gene False True False +NCIT:C201942 DPP6 wt Allele False True False +NCIT:C201943 Dipeptidyl Aminopeptidase-Like Protein 6 False True False +NCIT:C201944 NT5C1A Gene False True False +NCIT:C201945 NT5C1A wt Allele False True False +NCIT:C201946 DNA Polymerase Theta Inhibitor GSK4524101 False True False +NCIT:C201947 Cytosolic 5'-Nucleotidase 1A False True False +NCIT:C201948 CLEC6A Gene False True False +NCIT:C201949 CLEC6A wt Allele False True False NCIT:C20195 Gene Fusion False True False +NCIT:C201950 C-Type Lectin Domain Family 6 Member A False True False +NCIT:C201954 Anti-mutant Calreticulin Monoclonal Antibody INCA033989 False True False +NCIT:C201955 Hospital Outpatient Clinic False True False +NCIT:C201956 Hospital Outpatient Pediatric Clinic False True False +NCIT:C201957 Infectious Disease Specialty False True False +NCIT:C201958 Mental Health Specialty False True False +NCIT:C201959 Pain Management False True False +NCIT:C201962 Critical Care Medicine False True False +NCIT:C201963 Developmental and Behavioral Pediatrics False True False +NCIT:C201964 Transplant Hepatology False True False +NCIT:C201965 Hematology and Oncology False True False NCIT:C20197 Male False True False +NCIT:C201972 Lixumistat False True False +NCIT:C201974 Automated Terminology Harmonization, Extraction and Normalization for Analytics False True False +NCIT:C201979 Data Submitter False True False NCIT:C20198 Low Literacy Population False True False +NCIT:C201980 Diagnosis Related Group False True False +NCIT:C201981 Functional Tests Supplemental Qualifiers Dataset False True False +NCIT:C201982 Dual-activating Polyvalent STING Agonist ONM-501 False True False +NCIT:C201983 Transbronchial Mediastinal Cryobiopsy False True False +NCIT:C201984 ASTCT CRS Grade False True False +NCIT:C201985 ASTCT CRS Grade 1 False True False +NCIT:C201986 ASTCT CRS Grade 2 False True False +NCIT:C201987 ASTCT CRS Grade 3 False True False +NCIT:C201988 ASTCT CRS Grade 4 False True False +NCIT:C201989 ASTCT CRS Grade 5 False True False NCIT:C20199 Unspecified Risk Factor False True False +NCIT:C201990 Caffeine Use History False True False +NCIT:C201991 Autologous Anti-CD19/Anti-CD79b CAR-expressing Bispecific T-cells False True False +NCIT:C201992 Condition Stop Reason False True False +NCIT:C201993 PSA Level Less than 0.4 False True False +NCIT:C201994 Lower Anterior Resection Syndrome Score False True False +NCIT:C201995 Have Occasions When Cannot Control Flatus False True False +NCIT:C201996 Have Accidental Leakage of Liquid Stool False True False +NCIT:C201997 How Often Open Bowels False True False +NCIT:C201998 Have to Open Bowels Within One Hour of Last Bowel Opening False True False +NCIT:C201999 Have Urge to Open Bowels Strong Enough to Cause Rush to Toilet False True False NCIT:C202 Aclarubicin False True False NCIT:C2020 Farnesyl Transferase Inhibitor False True False NCIT:C20200 Outcome False True False +NCIT:C202000 How Much Does Bowel Function Affect Overall Quality of Life False True False +NCIT:C202001 Fecal Incontinence Severity Index False True False +NCIT:C202002 How Often Experience Accidental Bowel Leakage of Gas False True False +NCIT:C202003 How Often Experience Accidental Bowel Leakage of Mucus False True False +NCIT:C202004 How Often Experience Accidental Bowel Leakage of Liquid Stool False True False +NCIT:C202005 How Often Experience Accidental Bowel Leakage of Solid Stool False True False +NCIT:C202006 Two or More Times a Day False True False +NCIT:C202007 Two or More Times a Week False True False +NCIT:C202008 One to Three Times a Month False True False +NCIT:C202009 Pan-KRAS Inhibitor YL-17231 False True False NCIT:C20201 Lifestyle Factors, Unspecified False True False +NCIT:C202011 Autoimmune Pulmonary Alveolar Proteinosis False True False +NCIT:C202012 Isaacs Syndrome False True False +NCIT:C202013 Prostate Ablation False True False +NCIT:C202014 NCI Data Commons Framework Services False True False +NCIT:C202015 Indexd False True False +NCIT:C202016 Allogeneic Anti-CD33 CAR T-cells VCAR33 False True False +NCIT:C202017 Acute Encephalopathy with Biphasic Seizures and Late Reduced Diffusion False True False +NCIT:C202018 Autosomal Recessive Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy False True False +NCIT:C202019 Psychiatric Hospital False True False NCIT:C20202 Wireless Technology False True False +NCIT:C202020 Rehabilitation Hospital False True False +NCIT:C202021 Male Homosexual False True False +NCIT:C202022 Home Isolation False True False +NCIT:C202023 Ancillary Treatment Report False True False +NCIT:C202024 Nursing Report False True False +NCIT:C202026 Prescription Issue Record False True False +NCIT:C202027 Reference Laboratory False True False +NCIT:C202028 Hospital Admission False True False +NCIT:C202029 Immediate Cause of Death False True False NCIT:C20203 Laser-Induced Fluorescence Endoscopy False True False +NCIT:C202030 Postoperative Diagnosis False True False +NCIT:C202031 Preoperative Diagnosis False True False +NCIT:C202032 Primary Diagnosis at Admission False True False +NCIT:C202033 Primary Diagnosis False True False +NCIT:C202034 Primary Diagnosis at Discharge False True False +NCIT:C202035 Secondary Diagnosis False True False +NCIT:C202036 Secondary Diagnosis at Discharge False True False +NCIT:C202037 Referral for Diagnosis False True False +NCIT:C202038 Underlying Cause of Death False True False +NCIT:C202039 Admitting Department False True False NCIT:C20204 Preneoplastic Change False True False +NCIT:C202040 Against Medical Advice False True False +NCIT:C202041 Sexually Transmitted Disease Health Center False True False +NCIT:C202042 Substance Abuse Treatment Center False True False +NCIT:C202043 Vitamin A/Vitamin C/Vitamin E/Zinc Gluconate/Selenium/Coenzyme Q10/L-Glutathione/L-Methionine/Taurine/N-Acetyl-L-Cysteine/Superoxide Dismutase/Catalase-containing Supplement False True False +NCIT:C202044 Calcium Lactate Supplement False True False +NCIT:C202045 Calcium Lactate/Protease/Amylase/Lipase-containing Supplement False True False +NCIT:C202046 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome False True False +NCIT:C202047 Dyskinesia with Orofacial Involvement False True False +NCIT:C202048 Patient Dead False True False +NCIT:C202049 Health Information False True False NCIT:C20205 Marker of Preneoplastic Change False True False +NCIT:C202050 Contributory Cause of Death False True False +NCIT:C202051 Surgical Ciliated Cyst False True False +NCIT:C202052 Primary Diagnosis for Referral False True False +NCIT:C202053 Secondary Diagnosis for Referral False True False +NCIT:C202054 Diagnosis Not Present at Admission False True False +NCIT:C202055 Diagnosis Present at Admission False True False +NCIT:C202056 AMBN Gene Mutation False True False NCIT:C20206 Sentinel Lymph Node Mapping False True False +NCIT:C202060 ACTA2 Positive False True False +NCIT:C202062 Fruquintinib Regimen False True False +NCIT:C202063 Porcupine Inhibitor False True False +NCIT:C202064 Wnt Signaling Pathway Inhibitor False True False +NCIT:C202065 AMBN Gene False True False +NCIT:C202066 AMBN wt Allele False True False +NCIT:C202067 Ameloblastin False True False +NCIT:C202068 Fermented Dairy Product False True False +NCIT:C202069 Intellectual Developmental Disorder, X-Linked, Syndromic, Nascimento Type False True False NCIT:C20207 Nonhomologous DNA End Joining False True False +NCIT:C202070 Late-Onset Retinal Degeneration False True False +NCIT:C202071 Ossification of the Ligamentum Flavum False True False +NCIT:C202072 Periventricular Nodular Heterotopia False True False +NCIT:C202073 Neurodegeneration with Brain Iron Accumulation 2A False True False +NCIT:C202074 Canadian Provincial Medical Plan False True False +NCIT:C202075 Transanal Endoscopic Surgery False True False +NCIT:C202076 Lipoprotein(a) Quantitative Trait Locus False True False NCIT:C20208 TEP1 Gene False True False +NCIT:C202082 Near Complete Clinical Response False True False +NCIT:C202083 No Clinical Response False True False +NCIT:C202084 Eating Assessment Tool-10 False True False +NCIT:C202085 Swallowing Problem Causes Weight Loss False True False +NCIT:C202086 Swallowing Problem Interferes with Ability to Go Out for Meals False True False +NCIT:C202087 Swallowing Liquid Takes Extra Effort False True False +NCIT:C202088 Swallowing Solids Takes Extra Effort False True False +NCIT:C202089 Swallowing Pills Takes Extra Effort False True False NCIT:C20209 Epithelial Cell Adhesion Molecule False True False +NCIT:C202090 Swallowing is Painful False True False +NCIT:C202091 Pleasure of Eating Affected by Swallowing Problem False True False +NCIT:C202092 Food Sticks in Throat When Swallowing False True False +NCIT:C202093 Cough When Eating False True False +NCIT:C202094 Swallowing is Stressful False True False +NCIT:C202095 Problem Score False True False +NCIT:C202096 Problem Score 0 False True False +NCIT:C202097 Problem Score 1 False True False +NCIT:C202098 Problem Score 2 False True False +NCIT:C202099 Problem Score 3 False True False NCIT:C2021 Thymidylate Synthase Inhibitor False True False NCIT:C20210 MLH3 Gene False True False +NCIT:C202100 Problem Score 4 False True False +NCIT:C202101 Androgen Receptor Degrader False True False +NCIT:C202102 Anti-TROP-2/MMAE Antibody-drug Conjugate LCB84 False True False +NCIT:C202103 Pediatric Eating Assessment Tool-10 False True False +NCIT:C202104 Child's Swallowing Problem Prevents Weight Gain False True False +NCIT:C202105 Child's Swallowing Problem Interferes with Ability to Go Out for Meals False True False +NCIT:C202106 Swallowing Liquid Takes Extra Effort for Child False True False +NCIT:C202107 Swallowing Solids Takes Extra Effort for Child False True False +NCIT:C202108 Child Gags During Swallowing False True False +NCIT:C202109 Child Acts Like Swallowing Is Painful False True False NCIT:C20211 MSH3 Gene False True False +NCIT:C202110 Child Does Not Want to Eat False True False +NCIT:C202111 Food Sticks in Child's Throat and Causes Choking While Eating False True False +NCIT:C202112 Swallowing Is Stressful for Child False True False +NCIT:C202113 Child Coughs While Eating False True False +NCIT:C202114 Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome-1 False True False +NCIT:C202115 Osteoarthritis with Mild Chondrodysplasia False True False +NCIT:C202116 Diffuse Panbronchiolitis False True False +NCIT:C202117 Mitochondrial Pyruvate Carrier Deficiency False True False +NCIT:C202118 Ossification of Anterior Longitudinal Ligament False True False +NCIT:C202119 TROP2-targeting Agent False True False NCIT:C20212 Base Excision Repair False True False +NCIT:C202121 Generalized Pustular Psoriasis False True False +NCIT:C202122 Intensity-modulated Radiation Therapy with Static Fields False True False +NCIT:C202123 Rotational Intensity-modulated Radiation Therapy False True False +NCIT:C202124 Transanal Minimally Invasive Surgery False True False +NCIT:C202125 Transanal Endoscopic Operation False True False +NCIT:C202126 Defect Closure False True False +NCIT:C202129 Chronic Non-Specific Multiple Ulcers of the Small Intestine False True False NCIT:C20213 Nucleotide Excision Repair False True False +NCIT:C202134 Number of Days Between Index Date and Pathology Review False True False +NCIT:C202135 Surgical Platform False True False +NCIT:C202136 Average Number of Exercise Days per Week False True False +NCIT:C202137 Extracapsular Extension Present Indicator False True False +NCIT:C202138 Extrathyroid Extent Indicator False True False +NCIT:C202139 Histological Progression Type False True False NCIT:C20214 Hypoxia-Inducible Factor 1-Alpha False True False +NCIT:C202140 Micrometastasis Present Indicator False True False +NCIT:C202141 CDISC Questionnaire PROMIS Item Bank Version 2.0 Cognitive Function Short Form 6a Test Name Terminology False True False +NCIT:C202142 CDISC Questionnaire PROMIS Item Bank Version 2.0 Cognitive Function Short Form 6a Test Code Terminology False True False +NCIT:C202143 CDISC Questionnaire PROMIS Item Bank Version 1.0 Fatigue Short Form 7a Test Name Terminology False True False +NCIT:C202144 CDISC Questionnaire PROMIS Item Bank Version 1.0 Fatigue Short Form 7a Test Code Terminology False True False +NCIT:C202145 CDISC Clinical Classification Minnesota Tobacco Withdrawal Scale-Revised Test Name Terminology False True False +NCIT:C202146 CDISC Clinical Classification Minnesota Tobacco Withdrawal Scale-Revised Test Code Terminology False True False +NCIT:C202147 CDISC Clinical Classification Minnesota Tobacco Withdrawal Scale-Revised MTWSR101 Through MTWSR115 Original Response Terminology False True False +NCIT:C202148 CDISC Clinical Classification Minnesota Tobacco Withdrawal Scale-Revised MTWSR101 Through MTWSR115 Standardized Character Response Terminology False True False +NCIT:C202149 PROMIS Item Bank Version 2.0 Cognitive Function Short Form 6a Questionnaire Question False True False NCIT:C20215 Secondary Cell Culture False True False +NCIT:C202150 PROMIS Item Bank Version 1.0 Fatigue Short Form 7a Questionnaire Question False True False +NCIT:C202151 Minnesota Tobacco Withdrawal Scale-Revised Clinical Classification Question False True False +NCIT:C202152 Minnesota Tobacco Withdrawal Scale-Revised MTWSR101 Through MTWSR115 Question Clinical Classification Original Response False True False +NCIT:C202153 Minnesota Tobacco Withdrawal Scale-Revised MTWSR101 Through MTWSR115 Question Clinical Classification Standardized Character Response False True False +NCIT:C202154 PROMIS-29 Adult Profile False True False +NCIT:C202155 Non-Oncologic Therapeutic Agent False True False +NCIT:C202156 PROMIS Pediatric-25 Profile False True False +NCIT:C202157 Therapeutic Oxygen Use Indicator False True False +NCIT:C202158 Home Oxygen Therapy Use Duration Indicator False True False +NCIT:C202159 Radiosensitizing Agent Used Indicator False True False NCIT:C20216 Adherent Culture False True False +NCIT:C202160 Number of Values in Staining Intensity Scale False True False +NCIT:C202161 Segmental Odontomaxillary Dysplasia False True False NCIT:C20217 Suspension Culture False True False NCIT:C20218 Human Cell Line False True False NCIT:C20219 Monkey Cell Line False True False NCIT:C20220 Mouse Cell Line False True False +NCIT:C202206 RASAL1 Gene Amplification False True False +NCIT:C202207 BCL6 Degrader BMS-986458 False True False +NCIT:C202208 Ossicle Pattern False True False NCIT:C20221 Hamster Cell Line False True False +NCIT:C202210 B. infantis-based Formulation PBCLN-014 False True False +NCIT:C202211 Human Milk Oligosaccharides-based Formulation PBCLN-010 False True False +NCIT:C202212 Exercised Five or More Days per Week False True False +NCIT:C202213 Exercised Three to Four Days per Week False True False +NCIT:C202214 Exercised One to Two Days per Week False True False +NCIT:C202215 0-30 Days False True False +NCIT:C202216 31-90 Days False True False +NCIT:C202217 91-180 Days False True False +NCIT:C202218 Greater than or Equal to 181 Days False True False +NCIT:C202219 Gigantiform Cementoma False True False NCIT:C20222 Rat Cell Line False True False +NCIT:C202220 No Problem False True False +NCIT:C202221 Mild Problem False True False +NCIT:C202222 Mild to Moderate Problem False True False +NCIT:C202223 Moderate Problem False True False +NCIT:C202224 Severe Problem False True False +NCIT:C202225 Allogeneic Anti-CD19 CAR-gamma/delta T-cells QH103 False True False +NCIT:C202226 Allogeneic Anti-CD19 Gamma-delta CAR-T Cells UTAA09 False True False +NCIT:C202227 Anti-CD147 Monoclonal Antibody DS-1471 False True False +NCIT:C202228 Anti-CD73 Monoclonal Antibody HB0045 False True False +NCIT:C202229 Anti-CLDN18.2/Anti-PD-L1 CAR-T Cells False True False NCIT:C20223 hGH Gene False True False +NCIT:C202230 Anti-GPRC5D/anti-CD3 Bispecific Antibody LBL-034 False True False +NCIT:C202231 Anti-LILRB2 Monoclonal Antibody OR502 False True False +NCIT:C202232 Autologous Anti-MSLN CAR/HLA-A*02-gated Inhibitory Receptor/B2M shRNA-expressing T-lymphocytes A2B694 False True False +NCIT:C202233 Autologous CAR T Cells KITE-197 False True False +NCIT:C202234 Autologous dnTGF-BRII-armored Anti-GPC3 CAR T-cells AZD5851 False True False +NCIT:C202235 Autologous TROP2-CAR-transduced PD-1-positive T Cells T60c False True False +NCIT:C202236 Autologous Tumor Infiltrating Lymphocytes GT101 False True False +NCIT:C202237 BCR-ABL Inhibitor TGRX-678 False True False +NCIT:C202238 DGK-alpha Inhibitor GS-9911 False True False +NCIT:C202239 ENPP1 Inhibitor SR-8541A False True False NCIT:C20224 TK Gene False True False +NCIT:C202240 Fc-VEGFR1 Fusion Protein PB101 False True False +NCIT:C202241 Fractalkine Receptor Antagonist KAND567 False True False +NCIT:C202242 Gallium Ga 68 labeled PSMA-targeting Radiodiagnostic Agent HRS-9815 False True False +NCIT:C202243 GPC3-targeted Plasmid DNA Vaccine NWRD06 False True False +NCIT:C202244 GPRC5D/BCMA/CD3-targeting T-cell Engager IBI3003 False True False +NCIT:C202245 HIF-2alpha Inhibitor HS-10516 False True False +NCIT:C202246 IL-12-Fc Fusion Protein KGX101 False True False +NCIT:C202247 KRAS Inhibitor BI 3706674 False True False +NCIT:C202248 Lipid Nanoparticle Encapsulated mRNA Encoding Human Single-chain IL-12 ABO2011 False True False +NCIT:C202249 PI3K/HDAC Inhibitor BEBT-908 False True False NCIT:C20225 DNA Interstrand Cross-Link Repair False True False +NCIT:C202250 Rac/Cdc42 Inhibitor MBQ-167 False True False +NCIT:C202251 CT2584 Mesylate False True False +NCIT:C202255 Feature Barcoding False True False +NCIT:C202259 Number of Cells False True False NCIT:C20226 HeLa False True False +NCIT:C202266 BEBT-908 Free Base False True False +NCIT:C202267 Treatment not Administered per the Discretion of the Health Care Provider False True False +NCIT:C202268 Three Point Scale for Staining Intensity False True False +NCIT:C202269 Four Point Scale for Staining Intensity False True False NCIT:C20227 HeLa S3 False True False +NCIT:C202270 3'-End Bias False True False +NCIT:C202271 5'-End Bias False True False +NCIT:C202272 Full-Length Transcript False True False +NCIT:C202273 Staining Intensity 4+ False True False +NCIT:C202274 Mitotic Count Reported Indicator False True False +NCIT:C202275 Staining Intensity Value Reported Indicator False True False +NCIT:C202276 Once a Week for at Least a Year False True False +NCIT:C202277 Affymetrix Genome-Wide Human SNP Array 6.0 False True False +NCIT:C202278 Anti-HER3 Antibody-drug Conjugate SHR-A2009 False True False +NCIT:C202279 iPSC-derived Anti-CD19 CAR/CD16/IL-15RF/ADR-expressing CD38-eliminated NK Cells FT522 False True False NCIT:C20228 HeLa/SF False True False +NCIT:C202280 Eating Answer False True False +NCIT:C202281 NUDT15 Gene False True False +NCIT:C202282 NUDT15 wt Allele False True False +NCIT:C202283 Nucleotide Triphosphate Diphosphatase NUDT15 False True False +NCIT:C202284 EWSR1/TFCP2 Fusion Gene False True False +NCIT:C202285 FUS/TFCP2 Fusion Gene False True False +NCIT:C202286 Adult Day Care Center False True False +NCIT:C202287 Ambulatory Military Outpatient Operational (Transportable) Component Clinic False True False +NCIT:C202288 Inpatient Admission from Emergency Room Visit False True False +NCIT:C202289 Non-Hospital Care Facility Visit False True False NCIT:C20229 HL-60/MX2 False True False +NCIT:C202290 Discharge Summary False True False +NCIT:C202291 External Common Data Model Instance False True False +NCIT:C202292 Insurance Claim Detail False True False +NCIT:C202293 Insurance Claim Header False True False +NCIT:C202294 Home-related Exposure False True False +NCIT:C202295 Social Setting-related Exposure False True False +NCIT:C202296 Continuous Oxygen Administration False True False +NCIT:C202297 Intermittent Oxygen Administration False True False NCIT:C2023 Autologous-Cell Leukemia Vaccine False True False NCIT:C20230 HL-60/MX1 False True False +NCIT:C202300 Mail Order Record False True False +NCIT:C202301 Payer System Record False True False +NCIT:C202302 Pre-Qualification Time Period False True False +NCIT:C202303 Provider Charge List False True False +NCIT:C202304 Dorsal Root Ganglion Stimulation False True False +NCIT:C202305 Provider Financial System False True False +NCIT:C202306 CDISC SDTM London Deauville Criteria Point Scale 2014 Response Terminology False True False +NCIT:C202307 Provider Incurred Cost Record False True False +NCIT:C202308 US Social Security Death Master File False True False +NCIT:C202309 Vision Claim False True False NCIT:C20231 EG Cell Line False True False +NCIT:C202310 Point-of-Care Laboratory False True False +NCIT:C202311 Patient Self-Testing False True False +NCIT:C202312 Condition to be Diagnosed by Procedure False True False +NCIT:C202313 Contained Casualty Setting False True False +NCIT:C202314 Geriatric Assessment Facility False True False +NCIT:C202315 Fee-for-Service Private Physicians Group Office False True False +NCIT:C202316 Free-standing Ambulatory Surgery Facility False True False +NCIT:C202317 Free-standing Birthing Center False True False +NCIT:C202318 Free-standing Geriatric Health Center False True False +NCIT:C202319 Free-standing Laboratory False True False NCIT:C20232 ES Cell Line False True False +NCIT:C202320 Free-standing Mental Health Center False True False +NCIT:C202321 Free-standing Radiology Facility False True False +NCIT:C202322 Other Site of Care False True False +NCIT:C202323 Other Hospital Outpatient Clinic False True False +NCIT:C202324 Children's Hospital False True False +NCIT:C202325 Community Hospital False True False +NCIT:C202326 Government Hospital False True False +NCIT:C202327 Hospital Trauma Center False True False +NCIT:C202329 Other Independent Ambulatory Care Provider Facility False True False NCIT:C20233 BG01 False True False +NCIT:C202330 Physician Group False True False +NCIT:C202331 Private Residential Care Home False True False +NCIT:C202332 Psychogeriatric Day Hospital False True False +NCIT:C202333 Residential School Infirmary False True False +NCIT:C202334 Private Practice False True False +NCIT:C202336 Sports Facility False True False +NCIT:C202337 Traveler Aid Clinic False True False +NCIT:C202338 Dose Omitted False True False +NCIT:C202339 Dose Given Early False True False NCIT:C20234 BG02 False True False +NCIT:C202340 Crushed Tablet Dosage Form False True False +NCIT:C202341 Refrigerate False True False +NCIT:C202342 Mount False True False +NCIT:C202343 Expected Remaining Amount False True False +NCIT:C202344 Posteromedial False True False +NCIT:C202345 Film Coated Immediate Release Crushed Tablet Dosage Form False True False +NCIT:C202346 Film Coated Immediate Release Tablet Dosage Form False True False +NCIT:C202347 Sustained Atrial Tachycardia by ECG Finding False True False +NCIT:C202348 Non-Sustained Accelerated Idioventricular Rhythm by ECG Finding False True False +NCIT:C202349 Sustained Accelerated Idioventricular Rhythm by ECG Finding False True False NCIT:C20235 BG03 False True False +NCIT:C202350 Beta Lactoglobulin False True False +NCIT:C202351 Budgerigar Feather Antigen False True False +NCIT:C202352 Budgerigar Dropping Antigen False True False +NCIT:C202353 Budgerigar Serum Proteins False True False +NCIT:C202354 Japanese Cypress Pollen False True False +NCIT:C202355 Japanese Alder Pollen False True False +NCIT:C202356 Tomato Antigen False True False +NCIT:C202357 Sweet Vernal Grass Pollen Antigen False True False +NCIT:C202358 Beef Antigen False True False +NCIT:C202359 Common Buckwheat Antigen False True False NCIT:C20236 BG04 False True False +NCIT:C202360 Incense Cedar Pollen False True False +NCIT:C202361 Cancer pagurus Antigen False True False +NCIT:C202362 Green Kiwifruit Antigen False True False +NCIT:C202363 Natural Rubber Latex Antigen False True False +NCIT:C202364 Ovomucoid False True False +NCIT:C202366 Peach Antigen False True False +NCIT:C202367 Pork Antigen False True False +NCIT:C202368 Rice Antigen False True False +NCIT:C202369 Thunnus albacares Antigen False True False NCIT:C20237 CY12 False True False +NCIT:C202370 White Birch Pollen False True False +NCIT:C202371 Mitochondria M2-3E Antigen False True False +NCIT:C202372 Salmonella Typhi O Antigen False True False +NCIT:C202373 MAST 5-Grade False True False +NCIT:C202374 MAST 7-Grade False True False +NCIT:C202375 NephroCheck AKI Risk 2013 Formula False True False +NCIT:C202376 S-Pancreas-1 Antigen Measurement False True False +NCIT:C202377 Ketovaline Measurement False True False +NCIT:C202378 Ketoleucine Measurement False True False +NCIT:C202379 Ketoisoleucine Measurement False True False NCIT:C20238 CY30 False True False +NCIT:C202380 Urea Excretion Rate False True False +NCIT:C202381 Plasmin Alpha-2 Antiplasmin Complex Measurement False True False +NCIT:C202382 Aldosterone Excretion Rate False True False +NCIT:C202383 3-Nitrotyrosine Measurement False True False +NCIT:C202384 Acute Kidney Injury Risk Score False True False +NCIT:C202385 Activin A Measurement False True False +NCIT:C202386 Activin AB Measurement False True False +NCIT:C202387 Activin B Measurement False True False +NCIT:C202388 Phosphorylated Tau Protein 231 Measurement False True False +NCIT:C202389 Phosphorylated Tau Protein 217 Measurement False True False NCIT:C20239 CY40 False True False +NCIT:C202390 Phosphorylated Tau Protein 212 Measurement False True False +NCIT:C202391 Free Tissue Factor Pathway Inhibitor Antigen Measurement False True False +NCIT:C202392 Free Immunoglobulin E Measurement False True False +NCIT:C202393 Soluble Tumor Necrosis Factor Receptor Superfamily Member 9 Measurement False True False +NCIT:C202394 Complement C2 Measurement False True False +NCIT:C202395 Extranodal Region False True False +NCIT:C202396 Intra-Arterial Differential Pressure Transduction False True False +NCIT:C202397 Indirect Immunofluorescent Microscopy False True False +NCIT:C202398 Thromboelastography False True False +NCIT:C202399 Focus Forming Assay False True False NCIT:C2024 H-ras Antisense Oligodeoxynucleotide ISIS 2503 False True False NCIT:C20240 CY51 False True False +NCIT:C202400 Immunoagglutination Assay False True False +NCIT:C202401 Cell Based Neutralizing Antibody Assay False True False +NCIT:C202402 Semi-Quantitative Reverse Transcriptase Polymerase Chain Reaction False True False +NCIT:C202403 High Performance Liquid Chromatography/Accelerator Mass Spectrometry False True False +NCIT:C202404 Fluorescence Resonance Energy Transfer False True False +NCIT:C202405 Interferon Gamma Release Assay False True False +NCIT:C202406 Dye Dilution Method False True False +NCIT:C202407 Volume Conductivity Scatter Method False True False +NCIT:C202408 Computed Tomography Angiography False True False +NCIT:C202409 Modified Vaccinia Ankara Virus False True False NCIT:C20241 CY81 False True False +NCIT:C202410 Vaccinia Virus Western Reserve False True False +NCIT:C202411 Legionella longbeachae Serogroup 1 False True False +NCIT:C202412 Streptococcus pneumoniae Danish Serotype 6A False True False +NCIT:C202413 Aerobic Gram-Negative Bacteria False True False +NCIT:C202414 Aerobic Gram-Positive Bacteria False True False +NCIT:C202415 Alloiococcus otitis False True False +NCIT:C202416 Carbapenem Resistant Acinetobacter baumannii False True False +NCIT:C202417 Borreliella mayonii False True False +NCIT:C202418 B-Cell Lymphoma 6 Protein Measurement False True False +NCIT:C202419 Cyclin D1 Measurement False True False NCIT:C20242 CY82 False True False +NCIT:C202420 c-Myc Measurement False True False +NCIT:C202421 Integrin Subunit Beta 3 Measurement False True False +NCIT:C202422 Interferon Regulatory Factor 4 Measurement False True False +NCIT:C202423 SRY-Box Transcription Factor 10 Measurement False True False +NCIT:C202424 Scavenger Receptor Class D, Member 1 Measurement False True False +NCIT:C202425 S100 Calcium Binding Protein Measurement False True False +NCIT:C202426 MART-1 Antigen Measurement False True False +NCIT:C202427 Melanocyte Protein PMEL Measurement False True False +NCIT:C202428 T-Cell Surface Glycoprotein CD5 Measurement False True False +NCIT:C202429 Membrane Spanning 4-Domains A1 Measurement False True False NCIT:C20243 CY91 False True False +NCIT:C202430 Neural Cell Adhesion Molecule 1 Measurement False True False +NCIT:C202431 CD3 T-Cell Marker Measurement False True False +NCIT:C202432 T-Cell Surface Glycoprotein CD4 Measurement False True False +NCIT:C202433 T-Cell Surface Glycoprotein CD8 Measurement False True False +NCIT:C202434 Postural Tremor Evaluation False True False +NCIT:C202435 Glutamate to Creatine Ratio Measurement False True False +NCIT:C202436 Lactate to Creatine Ratio Measurement False True False +NCIT:C202437 Glutamine to Creatine Ratio Measurement False True False +NCIT:C202438 Tricarboxylic Acid Cycle Rate Measurement False True False +NCIT:C202439 Glutamate-Creatine Cycle Rate Measurement False True False NCIT:C20244 CY92 False True False +NCIT:C202440 Target Nodal Response False True False +NCIT:C202441 Circulating Lymphocyte Response False True False +NCIT:C202442 Platelet Response False True False +NCIT:C202443 Hemoglobin Response False True False +NCIT:C202444 Informed Consent Obtained For Protocol-Specified Activity False True False +NCIT:C202445 Informed Consent Declined For Protocol-Specified Activity False True False +NCIT:C202446 First Ventilatory Threshold False True False +NCIT:C202447 Gastrojejunal Route of Administration False True False +NCIT:C202448 Transplant Study False True False +NCIT:C202449 Hepatomegaly Indicator False True False NCIT:C20245 CY10 False True False +NCIT:C202450 Splenomegaly Indicator False True False +NCIT:C202451 Microliter per Liter False True False +NCIT:C202452 Per 50 Cells False True False +NCIT:C202453 Per 100 Cells False True False +NCIT:C202454 Per Cell False True False +NCIT:C202455 Normochromatic Erythrocytes Scored Count False True False +NCIT:C202456 Aberrant Craniopharyngeal Structures False True False +NCIT:C202457 Persistent Rathke's Pouch False True False +NCIT:C202458 Cystic Follicle False True False +NCIT:C202459 Schwann Cell Laminar Accumulation False True False NCIT:C20246 CyThera ES Cell Line False True False +NCIT:C202460 Matrix Accumulation False True False +NCIT:C202461 Compound Follicle False True False +NCIT:C202462 Postnatal Weaning Day False True False +NCIT:C202463 Litter Identifier False True False +NCIT:C202464 Mesenteric Ganglion False True False +NCIT:C202465 Compendial Name False True False +NCIT:C202466 Anti-PSMA/Anti-CD28 Bispecific Antibody JNJ-87189401 False True False +NCIT:C202467 Adenosine A2A Receptor Antagonist JNJ-86974680 False True False +NCIT:C202468 PI3K Alpha Inhibitor False True False +NCIT:C202469 Claim Enrollment Record False True False NCIT:C20247 BresaGen ES Cell Line False True False +NCIT:C202470 Cost Report False True False +NCIT:C202471 Government Report False True False +NCIT:C202472 Health Information Exchange Record False True False +NCIT:C202473 Helicopter-Based Care False True False +NCIT:C202474 PIK3CA NM_006218.4:c.263G>A False True False +NCIT:C202475 PIK3CA NP_006209.2:p.R88Q False True False +NCIT:C202476 PIK3CA NM_006218.4:c.1035T>A False True False +NCIT:C202477 PIK3CA NP_006209.2:p.N345K False True False +NCIT:C202478 PIK3CA NP_006209.2:p.Q546X False True False +NCIT:C202479 PIK3CA NM_006218.4:c.3129G>A False True False NCIT:C20248 ES ES Cell Line False True False +NCIT:C202480 PIK3CA NM_006218.4:c.3129G>C False True False +NCIT:C202481 PIK3CA NM_006218.4:c.3129G>T False True False +NCIT:C202482 PIK3CA NP_006209.2:p.M1043I False True False +NCIT:C202483 PIK3CA NM_006218.4:c.3145G>C False True False +NCIT:C202484 PIK3CA NP_006209.2:p.G1049R False True False +NCIT:C202485 Implantation Gel Dosage Form False True False +NCIT:C202486 Active Substance False True False +NCIT:C202487 Screening Epoch False True False +NCIT:C202488 Dispersion for Implantation Gel Dosage Form False True False +NCIT:C202489 Dispersion Dosage Form False True False NCIT:C20249 ES01 False True False +NCIT:C202490 Solution for Implantation Gel False True False +NCIT:C202491 Dispersion and Solution for Implantation Gel False True False +NCIT:C202492 Acinetobacter baumanii False True False +NCIT:C202493 Biomedical Concept Property False True False +NCIT:C202494 Biomedical Concept Property Name False True False +NCIT:C202495 Biomedical Concept Property Required Indicator False True False +NCIT:C202496 Biomedical Concept Property Enabled Indicator False True False +NCIT:C202498 PROMIS Pediatric and Parent Proxy Social Health Domain False True False +NCIT:C202499 PROMIS Relationships/Social Support Subordinate Domain False True False NCIT:C2025 Tyrphostin A8 False True False NCIT:C20250 ES02 False True False +NCIT:C202501 PROMIS Item Bank Version 2.0 Cognitive Function Short Form 6a Questionnaire False True False +NCIT:C202502 PROMIS Item Bank Version 1.0 Fatigue Short Form 7a Questionnaire False True False +NCIT:C202503 Minnesota Tobacco Withdrawal Scale-Revised Clinical Classification False True False +NCIT:C202504 PROMIS IB Version 2.0 Cognitive Function SF 6a - My Thinking Has Been Slow False True False +NCIT:C202505 PROMIS IB Version 2.0 Cognitive Function SF 6a - Brain Not Working as Well as Usual False True False +NCIT:C202506 PROMIS IB Version 2.0 Cognitive Function SF 6a - Had to Work Harder to Keep Track False True False +NCIT:C202507 PROMIS IB Version 2.0 Cognitive Function SF 6a - Trouble Shift Activities Thinking False True False +NCIT:C202508 PROMIS IB Version 2.0 Cognitive Function SF 6a - Had Trouble Concentrating False True False +NCIT:C202509 PROMIS IB Version 2.0 Cognitive Function SF 6a - Work Hard Pay Attention or Mistake False True False NCIT:C20251 ES03 False True False +NCIT:C202510 PROMIS IB Version 1.0 Fatigue SF 7a - Often Feel Tired False True False +NCIT:C202511 PROMIS IB Version 1.0 Fatigue SF 7a - Often Extreme Exhaustion False True False +NCIT:C202512 PROMIS IB Version 1.0 Fatigue SF 7a - Often Run Out of Energy False True False +NCIT:C202513 PROMIS IB Version 1.0 Fatigue SF 7a - Often Fatigue Limit You at Work False True False +NCIT:C202514 PROMIS IB Version 1.0 Fatigue SF 7a - Often Too Tired to Think Clearly False True False +NCIT:C202515 PROMIS IB Version 1.0 Fatigue SF 7a - Often Too Tired Take Bath or Shower False True False +NCIT:C202516 PROMIS IB Version 1.0 Fatigue SF 7a - Often Energy Exercise Strenuously False True False +NCIT:C202517 MTWS-Revised Version - Angry, Irritable, Frustrated False True False +NCIT:C202518 MTWS-Revised Version - Anxious, Nervous False True False +NCIT:C202519 MTWS-Revised Version - Depressed Mood, Sad False True False NCIT:C20252 ES04 False True False +NCIT:C202520 MTWS-Revised Version - Difficulty Concentrating False True False +NCIT:C202521 MTWS-Revised Version - Increased Appetite, Hungry, Weight Gain False True False +NCIT:C202522 MTWS-Revised Version - Sleep Problems, Awakening at Night False True False +NCIT:C202523 MTWS-Revised Version - Restless False True False +NCIT:C202524 MTWS-Revised Version - Impatient False True False +NCIT:C202525 MTWS-Revised Version - Craving to Smoke False True False +NCIT:C202526 MTWS-Revised Version - Constipation False True False +NCIT:C202527 MTWS-Revised Version - Dizziness False True False +NCIT:C202528 MTWS-Revised Version - Coughing False True False +NCIT:C202529 MTWS-Revised Version - Dreaming or Nightmares False True False NCIT:C20253 ES05 False True False +NCIT:C202530 MTWS-Revised Version - Nausea False True False +NCIT:C202531 MTWS-Revised Version - Sore Throat False True False +NCIT:C202532 MTWS-Revised Version - Total Withdrawal Discomfort Score False True False +NCIT:C202533 Minnesota Tobacco Withdrawal Scale-Revised MTWSR101 Through MTWSR115 Original Result - None False True False +NCIT:C202534 Minnesota Tobacco Withdrawal Scale-Revised MTWSR101 Through MTWSR115 Original Result - Slight False True False +NCIT:C202535 Minnesota Tobacco Withdrawal Scale-Revised MTWSR101 Through MTWSR115 Original Result - Mild False True False +NCIT:C202536 Minnesota Tobacco Withdrawal Scale-Revised MTWSR101 Through MTWSR115 Original Result - Moderate False True False +NCIT:C202537 Minnesota Tobacco Withdrawal Scale-Revised MTWSR101 Through MTWSR115 Original Result - Severe False True False +NCIT:C202538 Minnesota Tobacco Withdrawal Scale-Revised MTWSR101 Through MTWSR115 Standardized Character Result 4 False True False +NCIT:C202539 Minnesota Tobacco Withdrawal Scale-Revised MTWSR101 Through MTWSR115 Standardized Character Result 3 False True False NCIT:C20254 ES06 False True False +NCIT:C202540 Minnesota Tobacco Withdrawal Scale-Revised MTWSR101 Through MTWSR115 Standardized Character Result 2 False True False +NCIT:C202541 Minnesota Tobacco Withdrawal Scale-Revised MTWSR101 Through MTWSR115 Standardized Character Result 1 False True False +NCIT:C202542 Minnesota Tobacco Withdrawal Scale-Revised MTWSR101 Through MTWSR115 Standardized Character Result 0 False True False +NCIT:C202543 46,XY Sex Reversal 2 False True False +NCIT:C202544 Alacrima, Achalasia, and Impaired Intellectual Development Syndrome False True False +NCIT:C202545 Autosomal Dominant Congenital Myopathy-1A False True False +NCIT:C202546 Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress False True False +NCIT:C202547 Developmental and Epileptic Encephalopathy 44 False True False +NCIT:C202548 Developmental and Epileptic Encephalopathy 85 with or without Midline Brain Defects False True False +NCIT:C202549 Functional Oral Intake Scale False True False NCIT:C20255 Geron ES Cell Line False True False +NCIT:C202550 Modified Functional Oral Intake Scale False True False +NCIT:C202551 Takes Nothing by Mouth False True False +NCIT:C202552 Tube Dependent with Minimal Oral Intake False True False +NCIT:C202553 Tube Dependent with Consistent Oral Intake False True False +NCIT:C202554 Oral Diet of Single Consistency False True False +NCIT:C202555 Oral Diet of Multiple Consistencies with Special Preparation or Compensation False True False +NCIT:C202556 Oral Diet of Multiple Consistencies with Specific Preparation False True False +NCIT:C202557 Total Oral Diet False True False +NCIT:C202558 Takes Nothing by Mouth, Non-nutritive Sucking/Dummy Dips/Mouthcare Only False True False +NCIT:C202559 Tube Dependent with Minimal Oral Intake for Experience or Pleasure False True False NCIT:C20256 GE01 False True False +NCIT:C202560 Tube Dependent with Consistent Oral Intake to Meet Some Nutrition/Hydration Needs False True False +NCIT:C202561 Total Oral Intake, Special Preparation Required False True False +NCIT:C202562 Total Oral Intake, Special Conditions or Modifications Required False True False +NCIT:C202563 Total Age-Appropriate Oral Intake False True False +NCIT:C202564 Oral Intake Ability False True False +NCIT:C202565 Friend Question False True False +NCIT:C202566 Felt Accepted by Kids My Age False True False +NCIT:C202567 Able to Count on Friends False True False +NCIT:C202568 Friends and I Helped Each Other False True False +NCIT:C202569 Other Kids Wanted to be Friends False True False NCIT:C20257 GE07 False True False +NCIT:C202570 Anti-CD19/Anti-CD3/Anti-CD2 Trispecific Antibody PIT565 False True False +NCIT:C202571 Capivasertib/Fulvestrant Regimen False True False +NCIT:C202572 Chondrodermatitis Nodularis Chronica Helicis False True False +NCIT:C202573 Cystic Chondromalacia False True False +NCIT:C202575 Pharmaceutical Product Ingredient False True False +NCIT:C202576 Disease Contact Investigation Indicator False True False +NCIT:C202577 Long-term Follow-up Epoch False True False +NCIT:C202578 Follow-Up Epoch False True False +NCIT:C202579 Investigational Medicinal Product False True False NCIT:C20258 GE09 False True False +NCIT:C202580 Basket Trial Design False True False +NCIT:C202581 Platform Trial Design False True False +NCIT:C202586 R-mini-CHOP Regimen False True False +NCIT:C202587 Pola-R-CHP Regimen False True False +NCIT:C202588 Multiplex PCR with Matrix-Assisted Laser Desorption Ionization Mass Spectrometry False True False +NCIT:C202589 Umbrella Trial Design False True False NCIT:C20259 GE13 False True False +NCIT:C202590 Low Penetrance Risk Allele False True False +NCIT:C202591 Percent Risk of Recurrence in 3 Years False True False +NCIT:C202592 Shifted Termination Assay False True False +NCIT:C202593 Genomic Scar Score False True False +NCIT:C202595 PSA Decline Greater than or Equal to 30 Percent False True False +NCIT:C202596 PROMIS Pain Intensity Subordinate Domain False True False +NCIT:C202597 Microfluidic Cell Isolation False True False +NCIT:C202598 Droplet-based Single-cell Isolation False True False +NCIT:C202599 Nucleic Acid Capture False True False NCIT:C2026 Tyrphostin A9 False True False NCIT:C20260 GE14 False True False +NCIT:C202600 Sequencing Library Preparation False True False +NCIT:C202601 Allogeneic Natural Killer Cells IDP-023 False True False +NCIT:C202602 Early-Onset Progressive Encephalopathy with Brain Atrophy and Thin Corpus Callosum False True False +NCIT:C202603 Episodic Ataxia Type 2 False True False +NCIT:C202604 Focal Segmental Glomerulosclerosis 7 False True False +NCIT:C202605 Acetylcholine Releasing Agent ST101 False True False +NCIT:C202606 Mental Retardation, Autosomal Dominant 18 False True False +NCIT:C202607 Geleophysic Dysplasia 1 False True False +NCIT:C202608 Multiple Mitochondrial Dysfunctions Syndrome Type 3 False True False NCIT:C20261 GE91 False True False +NCIT:C202610 Primary Ciliary Dyskinesia 42 False True False +NCIT:C202612 Progressive Pseudorheumatoid Dysplasia False True False +NCIT:C202614 KCNC1 Gene False True False +NCIT:C202615 KCNC1 wt Allele False True False +NCIT:C202616 Potassium Voltage-Gated Channel Subfamily C Member 1 False True False +NCIT:C202617 KCND3 Gene False True False +NCIT:C202618 KCND3 wt Allele False True False +NCIT:C202619 Potassium Voltage-Gated Channel Subfamily D Member 3 False True False NCIT:C20262 GE92 False True False +NCIT:C202626 KCNE1 Gene False True False +NCIT:C202627 Total Lesion Uptake False True False +NCIT:C202628 KCNE1 wt Allele False True False +NCIT:C202629 Total Metabolic Tumor Volume False True False NCIT:C20263 Goteborg ES Cell Line False True False +NCIT:C202630 Potassium Voltage-Gated Channel Subfamily E Member 1 False True False +NCIT:C202631 Proximal Colon False True False +NCIT:C202632 Distal Colon False True False +NCIT:C202636 KCNH2 Gene False True False +NCIT:C202637 KCNH2 wt Allele False True False +NCIT:C202638 Potassium Voltage-Gated Channel Subfamily H Member 2 False True False +NCIT:C202639 KCNJ11 Gene False True False NCIT:C20264 SA01 False True False +NCIT:C202640 KCNJ11 wt Allele False True False +NCIT:C202641 Normocellular Bone Marrow False True False +NCIT:C202642 ATP-Sensitive Inward Rectifier Potassium Channel 11 False True False +NCIT:C202643 KCNJ2 Gene False True False +NCIT:C202644 KCNJ2 wt Allele False True False +NCIT:C202645 Inward Rectifier Potassium Channel 2 False True False +NCIT:C202648 CD33-specific CAR Lentiviral Vector-transduced Allogeneic T-lymphocytes False True False +NCIT:C202649 FN1 Gene Product False True False NCIT:C20265 SA02 False True False +NCIT:C202650 Extra Domain B Fibronectin False True False +NCIT:C202651 FOSB Gene Rearrangement False True False +NCIT:C202653 EDB-FN-targeting Gadolinium-based Contrast Agent MT218 False True False +NCIT:C202657 Quizartinib Regimen False True False +NCIT:C202658 KCNQ2 Gene False True False +NCIT:C202659 KCNQ2 wt Allele False True False NCIT:C20266 SA03 False True False +NCIT:C202660 Potassium Voltage-Gated Channel Subfamily KQT Member 2 False True False +NCIT:C202663 Unresectable or Metastatic Non-Clear Cell Renal Cell Carcinoma, Excluding Chromophobe Renal Cell Carcinoma False True False +NCIT:C202664 KCNV2 Gene False True False +NCIT:C202665 KCNV2 wt Allele False True False +NCIT:C202666 Potassium Voltage-Gated Channel Subfamily V Member 2 False True False +NCIT:C202667 Appetite Stimulant False True False +NCIT:C202668 Tisagenlecleucel Regimen False True False +NCIT:C202669 Brexucabtagene Autoleucel Regimen False True False NCIT:C20267 Karolinska ES Cell Line False True False +NCIT:C202670 Trastuzumab Emtansine Regimen False True False +NCIT:C202671 Tisotumab Vedotin Regimen False True False +NCIT:C202672 Futibatinib Regimen False True False +NCIT:C202673 KIT Non-Exon 9 Mutation False True False +NCIT:C202674 KLHL24 Gene False True False +NCIT:C202675 KLHL24 wt Allele False True False +NCIT:C202676 Kelch-Like Protein 24 False True False +NCIT:C202677 KLHL40 Gene False True False +NCIT:C202678 KLHL40 wt Allele False True False +NCIT:C202679 Kelch-Like Protein 40 False True False NCIT:C20268 KA08 False True False +NCIT:C202680 KLK5 Gene False True False +NCIT:C202681 KLK5 wt Allele False True False +NCIT:C202682 Kallikrein-5 False True False +NCIT:C202683 KLK7 Gene False True False +NCIT:C202685 KLK7 wt Allele False True False +NCIT:C202686 Kallikrein-7 False True False +NCIT:C202687 LAMA2 Gene False True False +NCIT:C202688 LAMA2 wt Allele False True False +NCIT:C202689 Laminin Subunit Alpha-2 False True False NCIT:C20269 KA09 False True False +NCIT:C202690 LAMB2 Gene False True False +NCIT:C202691 LAMB2 wt Allele False True False +NCIT:C202692 Laminin Subunit Beta-2 False True False +NCIT:C202693 Cosmetic Product Category False True False +NCIT:C202694 Baby Product Cosmetic Product Category False True False +NCIT:C202695 Bath Preparation Cosmetic Product Category False True False +NCIT:C202696 Eye Makeup Preparation Cosmetic Product Category False True False +NCIT:C202697 Child Eye Makeup Preparation Cosmetic Product Category False True False +NCIT:C202698 Fragrance Preparation Cosmetic Product Category False True False +NCIT:C202699 Non-Coloring Hair Preparation Cosmetic Product Category False True False NCIT:C2027 Tyrphostin A48 False True False NCIT:C20270 KA40 False True False +NCIT:C202700 Hair Coloring Preparation Cosmetic Product Category False True False +NCIT:C202701 Makeup Preparation Cosmetic Product Category False True False +NCIT:C202702 Child Makeup Preparation Cosmetic Product Category False True False +NCIT:C202703 Manicuring Preparation Cosmetic Product Category False True False +NCIT:C202704 Oral Product Cosmetic Product Category False True False +NCIT:C202705 Personal Cleanliness Cosmetic Product Category False True False +NCIT:C202706 Shaving Preparation Cosmetic Product Category False True False +NCIT:C202707 Skin Care Preparation Cosmetic Product Category False True False +NCIT:C202708 Suntan Preparation Cosmetic Product Category False True False +NCIT:C202709 Tattoo Preparation Cosmetic Product Category False True False NCIT:C20271 KA41 False True False +NCIT:C202710 Other Preparation Cosmetic Product Category False True False +NCIT:C202712 Baby Shampoo Cosmetic Product False True False +NCIT:C202713 Baby Lotion, Oil, Powder and Cream Cosmetic Product False True False +NCIT:C202714 Baby Wipe Cosmetic Product False True False +NCIT:C202715 Other Baby Cosmetic Product False True False +NCIT:C202716 Other Leave-On Baby Cosmetic Product False True False +NCIT:C202717 Other Rinse-Off Baby Cosmetic Product False True False +NCIT:C202718 Bath Oil, Tablet and Salt Cosmetic Product False True False +NCIT:C202719 Bubble Bath Cosmetic Product False True False NCIT:C20272 KA42 False True False +NCIT:C202720 Bath Capsule Cosmetic Product False True False +NCIT:C202721 Other Cosmetic Bath Product False True False +NCIT:C202722 Eyebrow Pencil Cosmetic Product False True False +NCIT:C202723 Eyeliner Cosmetic Product False True False +NCIT:C202724 Eye Shadow Cosmetic Product False True False +NCIT:C202725 Eye Lotion Cosmetic Product False True False +NCIT:C202726 Eye Makeup Remover Cosmetic Product False True False +NCIT:C202727 False Eyelash Cosmetic Product False True False +NCIT:C202728 Mascara Cosmetic Product False True False +NCIT:C202729 Eyelash and Eyebrow Adhesive, Glue and Sealant Cosmetic Product False True False NCIT:C20273 KA43 False True False +NCIT:C202730 Eyelash and Eyebrow Preparation Cosmetic Product False True False +NCIT:C202731 Eyelash Cleanser Cosmetic Product False True False +NCIT:C202732 Other Eye Makeup Preparation Cosmetic Product False True False +NCIT:C202733 Child Eyeshadow Cosmetic Product False True False +NCIT:C202734 Other Child Eye Makeup Cosmetic Product False True False +NCIT:C202735 Cologne and Toilet Water Cosmetic Product False True False +NCIT:C202736 Perfume Cosmetic Product False True False +NCIT:C202737 Fragrance Powder Cosmetic Product False True False +NCIT:C202738 Other Fragrance Cosmetic Product False True False +NCIT:C202739 Non-Coloring Hair Conditioner Cosmetic Product False True False NCIT:C20274 Maria ES Cell Line False True False +NCIT:C202740 Leave-On Non-Coloring Hair Conditioner Cosmetic Product False True False +NCIT:C202741 Rinse-Off Non-Coloring Hair Conditioner Cosmetic Product False True False +NCIT:C202742 Non-Coloring Hair Spray Cosmetic Product False True False +NCIT:C202743 Non-Coloring Hair Straightener Cosmetic Product False True False +NCIT:C202744 Non-Coloring Permanent Hair Wave Cosmetic Product False True False +NCIT:C202745 Non-Coloring Hair Rinse Cosmetic Product False True False +NCIT:C202746 Non-Coloring Hair Shampoo Cosmetic Product False True False +NCIT:C202747 Leave-On Non-Coloring Hair Shampoo Cosmetic Product False True False +NCIT:C202748 Rinse-Off Non-Coloring Hair Shampoo Cosmetic Product False True False +NCIT:C202749 Non-Coloring Hair Tonic, Dressing, and Other Grooming Aid Cosmetic Product False True False NCIT:C20275 MB01 False True False +NCIT:C202750 Non-Coloring Hair Wave Set Cosmetic Product False True False +NCIT:C202751 Other Non-Coloring Hair Preparation Cosmetic Product False True False +NCIT:C202752 Other Leave-On Non-Coloring Hair Cosmetic Product False True False +NCIT:C202753 Other Rinse-Off Non-Coloring Hair Cosmetic Product False True False +NCIT:C202754 Hair Dye and Color Cosmetic Product False True False +NCIT:C202755 Hair Tint Cosmetic Product False True False +NCIT:C202756 Hair Coloring Rinse Cosmetic Product False True False +NCIT:C202757 Leave-On Hair Coloring Rinse Cosmetic Product False True False +NCIT:C202758 Rinse-Off Hair Coloring Rinse Cosmetic Product False True False +NCIT:C202759 Hair Coloring Shampoo Cosmetic Product False True False NCIT:C20276 MB02 False True False +NCIT:C202760 Leave-On Hair Coloring Shampoo Cosmetic Product False True False +NCIT:C202761 Rinse-Off Hair Coloring Shampoo Cosmetic Product False True False +NCIT:C202762 Hair Color Spray Cosmetic Product False True False +NCIT:C202763 Hair Lighteners with Color Cosmetic Product False True False +NCIT:C202764 Hair Bleach Cosmetic Product False True False +NCIT:C202765 Eyelash and Eyebrow Dye Cosmetic Product False True False +NCIT:C202766 Other Hair Coloring Cosmetic Product False True False +NCIT:C202767 Other Leave-On Hair Coloring Cosmetic Product False True False +NCIT:C202768 Other Rinse-Off Hair Coloring Cosmetic Product False True False +NCIT:C202769 Blush and Rouge Cosmetic Product False True False NCIT:C20277 MB03 False True False +NCIT:C202770 Face Powder Cosmetic Product False True False +NCIT:C202771 Makeup Foundation Cosmetic Product False True False +NCIT:C202772 Traditional Makeup Foundation Application Cosmetic Product False True False +NCIT:C202773 Airbrush Makeup Base Application Cosmetic Product False True False +NCIT:C202774 Makeup Leg and Body Paint Cosmetic Product False True False +NCIT:C202777 Makeup Lipstick and Lip Gloss Cosmetic Product False True False +NCIT:C202778 Makeup Base Cosmetic Product False True False +NCIT:C202779 Traditional Makeup Base Application Cosmetic Product False True False NCIT:C20278 MizMedi ES Cell Line False True False +NCIT:C202780 Airbrush Makeup Application Cosmetic Product False True False +NCIT:C202781 Makeup Fixative Cosmetic Product False True False +NCIT:C202782 Other Makeup Cosmetic Product False True False +NCIT:C202783 Other Traditional Makeup Application Cosmetic Product False True False +NCIT:C202784 Other Airbrush Makeup Application Cosmetic Product False True False +NCIT:C202785 Child Blush and Rouge Cosmetic Product False True False +NCIT:C202786 Child Face Paint Cosmetic Product False True False +NCIT:C202787 Child Face Powder Cosmetic Product False True False +NCIT:C202788 Child Makeup Foundation Cosmetic Product False True False +NCIT:C202789 Child Lipstick and Lip Gloss Cosmetic Product False True False NCIT:C20279 MI01 False True False +NCIT:C202790 Child Color Hairspray Cosmetic Product False True False +NCIT:C202791 Other Child Makeup Cosmetic Product False True False +NCIT:C202792 Nail Basecoat and Undercoat Cosmetic Product False True False +NCIT:C202793 Nail Cuticle Softener Cosmetic Product False True False +NCIT:C202794 Nail Cream and Lotion Cosmetic Product False True False +NCIT:C202795 Nail Extender Cosmetic Product False True False +NCIT:C202796 Nail Polish and Enamel Cosmetic Product False True False +NCIT:C202797 Nail Polish and Enamel Remover Cosmetic Product False True False +NCIT:C202798 Other Manicuring Cosmetic Product False True False +NCIT:C202799 Oral Dentifrice Cosmetic Product False True False NCIT:C2028 Tyrphostin AG 370 False True False NCIT:C20280 Tara ES Cell Line False True False +NCIT:C202800 Oral Mouthwash and Breath Freshener Cosmetic Product False True False +NCIT:C202801 Other Oral Product Cosmetic Product False True False +NCIT:C202802 Bath Soap and Body Wash Cosmetic Product False True False +NCIT:C202803 Deodorant Cosmetic Product False True False +NCIT:C202804 Stick, Roll-On, Gel, Cream, and Wipe Deodorant Cosmetic Product False True False +NCIT:C202805 Spray Deodorant Cosmetic Product False True False +NCIT:C202806 Douche Cosmetic Product False True False +NCIT:C202807 Feminine Deodorant Cosmetic Product False True False +NCIT:C202808 Leave-On Feminine Deodorant Cosmetic Product False True False +NCIT:C202809 Rinse-Off Feminine Deodorant Cosmetic Product False True False NCIT:C20281 NC01 False True False +NCIT:C202810 Personal Disposable Wipe Cosmetic Product False True False +NCIT:C202811 Other Personal Cleanliness Product Cosmetic Product False True False +NCIT:C202812 Other Leave-On Personal Cleanliness Cosmetic Product False True False +NCIT:C202813 Other Rinse-Off Personal Cleanliness Cosmetic Product False True False +NCIT:C202814 Aftershave Lotion Cosmetic Product False True False +NCIT:C202815 Beard Softener Cosmetic Product False True False +NCIT:C202816 Shaving Talcum Cosmetic Product False True False +NCIT:C202817 Pre-Shave Lotion Cosmetic Product False True False +NCIT:C202818 Shaving Cream Cosmetic Product False True False +NCIT:C202819 Shaving Soap Cosmetic Product False True False NCIT:C20282 NC02 False True False +NCIT:C202820 Other Shaving Preparation Cosmetic Product False True False +NCIT:C202821 Cleansing Cold Cream, Lotion, Liquid and Pad Cosmetic Product False True False +NCIT:C202822 Depilatory Skin Care Cosmetic Product False True False +NCIT:C202823 Face and Neck Skin Care Cosmetic Product False True False +NCIT:C202824 Leave-On Face and Neck Skin Care Cosmetic Product False True False +NCIT:C202825 Rinse-Off Face and Neck Skin Care Cosmetic Product False True False +NCIT:C202826 Body and Hand Skin Care Cosmetic Product False True False +NCIT:C202827 Leave-On Body and Hand Skin Care Cosmetic Product False True False +NCIT:C202828 Rinse-Off Body and Hand Skin Care Cosmetic Product False True False +NCIT:C202829 Foot Powder and Spray Cosmetic Product False True False NCIT:C20283 NC03 False True False +NCIT:C202830 Moisturizing Skin Care Cosmetic Product False True False +NCIT:C202831 Night Skin Care Cosmetic Product False True False +NCIT:C202832 Paste Mask and Mud Pack Skin Care Cosmetic Product False True False +NCIT:C202833 Skin Freshener Cosmetic Product False True False +NCIT:C202834 Other Skin Care Cosmetic Product False True False +NCIT:C202835 Other Leave-On Skin Care Cosmetic Product False True False +NCIT:C202836 Other Rinse-Off Skin Care Cosmetic Product False True False +NCIT:C202837 Suntan Gel, Cream and Liquid Cosmetic Product False True False +NCIT:C202838 Indoor Tanning Cosmetic Product False True False +NCIT:C202839 Traditional Suntan Application Cosmetic Product False True False NCIT:C20284 Pochon ES Cell Line False True False +NCIT:C202840 Airbrush Suntan Application Cosmetic Product False True False +NCIT:C202841 Spray Suntan Application Cosmetic Product False True False +NCIT:C202842 Professional Airbrush Tanning Application Cosmetic Product False True False +NCIT:C202843 Professional Spray Tanning Application Cosmetic Product False True False +NCIT:C202844 Other Suntan Preparation Cosmetic Product False True False +NCIT:C202845 Permanent Tattoo Ink Cosmetic Product False True False +NCIT:C202846 Temporary Tattoo Ink Cosmetic Product False True False +NCIT:C202847 Other Tattoo Preparation Cosmetic Product False True False +NCIT:C202848 Traditional Leg and Body Paint Application Cosmetic Product False True False NCIT:C20285 CH01 False True False +NCIT:C202850 Airbrush Leg and Body Paint Application Cosmetic Product False True False +NCIT:C202854 Age at Specimen Collection False True False +NCIT:C202855 Age at Recurrence False True False +NCIT:C202857 SPL Cosmetic Product Category Terminology False True False NCIT:C20286 CH02 False True False +NCIT:C202862 PLZ4-coated Paclitaxel-loaded Micelle Formulation False True False +NCIT:C202863 LAP3 Gene False True False +NCIT:C202864 LAP3 wt Allele False True False +NCIT:C202865 Cytosol Aminopeptidase False True False +NCIT:C202866 LARGE1 Gene False True False +NCIT:C202867 LARGE1 wt Allele False True False +NCIT:C202868 Xylosyl- and Glucuronyltransferase LARGE1 False True False +NCIT:C202869 LBR Gene False True False NCIT:C20287 Reliance ES Cell Line False True False +NCIT:C202870 LBR wt Allele False True False +NCIT:C202871 Delta(14)-Sterol Reductase LBR False True False +NCIT:C202872 LCAT Gene False True False +NCIT:C202873 LCAT wt Allele False True False +NCIT:C202874 Phosphatidylcholine-Sterol Acyltransferase False True False +NCIT:C202875 Intimate Relationship False True False NCIT:C20288 RL05 False True False +NCIT:C202885 RAS/BRAF/NF1 Triple Wild Type False True False +NCIT:C202886 Ciltacabtagene Autoleucel Regimen False True False +NCIT:C202887 Idecabtagene Vicleucel Regimen False True False +NCIT:C202888 Teclistamab Regimen False True False +NCIT:C202889 Neck Lymph Node Boundary Level II False True False NCIT:C20289 RL07 False True False +NCIT:C202890 Neck Lymph Node Boundary Level V False True False +NCIT:C202891 Spigelman Classification for Duodenal Polyposis False True False +NCIT:C202892 Naxitamab Regimen False True False +NCIT:C202893 Lisocabtagene Maraleucel Regimen False True False +NCIT:C202895 Cobimetinib Regimen False True False NCIT:C2029 Tyrphostin B44(-) False True False NCIT:C20290 RL10 False True False +NCIT:C202900 Alpha-PD1/IL2 Fusion Protein AWT020 False True False +NCIT:C202902 Base Edited Natural Killer Cells NK510 False True False +NCIT:C202903 Topical AKT Inhibitor SM-020 False True False +NCIT:C202905 Engineered Interferon Alpha-2b Prodrug JZP898 False True False +NCIT:C202906 Multi-kinase Inhibitor ST-1898 False True False +NCIT:C202907 Cardioprotective Agent DH001 False True False +NCIT:C202908 LDB3 Gene False True False +NCIT:C202909 LDB3 wt Allele False True False NCIT:C20291 RL13 False True False +NCIT:C202910 LIM Domain-Binding Protein 3 False True False +NCIT:C202911 LDLRAP1 Gene False True False +NCIT:C202912 LDLRAP1 wt Allele False True False +NCIT:C202913 Low Density Lipoprotein Receptor Adapter Protein 1 False True False +NCIT:C202915 LDHB Gene False True False +NCIT:C202916 LDHB wt Allele False True False +NCIT:C202917 L-Lactate Dehydrogenase B Chain False True False +NCIT:C202918 LMBRD1 Gene False True False +NCIT:C202919 LMBRD1 wt Allele False True False NCIT:C20292 RL15 False True False +NCIT:C202920 Lysosomal Cobalamin Transport Escort Protein LMBD1 False True False +NCIT:C202928 Molecular Glue Degrader GLB-001 False True False NCIT:C20293 RL20 False True False +NCIT:C202931 CD19-CD34tagged Metabolically Programmed CAR T-cells False True False +NCIT:C202933 Anti-EpCAM/Anti-CD3 Bispecific Antibody A-337 False True False +NCIT:C202934 G-Quadruplex-selective Transcription Inhibitor QN-302 False True False +NCIT:C202937 Allogeneic NKG2D CAR Memory T-cells False True False +NCIT:C202938 NKp46/CD16/CD20/IL-2-variant-specific NK Cell Engager IPH6501 False True False +NCIT:C202939 Autologous Anti-CSPG4 CAR-iC9-expressing T-lymphocytes False True False NCIT:C20294 RL21 False True False +NCIT:C202940 LONP1 Gene False True False +NCIT:C202941 LONP1 wt Allele False True False +NCIT:C202942 Lon Protease Homolog, Mitochondrial False True False +NCIT:C202943 LOXL1 Gene False True False +NCIT:C202944 LOXL1 wt Allele False True False +NCIT:C202945 Lysyl Oxidase Homolog 1 False True False +NCIT:C202946 LPIN2 Gene False True False +NCIT:C202947 LPIN2 wt Allele False True False +NCIT:C202948 Phosphatidate Phosphatase LPIN2 False True False +NCIT:C202949 LRPAP1 Gene False True False NCIT:C20295 Technion ES Cell Line False True False +NCIT:C202950 LRPAP1 wt Allele False True False +NCIT:C202951 Alpha-2-Macroglobulin Receptor-Associated Protein False True False +NCIT:C202956 Androgen Receptor Inhibitor ONCT-534 False True False +NCIT:C202957 Anti-STEAP1 CAR T-cells False True False +NCIT:C202959 GNPTAB Gene False True False NCIT:C20296 TE03 False True False +NCIT:C202960 GNPTAB wt Allele False True False +NCIT:C202961 N-Acetylglucosamine-1-Phosphotransferase Subunits Alpha/Beta False True False +NCIT:C202962 PRKD1 Protein Variant False True False +NCIT:C202963 PRKD1 NP_002733.2:p.E710D False True False +NCIT:C202964 PRKD1 NM_002742.3:c.2130A>C False True False +NCIT:C202965 PRKD1 NM_002742.3:c.2130A>T False True False +NCIT:C202968 KIF7 Gene False True False +NCIT:C202969 KIF7 wt Allele False True False NCIT:C20297 TE32 False True False +NCIT:C202970 Kinesin-Like Protein KIF7 False True False +NCIT:C202974 Lymphoepithelial Cyst False True False +NCIT:C202976 Eflornithine Regimen False True False NCIT:C20298 TE33 False True False +NCIT:C202988 Ligand Directed Degrader BMS-986460 False True False NCIT:C20299 TE04 False True False +NCIT:C202999 BTK Inhibitor LP-168 False True False NCIT:C203 Acridine False True False NCIT:C2030 Tyrphostin AG 1288 False True False NCIT:C20300 TE06 False True False +NCIT:C203000 Therapeutic Allogeneic Hematopoietic Stem Cells False True False +NCIT:C203001 Therapeutic Autologous Hematopoietic Stem Cells False True False +NCIT:C203003 Engineered Interferon ORB-011 False True False NCIT:C20301 TE62 False True False +NCIT:C203019 Emilumenib False True False NCIT:C20302 TE07 False True False +NCIT:C203020 CD73 Inhibitor False True False +NCIT:C203021 CD73-targeting Agent False True False +NCIT:C203022 MALT1 Inhibitor False True False +NCIT:C203023 Chest Wall Radiation Therapy False True False +NCIT:C203024 PSA Decline Greater than or Equal to 90 Percent False True False +NCIT:C203025 Admilparant False True False +NCIT:C203026 Follitropin Alfa False True False +NCIT:C203027 Umizortamig False True False +NCIT:C203028 Budoprutug False True False +NCIT:C203029 Dazagamglogene Autogedtemcel False True False NCIT:C20303 TE72 False True False +NCIT:C203030 Renizgamglogene Autogedtemcel False True False +NCIT:C203031 Cinsebrutinib False True False +NCIT:C203032 Civorebrutinib False True False +NCIT:C203033 Rocbrutinib False True False +NCIT:C203034 Vilastobart False True False +NCIT:C203035 Lesabelimab False True False +NCIT:C203036 Sefaxersen Sodium False True False +NCIT:C203037 Cibrigirsen False True False +NCIT:C203038 Opemalirsen False True False +NCIT:C203039 Sefaxersen False True False NCIT:C20304 UCSF ES Cell Line False True False +NCIT:C203040 Limaresiquimod False True False +NCIT:C203041 Sontigidomide False True False +NCIT:C203042 Cibotercept False True False +NCIT:C203043 Bezetabart False True False +NCIT:C203044 Ciduvectamig False True False +NCIT:C203045 Raludotatug False True False +NCIT:C203046 Sigvotatug False True False +NCIT:C203047 Sigvotatug Vedotin False True False +NCIT:C203048 Izalontamab Brengitecan False True False +NCIT:C203049 Tegeprotafib False True False NCIT:C20305 UC01 False True False +NCIT:C203050 Vibapapogene Autoleucel False True False +NCIT:C203051 Rezatapopt False True False +NCIT:C203052 Vimekofusp False True False +NCIT:C203053 Ibuprofen Trelamine False True False +NCIT:C203054 Ibuprofen Trelamine Hydrochloride False True False +NCIT:C203055 Abiprubart False True False +NCIT:C203056 Fanastomig False True False +NCIT:C203057 Arlocabtagene Autoleucel False True False +NCIT:C203058 Hypericin Sodium False True False +NCIT:C203059 Zimislecel False True False NCIT:C20306 UC06 False True False +NCIT:C203060 Sitocabnagene Loxiveleucel False True False +NCIT:C203061 Alisvetcel False True False +NCIT:C203062 Volamcabtagene Durzigedleucel False True False +NCIT:C203063 Dalmelitinib False True False +NCIT:C203064 Efercoleukin Alfa False True False +NCIT:C203065 Taplitumomab Paptox False True False +NCIT:C203066 Zeleciment Rostudirsen False True False +NCIT:C203067 Lunaxafusp False True False +NCIT:C203068 Torulimogene Lonferencel False True False +NCIT:C203069 Uplarafenib False True False NCIT:C20307 Wisconsin ES Cell Line False True False +NCIT:C203070 Dasatinib Laurylsulfate False True False +NCIT:C203071 Trastuzumab Brengitecan False True False +NCIT:C203072 Ragistomig False True False +NCIT:C203073 Anizatrectinib False True False +NCIT:C203074 Labuxtinib False True False +NCIT:C203075 Lacutoclax False True False +NCIT:C203076 Opelkibart False True False +NCIT:C203077 Bemfivastatin False True False +NCIT:C203078 Oximbomotide False True False +NCIT:C203079 Omramotide False True False NCIT:C20308 WA01 False True False +NCIT:C203080 Sucantomotide False True False +NCIT:C203081 Lepzacitinib False True False +NCIT:C203082 Lomedeucitinib False True False +NCIT:C203083 Londamocitinib False True False +NCIT:C203084 Velucovacap False True False +NCIT:C203085 Upalsecovatein False True False +NCIT:C203086 Pemivibart False True False +NCIT:C203087 Timcevibart False True False +NCIT:C203088 Migaldendranib False True False +NCIT:C203089 Enavermotide False True False NCIT:C20309 WA07 False True False +NCIT:C203090 Acmucabtagene Autoleucel False True False +NCIT:C203091 Plixacabtagene Autoleucel False True False +NCIT:C203092 Ribrecabtagene Autoleucel False True False +NCIT:C203093 Xempritolimod False True False +NCIT:C203094 Onacrisantaspase False True False +NCIT:C203095 Vecilmeran False True False +NCIT:C203096 Vintesomeran False True False +NCIT:C203097 Andusomeran False True False +NCIT:C203098 Tegrenmeran False True False +NCIT:C203099 Pitozinameran False True False NCIT:C2031 Tyrphostin AG 1295 False True False NCIT:C20310 WA09 False True False +NCIT:C203100 Zeldesmeran False True False +NCIT:C203101 Raxtozinameran False True False +NCIT:C203102 Roconkibart False True False +NCIT:C203103 Bleximenib False True False +NCIT:C203104 Ibuzatrelvir False True False +NCIT:C203105 Olgotrelvir Sodium False True False +NCIT:C203106 Olgotrelvir False True False +NCIT:C203107 Imdatifan False True False +NCIT:C203108 Crozbaciclib False True False +NCIT:C203109 Ulecaciclib False True False NCIT:C20311 WA13 False True False +NCIT:C203110 Linvekinogene Treniplasmid False True False +NCIT:C203111 Brinretigene Vesgedparvovec False True False +NCIT:C203112 Nimatpagene Pariparvovec False True False +NCIT:C203113 Clemidsogene Lanparvovec False True False +NCIT:C203114 Raxorulimogene Belzovacirepvec False True False +NCIT:C203115 Pozetaldogene Ormesparvovec False True False +NCIT:C203116 Zopocianine Sodium False True False +NCIT:C203117 Zopocianine False True False +NCIT:C203118 Zanzalintinib Fumarate False True False +NCIT:C203119 Sacibertinib False True False NCIT:C20312 WA14 False True False +NCIT:C203120 Ansornitinib False True False +NCIT:C203121 Canlitinib False True False +NCIT:C203122 Narmafotinib False True False +NCIT:C203123 Divarasib Adipate False True False +NCIT:C203124 Evoncabtagene Pazurgedleucel False True False +NCIT:C203125 Pomlucabtagene Autoleucel False True False +NCIT:C203126 Firicabtagene Autoleucel False True False +NCIT:C203127 Cabotamig False True False +NCIT:C203128 Itezocabtagene Autoleucel False True False +NCIT:C203129 Pelgifatamab False True False NCIT:C20313 Tumor Cell Line False True False +NCIT:C203130 Dorocubicel False True False +NCIT:C203131 Tesrivetcel False True False +NCIT:C203132 Latovetcel False True False +NCIT:C203133 Solizmestrocel False True False +NCIT:C203134 Imdusiran False True False +NCIT:C203135 Mivelsiran False True False +NCIT:C203136 Lefelsiran False True False +NCIT:C203137 Zodasiran Sodium False True False +NCIT:C203138 Lepodisiran Sodium False True False +NCIT:C203139 Solbinsiran False True False NCIT:C20314 Protein Truncation False True False +NCIT:C203140 Zotresiran False True False +NCIT:C203141 Imdusiran Sodium False True False +NCIT:C203142 Tivanisiran Sodium False True False +NCIT:C203143 Lepodisiran False True False +NCIT:C203144 Lefelsiran Sodium False True False +NCIT:C203145 Omoprubart False True False +NCIT:C203146 Coramitug False True False +NCIT:C203147 Galvokimig False True False +NCIT:C203148 Navenibart False True False +NCIT:C203149 Ucenprubart False True False NCIT:C20315 Trace Metal Storage Protein False True False +NCIT:C203150 Vobramitamab False True False +NCIT:C203151 Eglatoprutug False True False +NCIT:C203152 Seniprutug False True False +NCIT:C203153 Zeleciment False True False +NCIT:C203154 Cepeprubart False True False +NCIT:C203155 Donzakimig False True False +NCIT:C203156 Verekitug False True False +NCIT:C203157 Zeleciment Basivarsen False True False +NCIT:C203158 Lunsekimig False True False +NCIT:C203159 Solrikitug False True False NCIT:C20316 Werner Syndrome ATP-Dependent Helicase False True False +NCIT:C203160 Luvagrobart False True False +NCIT:C203161 Usilnetug False True False +NCIT:C203162 Roginolisib False True False +NCIT:C203163 Vulolisib False True False +NCIT:C203164 Davelizomib False True False +NCIT:C203165 Tibremciclib False True False +NCIT:C203166 Culmerciclib False True False +NCIT:C203167 Vicatertide False True False +NCIT:C203168 Aneratrigine False True False +NCIT:C203169 Reflocibart False True False NCIT:C20317 Consumer Advocates in Research and Related Activities False True False +NCIT:C203170 Aspirin Trelamine Hydrochloride False True False +NCIT:C203171 Aspirin Trelamine False True False +NCIT:C203172 Usnoflast False True False +NCIT:C203173 Sutidiazine False True False +NCIT:C203174 Pobrolitide False True False +NCIT:C203175 Bevemipretide False True False +NCIT:C203176 Ensitrelvir Fumarate False True False +NCIT:C203177 Zevotrelvir False True False +NCIT:C203178 Mosnodenvir False True False +NCIT:C203179 Deunirmatrelvir False True False NCIT:C20318 ATP-Dependent DNA Helicase Q4 False True False +NCIT:C203180 Stannic Protoporfin False True False +NCIT:C203181 Arbemnifosbuvir False True False +NCIT:C203182 Tirfipiravir False True False +NCIT:C203183 Canvircept False True False +NCIT:C203184 Talovirtide False True False +NCIT:C203185 Atilotrelvir False True False +NCIT:C203186 Zelicapavir False True False +NCIT:C203187 Traxivitug False True False +NCIT:C203188 Silevimig False True False +NCIT:C203189 Umitrelimorgene Autodencel False True False NCIT:C20319 Licensing Factor False True False +NCIT:C203190 Tacatresgene Autoleucel False True False +NCIT:C203191 Cenzileucel False True False +NCIT:C203192 Plozasiran Sodium False True False +NCIT:C203193 Plozasiran False True False +NCIT:C203194 Zodasiran False True False +NCIT:C203195 Bimatoprost Grenod False True False +NCIT:C203196 Avenciguat False True False +NCIT:C203197 Osavampator False True False +NCIT:C203198 Zelatriazin False True False +NCIT:C203199 Monlunabant False True False NCIT:C2032 Tyrphostin AG 1433 False True False NCIT:C20320 Replication Initiation Point Mapping False True False +NCIT:C203200 Nerigliatin False True False +NCIT:C203201 Petrelintide False True False +NCIT:C203202 Ganipatide False True False +NCIT:C203203 Bivamelagon False True False +NCIT:C203204 Tarumase False True False +NCIT:C203205 Ziclumeran False True False +NCIT:C203206 Zelenectide False True False +NCIT:C203207 Sifarobocept False True False +NCIT:C203208 Pegmispotide False True False +NCIT:C203209 Tegomil Fumarate False True False +NCIT:C203210 Bezisterim False True False +NCIT:C203211 Rovunaptabin False True False +NCIT:C203212 Digadoglucitol False True False +NCIT:C203213 Igermetostat False True False +NCIT:C203214 Clofutriben False True False +NCIT:C203215 Redafamdastat False True False +NCIT:C203216 Friluglanstat False True False +NCIT:C203217 Irucalantide False True False +NCIT:C203218 Vamagloxistat False True False +NCIT:C203219 Bexicaserin False True False NCIT:C20322 High Mobility Group Protein HMG-I False True False +NCIT:C203220 Zalfermin False True False +NCIT:C203221 Efpegerglucagon False True False +NCIT:C203222 Zaloganan False True False +NCIT:C203223 Fidrisertib Succinate False True False +NCIT:C203224 Lerzeparib False True False +NCIT:C203225 Ucasareotide Dasaroxetan False True False +NCIT:C203226 Tisolagiline False True False +NCIT:C203227 Icalcaprant False True False +NCIT:C203228 Edelinontrine False True False +NCIT:C203229 Nerandomilast False True False NCIT:C20323 High Mobility Group Protein HMG-Y False True False +NCIT:C203230 Fosigotifator False True False +NCIT:C203231 Votoplam False True False +NCIT:C203232 Deupsilocin False True False +NCIT:C203233 Leramistat False True False +NCIT:C203234 Tebapivat False True False +NCIT:C203235 Invopressin False True False +NCIT:C203236 Orziloben False True False +NCIT:C203237 Lucoridalines False True False +NCIT:C203238 Mavodelpar Sodium False True False +NCIT:C203239 Nesvategrast False True False NCIT:C20324 High-Mobility Group Protein HMGI-C False True False +NCIT:C203240 Gildeuretinol Acetate False True False +NCIT:C203241 Gildeuretinol False True False +NCIT:C203242 Bemiltenase Alfa False True False +NCIT:C203243 Rondaptivon Pegol False True False +NCIT:C203244 Vanzacaftor Calcium False True False +NCIT:C203245 Lingdolinurad False True False +NCIT:C203246 Pozdeutinurad False True False +NCIT:C203247 Bavtavirine False True False +NCIT:C203248 Visepegenatide False True False +NCIT:C203249 Follitropin Beta False True False NCIT:C20325 HMGA Family Protein False True False +NCIT:C203254 Vixicovtogene Oboplasmid False True False +NCIT:C203255 NPM1 Gene Fusion Positive False True False +NCIT:C203256 SET/NUP214 Fusion Gene False True False +NCIT:C203257 CTPS1 Inhibitor STP938 False True False NCIT:C20326 HMGB Family Protein False True False +NCIT:C203261 Anti-CALRmut/Anti-CD3 Bispecific Antibody JNJ-88549968 False True False +NCIT:C203264 SET/NUP214 Fusion Protein False True False +NCIT:C203268 TACC3 Protein-Protein Interaction Inhibitor AO-252 False True False NCIT:C20327 HMGN Family Protein False True False +NCIT:C203275 Medicare Managed Care False True False +NCIT:C203276 Chronic Condition Special Needs Plan False True False +NCIT:C203277 Institutional Special Needs Plan False True False +NCIT:C203278 Preferred Provider Organization False True False +NCIT:C203279 Health Maintenance Organization Point of Service False True False NCIT:C20328 High Mobility Group Protein B1 False True False +NCIT:C203280 Other Medicare Managed Care False True False +NCIT:C203281 Medicare Non-Managed Care False True False +NCIT:C203287 Medicare Drug Coverage False True False +NCIT:C203288 Medicare Medical Savings Account Plan False True False +NCIT:C203289 Other Medicare Non-managed Care Plan False True False NCIT:C20329 High Mobility Group Protein B3 False True False +NCIT:C203290 Medicare Hospice Care Coverage False True False +NCIT:C203291 Dual Eligible Health Plan False True False +NCIT:C203292 Dual Eligible Special Needs Plan False True False +NCIT:C203293 Fully Integrated Dual Eligible Special Needs Plan False True False +NCIT:C203294 Other Medicare Plan False True False +NCIT:C203295 Pharmacy Benefit Manager False True False +NCIT:C203296 Medicaid Managed Care False True False +NCIT:C203297 Primary Care Case Management False True False +NCIT:C203298 Other Medicaid Plan or Service False True False +NCIT:C203299 Other Medicaid Managed Care False True False NCIT:C2033 Bis-Tyrphostin False True False NCIT:C20330 High Mobility Group Protein B2 False True False +NCIT:C203300 Medicaid Non-managed Care Plan False True False +NCIT:C203301 Medicaid State-sponsored Children's Health Insurance Program False True False +NCIT:C203303 Medicaid Out-of-State Exception False True False +NCIT:C203304 Medicaid Long Term Services and Supports False True False +NCIT:C203305 Medicaid Dental Coverage False True False +NCIT:C203306 Other Government Health Care Funding False True False NCIT:C20331 High Mobility Group Protein HMG-R False True False +NCIT:C203317 SARS Coronavirus 2 JN.1 False True False +NCIT:C203318 SARS Coronavirus 2 JD.1.1 False True False +NCIT:C203319 SARS Coronavirus 2 JG.3 False True False NCIT:C20332 High Mobility Group Nucleosome-Binding Domain-Containing Protein 3 False True False +NCIT:C203320 SARS Coronavirus 2 JF.1 False True False +NCIT:C203321 CTPS1 Gene False True False +NCIT:C203322 CTPS1 wt Allele False True False +NCIT:C203323 CTP Synthase 1 False True False +NCIT:C203324 HRAS NP_005334.1:p.G13X False True False +NCIT:C203325 HRAS NP_005334.1:p.Q61X False True False +NCIT:C203326 Anti-CEACAM5 ADC SGN-CEACAM5C False True False +NCIT:C203327 Social Security Administration False True False +NCIT:C203328 Anti-BCMA/Anti-GPRC5D CAR-T Cells BMS-986453 False True False +NCIT:C203329 STING Agonist BI 1703880 False True False NCIT:C20333 High Mobility Group Nucleosome-Binding Domain-Containing Protein 4 False True False +NCIT:C203330 Cold-cup Biopsy False True False +NCIT:C203332 Pegylated Topoisomerase Inhibitor False True False +NCIT:C203333 F5 Gene Mutation False True False +NCIT:C203334 F5 Protein Variant False True False +NCIT:C203335 F5 NP_000121.2:p.R534Q False True False +NCIT:C203336 FGFR1/2/3 Inhibitor TYRA-200 False True False +NCIT:C203337 Estrogen Receptor Positive by Immunohistochemistry Less than or Equal to 9 Percent False True False +NCIT:C203338 Progesterone Receptor Positive by Immunohistochemistry Less than or Equal to 9 Percent False True False NCIT:C20334 XRCC2 Gene False True False +NCIT:C203340 PROCR/PDGFRA/ZEB1 Positive Cells False True False +NCIT:C203345 PQ/CMC Capsule Shell Classification Terminology False True False +NCIT:C203346 PQ/CMC Release Mechanism Terminology False True False +NCIT:C203347 PQ/CMC Substance Name Type Terminology False True False +NCIT:C203348 Hard Gelatin Capsule Shell False True False +NCIT:C203349 Hard HPMC Capsule Shell False True False NCIT:C20335 XRCC3 Gene False True False +NCIT:C203350 Hard Pullulan Capsule Shell False True False +NCIT:C203351 Hard PVA Capsule Shell False True False +NCIT:C203352 Hard Starch Capsule Shell False True False +NCIT:C203353 Soft Gelatin Capsule Shell False True False +NCIT:C203354 Company Identifier False True False +NCIT:C203355 GSRS Preferred Term False True False +NCIT:C203356 IUPAC Name False True False +NCIT:C203357 Chemical Systematic Name False True False +NCIT:C203358 USP-NF Established Name False True False +NCIT:C203359 Matrix Drug Release False True False NCIT:C20336 Telomere Length Maintenance False True False +NCIT:C203360 Osmotic Pump Drug Release False True False +NCIT:C203361 Reservoir Drug Release False True False +NCIT:C203363 CKS2 Gene False True False +NCIT:C203364 CKS2 wt Allele False True False +NCIT:C203365 Cyclin-Dependent Kinases Regulatory Subunit 2 False True False +NCIT:C203366 TMEM30B Gene False True False +NCIT:C203367 TMEM30B wt Allele False True False +NCIT:C203368 Cell Cycle Control Protein 50B False True False NCIT:C20337 PRKDC Gene False True False +NCIT:C203371 FBLIM1 Gene False True False +NCIT:C203372 FBLIM1 wt Allele False True False +NCIT:C203373 Filamin-Binding LIM Protein 1 False True False +NCIT:C203377 LINC02593 Gene False True False +NCIT:C203378 LINC02593 wt Allele False True False +NCIT:C203379 Long Intergenic Non-Protein Coding RNA 2593 False True False NCIT:C20338 Telomere Maintenance Gene False True False +NCIT:C203382 Disease Relapse/Refractory False True False +NCIT:C203383 Tumor Surveillance False True False NCIT:C20339 Telomere Capping False True False +NCIT:C203396 Replication Competent Lentivirus False True False +NCIT:C203397 Germline PALB2 Gene Mutation False True False +NCIT:C203398 Somatic PALB2 Gene Mutation False True False +NCIT:C203399 Germline ATM Gene Mutation False True False NCIT:C2034 Tyrphostin A63 False True False NCIT:C20340 Telomere Recombination False True False +NCIT:C203400 Somatic ATM Gene Mutation False True False +NCIT:C203401 Germline CHEK2 Gene Mutation False True False +NCIT:C203402 Somatic CHEK2 Gene Mutation False True False +NCIT:C203403 USP1 Inhibitor ISM3091 False True False +NCIT:C203404 Age at Start of Time Period False True False +NCIT:C203405 Age at End of Time Period False True False NCIT:C20341 Elongation by Telomerase False True False +NCIT:C203414 Allogeneic Organ Transplantation False True False +NCIT:C203416 Parotid Duct-Sparing Radiation Therapy False True False +NCIT:C203417 CDC7 Inhibitor SGR-2921 False True False +NCIT:C203418 Antibody ROSE12 False True False +NCIT:C203419 Armed Forces Americas (except Canada) False True False NCIT:C20342 Internet False True False +NCIT:C203420 Armed Forces Europe, the Middle East, and Canada False True False +NCIT:C203421 Armed Forces Pacific False True False +NCIT:C203423 ATAD1 Gene False True False +NCIT:C203424 ATAD1 wt Allele False True False +NCIT:C203425 Outer Mitochondrial Transmembrane Helix Translocase False True False +NCIT:C203427 Aberrant HOXA Family Gene Expression False True False +NCIT:C203429 SPI1 Gene Rearrangement False True False NCIT:C20343 Human Glandular Kallikrein False True False +NCIT:C203436 Thrombocytopenia 5 False True False +NCIT:C203438 Non-IgM Secreting Waldenstrom Macroglobulinemia False True False +NCIT:C203439 IgM Secreting Waldenstrom Macroglobulinemia False True False NCIT:C20344 OGG1 Gene False True False +NCIT:C203441 Abiraterone/Olaparib/Prednisone Regimen False True False +NCIT:C203442 Markedly Elevated White Blood Cell Count Present False True False +NCIT:C203445 Abiraterone/Olaparib/Methylprednisolone Regimen False True False +NCIT:C203446 Abiraterone/Niraparib/Methylprednisolone Regimen False True False +NCIT:C203447 Adagrasib/Cetuximab Regimen False True False +NCIT:C203448 Thrombocytopenic Disorder False True False +NCIT:C203449 Adagrasib/Panitumumab Regimen False True False NCIT:C20345 EXO1 Gene False True False +NCIT:C203450 Azacitidine/Enasidenib Regimen False True False +NCIT:C203451 Azacitidine/Gilteritinib Regimen False True False +NCIT:C203452 Atezolizumab/Cisplatin/Etoposide Regimen False True False +NCIT:C203453 Severe Combined Immunodeficiency due to RAG Deficiency False True False +NCIT:C203454 Asparaginase Erwinia chrysanthemi Regimen False True False +NCIT:C203455 Severe Combined Immunodeficiency with Absence of T, B, and NK Cells False True False +NCIT:C203456 Two-Dimensional Imaging False True False +NCIT:C203457 One-Dimensional Imaging False True False +NCIT:C203458 Activated PI3K Delta Syndrome False True False +NCIT:C203459 Activated PI3K-Delta Syndrome 1 False True False NCIT:C20346 Atomic Resolution Microscopy False True False +NCIT:C203460 Less than Five Times False True False +NCIT:C203461 Familial Hemophagocytic Lymphohistiocytosis Type 4 False True False +NCIT:C203462 Familial Hemophagocytic Lymphohistiocytosis Type 2 False True False +NCIT:C203463 Familial Hemophagocytic Lymphohistiocytosis Type 3 False True False +NCIT:C203464 Familial Hemophagocytic Lymphohistiocytosis Type 5 False True False +NCIT:C203465 Immunodeficiency 66 False True False +NCIT:C203466 Bendamustine/Dexamethasone Regimen False True False +NCIT:C203467 Binimetinib/Imatinib Regimen False True False +NCIT:C203468 BV-ICE Regimen False True False NCIT:C20347 Apoptosis Inhibitor Gene False True False +NCIT:C203470 Regimen Used to Treat Malignant Digestive System Neoplasm False True False +NCIT:C203471 TRICARE Prime False True False +NCIT:C203472 TRICARE Extra False True False +NCIT:C203473 Regimen Used to Treat Ampullary Adenocarcinoma False True False +NCIT:C203474 TRICARE Standard False True False +NCIT:C203475 TRICARE For Life False True False +NCIT:C203476 TRICARE Reserve Select False True False +NCIT:C203477 TRICARE Select False True False +NCIT:C203478 Uniformed Services Family Health Plan False True False +NCIT:C203479 Enrolled False True False NCIT:C20348 Apoptosis Promoter Gene False True False +NCIT:C203480 Stand-Alone Dental Plan False True False +NCIT:C203481 VA Healthcare Facility False True False +NCIT:C203482 Outside Facility False True False +NCIT:C203483 VA Fee Basis Medical Program False True False +NCIT:C203484 VA Foreign Medical Program False True False +NCIT:C203485 Beta-catenin Inhibitor False True False +NCIT:C203486 VA Community Nursing Home False True False +NCIT:C203487 State Veterans Home False True False +NCIT:C203488 Sharing Agreements False True False +NCIT:C203489 Federal Agency False True False NCIT:C20349 M Phase Process False True False +NCIT:C203490 Non-Veterans Health Administration Health Care False True False +NCIT:C203491 Children of Women Vietnam Veterans Health Care Benefits Program False True False +NCIT:C203492 State Government False True False +NCIT:C203493 Local Government False True False +NCIT:C203494 Local Managed Health Care False True False +NCIT:C203495 Fee for Service Healthcare Plan False True False +NCIT:C203496 Federal Employees Health Benefits Program False True False +NCIT:C203497 Selenium/Fermented Organic Mushroom Blend/Uncaria tomentosa Bark-based supplement False True False +NCIT:C203498 Red Yeast Rice Extract False True False +NCIT:C203499 Pygeum Extract False True False NCIT:C2035 Tyrphostin A1 False True False NCIT:C20350 BIRC5 Gene False True False +NCIT:C203500 Saw Palmetto Berry Extract/Lycopene/Beta-Sitosterol/Vitamin D3/Zinc/Selenium/Quercetin-based Supplement False True False +NCIT:C203501 Garlic Extract/Olive Leaf Extract/Elderberry/Oregano Oil/Arabinogalactans/Rosemary Oil-based Supplement False True False +NCIT:C203502 Nattokinase/Serrapeptase-based Supplement False True False +NCIT:C203503 Vitamin A/C/E-Zinc/Copper-based Supplement False True False +NCIT:C203504 Dorzolamide Hydrochloride/Timolol Maleate Ophthalmic Solution False True False +NCIT:C203505 Papaverine Hydrochloride/Phentolamine Mesylate Injectable Formulation False True False +NCIT:C203506 Zinc Monomethionine/Copper-based Supplement False True False +NCIT:C203507 Marigold Extract/Saffron Extract-based Supplement False True False +NCIT:C203508 c-Myb mRNA Degrader REM-422 False True False +NCIT:C203509 Anti-CD123/TOP1i Antibody-drug Conjugate AZD9829 False True False +NCIT:C203510 Space-Available Care False True False +NCIT:C203512 USP1 Inhibitor TNG348 False True False +NCIT:C203514 Engineered IL-12 Variant/Aluminum Hydroxide Complex ANK-101 False True False +NCIT:C203516 Fluorine F 18-labeled MeFAMP False True False +NCIT:C203517 CD123-targeting Agent False True False +NCIT:C203518 Anti-CD123 Antibody-drug Conjugate False True False +NCIT:C203519 Exhaled Carbon Monoxide Concentration Less than or Equal to 5 ppm False True False NCIT:C20352 BIRC6 Gene False True False +NCIT:C203520 Sequenced Acquisition False True False +NCIT:C203521 Spiral Acquisition False True False +NCIT:C203522 Constant Angle Acquisition False True False +NCIT:C203524 Stationary Acquisition False True False +NCIT:C203525 Free Acquisition False True False +NCIT:C203527 PD-L1 Combined Positive Score Less than 5 False True False +NCIT:C203528 EBV-Related Hemophagocytic Lymphohistiocytosis False True False +NCIT:C203529 Molecular Characterization Initiative for Childhood Cancers False True False NCIT:C20353 BIRC7 Gene False True False +NCIT:C203530 Marrow Space False True False +NCIT:C203531 Anti-DLL3 ADC ZL-1310 False True False +NCIT:C203532 National Health Service False True False +NCIT:C203533 ADC TORL-4-500 False True False +NCIT:C203534 Parkinson Disease 9 False True False +NCIT:C203535 Parkinson Disease 20, Early-Onset False True False +NCIT:C203536 Parkinson Disease 23, Autosomal Recessive, Early Onset False True False +NCIT:C203537 Carboplatin/Cemiplimab/Paclitaxel Regimen False True False +NCIT:C203538 Cisplatin/Cemiplimab/Paclitaxel Regimen False True False +NCIT:C203539 Carboplatin/Cemiplimab/Pemetrexed Regimen False True False NCIT:C20354 NAIP Gene False True False +NCIT:C203540 Cisplatin/Cemiplimab/Pemetrexed Regimen False True False +NCIT:C203541 Cladribine/High-dose Cytarabine/Idarubicin/Filgrastim Regimen False True False +NCIT:C203542 Clofarabine/High-dose Cytarabine Regimen False True False +NCIT:C203543 Clofarabine Regimen False True False +NCIT:C203544 Topical Clobetasol/Mechlorethamine Regimen False True False +NCIT:C203545 CAPOX-Pembrolizumab-Trastuzumab Regimen False True False +NCIT:C203546 Topical Clobetasol Regimen False True False NCIT:C20355 BIRC2 Gene False True False +NCIT:C203557 Treatment Arm for COG ACNS0331 Comparison of Radiation Therapy Regimens in Combination with Chemotherapy in Treating Young Patients with Newly Diagnosed Standard-Risk Medulloblastoma False True False +NCIT:C203558 Treatment Arm for COG ACNS0332 Chemotherapy and Radiation Therapy in Treating Young Patients with Newly Diagnosed, Previously Untreated, High-Risk Medulloblastoma/ PNET False True False +NCIT:C203559 Treatment Arm for COG ACNS0333 Combination Chemotherapy, Radiation Therapy, and an Autologous Peripheral Blood Stem Cell Transplant in Treating Young Patients with Atypical Teratoid/Rhabdoid Tumor of the Central Nervous System False True False NCIT:C20356 BIRC3 Gene False True False +NCIT:C203560 Treatment Arm for COG ACNS0334 Combination Chemotherapy Followed By Peripheral Stem Cell Transplant in Treating Young Patients with Newly Diagnosed Supratentorial Primitive Neuroectodermal Tumors or High-Risk Medulloblastoma False True False +NCIT:C203561 Treatment Arm for EURO-E.W.I.N.G.99 Combination Chemotherapy with or without Peripheral Stem Cell Transplantation, Radiation Therapy, and/or Surgery in Treating Patients with Ewing's Sarcoma False True False +NCIT:C203562 ACNS0331 Arm I Includes 3-7 Years of Age, LDCSI, IFRT False True False +NCIT:C203563 ACNS0331 Arm II Includes 3-7 Years of Age, LDCSI, PFRT False True False +NCIT:C203564 ACNS0331 Arm III Includes 3-7 Years of Age, SDCSI, IFRT False True False +NCIT:C203565 ACNS0331 Arm IV Includes 3-7 Years of Age, SDCSI, PFRT False True False +NCIT:C203566 ACNS0331 Arm V Includes 8-21 Years of Age, SDCSI, IFRT False True False +NCIT:C203567 ACNS0331 Arm VI Includes 8-21 Years of Age, SDCSI, PFRT False True False +NCIT:C203568 ACNS0332 Arm A False True False +NCIT:C203569 ACNS0332 Arm B Includes Carboplatin False True False NCIT:C20357 XIAP Gene False True False +NCIT:C203570 ACNS0332 Arm C Includes Isotretinoin False True False +NCIT:C203571 ACNS0332 Arm D Includes Carboplatin and Isotretinoin False True False +NCIT:C203572 ACNS0333 Arm I Includes Chemotherapy, Autologous PBSC, 3D-CRT False True False +NCIT:C203573 ACNS0333 Arm II Includes Chemotherapy, 3D-CRT, Autologous PBSC False True False +NCIT:C203574 ACNS0334 Arm A Includes Induction Plus Consolidation Chemotherapy, Autologous PBSC False True False +NCIT:C203575 ACNS0334 Arm B Includes Induction Plus Consolidation Chemotherapy, Autologous PBSC False True False +NCIT:C203576 EE99 Not Randomized False True False +NCIT:C203577 EE99 R1-VAC False True False +NCIT:C203578 EE99 R1-VAI False True False +NCIT:C203579 EE99 R2Loc-BuMel False True False NCIT:C20358 APAF1 Gene False True False +NCIT:C203580 EE99 R2Loc-VAI False True False +NCIT:C203581 EE99 R2Pulm-BuMel False True False +NCIT:C203582 EE99 R2Pulm-VAI Plus Lung RT False True False +NCIT:C203584 Dental Care False True False +NCIT:C203585 Vision Care False True False +NCIT:C203586 Spina Bifida Health Care Benefits Program False True False +NCIT:C203587 FNCLCC Sarcoma Grade False True False +NCIT:C203588 Indian Health Care Program Services False True False +NCIT:C203589 Indian Health Care Contracted Services False True False NCIT:C20359 TOPBP1 Gene False True False +NCIT:C203590 Indian Managed Care Entity False True False +NCIT:C203591 Tribally-Sponsored Health Insurance Program False True False +NCIT:C203592 Title V Mother and Child Health Block Grant False True False +NCIT:C203593 Migrant Health Program False True False +NCIT:C203594 Ryan White HIV/AIDS Program False True False +NCIT:C203595 Disaster Assistance False True False +NCIT:C203596 Black Lung Benefits Act False True False +NCIT:C203597 Department of Corrections False True False +NCIT:C203598 Federal Bureau of Prisons False True False +NCIT:C203599 State Department of Corrections False True False NCIT:C2036 Ketanserin Tartrate False True False NCIT:C20360 SIDT1 Gene False True False +NCIT:C203600 Local Department of Corrections False True False +NCIT:C203602 Age-Weeks False True False +NCIT:C203603 Blue Cross Blue Shield False True False +NCIT:C203604 Self-funded Insurance Plan False True False +NCIT:C203605 Administrative Services Only Health Plan False True False +NCIT:C203606 Disability Insurance False True False +NCIT:C203607 Long-term Care Insurance False True False +NCIT:C203608 Peritumoral Lesion False True False +NCIT:C203609 Acute Myeloid Leukemia due to Lineage Switch from B Acute Lymphoblastic Leukemia, KMT2A-Rearranged False True False NCIT:C20361 XPA Gene False True False +NCIT:C203610 Recurrent Acute Myeloid Leukemia due to Lineage Switch from B Acute Lymphoblastic Leukemia, KMT2A-Rearranged False True False +NCIT:C203611 Refractory Acute Myeloid Leukemia due to Lineage Switch from B Acute Lymphoblastic Leukemia, KMT2A-Rearranged False True False +NCIT:C203612 Acute Myeloid Leukemia due to Lineage Switch from Acute Leukemia of Ambiguous Lineage False True False +NCIT:C203613 Recurrent Acute Myeloid Leukemia due to Lineage Switch from Acute Leukemia of Ambiguous Lineage False True False +NCIT:C203614 Refractory Acute Myeloid Leukemia due to Lineage Switch from Acute Leukemia of Ambiguous Lineage False True False +NCIT:C203615 Acute Myeloid Leukemia due to Lineage Switch from Mixed Phenotype Acute Leukemia False True False +NCIT:C203616 Recurrent Acute Myeloid Leukemia due to Lineage Switch from Mixed Phenotype Acute Leukemia False True False +NCIT:C203617 Refractory Acute Myeloid Leukemia due to Lineage Switch from Mixed Phenotype Acute Leukemia False True False NCIT:C20362 XRCC4 Gene False True False +NCIT:C203620 Autologous Anti-EGFRvIII synNotch Receptor-induced Anti-EphA2/IL-13Ralpha2 CAR-T Cells False True False +NCIT:C203621 Exhaled Carbon Monoxide Concentration Greater than 8 ppm False True False +NCIT:C203622 CBLIF Gene False True False +NCIT:C203623 CBLIF wt Allele False True False +NCIT:C203624 Cobalamin Binding Intrinsic Factor False True False +NCIT:C203625 Glycoprotein Ib/IX Complex False True False +NCIT:C203626 LRP4 Gene False True False +NCIT:C203627 LRP4 wt Allele False True False +NCIT:C203628 Autologous Anti-GPRC5D CAR-T Cells BMS-986393 False True False +NCIT:C203629 Low-Density Lipoprotein Receptor-Related Protein 4 False True False NCIT:C20363 XRCC5 Gene False True False +NCIT:C203630 Androgen Receptor Degrader RO7656594 False True False +NCIT:C203631 PSA Level Less than 0.01 False True False +NCIT:C203632 Level of Diagnostic Certainty False True False +NCIT:C203633 Anti-EpCAM/Anti-4-1BB Bispecific Antibody BNT314 False True False +NCIT:C203634 Commercial Managed Healthcare Plan False True False +NCIT:C203635 Exclusive Provider Organization Plan False True False +NCIT:C203636 Gatekeeper Preferred Provider Organization False True False +NCIT:C203637 Organized Delivery System False True False +NCIT:C203638 Small Employer Purchasing Group False True False +NCIT:C203639 Specialized Stand-Alone Insurance Plan False True False NCIT:C20364 Lymphotactin False True False +NCIT:C203640 Dental Insurance False True False +NCIT:C203641 Vision Insurance False True False +NCIT:C203642 Automobile Insurance False True False +NCIT:C203643 Liability Insurance False True False +NCIT:C203644 Not Listed False True False +NCIT:C203645 Listed False True False +NCIT:C203646 No Charge False True False +NCIT:C203647 Charity False True False +NCIT:C203648 Professional Courtesy False True False +NCIT:C203649 Refusal to Pay False True False NCIT:C20365 Replication Licensing False True False +NCIT:C203650 Bad Debt False True False +NCIT:C203651 Hill-Burton Act False True False +NCIT:C203652 Foreign National False True False +NCIT:C203653 Nanoparticle Encapsulated AChR Epitopes CNP-106 False True False +NCIT:C203654 KRAS G12C Inhibitor BEBT-607 False True False +NCIT:C203655 Modified Interleukin-2 DF6215 False True False +NCIT:C203656 Anti-CLL-1/Anti-CD38 CAR T Cells False True False +NCIT:C203657 Acylfulvene-derived Prodrug LP-184 False True False +NCIT:C203658 Autologous Tumor-draining Lymph Node-derived Lymphocytes False True False +NCIT:C203660 CDK4 Inhibitor BGB-43395 False True False +NCIT:C203661 Clinical Data Model False True False +NCIT:C203662 Data Warehouse False True False +NCIT:C203663 HL7 Feed False True False +NCIT:C203664 PCORNet ETL False True False +NCIT:C203665 Laboratory Instrument False True False +NCIT:C203666 Anti-CD19 CAR-IL-18-expressing Autologous T-lymphocytes False True False +NCIT:C203668 Circulating Tumor HPV-16 DNA False True False NCIT:C20367 MCM Protein False True False +NCIT:C203670 HPV16 Vaccine False True False +NCIT:C203671 Ultima Sequencing Platform False True False +NCIT:C203672 HIC File Format False True False +NCIT:C203674 Esophagus and Gastroesophageal Junction False True False +NCIT:C203676 ESR1 Gene Mutation Negative False True False +NCIT:C203677 ER-targeting Agent False True False +NCIT:C203678 Topical Leptospermum Honey False True False +NCIT:C203679 PRMT5 Inhibitor AZD3470 False True False NCIT:C20368 Research Technique False True False +NCIT:C203680 FGFR1 Overexpression Positive False True False +NCIT:C203681 FGFR2 Overexpression Positive False True False +NCIT:C203682 FGFR3 Overexpression Positive False True False +NCIT:C203683 MUC5AC Positive False True False +NCIT:C203684 Cyclophosphamide/Cytarabine/Mercaptopurine/Methotrexate Regimen False True False +NCIT:C203685 Carboplatin/Dostarlimab/Paclitaxel Regimen False True False +NCIT:C203686 Carboplatin/Durvalumab/Pemetrexed/Tremelimumab Regimen False True False +NCIT:C203687 Cisplatin/Durvalumab/Pemetrexed/Tremelimumab Regimen False True False +NCIT:C203688 Carboplatin/Durvalumab/Gemcitabine/Tremelimumab Regimen False True False +NCIT:C203689 Cisplatin/Durvalumab/Gemcitabine/Tremelimumab Regimen False True False NCIT:C20369 Microtechnique False True False +NCIT:C203690 Carboplatin/Durvalumab/Nab-paclitaxel/Tremelimumab Regimen False True False +NCIT:C203691 Elranatamab Regimen False True False +NCIT:C203692 Enfortumab Vedotin/Pembrolizumab Regimen False True False +NCIT:C203693 Enzalutamide/Talazoparib Regimen False True False +NCIT:C203694 Epcoritamab Regimen False True False +NCIT:C203695 Mirvetuximab Soravtansine Regimen False True False +NCIT:C203696 Medroxyprogesterone Regimen False True False +NCIT:C203697 Topical Mechlorethamine Regimen False True False +NCIT:C203698 Isotretinoin Regimen False True False +NCIT:C203699 Dexamethasone/Imatinib/Vincristine Regimen False True False NCIT:C2037 IMC-1C11 False True False NCIT:C20370 Replication Initiation Gene False True False +NCIT:C203701 Anti-HER2 ADC BB-1701 False True False +NCIT:C203702 Medroxyprogesterone Alternating with Tamoxifen Regimen False True False +NCIT:C203703 Critical Access Hospital False True False +NCIT:C203704 Acute Care Hospital False True False +NCIT:C203705 Specialty Hospital False True False +NCIT:C203706 Women's Hospital False True False +NCIT:C203707 Off Campus-Outpatient Hospital False True False +NCIT:C203708 Inpatient Isolation False True False +NCIT:C203709 Alternate Care Site False True False NCIT:C20371 ORC Subunit Gene False True False +NCIT:C203710 Religious Nonmedical Health Care Institution False True False +NCIT:C203711 Fluorouracil/Liposomal Irinotecan/Leucovorin/Oxaliplatin Regimen False True False +NCIT:C203712 Multi-Specialty Group False True False +NCIT:C203713 Single Specialty Group False True False +NCIT:C203714 Epilepsy Hospital Unit False True False +NCIT:C203715 Chronic Disease Hospital Unit False True False +NCIT:C203716 Inpatient Cardiac Care Facility False True False +NCIT:C203717 Hospital Nursery False True False +NCIT:C203718 Tribal 638 Free-standing Facility False True False +NCIT:C203719 End-Stage Renal Disease Treatment Facility False True False NCIT:C20372 Licensing Factor Gene False True False +NCIT:C203720 Tribal 638 Provider-based Facility False True False +NCIT:C203721 Federally Qualified Health Center False True False +NCIT:C203722 Indian Health Service Free-standing Facility False True False +NCIT:C203723 Indian Health Service Provider-based Facility False True False +NCIT:C203724 Substance Use Disorder Rehabilitation Hospital Unit False True False +NCIT:C203725 Children's Hospital Rehabilitation Center False True False +NCIT:C203726 Dental Laboratory False True False +NCIT:C203727 Physiological Laboratory False True False +NCIT:C203728 Mental Illness Assisted Living Facility False True False +NCIT:C203729 Abiraterone/Niraparib/Prednisone Regimen False True False NCIT:C20373 MCM2 Gene False True False +NCIT:C203730 Behavioral Disturbances Assisted Living Facility False True False +NCIT:C203731 Alzheimer Nursing Center False True False +NCIT:C203732 Custodial Care Facility False True False +NCIT:C203733 Skilled Pediatric Nursing Facility False True False +NCIT:C203734 Residential Mental Retardation and Developmental Disabilities Treatment Facility False True False +NCIT:C203735 Residential Physical Disabilities Treatment Facility False True False +NCIT:C203736 Community Based Residential Mental Illness Treatment Facility False True False +NCIT:C203737 Community Based Mental Retardation and Developmental Disabilities Residential Treatment Facility False True False +NCIT:C203738 Residential Emotionally Disturbed Children Treatment Facility False True False +NCIT:C203739 Residential Children Substance Abuse Treatment Facility False True False NCIT:C20374 MCM4 Gene False True False +NCIT:C203740 Autologous Anti-CD19 CAR-T Cells CABA-201 False True False +NCIT:C203741 Independent Diagnostic Testing Facility False True False +NCIT:C203742 Slide Preparation Facility False True False +NCIT:C203743 Emergency Room Critical Care Facility False True False +NCIT:C203744 Group Home False True False +NCIT:C203745 Psychiatric Facility-Partial Hospitalization False True False +NCIT:C203746 Comprehensive Inpatient Rehabilitation Facility False True False +NCIT:C203747 Community Mental Health Center False True False +NCIT:C203748 Non-residential Substance Abuse Treatment Facility False True False +NCIT:C203749 Psychiatric Residential Treatment Center False True False NCIT:C20375 MCM5 Gene False True False +NCIT:C203750 Transcutaneous Auricular Vagus Nerve Stimulation False True False +NCIT:C203751 Gemcitabine/Ramucirumab Regimen False True False +NCIT:C203752 Panitumumab/Sotorasib Regimen False True False +NCIT:C203753 Cetuximab/Sotorasib Regimen False True False +NCIT:C203754 Talquetamab Regimen False True False +NCIT:C203755 Doxorubicin/Trabectedin Regimen False True False +NCIT:C203756 MAN2B1 Gene False True False +NCIT:C203757 MAN2B1 wt Allele False True False +NCIT:C203758 Lysosomal Alpha-Mannosidase False True False +NCIT:C203759 MANBA Gene False True False NCIT:C20376 MCM6 Gene False True False +NCIT:C203760 Dabrafenib/Pembrolizumab/Trametinib Regimen False True False +NCIT:C203761 MANBA wt Allele False True False +NCIT:C203762 Beta-Mannosidase False True False +NCIT:C203763 Trastuzumab/Tucatinib Regimen False True False +NCIT:C203764 PTGR1 Gene False True False +NCIT:C203765 PTGR1 wt Allele False True False +NCIT:C203766 Prostaglandin Reductase 1 False True False +NCIT:C203767 CD93 Gene False True False +NCIT:C203768 CD93 wt Allele False True False +NCIT:C203769 Complement Component C1q Receptor False True False NCIT:C20377 MCM3 Gene False True False +NCIT:C203770 WHO CNS5 Diagnosis False True False +NCIT:C203771 MAT1A Gene False True False +NCIT:C203772 MAT1A wt Allele False True False +NCIT:C203773 S-Adenosylmethionine Synthase Isoform Type-1 False True False +NCIT:C203774 MBTPS2 Gene False True False +NCIT:C203775 MBTPS2 wt Allele False True False +NCIT:C203776 Membrane-Bound Transcription Factor Site-2 Protease False True False +NCIT:C203777 PQ/CMC Ingredient Location Terminology False True False +NCIT:C203778 PQ/CMC Release Profile Terminology False True False +NCIT:C203779 PQ/CMC Coating Purpose Terminology False True False NCIT:C20378 MCM7 Gene False True False +NCIT:C203780 PQ/CMC Product Part Type Terminology False True False +NCIT:C203781 Exhaled Carbon Monoxide Concentration Finding False True False +NCIT:C203782 Exhaled Carbon Monoxide Concentration Less than 10 ppm False True False +NCIT:C203783 MCOLN1 Gene False True False +NCIT:C203784 MCOLN1 wt Allele False True False +NCIT:C203785 Mucolipin-1 False True False +NCIT:C203786 MEFV Gene False True False +NCIT:C203787 MEFV wt Allele False True False +NCIT:C203788 Pyrin False True False +NCIT:C203789 MMAA Gene False True False NCIT:C20379 CDC45 Gene False True False +NCIT:C203790 MMAA wt Allele False True False +NCIT:C203791 Methylmalonic Aciduria Type A Protein, Mitochondrial False True False +NCIT:C203792 MMAB Gene False True False +NCIT:C203793 MMAB wt Allele False True False +NCIT:C203794 Corrinoid Adenosyltransferase MMAB False True False +NCIT:C203796 MMACHC Gene False True False +NCIT:C203797 MMACHC wt Allele False True False +NCIT:C203798 Cyanocobalamin Reductase / Alkylcobalamin Dealkylase False True False +NCIT:C203799 Proliferative Actinic Keratosis False True False NCIT:C2038 Monoclonal Antibody DC101 False True False NCIT:C20380 ORC2 Gene False True False +NCIT:C203800 Hypertrophic Actinic Keratosis False True False +NCIT:C203801 Lichenoid Actinic Keratosis False True False +NCIT:C203802 Atrophic Actinic Keratosis False True False +NCIT:C203803 Acantholytic Actinic Keratosis False True False +NCIT:C203804 Pigmented Actinic Keratosis False True False +NCIT:C203805 Increased Melanin Pigmentation in Basal Keratinocytes Present False True False +NCIT:C203806 Bowenoid Actinic Keratosis False True False +NCIT:C203807 Full-Thickness Epidermal Atypia False True False +NCIT:C203808 Nearly Full-Thickness Epidermal Atypia False True False +NCIT:C203809 MOCS1 Gene False True False NCIT:C20381 CDT1 Gene False True False +NCIT:C203810 MOCS1 wt Allele False True False +NCIT:C203811 Molybdenum Cofactor Biosynthesis Protein 1 False True False +NCIT:C203812 MPLKIP Gene False True False +NCIT:C203813 MPLKIP wt Allele False True False +NCIT:C203814 M-Phase-Specific PLK1-Interacting Protein False True False +NCIT:C203816 MPZ Gene False True False +NCIT:C203817 MPZ wt Allele False True False +NCIT:C203818 Myelin Protein P0 False True False +NCIT:C203819 MT-ATP6 Gene False True False NCIT:C20382 CDC6 Gene False True False +NCIT:C203820 MT-ATP6 wt Allele False True False +NCIT:C203821 ATP Synthase Subunit a False True False +NCIT:C203822 MTM1 Gene False True False +NCIT:C203823 MTM1 wt Allele False True False +NCIT:C203824 Myotubularin False True False +NCIT:C203825 IL-7R-Alpha-deficient Severe Combined Immunodeficiency False True False +NCIT:C203826 Oncolytic HSV-1 Expressing IL-2 and IL-12 KB707 False True False +NCIT:C203827 T-cell Engaging Trispecific Antibody False True False +NCIT:C203828 T-cell Engaging Antibody False True False +NCIT:C203829 MMUT Gene False True False NCIT:C20383 MCM10 Gene False True False +NCIT:C203830 MMUT wt Allele False True False +NCIT:C203831 Methylmalonyl-CoA Mutase, Mitochondrial False True False +NCIT:C203832 Family Planning Facility False True False +NCIT:C203833 Fertility Clinic False True False +NCIT:C203834 Amputee Clinic False True False +NCIT:C203835 MYH3 Gene False True False +NCIT:C203836 MYH3 wt Allele False True False +NCIT:C203837 Augmentative Communication Clinic False True False +NCIT:C203838 Corporate Health Clinic False True False +NCIT:C203839 Developmental Disabilities Clinic False True False NCIT:C20384 CDC7 Gene False True False +NCIT:C203840 Endoscopy Clinic False True False +NCIT:C203841 Myosin-3 False True False +NCIT:C203842 Genetics Clinic False True False +NCIT:C203843 NAGS Gene False True False +NCIT:C203844 NAGS wt Allele False True False +NCIT:C203845 N-Acetylglutamate Synthase, Mitochondrial False True False +NCIT:C203846 Non-Surgical Family Planning Clinic False True False +NCIT:C203847 Hearing and Speech Clinic False True False +NCIT:C203848 Lithotripsy Clinic False True False +NCIT:C203849 Adolescent and Children Mental Health Clinic False True False NCIT:C20385 DBF4 Gene False True False +NCIT:C203850 Migrant Health Clinic False True False +NCIT:C203852 Multi-Specialty Clinic False True False +NCIT:C203853 NAGLU Gene False True False +NCIT:C203854 Medical Specialty Clinic False True False +NCIT:C203855 NAGLU wt Allele False True False +NCIT:C203856 Alpha-N-Acetylglucosaminidase False True False +NCIT:C203857 NAPB Gene False True False +NCIT:C203858 NAPB wt Allele False True False +NCIT:C203859 Methadone Clinic False True False NCIT:C20386 ORC1 Gene False True False +NCIT:C203860 Medically Fragile Infants and Children Day Care Clinic False True False +NCIT:C203861 Podiatric Clinic False True False +NCIT:C203862 Mammography Clinic False True False +NCIT:C203863 Mobile Mammography Clinic False True False +NCIT:C203864 Mobile Radiology Clinic False True False +NCIT:C203865 Ambulatory Cardiac Rehabilitation Facility False True False +NCIT:C203866 Outpatient Research Clinic False True False +NCIT:C203867 Oral and Maxillofacial Surgery Clinic False True False +NCIT:C203868 Beta-Soluble NSF Attachment Protein False True False +NCIT:C203869 Sleep Disorder Diagnostic Clinic False True False NCIT:C20387 ORC4 Gene False True False +NCIT:C203870 Local Education Agency False True False +NCIT:C203871 Home Infusion Therapy Services Agency False True False +NCIT:C203872 Community Based Hospice Care Agency False True False +NCIT:C203873 Nursing Care Agency False True False +NCIT:C203874 Public Health Agency False True False +NCIT:C203875 Public Welfare Agency False True False +NCIT:C203876 Program of All-Inclusive Care for the Elderly False True False +NCIT:C203877 Support Brokerage Agency False True False +NCIT:C203878 Early Intervention Provider Agency False True False +NCIT:C203879 Foster Care Agency False True False NCIT:C20388 ORC5 Gene False True False +NCIT:C203880 Voluntary Health or Charitable Agency False True False +NCIT:C203881 Active Core Granule False True False +NCIT:C203882 Extragranular Ingredient False True False +NCIT:C203883 Intragranular Ingredient False True False +NCIT:C203884 Appearance Promoting Coating False True False +NCIT:C203885 Consumption Promoting Coating False True False +NCIT:C203886 Isolate Promoting Coating False True False +NCIT:C203887 Delayed Release Coating False True False +NCIT:C203888 Drug Layering Coating False True False +NCIT:C203889 Extended Release Coating False True False NCIT:C20389 ORC6 Gene False True False +NCIT:C203890 Irritant Suppression Coating False True False +NCIT:C203891 Odor Masking Coating False True False +NCIT:C203892 Protective Coating False True False +NCIT:C203893 Seal Coating False True False +NCIT:C203894 Site Delivery Coating False True False +NCIT:C203895 Taste Masking Coating False True False +NCIT:C203896 Blended Dry Mixture False True False +NCIT:C203897 Capsule Shell False True False +NCIT:C203898 Minitablet Dosage Form False True False +NCIT:C203899 NDP Gene False True False NCIT:C2039 Bevacizumab False True False NCIT:C20390 ORC3 Gene False True False +NCIT:C203900 NDP wt Allele False True False +NCIT:C203901 Norrin False True False +NCIT:C203902 PD-L1 Combined Positive Score Greater than or Equal to 20 False True False +NCIT:C203903 Anti-CCR8 Monoclonal Antibody BGB-A3055 False True False +NCIT:C203905 Target Antigen False True False +NCIT:C203906 NEB Gene False True False +NCIT:C203907 NEB wt Allele False True False +NCIT:C203908 Nebulin False True False +NCIT:C203909 NEU1 Gene False True False NCIT:C20391 Neurotrophic Factor False True False +NCIT:C203910 NEU1 wt Allele False True False +NCIT:C203911 Sialidase-1 False True False +NCIT:C203912 CDISC MRCT Center Clinical Research Glossary False True False +NCIT:C203913 To Volunteer False True False +NCIT:C203914 Additive Effect False True False +NCIT:C203915 Benefits of a Research Study False True False +NCIT:C203916 Comparative Effectiveness Research False True False +NCIT:C203917 Confound False True False +NCIT:C203918 Dissent False True False +NCIT:C203919 Drug Holiday False True False NCIT:C20392 Neuropoietic Cytokine False True False +NCIT:C203920 Electronic Consent Form False True False +NCIT:C203921 Equivalent Effect False True False +NCIT:C203922 Negligible False True False +NCIT:C203923 Participate False True False +NCIT:C203924 Periodically False True False +NCIT:C203925 Placebo-Controlled Study False True False +NCIT:C203926 Pseudonymize False True False +NCIT:C203927 Study Rationale False True False +NCIT:C203928 Risk-Benefit Ratio False True False +NCIT:C203929 Study Life Cycle False True False NCIT:C20393 Heparin-Binding Neurotrophic Factor False True False +NCIT:C203930 Study Results False True False +NCIT:C203931 Synergistic Effect False True False +NCIT:C203932 Study Intervention Tolerability False True False +NCIT:C203933 Voluntary Participation False True False +NCIT:C203934 Assent Form False True False +NCIT:C203935 Research Database False True False +NCIT:C203936 Research Repository False True False +NCIT:C203937 OMOP Common Data Model False True False +NCIT:C203938 OMOP Common Data Model v5.4 False True False +NCIT:C203939 PCORnet Common Data Model False True False NCIT:C20394 WNT Family Protein False True False +NCIT:C203940 PCORnet Common Data Model v6.1 False True False +NCIT:C203941 Recovery Care Clinic False True False +NCIT:C203942 Multiplexed Tissue Imaging False True False +NCIT:C203943 NGLY1 Gene False True False +NCIT:C203944 NGLY1 wt Allele False True False +NCIT:C203945 Peptide-N(4)-(N-Acetyl-Beta-Glucosaminyl)Asparagine Amidase False True False +NCIT:C203947 IDA-FLAG/Venetoclax Regimen False True False NCIT:C20395 GMNN Gene False True False +NCIT:C203950 CapOX/Panitumumab Regimen False True False +NCIT:C203951 Intracameral Implant in Applicator Dosage Form False True False +NCIT:C203952 Intravitreal Implant Dosage Form False True False +NCIT:C203953 Intracameral Implant Dosage Form False True False +NCIT:C203954 Carboplatin/Paclitaxel/Pertuzumab/Trastuzumab Regimen False True False +NCIT:C203955 Cisplatin/Gemcitabine/Pembrolizumab Regimen False True False +NCIT:C203956 Cisplatin/Docetaxel/Fluorouracil/Trastuzumab Regimen False True False +NCIT:C203957 Cisplatin/Docetaxel/Trastuzumab Regimen False True False +NCIT:C203958 Capecitabine/Cisplatin/Pembrolizumab/Trastuzumab Regimen False True False +NCIT:C203959 Cisplatin/Fluorouracil/Pembrolizumab/Trastuzumab Regimen False True False NCIT:C20396 Protein Phosphatase 2A Subunit Gene False True False +NCIT:C203960 FOLFOX-Pembrolizumab/Trastuzumab Regimen False True False +NCIT:C203961 mFOLFOX6 -Trastuzumab Regimen False True False +NCIT:C203962 Cisplatin/Paclitaxel/Trastuzumab Regimen False True False +NCIT:C203963 FOLFIRI-Trastuzumab Regimen False True False +NCIT:C203964 Fluorouracil/Trastuzumab Regimen False True False +NCIT:C203965 Docetaxel/Fluorouracil/Oxaliplatin/Trastuzumab Regimen False True False +NCIT:C203966 Cisplatin/Gemcitabine/Nivolumab Regimen False True False +NCIT:C203967 Total Laparoscopic Hysterectomy False True False NCIT:C20397 PPP2R3B Gene False True False +NCIT:C203970 Flat-Topped Papular Lesion False True False +NCIT:C203971 mFOLFOX6/Nivolumab Regimen False True False +NCIT:C203972 Cisplatin/Fluorouracil/Nivolumab Regimen False True False +NCIT:C203973 Capecitabine/Cisplatin/Nivolumab Regimen False True False +NCIT:C203974 ICE/Nivolumab Regimen False True False +NCIT:C203975 Cisplatin/Gemcitabine/Nivolumab Followed by Nivolumab Regimen False True False +NCIT:C203976 Selective Estrogen Receptor Covalent Antagonist False True False +NCIT:C203977 Complete Estrogen Receptor Antagonist False True False +NCIT:C203978 NLRP12 Gene False True False +NCIT:C203979 NLRP12 wt Allele False True False NCIT:C20398 PPP2CA Gene False True False +NCIT:C203980 Methotrexate/Pegaspargase Regimen False True False +NCIT:C203981 Daunorubicin/Pegaspargase/Prednisone/Vincristine Regimen False True False +NCIT:C203982 Gemcitabine/Oxaliplatin/Pegaspargase Regimen False True False +NCIT:C203983 Predisposition to Malignant Neoplasm False True False +NCIT:C203984 NOP56 Gene False True False +NCIT:C203985 NOP56 wt Allele False True False +NCIT:C203986 Cisplatin/Dexamethasone/Gemcitabine/Pegaspargase Regimen False True False +NCIT:C203987 Nucleolar Protein 56 False True False +NCIT:C203988 Dexamethasone/Etoposide/Gemcitabine/Pegaspargase Regimen False True False +NCIT:C203989 NPC1 Gene False True False NCIT:C20399 PPP2CB Gene False True False +NCIT:C203990 NPC1 wt Allele False True False +NCIT:C203991 Cytarabine/Etoposide/Rituximab Regimen False True False +NCIT:C203992 NPC Intracellular Cholesterol Transporter 1 False True False +NCIT:C203993 NPC2 Gene False True False +NCIT:C203994 NPC2 wt Allele False True False +NCIT:C203995 NPC Intracellular Cholesterol Transporter 2 False True False +NCIT:C203996 MPC1 Gene False True False +NCIT:C203997 MPC1 wt Allele False True False +NCIT:C203998 Mitochondrial Pyruvate Carrier 1 False True False +NCIT:C203999 MCIDAS Gene False True False NCIT:C204 Actinomycin Antineoplastic Antibiotic False True False NCIT:C2040 Texaphyrin False True False +NCIT:C204000 MCIDAS wt Allele False True False +NCIT:C204001 Multicilin False True False +NCIT:C204002 Dexamethasone/Cytarabine/Oxaliplatin/Rituximab Regimen False True False +NCIT:C204003 MAN2C1 Gene False True False +NCIT:C204004 Etoposide/Ifosfamide/Mesna/Mitoxantrone/Rituximab Regimen False True False +NCIT:C204005 MAN2C1 wt Allele False True False +NCIT:C204006 Alpha-Mannosidase 2C1 False True False +NCIT:C204007 Cytarabine/Fludarabine/Oxaliplatin/Rituximab Regimen False True False +NCIT:C204008 Liposomal Doxorubicin/Rituximab Regimen False True False +NCIT:C204009 Liposomal Doxorubicin/Prednisone/Rituximab Regimen False True False NCIT:C20401 Monoclonal Antibody False True False +NCIT:C204010 Military Hospital False True False +NCIT:C204011 Military Operational Hospital False True False +NCIT:C204012 Ground Ambulance False True False +NCIT:C204013 Air Ambulance False True False +NCIT:C204014 Water Ambulance False True False +NCIT:C204015 Non-Pharmacy Dispensing Site False True False +NCIT:C204016 Clinic Pharmacy False True False +NCIT:C204017 Retail Community Pharmacy False True False +NCIT:C204018 Compounding Pharmacy False True False +NCIT:C204019 Home Infusion Pharmacy False True False NCIT:C20402 PPP2R5A Gene False True False +NCIT:C204020 Institutional Pharmacy False True False +NCIT:C204021 Long-Term Care Pharmacy False True False +NCIT:C204022 Mail-Order Pharmacy False True False +NCIT:C204023 Nuclear Pharmacy False True False +NCIT:C204024 Specialty Pharmacy False True False +NCIT:C204025 Autologous Retroviral Vector MSGV1-transduced Anti-PSCA-8T28Z CAR Gamma Delta T-cells False True False +NCIT:C204026 Bunker Gear False True False +NCIT:C204027 Medical Supply Company with Pharmacist False True False +NCIT:C204028 Non-emergency Medical Transportation False True False +NCIT:C204029 Secured Medical Transportation False True False NCIT:C20403 PPP2R5B Gene False True False +NCIT:C204030 Air Transportation Carrier False True False +NCIT:C204031 Bus False True False +NCIT:C204032 Train False True False +NCIT:C204033 Medical Transportation Broker False True False +NCIT:C204034 Homeless Shelter False True False +NCIT:C204039 Allogeneic CRISPR-edited Anti-CLL-1 CAR-T Cells CB-012 False True False NCIT:C20404 PPP2R5C Gene False True False +NCIT:C204040 Country Dial-in Code False True False +NCIT:C204041 Personal Pronouns False True False +NCIT:C204042 Service Provider False True False +NCIT:C204043 Rehabilitation Assistive Technology Supplier False True False +NCIT:C204044 Audiology Assistive Technology Supplier False True False +NCIT:C204045 Durable Medical Equipment Supplier False True False +NCIT:C204046 Customized Equipment Supplier False True False +NCIT:C204047 Dialysis Equipment Supplier False True False +NCIT:C204048 Nursing Facility Supplier False True False +NCIT:C204049 Parenteral and Enteral Nutrition Supplier False True False NCIT:C20405 PPP2R5D Gene False True False +NCIT:C204050 Oxygen Equipment Supplier False True False +NCIT:C204051 Eyewear Supplier False True False +NCIT:C204052 Hearing Aid Equipment Supplier False True False +NCIT:C204053 Home-delivered Meal Supplier False True False +NCIT:C204054 Emergency Response System Supplier False True False +NCIT:C204055 Prosthetic Supplier False True False +NCIT:C204056 Orthotic Supplier False True False +NCIT:C204057 Medical Food Supplier False True False +NCIT:C204058 Portable Diagnostic Imaging Supplier False True False +NCIT:C204059 Oxygen Supplier False True False NCIT:C20406 PPP2R5E Gene False True False +NCIT:C204060 Portable X-Ray Supplier False True False +NCIT:C204061 Other Medical Supply Company False True False +NCIT:C204062 Medical Supply Company with Orthotist False True False +NCIT:C204063 Medical Supply Company with Prosthetist False True False +NCIT:C204064 Medical Supply Company with Respiratory Therapist False True False +NCIT:C204065 Medical Supply Company with Pedorthist False True False +NCIT:C204066 Organ Procurement Organization False True False +NCIT:C204067 Department Store False True False +NCIT:C204068 Independent Laboratory False True False +NCIT:C204069 Nursing Episode False True False NCIT:C20407 PTPA Gene False True False +NCIT:C204070 Medicare Part B Competitive Acquisition Program Drug Vendor False True False +NCIT:C204071 Well Child Care False True False +NCIT:C204072 Respite Care Camp False True False +NCIT:C204073 Child Mental Illness Respite Care False True False +NCIT:C204074 Child Mental Retardation and / or Developmental Disability Respite Care False True False +NCIT:C204075 Child Physical Disability Respite Care False True False +NCIT:C204076 YAG Laser Posterior Capsulotomy False True False +NCIT:C204077 Anti-TA-MUC1/DXd Antibody-drug Conjugate DS-3939a False True False +NCIT:C204078 Lung Radiation Therapy False True False +NCIT:C204079 Liver Radiation Therapy False True False NCIT:C20408 VAV Family Gene False True False +NCIT:C204080 Kidney Radiation Therapy False True False +NCIT:C204081 SEZ6 Gene False True False +NCIT:C204082 SEZ6 wt Allele False True False +NCIT:C204083 Seizure Protein 6 Homolog False True False +NCIT:C204084 Alpha-Mannosidase 2 False True False +NCIT:C204085 MAN2A1 Gene False True False +NCIT:C204086 MAN2A1 wt Allele False True False +NCIT:C204087 MAN2A2 Gene False True False +NCIT:C204088 MAN2A2 wt Allele False True False +NCIT:C204089 Alpha-Mannosidase 2x False True False NCIT:C20409 BCL-2 Gene Family False True False +NCIT:C204090 Copy Identifier False True False +NCIT:C204091 Genomic Inheritability Type False True False +NCIT:C204092 Genomic Symbol Entity Type False True False +NCIT:C204093 Reagent Cycle Number False True False +NCIT:C204094 Reagent Sub-Cycle Number False True False +NCIT:C204095 Excitation Wavelength False True False +NCIT:C204096 Excitation Bandwidth False True False +NCIT:C204097 Emission Bandwidth False True False +NCIT:C204098 Study Outcome False True False +NCIT:C204099 Autologous KRAS G12D-specific HLA-C*08:02-restricted TCR Gene Engineered T-lymphocytes NT-112 False True False NCIT:C2041 Radicicol Derivative KF58333 False True False NCIT:C20410 BCL2L1 Gene False True False +NCIT:C204100 Autologous CRISPR-Cas9 Engineered Tumor Infiltrating Lymphocytes KSQ-001EX False True False +NCIT:C204101 Emission Wavelength False True False +NCIT:C204102 Broccoli/Turmeric/Pomegranate/Green Tea Extract-based Supplement False True False +NCIT:C204103 CDK2 Inhibitor AZD8421 False True False +NCIT:C204104 OAT Gene False True False +NCIT:C204105 OAT wt Allele False True False +NCIT:C204106 Ornithine Aminotransferase, Mitochondrial False True False +NCIT:C204107 OCRL Gene False True False +NCIT:C204108 iPSC-derived Allogeneic Anti-HER2 CAR T-cells FT825 False True False +NCIT:C204109 OCRL wt Allele False True False NCIT:C20411 BCL2L2 Gene False True False +NCIT:C204110 Inositol Polyphosphate 5-Phosphatase OCRL False True False +NCIT:C204111 OLR1 Gene False True False +NCIT:C204112 OLR1 wt Allele False True False +NCIT:C204113 Oxidized Low-Density Lipoprotein Receptor 1 False True False +NCIT:C204114 CALHM1 Gene False True False +NCIT:C204115 CALHM1 wt Allele False True False +NCIT:C204116 Calcium Homeostasis Modulator Protein 1 False True False +NCIT:C204117 Face Wash False True False +NCIT:C204118 Ki-67 Positive Cells Less than or Equal to 30 Percent False True False +NCIT:C204119 Ki-67 Positive Cells Less than or Equal to 50 Percent False True False NCIT:C20412 MCL1 Gene False True False +NCIT:C204120 Ki-67 Positive Cells Greater than 50 Percent False True False +NCIT:C204121 CALHM3 Gene False True False +NCIT:C204122 CALHM3 wt Allele False True False +NCIT:C204123 Calcium Homeostasis Modulator Protein 3 False True False +NCIT:C204125 Anti-HHLA2 Monoclonal Antibody NPX887 False True False +NCIT:C204127 Developmentally Disabled Service Agency False True False +NCIT:C204128 Age at Start of Medication Administration False True False +NCIT:C204129 Age at End of Medication Administration False True False NCIT:C20413 BAK1 Gene False True False +NCIT:C204131 Response Evaluation Criteria in Prostate-specific Membrane Antigen (PSMA) PET/CT 1.0 False True False +NCIT:C204132 RECIP 1.0 Complete Response False True False +NCIT:C204133 RECIP 1.0 Partial Response False True False +NCIT:C204134 RECIP 1.0 Progressive Disease False True False +NCIT:C204135 RECIP 1.0 Stable Disease False True False +NCIT:C204136 NACHT, LRR and PYD Domains-Containing Protein 12 False True False +NCIT:C204137 Anti-CD47/Anti-HER2 Bispecific Antibody D3L-001 False True False +NCIT:C204138 Avitotamig False True False +NCIT:C204139 Bersiporocin Hydrochloride False True False NCIT:C20414 BAD Gene False True False +NCIT:C204140 Crelosidenib Gentisate False True False +NCIT:C204141 Dordaviprone Hydrochloride False True False +NCIT:C204142 Esepapogene Zalarnarepvec False True False +NCIT:C204143 Givinostat Hydrochloride False True False +NCIT:C204144 Lorundrostat Hydrobromide False True False +NCIT:C204145 Lotiglipron Tromethamine False True False +NCIT:C204146 Neltependocel False True False +NCIT:C204147 Ninsipapogene Sibarnarepvec False True False +NCIT:C204148 Opelkibart Elmanitin False True False +NCIT:C204149 Revumenib Citrate False True False NCIT:C20415 Bcl-X(S) False True False +NCIT:C204150 Volenrelaxin False True False +NCIT:C204151 Xalnesiran Sodium False True False +NCIT:C204152 Hpk1 Inhibitor BB3008 False True False +NCIT:C204153 PIGR Gene False True False +NCIT:C204154 BCL-XL Inhibitor False True False +NCIT:C204155 PIGR wt Allele False True False +NCIT:C204156 Polymeric Immunoglobulin Receptor False True False +NCIT:C204157 P2RX2 Gene False True False +NCIT:C204158 Anti-CCR8 Monoclonal Antibody AMG 355 False True False +NCIT:C204159 P2RX2 wt Allele False True False NCIT:C20416 BCL2L11 Gene False True False +NCIT:C204160 P2X Purinoceptor 2 False True False +NCIT:C204161 Anti-PD-L1/VEGF/TGF-beta Trispecific Antibody DR30206 False True False +NCIT:C204162 PABPN1 Gene False True False +NCIT:C204163 PABPN1 wt Allele False True False +NCIT:C204164 Polyadenylate-Binding Protein 2 False True False +NCIT:C204165 Anti-B7-H4/Anti-4-1BB Bispecific Antibody ABL103 False True False +NCIT:C204166 Anti-CD30 Antibody-drug Conjugate SGN-35T False True False +NCIT:C204167 Anti-PD-1/Anti-PD-L1 Bispecific Antibody CTX-8371 False True False +NCIT:C204168 Anti-PD-L1 Antibody-drug Conjugate HLX43 False True False +NCIT:C204169 Anti-TROP-2 Antibody-drug Conjugate HS-20105 False True False NCIT:C20417 BIK Gene False True False +NCIT:C204170 Autologous Anti-CLL-1-CAR T-lymphocytes BG1805 False True False +NCIT:C204171 Autologous Anti-GPC3 CAR T-lymphocytes JWAT204 False True False +NCIT:C204172 Autologous Anti-TIM-3/Anti-CD123 CAR T-cells False True False +NCIT:C204173 Autologous CRISPR-edited Tumor Infiltrating Lymphocytes GT316 False True False +NCIT:C204174 Autologous Tumor-infiltrating Lymphocytes GC101 False True False +NCIT:C204175 Crisaborole Ointment False True False +NCIT:C204176 Gallium Ga 68-DOTA-MGS5 False True False +NCIT:C204177 IL-15(N72D)/IL-15Ralpha-sFc Fusion Protein Complex FL115 False True False +NCIT:C204178 ROS1 Inhibitor JYP0322 False True False +NCIT:C204179 PACS2 Gene False True False NCIT:C20418 HRK Gene False True False +NCIT:C204180 PACS2 wt Allele False True False +NCIT:C204181 Phosphofurin Acidic Cluster Sorting Protein 2 False True False +NCIT:C204182 Donor-specific Antibody False True False +NCIT:C204183 PAH Gene False True False +NCIT:C204184 PAH wt Allele False True False +NCIT:C204185 Phenylalanine-4-Hydroxylase False True False +NCIT:C204186 PATL2 Gene False True False +NCIT:C204187 PATL2 wt Allele False True False +NCIT:C204188 Protein PAT1 Homolog 2 False True False +NCIT:C204189 PCDH19 Gene False True False NCIT:C20419 BID Gene False True False +NCIT:C204190 PCDH19 wt Allele False True False +NCIT:C204191 Protocadherin-19 False True False +NCIT:C204192 PDE6C Gene False True False +NCIT:C204193 PDE6C wt Allele False True False +NCIT:C204194 Molecular Sequence Alteration Region False True False +NCIT:C204195 Molecular Sequence Alteration Effect False True False +NCIT:C204196 Cone cGMP-Specific 3',5'-Cyclic Phosphodiesterase Subunit Alpha' False True False +NCIT:C204197 Breast Cancer IHC4 False True False +NCIT:C204198 Extracorporeal Hemodialysis Route of Administration False True False +NCIT:C204199 Intracolonic Route of Administration False True False NCIT:C2042 AG 1732 False True False NCIT:C20420 Transcription Factor Gene False True False +NCIT:C204200 PDSS2 Gene False True False +NCIT:C204201 PDSS2 wt Allele False True False +NCIT:C204202 All Trans-Polyprenyl-Diphosphate Synthase PDSS2 False True False +NCIT:C204204 Intradialytic Route of Administration False True False +NCIT:C204205 Sublabial Route of Administration False True False +NCIT:C204206 Autologous PSMA-inducible Anti-CA9 CAR T-cells AB-2100 False True False +NCIT:C204207 CA9-targeting Agent False True False +NCIT:C204208 Exhaled Carbon Monoxide Concentration Greater than or Equal to 8 ppm False True False +NCIT:C204209 PEX1 Gene False True False NCIT:C20421 TAF1 Gene False True False +NCIT:C204210 PEX1 wt Allele False True False +NCIT:C204211 Peroxisomal ATPase PEX1 False True False +NCIT:C204212 PEX10 Gene False True False +NCIT:C204213 Cisplatin Nano-engineered Intraoperative System PRV211 False True False +NCIT:C204214 PEX10 wt Allele False True False +NCIT:C204215 Peroxisome Biogenesis Factor 10 False True False +NCIT:C204216 PEX12 Gene False True False +NCIT:C204217 PEX12 wt Allele False True False +NCIT:C204218 Peroxisome Assembly Protein 12 False True False +NCIT:C204219 CDISC Questionnaire Perianal Crohn's Disease Activity Index Test Name Terminology False True False NCIT:C20422 Mitochondrial Membrane Protein False True False +NCIT:C204220 CDISC Questionnaire Perianal Crohn's Disease Activity Index Test Code Terminology False True False +NCIT:C204221 CDISC Questionnaire Penn State Electronic Cigarette Dependence Index Test Name Terminology False True False +NCIT:C204222 CDISC Questionnaire Penn State Electronic Cigarette Dependence Index Test Code Terminology False True False +NCIT:C204223 CDISC Questionnaire Sepsis-related Organ Failure Assessment Test Name Terminology False True False +NCIT:C204224 CDISC Questionnaire Sepsis-related Organ Failure Assessment Test Code Terminology False True False +NCIT:C204225 CDISC Questionnaire Sepsis-related Organ Failure Assessment SOFA0101 Original Response Terminology False True False +NCIT:C204226 CDISC Questionnaire Sepsis-related Organ Failure Assessment SOFA0101 Standardized Character Response Terminology False True False +NCIT:C204227 CDISC Questionnaire Sepsis-related Organ Failure Assessment SOFA0102 Original Response Terminology False True False +NCIT:C204228 CDISC Questionnaire Sepsis-related Organ Failure Assessment SOFA0102 Standardized Character Response Terminology False True False +NCIT:C204229 CDISC Questionnaire Sepsis-related Organ Failure Assessment SOFA0103 Original Response Terminology False True False NCIT:C20423 Helicase False True False +NCIT:C204230 CDISC Questionnaire Sepsis-related Organ Failure Assessment SOFA0103 Standardized Character Response Terminology False True False +NCIT:C204231 CDISC Questionnaire Sepsis-related Organ Failure Assessment SOFA0104 Original Response Terminology False True False +NCIT:C204232 CDISC Questionnaire Sepsis-related Organ Failure Assessment SOFA0104 Standardized Character Response Terminology False True False +NCIT:C204233 CDISC Questionnaire Sepsis-related Organ Failure Assessment SOFA0105 Original Response Terminology False True False +NCIT:C204234 CDISC Questionnaire Sepsis-related Organ Failure Assessment SOFA0105 Standardized Character Response Terminology False True False +NCIT:C204235 CDISC Questionnaire Sepsis-related Organ Failure Assessment SOFA0106 Original Response Terminology False True False +NCIT:C204236 CDISC Questionnaire Sepsis-related Organ Failure Assessment SOFA0106 Standardized Character Response Terminology False True False +NCIT:C204237 Perianal Crohn's Disease Activity Index Questionnaire Question False True False +NCIT:C204238 Penn State Electronic Cigarette Dependence Index Questionnaire Question False True False +NCIT:C204239 Sepsis-related Organ Failure Assessment Questionnaire Question False True False NCIT:C20424 Growth Factor False True False +NCIT:C204240 Sepsis-related Organ Failure Assessment SOFA0101 Question Questionnaire Original Response False True False +NCIT:C204241 Sepsis-related Organ Failure Assessment SOFA0101 Question Questionnaire Standardized Character Response False True False +NCIT:C204242 Sepsis-related Organ Failure Assessment SOFA0102 Question Questionnaire Original Response False True False +NCIT:C204243 Sepsis-related Organ Failure Assessment SOFA0102 Question Questionnaire Standardized Character Response False True False +NCIT:C204244 Sepsis-related Organ Failure Assessment SOFA0103 Question Questionnaire Original Response False True False +NCIT:C204245 Sepsis-related Organ Failure Assessment SOFA0103 Question Questionnaire Standardized Character Response False True False +NCIT:C204246 Sepsis-related Organ Failure Assessment SOFA0104 Question Questionnaire Original Response False True False +NCIT:C204247 Sepsis-related Organ Failure Assessment SOFA0104 Question Questionnaire Standardized Character Response False True False +NCIT:C204248 Sepsis-related Organ Failure Assessment SOFA0105 Question Questionnaire Original Response False True False +NCIT:C204249 Sepsis-related Organ Failure Assessment SOFA0105 Question Questionnaire Standardized Character Response False True False NCIT:C20425 Epidermal Growth Factor False True False +NCIT:C204250 Sepsis-related Organ Failure Assessment SOFA0106 Question Questionnaire Original Response False True False +NCIT:C204251 Sepsis-related Organ Failure Assessment SOFA0106 Question Questionnaire Standardized Character Response False True False +NCIT:C204252 Autologous KRAS Mutant-specific TCRs Gene Engineered PBLs False True False +NCIT:C204253 PEX16 Gene False True False +NCIT:C204254 PEX16 wt Allele False True False +NCIT:C204255 Peroxisomal Membrane Protein PEX16 False True False +NCIT:C204256 Adenovirus Serotype 5-based Therapeutic Agent False True False +NCIT:C204257 Sepsis-related Organ Failure Assessment SOFA0101 Original Result - >= 400 False True False +NCIT:C204258 Sepsis-related Organ Failure Assessment SOFA0101 Original Result - < 400 False True False +NCIT:C204259 Sepsis-related Organ Failure Assessment SOFA0101 Original Result - < 300 False True False NCIT:C20426 Fibroblast Growth Factor False True False +NCIT:C204260 Sepsis-related Organ Failure Assessment SOFA0101 Original Result - < 200 with respiratory support (mechanical ventilation including CPAP) False True False +NCIT:C204261 Sepsis-related Organ Failure Assessment SOFA0101 Original Result - < 100 with respiratory support (mechanical ventilation including CPAP) False True False +NCIT:C204262 Sepsis-related Organ Failure Assessment SOFA0101 Standardized Character Result 0 False True False +NCIT:C204263 Sepsis-related Organ Failure Assessment SOFA0101 Standardized Character Result 1 False True False +NCIT:C204264 Sepsis-related Organ Failure Assessment SOFA0101 Standardized Character Result 2 False True False +NCIT:C204265 Sepsis-related Organ Failure Assessment SOFA0101 Standardized Character Result 3 False True False +NCIT:C204266 Sepsis-related Organ Failure Assessment SOFA0101 Standardized Character Result 4 False True False +NCIT:C204267 Sepsis-related Organ Failure Assessment SOFA0102 Original Result - >= 150 False True False +NCIT:C204268 Sepsis-related Organ Failure Assessment SOFA0102 Original Result - < 150 False True False +NCIT:C204269 Sepsis-related Organ Failure Assessment SOFA0102 Original Result - < 100 False True False NCIT:C20427 Hematopoietic Growth Factor False True False +NCIT:C204270 Sepsis-related Organ Failure Assessment SOFA0102 Original Result - < 50 False True False +NCIT:C204271 Sepsis-related Organ Failure Assessment SOFA0102 Original Result - < 20 False True False +NCIT:C204272 Sepsis-related Organ Failure Assessment SOFA0102 Standardized Character Result 0 False True False +NCIT:C204273 Sepsis-related Organ Failure Assessment SOFA0102 Standardized Character Result 1 False True False +NCIT:C204274 Sepsis-related Organ Failure Assessment SOFA0102 Standardized Character Result 2 False True False +NCIT:C204275 Sepsis-related Organ Failure Assessment SOFA0102 Standardized Character Result 3 False True False +NCIT:C204276 Sepsis-related Organ Failure Assessment SOFA0102 Standardized Character Result 4 False True False +NCIT:C204277 Sepsis-related Organ Failure Assessment SOFA0103 Original Result - < 1.2; < 20 False True False +NCIT:C204278 Sepsis-related Organ Failure Assessment SOFA0103 Original Result - 1.2 - 1.9; 20 - 32 False True False +NCIT:C204279 Sepsis-related Organ Failure Assessment SOFA0103 Original Result - 2.0 - 5.9; 33 - 101 False True False NCIT:C20428 Hepatocyte Growth Factor False True False +NCIT:C204280 Sepsis-related Organ Failure Assessment SOFA0103 Original Result - 6.0 - 11.9; 102 - 204 False True False +NCIT:C204281 Sepsis-related Organ Failure Assessment SOFA0103 Original Result - > 12.0; > 204 False True False +NCIT:C204282 Sepsis-related Organ Failure Assessment SOFA0103 Standardized Character Result 0 False True False +NCIT:C204283 Sepsis-related Organ Failure Assessment SOFA0103 Standardized Character Result 1 False True False +NCIT:C204284 Sepsis-related Organ Failure Assessment SOFA0103 Standardized Character Result 2 False True False +NCIT:C204285 Sepsis-related Organ Failure Assessment SOFA0103 Standardized Character Result 3 False True False +NCIT:C204286 Sepsis-related Organ Failure Assessment SOFA0103 Standardized Character Result 4 False True False +NCIT:C204287 Sepsis-related Organ Failure Assessment SOFA0104 Original Result - MAP >= 70 False True False +NCIT:C204288 Sepsis-related Organ Failure Assessment SOFA0104 Original Result - MAP < 70 False True False +NCIT:C204289 Sepsis-related Organ Failure Assessment SOFA0104 Original Result - Dopamine <= 5; Dobutamine (any dose) False True False NCIT:C20429 Erythropoietin False True False +NCIT:C204290 Sepsis-related Organ Failure Assessment SOFA0104 Original Result - Dopamine > 5; Epinephrine <= 0.1; Norepinephrine <= 0.1 False True False +NCIT:C204291 Sepsis-related Organ Failure Assessment SOFA0104 Original Result - Dopamine > 15; Epinephrine > 0.1; Norepinephrine > 0.1 False True False +NCIT:C204292 Sepsis-related Organ Failure Assessment SOFA0104 Standardized Character Result 0 False True False +NCIT:C204293 Sepsis-related Organ Failure Assessment SOFA0104 Standardized Character Result 1 False True False +NCIT:C204294 Sepsis-related Organ Failure Assessment SOFA0104 Standardized Character Result 2 False True False +NCIT:C204295 Sepsis-related Organ Failure Assessment SOFA0104 Standardized Character Result 3 False True False +NCIT:C204296 Sepsis-related Organ Failure Assessment SOFA0104 Standardized Character Result 4 False True False +NCIT:C204297 Sepsis-related Organ Failure Assessment SOFA0105 Original Result - 15 False True False +NCIT:C204298 Sepsis-related Organ Failure Assessment SOFA0105 Original Result - 13 - 14 False True False +NCIT:C204299 Sepsis-related Organ Failure Assessment SOFA0105 Original Result - 10 - 12 False True False NCIT:C2043 Labetuzumab False True False NCIT:C20430 Angiogenin False True False +NCIT:C204300 Sepsis-related Organ Failure Assessment SOFA0105 Original Result - 6 - 9 False True False +NCIT:C204301 Sepsis-related Organ Failure Assessment SOFA0105 Original Result - < 6 False True False +NCIT:C204302 Sepsis-related Organ Failure Assessment SOFA0105 Standardized Character Result 0 False True False +NCIT:C204303 Sepsis-related Organ Failure Assessment SOFA0105 Standardized Character Result 1 False True False +NCIT:C204304 Sepsis-related Organ Failure Assessment SOFA0105 Standardized Character Result 2 False True False +NCIT:C204305 Sepsis-related Organ Failure Assessment SOFA0105 Standardized Character Result 3 False True False +NCIT:C204306 Sepsis-related Organ Failure Assessment SOFA0105 Standardized Character Result 4 False True False +NCIT:C204307 Sepsis-related Organ Failure Assessment SOFA0106 Original Result - < 1.2; < 110 False True False +NCIT:C204308 Sepsis-related Organ Failure Assessment SOFA0106 Original Result - 1.2 - 1.9; 110 - 170 False True False +NCIT:C204309 Sepsis-related Organ Failure Assessment SOFA0106 Original Result - 2.0 - 3.4; 171 - 299 False True False NCIT:C20431 Amphiregulin False True False +NCIT:C204310 Sepsis-related Organ Failure Assessment SOFA0106 Original Result -3.5 - 4.9; 300 - 440; < 500 False True False +NCIT:C204311 Sepsis-related Organ Failure Assessment SOFA0106 Original Result - > 5; > 440; < 200 False True False +NCIT:C204312 Sepsis-related Organ Failure Assessment SOFA0106 Standardized Character Result 0 False True False +NCIT:C204313 Sepsis-related Organ Failure Assessment SOFA0106 Standardized Character Result 1 False True False +NCIT:C204314 Sepsis-related Organ Failure Assessment SOFA0106 Standardized Character Result 2 False True False +NCIT:C204315 Sepsis-related Organ Failure Assessment SOFA0106 Standardized Character Result 3 False True False +NCIT:C204316 Sepsis-related Organ Failure Assessment SOFA0106 Standardized Character Result 4 False True False +NCIT:C204317 Perianal Crohn's Disease Activity Index Questionnaire False True False +NCIT:C204318 Penn State Electronic Cigarette Dependence Index Questionnaire False True False +NCIT:C204319 Sepsis-related Organ Failure Assessment Questionnaire False True False NCIT:C20432 Betacellulin False True False +NCIT:C204320 PDAI - Discharge False True False +NCIT:C204321 PDAI - Pain/Restriction of Activities False True False +NCIT:C204322 PDAI - Restriction of Sexual Activity False True False +NCIT:C204323 PDAI - Type of Perianal Disease False True False +NCIT:C204324 PDAI - Degree of Induration False True False +NCIT:C204325 PDAI - Total Score False True False +NCIT:C204326 PSECDI - Times per Day You Use Your Electronic Cigarette False True False +NCIT:C204327 PSECDI - First Use Electronic Cigarette After Wake Up False True False +NCIT:C204328 PSECDI - Sometimes Awaken Night Use Electronic Cigarette False True False +NCIT:C204329 PSECDI - Nights per Week Awaken Use Electronic Cigarette False True False NCIT:C20433 Neuregulin False True False +NCIT:C204330 PSECDI - Use an Electronic Cigarette Because Hard to Quit False True False +NCIT:C204331 PSECDI - Have Strong Cravings to Use Electronic Cigarette False True False +NCIT:C204332 PSECDI - How Strong Urges to Use Electronic Cigarette False True False +NCIT:C204333 PSECDI - Hard Keep From Using Electronic Cigarette False True False +NCIT:C204334 PSECDI - More Irritable Couldn't Use Electronic Cigarette False True False +NCIT:C204335 PSECDI - Nervous Couldn't Use Electronic Cigarette False True False +NCIT:C204336 PSECDI - Total Score False True False +NCIT:C204337 SOFA - Respiration: PaO2/FiO2 False True False +NCIT:C204338 SOFA - Coagulation: Platelets False True False +NCIT:C204339 SOFA - Liver: Bilirubin False True False NCIT:C20434 Fibroblast Growth Factor 5 False True False +NCIT:C204340 SOFA - Cardiovascular: Hypotension False True False +NCIT:C204341 SOFA - CNS: Glasgow Coma Score False True False +NCIT:C204342 SOFA - Renal: Creatinine or Urine Output False True False +NCIT:C204343 SOFA - Total SOFA Score False True False +NCIT:C204344 PSA Level Less than or Equal to 0.5 False True False +NCIT:C204345 RAD51 Low False True False +NCIT:C204346 RAD51 Negative False True False +NCIT:C204347 EPHA5 Negative False True False +NCIT:C204348 EPHA5 Positive False True False +NCIT:C204349 Anti-EphA5/MMAE Antibody-drug Conjugate MBRC-101 False True False NCIT:C20435 Fibroblast Growth Factor 6 False True False +NCIT:C204350 Anti-PTK7/MMAE ADC PRO1107 False True False +NCIT:C204351 Hypertransfusion False True False +NCIT:C204352 Genomic Variant Call Format False True False +NCIT:C204353 Cannabis sativa Extract False True False +NCIT:C204354 Dactinomycin Regimen False True False +NCIT:C204356 Lenalidomide/Prednisone Regimen False True False +NCIT:C204357 Drama Therapist False True False +NCIT:C204358 Substance Abuse Counselor False True False +NCIT:C204359 Professional Counselor False True False NCIT:C20436 Fibroblast Growth Factor 7 False True False +NCIT:C204360 School Counselor False True False +NCIT:C204361 Psychoanalyst False True False +NCIT:C204362 Poetry Therapist False True False +NCIT:C204363 Clinical Neuropsychologist False True False +NCIT:C204364 Behavioral Analyst False True False +NCIT:C204365 Substance Abuse Psychologist False True False +NCIT:C204366 Adult Development and Aging Psychologist False True False +NCIT:C204367 Cognitive and Behavioral Psychologist False True False +NCIT:C204368 Clinical Psychologist False True False +NCIT:C204369 Counseling Psychologist False True False NCIT:C20437 Macrophage Colony-Stimulating Factor 1 False True False +NCIT:C204370 Clinical Child and Adolescent Psychologist False True False +NCIT:C204371 Educational Psychologist False True False +NCIT:C204372 Exercise and Sports Psychologist False True False +NCIT:C204373 Family Psychologist False True False +NCIT:C204374 Forensic Psychologist False True False +NCIT:C204375 Health Psychologist False True False +NCIT:C204376 Health Service Psychologist False True False +NCIT:C204377 Men and Masculinity Psychologist False True False +NCIT:C204378 Intellectual and Developmental Disabilities Psychologist False True False +NCIT:C204379 Prescribing Psychologist False True False +NCIT:C204380 Psychoanalytic Psychologist False True False +NCIT:C204381 Rehabilitation Psychologist False True False +NCIT:C204382 Feminine Psychology False True False +NCIT:C204384 Merkel Cell Polyoma Virus Positive False True False +NCIT:C204386 L-Type Amino Acid Transporter 1 Complex False True False +NCIT:C204387 Cisplatin/Docetaxel/Pembrolizumab Regimen False True False +NCIT:C204388 Assistant Behavioral Analyst False True False +NCIT:C204389 Marriage and Family Therapist False True False NCIT:C20439 Interleukin-3 False True False +NCIT:C204390 Behavioral Technician False True False +NCIT:C204391 Chiropractor False True False +NCIT:C204392 Chiropractic Independent Medical Examiner False True False +NCIT:C204393 Chiropractic Internist False True False +NCIT:C204394 Chiropractic Neurologist False True False +NCIT:C204395 Chiropractic Nutritionist False True False +NCIT:C204396 Pediatric Chiropractor False True False +NCIT:C204397 Carboplatin/Docetaxel/Pembrolizumab Regimen False True False +NCIT:C204398 Intravesical Docetaxel/Gemcitabine Regimen False True False +NCIT:C204399 Chiropractic Radiologist False True False NCIT:C2044 In 111 DAC False True False NCIT:C20440 Kit Ligand False True False +NCIT:C204400 Chiropractic Rehabilitation False True False +NCIT:C204401 Chiropractic Sports Physician False True False +NCIT:C204402 Chiropractor Thermography False True False +NCIT:C204403 Occupational Health Chiropractor False True False +NCIT:C204404 Orthopedic Chiropractor False True False +NCIT:C204405 Action Taken with Study Product False True False +NCIT:C204406 Wattage False True False +NCIT:C204407 Puff Device Setting False True False +NCIT:C204408 Glomerular Filtration Rate Estimation Formula False True False +NCIT:C204409 Porosity False True False NCIT:C20441 Thrombopoietin False True False +NCIT:C204410 CDISC ADaM Input Parameter Terminology False True False +NCIT:C204411 CDISC ADaM Analysis Stratum Terminology False True False +NCIT:C204412 CDISC ADaM Tobacco Use Transition Response Terminology False True False +NCIT:C204413 CDISC ADaM Tobacco Product Use Status Response Terminology False True False +NCIT:C204414 CDISC ADaM Tobacco Product Category Response Terminology False True False +NCIT:C204415 CDISC SEND Reference ID Level Description Response Terminology False True False +NCIT:C204416 CDISC SEND Genetic Toxicology In vitro Test Name Terminology False True False +NCIT:C204417 CDISC SEND Genetic Toxicology In vitro Test Code Terminology False True False +NCIT:C204418 CDISC SDTM Tobacco Product Testing Specimen Type Terminology False True False +NCIT:C204419 CDISC SDTM Tobacco Study Completion/Reason for Non-Completion Terminology False True False NCIT:C20442 Insulin-Like Growth Factor False True False +NCIT:C204420 CDISC SDTM Action Taken with Tobacco Product Terminology False True False +NCIT:C204421 CDISC SDTM Environmental Storage Conditions Parameter Code Terminology False True False +NCIT:C204422 CDISC SDTM Environmental Storage Conditions Parameter Name Terminology False True False +NCIT:C204423 CDISC SDTM Ingredient Complexity Response Terminology False True False +NCIT:C204424 CDISC SDTM Category of Ingredient Quantities by Component Terminology False True False +NCIT:C204425 CDISC SDTM Tobacco Product Design Parameters Code Terminology False True False +NCIT:C204426 CDISC SDTM Tobacco Product Design Parameters Name Terminology False True False +NCIT:C204427 CDISC SDTM Tobacco Product Testing Test Code Terminology False True False +NCIT:C204428 CDISC SDTM Tobacco Product Testing Test Name Terminology False True False +NCIT:C204429 CDISC SDTM Category of Product Testing Terminology False True False +NCIT:C204430 CDISC SDTM Tobacco Findings About Test Code Terminology False True False +NCIT:C204431 CDISC SDTM Tobacco Findings About Test Name Terminology False True False +NCIT:C204432 CDISC SDTM Tobacco Products Parameter Code Terminology False True False +NCIT:C204433 CDISC SDTM Tobacco Products Parameter Name Terminology False True False +NCIT:C204434 CDISC SDTM Category of Tobacco Products Terminology False True False +NCIT:C204435 IFNA1 Gene False True False +NCIT:C204436 IFNA1 wt Allele False True False +NCIT:C204438 Holmium Laser Enucleation of the Prostate False True False +NCIT:C204439 Transurethral Vaporesection of the Prostate False True False NCIT:C20444 Beta-Nerve Growth Factor False True False +NCIT:C204440 PD-L1 Expression Positive in Myeloid-Derived Suppressor Cells False True False +NCIT:C204441 Vesicular Stomatitis Virus-based Therapeutic Agent False True False +NCIT:C204442 Hemodiafiltration Route of Administration False True False +NCIT:C204443 PEX2 Gene False True False +NCIT:C204444 PEX2 wt Allele False True False +NCIT:C204445 Peroxisome Biogenesis Factor 2 False True False +NCIT:C204446 Peroxisome Biogenesis Factor Gene False True False +NCIT:C204447 Bevacizumab/Docetaxel/Oxaliplatin Regimen False True False +NCIT:C204448 PEX26 Gene False True False +NCIT:C204449 PEX26 wt Allele False True False NCIT:C20445 Brain-Derived Neurotrophic Factor False True False +NCIT:C204450 Cytarabine/Etoposide/Mercaptopurine/Methotrexate Regimen False True False +NCIT:C204451 Peroxisome Assembly Protein 26 False True False +NCIT:C204452 PEX5 Gene False True False +NCIT:C204453 PEX5 wt Allele False True False +NCIT:C204454 Peroxisomal Targeting Signal 1 Receptor False True False +NCIT:C204455 PEX6 Gene False True False +NCIT:C204456 PEX6 wt Allele False True False +NCIT:C204457 Peroxisomal ATPase PEX6 False True False +NCIT:C204458 PEX7 Gene False True False +NCIT:C204459 PEX7 wt Allele False True False NCIT:C20446 Glial Cell Line-Derived Neurotrophic Factor False True False +NCIT:C204460 Peroxisomal Targeting Signal 2 Receptor False True False +NCIT:C204461 Estrogen Receptor Positive by Immunohistochemistry Less than 10 Percent False True False +NCIT:C204462 Progesterone Receptor Positive by Immunohistochemistry Less than 10 Percent False True False +NCIT:C204463 Therapeutic Bacterial Strain CJRB-101 False True False +NCIT:C204464 Cell Suspension for Single-Cell Assay False True False +NCIT:C204465 Nuclei Suspension for Single-Nuclei Assay False True False +NCIT:C204466 Body Fluid Specimen False True False +NCIT:C204467 IL-15 Superagonist SOT201 False True False +NCIT:C204468 Dexamethasone/Mercaptopurine/Methotrexate/Vincristine Regimen False True False +NCIT:C204469 Cytarabine/Fludarabine/Mitoxantrone Regimen False True False NCIT:C20447 Parathyroid Hormone-Related Protein False True False +NCIT:C204470 Prednisone/Vinblastine Regimen False True False +NCIT:C204471 PGAM2 Gene False True False +NCIT:C204472 Skin Concentric Pigmentation False True False +NCIT:C204473 PGAM2 wt Allele False True False +NCIT:C204474 Phosphoglycerate Mutase 2 False True False +NCIT:C204476 Dark Small Macules and Papules Present False True False +NCIT:C204477 Autologous dnTGF-BRII-armored Anti-STEAP2 CAR T-cells AZD0754 False True False +NCIT:C204478 PHEX Gene False True False +NCIT:C204479 PHEX wt Allele False True False NCIT:C20448 Platelet-Derived Growth Factor False True False +NCIT:C204480 Phosphate-Regulating Neutral Endopeptidase PHEX False True False +NCIT:C204481 Anti-interleukin-1 Beta Monoclonal Antibody False True False +NCIT:C204483 WRN Inhibitor RO7589831 False True False +NCIT:C204484 PHYH Gene False True False +NCIT:C204485 PHYH wt Allele False True False +NCIT:C204486 Phytanoyl-CoA Dioxygenase, Peroxisomal False True False +NCIT:C204487 PIGN Gene False True False +NCIT:C204488 PIGN wt Allele False True False +NCIT:C204489 GPI Ethanolamine Phosphate Transferase 1 False True False NCIT:C20449 Platelet-Derived Growth Factor Subunit B False True False +NCIT:C204490 PINK1 Gene False True False +NCIT:C204491 PINK1 wt Allele False True False +NCIT:C204492 Serine/Threonine-Protein Kinase PINK1, Mitochondrial False True False +NCIT:C204493 PITX1 Gene False True False +NCIT:C204494 Target of Interest False True False +NCIT:C204495 PITX1 wt Allele False True False +NCIT:C204496 NCI-MATCH False True False +NCIT:C204497 Pituitary Homeobox 1 False True False +NCIT:C204498 PLN Gene False True False +NCIT:C204499 PLN wt Allele False True False NCIT:C2045 Matrix Metalloproteinase Inhibitor MMI270 False True False NCIT:C20450 Vascular Endothelial Growth Factor A False True False +NCIT:C204500 Cardiac Phospholamban False True False +NCIT:C204501 EGFRt/19-28z/IL-12 CAR T-lymphocytes False True False +NCIT:C204502 EGFR Mutant-selective Inhibitor WZ4002 False True False +NCIT:C204503 Anti-CD47/CD20 Bispecific Antibody CC-96673 False True False +NCIT:C204505 TACSTD2 Positive False True False +NCIT:C204506 TACSTD2 Expression by Immunohistochemistry 2+ False True False +NCIT:C204507 TACSTD2 Expression by Immunohistochemistry 3+ False True False +NCIT:C204508 NECTIN4 Status by Immunohistochemistry False True False +NCIT:C204509 NECTIN4 Expression by Immunohistochemistry 2+ False True False NCIT:C20451 Interleukin-6 False True False +NCIT:C204510 NECTIN4 Expression by Immunohistochemistry 3+ False True False +NCIT:C204511 STEAP2 Gene False True False +NCIT:C204512 STEAP2 wt Allele False True False +NCIT:C204513 Metalloreductase STEAP2 False True False +NCIT:C204515 MAPK Pathway Activated False True False +NCIT:C204517 PLOD1 Gene False True False +NCIT:C204518 Dentist Anesthesiologist False True False +NCIT:C204519 PLOD1 wt Allele False True False NCIT:C20452 Pleiotrophin False True False +NCIT:C204520 Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 False True False +NCIT:C204521 POGLUT1 Gene False True False +NCIT:C204522 POGLUT1 wt Allele False True False +NCIT:C204523 Oral and Maxillofacial Pathologist False True False +NCIT:C204524 Oral and Maxillofacial Radiologist False True False +NCIT:C204525 Protein O-Glucosyltransferase 1 False True False +NCIT:C204526 Orofacial Pain Dentist False True False +NCIT:C204527 POMGNT1 Gene False True False +NCIT:C204528 POMGNT1 wt Allele False True False +NCIT:C204529 Protein O-Linked-Mannose Beta-1,2-N-Acetylglucosaminyltransferase 1 False True False NCIT:C20453 Transforming Growth Factor False True False +NCIT:C204530 POMT1 Gene False True False +NCIT:C204531 POMT1 wt Allele False True False +NCIT:C204532 Protein O-Mannosyl-Transferase 1 False True False +NCIT:C204533 POMT2 Gene False True False +NCIT:C204534 POMT2 wt Allele False True False +NCIT:C204535 Protein O-Mannosyl-Transferase 2 False True False +NCIT:C204536 PLIN1 Gene False True False +NCIT:C204537 PLIN1 wt Allele False True False +NCIT:C204538 Perilipin-1 False True False +NCIT:C204539 Health Benefit Plan Stop Reason False True False NCIT:C20454 Transforming Growth Factor Alpha False True False +NCIT:C204540 Family Identifier False True False +NCIT:C204541 Medical Device Exposure False True False +NCIT:C204542 Dental Care Professional False True False +NCIT:C204543 Dental Therapist False True False +NCIT:C204544 Advanced Dental Therapist False True False +NCIT:C204545 Dentofacial Orthopedist False True False +NCIT:C204546 Dental Laboratory Technician False True False +NCIT:C204547 Dietary Manager False True False +NCIT:C204548 Registered Pediatric Dietitian False True False +NCIT:C204549 Registered Renal Dietitian False True False NCIT:C20455 Transforming Growth Factor-Beta Superfamily False True False +NCIT:C204550 Registered Metabolic Dietitian False True False +NCIT:C204551 Registered Gerontological Dietitian False True False +NCIT:C204552 Registered Obesity and Weight Management Dietitian False True False +NCIT:C204553 Registered Oncology Dietitian False True False +NCIT:C204554 Registered Pediatric Critical Care Dietitian False True False +NCIT:C204555 Registered Sports Dietitian False True False +NCIT:C204556 Registered Dietetic Technician False True False +NCIT:C204557 Personal Emergency Response Attendant False True False +NCIT:C204558 Intermediate Emergency Medical Technician False True False +NCIT:C204559 Basic Emergency Medical Technician False True False NCIT:C20456 Activin False True False +NCIT:C204560 Continence Care Nurse False True False +NCIT:C204561 Infusion Therapy Nurse False True False +NCIT:C204562 Nurse Lactation Consultant False True False +NCIT:C204563 Neonatal Intensive Care Nurse False True False +NCIT:C204564 Low-Risk Neonatal Nurse False True False +NCIT:C204565 Child and Adolescent Mental Health Nurse False True False +NCIT:C204566 Adult Mental Health Nurse False True False +NCIT:C204567 Registered Perinatal Nurse False True False +NCIT:C204568 Registered Nurse First Assistant False True False +NCIT:C204569 Registered Reproductive Endocrinology and Infertility Nurse False True False NCIT:C20457 Transforming Growth Factor Beta-1 False True False +NCIT:C204570 Registered High Risk Obstetric Nurse False True False +NCIT:C204571 Registered Ostomy Care Nurse False True False +NCIT:C204572 PRKAR1A Gene Inactivation False True False +NCIT:C204576 HNF1A Gene Mutation False True False +NCIT:C204577 Dendritic Cell to Leukocyte Ratio Measurement False True False +NCIT:C204578 Memory B-Lymphocyte Subpopulation to Memory B-Lymphocyte Ratio Measurement False True False +NCIT:C204579 Memory B-Lymphocyte Subpopulation to Memory B-Lymphocyte Subpopulation Ratio Measurement False True False NCIT:C20458 Transforming Growth Factor Beta-2 False True False +NCIT:C204580 Atypical B-Lymphocyte to B-Lymphocyte Ratio Measurement False True False +NCIT:C204581 US FDA Tobacco Product Applicant False True False +NCIT:C204582 CAPOX-Cetuximab Regimen False True False +NCIT:C204583 mFOLFOX6-Cetuximab Regimen False True False +NCIT:C204584 Next Observation Carried Backward Imputation Technique False True False +NCIT:C204585 Overall Hearing Assessment False True False +NCIT:C204586 Hearing Loss Type False True False +NCIT:C204587 Natural Killer Cell Subpopulation to Natural Killer Cell Subpopulation Ratio Measurement False True False +NCIT:C204588 Natural Killer T-Lymphocyte Subpopulation to Natural Killer T-Lymphocyte Subpopulation Ratio Measurement False True False +NCIT:C204589 B-Lymphocyte to Non-TNK Leukocyte Ratio Measurement False True False NCIT:C20459 Transforming Growth Factor Beta-3 False True False +NCIT:C204590 Non-TBNK Leukocyte Subpopulation to Non-TBNK Leukocyte Ratio Measurement False True False +NCIT:C204591 Myeloid Derived Suppressor Cell Subpopulation to Non-TBNK Leukocyte Ratio Measurement False True False +NCIT:C204592 Natural Killer Cell to Non-TB Leukocyte Ratio Measurement False True False +NCIT:C204593 Dendritic Cell to Non-TBNK Leukocyte Ratio Measurement False True False +NCIT:C204594 Myeloid Derived Suppressor Cell Subpopulation to Leukocyte Ratio Measurement False True False +NCIT:C204595 Type 1 Myeloid Dendritic Cell Subpopulation to Type 1 Myeloid Dendritic Cell Ratio Measurement False True False +NCIT:C204596 Type 2 Myeloid Dendritic Cell Subpopulation to Type 2 Myeloid Dendritic Cell Ratio Measurement False True False +NCIT:C204597 Dendritic Cell Subpopulation to Dendritic Cell Ratio Measurement False True False +NCIT:C204598 Classical Memory B-Lymphocyte to B-Lymphocyte Ratio Measurement False True False +NCIT:C204599 Classical Memory B-Lymphocyte Subpopulation to Classical Memory B-Lymphocyte Ratio Measurement False True False NCIT:C20460 TBP Gene False True False +NCIT:C204600 Classical Memory B-Lymphocyte Subpopulation to Classical Memory B-Lymphocyte Subpopulation Ratio Measurement False True False +NCIT:C204601 Atypical B-Lymphocyte Subpopulation to Atypical B-Lymphocyte Ratio Measurement False True False +NCIT:C204602 Atypical B-Lymphocyte Subpopulation to Atypical B-Lymphocyte Subpopulation Ratio Measurement False True False +NCIT:C204603 B-Lymphocyte Subpopulation to B-Lymphocyte Subpopulation Ratio Measurement False True False +NCIT:C204604 Mucosal-Associated Invariant T-Lymphocyte to Leukocyte Ratio Measurement False True False +NCIT:C204605 Mucosal-Associated Invariant T-Lymphocyte Count False True False +NCIT:C204606 Mucosal-Associated Invariant T-Lymphocyte to T-Lymphocyte Ratio Measurement False True False +NCIT:C204607 Mucosal-Associated Invariant T-Lymphocyte Subpopulation to Mucosal-Associated T-Lymphocyte Ratio Measurement False True False +NCIT:C204608 Transcription Factor 7 Expression Measurement False True False +NCIT:C204609 TOX1 and TOX2 Expression Measurement False True False NCIT:C20461 World Wide Web False True False +NCIT:C204610 CD163 Expression Measurement False True False +NCIT:C204611 Reference Data Structure False True False +NCIT:C204612 Tobacco Product Testing Domain False True False +NCIT:C204613 Tobacco Product Design Parameters Domain False True False +NCIT:C204614 Tobacco Ingredients Domain False True False +NCIT:C204615 Non-Tobacco Ingredients Domain False True False +NCIT:C204616 Ingredient Quantities by Component Domain False True False +NCIT:C204617 Tobacco Product Identifiers and Descriptors Domain False True False +NCIT:C204618 Environmental Storage Conditions Domain False True False +NCIT:C204619 15 Lead Placement Including V7-V9 False True False NCIT:C20462 Apoptosis Regulation Gene False True False +NCIT:C204620 15 Lead Placement Including V3R-V5R False True False +NCIT:C204621 Esophageal Obstruction Indicator False True False +NCIT:C204622 Endomysial Autoantigens False True False +NCIT:C204623 Deamidated Gliadin Peptide False True False +NCIT:C204624 IgG1 Autoantibody Measurement False True False +NCIT:C204625 IgG2 Autoantibody Measurement False True False +NCIT:C204626 IgG3 Autoantibody Measurement False True False +NCIT:C204627 Cytokine-Secreting T Lymphocyte Count False True False +NCIT:C204628 Factor IX Inhibitor Measurement False True False +NCIT:C204629 Friedewald 1972 Formula False True False NCIT:C20463 TERC Gene False True False +NCIT:C204630 CKD U25 Cystatin C Based eGFR 2021 Formula False True False +NCIT:C204631 2010 Japanese Modification of 2009 CKD-EPI Formula False True False +NCIT:C204632 CKD-EPI Collaboration 2021 Formula False True False +NCIT:C204633 Free Complement C2 to Complement C2 Ratio Measurement False True False +NCIT:C204634 Free Complement C2 Measurement False True False +NCIT:C204635 Smear Examination False True False +NCIT:C204636 Heparin-Binding Protein Measurement False True False +NCIT:C204637 Erythroid Cell Count False True False +NCIT:C204638 1,3-Butadiene Measurement False True False +NCIT:C204639 1-Aminonaphthalene Measurement False True False NCIT:C20464 Cytokine False True False +NCIT:C204640 2-Aminonaphthalene Measurement False True False +NCIT:C204641 4-Aminobiphenyl Measurement False True False +NCIT:C204642 Acetaldehyde Measurement False True False +NCIT:C204643 Acrolein Measurement False True False +NCIT:C204644 Acrylonitrile Measurement False True False +NCIT:C204645 Benzene Measurement False True False +NCIT:C204646 Benzo[a]pyrene Measurement False True False +NCIT:C204647 Cadmium Measurement False True False +NCIT:C204648 Crotonaldehyde Measurement False True False +NCIT:C204649 Formaldehyde Measurement False True False NCIT:C20465 Thioredoxin False True False +NCIT:C204650 Isoprene Measurement False True False +NCIT:C204651 Nicotine-Derived Nitrosamine Ketone Measurement False True False +NCIT:C204652 N-Nitrosonornicotine Measurement False True False +NCIT:C204653 Toluene Measurement False True False +NCIT:C204654 Shoulder Abductor Muscles False True False +NCIT:C204655 Knee Extensor Muscles False True False +NCIT:C204656 Hip Abductor Muscles False True False +NCIT:C204657 Hip Adductor Muscles False True False +NCIT:C204658 Neck Extensor Muscles False True False +NCIT:C204659 Shoulder External Rotator Muscles False True False NCIT:C20466 Chemokine False True False +NCIT:C204660 Hip Extensor Muscles False True False +NCIT:C204661 Ankle Dorsiflexor Muscles False True False +NCIT:C204662 Most Recent Disease Relapse False True False +NCIT:C204663 Orientia tsutsugamushi False True False +NCIT:C204664 Plasmodium Lactate Dehydrogenase Measurement False True False +NCIT:C204665 Plasmodium Histidine Rich Protein 2 Measurement False True False +NCIT:C204666 Plasmodium Antigen Measurement False True False +NCIT:C204667 Positive Cells Area False True False +NCIT:C204668 Average Shortest Distances to Invasive Margin-Whole Tumor Region Boundary Measurement False True False +NCIT:C204669 Mean Staining Intensity False True False NCIT:C20467 Alpha Chemokine False True False +NCIT:C204670 Combined Positive Score False True False +NCIT:C204671 Erythroid Proliferation Measurement False True False +NCIT:C204672 Granulocyte Proliferation Measurement False True False +NCIT:C204673 Megakaryocyte Proliferation Measurement False True False +NCIT:C204674 Collagen Fibrosis Assessment False True False +NCIT:C204675 Reticulin Fibrosis Assessment False True False +NCIT:C204676 Tumor Associated Calcium Signal Transducer 2 Measurement False True False +NCIT:C204677 T-Cell Immunoreceptor with Ig and ITIM Domains Measurement False True False +NCIT:C204678 Tumor-Infiltrating Lymphocyte Count False True False +NCIT:C204679 Tertiary Lymphoid Structure Assessment False True False NCIT:C20468 Beta-Thromboglobulin False True False +NCIT:C204680 Dysplasia Assessment False True False +NCIT:C204681 Myeloid Proliferation Measurement False True False +NCIT:C204682 Leukoerythroblastosis Measurement False True False +NCIT:C204683 Central Nervous System Disease Response Status Assessment False True False +NCIT:C204684 Bone Marrow Disease Response Status Assessment False True False +NCIT:C204685 Extramedullary Disease Response Assessment False True False +NCIT:C204686 Peripheral Blasts Indicator False True False +NCIT:C204687 Testicular Disease Indicator False True False +NCIT:C204688 Neurological Disease Response Status Assessment False True False +NCIT:C204689 M1 Marrow False True False NCIT:C20469 Connective Tissue-Activating Peptide III False True False +NCIT:C204690 M2 Marrow False True False +NCIT:C204691 M3 Marrow False True False +NCIT:C204692 Subject Entered Additional Research Study False True False +NCIT:C204693 Second Ventilatory Threshold False True False +NCIT:C204694 Menarche Indicator False True False +NCIT:C204695 Actively Menstruating Indicator False True False +NCIT:C204696 Information Source for Survival Status False True False +NCIT:C204697 Precipitated Specimen False True False +NCIT:C204698 Recurrent Disease Clinical Trial Setting False True False +NCIT:C204699 Ongoing Study Indicator False True False NCIT:C2047 Prolactin 16-kD Fragment False True False NCIT:C20470 C-X-C Motif Chemokine 5 False True False +NCIT:C204700 CDISC Tobacco Implementation Guide Version False True False +NCIT:C204701 Per Plate False True False +NCIT:C204702 Cuts per Inch False True False +NCIT:C204703 Coresta Unit False True False +NCIT:C204704 Square Centimeter per Second False True False +NCIT:C204705 Gram per 9000 Meters False True False +NCIT:C204706 Gram per Cubic Centimeter False True False +NCIT:C204707 Milliampere Hour False True False +NCIT:C204708 Millipascal per Second False True False +NCIT:C204709 Per Cubic Centimeter False True False NCIT:C20471 Growth-Regulated Alpha Protein False True False +NCIT:C204710 Liter per Square Meter per Second False True False +NCIT:C204711 Euthanasia by Carbon Dioxide/Cervical Dislocation False True False +NCIT:C204712 Bile Plug False True False +NCIT:C204713 Phase-Specific Control False True False +NCIT:C204714 Genetic Toxicology In vitro Test Results Domain False True False +NCIT:C204715 Adverse Experience False True False +NCIT:C204716 Universal Product Code False True False +NCIT:C204717 FDA CTP Submission Tracking Number False True False +NCIT:C204718 mFOLFOX7 Regimen False True False +NCIT:C204719 Axillary Radiation Therapy False True False +NCIT:C204720 R-DHAX Followed by R-CHOP False True False +NCIT:C204721 Breast Fibrotic Tissue False True False +NCIT:C204722 Inflammatory Cyst False True False +NCIT:C204723 Corneal and Contact Lens Management Optometrist False True False +NCIT:C204724 Low Vision Rehabilitation Optometrist False True False +NCIT:C204725 Sports Vision Optometrist False True False +NCIT:C204726 Vision Therapy Optometrist False True False +NCIT:C204727 Occupational Vision Optometrist False True False +NCIT:C204728 Contact Lens Technician False True False +NCIT:C204729 Contact Lens Fitter False True False NCIT:C20473 Interleukin-8 False True False +NCIT:C204730 Ophthalmic Technician False True False +NCIT:C204731 Ophthalmic Assistant False True False +NCIT:C204732 Optometric Technician False True False +NCIT:C204733 Ocularist False True False +NCIT:C204734 Optician False True False +NCIT:C204735 Orthoptist False True False +NCIT:C204736 Optometric Assistant False True False +NCIT:C204737 Autologous 19-28z/IL-18 CAR T-lymphocytes False True False +NCIT:C204738 Staining Intensity Index False True False NCIT:C20474 C-X-C Motif Chemokine 2 False True False +NCIT:C204742 MITF Gene Rearrangement False True False +NCIT:C204743 MITF Pathway Activated False True False +NCIT:C204744 Melanocyte with Clear Cytoplasm False True False +NCIT:C204745 AlphaVbeta1/8 Inhibitor PLN-101095 False True False +NCIT:C204746 Group Health Insurance False True False +NCIT:C204747 Fully-insured Health Insurance False True False +NCIT:C204748 Small Group Health Insurance False True False +NCIT:C204749 Large Group Health Insurance False True False NCIT:C20475 C-X-C Motif Chemokine 3 False True False +NCIT:C204750 ACTIN/MITF Fusion Gene False True False +NCIT:C204751 ACTB/MITF Fusion Gene False True False +NCIT:C204752 ACTG1/MITF Fusion Gene False True False +NCIT:C204753 MITF/CREM Fusion Gene False True False +NCIT:C204754 CDK2 Inhibitor NKT3447 False True False +NCIT:C204757 KMT2A Gene Rearrangement Negative False True False +NCIT:C204758 Prednisone/Vincristine Regimen False True False +NCIT:C204759 Dacarbazine/Gemcitabine Regimen False True False NCIT:C20476 Beta Chemokine False True False +NCIT:C204760 Augmented HyperCVAD/Pegaspargase Regimen False True False +NCIT:C204761 Doxorubicin/Gemcitabine/Ifosfamide Regimen False True False +NCIT:C204762 Cytarabine/High-dose Methotrexate/Pegaspargase Regimen False True False +NCIT:C204763 Carboplatin/Osimertinib/Pemetrexed Regimen False True False +NCIT:C204764 Cisplatin/Osimertinib/Pemetrexed Regimen False True False +NCIT:C204765 Amivantamab/Carboplatin/Pemetrexed Regimen False True False +NCIT:C204766 Obinutuzumab/Zanubrutinib Regimen False True False +NCIT:C204767 Lifileucel Regimen False True False +NCIT:C204768 Treehouse Childhood Cancer Initiative False True False +NCIT:C204769 Pemetrexed Intrathecal Regimen False True False NCIT:C20477 C-C Motif Chemokine 4 False True False +NCIT:C204770 Termination of Employment False True False +NCIT:C204771 Reduction of Hours False True False +NCIT:C204772 Divorce or Separation from Covered Spouse False True False +NCIT:C204773 Death of Covered Employee False True False +NCIT:C204774 Termination of Group Health Plan by Sponsor False True False +NCIT:C204775 Failure to Pay Premiums False True False +NCIT:C204776 Coverage Under Another Plan False True False +NCIT:C204777 Loss of Social Security Disability Status False True False +NCIT:C204778 Entitlement to Medicare False True False +NCIT:C204779 Coverage Terminated by Person False True False NCIT:C20478 C-C Motif Chemokine 1 False True False +NCIT:C204780 Coverage Terminated by Contract Owner False True False +NCIT:C204781 Modified CODOX-M Regimen False True False +NCIT:C204782 Dactinomycin/Etoposide/Ifosfamide/Vincristine Regimen False True False +NCIT:C204783 Allogeneic CD33CAR-CD3zeta-4-1BB-expressing T-lymphocytes False True False +NCIT:C204784 Allogeneic Gene-edited CD33-knockout Hematopoietic Stem and Progenitor Cells False True False +NCIT:C204785 COPAD Regimen False True False NCIT:C20479 C-C Motif Chemokine 8 False True False +NCIT:C204791 MAP3K8 Fusion Positive False True False +NCIT:C204792 Anti-DKK1 Monoclonal Antibody False True False +NCIT:C204793 Lineage Switching False True False +NCIT:C204794 Autologous Total Tumor mRNA Loaded Liposome Vaccine False True False +NCIT:C204795 Chemotherapy Backbone False True False +NCIT:C204796 Oncotype DX Colon Recurrence Score False True False +NCIT:C204797 R-COPADM Regimen False True False +NCIT:C204798 mini-CHOP Regimen False True False +NCIT:C204799 Autologous HLA-A*11:01 KRASG12V-specific TCR-expressing CD8- and CD4-positive T-lymphocytes AFNT-211 False True False NCIT:C2048 A-65 False True False NCIT:C20480 Cellular Process False True False +NCIT:C204800 Akt Inhibitor NTQ1062 False True False +NCIT:C204801 Androgen Receptor Degrader HP518 False True False +NCIT:C204802 Anti-CLDN18.2/CD47 Bispecific Antibody AK132 False True False +NCIT:C204803 Anti-HER2/Topoisomerase I Inhibitor ADC GQ1005 False True False +NCIT:C204804 Anti-HER3/Topoisomerase I Inhibitor Antibody-drug Conjugate IBI133 False True False +NCIT:C204805 Anti-LILRB4/MMAE ADC SG2918 False True False +NCIT:C204806 Anti-PD-L1/4-1BB Bispecific Antibody LBL-024 False True False +NCIT:C204807 Autologous GCC-targeting CAR T-cells LCAR-G08 False True False +NCIT:C204808 TRK/RET Inhibitor ND-003 False True False +NCIT:C204809 HER2 Inhibitor IAM1363 False True False NCIT:C20481 C-C Motif Chemokine 3 False True False +NCIT:C204810 Autologous CD34+ enriched Alpha-L-iduronidase-expressing Hematopoietic Stem Cells OTL-203 False True False +NCIT:C204811 Viral RNA False True False +NCIT:C204812 MEK Inhibitor IMM-6-415 False True False +NCIT:C204813 Amplicon Sequencing False True False +NCIT:C204814 Clone-Based Sequencing False True False +NCIT:C204815 Clone End Sequencing False True False +NCIT:C204816 Concatenated Tag Sequencing False True False +NCIT:C204817 Full-length cDNA Sequencing False True False +NCIT:C204818 Finish Sequencing False True False +NCIT:C204819 Hi-C Sequencing False True False +NCIT:C204820 Methyl-binding Domain Sequencing False True False +NCIT:C204821 Methylated DNA Immunoprecipitation Sequencing False True False +NCIT:C204822 Methylation-Sensitive Restriction Enzyme Sequencing False True False +NCIT:C204823 Pooled DNA Sequencing False True False +NCIT:C204824 Restriction-site Associated DNA Sequencing False True False +NCIT:C204825 Direct Sequencing of RNA Immunoprecipitates False True False +NCIT:C204826 Systematic Evolution of Ligands by Exponential Enrichment False True False +NCIT:C204827 Synthetic Long-Read Sequencing False True False +NCIT:C204828 Targeted Capture Sequencing False True False +NCIT:C204829 Tethered Chromatin Conformation Capture Sequencing False True False NCIT:C20483 C-C Motif Chemokine 5 False True False +NCIT:C204830 Transposon Sequencing False True False +NCIT:C204831 Whole Chromosome Random Shotgun Sequencing False True False +NCIT:C204832 Deep Sequencing False True False +NCIT:C204833 R-DHAC Followed by R-CHOP Regimen False True False +NCIT:C204834 R-DHAP Followed by R-CHOP Regimen False True False +NCIT:C204835 IDUA Gene Mutation False True False +NCIT:C204836 Biallelic IDUA Gene Mutation False True False +NCIT:C204837 Potassium Chloride in D5NS False True False +NCIT:C204838 Peritoneal Supernatant False True False +NCIT:C204839 Anti-4-1BB/PD-L1 Bispecific Antibody BH3120 False True False NCIT:C20484 C-C Motif Chemokine 21 False True False +NCIT:C204841 Intermittent Sun Exposure False True False +NCIT:C204842 CHOP Followed by IVE/Methotrexate Regimen False True False +NCIT:C204844 Pharmacologic Assay False True False +NCIT:C204845 Active Ingredient Assay False True False +NCIT:C204846 Comedo, Cribriform False True False +NCIT:C204847 Comedo, Cribriform, Micropapillary False True False +NCIT:C204848 Comedo, Clinging False True False +NCIT:C204849 Comedo, Cribriform, Solid False True False NCIT:C20485 Eotaxin False True False +NCIT:C204850 Comedo, Solid, Micropapillary False True False +NCIT:C204851 Comedo, Micropapillary False True False +NCIT:C204852 Comedo, Solid False True False +NCIT:C204853 Comedo, Solid, Cribriform, Micropapillary False True False +NCIT:C204854 Cribriform, Micropapillary False True False +NCIT:C204855 Cribriform, Papillary False True False +NCIT:C204856 Cribriform, Solid False True False +NCIT:C204857 Cribriform, Solid, Micropapillary False True False +NCIT:C204858 Cribriform, Solid, Apocrine False True False +NCIT:C204859 Mammary Region False True False NCIT:C20486 Chemokine, Other False True False +NCIT:C204860 Solid, Micropapillary False True False +NCIT:C204861 RGD-modified COX-2 Promoter-controlled Conditionally Replicative Adenovirus RGDCRAdCox2F False True False +NCIT:C204862 PQ/CMC Test Subcategory Terminology False True False +NCIT:C204863 Hypertransfused False True False +NCIT:C204869 PPCS Gene False True False NCIT:C20487 C5a Anaphylatoxin False True False +NCIT:C204870 PPCS wt Allele False True False +NCIT:C204871 Phosphopantothenate-Cysteine Ligase False True False +NCIT:C204872 Chronic Sun Exposure False True False +NCIT:C204873 PPP2R2B Gene False True False +NCIT:C204874 PPP2R2B wt Allele False True False +NCIT:C204875 Serine/Threonine-Protein Phosphatase 2A 55 kDa Regulatory Subunit B Beta Isoform False True False +NCIT:C204876 Honokiol-based Supplement False True False +NCIT:C204877 Hericium erinaceus-based Supplement False True False +NCIT:C204878 Curcuma zedoaria/Cyperus rotundus/Astragalus membranaceus/Notopterygium incisum-based Herbal Supplement False True False +NCIT:C204879 Frankincense/Orange/Litsea/Thyme/Clove/Summer Savory/Niaouli/Lemongrass Essential Oil False True False NCIT:C20488 Delta Chemokine False True False +NCIT:C204880 Marigold Extract-based Supplement False True False +NCIT:C204881 DNA Damage Response Deficiency Negative False True False +NCIT:C204882 Ascorbic Acid/Carbonyl Iron False True False +NCIT:C204884 KRAS Mutant Inhibitor QTX3034 False True False +NCIT:C204885 Palms of Hands, Soles of Feet, and Nails False True False +NCIT:C204886 Subungual Space False True False NCIT:C20489 Fractalkine False True False +NCIT:C204890 Chemical Impurity Test False True False +NCIT:C204891 Uniformity Analysis False True False +NCIT:C204892 Substance Weight Analysis False True False +NCIT:C204893 PRKRA Gene False True False +NCIT:C204894 PRKRA wt Allele False True False +NCIT:C204895 Interferon-Inducible Double-Stranded RNA-Dependent Protein Kinase Activator A False True False +NCIT:C204896 PTGDR2 Gene False True False +NCIT:C204897 PTGDR2 wt Allele False True False +NCIT:C204898 Prostaglandin D2 Receptor 2 False True False +NCIT:C204899 PTH1R Gene False True False NCIT:C2049 Indibulin False True False NCIT:C20490 Gamma Chemokine False True False +NCIT:C204900 PTH1R wt Allele False True False +NCIT:C204901 Parathyroid Hormone/Parathyroid Hormone-Related Peptide Receptor False True False +NCIT:C204902 Locoregional Disease False True False +NCIT:C204903 PTS Gene False True False +NCIT:C204904 Anti-nectin-4 Antibody-drug Conjugate LY4101174 False True False +NCIT:C204905 PTS wt Allele False True False +NCIT:C204906 6-Pyruvoyl Tetrahydrobiopterin Synthase False True False +NCIT:C204908 Melanosis False True False +NCIT:C204909 Dendritic Melanocyte False True False NCIT:C20491 Molecular Nanotechnology False True False +NCIT:C204912 PYGB Gene False True False +NCIT:C204913 PYGB wt Allele False True False +NCIT:C204914 Glycogen Phosphorylase, Brain Form False True False +NCIT:C204915 PYGL Gene False True False +NCIT:C204916 PYGL wt Allele False True False +NCIT:C204917 Glycogen Phosphorylase, Liver Form False True False +NCIT:C204918 PYGM Gene False True False +NCIT:C204919 PYGM wt Allele False True False NCIT:C20492 Fms-Related Tyrosine Kinase 3 Ligand False True False +NCIT:C204920 Glycogen Phosphorylase, Muscle Form False True False +NCIT:C204921 QDPR Gene False True False +NCIT:C204922 QDPR wt Allele False True False +NCIT:C204923 Dihydropteridine Reductase False True False +NCIT:C204924 Autologous Anti-B7-H3 CAR-iC9-expressing T-lymphocytes False True False +NCIT:C204925 RAB39B Gene False True False +NCIT:C204926 RAB39B wt Allele False True False +NCIT:C204927 Ras-Related Protein Rab-39B False True False +NCIT:C204928 RBM20 Gene False True False +NCIT:C204929 RBM20 wt Allele False True False NCIT:C20493 Interferon False True False +NCIT:C204930 RNA-Binding Protein 20 False True False +NCIT:C204931 Chamomilla/Mercurius Solubilis/Sulfur-containing Homeopathic Ear Drops False True False +NCIT:C204932 Steroid-Dependent Gastrointestinal Tract Acute Graft Versus Host Disease False True False +NCIT:C204933 RBP1 Gene False True False +NCIT:C204934 RBP1 wt Allele False True False +NCIT:C204935 Retinol-Binding Protein 1 False True False +NCIT:C204936 RBP2 Gene False True False +NCIT:C204937 RBP2 wt Allele False True False +NCIT:C204938 Retinol-Binding Protein 2 False True False +NCIT:C204939 RBP3 Gene False True False NCIT:C20494 Interferon Alpha False True False +NCIT:C204940 RBP3 wt Allele False True False +NCIT:C204941 Retinol-Binding Protein 3 False True False +NCIT:C204942 Lipid Nanoparticle Encapsulating mRNA Encoding Cas9 Protein and TTR-targeting Single Guide RNA NTLA-2001 False True False +NCIT:C204943 Tislelizumab Regimen False True False +NCIT:C204944 RCBTB1 Gene False True False +NCIT:C204945 RCBTB1 wt Allele False True False +NCIT:C204946 RCC1 and BTB Domain-Containing Protein 1 False True False +NCIT:C204947 REEP1 Gene False True False +NCIT:C204948 REEP1 wt Allele False True False +NCIT:C204949 Receptor Expression-Enhancing Protein 1 False True False NCIT:C20495 Interferon Beta False True False +NCIT:C204950 RNASEH2B Gene False True False +NCIT:C204951 RNASEH2B wt Allele False True False +NCIT:C204952 Ribonuclease H2 Subunit B False True False +NCIT:C204953 RORB Gene False True False +NCIT:C204954 RORB wt Allele False True False +NCIT:C204955 Nuclear Receptor ROR-Beta False True False +NCIT:C204956 RPGRIP1L Gene False True False +NCIT:C204957 RPGRIP1L wt Allele False True False +NCIT:C204958 Protein Fantom False True False +NCIT:C204959 RYR2 Gene False True False NCIT:C20496 Interferon Gamma False True False +NCIT:C204960 RYR2 wt Allele False True False +NCIT:C204961 Ryanodine Receptor 2 False True False +NCIT:C204962 SACS Gene False True False +NCIT:C204963 SACS wt Allele False True False +NCIT:C204964 Sacsin False True False +NCIT:C204965 SALL1 Gene False True False +NCIT:C204966 SALL1 wt Allele False True False +NCIT:C204967 Sal-Like Protein 1 False True False +NCIT:C204968 Dimension Measurement False True False +NCIT:C204969 DACT1 Gene False True False NCIT:C20497 Interleukin False True False +NCIT:C204970 DACT1 wt Allele False True False +NCIT:C204971 Impurity Test False True False +NCIT:C204972 Dapper Homolog 1 False True False +NCIT:C204973 Carbon C 11 AZ14193391 False True False +NCIT:C204974 Skin Lesion More Than 200 mm False True False +NCIT:C204975 Skin Lesion 15-200 mm False True False NCIT:C20498 Lymphokine False True False +NCIT:C204983 c-Met-targeting Tri-specific Natural Killer Cell Engager ABBV-303 False True False +NCIT:C204989 SBF1 Gene False True False NCIT:C20499 Oncostatin-M False True False +NCIT:C204990 SBF1 wt Allele False True False +NCIT:C204992 Myotubularin-Related Protein 5 False True False +NCIT:C204993 SCARB2 Gene False True False +NCIT:C204994 SCARB2 wt Allele False True False +NCIT:C204995 Lysosome Membrane Protein 2 False True False +NCIT:C204996 Myelodysplastic Syndrome Overall Response Rate False True False +NCIT:C204997 Myelodysplastic Syndrome Complete Response Equivalent False True False +NCIT:C204998 Myelodysplastic Syndrome Complete Response with Limited Count Recovery False True False +NCIT:C204999 Topoisomerase I inhibitor-containing Antibody-drug Conjugate False True False NCIT:C205 Acyclovir False True False NCIT:C2050 Alpha V Beta Inhibitor False True False NCIT:C20500 Tumor Necrosis Factor Family Protein False True False +NCIT:C205000 Active Substance Functional Assay False True False +NCIT:C205001 Adventitious Agent Assay False True False +NCIT:C205002 Amidation Assay False True False +NCIT:C205003 Bioburden Test False True False +NCIT:C205004 Blend Uniformity Test False True False +NCIT:C205005 Capsule Lock Length Measurement False True False +NCIT:C205006 Cell and Gene Therapy Product Characterization Assay False True False +NCIT:C205007 Counterion Content Assessment False True False +NCIT:C205008 Deamidation Assessment False True False +NCIT:C205009 Dose Orifice Depth Drilled Measurement False True False NCIT:C20501 TAF2 Gene False True False +NCIT:C205010 Dose Orifice Diameter Drilled Measurement False True False +NCIT:C205011 Dose Orifice Location Measurement False True False +NCIT:C205012 Droplet Size Test Measurement False True False +NCIT:C205013 Elemental Analysis False True False +NCIT:C205014 Elemental Impurity Analysis False True False +NCIT:C205015 Excipient Measurement False True False +NCIT:C205016 Group Fill Substance Weight Measurement False True False +NCIT:C205017 Group Substance Weight Measurement False True False +NCIT:C205018 Host Cell DNA Measurement False True False +NCIT:C205019 In Process Control Content Uniformity Tests False True False NCIT:C20502 TAF3 Gene False True False +NCIT:C205020 In Vitro or In Vivo Test for Viral Contaminants False True False +NCIT:C205021 Individual Substance Fill Weight Measurement False True False +NCIT:C205022 Individual Substance Weight Measurement False True False +NCIT:C205023 Mechanical Integrity Test False True False +NCIT:C205024 Metal Level Detection Test False True False +NCIT:C205025 Number of Dose Orifices Drilled Count False True False +NCIT:C205026 Organoleptic Examination False True False +NCIT:C205027 Osmolality/Osmolarity Measurement False True False +NCIT:C205028 Percent Conjugated Protein Measurement False True False +NCIT:C205029 pH Measurement False True False NCIT:C20503 TAF4 Gene False True False +NCIT:C205030 Porosity Measurement False True False +NCIT:C205031 Protein Sialylation False True False +NCIT:C205032 Refractive Index Measurement False True False +NCIT:C205033 Ribbon Density False True False +NCIT:C205034 Ribbon Thickness False True False +NCIT:C205035 Seam Thickness Measurement False True False +NCIT:C205036 Shell Weight Measurement False True False +NCIT:C205037 Single or Double Drilled Side Assessment False True False +NCIT:C205038 Solvate Content Identification False True False +NCIT:C205039 Specified Identified Impurity Test False True False NCIT:C20504 Cell Maintenance False True False +NCIT:C205040 Specified Unidentified Impurity Test False True False +NCIT:C205041 Surface Area Measurement False True False +NCIT:C205042 Tablet Thickness Measurement False True False +NCIT:C205043 Tablet/Capsule Diameter Measurement False True False +NCIT:C205044 Tablet/Capsule Length Measurement False True False +NCIT:C205045 Target Group Product Weight Gain Percentage False True False +NCIT:C205047 Total Product Impurity above Threshold Assay False True False +NCIT:C205048 Total Product Unknown Impurity Assay False True False +NCIT:C205049 Transdermal Device Property Test False True False NCIT:C20505 TAF5 Gene False True False +NCIT:C205050 Content Uniformity in Container False True False +NCIT:C205051 Unspecified Product Impurity below ICH Identification Threshold False True False +NCIT:C205052 Unspecified Product Impurity Test False True False +NCIT:C205053 Weight/Concentration Variation Test False True False +NCIT:C205054 Thrombin Peptide Map False True False +NCIT:C205055 Microbiology Laboratory Test Result False True False +NCIT:C205056 Measurable Residual Disease Result False True False +NCIT:C205058 OMOP Concept Identifier False True False +NCIT:C205059 SGCE Gene False True False NCIT:C20506 Interleukin-1 False True False +NCIT:C205060 SGCE wt Allele False True False +NCIT:C205061 Epsilon-Sarcoglycan False True False +NCIT:C205062 SCN11A Gene False True False +NCIT:C205063 SCN11A wt Allele False True False +NCIT:C205064 Sodium Channel Protein Type 11 Subunit Alpha False True False +NCIT:C205065 SCN4A Gene False True False +NCIT:C205066 SCN4A wt Allele False True False +NCIT:C205067 Sodium Channel Protein Type 4 Subunit Alpha False True False +NCIT:C205068 Autologous Anti-BCMA-CAR-4-1BB-expressing T-cells NXC-201 False True False NCIT:C20507 Interleukin-2 False True False +NCIT:C205070 OMOP Coding System False True False +NCIT:C205071 SELENON Gene False True False +NCIT:C205072 SELENON wt Allele False True False +NCIT:C205073 Selenoprotein N False True False +NCIT:C205074 Licensed Psychiatric Technician False True False +NCIT:C205075 Health and Wellness Coach False True False +NCIT:C205076 Naprapath False True False +NCIT:C205077 Homeopath False True False +NCIT:C205078 Pharmacy Technician False True False +NCIT:C205079 Reflexologist False True False NCIT:C20508 Interleukin-4 False True False +NCIT:C205080 Addiction Medicine Anesthesiologist False True False +NCIT:C205081 Critical Care Anesthesiologist False True False +NCIT:C205082 Hospice and Palliative Care Anesthesiologist False True False +NCIT:C205083 Pain Medicine Anesthesiologist False True False +NCIT:C205084 Mechanotherapist False True False +NCIT:C205085 Lactation Consultant, Non-RN False True False +NCIT:C205086 Clinical Ethicist False True False +NCIT:C205087 Clinical and Laboratory Immunologist False True False +NCIT:C205088 Compounding Pharmacist False True False +NCIT:C205089 Emergency Medicine Pharmacist False True False NCIT:C20509 Interleukin-5 False True False +NCIT:C205090 Nuclear Pharmacist False True False +NCIT:C205091 Clinical Pharmacy Specialist False True False +NCIT:C205092 Ambulatory Care Pharmacist False True False +NCIT:C205093 Solid Organ Transplant Pharmacist False True False +NCIT:C205094 Community Health Worker False True False +NCIT:C205095 Specialist False True False +NCIT:C205096 Sleep Medicine Specialist False True False +NCIT:C205097 Phlebology Doctor False True False +NCIT:C205098 Electrodiagnostic Medical Doctor False True False +NCIT:C205099 Case Manager False True False NCIT:C2051 Spongistatin False True False NCIT:C20510 Interleukin-7 False True False +NCIT:C205100 Prosthetics Case Manager False True False +NCIT:C205101 Independent Duty Corpsman False True False +NCIT:C205102 Independent Duty Medical Technician False True False +NCIT:C205103 Sports Medicine Osteopathic Doctor False True False +NCIT:C205104 Neuromusculoskeletal and Osteopathic Manipulative Medicine Doctor False True False +NCIT:C205105 Research Study Specialist False True False +NCIT:C205106 Research Data Abstracter or Coder False True False +NCIT:C205107 Graphic Designer False True False +NCIT:C205108 Vehicle Modifications Contractor False True False +NCIT:C205109 Home Modifications Contractor False True False NCIT:C20511 Interleukin-9 False True False +NCIT:C205110 Peer Specialist False True False +NCIT:C205111 Independent Medical Examiner False True False +NCIT:C205112 SERPINA12 Gene False True False +NCIT:C205113 Lay Midwife False True False +NCIT:C205114 Driver False True False +NCIT:C205115 SERPINA12 wt Allele False True False +NCIT:C205116 Serpin A12 False True False +NCIT:C205117 Health Educator False True False +NCIT:C205118 Medical Research Veterinarian False True False +NCIT:C205119 Blood and Marrow Transplant Clinical Trials Network False True False NCIT:C20512 Interleukin-10 False True False +NCIT:C205120 Integrative Medicine Doctor False True False +NCIT:C205121 Spatial Transcriptome Analysis False True False +NCIT:C205122 Meal Provider False True False +NCIT:C205123 Single-cell Multiome Analysis False True False +NCIT:C205124 Funeral Director False True False +NCIT:C205126 PD-L1 Tumor Proportion Score Less than 1 False True False +NCIT:C205128 PD-L1 Tumor Proportion Score Greater than or Equal to 50 False True False NCIT:C20513 Interleukin-11 False True False +NCIT:C205133 ALDH3A2 Gene False True False +NCIT:C205134 ALDH3A2 wt Allele False True False +NCIT:C205137 Emergency Medical Palliative Care Physician False True False +NCIT:C205138 Emergency Medical Pediatrician False True False +NCIT:C205139 Emergency Medical Toxicologist False True False NCIT:C20514 Interleukin-12 False True False +NCIT:C205140 Adult Congenital Heart Disease Internist False True False +NCIT:C205141 Advanced Heart Failure and Transplant Cardiology Internist False True False +NCIT:C205142 Advanced Heart Failure and Transplant Internist False True False +NCIT:C205143 Nuclear Medicine Cardiologist False True False +NCIT:C205144 Nuclear Medicine Nuclear Imaging and Therapy Specialist False True False +NCIT:C205145 Dermatopathologist False True False +NCIT:C205146 Molecular Genetic Pathologist False True False +NCIT:C205147 Procedural Dermatologist False True False +NCIT:C205148 Diabetes and Metabolism Endocrinologist False True False +NCIT:C205149 Ophthalmology Cornea and External Diseases Specialist False True False NCIT:C20515 Interleukin-13 False True False +NCIT:C205150 Ophthalmology Glaucoma Specialist False True False +NCIT:C205151 Ophthalmology Neuro-ophthalmology Specialist False True False +NCIT:C205152 Ophthalmology Ophthalmic Plastic and Reconstructive Surgery Specialist False True False +NCIT:C205153 Ophthalmology Pediatric Ophthalmology and Strabismus Specialist False True False +NCIT:C205154 Ophthalmology Retina Specialist False True False +NCIT:C205155 Ophthalmology Uveitis and Ocular Inflammatory Disease Specialist False True False +NCIT:C205156 Internal Medicine Adult Congenital Heart Disease Specialist False True False +NCIT:C205157 Allergy and Immunology Physician False True False +NCIT:C205158 Clinical and Laboratory Immunologist False True False +NCIT:C205159 Internal Medicine Clinical Cardiac Electrophysiology Specialist False True False +NCIT:C205160 Internal Medicine Hypertension Specialist False True False +NCIT:C205161 Internal Medicine Obesity Medicine Specialist False True False +NCIT:C205162 Internal Medicine Sleep Medicine Specialist False True False +NCIT:C205163 Internal Medicine Transplant Hepatology Specialist False True False +NCIT:C205164 Immunological Dermatologist False True False +NCIT:C205165 In Vivo and In Vitro Nuclear Medicine Physician False True False +NCIT:C205166 Internal Medicine Addiction Medicine Specialist False True False +NCIT:C205167 Internal Medicine Adolescent Medicine Specialist False True False +NCIT:C205168 Emergency Medicine Undersea and Hyperbaric Medicine Specialist False True False +NCIT:C205169 Family Medicine Obesity Medicine Specialist False True False NCIT:C20517 Interleukin-15 False True False +NCIT:C205170 Family Medicine Sleep Medicine Specialist False True False +NCIT:C205171 Clinical Biochemical Geneticist False True False +NCIT:C205172 Clinical Cytogeneticist False True False +NCIT:C205173 Clinical Medical Geneticist False True False +NCIT:C205174 Clinical Molecular Geneticist False True False +NCIT:C205175 Obstetrics and Gynecology Complex Family Planning Specialist False True False +NCIT:C205176 Obstetrics and Gynecology Female Pelvic Medicine and Reconstructive Surgery Specialist False True False +NCIT:C205177 Obstetrics and Gynecology Hospice and Palliative Medicine Specialist False True False +NCIT:C205178 Obstetrics and Gynecology Maternal and Fetal Medicine Specialist False True False +NCIT:C205179 Obstetrics and Gynecology Obesity Medicine Specialist False True False NCIT:C20518 Interleukin-16 False True False +NCIT:C205180 Aldehyde Dehydrogenase Family 3 Member A2 False True False +NCIT:C205181 Oncolytic HSV-1 JNJ-87704916 False True False +NCIT:C205182 MBD4 Gene Mutation False True False +NCIT:C205183 MITF Gene Mutation False True False +NCIT:C205184 RPS20 Gene Mutation False True False +NCIT:C205185 TMEM127 Gene Mutation False True False +NCIT:C205186 Medical Geneticist False True False +NCIT:C205189 Aortography False True False NCIT:C20519 Interleukin-17A False True False +NCIT:C205190 Etonogestrel Implant False True False +NCIT:C205191 SMO NM_005631.5:c.1234C>T False True False +NCIT:C205192 SMO NP_005622.1:p.L412F False True False +NCIT:C205193 SMO NM_005631.5:c.1921C>G False True False +NCIT:C205194 SMO NP_005622.1:p.P641A False True False +NCIT:C205195 SMO NM_005631.5:c.1598G>A False True False +NCIT:C205196 SMO NP_005622.1:p.S533N False True False +NCIT:C205197 PTCH1 NM_000264.5:c.2532G>T False True False +NCIT:C205198 PTCH1 NM_000264.5:c.2532G>C False True False +NCIT:C205199 PTCH1 NP_000255.2:p.W844C False True False NCIT:C2052 Cephalostatin False True False NCIT:C20520 Interleukin-18 False True False +NCIT:C205200 SMO NM_005631.5:c.1573A>T False True False +NCIT:C205201 SMO NP_005622.1:p.M525L False True False +NCIT:C205202 Near Infrared Imaging Agent IS-001 False True False +NCIT:C205203 SMO NM_005631.5:c.961G>A False True False +NCIT:C205204 SMO NP_005622.1:p.V321M False True False +NCIT:C205205 SMO NM_005631.5:c.1222A>G False True False +NCIT:C205206 Average Fill Substance Weight Measurement False True False +NCIT:C205207 SMO NP_005622.1:p.I408V False True False +NCIT:C205208 SMO NM_005631.5:c.655A>G False True False +NCIT:C205209 Average Substance Weight Measurement False True False NCIT:C20521 Interleukin-1 Alpha False True False +NCIT:C205210 SMO NP_005622.1:p.N219D False True False +NCIT:C205211 SMO NM_005631.5:c.662T>G False True False +NCIT:C205212 SMO NP_005622.1:p.L221R False True False +NCIT:C205213 Lutetium Lu 177 FF58 False True False +NCIT:C205214 Complete Remission in Myelodysplastic Syndrome with Partial Hematologic Recovery False True False +NCIT:C205215 WAIS-IV Subtest False True False +NCIT:C205216 Arithmetic Subtest (WAIS-IV) False True False +NCIT:C205217 Comprehension Subtest (WAIS-IV) False True False +NCIT:C205218 Information Subtest (WAIS-IV) False True False +NCIT:C205219 Matrix Reasoning Subtest (WAIS-IV) False True False NCIT:C20522 Interleukin-1 Beta False True False +NCIT:C205220 Similarities Subtest (WAIS-IV) False True False +NCIT:C205221 Visual Puzzles Subtest (WAIS-IV) False True False +NCIT:C205222 WAIS-IV Index or Composite Score False True False +NCIT:C205223 Full Scale Intelligence Quotient (WAIS-IV) False True False +NCIT:C205224 General Ability Index (WAIS-IV) False True False +NCIT:C205225 Perceptual Reasoning Index (WAIS-IV) False True False +NCIT:C205227 SMO NM_005631.5:c.1552G>A False True False +NCIT:C205228 SMO NP_005622.1:p.E518K False True False +NCIT:C205229 Processing Speed Index (WAIS-IV) False True False +NCIT:C205230 Verbal Comprehension Index (WAIS-IV) False True False +NCIT:C205231 Working Memory Index (WAIS-IV) False True False +NCIT:C205232 WPPSI-IV Subtest False True False +NCIT:C205233 WPPSI-IV Index or Composite Score False True False +NCIT:C205234 SMO NM_005631.5:c.1553A>C False True False +NCIT:C205235 SMO NP_005622.1:p.E518A False True False +NCIT:C205236 TP/TE Regimen False True False +NCIT:C205237 Cetuximab/Paclitaxel Regimen False True False +NCIT:C205239 DNAJC6 Gene False True False NCIT:C20524 Leukemia Inhibitory Factor False True False +NCIT:C205240 DNAJC6 wt Allele False True False +NCIT:C205241 Capecitabine/Paclitaxel Regimen False True False +NCIT:C205242 Auxilin False True False +NCIT:C205243 Animal Coding Subtest (WPPSI-IV) False True False +NCIT:C205244 Comprehension Subtest (WPPSI-IV) False True False +NCIT:C205245 Information Subtest (WPPSI-IV) False True False +NCIT:C205246 Matrix Reasoning Subtest (WPPSI-IV) False True False +NCIT:C205247 Object Assembly Subtest (WPPSI-IV) False True False +NCIT:C205248 Picture Concepts Subtest (WPPSI-IV) False True False +NCIT:C205249 Similarities Subtest (WPPSI-IV) False True False NCIT:C20525 Leukoregulin False True False +NCIT:C205250 Fluid Reasoning Index (WPPSI-IV) False True False +NCIT:C205251 Full Scale Intelligence Quotient (WPPSI-IV) False True False +NCIT:C205252 Processing Speed Index (WPPSI-IV) False True False +NCIT:C205253 Verbal Comprehension Index (WPPSI-IV) False True False +NCIT:C205254 Visual Spatial Index (WPPSI-IV) False True False +NCIT:C205255 Working Memory Index (WPPSI-IV) False True False +NCIT:C205256 WISC-V Subtest False True False +NCIT:C205257 WISC-V Index or Composite Score False True False +NCIT:C205258 Intraperitoneal Carboplatin/Paclitaxel Regimen False True False +NCIT:C205259 FBXO7 Gene False True False NCIT:C20526 TAF6 Gene False True False +NCIT:C205260 Arithmetic Subtest (WISC-V) False True False +NCIT:C205261 Cancellation Subtest (WISC-V) False True False +NCIT:C205262 FBXO7 wt Allele False True False +NCIT:C205263 Comprehension Subtest (WISC-V) False True False +NCIT:C205264 Digit Span Subtest (WISC-V) False True False +NCIT:C205265 F-Box Only Protein 7 False True False +NCIT:C205266 Figure Weights Subtest (WISC-V) False True False +NCIT:C205267 Information Subtest (WISC-V) False True False +NCIT:C205268 Letter Numbering Sequence Subtest (WISC-V) False True False +NCIT:C205269 Matrix Reasoning Subtest (WISC-V) False True False NCIT:C20527 TAF7 Gene False True False +NCIT:C205270 Picture Concepts Subtest (WISC-V) False True False +NCIT:C205271 Picture Span Subtest (WISC-V) False True False +NCIT:C205272 Similarities Subtest (WISC-V) False True False +NCIT:C205273 MTMR2 Gene False True False +NCIT:C205274 Visual Puzzles Subtest (WISC-V) False True False +NCIT:C205275 Fluid Reasoning Index (WISC-V) False True False +NCIT:C205276 Processing Speed Index (WISC-V) False True False +NCIT:C205277 Verbal Comprehension Index (WISC-V) False True False +NCIT:C205278 MTMR2 wt Allele False True False +NCIT:C205279 Visual Spatial Index (WISC-V) False True False NCIT:C20528 CD40 Ligand False True False +NCIT:C205280 Working Memory Index (WISC-V) False True False +NCIT:C205281 Myotubularin-Related Protein 2 False True False +NCIT:C205282 Intraperitoneal Carboplatin/Paclitaxel/Intraperitoneal Paclitaxel Regimen False True False +NCIT:C205283 Fluorouracil/Paclitaxel Regimen False True False +NCIT:C205284 PSMA-Positive Extracellular Vesicles High False True False +NCIT:C205285 PSMA-Positive Extracellular Vesicles Low False True False +NCIT:C205288 CUX1 Gene Product False True False NCIT:C20529 Tumor Necrosis Factor Ligand Superfamily Member 6 False True False +NCIT:C205291 Orthopedic Surgeon False True False +NCIT:C205292 Adult Reconstructive Orthopedic Surgeon False True False +NCIT:C205293 Foot and Ankle Orthopedic Surgeon False True False +NCIT:C205294 Trauma Orthopedic Surgeon False True False +NCIT:C205296 Pediatric Otolaryngologist False True False +NCIT:C205297 Otolaryngologist Sleep Medicine False True False +NCIT:C205299 Otolaryngology Plastic Surgery within the Head and Neck False True False NCIT:C2053 T-1622 False True False NCIT:C20530 Lymphotoxin-Beta False True False +NCIT:C205300 NCBI Taxonomy False True False +NCIT:C205302 Otolaryngic Allergy Otolaryngologist False True False +NCIT:C205304 Otology and Neurotology Otolaryngologist False True False +NCIT:C205305 Facial Plastic Surgery Otolaryngologist False True False NCIT:C20531 TAF7L Gene False True False +NCIT:C205312 PARP1 Inhibitor IMP1734 False True False +NCIT:C205315 Cytopathologist False True False +NCIT:C205316 Medical Microbiology Pathologist False True False +NCIT:C205318 Anatomic Pathologist False True False +NCIT:C205319 Cisplatin Followed by Carboplatin/Paclitaxel Regimen False True False NCIT:C20532 Tumor Necrosis Factor Ligand Superfamily Member 4 False True False +NCIT:C205320 Anatomic and Clinical Pathologist False True False +NCIT:C205321 Chemical Pathologist False True False +NCIT:C205322 Clinical Pathology and Laboratory Medicine Pathologist False True False +NCIT:C205323 Pediatric Pathologist False True False +NCIT:C205324 Adolescent Medicine Pediatrician False True False +NCIT:C205325 Obestity Medicine Pediatrician False True False +NCIT:C205326 Child Abuse Pediatrician False True False +NCIT:C205327 Clinical Laboratory and Immunology Pediatrician False True False +NCIT:C205328 Neonatal-Perinatal Medicine Pediatrician False True False NCIT:C20533 Tumor Necrosis Factor Ligand Superfamily Member 10 False True False +NCIT:C205330 Neurodevelopmental Disabilities Pediatrician False True False +NCIT:C205331 Emergency Medicine Physician False True False +NCIT:C205332 Sleep Medicine Pediatrician False True False +NCIT:C205333 Medical Toxicology Pediatrician False True False +NCIT:C205334 Transplant Hepatology Pediatrician False True False +NCIT:C205335 Hospice and Palliative Medicine Physiatrist False True False +NCIT:C205336 Neuromuscular Medicine Physiatrist False True False +NCIT:C205337 Plastic Surgery within the Head and Neck Plastic Surgeon False True False +NCIT:C205338 Pediatric Physiatrist False True False +NCIT:C205339 Pain Medicine Physiatrist False True False NCIT:C20534 TAF8 Gene False True False +NCIT:C205340 Brain Injury Medicine Physiatrist False True False +NCIT:C205341 Sports Medicine Physiatrist False True False +NCIT:C205342 Blood Banking and Transfusion Medicine Pathologist False True False +NCIT:C205343 Preventive Medicine Physician False True False +NCIT:C205344 Preventive Medicine Aerospace Physician False True False +NCIT:C205345 Preventive Medicine Obesity Medicine Physician False True False +NCIT:C205346 Preventive Medicine Addiction Medicine Physician False True False +NCIT:C205347 Preventive Medicine Clinical Informatics Physician False True False +NCIT:C205348 Preventive Medicine Undersea and Hyperbaric Medicine Physician False True False +NCIT:C205349 Preventive Medicine Preventive Medicine/Occupational Environmental Medicine Physician False True False NCIT:C20535 Tumor Necrosis Factor False True False +NCIT:C205350 Preventive Medicine Sports Medicine Physician False True False +NCIT:C205351 Preventive Medicine Medical Toxicology Physician False True False +NCIT:C205352 Preventive Medicine Occupational Medicine Physician False True False +NCIT:C205353 Anti-ROR1/Anti-CD3/Anti-HSA Trispecific Antibody NM32-2668 False True False +NCIT:C205354 Bevacizumab/Carboplatin/Paclitaxel/Pembrolizumab Regimen False True False +NCIT:C205355 Family Medicine Physician False True False +NCIT:C205356 Bevacizumab/Cisplatin/Paclitaxel/Pembrolizumab Regimen False True False +NCIT:C205358 KRAS G12C Inhibitor BBO-8520 False True False +NCIT:C205359 PSA Level Greater than or Equal to Eight False True False NCIT:C20536 Lymphotoxin-Alpha False True False +NCIT:C205360 Post Neoadjuvant Pathological Staging False True False +NCIT:C205362 Ventrogluteal Region False True False +NCIT:C205363 Familial Cylindromatosis False True False +NCIT:C205364 Multiple Familial Trichoepithelioma False True False +NCIT:C205365 Omics False True False +NCIT:C205366 Vaccine Administered Code False True False +NCIT:C205367 External Data Feed False True False +NCIT:C205368 Patient Objection False True False +NCIT:C205369 Immunization Information System False True False NCIT:C20537 TAF9 Gene False True False +NCIT:C205372 FOXK1-GRHL Fusion Protein Expression False True False +NCIT:C205373 GPS2-GRHL Fusion Protein Expression False True False +NCIT:C205374 Paired Tumor-Normal DNA Sequencing False True False +NCIT:C205375 mTORC1/mTORC2 Inhibitor XL388 False True False +NCIT:C205376 mTORC1/mTORC2 Inhibitor Palomid 529 False True False +NCIT:C205377 Psychiatrist or Neurologist False True False +NCIT:C205378 Psychiatrist or Neurologist Addiction Medicine Physician False True False +NCIT:C205379 Neurocritical Care Neurologist False True False NCIT:C20538 TAF10 Gene False True False +NCIT:C205380 Psychiatrist or Neurologist Obesity Medicine Physician False True False +NCIT:C205381 Epileptologist False True False +NCIT:C205382 Forensic Psychiatrist False True False +NCIT:C205383 Neuromuscular Medicine Neurologist False True False +NCIT:C205384 FOXK1/GRHL Fusion Gene False True False +NCIT:C205385 GPS2/GRHL Fusion Gene False True False +NCIT:C205386 Online Adaptive Proton Stereotactic Body Radiation Therapy False True False +NCIT:C205387 FOXK1 Gene False True False +NCIT:C205388 FOXK1 wt Allele False True False +NCIT:C205389 Forkhead Box Protein K1 False True False NCIT:C20539 TBP-Associated Factor Gene False True False +NCIT:C205390 GRHL1 Gene False True False +NCIT:C205391 GRHL1 wt Allele False True False +NCIT:C205392 Psychiatrist or Neurologist Diagnostic Neuroimaging Physician False True False +NCIT:C205393 Grainyhead-Like Protein 1 Homolog False True False +NCIT:C205394 GRHL3 Gene False True False +NCIT:C205395 GRHL3 wt Allele False True False +NCIT:C205396 Grainyhead-Like Protein 3 Homolog False True False +NCIT:C205397 Repotrectinib Regimen False True False +NCIT:C205398 ICD-9-CM Diagnosis Codes False True False +NCIT:C205399 ICD-9-CM Procedure Codes False True False NCIT:C2054 BCI Immune Activator False True False NCIT:C20540 TAF11 Gene False True False +NCIT:C205400 User-defined Source False True False +NCIT:C205401 Locally-defined Death File False True False +NCIT:C205402 State Death File False True False +NCIT:C205403 Tumor Data Death File False True False +NCIT:C205404 Bevacizumab/Cyclophosphamide/Pembrolizumab Regimen False True False +NCIT:C205405 Bevacizumab/Carboplatin/Docetaxel Followed by Bevacizumab Regimen False True False +NCIT:C205406 Respiratory Tract Route of Administration False True False +NCIT:C205407 Survey System Mobile Application Source False True False +NCIT:C205408 Bevacizumab/Docetaxel/Oxaliplatin Followed by Bevacizumab Regimen False True False NCIT:C20541 TAF12 Gene False True False +NCIT:C205410 Psychiatrist or Neurologist Behavioral Neurology and Neuropsychiatry Physician False True False +NCIT:C205411 Psychiatrist or Neurologist Hospice and Palliative Medicine Physician False True False +NCIT:C205412 Clinical Neurophysiologist False True False +NCIT:C205413 Neurodevelopmental Neurologist False True False +NCIT:C205414 Psychosomatic Medicine Psychiatrist False True False +NCIT:C205415 Psychiatrist or Neurologist Brain Injury Physician False True False +NCIT:C205416 Addiction Psychiatrist False True False +NCIT:C205417 Adolescent Psychiatrist False True False +NCIT:C205418 Geriatric Psychiatrist False True False +NCIT:C205419 Psychiatrist or Neurologist Pain Medicine Physician False True False NCIT:C20542 TAF13 Gene False True False +NCIT:C205420 Psychiatrist or Neurologist Sports Medicine Physician False True False +NCIT:C205421 Psychiatrist or Neurologist Sleep Medicine Physician False True False +NCIT:C205422 Vascular Neurologist False True False +NCIT:C205423 Body Imaging Radiologist False True False +NCIT:C205424 Diagnostic Neuroradiologist False True False +NCIT:C205425 Hospice and Palliative Medicine Radiologist False True False +NCIT:C205426 Radiation Physics Radiologist False True False +NCIT:C205427 Hospice and Palliative Medicine Surgeon False True False +NCIT:C205428 Critical Care Surgeon False True False +NCIT:C205429 Female Pelvic Medicine and Reconstructive Surgery Urologist False True False NCIT:C20543 TFIID Subunit Gene False True False +NCIT:C205430 Hospitalist False True False +NCIT:C205431 Pain Medicine Physician False True False +NCIT:C205432 Interventional Pain Physician False True False +NCIT:C205433 Podiatric Radiologist False True False +NCIT:C205434 Podiatric Foot and Ankle Surgeon False True False +NCIT:C205435 Anti-CEA/Anti-4-1BB Bispecific Antibody LM-24C5 False True False +NCIT:C205436 Anti-PD-1/Anti-CD73 Bispecific Antibody AK131 False True False +NCIT:C205437 ATR Inhibitor TQB3015 False True False +NCIT:C205438 Autologous Tumor Infiltrating Lymphocytes BST02 False True False +NCIT:C205439 Dalpiciclib Isethionate False True False NCIT:C20544 TFIIA Subunit Gene False True False +NCIT:C205440 EGFR Mutant-selective Inhibitor TRX-221 False True False +NCIT:C205441 Oncolytic Vaccinia Virus Expressing Leptin/IL-2 Fusion Protein ASP1012 False True False +NCIT:C205442 PARP1 Inhibitor GS-0201 False True False +NCIT:C205443 PD-1 Targeted IL-2 Mutein Fusion Protein KY-0118 False True False +NCIT:C205444 Recombinant Oncolytic Adenovirus 5 Encoding Non-secreting Interleukin-12 BioTTT001 False True False +NCIT:C205445 Occupational Therapy Assistant False True False +NCIT:C205446 Environmental Modification Occupational Therapy Assistant False True False +NCIT:C205447 Feeding, Eating and Swallowing Occupational Therapy Assistant False True False +NCIT:C205448 Low Vision Occupational Therapy Assistant False True False +NCIT:C205449 Driving and Community Mobility Occupational Therapy Assistant False True False NCIT:C20545 Granulocyte-Macrophage Colony-Stimulating Factor False True False +NCIT:C205450 Prosthetist False True False +NCIT:C205451 Art Therapist False True False +NCIT:C205452 PD-L1 Expression Greater than 50 Percent False True False +NCIT:C205453 Developmental Therapist False True False +NCIT:C205454 Orthotist False True False +NCIT:C205455 Mastectomy Fitter False True False +NCIT:C205456 Pedorthist False True False +NCIT:C205457 Clinical Exercise Physiologist False True False +NCIT:C205458 CA19-9 Greater than 500 U/mL False True False +NCIT:C205460 Papillary Projections Present False True False +NCIT:C205461 Bevacizumab/Gemcitabine Regimen False True False +NCIT:C205464 Female Gender, Self Reported False True False +NCIT:C205465 Male Gender, Self Reported False True False +NCIT:C205466 Female Gender Identity False True False +NCIT:C205467 Male Gender Identity False True False +NCIT:C205468 Non-Binary Gender Identity False True False +NCIT:C205469 Agender False True False NCIT:C20547 Fibroblast Growth Factor 2 False True False +NCIT:C205470 Gender Fluid False True False +NCIT:C205471 Transgender False True False +NCIT:C205472 Sex Assigned at Birth False True False +NCIT:C205473 Assigned Male at Birth False True False +NCIT:C205474 Assigned Female at Birth False True False +NCIT:C205477 PQ/CMC Substance Classification Terminology False True False +NCIT:C205478 Microgram per Actuation False True False +NCIT:C205479 Bait Dosing Unit False True False NCIT:C20548 Fibroblast Growth Factor 1 False True False +NCIT:C205480 Oral Suspension Bait Dosage Form False True False +NCIT:C205481 Bait Dosage Form Category False True False +NCIT:C205482 Somali False True False +NCIT:C205483 Ghanian False True False +NCIT:C205484 Prednisone/Sirolimus Regimen False True False +NCIT:C205485 Salvadoran False True False +NCIT:C205486 Guatemalan False True False +NCIT:C205487 Honduran False True False +NCIT:C205488 Colombian False True False +NCIT:C205489 Moroccan False True False NCIT:C20549 Fibroblast Growth Factor 3 False True False +NCIT:C205490 Yemeni False True False +NCIT:C205491 Kurdish False True False +NCIT:C205492 MYC Gene Rearrangement and BCL2 Gene Rearrangement Positive False True False +NCIT:C205493 Congolese False True False +NCIT:C205494 MYC Gene Rearrangement and BCL6 Gene Rearrangement Positive False True False +NCIT:C205495 YAP1/MAML2 Fusion Gene False True False +NCIT:C205496 YAP1/NUTM1 Fusion Gene False True False +NCIT:C205497 MYC Gene Rearrangement, BCL2 Gene Rearrangement, and BCL6 Gene Rearrangement Positive False True False +NCIT:C205498 Bortezomib/Dexamethasone/Isatuximab/Lenalidomide Regimen False True False +NCIT:C205499 Fitter False True False NCIT:C2055 Allogenic Glioma Cancer Vaccine False True False NCIT:C20550 Fibroblast Growth Factor 4 False True False +NCIT:C205500 Orthotic Fitter False True False +NCIT:C205501 Ergonomics Physical Therapist False True False +NCIT:C205502 Clinical Electrophysiologic Physical Therapist False True False +NCIT:C205503 Human Factors Physical Therapist False True False +NCIT:C205504 Sports Physical Therapist False True False +NCIT:C205505 Physical Therapy Assistant False True False +NCIT:C205506 Tovorafenib Regimen False True False +NCIT:C205507 Nogapendekin Alfa Inbakicept False True False +NCIT:C205508 Can't Afford Balanced Meals False True False +NCIT:C205509 Adults Cut Meal Size or Skipped Meals Because Not Enough Money False True False NCIT:C20551 TBPL1 Gene False True False +NCIT:C205510 Ate Less Than Should Because Not Enough Money False True False +NCIT:C205511 Hungry and Didn't Eat Because Couldn't Afford Food False True False +NCIT:C205512 Almost Every Month False True False +NCIT:C205513 Some Months, but Not Every Month False True False +NCIT:C205514 One or Two Months False True False +NCIT:C205515 Soda False True False +NCIT:C205516 Boredom False True False +NCIT:C205517 Loose False True False +NCIT:C205518 Intravesical Nogapendekin Alfa Inbakicept/BCG Regimen False True False +NCIT:C205519 Intravesical Mitomycin Regimen False True False NCIT:C20552 PMS2P1 Gene False True False +NCIT:C205520 Intraperitoneal Mitomycin Regimen False True False +NCIT:C205521 Delayed Medical Care Due to Cost False True False +NCIT:C205522 Did Not Get Medical Care Due to Cost False True False +NCIT:C205523 How Often Visited Urgent Care Center or Drug/Grocery Store Clinic About Health False True False +NCIT:C205524 Two to Three Years False True False +NCIT:C205525 Five to Ten Years False True False +NCIT:C205526 Ten or More Years False True False +NCIT:C205527 Does Not Go to One Place Most Often False True False +NCIT:C205528 Homeowner False True False +NCIT:C205529 Renter False True False NCIT:C20553 APEX2 Gene False True False +NCIT:C205530 Fiance(e) False True False +NCIT:C205531 Within the Last Year False True False +NCIT:C205532 One to Two Years Ago False True False +NCIT:C205533 Two to Three Years Ago False True False +NCIT:C205534 Three to Five Years Ago False True False +NCIT:C205535 Five to Ten Years Ago False True False +NCIT:C205536 Ten or More Years Ago False True False +NCIT:C205537 Regimen Used to Treat Histiocytic and Dendritic Cell Neoplasm False True False +NCIT:C205538 CRTC3-MAML2 Fusion Protein Expression False True False NCIT:C20554 ERCC1 Gene False True False +NCIT:C205540 ALPK1 Gene Mutation False True False +NCIT:C205541 CYLD Cutaneous Syndrome False True False +NCIT:C205542 Massage Therapist False True False +NCIT:C205543 Dance Therapist False True False +NCIT:C205544 Recreation Therapist False True False +NCIT:C205545 Music Therapist False True False +NCIT:C205546 Critical Care Respiratory Therapist False True False +NCIT:C205547 Emergency Care Respiratory Therapist False True False +NCIT:C205548 Educational Respiratory Therapist False True False +NCIT:C205549 Geriatric Respiratory Therapist False True False NCIT:C20555 ERCC2 Gene False True False +NCIT:C205550 General Care Respiratory Therapist False True False +NCIT:C205552 Home Health Respiratory Therapist False True False +NCIT:C205553 Pulmonary Diagnostics Respiratory Therapist False True False +NCIT:C205554 Pulmonary Rehabilitation Respiratory Therapist False True False +NCIT:C205555 Pulmonary Function Technologist Respiratory Therapist False True False +NCIT:C205556 Palliative/Hospice Respiratory Therapist False True False +NCIT:C205557 Neonatal/Pediatrics Respiratory Therapist False True False +NCIT:C205558 Patient Transport Respiratory Therapist False True False +NCIT:C205559 Skilled Nursing Facility/Subacute Care Respiratory Therapist False True False NCIT:C20556 ERCC3 Gene False True False +NCIT:C205560 Registered Respiratory Therapist False True False +NCIT:C205561 Registered Critical Care Respiratory Therapist False True False +NCIT:C205562 Registered Emergency Care Respiratory Therapist False True False +NCIT:C205563 Registered Educational Respiratory Therapist False True False +NCIT:C205564 Registered Geriatric Respiratory Therapist False True False +NCIT:C205565 Registered General Care Respiratory Therapist False True False +NCIT:C205566 Registered Home Health Respiratory Therapist False True False +NCIT:C205567 Registered Pulmonary Diagnostics Respiratory Therapist False True False +NCIT:C205568 Registered Pulmonary Rehabilitation Respiratory Therapist False True False +NCIT:C205569 Registered Pulmonary Function Technologist Respiratory Therapist False True False NCIT:C20557 ERCC5 Gene False True False +NCIT:C205570 Registered Palliative/Hospice Respiratory Therapist False True False +NCIT:C205571 Registered Neonatal/Pediatrics Respiratory Therapist False True False +NCIT:C205572 Registered Patient Transport Respiratory Therapist False True False +NCIT:C205573 Registered Skilled Nursing Facility/Subacute Care Respiratory Therapist False True False +NCIT:C205574 Environmental Modification Occupational Therapist False True False +NCIT:C205575 Ergonomics Occupational Therapist False True False +NCIT:C205576 Feeding, Eating & Swallowing Occupational Therapist False True False +NCIT:C205577 Human Factors Occupational Therapist False True False +NCIT:C205578 Low Vision Occupational Therapist False True False +NCIT:C205579 Mental Health Occupational Therapist False True False NCIT:C20558 ERCC4 Gene False True False +NCIT:C205580 Neurorehabilitation Occupational Therapist False True False +NCIT:C205581 Driving and Community Mobility Occupational Therapist False True False +NCIT:C205582 Nirogacestat Regimen False True False +NCIT:C205583 Rituximab Followed by Prednisone False True False +NCIT:C205584 Etoposide/Rituximab Regimen False True False +NCIT:C205585 Toripalimab Regimen False True False +NCIT:C205586 Certified Respiratory Therapist False True False +NCIT:C205587 Cytarabine/Quizartinib Regimen False True False +NCIT:C205588 Cytarabine/Daunorubicin/Quizartinib Regimen False True False +NCIT:C205589 Cytarabine/Idarubicin/Quizartinib Regimen False True False NCIT:C20559 TREX1 Gene False True False +NCIT:C205590 Rehabilitation Counselor False True False +NCIT:C205591 Assistive Technology Practitioner Audiologist False True False +NCIT:C205592 Assistive Technology Supplier Audiologist False True False +NCIT:C205593 Recreational Therapist Assistant False True False +NCIT:C205594 Assistive Technology Supplier Rehabilitation Counselor False True False +NCIT:C205595 Assistive Technology Practitioner Rehabilitation Counselor False True False +NCIT:C205596 Anaplastologist False True False +NCIT:C205597 Kinesiotherapist False True False +NCIT:C205598 Speech Therapist Assistant False True False +NCIT:C205599 Athletic Trainer False True False NCIT:C2056 Neu-Sensamide False True False NCIT:C20560 ATR Gene False True False +NCIT:C205600 Audiology Assistant False True False +NCIT:C205601 Blind Rehabilitation Specialist False True False +NCIT:C205602 Pulmonary Function Technologist False True False +NCIT:C205603 Orientation and Mobility Training Provider Rehabilitation Counselor False True False +NCIT:C205605 Dacarbazine/Fluorouracil Regimen False True False +NCIT:C205606 Doxorubicin/Ifosfamide Alternating with Cisplatin/Etoposide Regimen False True False NCIT:C20561 TREX2 Gene False True False NCIT:C20562 TERF2 Gene False True False NCIT:C20563 TERF1 Gene False True False @@ -114964,7 +118928,7 @@ NCIT:C20751 Inhibition of Cell Proliferation False True False NCIT:C20752 GAS8 Gene False True False NCIT:C20754 ACRBP Gene False True False NCIT:C20755 AGR2 Gene False True False -NCIT:C20756 ANP32C Gene False True False +NCIT:C20756 ANP32CP Gene False True False NCIT:C20757 HMMR Gene False True False NCIT:C20758 Hyaluronic Acid Binding False True False NCIT:C20759 ANP32D Gene False True False @@ -115705,7 +119669,7 @@ NCIT:C21480 Relative False True False NCIT:C21481 First Degree Relative False True False NCIT:C21482 Anterior Gradient Protein 2 Homolog False True False NCIT:C21483 DNA-Dependent Protein Kinase Catalytic Subunit False True False -NCIT:C21484 Acidic Leucine-Rich Nuclear Phosphoprotein 32 Family Member C False True False +NCIT:C21484 Putative Uncharacterized Protein ANP32CP False True False NCIT:C21485 Acidic Leucine-Rich Nuclear Phosphoprotein 32 Family Member D False True False NCIT:C21486 Amyloid Protein-Binding Protein 2 False True False NCIT:C21487 GTP-Binding Protein Di-Ras3 False True False @@ -117048,7 +121012,7 @@ NCIT:C2481 Cetrorelix False True False NCIT:C24810 SHH Gene False True False NCIT:C24811 SIRPB1 Gene False True False NCIT:C24812 SKIL Gene False True False -NCIT:C24813 SKIV2L Gene False True False +NCIT:C24813 SKIC2 Gene False True False NCIT:C24814 SKP2 Gene False True False NCIT:C24815 SLC26A3 Gene False True False NCIT:C24816 SHC2 Gene False True False @@ -117888,7 +121852,7 @@ NCIT:C25606 Palpable False True False NCIT:C25607 Parametrial False True False NCIT:C25608 Participation False True False NCIT:C25609 Past False True False -NCIT:C2561 T-cell Receptor Excision Circle False True False +NCIT:C2561 T-Cell Receptor Excision Circle False True False NCIT:C25610 Pathologic False True False NCIT:C25611 Pectoral False True False NCIT:C25612 Penetration False True False @@ -118533,7 +122497,7 @@ NCIT:C2632 Annamycin False True False NCIT:C26320 Caribbean False True False NCIT:C26321 Leukemia Inhibitory Factor Receptor False True False NCIT:C26322 Growth/Differentiation Factor 5 False True False -NCIT:C26324 Non-Neoplastic Hematologic and Lymphocytic Disorder False True False +NCIT:C26324 Non-Neoplastic Hematopoietic and Lymphoid Cell Disorder False True False NCIT:C26326 Non-Neoplastic Connective and Soft Tissue Disorder False True False NCIT:C26327 Protein-Lysine 6-Oxidase False True False NCIT:C26328 Growth/Differentiation Factor 8 False True False @@ -120925,7 +124889,7 @@ NCIT:C29830 Putative Hydrolase RBBP9 False True False NCIT:C29831 Retinoblastoma-Like Protein 2 False True False NCIT:C29832 RNA-Binding Protein 5 False True False NCIT:C29833 RNA-Binding Protein 6 False True False -NCIT:C29834 RING Box Protein 1 False True False +NCIT:C29834 E3 Ubiquitin-Protein Ligase RBX1 False True False NCIT:C29835 Reticulocalbin-2 False True False NCIT:C29836 DNA Topology Regulation False True False NCIT:C29837 Zinc-Finger Protein RFP False True False @@ -121061,7 +125025,7 @@ NCIT:C29968 16p13.13-p13.12 False True False NCIT:C29969 Signal-Regulatory Protein Beta-1 False True False NCIT:C2997 Dyspareunia False True False NCIT:C29970 SKI-Like Protein False True False -NCIT:C29971 Helicase SKI2W False True False +NCIT:C29971 Superkiller Complex Protein 2 False True False NCIT:C29972 S-Phase Kinase-Associated Protein 2 False True False NCIT:C29973 PUVA Photochemotherapy False True False NCIT:C29974 Sodium Chloride False True False @@ -121069,7 +125033,7 @@ NCIT:C29977 Chloride Anion Exchanger False True False NCIT:C29978 SHC-Transforming Protein 2 False True False NCIT:C29979 Antileukoproteinase False True False NCIT:C2998 Dyspnea False True False -NCIT:C29980 Smoothened Homolog False True False +NCIT:C29980 Protein Smoothened False True False NCIT:C29981 Ibritumomab Tiuxetan False True False NCIT:C29982 ALVAC-CEA (6D)-B7.1 Vaccine False True False NCIT:C29983 Anti-MUC-1 Monoclonal Antibody False True False @@ -121236,7 +125200,7 @@ NCIT:C30175 Histone-Lysine N-Methyltransferase EZH2 False True False NCIT:C30176 Fatty Acid-Binding Protein, Epidermal False True False NCIT:C3018 Sebaceous Cyst False True False NCIT:C302 Benzene False True False -NCIT:C3023 Petit Mal Epilepsy False True False +NCIT:C3023 Absence Epilepsy False True False NCIT:C3026 Esophageal Cyst False True False NCIT:C303 Betamethasone False True False NCIT:C3036 Fatigue False True False @@ -126091,7 +130055,7 @@ NCIT:C37915 Auditory False True False NCIT:C37916 Autoimmune False True False NCIT:C37917 Average False True False NCIT:C37918 Bicarbonate Ion False True False -NCIT:C37919 Blur False True False +NCIT:C37919 Blurry False True False NCIT:C37920 Bradycardia False True False NCIT:C37921 Bruise False True False NCIT:C37922 Callback False True False @@ -126364,7 +130328,7 @@ NCIT:C38231 Intracavitary Route of Administration False True False NCIT:C38232 Intracerebral Route of Administration False True False NCIT:C38233 Intracisternal Route of Administration False True False NCIT:C38234 Intracorneal Route of Administration False True False -NCIT:C38235 Intracorporus Cavernosum Route of Administration False True False +NCIT:C38235 Intracorpus Cavernosum Route of Administration False True False NCIT:C38236 Intracranial Route of Administration False True False NCIT:C38238 Intradermal Route of Administration False True False NCIT:C38239 Intradiscal Route of Administration False True False @@ -127584,7 +131548,7 @@ NCIT:C39507 Reporting Period for Cancer Center Support Grant False True False NCIT:C39508 Robert H. Lurie Comprehensive Cancer Center False True False NCIT:C39509 Roswell Park Cancer Institute False True False NCIT:C3951 Leukoplakia of Lip False True False -NCIT:C39510 Saint Jude Children's Research Hospital False True False +NCIT:C39510 St. Jude Children's Research Hospital False True False NCIT:C39511 Cancer Therapy and Research Center False True False NCIT:C39512 Secretarial and Word Processing Shared Resource False True False NCIT:C39513 Shared Resource Cancer Center False True False @@ -130122,7 +134086,7 @@ NCIT:C43233 Drug Package False True False NCIT:C43234 Not Reported False True False NCIT:C43236 WAS Gene False True False NCIT:C43237 Xp11.4-p11.21 False True False -NCIT:C43238 Wiskott-Aldrich Syndrome Protein False True False +NCIT:C43238 Actin Nucleation-Promoting Factor WAS False True False NCIT:C43239 PNP Gene False True False NCIT:C43241 Purine Nucleoside Phosphorylase False True False NCIT:C43242 Pharmaceutical Product Characteristics False True False @@ -130131,11 +134095,10 @@ NCIT:C43245 Pyramidal Tract Dysfunction False True False NCIT:C43246 Mass False True False NCIT:C43247 Babinski Sign False True False NCIT:C43248 Hyperreflexia False True False -NCIT:C43249 Mature Tissue Histiocyte False True False NCIT:C43251 Histiocytic and Dendritic Cell False True False NCIT:C43253 Neoplastic Histiocytic and Dendritic Cell False True False -NCIT:C43255 Large Malignant Histiocyte False True False -NCIT:C43256 Large Multinucleated Malignant Histiocyte False True False +NCIT:C43255 Malignant Large Histiocyte False True False +NCIT:C43256 Malignant Large Multinucleated Histiocyte False True False NCIT:C43257 Unifocal Disease False True False NCIT:C43258 Multifocal Unisystem Disease False True False NCIT:C43259 Multifocal Multisystem Disease False True False @@ -132431,8 +136394,8 @@ NCIT:C46110 Female Gender False True False NCIT:C46112 Male Phenotype False True False NCIT:C46113 Female Phenotype False True False NCIT:C46117 Transsexual False True False -NCIT:C46120 Male-to-Female Transsexual False True False -NCIT:C46121 Female-to-Male Transsexual False True False +NCIT:C46120 Transgender Woman False True False +NCIT:C46121 Transgender Man False True False NCIT:C46126 Ordinal Position False True False NCIT:C46128 Capsular Invasion False True False NCIT:C462 Echinomycin False True False @@ -133330,7 +137293,7 @@ NCIT:C48366 Lossy Compression False True False NCIT:C48367 Pixel False True False NCIT:C48368 Adenovector Encoding MDA7 False True False NCIT:C48369 Multikinase Inhibitor AEE788 False True False -NCIT:C4837 Dysplasia of Vocal Cord False True False +NCIT:C4837 Vocal Cord Epithelial Dysplasia False True False NCIT:C48370 Aminoflavone Prodrug AFP464 False True False NCIT:C48371 Allogeneic GM-CSF-Secreting Breast Cancer Vaccine False True False NCIT:C48372 Alpha Fetoprotein Adenoviral Vector Vaccine False True False @@ -133341,7 +137304,7 @@ NCIT:C48376 Autologous Dendritic Cell-Allogeneic Melanoma Tumor Cell Lysate Vacc NCIT:C48377 Autologous EBV-Transformed B Lymphoblastoid-Tumor Fusion Cell Vaccine False True False NCIT:C48378 Saracatinib False True False NCIT:C48379 Cediranib Maleate False True False -NCIT:C4838 Dysplasia of Larynx False True False +NCIT:C4838 Laryngeal Epithelial Dysplasia False True False NCIT:C48380 pan-HER Kinase Inhibitor AC480 False True False NCIT:C48381 Bowman-Birk Inhibitor Concentrate False True False NCIT:C48382 Bardoxolone False True False @@ -134103,7 +138066,7 @@ NCIT:C49201 Primitive Malignant Skeletal Spindle Cell False True False NCIT:C49202 Primitive Malignant Skeletal Muscle Cell False True False NCIT:C49203 Fibrovascular Septa Present False True False NCIT:C49205 NUDT1 Gene False True False -NCIT:C49206 7,8-Dihydro-8-Oxoguanine Triphosphatase False True False +NCIT:C49206 Oxidized Purine Nucleoside Triphosphate Hydrolase False True False NCIT:C49207 Bronchus Basal Lamina False True False NCIT:C49208 Bronchus Basement Membrane False True False NCIT:C49209 Bronchus Cartilage False True False @@ -134305,7 +138268,7 @@ NCIT:C49408 RAD54B wt Allele False True False NCIT:C49409 RECQL4 wt Allele False True False NCIT:C49410 RECQL5 wt Allele False True False NCIT:C49411 RECQL wt Allele False True False -NCIT:C49412 SKIV2L wt Allele False True False +NCIT:C49412 SKIC2 wt Allele False True False NCIT:C49413 WRN wt Allele False True False NCIT:C49414 HPSE wt Allele False True False NCIT:C49415 NUDT1 wt Allele False True False @@ -134906,7 +138869,6 @@ NCIT:C50033 Line Conditioner Device False True False NCIT:C50034 Load Device False True False NCIT:C50035 Lock Device False True False NCIT:C50036 Locking Sleeve Device False True False -NCIT:C50037 Logic Board Device False True False NCIT:C50038 Lower Piston Bearing Device False True False NCIT:C50039 Magazine Device False True False NCIT:C50040 Magnet Device False True False @@ -135306,7 +139268,7 @@ NCIT:C50432 Misdiagnosis False True False NCIT:C50433 Delamination False True False NCIT:C50434 Drainage False True False NCIT:C50435 Skin Wrinkling False True False -NCIT:C50436 Petit Mal Seizure False True False +NCIT:C50436 Absence Seizure False True False NCIT:C50437 Body Substance Discharge False True False NCIT:C50438 Intracranial Hemorrhage False True False NCIT:C5044 Fluid and Electrolyte Manifestation False True False @@ -135431,7 +139393,7 @@ NCIT:C50570 Follow-Up Intestinal Resection Required False True False NCIT:C50571 Foot Or Leg Hypoesthesia False True False NCIT:C50572 Foreign Body Sensation False True False NCIT:C50573 Gangrene False True False -NCIT:C50574 Grand Mal Seizure False True False +NCIT:C50574 Tonic-Clonic Seizure False True False NCIT:C50576 Hearing Impairment False True False NCIT:C50578 Heavier Menses False True False NCIT:C50579 Hematoma False True False @@ -136776,7 +140738,6 @@ NCIT:C51978 Recombinant Vaccinia-Mgp100 Vaccine False True False NCIT:C51979 Recombinant Human CD4 Immunoglobulin False True False NCIT:C51980 Product False True False NCIT:C51981 Ingredient False True False -NCIT:C51982 Implantation False True False NCIT:C51985 Oral Prosthesis False True False NCIT:C51986 Laser Lithotripsy False True False NCIT:C51987 Adjuvant Radiation Therapy False True False @@ -138700,7 +142661,7 @@ NCIT:C54014 Castrated Female False True False NCIT:C54015 Elastin Fibers Present False True False NCIT:C54016 Valve Cam Device False True False NCIT:C54017 Significant Stabilization False True False -NCIT:C54018 Amorphous, Eosinophilic, and Acellular Deposit False True False +NCIT:C54018 Amyloid Deposition False True False NCIT:C54019 Apple Green Dichromism Present in Polarized Congo-Red Stained Sections False True False NCIT:C54020 Jaw Device False True False NCIT:C54021 Knife Device False True False @@ -138820,7 +142781,6 @@ NCIT:C54142 Mutual False True False NCIT:C54144 Employer False True False NCIT:C54145 Mixture of Germ Cell Neoplastic Components Present False True False NCIT:C54146 Clinical Resource Contractor False True False -NCIT:C54147 Correctional Institute False True False NCIT:C54148 Contract Research Organization False True False NCIT:C54149 Drug Company False True False NCIT:C5415 Multiple Spinal Meningeal Cysts False True False @@ -138971,7 +142931,7 @@ NCIT:C54321 CRYBG1 wt Allele False True False NCIT:C54322 IRAG1 wt Allele False True False NCIT:C54324 AIM2 wt Allele False True False NCIT:C54325 ANP32B wt Allele False True False -NCIT:C54326 ANP32C wt Allele False True False +NCIT:C54326 ANP32CP wt Allele False True False NCIT:C54327 MSC wt Allele False True False NCIT:C54328 ANP32D wt Allele False True False NCIT:C54329 MSLN wt Allele False True False @@ -144306,6 +148266,7 @@ NCIT:C59706 Grade 4 External Ear Infection Documented Clinically or Microbiologi NCIT:C59707 Grade 4 External Ear Infection with Normal Absolute Neutrophil Count or Grade 1 or 2 Neutrophils, CTCAE False True False NCIT:C59708 Grade 4 External Ear Infection with Unknown Absolute Neutrophil Count, CTCAE False True False NCIT:C59709 Grade 4 Eye Infection NOS Documented Clinically or Microbiologically with Grade 3 or 4 Neutrophils, CTCAE False True False +NCIT:C5971 Ear Polyp False True False NCIT:C59710 Grade 4 Eye Infection NOS with Normal Absolute Neutrophil Count or Grade 1 or 2 Neutrophils, CTCAE False True False NCIT:C59711 Grade 4 Eye Infection NOS with Unknown Absolute Neutrophil Count, CTCAE False True False NCIT:C59712 Grade 4 Fallopian Tube Infection Documented Clinically or Microbiologically with Grade 3 or 4 Neutrophils, CTCAE False True False @@ -145690,9 +149651,7 @@ NCIT:C61395 R On T Phenomenon by ECG Finding False True False NCIT:C61396 Polyvesicular Vitelline Pattern False True False NCIT:C61397 Science False True False NCIT:C61398 Radiation Exposure False True False -NCIT:C61399 Radiation Underexposure False True False NCIT:C614 Lidocaine False True False -NCIT:C61400 Radiation Overexposure False True False NCIT:C61401 Unintended Radiation Exposure False True False NCIT:C61402 Computer Hardware Device False True False NCIT:C61403 Dialysate Concentrate Device False True False @@ -145740,7 +149699,7 @@ NCIT:C61447 Retiform Structures Comprise 90% or More of the Tumor False True Fal NCIT:C61448 Retiform Structures Comprise More than 10% and Less than 90% of the Tumor False True False NCIT:C61449 Ovarian Hilus False True False NCIT:C61450 Neoplastic Sex Cord-Stromal Cell Resembling Steroid Hormone-Secreting Cell False True False -NCIT:C61451 Small Lesion False True False +NCIT:C61451 Skin Lesion Less Than 15 mm False True False NCIT:C61452 Annular Tubules Present False True False NCIT:C61453 Cardiomegaly False True False NCIT:C61454 Basilar Rales False True False @@ -146608,7 +150567,7 @@ NCIT:C62348 Nanoscale Mechanism False True False NCIT:C62349 Nanoparticle Surface Characteristic False True False NCIT:C62350 Nanoparticle Topology False True False NCIT:C62351 Physical Composition False True False -NCIT:C62352 Purity False True False +NCIT:C62352 Purity Assessment False True False NCIT:C62353 Stalk False True False NCIT:C62354 Zeta Potential False True False NCIT:C62355 With False True False @@ -147545,8 +151504,8 @@ NCIT:C63374 Citrate False True False NCIT:C63375 Acid-Citrate-Dextrose False True False NCIT:C63376 chlVPP Regimen False True False NCIT:C63377 ESHAP Regimen False True False -NCIT:C63379 CAE Regimen False True False -NCIT:C63380 CAV Regimen False True False +NCIT:C63379 CDE Regimen False True False +NCIT:C63380 Cyclophosphamide/Doxorubicin/Vincristine Regimen False True False NCIT:C63381 Carboplatin/Etoposide Regimen False True False NCIT:C63382 EP Regimen False True False NCIT:C63383 Cisplatin/Irinotecan Regimen False True False @@ -147560,7 +151519,7 @@ NCIT:C63390 Vapor False True False NCIT:C63391 Slurry False True False NCIT:C63392 Cryobath False True False NCIT:C63393 Cryostat False True False -NCIT:C63394 Melting Point False True False +NCIT:C63394 Melting Point Determination False True False NCIT:C63395 FAM Regimen False True False NCIT:C63396 FAMTX Regimen False True False NCIT:C63397 FUP Regimen False True False @@ -147624,7 +151583,6 @@ NCIT:C63465 R-ICE Regimen False True False NCIT:C63466 Rituximab/Thalidomide Regimen False True False NCIT:C63467 Regimen Used to Treat Bladder Carcinoma False True False NCIT:C63468 Regimen Used to Treat Prostate Carcinoma False True False -NCIT:C63469 CDE Regimen False True False NCIT:C63470 Regimen Used to Treat Malignant Brain Neoplasm False True False NCIT:C63471 Cancel False True False NCIT:C63472 HyperCVAD Alternating with High-dose MTX AraC Regimen False True False @@ -147856,7 +151814,7 @@ NCIT:C63718 Dental Implant False True False NCIT:C63719 Regimen Used to Treat Esophageal Carcinoma False True False NCIT:C63720 Denture False True False NCIT:C63723 Periradicular False True False -NCIT:C63724 CAP Regimen False True False +NCIT:C63724 CISCA Regimen False True False NCIT:C63726 TIC Regimen False True False NCIT:C63727 PFL Regimen False True False NCIT:C63729 BV Regimen False True False @@ -148024,7 +151982,6 @@ NCIT:C64186 Allylisopropylacetamide False True False NCIT:C64187 Juvenile Hormone III False True False NCIT:C64188 Chaetomellic Acid A Disodium False True False NCIT:C64189 N-Desmethyltamoxifen False True False -NCIT:C64190 CISCA Regimen False True False NCIT:C64191 IFL-FOLFIRI Regimen False True False NCIT:C64192 Waist False True False NCIT:C64193 Hip False True False @@ -148718,7 +152675,7 @@ NCIT:C64968 Sunday False True False NCIT:C64969 Therapeutic Thoracoscopy False True False NCIT:C64970 Therapeutic Videothoracoscopy False True False NCIT:C64971 Therapeutic Bronchoscopy False True False -NCIT:C64973 Administration via Gastro-Intestinal Stoma False True False +NCIT:C64973 Gastrointestinal Stoma Route of Administration False True False NCIT:C64974 Give False True False NCIT:C64975 Good False True False NCIT:C64976 Cardiovascular Complications Management False True False @@ -150823,8 +154780,7 @@ NCIT:C67220 Percent of Total Hemoglobin False True False NCIT:C67226 Software Development False True False NCIT:C67227 Software Maintenance False True False NCIT:C67229 Regimen Used to Treat Ewing's Family of Tumors False True False -NCIT:C67231 VAdriaC Regimen False True False -NCIT:C67232 VAdriaC Alternating with IE Regimen False True False +NCIT:C67232 Cyclophosphamide/Doxorubicin/Vincristine Alternating with IE Regimen False True False NCIT:C67233 Cyclophosphamide/Topotecan Regimen False True False NCIT:C67234 Thousand False True False NCIT:C67236 Phosphaturia False True False @@ -153615,7 +157571,7 @@ NCIT:C71945 Brown Sugar False True False NCIT:C71946 Popcorn False True False NCIT:C71947 Whey False True False NCIT:C71948 Mutton False True False -NCIT:C71949 Mushroom False True False +NCIT:C71949 Mushroom Extract False True False NCIT:C71950 Lima Bean False True False NCIT:C71951 String Bean False True False NCIT:C71952 Fruit Juice False True False @@ -156106,7 +160062,7 @@ NCIT:C74457 CDISC SDTM Race Terminology False True False NCIT:C74458 Almond False True False NCIT:C74460 NPC1L1 Gene False True False NCIT:C74461 NPC1L1 wt Allele False True False -NCIT:C74462 Niemann-Pick C1-Like Protein 1 False True False +NCIT:C74462 NPC1-Like Intracellular Cholesterol Transporter 1 False True False NCIT:C74463 Aloe ferox False True False NCIT:C74464 Cardamom False True False NCIT:C74465 MMADHC Gene False True False @@ -158726,7 +162682,6 @@ NCIT:C77182 Aspergillus fumigatus False True False NCIT:C77183 Aspergillus brasiliensis False True False NCIT:C77184 Cryptococcus False True False NCIT:C77185 Fusarium False True False -NCIT:C77186 Ajellomyces capsulatus False True False NCIT:C77187 Bordetella pertussis Antigen, A False True False NCIT:C77188 Cefprozil Anhydrous, (E)- False True False NCIT:C77189 Cefprozil, (E)- False True False @@ -161305,7 +165260,7 @@ NCIT:C80123 Acacia False True False NCIT:C80124 Gadoterate Meglumine False True False NCIT:C80125 Aminopentamide Hydrochloride False True False NCIT:C80126 Azalanstat Dihydrochloride False True False -NCIT:C80127 Merkel Cell Polyomavirus Infection False True False +NCIT:C80127 Merkel Cell Polyoma Virus Infection False True False NCIT:C80129 Iodohippurate Sodium I-125 False True False NCIT:C80130 Lactic Acid, DL- False True False NCIT:C80131 Polyethylene Glycol 3350 False True False @@ -162070,7 +166025,7 @@ NCIT:C80932 Guar Gum False True False NCIT:C80933 Hydroxyethylpiperazine Ethane Sulfonic Acid False True False NCIT:C80934 Myristyl Alcohol False True False NCIT:C80935 Octoxynol 9 False True False -NCIT:C80936 Poloxamer 188 False True False +NCIT:C80936 Vepoloxamer False True False NCIT:C80937 Polysorbate 20 False True False NCIT:C80938 Potassium Bicarbonate False True False NCIT:C80939 Potassium Bitartrate False True False @@ -164761,7 +168716,6 @@ NCIT:C83716 Ferumoxides Non-Stoichiometric Magnetite False True False NCIT:C83717 Filibuvir False True False NCIT:C83718 Flunarizine False True False NCIT:C83719 Formic Acid False True False -NCIT:C8372 Hamartomatous Polyp False True False NCIT:C83720 Fosamprenavir False True False NCIT:C83721 Fosbretabulin Tromethamine False True False NCIT:C83722 Fosfonet Sodium Anhydrous False True False @@ -165353,7 +169307,7 @@ NCIT:C84319 BLAST Raw Score False True False NCIT:C84320 BLAST E-Value False True False NCIT:C84321 CD38 Gene False True False NCIT:C84322 CD38 wt Allele False True False -NCIT:C84323 ADP-Ribosyl Cyclase 1 False True False +NCIT:C84323 ADP-Ribosyl Cyclase/Cyclic ADP-Ribose Hydrolase 1 False True False NCIT:C84324 CFD Gene False True False NCIT:C84325 CFD wt Allele False True False NCIT:C84326 Complement Factor D False True False @@ -168570,7 +172524,7 @@ NCIT:C88268 Agaricus blazei Murill Extract False True False NCIT:C88269 High-Selenium Baker's Yeast False True False NCIT:C88270 Omipalisib False True False NCIT:C88271 PDK1 Inhibitor AR-12 False True False -NCIT:C88272 FGFR Inhibitor AZD4547 False True False +NCIT:C88272 Fexagratinib False True False NCIT:C88274 Smac Mimetic GDC-0152 False True False NCIT:C88275 THL-P False True False NCIT:C88276 Technetium Tc-99m Demobesin-4 False True False @@ -169221,7 +173175,7 @@ NCIT:C88939 Lip and Oral Cavity Cancer Pathologic TNM Finding v7 False True Fals NCIT:C88940 Lip and Oral Cavity Cancer Pathologic Primary Tumor TNM Finding v7 False True False NCIT:C88941 MYCBP2 Gene False True False NCIT:C88942 MYCBP2 wt Allele False True False -NCIT:C88943 Probable E3 Ubiquitin-Protein Ligase MYCBP2 False True False +NCIT:C88943 E3 Ubiquitin-Protein Ligase MYCBP2 False True False NCIT:C88944 SNED1 Gene False True False NCIT:C88945 SNED1 wt Allele False True False NCIT:C88946 Sushi, Nidogen and EGF-Like Domain-Containing Protein 1 False True False @@ -171377,7 +175331,7 @@ NCIT:C91264 LMO1 wt Allele False True False NCIT:C91265 Rhombotin-1 False True False NCIT:C91266 TRIP12 Gene False True False NCIT:C91267 TRIP12 wt Allele False True False -NCIT:C91268 Probable E3 Ubiquitin-Protein Ligase TRIP12 False True False +NCIT:C91268 E3 Ubiquitin-Protein Ligase TRIP12 False True False NCIT:C91269 LIG1 Gene False True False NCIT:C91270 LIG1 wt Allele False True False NCIT:C91271 Dynamic Extension False True False @@ -171443,7 +175397,7 @@ NCIT:C91330 Feeding Amino Groups into the Urea Cycle False True False NCIT:C91331 Transcriptional Repression by DNA Methylation Pathway False True False NCIT:C91332 F5 Gene False True False NCIT:C91333 F5 wt Allele False True False -NCIT:C91334 F5 Leiden Allele False True False +NCIT:C91334 F5 NM_000130.4:c.1601G>A False True False NCIT:C91335 Coagulation Factor V False True False NCIT:C91336 MAGEA11 Gene False True False NCIT:C91337 MAGEA11 wt Allele False True False @@ -172128,7 +176082,7 @@ NCIT:C92015 Device Tissue Engineering Evaluation Method False True False NCIT:C92016 Device to Device Interaction Testing Evaluation Method False True False NCIT:C92017 Device to Human Interaction Testing Evaluation Method False True False NCIT:C92018 Device Ultrasonic Sound Testing Evaluation Method False True False -NCIT:C92019 Device Unit Testing Evaluation Method False True False +NCIT:C92019 Device Unit Testing False True False NCIT:C92020 Device Use Testing Evaluation Method False True False NCIT:C92021 Device User Survey Evaluation Method False True False NCIT:C92022 Device Vibration Testing Evaluation Method False True False @@ -172298,7 +176252,6 @@ NCIT:C92199 Mental Disorder Due to a General Medical Condition False True False NCIT:C922 Uridine False True False NCIT:C92201 Schizophrenia and Other Psychotic Disorders False True False NCIT:C92205 Trail Making Test False True False -NCIT:C92206 Short Limb Dwarfism-Saddle Nose-Spinal Alterations-Metaphyseal Striation Syndrome False True False NCIT:C92207 Stage Unknown False True False NCIT:C92208 Extraperitoneal Space False True False NCIT:C92209 Intercept False True False @@ -173123,7 +177076,7 @@ NCIT:C93064 CD276 wt Allele False True False NCIT:C93065 Nephrologist False True False NCIT:C93066 CD276 Antigen False True False NCIT:C93067 Anesthesiologist False True False -NCIT:C93068 Physical Medicine Specialist False True False +NCIT:C93068 Physiatrist False True False NCIT:C93069 CUL4B Gene False True False NCIT:C9307 Lymphadenopathy with Polyclonal Hypergammaglobulinemia False True False NCIT:C93070 CUL4B wt Allele False True False @@ -176702,7 +180655,7 @@ NCIT:C96755 Solabegron Hydrochloride False True False NCIT:C96757 Onercept False True False NCIT:C9676 Chlorambucil/Dactinomycin/Methotrexate False True False NCIT:C96762 Baminercept Alfa False True False -NCIT:C96763 HNF1A Gene Mutation False True False +NCIT:C96763 Inactivating HNF1A Gene Mutation False True False NCIT:C96764 Valomaciclovir False True False NCIT:C96766 Aminacrine Pyruvate False True False NCIT:C96769 Aminacrine Undecylate False True False @@ -176941,7 +180894,7 @@ NCIT:C97068 Adult Extramedullary Hematopoiesis False True False NCIT:C9707 Cyclophosphamide/Etoposide/Vincristine False True False NCIT:C97070 Intrahepatic Biliary Atresia False True False NCIT:C97072 Ductal Plate Malformation False True False -NCIT:C97078 Benign Lymphoid Hyperplasia False True False +NCIT:C97078 Reactive Lymphoid Hyperplasia False True False NCIT:C97079 Bronchial Epithelial Hyperplasia False True False NCIT:C9708 Mitoxantrone/Prednisone/Procarbazine/Vincristine False True False NCIT:C97080 Denture-Induced Fibrous Hyperplasia False True False @@ -176988,7 +180941,7 @@ NCIT:C97127 Vi Capsular Polysaccharide Typhoid Vaccine False True False NCIT:C97128 Acute Rejection False True False NCIT:C97129 Pedunculate False True False NCIT:C9713 Cyclophosphamide/Etoposide Regimen False True False -NCIT:C97130 Radiosensitizer RRx-001 False True False +NCIT:C97130 Nibrozetone False True False NCIT:C97131 5-Fluorouracil/Salicylic Acid Topical Solution False True False NCIT:C97133 Topical Wound Spray HP802-247 False True False NCIT:C97134 Fluorine F 18 CP18 Peptide False True False @@ -180190,7 +184143,7 @@ NCIT:C186279 Canine Cutaneous T-Cell Lymphoma True False False NCIT:C188051 Malignant Pylorus Neoplasm True False False NCIT:C189247 SMARCB1-Deficient Kidney Medullary Carcinoma True False False NCIT:C25765 Secondary Acute Myeloid Leukemia True False False -NCIT:C26323 Hematologic and Lymphocytic Disorder True False False +NCIT:C26323 Hematopoietic and Lymphoid Cell Disorder True False False NCIT:C26684 Radiation-Induced Disorder True False False NCIT:C26690 Adrenal Gland Disorder True False False NCIT:C26695 Anal Disorder True False False @@ -180255,7 +184208,7 @@ NCIT:C27065 Middle Ear Disorder True False False NCIT:C27067 Endocrine Pancreas Disorder True False False NCIT:C27080 Refractory Anemia with Excess Blasts in Transformation True False False NCIT:C27081 Juvenile Pilocytic Astrocytoma True False False -NCIT:C27084 Spindle Cell Squamous Cell Carcinoma True False False +NCIT:C27084 Spindle Cell Squamous Carcinoma True False False NCIT:C27087 Verruca Vulgaris True False False NCIT:C27091 Malignant Spindle Cell Neoplasm True False False NCIT:C27093 Stage 0 Squamous Cell Carcinoma True False False @@ -180345,7 +184298,7 @@ NCIT:C27471 Peripheral Primitive Neuroectodermal Tumor of Soft Tissues True Fals NCIT:C27472 Proximal-Type Epithelioid Sarcoma True False False NCIT:C27473 Distal-Type Epithelioid Sarcoma True False False NCIT:C27474 Non-Muscle Invasive Bladder Carcinoma True False False -NCIT:C27479 Nasopharyngeal Angiofibroma True False False +NCIT:C27479 Sinonasal Tract Angiofibroma True False False NCIT:C27481 Mesenchymal Extraskeletal Chondrosarcoma True False False NCIT:C27483 Lipoblastoma True False False NCIT:C27485 Liver Angiomyolipoma True False False @@ -180364,7 +184317,7 @@ NCIT:C27507 Hemangioma of Peripheral Nerve True False False NCIT:C27509 Skin Lymphangioma True False False NCIT:C27510 Kaposiform Hemangioendothelioma True False False NCIT:C27511 Retiform Hemangioendothelioma True False False -NCIT:C27514 Adult Xanthogranuloma True False False +NCIT:C27514 Cutaneous Adult Xanthogranuloma True False False NCIT:C27516 Epidermolytic Acanthoma True False False NCIT:C27517 Acantholytic Acanthoma True False False NCIT:C27518 Large Cell Acanthoma True False False @@ -180378,7 +184331,7 @@ NCIT:C27539 Skin Infiltrating Basal Cell Carcinoma True False False NCIT:C27540 Skin Infundibulocystic Basal Cell Carcinoma True False False NCIT:C27541 Skin Micronodular Basal Cell Carcinoma True False False NCIT:C27542 Skin Pseudovascular Squamous Cell Carcinoma True False False -NCIT:C27543 Skin Basaloid Carcinoma True False False +NCIT:C27543 Skin Basaloid Squamous Cell Carcinoma True False False NCIT:C27548 Melanoacanthoma True False False NCIT:C27571 Head and Neck Disorder True False False NCIT:C27580 Peripheral Nervous System Disorder True False False @@ -180400,7 +184353,7 @@ NCIT:C27721 Digestive System Neuroendocrine Neoplasm True False False NCIT:C27729 Thyroid Gland Well-Differentiated Tumor of Uncertain Malignant Potential True False False NCIT:C27730 Childhood Kidney Wilms Tumor True False False NCIT:C27735 Colorectal Gastrointestinal Stromal Tumor True False False -NCIT:C27753 Acute Myeloid Leukemia Not Otherwise Specified True False False +NCIT:C27753 Acute Myeloid Leukemia, Not Otherwise Specified True False False NCIT:C27777 Giant Hemangioma True False False NCIT:C27779 Lymphohistiocytoid Mesothelioma True False False NCIT:C27781 Myxoid Liposarcoma True False False @@ -180423,7 +184376,6 @@ NCIT:C27885 Invasive Bladder Urothelial Carcinoma True False False NCIT:C27888 Classic Variant of Chromophobe Renal Cell Carcinoma True False False NCIT:C27889 Eosinophilic Variant of Chromophobe Renal Cell Carcinoma True False False NCIT:C27891 TFE3-Rearranged Renal Cell Carcinoma True False False -NCIT:C27892 Unclassified Renal Cell Carcinoma True False False NCIT:C27893 Sarcomatoid Renal Cell Carcinoma True False False NCIT:C27904 Retroperitoneal Leiomyosarcoma True False False NCIT:C27907 B-Cell Neoplasm True False False @@ -180467,7 +184419,6 @@ NCIT:C2906 Skin Squamous Cell Carcinoma In Situ True False False NCIT:C2907 Brain Neoplasm True False False NCIT:C2910 Breast Neoplasm True False False NCIT:C2912 Burkitt Lymphoma True False False -NCIT:C2915 Carcinoid Tumor True False False NCIT:C2916 Carcinoma True False False NCIT:C2917 Carcinoma In Situ True False False NCIT:C2918 Female Breast Carcinoma True False False @@ -180716,7 +184667,7 @@ NCIT:C3434 Uterine Corpus Leiomyoma True False False NCIT:C3435 Uterine Neoplasm True False False NCIT:C3436 Uveal Neoplasm True False False NCIT:C3437 Vaginal Neoplasm True False False -NCIT:C34417 Benign Neoplasm of Lower Jaw Bone True False False +NCIT:C34417 Benign Neoplasm of Mandible True False False NCIT:C3443 Vulvar Neoplasm True False False NCIT:C34433 Bone Marrow Disorder True False False NCIT:C34447 Head and Neck Squamous Cell Carcinoma True False False @@ -180762,7 +184713,7 @@ NCIT:C3513 Esophageal Carcinoma True False False NCIT:C3516 Aneurysmal Bone Cyst True False False NCIT:C3517 Mixed Cellularity Classic Hodgkin Lymphoma True False False NCIT:C35177 Malignant Uvula Neoplasm True False False -NCIT:C35178 Malignant Neoplasm of Lower Jaw Bone True False False +NCIT:C35178 Malignant Neoplasm of Mandible True False False NCIT:C3518 Nodular Sclerosis Classic Hodgkin Lymphoma True False False NCIT:C3519 Atypical Chronic Myeloid Leukemia True False False NCIT:C3520 Myeloid Sarcoma True False False @@ -180841,12 +184792,12 @@ NCIT:C3576 Malignant Thoracic Neoplasm True False False NCIT:C35765 Histiocytoma True False False NCIT:C35775 Ciliary Body Disorder True False False NCIT:C35780 Uveal Epithelioid Cell Melanoma True False False -NCIT:C35781 Uveal Mixed Cell Melanoma True False False -NCIT:C35782 Choroid Mixed Cell Melanoma True False False -NCIT:C35783 Ciliary Body Mixed Cell Melanoma True False False +NCIT:C35781 Uveal Mixed Epithelioid and Spindle Cell Melanoma True False False +NCIT:C35782 Choroid Mixed Epithelioid and Spindle Cell Melanoma True False False +NCIT:C35783 Ciliary Body Mixed Epithelioid and Spindle Cell Melanoma True False False NCIT:C35794 Pagetoid Reticulosis True False False NCIT:C35812 Malignant Lymph Node Neoplasm True False False -NCIT:C35813 Hematopoietic and Lymphoid System Neoplasm True False False +NCIT:C35813 Hematopoietic and Lymphatic System Neoplasm True False False NCIT:C35815 Granulocytic Sarcoma True False False NCIT:C35823 Splenic Disorder True False False NCIT:C35830 Columnar Cell Variant Thyroid Gland Papillary Carcinoma True False False @@ -181305,7 +185256,7 @@ NCIT:C40181 Uterine Corpus Mixed Epithelial and Mesenchymal Neoplasm True False NCIT:C40182 Uterine Corpus Carcinofibroma True False False NCIT:C40187 Cervical Keratinizing Squamous Cell Carcinoma True False False NCIT:C40188 Cervical Non-Keratinizing Squamous Cell Carcinoma True False False -NCIT:C40189 Cervical Basaloid Carcinoma True False False +NCIT:C40189 Cervical Basaloid Squamous Cell Carcinoma True False False NCIT:C40190 Cervical Verrucous Carcinoma True False False NCIT:C40193 Cervical Lymphoepithelioma-Like Carcinoma True False False NCIT:C4020 Fibroblastic Osteosarcoma True False False @@ -181360,7 +185311,7 @@ NCIT:C40280 Benign Vaginal Mixed Tumor True False False NCIT:C40283 Vulvar Squamous Neoplasm True False False NCIT:C40284 Vulvar Keratinizing Squamous Cell Carcinoma True False False NCIT:C40285 Vulvar Non-Keratinizing Squamous Cell Carcinoma True False False -NCIT:C40286 Vulvar Basaloid Carcinoma True False False +NCIT:C40286 Vulvar Basaloid Squamous Cell Carcinoma True False False NCIT:C4029 Cervical Adenocarcinoma True False False NCIT:C40290 Vulvar Squamous Papillomatosis True False False NCIT:C40291 Vulvar Inverted Follicular Keratosis True False False @@ -181374,7 +185325,7 @@ NCIT:C40299 Bartholin Gland Adenoma True False False NCIT:C4030 Urothelial Carcinoma True False False NCIT:C40300 Bartholin Gland Adenomyoma True False False NCIT:C40301 Adenoma of Minor Vestibular Glands True False False -NCIT:C40302 Vulvar Chondroid Syringoma True False False +NCIT:C40302 Benign Mixed Tumor of the Vulva True False False NCIT:C40305 Vulvar Eccrine Adenocarcinoma True False False NCIT:C40306 Vulvar Porocarcinoma True False False NCIT:C40307 Vulvar Clear Cell Hidradenocarcinoma True False False @@ -181384,7 +185335,7 @@ NCIT:C4031 Bladder Squamous Cell Carcinoma True False False NCIT:C40310 Sebaceous Carcinoma True False False NCIT:C40311 Vulvar Syringoma True False False NCIT:C40312 Vulvar Nodular Hidradenoma True False False -NCIT:C40314 Vulvar Trichoepithelioma True False False +NCIT:C40314 Vulvar Trichoblastoma True False False NCIT:C40315 Pilomyxoid Astrocytoma True False False NCIT:C40317 Vulvar Sarcoma True False False NCIT:C40318 Vulvar Leiomyosarcoma True False False @@ -181414,7 +185365,7 @@ NCIT:C40368 Glycogen-Rich, Clear Cell Breast Carcinoma True False False NCIT:C40369 Breast Sebaceous Carcinoma True False False NCIT:C40370 Synchronous Bilateral Breast Carcinoma True False False NCIT:C40375 Breast Diffuse Large B-Cell Lymphoma True False False -NCIT:C4038 Lung Carcinoid Tumor True False False +NCIT:C4038 Lung Neuroendocrine Tumor True False False NCIT:C40381 Breast Angiomatosis True False False NCIT:C40382 Breast Adenoma True False False NCIT:C40383 Breast Apocrine Adenoma True False False @@ -181525,7 +185476,6 @@ NCIT:C4169 Apocrine Carcinoma True False False NCIT:C4170 Spiradenoma True False False NCIT:C4171 Hidradenoma Papilliferum True False False NCIT:C4172 Syringocystadenoma Papilliferum True False False -NCIT:C4173 Papillary Eccrine Adenoma True False False NCIT:C4174 Sebaceous Adenoma True False False NCIT:C4176 Ceruminous Adenocarcinoma True False False NCIT:C4179 Papillary Cystic Neoplasm True False False @@ -181553,7 +185503,7 @@ NCIT:C4222 Glomangioma True False False NCIT:C4223 Glomangiomyoma True False False NCIT:C4225 Cutaneous Nodular Melanoma True False False NCIT:C4227 Balloon Cell Melanoma True False False -NCIT:C4234 Giant Congenital Nevus True False False +NCIT:C4234 Giant Congenital Melanocytic Nevus True False False NCIT:C4236 Epithelioid Cell Melanoma True False False NCIT:C4237 Spindle Cell Melanoma True False False NCIT:C4242 Benign Soft Tissue Neoplasm True False False @@ -181623,7 +185573,6 @@ NCIT:C4334 Meningeal Sarcomatosis True False False NCIT:C43340 Eye Sebaceous Carcinoma True False False NCIT:C43345 Ductal Eccrine Adenocarcinoma True False False NCIT:C4335 Malignant Triton Tumor True False False -NCIT:C43352 Turban Tumor True False False NCIT:C43356 Syringofibroadenoma True False False NCIT:C4336 Malignant Granular Cell Tumor True False False NCIT:C4337 Mantle Cell Lymphoma True False False @@ -181655,7 +185604,6 @@ NCIT:C43606 Gallbladder Biliary Intraepithelial Neoplasia True False False NCIT:C4361 Corneal Neoplasm True False False NCIT:C4364 Ciliary Body Neoplasm True False False NCIT:C4365 Primary Retinal Non-Hodgkin Lymphoma True False False -NCIT:C4366 External Ear Polyp True False False NCIT:C4369 Nasal Vestibule Squamous Papilloma True False False NCIT:C4374 Pancreatic Cystadenoma True False False NCIT:C4380 Scrotal Neoplasm True False False @@ -181716,7 +185664,7 @@ NCIT:C4468 Pilar Sheath Acanthoma True False False NCIT:C4469 Tumor of the Follicular Infundibulum True False False NCIT:C4471 Adenoid Cystic Skin Carcinoma True False False NCIT:C4472 Skin Mucoepidermoid Carcinoma True False False -NCIT:C4474 Chondroid Syringoma True False False +NCIT:C4474 Benign Mixed Tumor of the Skin True False False NCIT:C4475 Dermal Neoplasm True False False NCIT:C4481 Cutaneous Ganglioneuroma True False False NCIT:C4482 Skin Leiomyoma True False False @@ -181852,7 +185800,7 @@ NCIT:C4621 Benign Endocrine Neoplasm True False False NCIT:C4623 Metastatic Jugulotympanic Paraganglioma True False False NCIT:C4627 Malignant Central Nervous System Neoplasm True False False NCIT:C4628 Malignant Meningeal Neoplasm True False False -NCIT:C4632 Dermoid Cyst of the Skin True False False +NCIT:C4632 Skin Dermoid Cyst True False False NCIT:C4633 Amelanotic Cutaneous Melanoma True False False NCIT:C4635 Gastric Neuroendocrine Tumor G1 True False False NCIT:C4636 Gastric Lymphoma True False False @@ -182250,7 +186198,7 @@ NCIT:C54287 Sinonasal Non-Keratinizing Squamous Cell Carcinoma True False False NCIT:C5429 Childhood Mediastinal Neurogenic Neoplasm True False False NCIT:C54293 Sinonasal Carcinoma True False False NCIT:C54294 Sinonasal Undifferentiated Carcinoma True False False -NCIT:C54295 Primary Intraosseous Squamous Cell Carcinoma True False False +NCIT:C54295 Primary Intraosseous Carcinoma, Not Otherwise Specified True False False NCIT:C54301 Calcifying Epithelial Odontogenic Tumor True False False NCIT:C5432 Intracranial Cavernous Hemangioma True False False NCIT:C5433 Cerebral Hemangioma True False False @@ -182293,9 +186241,7 @@ NCIT:C5498 Colon Mucosa-Associated Lymphoid Tissue Lymphoma True False False NCIT:C5500 Colon Lymphangioma True False False NCIT:C5501 Cecum Neuroendocrine Tumor G1 True False False NCIT:C5502 Benign Peripheral Nerve Granular Cell Tumor True False False -NCIT:C5503 Central Nervous System Hematopoietic Neoplasm True False False -NCIT:C5504 Central Nervous System Melanocytic Neoplasm True False False -NCIT:C5505 Central Nervous System Melanoma True False False +NCIT:C5503 Central Nervous System Hematopoietic and Lymphoid Cell Neoplasm True False False NCIT:C5511 Appendix Mucinous Cystadenocarcinoma True False False NCIT:C5512 Appendix Villous Adenoma True False False NCIT:C5513 Appendix Lymphoma True False False @@ -182661,7 +186607,7 @@ NCIT:C6450 Thymic Epithelial Neoplasm True False False NCIT:C6451 Thymic Lymphoma True False False NCIT:C6454 Thymoma Type A True False False NCIT:C6455 Thymic Squamous Cell Carcinoma True False False -NCIT:C6456 Thymic Basaloid Carcinoma True False False +NCIT:C6456 Thymic Basaloid Squamous Cell Carcinoma True False False NCIT:C6457 Thymic Mucoepidermoid Carcinoma True False False NCIT:C6458 Thymic Adenosquamous Carcinoma True False False NCIT:C6459 Thymic Adenocarcinoma True False False @@ -182785,7 +186731,6 @@ NCIT:C6683 Occult Lung Small Cell Carcinoma True False False NCIT:C66845 Malignant Peripheral Nerve Sheath Tumor with Perineurial Differentiation True False False NCIT:C6685 Occult Lung Large Cell Carcinoma True False False NCIT:C6686 Occult Lung Squamous Cell Carcinoma True False False -NCIT:C66903 Skin Metatypical Carcinoma True False False NCIT:C66950 Hepatoid Adenocarcinoma True False False NCIT:C66989 Ovarian Thecoma True False False NCIT:C6699 Occult Lung Adenocarcinoma True False False @@ -182853,7 +186798,7 @@ NCIT:C6810 Testicular Lymphoma True False False NCIT:C6811 Plantar Verrucous Carcinoma True False False NCIT:C6812 Mediastinal Seminoma True False False NCIT:C6814 Superficial Fibromatosis True False False -NCIT:C6834 Middle Ear Adenoma True False False +NCIT:C6834 Middle Ear Neuroendocrine Tumor True False False NCIT:C6835 Paranasal Sinus Papilloma True False False NCIT:C6836 Ethmoid Sinus Papilloma True False False NCIT:C6837 Frontal Sinus Papilloma True False False @@ -182874,7 +186819,7 @@ NCIT:C6870 Breast Solid Papillary Carcinoma True False False NCIT:C68744 Childhood Myelodysplastic Syndrome True False False NCIT:C6875 Large Cell Neuroendocrine Carcinoma True False False NCIT:C6876 Lung Large Cell Carcinoma with Rhabdoid Phenotype True False False -NCIT:C6879 Pancreatic Mixed Ductal-Neuroendocrine Carcinoma True False False +NCIT:C6879 Pancreatic Mixed Ductal Adenocarcinoma-Neuroendocrine Carcinoma True False False NCIT:C6880 Glandular Papilloma True False False NCIT:C6881 Bile Duct Intraductal Papillary Neoplasm True False False NCIT:C6882 Micropapillary Serous Carcinoma True False False @@ -182909,7 +186854,6 @@ NCIT:C6923 Acute Bilineal Leukemia True False False NCIT:C6925 Anal Margin Squamous Cell Carcinoma True False False NCIT:C6926 Stromal Sarcoma True False False NCIT:C6930 Mixed Neoplasm True False False -NCIT:C6933 Middle Ear Polyp True False False NCIT:C6934 Gangliocytoma True False False NCIT:C6935 Spinal Cord Meningioma True False False NCIT:C6938 Sweat Gland Carcinoma True False False @@ -182954,7 +186898,7 @@ NCIT:C7017 Granular Cell Tumor of the Sellar Region True False False NCIT:C7018 Nerve Sheath Myxoma True False False NCIT:C7019 Trilateral Retinoblastoma True False False NCIT:C7027 Barrett Adenocarcinoma True False False -NCIT:C7032 Esophageal Basaloid Carcinoma True False False +NCIT:C7032 Esophageal Basaloid Squamous Cell Carcinoma True False False NCIT:C7049 Adult Astrocytic Tumor True False False NCIT:C7052 Myofibroma True False False NCIT:C7053 Cavernous Hemangioma of the Face True False False @@ -183004,12 +186948,12 @@ NCIT:C71720 Primary Diffuse Large B-Cell Lymphoma of the Central Nervous System NCIT:C7173 Diffuse Astrocytoma True False False NCIT:C71732 Triple-Negative Breast Carcinoma True False False NCIT:C7175 Acute Myeloid Leukemia with Recurrent Genetic Abnormalities True False False -NCIT:C7184 Methotrexate- Associated Lymphoproliferative Disorder True False False +NCIT:C7184 Methotrexate-Associated Lymphoproliferative Disorder True False False NCIT:C7185 Lymphoma by Site True False False NCIT:C7190 Malignant Hypopharyngeal Neoplasm True False False NCIT:C7202 Malignant Histiocytosis True False False NCIT:C7203 Blastic Plasmacytoid Dendritic Cell Neoplasm True False False -NCIT:C72074 Atypical Carcinoid Tumor True False False +NCIT:C72074 Neuroendocrine Tumor G2 True False False NCIT:C7208 Small Cell Variant Anaplastic Large Cell Lymphoma True False False NCIT:C7210 Childhood T Lymphoblastic Lymphoma True False False NCIT:C7217 Primary Cutaneous Follicle Center Lymphoma True False False @@ -183210,7 +187154,7 @@ NCIT:C7904 Invasive Malignant Thymoma True False False NCIT:C7913 Ocular Melanoma with Extraocular Extension True False False NCIT:C7915 Thyrotroph Pituitary Neuroendocrine Tumor True False False NCIT:C7925 Adult Extraskeletal Osteosarcoma True False False -NCIT:C7927 Liver and Intrahepatic Bile Duct Carcinoma True False False +NCIT:C7927 Liver Carcinoma True False False NCIT:C7928 Childhood Germ Cell Tumor True False False NCIT:C7930 Lymphomatoid Granulomatosis True False False NCIT:C7942 Adult Nodular Lymphocyte Predominant B-Cell Lymphoma True False False @@ -183306,7 +187250,7 @@ NCIT:C82423 Acute Myeloid Leukemia with t(6;9)(p22.3;q34.1); DEK-NUP214 True Fal NCIT:C82431 Acute Myeloid Leukemia with NPM1 Mutation True False False NCIT:C82433 Acute Myeloid Leukemia with CEBPA Mutation True False False NCIT:C8255 Anal Canal Cloacogenic Carcinoma True False False -NCIT:C8256 Anal Basaloid Carcinoma True False False +NCIT:C8256 Anal Basaloid Squamous Cell Carcinoma True False False NCIT:C82591 Myelodysplastic Syndrome, Not Otherwise Specified with Single Lineage Dysplasia True False False NCIT:C82596 Refractory Cytopenia of Childhood True False False NCIT:C8263 Adult Acute Monocytic Leukemia True False False @@ -183591,7 +187535,7 @@ NCIT:C9347 Tracheal Carcinoma True False False NCIT:C9348 Mast Cell Sarcoma True False False NCIT:C9349 Plasmacytoma True False False NCIT:C9351 Pleural Mesothelial Neoplasm True False False -NCIT:C9356 Regional Ureter Carcinoma True False False +NCIT:C9356 Locally Advanced Ureter Carcinoma True False False NCIT:C9357 Hodgkin Lymphoma True False False NCIT:C9359 Skin Pigmented Basal Cell Carcinoma True False False NCIT:C9360 Lymphoblastic Lymphoma True False False @@ -183607,7 +187551,6 @@ NCIT:C9382 Rectal Carcinoma True False False NCIT:C9383 Rectal Adenocarcinoma True False False NCIT:C9384 Kidney Carcinoma True False False NCIT:C9385 Renal Cell Carcinoma True False False -NCIT:C9419 AJCC Grade 1 Sarcoma True False False NCIT:C9423 Combined Lung Small Cell and Squamous Cell Carcinoma True False False NCIT:C9425 Conventional Malignant Hemangiopericytoma True False False NCIT:C9426 Conventional Angiosarcoma True False False @@ -183633,7 +187576,6 @@ NCIT:C9480 Invasive Carcinoma True False False NCIT:C9482 Soft Tissue Chondroma True False False NCIT:C9496 T-Cell/Histiocyte-Rich Large B-Cell Lymphoma True False False NCIT:C9497 Melanocytic Medulloblastoma True False False -NCIT:C9499 Melanomatosis True False False NCIT:C9503 Juvenile Breast Papillomatosis True False False NCIT:C9505 Dysembryoplastic Neuroepithelial Tumor True False False NCIT:C95404 Digestive System Neuroendocrine Tumor True False False @@ -183679,18 +187621,28 @@ NCIT:C97093 Lipodystrophy True False False NCIT:C97110 Spinal Cord Disorder True False False NCIT:C98291 Gonadal Teratoma True False False NCIT:C99055 Sacrococcygeal Teratoma True False False +NCIT:C27892 Unclassified Renal Cell Carcinoma True False True +NCIT:C2915 Carcinoid Tumor True False True NCIT:C3234 Mesothelioma True False True NCIT:C34801 Male Erectile Disorder True False True +NCIT:C35439 Hemophagocytic Syndrome True False True +NCIT:C3963 Purine-Nucleoside Phosphorylase Deficiency True False True NCIT:C39822 Infiltrating Bladder Urothelial Carcinoma, Lymphoma-Like Variant True False True NCIT:C40257 Vaginal Tubular Adenoma True False True +NCIT:C4173 Papillary Eccrine Adenoma True False True NCIT:C4462 Skin Squamous Papilloma True False True NCIT:C4743 Benign Basal Cell Neoplasm True False True +NCIT:C5504 Central Nervous System Melanocytic Neoplasm True False True +NCIT:C5505 Central Nervous System Melanoma True False True +NCIT:C66903 Skin Metatypical Carcinoma True False True NCIT:C6977 Breast Papillomatosis True False True NCIT:C7150 Indolent Multiple Myeloma True False True NCIT:C7167 Myelodysplastic Syndrome with Excess Blasts-1 True False True NCIT:C75007 Marfan Syndrome Type II True False True NCIT:C7586 Malignant Basal Cell Neoplasm True False True NCIT:C8998 Medullary Carcinoma True False True +NCIT:C9419 AJCC Grade 1 Sarcoma True False True +NCIT:C9499 Melanomatosis True False True NCIT:C101024 Colon Atresia True True False NCIT:C101025 Duodenal Atresia True True False NCIT:C101029 Atrioventricular Septal Defect True True False @@ -184912,7 +188864,7 @@ NCIT:C26836 Nutritional Disorder True True False NCIT:C26837 Osteogenesis Imperfecta True True False NCIT:C26838 Osteomalacia True True False NCIT:C26840 Osteopetrosis True True False -NCIT:C26845 Parkinson's Disease True True False +NCIT:C26845 Parkinson Disease True True False NCIT:C26847 Polyarteritis Nodosa True True False NCIT:C26849 Peritonitis True True False NCIT:C26851 Pharyngitis True True False @@ -185179,7 +189131,7 @@ NCIT:C3001 Eczema True True False NCIT:C3014 Endometriosis True True False NCIT:C3020 Seizure Disorder True True False NCIT:C3021 Generalized Epilepsy True True False -NCIT:C3022 Grand Mal Epilepsy True True False +NCIT:C3022 Tonic-Clonic Epilepsy True True False NCIT:C3024 Erythema Multiforme True True False NCIT:C3025 Erythroplakia True True False NCIT:C3029 Exostosis True True False @@ -185454,7 +189406,7 @@ NCIT:C34589 Epicondylitis True True False NCIT:C34590 Epidemic Keratoconjunctivitis True True False NCIT:C34591 Erythematosquamous Dermatosis True True False NCIT:C34593 Erythromelalgia True True False -NCIT:C34594 Escherichia Coli Infection True True False +NCIT:C34594 Escherichia coli Infection True True False NCIT:C34596 Internal Strabismus True True False NCIT:C34597 Ethmoidal Sinusitis True True False NCIT:C34601 Divergent Strabismus True True False @@ -185829,7 +189781,6 @@ NCIT:C35434 Polycythaemia due to Excess Erythropoetin Production True True False NCIT:C35436 Cauda Equina Syndrome True True False NCIT:C35437 Familial Idiopathic Dystonia True True False NCIT:C35438 Non-Familial Idiopathic Dystonia True True False -NCIT:C35439 Hemophagocytic Syndrome True True False NCIT:C35441 Cerebral Sarcoidosis True True False NCIT:C35443 Post-Streptococcal Glomerulonephritis True True False NCIT:C35444 Crescentic Glomerulonephritis True True False @@ -185977,7 +189928,7 @@ NCIT:C3937 Non-Neoplastic Nevus True True False NCIT:C3939 Bannayan-Riley-Ruvalcaba Syndrome True True False NCIT:C3940 Hereditary Benign Intraepithelial Dyskeratosis True True False NCIT:C3943 Nevus Anemicus True True False -NCIT:C3945 Mongolian Spot True True False +NCIT:C3945 Congenital Dermal Melanocytosis True True False NCIT:C3946 Nevus Comedonicus True True False NCIT:C3948 Gingival Polyp True True False NCIT:C3949 Benign Lymphoepithelial Lesion of the Salivary Gland True True False @@ -185987,7 +189938,6 @@ NCIT:C39577 Autoimmune Lymphoproliferative Syndrome-Unknown Underlying Mutation NCIT:C39594 Skin Rash True True False NCIT:C39611 Intestinal Perforation True True False NCIT:C3962 Adenosine Deaminase Deficiency True True False -NCIT:C3963 Purine-Nucleoside Phosphorylase Deficiency True True False NCIT:C39646 Erythroderma True True False NCIT:C3965 Xeroderma Pigmentosum, Complementation Group A True True False NCIT:C39658 Bronchiolitis True True False @@ -186036,8 +189986,10 @@ NCIT:C42086 Downward Ocular Deviation True True False NCIT:C42088 Cortical Dysplasia True True False NCIT:C4293 Partial Hydatidiform Mole True True False NCIT:C43263 Diabetes Insipidus True True False +NCIT:C43352 Turban Tumor Syndrome True True False NCIT:C4350 Limbic Encephalitis True True False NCIT:C4351 Choroid Plexus Cyst True True False +NCIT:C4366 External Ear Polyp True True False NCIT:C4367 Frontal Sinus Polyp True True False NCIT:C4373 Gastric Hamartomatous Polyp True True False NCIT:C4375 Nesidioblastosis True True False @@ -186062,7 +190014,7 @@ NCIT:C45525 Valvular Heart Disorder True True False NCIT:C45745 Conduction System Hamartoma True True False NCIT:C4657 Central Nervous System Cyst True True False NCIT:C4674 Verrucous Nevus True True False -NCIT:C4675 Congenital Epulis True True False +NCIT:C4675 Congenital Granular Cell Epulis True True False NCIT:C4678 Organoid Nevus True True False NCIT:C4681 Roberts-SC Phocomelia Syndrome True True False NCIT:C4682 X-Linked Severe Combined Immunodeficiency True True False @@ -186248,6 +190200,7 @@ NCIT:C6729 Attenuated Familial Adenomatous Polyposis True True False NCIT:C67383 Epidermolysis Bullosa True True False NCIT:C6857 Vulvar Fibroepithelial Stromal Polyp True True False NCIT:C68677 von Willebrand Disease True True False +NCIT:C6933 Middle Ear Polyp True True False NCIT:C6940 Breast Fibrocystic Change, Proliferative Type True True False NCIT:C6943 Breast Fibrocystic Change, Non-Proliferative Type True True False NCIT:C6996 Uterine Corpus Adenomyosis True True False diff --git a/src/ontology/reports/ncit_term_exclusions.txt b/src/ontology/reports/ncit_term_exclusions.txt index 465808a7..2f722b57 100644 --- a/src/ontology/reports/ncit_term_exclusions.txt +++ b/src/ontology/reports/ncit_term_exclusions.txt @@ -24685,7 +24685,6 @@ NCIT:C122828 NCIT:C122829 NCIT:C122830 NCIT:C122831 -NCIT:C122832 NCIT:C122833 NCIT:C122834 NCIT:C122835 @@ -47811,7 +47810,6 @@ NCIT:C147308 NCIT:C147309 NCIT:C147310 NCIT:C147311 -NCIT:C147312 NCIT:C147313 NCIT:C147314 NCIT:C147315 @@ -53102,7 +53100,6 @@ NCIT:C154136 NCIT:C154137 NCIT:C154138 NCIT:C154139 -NCIT:C15414 NCIT:C154140 NCIT:C154141 NCIT:C154142 @@ -54824,7 +54821,6 @@ NCIT:C156048 NCIT:C156049 NCIT:C15605 NCIT:C156051 -NCIT:C156052 NCIT:C156053 NCIT:C156054 NCIT:C156055 @@ -57771,7 +57767,6 @@ NCIT:C15925 NCIT:C159253 NCIT:C159254 NCIT:C159255 -NCIT:C159256 NCIT:C159257 NCIT:C159258 NCIT:C159259 @@ -68352,7 +68347,6 @@ NCIT:C171536 NCIT:C171537 NCIT:C171538 NCIT:C171539 -NCIT:C17154 NCIT:C171540 NCIT:C171541 NCIT:C171542 @@ -69550,7 +69544,6 @@ NCIT:C172801 NCIT:C172802 NCIT:C172805 NCIT:C172807 -NCIT:C172809 NCIT:C17281 NCIT:C172816 NCIT:C172817 @@ -70148,7 +70141,6 @@ NCIT:C173527 NCIT:C173528 NCIT:C17353 NCIT:C173535 -NCIT:C173536 NCIT:C173537 NCIT:C173538 NCIT:C173539 @@ -70353,7 +70345,6 @@ NCIT:C173791 NCIT:C173792 NCIT:C173794 NCIT:C173796 -NCIT:C173798 NCIT:C17380 NCIT:C173800 NCIT:C173801 @@ -72374,7 +72365,6 @@ NCIT:C175852 NCIT:C175853 NCIT:C175854 NCIT:C175855 -NCIT:C175856 NCIT:C175857 NCIT:C175858 NCIT:C175859 @@ -73180,7 +73170,6 @@ NCIT:C176619 NCIT:C17662 NCIT:C176620 NCIT:C176621 -NCIT:C176622 NCIT:C176623 NCIT:C176624 NCIT:C176625 @@ -78847,6 +78836,7 @@ NCIT:C182353 NCIT:C182354 NCIT:C182355 NCIT:C182356 +NCIT:C182357 NCIT:C182358 NCIT:C182359 NCIT:C182360 @@ -83778,7 +83768,6 @@ NCIT:C187030 NCIT:C187031 NCIT:C187032 NCIT:C187033 -NCIT:C187034 NCIT:C187035 NCIT:C187036 NCIT:C187037 @@ -86614,7 +86603,6 @@ NCIT:C189902 NCIT:C189903 NCIT:C189904 NCIT:C189905 -NCIT:C189906 NCIT:C189907 NCIT:C189908 NCIT:C189909 @@ -88422,7 +88410,6 @@ NCIT:C191756 NCIT:C191757 NCIT:C191758 NCIT:C191759 -NCIT:C191760 NCIT:C191761 NCIT:C191762 NCIT:C191765 @@ -94962,7 +94949,6 @@ NCIT:C198024 NCIT:C198025 NCIT:C198026 NCIT:C198028 -NCIT:C198029 NCIT:C19803 NCIT:C198033 NCIT:C198037 @@ -97325,7 +97311,6 @@ NCIT:C200519 NCIT:C20052 NCIT:C200521 NCIT:C200522 -NCIT:C200523 NCIT:C200525 NCIT:C200526 NCIT:C200527 @@ -98412,441 +98397,4021 @@ NCIT:C201554 NCIT:C201555 NCIT:C201556 NCIT:C201557 +NCIT:C201558 +NCIT:C201559 NCIT:C20156 +NCIT:C201560 +NCIT:C201561 +NCIT:C201562 +NCIT:C201563 +NCIT:C201564 +NCIT:C201565 +NCIT:C201566 +NCIT:C201567 +NCIT:C201568 +NCIT:C201569 NCIT:C20157 +NCIT:C201570 +NCIT:C201571 +NCIT:C201572 +NCIT:C201573 +NCIT:C201574 +NCIT:C201576 +NCIT:C201577 +NCIT:C201578 +NCIT:C201579 NCIT:C20158 +NCIT:C201580 +NCIT:C201581 +NCIT:C201582 +NCIT:C201583 +NCIT:C201584 +NCIT:C201585 +NCIT:C201586 +NCIT:C201587 +NCIT:C201588 +NCIT:C201589 NCIT:C20159 +NCIT:C201590 +NCIT:C201591 +NCIT:C201592 +NCIT:C201593 +NCIT:C201594 +NCIT:C201595 +NCIT:C201596 +NCIT:C201597 +NCIT:C201598 +NCIT:C201599 NCIT:C2016 NCIT:C20160 +NCIT:C201600 +NCIT:C201601 +NCIT:C201602 +NCIT:C201603 +NCIT:C201604 +NCIT:C201605 +NCIT:C201606 +NCIT:C201607 +NCIT:C201608 +NCIT:C201609 NCIT:C20161 +NCIT:C201610 +NCIT:C201611 +NCIT:C201612 +NCIT:C201613 +NCIT:C201614 +NCIT:C201615 +NCIT:C201616 +NCIT:C201617 +NCIT:C201618 +NCIT:C201619 NCIT:C20162 +NCIT:C201621 +NCIT:C201622 +NCIT:C201623 +NCIT:C201624 +NCIT:C201625 +NCIT:C201626 +NCIT:C201627 +NCIT:C201628 +NCIT:C201629 NCIT:C20163 +NCIT:C201630 +NCIT:C201631 +NCIT:C201632 +NCIT:C201633 +NCIT:C201638 +NCIT:C201639 NCIT:C20164 +NCIT:C201640 +NCIT:C201641 +NCIT:C201642 +NCIT:C201643 +NCIT:C201644 +NCIT:C201645 +NCIT:C201646 +NCIT:C201647 +NCIT:C201648 +NCIT:C201649 NCIT:C20165 +NCIT:C201650 +NCIT:C201651 +NCIT:C201652 +NCIT:C201653 +NCIT:C201654 +NCIT:C201655 +NCIT:C201656 +NCIT:C201657 +NCIT:C201658 +NCIT:C201659 NCIT:C20166 +NCIT:C201660 +NCIT:C201661 +NCIT:C201662 +NCIT:C201663 +NCIT:C201664 +NCIT:C201665 +NCIT:C201666 +NCIT:C201667 +NCIT:C201668 +NCIT:C201669 NCIT:C20167 +NCIT:C201670 +NCIT:C201671 +NCIT:C201672 +NCIT:C201673 +NCIT:C201674 +NCIT:C201675 +NCIT:C201676 +NCIT:C201677 +NCIT:C201678 +NCIT:C201679 NCIT:C20168 +NCIT:C201680 +NCIT:C201681 +NCIT:C201682 +NCIT:C201683 +NCIT:C201684 +NCIT:C201685 +NCIT:C201686 +NCIT:C201687 +NCIT:C201688 +NCIT:C201689 NCIT:C20169 +NCIT:C201690 +NCIT:C201691 +NCIT:C201692 +NCIT:C201693 +NCIT:C201694 +NCIT:C201695 +NCIT:C201696 +NCIT:C201697 +NCIT:C201698 +NCIT:C201699 NCIT:C2017 NCIT:C20170 +NCIT:C201700 +NCIT:C201701 +NCIT:C201702 +NCIT:C201703 +NCIT:C201704 +NCIT:C201705 +NCIT:C201706 +NCIT:C201707 +NCIT:C201708 +NCIT:C201709 NCIT:C20171 +NCIT:C201710 +NCIT:C201711 +NCIT:C201712 +NCIT:C201713 +NCIT:C201714 +NCIT:C201715 +NCIT:C201716 +NCIT:C201717 +NCIT:C201718 +NCIT:C201719 NCIT:C20172 +NCIT:C201720 +NCIT:C201721 +NCIT:C201722 +NCIT:C201723 +NCIT:C201724 +NCIT:C201725 +NCIT:C201726 +NCIT:C201727 +NCIT:C201728 +NCIT:C201729 NCIT:C20173 +NCIT:C201730 +NCIT:C201731 +NCIT:C201732 +NCIT:C201733 +NCIT:C201734 +NCIT:C201735 +NCIT:C201736 +NCIT:C201737 +NCIT:C201738 +NCIT:C201739 NCIT:C20174 +NCIT:C201740 +NCIT:C201741 +NCIT:C201744 +NCIT:C201745 NCIT:C20175 +NCIT:C201750 +NCIT:C201751 +NCIT:C201752 +NCIT:C201753 +NCIT:C201754 +NCIT:C201755 +NCIT:C201756 +NCIT:C201757 +NCIT:C201758 +NCIT:C201759 NCIT:C20176 +NCIT:C201760 +NCIT:C201761 +NCIT:C201762 +NCIT:C201763 +NCIT:C201765 +NCIT:C201769 NCIT:C20177 +NCIT:C201771 +NCIT:C201773 +NCIT:C201774 +NCIT:C201775 +NCIT:C201776 +NCIT:C201777 +NCIT:C201778 +NCIT:C201779 NCIT:C20178 +NCIT:C201780 +NCIT:C201782 +NCIT:C201783 +NCIT:C201784 +NCIT:C201785 +NCIT:C201787 +NCIT:C201788 +NCIT:C201789 NCIT:C20179 +NCIT:C201790 +NCIT:C201791 +NCIT:C201792 +NCIT:C201793 +NCIT:C201794 +NCIT:C201795 +NCIT:C201796 +NCIT:C201797 +NCIT:C201798 +NCIT:C201799 NCIT:C2018 NCIT:C20180 +NCIT:C201800 +NCIT:C201801 +NCIT:C201802 +NCIT:C201803 +NCIT:C201804 +NCIT:C201805 +NCIT:C201806 +NCIT:C201807 +NCIT:C201808 +NCIT:C201809 NCIT:C20181 +NCIT:C201810 +NCIT:C201811 +NCIT:C201812 +NCIT:C201813 +NCIT:C201814 +NCIT:C201815 +NCIT:C201816 +NCIT:C201817 +NCIT:C201818 +NCIT:C201819 NCIT:C20182 +NCIT:C201820 +NCIT:C201822 +NCIT:C201824 +NCIT:C201825 +NCIT:C201826 +NCIT:C201827 +NCIT:C201828 +NCIT:C201829 NCIT:C20183 +NCIT:C201830 +NCIT:C201831 +NCIT:C201833 +NCIT:C201834 +NCIT:C201835 +NCIT:C201836 NCIT:C20184 +NCIT:C201840 +NCIT:C201841 +NCIT:C201842 +NCIT:C201843 +NCIT:C201844 +NCIT:C201845 +NCIT:C201846 +NCIT:C201847 +NCIT:C201848 NCIT:C20185 +NCIT:C201850 +NCIT:C201851 +NCIT:C201852 +NCIT:C201853 +NCIT:C201854 +NCIT:C201855 +NCIT:C201856 +NCIT:C201857 +NCIT:C201858 +NCIT:C201859 NCIT:C20186 +NCIT:C201860 +NCIT:C201861 +NCIT:C201862 +NCIT:C201863 +NCIT:C201864 +NCIT:C201865 +NCIT:C201866 +NCIT:C201867 +NCIT:C201868 +NCIT:C201869 NCIT:C20187 +NCIT:C201870 +NCIT:C201871 +NCIT:C201872 +NCIT:C201873 +NCIT:C201874 +NCIT:C201875 +NCIT:C201876 +NCIT:C201877 +NCIT:C201879 NCIT:C20188 +NCIT:C201881 +NCIT:C201882 +NCIT:C201883 +NCIT:C201884 +NCIT:C201885 +NCIT:C201886 +NCIT:C201887 +NCIT:C201889 NCIT:C20189 +NCIT:C201890 +NCIT:C201891 +NCIT:C201892 +NCIT:C201893 +NCIT:C201894 +NCIT:C201895 +NCIT:C201896 +NCIT:C201897 +NCIT:C201898 +NCIT:C201899 NCIT:C2019 NCIT:C20190 +NCIT:C201901 +NCIT:C201902 +NCIT:C201903 +NCIT:C201908 +NCIT:C201909 NCIT:C20191 +NCIT:C201910 +NCIT:C201911 +NCIT:C201912 +NCIT:C201913 +NCIT:C201914 +NCIT:C201915 +NCIT:C201916 +NCIT:C201917 +NCIT:C201918 +NCIT:C201919 +NCIT:C201920 +NCIT:C201921 +NCIT:C201922 +NCIT:C201923 +NCIT:C201924 +NCIT:C201925 +NCIT:C201926 +NCIT:C201927 +NCIT:C201928 +NCIT:C201929 NCIT:C20193 +NCIT:C201930 +NCIT:C201931 +NCIT:C201932 +NCIT:C201933 +NCIT:C201934 +NCIT:C201935 +NCIT:C201936 +NCIT:C201937 +NCIT:C201938 +NCIT:C201939 NCIT:C20194 +NCIT:C201940 +NCIT:C201941 +NCIT:C201942 +NCIT:C201943 +NCIT:C201944 +NCIT:C201945 +NCIT:C201946 +NCIT:C201947 +NCIT:C201948 +NCIT:C201949 NCIT:C20195 +NCIT:C201950 +NCIT:C201954 +NCIT:C201955 +NCIT:C201956 +NCIT:C201957 +NCIT:C201958 +NCIT:C201959 +NCIT:C201962 +NCIT:C201963 +NCIT:C201964 +NCIT:C201965 NCIT:C20197 +NCIT:C201972 +NCIT:C201974 +NCIT:C201979 NCIT:C20198 +NCIT:C201980 +NCIT:C201981 +NCIT:C201982 +NCIT:C201983 +NCIT:C201984 +NCIT:C201985 +NCIT:C201986 +NCIT:C201987 +NCIT:C201988 +NCIT:C201989 NCIT:C20199 +NCIT:C201990 +NCIT:C201991 +NCIT:C201992 +NCIT:C201993 +NCIT:C201994 +NCIT:C201995 +NCIT:C201996 +NCIT:C201997 +NCIT:C201998 +NCIT:C201999 NCIT:C202 NCIT:C2020 NCIT:C20200 +NCIT:C202000 +NCIT:C202001 +NCIT:C202002 +NCIT:C202003 +NCIT:C202004 +NCIT:C202005 +NCIT:C202006 +NCIT:C202007 +NCIT:C202008 +NCIT:C202009 NCIT:C20201 +NCIT:C202011 +NCIT:C202012 +NCIT:C202013 +NCIT:C202014 +NCIT:C202015 +NCIT:C202016 +NCIT:C202017 +NCIT:C202018 +NCIT:C202019 NCIT:C20202 +NCIT:C202020 +NCIT:C202021 +NCIT:C202022 +NCIT:C202023 +NCIT:C202024 +NCIT:C202026 +NCIT:C202027 +NCIT:C202028 +NCIT:C202029 NCIT:C20203 +NCIT:C202030 +NCIT:C202031 +NCIT:C202032 +NCIT:C202033 +NCIT:C202034 +NCIT:C202035 +NCIT:C202036 +NCIT:C202037 +NCIT:C202038 +NCIT:C202039 NCIT:C20204 +NCIT:C202040 +NCIT:C202041 +NCIT:C202042 +NCIT:C202043 +NCIT:C202044 +NCIT:C202045 +NCIT:C202046 +NCIT:C202047 +NCIT:C202048 +NCIT:C202049 NCIT:C20205 +NCIT:C202050 +NCIT:C202051 +NCIT:C202052 +NCIT:C202053 +NCIT:C202054 +NCIT:C202055 +NCIT:C202056 NCIT:C20206 +NCIT:C202060 +NCIT:C202062 +NCIT:C202063 +NCIT:C202064 +NCIT:C202065 +NCIT:C202066 +NCIT:C202067 +NCIT:C202068 +NCIT:C202069 NCIT:C20207 +NCIT:C202070 +NCIT:C202071 +NCIT:C202072 +NCIT:C202073 +NCIT:C202074 +NCIT:C202075 +NCIT:C202076 NCIT:C20208 +NCIT:C202082 +NCIT:C202083 +NCIT:C202084 +NCIT:C202085 +NCIT:C202086 +NCIT:C202087 +NCIT:C202088 +NCIT:C202089 NCIT:C20209 +NCIT:C202090 +NCIT:C202091 +NCIT:C202092 +NCIT:C202093 +NCIT:C202094 +NCIT:C202095 +NCIT:C202096 +NCIT:C202097 +NCIT:C202098 +NCIT:C202099 NCIT:C2021 NCIT:C20210 +NCIT:C202100 +NCIT:C202101 +NCIT:C202102 +NCIT:C202103 +NCIT:C202104 +NCIT:C202105 +NCIT:C202106 +NCIT:C202107 +NCIT:C202108 +NCIT:C202109 NCIT:C20211 +NCIT:C202110 +NCIT:C202111 +NCIT:C202112 +NCIT:C202113 +NCIT:C202114 +NCIT:C202115 +NCIT:C202116 +NCIT:C202117 +NCIT:C202118 +NCIT:C202119 NCIT:C20212 +NCIT:C202121 +NCIT:C202122 +NCIT:C202123 +NCIT:C202124 +NCIT:C202125 +NCIT:C202126 +NCIT:C202129 NCIT:C20213 +NCIT:C202134 +NCIT:C202135 +NCIT:C202136 +NCIT:C202137 +NCIT:C202138 +NCIT:C202139 NCIT:C20214 +NCIT:C202140 +NCIT:C202141 +NCIT:C202142 +NCIT:C202143 +NCIT:C202144 +NCIT:C202145 +NCIT:C202146 +NCIT:C202147 +NCIT:C202148 +NCIT:C202149 NCIT:C20215 +NCIT:C202150 +NCIT:C202151 +NCIT:C202152 +NCIT:C202153 +NCIT:C202154 +NCIT:C202155 +NCIT:C202156 +NCIT:C202157 +NCIT:C202158 +NCIT:C202159 NCIT:C20216 +NCIT:C202160 +NCIT:C202161 NCIT:C20217 NCIT:C20218 NCIT:C20219 NCIT:C20220 +NCIT:C202206 +NCIT:C202207 +NCIT:C202208 NCIT:C20221 +NCIT:C202210 +NCIT:C202211 +NCIT:C202212 +NCIT:C202213 +NCIT:C202214 +NCIT:C202215 +NCIT:C202216 +NCIT:C202217 +NCIT:C202218 +NCIT:C202219 NCIT:C20222 +NCIT:C202220 +NCIT:C202221 +NCIT:C202222 +NCIT:C202223 +NCIT:C202224 +NCIT:C202225 +NCIT:C202226 +NCIT:C202227 +NCIT:C202228 +NCIT:C202229 NCIT:C20223 +NCIT:C202230 +NCIT:C202231 +NCIT:C202232 +NCIT:C202233 +NCIT:C202234 +NCIT:C202235 +NCIT:C202236 +NCIT:C202237 +NCIT:C202238 +NCIT:C202239 NCIT:C20224 +NCIT:C202240 +NCIT:C202241 +NCIT:C202242 +NCIT:C202243 +NCIT:C202244 +NCIT:C202245 +NCIT:C202246 +NCIT:C202247 +NCIT:C202248 +NCIT:C202249 NCIT:C20225 +NCIT:C202250 +NCIT:C202251 +NCIT:C202255 +NCIT:C202259 NCIT:C20226 +NCIT:C202266 +NCIT:C202267 +NCIT:C202268 +NCIT:C202269 NCIT:C20227 +NCIT:C202270 +NCIT:C202271 +NCIT:C202272 +NCIT:C202273 +NCIT:C202274 +NCIT:C202275 +NCIT:C202276 +NCIT:C202277 +NCIT:C202278 +NCIT:C202279 NCIT:C20228 +NCIT:C202280 +NCIT:C202281 +NCIT:C202282 +NCIT:C202283 +NCIT:C202284 +NCIT:C202285 +NCIT:C202286 +NCIT:C202287 +NCIT:C202288 +NCIT:C202289 NCIT:C20229 +NCIT:C202290 +NCIT:C202291 +NCIT:C202292 +NCIT:C202293 +NCIT:C202294 +NCIT:C202295 +NCIT:C202296 +NCIT:C202297 NCIT:C2023 NCIT:C20230 +NCIT:C202300 +NCIT:C202301 +NCIT:C202302 +NCIT:C202303 +NCIT:C202304 +NCIT:C202305 +NCIT:C202306 +NCIT:C202307 +NCIT:C202308 +NCIT:C202309 NCIT:C20231 +NCIT:C202310 +NCIT:C202311 +NCIT:C202312 +NCIT:C202313 +NCIT:C202314 +NCIT:C202315 +NCIT:C202316 +NCIT:C202317 +NCIT:C202318 +NCIT:C202319 NCIT:C20232 +NCIT:C202320 +NCIT:C202321 +NCIT:C202322 +NCIT:C202323 +NCIT:C202324 +NCIT:C202325 +NCIT:C202326 +NCIT:C202327 +NCIT:C202329 NCIT:C20233 +NCIT:C202330 +NCIT:C202331 +NCIT:C202332 +NCIT:C202333 +NCIT:C202334 +NCIT:C202336 +NCIT:C202337 +NCIT:C202338 +NCIT:C202339 NCIT:C20234 +NCIT:C202340 +NCIT:C202341 +NCIT:C202342 +NCIT:C202343 +NCIT:C202344 +NCIT:C202345 +NCIT:C202346 +NCIT:C202347 +NCIT:C202348 +NCIT:C202349 NCIT:C20235 +NCIT:C202350 +NCIT:C202351 +NCIT:C202352 +NCIT:C202353 +NCIT:C202354 +NCIT:C202355 +NCIT:C202356 +NCIT:C202357 +NCIT:C202358 +NCIT:C202359 NCIT:C20236 +NCIT:C202360 +NCIT:C202361 +NCIT:C202362 +NCIT:C202363 +NCIT:C202364 +NCIT:C202366 +NCIT:C202367 +NCIT:C202368 +NCIT:C202369 NCIT:C20237 +NCIT:C202370 +NCIT:C202371 +NCIT:C202372 +NCIT:C202373 +NCIT:C202374 +NCIT:C202375 +NCIT:C202376 +NCIT:C202377 +NCIT:C202378 +NCIT:C202379 NCIT:C20238 +NCIT:C202380 +NCIT:C202381 +NCIT:C202382 +NCIT:C202383 +NCIT:C202384 +NCIT:C202385 +NCIT:C202386 +NCIT:C202387 +NCIT:C202388 +NCIT:C202389 NCIT:C20239 +NCIT:C202390 +NCIT:C202391 +NCIT:C202392 +NCIT:C202393 +NCIT:C202394 +NCIT:C202395 +NCIT:C202396 +NCIT:C202397 +NCIT:C202398 +NCIT:C202399 NCIT:C2024 NCIT:C20240 +NCIT:C202400 +NCIT:C202401 +NCIT:C202402 +NCIT:C202403 +NCIT:C202404 +NCIT:C202405 +NCIT:C202406 +NCIT:C202407 +NCIT:C202408 +NCIT:C202409 NCIT:C20241 +NCIT:C202410 +NCIT:C202411 +NCIT:C202412 +NCIT:C202413 +NCIT:C202414 +NCIT:C202415 +NCIT:C202416 +NCIT:C202417 +NCIT:C202418 +NCIT:C202419 NCIT:C20242 +NCIT:C202420 +NCIT:C202421 +NCIT:C202422 +NCIT:C202423 +NCIT:C202424 +NCIT:C202425 +NCIT:C202426 +NCIT:C202427 +NCIT:C202428 +NCIT:C202429 NCIT:C20243 +NCIT:C202430 +NCIT:C202431 +NCIT:C202432 +NCIT:C202433 +NCIT:C202434 +NCIT:C202435 +NCIT:C202436 +NCIT:C202437 +NCIT:C202438 +NCIT:C202439 NCIT:C20244 +NCIT:C202440 +NCIT:C202441 +NCIT:C202442 +NCIT:C202443 +NCIT:C202444 +NCIT:C202445 +NCIT:C202446 +NCIT:C202447 +NCIT:C202448 +NCIT:C202449 NCIT:C20245 +NCIT:C202450 +NCIT:C202451 +NCIT:C202452 +NCIT:C202453 +NCIT:C202454 +NCIT:C202455 +NCIT:C202456 +NCIT:C202457 +NCIT:C202458 +NCIT:C202459 NCIT:C20246 +NCIT:C202460 +NCIT:C202461 +NCIT:C202462 +NCIT:C202463 +NCIT:C202464 +NCIT:C202465 +NCIT:C202466 +NCIT:C202467 +NCIT:C202468 +NCIT:C202469 NCIT:C20247 +NCIT:C202470 +NCIT:C202471 +NCIT:C202472 +NCIT:C202473 +NCIT:C202474 +NCIT:C202475 +NCIT:C202476 +NCIT:C202477 +NCIT:C202478 +NCIT:C202479 NCIT:C20248 +NCIT:C202480 +NCIT:C202481 +NCIT:C202482 +NCIT:C202483 +NCIT:C202484 +NCIT:C202485 +NCIT:C202486 +NCIT:C202487 +NCIT:C202488 +NCIT:C202489 NCIT:C20249 +NCIT:C202490 +NCIT:C202491 +NCIT:C202492 +NCIT:C202493 +NCIT:C202494 +NCIT:C202495 +NCIT:C202496 +NCIT:C202498 +NCIT:C202499 NCIT:C2025 NCIT:C20250 +NCIT:C202501 +NCIT:C202502 +NCIT:C202503 +NCIT:C202504 +NCIT:C202505 +NCIT:C202506 +NCIT:C202507 +NCIT:C202508 +NCIT:C202509 NCIT:C20251 +NCIT:C202510 +NCIT:C202511 +NCIT:C202512 +NCIT:C202513 +NCIT:C202514 +NCIT:C202515 +NCIT:C202516 +NCIT:C202517 +NCIT:C202518 +NCIT:C202519 NCIT:C20252 +NCIT:C202520 +NCIT:C202521 +NCIT:C202522 +NCIT:C202523 +NCIT:C202524 +NCIT:C202525 +NCIT:C202526 +NCIT:C202527 +NCIT:C202528 +NCIT:C202529 NCIT:C20253 +NCIT:C202530 +NCIT:C202531 +NCIT:C202532 +NCIT:C202533 +NCIT:C202534 +NCIT:C202535 +NCIT:C202536 +NCIT:C202537 +NCIT:C202538 +NCIT:C202539 NCIT:C20254 +NCIT:C202540 +NCIT:C202541 +NCIT:C202542 +NCIT:C202543 +NCIT:C202544 +NCIT:C202545 +NCIT:C202546 +NCIT:C202547 +NCIT:C202548 +NCIT:C202549 NCIT:C20255 +NCIT:C202550 +NCIT:C202551 +NCIT:C202552 +NCIT:C202553 +NCIT:C202554 +NCIT:C202555 +NCIT:C202556 +NCIT:C202557 +NCIT:C202558 +NCIT:C202559 NCIT:C20256 +NCIT:C202560 +NCIT:C202561 +NCIT:C202562 +NCIT:C202563 +NCIT:C202564 +NCIT:C202565 +NCIT:C202566 +NCIT:C202567 +NCIT:C202568 +NCIT:C202569 NCIT:C20257 +NCIT:C202570 +NCIT:C202571 +NCIT:C202572 +NCIT:C202573 +NCIT:C202575 +NCIT:C202576 +NCIT:C202577 +NCIT:C202578 +NCIT:C202579 NCIT:C20258 +NCIT:C202580 +NCIT:C202581 +NCIT:C202586 +NCIT:C202587 +NCIT:C202588 +NCIT:C202589 NCIT:C20259 +NCIT:C202590 +NCIT:C202591 +NCIT:C202592 +NCIT:C202593 +NCIT:C202595 +NCIT:C202596 +NCIT:C202597 +NCIT:C202598 +NCIT:C202599 NCIT:C2026 NCIT:C20260 +NCIT:C202600 +NCIT:C202601 +NCIT:C202602 +NCIT:C202603 +NCIT:C202604 +NCIT:C202605 +NCIT:C202606 +NCIT:C202607 +NCIT:C202608 NCIT:C20261 +NCIT:C202610 +NCIT:C202612 +NCIT:C202614 +NCIT:C202615 +NCIT:C202616 +NCIT:C202617 +NCIT:C202618 +NCIT:C202619 NCIT:C20262 +NCIT:C202626 +NCIT:C202627 +NCIT:C202628 +NCIT:C202629 NCIT:C20263 +NCIT:C202630 +NCIT:C202631 +NCIT:C202632 +NCIT:C202636 +NCIT:C202637 +NCIT:C202638 +NCIT:C202639 NCIT:C20264 +NCIT:C202640 +NCIT:C202641 +NCIT:C202642 +NCIT:C202643 +NCIT:C202644 +NCIT:C202645 +NCIT:C202648 +NCIT:C202649 NCIT:C20265 +NCIT:C202650 +NCIT:C202651 +NCIT:C202653 +NCIT:C202657 +NCIT:C202658 +NCIT:C202659 NCIT:C20266 +NCIT:C202660 +NCIT:C202663 +NCIT:C202664 +NCIT:C202665 +NCIT:C202666 +NCIT:C202667 +NCIT:C202668 +NCIT:C202669 NCIT:C20267 +NCIT:C202670 +NCIT:C202671 +NCIT:C202672 +NCIT:C202673 +NCIT:C202674 +NCIT:C202675 +NCIT:C202676 +NCIT:C202677 +NCIT:C202678 +NCIT:C202679 NCIT:C20268 +NCIT:C202680 +NCIT:C202681 +NCIT:C202682 +NCIT:C202683 +NCIT:C202685 +NCIT:C202686 +NCIT:C202687 +NCIT:C202688 +NCIT:C202689 NCIT:C20269 +NCIT:C202690 +NCIT:C202691 +NCIT:C202692 +NCIT:C202693 +NCIT:C202694 +NCIT:C202695 +NCIT:C202696 +NCIT:C202697 +NCIT:C202698 +NCIT:C202699 NCIT:C2027 NCIT:C20270 +NCIT:C202700 +NCIT:C202701 +NCIT:C202702 +NCIT:C202703 +NCIT:C202704 +NCIT:C202705 +NCIT:C202706 +NCIT:C202707 +NCIT:C202708 +NCIT:C202709 NCIT:C20271 +NCIT:C202710 +NCIT:C202712 +NCIT:C202713 +NCIT:C202714 +NCIT:C202715 +NCIT:C202716 +NCIT:C202717 +NCIT:C202718 +NCIT:C202719 NCIT:C20272 +NCIT:C202720 +NCIT:C202721 +NCIT:C202722 +NCIT:C202723 +NCIT:C202724 +NCIT:C202725 +NCIT:C202726 +NCIT:C202727 +NCIT:C202728 +NCIT:C202729 NCIT:C20273 +NCIT:C202730 +NCIT:C202731 +NCIT:C202732 +NCIT:C202733 +NCIT:C202734 +NCIT:C202735 +NCIT:C202736 +NCIT:C202737 +NCIT:C202738 +NCIT:C202739 NCIT:C20274 +NCIT:C202740 +NCIT:C202741 +NCIT:C202742 +NCIT:C202743 +NCIT:C202744 +NCIT:C202745 +NCIT:C202746 +NCIT:C202747 +NCIT:C202748 +NCIT:C202749 NCIT:C20275 +NCIT:C202750 +NCIT:C202751 +NCIT:C202752 +NCIT:C202753 +NCIT:C202754 +NCIT:C202755 +NCIT:C202756 +NCIT:C202757 +NCIT:C202758 +NCIT:C202759 NCIT:C20276 +NCIT:C202760 +NCIT:C202761 +NCIT:C202762 +NCIT:C202763 +NCIT:C202764 +NCIT:C202765 +NCIT:C202766 +NCIT:C202767 +NCIT:C202768 +NCIT:C202769 NCIT:C20277 +NCIT:C202770 +NCIT:C202771 +NCIT:C202772 +NCIT:C202773 +NCIT:C202774 +NCIT:C202777 +NCIT:C202778 +NCIT:C202779 NCIT:C20278 +NCIT:C202780 +NCIT:C202781 +NCIT:C202782 +NCIT:C202783 +NCIT:C202784 +NCIT:C202785 +NCIT:C202786 +NCIT:C202787 +NCIT:C202788 +NCIT:C202789 NCIT:C20279 +NCIT:C202790 +NCIT:C202791 +NCIT:C202792 +NCIT:C202793 +NCIT:C202794 +NCIT:C202795 +NCIT:C202796 +NCIT:C202797 +NCIT:C202798 +NCIT:C202799 NCIT:C2028 NCIT:C20280 +NCIT:C202800 +NCIT:C202801 +NCIT:C202802 +NCIT:C202803 +NCIT:C202804 +NCIT:C202805 +NCIT:C202806 +NCIT:C202807 +NCIT:C202808 +NCIT:C202809 NCIT:C20281 +NCIT:C202810 +NCIT:C202811 +NCIT:C202812 +NCIT:C202813 +NCIT:C202814 +NCIT:C202815 +NCIT:C202816 +NCIT:C202817 +NCIT:C202818 +NCIT:C202819 NCIT:C20282 +NCIT:C202820 +NCIT:C202821 +NCIT:C202822 +NCIT:C202823 +NCIT:C202824 +NCIT:C202825 +NCIT:C202826 +NCIT:C202827 +NCIT:C202828 +NCIT:C202829 NCIT:C20283 +NCIT:C202830 +NCIT:C202831 +NCIT:C202832 +NCIT:C202833 +NCIT:C202834 +NCIT:C202835 +NCIT:C202836 +NCIT:C202837 +NCIT:C202838 +NCIT:C202839 NCIT:C20284 +NCIT:C202840 +NCIT:C202841 +NCIT:C202842 +NCIT:C202843 +NCIT:C202844 +NCIT:C202845 +NCIT:C202846 +NCIT:C202847 +NCIT:C202848 NCIT:C20285 +NCIT:C202850 +NCIT:C202854 +NCIT:C202855 +NCIT:C202857 NCIT:C20286 +NCIT:C202862 +NCIT:C202863 +NCIT:C202864 +NCIT:C202865 +NCIT:C202866 +NCIT:C202867 +NCIT:C202868 +NCIT:C202869 NCIT:C20287 +NCIT:C202870 +NCIT:C202871 +NCIT:C202872 +NCIT:C202873 +NCIT:C202874 +NCIT:C202875 NCIT:C20288 +NCIT:C202885 +NCIT:C202886 +NCIT:C202887 +NCIT:C202888 +NCIT:C202889 NCIT:C20289 +NCIT:C202890 +NCIT:C202891 +NCIT:C202892 +NCIT:C202893 +NCIT:C202895 NCIT:C2029 NCIT:C20290 +NCIT:C202900 +NCIT:C202902 +NCIT:C202903 +NCIT:C202905 +NCIT:C202906 +NCIT:C202907 +NCIT:C202908 +NCIT:C202909 NCIT:C20291 +NCIT:C202910 +NCIT:C202911 +NCIT:C202912 +NCIT:C202913 +NCIT:C202915 +NCIT:C202916 +NCIT:C202917 +NCIT:C202918 +NCIT:C202919 NCIT:C20292 +NCIT:C202920 +NCIT:C202928 NCIT:C20293 +NCIT:C202931 +NCIT:C202933 +NCIT:C202934 +NCIT:C202937 +NCIT:C202938 +NCIT:C202939 NCIT:C20294 +NCIT:C202940 +NCIT:C202941 +NCIT:C202942 +NCIT:C202943 +NCIT:C202944 +NCIT:C202945 +NCIT:C202946 +NCIT:C202947 +NCIT:C202948 +NCIT:C202949 NCIT:C20295 +NCIT:C202950 +NCIT:C202951 +NCIT:C202956 +NCIT:C202957 +NCIT:C202959 NCIT:C20296 +NCIT:C202960 +NCIT:C202961 +NCIT:C202962 +NCIT:C202963 +NCIT:C202964 +NCIT:C202965 +NCIT:C202968 +NCIT:C202969 NCIT:C20297 +NCIT:C202970 +NCIT:C202974 +NCIT:C202976 NCIT:C20298 +NCIT:C202988 NCIT:C20299 +NCIT:C202999 NCIT:C203 NCIT:C2030 NCIT:C20300 +NCIT:C203000 +NCIT:C203001 +NCIT:C203003 NCIT:C20301 +NCIT:C203019 NCIT:C20302 +NCIT:C203020 +NCIT:C203021 +NCIT:C203022 +NCIT:C203023 +NCIT:C203024 +NCIT:C203025 +NCIT:C203026 +NCIT:C203027 +NCIT:C203028 +NCIT:C203029 NCIT:C20303 +NCIT:C203030 +NCIT:C203031 +NCIT:C203032 +NCIT:C203033 +NCIT:C203034 +NCIT:C203035 +NCIT:C203036 +NCIT:C203037 +NCIT:C203038 +NCIT:C203039 NCIT:C20304 +NCIT:C203040 +NCIT:C203041 +NCIT:C203042 +NCIT:C203043 +NCIT:C203044 +NCIT:C203045 +NCIT:C203046 +NCIT:C203047 +NCIT:C203048 +NCIT:C203049 NCIT:C20305 +NCIT:C203050 +NCIT:C203051 +NCIT:C203052 +NCIT:C203053 +NCIT:C203054 +NCIT:C203055 +NCIT:C203056 +NCIT:C203057 +NCIT:C203058 +NCIT:C203059 NCIT:C20306 +NCIT:C203060 +NCIT:C203061 +NCIT:C203062 +NCIT:C203063 +NCIT:C203064 +NCIT:C203065 +NCIT:C203066 +NCIT:C203067 +NCIT:C203068 +NCIT:C203069 NCIT:C20307 +NCIT:C203070 +NCIT:C203071 +NCIT:C203072 +NCIT:C203073 +NCIT:C203074 +NCIT:C203075 +NCIT:C203076 +NCIT:C203077 +NCIT:C203078 +NCIT:C203079 NCIT:C20308 +NCIT:C203080 +NCIT:C203081 +NCIT:C203082 +NCIT:C203083 +NCIT:C203084 +NCIT:C203085 +NCIT:C203086 +NCIT:C203087 +NCIT:C203088 +NCIT:C203089 NCIT:C20309 +NCIT:C203090 +NCIT:C203091 +NCIT:C203092 +NCIT:C203093 +NCIT:C203094 +NCIT:C203095 +NCIT:C203096 +NCIT:C203097 +NCIT:C203098 +NCIT:C203099 NCIT:C2031 NCIT:C20310 +NCIT:C203100 +NCIT:C203101 +NCIT:C203102 +NCIT:C203103 +NCIT:C203104 +NCIT:C203105 +NCIT:C203106 +NCIT:C203107 +NCIT:C203108 +NCIT:C203109 NCIT:C20311 +NCIT:C203110 +NCIT:C203111 +NCIT:C203112 +NCIT:C203113 +NCIT:C203114 +NCIT:C203115 +NCIT:C203116 +NCIT:C203117 +NCIT:C203118 +NCIT:C203119 NCIT:C20312 +NCIT:C203120 +NCIT:C203121 +NCIT:C203122 +NCIT:C203123 +NCIT:C203124 +NCIT:C203125 +NCIT:C203126 +NCIT:C203127 +NCIT:C203128 +NCIT:C203129 NCIT:C20313 +NCIT:C203130 +NCIT:C203131 +NCIT:C203132 +NCIT:C203133 +NCIT:C203134 +NCIT:C203135 +NCIT:C203136 +NCIT:C203137 +NCIT:C203138 +NCIT:C203139 NCIT:C20314 +NCIT:C203140 +NCIT:C203141 +NCIT:C203142 +NCIT:C203143 +NCIT:C203144 +NCIT:C203145 +NCIT:C203146 +NCIT:C203147 +NCIT:C203148 +NCIT:C203149 NCIT:C20315 +NCIT:C203150 +NCIT:C203151 +NCIT:C203152 +NCIT:C203153 +NCIT:C203154 +NCIT:C203155 +NCIT:C203156 +NCIT:C203157 +NCIT:C203158 +NCIT:C203159 NCIT:C20316 +NCIT:C203160 +NCIT:C203161 +NCIT:C203162 +NCIT:C203163 +NCIT:C203164 +NCIT:C203165 +NCIT:C203166 +NCIT:C203167 +NCIT:C203168 +NCIT:C203169 NCIT:C20317 +NCIT:C203170 +NCIT:C203171 +NCIT:C203172 +NCIT:C203173 +NCIT:C203174 +NCIT:C203175 +NCIT:C203176 +NCIT:C203177 +NCIT:C203178 +NCIT:C203179 NCIT:C20318 +NCIT:C203180 +NCIT:C203181 +NCIT:C203182 +NCIT:C203183 +NCIT:C203184 +NCIT:C203185 +NCIT:C203186 +NCIT:C203187 +NCIT:C203188 +NCIT:C203189 NCIT:C20319 +NCIT:C203190 +NCIT:C203191 +NCIT:C203192 +NCIT:C203193 +NCIT:C203194 +NCIT:C203195 +NCIT:C203196 +NCIT:C203197 +NCIT:C203198 +NCIT:C203199 NCIT:C2032 NCIT:C20320 +NCIT:C203200 +NCIT:C203201 +NCIT:C203202 +NCIT:C203203 +NCIT:C203204 +NCIT:C203205 +NCIT:C203206 +NCIT:C203207 +NCIT:C203208 +NCIT:C203209 +NCIT:C203210 +NCIT:C203211 +NCIT:C203212 +NCIT:C203213 +NCIT:C203214 +NCIT:C203215 +NCIT:C203216 +NCIT:C203217 +NCIT:C203218 +NCIT:C203219 NCIT:C20322 +NCIT:C203220 +NCIT:C203221 +NCIT:C203222 +NCIT:C203223 +NCIT:C203224 +NCIT:C203225 +NCIT:C203226 +NCIT:C203227 +NCIT:C203228 +NCIT:C203229 NCIT:C20323 +NCIT:C203230 +NCIT:C203231 +NCIT:C203232 +NCIT:C203233 +NCIT:C203234 +NCIT:C203235 +NCIT:C203236 +NCIT:C203237 +NCIT:C203238 +NCIT:C203239 NCIT:C20324 +NCIT:C203240 +NCIT:C203241 +NCIT:C203242 +NCIT:C203243 +NCIT:C203244 +NCIT:C203245 +NCIT:C203246 +NCIT:C203247 +NCIT:C203248 +NCIT:C203249 NCIT:C20325 +NCIT:C203254 +NCIT:C203255 +NCIT:C203256 +NCIT:C203257 NCIT:C20326 +NCIT:C203261 +NCIT:C203264 +NCIT:C203268 NCIT:C20327 +NCIT:C203275 +NCIT:C203276 +NCIT:C203277 +NCIT:C203278 +NCIT:C203279 NCIT:C20328 +NCIT:C203280 +NCIT:C203281 +NCIT:C203287 +NCIT:C203288 +NCIT:C203289 NCIT:C20329 +NCIT:C203290 +NCIT:C203291 +NCIT:C203292 +NCIT:C203293 +NCIT:C203294 +NCIT:C203295 +NCIT:C203296 +NCIT:C203297 +NCIT:C203298 +NCIT:C203299 NCIT:C2033 NCIT:C20330 +NCIT:C203300 +NCIT:C203301 +NCIT:C203303 +NCIT:C203304 +NCIT:C203305 +NCIT:C203306 NCIT:C20331 +NCIT:C203317 +NCIT:C203318 +NCIT:C203319 NCIT:C20332 +NCIT:C203320 +NCIT:C203321 +NCIT:C203322 +NCIT:C203323 +NCIT:C203324 +NCIT:C203325 +NCIT:C203326 +NCIT:C203327 +NCIT:C203328 +NCIT:C203329 NCIT:C20333 +NCIT:C203330 +NCIT:C203332 +NCIT:C203333 +NCIT:C203334 +NCIT:C203335 +NCIT:C203336 +NCIT:C203337 +NCIT:C203338 NCIT:C20334 +NCIT:C203340 +NCIT:C203345 +NCIT:C203346 +NCIT:C203347 +NCIT:C203348 +NCIT:C203349 NCIT:C20335 +NCIT:C203350 +NCIT:C203351 +NCIT:C203352 +NCIT:C203353 +NCIT:C203354 +NCIT:C203355 +NCIT:C203356 +NCIT:C203357 +NCIT:C203358 +NCIT:C203359 NCIT:C20336 +NCIT:C203360 +NCIT:C203361 +NCIT:C203363 +NCIT:C203364 +NCIT:C203365 +NCIT:C203366 +NCIT:C203367 +NCIT:C203368 NCIT:C20337 +NCIT:C203371 +NCIT:C203372 +NCIT:C203373 +NCIT:C203377 +NCIT:C203378 +NCIT:C203379 NCIT:C20338 +NCIT:C203382 +NCIT:C203383 NCIT:C20339 +NCIT:C203396 +NCIT:C203397 +NCIT:C203398 +NCIT:C203399 NCIT:C2034 NCIT:C20340 +NCIT:C203400 +NCIT:C203401 +NCIT:C203402 +NCIT:C203403 +NCIT:C203404 +NCIT:C203405 NCIT:C20341 +NCIT:C203414 +NCIT:C203416 +NCIT:C203417 +NCIT:C203418 +NCIT:C203419 NCIT:C20342 +NCIT:C203420 +NCIT:C203421 +NCIT:C203423 +NCIT:C203424 +NCIT:C203425 +NCIT:C203427 +NCIT:C203429 NCIT:C20343 +NCIT:C203436 +NCIT:C203438 +NCIT:C203439 NCIT:C20344 +NCIT:C203441 +NCIT:C203442 +NCIT:C203445 +NCIT:C203446 +NCIT:C203447 +NCIT:C203448 +NCIT:C203449 NCIT:C20345 +NCIT:C203450 +NCIT:C203451 +NCIT:C203452 +NCIT:C203453 +NCIT:C203454 +NCIT:C203455 +NCIT:C203456 +NCIT:C203457 +NCIT:C203458 +NCIT:C203459 NCIT:C20346 +NCIT:C203460 +NCIT:C203461 +NCIT:C203462 +NCIT:C203463 +NCIT:C203464 +NCIT:C203465 +NCIT:C203466 +NCIT:C203467 +NCIT:C203468 NCIT:C20347 +NCIT:C203470 +NCIT:C203471 +NCIT:C203472 +NCIT:C203473 +NCIT:C203474 +NCIT:C203475 +NCIT:C203476 +NCIT:C203477 +NCIT:C203478 +NCIT:C203479 NCIT:C20348 +NCIT:C203480 +NCIT:C203481 +NCIT:C203482 +NCIT:C203483 +NCIT:C203484 +NCIT:C203485 +NCIT:C203486 +NCIT:C203487 +NCIT:C203488 +NCIT:C203489 NCIT:C20349 +NCIT:C203490 +NCIT:C203491 +NCIT:C203492 +NCIT:C203493 +NCIT:C203494 +NCIT:C203495 +NCIT:C203496 +NCIT:C203497 +NCIT:C203498 +NCIT:C203499 NCIT:C2035 NCIT:C20350 +NCIT:C203500 +NCIT:C203501 +NCIT:C203502 +NCIT:C203503 +NCIT:C203504 +NCIT:C203505 +NCIT:C203506 +NCIT:C203507 +NCIT:C203508 +NCIT:C203509 +NCIT:C203510 +NCIT:C203512 +NCIT:C203514 +NCIT:C203516 +NCIT:C203517 +NCIT:C203518 +NCIT:C203519 NCIT:C20352 +NCIT:C203520 +NCIT:C203521 +NCIT:C203522 +NCIT:C203524 +NCIT:C203525 +NCIT:C203527 +NCIT:C203528 +NCIT:C203529 NCIT:C20353 +NCIT:C203530 +NCIT:C203531 +NCIT:C203532 +NCIT:C203533 +NCIT:C203534 +NCIT:C203535 +NCIT:C203536 +NCIT:C203537 +NCIT:C203538 +NCIT:C203539 NCIT:C20354 +NCIT:C203540 +NCIT:C203541 +NCIT:C203542 +NCIT:C203543 +NCIT:C203544 +NCIT:C203545 +NCIT:C203546 NCIT:C20355 +NCIT:C203557 +NCIT:C203558 +NCIT:C203559 NCIT:C20356 +NCIT:C203560 +NCIT:C203561 +NCIT:C203562 +NCIT:C203563 +NCIT:C203564 +NCIT:C203565 +NCIT:C203566 +NCIT:C203567 +NCIT:C203568 +NCIT:C203569 NCIT:C20357 +NCIT:C203570 +NCIT:C203571 +NCIT:C203572 +NCIT:C203573 +NCIT:C203574 +NCIT:C203575 +NCIT:C203576 +NCIT:C203577 +NCIT:C203578 +NCIT:C203579 NCIT:C20358 +NCIT:C203580 +NCIT:C203581 +NCIT:C203582 +NCIT:C203584 +NCIT:C203585 +NCIT:C203586 +NCIT:C203587 +NCIT:C203588 +NCIT:C203589 NCIT:C20359 +NCIT:C203590 +NCIT:C203591 +NCIT:C203592 +NCIT:C203593 +NCIT:C203594 +NCIT:C203595 +NCIT:C203596 +NCIT:C203597 +NCIT:C203598 +NCIT:C203599 NCIT:C2036 NCIT:C20360 +NCIT:C203600 +NCIT:C203602 +NCIT:C203603 +NCIT:C203604 +NCIT:C203605 +NCIT:C203606 +NCIT:C203607 +NCIT:C203608 +NCIT:C203609 NCIT:C20361 +NCIT:C203610 +NCIT:C203611 +NCIT:C203612 +NCIT:C203613 +NCIT:C203614 +NCIT:C203615 +NCIT:C203616 +NCIT:C203617 NCIT:C20362 +NCIT:C203620 +NCIT:C203621 +NCIT:C203622 +NCIT:C203623 +NCIT:C203624 +NCIT:C203625 +NCIT:C203626 +NCIT:C203627 +NCIT:C203628 +NCIT:C203629 NCIT:C20363 +NCIT:C203630 +NCIT:C203631 +NCIT:C203632 +NCIT:C203633 +NCIT:C203634 +NCIT:C203635 +NCIT:C203636 +NCIT:C203637 +NCIT:C203638 +NCIT:C203639 NCIT:C20364 +NCIT:C203640 +NCIT:C203641 +NCIT:C203642 +NCIT:C203643 +NCIT:C203644 +NCIT:C203645 +NCIT:C203646 +NCIT:C203647 +NCIT:C203648 +NCIT:C203649 NCIT:C20365 +NCIT:C203650 +NCIT:C203651 +NCIT:C203652 +NCIT:C203653 +NCIT:C203654 +NCIT:C203655 +NCIT:C203656 +NCIT:C203657 +NCIT:C203658 +NCIT:C203660 +NCIT:C203661 +NCIT:C203662 +NCIT:C203663 +NCIT:C203664 +NCIT:C203665 +NCIT:C203666 +NCIT:C203668 NCIT:C20367 +NCIT:C203670 +NCIT:C203671 +NCIT:C203672 +NCIT:C203674 +NCIT:C203676 +NCIT:C203677 +NCIT:C203678 +NCIT:C203679 NCIT:C20368 +NCIT:C203680 +NCIT:C203681 +NCIT:C203682 +NCIT:C203683 +NCIT:C203684 +NCIT:C203685 +NCIT:C203686 +NCIT:C203687 +NCIT:C203688 +NCIT:C203689 NCIT:C20369 +NCIT:C203690 +NCIT:C203691 +NCIT:C203692 +NCIT:C203693 +NCIT:C203694 +NCIT:C203695 +NCIT:C203696 +NCIT:C203697 +NCIT:C203698 +NCIT:C203699 NCIT:C2037 NCIT:C20370 +NCIT:C203701 +NCIT:C203702 +NCIT:C203703 +NCIT:C203704 +NCIT:C203705 +NCIT:C203706 +NCIT:C203707 +NCIT:C203708 +NCIT:C203709 NCIT:C20371 +NCIT:C203710 +NCIT:C203711 +NCIT:C203712 +NCIT:C203713 +NCIT:C203714 +NCIT:C203715 +NCIT:C203716 +NCIT:C203717 +NCIT:C203718 +NCIT:C203719 NCIT:C20372 +NCIT:C203720 +NCIT:C203721 +NCIT:C203722 +NCIT:C203723 +NCIT:C203724 +NCIT:C203725 +NCIT:C203726 +NCIT:C203727 +NCIT:C203728 +NCIT:C203729 NCIT:C20373 +NCIT:C203730 +NCIT:C203731 +NCIT:C203732 +NCIT:C203733 +NCIT:C203734 +NCIT:C203735 +NCIT:C203736 +NCIT:C203737 +NCIT:C203738 +NCIT:C203739 NCIT:C20374 +NCIT:C203740 +NCIT:C203741 +NCIT:C203742 +NCIT:C203743 +NCIT:C203744 +NCIT:C203745 +NCIT:C203746 +NCIT:C203747 +NCIT:C203748 +NCIT:C203749 NCIT:C20375 +NCIT:C203750 +NCIT:C203751 +NCIT:C203752 +NCIT:C203753 +NCIT:C203754 +NCIT:C203755 +NCIT:C203756 +NCIT:C203757 +NCIT:C203758 +NCIT:C203759 NCIT:C20376 +NCIT:C203760 +NCIT:C203761 +NCIT:C203762 +NCIT:C203763 +NCIT:C203764 +NCIT:C203765 +NCIT:C203766 +NCIT:C203767 +NCIT:C203768 +NCIT:C203769 NCIT:C20377 +NCIT:C203770 +NCIT:C203771 +NCIT:C203772 +NCIT:C203773 +NCIT:C203774 +NCIT:C203775 +NCIT:C203776 +NCIT:C203777 +NCIT:C203778 +NCIT:C203779 NCIT:C20378 +NCIT:C203780 +NCIT:C203781 +NCIT:C203782 +NCIT:C203783 +NCIT:C203784 +NCIT:C203785 +NCIT:C203786 +NCIT:C203787 +NCIT:C203788 +NCIT:C203789 NCIT:C20379 +NCIT:C203790 +NCIT:C203791 +NCIT:C203792 +NCIT:C203793 +NCIT:C203794 +NCIT:C203796 +NCIT:C203797 +NCIT:C203798 +NCIT:C203799 NCIT:C2038 NCIT:C20380 +NCIT:C203800 +NCIT:C203801 +NCIT:C203802 +NCIT:C203803 +NCIT:C203804 +NCIT:C203805 +NCIT:C203806 +NCIT:C203807 +NCIT:C203808 +NCIT:C203809 NCIT:C20381 +NCIT:C203810 +NCIT:C203811 +NCIT:C203812 +NCIT:C203813 +NCIT:C203814 +NCIT:C203816 +NCIT:C203817 +NCIT:C203818 +NCIT:C203819 NCIT:C20382 +NCIT:C203820 +NCIT:C203821 +NCIT:C203822 +NCIT:C203823 +NCIT:C203824 +NCIT:C203825 +NCIT:C203826 +NCIT:C203827 +NCIT:C203828 +NCIT:C203829 NCIT:C20383 +NCIT:C203830 +NCIT:C203831 +NCIT:C203832 +NCIT:C203833 +NCIT:C203834 +NCIT:C203835 +NCIT:C203836 +NCIT:C203837 +NCIT:C203838 +NCIT:C203839 NCIT:C20384 +NCIT:C203840 +NCIT:C203841 +NCIT:C203842 +NCIT:C203843 +NCIT:C203844 +NCIT:C203845 +NCIT:C203846 +NCIT:C203847 +NCIT:C203848 +NCIT:C203849 NCIT:C20385 +NCIT:C203850 +NCIT:C203852 +NCIT:C203853 +NCIT:C203854 +NCIT:C203855 +NCIT:C203856 +NCIT:C203857 +NCIT:C203858 +NCIT:C203859 NCIT:C20386 +NCIT:C203860 +NCIT:C203861 +NCIT:C203862 +NCIT:C203863 +NCIT:C203864 +NCIT:C203865 +NCIT:C203866 +NCIT:C203867 +NCIT:C203868 +NCIT:C203869 NCIT:C20387 +NCIT:C203870 +NCIT:C203871 +NCIT:C203872 +NCIT:C203873 +NCIT:C203874 +NCIT:C203875 +NCIT:C203876 +NCIT:C203877 +NCIT:C203878 +NCIT:C203879 NCIT:C20388 +NCIT:C203880 +NCIT:C203881 +NCIT:C203882 +NCIT:C203883 +NCIT:C203884 +NCIT:C203885 +NCIT:C203886 +NCIT:C203887 +NCIT:C203888 +NCIT:C203889 NCIT:C20389 +NCIT:C203890 +NCIT:C203891 +NCIT:C203892 +NCIT:C203893 +NCIT:C203894 +NCIT:C203895 +NCIT:C203896 +NCIT:C203897 +NCIT:C203898 +NCIT:C203899 NCIT:C2039 NCIT:C20390 +NCIT:C203900 +NCIT:C203901 +NCIT:C203902 +NCIT:C203903 +NCIT:C203905 +NCIT:C203906 +NCIT:C203907 +NCIT:C203908 +NCIT:C203909 NCIT:C20391 +NCIT:C203910 +NCIT:C203911 +NCIT:C203912 +NCIT:C203913 +NCIT:C203914 +NCIT:C203915 +NCIT:C203916 +NCIT:C203917 +NCIT:C203918 +NCIT:C203919 NCIT:C20392 +NCIT:C203920 +NCIT:C203921 +NCIT:C203922 +NCIT:C203923 +NCIT:C203924 +NCIT:C203925 +NCIT:C203926 +NCIT:C203927 +NCIT:C203928 +NCIT:C203929 NCIT:C20393 +NCIT:C203930 +NCIT:C203931 +NCIT:C203932 +NCIT:C203933 +NCIT:C203934 +NCIT:C203935 +NCIT:C203936 +NCIT:C203937 +NCIT:C203938 +NCIT:C203939 NCIT:C20394 +NCIT:C203940 +NCIT:C203941 +NCIT:C203942 +NCIT:C203943 +NCIT:C203944 +NCIT:C203945 +NCIT:C203947 NCIT:C20395 +NCIT:C203950 +NCIT:C203951 +NCIT:C203952 +NCIT:C203953 +NCIT:C203954 +NCIT:C203955 +NCIT:C203956 +NCIT:C203957 +NCIT:C203958 +NCIT:C203959 NCIT:C20396 +NCIT:C203960 +NCIT:C203961 +NCIT:C203962 +NCIT:C203963 +NCIT:C203964 +NCIT:C203965 +NCIT:C203966 +NCIT:C203967 NCIT:C20397 +NCIT:C203970 +NCIT:C203971 +NCIT:C203972 +NCIT:C203973 +NCIT:C203974 +NCIT:C203975 +NCIT:C203976 +NCIT:C203977 +NCIT:C203978 +NCIT:C203979 NCIT:C20398 +NCIT:C203980 +NCIT:C203981 +NCIT:C203982 +NCIT:C203983 +NCIT:C203984 +NCIT:C203985 +NCIT:C203986 +NCIT:C203987 +NCIT:C203988 +NCIT:C203989 NCIT:C20399 +NCIT:C203990 +NCIT:C203991 +NCIT:C203992 +NCIT:C203993 +NCIT:C203994 +NCIT:C203995 +NCIT:C203996 +NCIT:C203997 +NCIT:C203998 +NCIT:C203999 NCIT:C204 NCIT:C2040 +NCIT:C204000 +NCIT:C204001 +NCIT:C204002 +NCIT:C204003 +NCIT:C204004 +NCIT:C204005 +NCIT:C204006 +NCIT:C204007 +NCIT:C204008 +NCIT:C204009 NCIT:C20401 +NCIT:C204010 +NCIT:C204011 +NCIT:C204012 +NCIT:C204013 +NCIT:C204014 +NCIT:C204015 +NCIT:C204016 +NCIT:C204017 +NCIT:C204018 +NCIT:C204019 NCIT:C20402 +NCIT:C204020 +NCIT:C204021 +NCIT:C204022 +NCIT:C204023 +NCIT:C204024 +NCIT:C204025 +NCIT:C204026 +NCIT:C204027 +NCIT:C204028 +NCIT:C204029 NCIT:C20403 +NCIT:C204030 +NCIT:C204031 +NCIT:C204032 +NCIT:C204033 +NCIT:C204034 +NCIT:C204039 NCIT:C20404 +NCIT:C204040 +NCIT:C204041 +NCIT:C204042 +NCIT:C204043 +NCIT:C204044 +NCIT:C204045 +NCIT:C204046 +NCIT:C204047 +NCIT:C204048 +NCIT:C204049 NCIT:C20405 +NCIT:C204050 +NCIT:C204051 +NCIT:C204052 +NCIT:C204053 +NCIT:C204054 +NCIT:C204055 +NCIT:C204056 +NCIT:C204057 +NCIT:C204058 +NCIT:C204059 NCIT:C20406 +NCIT:C204060 +NCIT:C204061 +NCIT:C204062 +NCIT:C204063 +NCIT:C204064 +NCIT:C204065 +NCIT:C204066 +NCIT:C204067 +NCIT:C204068 +NCIT:C204069 NCIT:C20407 +NCIT:C204070 +NCIT:C204071 +NCIT:C204072 +NCIT:C204073 +NCIT:C204074 +NCIT:C204075 +NCIT:C204076 +NCIT:C204077 +NCIT:C204078 +NCIT:C204079 NCIT:C20408 +NCIT:C204080 +NCIT:C204081 +NCIT:C204082 +NCIT:C204083 +NCIT:C204084 +NCIT:C204085 +NCIT:C204086 +NCIT:C204087 +NCIT:C204088 +NCIT:C204089 NCIT:C20409 +NCIT:C204090 +NCIT:C204091 +NCIT:C204092 +NCIT:C204093 +NCIT:C204094 +NCIT:C204095 +NCIT:C204096 +NCIT:C204097 +NCIT:C204098 +NCIT:C204099 NCIT:C2041 NCIT:C20410 +NCIT:C204100 +NCIT:C204101 +NCIT:C204102 +NCIT:C204103 +NCIT:C204104 +NCIT:C204105 +NCIT:C204106 +NCIT:C204107 +NCIT:C204108 +NCIT:C204109 NCIT:C20411 +NCIT:C204110 +NCIT:C204111 +NCIT:C204112 +NCIT:C204113 +NCIT:C204114 +NCIT:C204115 +NCIT:C204116 +NCIT:C204117 +NCIT:C204118 +NCIT:C204119 NCIT:C20412 +NCIT:C204120 +NCIT:C204121 +NCIT:C204122 +NCIT:C204123 +NCIT:C204125 +NCIT:C204127 +NCIT:C204128 +NCIT:C204129 NCIT:C20413 +NCIT:C204131 +NCIT:C204132 +NCIT:C204133 +NCIT:C204134 +NCIT:C204135 +NCIT:C204136 +NCIT:C204137 +NCIT:C204138 +NCIT:C204139 NCIT:C20414 +NCIT:C204140 +NCIT:C204141 +NCIT:C204142 +NCIT:C204143 +NCIT:C204144 +NCIT:C204145 +NCIT:C204146 +NCIT:C204147 +NCIT:C204148 +NCIT:C204149 NCIT:C20415 +NCIT:C204150 +NCIT:C204151 +NCIT:C204152 +NCIT:C204153 +NCIT:C204154 +NCIT:C204155 +NCIT:C204156 +NCIT:C204157 +NCIT:C204158 +NCIT:C204159 NCIT:C20416 +NCIT:C204160 +NCIT:C204161 +NCIT:C204162 +NCIT:C204163 +NCIT:C204164 +NCIT:C204165 +NCIT:C204166 +NCIT:C204167 +NCIT:C204168 +NCIT:C204169 NCIT:C20417 +NCIT:C204170 +NCIT:C204171 +NCIT:C204172 +NCIT:C204173 +NCIT:C204174 +NCIT:C204175 +NCIT:C204176 +NCIT:C204177 +NCIT:C204178 +NCIT:C204179 NCIT:C20418 +NCIT:C204180 +NCIT:C204181 +NCIT:C204182 +NCIT:C204183 +NCIT:C204184 +NCIT:C204185 +NCIT:C204186 +NCIT:C204187 +NCIT:C204188 +NCIT:C204189 NCIT:C20419 +NCIT:C204190 +NCIT:C204191 +NCIT:C204192 +NCIT:C204193 +NCIT:C204194 +NCIT:C204195 +NCIT:C204196 +NCIT:C204197 +NCIT:C204198 +NCIT:C204199 NCIT:C2042 NCIT:C20420 +NCIT:C204200 +NCIT:C204201 +NCIT:C204202 +NCIT:C204204 +NCIT:C204205 +NCIT:C204206 +NCIT:C204207 +NCIT:C204208 +NCIT:C204209 NCIT:C20421 +NCIT:C204210 +NCIT:C204211 +NCIT:C204212 +NCIT:C204213 +NCIT:C204214 +NCIT:C204215 +NCIT:C204216 +NCIT:C204217 +NCIT:C204218 +NCIT:C204219 NCIT:C20422 +NCIT:C204220 +NCIT:C204221 +NCIT:C204222 +NCIT:C204223 +NCIT:C204224 +NCIT:C204225 +NCIT:C204226 +NCIT:C204227 +NCIT:C204228 +NCIT:C204229 NCIT:C20423 +NCIT:C204230 +NCIT:C204231 +NCIT:C204232 +NCIT:C204233 +NCIT:C204234 +NCIT:C204235 +NCIT:C204236 +NCIT:C204237 +NCIT:C204238 +NCIT:C204239 NCIT:C20424 +NCIT:C204240 +NCIT:C204241 +NCIT:C204242 +NCIT:C204243 +NCIT:C204244 +NCIT:C204245 +NCIT:C204246 +NCIT:C204247 +NCIT:C204248 +NCIT:C204249 NCIT:C20425 +NCIT:C204250 +NCIT:C204251 +NCIT:C204252 +NCIT:C204253 +NCIT:C204254 +NCIT:C204255 +NCIT:C204256 +NCIT:C204257 +NCIT:C204258 +NCIT:C204259 NCIT:C20426 +NCIT:C204260 +NCIT:C204261 +NCIT:C204262 +NCIT:C204263 +NCIT:C204264 +NCIT:C204265 +NCIT:C204266 +NCIT:C204267 +NCIT:C204268 +NCIT:C204269 NCIT:C20427 +NCIT:C204270 +NCIT:C204271 +NCIT:C204272 +NCIT:C204273 +NCIT:C204274 +NCIT:C204275 +NCIT:C204276 +NCIT:C204277 +NCIT:C204278 +NCIT:C204279 NCIT:C20428 +NCIT:C204280 +NCIT:C204281 +NCIT:C204282 +NCIT:C204283 +NCIT:C204284 +NCIT:C204285 +NCIT:C204286 +NCIT:C204287 +NCIT:C204288 +NCIT:C204289 NCIT:C20429 +NCIT:C204290 +NCIT:C204291 +NCIT:C204292 +NCIT:C204293 +NCIT:C204294 +NCIT:C204295 +NCIT:C204296 +NCIT:C204297 +NCIT:C204298 +NCIT:C204299 NCIT:C2043 NCIT:C20430 +NCIT:C204300 +NCIT:C204301 +NCIT:C204302 +NCIT:C204303 +NCIT:C204304 +NCIT:C204305 +NCIT:C204306 +NCIT:C204307 +NCIT:C204308 +NCIT:C204309 NCIT:C20431 +NCIT:C204310 +NCIT:C204311 +NCIT:C204312 +NCIT:C204313 +NCIT:C204314 +NCIT:C204315 +NCIT:C204316 +NCIT:C204317 +NCIT:C204318 +NCIT:C204319 NCIT:C20432 +NCIT:C204320 +NCIT:C204321 +NCIT:C204322 +NCIT:C204323 +NCIT:C204324 +NCIT:C204325 +NCIT:C204326 +NCIT:C204327 +NCIT:C204328 +NCIT:C204329 NCIT:C20433 +NCIT:C204330 +NCIT:C204331 +NCIT:C204332 +NCIT:C204333 +NCIT:C204334 +NCIT:C204335 +NCIT:C204336 +NCIT:C204337 +NCIT:C204338 +NCIT:C204339 NCIT:C20434 +NCIT:C204340 +NCIT:C204341 +NCIT:C204342 +NCIT:C204343 +NCIT:C204344 +NCIT:C204345 +NCIT:C204346 +NCIT:C204347 +NCIT:C204348 +NCIT:C204349 NCIT:C20435 +NCIT:C204350 +NCIT:C204351 +NCIT:C204352 +NCIT:C204353 +NCIT:C204354 +NCIT:C204356 +NCIT:C204357 +NCIT:C204358 +NCIT:C204359 NCIT:C20436 +NCIT:C204360 +NCIT:C204361 +NCIT:C204362 +NCIT:C204363 +NCIT:C204364 +NCIT:C204365 +NCIT:C204366 +NCIT:C204367 +NCIT:C204368 +NCIT:C204369 NCIT:C20437 +NCIT:C204370 +NCIT:C204371 +NCIT:C204372 +NCIT:C204373 +NCIT:C204374 +NCIT:C204375 +NCIT:C204376 +NCIT:C204377 +NCIT:C204378 +NCIT:C204379 +NCIT:C204380 +NCIT:C204381 +NCIT:C204382 +NCIT:C204384 +NCIT:C204386 +NCIT:C204387 +NCIT:C204388 +NCIT:C204389 NCIT:C20439 +NCIT:C204390 +NCIT:C204391 +NCIT:C204392 +NCIT:C204393 +NCIT:C204394 +NCIT:C204395 +NCIT:C204396 +NCIT:C204397 +NCIT:C204398 +NCIT:C204399 NCIT:C2044 NCIT:C20440 +NCIT:C204400 +NCIT:C204401 +NCIT:C204402 +NCIT:C204403 +NCIT:C204404 +NCIT:C204405 +NCIT:C204406 +NCIT:C204407 +NCIT:C204408 +NCIT:C204409 NCIT:C20441 +NCIT:C204410 +NCIT:C204411 +NCIT:C204412 +NCIT:C204413 +NCIT:C204414 +NCIT:C204415 +NCIT:C204416 +NCIT:C204417 +NCIT:C204418 +NCIT:C204419 NCIT:C20442 +NCIT:C204420 +NCIT:C204421 +NCIT:C204422 +NCIT:C204423 +NCIT:C204424 +NCIT:C204425 +NCIT:C204426 +NCIT:C204427 +NCIT:C204428 +NCIT:C204429 +NCIT:C204430 +NCIT:C204431 +NCIT:C204432 +NCIT:C204433 +NCIT:C204434 +NCIT:C204435 +NCIT:C204436 +NCIT:C204438 +NCIT:C204439 NCIT:C20444 +NCIT:C204440 +NCIT:C204441 +NCIT:C204442 +NCIT:C204443 +NCIT:C204444 +NCIT:C204445 +NCIT:C204446 +NCIT:C204447 +NCIT:C204448 +NCIT:C204449 NCIT:C20445 +NCIT:C204450 +NCIT:C204451 +NCIT:C204452 +NCIT:C204453 +NCIT:C204454 +NCIT:C204455 +NCIT:C204456 +NCIT:C204457 +NCIT:C204458 +NCIT:C204459 NCIT:C20446 +NCIT:C204460 +NCIT:C204461 +NCIT:C204462 +NCIT:C204463 +NCIT:C204464 +NCIT:C204465 +NCIT:C204466 +NCIT:C204467 +NCIT:C204468 +NCIT:C204469 NCIT:C20447 +NCIT:C204470 +NCIT:C204471 +NCIT:C204472 +NCIT:C204473 +NCIT:C204474 +NCIT:C204476 +NCIT:C204477 +NCIT:C204478 +NCIT:C204479 NCIT:C20448 +NCIT:C204480 +NCIT:C204481 +NCIT:C204483 +NCIT:C204484 +NCIT:C204485 +NCIT:C204486 +NCIT:C204487 +NCIT:C204488 +NCIT:C204489 NCIT:C20449 +NCIT:C204490 +NCIT:C204491 +NCIT:C204492 +NCIT:C204493 +NCIT:C204494 +NCIT:C204495 +NCIT:C204496 +NCIT:C204497 +NCIT:C204498 +NCIT:C204499 NCIT:C2045 NCIT:C20450 +NCIT:C204500 +NCIT:C204501 +NCIT:C204502 +NCIT:C204503 +NCIT:C204505 +NCIT:C204506 +NCIT:C204507 +NCIT:C204508 +NCIT:C204509 NCIT:C20451 +NCIT:C204510 +NCIT:C204511 +NCIT:C204512 +NCIT:C204513 +NCIT:C204515 +NCIT:C204517 +NCIT:C204518 +NCIT:C204519 NCIT:C20452 +NCIT:C204520 +NCIT:C204521 +NCIT:C204522 +NCIT:C204523 +NCIT:C204524 +NCIT:C204525 +NCIT:C204526 +NCIT:C204527 +NCIT:C204528 +NCIT:C204529 NCIT:C20453 +NCIT:C204530 +NCIT:C204531 +NCIT:C204532 +NCIT:C204533 +NCIT:C204534 +NCIT:C204535 +NCIT:C204536 +NCIT:C204537 +NCIT:C204538 +NCIT:C204539 NCIT:C20454 +NCIT:C204540 +NCIT:C204541 +NCIT:C204542 +NCIT:C204543 +NCIT:C204544 +NCIT:C204545 +NCIT:C204546 +NCIT:C204547 +NCIT:C204548 +NCIT:C204549 NCIT:C20455 +NCIT:C204550 +NCIT:C204551 +NCIT:C204552 +NCIT:C204553 +NCIT:C204554 +NCIT:C204555 +NCIT:C204556 +NCIT:C204557 +NCIT:C204558 +NCIT:C204559 NCIT:C20456 +NCIT:C204560 +NCIT:C204561 +NCIT:C204562 +NCIT:C204563 +NCIT:C204564 +NCIT:C204565 +NCIT:C204566 +NCIT:C204567 +NCIT:C204568 +NCIT:C204569 NCIT:C20457 +NCIT:C204570 +NCIT:C204571 +NCIT:C204572 +NCIT:C204576 +NCIT:C204577 +NCIT:C204578 +NCIT:C204579 NCIT:C20458 +NCIT:C204580 +NCIT:C204581 +NCIT:C204582 +NCIT:C204583 +NCIT:C204584 +NCIT:C204585 +NCIT:C204586 +NCIT:C204587 +NCIT:C204588 +NCIT:C204589 NCIT:C20459 +NCIT:C204590 +NCIT:C204591 +NCIT:C204592 +NCIT:C204593 +NCIT:C204594 +NCIT:C204595 +NCIT:C204596 +NCIT:C204597 +NCIT:C204598 +NCIT:C204599 NCIT:C20460 +NCIT:C204600 +NCIT:C204601 +NCIT:C204602 +NCIT:C204603 +NCIT:C204604 +NCIT:C204605 +NCIT:C204606 +NCIT:C204607 +NCIT:C204608 +NCIT:C204609 NCIT:C20461 +NCIT:C204610 +NCIT:C204611 +NCIT:C204612 +NCIT:C204613 +NCIT:C204614 +NCIT:C204615 +NCIT:C204616 +NCIT:C204617 +NCIT:C204618 +NCIT:C204619 NCIT:C20462 +NCIT:C204620 +NCIT:C204621 +NCIT:C204622 +NCIT:C204623 +NCIT:C204624 +NCIT:C204625 +NCIT:C204626 +NCIT:C204627 +NCIT:C204628 +NCIT:C204629 NCIT:C20463 +NCIT:C204630 +NCIT:C204631 +NCIT:C204632 +NCIT:C204633 +NCIT:C204634 +NCIT:C204635 +NCIT:C204636 +NCIT:C204637 +NCIT:C204638 +NCIT:C204639 NCIT:C20464 +NCIT:C204640 +NCIT:C204641 +NCIT:C204642 +NCIT:C204643 +NCIT:C204644 +NCIT:C204645 +NCIT:C204646 +NCIT:C204647 +NCIT:C204648 +NCIT:C204649 NCIT:C20465 +NCIT:C204650 +NCIT:C204651 +NCIT:C204652 +NCIT:C204653 +NCIT:C204654 +NCIT:C204655 +NCIT:C204656 +NCIT:C204657 +NCIT:C204658 +NCIT:C204659 NCIT:C20466 +NCIT:C204660 +NCIT:C204661 +NCIT:C204662 +NCIT:C204663 +NCIT:C204664 +NCIT:C204665 +NCIT:C204666 +NCIT:C204667 +NCIT:C204668 +NCIT:C204669 NCIT:C20467 +NCIT:C204670 +NCIT:C204671 +NCIT:C204672 +NCIT:C204673 +NCIT:C204674 +NCIT:C204675 +NCIT:C204676 +NCIT:C204677 +NCIT:C204678 +NCIT:C204679 NCIT:C20468 +NCIT:C204680 +NCIT:C204681 +NCIT:C204682 +NCIT:C204683 +NCIT:C204684 +NCIT:C204685 +NCIT:C204686 +NCIT:C204687 +NCIT:C204688 +NCIT:C204689 NCIT:C20469 +NCIT:C204690 +NCIT:C204691 +NCIT:C204692 +NCIT:C204693 +NCIT:C204694 +NCIT:C204695 +NCIT:C204696 +NCIT:C204697 +NCIT:C204698 +NCIT:C204699 NCIT:C2047 NCIT:C20470 +NCIT:C204700 +NCIT:C204701 +NCIT:C204702 +NCIT:C204703 +NCIT:C204704 +NCIT:C204705 +NCIT:C204706 +NCIT:C204707 +NCIT:C204708 +NCIT:C204709 NCIT:C20471 +NCIT:C204710 +NCIT:C204711 +NCIT:C204712 +NCIT:C204713 +NCIT:C204714 +NCIT:C204715 +NCIT:C204716 +NCIT:C204717 +NCIT:C204718 +NCIT:C204719 +NCIT:C204720 +NCIT:C204721 +NCIT:C204722 +NCIT:C204723 +NCIT:C204724 +NCIT:C204725 +NCIT:C204726 +NCIT:C204727 +NCIT:C204728 +NCIT:C204729 NCIT:C20473 +NCIT:C204730 +NCIT:C204731 +NCIT:C204732 +NCIT:C204733 +NCIT:C204734 +NCIT:C204735 +NCIT:C204736 +NCIT:C204737 +NCIT:C204738 NCIT:C20474 +NCIT:C204742 +NCIT:C204743 +NCIT:C204744 +NCIT:C204745 +NCIT:C204746 +NCIT:C204747 +NCIT:C204748 +NCIT:C204749 NCIT:C20475 +NCIT:C204750 +NCIT:C204751 +NCIT:C204752 +NCIT:C204753 +NCIT:C204754 +NCIT:C204757 +NCIT:C204758 +NCIT:C204759 NCIT:C20476 +NCIT:C204760 +NCIT:C204761 +NCIT:C204762 +NCIT:C204763 +NCIT:C204764 +NCIT:C204765 +NCIT:C204766 +NCIT:C204767 +NCIT:C204768 +NCIT:C204769 NCIT:C20477 +NCIT:C204770 +NCIT:C204771 +NCIT:C204772 +NCIT:C204773 +NCIT:C204774 +NCIT:C204775 +NCIT:C204776 +NCIT:C204777 +NCIT:C204778 +NCIT:C204779 NCIT:C20478 +NCIT:C204780 +NCIT:C204781 +NCIT:C204782 +NCIT:C204783 +NCIT:C204784 +NCIT:C204785 NCIT:C20479 +NCIT:C204791 +NCIT:C204792 +NCIT:C204793 +NCIT:C204794 +NCIT:C204795 +NCIT:C204796 +NCIT:C204797 +NCIT:C204798 +NCIT:C204799 NCIT:C2048 NCIT:C20480 +NCIT:C204800 +NCIT:C204801 +NCIT:C204802 +NCIT:C204803 +NCIT:C204804 +NCIT:C204805 +NCIT:C204806 +NCIT:C204807 +NCIT:C204808 +NCIT:C204809 NCIT:C20481 +NCIT:C204810 +NCIT:C204811 +NCIT:C204812 +NCIT:C204813 +NCIT:C204814 +NCIT:C204815 +NCIT:C204816 +NCIT:C204817 +NCIT:C204818 +NCIT:C204819 +NCIT:C204820 +NCIT:C204821 +NCIT:C204822 +NCIT:C204823 +NCIT:C204824 +NCIT:C204825 +NCIT:C204826 +NCIT:C204827 +NCIT:C204828 +NCIT:C204829 NCIT:C20483 +NCIT:C204830 +NCIT:C204831 +NCIT:C204832 +NCIT:C204833 +NCIT:C204834 +NCIT:C204835 +NCIT:C204836 +NCIT:C204837 +NCIT:C204838 +NCIT:C204839 NCIT:C20484 +NCIT:C204841 +NCIT:C204842 +NCIT:C204844 +NCIT:C204845 +NCIT:C204846 +NCIT:C204847 +NCIT:C204848 +NCIT:C204849 NCIT:C20485 +NCIT:C204850 +NCIT:C204851 +NCIT:C204852 +NCIT:C204853 +NCIT:C204854 +NCIT:C204855 +NCIT:C204856 +NCIT:C204857 +NCIT:C204858 +NCIT:C204859 NCIT:C20486 +NCIT:C204860 +NCIT:C204861 +NCIT:C204862 +NCIT:C204863 +NCIT:C204869 NCIT:C20487 +NCIT:C204870 +NCIT:C204871 +NCIT:C204872 +NCIT:C204873 +NCIT:C204874 +NCIT:C204875 +NCIT:C204876 +NCIT:C204877 +NCIT:C204878 +NCIT:C204879 NCIT:C20488 +NCIT:C204880 +NCIT:C204881 +NCIT:C204882 +NCIT:C204884 +NCIT:C204885 +NCIT:C204886 NCIT:C20489 +NCIT:C204890 +NCIT:C204891 +NCIT:C204892 +NCIT:C204893 +NCIT:C204894 +NCIT:C204895 +NCIT:C204896 +NCIT:C204897 +NCIT:C204898 +NCIT:C204899 NCIT:C2049 NCIT:C20490 +NCIT:C204900 +NCIT:C204901 +NCIT:C204902 +NCIT:C204903 +NCIT:C204904 +NCIT:C204905 +NCIT:C204906 +NCIT:C204908 +NCIT:C204909 NCIT:C20491 +NCIT:C204912 +NCIT:C204913 +NCIT:C204914 +NCIT:C204915 +NCIT:C204916 +NCIT:C204917 +NCIT:C204918 +NCIT:C204919 NCIT:C20492 +NCIT:C204920 +NCIT:C204921 +NCIT:C204922 +NCIT:C204923 +NCIT:C204924 +NCIT:C204925 +NCIT:C204926 +NCIT:C204927 +NCIT:C204928 +NCIT:C204929 NCIT:C20493 +NCIT:C204930 +NCIT:C204931 +NCIT:C204932 +NCIT:C204933 +NCIT:C204934 +NCIT:C204935 +NCIT:C204936 +NCIT:C204937 +NCIT:C204938 +NCIT:C204939 NCIT:C20494 +NCIT:C204940 +NCIT:C204941 +NCIT:C204942 +NCIT:C204943 +NCIT:C204944 +NCIT:C204945 +NCIT:C204946 +NCIT:C204947 +NCIT:C204948 +NCIT:C204949 NCIT:C20495 +NCIT:C204950 +NCIT:C204951 +NCIT:C204952 +NCIT:C204953 +NCIT:C204954 +NCIT:C204955 +NCIT:C204956 +NCIT:C204957 +NCIT:C204958 +NCIT:C204959 NCIT:C20496 +NCIT:C204960 +NCIT:C204961 +NCIT:C204962 +NCIT:C204963 +NCIT:C204964 +NCIT:C204965 +NCIT:C204966 +NCIT:C204967 +NCIT:C204968 +NCIT:C204969 NCIT:C20497 +NCIT:C204970 +NCIT:C204971 +NCIT:C204972 +NCIT:C204973 +NCIT:C204974 +NCIT:C204975 NCIT:C20498 +NCIT:C204983 +NCIT:C204989 NCIT:C20499 +NCIT:C204990 +NCIT:C204992 +NCIT:C204993 +NCIT:C204994 +NCIT:C204995 +NCIT:C204996 +NCIT:C204997 +NCIT:C204998 +NCIT:C204999 NCIT:C205 NCIT:C2050 NCIT:C20500 +NCIT:C205000 +NCIT:C205001 +NCIT:C205002 +NCIT:C205003 +NCIT:C205004 +NCIT:C205005 +NCIT:C205006 +NCIT:C205007 +NCIT:C205008 +NCIT:C205009 NCIT:C20501 +NCIT:C205010 +NCIT:C205011 +NCIT:C205012 +NCIT:C205013 +NCIT:C205014 +NCIT:C205015 +NCIT:C205016 +NCIT:C205017 +NCIT:C205018 +NCIT:C205019 NCIT:C20502 +NCIT:C205020 +NCIT:C205021 +NCIT:C205022 +NCIT:C205023 +NCIT:C205024 +NCIT:C205025 +NCIT:C205026 +NCIT:C205027 +NCIT:C205028 +NCIT:C205029 NCIT:C20503 +NCIT:C205030 +NCIT:C205031 +NCIT:C205032 +NCIT:C205033 +NCIT:C205034 +NCIT:C205035 +NCIT:C205036 +NCIT:C205037 +NCIT:C205038 +NCIT:C205039 NCIT:C20504 +NCIT:C205040 +NCIT:C205041 +NCIT:C205042 +NCIT:C205043 +NCIT:C205044 +NCIT:C205045 +NCIT:C205047 +NCIT:C205048 +NCIT:C205049 NCIT:C20505 +NCIT:C205050 +NCIT:C205051 +NCIT:C205052 +NCIT:C205053 +NCIT:C205054 +NCIT:C205055 +NCIT:C205056 +NCIT:C205058 +NCIT:C205059 NCIT:C20506 +NCIT:C205060 +NCIT:C205061 +NCIT:C205062 +NCIT:C205063 +NCIT:C205064 +NCIT:C205065 +NCIT:C205066 +NCIT:C205067 +NCIT:C205068 NCIT:C20507 +NCIT:C205070 +NCIT:C205071 +NCIT:C205072 +NCIT:C205073 +NCIT:C205074 +NCIT:C205075 +NCIT:C205076 +NCIT:C205077 +NCIT:C205078 +NCIT:C205079 NCIT:C20508 +NCIT:C205080 +NCIT:C205081 +NCIT:C205082 +NCIT:C205083 +NCIT:C205084 +NCIT:C205085 +NCIT:C205086 +NCIT:C205087 +NCIT:C205088 +NCIT:C205089 NCIT:C20509 +NCIT:C205090 +NCIT:C205091 +NCIT:C205092 +NCIT:C205093 +NCIT:C205094 +NCIT:C205095 +NCIT:C205096 +NCIT:C205097 +NCIT:C205098 +NCIT:C205099 NCIT:C2051 NCIT:C20510 +NCIT:C205100 +NCIT:C205101 +NCIT:C205102 +NCIT:C205103 +NCIT:C205104 +NCIT:C205105 +NCIT:C205106 +NCIT:C205107 +NCIT:C205108 +NCIT:C205109 NCIT:C20511 +NCIT:C205110 +NCIT:C205111 +NCIT:C205112 +NCIT:C205113 +NCIT:C205114 +NCIT:C205115 +NCIT:C205116 +NCIT:C205117 +NCIT:C205118 +NCIT:C205119 NCIT:C20512 +NCIT:C205120 +NCIT:C205121 +NCIT:C205122 +NCIT:C205123 +NCIT:C205124 +NCIT:C205126 +NCIT:C205128 NCIT:C20513 +NCIT:C205133 +NCIT:C205134 +NCIT:C205137 +NCIT:C205138 +NCIT:C205139 NCIT:C20514 +NCIT:C205140 +NCIT:C205141 +NCIT:C205142 +NCIT:C205143 +NCIT:C205144 +NCIT:C205145 +NCIT:C205146 +NCIT:C205147 +NCIT:C205148 +NCIT:C205149 NCIT:C20515 +NCIT:C205150 +NCIT:C205151 +NCIT:C205152 +NCIT:C205153 +NCIT:C205154 +NCIT:C205155 +NCIT:C205156 +NCIT:C205157 +NCIT:C205158 +NCIT:C205159 +NCIT:C205160 +NCIT:C205161 +NCIT:C205162 +NCIT:C205163 +NCIT:C205164 +NCIT:C205165 +NCIT:C205166 +NCIT:C205167 +NCIT:C205168 +NCIT:C205169 NCIT:C20517 +NCIT:C205170 +NCIT:C205171 +NCIT:C205172 +NCIT:C205173 +NCIT:C205174 +NCIT:C205175 +NCIT:C205176 +NCIT:C205177 +NCIT:C205178 +NCIT:C205179 NCIT:C20518 +NCIT:C205180 +NCIT:C205181 +NCIT:C205182 +NCIT:C205183 +NCIT:C205184 +NCIT:C205185 +NCIT:C205186 +NCIT:C205189 NCIT:C20519 +NCIT:C205190 +NCIT:C205191 +NCIT:C205192 +NCIT:C205193 +NCIT:C205194 +NCIT:C205195 +NCIT:C205196 +NCIT:C205197 +NCIT:C205198 +NCIT:C205199 NCIT:C2052 NCIT:C20520 +NCIT:C205200 +NCIT:C205201 +NCIT:C205202 +NCIT:C205203 +NCIT:C205204 +NCIT:C205205 +NCIT:C205206 +NCIT:C205207 +NCIT:C205208 +NCIT:C205209 NCIT:C20521 +NCIT:C205210 +NCIT:C205211 +NCIT:C205212 +NCIT:C205213 +NCIT:C205214 +NCIT:C205215 +NCIT:C205216 +NCIT:C205217 +NCIT:C205218 +NCIT:C205219 NCIT:C20522 +NCIT:C205220 +NCIT:C205221 +NCIT:C205222 +NCIT:C205223 +NCIT:C205224 +NCIT:C205225 +NCIT:C205227 +NCIT:C205228 +NCIT:C205229 +NCIT:C205230 +NCIT:C205231 +NCIT:C205232 +NCIT:C205233 +NCIT:C205234 +NCIT:C205235 +NCIT:C205236 +NCIT:C205237 +NCIT:C205239 NCIT:C20524 +NCIT:C205240 +NCIT:C205241 +NCIT:C205242 +NCIT:C205243 +NCIT:C205244 +NCIT:C205245 +NCIT:C205246 +NCIT:C205247 +NCIT:C205248 +NCIT:C205249 NCIT:C20525 +NCIT:C205250 +NCIT:C205251 +NCIT:C205252 +NCIT:C205253 +NCIT:C205254 +NCIT:C205255 +NCIT:C205256 +NCIT:C205257 +NCIT:C205258 +NCIT:C205259 NCIT:C20526 +NCIT:C205260 +NCIT:C205261 +NCIT:C205262 +NCIT:C205263 +NCIT:C205264 +NCIT:C205265 +NCIT:C205266 +NCIT:C205267 +NCIT:C205268 +NCIT:C205269 NCIT:C20527 +NCIT:C205270 +NCIT:C205271 +NCIT:C205272 +NCIT:C205273 +NCIT:C205274 +NCIT:C205275 +NCIT:C205276 +NCIT:C205277 +NCIT:C205278 +NCIT:C205279 NCIT:C20528 +NCIT:C205280 +NCIT:C205281 +NCIT:C205282 +NCIT:C205283 +NCIT:C205284 +NCIT:C205285 +NCIT:C205288 NCIT:C20529 +NCIT:C205291 +NCIT:C205292 +NCIT:C205293 +NCIT:C205294 +NCIT:C205296 +NCIT:C205297 +NCIT:C205299 NCIT:C2053 NCIT:C20530 +NCIT:C205300 +NCIT:C205302 +NCIT:C205304 +NCIT:C205305 NCIT:C20531 +NCIT:C205312 +NCIT:C205315 +NCIT:C205316 +NCIT:C205318 +NCIT:C205319 NCIT:C20532 +NCIT:C205320 +NCIT:C205321 +NCIT:C205322 +NCIT:C205323 +NCIT:C205324 +NCIT:C205325 +NCIT:C205326 +NCIT:C205327 +NCIT:C205328 NCIT:C20533 +NCIT:C205330 +NCIT:C205331 +NCIT:C205332 +NCIT:C205333 +NCIT:C205334 +NCIT:C205335 +NCIT:C205336 +NCIT:C205337 +NCIT:C205338 +NCIT:C205339 NCIT:C20534 +NCIT:C205340 +NCIT:C205341 +NCIT:C205342 +NCIT:C205343 +NCIT:C205344 +NCIT:C205345 +NCIT:C205346 +NCIT:C205347 +NCIT:C205348 +NCIT:C205349 NCIT:C20535 +NCIT:C205350 +NCIT:C205351 +NCIT:C205352 +NCIT:C205353 +NCIT:C205354 +NCIT:C205355 +NCIT:C205356 +NCIT:C205358 +NCIT:C205359 NCIT:C20536 +NCIT:C205360 +NCIT:C205362 +NCIT:C205363 +NCIT:C205364 +NCIT:C205365 +NCIT:C205366 +NCIT:C205367 +NCIT:C205368 +NCIT:C205369 NCIT:C20537 +NCIT:C205372 +NCIT:C205373 +NCIT:C205374 +NCIT:C205375 +NCIT:C205376 +NCIT:C205377 +NCIT:C205378 +NCIT:C205379 NCIT:C20538 +NCIT:C205380 +NCIT:C205381 +NCIT:C205382 +NCIT:C205383 +NCIT:C205384 +NCIT:C205385 +NCIT:C205386 +NCIT:C205387 +NCIT:C205388 +NCIT:C205389 NCIT:C20539 +NCIT:C205390 +NCIT:C205391 +NCIT:C205392 +NCIT:C205393 +NCIT:C205394 +NCIT:C205395 +NCIT:C205396 +NCIT:C205397 +NCIT:C205398 +NCIT:C205399 NCIT:C2054 NCIT:C20540 +NCIT:C205400 +NCIT:C205401 +NCIT:C205402 +NCIT:C205403 +NCIT:C205404 +NCIT:C205405 +NCIT:C205406 +NCIT:C205407 +NCIT:C205408 NCIT:C20541 +NCIT:C205410 +NCIT:C205411 +NCIT:C205412 +NCIT:C205413 +NCIT:C205414 +NCIT:C205415 +NCIT:C205416 +NCIT:C205417 +NCIT:C205418 +NCIT:C205419 NCIT:C20542 +NCIT:C205420 +NCIT:C205421 +NCIT:C205422 +NCIT:C205423 +NCIT:C205424 +NCIT:C205425 +NCIT:C205426 +NCIT:C205427 +NCIT:C205428 +NCIT:C205429 NCIT:C20543 +NCIT:C205430 +NCIT:C205431 +NCIT:C205432 +NCIT:C205433 +NCIT:C205434 +NCIT:C205435 +NCIT:C205436 +NCIT:C205437 +NCIT:C205438 +NCIT:C205439 NCIT:C20544 +NCIT:C205440 +NCIT:C205441 +NCIT:C205442 +NCIT:C205443 +NCIT:C205444 +NCIT:C205445 +NCIT:C205446 +NCIT:C205447 +NCIT:C205448 +NCIT:C205449 NCIT:C20545 +NCIT:C205450 +NCIT:C205451 +NCIT:C205452 +NCIT:C205453 +NCIT:C205454 +NCIT:C205455 +NCIT:C205456 +NCIT:C205457 +NCIT:C205458 +NCIT:C205460 +NCIT:C205461 +NCIT:C205464 +NCIT:C205465 +NCIT:C205466 +NCIT:C205467 +NCIT:C205468 +NCIT:C205469 NCIT:C20547 +NCIT:C205470 +NCIT:C205471 +NCIT:C205472 +NCIT:C205473 +NCIT:C205474 +NCIT:C205477 +NCIT:C205478 +NCIT:C205479 NCIT:C20548 +NCIT:C205480 +NCIT:C205481 +NCIT:C205482 +NCIT:C205483 +NCIT:C205484 +NCIT:C205485 +NCIT:C205486 +NCIT:C205487 +NCIT:C205488 +NCIT:C205489 NCIT:C20549 +NCIT:C205490 +NCIT:C205491 +NCIT:C205492 +NCIT:C205493 +NCIT:C205494 +NCIT:C205495 +NCIT:C205496 +NCIT:C205497 +NCIT:C205498 +NCIT:C205499 NCIT:C2055 NCIT:C20550 +NCIT:C205500 +NCIT:C205501 +NCIT:C205502 +NCIT:C205503 +NCIT:C205504 +NCIT:C205505 +NCIT:C205506 +NCIT:C205507 +NCIT:C205508 +NCIT:C205509 NCIT:C20551 +NCIT:C205510 +NCIT:C205511 +NCIT:C205512 +NCIT:C205513 +NCIT:C205514 +NCIT:C205515 +NCIT:C205516 +NCIT:C205517 +NCIT:C205518 +NCIT:C205519 NCIT:C20552 +NCIT:C205520 +NCIT:C205521 +NCIT:C205522 +NCIT:C205523 +NCIT:C205524 +NCIT:C205525 +NCIT:C205526 +NCIT:C205527 +NCIT:C205528 +NCIT:C205529 NCIT:C20553 +NCIT:C205530 +NCIT:C205531 +NCIT:C205532 +NCIT:C205533 +NCIT:C205534 +NCIT:C205535 +NCIT:C205536 +NCIT:C205537 +NCIT:C205538 NCIT:C20554 +NCIT:C205540 +NCIT:C205541 +NCIT:C205542 +NCIT:C205543 +NCIT:C205544 +NCIT:C205545 +NCIT:C205546 +NCIT:C205547 +NCIT:C205548 +NCIT:C205549 NCIT:C20555 +NCIT:C205550 +NCIT:C205552 +NCIT:C205553 +NCIT:C205554 +NCIT:C205555 +NCIT:C205556 +NCIT:C205557 +NCIT:C205558 +NCIT:C205559 NCIT:C20556 +NCIT:C205560 +NCIT:C205561 +NCIT:C205562 +NCIT:C205563 +NCIT:C205564 +NCIT:C205565 +NCIT:C205566 +NCIT:C205567 +NCIT:C205568 +NCIT:C205569 NCIT:C20557 +NCIT:C205570 +NCIT:C205571 +NCIT:C205572 +NCIT:C205573 +NCIT:C205574 +NCIT:C205575 +NCIT:C205576 +NCIT:C205577 +NCIT:C205578 +NCIT:C205579 NCIT:C20558 +NCIT:C205580 +NCIT:C205581 +NCIT:C205582 +NCIT:C205583 +NCIT:C205584 +NCIT:C205585 +NCIT:C205586 +NCIT:C205587 +NCIT:C205588 +NCIT:C205589 NCIT:C20559 +NCIT:C205590 +NCIT:C205591 +NCIT:C205592 +NCIT:C205593 +NCIT:C205594 +NCIT:C205595 +NCIT:C205596 +NCIT:C205597 +NCIT:C205598 +NCIT:C205599 NCIT:C2056 NCIT:C20560 +NCIT:C205600 +NCIT:C205601 +NCIT:C205602 +NCIT:C205603 +NCIT:C205605 +NCIT:C205606 NCIT:C20561 NCIT:C20562 NCIT:C20563 @@ -109105,7 +112670,6 @@ NCIT:C35435 NCIT:C35436 NCIT:C35437 NCIT:C35438 -NCIT:C35439 NCIT:C35440 NCIT:C35441 NCIT:C35443 @@ -112944,7 +116508,6 @@ NCIT:C39626 NCIT:C39627 NCIT:C39628 NCIT:C39629 -NCIT:C3963 NCIT:C39630 NCIT:C39631 NCIT:C39632 @@ -115426,7 +118989,6 @@ NCIT:C43245 NCIT:C43246 NCIT:C43247 NCIT:C43248 -NCIT:C43249 NCIT:C43251 NCIT:C43253 NCIT:C43255 @@ -115482,6 +119044,7 @@ NCIT:C43320 NCIT:C43337 NCIT:C43338 NCIT:C43339 +NCIT:C43352 NCIT:C43358 NCIT:C43359 NCIT:C43360 @@ -115710,6 +119273,7 @@ NCIT:C43647 NCIT:C43648 NCIT:C43649 NCIT:C43650 +NCIT:C4366 NCIT:C4367 NCIT:C43670 NCIT:C43671 @@ -120267,7 +123831,6 @@ NCIT:C50033 NCIT:C50034 NCIT:C50035 NCIT:C50036 -NCIT:C50037 NCIT:C50038 NCIT:C50039 NCIT:C50040 @@ -122179,7 +125742,6 @@ NCIT:C51979 NCIT:C5198 NCIT:C51980 NCIT:C51981 -NCIT:C51982 NCIT:C51985 NCIT:C51986 NCIT:C51987 @@ -124237,7 +127799,6 @@ NCIT:C54142 NCIT:C54144 NCIT:C54145 NCIT:C54146 -NCIT:C54147 NCIT:C54148 NCIT:C54149 NCIT:C5415 @@ -129735,6 +133296,7 @@ NCIT:C59706 NCIT:C59707 NCIT:C59708 NCIT:C59709 +NCIT:C5971 NCIT:C59710 NCIT:C59711 NCIT:C59712 @@ -131159,9 +134721,7 @@ NCIT:C61395 NCIT:C61396 NCIT:C61397 NCIT:C61398 -NCIT:C61399 NCIT:C614 -NCIT:C61400 NCIT:C61401 NCIT:C61402 NCIT:C61403 @@ -133115,7 +136675,6 @@ NCIT:C63465 NCIT:C63466 NCIT:C63467 NCIT:C63468 -NCIT:C63469 NCIT:C63470 NCIT:C63471 NCIT:C63472 @@ -133519,7 +137078,6 @@ NCIT:C64186 NCIT:C64187 NCIT:C64188 NCIT:C64189 -NCIT:C64190 NCIT:C64191 NCIT:C64192 NCIT:C64193 @@ -136321,7 +139879,6 @@ NCIT:C67220 NCIT:C67226 NCIT:C67227 NCIT:C67229 -NCIT:C67231 NCIT:C67232 NCIT:C67233 NCIT:C67234 @@ -137648,6 +141205,7 @@ NCIT:C69317 NCIT:C69318 NCIT:C69319 NCIT:C69320 +NCIT:C6933 NCIT:C694 NCIT:C6940 NCIT:C69402 @@ -144318,7 +147876,6 @@ NCIT:C77182 NCIT:C77183 NCIT:C77184 NCIT:C77185 -NCIT:C77186 NCIT:C77187 NCIT:C77188 NCIT:C77189 @@ -150419,7 +153976,6 @@ NCIT:C83716 NCIT:C83717 NCIT:C83718 NCIT:C83719 -NCIT:C8372 NCIT:C83720 NCIT:C83721 NCIT:C83722 @@ -158456,7 +162012,6 @@ NCIT:C92201 NCIT:C92202 NCIT:C92203 NCIT:C92205 -NCIT:C92206 NCIT:C92207 NCIT:C92208 NCIT:C92209 diff --git a/src/ontology/reports/ncit_unmapped_terms.tsv b/src/ontology/reports/ncit_unmapped_terms.tsv index 6ae1dc42..2e526ca9 100644 --- a/src/ontology/reports/ncit_unmapped_terms.tsv +++ b/src/ontology/reports/ncit_unmapped_terms.tsv @@ -27,13 +27,11 @@ NCIT:C5052 AIDS-Related Malignant Cervical Neoplasm NCIT:C4046 AIDS-Related Malignant Neoplasm NCIT:C5051 AIDS-Related Non-Hodgkin Lymphoma NCIT:C7434 AIDS-Related Non-Hodgkin Lymphoma of the Cervix +NCIT:C9016 AIDS-Related Oral Cavity Plasmablastic Lymphoma NCIT:C27859 AIDS-Related Plasmablastic Lymphoma NCIT:C38160 AIDS-Related Plasmablastic Lymphoma of Mucosa Site -NCIT:C9016 AIDS-Related Plasmablastic Lymphoma of the Oral Mucosa NCIT:C186660 AIDS-Related Primary Diffuse Large B-Cell Lymphoma of the Central Nervous System NCIT:C9017 AIDS-Related Primary Effusion Lymphoma -NCIT:C9420 AJCC Grade 2 Sarcoma -NCIT:C9421 AJCC Grade 3 Sarcoma NCIT:C9422 AJCC Grade 4 Sarcoma NCIT:C200105 ALK-Positive Histiocytosis NCIT:C189249 ALK-Rearranged Renal Cell Carcinoma @@ -65,9 +63,11 @@ NCIT:C23117 Acinic Cell Carcinoma of the Mouse Larynx NCIT:C23141 Acinic Cell Carcinoma of the Mouse Salivary Glands NCIT:C22944 Acquired Tufted Hemangioma of the Mouse Blood Vessel NCIT:C121713 Acral Fibromyxoma +NCIT:C204883 Acral Melanoma NCIT:C54659 Acral Nevus NCIT:C36265 Acute Adult T-Cell Leukemia/Lymphoma NCIT:C22079 Acute Enteritis of the Mouse Intestinal Tract +NCIT:C203437 Acute Leukemia of Ambiguous Lineage with BCL11B Rearrangement NCIT:C200494 Acute Leukemia of Ambiguous Lineage with Defining Genetic Abnormalities NCIT:C151975 Acute Leukemia of Ambiguous Lineage, Not Otherwise Specified NCIT:C121973 Acute Lymphoblastic Leukemia by Gene Expression Profile @@ -132,6 +132,7 @@ NCIT:C9288 Acute Myeloid Leukemia with t(8;21)(q22; q22.1); RUNX1-RUNX1T1 NCIT:C9020 Acute Myelomonocytic Leukemia with Abnormal Eosinophils NCIT:C42779 Acute Myelomonocytic Leukemia without Abnormal Eosinophils NCIT:C22086 Acute Ulcerative Enteritis of the Mouse Intestinal Tract +NCIT:C43312 Adamantinoid Trichoblastoma NCIT:C64005 Adenocarcinoma Arising In Fibroadenoma of the Rat Mammary Gland NCIT:C7678 Adenocarcinoma In Situ in Adenomatous Polyp NCIT:C7679 Adenocarcinoma In Situ in Tubular Adenoma @@ -194,6 +195,7 @@ NCIT:C66745 Adenocarcinoma with Neuroendocrine Differentiation NCIT:C7684 Adenocarcinoma with Osseous Metaplasia NCIT:C4201 Adenocarcinoma with Spindle Cell Metaplasia NCIT:C4200 Adenocarcinoma with Squamous Metaplasia +NCIT:C202061 Adenoid Ameloblastoma NCIT:C23115 Adenoid Cystic Carcinoma of the Mouse Larynx NCIT:C23142 Adenoid Cystic Carcinoma of the Mouse Salivary Glands NCIT:C64015 Adenolipoma of the Rat Mammary Gland @@ -317,6 +319,7 @@ NCIT:C9376 Adult Brain Oligodendroglioma NCIT:C7954 Adult Burkitt Leukemia NCIT:C9062 Adult Burkitt Lymphoma NCIT:C45747 Adult Cardiac Cellular Rhabdomyoma +NCIT:C115253 Adult Central Nervous System Melanocytic Neoplasm NCIT:C5131 Adult Central Nervous System Neoplasm NCIT:C8265 Adult Cholangiocarcinoma NCIT:C69138 Adult Classic Hodgkin Lymphoma @@ -389,7 +392,6 @@ NCIT:C114993 Adult Pleomorphic Hepatocellular Carcinoma NCIT:C188945 Adult Posterior Fossa Ependymoma NCIT:C114599 Adult Pre-B Acute Lymphoblastic Leukemia NCIT:C27365 Adult Primary Cutaneous Anaplastic Large Cell Lymphoma -NCIT:C115253 Adult Primary Meningeal Melanocytic Neoplasm NCIT:C68693 Adult Pure Erythroid Leukemia NCIT:C9130 Adult Rhabdomyosarcoma NCIT:C118825 Adult Salivary Gland Carcinoma @@ -432,7 +434,6 @@ NCIT:C162762 Advanced Bone Sarcoma NCIT:C165700 Advanced Breast Adenocarcinoma NCIT:C162648 Advanced Breast Carcinoma NCIT:C180922 Advanced Bronchogenic Carcinoma -NCIT:C156487 Advanced Carcinoid Tumor NCIT:C153171 Advanced Carcinoma NCIT:C170960 Advanced Carcinoma Of Unknown Primary NCIT:C170928 Advanced Carcinosarcoma @@ -440,8 +441,8 @@ NCIT:C156304 Advanced Cervical Adenocarcinoma NCIT:C174032 Advanced Cervical Adenosquamous Carcinoma NCIT:C156294 Advanced Cervical Carcinoma NCIT:C174030 Advanced Cervical Squamous Cell Carcinoma -NCIT:C187213 Advanced Childhood Malignant Brain Neoplasm NCIT:C187210 Advanced Childhood Malignant Solid Neoplasm +NCIT:C187213 Advanced Childhood Primary Malignant Brain Neoplasm NCIT:C162752 Advanced Cholangiocarcinoma NCIT:C173333 Advanced Chordoma NCIT:C171579 Advanced Chromophobe Renal Cell Carcinoma @@ -458,9 +459,12 @@ NCIT:C168715 Advanced Dedifferentiated Liposarcoma NCIT:C173980 Advanced Differentiated Thyroid Gland Carcinoma NCIT:C171264 Advanced Diffuse Large B-Cell Lymphoma NCIT:C156746 Advanced Digestive System Carcinoma +NCIT:C203253 Advanced Digestive System Neuroendocrine Carcinoma NCIT:C158089 Advanced Digestive System Neuroendocrine Neoplasm +NCIT:C204036 Advanced Digestive System Neuroendocrine Tumor NCIT:C179418 Advanced Digestive System Neuroendocrine Tumor G1 NCIT:C190711 Advanced Digestive System Neuroendocrine Tumor G2 +NCIT:C203252 Advanced Digestive System Neuroendocrine Tumor G3 NCIT:C176888 Advanced Distal Bile Duct Adenocarcinoma NCIT:C170805 Advanced Endometrial Adenocarcinoma NCIT:C159676 Advanced Endometrial Carcinoma @@ -482,6 +486,7 @@ NCIT:C191990 Advanced Extrapulmonary Large Cell Neuroendocrine Carcinoma NCIT:C191982 Advanced Extrapulmonary Neuroendocrine Carcinoma NCIT:C191993 Advanced Extrapulmonary Small Cell Neuroendocrine Carcinoma NCIT:C167395 Advanced Fallopian Tube Carcinoma +NCIT:C203311 Advanced Fallopian Tube High Grade Serous Adenocarcinoma NCIT:C68662 Advanced Favorable Hodgkin Lymphoma NCIT:C53283 Advanced Favorable Non-Hodgkin Lymphoma NCIT:C185067 Advanced Fibrolamellar Carcinoma @@ -518,11 +523,11 @@ NCIT:C165780 Advanced Leiomyosarcoma NCIT:C168701 Advanced Liposarcoma NCIT:C176727 Advanced Lung Adenocarcinoma NCIT:C181967 Advanced Lung Adenosquamous Carcinoma -NCIT:C177245 Advanced Lung Carcinoid Tumor NCIT:C153203 Advanced Lung Carcinoma NCIT:C187163 Advanced Lung Large Cell Neuroendocrine Carcinoma NCIT:C192798 Advanced Lung Neuroendocrine Carcinoma NCIT:C165446 Advanced Lung Neuroendocrine Neoplasm +NCIT:C177245 Advanced Lung Neuroendocrine Tumor NCIT:C162158 Advanced Lung Non-Small Cell Carcinoma NCIT:C153201 Advanced Lung Non-Small Cell Squamous Carcinoma NCIT:C147924 Advanced Lung Non-Squamous Non-Small Cell Carcinoma @@ -576,6 +581,7 @@ NCIT:C190633 Advanced Ovarian High Grade Serous Adenocarcinoma NCIT:C170937 Advanced Ovarian Serous Adenocarcinoma NCIT:C187235 Advanced Ovarian Serous Cystadenocarcinoma NCIT:C162153 Advanced Pancreatic Adenocarcinoma +NCIT:C204035 Advanced Pancreatic Adenosquamous Carcinoma NCIT:C165452 Advanced Pancreatic Carcinoma NCIT:C164214 Advanced Pancreatic Ductal Adenocarcinoma NCIT:C165448 Advanced Pancreatic Neuroendocrine Neoplasm @@ -589,6 +595,7 @@ NCIT:C170790 Advanced Penile Carcinoma NCIT:C8703 Advanced Pericardial Malignant Mesothelioma NCIT:C170784 Advanced Pharyngeal Carcinoma NCIT:C173694 Advanced Pharyngeal Squamous Cell Carcinoma +NCIT:C204866 Advanced Platinum-Refractory Ovarian Carcinoma NCIT:C170958 Advanced Platinum-Resistant Malignant Germ Cell Tumor NCIT:C189977 Advanced Platinum-Resistant Ovarian Carcinoma NCIT:C182026 Advanced Pleomorphic Liposarcoma @@ -597,15 +604,18 @@ NCIT:C172442 Advanced Primary Cutaneous T-Cell Non-Hodgkin Lymphoma NCIT:C175549 Advanced Primary Malignant Brain Neoplasm NCIT:C170966 Advanced Primary Malignant Central Nervous System Neoplasm NCIT:C167396 Advanced Primary Peritoneal Carcinoma +NCIT:C203312 Advanced Primary Peritoneal High Grade Serous Adenocarcinoma NCIT:C200573 Advanced Progesterone Receptor-Positive Breast Carcinoma NCIT:C156286 Advanced Prostate Adenocarcinoma NCIT:C186456 Advanced Prostate Adenocarcinoma with Neuroendocrine Differentiation NCIT:C156284 Advanced Prostate Carcinoma +NCIT:C202894 Advanced Prostate Small Cell Neuroendocrine Carcinoma NCIT:C192677 Advanced Rare Malignant Solid Neoplasm NCIT:C175363 Advanced Rectal Adenocarcinoma NCIT:C170777 Advanced Rectal Carcinoma NCIT:C170780 Advanced Rectal Squamous Cell Carcinoma NCIT:C153170 Advanced Renal Cell Carcinoma +NCIT:C171582 Advanced Renal Cell Carcinoma, Not Otherwise Specified NCIT:C163966 Advanced Renal Pelvis Carcinoma NCIT:C172278 Advanced Renal Pelvis Urothelial Carcinoma NCIT:C172276 Advanced Renal Pelvis and Ureter Urothelial Carcinoma @@ -633,11 +643,10 @@ NCIT:C163964 Advanced Thyroid Gland Medullary Carcinoma NCIT:C172361 Advanced Transformed Non-Hodgkin Lymphoma NCIT:C172091 Advanced Transitional Cell Carcinoma NCIT:C175236 Advanced Triple-Negative Breast Carcinoma -NCIT:C171582 Advanced Unclassified Renal Cell Carcinoma NCIT:C165781 Advanced Undifferentiated Pleomorphic Sarcoma NCIT:C68665 Advanced Unfavorable Hodgkin Lymphoma NCIT:C53284 Advanced Unfavorable Non-Hodgkin Lymphoma -NCIT:C153317 Advanced Unresectable Gastric Adenocarcinoma +NCIT:C8716 Advanced Ureter Carcinoma NCIT:C163955 Advanced Ureter Urothelial Carcinoma NCIT:C163963 Advanced Urethral Urothelial Carcinoma NCIT:C148493 Advanced Urothelial Carcinoma @@ -683,10 +692,10 @@ NCIT:C7496 Ameloblastic Carcinoma-Secondary Type (Dedifferentiated) NCIT:C54298 Ameloblastic Carcinoma-Secondary Type (Dedifferentiated), Intraosseous NCIT:C54299 Ameloblastic Carcinoma-Secondary Type (Dedifferentiated), Peripheral NCIT:C3710 Ameloblastic Fibro-Odontoma +NCIT:C173740 Ameloblastic Fibro-Odontosarcoma NCIT:C66800 Ameloblastic Fibrodentinoma NCIT:C173739 Ameloblastic Fibrodentinosarcoma NCIT:C4316 Ameloblastic Fibroma -NCIT:C173740 Ameloblastic Fibroodontosarcoma NCIT:C4317 Ameloblastic Fibrosarcoma NCIT:C63901 Amphophilic Focus of Cellular Alteration of the Rat NCIT:C6657 Ampulla of Vater Adenoma, Intestinal-Type @@ -1025,8 +1034,11 @@ NCIT:C6062 Anterior Tongue Neoplasm NCIT:C8169 Anterior Tongue Squamous Cell Carcinoma NCIT:C21646 Aplasia of the Mouse Mammary Gland NCIT:C21705 Aplasia of the Mouse Prostate Gland +NCIT:C205459 Apocrine Cystadenoma NCIT:C43342 Apocrine Hidrocystoma NCIT:C21828 Apocrine Neoplasms of the Mouse Skin +NCIT:C205463 Apocrine Poroma +NCIT:C202880 Appendicular Skeleton Phosphaturic Mesenchymal Tumor NCIT:C133733 Appendix Carcinoma by AJCC v7 Stage NCIT:C134117 Appendix Carcinoma by AJCC v8 Stage NCIT:C173799 Appendix Disorder @@ -1058,6 +1070,8 @@ NCIT:C27775 Aromatic Dyes-Related Malignant Neoplasm NCIT:C84472 Asbestos-Related Lung Disorder NCIT:C27926 Asbestos-Related Malignant Mesothelioma NCIT:C27774 Asbestos-Related Malignant Neoplasm +NCIT:C203387 Ascending Colon Neuroendocrine Tumor +NCIT:C203391 Ascending Colon Neuroendocrine Tumor G2 NCIT:C36202 Astler-Coller A Colon Carcinoma NCIT:C5927 Astler-Coller A Colorectal Carcinoma NCIT:C5924 Astler-Coller A Rectal Carcinoma @@ -1105,7 +1119,6 @@ NCIT:C178255 Atypical Neurofibromatous Neoplasm of Uncertain Biologic Potential NCIT:C48285 Atypical Parathyroid Gland Tumor NCIT:C132296 Atypical Pituitary Neuroendocrine Tumor NCIT:C37268 Atypical Small Acinar Proliferation of the Prostate Gland -NCIT:C136825 Atypical Spitz Nevus NCIT:C200597 Atypical Teratoid/Rhabdoid Tumor Molecular Subtypes NCIT:C200599 Atypical Teratoid/Rhabdoid Tumor-MYC NCIT:C200598 Atypical Teratoid/Rhabdoid Tumor-SHH @@ -1167,7 +1180,6 @@ NCIT:C21922 B-NK Cell Lymphoma of the Mouse Hematologic System NCIT:C21850 B-cell Lymphomas of the Mouse Skin NCIT:C16317 B16 Malignant Melanoma NCIT:C165525 BAP1-Inactivated Melanocytoma -NCIT:C165522 BAP1-Inactivated Skin Melanocytic Neoplasm NCIT:C157614 BAP1-Mutant Clear Cell Renal Cell Carcinoma NCIT:C199467 BCL2-R-Negative, CD23-Positive Follicle Center Lymphoma NCIT:C115139 BCLC Stage 0 Adult Hepatocellular Carcinoma @@ -1254,6 +1266,7 @@ NCIT:C64031 Benign Granulosa Cell Tumor of the Rat Testis NCIT:C8539 Benign Great Vessel Neoplasm NCIT:C27520 Benign Hair Follicle Neoplasm NCIT:C173932 Benign Head and Neck Neoplasm +NCIT:C202624 Benign Head and Neck Soft Tissue Neoplasm NCIT:C66779 Benign Hemangioendothelioma NCIT:C4300 Benign Hemangiopericytoma NCIT:C21857 Benign Histiocytic Neoplasms of the Mouse Skin @@ -1284,7 +1297,6 @@ NCIT:C21831 Benign Mesenchymal Neoplasms of the Mouse Skin NCIT:C64106 Benign Mesothelioma of the Rat Pericardium NCIT:C64107 Benign Mesothelioma of the Rat Peritoneum NCIT:C64108 Benign Mesothelioma of the Rat Pleura -NCIT:C43322 Benign Mixed Epithelial and Mesenchymal Hair Follicle Neoplasm NCIT:C64034 Benign Mixed Glioma of the Rat Spinal Cord NCIT:C63968 Benign Mixed Muellerian Tumor of the Rat Uterine Cervix NCIT:C63969 Benign Mixed Muellerian Tumor of the Rat Uterus @@ -1506,8 +1518,11 @@ NCIT:C40140 Borderline Uterine Ligament Neoplasm NCIT:C181907 Borderline Vulvar Phyllodes Tumor NCIT:C45163 Borrelia Burgdoferi-Associated Primary Cutaneous Marginal Zone Lymphoproliferative Disorder NCIT:C156462 Brain Ependymoma +NCIT:C201977 Brain Low Grade Glioma +NCIT:C201975 Brain Pilocytic Astrocytoma NCIT:C5097 Brain Stem Glioblastoma NCIT:C113665 Branch Duct Pancreatic Intraductal Papillary-Mucinous Neoplasm +NCIT:C53595 Branchioma NCIT:C40360 Breast Adenocarcinoma with Spindle Cell Metaplasia NCIT:C5163 Breast Adenocarcinoma with Squamous Metaplasia NCIT:C176255 Breast Angiolipoma @@ -1521,12 +1536,6 @@ NCIT:C91230 Breast Cancer by AJCC v7 Stage NCIT:C139533 Breast Cancer by AJCC v8 Anatomic Stage NCIT:C139554 Breast Cancer by AJCC v8 Prognostic Stage NCIT:C139532 Breast Cancer by AJCC v8 Stage -NCIT:C36303 Breast Carcinoma Metastatic in the Bone -NCIT:C36301 Breast Carcinoma Metastatic in the Brain -NCIT:C133501 Breast Carcinoma Metastatic in the Central Nervous System -NCIT:C36302 Breast Carcinoma Metastatic in the Liver -NCIT:C36300 Breast Carcinoma Metastatic in the Lung -NCIT:C153227 Breast Carcinoma Metastatic in the Lymph Nodes NCIT:C153226 Breast Carcinoma Metastatic in the Spine NCIT:C47847 Breast Carcinoma with Chondroid Metaplasia NCIT:C40350 Breast Carcinoma with Choriocarcinomatous Features @@ -1553,11 +1562,13 @@ NCIT:C6987 Breast Ductal Carcinoma with Squamous Metaplasia NCIT:C9492 Breast Ductal Hyperplasia NCIT:C175950 Breast Florid Lobular Carcinoma In Situ NCIT:C40377 Breast Follicular Lymphoma +NCIT:C5167 Breast High Grade Mucoepidermoid Carcinoma NCIT:C157235 Breast Histiocytoid Carcinoma NCIT:C4804 Breast Hyperplasia NCIT:C139012 Breast Implant-Associated Anaplastic Large Cell Lymphoma NCIT:C40398 Breast Inflammatory Myofibroblastic Tumor NCIT:C7645 Breast Intracystic Papillary Carcinoma +NCIT:C5168 Breast Low Grade Mucoepidermoid Carcinoma NCIT:C5139 Breast Micropapillary Ductal Carcinoma In Situ NCIT:C40347 Breast Mixed Carcinoma NCIT:C175581 Breast Neuroendocrine Carcinoma @@ -1602,6 +1613,7 @@ NCIT:C45601 Bronchial Glandular Papilloma NCIT:C7436 Bronchial Intraepithelial Neoplasia NCIT:C45602 Bronchial Mixed Squamous Cell and Glandular Papilloma NCIT:C183045 Bronchiolar Adenoma/Ciliated Muconodular Papillary Tumor +NCIT:C202609 Buccal Mucosa Lipoma NCIT:C8175 Buccal Mucosa Verrucous Carcinoma NCIT:C134943 Budgerigar Fibrosarcoma NCIT:C135003 Budgerigar Testicular Carcinoma @@ -1677,6 +1689,8 @@ NCIT:C153336 Castration-Sensitive Prostate Carcinoma NCIT:C5324 Cauda Equina Neuroendocrine Tumor NCIT:C49115 Cavernous Angioleiomyoma NCIT:C22922 Cavernous Hemangioma of the Mouse Blood Vessel +NCIT:C203386 Cecum Neuroendocrine Tumor +NCIT:C203392 Cecum Neuroendocrine Tumor G2 NCIT:C5521 Cecum Non-Hodgkin Lymphoma NCIT:C27257 Cellular Angiofibroma NCIT:C4241 Cellular Blue Nevus @@ -1718,6 +1732,7 @@ NCIT:C7006 Central Nervous System Kaposi Sarcoma NCIT:C129806 Central Nervous System Langerhans Cell Histiocytosis NCIT:C186662 Central Nervous System Lymphomatoid Granulomatosis NCIT:C129600 Central Nervous System Mature T-Cell and NK-Cell Non-Hodgkin Lymphoma +NCIT:C4661 Central Nervous System Melanocytic Neoplasm NCIT:C129534 Central Nervous System Mesenchymal Chondrosarcoma NCIT:C129551 Central Nervous System Myofibroblastoma NCIT:C186547 Central Nervous System Neuroblastoma, FOXR2-Activated @@ -1734,6 +1749,8 @@ NCIT:C5409 Central Nervous System T-Cell Non-Hodgkin Lymphoma NCIT:C7015 Central Nervous System Teratoma with Malignant Transformation NCIT:C186556 Central Nervous System Tumor with BCOR Internal Tandem Duplication NCIT:C129566 Central Nervous System Undifferentiated Pleomorphic Sarcoma +NCIT:C202077 Central Odontogenic Fibroma +NCIT:C202253 Central Osteoma NCIT:C22955 Central Osteosarcoma of the Mouse Skeletal System NCIT:C21913 Centroblastic Diffuse Large B Cell Lymphoma of the Mouse Hematologic System NCIT:C4074 Centroblastic Lymphoma @@ -2018,6 +2035,7 @@ NCIT:C190020 Childhood Liver Angiosarcoma NCIT:C189934 Childhood Liver Embryonal Sarcoma NCIT:C27368 Childhood Liver Neoplasm NCIT:C188970 Childhood Low Grade Fibromyxoid Sarcoma +NCIT:C202299 Childhood Low Grade Glioma NCIT:C188973 Childhood Low Grade Myofibroblastic Sarcoma NCIT:C190095 Childhood Lung Neoplasm NCIT:C118814 Childhood Lung Non-Small Cell Carcinoma @@ -2035,6 +2053,7 @@ NCIT:C5448 Childhood Malignant Central Nervous System Neoplasm NCIT:C189870 Childhood Malignant Digestive System Neoplasm NCIT:C190070 Childhood Malignant Endocrine Neoplasm NCIT:C189269 Childhood Malignant Genitourinary System Neoplasm +NCIT:C202298 Childhood Malignant Glioma NCIT:C190121 Childhood Malignant Head and Neck Neoplasm NCIT:C198104 Childhood Malignant Kidney Neoplasm Excluding Renal Cell Carcinoma by Toronto Guidelines v2 Stage NCIT:C198085 Childhood Malignant Kidney Neoplasm Excluding Renal Cell Carcinoma by Toronto Guidelines v2 Stage, Children's Oncology Group (COG) Protocol @@ -2256,6 +2275,7 @@ NCIT:C130035 Chronic Myelomonocytic Leukemia-0 NCIT:C36061 Chronic Myelomonocytic Leukemia-1 NCIT:C36062 Chronic Myelomonocytic Leukemia-2 NCIT:C3175 Chronic Phase Chronic Myeloid Leukemia, BCR-ABL1 Positive +NCIT:C203904 Chronic Phase Chronic Myeloid Leukemia, Philadelphia Chromosome Positive, BCR-ABL1 Positive NCIT:C188314 Chronic Phase Primary Myelofibrosis NCIT:C22094 Chronic Ulcerative Enteritis of the Mouse Intestinal Tract NCIT:C27772 Cigarette Smoking-Related Carcinoma @@ -2273,6 +2293,7 @@ NCIT:C21917 Classic Burkitt Lymphoma of the Mouse Hematologic System NCIT:C200669 Classic Follicular Lymphoma NCIT:C7243 Classic Hodgkin Lymphoma Post-Transplant Lymphoproliferative Disorder NCIT:C199676 Classic Hydroa Vacciniforme Lymphoproliferative Disorder +NCIT:C43353 Classic Poroma NCIT:C27480 Classic Rhabdomyoma NCIT:C187644 Classic Thyroid Gland Papillary Carcinoma NCIT:C27545 Classic Type Atypical Fibroxanthoma @@ -2280,9 +2301,9 @@ NCIT:C27521 Classic Type Trichilemmoma NCIT:C27523 Classic Type Trichoepithelioma NCIT:C7188 Classical Burkitt Lymphoma NCIT:C45210 Classical Low Grade Fibromyxoid Sarcoma -NCIT:C43353 Classical Poroma NCIT:C191768 Clear Cell Adenocarcinoma of the Urinary Tract NCIT:C23134 Clear Cell Adenoma of the Mouse Salivary Glands +NCIT:C202057 Clear Cell Calcifying Epithelial Odontogenic Tumor NCIT:C22976 Clear Cell Chondrosarcoma of the Mouse Skeletal System NCIT:C63900 Clear Cell Focus of Cellular Alteration of the Rat NCIT:C43848 Clear Cell Intrahepatic Cholangiocarcinoma @@ -2291,57 +2312,61 @@ NCIT:C38154 Clear Cell Myomelanocytic Tumor of the Falciform Ligament/Ligamentum NCIT:C66752 Clear Cell Neoplasm NCIT:C54300 Clear Cell Odontogenic Carcinoma NCIT:C121955 Clear Cell Papillary Renal Tumor +NCIT:C204755 Clear Cell Tumor with Melanocytic Differentiation and ACTB-MITF Translocation +NCIT:C204756 Clear Cell Tumor with Melanocytic Differentiation and ACTG1-MITF Translocation +NCIT:C204740 Clear Cell Tumor with Melanocytic Differentiation and ACTIN-MITF Translocation +NCIT:C204741 Clear Cell Tumor with Melanocytic Differentiation and MITF-CREM Translocation NCIT:C46094 Clear Cell Variant Thyroid Gland Papillary Carcinoma NCIT:C137647 Clinical Stage 0 Cutaneous Melanoma AJCC v8 +NCIT:C136872 Clinical Stage 0 Cutaneous Merkel Cell Carcinoma AJCC v8 NCIT:C133402 Clinical Stage 0 Esophageal Adenocarcinoma AJCC v8 NCIT:C133447 Clinical Stage 0 Esophageal Squamous Cell Carcinoma AJCC v8 NCIT:C133647 Clinical Stage 0 Gastric Cancer AJCC v8 NCIT:C133550 Clinical Stage 0 Gastroesophageal Junction Adenocarcinoma AJCC v8 -NCIT:C136872 Clinical Stage 0 Merkel Cell Carcinoma AJCC v8 NCIT:C137648 Clinical Stage I Cutaneous Melanoma AJCC v8 +NCIT:C136873 Clinical Stage I Cutaneous Merkel Cell Carcinoma AJCC v8 NCIT:C133403 Clinical Stage I Esophageal Adenocarcinoma AJCC v8 NCIT:C133448 Clinical Stage I Esophageal Squamous Cell Carcinoma AJCC v8 NCIT:C133648 Clinical Stage I Gastric Cancer AJCC v8 NCIT:C133552 Clinical Stage I Gastroesophageal Junction Adenocarcinoma AJCC v8 NCIT:C132885 Clinical Stage I HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8 -NCIT:C136873 Clinical Stage I Merkel Cell Carcinoma AJCC v8 NCIT:C140752 Clinical Stage I Retinoblastoma AJCC v8 NCIT:C137649 Clinical Stage IA Cutaneous Melanoma AJCC v8 NCIT:C137650 Clinical Stage IB Cutaneous Melanoma AJCC v8 NCIT:C137651 Clinical Stage II Cutaneous Melanoma AJCC v8 +NCIT:C136874 Clinical Stage II Cutaneous Merkel Cell Carcinoma AJCC v8 NCIT:C133404 Clinical Stage II Esophageal Adenocarcinoma AJCC v8 NCIT:C133449 Clinical Stage II Esophageal Squamous Cell Carcinoma AJCC v8 NCIT:C133649 Clinical Stage II Gastric Cancer AJCC v8 NCIT:C133553 Clinical Stage II Gastroesophageal Junction Adenocarcinoma AJCC v8 NCIT:C132886 Clinical Stage II HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8 -NCIT:C136874 Clinical Stage II Merkel Cell Carcinoma AJCC v8 NCIT:C140753 Clinical Stage II Retinoblastoma AJCC v8 NCIT:C137652 Clinical Stage IIA Cutaneous Melanoma AJCC v8 +NCIT:C136875 Clinical Stage IIA Cutaneous Merkel Cell Carcinoma AJCC v8 NCIT:C133405 Clinical Stage IIA Esophageal Adenocarcinoma AJCC v8 NCIT:C133681 Clinical Stage IIA Gastric Cancer AJCC v8 NCIT:C133554 Clinical Stage IIA Gastroesophageal Junction Adenocarcinoma AJCC v8 -NCIT:C136875 Clinical Stage IIA Merkel Cell Carcinoma AJCC v8 NCIT:C137653 Clinical Stage IIB Cutaneous Melanoma AJCC v8 +NCIT:C136876 Clinical Stage IIB Cutaneous Merkel Cell Carcinoma AJCC v8 NCIT:C133406 Clinical Stage IIB Esophageal Adenocarcinoma AJCC v8 NCIT:C133682 Clinical Stage IIB Gastric Cancer AJCC v8 NCIT:C133555 Clinical Stage IIB Gastroesophageal Junction Adenocarcinoma AJCC v8 -NCIT:C136876 Clinical Stage IIB Merkel Cell Carcinoma AJCC v8 NCIT:C137654 Clinical Stage IIC Cutaneous Melanoma AJCC v8 NCIT:C137655 Clinical Stage III Cutaneous Melanoma AJCC v8 +NCIT:C136877 Clinical Stage III Cutaneous Merkel Cell Carcinoma AJCC v8 NCIT:C133407 Clinical Stage III Esophageal Adenocarcinoma AJCC v8 NCIT:C133450 Clinical Stage III Esophageal Squamous Cell Carcinoma AJCC v8 NCIT:C133650 Clinical Stage III Gastric Cancer AJCC v8 NCIT:C133556 Clinical Stage III Gastroesophageal Junction Adenocarcinoma AJCC v8 NCIT:C132891 Clinical Stage III HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8 -NCIT:C136877 Clinical Stage III Merkel Cell Carcinoma AJCC v8 NCIT:C140754 Clinical Stage III Retinoblastoma AJCC v8 NCIT:C137656 Clinical Stage IV Cutaneous Melanoma AJCC v8 +NCIT:C136878 Clinical Stage IV Cutaneous Merkel Cell Carcinoma AJCC v8 NCIT:C133408 Clinical Stage IV Esophageal Adenocarcinoma AJCC v8 NCIT:C133451 Clinical Stage IV Esophageal Squamous Cell Carcinoma AJCC v8 NCIT:C133651 Clinical Stage IV Gastric Cancer AJCC v8 NCIT:C133557 Clinical Stage IV Gastroesophageal Junction Adenocarcinoma AJCC v8 NCIT:C132893 Clinical Stage IV HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8 -NCIT:C136878 Clinical Stage IV Merkel Cell Carcinoma AJCC v8 NCIT:C140755 Clinical Stage IV Retinoblastoma AJCC v8 NCIT:C133409 Clinical Stage IVA Esophageal Adenocarcinoma AJCC v8 NCIT:C133452 Clinical Stage IVA Esophageal Squamous Cell Carcinoma AJCC v8 @@ -2375,6 +2400,7 @@ NCIT:C170977 Colon Large Cell Neuroendocrine Carcinoma NCIT:C156279 Colon Liposarcoma NCIT:C27411 Colon Mantle Cell Lymphoma NCIT:C96492 Colon Micropapillary Adenocarcinoma +NCIT:C203384 Colon Neuroendocrine Carcinoma NCIT:C160443 Colon Neuroendocrine Tumor G2 NCIT:C172702 Colon Neuroendocrine Tumor G3 NCIT:C135214 Colon Neuroendocrine Tumor by AJCC v8 Stage @@ -2436,7 +2462,8 @@ NCIT:C43591 Colorectal Undifferentiated Carcinoma NCIT:C5676 Colorectal Villous Adenoma NCIT:C54181 Columnar Cell Change of the Breast NCIT:C54182 Columnar Cell Change of the Breast with Atypia -NCIT:C165523 Combined BAP1-Inactivated Nevus +NCIT:C27524 Columnar Trichoblastoma +NCIT:C165523 Combined BAP1-Inactivated Melanocytoma NCIT:C21727 Combined Epithelial / Stromal Atypical Hyperplasia of the Mouse Prostate Gland NCIT:C21714 Combined Epithelial / Stromal Diffuse Hyperplasia of the Mouse Prostate Gland NCIT:C21720 Combined Epithelial / Stromal Focal Hyperplasia of the Mouse Prostate Gland @@ -2452,6 +2479,7 @@ NCIT:C188229 Composite Gangliocytoma/Neuroma and Neuroendocrine Tumor NCIT:C157246 Composite Paraganglioma NCIT:C21785 Compound Melanocytic Hyperplasia of Mouse NCIT:C3901 Compound Nevus +NCIT:C204787 Compound Spitz Nevus NCIT:C2960 Condyloma Acuminatum NCIT:C97057 Condyloma Acuminatum with Dysplasia NCIT:C116899 Congenital Cystic Hygroma @@ -2459,6 +2487,7 @@ NCIT:C142823 Congenital Peribronchial Myofibroblastic Tumor NCIT:C22105 Congestion of the Mouse Intestinal Tract NCIT:C174402 Conjunctival Adenosquamous Carcinoma NCIT:C175499 Conjunctival Angiosarcoma +NCIT:C204978 Conjunctival Balloon Cell Nevus NCIT:C174452 Conjunctival Blue Nevus NCIT:C174403 Conjunctival Carcinoma NCIT:C174418 Conjunctival Compound Nevus @@ -2470,7 +2499,9 @@ NCIT:C4578 Conjunctival Kaposi Sarcoma NCIT:C174390 Conjunctival Keratoacanthoma NCIT:C175500 Conjunctival Leiomyosarcoma NCIT:C175498 Conjunctival Lymphangioma -NCIT:C100054 Conjunctival Melanocytic Intraepithelial Neoplasia +NCIT:C100054 Conjunctival Melanocytic Intraepithelial Lesion +NCIT:C204977 Conjunctival Melanocytic Neoplasm +NCIT:C204981 Conjunctival Melanoma In Situ NCIT:C175431 Conjunctival Mucosa-Associated Lymphoid Tissue Lymphoma NCIT:C175495 Conjunctival Myxoma NCIT:C175432 Conjunctival Non-Hodgkin Lymphoma @@ -2482,11 +2513,12 @@ NCIT:C174398 Conjunctival Spindle Cell Carcinoma NCIT:C174493 Conjunctival Spitz Nevus NCIT:C6224 Conjunctival Squamous Papilloma NCIT:C175494 Conjunctival Stromal Tumor -NCIT:C174426 Conjunctival Subepithelial Nevus +NCIT:C174426 Conjunctival Subepithelial (Stromal) Nevus NCIT:C27574 Connective and Soft Tissue Disorder NCIT:C62277 Connective and Soft Tissue Neoplasm (Antiquated) NCIT:C99390 Contralateral Breast Carcinoma NCIT:C27492 Conventional Alveolar Rhabdomyosarcoma +NCIT:C39755 Conventional Ameloblastoma NCIT:C49179 Conventional Cardiac Rhabdomyoma NCIT:C178563 Conventional Chordoma NCIT:C49104 Conventional Dermatofibrosarcoma Protuberans @@ -2501,6 +2533,7 @@ NCIT:C160974 Cribriform Adenocarcinoma of Minor Salivary Gland NCIT:C201124 Cribriform Comedo-Type Adenocarcinoma NCIT:C21683 Cribriform Mammary Carcinoma of Mouse NCIT:C121963 Cribriform Neuroepithelial Tumor +NCIT:C43322 Cribriform Trichoblastoma NCIT:C96497 Crohn Disease-Associated Colorectal Adenocarcinoma NCIT:C154342 Crooke Cell Tumor NCIT:C45272 Cutaneous Adult T-Cell Leukemia/Lymphoma @@ -2513,6 +2546,7 @@ NCIT:C7218 Cutaneous Follicular Lymphoma NCIT:C45240 Cutaneous Hematopoietic and Lymphoid Cell Neoplasm NCIT:C168980 Cutaneous Histiocytic and Dendritic Cell Neoplasm NCIT:C168984 Cutaneous Indeterminate Dendritic Cell Histiocytosis +NCIT:C202966 Cutaneous Juvenile Xanthogranuloma NCIT:C168983 Cutaneous Langerhans Cell Histiocytosis NCIT:C171101 Cutaneous Lymphoma NCIT:C45267 Cutaneous Lymphomatoid Granulomatosis @@ -2527,6 +2561,11 @@ NCIT:C137646 Cutaneous Melanoma by AJCC v8 Clinical Stage NCIT:C137657 Cutaneous Melanoma by AJCC v8 Pathologic Stage NCIT:C137645 Cutaneous Melanoma by AJCC v8 Stage NCIT:C155305 Cutaneous Melanoma of the Extremity +NCIT:C173385 Cutaneous Merkel Cell Carcinoma +NCIT:C136869 Cutaneous Merkel Cell Carcinoma by AJCC v7 Stage +NCIT:C136871 Cutaneous Merkel Cell Carcinoma by AJCC v8 Clinical Stage +NCIT:C136880 Cutaneous Merkel Cell Carcinoma by AJCC v8 Pathologic Stage +NCIT:C136870 Cutaneous Merkel Cell Carcinoma by AJCC v8 Stage NCIT:C45268 Cutaneous Nasal Type Extranodal NK/T-Cell Lymphoma NCIT:C4479 Cutaneous Neural Neoplasm NCIT:C128451 Cutaneous Neurofibroma @@ -2548,6 +2587,7 @@ NCIT:C21673 Cystic Mouse MIN NOS NCIT:C82890 Cystic Oncocytic Neoplasm NCIT:C192105 Cystic Trophoblastic Tumor NCIT:C45754 Cystic Tumor of the Atrioventricular Node +NCIT:C202058 Cystic/Microcystic Calcifying Epithelial Odontogenic Tumor NCIT:C122687 Cytogenetically Normal Acute Myeloid Leukemia NCIT:C186730 Cytogenetically Normal Acute Myeloid Leukemia Post Cytotoxic Therapy NCIT:C21900 Cytopenia with Increased Blasts of Mouse @@ -2564,6 +2604,7 @@ NCIT:C7852 DS Stage III Multiple Myeloma NCIT:C181865 DS Stage IIIA Multiple Myeloma NCIT:C181866 DS Stage IIIB Multiple Myeloma NCIT:C200050 DUSP22-R Anaplastic Large Cell Lymphoma, ALK-Negative +NCIT:C205127 De Novo Nodular Melanoma NCIT:C63978 Decidual Reaction of the Rat Uterine Cervix NCIT:C63979 Decidual Reaction of the Rat Uterus NCIT:C22977 Dedifferentiated Chondrosarcoma of the Mouse Skeletal System @@ -2573,10 +2614,11 @@ NCIT:C179932 Dedifferentiated Gastrointestinal Stromal Tumor NCIT:C178222 Dedifferentiated Leiomyosarcoma NCIT:C6936 Deep (Aggressive) Angiomyxoma NCIT:C6498 Deep Lipoma -NCIT:C7576 Deep Penetrating Nevus +NCIT:C7576 Deep Penetrating Melanocytoma NCIT:C5305 Deletion of Chromosome 22 Associated Meningioma NCIT:C5306 Deletion of Chromosome 3p Associated Meningioma NCIT:C5294 Deletion of the Short Arm of Chromosome 1 (1p) Associated Meningioma +NCIT:C204910 Dendritic Blue Nevus NCIT:C154339 Densely Granulated Corticotroph Pituitary Neuroendocrine Tumor NCIT:C45931 Densely Granulated Lactotroph Pituitary Neuroendocrine Tumor NCIT:C45925 Densely Granulated Somatotroph Pituitary Neuroendocrine Tumor @@ -2584,18 +2626,21 @@ NCIT:C54323 Dentinogenic Ghost Cell Tumor NCIT:C4473 Dermal Duct Tumor NCIT:C6484 Dermal Fibroma NCIT:C21784 Dermal Melanocytic Hyperplasia of Mouse +NCIT:C205129 Dermal Melanoma NCIT:C121680 Dermal Nerve Sheath Myxoma +NCIT:C204789 Dermal Spitz Nevus NCIT:C38108 Dermatofibrosarcoma Protuberans with Giant Cell Fibroblastoma-Like Differentiation NCIT:C38105 Dermatofibrosarcoma Protuberans with Myoid Differentiation NCIT:C170888 Dermatomyofibroma +NCIT:C203388 Descending Colon Neuroendocrine Tumor NCIT:C6428 Descending Colon Neuroendocrine Tumor G1 +NCIT:C203393 Descending Colon Neuroendocrine Tumor G2 NCIT:C27515 Desmoplastic Fibroblastoma NCIT:C3740 Desmoplastic Fibroma NCIT:C6747 Desmoplastic Mesothelioma NCIT:C178507 Desmoplastic Myxoid Tumor of the Pineal Region, SMARCB1-Mutant NCIT:C48614 Desmoplastic Neurotropic Melanoma NCIT:C27522 Desmoplastic Trichilemmoma -NCIT:C27524 Desmoplastic Trichoepithelioma NCIT:C136978 Devil Facial Tumor Disease NCIT:C176223 Devil Facial Tumor Disease 1 NCIT:C176224 Devil Facial Tumor Disease 2 @@ -2645,6 +2690,7 @@ NCIT:C185218 Diffuse Low Grade Glioma, MAPK Pathway-Altered NCIT:C27822 Diffuse Malignant Lymphoma NCIT:C8420 Diffuse Malignant Mesothelioma NCIT:C22052 Diffuse Melanocytosis of the Mouse Nervous System +NCIT:C205069 Diffuse Meningeal Melanocytic Neoplasm NCIT:C182151 Diffuse Midline Glioma NCIT:C185370 Diffuse Midline Glioma with EZHIP Overexpression NCIT:C185369 Diffuse Midline Glioma, EGFR-Mutant @@ -2660,7 +2706,6 @@ NCIT:C185468 Diffuse Pediatric-Type High Grade Glioma RTK2 NCIT:C185467 Diffuse Pediatric-Type High Grade Glioma, H3-Wildtype and IDH-Wildtype NCIT:C45630 Diffuse Pulmonary Lymphangiomatosis NCIT:C66815 Diffuse Retinoblastoma -NCIT:C182357 Diffusion Restriction NCIT:C35180 Digestive System Carcinoma In Situ NCIT:C172850 Digestive System Diffuse Large B-Cell Lymphoma NCIT:C96466 Digestive System Filiform Serrated Adenoma @@ -2685,7 +2730,6 @@ NCIT:C172849 Digestive System Sarcoma NCIT:C154641 Digestive System Small Cell Neuroendocrine Carcinoma NCIT:C172852 Digestive System Soft Tissue Neoplasm NCIT:C172940 Digestive System Solitary Fibrous Tumor -NCIT:C162848 Digital Papillary Adenoma NCIT:C21864 Disorders of Pigmentation of the Mouse Skin NCIT:C21865 Disorders of the Mouse Hair Follicle NCIT:C21863 Disorders of the Squamous Epithelium of the Mouse Skin @@ -2697,6 +2741,7 @@ NCIT:C4829 Disseminated Squamous Cell Carcinoma NCIT:C7976 Distal Bile Duct Adenocarcinoma NCIT:C134810 Distal Bile Duct Cancer by AJCC v7 Stage NCIT:C134811 Distal Bile Duct Cancer by AJCC v8 Stage +NCIT:C202634 Distal Colon Carcinoma NCIT:C152036 Distal Esophagus Adenocarcinoma NCIT:C150037 Distal Esophagus Squamous Cell Carcinoma NCIT:C115210 Distal Urethral Carcinoma @@ -2744,6 +2789,8 @@ NCIT:C27693 EBV-Related Non-Hodgkin Lymphoma NCIT:C27696 EBV-Related Post-Transplant Lymphoproliferative Disorder NCIT:C162305 EBV-Related Sarcoma NCIT:C190402 EBV-Related T/NK-Cell Lymphoproliferative Disorder +NCIT:C202130 EGFR-Positive Lung Adenocarcinoma +NCIT:C202131 EGFR-Positive Lung Non-Small Cell Carcinoma NCIT:C191375 ELOC-Mutated Renal Cell Carcinoma NCIT:C186591 ELP1-Associated Medulloblastoma NCIT:C104031 ENSAT Stage I Adrenal Cortical Carcinoma @@ -2753,13 +2800,22 @@ NCIT:C104034 ENSAT Stage IV Adrenal Cortical Carcinoma NCIT:C177278 EWSR1-SMAD3-Positive Fibroblastic Tumor NCIT:C148398 EZB Diffuse Large B-Cell Lymphoma NCIT:C54262 Ear Carcinoma -NCIT:C5971 Ear Polyp +NCIT:C202574 Ear Osteoma NCIT:C68661 Early Favorable Hodgkin Lymphoma NCIT:C53280 Early Favorable Non-Hodgkin Lymphoma NCIT:C96772 Early Hepatocellular Carcinoma NCIT:C180374 Early Primary Cutaneous T-Cell Non-Hodgkin Lymphoma +NCIT:C205286 Early Stage Bladder Urothelial Carcinoma NCIT:C94774 Early Stage Breast Carcinoma +NCIT:C205287 Early Stage Cervical Carcinoma +NCIT:C205289 Early Stage Clear Cell Renal Cell Carcinoma +NCIT:C205290 Early Stage Colorectal Carcinoma +NCIT:C205295 Early Stage Endometrial Carcinoma +NCIT:C205298 Early Stage Esophageal Carcinoma NCIT:C190215 Early Stage HER2-Negative Breast Carcinoma +NCIT:C205301 Early Stage Hepatocellular Carcinoma +NCIT:C205303 Early Stage Lung Non-Small Cell Carcinoma +NCIT:C205307 Early Stage Malignant Skin Neoplasm NCIT:C158961 Early Stage Pancreatic Ductal Adenocarcinoma NCIT:C181081 Early Stage Triple-Negative Breast Carcinoma NCIT:C199171 Early T Precursor Acute Lymphoblastic Leukemia with BCL11B Rearrangement @@ -2768,15 +2824,16 @@ NCIT:C199170 Early T Precursor Lymphoblastic Leukemia/Lymphoma NCIT:C68664 Early Unfavorable Hodgkin Lymphoma NCIT:C53282 Early Unfavorable Non-Hodgkin Lymphoma NCIT:C7565 Eccrine Hidrocystoma +NCIT:C205462 Eccrine Poroma NCIT:C121785 Ectomesenchymal Chondromyxoid Tumor NCIT:C95048 Ectopic Cervical Thymoma -NCIT:C53595 Ectopic Hamartomatous Thymoma NCIT:C5308 Ectopic Meningioma NCIT:C173345 Ectopic Pituitary Neuroendocrine Tumor NCIT:C22064 Embryonal Carcinoma of the Mouse Nervous System NCIT:C23108 Embryonal Rhabdomyosarcoma of the Mouse Nose and Paranasal Sinuses NCIT:C23078 Embryonal Rhabdomyosarcoma of the Mouse Pharynx NCIT:C186534 Embryonal Tumor with Multilayered Rosettes +NCIT:C202010 Embryonal Tumor with Multilayered Rosettes of the Fourth Ventricle NCIT:C129499 Embryonal Tumor with Multilayered Rosettes without C19MC Alteration NCIT:C186535 Embryonal Tumor with Multilayered Rosettes, DICER1-Mutated NCIT:C176009 Encapsulated Breast Papillary Carcinoma @@ -2801,7 +2858,9 @@ NCIT:C27844 Endometrial Endometrioid Adenocarcinoma with a Poorly Differentiated NCIT:C27845 Endometrial Endometrioid Adenocarcinoma with an Undifferentiated Carcinomatous Component NCIT:C27848 Endometrial Endometrioid Adenocarcinoma, Ciliated Variant NCIT:C6290 Endometrial Endometrioid Adenocarcinoma, Variant with Squamous Differentiation +NCIT:C40148 Endometrial High Grade Endometrioid Adenocarcinoma NCIT:C126772 Endometrial Large Cell Neuroendocrine Carcinoma +NCIT:C180510 Endometrial Low Grade Endometrioid Adenocarcinoma NCIT:C179322 Endometrial Mesonephric-Like Adenocarcinoma NCIT:C180537 Endometrial Mucinous Adenocarcinoma, Gastric-Type NCIT:C180536 Endometrial Mucinous Adenocarcinoma, Intestinal-Type @@ -2818,7 +2877,6 @@ NCIT:C158610 Endometrioid Adenocarcinoma, Variant with Squamous Differentiation NCIT:C158620 Endometrioid Tumor, Variant with Squamous Differentiation NCIT:C63887 Endophytic Squamous Cell Carcinoma of the Rat Esophagus NCIT:C22935 Endovascular Papillary Angioendothelioma of the Mouse Blood Vessel -NCIT:C121924 Enostosis NCIT:C27252 Enterochromaffin-Like Cell Neuroendocrine Tumor G1 NCIT:C66925 Enteroglucagonoma NCIT:C141295 Enteropathy-Associated T-Cell Lymphoma by Ann Arbor Stage @@ -2922,11 +2980,14 @@ NCIT:C133443 Esophageal Squamous Cell Carcinoma by AJCC v8 Stage NCIT:C27423 Esophageal Squamous Intraepithelial Neoplasia NCIT:C95624 Esophageal Synovial Sarcoma NCIT:C95610 Esophageal Well Differentiated Squamous Cell Carcinoma +NCIT:C203673 Esophageal and Gastroesophageal Junction Carcinoma NCIT:C188366 Estrogen Receptor-Positive Breast Carcinoma NCIT:C48456 Estrogen-Producing Adrenal Cortical Adenoma NCIT:C63888 Exophytic Squamous Cell Carcinoma of the Rat Esophagus NCIT:C16835 Experimental Malignant Melanoma NCIT:C9049 Extensive Stage Lung Small Cell Carcinoma +NCIT:C202594 External Auditory Canal Squamous Cell Carcinoma +NCIT:C91741 External Auditory Canal Squamous Cell Carcinoma In Situ NCIT:C6080 External Ear Actinic Keratosis NCIT:C3309 Extra-Adrenal Paraganglioma NCIT:C5328 Extra-Adrenal Retroperitoneal Paraganglioma @@ -3029,9 +3090,6 @@ NCIT:C128094 FIGO Stage IVA Ovarian Cancer NCIT:C6406 FIGO Stage IVB Gestational Trophoblastic Tumor NCIT:C128095 FIGO Stage IVB Ovarian Cancer NCIT:C6407 FIGO Stage IVC Gestational Trophoblastic Tumor -NCIT:C9024 FNCLCC Sarcoma Grade 1 -NCIT:C9028 FNCLCC Sarcoma Grade 2 -NCIT:C9029 FNCLCC Sarcoma Grade 3 NCIT:C189329 FOXL2 c.402C>G (p.Cys134Trp)-Mutant Ovarian Sertoli-Leydig Cell Tumor NCIT:C121152 FSH-Producing Pituitary Neuroendocrine Tumor NCIT:C90499 Fallopian Tube Cancer by AJCC v6 Stage @@ -3114,15 +3172,17 @@ NCIT:C7264 Follicular Lymphoma with Predominantly Diffuse Growth Pattern NCIT:C200684 Follicular Lymphoma with Unusual Cytological Features NCIT:C27526 Follicular Myxoma NCIT:C21813 Follicular Neoplasms of the Mouse Skin -NCIT:C187645 Follicular-Derived Thyroid Gland Carcinoma, High Grade -NCIT:C6421 Foregut Neuroendocrine Tumor G1 +NCIT:C6421 Foregut Neuroendocrine Tumor +NCIT:C203258 Foregut Neuroendocrine Tumor G1 +NCIT:C203259 Foregut Neuroendocrine Tumor G2 +NCIT:C203260 Foregut Neuroendocrine Tumor G3 NCIT:C156039 Fourth Ventricle Medulloblastoma NCIT:C95779 Foveolar-Type Adenoma NCIT:C134771 Frog Pronephric Kidney Tumor NCIT:C156035 Frontal Lobe Anaplastic Astrocytoma NCIT:C156120 Frontal Lobe Anaplastic Oligodendroglioma NCIT:C164156 Fumarate Hydratase-Deficient Renal Cell Carcinoma -NCIT:C176705 Functioning Lung Carcinoid Tumor +NCIT:C176705 Functioning Lung Neuroendocrine Tumor NCIT:C45841 Functioning Pancreatic Neuroendocrine Tumor G2 NCIT:C121720 Functioning Pituitary Neuroendocrine Tumor/Macroadenoma NCIT:C121679 Functioning Pituitary Neuroendocrine Tumor/Microadenoma @@ -3131,6 +3191,7 @@ NCIT:C123732 Fusion-Negative Alveolar Rhabdomyosarcoma NCIT:C123736 Fusion-Negative Rhabdomyosarcoma NCIT:C123731 Fusion-Positive Alveolar Rhabdomyosarcoma NCIT:C123735 Fusion-Positive Rhabdomyosarcoma +NCIT:C202896 GLI1-Altered Soft Tissue Tumor NCIT:C9169 Gallbladder Adenocarcinoma with Squamous Metaplasia NCIT:C96915 Gallbladder Adenocarcinoma, Biliary Type NCIT:C96916 Gallbladder Adenocarcinoma, Gastric Foveolar Type @@ -3224,6 +3285,7 @@ NCIT:C133549 Gastroesophageal Junction Adenocarcinoma by AJCC v8 Clinical Stage NCIT:C133563 Gastroesophageal Junction Adenocarcinoma by AJCC v8 Pathologic Stage NCIT:C133583 Gastroesophageal Junction Adenocarcinoma by AJCC v8 Postneoadjuvant Therapy Stage NCIT:C133548 Gastroesophageal Junction Adenocarcinoma by AJCC v8 Stage +NCIT:C203675 Gastroesophageal Junction Carcinoma NCIT:C126323 Gastroesophageal Junction Large Cell Neuroendocrine Carcinoma NCIT:C126324 Gastroesophageal Junction Neuroendocrine Carcinoma NCIT:C126325 Gastroesophageal Junction Small Cell Neuroendocrine Carcinoma @@ -3266,6 +3328,7 @@ NCIT:C5699 Giant Fibrovascular Esophageal Polyp NCIT:C134774 Gibbon Lymphosarcoma NCIT:C27478 Gingival Angiofibroma NCIT:C7721 Gingival Carcinoma +NCIT:C202622 Gingival Low Grade Myofibroblastic Sarcoma NCIT:C129289 Gingival Spindle Cell Carcinoma NCIT:C129857 Gingival Squamous Cell Carcinoma NCIT:C27269 Glandular Cell Intraepithelial Neoplasia @@ -3368,6 +3431,7 @@ NCIT:C132884 HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma by AJCC v8 Path NCIT:C132882 HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma by AJCC v8 Stage NCIT:C27685 HTLV-1-Related Malignant Neoplasm NCIT:C22104 Hamartoma of the Mouse Intestinal Tract +NCIT:C8372 Hamartomatous Polyp NCIT:C134990 Hamster Adrenal Carcinoma NCIT:C134565 Hamster Buccal Pouch Carcinoma NCIT:C134566 Hamster Cholangiocarcinoma @@ -3392,16 +3456,45 @@ NCIT:C6214 Hard Palate Mucoepidermoid Carcinoma NCIT:C6212 Hard Palate Pleomorphic Adenoma NCIT:C8170 Hard Palate Squamous Cell Carcinoma NCIT:C16662 Harding-Passey Malignant Melanoma -NCIT:C37290 Head and Neck Basaloid Carcinoma +NCIT:C202656 Head and Neck Angiosarcoma +NCIT:C37290 Head and Neck Basaloid Squamous Cell Carcinoma +NCIT:C202935 Head and Neck Burkitt Lymphoma NCIT:C162595 Head and Neck Carcinoma of Unknown Primary +NCIT:C202975 Head and Neck Dermoid Cyst +NCIT:C202930 Head and Neck Diffuse Large B-Cell Lymphoma +NCIT:C202849 Head and Neck EBV-Associated Smooth Muscle Tumor +NCIT:C202655 Head and Neck Epithelioid Hemangioendothelioma +NCIT:C202652 Head and Neck Epithelioid Hemangioma +NCIT:C202972 Head and Neck Erdheim-Chester Disease +NCIT:C202904 Head and Neck Ewing Sarcoma +NCIT:C202924 Head and Neck Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue +NCIT:C202881 Head and Neck Extraskeletal Myxoid Chondrosarcoma NCIT:C173580 Head and Neck Follicular Dendritic Cell Sarcoma +NCIT:C202926 Head and Neck Follicular Lymphoma +NCIT:C202897 Head and Neck GLI1-Altered Soft Tissue Tumor +NCIT:C202977 Head and Neck Germ Cell Tumor +NCIT:C202647 Head and Neck Hemangioma +NCIT:C202954 Head and Neck Hematopoietic and Lymphoid Cell Neoplasm NCIT:C173588 Head and Neck Heterotopia-Associated Carcinoma NCIT:C173485 Head and Neck Histiocytic and Dendritic Cell Neoplasm +NCIT:C202922 Head and Neck Hodgkin Lymphoma +NCIT:C202635 Head and Neck Inflammatory Myofibroblastic Tumor +NCIT:C202967 Head and Neck Juvenile Xanthogranuloma NCIT:C54283 Head and Neck Keratinizing Squamous Cell Carcinoma NCIT:C173486 Head and Neck Langerhans Cell Histiocytosis +NCIT:C202929 Head and Neck Large B-Cell Lymphoma with IRF4 Rearrangement NCIT:C160982 Head and Neck Large Cell Neuroendocrine Carcinoma +NCIT:C202711 Head and Neck Leiomyoma +NCIT:C202853 Head and Neck Leiomyosarcoma +NCIT:C202646 Head and Neck Lipoma +NCIT:C202611 Head and Neck Liposarcoma +NCIT:C202654 Head and Neck Lymphangioma +NCIT:C202921 Head and Neck Lymphoma +NCIT:C202878 Head and Neck Malignant Peripheral Nerve Sheath Tumor +NCIT:C202925 Head and Neck Mantle Cell Lymphoma NCIT:C173488 Head and Neck Melanocytic Neoplasm NCIT:C173587 Head and Neck Merkel Cell Carcinoma +NCIT:C202914 Head and Neck Myeloid Sarcoma NCIT:C173087 Head and Neck NUT Carcinoma NCIT:C160980 Head and Neck Neuroendocrine Carcinoma NCIT:C188222 Head and Neck Neuroendocrine Neoplasm @@ -3409,9 +3502,22 @@ NCIT:C173387 Head and Neck Neuroendocrine Tumor NCIT:C188224 Head and Neck Neuroendocrine Tumor G1 NCIT:C173388 Head and Neck Neuroendocrine Tumor G2 NCIT:C54661 Head and Neck Nevus +NCIT:C202613 Head and Neck Nodular Fasciitis +NCIT:C202923 Head and Neck Non-Hodgkin Lymphoma +NCIT:C202927 Head and Neck Pediatric-Type Follicular Lymphoma +NCIT:C202879 Head and Neck Phosphaturic Mesenchymal Tumor +NCIT:C202936 Head and Neck Plasmablastic Lymphoma +NCIT:C202973 Head and Neck Plasmacytoma +NCIT:C202858 Head and Neck Rhabdomyoma +NCIT:C202859 Head and Neck Rhabdomyosarcoma +NCIT:C202971 Head and Neck Rosai-Dorfman-Destombes Disease NCIT:C164198 Head and Neck Sarcoma NCIT:C160978 Head and Neck Sebaceous Carcinoma NCIT:C160981 Head and Neck Small Cell Neuroendocrine Carcinoma +NCIT:C202623 Head and Neck Soft Tissue Neoplasm +NCIT:C202884 Head and Neck Synovial Sarcoma +NCIT:C202980 Head and Neck Teratoma +NCIT:C202901 Head and Neck Undifferentiated Pleomorphic Sarcoma NCIT:C199457 Heavy Chain Class-Switched Primary Cutaneous Marginal Zone Lymphoproliferative Disorder NCIT:C27763 Helicobacter Pylori-Associated Gastric Mucosa-Associated Lymphoid Tissue Lymphoma NCIT:C27764 Helicobacter Pylori-Related Carcinoma @@ -3455,8 +3561,8 @@ NCIT:C23099 Hematopoietic Neoplasms of the Mouse Nose and Paranasal Sinuses NCIT:C23063 Hematopoietic Neoplasms of the Mouse Oral Cavity NCIT:C23083 Hematopoietic Neoplasms of the Mouse Pharynx NCIT:C23147 Hematopoietic Neoplasms of the Mouse Salivary Glands +NCIT:C35814 Hematopoietic and Lymphatic System Disorder NCIT:C7340 Hematopoietic and Lymphoid Neoplasm (Antiquated) -NCIT:C35814 Hematopoietic and Lymphoid System Disorder NCIT:C5123 Hemispheric Anaplastic Astrocytoma NCIT:C66792 Hemolymphangioma NCIT:C121752 Hemosiderotic Fibrolipomatous Tumor @@ -3490,6 +3596,7 @@ NCIT:C5329 Hereditary Paraganglioma NCIT:C46099 Hereditary Thyroid Gland Medullary Carcinoma NCIT:C22032 Hibernoma of the Mouse Nervous System NCIT:C21835 Hibernoma of the Mouse Skin +NCIT:C205475 Hidroacanthoma Simplex NCIT:C9109 High Grade Adult Non-Hodgkin's Lymphoma NCIT:C27275 High Grade Anal Canal Intraepithelial Neoplasia NCIT:C172706 High Grade Anal Intraepithelial Neoplasia @@ -3504,21 +3611,21 @@ NCIT:C199618 High Grade B-Cell Lymphoma with MYC and BCL6 Rearrangements NCIT:C131913 High Grade B-Cell Lymphoma with MYC, BCL2, and BCL6 Rearrangements NCIT:C80291 High Grade B-Cell Lymphoma, Not Otherwise Specified NCIT:C6817 High Grade B-Cell Non-Hodgkin's Lymphoma -NCIT:C5167 High Grade Breast Mucoepidermoid Carcinoma NCIT:C5005 High Grade Burkitt-Like Lymphoma NCIT:C7675 High Grade Cervical Glandular Intraepithelial Neoplasia NCIT:C7670 High Grade Cervical Intraepithelial Neoplasia NCIT:C40197 High Grade Cervical Squamous Intraepithelial Neoplasia +NCIT:C204980 High Grade Conjunctival Melanocytic Intraepithelial Lesion NCIT:C7668 High Grade Conjunctival Squamous Intraepithelial Neoplasia NCIT:C7669 High Grade Corneal Squamous Intraepithelial Neoplasia NCIT:C190680 High Grade Endometrial Carcinoma -NCIT:C40148 High Grade Endometrial Endometrioid Adenocarcinoma NCIT:C199149 High Grade Endometrioid Adenocarcinoma NCIT:C27429 High Grade Esophageal Glandular Intraepithelial Neoplasia NCIT:C27426 High Grade Esophageal Squamous Intraepithelial Neoplasia NCIT:C22132 High Grade Flat Tubular Dysplasia of the Mouse Intestinal Tract NCIT:C22138 High Grade Flat Tubulovillous Dysplasia of the Mouse Intestinal Tract NCIT:C22135 High Grade Flat Villous Dysplasia of the Mouse Intestinal Tract +NCIT:C187645 High Grade Follicular Cell-Derived Non-Anaplastic Thyroid Gland Carcinoma NCIT:C27437 High Grade Gastric Intraepithelial Neoplasia NCIT:C7662 High Grade Glandular Intraepithelial Neoplasia NCIT:C7348 High Grade Intraepithelial Neoplasia @@ -3527,9 +3634,10 @@ NCIT:C3458 High Grade Lymphoma NCIT:C9030 High Grade Malignant Peripheral Nerve Sheath Tumor NCIT:C21676 High Grade Mouse MIN NCIT:C21730 High Grade Mouse Prostatic Intraepithelial Neoplasia +NCIT:C203948 High Grade Mucinous Carcinoma Peritonei +NCIT:C203949 High Grade Mucinous Carcinoma Peritonei with Signet Ring Cells NCIT:C23139 High Grade Mucoepidermoid Tumor of the Mouse Salivary Glands NCIT:C197813 High Grade Osteosarcoma -NCIT:C199166 High Grade Ovarian Endometrioid Adenocarcinoma NCIT:C95432 High Grade Pancreatic Intraepithelial Neoplasia NCIT:C6850 High Grade Paranasal Sinus Sarcoma NCIT:C22142 High Grade Pedunculated Tubular Dysplasia of the Mouse Intestinal Tract @@ -3541,8 +3649,6 @@ NCIT:C39890 High Grade Prostatic Intraepithelial Neoplasia, Inverted Variant NCIT:C39888 High Grade Prostatic Intraepithelial Neoplasia, Mucinous Variant NCIT:C39887 High Grade Prostatic Intraepithelial Neoplasia, Signet Ring Variant NCIT:C39891 High Grade Prostatic Intraepithelial Neoplasia, Small Cell Neuroendocrine Variant -NCIT:C8018 High Grade Salivary Gland Carcinoma -NCIT:C8019 High Grade Salivary Gland Mucoepidermoid Carcinoma NCIT:C9418 High Grade Sarcoma NCIT:C22122 High Grade Sessile Tubular Dysplasia of the Mouse Intestinal Tract NCIT:C22128 High Grade Sessile Tubulovillous Dysplasia of the Mouse Intestinal Tract @@ -3563,8 +3669,12 @@ NCIT:C165659 High-CSD Melanoma NCIT:C67493 High-Grade Biliary Intraepithelial Neoplasia NCIT:C134742 Hilar Cholangiocarcinoma by AJCC v7 Stage NCIT:C134743 Hilar Cholangiocarcinoma by AJCC v8 Stage -NCIT:C6423 Hindgut Neuroendocrine Tumor G1 +NCIT:C6423 Hindgut Neuroendocrine Tumor +NCIT:C203262 Hindgut Neuroendocrine Tumor G1 +NCIT:C203265 Hindgut Neuroendocrine Tumor G2 +NCIT:C203266 Hindgut Neuroendocrine Tumor G3 NCIT:C21915 Histiocyte-Associated Diffuse Large B Cell Lymphoma of the Mouse Hematologic System +NCIT:C203422 Histiocytic Disorder NCIT:C23121 Histiocytic Neoplasms of the Mouse Larynx NCIT:C21856 Histiocytic Neoplasms of the Mouse Skin NCIT:C21874 Histiocytosis in Association with a Hematopoietic Neoplasm of Mouse @@ -3586,10 +3696,10 @@ NCIT:C200652 Hormone Therapy Refractory Neoplasm NCIT:C180848 Human Papillomavirus-Independent Cervical Adenocarcinoma NCIT:C180846 Human Papillomavirus-Independent Cervical Adenocarcinoma In Situ NCIT:C180841 Human Papillomavirus-Independent Cervical Squamous Cell Carcinoma +NCIT:C164250 Human Papillomavirus-Independent Squamous Cell Carcinoma NCIT:C180919 Human Papillomavirus-Independent Vaginal Squamous Cell Carcinoma NCIT:C181903 Human Papillomavirus-Independent Vulvar Squamous Cell Carcinoma -NCIT:C190149 Human Papillomavirus-Negative Head and Neck Squamous Cell Carcinoma of Unknown Primary -NCIT:C164250 Human Papillomavirus-Negative Squamous Cell Carcinoma +NCIT:C190149 Human Papillomavirus-Negative Neck Squamous Cell Carcinoma of Unknown Primary NCIT:C27684 Human Papillomavirus-Related Adenocarcinoma NCIT:C97046 Human Papillomavirus-Related Adenosquamous Carcinoma NCIT:C27681 Human Papillomavirus-Related Anal Squamous Cell Carcinoma @@ -3599,18 +3709,20 @@ NCIT:C180845 Human Papillomavirus-Related Cervical Adenocarcinoma In Situ NCIT:C27675 Human Papillomavirus-Related Cervical Carcinoma NCIT:C27676 Human Papillomavirus-Related Cervical Squamous Cell Carcinoma NCIT:C27680 Human Papillomavirus-Related Esophageal Squamous Cell Carcinoma -NCIT:C187051 Human Papillomavirus-Related Head and Neck Squamous Cell Carcinoma of Unknown Primary NCIT:C27718 Human Papillomavirus-Related Malignant Neoplasm NCIT:C102884 Human Papillomavirus-Related Malignant Neoplasm in AIDS Patient NCIT:C171023 Human Papillomavirus-Related Mucosal Head and Neck Squamous Cell Carcinoma +NCIT:C187051 Human Papillomavirus-Related Neck Squamous Cell Carcinoma of Unknown Primary NCIT:C162541 Human Papillomavirus-Related Penile Intraepithelial Neoplasia NCIT:C39862 Human Papillomavirus-Related Urethral Squamous Cell Carcinoma NCIT:C180943 Human Papillomavirus-Related Vaginal Adenocarcinoma NCIT:C180917 Human Papillomavirus-Related Vaginal Squamous Cell Carcinoma NCIT:C27678 Human Papillomavirus-Related Verrucous Carcinoma NCIT:C27679 Human Papillomavirus-Related Vulvar Squamous Cell Carcinoma +NCIT:C201821 Hyalinizing Clear Cell Carcinoma NCIT:C121686 Hybrid Nerve Sheath Tumor NCIT:C7448 Hybrid Odontogenic Fibroma +NCIT:C202081 Hybrid Odontogenic Fibroma with Central Giant Cell Granuloma NCIT:C181079 Hybrid Salivary Gland Carcinoma NCIT:C181078 Hybrid Salivary Gland Tumor NCIT:C80344 Hyperdiploid B Acute Lymphoblastic Leukemia @@ -3620,9 +3732,13 @@ NCIT:C21652 Hyperplasia of the Mouse Mammary Gland NCIT:C21708 Hyperplasia of the Mouse Prostate Gland NCIT:C21756 Hyperplasia of the Mouse Pulmonary System NCIT:C80345 Hypodiploid B Acute Lymphoblastic Leukemia +NCIT:C201746 Hypopharyngeal Basaloid Squamous Cell Carcinoma NCIT:C90524 Hypopharyngeal Carcinoma by AJCC v6 Stage NCIT:C91251 Hypopharyngeal Carcinoma by AJCC v7 Stage NCIT:C133003 Hypopharyngeal Carcinoma by AJCC v8 Stage +NCIT:C201748 Hypopharyngeal Papillary Squamous Cell Carcinoma +NCIT:C201749 Hypopharyngeal Spindle Cell Squamous Carcinoma +NCIT:C201743 Hypopharyngeal Verrucous Carcinoma NCIT:C21647 Hypoplasia of the Mouse Mammary Gland NCIT:C21706 Hypoplasia of the Mouse Prostate Gland NCIT:C122686 Hypoplastic Myelodysplastic Syndrome @@ -3694,13 +3810,13 @@ NCIT:C9407 Inflammatory Malignant Fibrous Histiocytoma NCI Grade 2 NCIT:C9408 Inflammatory Malignant Fibrous Histiocytoma NCI Grade 3 NCIT:C21657 Inflammatory Nodule of the Mouse Mammary Gland NCIT:C5148 Infratentorial Glioblastoma -NCIT:C7201 Infrequent Neoplasm NCIT:C45473 Intermediate (Locally Aggressive) Blood Vessel Neoplasm NCIT:C45474 Intermediate (Rarely Metastasizing) Blood Vessel Neoplasm NCIT:C136972 Intermediate Atypical Prostate Carcinoma NCIT:C7391 Intermediate Blood Vessel Neoplasm NCIT:C121926 Intermediate Bone Neoplasm NCIT:C121846 Intermediate Chondrogenic Neoplasm +NCIT:C204976 Intermediate Congenital Melanocytic Nevus NCIT:C7333 Intermediate Fibroblastic Neoplasm NCIT:C6491 Intermediate Fibrohistiocytic Neoplasm NCIT:C9108 Intermediate Grade Adult Non-Hodgkin's Lymphoma @@ -3709,7 +3825,6 @@ NCIT:C45568 Intermediate Grade Lung Neuroendocrine Neoplasm NCIT:C3459 Intermediate Grade Lymphoma NCIT:C36047 Intermediate Grade Malignant Neoplasm NCIT:C197814 Intermediate Grade Osteosarcoma -NCIT:C8017 Intermediate Grade Salivary Gland Mucoepidermoid Carcinoma NCIT:C7630 Intermediate Lipomatous Neoplasm NCIT:C121931 Intermediate Osteoclastic Giant Cell-Rich Tumor of Bone NCIT:C121925 Intermediate Osteogenic Neoplasm @@ -3842,10 +3957,15 @@ NCIT:C65165 Inverted Squamous Papilloma NCIT:C27930 Ionizing Radiation-Related Malignant Neoplasm NCIT:C190746 Iridociliary Melanoma NCIT:C174498 Iris Epithelioid Cell Melanoma -NCIT:C174506 Iris Mixed Cell Melanoma +NCIT:C174506 Iris Mixed Epithelioid and Spindle Cell Melanoma NCIT:C4556 Iris Nevus NCIT:C65184 Islet Cell Adenoma -NCIT:C121923 Ivory Exostosis +NCIT:C202257 Jaw Chondromyxoid Fibroma +NCIT:C202258 Jaw Desmoplastic Fibroma +NCIT:C202256 Jaw Osteoblastoma +NCIT:C202254 Jaw Osteoma +NCIT:C202261 Jaw Osteosarcoma +NCIT:C202265 Jaw Rhabdomyosarcoma with TFCP2 Rearrangement NCIT:C181157 Jejunal Carcinoma NCIT:C188067 Jejunal Melanoma NCIT:C160437 Jejunal Neuroendocrine Tumor G2 @@ -3854,6 +3974,7 @@ NCIT:C135119 Jejunal Neuroendocrine Tumor by AJCC v8 Stage NCIT:C5589 Jugular Foramen Neoplasm NCIT:C21783 Junctional Melanocytic Hyperplasia of Mouse NCIT:C4231 Junctional Nevus +NCIT:C204788 Junctional Spitz Nevus NCIT:C40434 Juvenile Bilateral Ovarian Granulosa Cell Tumor NCIT:C4276 Juvenile Breast Fibroadenoma NCIT:C4207 Juvenile Granulosa Cell Tumor @@ -3861,6 +3982,7 @@ NCIT:C198680 Juvenile Myelomonocytic Leukemia Associated with Neurofibromatosis NCIT:C198682 Juvenile Myelomonocytic Leukemia Associated with Noonan Syndrome-Like Disorder NCIT:C198661 Juvenile Myelomonocytic Leukemia-Like Neoplasm NCIT:C7289 Juvenile Ovarian Granulosa Cell Tumor +NCIT:C202205 Juvenile Trabecular Ossifying Fibroma NCIT:C6580 Juxta-Articular Myxoma NCIT:C22969 Juxtacortical Chondroma of the Mouse Skeletal System NCIT:C22970 Juxtacortical Chondrosarcoma of the Mouse Skeletal System @@ -3948,7 +4070,7 @@ NCIT:C133494 Large B-Cell Lymphoma with IRF4 Rearrangement NCIT:C21926 Large Cell Anaplastic Lymphoma of the Mouse Hematologic System NCIT:C54337 Laryngeal Acantholytic Squamous Cell Carcinoma NCIT:C54338 Laryngeal Adenosquamous Carcinoma -NCIT:C54334 Laryngeal Basaloid Carcinoma +NCIT:C54334 Laryngeal Basaloid Squamous Cell Carcinoma NCIT:C90527 Laryngeal Cancer by AJCC v6 Stage NCIT:C91256 Laryngeal Cancer by AJCC v7 Stage NCIT:C133156 Laryngeal Cancer by AJCC v8 Stage @@ -3969,7 +4091,7 @@ NCIT:C6409 Laryngeal Paraganglioma NCIT:C173412 Laryngeal Pleomorphic Adenoma NCIT:C173397 Laryngeal Soft Tissue Neoplasm NCIT:C173408 Laryngeal Soft Tissue Sarcoma -NCIT:C54336 Laryngeal Squamous Cell Carcinoma, Spindle Cell Variant +NCIT:C54336 Laryngeal Spindle Cell Squamous Carcinoma NCIT:C54339 Laryngeal Undifferentiated Carcinoma NCIT:C4791 Left Atrial Myxoma NCIT:C22147 Leiomyoma of the Mouse Intestinal Tract @@ -3985,6 +4107,7 @@ NCIT:C23106 Leiomyosarcoma of the Mouse Nose and Paranasal Sinuses NCIT:C23055 Leiomyosarcoma of the Mouse Oral Cavity NCIT:C21749 Leiomyosarcoma of the Mouse Prostate Gland NCIT:C21844 Leiomyosarcoma of the Mouse Skin +NCIT:C204482 Lentiginous Melanocytic Nevus NCIT:C43372 Lentigo Maligna NCIT:C123160 Lepidic Adenocarcinoma NCIT:C134530 Leporine Experimental Organism Diagnosis @@ -4110,7 +4233,9 @@ NCIT:C27903 Localized Peripheral Primitive Neuroectodermal Tumor NCIT:C27353 Localized Peripheral Primitive Neuroectodermal Tumor of Bone NCIT:C45666 Localized Pleural Malignant Mesothelioma NCIT:C27294 Localized Primitive Neuroectodermal Tumor +NCIT:C201849 Localized Prostate Adenocarcinoma NCIT:C176517 Localized Prostate Carcinoma +NCIT:C205361 Localized Renal Cell Carcinoma NCIT:C8167 Localized Renal Pelvis and Ureter Urothelial Carcinoma NCIT:C9064 Localized Resectable Adult Hepatocellular Carcinoma NCIT:C7877 Localized Resectable Adult Liver Carcinoma @@ -4129,15 +4254,18 @@ NCIT:C164076 Locally Advanced Alveolar Soft Part Sarcoma NCIT:C171327 Locally Advanced Ampulla of Vater Carcinoma NCIT:C168977 Locally Advanced Anal Carcinoma NCIT:C146856 Locally Advanced Angiosarcoma +NCIT:C203618 Locally Advanced Appendix Adenocarcinoma NCIT:C156770 Locally Advanced Basal Cell Carcinoma NCIT:C151971 Locally Advanced Bile Duct Carcinoma NCIT:C168981 Locally Advanced Biliary Tract Carcinoma +NCIT:C203407 Locally Advanced Bladder Adenocarcinoma NCIT:C167071 Locally Advanced Bladder Carcinoma +NCIT:C203415 Locally Advanced Bladder Small Cell Neuroendocrine Carcinoma +NCIT:C203410 Locally Advanced Bladder Squamous Cell Carcinoma NCIT:C162618 Locally Advanced Bladder Urothelial Carcinoma NCIT:C153070 Locally Advanced Bone Sarcoma NCIT:C165699 Locally Advanced Breast Adenocarcinoma NCIT:C160920 Locally Advanced Breast Carcinoma -NCIT:C187328 Locally Advanced Carcinoid Tumor NCIT:C148130 Locally Advanced Carcinoma NCIT:C156297 Locally Advanced Cervical Adenocarcinoma NCIT:C156295 Locally Advanced Cervical Carcinoma @@ -4159,6 +4287,7 @@ NCIT:C200083 Locally Advanced Differentiated Thyroid Gland Carcinoma NCIT:C153358 Locally Advanced Digestive System Carcinoma NCIT:C155934 Locally Advanced Digestive System Neuroendocrine Carcinoma NCIT:C178271 Locally Advanced Digestive System Neuroendocrine Neoplasm +NCIT:C204038 Locally Advanced Digestive System Neuroendocrine Tumor NCIT:C187332 Locally Advanced Digestive System Neuroendocrine Tumor G1 NCIT:C187341 Locally Advanced Digestive System Neuroendocrine Tumor G2 NCIT:C192773 Locally Advanced Digestive System Neuroendocrine Tumor G3 @@ -4178,6 +4307,7 @@ NCIT:C187244 Locally Advanced Extrahepatic Bile Duct Carcinoma NCIT:C191991 Locally Advanced Extrapulmonary Large Cell Neuroendocrine Carcinoma NCIT:C191983 Locally Advanced Extrapulmonary Neuroendocrine Carcinoma NCIT:C191992 Locally Advanced Extrapulmonary Small Cell Neuroendocrine Carcinoma +NCIT:C201951 Locally Advanced Extraskeletal Myxoid Chondrosarcoma NCIT:C167202 Locally Advanced Fallopian Tube Carcinoma NCIT:C171317 Locally Advanced Fibrosarcoma NCIT:C170462 Locally Advanced Gallbladder Carcinoma @@ -4188,6 +4318,7 @@ NCIT:C150739 Locally Advanced Gastrointestinal Stromal Tumor NCIT:C167069 Locally Advanced Genitourinary System Carcinoma NCIT:C170980 Locally Advanced Glioblastoma NCIT:C180876 Locally Advanced Glioma +NCIT:C204437 Locally Advanced HER2-Low Breast Carcinoma NCIT:C178348 Locally Advanced HER2-Negative Breast Carcinoma NCIT:C181793 Locally Advanced HER2-Positive Breast Carcinoma NCIT:C153213 Locally Advanced Head and Neck Carcinoma @@ -4199,6 +4330,7 @@ NCIT:C171280 Locally Advanced Hypopharyngeal Carcinoma NCIT:C165701 Locally Advanced Hypopharyngeal Squamous Cell Carcinoma NCIT:C173814 Locally Advanced Intrahepatic Cholangiocarcinoma NCIT:C172618 Locally Advanced Kidney Carcinoma +NCIT:C203412 Locally Advanced Kidney Medullary Carcinoma NCIT:C158910 Locally Advanced Large Cell Neuroendocrine Carcinoma NCIT:C165560 Locally Advanced Laryngeal Carcinoma NCIT:C165473 Locally Advanced Laryngeal Squamous Cell Carcinoma @@ -4235,12 +4367,14 @@ NCIT:C167330 Locally Advanced Midgut Neuroendocrine Tumor NCIT:C168671 Locally Advanced Myxofibrosarcoma NCIT:C185350 Locally Advanced Nasal Cavity Squamous Cell Carcinoma NCIT:C167352 Locally Advanced Nasopharyngeal Squamous Cell Carcinoma +NCIT:C203526 Locally Advanced Neuroblastoma NCIT:C158909 Locally Advanced Neuroendocrine Carcinoma NCIT:C167332 Locally Advanced Neuroendocrine Neoplasm NCIT:C167333 Locally Advanced Neuroendocrine Tumor NCIT:C171297 Locally Advanced Non-Cutaneous Melanoma NCIT:C190773 Locally Advanced Non-Muscle Invasive Bladder Carcinoma NCIT:C171296 Locally Advanced Ocular Melanoma +NCIT:C203513 Locally Advanced Olfactory Neuroblastoma NCIT:C171281 Locally Advanced Oral Cavity Carcinoma NCIT:C165472 Locally Advanced Oral Cavity Squamous Cell Carcinoma NCIT:C170782 Locally Advanced Oropharyngeal Carcinoma @@ -4263,8 +4397,10 @@ NCIT:C165563 Locally Advanced Paranasal Sinus Carcinoma NCIT:C185351 Locally Advanced Paranasal Sinus Squamous Cell Carcinoma NCIT:C163958 Locally Advanced Parathyroid Gland Carcinoma NCIT:C170789 Locally Advanced Penile Carcinoma +NCIT:C203413 Locally Advanced Penile Squamous Cell Carcinoma NCIT:C165561 Locally Advanced Pharyngeal Carcinoma NCIT:C163956 Locally Advanced Pituitary Neuroendocrine Tumor +NCIT:C204868 Locally Advanced Platinum-Refractory Ovarian Carcinoma NCIT:C189978 Locally Advanced Platinum-Resistant Ovarian Carcinoma NCIT:C175936 Locally Advanced Pleural Malignant Mesothelioma NCIT:C180874 Locally Advanced Primary Malignant Brain Neoplasm @@ -4277,6 +4413,7 @@ NCIT:C174122 Locally Advanced Rectal Adenocarcinoma NCIT:C170778 Locally Advanced Rectal Carcinoma NCIT:C170781 Locally Advanced Rectal Squamous Cell Carcinoma NCIT:C168995 Locally Advanced Renal Cell Carcinoma +NCIT:C172222 Locally Advanced Renal Cell Carcinoma, Not Otherwise Specified NCIT:C172277 Locally Advanced Renal Pelvis Carcinoma NCIT:C162617 Locally Advanced Renal Pelvis Urothelial Carcinoma NCIT:C164159 Locally Advanced Renal Pelvis and Ureter Urothelial Carcinoma @@ -4284,6 +4421,7 @@ NCIT:C166415 Locally Advanced Rhabdomyosarcoma NCIT:C158464 Locally Advanced Salivary Gland Carcinoma NCIT:C153071 Locally Advanced Sarcoma NCIT:C172219 Locally Advanced Sarcomatoid Renal Cell Carcinoma +NCIT:C203515 Locally Advanced Sinonasal Carcinoma NCIT:C154322 Locally Advanced Sinonasal Squamous Cell Carcinoma NCIT:C153182 Locally Advanced Skin Squamous Cell Carcinoma NCIT:C158915 Locally Advanced Small Cell Neuroendocrine Carcinoma @@ -4301,7 +4439,6 @@ NCIT:C168543 Locally Advanced Thyroid Gland Medullary Carcinoma NCIT:C175507 Locally Advanced Thyroid Gland Oncocytic Carcinoma NCIT:C175493 Locally Advanced Transitional Cell Carcinoma NCIT:C175237 Locally Advanced Triple-Negative Breast Carcinoma -NCIT:C172222 Locally Advanced Unclassified Renal Cell Carcinoma NCIT:C160919 Locally Advanced Undifferentiated Pleomorphic Sarcoma NCIT:C156789 Locally Advanced Unresectable Basal Cell Carcinoma NCIT:C153475 Locally Advanced Unresectable Bone Sarcoma @@ -4312,6 +4449,7 @@ NCIT:C156300 Locally Advanced Unresectable Cervical Carcinoma NCIT:C187412 Locally Advanced Unresectable Cholangiocarcinoma NCIT:C162271 Locally Advanced Unresectable Colon Adenocarcinoma NCIT:C162270 Locally Advanced Unresectable Colorectal Adenocarcinoma +NCIT:C202500 Locally Advanced Unresectable Digestive System Adenocarcinoma NCIT:C158090 Locally Advanced Unresectable Digestive System Neuroendocrine Neoplasm NCIT:C187406 Locally Advanced Unresectable Endometrial Carcinoma NCIT:C162113 Locally Advanced Unresectable Esophageal Adenocarcinoma @@ -4327,6 +4465,7 @@ NCIT:C153278 Locally Advanced Unresectable Malignant Neoplasm NCIT:C164247 Locally Advanced Unresectable Malignant PEComa NCIT:C187393 Locally Advanced Unresectable Ovarian High Grade Serous Adenocarcinoma NCIT:C155743 Locally Advanced Unresectable Pancreatic Adenocarcinoma +NCIT:C205226 Locally Advanced Unresectable Pancreatic Ductal Adenocarcinoma NCIT:C176728 Locally Advanced Unresectable Primary Central Chondrosarcoma NCIT:C187389 Locally Advanced Unresectable Primary Peritoneal Carcinoma NCIT:C156289 Locally Advanced Unresectable Prostate Adenocarcinoma @@ -4338,6 +4477,7 @@ NCIT:C153476 Locally Advanced Unresectable Soft Tissue Sarcoma NCIT:C187402 Locally Advanced Unresectable Triple-Negative Breast Carcinoma NCIT:C190138 Locally Advanced Unresectable Uveal Melanoma NCIT:C162616 Locally Advanced Ureter Urothelial Carcinoma +NCIT:C7639 Locally Advanced Urethral Carcinoma NCIT:C162619 Locally Advanced Urethral Urothelial Carcinoma NCIT:C157636 Locally Advanced Urothelial Carcinoma NCIT:C188208 Locally Advanced Uterine Corpus Leiomyosarcoma @@ -4371,14 +4511,13 @@ NCIT:C42598 Low Grade Appendix Mucinous Neoplasm NCIT:C6816 Low Grade B-Cell Non-Hodgkin's Lymphoma NCIT:C172804 Low Grade Biliary Intraepithelial Neoplasia NCIT:C40362 Low Grade Breast Adenosquamous Carcinoma -NCIT:C5168 Low Grade Breast Mucoepidermoid Carcinoma NCIT:C126480 Low Grade Broad Ligament Serous Adenocarcinoma NCIT:C7674 Low Grade Cervical Glandular Intraepithelial Neoplasia NCIT:C4630 Low Grade Cervical Intraepithelial Neoplasia NCIT:C40196 Low Grade Cervical Squamous Intraepithelial Neoplasia +NCIT:C204979 Low Grade Conjunctival Melanocytic Intraepithelial Lesion NCIT:C6097 Low Grade Conjunctival Squamous Intraepithelial Neoplasia NCIT:C6094 Low Grade Corneal Squamous Intraepithelial Neoplasia -NCIT:C180510 Low Grade Endometrial Endometrioid Adenocarcinoma NCIT:C199146 Low Grade Endometrioid Adenocarcinoma NCIT:C4263 Low Grade Endometrioid Stromal Sarcoma NCIT:C27428 Low Grade Esophageal Glandular Intraepithelial Neoplasia @@ -4397,10 +4536,10 @@ NCIT:C36048 Low Grade Malignant Neoplasm NCIT:C9026 Low Grade Malignant Peripheral Nerve Sheath Tumor NCIT:C21668 Low Grade Mouse MIN NCIT:C21729 Low Grade Mouse Prostatic Intraepithelial Neoplasia +NCIT:C203946 Low Grade Mucinous Carcinoma Peritonei NCIT:C23138 Low Grade Mucoepidermoid Tumor of the Mouse Salivary Glands NCIT:C49024 Low Grade Myofibroblastic Sarcoma NCIT:C197815 Low Grade Osteosarcoma -NCIT:C199159 Low Grade Ovarian Endometrioid Adenocarcinoma NCIT:C172803 Low Grade Pancreatic Intraepithelial Neoplasia NCIT:C180670 Low Grade Papillary Schneiderian Carcinoma NCIT:C6851 Low Grade Paranasal Sinus Sarcoma @@ -4408,8 +4547,6 @@ NCIT:C22141 Low Grade Pedunculated Tubular Dysplasia of the Mouse Intestinal Tra NCIT:C22144 Low Grade Pedunculated Tubulovillous Dysplasia of the Mouse Intestinal Tract NCIT:C7666 Low Grade Penile Intraepithelial Neoplasia NCIT:C5542 Low Grade Prostatic Intraepithelial Neoplasia -NCIT:C8012 Low Grade Salivary Gland Carcinoma -NCIT:C8015 Low Grade Salivary Gland Mucoepidermoid Carcinoma NCIT:C9417 Low Grade Sarcoma NCIT:C22121 Low Grade Sessile Tubular Dysplasia of the Mouse Intestinal Tract NCIT:C22127 Low Grade Sessile Tubulovillous Dysplasia of the Mouse Intestinal Tract @@ -4423,6 +4560,7 @@ NCIT:C27239 Low Risk Gastric Gastrointestinal Stromal Tumor NCIT:C27242 Low Risk Gastrointestinal Stromal Tumor NCIT:C27244 Low Risk Small Intestinal Gastrointestinal Stromal Tumor NCIT:C187273 Low Risk Thyroid Gland Neoplasm +NCIT:C204843 Low-CSD Melanoma, Superficial Spreading Melanoma Subtype NCIT:C199213 Low-Hypodiploid B Acute Lymphoblastic Leukemia NCIT:C170776 Lower Alveolar Ridge Squamous Cell Carcinoma NCIT:C8393 Lower Gingival Carcinoma @@ -4485,16 +4623,11 @@ NCIT:C133091 Lung Adenofibroma NCIT:C136492 Lung Adenosquamous Carcinoma by AJCC v7 Stage NCIT:C173809 Lung Alveolar Soft Part Sarcoma NCIT:C188082 Lung Anaplastic Large Cell Lymphoma -NCIT:C45551 Lung Atypical Carcinoid Tumor NCIT:C45507 Lung Basaloid Squamous Cell Carcinoma NCIT:C45632 Lung Biphasic Synovial Sarcoma NCIT:C90519 Lung Cancer by AJCC v6 Stage NCIT:C91232 Lung Cancer by AJCC v7 Stage NCIT:C136467 Lung Cancer by AJCC v8 Stage -NCIT:C36305 Lung Carcinoma Metastatic in the Bone -NCIT:C36304 Lung Carcinoma Metastatic in the Brain -NCIT:C133503 Lung Carcinoma Metastatic in the Central Nervous System -NCIT:C36306 Lung Carcinoma Metastatic in the Liver NCIT:C45543 Lung Carcinosarcoma NCIT:C45629 Lung Chondroma NCIT:C45516 Lung Clear Cell Adenocarcinoma @@ -4520,6 +4653,8 @@ NCIT:C142828 Lung Myoepithelial Tumor NCIT:C142829 Lung Myoepithelioma NCIT:C5657 Lung Myolipoma NCIT:C45569 Lung Neuroendocrine Carcinoma +NCIT:C45550 Lung Neuroendocrine Tumor G1 +NCIT:C45551 Lung Neuroendocrine Tumor G2 NCIT:C136714 Lung Non-Keratinizing Squamous Cell Carcinoma NCIT:C136716 Lung Non-Mucinous Adenocarcinoma In Situ NCIT:C136491 Lung Non-Small Cell Cancer by AJCC v7 Stage @@ -4550,7 +4685,6 @@ NCIT:C45504 Lung Squamous Cell Carcinoma, Small Cell Variant NCIT:C45573 Lung Squamous Papilloma NCIT:C45631 Lung Synovial Sarcoma NCIT:C45637 Lung Teratoma -NCIT:C45550 Lung Typical Carcinoid Tumor NCIT:C27500 Lymphadenopathic Kaposi Sarcoma NCIT:C45485 Lymphangioma Circumscriptum NCIT:C8373 Lymphangiomatosis @@ -4589,6 +4723,7 @@ NCIT:C21881 MAIDS NCIT:C148394 MCD Diffuse Large B-Cell Lymphoma NCIT:C154335 MGMT-Methylated Glioblastoma NCIT:C132902 MGMT-Unmethylated Glioblastoma +NCIT:C204739 MITF Pathway-Activated Melanocytic Tumor NCIT:C198069 MS Childhood Neuroblastoma by Toronto Guidelines v2 NCIT:C178235 MYOD1-Mutant Spindle Cell/Sclerosing Rhabdomyosarcoma NCIT:C182077 Macaca mulatta Hepatocellular Carcinoma @@ -4639,6 +4774,8 @@ NCIT:C64046 Malignant Glioma of the Rat Spinal Cord NCIT:C4205 Malignant Granulosa Cell Tumor NCIT:C63986 Malignant Granulosa Cell Tumor of the Rat Ovary NCIT:C43310 Malignant Hair Follicle Neoplasm +NCIT:C202983 Malignant Head and Neck Germ Cell Tumor +NCIT:C202625 Malignant Head and Neck Soft Tissue Neoplasm NCIT:C9393 Malignant Hemangiopericytoma NCI Grade 2 NCIT:C9394 Malignant Hemangiopericytoma NCI Grade 3 NCIT:C8609 Malignant Hepatobiliary Neoplasm @@ -4649,7 +4786,6 @@ NCIT:C5377 Malignant Inferior Vena Cava Neoplasm NCIT:C174026 Malignant Inner Ear Neoplasm NCIT:C5403 Malignant Intracranial Germ Cell Tumor NCIT:C5114 Malignant Intracranial Neoplasm -NCIT:C7045 Malignant Intracranial Neoplasm by Morphology NCIT:C64047 Malignant Intraocular Schwannoma of the Rat Eyeball NCIT:C170919 Malignant Jejunal Neoplasm NCIT:C120456 Malignant Kidney Neoplasm Except Pelvis @@ -4672,11 +4808,11 @@ NCIT:C27258 Malignant Lymphoma, Non-Cleaved Cell Type NCIT:C27266 Malignant Lymphoma, Non-Cleaved, Diffuse NCIT:C22059 Malignant Lymphomas of the Mouse Nervous System NCIT:C8991 Malignant Mastocytosis +NCIT:C202262 Malignant Maxillofacial Neoplasm NCIT:C146848 Malignant Mediastinal Germ Cell Tumor Stage Grouping of the Pediatric Study Group NCIT:C45733 Malignant Mediastinal Germ Cell Tumor with Associated Hematologic Malignancy NCIT:C6439 Malignant Mediastinal Nongerminomatous Germ Cell Tumor NCIT:C63917 Malignant Medullary Tumor of the Rat Adrenal Gland -NCIT:C66753 Malignant Melanoma in Precancerous Melanosis NCIT:C22054 Malignant Melanoma of the Mouse Nervous System NCIT:C64048 Malignant Melanoma of the Rat Cerebral Meninx NCIT:C64123 Malignant Melanoma of the Rat Skin @@ -4725,13 +4861,13 @@ NCIT:C24102 Malignant Mouse Uterine Corpus Mixed Neoplasm NCIT:C24087 Malignant Mouse Uterine Corpus Neoplasm NCIT:C24066 Malignant Mouse Uterine Neoplasms NCIT:C166357 Malignant Musculoskeletal Neoplasm +NCIT:C202985 Malignant Nasopharyngeal Germ Cell Tumor NCIT:C36041 Malignant Neoplasm by Grade NCIT:C139565 Malignant Neoplasm of Lung - Multiple Primary Sites NCIT:C35427 Malignant Neoplasm of Multiple Primary Sites NCIT:C3535 Malignant Neoplasm of the Lower Third of the Esophagus NCIT:C3534 Malignant Neoplasm of the Middle Third of the Esophagus NCIT:C3533 Malignant Neoplasm of the Upper Third of the Esophagus -NCIT:C8512 Malignant Neoplasm with Regional Lymph Node Involvement NCIT:C65153 Malignant Neoplasm, Uncertain Whether Primary or Metastatic NCIT:C38772 Malignant Neoplasms of Mouse Liver NCIT:C22151 Malignant Neoplasms of the Mouse Intestinal Tract @@ -4791,6 +4927,7 @@ NCIT:C161644 Malignant Seminal Vesicle Neoplasm NCIT:C63989 Malignant Sertoli Cell Tumor of the Rat Ovary NCIT:C64058 Malignant Sertoli Cell Tumor of the Rat Testis NCIT:C67561 Malignant Sex Cord-Stromal Tumor +NCIT:C202984 Malignant Sinonasal Germ Cell Tumor NCIT:C173097 Malignant Sinonasal Neoplasm NCIT:C173176 Malignant Sinonasal Soft Tissue Neoplasm NCIT:C4573 Malignant Skin Appendage Neoplasm @@ -4862,9 +4999,11 @@ NCIT:C173900 Maxillofacial Desmoplastic Fibroma NCIT:C173843 Maxillofacial Mesenchymal Chondrosarcoma NCIT:C173845 Maxillofacial Neoplasm NCIT:C173899 Maxillofacial Osteoblastoma +NCIT:C202260 Maxillofacial Osteochondroma NCIT:C173898 Maxillofacial Osteoid Osteoma NCIT:C173894 Maxillofacial Osteoma NCIT:C173844 Maxillofacial Osteosarcoma +NCIT:C202264 Maxillofacial Rhabdomyosarcoma with TFCP2 Rearrangement NCIT:C173841 Maxillofacial Sarcoma NCIT:C6424 Meckel Diverticulum Neuroendocrine Tumor G1 NCIT:C134571 Medaka Hepatoma @@ -4920,12 +5059,13 @@ NCIT:C23061 Melanocytic Neoplasms of the Mouse Oral Cavity NCIT:C21782 Melanocytic Proliferative Disorders of Mouse NCIT:C9498 Melanocytoma NCIT:C22053 Melanocytoma of the Mouse Nervous System -NCIT:C4240 Melanoma Arising from Blue Nevus +NCIT:C4240 Melanoma Arising in Blue Nevus +NCIT:C48613 Melanoma Arising in Congenital Melanocytic Nevus NCIT:C4235 Melanoma Arising in Giant Congenital Nevus -NCIT:C179206 Melanoma Metastatic in the Brain -NCIT:C133504 Melanoma Metastatic in the Central Nervous System -NCIT:C48613 Melanoma in Congenital Melanocytic Nevus +NCIT:C204864 Melanoma in Chronically Sun-Exposed Skin +NCIT:C204840 Melanoma in Intermittently Sun-Exposed Skin NCIT:C4232 Melanoma in Junctional Nevus +NCIT:C66753 Melanoma in Precancerous Melanosis NCIT:C154473 Melanoma of Unknown Primary NCIT:C23098 Melanoma of the Mouse Nose and Paranasal Sinuses NCIT:C23062 Melanoma of the Mouse Oral Cavity @@ -4943,10 +5083,8 @@ NCIT:C64061 Meningeal Sarcoma of the Rat Spinal Meninx NCIT:C7051 Meningioma by Site NCIT:C3707 Meningiomatosis NCIT:C6971 Meningothelial Cell Neoplasm -NCIT:C136869 Merkel Cell Carcinoma by AJCC v7 Stage -NCIT:C136871 Merkel Cell Carcinoma by AJCC v8 Clinical Stage -NCIT:C136880 Merkel Cell Carcinoma by AJCC v8 Pathologic Stage -NCIT:C136870 Merkel Cell Carcinoma by AJCC v8 Stage +NCIT:C204385 Merkel Cell Polyoma Virus-Negative Merkel Cell Carcinoma +NCIT:C204383 Merkel Cell Polyoma Virus-Positive Merkel Cell Carcinoma NCIT:C53493 Mesenchymal Chondrosarcoma of Bone NCIT:C22974 Mesenchymal Chondrosarcoma of the Mouse Skeletal System NCIT:C22029 Mesenchymal Non-meningothelial Tumours of the Mouse Nervous System @@ -4993,6 +5131,7 @@ NCIT:C156769 Metastatic Basal Cell Carcinoma NCIT:C36264 Metastatic Benign Neoplasm NCIT:C142869 Metastatic Bile Duct Carcinoma NCIT:C162751 Metastatic Biliary Tract Carcinoma +NCIT:C203406 Metastatic Bladder Adenocarcinoma NCIT:C156062 Metastatic Bladder Carcinoma NCIT:C157768 Metastatic Bladder Clear Cell (Glycogen-Rich) Urothelial Carcinoma NCIT:C157769 Metastatic Bladder Giant Cell Urothelial Carcinoma @@ -5010,6 +5149,12 @@ NCIT:C6621 Metastatic Bone Ewing Sarcoma NCIT:C153073 Metastatic Bone Sarcoma NCIT:C165698 Metastatic Breast Adenocarcinoma NCIT:C153238 Metastatic Breast Carcinoma +NCIT:C36303 Metastatic Breast Carcinoma in the Bone +NCIT:C36301 Metastatic Breast Carcinoma in the Brain +NCIT:C133501 Metastatic Breast Carcinoma in the Central Nervous System +NCIT:C36302 Metastatic Breast Carcinoma in the Liver +NCIT:C36300 Metastatic Breast Carcinoma in the Lung +NCIT:C153227 Metastatic Breast Carcinoma in the Lymph Nodes NCIT:C28311 Metastatic Breast Carcinoma in the Skin NCIT:C76326 Metastatic Breast Ductal Carcinoma NCIT:C181787 Metastatic Breast Inflammatory Carcinoma @@ -5018,7 +5163,6 @@ NCIT:C156493 Metastatic Breast Neuroendocrine Neoplasm NCIT:C5171 Metastatic Breast Neuroendocrine Tumor G1 NCIT:C5176 Metastatic Breast Signet Ring Cell Carcinoma NCIT:C5178 Metastatic Breast Squamous Cell Carcinoma -NCIT:C6431 Metastatic Carcinoid Tumor NCIT:C27381 Metastatic Carcinoma in the Adrenal Cortex NCIT:C96767 Metastatic Carcinoma in the Liver NCIT:C27408 Metastatic Carcinoma in the Lung @@ -5042,7 +5186,6 @@ NCIT:C198487 Metastatic Childhood Ependymoma by Toronto Guidelines v2 NCIT:C198189 Metastatic Childhood Hepatoblastoma by Toronto Guidelines v2, Tier 1 NCIT:C198192 Metastatic Childhood Hepatoblastoma by Toronto Guidelines v2, Tier 2 NCIT:C198173 Metastatic Childhood Malignant Bone Neoplasm by Toronto Guidelines v2 -NCIT:C187212 Metastatic Childhood Malignant Brain Neoplasm NCIT:C198088 Metastatic Childhood Malignant Kidney Neoplasm Excluding Renal Cell Carcinoma by Toronto Guidelines v2, Children's Oncology Group (COG) Protocol NCIT:C198079 Metastatic Childhood Malignant Kidney Neoplasm Excluding Renal Cell Carcinoma by Toronto Guidelines v2, International Society of Pediatric Oncology (SIOP) Protocol NCIT:C187211 Metastatic Childhood Malignant Neoplasm in the Brain @@ -5050,6 +5193,7 @@ NCIT:C198477 Metastatic Childhood Medulloblastoma by Toronto Guidelines v2 NCIT:C198067 Metastatic Childhood Neuroblastoma by Toronto Guidelines v2 NCIT:C198163 Metastatic Childhood Non-Rhabdomyosarcoma Soft Tissue Sarcoma by Toronto Guidelines v2 NCIT:C198441 Metastatic Childhood Ovarian Germ Cell Tumor by Toronto Guidelines v2 +NCIT:C187212 Metastatic Childhood Primary Malignant Brain Neoplasm NCIT:C198178 Metastatic Childhood Retinoblastoma by Toronto Guidelines v2 NCIT:C198154 Metastatic Childhood Rhabdomyosarcoma by Toronto Guidelines v2 NCIT:C8066 Metastatic Childhood Soft Tissue Sarcoma @@ -5077,6 +5221,7 @@ NCIT:C133839 Metastatic Digestive System Carcinoma NCIT:C163967 Metastatic Digestive System Mixed Adenoneuroendocrine Carcinoma NCIT:C155936 Metastatic Digestive System Neuroendocrine Carcinoma NCIT:C156492 Metastatic Digestive System Neuroendocrine Neoplasm +NCIT:C204037 Metastatic Digestive System Neuroendocrine Tumor NCIT:C115245 Metastatic Digestive System Neuroendocrine Tumor G1 NCIT:C179415 Metastatic Digestive System Neuroendocrine Tumor G2 NCIT:C192769 Metastatic Digestive System Neuroendocrine Tumor G3 @@ -5160,11 +5305,15 @@ NCIT:C178559 Metastatic Low Grade Astrocytoma NCIT:C178558 Metastatic Low Grade Glioma NCIT:C155908 Metastatic Lung Adenocarcinoma NCIT:C156093 Metastatic Lung Adenosquamous Carcinoma -NCIT:C177243 Metastatic Lung Carcinoid Tumor NCIT:C153202 Metastatic Lung Carcinoma +NCIT:C36305 Metastatic Lung Carcinoma in the Bone +NCIT:C36304 Metastatic Lung Carcinoma in the Brain +NCIT:C133503 Metastatic Lung Carcinoma in the Central Nervous System +NCIT:C36306 Metastatic Lung Carcinoma in the Liver NCIT:C177799 Metastatic Lung Large Cell Neuroendocrine Carcinoma NCIT:C192797 Metastatic Lung Neuroendocrine Carcinoma NCIT:C157602 Metastatic Lung Neuroendocrine Neoplasm +NCIT:C177243 Metastatic Lung Neuroendocrine Tumor NCIT:C156094 Metastatic Lung Non-Small Cell Carcinoma NCIT:C157364 Metastatic Lung Non-Small Cell Squamous Carcinoma NCIT:C128798 Metastatic Lung Non-Squamous Non-Small Cell Carcinoma @@ -5277,6 +5426,11 @@ NCIT:C127155 Metastatic Malignant Solid Neoplasm NCIT:C25771 Metastatic Malignant Testicular Germ Cell Tumor NCIT:C176862 Metastatic Malignant Thoracic Neoplasm NCIT:C177725 Metastatic Medulloblastoma +NCIT:C179206 Metastatic Melanoma in the Brain +NCIT:C133504 Metastatic Melanoma in the Central Nervous System +NCIT:C205131 Metastatic Melanoma in the Lymph Nodes +NCIT:C205130 Metastatic Melanoma in the Skin +NCIT:C205132 Metastatic Melanoma in the Viscera NCIT:C5274 Metastatic Meningioma NCIT:C162572 Metastatic Merkel Cell Carcinoma NCIT:C185381 Metastatic Mesonephric Adenocarcinoma @@ -5296,7 +5450,7 @@ NCIT:C160297 Metastatic NUT Carcinoma NCIT:C167236 Metastatic Nasal Cavity Squamous Cell Carcinoma NCIT:C156079 Metastatic Nasopharyngeal Carcinoma NCIT:C156077 Metastatic Nasopharyngeal Keratinizing Squamous Cell Carcinoma -NCIT:C177153 Metastatic Nasopharyngeal Nonkeratinizing Carcinoma +NCIT:C177153 Metastatic Nasopharyngeal Non-Keratinizing Carcinoma NCIT:C150209 Metastatic Nasopharyngeal Squamous Cell Carcinoma NCIT:C156078 Metastatic Nasopharyngeal Undifferentiated Carcinoma NCIT:C24162 Metastatic Neoplasm to the Mouse Gallbladder @@ -5311,6 +5465,7 @@ NCIT:C140329 Metastatic Non-Functioning Neuroendocrine Tumor NCIT:C190772 Metastatic Non-Muscle Invasive Bladder Carcinoma NCIT:C165537 Metastatic Non-Small Cell Carcinoma NCIT:C171295 Metastatic Ocular Melanoma +NCIT:C203511 Metastatic Olfactory Neuroblastoma NCIT:C156089 Metastatic Oral Cavity Adenoid Cystic Carcinoma NCIT:C156087 Metastatic Oral Cavity Carcinoma NCIT:C156090 Metastatic Oral Cavity Mucoepidermoid Carcinoma @@ -5356,8 +5511,11 @@ NCIT:C179462 Metastatic Peritoneal Malignant Mesothelioma NCIT:C156080 Metastatic Pharyngeal Carcinoma NCIT:C173685 Metastatic Pharyngeal Squamous Cell Carcinoma NCIT:C191697 Metastatic Plasmacytoid Urothelial Carcinoma +NCIT:C204865 Metastatic Platinum-Refractory Ovarian Carcinoma +NCIT:C203313 Metastatic Platinum-Resistant Fallopian Tube Carcinoma NCIT:C170957 Metastatic Platinum-Resistant Malignant Germ Cell Tumor NCIT:C179460 Metastatic Platinum-Resistant Ovarian Carcinoma +NCIT:C203314 Metastatic Platinum-Resistant Primary Peritoneal Carcinoma NCIT:C182025 Metastatic Pleomorphic Liposarcoma NCIT:C168545 Metastatic Pleural Malignant Mesothelioma NCIT:C174046 Metastatic Poorly Differentiated Thyroid Gland Carcinoma @@ -5378,6 +5536,7 @@ NCIT:C160820 Metastatic Rectal Adenocarcinoma NCIT:C156098 Metastatic Rectal Carcinoma NCIT:C170779 Metastatic Rectal Squamous Cell Carcinoma NCIT:C150595 Metastatic Renal Cell Carcinoma +NCIT:C171583 Metastatic Renal Cell Carcinoma, Not Otherwise Specified NCIT:C163965 Metastatic Renal Pelvis Carcinoma NCIT:C150514 Metastatic Renal Pelvis Urothelial Carcinoma NCIT:C8064 Metastatic Renal Pelvis and Ureter Urothelial Carcinoma @@ -5388,6 +5547,7 @@ NCIT:C199662 Metastatic Salivary Duct Carcinoma NCIT:C199665 Metastatic Salivary Gland Adenocarcinoma NCIT:C199664 Metastatic Salivary Gland Adenocarcinoma, Not Otherwise Specified NCIT:C158463 Metastatic Salivary Gland Carcinoma +NCIT:C203380 Metastatic Salivary Gland Secretory Carcinoma NCIT:C172649 Metastatic Salivary Gland Squamous Cell Carcinoma NCIT:C152076 Metastatic Sarcoma NCIT:C179657 Metastatic Sarcoma in the Peritoneum @@ -5421,7 +5581,6 @@ NCIT:C129828 Metastatic Transitional Cell Carcinoma NCIT:C153348 Metastatic Triple-Negative Breast Carcinoma NCIT:C185954 Metastatic Triple-Negative Breast Inflammatory Carcinoma NCIT:C22077 Metastatic Tumours of the Mouse Nervous System -NCIT:C171583 Metastatic Unclassified Renal Cell Carcinoma NCIT:C4926 Metastatic Undifferentiated Pleomorphic Sarcoma NCIT:C156788 Metastatic Unresectable Basal Cell Carcinoma NCIT:C153315 Metastatic Unresectable Carcinoma @@ -5470,8 +5629,11 @@ NCIT:C180335 Microsatellite Stable Endometrial Carcinoma NCIT:C180332 Microsatellite Stable Ovarian Carcinoma NCIT:C177776 Microsatellite Stable Rectal Carcinoma NCIT:C45708 Microscopic Thymoma -NCIT:C91741 Middle Ear Carcinoma In Situ NCIT:C188115 Middle Ear Embryonal Rhabdomyosarcoma +NCIT:C202584 Middle Ear Exophytic Sinonasal-Type Papilloma +NCIT:C202583 Middle Ear Inverted Sinonasal-Type Papilloma +NCIT:C202585 Middle Ear Oncocytic Sinonasal-Type Papilloma +NCIT:C202582 Middle Ear Papilloma NCIT:C6085 Middle Ear Paraganglioma NCIT:C167327 Midgut Neuroendocrine Tumor NCIT:C6422 Midgut Neuroendocrine Tumor G1 @@ -5486,6 +5648,7 @@ NCIT:C5976 Minor Salivary Gland Carcinoma ex Pleomorphic Adenoma NCIT:C180880 Minor Salivary Gland Intraductal Papillary Neoplasm NCIT:C180881 Minor Salivary Gland Intraductal Papillary-Mucinous Neoplasm NCIT:C5953 Minor Salivary Gland Mucoepidermoid Carcinoma +NCIT:C201832 Minor Salivary Gland Sclerosing Microcystic Adenocarcinoma NCIT:C5956 Minor Salivary Gland Small Cell Neuroendocrine Carcinoma NCIT:C5959 Minor Salivary Gland Squamous Cell Carcinoma NCIT:C5954 Minor Salivary Gland Undifferentiated Carcinoma @@ -5497,7 +5660,6 @@ NCIT:C3210 Mixed Cell Lymphoma NCIT:C27793 Mixed Cell Type Gastrointestinal Stromal Tumor NCIT:C141224 Mixed Cellularity Classic Hodgkin Lymphoma by Ann Arbor Stage NCIT:C97058 Mixed Congenital Mesoblastic Nephroma -NCIT:C43312 Mixed Epithelial and Mesenchymal Hair Follicle Neoplasm NCIT:C63903 Mixed Focus of Cellular Alteration of the Rat NCIT:C155767 Mixed Gangliocytoma-Pituitary Neuroendocrine Tumor NCIT:C22071 Mixed Germ Cell Tumours of the Mouse Nervous System @@ -6025,6 +6187,7 @@ NCIT:C178443 Mucosal Melanoma of the Genitourinary System NCIT:C133187 Mucosal Melanoma of the Head and Neck NCIT:C133186 Mucosal Melanoma of the Head and Neck by AJCC v7 Stage NCIT:C178453 Mucosal Melanoma of the Urinary System +NCIT:C204907 Mucosal Nevus NCIT:C166405 Mucosal Nodular Melanoma NCIT:C7744 Mucous Membrane Hemangioma NCIT:C64296 Mucus Cell Hyperplasia of the Rat Bronchiole @@ -6065,6 +6228,7 @@ NCIT:C9265 Mycosis Fungoides and Sezary Syndrome NCIT:C141142 Mycosis Fungoides and Sezary Syndrome by AJCC v7 Stage NCIT:C141346 Mycosis Fungoides and Sezary Syndrome by AJCC v8 Stage NCIT:C141143 Mycosis Fungoides by AJCC v7 Stage +NCIT:C203443 Myelodysplastic Chronic Myelomonocytic Leukemia NCIT:C27722 Myelodysplastic Syndrome Post Cytotoxic Therapy NCIT:C200376 Myelodysplastic Syndrome with Biallelic TP53 Inactivation NCIT:C200381 Myelodysplastic Syndrome with Biallelic TP53 Mutation @@ -6094,10 +6258,11 @@ NCIT:C198581 Myelodysplastic/Myeloproliferative Neoplasm with SF3B1 Mutation and NCIT:C27780 Myelodysplastic/Myeloproliferative Neoplasm, Not Otherwise Specified NCIT:C21898 Myeloid Dysplasia of Mouse NCIT:C43223 Myeloid Leukemia Associated with Down Syndrome -NCIT:C3176 Myeloid Leukemia, Philadelphia- Negative +NCIT:C3176 Myeloid Leukemia, Philadelphia-Negative NCIT:C198593 Myeloid Neoplasm with Mutated TP53 NCIT:C198565 Myeloid/Lymphoid Neoplasms with ETV6-ABL1 NCIT:C198559 Myeloid/Lymphoid Neoplasms with FLT3 Rearrangement +NCIT:C203444 Myeloproliferative Chronic Myelomonocytic Leukemia NCIT:C198555 Myeloproliferative Neoplasm, BCR-ABL1 Negative NCIT:C21687 Myoepithelial Carcinoma of the Mouse Mammary Gland NCIT:C21688 Myoepithelial and Mixed Glandular Myoepithelial Carcinoma of the Mouse Mammary Gland @@ -6116,36 +6281,48 @@ NCIT:C148396 N1 Diffuse Large B-Cell Lymphoma NCIT:C164313 NF1-Associated Malignant Peripheral Nerve Sheath Tumor NCIT:C128697 NK-Cell Lymphoma, Unclassifiable NCIT:C178426 NTRK-Rearranged Spindle Cell Neoplasm +NCIT:C204889 Nail Apparatus Melanoma NCIT:C165662 Nail Matrix Nevus NCIT:C188081 Nasal Cavity Diffuse Large B-Cell Lymphoma NCIT:C54347 Nasal Cavity Exophytic Papilloma NCIT:C173173 Nasal Cavity Extranodal NK/T-Cell Lymphoma NCIT:C54285 Nasal Cavity Keratinizing Squamous Cell Carcinoma +NCIT:C203005 Nasal Cavity Large Cell Neuroendocrine Carcinoma +NCIT:C202996 Nasal Cavity Neuroendocrine Carcinoma +NCIT:C202992 Nasal Cavity Neuroendocrine Neoplasm +NCIT:C202994 Nasal Cavity Neuroendocrine Tumor +NCIT:C203008 Nasal Cavity Neuroendocrine Tumor G1 +NCIT:C203011 Nasal Cavity Neuroendocrine Tumor G2 NCIT:C6075 Nasal Cavity Non-Hodgkin Lymphoma NCIT:C164256 Nasal Cavity Papilloma +NCIT:C203002 Nasal Cavity Small Cell Neuroendocrine Carcinoma NCIT:C141296 Nasal Type NK/T-Cell Lymphoma by Ann Arbor Stage NCIT:C175259 Nasolacrimal Duct Neoplasm NCIT:C173340 Nasopharyngeal Adenoid Cystic Carcinoma -NCIT:C54360 Nasopharyngeal Basaloid Carcinoma +NCIT:C54360 Nasopharyngeal Basaloid Squamous Cell Carcinoma NCIT:C90522 Nasopharyngeal Carcinoma by AJCC v6 Stage NCIT:C91244 Nasopharyngeal Carcinoma by AJCC v7 Stage NCIT:C132816 Nasopharyngeal Carcinoma by AJCC v8 Stage NCIT:C54389 Nasopharyngeal Differentiated Carcinoma +NCIT:C202979 Nasopharyngeal Germ Cell Tumor NCIT:C173361 Nasopharyngeal Hodgkin Lymphoma NCIT:C7992 Nasopharyngeal Keratinizing Squamous Cell Carcinoma +NCIT:C203015 Nasopharyngeal Large Cell Neuroendocrine Carcinoma +NCIT:C54400 Nasopharyngeal Low Grade Papillary Adenocarcinoma NCIT:C173357 Nasopharyngeal Lymphoma NCIT:C178522 Nasopharyngeal Melanoma +NCIT:C203013 Nasopharyngeal Neuroendocrine Carcinoma NCIT:C173359 Nasopharyngeal Non-Hodgkin Lymphoma -NCIT:C7373 Nasopharyngeal Nonkeratinizing Carcinoma -NCIT:C54400 Nasopharyngeal Papillary Adenocarcinoma +NCIT:C7373 Nasopharyngeal Non-Keratinizing Carcinoma NCIT:C48316 Nasopharyngeal Paraganglioma NCIT:C173352 Nasopharyngeal Pituitary Neuroendocrine Tumor NCIT:C6034 Nasopharyngeal Polyp +NCIT:C203014 Nasopharyngeal Small Cell Neuroendocrine Carcinoma NCIT:C6037 Nasopharyngeal Squamous Papilloma +NCIT:C202982 Nasopharyngeal Teratoma NCIT:C82217 Natural Killer Cell Lymphoblastic Leukemia/Lymphoma NCIT:C199215 Near-Haploid B Acute Lymphoblastic Leukemia NCIT:C6077 Neck Carcinoma -NCIT:C173585 Neck Carcinoma of Unknown Primary NCIT:C27648 Neck Disorder NCIT:C7713 Neck Squamous Cell Carcinoma of Unknown Primary NCIT:C36029 Necrotic Neoplasm @@ -6177,13 +6354,14 @@ NCIT:C21979 Neuroblastomas of the Mouse Adrenal Gland and Sympathetic Nervous Sy NCIT:C22150 Neuroendocrine Adenoma of the Mouse Intestinal Tract NCIT:C163975 Neuroendocrine Carcinoma of Unknown Primary NCIT:C21778 Neuroendocrine Carcinoma of the Mouse Pulmonary System -NCIT:C173385 Neuroendocrine Carcinoma, Excluding Head and Neck NCIT:C22163 Neuroendocrine Cell Carcinoma of the Mouse Intestinal Tract NCIT:C22101 Neuroendocrine Cell Hyperplasia of the Mouse Intestinal Tract NCIT:C63890 Neuroendocrine Cell Hyperplasia of the Rat Glandular Stomach NCIT:C21758 Neuroendocrine Hyperplasia of the Mouse Pulmonary System NCIT:C23123 Neuroendocrine Neoplasms of the Mouse Larynx NCIT:C188218 Neuroendocrine Tumor +NCIT:C203250 Neuroendocrine Tumor G1 +NCIT:C203251 Neuroendocrine Tumor G3 NCIT:C35562 Neuroepithelial, Perineurial, and Schwann Cell Neoplasm NCIT:C23058 Neurofibroma of the Mouse Oral Cavity NCIT:C21837 Neurofibroma of the Mouse Skin @@ -6198,16 +6376,19 @@ NCIT:C60316 No Proliferative Lesion Detected NCIT:C180516 No Specific Molecular Profile Endometrial Endometrioid Adenocarcinoma NCIT:C141261 Nodal Marginal Zone Lymphoma by Ann Arbor Stage NCIT:C141225 Nodular Lymphocyte Predominant B-Cell Lymphoma by Ann Arbor Stage +NCIT:C205125 Nodular Melanoma NCIT:C36012 Nodular Neoplasm NCIT:C141223 Nodular Sclerosis Classic Hodgkin Lymphoma by Ann Arbor Stage NCIT:C67171 Nodular Sclerosis Classic Hodgkin Lymphoma, Cellular Phase NCIT:C27807 Nodular Sclerosis Classic Hodgkin Lymphoma, Syncytial Variant NCIT:C7187 Non-Burkitt's Lymphoma +NCIT:C202059 Non-Calcifying/Langerhans Cell-Rich Calcifying Epithelial Odontogenic Tumor +NCIT:C202497 Non-Clear Cell Renal Cell Carcinoma NCIT:C121583 Non-Cutaneous Leiomyosarcoma NCIT:C36036 Non-Encapsulated Neoplasm NCIT:C154429 Non-Functioning Corticotroph Pituitary Neuroendocrine Tumor NCIT:C154431 Non-Functioning Densely Granulated Corticotroph Pituitary Neuroendocrine Tumor -NCIT:C176706 Non-Functioning Lung Carcinoid Tumor +NCIT:C176706 Non-Functioning Lung Neuroendocrine Tumor NCIT:C95585 Non-Functioning Pancreatic Neuroendocrine Tumor G1 NCIT:C45838 Non-Functioning Pancreatic Neuroendocrine Tumor G2 NCIT:C121721 Non-Functioning Pituitary Neuroendocrine Tumor/Macroadenoma @@ -6234,7 +6415,7 @@ NCIT:C23073 Non-Keratinizing Carcinoma of the Mouse Pharynx With Lymphoid Stroma NCIT:C23072 Non-Keratinizing Carcinoma of the Mouse Pharynx Without Lymphoid Stroma NCIT:C64125 Non-Keratinizing Epithelioma of the Rat Lung NCIT:C65173 Non-Keratinizing Large Cell Squamous Cell Carcinoma -NCIT:C7499 Non-Keratinizing Primary Intraosseous Squamous Cell Carcinoma -Solid Type +NCIT:C7499 Non-Keratinizing Primary Intraosseous Squamous Cell Carcinoma-Solid Type NCIT:C65175 Non-Keratinizing Small Cell Squamous Cell Carcinoma NCIT:C21883 Non-Lymphoid Hematopoietic Neoplasm of Mouse NCIT:C163003 Non-Malignant Neoplasm @@ -6251,6 +6432,7 @@ NCIT:C21868 Non-Neoplastic Non-Lymphoid Hematopoietic Disorders of Mouse NCIT:C38752 Non-Neoplastic Proliferation of the Mouse Liver NCIT:C21651 Non-Neoplastic Proliferation of the Mouse Mammary Gland NCIT:C21870 Non-Neoplastic Splenic Myeloid Hyperplasia of Mouse +NCIT:C173798 Non-Neoplastic Tonsillar Disorder NCIT:C121929 Non-Ossifying Fibroma NCIT:C27745 Non-Small Cell Adenocarcinoma NCIT:C65151 Non-Small Cell Carcinoma @@ -6288,6 +6470,9 @@ NCIT:C54317 Odontoameloblastoma NCIT:C173720 Odontogenic Carcinoma NCIT:C173735 Odontogenic Carcinosarcoma NCIT:C4314 Odontogenic Fibroma +NCIT:C202078 Odontogenic Fibroma, Amyloid Subtype +NCIT:C202079 Odontogenic Fibroma, Granular Cell Subtype +NCIT:C202080 Odontogenic Fibroma, Ossifying Subtype NCIT:C7452 Odontogenic Myxofibroma NCIT:C7501 Odontogenic Myxoma NCIT:C173738 Odontogenic Sarcoma @@ -6314,6 +6499,7 @@ NCIT:C171265 Oligometastatic Prostate Carcinoma NCIT:C40340 Omentum Gastrointestinal Stromal Tumor NCIT:C3679 Oncocytic Adenocarcinoma NCIT:C46093 Oncocytic Variant Thyroid Gland Papillary Carcinoma +NCIT:C201839 Oncocytic Variant of Chromophobe Renal Cell Carcinoma NCIT:C27769 Opisthorchis Viverrini-Related Cholangiocarcinoma NCIT:C179886 Optic Chiasm Neoplasm NCIT:C4230 Optic Disc Melanocytoma @@ -6333,8 +6519,11 @@ NCIT:C173478 Oral Cavity Low Grade Myofibroblastic Sarcoma NCIT:C6845 Oral Cavity Monomorphic Adenoma NCIT:C5915 Oral Cavity Mucosal Melanoma NCIT:C173489 Oral Cavity Myeloid Sarcoma +NCIT:C202860 Oral Cavity Neurofibroma +NCIT:C80290 Oral Cavity Plasmablastic Lymphoma NCIT:C6242 Oral Cavity Pleomorphic Adenoma NCIT:C5916 Oral Cavity Sarcoma +NCIT:C202876 Oral Cavity Schwannoma NCIT:C173479 Oral Cavity Soft Tissue Neoplasm NCIT:C173481 Oral Cavity Soft Tissue Sarcoma NCIT:C7425 Oral Cavity and Lip Precancerous Condition @@ -6346,24 +6535,33 @@ NCIT:C8989 Oral Neoplasm NCIT:C173476 Oral Squamous Papilloma NCIT:C173475 Oral Verruca Vulgaris NCIT:C4545 Orbit Capillary Hemangioma +NCIT:C202882 Orbit Extraskeletal Myxoid Chondrosarcoma NCIT:C4547 Orbit Hemangiopericytoma NCIT:C6408 Orbit Paraganglioma +NCIT:C202620 Orbit Solitary Fibrous Tumor NCIT:C156276 Orbital Alveolar Soft Part Sarcoma NCIT:C118828 Orbital Melanoma NCIT:C60317 Organ not Available for Histological Examination NCIT:C132994 Oropharyngeal (p16-Negative) Carcinoma by AJCC v8 Stage -NCIT:C126751 Oropharyngeal Basaloid Carcinoma +NCIT:C126751 Oropharyngeal Basaloid Squamous Cell Carcinoma NCIT:C90523 Oropharyngeal Carcinoma by AJCC v6 Stage NCIT:C91248 Oropharyngeal Carcinoma by AJCC v7 Stage NCIT:C173578 Oropharyngeal Hodgkin Lymphoma -NCIT:C173414 Oropharyngeal Human Papillomavirus-Negative Squamous Cell Carcinoma -NCIT:C87055 Oropharyngeal Human Papillomavirus-Positive Squamous Cell Carcinoma +NCIT:C201905 Oropharyngeal Human Papillomavirus-Independent Keratinizing Squamous Cell Carcinoma +NCIT:C173414 Oropharyngeal Human Papillomavirus-Independent Squamous Cell Carcinoma +NCIT:C201906 Oropharyngeal Human Papillomavirus-Related Keratinizing Squamous Cell Carcinoma +NCIT:C201907 Oropharyngeal Human Papillomavirus-Related Non-Keratinizing Squamous Cell Carcinoma +NCIT:C87055 Oropharyngeal Human Papillomavirus-Related Squamous Cell Carcinoma +NCIT:C201904 Oropharyngeal Keratinizing Squamous Cell Carcinoma +NCIT:C203018 Oropharyngeal Large Cell Neuroendocrine Carcinoma NCIT:C173577 Oropharyngeal Lymphoma +NCIT:C203016 Oropharyngeal Neuroendocrine Carcinoma NCIT:C173579 Oropharyngeal Non-Hodgkin Lymphoma NCIT:C173575 Oropharyngeal Pleomorphic Adenoma NCIT:C173576 Oropharyngeal Polymorphous Adenocarcinoma NCIT:C5988 Oropharyngeal Polyp NCIT:C126750 Oropharyngeal Poorly Differentiated Carcinoma +NCIT:C203017 Oropharyngeal Small Cell Neuroendocrine Carcinoma NCIT:C6038 Oropharyngeal Squamous Papilloma NCIT:C68610 Oropharyngeal Undifferentiated Carcinoma NCIT:C147906 Oropharyngeal p16INK4a-Negative Squamous Cell Carcinoma @@ -6403,7 +6601,6 @@ NCIT:C126331 Ovarian Adenomatoid Tumor NCIT:C128106 Ovarian Cancer by AJCC v6 and v7 Stage NCIT:C139963 Ovarian Cancer by AJCC v8 Stage NCIT:C128081 Ovarian Cancer by FIGO Stage -NCIT:C5229 Ovarian Carcinoid Tumor NCIT:C7291 Ovarian Cellular Fibroma NCIT:C179334 Ovarian Dedifferentiated Carcinoma NCIT:C39999 Ovarian Dermoid Cyst with Adenocarcinoma @@ -6426,6 +6623,7 @@ NCIT:C39998 Ovarian Dermoid Cyst with Squamous Cell Carcinoma NCIT:C6257 Ovarian Endometrioid Tumor NCIT:C5233 Ovarian Fibrosarcoma NCIT:C7287 Ovarian Granulosa-Stromal Cell Tumor +NCIT:C199166 Ovarian High Grade Endometrioid Adenocarcinoma NCIT:C105555 Ovarian High Grade Serous Adenocarcinoma NCIT:C4214 Ovarian Hilus Cell Tumor NCIT:C40013 Ovarian Insular Carcinoid Tumor @@ -6433,6 +6631,7 @@ NCIT:C179360 Ovarian Leiomyoma NCIT:C5231 Ovarian Leydig Cell Tumor NCIT:C39983 Ovarian Leydig Cell Tumor, Non-Hilar Type NCIT:C39984 Ovarian Leydig Cell Tumor, Not Otherwise Specified +NCIT:C199159 Ovarian Low Grade Endometrioid Adenocarcinoma NCIT:C40063 Ovarian Low Grade Endometrioid Stromal Sarcoma NCIT:C105556 Ovarian Low Grade Serous Adenocarcinoma NCIT:C4203 Ovarian Luteinized Thecoma @@ -6447,6 +6646,7 @@ NCIT:C40042 Ovarian Mucinous Cystic Tumor with Mural Nodules NCIT:C5245 Ovarian Myxoma NCIT:C179474 Ovarian Neuroectodermal-Type Tumor NCIT:C171032 Ovarian Neuroendocrine Carcinoma +NCIT:C5229 Ovarian Neuroendocrine Tumor NCIT:C39971 Ovarian Retiform Sertoli-Leydig Cell Tumor NCIT:C126322 Ovarian Retiform Sertoli-Leydig Cell Tumor, Variant with Heterologous Elements NCIT:C4204 Ovarian Sclerosing Stromal Tumor @@ -6488,9 +6688,11 @@ NCIT:C7139 PRETEXT I Hepatoblastoma NCIT:C7140 PRETEXT II Hepatoblastoma NCIT:C7141 PRETEXT III Hepatoblastoma NCIT:C7142 PRETEXT IV Hepatoblastoma +NCIT:C204574 PRKAR1A-Inactivated Pigmented Epithelioid Melanocytoma NCIT:C8463 Palate Carcinoma NCIT:C6749 Palate Kaposi Sarcoma NCIT:C4649 Palate Squamous Cell Carcinoma +NCIT:C201900 Palatine Tonsil Hamartomatous Polyp NCIT:C95542 Pancreatic Acinar Cell Neoplasm NCIT:C67455 Pancreatic Alpha Cell Adenoma NCIT:C67457 Pancreatic Beta Cell Adenoma @@ -6518,10 +6720,11 @@ NCIT:C188065 Pancreatic Leiomyosarcoma NCIT:C95471 Pancreatic Macrocystic Serous Cystadenoma NCIT:C95559 Pancreatic Mature Teratoma NCIT:C95466 Pancreatic Medullary Carcinoma +NCIT:C6878 Pancreatic Mixed Acinar Carcinoma-Neuroendocrine Carcinoma NCIT:C95458 Pancreatic Mixed Acinar-Ductal Carcinoma -NCIT:C95460 Pancreatic Mixed Acinar-Ductal Neuroendocrine Carcinoma -NCIT:C6878 Pancreatic Mixed Acinar-Neuroendocrine Carcinoma -NCIT:C188217 Pancreatic Mixed Ductal-Neuroendocrine Neoplasm +NCIT:C95460 Pancreatic Mixed Ductal Adenocarcinoma-Acinar Carcinoma-Neuroendocrine Carcinoma +NCIT:C188217 Pancreatic Mixed Ductal Adenocarcinoma-Neuroendocrine Neoplasm +NCIT:C203795 Pancreatic Mixed Ductal Adenocarcinoma-Neuroendocrine Tumor NCIT:C95427 Pancreatic Moderately Differentiated Ductal Adenocarcinoma NCIT:C6883 Pancreatic Mucinous-Cystic Neoplasm with Intermediate Grade Dysplasia NCIT:C95493 Pancreatic Mucinous-Cystic Neoplasm, High Grade @@ -6570,8 +6773,15 @@ NCIT:C6017 Paranasal Sinus Adenocarcinoma NCIT:C6073 Paranasal Sinus Diffuse Large B-Cell Lymphoma NCIT:C8195 Paranasal Sinus Inverted Papilloma NCIT:C54284 Paranasal Sinus Keratinizing Squamous Cell Carcinoma +NCIT:C203006 Paranasal Sinus Large Cell Neuroendocrine Carcinoma +NCIT:C202997 Paranasal Sinus Neuroendocrine Carcinoma +NCIT:C202993 Paranasal Sinus Neuroendocrine Neoplasm +NCIT:C202995 Paranasal Sinus Neuroendocrine Tumor +NCIT:C203009 Paranasal Sinus Neuroendocrine Tumor G1 +NCIT:C203012 Paranasal Sinus Neuroendocrine Tumor G2 NCIT:C6069 Paranasal Sinus Non-Hodgkin Lymphoma NCIT:C6016 Paranasal Sinus Olfactory Neuroblastoma +NCIT:C203004 Paranasal Sinus Small Cell Neuroendocrine Carcinoma NCIT:C162820 Parapharyngeal Neoplasm NCIT:C27767 Parasite-Related Carcinoma NCIT:C27766 Parasite-Related Malignant Neoplasm @@ -6614,6 +6824,7 @@ NCIT:C173719 Parotid Gland Diffuse Large B-Cell Lymphoma NCIT:C173716 Parotid Gland Follicular Lymphoma NCIT:C5397 Parotid Gland Hemangioma NCIT:C5952 Parotid Gland Kaposi Sarcoma +NCIT:C201770 Parotid Gland Keratocystoma NCIT:C5982 Parotid Gland Lipoma NCIT:C156281 Parotid Gland Liposarcoma NCIT:C5393 Parotid Gland Lymphangioma @@ -6629,18 +6840,18 @@ NCIT:C173684 Parotid Gland Sialolipoma NCIT:C5946 Parotid Gland Undifferentiated Carcinoma NCIT:C66865 Parotid Gland Warthin Tumor NCIT:C137662 Pathologic Stage 0 Cutaneous Melanoma AJCC v8 +NCIT:C136881 Pathologic Stage 0 Cutaneous Merkel Cell Carcinoma AJCC v8 NCIT:C133413 Pathologic Stage 0 Esophageal Adenocarcinoma AJCC v8 NCIT:C133519 Pathologic Stage 0 Esophageal Squamous Cell Carcinoma AJCC v8 NCIT:C133654 Pathologic Stage 0 Gastric Cancer AJCC v8 NCIT:C133564 Pathologic Stage 0 Gastroesophageal Junction Adenocarcinoma AJCC v8 -NCIT:C136881 Pathologic Stage 0 Merkel Cell Carcinoma AJCC v8 NCIT:C137663 Pathologic Stage I Cutaneous Melanoma AJCC v8 +NCIT:C136882 Pathologic Stage I Cutaneous Merkel Cell Carcinoma AJCC v8 NCIT:C133414 Pathologic Stage I Esophageal Adenocarcinoma AJCC v8 NCIT:C133521 Pathologic Stage I Esophageal Squamous Cell Carcinoma AJCC v8 NCIT:C133655 Pathologic Stage I Gastric Cancer AJCC v8 NCIT:C133565 Pathologic Stage I Gastroesophageal Junction Adenocarcinoma AJCC v8 NCIT:C132898 Pathologic Stage I HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8 -NCIT:C136882 Pathologic Stage I Merkel Cell Carcinoma AJCC v8 NCIT:C140757 Pathologic Stage I Retinoblastoma AJCC v8 NCIT:C137664 Pathologic Stage IA Cutaneous Melanoma AJCC v8 NCIT:C133415 Pathologic Stage IA Esophageal Adenocarcinoma AJCC v8 @@ -6655,56 +6866,56 @@ NCIT:C133567 Pathologic Stage IB Gastroesophageal Junction Adenocarcinoma AJCC v NCIT:C133417 Pathologic Stage IC Esophageal Adenocarcinoma AJCC v8 NCIT:C133568 Pathologic Stage IC Gastroesophageal Junction Adenocarcinoma AJCC v8 NCIT:C137666 Pathologic Stage II Cutaneous Melanoma AJCC v8 +NCIT:C136883 Pathologic Stage II Cutaneous Merkel Cell Carcinoma AJCC v8 NCIT:C133418 Pathologic Stage II Esophageal Adenocarcinoma AJCC v8 NCIT:C133532 Pathologic Stage II Esophageal Squamous Cell Carcinoma AJCC v8 NCIT:C133659 Pathologic Stage II Gastric Cancer AJCC v8 NCIT:C133570 Pathologic Stage II Gastroesophageal Junction Adenocarcinoma AJCC v8 NCIT:C132899 Pathologic Stage II HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8 -NCIT:C136883 Pathologic Stage II Merkel Cell Carcinoma AJCC v8 NCIT:C140758 Pathologic Stage II Retinoblastoma AJCC v8 NCIT:C137667 Pathologic Stage IIA Cutaneous Melanoma AJCC v8 +NCIT:C136884 Pathologic Stage IIA Cutaneous Merkel Cell Carcinoma AJCC v8 NCIT:C133419 Pathologic Stage IIA Esophageal Adenocarcinoma AJCC v8 NCIT:C133534 Pathologic Stage IIA Esophageal Squamous Cell Carcinoma AJCC v8 NCIT:C133660 Pathologic Stage IIA Gastric Cancer AJCC v8 NCIT:C133572 Pathologic Stage IIA Gastroesophageal Junction Adenocarcinoma AJCC v8 -NCIT:C136884 Pathologic Stage IIA Merkel Cell Carcinoma AJCC v8 NCIT:C137668 Pathologic Stage IIB Cutaneous Melanoma AJCC v8 +NCIT:C136885 Pathologic Stage IIB Cutaneous Merkel Cell Carcinoma AJCC v8 NCIT:C133420 Pathologic Stage IIB Esophageal Adenocarcinoma AJCC v8 NCIT:C133535 Pathologic Stage IIB Esophageal Squamous Cell Carcinoma AJCC v8 NCIT:C133662 Pathologic Stage IIB Gastric Cancer AJCC v8 NCIT:C133573 Pathologic Stage IIB Gastroesophageal Junction Adenocarcinoma AJCC v8 -NCIT:C136885 Pathologic Stage IIB Merkel Cell Carcinoma AJCC v8 NCIT:C137669 Pathologic Stage IIC Cutaneous Melanoma AJCC v8 NCIT:C137670 Pathologic Stage III Cutaneous Melanoma AJCC v8 +NCIT:C136886 Pathologic Stage III Cutaneous Merkel Cell Carcinoma AJCC v8 NCIT:C133421 Pathologic Stage III Esophageal Adenocarcinoma AJCC v8 NCIT:C133536 Pathologic Stage III Esophageal Squamous Cell Carcinoma AJCC v8 NCIT:C133663 Pathologic Stage III Gastric Cancer AJCC v8 NCIT:C133575 Pathologic Stage III Gastroesophageal Junction Adenocarcinoma AJCC v8 NCIT:C132900 Pathologic Stage III HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8 -NCIT:C136886 Pathologic Stage III Merkel Cell Carcinoma AJCC v8 NCIT:C140759 Pathologic Stage III Retinoblastoma AJCC v8 NCIT:C137671 Pathologic Stage IIIA Cutaneous Melanoma AJCC v8 +NCIT:C136887 Pathologic Stage IIIA Cutaneous Merkel Cell Carcinoma AJCC v8 NCIT:C133422 Pathologic Stage IIIA Esophageal Adenocarcinoma AJCC v8 NCIT:C133537 Pathologic Stage IIIA Esophageal Squamous Cell Carcinoma AJCC v8 NCIT:C133665 Pathologic Stage IIIA Gastric Cancer AJCC v8 NCIT:C133577 Pathologic Stage IIIA Gastroesophageal Junction Adenocarcinoma AJCC v8 -NCIT:C136887 Pathologic Stage IIIA Merkel Cell Carcinoma AJCC v8 NCIT:C137672 Pathologic Stage IIIB Cutaneous Melanoma AJCC v8 +NCIT:C136888 Pathologic Stage IIIB Cutaneous Merkel Cell Carcinoma AJCC v8 NCIT:C133423 Pathologic Stage IIIB Esophageal Adenocarcinoma AJCC v8 NCIT:C133538 Pathologic Stage IIIB Esophageal Squamous Cell Carcinoma AJCC v8 NCIT:C133666 Pathologic Stage IIIB Gastric Cancer AJCC v8 NCIT:C133579 Pathologic Stage IIIB Gastroesophageal Junction Adenocarcinoma AJCC v8 -NCIT:C136888 Pathologic Stage IIIB Merkel Cell Carcinoma AJCC v8 NCIT:C137673 Pathologic Stage IIIC Cutaneous Melanoma AJCC v8 NCIT:C133667 Pathologic Stage IIIC Gastric Cancer AJCC v8 NCIT:C137675 Pathologic Stage IIID Cutaneous Melanoma AJCC v8 NCIT:C137677 Pathologic Stage IV Cutaneous Melanoma AJCC v8 +NCIT:C136889 Pathologic Stage IV Cutaneous Merkel Cell Carcinoma AJCC v8 NCIT:C133424 Pathologic Stage IV Esophageal Adenocarcinoma AJCC v8 NCIT:C133539 Pathologic Stage IV Esophageal Squamous Cell Carcinoma AJCC v8 NCIT:C133668 Pathologic Stage IV Gastric Cancer AJCC v8 NCIT:C133580 Pathologic Stage IV Gastroesophageal Junction Adenocarcinoma AJCC v8 NCIT:C132901 Pathologic Stage IV HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8 -NCIT:C136889 Pathologic Stage IV Merkel Cell Carcinoma AJCC v8 NCIT:C140760 Pathologic Stage IV Retinoblastoma AJCC v8 NCIT:C133425 Pathologic Stage IVA Esophageal Adenocarcinoma AJCC v8 NCIT:C133541 Pathologic Stage IVA Esophageal Squamous Cell Carcinoma AJCC v8 @@ -6819,8 +7030,14 @@ NCIT:C43332 Pilar Leiomyoma NCIT:C43313 Pilar-Associated Mesenchyme Neoplasm NCIT:C21815 Pilomatrixoma Type of Basaloid Follicular Neoplasm of the Mouse Skin NCIT:C4659 Pineal Region Germ Cell Tumor +NCIT:C201966 Pineoblastoma Molecular Subtypes +NCIT:C201967 Pineoblastoma miRNA Processing Altered 1 +NCIT:C201968 Pineoblastoma miRNA Processing Altered 2 +NCIT:C201973 Pineoblastoma, MYC/FOXR2-Activated +NCIT:C201969 Pineoblastoma, RB1-Altered NCIT:C4147 Pituitary Gland Acidophil Carcinoma NCIT:C155304 Pituitary Gland Blastoma +NCIT:C155797 Pituitary Gland Diffuse Large B-Cell Lymphoma NCIT:C4149 Pituitary Gland Mixed Acidophil-Basophil Carcinoma NCIT:C45922 Pituitary Gland Neoplasm (Antiquated) NCIT:C155796 Pituitary Gland Non-Hodgkin Lymphoma @@ -6844,7 +7061,6 @@ NCIT:C23150 Plasma Cell Neoplasms of the Mouse Salivary Glands NCIT:C21853 Plasma Cell Neoplasms of the Mouse Skin NCIT:C7240 Plasma Cell Post-Transplant Lymphoproliferative Disorder NCIT:C38159 Plasmablastic Lymphoma of Mucosa Site -NCIT:C80290 Plasmablastic Lymphoma of the Oral Mucosa NCIT:C21919 Plasmacytoma of the Mouse Hematologic System NCIT:C22060 Plasmacytoma of the Mouse Nervous System NCIT:C23104 Plasmacytoma of the Mouse Nose and Paranasal Sinuses @@ -6853,10 +7069,14 @@ NCIT:C23087 Plasmacytoma of the Mouse Pharynx NCIT:C23151 Plasmacytoma of the Mouse Salivary Glands NCIT:C7241 Plasmacytoma-Like Post-Transplant Lymphoproliferative Disorder NCIT:C178698 Platinum-Refractory Fallopian Tube Carcinoma +NCIT:C204988 Platinum-Refractory Fallopian Tube High Grade Serous Adenocarcinoma NCIT:C178697 Platinum-Refractory Malignant Female Reproductive System Neoplasm NCIT:C178700 Platinum-Refractory Ovarian Carcinoma +NCIT:C204987 Platinum-Refractory Ovarian High Grade Serous Adenocarcinoma NCIT:C178702 Platinum-Refractory Primary Peritoneal Carcinoma +NCIT:C204991 Platinum-Refractory Primary Peritoneal High Grade Serous Adenocarcinoma NCIT:C157621 Platinum-Resistant Fallopian Tube Carcinoma +NCIT:C204982 Platinum-Resistant Fallopian Tube High Grade Serous Adenocarcinoma NCIT:C179151 Platinum-Resistant Head and Neck Carcinoma NCIT:C158493 Platinum-Resistant Lung Small Cell Carcinoma NCIT:C169021 Platinum-Resistant Malignant Female Reproductive System Neoplasm @@ -6864,7 +7084,9 @@ NCIT:C170955 Platinum-Resistant Malignant Germ Cell Tumor NCIT:C147561 Platinum-Resistant Ovarian Carcinoma NCIT:C199567 Platinum-Resistant Ovarian High Grade Serous Adenocarcinoma NCIT:C157622 Platinum-Resistant Primary Peritoneal Carcinoma +NCIT:C204985 Platinum-Resistant Primary Peritoneal High Grade Serous Adenocarcinoma NCIT:C150365 Platinum-Resistant Urothelial Carcinoma +NCIT:C205187 Platinum-Sensitive Endometrial Carcinoma NCIT:C187374 Platinum-Sensitive Endometrial Serous Adenocarcinoma NCIT:C160873 Platinum-Sensitive Fallopian Tube Carcinoma NCIT:C158495 Platinum-Sensitive Lung Small Cell Carcinoma @@ -6892,6 +7114,7 @@ NCIT:C188055 Pleural Proximal-Type Epithelioid Sarcoma NCIT:C45696 Pleural Synovial Sarcoma NCIT:C45660 Pleural Well Differentiated Papillary Mesothelial Tumor NCIT:C6493 Plexiform Fibrohistiocytic Tumor +NCIT:C204516 Plexiform Spindle Cell Melanocytoma NCIT:C45916 Plurihormonal Pituitary Neuroendocrine Tumor NCIT:C154505 Plurimorphous Plurihormonal Pituitary Neuroendocrine Tumor NCIT:C134962 Poeciliopsis Lucida Hepatocellular Carcinoma @@ -6915,8 +7138,10 @@ NCIT:C42047 Poorly Differentiated Neuroblastoma NCIT:C4210 Poorly Differentiated Ovarian Sertoli-Leydig Cell Tumor NCIT:C39973 Poorly Differentiated Ovarian Sertoli-Leydig Cell Tumor, Variant with Heterologous Elements NCIT:C27916 Poorly Differentiated Prostate Adenocarcinoma +NCIT:C202883 Poorly Differentiated Synovial Sarcoma NCIT:C21809 Poorly-differentiated Squamous Cell Carcinoma of the Mouse Skin NCIT:C43354 Porocarcinoma In Situ +NCIT:C205476 Poroid Hidradenoma NCIT:C126806 Post-Essential Thrombocythemia Myelofibrosis NCIT:C8595 Postcricoid Carcinoma NCIT:C8185 Postcricoid Squamous Cell Carcinoma @@ -6986,6 +7211,7 @@ NCIT:C121930 Primary Bone Non-Hodgkin Lymphoma NCIT:C4834 Primary Bone Osteosarcoma NCIT:C4975 Primary Brain Stem Neoplasm NCIT:C176251 Primary Breast Angiosarcoma +NCIT:C202952 Primary CD30-Positive T-Cell Lymphoproliferative Disorder NCIT:C178476 Primary Central Atypical Cartilaginous Tumor/Chondrosarcoma, Grade 1 NCIT:C7155 Primary Central Chondrosarcoma NCIT:C102871 Primary Central Nervous System Neoplasm @@ -7005,15 +7231,16 @@ NCIT:C45340 Primary Cutaneous Gamma-Delta T-Cell Lymphoma NCIT:C7221 Primary Cutaneous Hodgkin Lymphoma NCIT:C45214 Primary Cutaneous Intravascular Large B-Cell Lymphoma NCIT:C27533 Primary Cutaneous Mucinous Carcinoma +NCIT:C205357 Primary Cutaneous NUT Adnexal Carcinoma NCIT:C188114 Primary Cutaneous Non-Hodgkin Lymphoma NCIT:C201080 Primary Cutaneous Peripheral T-Cell Lymphoma, Not Otherwise Specified NCIT:C45332 Primary Cutaneous Peripheral T-Cell Lymphoma, Rare Subtype NCIT:C45216 Primary Cutaneous Plasmablastic Lymphoma NCIT:C45215 Primary Cutaneous T-Cell/Histiocyte-Rich Large B-Cell Lymphoma -NCIT:C162467 Primary Diffuse Large B-Cell Lymphoma of the Testis +NCIT:C202953 Primary Head and Neck Mucosal CD30-Positive T-Cell Lymphoproliferative Disorder NCIT:C186610 Primary Intracranial Sarcoma, DICER1-Mutant -NCIT:C54303 Primary Intraosseous Squamous Cell Carcinoma Derived From Keratocystic Odontogenic Tumor -NCIT:C7500 Primary Intraosseous Squamous Cell Carcinoma Derived From Odontogenic Cyst +NCIT:C7500 Primary Intraosseous Carcinoma, Not Otherwise Specified, Derived from Odontogenic Cyst +NCIT:C54303 Primary Intraosseous Carcinoma, Not Otherwise Specified, Derived from Odontogenic Keratocyst NCIT:C7491 Primary Intraosseous Squamous Cell Carcinoma-Solid Type NCIT:C175467 Primary Iris Non-Hodgkin Lymphoma NCIT:C200687 Primary Large B-Cell Lymphoma of Immune-Privileged Site @@ -7025,11 +7252,11 @@ NCIT:C183184 Primary Malignant Pelvic Neoplasm NCIT:C141262 Primary Mediastinal Large B-Cell Lymphoma by Ann Arbor Stage NCIT:C21916 Primary Mediastinal Thymic Diffuse Large B Cell Lymphoma of the Mouse Hematologic System NCIT:C22051 Primary Melanocytic Lesions of the Mouse Nervous System -NCIT:C4661 Primary Meningeal Melanocytic Neoplasm NCIT:C174033 Primary Middle Ear Meningioma NCIT:C24238 Primary Mouse Gastric Non-Hodgkin's Lymphoma NCIT:C8509 Primary Neoplasm NCIT:C139288 Primary Nodal EBV-Positive T-Cell/NK-Cell Lymphoma +NCIT:C202955 Primary Oral Cavity CD30-Positive T-Cell Lymphoproliferative Disorder NCIT:C170733 Primary Peritoneal Adenocarcinoma NCIT:C140003 Primary Peritoneal Cancer by AJCC v7 Stage NCIT:C140004 Primary Peritoneal Cancer by AJCC v8 Stage @@ -7040,7 +7267,6 @@ NCIT:C126353 Primary Peritoneal High Grade Serous Adenocarcinoma NCIT:C126354 Primary Peritoneal Low Grade Serous Adenocarcinoma NCIT:C162564 Primary Peritoneal Transitional Cell Carcinoma NCIT:C162562 Primary Peritoneal Undifferentiated Carcinoma -NCIT:C155797 Primary Pituitary Gland Diffuse Large B-Cell Lymphoma NCIT:C142827 Primary Pulmonary Myxoid Sarcoma with EWSR1-CREB1 Fusion NCIT:C173163 Primary Sinonasal Meningioma NCIT:C175451 Primary Uveal Non-Hodgkin Lymphoma @@ -7130,14 +7356,17 @@ NCIT:C161607 Prostate Wilms Tumor NCIT:C39901 Prostatic Duct Urothelial Carcinoma NCIT:C21728 Prostatic Intraepithelial Neoplasia of the Mouse Prostate Gland NCIT:C191961 Prostatic Intraepithelial Neoplasia-Like Adenocarcinoma +NCIT:C202633 Proximal Colon Carcinoma NCIT:C165628 Proximal Gastric Adenocarcinoma NCIT:C115334 Proximal Urethral Carcinoma NCIT:C176887 Psammocarcinoma +NCIT:C202209 Psammomatoid Ossifying Fibroma NCIT:C121668 Pseudomyogenic Hemangioendothelioma NCIT:C3763 Pulmonary Adenomatosis NCIT:C6746 Pulmonary Artery Angiosarcoma NCIT:C142825 Pulmonary Artery Intimal Sarcoma NCIT:C45607 Pulmonary Lymphomatoid Granulomatosis +NCIT:C201978 Pulmonary Mucinous Cystic Tumor of Borderline Malignancy NCIT:C7435 Pulmonary Precancerous Condition NCIT:C28620 Pulmonary Proliferative Lesions of the Mouse NCIT:C43277 Pure Cutaneous Mastocytosis @@ -7170,6 +7399,7 @@ NCIT:C93125 Radiation-Related Sarcoma NCIT:C134573 Rainbow Trout Hepatoma NCIT:C136977 Rainbow Trout Mesothelioma NCIT:C192672 Rare Malignant Solid Neoplasm +NCIT:C7201 Rare Neoplasm NCIT:C63820 Rat Acanthomatous Ameloblastoma NCIT:C60318 Rat Acinar Cell Adenocarcinoma NCIT:C60319 Rat Acinar Cell Adenoma @@ -7440,6 +7670,7 @@ NCIT:C188079 Rectal Epithelioid Cell Melanoma NCIT:C193420 Rectal Gastrointestinal Stromal Tumor NCIT:C176697 Rectal Large Cell Neuroendocrine Carcinoma NCIT:C96493 Rectal Micropapillary Adenocarcinoma +NCIT:C203385 Rectal Neuroendocrine Carcinoma NCIT:C160451 Rectal Neuroendocrine Tumor G2 NCIT:C172703 Rectal Neuroendocrine Tumor G3 NCIT:C135527 Rectal Neuroendocrine Tumor by AJCC v8 Stage @@ -7530,6 +7761,7 @@ NCIT:C179174 Recurrent Appendix Adenocarcinoma NCIT:C153802 Recurrent Appendix Carcinoma NCIT:C153579 Recurrent Appendix Mucinous Adenocarcinoma NCIT:C27900 Recurrent Askin Tumor +NCIT:C203274 Recurrent Astrocytic Tumor NCIT:C188127 Recurrent Astrocytoma, IDH-Mutant NCIT:C191197 Recurrent Astrocytoma, IDH-Mutant, Grade 3 NCIT:C182018 Recurrent Astrocytoma, IDH-Mutant, Grade 4 @@ -7541,6 +7773,7 @@ NCIT:C177895 Recurrent B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); NCIT:C134834 Recurrent B Acute Lymphoblastic Leukemia, BCR-ABL1-Like NCIT:C189042 Recurrent B Acute Lymphoblastic Leukemia, Philadelphia Chromosome Negative NCIT:C8869 Recurrent B Lymphoblastic Lymphoma +NCIT:C204124 Recurrent B-Cell Malignant Neoplasm NCIT:C8841 Recurrent B-Cell Non-Hodgkin Lymphoma NCIT:C158081 Recurrent B-Cell Prolymphocytic Leukemia NCIT:C148025 Recurrent BRCA- Associated Ovarian Carcinoma @@ -7549,6 +7782,7 @@ NCIT:C153360 Recurrent Bile Duct Carcinoma NCIT:C156782 Recurrent Biliary Tract Carcinoma NCIT:C4995 Recurrent Bladder Adenocarcinoma NCIT:C7899 Recurrent Bladder Carcinoma +NCIT:C203815 Recurrent Bladder Non-Invasive Papillary Urothelial Carcinoma, Low Grade NCIT:C191860 Recurrent Bladder Small Cell Neuroendocrine Carcinoma NCIT:C8902 Recurrent Bladder Squamous Cell Carcinoma NCIT:C126307 Recurrent Bladder Urothelial Carcinoma @@ -7561,16 +7795,22 @@ NCIT:C153568 Recurrent Breast Acinic Cell Carcinoma NCIT:C175588 Recurrent Breast Adenocarcinoma NCIT:C133092 Recurrent Breast Angiosarcoma NCIT:C7771 Recurrent Breast Carcinoma +NCIT:C203339 Recurrent Breast Ductal Carcinoma In Situ NCIT:C176680 Recurrent Breast Implant-Associated Anaplastic Large Cell Lymphoma NCIT:C8607 Recurrent Breast Inflammatory Carcinoma NCIT:C138023 Recurrent Breast Lymphoma +NCIT:C203341 Recurrent Breast Medullary Carcinoma +NCIT:C203342 Recurrent Breast Mucinous Carcinoma NCIT:C153588 Recurrent Breast Paget Disease +NCIT:C203344 Recurrent Breast Papillary Carcinoma NCIT:C170727 Recurrent Breast Sarcoma +NCIT:C203362 Recurrent Breast Tubular Carcinoma NCIT:C180923 Recurrent Bronchogenic Carcinoma NCIT:C151976 Recurrent Burkitt Leukemia NCIT:C5008 Recurrent Burkitt Lymphoma NCIT:C7619 Recurrent Carcinoma NCIT:C9181 Recurrent Carcinoma of Unknown Primary +NCIT:C205238 Recurrent Castration-Sensitive Prostate Carcinoma NCIT:C138019 Recurrent Central Nervous System Lymphoma NCIT:C146990 Recurrent Central Nervous System Non-Hodgkin Lymphoma NCIT:C8926 Recurrent Centroblastic Lymphoma @@ -7661,12 +7901,15 @@ NCIT:C155875 Recurrent Desmoid Fibromatosis NCIT:C158426 Recurrent Desmoplastic Small Round Cell Tumor NCIT:C165611 Recurrent Differentiated Thyroid Gland Carcinoma NCIT:C167081 Recurrent Diffuse Astrocytoma +NCIT:C203285 Recurrent Diffuse Glioma +NCIT:C203273 Recurrent Diffuse Hemispheric Glioma, H3 G34-Mutant NCIT:C136518 Recurrent Diffuse Intrinsic Pontine Glioma NCIT:C8852 Recurrent Diffuse Large B-Cell Lymphoma NCIT:C160231 Recurrent Diffuse Large B-Cell Lymphoma Activated B-Cell Type NCIT:C183140 Recurrent Diffuse Large B-Cell Lymphoma Associated with Chronic Inflammation NCIT:C160230 Recurrent Diffuse Large B-Cell Lymphoma Germinal Center B-Cell Type NCIT:C165240 Recurrent Diffuse Large B-Cell Lymphoma, Not Otherwise Specified +NCIT:C203267 Recurrent Diffuse Midline Glioma NCIT:C179222 Recurrent Diffuse Midline Glioma, H3 K27M-Mutant NCIT:C7622 Recurrent Digestive System Carcinoma NCIT:C155938 Recurrent Digestive System Neuroendocrine Carcinoma @@ -7685,6 +7928,8 @@ NCIT:C150094 Recurrent Endometrial Carcinoma NCIT:C155816 Recurrent Endometrial Clear Cell Adenocarcinoma NCIT:C165282 Recurrent Endometrial Dedifferentiated Carcinoma NCIT:C150097 Recurrent Endometrial Endometrioid Adenocarcinoma +NCIT:C199156 Recurrent Endometrial High Grade Endometrioid Adenocarcinoma +NCIT:C199153 Recurrent Endometrial Low Grade Endometrioid Adenocarcinoma NCIT:C155819 Recurrent Endometrial Mixed Cell Adenocarcinoma NCIT:C165291 Recurrent Endometrial Mucinous Adenocarcinoma NCIT:C132294 Recurrent Endometrial Serous Adenocarcinoma @@ -7749,6 +7994,7 @@ NCIT:C126306 Recurrent Glioblastoma NCIT:C182019 Recurrent Glioblastoma, IDH-Wildtype NCIT:C132506 Recurrent Glioma NCIT:C179221 Recurrent Gliomatosis Cerebri +NCIT:C203302 Recurrent Glioneuronal and Neuronal Tumors NCIT:C131209 Recurrent Gliosarcoma NCIT:C8155 Recurrent Grade 1 Follicular Lymphoma NCIT:C8156 Recurrent Grade 2 Follicular Lymphoma @@ -7761,6 +8007,7 @@ NCIT:C69144 Recurrent Grade III Lymphomatoid Granulomatosis NCIT:C138013 Recurrent Gray-Zone Lymphoma NCIT:C168783 Recurrent HER2-Negative Breast Carcinoma NCIT:C182108 Recurrent HER2-Positive Breast Carcinoma +NCIT:C202986 Recurrent HHV8-Positive Diffuse Large B-Cell Lymphoma, Not Otherwise Specified NCIT:C157685 Recurrent HIV-Related Lymphoproliferative Disorder NCIT:C142882 Recurrent Hairy Cell Leukemia NCIT:C171065 Recurrent Hairy Cell Leukemia Variant @@ -7777,9 +8024,7 @@ NCIT:C151980 Recurrent High Grade B-Cell Lymphoma with MYC and BCL2 or BCL6 Rear NCIT:C162451 Recurrent High Grade B-Cell Lymphoma with MYC, BCL2, and BCL6 Rearrangements NCIT:C188788 Recurrent High Grade B-Cell Lymphoma, Not Otherwise Specified NCIT:C5004 Recurrent High Grade Burkitt-Like Lymphoma -NCIT:C199156 Recurrent High Grade Endometrial Endometrioid Adenocarcinoma NCIT:C199152 Recurrent High Grade Endometrioid Adenocarcinoma -NCIT:C199168 Recurrent High Grade Ovarian Endometrioid Adenocarcinoma NCIT:C134172 Recurrent Histiocytic and Dendritic Cell Neoplasm NCIT:C4937 Recurrent Hodgkin Lymphoma NCIT:C8828 Recurrent Hodgkin's Disease Lymphocyte Predominance Type @@ -7819,11 +8064,9 @@ NCIT:C7110 Recurrent Liver Carcinoma NCIT:C153584 Recurrent Lobular Breast Carcinoma NCIT:C8153 Recurrent Low Grade Adult Non-Hodgkin's Lymphoma NCIT:C176464 Recurrent Low Grade Astrocytoma -NCIT:C199153 Recurrent Low Grade Endometrial Endometrioid Adenocarcinoma NCIT:C199150 Recurrent Low Grade Endometrioid Adenocarcinoma NCIT:C156456 Recurrent Low Grade Fallopian Tube Serous Adenocarcinoma NCIT:C177794 Recurrent Low Grade Glioma -NCIT:C199167 Recurrent Low Grade Ovarian Endometrioid Adenocarcinoma NCIT:C8757 Recurrent Lung Adenocarcinoma NCIT:C8747 Recurrent Lung Adenosquamous Carcinoma NCIT:C8953 Recurrent Lung Carcinoma @@ -7977,7 +8220,9 @@ NCIT:C153618 Recurrent Ovarian Clear Cell Adenocarcinoma NCIT:C153617 Recurrent Ovarian Cystadenocarcinoma NCIT:C150095 Recurrent Ovarian Endometrioid Adenocarcinoma NCIT:C8087 Recurrent Ovarian Germ Cell Tumor +NCIT:C199168 Recurrent Ovarian High Grade Endometrioid Adenocarcinoma NCIT:C165262 Recurrent Ovarian High Grade Serous Adenocarcinoma +NCIT:C199167 Recurrent Ovarian Low Grade Endometrioid Adenocarcinoma NCIT:C156455 Recurrent Ovarian Low Grade Serous Adenocarcinoma NCIT:C153616 Recurrent Ovarian Mucinous Adenocarcinoma NCIT:C178669 Recurrent Ovarian Seromucinous Carcinoma @@ -8016,9 +8261,12 @@ NCIT:C193433 Recurrent Plasma Cell Leukemia NCIT:C172289 Recurrent Plasma Cell Neoplasm NCIT:C157683 Recurrent Plasmablastic Lymphoma NCIT:C170750 Recurrent Platinum-Resistant Fallopian Tube Carcinoma +NCIT:C204984 Recurrent Platinum-Resistant Fallopian Tube High Grade Serous Adenocarcinoma NCIT:C170748 Recurrent Platinum-Resistant Ovarian Carcinoma NCIT:C200719 Recurrent Platinum-Resistant Ovarian High Grade Serous Adenocarcinoma NCIT:C170751 Recurrent Platinum-Resistant Primary Peritoneal Carcinoma +NCIT:C204986 Recurrent Platinum-Resistant Primary Peritoneal High Grade Serous Adenocarcinoma +NCIT:C205188 Recurrent Platinum-Sensitive Endometrial Carcinoma NCIT:C191395 Recurrent Platinum-Sensitive Fallopian Tube Carcinoma NCIT:C188391 Recurrent Platinum-Sensitive Ovarian Carcinoma NCIT:C191407 Recurrent Platinum-Sensitive Primary Peritoneal Carcinoma @@ -8031,6 +8279,7 @@ NCIT:C157681 Recurrent Primary Bone Lymphoma NCIT:C71700 Recurrent Primary Central Nervous System Neoplasm NCIT:C181044 Recurrent Primary Cutaneous Anaplastic Large Cell Lymphoma NCIT:C191823 Recurrent Primary Cutaneous CD8-Positive Aggressive Epidermotropic Cytotoxic T-Cell Lymphoma +NCIT:C203667 Recurrent Primary Cutaneous Diffuse Large B-Cell Lymphoma NCIT:C138027 Recurrent Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type NCIT:C191818 Recurrent Primary Cutaneous Gamma-Delta T-Cell Lymphoma NCIT:C142876 Recurrent Primary Cutaneous Lymphoma @@ -8074,6 +8323,7 @@ NCIT:C153611 Recurrent Salivary Duct Carcinoma NCIT:C199666 Recurrent Salivary Gland Adenocarcinoma NCIT:C199663 Recurrent Salivary Gland Adenocarcinoma, Not Otherwise Specified NCIT:C7926 Recurrent Salivary Gland Carcinoma +NCIT:C203381 Recurrent Salivary Gland Mucoepidermoid Carcinoma NCIT:C172650 Recurrent Salivary Gland Squamous Cell Carcinoma NCIT:C148302 Recurrent Sarcoma NCIT:C155648 Recurrent Sarcoma of the Extremity @@ -8207,6 +8457,7 @@ NCIT:C179429 Refractory B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2) NCIT:C134835 Refractory B Acute Lymphoblastic Leukemia, BCR-ABL1-Like NCIT:C189043 Refractory B Acute Lymphoblastic Leukemia, Philadelphia Chromosome Negative NCIT:C8870 Refractory B Lymphoblastic Lymphoma +NCIT:C204126 Refractory B-Cell Malignant Neoplasm NCIT:C8842 Refractory B-Cell Non-Hodgkin Lymphoma NCIT:C157697 Refractory B-Cell Prolymphocytic Leukemia NCIT:C199640 Refractory Basal Cell Carcinoma @@ -8343,6 +8594,7 @@ NCIT:C172318 Refractory Grade 3b Follicular Lymphoma NCIT:C138014 Refractory Gray-Zone Lymphoma NCIT:C168784 Refractory HER2-Negative Breast Carcinoma NCIT:C182110 Refractory HER2-Positive Breast Carcinoma +NCIT:C202987 Refractory HHV8-Positive Diffuse Large B-Cell Lymphoma, Not Otherwise Specified NCIT:C157687 Refractory HIV-Related Lymphoproliferative Disorder NCIT:C171064 Refractory Hairy Cell Leukemia Variant NCIT:C151907 Refractory Head and Neck Carcinoma @@ -8369,6 +8621,7 @@ NCIT:C173046 Refractory Indolent Non-Hodgkin Lymphoma NCIT:C183515 Refractory Indolent T-Cell Non-Hodgkin Lymphoma NCIT:C174247 Refractory Intrahepatic Cholangiocarcinoma NCIT:C138026 Refractory Intravascular Large B-Cell Lymphoma +NCIT:C203523 Refractory Juvenile Myelomonocytic Leukemia NCIT:C156474 Refractory Kaposi Sarcoma NCIT:C172623 Refractory Kidney Carcinoma NCIT:C162727 Refractory Kidney Medullary Carcinoma @@ -8393,6 +8646,7 @@ NCIT:C151978 Refractory Lymphoblastic Lymphoma NCIT:C8650 Refractory Lymphocyte-Depleted Classic Hodgkin Lymphoma NCIT:C142982 Refractory Lymphocyte-Rich Classic Hodgkin Lymphoma NCIT:C134154 Refractory Lymphoma +NCIT:C202989 Refractory Lymphomatoid Granulomatosis NCIT:C8652 Refractory Lymphoplasmacytic Lymphoma NCIT:C157686 Refractory Lymphoproliferative Disorder NCIT:C177149 Refractory Male Reproductive System Carcinoma @@ -8470,6 +8724,7 @@ NCIT:C7260 Refractory Nodular Lymphocyte Predominant B-Cell Lymphoma NCIT:C8838 Refractory Nodular Sclerosis Classic Hodgkin Lymphoma NCIT:C173328 Refractory Non-Cutaneous Melanoma NCIT:C8701 Refractory Non-Hodgkin Lymphoma +NCIT:C202899 Refractory Non-Muscle Invasive Bladder Carcinoma NCIT:C180530 Refractory Non-Muscle Invasive Bladder Urothelial Carcinoma NCIT:C173329 Refractory Ocular Melanoma NCIT:C148384 Refractory Oral Cavity Squamous Cell Carcinoma @@ -8509,6 +8764,7 @@ NCIT:C157682 Refractory Primary Bone Lymphoma NCIT:C71701 Refractory Primary Central Nervous System Neoplasm NCIT:C181045 Refractory Primary Cutaneous Anaplastic Large Cell Lymphoma NCIT:C191824 Refractory Primary Cutaneous CD8-Positive Aggressive Epidermotropic Cytotoxic T-Cell Lymphoma +NCIT:C203669 Refractory Primary Cutaneous Diffuse Large B-Cell Lymphoma NCIT:C138028 Refractory Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type NCIT:C191820 Refractory Primary Cutaneous Gamma-Delta T-Cell Lymphoma NCIT:C142877 Refractory Primary Cutaneous Lymphoma @@ -8607,6 +8863,7 @@ NCIT:C185304 Refractory Vulvar Squamous Cell Carcinoma NCIT:C177798 Refractory WHO Grade 1 Glioma NCIT:C158104 Refractory WHO Grade 2 Glioma NCIT:C153865 Refractory WHO Grade 3 Glioma +NCIT:C203369 Refractory WHO Grade 4 Glioma NCIT:C142149 Refractory Waldenstrom Macroglobulinemia NCIT:C188038 Refractory Wilms Tumor NCIT:C5402 Region 17p13 Allelic Loss Associated Medulloblastoma @@ -8615,8 +8872,6 @@ NCIT:C198439 Regional Childhood Ovarian Germ Cell Tumor by Toronto Guidelines v2 NCIT:C198177 Regional Childhood Retinoblastoma by Toronto Guidelines v2 NCIT:C198416 Regional Childhood Testicular Germ Cell Tumor by Toronto Guidelines v2 NCIT:C7862 Regional Digestive System Neuroendocrine Tumor G1 -NCIT:C8716 Regional Malignant Ureter Neoplasm -NCIT:C7639 Regional Malignant Urethral Neoplasm NCIT:C7836 Regional Neuroblastoma NCIT:C8168 Regional Renal Pelvis and Ureter Urothelial Carcinoma NCIT:C162139 Regressed Testicular Germ Cell Tumor @@ -8653,7 +8908,9 @@ NCIT:C188032 Resectable Bladder Urothelial Carcinoma NCIT:C188035 Resectable Breast Carcinoma NCIT:C150604 Resectable Carcinoma NCIT:C170961 Resectable Carcinoma of Unknown Primary +NCIT:C205308 Resectable Cervical Carcinoma NCIT:C27326 Resectable Cholangiocarcinoma +NCIT:C205309 Resectable Clear Cell Renal Cell Carcinoma NCIT:C167237 Resectable Colon Carcinoma NCIT:C162257 Resectable Colorectal Carcinoma NCIT:C190240 Resectable Cutaneous Melanoma @@ -8661,7 +8918,9 @@ NCIT:C162943 Resectable Cutaneous Squamous Cell Carcinoma of the Head and Neck NCIT:C150607 Resectable Dedifferentiated Liposarcoma NCIT:C156909 Resectable Digestive System Carcinoma NCIT:C27323 Resectable Duodenal Carcinoma +NCIT:C205310 Resectable Endometrial Carcinoma NCIT:C198615 Resectable Esophageal Adenocarcinoma +NCIT:C205311 Resectable Esophageal Carcinoma NCIT:C156911 Resectable Extrahepatic Bile Duct Adenocarcinoma NCIT:C8640 Resectable Extrahepatic Bile Duct Carcinoma NCIT:C198617 Resectable Gallbladder Adenocarcinoma @@ -8675,7 +8934,7 @@ NCIT:C7691 Resectable Hepatocellular Carcinoma NCIT:C156908 Resectable Intrahepatic Cholangiocarcinoma NCIT:C175505 Resectable Leiomyosarcoma NCIT:C150606 Resectable Liposarcoma -NCIT:C165293 Resectable Liver and Intrahepatic Bile Duct Carcinoma +NCIT:C165293 Resectable Liver Carcinoma NCIT:C190954 Resectable Lung Adenocarcinoma NCIT:C190952 Resectable Lung Carcinoma NCIT:C165767 Resectable Lung Non-Small Cell Carcinoma @@ -8685,6 +8944,7 @@ NCIT:C170963 Resectable Malignant Female Reproductive System Neoplasm NCIT:C7692 Resectable Malignant Liver Neoplasm NCIT:C154442 Resectable Malignant Mesothelioma NCIT:C150602 Resectable Malignant Neoplasm +NCIT:C205313 Resectable Malignant Solid Neoplasm NCIT:C190239 Resectable Melanoma NCIT:C193450 Resectable Merkel Cell Carcinoma NCIT:C150620 Resectable Neuroblastoma @@ -8706,6 +8966,8 @@ NCIT:C170465 Resectable Skin Carcinoma NCIT:C170464 Resectable Skin Squamous Cell Carcinoma NCIT:C8639 Resectable Small Intestinal Carcinoma NCIT:C153086 Resectable Soft Tissue Sarcoma +NCIT:C201952 Resectable Soft Tissue Sarcoma of the Trunk and Extremities +NCIT:C205314 Resectable Triple-Negative Breast Carcinoma NCIT:C150611 Resectable Undifferentiated Pleomorphic Sarcoma NCIT:C26959 Reticulosarcoma Involving Spleen NCIT:C174539 Retinal Astrocytoma @@ -8728,6 +8990,7 @@ NCIT:C24161 Rhabdomyosarcoma of the Mouse Gallbladder NCIT:C22040 Rhabdomyosarcoma of the Mouse Nervous System NCIT:C21750 Rhabdomyosarcoma of the Mouse Prostate Gland NCIT:C21845 Rhabdomyosarcoma of the Mouse Skin +NCIT:C202263 Rhabdomyosarcoma with TFCP2 Rearrangement NCIT:C134783 Rhesus Monkey Lymphoma NCIT:C134784 Rhesus Monkey Mammary Tumor NCIT:C4792 Right Atrial Myxoma @@ -8741,8 +9004,12 @@ NCIT:C178462 Round Cell Sarcoma with FUS-NFATC2 Gene Fusion NCIT:C168746 SAMD9-Associated Hereditary Myelodysplastic Syndrome NCIT:C168747 SAMD9L-Associated Hereditary Myelodysplastic Syndrome NCIT:C21880 SJL Disease of the Mouse Hematologic System +NCIT:C201637 SMARCA4 -Deficient Sinonasal Carcinoma NCIT:C186703 SMARCB1 Schwannomatosis 1 +NCIT:C201636 SMARCB1-Deficient Sinonasal Adenocarcinoma +NCIT:C201635 SMARCB1-Deficient Sinonasal Carcinoma NCIT:C187445 ST2 Diffuse Large B-Cell Lymphoma +NCIT:C201634 SWI/SNF Complex-Deficient Sinonasal Carcinoma NCIT:C129927 Sacral Chordoma NCIT:C168674 Sacral Spine Neoplasm NCIT:C8021 Salivary Gland Adenocarcinoma @@ -8757,15 +9024,27 @@ NCIT:C173717 Salivary Gland Diffuse Large B-Cell Lymphoma NCIT:C35839 Salivary Gland Ductal Papilloma NCIT:C173715 Salivary Gland Follicular Lymphoma NCIT:C173680 Salivary Gland Hemangioma +NCIT:C203370 Salivary Gland High Grade Adenocarcinoma, Not Otherwise Specified +NCIT:C8018 Salivary Gland High Grade Carcinoma +NCIT:C8019 Salivary Gland High Grade Mucoepidermoid Carcinoma NCIT:C173692 Salivary Gland Hodgkin Lymphoma +NCIT:C201823 Salivary Gland Hyalinizing Clear Cell Carcinoma +NCIT:C201764 Salivary Gland Intercalated Duct Adenoma +NCIT:C203375 Salivary Gland Intermediate Grade Adenocarcinoma, Not Otherwise Specified +NCIT:C8017 Salivary Gland Intermediate Grade Mucoepidermoid Carcinoma +NCIT:C203376 Salivary Gland Intestinal-Type Adenocarcinoma NCIT:C62192 Salivary Gland Intraductal Carcinoma NCIT:C35834 Salivary Gland Intraductal Papilloma NCIT:C35835 Salivary Gland Inverted Ductal Papilloma NCIT:C173650 Salivary Gland Large Cell Neuroendocrine Carcinoma NCIT:C173681 Salivary Gland Lipoma +NCIT:C203374 Salivary Gland Low Grade Adenocarcinoma, Not Otherwise Specified +NCIT:C8012 Salivary Gland Low Grade Carcinoma +NCIT:C8015 Salivary Gland Low Grade Mucoepidermoid Carcinoma NCIT:C173659 Salivary Gland Lymphadenoma NCIT:C35736 Salivary Gland Lymphoepithelial Carcinoma NCIT:C173690 Salivary Gland Lymphoma +NCIT:C201772 Salivary Gland Microsecretory Adenocarcinoma NCIT:C3686 Salivary Gland Monomorphic Adenoma NCIT:C62193 Salivary Gland Mucinous Adenocarcinoma NCIT:C173693 Salivary Gland Mucosa-Associated Lymphoid Tissue Lymphoma @@ -8775,10 +9054,12 @@ NCIT:C5978 Salivary Gland Myoepithelioma NCIT:C173653 Salivary Gland Neuroendocrine Carcinoma NCIT:C173687 Salivary Gland Nodular Fasciitis NCIT:C173691 Salivary Gland Non-Hodgkin Lymphoma -NCIT:C62194 Salivary Gland Oncocytic Carcinoma +NCIT:C62194 Salivary Gland Oncocytic Adenocarcinoma NCIT:C5932 Salivary Gland Oncocytoma NCIT:C40409 Salivary Gland Pleomorphic Adenoma NCIT:C35702 Salivary Gland Polymorphous Adenocarcinoma +NCIT:C201781 Salivary Gland Polymorphous Adenocarcinoma, Conventional Subtype +NCIT:C201786 Salivary Gland Polymorphous Adenocarcinoma, Cribriform Subtype NCIT:C173649 Salivary Gland Poorly Differentiated Carcinoma NCIT:C8022 Salivary Gland Poorly Differentiated Squamous Cell Carcinoma NCIT:C35738 Salivary Gland Sebaceous Adenoma @@ -8788,11 +9069,14 @@ NCIT:C123384 Salivary Gland Secretory Carcinoma NCIT:C35836 Salivary Gland Sialadenoma Papilliferum NCIT:C200313 Salivary Gland Striated Duct Adenoma NCIT:C8024 Salivary Gland Undifferentiated Carcinoma +NCIT:C9024 Sarcoma G1 +NCIT:C9028 Sarcoma G2 +NCIT:C9029 Sarcoma G3 +NCIT:C203583 Sarcoma GX NCIT:C9388 Sarcoma NCI Grade 1 NCIT:C9400 Sarcoma NCI Grade 2 NCIT:C9415 Sarcoma NCI Grade 3 NCIT:C21753 Sarcoma NOS of the Mouse Prostate Gland -NCIT:C9416 Sarcoma by AJCC Grade NCIT:C9023 Sarcoma by FNCLCC Grade NCIT:C9387 Sarcoma by NCI Grade NCIT:C155647 Sarcoma of the Extremity @@ -8805,10 +9089,11 @@ NCIT:C39833 Schistosoma Hematobium-Related Bladder Verrucous Carcinoma NCIT:C21836 Schwannoma of the Mouse Skin NCIT:C188213 Schwannoma of the Seventh Cranial Nerve NCIT:C200533 Sclerosing Angiomatoid Nodular Transformation of Spleen +NCIT:C204911 Sclerosing Blue Nevus NCIT:C49027 Sclerosing Epithelioid Fibrosarcoma NCIT:C173733 Sclerosing Odontogenic Carcinoma NCIT:C121790 Sclerosing PEComa -NCIT:C97135 Sclerosing Polycystic Adenosis +NCIT:C97135 Sclerosing Polycystic Adenoma NCIT:C121655 Sclerosing Rhabdomyosarcoma NCIT:C45709 Sclerosing Thymoma NCIT:C156282 Scrotal Liposarcoma @@ -8894,7 +9179,9 @@ NCIT:C165546 Shared Neoantigen-Positive Malignant Solid Neoplasm NCIT:C35837 Sialoblastoma NCIT:C173682 Sialolipoma NCIT:C177680 Sigmoid Colon Carcinoma +NCIT:C203389 Sigmoid Colon Neuroendocrine Tumor NCIT:C188043 Sigmoid Colon Neuroendocrine Tumor G1 +NCIT:C203394 Sigmoid Colon Neuroendocrine Tumor G2 NCIT:C22156 Signet Ring Cell Adenocarcinoma of the Mouse Intestinal Tract NCIT:C63891 Signet Ring Cell Adenocarcinoma of the Rat Glandular Stomach NCIT:C167369 Signet Ring Cell/Histiocytoid Carcinoma @@ -8919,13 +9206,14 @@ NCIT:C133074 Sinonasal Cancer by AJCC v8 Stage NCIT:C173133 Sinonasal Desmoid Fibromatosis NCIT:C27647 Sinonasal Disorder NCIT:C173138 Sinonasal Epithelioid Hemangioendothelioma -NCIT:C173175 Sinonasal Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor +NCIT:C173175 Sinonasal Ewing Sarcoma NCIT:C164251 Sinonasal Exophytic Papilloma NCIT:C173172 Sinonasal Extranodal NK/T-Cell Lymphoma NCIT:C173120 Sinonasal Fibrosarcoma +NCIT:C202978 Sinonasal Germ Cell Tumor NCIT:C173136 Sinonasal Glomangiopericytoma NCIT:C173142 Sinonasal Hemangioma -NCIT:C173078 Sinonasal Human Papillomavirus-Related Carcinoma with Adenoid Cystic-Like Features +NCIT:C173078 Sinonasal Human Papillomavirus-Related Multiphenotypic Carcinoma NCIT:C6871 Sinonasal Inverted Papilloma NCIT:C173077 Sinonasal Keratinizing Squamous Cell Carcinoma NCIT:C173091 Sinonasal Large Cell Neuroendocrine Carcinoma @@ -8937,6 +9225,10 @@ NCIT:C173127 Sinonasal Malignant Peripheral Nerve Sheath Tumor NCIT:C166399 Sinonasal Mucosal Melanoma NCIT:C173088 Sinonasal NUT Carcinoma NCIT:C173089 Sinonasal Neuroendocrine Carcinoma +NCIT:C202990 Sinonasal Neuroendocrine Neoplasm +NCIT:C202991 Sinonasal Neuroendocrine Tumor +NCIT:C203007 Sinonasal Neuroendocrine Tumor G1 +NCIT:C203010 Sinonasal Neuroendocrine Tumor G2 NCIT:C173144 Sinonasal Neurofibroma NCIT:C173171 Sinonasal Non-Hodgkin Lymphoma NCIT:C173174 Sinonasal Olfactory Neuroblastoma @@ -8949,11 +9241,13 @@ NCIT:C173124 Sinonasal Rhabdomyosarcoma NCIT:C173118 Sinonasal Sarcoma NCIT:C173143 Sinonasal Schwannoma NCIT:C116318 Sinonasal Small Cell Neuroendocrine Carcinoma +NCIT:C202852 Sinonasal Smooth Muscle Tumor of Uncertain Malignant Potential NCIT:C173117 Sinonasal Soft Tissue Neoplasm NCIT:C173137 Sinonasal Solitary Fibrous Tumor -NCIT:C173079 Sinonasal Spindle Cell Squamous Cell Carcinoma +NCIT:C173079 Sinonasal Spindle Cell Squamous Carcinoma NCIT:C173128 Sinonasal Synovial Sarcoma NCIT:C173094 Sinonasal Teratocarcinosarcoma +NCIT:C202981 Sinonasal Teratoma NCIT:C190160 Sinonasal Tract Myxoma NCIT:C173121 Sinonasal Undifferentiated Pleomorphic Sarcoma NCIT:C21873 Sinus Histiocytosis of Mouse @@ -8980,12 +9274,13 @@ NCIT:C3550 Skin Kaposi Sarcoma NCIT:C54665 Skin Keratotic Basal Cell Carcinoma NCIT:C5566 Skin Lipomatous Neoplasm NCIT:C4370 Skin Lymphangioleiomyomatosis -NCIT:C165467 Skin Lymphoepithelioma-Like Carcinoma +NCIT:C165467 Skin Lymphoepithelial Carcinoma NCIT:C167370 Skin Myoepithelioma NCIT:C172632 Skin Myxofibrosarcoma NCIT:C6578 Skin Myxoma NCIT:C62282 Skin Nodular Basal Cell Carcinoma NCIT:C5616 Skin Nodular Solid Basal Cell Carcinoma +NCIT:C204355 Skin Nodulocystic Basal Cell Carcinoma NCIT:C170476 Skin Pleomorphic Lipoma NCIT:C170473 Skin Pleomorphic Liposarcoma NCIT:C27719 Skin Radiation-Related Angiosarcoma @@ -8995,6 +9290,7 @@ NCIT:C170475 Skin Spindle Cell Lipoma NCIT:C170474 Skin Spindle Cell/Pleomorphic Lipoma NCIT:C165466 Skin Squamous Cell Carcinoma with Osteoclast-Like Giant Cells NCIT:C165468 Skin Squamous Cell Carcinoma with Sarcomatoid Differentiation +NCIT:C205551 Skin Syncytial Myoepithelioma NCIT:C5354 Skin Vascular Neoplasm NCIT:C165465 Skin Verrucous Carcinoma NCIT:C192732 Skull Base Carcinoma @@ -9058,6 +9354,7 @@ NCIT:C188041 Smoldering Systemic Mastocytosis with an Associated Myeloid Neoplas NCIT:C155910 Smoldering Waldenstrom Macroglobulinemia NCIT:C23105 Smooth Muscle Neoplasms of the Mouse Nose and Paranasal Sinuses NCIT:C23053 Smooth Muscle Neoplasms of the Mouse Oral Cavity +NCIT:C202851 Smooth Muscle Tumor of Uncertain Malignant Potential NCIT:C6210 Soft Palate Benign Granular Cell Tumor NCIT:C6211 Soft Palate Pleomorphic Adenoma NCIT:C4941 Soft Palate Squamous Cell Carcinoma @@ -9077,6 +9374,7 @@ NCIT:C21764 Solid Adenoma of the Mouse Pulmonary System NCIT:C27493 Solid Alveolar Rhabdomyosarcoma NCIT:C49110 Solid Angioleiomyoma NCIT:C4137 Solid Carcinoma +NCIT:C205539 Solid Cystic Hidradenoma NCIT:C51133 Solid Glomus Tumor NCIT:C5651 Solid Lung Adenocarcinoma NCIT:C21685 Solid Mammary Carcinoma of Mouse @@ -9084,7 +9382,6 @@ NCIT:C21674 Solid Mouse MIN NOS NCIT:C9292 Solid Neoplasm NCIT:C201136 Solid Pseudopapillary Neoplasm NCIT:C165261 Solid Pseudopapillary Neoplasm of the Ovary -NCIT:C39755 Solid/Multicystic Ameloblastoma NCIT:C46095 Solid/Trabecular Variant Thyroid Gland Papillary Carcinoma NCIT:C5394 Solitary Adult Fibroma NCIT:C121681 Solitary Circumscribed Neuroma @@ -9097,6 +9394,7 @@ NCIT:C154340 Sparsely Granulated Corticotroph Pituitary Neuroendocrine Tumor NCIT:C45932 Sparsely Granulated Lactotroph Pituitary Neuroendocrine Tumor NCIT:C45926 Sparsely Granulated Somatotroph Pituitary Neuroendocrine Tumor NCIT:C186494 Spinal Cord Ependymoma, MYCN Amplified +NCIT:C201976 Spinal Cord Pilocytic Astrocytoma NCIT:C155948 Spinal Hemangioblastoma NCIT:C168693 Spinal Neoplasm NCIT:C21745 Spindle Cell / Sarcomatoid Carcinoma of the Mouse Prostate Gland @@ -9113,7 +9411,9 @@ NCIT:C21810 Spindle-cell Squamous Cell Carcinoma of the Mouse Skin NCIT:C167344 Spiradenocylindrocarcinoma NCIT:C167342 Spiradenocylindroma NCIT:C21820 Spiradenoma Type of Basaloid Follicular Neoplasm of the Mouse Skin +NCIT:C136825 Spitz Melanocytoma NCIT:C165497 Spitz Melanoma +NCIT:C204790 Spitz Tumor NCIT:C7310 Splenic B Lymphoblastic Lymphoma NCIT:C80308 Splenic B-Cell Lymphoma/Leukemia, Unclassifiable NCIT:C7309 Splenic Burkitt Lymphoma @@ -9269,6 +9569,7 @@ NCIT:C134271 Stage 0 Colon Cancer AJCC v8 NCIT:C8932 Stage 0 Colorectal Cancer AJCC v6 and v7 NCIT:C134182 Stage 0 Colorectal Cancer AJCC v8 NCIT:C8423 Stage 0 Cutaneous Melanoma AJCC v6 and v7 +NCIT:C85887 Stage 0 Cutaneous Merkel Cell Carcinoma AJCC v7 NCIT:C133255 Stage 0 Cutaneous Squamous Cell Carcinoma of the Head and Neck AJCC v8 NCIT:C88027 Stage 0 Digestive System Neuroendocrine Tumor AJCC v7 NCIT:C88089 Stage 0 Distal Bile Duct Cancer AJCC v7 @@ -9299,7 +9600,6 @@ NCIT:C35758 Stage 0 Lung Large Cell Carcinoma AJCC v6 and v7 NCIT:C9104 Stage 0 Lung Non-Small Cell Cancer AJCC v6 and v7 NCIT:C8763 Stage 0 Lung Squamous Cell Carcinoma AJCC v6 and v7 NCIT:C132783 Stage 0 Major Salivary Gland Cancer AJCC v8 -NCIT:C85887 Stage 0 Merkel Cell Carcinoma AJCC v7 NCIT:C6036 Stage 0 Nasopharyngeal Keratinizing Squamous Cell Carcinoma AJCC v6, v7, and v8 NCIT:C6035 Stage 0 Nasopharyngeal Undifferentiated Carcinoma AJCC v6, v7, and v8 NCIT:C6052 Stage 0 Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7 @@ -9419,6 +9719,7 @@ NCIT:C134185 Stage I Colorectal Cancer AJCC v8 NCIT:C135206 Stage I Colorectal Neuroendocrine Tumor AJCC v8 NCIT:C7916 Stage I Cutaneous Melanoma AJCC v6 NCIT:C88414 Stage I Cutaneous Melanoma AJCC v7 +NCIT:C85889 Stage I Cutaneous Merkel Cell Carcinoma AJCC v7 NCIT:C133256 Stage I Cutaneous Squamous Cell Carcinoma of the Head and Neck AJCC v8 NCIT:C7795 Stage I Cutaneous T-Cell Non-Hodgkin Lymphoma NCIT:C101540 Stage I Differentiated Thyroid Gland Carcinoma 45 Years and Older AJCC v7 @@ -9491,7 +9792,6 @@ NCIT:C8764 Stage I Lung Squamous Cell Carcinoma AJCC v7 NCIT:C5895 Stage I Major Salivary Gland Cancer AJCC v7 NCIT:C132781 Stage I Major Salivary Gland Cancer AJCC v8 NCIT:C146849 Stage I Malignant Mediastinal Germ Cell Tumor -NCIT:C85889 Stage I Merkel Cell Carcinoma AJCC v7 NCIT:C7796 Stage I Mycosis Fungoides AJCC v7 NCIT:C88150 Stage I Mycosis Fungoides and Sezary Syndrome AJCC v7 NCIT:C141347 Stage I Mycosis Fungoides and Sezary Syndrome AJCC v8 @@ -9612,6 +9912,7 @@ NCIT:C162227 Stage IA Cervical Cancer FIGO 2018 NCIT:C198043 Stage IA Childhood Hodgkin Lymphoma by Toronto Guidelines v2 NCIT:C198420 Stage IA Childhood Testicular Germ Cell Tumor by Toronto Guidelines v2 NCIT:C86026 Stage IA Cutaneous Melanoma AJCC v7 +NCIT:C85890 Stage IA Cutaneous Merkel Cell Carcinoma AJCC v7 NCIT:C88090 Stage IA Distal Bile Duct Cancer AJCC v7 NCIT:C87782 Stage IA Esophageal Adenocarcinoma AJCC v7 NCIT:C115117 Stage IA Esophageal Cancer AJCC v7 @@ -9634,7 +9935,6 @@ NCIT:C6661 Stage IA Lung Large Cell Carcinoma AJCC v7 NCIT:C5652 Stage IA Lung Non-Small Cell Carcinoma AJCC v7 NCIT:C6674 Stage IA Lung Small Cell Carcinoma AJCC v7 NCIT:C6687 Stage IA Lung Squamous Cell Carcinoma AJCC v7 -NCIT:C85890 Stage IA Merkel Cell Carcinoma AJCC v7 NCIT:C130951 Stage IA Mycosis Fungoides AJCC v7 NCIT:C88151 Stage IA Mycosis Fungoides and Sezary Syndrome AJCC v7 NCIT:C141348 Stage IA Mycosis Fungoides and Sezary Syndrome AJCC v8 @@ -9690,6 +9990,7 @@ NCIT:C162230 Stage IB Cervical Cancer FIGO 2018 NCIT:C198044 Stage IB Childhood Hodgkin Lymphoma by Toronto Guidelines v2 NCIT:C198421 Stage IB Childhood Testicular Germ Cell Tumor by Toronto Guidelines v2 NCIT:C86030 Stage IB Cutaneous Melanoma AJCC v7 +NCIT:C85892 Stage IB Cutaneous Merkel Cell Carcinoma AJCC v7 NCIT:C88091 Stage IB Distal Bile Duct Cancer AJCC v7 NCIT:C87783 Stage IB Esophageal Adenocarcinoma AJCC v7 NCIT:C115118 Stage IB Esophageal Cancer AJCC v7 @@ -9713,7 +10014,6 @@ NCIT:C6662 Stage IB Lung Large Cell Carcinoma AJCC v7 NCIT:C5653 Stage IB Lung Non-Small Cell Carcinoma AJCC v7 NCIT:C6675 Stage IB Lung Small Cell Carcinoma AJCC v7 NCIT:C6692 Stage IB Lung Squamous Cell Carcinoma AJCC v7 -NCIT:C85892 Stage IB Merkel Cell Carcinoma AJCC v7 NCIT:C130237 Stage IB Mycosis Fungoides AJCC v7 NCIT:C88152 Stage IB Mycosis Fungoides and Sezary Syndrome AJCC v7 NCIT:C141349 Stage IB Mycosis Fungoides and Sezary Syndrome AJCC v8 @@ -9819,6 +10119,7 @@ NCIT:C8475 Stage II Contiguous Adult Diffuse Large Cell Lymphoma NCIT:C8474 Stage II Contiguous Adult Diffuse Mixed Cell Lymphoma NCIT:C8471 Stage II Contiguous Adult Diffuse Small Cleaved Cell Lymphoma NCIT:C7917 Stage II Cutaneous Melanoma AJCC v6 and v7 +NCIT:C85893 Stage II Cutaneous Merkel Cell Carcinoma AJCC v7 NCIT:C133257 Stage II Cutaneous Squamous Cell Carcinoma of the Head and Neck AJCC v8 NCIT:C7797 Stage II Cutaneous T-Cell Non-Hodgkin Lymphoma NCIT:C101542 Stage II Differentiated Thyroid Gland Carcinoma 45 Years and Older AJCC v7 @@ -9891,7 +10192,6 @@ NCIT:C8765 Stage II Lung Squamous Cell Carcinoma AJCC v7 NCIT:C5896 Stage II Major Salivary Gland Cancer AJCC v7 NCIT:C132785 Stage II Major Salivary Gland Cancer AJCC v8 NCIT:C146850 Stage II Malignant Mediastinal Germ Cell Tumor -NCIT:C85893 Stage II Merkel Cell Carcinoma AJCC v7 NCIT:C7798 Stage II Mycosis Fungoides AJCC v7 NCIT:C88153 Stage II Mycosis Fungoides and Sezary Syndrome AJCC v7 NCIT:C141350 Stage II Mycosis Fungoides and Sezary Syndrome AJCC v8 @@ -10029,6 +10329,7 @@ NCIT:C87813 Stage IIA Colorectal Cancer AJCC v7 NCIT:C134187 Stage IIA Colorectal Cancer AJCC v8 NCIT:C135207 Stage IIA Colorectal Neuroendocrine Tumor AJCC v8 NCIT:C86033 Stage IIA Cutaneous Melanoma AJCC v6 and v7 +NCIT:C85894 Stage IIA Cutaneous Merkel Cell Carcinoma AJCC v7 NCIT:C88029 Stage IIA Digestive System Neuroendocrine Tumor AJCC v7 NCIT:C88092 Stage IIA Distal Bile Duct Cancer AJCC v7 NCIT:C134815 Stage IIA Distal Bile Duct Cancer AJCC v8 @@ -10049,7 +10350,6 @@ NCIT:C6666 Stage IIA Lung Large Cell Carcinoma AJCC v7 NCIT:C5655 Stage IIA Lung Non-Small Cell Carcinoma AJCC v7 NCIT:C6677 Stage IIA Lung Small Cell Carcinoma AJCC v7 NCIT:C6688 Stage IIA Lung Squamous Cell Carcinoma AJCC v7 -NCIT:C85894 Stage IIA Merkel Cell Carcinoma AJCC v7 NCIT:C88154 Stage IIA Mycosis Fungoides and Sezary Syndrome AJCC v7 NCIT:C141351 Stage IIA Mycosis Fungoides and Sezary Syndrome AJCC v8 NCIT:C5998 Stage IIA Nasopharyngeal Carcinoma @@ -10113,6 +10413,7 @@ NCIT:C87814 Stage IIB Colorectal Cancer AJCC v7 NCIT:C134188 Stage IIB Colorectal Cancer AJCC v8 NCIT:C135208 Stage IIB Colorectal Neuroendocrine Tumor AJCC v8 NCIT:C27742 Stage IIB Cutaneous Melanoma AJCC v6 and v7 +NCIT:C85895 Stage IIB Cutaneous Merkel Cell Carcinoma AJCC v7 NCIT:C88030 Stage IIB Digestive System Neuroendocrine Tumor AJCC v7 NCIT:C88093 Stage IIB Distal Bile Duct Cancer AJCC v7 NCIT:C134816 Stage IIB Distal Bile Duct Cancer AJCC v8 @@ -10133,7 +10434,6 @@ NCIT:C6663 Stage IIB Lung Large Cell Carcinoma AJCC v7 NCIT:C5654 Stage IIB Lung Non-Small Cell Carcinoma AJCC v7 NCIT:C6676 Stage IIB Lung Small Cell Carcinoma AJCC v7 NCIT:C6691 Stage IIB Lung Squamous Cell Carcinoma AJCC v7 -NCIT:C85895 Stage IIB Merkel Cell Carcinoma AJCC v7 NCIT:C88155 Stage IIB Mycosis Fungoides and Sezary Syndrome AJCC v7 NCIT:C141352 Stage IIB Mycosis Fungoides and Sezary Syndrome AJCC v8 NCIT:C5999 Stage IIB Nasopharyngeal Carcinoma @@ -10170,8 +10470,8 @@ NCIT:C134282 Stage IIC Colon Cancer AJCC v8 NCIT:C87815 Stage IIC Colorectal Cancer AJCC v7 NCIT:C134190 Stage IIC Colorectal Cancer AJCC v8 NCIT:C86034 Stage IIC Cutaneous Melanoma AJCC v6 and v7 +NCIT:C85896 Stage IIC Cutaneous Merkel Cell Carcinoma AJCC v7 NCIT:C6276 Stage IIC Fallopian Tube Cancer AJCC v6 and v7 -NCIT:C85896 Stage IIC Merkel Cell Carcinoma AJCC v7 NCIT:C5225 Stage IIC Ovarian Cancer AJCC v6 and v7 NCIT:C6294 Stage IIC Ovarian Germ Cell Tumor AJCC v6 and v7 NCIT:C140168 Stage IIC Prostate Cancer AJCC v8 @@ -10235,6 +10535,7 @@ NCIT:C89994 Stage III Colorectal Cancer AJCC v7 NCIT:C134191 Stage III Colorectal Cancer AJCC v8 NCIT:C7918 Stage III Cutaneous Melanoma AJCC v6 NCIT:C88415 Stage III Cutaneous Melanoma AJCC v7 +NCIT:C85897 Stage III Cutaneous Merkel Cell Carcinoma AJCC v7 NCIT:C133258 Stage III Cutaneous Squamous Cell Carcinoma of the Head and Neck AJCC v8 NCIT:C7799 Stage III Cutaneous T-Cell Non-Hodgkin Lymphoma NCIT:C87545 Stage III Differentiated Thyroid Gland Carcinoma AJCC v7 @@ -10305,7 +10606,6 @@ NCIT:C8766 Stage III Lung Squamous Cell Carcinoma AJCC v7 NCIT:C5897 Stage III Major Salivary Gland Cancer AJCC v7 NCIT:C132786 Stage III Major Salivary Gland Cancer AJCC v8 NCIT:C146851 Stage III Malignant Mediastinal Germ Cell Tumor -NCIT:C85897 Stage III Merkel Cell Carcinoma AJCC v7 NCIT:C87532 Stage III Mucosal Melanoma of the Head and Neck AJCC v7 NCIT:C7800 Stage III Mycosis Fungoides AJCC v7 NCIT:C88157 Stage III Mycosis Fungoides and Sezary Syndrome AJCC v7 @@ -10435,6 +10735,7 @@ NCIT:C87816 Stage IIIA Colorectal Cancer AJCC v7 NCIT:C134192 Stage IIIA Colorectal Cancer AJCC v8 NCIT:C135209 Stage IIIA Colorectal Neuroendocrine Tumor AJCC v8 NCIT:C86049 Stage IIIA Cutaneous Melanoma AJCC v7 +NCIT:C85898 Stage IIIA Cutaneous Merkel Cell Carcinoma AJCC v7 NCIT:C88031 Stage IIIA Digestive System Neuroendocrine Tumor AJCC v7 NCIT:C134818 Stage IIIA Distal Bile Duct Cancer AJCC v8 NCIT:C87784 Stage IIIA Esophageal Adenocarcinoma AJCC v7 @@ -10464,7 +10765,6 @@ NCIT:C6665 Stage IIIA Lung Large Cell Carcinoma AJCC v7 NCIT:C9102 Stage IIIA Lung Non-Small Cell Cancer AJCC v7 NCIT:C6680 Stage IIIA Lung Small Cell Carcinoma AJCC v7 NCIT:C6689 Stage IIIA Lung Squamous Cell Carcinoma AJCC v7 -NCIT:C85898 Stage IIIA Merkel Cell Carcinoma AJCC v7 NCIT:C88158 Stage IIIA Mycosis Fungoides and Sezary Syndrome AJCC v7 NCIT:C141354 Stage IIIA Mycosis Fungoides and Sezary Syndrome AJCC v8 NCIT:C6258 Stage IIIA Ovarian Cancer AJCC v6 and v7 @@ -10526,6 +10826,7 @@ NCIT:C87817 Stage IIIB Colorectal Cancer AJCC v7 NCIT:C134193 Stage IIIB Colorectal Cancer AJCC v8 NCIT:C135210 Stage IIIB Colorectal Neuroendocrine Tumor AJCC v8 NCIT:C86051 Stage IIIB Cutaneous Melanoma AJCC v7 +NCIT:C85899 Stage IIIB Cutaneous Merkel Cell Carcinoma AJCC v7 NCIT:C88032 Stage IIIB Digestive System Neuroendocrine Tumor AJCC v7 NCIT:C134819 Stage IIIB Distal Bile Duct Cancer AJCC v8 NCIT:C87785 Stage IIIB Esophageal Adenocarcinoma AJCC v7 @@ -10557,7 +10858,6 @@ NCIT:C6681 Stage IIIB Lung Small Cell Carcinoma AJCC v7 NCIT:C35756 Stage IIIB Lung Small Cell Carcinoma with Pleural Effusion AJCC v7 NCIT:C35757 Stage IIIB Lung Small Cell Carcinoma without Pleural Effusion AJCC v7 NCIT:C6690 Stage IIIB Lung Squamous Cell Carcinoma AJCC v7 -NCIT:C85899 Stage IIIB Merkel Cell Carcinoma AJCC v7 NCIT:C88159 Stage IIIB Mycosis Fungoides and Sezary Syndrome AJCC v7 NCIT:C141355 Stage IIIB Mycosis Fungoides and Sezary Syndrome AJCC v8 NCIT:C6259 Stage IIIB Ovarian Cancer AJCC v6 and v7 @@ -10704,6 +11004,7 @@ NCIT:C89998 Stage IV Colorectal Cancer AJCC v7 NCIT:C134195 Stage IV Colorectal Cancer AJCC v8 NCIT:C135211 Stage IV Colorectal Neuroendocrine Tumor AJCC v8 NCIT:C9096 Stage IV Cutaneous Melanoma AJCC v6 and v7 +NCIT:C85900 Stage IV Cutaneous Merkel Cell Carcinoma AJCC v7 NCIT:C133259 Stage IV Cutaneous Squamous Cell Carcinoma of the Head and Neck AJCC v8 NCIT:C7801 Stage IV Cutaneous T-Cell Non-Hodgkin Lymphoma NCIT:C140973 Stage IV Differentiated Thyroid Gland Carcinoma AJCC v8 @@ -10778,7 +11079,6 @@ NCIT:C132787 Stage IV Major Salivary Gland Cancer AJCC v8 NCIT:C5899 Stage IV Major Salivary Gland Carcinoma with Metastasis NCIT:C5900 Stage IV Major Salivary Gland Carcinoma without Metastasis NCIT:C146852 Stage IV Malignant Mediastinal Germ Cell Tumor -NCIT:C85900 Stage IV Merkel Cell Carcinoma AJCC v7 NCIT:C7802 Stage IV Mycosis Fungoides AJCC v7 NCIT:C88160 Stage IV Mycosis Fungoides and Sezary Syndrome AJCC v7 NCIT:C141356 Stage IV Mycosis Fungoides and Sezary Syndrome AJCC v8 @@ -11179,6 +11479,7 @@ NCIT:C5943 Submandibular Gland Squamous Cell Carcinoma NCIT:C5947 Submandibular Gland Undifferentiated Carcinoma NCIT:C23002 Subtypes of Diffuse Large B Cell Lymphoma of the Mouse Hematologic System NCIT:C121844 Subungual Exostosis +NCIT:C204887 Subungual Melanoma NCIT:C156464 Succinate Dehydrogenase-Deficient Renal Cell Carcinoma NCIT:C134951 Suncus Murinus Mammary Tumor NCIT:C40323 Superficial Angiomyxoma @@ -11203,6 +11504,7 @@ NCIT:C171013 Supratentorial Gliosarcoma NCIT:C7048 Supratentorial Meningioma NCIT:C3397 Supratentorial Neoplasm NCIT:C156041 Supratentorial Pleomorphic Xanthoastrocytoma +NCIT:C202252 Surface Osteoma NCIT:C3682 Sweat Gland Tubular Carcinoma NCIT:C200087 Synchronous Ipsilateral Breast Carcinoma NCIT:C176467 Synovial Chondrosarcoma @@ -11217,6 +11519,14 @@ NCIT:C37196 Systemic Anaplastic Large Cell Lymphoma, ALK-Negative NCIT:C37195 Systemic Anaplastic Large Cell Lymphoma, ALK-Positive NCIT:C199677 Systemic Hydroa Vacciniforme Lymphoproliferative Disorder NCIT:C186735 Systemic Mastocytosis with an Associated Germ Cell Tumor +NCIT:C203434 T Acute Lymphoblastic Leukemia with LMO1 Rearrangement +NCIT:C203435 T Acute Lymphoblastic Leukemia with LMO2 Rearrangement +NCIT:C203469 T Acute Lymphoblastic Leukemia with Recurrent Genetic Abnormalities +NCIT:C203428 T Acute Lymphoblastic Leukemia with SPI1 Rearrangement +NCIT:C203433 T Acute Lymphoblastic Leukemia with TAL1 Rearrangement +NCIT:C203431 T Acute Lymphoblastic Leukemia with TLX1 Rearrangement +NCIT:C203432 T Acute Lymphoblastic Leukemia with TLX3 Rearrangement +NCIT:C203426 T Acute Lymphoblastic Leukemia, HOXA Dysregulated NCIT:C199174 T Acute Lymphoblastic Leukemia, Not Otherwise Specified NCIT:C22999 T Cell Neoplasms of Undetermined Character of the Mouse Hematologic System NCIT:C21923 T Cell Neoplasms of the Mouse Hematologic System @@ -11249,6 +11559,7 @@ NCIT:C140241 Testicular Cancer by AJCC v6 and v7 Stage NCIT:C140225 Testicular Cancer by AJCC v8 Stage NCIT:C192106 Testicular Cystic Trophoblastic Tumor NCIT:C36092 Testicular Dermoid Cyst +NCIT:C162467 Testicular Diffuse Large B-Cell Lymphoma NCIT:C150589 Testicular Follicular Lymphoma NCIT:C40345 Testicular Germ Cell Neoplasia In Situ NCIT:C7326 Testicular Germ Cell Neoplasia In Situ with Extratubular Extension @@ -11301,8 +11612,6 @@ NCIT:C183115 Thoracic SMARCA4-Deficient Undifferentiated Tumor NCIT:C168672 Thoracic Spine Neoplasm NCIT:C35506 Throat Carcinoma NCIT:C183315 Thymic Adenocarcinoma, Not Otherwise Specified -NCIT:C45719 Thymic Atypical Carcinoid Tumor -NCIT:C6430 Thymic Carcinoid Tumor NCIT:C183313 Thymic Carcinoma with Adenoid Cystic Carcinoma-Like Features NCIT:C183316 Thymic Carcinoma, Not Otherwise Specified NCIT:C183314 Thymic Enteric-Type Adenocarcinoma @@ -11311,7 +11620,9 @@ NCIT:C146717 Thymic Hepatoid Adenocarcinoma NCIT:C95057 Thymic Hodgkin Lymphoma NCIT:C45380 Thymic Mucosa-Associated Lymphoid Tissue Lymphoma NCIT:C162460 Thymic Neuroendocrine Neoplasm -NCIT:C45720 Thymic Typical Carcinoid Tumor +NCIT:C6430 Thymic Neuroendocrine Tumor +NCIT:C45720 Thymic Neuroendocrine Tumor G1 +NCIT:C45719 Thymic Neuroendocrine Tumor G2 NCIT:C95038 Thymoliposarcoma NCIT:C136345 Thymoma by AJCC v8 Stage NCIT:C112006 Thymoma by Masaoka-Koga Stage @@ -11383,19 +11694,31 @@ NCIT:C171028 Tongue Adenoid Cystic Carcinoma NCIT:C173807 Tongue Adenosquamous Carcinoma NCIT:C156273 Tongue Alveolar Soft Part Sarcoma' NCIT:C4824 Tongue Carcinoma +NCIT:C201880 Tongue Ectomesenchymal Chondromyxoid Tumor +NCIT:C202898 Tongue GLI1-Altered Soft Tissue Tumor NCIT:C7734 Tongue Lipoma NCIT:C173404 Tongue Liposarcoma +NCIT:C202621 Tongue Low Grade Myofibroblastic Sarcoma NCIT:C181160 Tongue Mucoepidermoid Carcinoma +NCIT:C202861 Tongue Neurofibroma NCIT:C156274 Tongue Sarcoma +NCIT:C202877 Tongue Schwannoma +NCIT:C201878 Tongue Verrucous Carcinoma NCIT:C188072 Tonsillar Diffuse Large B-Cell Lymphoma NCIT:C173797 Tonsillar Disorder NCIT:C188080 Tonsillar Mantle Cell Lymphoma NCIT:C8184 Tonsillar Undifferentiated Carcinoma NCIT:C27755 Topoisomerase II Inhibitor-Related Acute Myeloid Leukemia NCIT:C3688 Trabecular Adenoma +NCIT:C201747 Tracheal Basaloid Squamous Cell Carcinoma +NCIT:C201742 Tracheal Verrucous Carcinoma NCIT:C38458 Traditional Serrated Adenoma NCIT:C179721 Transformed B-Cell Lymphoma, Unclassifiable, with Features Intermediate between Diffuse Large B-Cell Lymphoma and Classic Hodgkin Lymphoma to Diffuse Large B-Cell Lymphoma NCIT:C157624 Transformed Chronic Lymphocytic Leukemia to Diffuse Large B-Cell Lymphoma +NCIT:C201960 Transformed Chronic Lymphocytic Leukemia to Hodgkin Lymphoma +NCIT:C202133 Transformed EGFR-Positive Lung Adenocarcinoma to Small Cell Carcinoma +NCIT:C202128 Transformed EGFR-Positive Lung Adenocarcinoma to Squamous Cell Carcinoma +NCIT:C202132 Transformed EGFR-Positive Lung Non-Small Cell Carcinoma to Small Cell Carcinoma NCIT:C139681 Transformed Follicular Lymphoma to Diffuse Large B-Cell Lymphoma NCIT:C179717 Transformed Indolent B-Cell Non-Hodgkin Lymphoma to Diffuse Large B-Cell Lymphoma NCIT:C185134 Transformed Lymphoplasmacytic Lymphoma to Diffuse Large B-Cell Lymphoma @@ -11403,6 +11726,7 @@ NCIT:C156699 Transformed Marginal Zone Lymphoma to Diffuse Large B-Cell Lymphoma NCIT:C165783 Transformed Mycosis Fungoides NCIT:C151957 Transformed Non-Hodgkin Lymphoma NCIT:C157625 Transformed Small Lymphocytic Lymphoma to Diffuse Large B-Cell Lymphoma +NCIT:C201961 Transformed Small Lymphocytic Lymphoma to Hodgkin Lymphoma NCIT:C185135 Transformed Waldenstrom Macroglobulinemia to Diffuse Large B-Cell Lymphoma NCIT:C64158 Transitional Cell Carcinoma of the Rat Renal Pelvis NCIT:C64159 Transitional Cell Carcinoma of the Rat Ureter @@ -11428,7 +11752,9 @@ NCIT:C27632 Transplant-Related Malignant Neoplasm NCIT:C27638 Transplant-Related Renal Cell Carcinoma NCIT:C27636 Transplant-Related Skin Squamous Cell Carcinoma NCIT:C154700 Transplant-Related Squamous Cell Carcinoma +NCIT:C203390 Transverse Colon Neuroendocrine Tumor NCIT:C6426 Transverse Colon Neuroendocrine Tumor G1 +NCIT:C203395 Transverse Colon Neuroendocrine Tumor G2 NCIT:C191963 Treatment-Related Prostate Neuroendocrine Carcinoma NCIT:C43326 Trichilemmal Carcinoma NCIT:C4113 Trichilemmoma @@ -11440,6 +11766,7 @@ NCIT:C43328 Trichoepithelial Carcinoma NCIT:C21817 Trichoepithelioma Type of Basaloid Follicular Neoplasm of the Mouse Skin NCIT:C43329 Trichofollicular Carcinoma NCIT:C21818 Trichofolliculoma Type of Basaloid Follicular Neoplasm of the Mouse Skin +NCIT:C205371 Trichogerminoma NCIT:C178375 Triple-Class Refractory Multiple Myeloma NCIT:C35382 True Histiocytic Lymphoma NCIT:C22153 Tubular Adenocarcinoma of the Mouse Intestinal Tract @@ -11509,13 +11836,19 @@ NCIT:C165172 Unresectable Ampulla of Vater Carcinoma NCIT:C175384 Unresectable Anal Canal Squamous Cell Carcinoma NCIT:C173156 Unresectable Anal Squamous Cell Carcinoma NCIT:C168718 Unresectable Angiosarcoma +NCIT:C203619 Unresectable Appendix Adenocarcinoma +NCIT:C203282 Unresectable Astrocytic Tumor +NCIT:C203269 Unresectable Astrocytoma, IDH-Mutant NCIT:C157330 Unresectable Basal Cell Carcinoma NCIT:C171322 Unresectable Bile Duct Carcinoma NCIT:C176042 Unresectable Biliary Tract Carcinoma +NCIT:C203409 Unresectable Bladder Adenocarcinoma NCIT:C167075 Unresectable Bladder Carcinoma NCIT:C191857 Unresectable Bladder Small Cell Neuroendocrine Carcinoma +NCIT:C203411 Unresectable Bladder Squamous Cell Carcinoma NCIT:C158586 Unresectable Bladder Urothelial Carcinoma NCIT:C153072 Unresectable Bone Sarcoma +NCIT:C203331 Unresectable Breast Adenocarcinoma NCIT:C158752 Unresectable Breast Carcinoma NCIT:C158751 Unresectable Breast Inflammatory Carcinoma NCIT:C148124 Unresectable Carcinoma @@ -11526,6 +11859,7 @@ NCIT:C174024 Unresectable Cervical Carcinoma NCIT:C174025 Unresectable Cervical Squamous Cell Carcinoma NCIT:C27324 Unresectable Cholangiocarcinoma NCIT:C153325 Unresectable Chordoma +NCIT:C201953 Unresectable Chromophobe Renal Cell Carcinoma NCIT:C165449 Unresectable Clear Cell Renal Cell Carcinoma NCIT:C162116 Unresectable Colon Adenocarcinoma NCIT:C180406 Unresectable Colon Carcinoma @@ -11538,6 +11872,10 @@ NCIT:C150598 Unresectable Dedifferentiated Liposarcoma NCIT:C155877 Unresectable Desmoid Fibromatosis NCIT:C170826 Unresectable Desmoplastic Small Round Cell Tumor NCIT:C168572 Unresectable Differentiated Thyroid Gland Carcinoma +NCIT:C203286 Unresectable Diffuse Glioma +NCIT:C203272 Unresectable Diffuse Hemispheric Glioma, H3 G34-Mutant +NCIT:C203263 Unresectable Diffuse Midline Glioma +NCIT:C203271 Unresectable Diffuse Midline Glioma, H3 K27M-Mutant NCIT:C129654 Unresectable Digestive System Adenocarcinoma NCIT:C155903 Unresectable Digestive System Carcinoma NCIT:C172808 Unresectable Digestive System Mixed Adenoneuroendocrine Carcinoma @@ -11576,6 +11914,8 @@ NCIT:C180885 Unresectable Gastroesophageal Junction Neuroendocrine Carcinoma NCIT:C190783 Unresectable Genitourinary System Carcinoma NCIT:C176890 Unresectable Glioblastoma NCIT:C176889 Unresectable Glioma +NCIT:C203308 Unresectable Glioneuronal and Neuronal Tumors +NCIT:C203700 Unresectable HER2-Low Breast Carcinoma NCIT:C187161 Unresectable HER2-Negative Breast Carcinoma NCIT:C186284 Unresectable HER2-Positive Breast Carcinoma NCIT:C165174 Unresectable Head and Neck Carcinoma @@ -11594,14 +11934,14 @@ NCIT:C172810 Unresectable Large Cell Neuroendocrine Carcinoma NCIT:C172645 Unresectable Laryngeal Squamous Cell Carcinoma NCIT:C132147 Unresectable Leiomyosarcoma NCIT:C132148 Unresectable Liposarcoma -NCIT:C165171 Unresectable Liver and Intrahepatic Bile Duct Carcinoma +NCIT:C165171 Unresectable Liver Carcinoma NCIT:C155829 Unresectable Low Grade Glioma NCIT:C174510 Unresectable Lung Adenocarcinoma -NCIT:C177246 Unresectable Lung Carcinoid Tumor NCIT:C155902 Unresectable Lung Carcinoma NCIT:C187162 Unresectable Lung Large Cell Neuroendocrine Carcinoma NCIT:C192018 Unresectable Lung Neuroendocrine Carcinoma NCIT:C165454 Unresectable Lung Neuroendocrine Neoplasm +NCIT:C177246 Unresectable Lung Neuroendocrine Tumor NCIT:C155901 Unresectable Lung Non-Small Cell Carcinoma NCIT:C171612 Unresectable Lung Non-Small Cell Squamous Carcinoma NCIT:C162642 Unresectable Lung Non-Squamous Non-Small Cell Carcinoma @@ -11634,6 +11974,8 @@ NCIT:C172806 Unresectable Neuroendocrine Carcinoma NCIT:C168973 Unresectable Neuroendocrine Neoplasm NCIT:C165453 Unresectable Neuroendocrine Tumor NCIT:C153080 Unresectable Neuroendocrine Tumor G1 +NCIT:C203284 Unresectable Oligodendroglioma +NCIT:C203270 Unresectable Oligodendroglioma, IDH-Mutant and 1p/19q-Codeleted NCIT:C172644 Unresectable Oral Cavity Squamous Cell Carcinoma NCIT:C162833 Unresectable Oropharyngeal Squamous Cell Carcinoma NCIT:C190632 Unresectable Oropharyngeal Undifferentiated Carcinoma @@ -11658,12 +12000,18 @@ NCIT:C173611 Unresectable Paratesticular Biphasic Mesothelioma NCIT:C173609 Unresectable Paratesticular Epithelioid Mesothelioma NCIT:C173608 Unresectable Paratesticular Malignant Mesothelioma NCIT:C173610 Unresectable Paratesticular Sarcomatoid Mesothelioma +NCIT:C201837 Unresectable Penile Carcinoma +NCIT:C201838 Unresectable Penile Squamous Cell Carcinoma NCIT:C165173 Unresectable Periampullary Adenocarcinoma NCIT:C173615 Unresectable Peritoneal Biphasic Mesothelioma NCIT:C173613 Unresectable Peritoneal Epithelioid Mesothelioma NCIT:C173612 Unresectable Peritoneal Malignant Mesothelioma NCIT:C173614 Unresectable Peritoneal Sarcomatoid Mesothelioma +NCIT:C203283 Unresectable Pilocytic Astrocytoma +NCIT:C204867 Unresectable Platinum-Refractory Ovarian Carcinoma +NCIT:C203315 Unresectable Platinum-Resistant Fallopian Tube Carcinoma NCIT:C179459 Unresectable Platinum-Resistant Ovarian Carcinoma +NCIT:C203316 Unresectable Platinum-Resistant Primary Peritoneal Carcinoma NCIT:C182028 Unresectable Pleomorphic Liposarcoma NCIT:C173618 Unresectable Pleural Biphasic Mesothelioma NCIT:C173616 Unresectable Pleural Epithelioid Mesothelioma @@ -11672,6 +12020,8 @@ NCIT:C173617 Unresectable Pleural Sarcomatoid Mesothelioma NCIT:C179423 Unresectable Plexiform Neurofibroma NCIT:C174569 Unresectable Poorly Differentiated Thyroid Gland Carcinoma NCIT:C171070 Unresectable Primary Central Chondrosarcoma +NCIT:C203309 Unresectable Primary Central Nervous System Neoplasm +NCIT:C203310 Unresectable Primary Malignant Central Nervous System Neoplasm NCIT:C170974 Unresectable Primary Peritoneal Adenocarcinoma NCIT:C170973 Unresectable Primary Peritoneal Carcinoma NCIT:C186276 Unresectable Primary Peritoneal Endometrioid Adenocarcinoma @@ -11681,6 +12031,7 @@ NCIT:C171611 Unresectable Prostate Carcinoma NCIT:C191856 Unresectable Prostate Small Cell Neuroendocrine Carcinoma NCIT:C162117 Unresectable Rectal Adenocarcinoma NCIT:C154545 Unresectable Renal Cell Carcinoma +NCIT:C190508 Unresectable Renal Cell Carcinoma, Not Otherwise Specified NCIT:C158588 Unresectable Renal Pelvis Urothelial Carcinoma NCIT:C164160 Unresectable Renal Pelvis and Ureter Urothelial Carcinoma NCIT:C170829 Unresectable Rhabdoid Tumor @@ -11712,7 +12063,6 @@ NCIT:C174572 Unresectable Thyroid Gland Oncocytic Carcinoma NCIT:C174570 Unresectable Thyroid Gland Papillary Carcinoma NCIT:C129827 Unresectable Transitional Cell Carcinoma NCIT:C165491 Unresectable Triple-Negative Breast Carcinoma -NCIT:C190508 Unresectable Unclassified Renal Cell Carcinoma NCIT:C150610 Unresectable Undifferentiated Pleomorphic Sarcoma NCIT:C158587 Unresectable Ureter Urothelial Carcinoma NCIT:C158585 Unresectable Urethral Urothelial Carcinoma @@ -11782,6 +12132,7 @@ NCIT:C111020 Uveal Class 1 Melanoma NCIT:C111022 Uveal Class 1a Melanoma NCIT:C111023 Uveal Class 1b Melanoma NCIT:C111021 Uveal Class 2 Melanoma +NCIT:C205057 Uveal Melanocytic Neoplasm NCIT:C174503 Uveal Melanocytoma NCIT:C150130 Uveal Melanoma Metastatic in the Liver NCIT:C140672 Uveal Melanoma by AJCC v7 Stage @@ -11793,7 +12144,7 @@ NCIT:C180947 Vaginal Adenocarcinoma of Skene Gland Origin NCIT:C40262 Vaginal Adenoid Basal Carcinoma NCIT:C40260 Vaginal Adenosquamous Carcinoma NCIT:C45445 Vaginal Angiomyofibroblastoma -NCIT:C40245 Vaginal Basaloid Carcinoma +NCIT:C40245 Vaginal Basaloid Squamous Cell Carcinoma NCIT:C40282 Vaginal Blue Nevus NCIT:C90347 Vaginal Cancer by AJCC v6 Stage NCIT:C91204 Vaginal Cancer by AJCC v7 Stage @@ -11830,6 +12181,8 @@ NCIT:C23081 Vascular-fibrous Neoplasms of the Mouse Pharynx NCIT:C49111 Venous Angioleiomyoma NCIT:C22923 Venous Hemangioma of the Mouse Blood Vessel NCIT:C45748 Ventricular Myxoma +NCIT:C203968 Verruca Palmaris +NCIT:C203969 Verruca Plana NCIT:C23093 Verrucous Carcinoma of the Mouse Nose and Paranasal Sinuses NCIT:C23051 Verrucous Carcinoma of the Mouse Oral Cavity NCIT:C22939 Verrucous Keratotic Hemangioma of the Mouse Blood Vessel @@ -11841,7 +12194,6 @@ NCIT:C27731 Very Low Risk Gastrointestinal Stromal Tumor NCIT:C27734 Very Low Risk Small Intestinal Gastrointestinal Stromal Tumor NCIT:C22155 Villous Adenocarcinoma of the Mouse Intestinal Tract NCIT:C191750 Villous Adenoma of the Urinary Tract -NCIT:C36034 Villous Neoplasm NCIT:C27698 Virus-Related Carcinoma NCIT:C27699 Virus-Related Lymphoma NCIT:C27673 Virus-Related Malignant Neoplasm @@ -11850,11 +12202,11 @@ NCIT:C171026 Visceral Angiosarcoma NCIT:C175225 Visual Pathway Medulloepithelioma NCIT:C175224 Visual Pathway Melanocytoma NCIT:C6262 Visual Pathway Neoplasm +NCIT:C204888 Volar Melanoma NCIT:C95476 Von Hippel Lindau Syndrome-Associated Pancreatic Serous Adenoma NCIT:C40331 Vulvar Acquired Melanocytic Nevus NCIT:C128162 Vulvar Adenocarcinoma of Mammary Gland Type NCIT:C128164 Vulvar Adenocarcinoma of Sweat Gland Origin -NCIT:C128166 Vulvar Adenocarcinoma, Intestinal-Type NCIT:C128273 Vulvar Alveolar Rhabdomyosarcoma NCIT:C45446 Vulvar Angiomyofibroblastoma NCIT:C40325 Vulvar Angiomyxoma @@ -11885,6 +12237,7 @@ NCIT:C128270 Vulvar Lipoma NCIT:C40335 Vulvar Melanocytic Neoplasm NCIT:C128289 Vulvar Melanocytic Nevus NCIT:C128247 Vulvar Merkel Cell Carcinoma +NCIT:C128166 Vulvar Mucinous Adenocarcinoma, Intestinal-Type NCIT:C40303 Vulvar Neoplasm of Skin Appendage Origin NCIT:C181905 Vulvar Phyllodes Tumor NCIT:C181926 Vulvar Prepubertal Fibroma @@ -11904,6 +12257,7 @@ NCIT:C40287 Vulvar Warty Carcinoma NCIT:C128295 Vulvar Yolk Sac Tumor NCIT:C177797 WHO Grade 1 Glioma NCIT:C200758 WHO Grade 4 Glioma +NCIT:C204514 WNT-Activated Deep Penetrating/Plexiform Melanocytoma (Nevus) NCIT:C135002 Walleye Dermal Sarcoma NCIT:C23132 Warthin's Tumor of the Mouse Salivary Glands NCIT:C126409 Warthin-Like Variant Thyroid Gland Papillary Carcinoma diff --git a/src/ontology/reports/omim.subclass.added.robot.tsv b/src/ontology/reports/omim.subclass.added.robot.tsv index 1e865653..d9576957 100644 --- a/src/ontology/reports/omim.subclass.added.robot.tsv +++ b/src/ontology/reports/omim.subclass.added.robot.tsv @@ -117,7 +117,6 @@ MONDO:0012627 epilepsy, idiopathic generalized, susceptibility to, 13 MONDO:0010 MONDO:0012655 myoclonic epilepsy, juvenile, susceptibility to, 4 MONDO:0009696 OMIM:611364 OMIMPS:254770 juvenile myoclonic epilepsy MONDO:0012660 susceptibility to visceral leishmaniasis, 2 MONDO:0005445 OMIM:611381 OMIMPS:608207 visceral leishmaniasis MONDO:0012661 susceptibility to visceral leishmaniasis, 3 MONDO:0005445 OMIM:611382 OMIMPS:608207 visceral leishmaniasis -MONDO:0012682 immunodeficiency 35 MONDO:0021094 OMIM:611521 OMIMPS:300755 immunodeficiency disease MONDO:0012702 celiac disease, susceptibility to, 6 MONDO:0005130 OMIM:611598 OMIMPS:212750 celiac disease MONDO:0012710 Hirschsprung disease, susceptibility to, 9 MONDO:0018309 OMIM:611644 OMIMPS:142623 Hirschsprung disease MONDO:0012737 long QT syndrome 10 MONDO:0018054 OMIM:611819 OMIMPS:608583 familial atrial fibrillation @@ -136,7 +135,6 @@ MONDO:0012781 celiac disease, susceptibility to, 12 MONDO:0005130 OMIM:612010 OM MONDO:0012782 celiac disease, susceptibility to, 13 MONDO:0005130 OMIM:612011 OMIMPS:212750 celiac disease MONDO:0012786 juvenile cataract-microcornea-renal glucosuria syndrome MONDO:0005129 OMIM:612018 OMIMPS:116200 cataract MONDO:0012808 dilated cardiomyopathy 1AA MONDO:0024573 OMIM:612158 OMIMPS:192600 familial hypertrophic cardiomyopathy -MONDO:0012839 pyogenic bacterial infections due to MyD88 deficiency MONDO:0021094 OMIM:612260 OMIMPS:300755 immunodeficiency disease MONDO:0012843 epilepsy, childhood absence, susceptibility to, 5 MONDO:0010826 OMIM:612269 OMIMPS:600131 childhood absence epilepsy MONDO:0012896 psoriasis 10, susceptibility to MONDO:0005083 OMIM:612410 OMIMPS:177900 psoriasis MONDO:0012898 narcolepsy 4, susceptibility to MONDO:0100554 OMIM:612417 OMIMPS:161400 hereditary narcolepsy @@ -162,7 +160,6 @@ MONDO:0013340 Parkinson disease 5, autosomal dominant, susceptibility to MONDO:0 MONDO:0013383 Hirschsprung disease, susceptibility to, 3 MONDO:0018309 OMIM:613711 OMIMPS:142623 Hirschsprung disease MONDO:0013384 Hirschsprung disease, susceptibility to, 4 MONDO:0018309 OMIM:613712 OMIMPS:142623 Hirschsprung disease MONDO:0013409 age related macular degeneration 5 MONDO:0005150 OMIM:613761 OMIMPS:603075 age-related macular degeneration -MONDO:0013427 immunodeficiency 31B MONDO:0021094 OMIM:613796 OMIMPS:300755 immunodeficiency disease MONDO:0013468 retinitis pigmentosa 59 MONDO:0005500 OMIM:613861 OMIMPS:212065 congenital disorder of glycosylation type I MONDO:0013470 generalized epilepsy with febrile seizures plus, type 7 MONDO:0000032 OMIM:613863 OMIMPS:121210 febrile seizures, familial MONDO:0013500 immunodeficiency 51 MONDO:0021094 OMIM:613953 OMIMPS:300755 immunodeficiency disease @@ -210,6 +207,7 @@ MONDO:0014289 macrocephaly-developmental delay syndrome MONDO:0019502 OMIM:61563 MONDO:0014313 autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity MONDO:0021094 OMIM:615707 OMIMPS:300755 immunodeficiency disease MONDO:0014333 polymicrogyria, bilateral perisylvian, autosomal recessive MONDO:0000904 OMIM:615752 OMIMPS:614039 complex cortical dysplasia with other brain malformations MONDO:0014336 intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency MONDO:0100172 OMIM:615761 OMIMPS:156200 intellectual disability, autosomal dominant +MONDO:0014347 short stature with microcephaly and distinctive facies MONDO:0010002 OMIM:615789 OMIMPS:268400 Rothmund-Thomson syndrome MONDO:0014429 autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency MONDO:0021094 OMIM:615978 OMIMPS:300755 immunodeficiency disease MONDO:0014482 intellectual disability, autosomal dominant 29 MONDO:0100172 OMIM:616078 OMIMPS:156200 intellectual disability, autosomal dominant MONDO:0014486 intellectual disability, autosomal dominant 30 MONDO:0100172 OMIM:616083 OMIMPS:156200 intellectual disability, autosomal dominant diff --git a/src/ontology/reports/omim.subclass.confirmed.robot.tsv b/src/ontology/reports/omim.subclass.confirmed.robot.tsv index 742607a0..124e41a6 100644 --- a/src/ontology/reports/omim.subclass.confirmed.robot.tsv +++ b/src/ontology/reports/omim.subclass.confirmed.robot.tsv @@ -191,7 +191,7 @@ MONDO:0008271 polydactyly of an index finger MONDO:0017425 OMIM:174600 OMIMPS:17 MONDO:0008272 polysyndactyly 4 MONDO:0017425 OMIM:174700 OMIMPS:174400 preaxial polydactyly of fingers MONDO:0008289 brain small vessel disease 1 with or without ocular anomalies MONDO:0020496 OMIM:175780 OMIMPS:175780 familial porencephaly MONDO:0008291 porokeratosis plantaris palmaris et disseminata MONDO:0006602 OMIM:175850 OMIMPS:175800 porokeratosis -MONDO:0008302 centra precocious puberty 1 MONDO:0019165 OMIM:176400 OMIMPS:176400 central precocious puberty +MONDO:0008302 central precocious puberty 1 MONDO:0019165 OMIM:176400 OMIMPS:176400 central precocious puberty MONDO:0008310 Hutchinson-Gilford progeria syndrome MONDO:0020732 OMIM:176670 OMIMPS:176670 progeria MONDO:0008332 platelet-type von Willebrand disease MONDO:0000009 OMIM:177820 OMIMPS:231200 inherited bleeding disorder, platelet-type MONDO:0008338 contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A MONDO:0020937 OMIM:178110 OMIMPS:178110 contractures, pterygia, and variable skeletal fusions syndrome @@ -279,6 +279,7 @@ MONDO:0008958 Klippel-Feil syndrome 2, autosomal recessive MONDO:0001029 OMIM:21 MONDO:0008962 Griscelli syndrome type 1 MONDO:0018306 OMIM:214450 OMIMPS:214450 Griscelli syndrome MONDO:0008967 congenital bile acid synthesis defect 4 MONDO:0018841 OMIM:214950 OMIMPS:607765 congenital bile acid synthesis defect MONDO:0008972 rhizomelic chondrodysplasia punctata type 1 MONDO:0015776 OMIM:215100 OMIMPS:215100 rhizomelic chondrodysplasia punctata +MONDO:0008988 citrullinemia type I MONDO:0015991 OMIM:215700 OMIMPS:215700 citrullinemia MONDO:0009014 cornea plana 2 MONDO:0000733 OMIM:217300 OMIMPS:121400 cornea plana MONDO:0009035 craniometaphyseal dysplasia, autosomal recessive MONDO:0015465 OMIM:218400 OMIMPS:123000 craniometaphyseal dysplasia MONDO:0009050 Cushing disease due to pituitary adenoma MONDO:0017824 OMIM:219090 OMIMPS:102200 familial isolated pituitary adenoma @@ -1155,7 +1156,7 @@ MONDO:0012346 generalized epilepsy with febrile seizures plus, type 4 MONDO:0018 MONDO:0012353 erythrocytosis, familial, 3 MONDO:0001115 OMIM:609820 OMIMPS:133100 familial polycythemia MONDO:0012354 platelet-type bleeding disorder 8 MONDO:0000009 OMIM:609821 OMIMPS:231200 inherited bleeding disorder, platelet-type MONDO:0012355 autosomal recessive nonsyndromic hearing loss 28 MONDO:0019588 OMIM:609823 OMIMPS:220290 hearing loss, autosomal recessive -MONDO:0012360 congenital nongoitrous hypothryoidism 3 MONDO:0000045 OMIM:609893 OMIMPS:275200 hypothyroidism, congenital, nongoitrous +MONDO:0012360 congenital nongoitrous hypothyroidism 3 MONDO:0000045 OMIM:609893 OMIMPS:275200 hypothyroidism, congenital, nongoitrous MONDO:0012362 dilated cardiomyopathy 1P MONDO:0016333 OMIM:609909 OMIMPS:115200 familial dilated cardiomyopathy MONDO:0012363 retinitis pigmentosa 32 MONDO:0019200 OMIM:609913 OMIMPS:268000 retinitis pigmentosa MONDO:0012364 dilated cardiomyopathy 1Q MONDO:0016333 OMIM:609915 OMIMPS:115200 familial dilated cardiomyopathy @@ -1309,6 +1310,7 @@ MONDO:0012678 atrial fibrillation, familial, 5 MONDO:0018054 OMIM:611494 OMIMPS: MONDO:0012679 autosomal recessive osteopetrosis 6 MONDO:0019026 OMIM:611497 OMIMPS:259700 autosomal recessive osteopetrosis MONDO:0012680 nephronophthisis 7 MONDO:0019005 OMIM:611498 OMIMPS:256100 nephronophthisis MONDO:0012681 febrile seizures, familial, 7 MONDO:0000032 OMIM:611515 OMIMPS:121210 febrile seizures, familial +MONDO:0012682 immunodeficiency 35 MONDO:0021094 OMIM:611521 OMIMPS:300755 immunodeficiency disease MONDO:0012683 pontocerebellar hypoplasia type 6 MONDO:0020135 OMIM:611523 OMIMPS:607596 pontocerebellar hypoplasia MONDO:0012684 arrhythmogenic right ventricular dysplasia 12 MONDO:0016342 OMIM:611528 OMIMPS:107970 familial isolated arrhythmogenic right ventricular dysplasia MONDO:0012689 premature ovarian failure 5 MONDO:0019852 OMIM:611548 OMIMPS:311360 inherited primary ovarian failure @@ -1381,6 +1383,7 @@ MONDO:0012831 inflammatory bowel disease 13 MONDO:0005265 OMIM:612244 OMIMPS:266 MONDO:0012832 inflammatory bowel disease 14 MONDO:0005265 OMIM:612245 OMIMPS:266600 inflammatory bowel disease MONDO:0012837 inflammatory bowel disease 15 MONDO:0005265 OMIM:612255 OMIMPS:266600 inflammatory bowel disease MONDO:0012838 inflammatory bowel disease 16 MONDO:0005265 OMIM:612259 OMIMPS:266600 inflammatory bowel disease +MONDO:0012839 pyogenic bacterial infections due to MyD88 deficiency MONDO:0021094 OMIM:612260 OMIMPS:300755 immunodeficiency disease MONDO:0012840 inflammatory bowel disease 17 MONDO:0005265 OMIM:612261 OMIMPS:266600 inflammatory bowel disease MONDO:0012841 inflammatory bowel disease 18 MONDO:0005265 OMIM:612262 OMIMPS:266600 inflammatory bowel disease MONDO:0012842 melanoma, cutaneous malignant, susceptibility to, 7 MONDO:0024462 OMIM:612263 OMIMPS:155600 susceptibility to familial cutaneous melanoma @@ -1655,6 +1658,7 @@ MONDO:0013420 age related macular degeneration 12 MONDO:0005150 OMIM:613784 OMIM MONDO:0013423 immunodeficiency due to MASP-2 deficiency MONDO:0044209 OMIM:613791 OMIMPS:614372 disorder of lectin complement activation pathway MONDO:0013425 retinitis pigmentosa 20 MONDO:0019200 OMIM:613794 OMIMPS:268000 retinitis pigmentosa MONDO:0013426 aneurysm-osteoarthritis syndrome MONDO:0018954 OMIM:613795 OMIMPS:609192 Loeys-Dietz syndrome +MONDO:0013427 immunodeficiency 31B MONDO:0021094 OMIM:613796 OMIMPS:300755 immunodeficiency disease MONDO:0013428 Meier-Gorlin syndrome 2 MONDO:0016817 OMIM:613800 OMIMPS:224690 Meier-Gorlin syndrome MONDO:0013429 retinitis pigmentosa 40 MONDO:0019200 OMIM:613801 OMIMPS:268000 retinitis pigmentosa MONDO:0013430 Meier-Gorlin syndrome 3 MONDO:0016817 OMIM:613803 OMIMPS:224690 Meier-Gorlin syndrome @@ -1835,7 +1839,7 @@ MONDO:0013750 atrial septal defect 8 MONDO:0006664 OMIM:614433 OMIMPS:108800 atr MONDO:0013752 hypoplastic left heart syndrome 2 MONDO:0004933 OMIM:614435 OMIMPS:241550 hypoplastic left heart syndrome MONDO:0013755 PYCR1-related de Barsy syndrome MONDO:0100237 OMIM:614438 OMIMPS:123700 inherited cutis laxa MONDO:0013756 hypertrophic osteoarthropathy, primary, autosomal recessive, 2 MONDO:0016620 OMIM:614441 OMIMPS:259100 primary hypertrophic osteoarthropathy -MONDO:0013757 congenital nongoitrous hypothryoidism 6 MONDO:0000045 OMIM:614450 OMIMPS:275200 hypothyroidism, congenital, nongoitrous +MONDO:0013757 congenital nongoitrous hypothyroidism 6 MONDO:0000045 OMIM:614450 OMIMPS:275200 hypothyroidism, congenital, nongoitrous MONDO:0013759 melanoma, cutaneous malignant, susceptibility to, 8 MONDO:0024462 OMIM:614456 OMIMPS:155600 susceptibility to familial cutaneous melanoma MONDO:0013761 childhood encephalopathy due to thiamine pyrophosphokinase deficiency MONDO:0000152 OMIM:614458 OMIMPS:249270 thiamine-responsive dysfunction syndrome MONDO:0013762 lipoic acid synthetase deficiency MONDO:0019169 OMIM:614462 OMIMPS:312170 pyruvate dehydrogenase deficiency @@ -1904,7 +1908,7 @@ MONDO:0013862 immunodeficiency, common variable, 7 MONDO:0015517 OMIM:614699 OMI MONDO:0013863 combined immunodeficiency due to LRBA deficiency MONDO:0015517 OMIM:614700 OMIMPS:607594 common variable immunodeficiency MONDO:0013864 Cornelia de Lange syndrome 4 MONDO:0016033 OMIM:614701 OMIMPS:122470 Cornelia de Lange syndrome MONDO:0013865 mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency MONDO:0000732 OMIM:614702 OMIMPS:609060 combined oxidative phosphorylation deficiency -MONDO:0013867 brown-Vialetto-van Laere syndrome 2 MONDO:0008891 OMIM:614707 OMIMPS:211530 riboflavin transporter deficiency +MONDO:0013867 Brown-Vialetto-van Laere syndrome 2 MONDO:0008891 OMIM:614707 OMIMPS:211530 riboflavin transporter deficiency MONDO:0013870 TMEM165-congenital disorder of glycosylation MONDO:0005501 OMIM:614727 OMIMPS:212066 congenital disorder of glycosylation type II MONDO:0013871 Seckel syndrome 6 MONDO:0019342 OMIM:614728 OMIMPS:210600 Seckel syndrome MONDO:0013874 glucocorticoid deficiency 4 MONDO:0008733 OMIM:614736 OMIMPS:202200 familial glucocorticoid deficiency @@ -2598,6 +2602,8 @@ MONDO:0023664 spermatogenic failure 54 MONDO:0004983 OMIM:619379 OMIMPS:258150 s MONDO:0023670 Bardet-Biedl syndrome 20 MONDO:0015229 OMIM:619471 OMIMPS:209900 Bardet-Biedl syndrome MONDO:0023671 oculopharyngodistal myopathy 3 MONDO:0025193 OMIM:619473 OMIMPS:164310 oculopharyngodistal myopathy MONDO:0023691 maple syrup urine disease type 1A MONDO:0009563 OMIM:248600 OMIMPS:248600 maple syrup urine disease +MONDO:0023692 maple syrup urine disease type 1B MONDO:0009563 OMIM:620698 OMIMPS:248600 maple syrup urine disease +MONDO:0023693 maple syrup urine disease type 2 MONDO:0009563 OMIM:620699 OMIMPS:248600 maple syrup urine disease MONDO:0024264 hypothyroidism, congenital, nongoitrous, 2 MONDO:0000045 OMIM:218700 OMIMPS:275200 hypothyroidism, congenital, nongoitrous MONDO:0024265 Duane syndrome type 1 MONDO:0007473 OMIM:126800 OMIMPS:126800 Duane retraction syndrome MONDO:0024266 patent ductus arteriosus 3 MONDO:0011827 OMIM:617039 OMIMPS:607411 patent ductus arteriosus @@ -3763,6 +3769,10 @@ MONDO:0958330 developmental and epileptic encephalopathy 113 MONDO:0100062 OMIM: MONDO:0958331 developmental and epileptic encephalopathy 114 MONDO:0100062 OMIM:620774 OMIMPS:308350 developmental and epileptic encephalopathy MONDO:0958333 thrombocytopenia 13, syndromic MONDO:0100241 OMIM:620776 OMIMPS:313900 inherited thrombocytopenia MONDO:0968944 intellectual developmental disorder, autosomal recessive 82 MONDO:0019502 OMIM:620779 OMIMPS:249500 autosomal recessive non-syndromic intellectual disability +MONDO:0968946 developmental and epileptic encephalopathy 115 MONDO:0100062 OMIM:620783 OMIMPS:308350 developmental and epileptic encephalopathy +MONDO:0968980 otosclerosis 12 MONDO:0005349 OMIM:620792 OMIMPS:166800 otosclerosis +MONDO:0968981 autosomal recessive nonsyndromic hearing loss 124 MONDO:0019588 OMIM:620794 OMIMPS:220290 hearing loss, autosomal recessive +MONDO:0968983 proteasome-associated autoinflammatory syndrome 6 MONDO:0009726 OMIM:620796 OMIMPS:256040 proteosome-associated autoinflammatory syndrome MONDO:8000006 WHIM syndrome 1 MONDO:0023880 OMIM:193670 OMIMPS:193670 WHIM syndrome MONDO:8000008 Martsolf syndrome 1 MONDO:0023910 OMIM:212720 OMIMPS:212720 Martsolf syndrome MONDO:8000011 visceral neuropathy, familial, 1, autosomal recessive MONDO:0023961 OMIM:243180 OMIMPS:243180 visceral neuropathy, familial diff --git a/src/ontology/reports/omim_exclusion_reasons.robot.template.tsv b/src/ontology/reports/omim_exclusion_reasons.robot.template.tsv index f6f69534..ab6edb17 100644 --- a/src/ontology/reports/omim_exclusion_reasons.robot.template.tsv +++ b/src/ontology/reports/omim_exclusion_reasons.robot.template.tsv @@ -17531,6 +17531,22 @@ OMIM:620801 MONDO:excludeGene OMIM:620802 MONDO:excludeGene OMIM:620803 MONDO:excludeGene OMIM:620804 MONDO:excludeGene +OMIM:620805 MONDO:excludeGene +OMIM:620808 MONDO:excludeGene +OMIM:620809 MONDO:excludeGene +OMIM:620810 MONDO:excludeGene +OMIM:620811 MONDO:excludeGene +OMIM:620812 MONDO:excludeGene +OMIM:620821 MONDO:excludeGene +OMIM:620822 MONDO:excludeGene +OMIM:620823 MONDO:excludeGene +OMIM:620824 MONDO:excludeGene +OMIM:620826 MONDO:excludeGene +OMIM:620827 MONDO:excludeGene +OMIM:620828 MONDO:excludeGene +OMIM:620829 MONDO:excludeGene +OMIM:620831 MONDO:excludeGene +OMIMPS:151623 MONDO:excludeGrouping OMIM:100640 MONDO:excludeNonDisease OMIM:100660 MONDO:excludeNonDisease OMIM:100670 MONDO:excludeNonDisease @@ -18548,7 +18564,6 @@ OMIM:179837 MONDO:excludeNonDisease OMIM:179838 MONDO:excludeNonDisease OMIM:180190 MONDO:excludeNonDisease OMIM:180201 MONDO:excludeNonDisease -OMIM:180202 MONDO:excludeNonDisease OMIM:180230 MONDO:excludeNonDisease OMIM:180231 MONDO:excludeNonDisease OMIM:180245 MONDO:excludeNonDisease @@ -21436,6 +21451,7 @@ OMIM:603981 MONDO:excludeNonDisease OMIM:603982 MONDO:excludeNonDisease OMIM:603983 MONDO:excludeNonDisease OMIM:603984 MONDO:excludeNonDisease +OMIM:603988 MONDO:excludeNonDisease OMIM:603989 MONDO:excludeNonDisease OMIM:603994 MONDO:excludeNonDisease OMIM:603996 MONDO:excludeNonDisease @@ -26898,7 +26914,6 @@ OMIM:614011 MONDO:excludeNonDisease OMIM:614012 MONDO:excludeNonDisease OMIM:614013 MONDO:excludeNonDisease OMIM:614014 MONDO:excludeNonDisease -OMIM:614015 MONDO:excludeNonDisease OMIM:614016 MONDO:excludeNonDisease OMIM:614026 MONDO:excludeNonDisease OMIM:614027 MONDO:excludeNonDisease @@ -29870,6 +29885,21 @@ OMIM:620801 MONDO:excludeNonDisease OMIM:620802 MONDO:excludeNonDisease OMIM:620803 MONDO:excludeNonDisease OMIM:620804 MONDO:excludeNonDisease +OMIM:620805 MONDO:excludeNonDisease +OMIM:620808 MONDO:excludeNonDisease +OMIM:620809 MONDO:excludeNonDisease +OMIM:620810 MONDO:excludeNonDisease +OMIM:620811 MONDO:excludeNonDisease +OMIM:620812 MONDO:excludeNonDisease +OMIM:620821 MONDO:excludeNonDisease +OMIM:620822 MONDO:excludeNonDisease +OMIM:620823 MONDO:excludeNonDisease +OMIM:620824 MONDO:excludeNonDisease +OMIM:620826 MONDO:excludeNonDisease +OMIM:620827 MONDO:excludeNonDisease +OMIM:620828 MONDO:excludeNonDisease +OMIM:620829 MONDO:excludeNonDisease +OMIM:620831 MONDO:excludeNonDisease OMIM:123270 MONDO:excludePhenotype OMIM:130180 MONDO:excludePhenotype OMIM:131500 MONDO:excludePhenotype @@ -30369,7 +30399,6 @@ OMIM:168200 MONDO:excludeTrait OMIM:168710 MONDO:excludeTrait OMIM:168800 MONDO:excludeTrait OMIM:168830 MONDO:excludeTrait -OMIM:168885 MONDO:excludeTrait OMIM:169170 MONDO:excludeTrait OMIM:169200 MONDO:excludeTrait OMIM:169300 MONDO:excludeTrait @@ -31247,6 +31276,7 @@ OMIM:424500 MONDO:excludeTrait OMIM:425500 MONDO:excludeTrait OMIM:475000 MONDO:excludeTrait OMIM:489000 MONDO:excludeTrait +OMIM:500007 MONDO:excludeTrait OMIM:600000 MONDO:excludeTrait OMIM:600080 MONDO:excludeTrait OMIM:600084 MONDO:excludeTrait @@ -31445,7 +31475,6 @@ OMIM:603976 MONDO:excludeTrait OMIM:603979 MONDO:excludeTrait OMIM:603985 MONDO:excludeTrait OMIM:603987 MONDO:excludeTrait -OMIM:603988 MONDO:excludeTrait OMIM:603991 MONDO:excludeTrait OMIM:603992 MONDO:excludeTrait OMIM:603993 MONDO:excludeTrait @@ -37957,6 +37986,7 @@ OMIM:603981 MONDO:nonDisease OMIM:603982 MONDO:nonDisease OMIM:603983 MONDO:nonDisease OMIM:603984 MONDO:nonDisease +OMIM:603988 MONDO:nonDisease OMIM:603989 MONDO:nonDisease OMIM:603994 MONDO:nonDisease OMIM:603996 MONDO:nonDisease @@ -48942,3 +48972,18 @@ OMIM:620801 MONDO:nonDisease OMIM:620802 MONDO:nonDisease OMIM:620803 MONDO:nonDisease OMIM:620804 MONDO:nonDisease +OMIM:620805 MONDO:nonDisease +OMIM:620808 MONDO:nonDisease +OMIM:620809 MONDO:nonDisease +OMIM:620810 MONDO:nonDisease +OMIM:620811 MONDO:nonDisease +OMIM:620812 MONDO:nonDisease +OMIM:620821 MONDO:nonDisease +OMIM:620822 MONDO:nonDisease +OMIM:620823 MONDO:nonDisease +OMIM:620824 MONDO:nonDisease +OMIM:620826 MONDO:nonDisease +OMIM:620827 MONDO:nonDisease +OMIM:620828 MONDO:nonDisease +OMIM:620829 MONDO:nonDisease +OMIM:620831 MONDO:nonDisease diff --git a/src/ontology/reports/omim_mapped_deprecated_terms.robot.template.tsv b/src/ontology/reports/omim_mapped_deprecated_terms.robot.template.tsv index 3028a160..4adb3fcc 100644 --- a/src/ontology/reports/omim_mapped_deprecated_terms.robot.template.tsv +++ b/src/ontology/reports/omim_mapped_deprecated_terms.robot.template.tsv @@ -11,6 +11,7 @@ MONDO:0008091 OMIM:162820 MONDO:equivalentObsolete MONDO:0008126 OMIM:164891 MONDO:equivalentObsolete MONDO:0008204 OMIM:168850 MONDO:equivalentObsolete MONDO:0008415 OMIM:181515 MONDO:equivalentObsolete +MONDO:0008873 OMIM:210730 MONDO:equivalentObsolete MONDO:0009535 OMIM:247440 MONDO:equivalentObsolete MONDO:0009586 OMIM:249660 MONDO:equivalentObsolete MONDO:0009654 OMIM:252700 MONDO:equivalentObsolete diff --git a/src/ontology/reports/omim_mapping_status.tsv b/src/ontology/reports/omim_mapping_status.tsv index 20c495a6..a3a640e2 100644 --- a/src/ontology/reports/omim_mapping_status.tsv +++ b/src/ontology/reports/omim_mapping_status.tsv @@ -1,14 +1,9 @@ subject_id subject_label is_mapped is_excluded is_deprecated -OMIM:620785 neurodevelopmental disorder with progressive movement abnormalities False False False -OMIM:620786 basal ganglia calcification, idiopathic, 9, autosomal recessive False False False -OMIM:620789 aplasia cutis-enamel dysplasia syndrome False False False -OMIM:620790 neurodevelopmental disorder with hypotonia and seizures False False False -OMIM:620792 otosclerosis 12 False False False -OMIM:620794 deafness, autosomal recessive 124 False False False -OMIM:620795 autoinflammation with episodic fever and immune dysregulation False False False -OMIM:620796 proteasome-associated autoinflammatory syndrome 6 False False False -OMIMPS:151623 Li-Fraumeni syndrome False False False -OMIMPS:215700 Citrullinemia False False False +OMIM:500017 leigh syndrome, mitochondrial False False False +OMIM:620806 developmental and epileptic encephalopathy 116 False False False +OMIM:620819 rothmund-thomson syndrome, type 4 False False False +OMIM:620820 el hayek-chahrour neurodevelopmental syndrome False False False +OMIMPS:619539 Neuroocular syndrome False False False OMIM:100500 False False True OMIM:100680 False False True OMIM:100735 False False True @@ -7755,7 +7750,7 @@ OMIM:603983 ZNF101 False True False OMIM:603984 ZNF737 False True False OMIM:603985 zinc finger protein 103 False True False OMIM:603987 zinc finger protein 105 False True False -OMIM:603988 zinc finger protein 106 False True False +OMIM:603988 ZNF106 False True False OMIM:603989 ZNF107 False True False OMIM:603991 zinc finger protein 109 False True False OMIM:603992 zinc finger protein 110 False True False @@ -18941,6 +18936,22 @@ OMIM:620801 GK5 False True False OMIM:620802 WDSUB1 False True False OMIM:620803 HIGD1C False True False OMIM:620804 MOB3C False True False +OMIM:620805 ISOC1 False True False +OMIM:620808 SNHG17 False True False +OMIM:620809 ASCL5 False True False +OMIM:620810 SNORD94 False True False +OMIM:620811 SCARNA1 False True False +OMIM:620812 CLDN25 False True False +OMIM:620821 ITPRIPL1 False True False +OMIM:620822 RNU4-1 False True False +OMIM:620823 RNU4-2 False True False +OMIM:620824 GLTPD2 False True False +OMIM:620826 WDR54 False True False +OMIM:620827 ZNF229 False True False +OMIM:620828 OR9I1 False True False +OMIM:620829 HERPUD2 False True False +OMIM:620831 SCCPDH False True False +OMIMPS:151623 Li-Fraumeni syndrome False True False OMIM:616915 removed from database False True True OMIM:100070 aortic aneurysm, familial abdominal, 1 True False False OMIM:100100 prune belly syndrome True False False @@ -19725,6 +19736,7 @@ OMIM:168600 parkinson disease, late-onset True False False OMIM:168601 parkinson disease 1, autosomal dominant True False False OMIM:168605 perry syndrome True False False OMIM:168860 patella aplasia-hypoplasia True False False +OMIM:168885 neuroocular syndrome 2, paroxysmal type True False False OMIM:168900 patella, chondromalacia of True False False OMIM:169000 patella, familial recurrent dislocation of True False False OMIM:169100 char syndrome True False False @@ -20119,7 +20131,6 @@ OMIM:210500 biliary atresia, extrahepatic True False False OMIM:210600 seckel syndrome 1 True False False OMIM:210710 microcephalic osteodysplastic primordial dwarfism, type 1 True False False OMIM:210720 microcephalic osteodysplastic primordial dwarfism, type 2 True False False -OMIM:210730 microcephalic osteodysplastic primordial dwarfism, type 3 True False False OMIM:210745 blepharophimosis with ptosis, syndactyly, and short stature True False False OMIM:210750 skin/hair/eye pigmentation, variation in, 6 True False False OMIM:210900 bloom syndrome True False False @@ -20595,8 +20606,8 @@ OMIM:251950 mitochondrial myopathy with lactic acidosis True False False OMIM:252010 mitochondrial complex 1 deficiency, nuclear type 1 True False False OMIM:252011 mitochondrial complex 2 deficiency, nuclear type 1 True False False OMIM:252100 orofaciodigital syndrome 2 True False False -OMIM:252150 molybdenum cofactor deficiency, complementation group a True False False -OMIM:252160 molybdenum cofactor deficiency, complementation group B True False False +OMIM:252150 molybdenum cofactor deficiency, type a True False False +OMIM:252160 molybdenum cofactor deficiency, type B True False False OMIM:252270 monosomy 7 myelodysplasia and leukemia syndrome 1 True False False OMIM:252350 moyamoya disease 1 True False False OMIM:252500 mucolipidosis 2 alpha/beta True False False @@ -20655,7 +20666,7 @@ OMIM:255700 myotonia congenita, autosomal recessive True False False OMIM:255800 schwartz-jampel syndrome, type 1 True False False OMIM:255960 myxoma, intracardiac True False False OMIM:255995 congenital myopathy 13 True False False -OMIM:256000 leigh syndrome True False False +OMIM:256000 leigh syndrome, nuclear True False False OMIM:256020 focal segmental glomerulosclerosis 10 True False False OMIM:256030 nemaline myopathy 2 True False False OMIM:256040 proteasome-associated autoinflammatory syndrome 1 True False False @@ -21399,13 +21410,13 @@ OMIM:309545 intellectual developmental disorder, x-linked, syndromic 12 True Fal OMIM:309548 intellectual developmental disorder, X-linked 109 True False False OMIM:309549 intellectual developmental disorder, X-linked 9 True False False OMIM:309555 intellectual developmental disorder, x-linked, syndromic, gustavson type True False False -OMIM:309560 mental retardation with spastic paraplegia and palmoplantar hyperkeratosis True False False +OMIM:309560 impaired intellectual development with spastic paraplegia and palmoplantar hyperkeratosis True False False OMIM:309580 intellectual disability-hypotonic facies syndrome, x-linked, 1 True False False OMIM:309583 intellectual developmental disorder, x-linked, syndromic, snyder-robinson type True False False OMIM:309585 intellectual developmental disorder, x-linked, syndromic, wilson-turner type True False False OMIM:309590 intellectual developmental disorder, x-linked, syndromic, turner type True False False OMIM:309610 prieto syndrome True False False -OMIM:309620 mental retardation, skeletal dysplasia, and abducens palsy True False False +OMIM:309620 christian syndrome True False False OMIM:309630 metacarpal 4-5 fusion True False False OMIM:309800 microphthalmia, syndromic 1 True False False OMIM:309801 linear skin defects with multiple congenital anomalies 1 True False False @@ -21476,7 +21487,6 @@ OMIM:500003 striatonigral degeneration, infantile, mitochondrial True False Fals OMIM:500004 retinitis pigmentosa-deafness syndrome True False False OMIM:500005 hypomagnesemia, hypertension, and hypercholesterolemia, mitochondrial True False False OMIM:500006 cardiomyopathy, infantile hypertrophic True False False -OMIM:500007 cyclic vomiting syndrome True False False OMIM:500008 deafness, nonsyndromic sensorineural, mitochondrial True False False OMIM:500009 mitochondrial myopathy, infantile, transient True False False OMIM:500010 ataxia and polyneuropathy, adult-onset True False False @@ -21734,7 +21744,7 @@ OMIM:601775 megaloblastic anemia, folate-responsive True False False OMIM:601776 ehlers-danlos syndrome, musculocontractural type, 1 True False False OMIM:601777 cone-rod dystrophy 6 True False False OMIM:601780 ceroid lipofuscinosis, neuronal, 6a True False False -OMIM:601794 coloboma-obesity-hypogenitalism-mental retardation syndrome True False False +OMIM:601794 coloboma-obesity-hypogenitalism-impaired intellectual development syndrome True False False OMIM:601803 pallister-killian syndrome True False False OMIM:601808 chromosome 18q deletion syndrome True False False OMIM:601812 premature aging syndrome, penttinen type True False False @@ -21827,7 +21837,7 @@ OMIM:602594 retinitis pigmentosa 22 True False False OMIM:602629 dystonia 6, torsion True False False OMIM:602639 tooth agenesis, selective, 2 True False False OMIM:602668 myotonic dystrophy 2 True False False -OMIM:602685 mental retardation, severe, with spasticity and pigmentary tapetoretinal degeneration True False False +OMIM:602685 intellectual developmental disorder with spasticity and pigmentary tapetoretinal degeneration True False False OMIM:602722 renal tubular acidosis, distal, 3, with or without sensorineural hearing loss True False False OMIM:602723 psoriasis 2 True False False OMIM:602759 prostate cancer, hereditary, 8 True False False @@ -22126,7 +22136,7 @@ OMIM:606217 atrioventricular septal defect, susceptibility to, 2 True False Fals OMIM:606220 intellectual developmental disorder with short stature, facial anomalies, and speech defects True False False OMIM:606232 phelan-mcdermid syndrome True False False OMIM:606240 thyroid cancer, nonmedullary, 3 True False False -OMIM:606242 mental retardation, microcephaly, growth retardation, joint contractures, and facial dysmorphism True False False +OMIM:606242 kondoh syndrome True False False OMIM:606243 alveolar soft part sarcoma True False False OMIM:606263 paget disease of bone 4 True False False OMIM:606282 deafness, autosomal dominant 24 True False False @@ -22415,7 +22425,7 @@ OMIM:608115 ovarian hyperstimulation syndrome True False False OMIM:608118 zinc deficiency, transient neonatal True False False OMIM:608133 retinitis pigmentosa 7 True False False OMIM:608149 kagami-ogata syndrome True False False -OMIM:608154 lipodystrophy, generalized, with mental retardation, deafness, short stature, and slender bones True False False +OMIM:608154 lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones True False False OMIM:608156 nablus mask-like facial syndrome True False False OMIM:608158 coq-responsive oxphos deficiency True False False OMIM:608161 macular dystrophy, vitelliform, 3 True False False @@ -24196,7 +24206,7 @@ OMIM:614676 cardiomyopathy, familial hypertrophic, 21 True False False OMIM:614678 pontocerebellar hypoplasia, type 1b True False False OMIM:614679 ciliary dyskinesia, primary, 17 True False False OMIM:614680 influenza, severe, susceptibility to True False False -OMIM:614684 hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, mental retardation, and recurrent inflammatory episodes True False False +OMIM:614684 hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes True False False OMIM:614691 cataract 38 True False False OMIM:614692 membranous nephropathy, susceptibility to True False False OMIM:614699 immunodeficiency, common variable, 7 True False False @@ -24548,7 +24558,7 @@ OMIM:615490 charcot-marie-tooth disease, axonal, type 2r True False False OMIM:615491 spastic paraplegia 79b, autosomal recessive True False False OMIM:615493 intellectual developmental disorder, autosomal recessive 37 True False False OMIM:615500 ciliary dyskinesia, primary, 26 True False False -OMIM:615501 molybdenum cofactor deficiency, complementation group c True False False +OMIM:615501 molybdenum cofactor deficiency, type c True False False OMIM:615502 intellectual developmental disorder, autosomal dominant 21 True False False OMIM:615503 short-rib thoracic dysplasia 8 with or without polydactyly True False False OMIM:615504 ciliary dyskinesia, primary, 27 True False False @@ -24681,7 +24691,7 @@ OMIM:615777 desbuquois dysplasia 2 True False False OMIM:615779 congenital heart defects, multiple types, 4 True False False OMIM:615780 retinitis pigmentosa 69 True False False OMIM:615785 white sponge nevus 2 True False False -OMIM:615789 short stature with microcephaly and distinctive facies True False False +OMIM:615789 rothmund-thomson syndrome, type 3 True False False OMIM:615802 neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities True False False OMIM:615803 pontocerebellar hypoplasia, type 10 True False False OMIM:615807 seckel syndrome 8 True False False @@ -26477,7 +26487,7 @@ OMIM:619528 spermatogenic failure 57 True False False OMIM:619531 cone-rod dystrophy 22 True False False OMIM:619534 biliary, renal, neurologic, and skeletal syndrome True False False OMIM:619538 cerebral cavernous malformations 4 True False False -OMIM:619539 neuroocular syndrome True False False +OMIM:619539 neuroocular syndrome 1 True False False OMIM:619542 king-denborough syndrome True False False OMIM:619543 boudin-mortier syndrome True False False OMIM:619548 usmani-riazuddin syndrome, autosomal recessive True False False @@ -27064,6 +27074,14 @@ OMIM:620780 cutis laxa, autosomal recessive, type 1d True False False OMIM:620782 neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder True False False OMIM:620783 developmental and epileptic encephalopathy 115 True False False OMIM:620784 neurodevelopmental disorder plus optic atrophy True False False +OMIM:620785 neurodevelopmental disorder with progressive movement abnormalities True False False +OMIM:620786 basal ganglia calcification, idiopathic, 9, autosomal recessive True False False +OMIM:620789 aplasia cutis-enamel dysplasia syndrome True False False +OMIM:620790 neurodevelopmental disorder with hypotonia and seizures True False False +OMIM:620792 otosclerosis 12 True False False +OMIM:620794 deafness, autosomal recessive 124 True False False +OMIM:620795 autoinflammation with episodic fever and immune dysregulation True False False +OMIM:620796 proteasome-associated autoinflammatory syndrome 6 True False False OMIMPS:100070 Aortic aneurysm, familial abdominal True False False OMIMPS:100300 Adams-Oliver syndrome True False False OMIMPS:101800 Acrodysostosis True False False @@ -27319,6 +27337,7 @@ OMIMPS:214450 Griscelli syndrome True False False OMIMPS:214700 Diarrhea, congenital True False False OMIMPS:215100 Rhizomelic chondrodysplasia punctata True False False OMIMPS:215500 Choroidal dystrophy, central areolar True False False +OMIMPS:215700 Citrullinemia True False False OMIMPS:218330 Cranioectodermal dysplasia True False False OMIMPS:219000 Fraser syndrome True False False OMIMPS:220110 Mitochondrial complex IV deficiency, nuclear-type True False False @@ -27659,6 +27678,7 @@ OMIM:164891 True False True OMIM:168850 True False True OMIM:175020 True False True OMIM:181515 True False True +OMIM:210730 True False True OMIM:247440 True False True OMIM:249660 True False True OMIM:252700 True False True @@ -27727,7 +27747,7 @@ OMIM:106900 anonychia-ectrodactyly True True False OMIM:106990 anonychia-onychodystrophy with brachydactyly type B and ectrodactyly True True False OMIM:107320 antiphospholipid syndrome, familial True True False OMIM:107440 antiviral state repressor, regulator of True True False -OMIM:107500 aortic arch anomaly with peculiar facies and mental retardation True True False +OMIM:107500 aortic arch anomaly with peculiar facies and impaired intellectual development True True False OMIM:107550 aortic arch interruption, facial palsy, and retinal coloboma True True False OMIM:107640 apnea, central sleep True True False OMIM:107700 appendicitis, proneness to True True False @@ -27811,7 +27831,7 @@ OMIM:121070 arthrogryposis, distal, type 2e True True False OMIM:121270 copper deficiency, familial benign True True False OMIM:121350 coracoclavicular joint, anomalous True True False OMIM:121450 corneal degeneration, ribbonlike, with deafness True True False -OMIM:122430 corneal hypesthesia with retinal abnormalities, sensorineural deafness, unusual facies, persistent ductus arteriosus, and mental retardation True True False +OMIM:122430 ramos-arroyo syndrome True True False OMIM:122440 corneodermatoosseous syndrome True True False OMIM:122455 coronary artery dissection, spontaneous True True False OMIM:122580 costocoracoid ligament, congenitally short True True False @@ -27954,7 +27974,7 @@ OMIM:141405 hemifacial spasm, familial True True False OMIM:141700 hemolytic poikilocytic anemia due to reduced ankyrin binding sites True True False OMIM:142350 hernia, double inguinal True True False OMIM:142500 heterochromia iridis True True False -OMIM:142625 hirsutism, skeletal dysplasia, and mental retardation True True False +OMIM:142625 hirsutism, skeletal dysplasia, and impaired intellectual development True True False OMIM:142630 histiocytosis, progressive mucinous True True False OMIM:142730 histiocytic dermatoarthritis True True False OMIM:142770 hla modifier True True False @@ -28117,7 +28137,6 @@ OMIM:168100 paralysis agitans, juvenile, of hunt True True False OMIM:168200 paramolar tubercle of bolk True True False OMIM:168800 parotidomegaly, hereditary bilateral True True False OMIM:168830 passovoy factor defect True True False -OMIM:168885 paroxysmal tonic upgaze, benign childhood, with ataxia True True False OMIM:169170 patterson pseudoleprechaunism syndrome True True False OMIM:169200 pechet factor deficiency True True False OMIM:169300 pectus excavatum True True False @@ -28209,8 +28228,8 @@ OMIM:182255 skeletal dysplasia with delayed epiphyseal and carpal bone ossificat OMIM:182260 slipped femoral capital epiphyses True True False OMIM:182270 ketone compounds, ability to smell True True False OMIM:182400 somatomedin, embryonic True True False -OMIM:182610 spastic paraplegia, epilepsy, and mental retardation True True False -OMIM:182690 spastic paraplegia, sensorineural deafness, mental retardation, and progressive nephropathy True True False +OMIM:182610 spastic paraplegia, epilepsy, and impaired intellectual development True True False +OMIM:182690 spastic paraplegia, sensorineural deafness, impaired intellectual development, and progressive nephropathy True True False OMIM:182800 spastic paraplegia with associated extrapyramidal signs True True False OMIM:182815 spastic paraplegia with neuropathy and poikiloderma True True False OMIM:182820 spastic paraplegia with precocious puberty True True False @@ -28319,7 +28338,7 @@ OMIM:193450 vulvovaginitis, allergic seminal True True False OMIM:194000 widow's peak True True False OMIM:194320 woronets trait True True False OMIM:194400 xeroderma pigmentosum, autosomal dominant, mild True True False -OMIM:200130 absent eyebrows and eyelashes with mental retardation True True False +OMIM:200130 absent eyebrows and eyelashes with impaired intellectual development True True False OMIM:200170 acanthosis nigricans with muscle cramps and acral enlargement True True False OMIM:200300 acetophenetidin sensitivity True True False OMIM:200450 achalasia-microcephaly syndrome True True False @@ -28342,7 +28361,7 @@ OMIM:202660 pagod syndrome True True False OMIM:202900 alaninuria with microcephaly, dwarfism, enamel hypoplasia, and diabetes mellitus True True False OMIM:203000 frontonasal dysplasia with alar clefts True True False OMIM:203340 albinism-microcephaly-digital anomalies syndrome True True False -OMIM:203550 alopecia-contractures-dwarfism mental retardation syndrome True True False +OMIM:203550 intellectual developmental syndrome with alopecia, contractures, and dwarfism True True False OMIM:203600 alopecia-epilepsy-oligophrenia syndrome of moynahan True True False OMIM:203760 alpha-2-deficient collagen disease True True False OMIM:204110 amaurosis congenita, cone-rod type, with congenital hypertrichosis True True False @@ -28381,7 +28400,7 @@ OMIM:208910 ataxia-telangiectasia with generalized skin pigmentation and early d OMIM:209010 atherosclerosis, premature, with deafness, nephropathy, diabetes mellitus, photomyoclonus, and degenerative neurologic disease True True False OMIM:209050 athrombia, essential True True False OMIM:209600 atrioventricular dissociation True True False -OMIM:209770 aural atresia, multiple congenital anomalies, and mental retardation True True False +OMIM:209770 aural atresia, multiple congenital anomalies, and impaired intellectual development True True False OMIM:209800 australia antigen True True False OMIM:209970 beemer lethal malformation syndrome True True False OMIM:210050 berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification True True False @@ -28430,7 +28449,7 @@ OMIM:215050 chondrodysplasia calcificans metaphysealis True True False OMIM:215105 chondrodysplasia punctata syndrome True True False OMIM:215250 chondroitin-6-sulfaturia, defective cellular immunity, nephrotic syndrome True True False OMIM:215450 chorea, benign familial True True False -OMIM:215480 choroid plexus calcification and mental retardation True True False +OMIM:215480 choroid plexus calcification and impaired intellectual development True True False OMIM:215510 chromosomal instability with tissue-specific radiosensitivity True True False OMIM:215518 ciliary discoordination due to random ciliary orientation True True False OMIM:215550 circumvallate placenta syndrome True True False @@ -28453,17 +28472,17 @@ OMIM:218350 craniofacial dyssynostosis with short stature True True False OMIM:218450 craniostenosis, sagittal, with congenital heart disease, mental deficiency, and mandibular ankylosis True True False OMIM:218530 craniosynostosis with anomalies of the cranial base and digits True True False OMIM:218550 craniosynostosis with fibular aplasia True True False -OMIM:218649 craniosynostosis-mental retardation syndrome of 51n and gettig True True False -OMIM:218650 craniosynostosis-mental retardation-clefting syndrome True True False +OMIM:218649 lin-getting syndrome True True False +OMIM:218650 craniosynostosis-impaired intellectual development-clefting syndrome True True False OMIM:218670 craniotelencephalic dysplasia True True False OMIM:219070 curved nail of fourth toe True True False OMIM:219095 cutaneous photosensitivity and colitis, lethal True True False OMIM:219250 cutis marmorata telangiectatica congenita True True False -OMIM:219300 cutis verticis gyrata and mental retardation True True False +OMIM:219300 cutis verticis gyrata and impaired intellectual development True True False OMIM:219400 cyanosis and hepatic disease True True False OMIM:219550 cysteine peptiduria True True False -OMIM:219721 cystic fibrosis with helicobacter pylori gastritis, megaloblastic anemia, and mental retardation True True False -OMIM:220219 dandy-walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy True True False +OMIM:219721 cystic fibrosis with helicobacter pylori gastritis, megaloblastic anemia, and impaired intellectual development True True False +OMIM:220219 dandy-walker malformation with impaired intellectual development, macrocephaly, myopia, and brachytelephalangy True True False OMIM:220220 dandy-walker malformation with postaxial polydactyly True True False OMIM:220300 deafness, congenital, and familial myoclonic epilepsy True True False OMIM:220900 deafness, congenital, with total albinism True True False @@ -28478,7 +28497,7 @@ OMIM:221780 dermatoglyphics--hypothenar radial arch True True False OMIM:221790 dermatoleukodystrophy True True False OMIM:221810 dermatoosteolysis, kirghizian type True True False OMIM:221950 dextrocardia with unusual facies and microphthalmia True True False -OMIM:221995 diabetes insipidus, nephrogenic, with mental retardation and intracerebral calcification True True False +OMIM:221995 diabetes insipidus, nephrogenic, with impaired intellectual development and intracerebral calcification True True False OMIM:222350 diaminopentanuria True True False OMIM:222500 diastematomyelia True True False OMIM:223300 disseminated sclerosis with narcolepsy True True False @@ -28489,7 +28508,7 @@ OMIM:223350 dohle bodies and leukemia True True False OMIM:223380 dopamine beta-hydroxylase, plasma, thermolability of True True False OMIM:223400 duodenal atresia True True False OMIM:223500 dwarfism, low-birth-weight type, with unresponsiveness to growth hormone True True False -OMIM:223540 dwarfism, mental retardation, and eye abnormality True True False +OMIM:223540 mollica syndrome True True False OMIM:223550 dwarfism, proportionate, with hip dislocation True True False OMIM:224000 dysautonomia-like disorder True True False OMIM:224250 dysmyelination with jaundice True True False @@ -28509,9 +28528,9 @@ OMIM:226100 endocardial fibroelastosis and coarctation of abdominal aorta True T OMIM:226110 endothelial dystrophy, congenital hereditary, with nail hypoplasia True True False OMIM:226150 enterocolitis True True False OMIM:226350 eosinophilic fasciitis True True False -OMIM:226440 epidermolysis bullosa, late-onset localized junctional, with mental retardation True True False +OMIM:226440 epidermolysis bullosa, late-onset localized junctional, with impaired intellectual development True True False OMIM:226735 epidermolysis bullosa with diaphragmatic hernia True True False -OMIM:226800 epilepsy, photogenic, with spastic diplegia and mental retardation True True False +OMIM:226800 epilepsy, photogenic, with spastic diplegia and impaired intellectual development True True False OMIM:226810 epilepsy with bilateral occipital calcifications True True False OMIM:226850 epilepsy-telangiectasia True True False OMIM:226950 epiphyseal dysplasia of femoral head, myopia, and deafness True True False @@ -28519,7 +28538,7 @@ OMIM:226985 epithelial squamous dysplasia, keratinizing desquamative, of urinary OMIM:227000 erythema of acral regions True True False OMIM:227010 ermine phenotype True True False OMIM:227210 eyebrows, duplication of, with stretchable skin and syndactyly True True False -OMIM:227250 facial abnormalities, kyphoscoliosis, and mental retardation True True False +OMIM:227250 facial abnormalities, kyphoscoliosis, and impaired intellectual development True True False OMIM:227255 facial dysmorphism with multiple malformations True True False OMIM:227270 faciocardiomelic dysplasia, lethal True True False OMIM:227280 faciocardiorenal syndrome True True False @@ -28553,7 +28572,7 @@ OMIM:233450 goodpasture syndrome True True False OMIM:233800 grouped pigmentation of the retina True True False OMIM:233805 growth factors, combined defect of True True False OMIM:233810 growth retardation, small and puffy hands and feet, and eczema True True False -OMIM:234030 hair defect with photosensitivity and mental retardation True True False +OMIM:234030 hair defect with photosensitivity and impaired intellectual development True True False OMIM:234250 hall-riggs syndrome True True False OMIM:234280 hallux varus and preaxial polysyndactyly True True False OMIM:234300 halo nevi True True False @@ -28601,19 +28620,19 @@ OMIM:241120 hypohidrosis with abnormal palmar dermal ridges True True False OMIM:241519 hypophosphatemia, renal, with intracerebral calcifications True True False OMIM:241540 hypopituitarism, congenital, with central diabetes insipidus True True False OMIM:241550 hypoplastic left heart syndrome 1 True True False -OMIM:241760 hypospadias-mental retardation syndrome True True False +OMIM:241760 hypospadias-impaired intellectual development syndrome True True False OMIM:242050 hypouricemia, hypercalcinuria, and decreased bone density True True False OMIM:242400 ichthyosis congenita with biliary atresia True True False -OMIM:242510 ichthyosis with alopecia, eclabium, ectropion, and mental retardation True True False +OMIM:242510 ichthyosis with alopecia, eclabium, ectropion, and impaired intellectual development True True False OMIM:242520 ichthyosis, hepatosplenomegaly, and cerebellar degeneration True True False -OMIM:242530 ichthyosis, mental retardation, dwarfism, and renal impairment True True False +OMIM:242530 ichthyosis, impaired intellectual development, dwarfism, and renal impairment True True False OMIM:242550 ichthyosis, split hairs, and amino aciduria True True False OMIM:242680 ciliary dyskinesia with excessively long cilia True True False OMIM:242850 immune deficiency disease True True False OMIM:242870 immunodeficiency, partial combined, with absence of hla determinants and beta-2-microglobulin from lymphocytes True True False OMIM:242880 immunoerythromyeloid hypoplasia True True False OMIM:242890 immunoglobulin d level 1n plasma, low True True False -OMIM:243050 indolylacroyl glycinuria with mental retardation True True False +OMIM:243050 indolylacroyl glycinuria with impaired intellectual development True True False OMIM:243080 inosine phosphorylase deficiency, immune defect due to True True False OMIM:243100 internal carotid arteries, hypoplasia of True True False OMIM:243110 immunodeficiency with defective t-cell response to interleukin 1 True True False @@ -28632,9 +28651,9 @@ OMIM:245190 kniest-like dysplasia, lethal True True False OMIM:245550 lambert syndrome True True False OMIM:245650 larsen-like syndrome, lethal type True True False OMIM:246470 leukemia, acute myelocytic, with polyposis coli and colon cancer True True False -OMIM:246500 leukomelanoderma, infantilism, mental retardation, hypodontia, hypotrichosis True True False +OMIM:246500 leukomelanoderma, infantilism, impaired intellectual development, hypodontia, hypotrichosis True True False OMIM:246550 lichtenstein syndrome True True False -OMIM:246555 limb defects, distal transverse, with mental retardation and spasticity True True False +OMIM:246555 limb defects, distal transverse, with impaired intellectual development and spasticity True True False OMIM:246570 fibular aplasia, tibial campomelia, and oligosyndactyly syndrome True True False OMIM:247150 lip prints True True False OMIM:247410 lymphedema-hypoparathyroidism syndrome True True False @@ -28651,17 +28670,17 @@ OMIM:248100 macrosomia adiposa congenita True True False OMIM:248110 macrosomia with microphthalmia, lethal True True False OMIM:248260 magnesium, elevated red cell True True False OMIM:248350 malocclusion and short stature True True False -OMIM:248400 mandibulofacial dysostosis with mental retardation True True False +OMIM:248400 mandibulofacial dysostosis with impaired intellectual development True True False OMIM:248760 marfanoid habitus with microcephaly and glomerulonephritis True True False -OMIM:248770 marfanoid mental retardation syndrome, autosomal True True False +OMIM:248770 marfanoid impaired intellectual developmental syndrome, autosomal True True False OMIM:248910 cutaneous mastocytosis, conductive hearing loss and microtia True True False OMIM:248950 mcdonough syndrome True True False OMIM:249230 megaepiphyseal dwarfism True True False OMIM:249240 megalencephaly with dysmyelination True True False OMIM:249300 megalocornea True True False -OMIM:249599 mental retardation syndrome, belgian type True True False +OMIM:249599 intellectual developmental disorder, belgian type True True False OMIM:249600 mental retardation syndrome, mietens-weber type True True False -OMIM:249630 mental retardation, buenos aires type True True False +OMIM:249630 mutchinick syndrome True True False OMIM:249670 mesoaxial hexadactyly and cardiac malformation True True False OMIM:249710 mesomelic limb shortening and bowing True True False OMIM:250230 metaphyseal chondrodysplasia, kaitila type True True False @@ -28683,7 +28702,7 @@ OMIM:251945 mitochondrial myopathy with a defect 1n mitochondrial-protein transp OMIM:252250 monocyte chemotactic disorder True True False OMIM:252300 morquio syndrome c True True False OMIM:252320 motor neuropathy, peripheral, with dysautonomia True True False -OMIM:253320 multicore myopathy with mental retardation, short stature, and hypogonadotropic hypogonadism True True False +OMIM:253320 chudley syndrome True True False OMIM:253590 muscular dystrophy, adult-onset, with leukoencephalopathy True True False OMIM:254000 muscular dystrophy, congenital, with infantile cataract and hypogonadism True True False OMIM:254120 muscular hypertonia, lethal True True False @@ -28694,7 +28713,7 @@ OMIM:254700 myeloproliferative disease, autosomal recessive True True False OMIM:254950 myopathy, granulovacuolar lobular, with electrical myotonia True True False OMIM:254960 myopathy due to malate-aspartate shuttle defect True True False OMIM:255140 myopathy with giant abnormal mitochondria True True False -OMIM:255710 myotonia with skeletal abnormalities and mental retardation True True False +OMIM:255710 myotonia with skeletal abnormalities and impaired intellectual development True True False OMIM:255900 myxedema True True False OMIM:255990 nathalie syndrome True True False OMIM:256120 nephropathy, deafness, and hyperparathyroidism True True False @@ -28760,7 +28779,7 @@ OMIM:264060 prepapillary vascular loops True True False OMIM:264080 progesterone resistance True True False OMIM:264110 prolactin deficiency, isolated True True False OMIM:264120 prolactin deficiency with obesity and enlarged testes True True False -OMIM:264140 prune belly syndrome with pulmonic stenosis, mental retardation, and deafness True True False +OMIM:264140 prune belly syndrome with pulmonic stenosis, impaired intellectual development, and deafness True True False OMIM:264180 pseudodiastrophic dysplasia True True False OMIM:264420 fundus dystrophy, pseudoinflammatory, recessive form True True False OMIM:264475 pseudopapilledema, ocular hypotelorism, blepharophimosis, and hand anomalies True True False @@ -28787,7 +28806,7 @@ OMIM:267740 retinal degeneration and epilepsy True True False OMIM:267760 retinal degeneration with nanophthalmos, cystic macular degeneration, and angle closure glaucoma True True False OMIM:267900 retinal telangiectasia and hypogammaglobulinemia True True False OMIM:268010 retinitis pigmentosa inversa with deafness True True False -OMIM:268020 retinitis pigmentosa, deafness, mental retardation, and hypogonadism True True False +OMIM:268020 retinitis pigmentosa, deafness, impaired intellectual development, and hypogonadism True True False OMIM:268025 retinitis pigmentosa, late-adult onset True True False OMIM:268040 retinohepatoendocrinologic syndrome True True False OMIM:268050 mirhosseini-holmes-walton syndrome True True False @@ -28806,13 +28825,13 @@ OMIM:270220 sjogren-larsson-like ichthyosis without cns or eye involvement True OMIM:270350 anosmia for butyl mercaptan True True False OMIM:270425 sodium-potassium-atpase activity of red cell True True False OMIM:270460 sonoda syndrome True True False -OMIM:270500 ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and mental retardation True True False +OMIM:270500 ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and impaired intellectual development True True False OMIM:270805 spastic paraplegia with myoclonic epilepsy True True False -OMIM:270850 spastic paresis, glaucoma, and mental retardation True True False +OMIM:270850 spastic paresis, glaucoma, and impaired intellectual development True True False OMIM:270900 spastic pseudosclerosis True True False -OMIM:270950 spastic quadriplegia, retinitis pigmentosa, and mental retardation True True False -OMIM:271109 spinal muscular atrophy with mental retardation True True False -OMIM:271110 spinal muscular atrophy with microcephaly and mental subnormality True True False +OMIM:270950 spastic quadriplegia, retinitis pigmentosa, and impaired intellectual development True True False +OMIM:271109 spinal muscular atrophy with impaired intellectual development True True False +OMIM:271110 spinal muscular atrophy with microcephaly and impaired intellectual development True True False OMIM:271200 spinal muscular atrophy, ryukyuan type True True False OMIM:271220 spinal muscular atrophy, scapuloperoneal True True False OMIM:271270 spinocerebellar ataxia with dysmorphism True True False @@ -28821,7 +28840,7 @@ OMIM:271320 spinocerebellar degeneration with macular corneal dystrophy, congeni OMIM:271322 spinocerebellar degeneration with slow eye movements True True False OMIM:271500 splenoportal vascular anomalies True True False OMIM:271520 spondylocostal dysostosis with anal atresia and urogenital anomalies True True False -OMIM:271620 spondyloepiphyseal dysplasia tarda with mental retardation True True False +OMIM:271620 spondyloepiphyseal dysplasia tarda with impaired intellectual development True True False OMIM:271950 subaortic stenosis, membranous True True False OMIM:271960 subaortic stenosis--short stature syndrome True True False OMIM:272000 sucrosuria, hiatus hernia, and impaired intellectual development True True False @@ -28861,17 +28880,17 @@ OMIM:275450 trichoodontoonychial dysplasia with bone deficiency True True False OMIM:275595 trigonobrachycephaly, bulbous bifid nose, micrognathia, and abnormalities of the hands and feet True True False OMIM:276200 t-substance anomaly True True False OMIM:276800 tyrosinosis True True False -OMIM:276821 ulnar hypoplasia with mental retardation True True False +OMIM:276821 ulnar hypoplasia with impaired intellectual development True True False OMIM:276822 ulnar agenesis and endocardial fibroelastosis True True False OMIM:277175 vascular hyalinosis True True False OMIM:277200 right ventricular hypoplasia, isolated True True False -OMIM:277465 vitiligo, progressive, with mental retardation and urethral duplication True True False +OMIM:277465 vitiligo, progressive, with impaired intellectual development and urethral duplication True True False OMIM:277740 white forelock with malformations True True False -OMIM:277990 wolff mental retardation syndrome True True False +OMIM:277990 wolff syndrome True True False OMIM:278200 woolly hair, hypotrichosis, everted lower lip, and outstanding ears True True False OMIM:278900 xylosidase deficiency True True False OMIM:300042 alopecia, congenital True True False -OMIM:300064 mental retardation, x-linked, with craniofacial dysmorphism True True False +OMIM:300064 hyde-forster syndrome True True False OMIM:300073 fetal akinesia syndrome, X-linked True True False OMIM:300129 hematopoietic stem cell kinetics, control of True True False OMIM:300184 hypotonia, congenital nystagmus, ataxia, and abnormal auditory brainstem responses True True False @@ -28899,7 +28918,7 @@ OMIM:302803 charcot-marie-tooth peroneal muscular atrophy, x-linked, with aplasi OMIM:302900 charcot-marie-tooth peroneal muscular atrophy and friedreich ataxia, combined True True False OMIM:303650 colonic atresia True True False OMIM:304030 cone dystrophy, x-linked, with tapetal-like sheen True True False -OMIM:304200 cutis verticis gyrata, thyroid aplasia, and mental retardation True True False +OMIM:304200 cutis verticis gyrata, thyroid aplasia, and impaired intellectual development True True False OMIM:304300 cyanide, inability to smell True True False OMIM:304350 deafness-hypogonadism syndrome True True False OMIM:304900 diabetes insipidus, neurohypophyseal, X-linked True True False @@ -28917,7 +28936,7 @@ OMIM:306980 hirschsprung disease with type d brachydactyly True True False OMIM:306990 microhydranencephaly, X-linked True True False OMIM:306995 homosexuality 1 True True False OMIM:307010 hydrocephalus with cerebellar agenesis True True False -OMIM:307500 hypogonadism, male, with mental retardation and skeletal anomalies True True False +OMIM:307500 hypogonadism, male, with impaired intellectual development and skeletal anomalies True True False OMIM:307830 hypouricemia, familial renal, due to tubular hypersecretion True True False OMIM:308200 ichthyosis and male hypogonadism True True False OMIM:308220 immunodeficiency, x-linked, with deficiency of 115,000 dalton surface glycoprotein True True False @@ -28929,7 +28948,7 @@ OMIM:308830 keratosis follicularis, dwarfism, and cerebral atrophy True True Fal OMIM:308850 laryngeal abductor paralysis, X-linked True True False OMIM:308950 lesch-nyhan phenotype with normal hgprt True True False OMIM:308960 leukemia, acute, X-linked True True False -OMIM:309480 mental retardation and psoriasis True True False +OMIM:309480 impaired intellectual development and psoriasis True True False OMIM:309640 mental retardation with spastic paraplegia True True False OMIM:309840 modifier, x-linked, for neurofunctional defects True True False OMIM:309930 muscular dystrophy, cardiac type True True False @@ -28955,7 +28974,7 @@ OMIM:312210 radiation sensitivity of natural killer activity True True False OMIM:312550 retinal dysplasia, primary True True False OMIM:312780 russell-silver syndrome, X-linked True True False OMIM:312830 scarf syndrome True True False -OMIM:312840 schimke X-linked mental retardation syndrome True True False +OMIM:312840 schimke syndrome True True False OMIM:312910 spastic paraparesis and deafness True True False OMIM:313480 taqi polymorphism True True False OMIM:314000 thrombocytopenia with elevated serum iga and renal disease True True False @@ -28970,6 +28989,7 @@ OMIM:314800 xh antigen True True False OMIM:424500 gonadoblastoma True True False OMIM:425500 hairy ears, Y-linked True True False OMIM:489000 ubiquitin-activating enzyme, Y-linked True True False +OMIM:500007 cyclic vomiting syndrome True True False OMIM:600000 spondylocamptodactyly True True False OMIM:600080 myelocytic leukemia-like syndrome, familial, chronic True True False OMIM:600084 macrocytosis, familial True True False @@ -28977,9 +28997,9 @@ OMIM:600089 pancreatic beta cell agenesis with neonatal diabetes mellitus True T OMIM:600093 spondyloepiphyseal dysplasia tarda with characteristic facies True True False OMIM:600096 puerto rican infant hypotonia syndrome True True False OMIM:600117 dysphasia, familial developmental True True False -OMIM:600122 male pseudohermaphroditism/mental retardation syndrome, verloes type True True False +OMIM:600122 verloes syndrome True True False OMIM:600123 atrioventricular septal defect with blepharophimosis and anal and radial defects True True False -OMIM:600159 pterygium colli and mental retardation with facial and digital anomalies True True False +OMIM:600159 pterygium colli and impaired intellectual development with facial and digital anomalies True True False OMIM:600166 hyperparathyroidism, primary, caused by water clear cell hyperplasia True True False OMIM:600171 gonadal agenesis True True False OMIM:600252 lowry-maclean syndrome True True False @@ -29014,7 +29034,7 @@ OMIM:600801 isoproterenol-mediated vasodilatation True True False OMIM:600841 eukaryotic translation elongation factor 1 alpha-1-like 14 True True False OMIM:600851 mitochondrial import-stimulating factor True True False OMIM:600903 wiskott-aldrich syndrome, autosomal dominant True True False -OMIM:600906 ectodermal dysplasia with mental retardation and syndactyly True True False +OMIM:600906 ectodermal dysplasia with impaired intellectual development and syndactyly True True False OMIM:600907 enamel hypoplasia, cataracts, and aqueductal stenosis True True False OMIM:600931 protocadherin 3 True True False OMIM:600952 transsexuality True True False @@ -29023,7 +29043,7 @@ OMIM:600991 hydrocephalus, sprengel anomaly, and costovertebral dysplasia True T OMIM:601004 portal vein, cavernous transformation of True True False OMIM:601016 midline malformations, multiple, with limb abnormalities and hypopituitarism True True False OMIM:601027 tibia, absence or hypoplasia of, with polydactyly, retrocerebellar arachnoid cyst, and other anomalies True True False -OMIM:601039 ichthyosis-mental retardation syndrome with large keratohyalin granules 1n the skin True True False +OMIM:601039 ichthyosis-impaired intellectual developmental syndrome with large keratohyalin granules 1n the skin True True False OMIM:601075 aplasia cutis congenita, high myopia, and cone-rod dysfunction True True False OMIM:601083 cd4/cd8 t-cell ratio True True False OMIM:601095 harrod syndrome True True False @@ -29036,7 +29056,7 @@ OMIM:601165 cleft lip/palate with characteristic facies, intestinal malrotation, OMIM:601170 muscular dystrophy, congenital, with severe central nervous system atrophy and absence of large myelinated fibers True True False OMIM:601187 gurrieri syndrome True True False OMIM:601195 iron overload 1n africa True True False -OMIM:601217 alopecia-mental retardation syndrome with convulsions and hypergonadotropic hypogonadism True True False +OMIM:601217 alopecia-impaired intellectual developmental syndrome with convulsions and hypergonadotropic hypogonadism True True False OMIM:601220 osteoporosis and oculocutaneous hypopigmentation syndrome True True False OMIM:601223 neuronal intestinal dysplasia, type B True True False OMIM:601230 dermatitis herpetiformis, familial True True False @@ -29050,7 +29070,7 @@ OMIM:601347 myelodysplasia, immunodeficiency, facial dysmorphism, short stature, OMIM:601348 ectrodactyly of lower limbs, congenital heart defect, and micrognathia True True False OMIM:601350 short stature syndrome, brussels type True True False OMIM:601351 growth retardation, deafness, femoral epiphyseal dysplasia, and lacrimal duct obstruction True True False -OMIM:601352 mental retardation, microcephaly, epilepsy, and coarse face True True False +OMIM:601352 impaired intellectual development, microcephaly, epilepsy, and coarse face True True False OMIM:601355 microcephaly, congenital heart disease, unilateral renal agenesis, and hyposegmented lungs True True False OMIM:601370 holoprosencephaly, semilobar, with craniosynostosis True True False OMIM:601371 cataract, age-related nuclear True True False @@ -29099,20 +29119,20 @@ OMIM:602511 pseudoacromegaly with severe insulin resistance True True False OMIM:602551 jejunal atresia with renal adysplasia True True False OMIM:602553 anal atresia, hypospadias, and penoscrotal inversion True True False OMIM:602554 torsion dystonia with onset 1n infancy True True False -OMIM:602555 microcephaly, macrotia, and mental retardation True True False +OMIM:602555 microcephaly, macrotia, and impaired intellectual development True True False OMIM:602556 facial dysmorphism, cleft palate, hearing loss, and camptodactyly True True False OMIM:602558 craniomicromelic syndrome True True False OMIM:602561 brachydactyly, intraventricular septal defect, and deafness True True False OMIM:602562 mandibulofacial dysostosis with macroblepharon and macrostomia True True False -OMIM:602564 emphysema, congenital, with deafness, penoscrotal web, and mental retardation True True False +OMIM:602564 emphysema, congenital, with deafness, penoscrotal web, and intellectual developmental disorder True True False OMIM:602596 pancreatic lymphoma, familial True True False -OMIM:602611 spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and mental retardation True True False +OMIM:602611 spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and impaired intellectual development True True False OMIM:602612 camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye True True False OMIM:602613 skeletal dysplasia and progressive central nervous system degeneration, lethal True True False OMIM:602994 leukoregulin True True False OMIM:603117 spastic paraplegia, optic atrophy, microcephaly, and 10y sex reversal True True False OMIM:603119 apraxia of eyelid opening True True False -OMIM:603133 dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and mental retardation True True False +OMIM:603133 dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and impaired intellectual development True True False OMIM:603174 hyperhomocysteinemia True True False OMIM:603323 muscular dystrophy, congenital, with cerebellar atrophy True True False OMIM:603376 long chain fatty acids, defect 1n transport of True True False @@ -29121,13 +29141,13 @@ OMIM:603393 osteosclerotic chondrodysplasia, lethal, with intracellular inclusio OMIM:603394 microcephaly, severe, with skeletal anomalies including posterior rib-gap defects True True False OMIM:603396 tonoki syndrome True True False OMIM:603416 ribosomal protein l21 pseudogene 1 True True False -OMIM:603438 radioulnar synostosis with microcephaly, short stature, scoliosis, and mental retardation True True False +OMIM:603438 tsukahara syndrome True True False OMIM:603439 expansile bone lesions True True False OMIM:603446 oroacral syndrome, verloes-koulischer type True True False OMIM:603523 chylothorax, congenital True True False OMIM:603529 dyserythropoiesis, congenital, with ultrastructurally normal erythroblast heterochromatin True True False OMIM:603569 tracheobronchial stenosis, congenital True True False -OMIM:603572 microcephaly, facial abnormalities, micromelia, and mental retardation True True False +OMIM:603572 microcephaly, facial abnormalities, micromelia, and impaired intellectual development True True False OMIM:603587 follicular atrophoderma, perioral pigmented, with milia and epidermoid cysts True True False OMIM:603588 parotitis, juvenile recurrent True True False OMIM:603589 facial dysmorphism, selective tooth agenesis, and choroid calcification True True False @@ -29151,7 +29171,7 @@ OMIM:604211 hirschsprung disease with heart defects, laryngeal anomalies, and pr OMIM:604257 camera-marugo-cohen syndrome True True False OMIM:604287 carney triad True True False OMIM:604291 ascaris lumbricoides infection, susceptibility to True True False -OMIM:604315 anemia, congenital hypoplastic, with multiple congenital anomalies/mental retardation syndrome True True False +OMIM:604315 anemia, congenital hypoplastic, with multiple congenital anomalies/impaired intellectual development syndrome True True False OMIM:604324 acne, adult True True False OMIM:604335 reflex sympathetic dystrophy True True False OMIM:604363 myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders True True False @@ -29173,7 +29193,7 @@ OMIM:605067 tricuspid atresia True True False OMIM:605105 early response to neural induction gene True True False OMIM:605274 mesomelic dysplasia, savarirayan type True True False OMIM:605321 frontoocular syndrome True True False -OMIM:605400 fibromatosis, gingival, with hypertrichosis and mental retardation True True False +OMIM:605400 fibromatosis, gingival, with hypertrichosis and impaired intellectual development True True False OMIM:605463 radiation sensitivity/chromosome instability syndrome, autosomal dominant True True False OMIM:605618 tetralogy of fallot syndrome, autosomal recessive True True False OMIM:605672 cerebellar ataxia and hypergonadotropic hypogonadism True True False @@ -29197,7 +29217,7 @@ OMIM:606519 phace association True True False OMIM:606527 megarbane syndrome True True False OMIM:606529 craniosynostosis syndrome, autosomal recessive True True False OMIM:606752 acute hemorrhagic leukoencephalitis True True False -OMIM:606851 cree mental retardation syndrome True True False +OMIM:606851 cree impaired intellectual development syndrome True True False OMIM:606894 duodenojejunal atresia with volvulus, absent dorsal mesentery, and absent superior mesenteric artery True True False OMIM:606895 symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch True True False OMIM:607044 t-box 24 True True False @@ -29209,7 +29229,7 @@ OMIM:607395 streptococcus, group a, severity of infection by True True False OMIM:607504 headache associated with sexual activity True True False OMIM:607540 secretory diarrhea, myopathy, and deafness True True False OMIM:607543 spondylometaphyseal dysplasia with bowed forearms and facial dysmorphism True True False -OMIM:607565 spastic paraplegia, ataxia, and mental retardation True True False +OMIM:607565 spastic paraplegia, ataxia, and impaired intellectual development True True False OMIM:607578 breath-holding spells True True False OMIM:607597 microphthalmia with cyst, bilateral facial clefts, and limb anomalies True True False OMIM:607665 tubulointerstitial nephritis with uveitis True True False @@ -29220,7 +29240,7 @@ OMIM:608184 immunodeficiency with hyper-igm, type 4 True True False OMIM:608223 aspirin resistance True True False OMIM:608227 craniofacial abnormalities, cataracts, congenital heart disease, sacral neural tube defects, and growth and developmental retardation True True False OMIM:608257 mandibulofacial dysostosis with ptosis, autosomal dominant True True False -OMIM:608278 growth failure, microcephaly, mental retardation, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy True True False +OMIM:608278 growth failure, microcephaly, impaired intellectual development, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy True True False OMIM:608279 craniosynostosis with ocular abnormalities and hallucal defects True True False OMIM:608281 scimitar anomaly, multiple cardiac malformations, and craniofacial and central nervous system abnormalities True True False OMIM:608406 vater-like defects with pulmonary hypertension, laryngeal webs, and growth deficiency True True False @@ -29238,12 +29258,12 @@ OMIM:608809 leukoencephalopathy, arthritis, colitis, and hypogammaglobulinema Tr OMIM:608811 metaphyseal undermodeling, spondylar dysplasia, and overgrowth True True False OMIM:608814 lateral semicircular canal malformation, familial, with external and middle ear abnormalities True True False OMIM:609008 marfanoid habitus with situs inversus True True False -OMIM:609037 mental retardation with optic atrophy, facial dysmorphism, microcephaly, and short stature True True False +OMIM:609037 intellectual developmental disorder with optic atrophy, facial dysmorphism, microcephaly, and short stature True True False OMIM:609047 skeletal dysplasia, rhizomelic, with retinitis pigmentosa True True False OMIM:609250 hypotrichosis, progressive patterned scalp, with wiry hair, onycholysis, and cleft lip/palate True True False OMIM:609345 cerebrorenodigital syndrome with limb malformations and triradiate acetabula True True False OMIM:609363 colloid cysts of third ventricle True True False -OMIM:609438 mental retardation, keratoconus, febrile seizures, and sinoatrial block True True False +OMIM:609438 intellectual developmental disorder with keratoconus, febrile seizures, and sinoatrial block True True False OMIM:609442 valproate embryopathy, susceptibility to True True False OMIM:609466 cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss True True False OMIM:609515 iridogoniodysgenesis and skeletal anomalies True True False @@ -29282,7 +29302,7 @@ OMIM:612867 corneal dystrophy, subepithelial mucinous True True False OMIM:612916 zechi-ceide syndrome True True False OMIM:612917 giacheti syndrome True True False OMIM:612947 microcephaly, growth retardation, cataract, hearing loss, and unusual appearance True True False -OMIM:612948 stargardt macular degeneration, absent or hypoplastic corpus callosum, mental retardation, and dysmorphic facial features True True False +OMIM:612948 stargardt macular degeneration, absent or hypoplastic corpus callosum, impaired intellectual development, and dysmorphic facial features True True False OMIM:613005 santos syndrome True True False OMIM:613124 hydrops fetalis, nonimmune, with gracile bones and dysmorphism True True False OMIM:613241 pseudopili annulati True True False @@ -29290,7 +29310,7 @@ OMIM:613342 mseleni joint disease True True False OMIM:613600 torsade lange pointes, short-coupled variant True True False OMIM:613601 early repolarization associated with ventricular fibrillation True True False OMIM:613623 agenesis of the corpus callosum and congenital lymphedema True True False -OMIM:613627 brachydactyly, type a1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation True True False +OMIM:613627 tsukahara syndrome True True False OMIM:614033 hydroxyacyl glutathione hydrolase deficiency True True False OMIM:614036 alpha-2-macroglobulin deficiency True True False OMIM:614037 leukotriene c4 synthase deficiency True True False diff --git a/src/ontology/reports/omim_term_exclusions.txt b/src/ontology/reports/omim_term_exclusions.txt index 6c8cc877..a0cda27e 100644 --- a/src/ontology/reports/omim_term_exclusions.txt +++ b/src/ontology/reports/omim_term_exclusions.txt @@ -2078,7 +2078,6 @@ OMIM:168810 OMIM:168820 OMIM:168830 OMIM:168840 -OMIM:168885 OMIM:168890 OMIM:169170 OMIM:169190 @@ -4590,6 +4589,7 @@ OMIM:480100 OMIM:489000 OMIM:489500 OMIM:490000 +OMIM:500007 OMIM:502000 OMIM:516000 OMIM:516001 @@ -19230,3 +19230,19 @@ OMIM:620801 OMIM:620802 OMIM:620803 OMIM:620804 +OMIM:620805 +OMIM:620808 +OMIM:620809 +OMIM:620810 +OMIM:620811 +OMIM:620812 +OMIM:620821 +OMIM:620822 +OMIM:620823 +OMIM:620824 +OMIM:620826 +OMIM:620827 +OMIM:620828 +OMIM:620829 +OMIM:620831 +OMIMPS:151623 diff --git a/src/ontology/reports/omim_unmapped_terms.tsv b/src/ontology/reports/omim_unmapped_terms.tsv index 27c1acb6..401aee0d 100644 --- a/src/ontology/reports/omim_unmapped_terms.tsv +++ b/src/ontology/reports/omim_unmapped_terms.tsv @@ -1,11 +1,6 @@ subject_id subject_label -OMIMPS:215700 Citrullinemia -OMIMPS:151623 Li-Fraumeni syndrome -OMIM:620789 aplasia cutis-enamel dysplasia syndrome -OMIM:620795 autoinflammation with episodic fever and immune dysregulation -OMIM:620786 basal ganglia calcification, idiopathic, 9, autosomal recessive -OMIM:620794 deafness, autosomal recessive 124 -OMIM:620790 neurodevelopmental disorder with hypotonia and seizures -OMIM:620785 neurodevelopmental disorder with progressive movement abnormalities -OMIM:620792 otosclerosis 12 -OMIM:620796 proteasome-associated autoinflammatory syndrome 6 +OMIMPS:619539 Neuroocular syndrome +OMIM:620806 developmental and epileptic encephalopathy 116 +OMIM:620820 el hayek-chahrour neurodevelopmental syndrome +OMIM:500017 leigh syndrome, mitochondrial +OMIM:620819 rothmund-thomson syndrome, type 4 diff --git a/src/ontology/reports/ordo.subclass.added-obsolete.robot.tsv b/src/ontology/reports/ordo.subclass.added-obsolete.robot.tsv index f0d5e3a1..1886a229 100644 --- a/src/ontology/reports/ordo.subclass.added-obsolete.robot.tsv +++ b/src/ontology/reports/ordo.subclass.added-obsolete.robot.tsv @@ -179,6 +179,7 @@ MONDO:0004542 cervical adenosquamous carcinoma, glassy cell variant MONDO:001627 MONDO:0004604 Hodgkin's lymphoma, lymphocytic-histiocytic predominance MONDO:8000031 Orphanet:98845 Orphanet:557494 obsolete subtype of a disorder MONDO:0004620 Hodgkin's lymphoma, lymphocytic depletion MONDO:8000031 Orphanet:98846 Orphanet:557494 obsolete subtype of a disorder MONDO:0004633 Hodgkin's lymphoma, mixed cellularity MONDO:8000031 Orphanet:98844 Orphanet:557494 obsolete subtype of a disorder +MONDO:0004665 nodular sclerosis classical Hodgkin lymphoma MONDO:8000031 Orphanet:98843 Orphanet:557494 obsolete subtype of a disorder MONDO:0004691 autosomal dominant polycystic kidney disease MONDO:0018396 Orphanet:730 Orphanet:399824 obsolete rare male fertility disorder with obstructive azoospermia MONDO:0004691 autosomal dominant polycystic kidney disease MONDO:0018409 Orphanet:730 Orphanet:400003 obsolete rare genetic disorder with obstructive azoospermia MONDO:0004691 autosomal dominant polycystic kidney disease MONDO:0022409 Orphanet:730 Orphanet:156162 obsolete nephropathy-associated ciliopathy @@ -201,6 +202,7 @@ MONDO:0005100 systemic sclerosis MONDO:0015939 Orphanet:90291 Orphanet:182228 ob MONDO:0005103 well-differentiated liposarcoma MONDO:8000031 Orphanet:99971 Orphanet:557494 obsolete subtype of a disorder MONDO:0005116 Whipple disease MONDO:0015245 Orphanet:3452 Orphanet:117569 obsolete rare intestinal disease MONDO:0005116 Whipple disease MONDO:0015575 Orphanet:3452 Orphanet:163582 obsolete rare bacterial infectious disease +MONDO:0005116 Whipple disease MONDO:0015979 Orphanet:3452 Orphanet:183710 obsolete hereditary predisposition to infections MONDO:0005116 Whipple disease MONDO:0017652 Orphanet:3452 Orphanet:306753 obsolete rare disease with myoclonus as a major feature MONDO:0005124 leprosy MONDO:0015575 Orphanet:548 Orphanet:163582 obsolete rare bacterial infectious disease MONDO:0005124 leprosy MONDO:0016104 Orphanet:548 Orphanet:206613 obsolete infectious disease with peripheral neuropathy @@ -1245,6 +1247,7 @@ MONDO:0008101 familial supernumerary nipples MONDO:0015852 Orphanet:2456 Orphane MONDO:0008101 familial supernumerary nipples MONDO:8000030 Orphanet:2456 Orphanet:377791 obsolete morphological anomaly MONDO:0008108 oculocerebrocutaneous syndrome MONDO:0017120 Orphanet:1647 Orphanet:269531 obsolete other syndrome with a central nervous system malformation as major feature MONDO:0008108 oculocerebrocutaneous syndrome MONDO:8000032 Orphanet:1647 Orphanet:377789 obsolete malformation syndrome +MONDO:0008109 ocular cicatricial pemphigoid MONDO:0020198 Orphanet:99922 Orphanet:98610 obsolete rare conjunctival disease MONDO:0008111 oculodentodigital dysplasia MONDO:0015336 Orphanet:2710 Orphanet:139042 obsolete malformation syndrome with odontal and/or periodontal component MONDO:0008111 oculodentodigital dysplasia MONDO:0020225 Orphanet:2710 Orphanet:98641 obsolete syndromic cataract MONDO:0008111 oculodentodigital dysplasia MONDO:0026190 Orphanet:2710 Orphanet:183580 obsolete genetic malformation syndrome with odontal and/or periodontal component @@ -1396,7 +1399,7 @@ MONDO:0008286 crossed polysyndactyly MONDO:8000032 Orphanet:2935 Orphanet:377789 MONDO:0008287 Greig cephalopolysyndactyly syndrome MONDO:0017434 Orphanet:380 Orphanet:294959 obsolete syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy MONDO:0008287 Greig cephalopolysyndactyly syndrome MONDO:0043008 Orphanet:380 Orphanet:330206 obsolete genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability MONDO:0008287 Greig cephalopolysyndactyly syndrome MONDO:8000032 Orphanet:380 Orphanet:377789 obsolete malformation syndrome -MONDO:0008289 brain small vessel disease 1 with or without ocular anomalies MONDO:0018790 Orphanet:36383 Orphanet:477765 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendancy +MONDO:0008289 brain small vessel disease 1 with or without ocular anomalies MONDO:0018790 Orphanet:36383 Orphanet:477765 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendency MONDO:0008291 porokeratosis plantaris palmaris et disseminata MONDO:0016518 Orphanet:737 Orphanet:2338 obsolete isolated punctate palmoplantar keratoderma MONDO:0008291 porokeratosis plantaris palmaris et disseminata MONDO:0026152 Orphanet:737 Orphanet:183444 obsolete genetic porokeratosis MONDO:0008292 punctate palmoplantar keratoderma type 2 MONDO:0016518 Orphanet:79502 Orphanet:2338 obsolete isolated punctate palmoplantar keratoderma @@ -1469,7 +1472,7 @@ MONDO:0008365 recombinant 8 syndrome MONDO:8000032 Orphanet:96167 Orphanet:37778 MONDO:0008368 autosomal dominant distal renal tubular acidosis MONDO:8000031 Orphanet:93608 Orphanet:557494 obsolete subtype of a disorder MONDO:0008369 proximal renal tubular acidosis MONDO:0017828 Orphanet:47159 Orphanet:314822 obsolete primary renal tubular acidosis MONDO:0008371 Dowling-Degos disease MONDO:0018293 Orphanet:79145 Orphanet:371200 obsolete congenital disorder of glycosylation with skin involvement -MONDO:0008373 retinal arterial tortuosity MONDO:0018790 Orphanet:75326 Orphanet:477765 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendancy +MONDO:0008373 retinal arterial tortuosity MONDO:0018790 Orphanet:75326 Orphanet:477765 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendency MONDO:0008380 retinoblastoma MONDO:0015121 Orphanet:790 Orphanet:101950 obsolete rare eye tumor MONDO:0008387 ring dermoid of cornea MONDO:0015121 Orphanet:91481 Orphanet:101950 obsolete rare eye tumor MONDO:0008387 ring dermoid of cornea MONDO:0015966 Orphanet:91481 Orphanet:183619 obsolete hereditary eye tumor @@ -2060,6 +2063,7 @@ MONDO:0008900 camptodactyly with fibrous tissue hyperplasia and skeletal dysplas MONDO:0008900 camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia MONDO:8000032 Orphanet:1321 Orphanet:377789 obsolete malformation syndrome MONDO:0008901 Tel Hashomer camptodactyly syndrome MONDO:0018235 Orphanet:3292 Orphanet:364568 obsolete dysostosis with limb anomaly as a major feature MONDO:0008901 Tel Hashomer camptodactyly syndrome MONDO:8000032 Orphanet:3292 Orphanet:377789 obsolete malformation syndrome +MONDO:0008905 predisposition to invasive fungal disease due to CARD9 deficiency MONDO:0015979 Orphanet:457088 Orphanet:183710 obsolete hereditary predisposition to infections MONDO:0008907 PMM2-congenital disorder of glycosylation MONDO:0018287 Orphanet:79318 Orphanet:371071 obsolete congenital disorder of glycosylation with epilepsy as a major feature MONDO:0008907 PMM2-congenital disorder of glycosylation MONDO:0018288 Orphanet:79318 Orphanet:371157 obsolete congenital disorder of glycosylation with hepatic involvement MONDO:0008907 PMM2-congenital disorder of glycosylation MONDO:0018293 Orphanet:79318 Orphanet:371200 obsolete congenital disorder of glycosylation with skin involvement @@ -4054,6 +4058,7 @@ MONDO:0010654 Partington syndrome MONDO:0035862 Orphanet:94083 Orphanet:611314 o MONDO:0010654 Partington syndrome MONDO:8000032 Orphanet:94083 Orphanet:377789 obsolete malformation syndrome MONDO:0010655 X-linked intellectual disability with marfanoid habitus MONDO:0035863 Orphanet:776 Orphanet:611327 obsolete genetic multiple congenital anomalies/dysmorphic syndrome-intellectual disability MONDO:0010655 X-linked intellectual disability with marfanoid habitus MONDO:8000032 Orphanet:776 Orphanet:377789 obsolete malformation syndrome +MONDO:0010656 intellectual disability, X-linked 1 MONDO:0035862 Orphanet:397933 Orphanet:611314 obsolete rare syndromic intellectual disability without multiple congenital anomalies/dysmorphic syndrome MONDO:0010657 methylmalonic acidemia with homocystinuria, type cblX MONDO:8000031 Orphanet:369962 Orphanet:557494 obsolete subtype of a disorder MONDO:0010658 syndromic X-linked intellectual disability 12 MONDO:0035862 Orphanet:85290 Orphanet:611314 obsolete rare syndromic intellectual disability without multiple congenital anomalies/dysmorphic syndrome MONDO:0010658 syndromic X-linked intellectual disability 12 MONDO:8000032 Orphanet:85290 Orphanet:377789 obsolete malformation syndrome @@ -4916,6 +4921,7 @@ MONDO:0011884 hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma sy MONDO:0011884 hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome MONDO:0020095 Orphanet:307936 Orphanet:98353 obsolete autosomal dominant disease associated with focal palmoplantar keratoderma as a major feature MONDO:0011885 tubulointerstitial nephritis and uveitis syndrome MONDO:0017259 Orphanet:91500 Orphanet:280926 obsolete systemic diseases with anterior uveitis MONDO:0011885 tubulointerstitial nephritis and uveitis syndrome MONDO:0019744 Orphanet:91500 Orphanet:93603 obsolete rare renal tubular disease +MONDO:0011888 immunodeficiency 67 MONDO:0015979 Orphanet:70592 Orphanet:183710 obsolete hereditary predisposition to infections MONDO:0011897 leukoencephalopathy-ataxia-hypodontia-hypomyelination syndrome MONDO:0017333 Orphanet:137639 Orphanet:289494 obsolete hypomyelinating leukodystrophy with or without oligondontia and/or hypogonadism MONDO:0011897 leukoencephalopathy-ataxia-hypodontia-hypomyelination syndrome MONDO:8000031 Orphanet:137639 Orphanet:557494 obsolete subtype of a disorder MONDO:0011899 Noonan syndrome-like disorder with loose anagen hair MONDO:0020167 Orphanet:2701 Orphanet:98576 obsolete malposition of external canthus @@ -5252,6 +5258,7 @@ MONDO:0012520 insulin-resistance syndrome type A MONDO:0015885 Orphanet:2297 Orp MONDO:0012520 insulin-resistance syndrome type A MONDO:0018401 Orphanet:2297 Orphanet:399853 obsolete female infertility due to an anomaly of ovarian function MONDO:0012520 insulin-resistance syndrome type A MONDO:0018413 Orphanet:2297 Orphanet:400022 obsolete female infertility due to an anomaly of ovarian function of genetic origin MONDO:0012521 herpes simplex encephalitis MONDO:0015659 Orphanet:1930 Orphanet:166490 obsolete infectious disease with epilepsy +MONDO:0012521 herpes simplex encephalitis MONDO:0015979 Orphanet:1930 Orphanet:183710 obsolete hereditary predisposition to infections MONDO:0012521 herpes simplex encephalitis MONDO:0020141 Orphanet:1930 Orphanet:98542 obsolete infectious disease with dementia MONDO:0012526 hereditary angioedema type 3 MONDO:8000031 Orphanet:100054 Orphanet:557494 obsolete subtype of a disorder MONDO:0012530 palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome MONDO:0017671 Orphanet:85112 Orphanet:307804 obsolete autosomal recessive disease with diffuse palmoplantar keratoderma as a major feature @@ -5350,7 +5357,7 @@ MONDO:0012721 progressive myoclonic epilepsy type 3 MONDO:0018284 Orphanet:26351 MONDO:0012721 progressive myoclonic epilepsy type 3 MONDO:0035862 Orphanet:263516 Orphanet:611314 obsolete rare syndromic intellectual disability without multiple congenital anomalies/dysmorphic syndrome MONDO:0012721 progressive myoclonic epilepsy type 3 MONDO:8000031 Orphanet:263516 Orphanet:557494 obsolete subtype of a disorder MONDO:0012724 familial cold autoinflammatory syndrome 2 MONDO:0017370 Orphanet:247868 Orphanet:290842 obsolete autoinflammatory syndrome with skin involvement -MONDO:0012726 autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome MONDO:0018790 Orphanet:73229 Orphanet:477765 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendancy +MONDO:0012726 autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome MONDO:0018790 Orphanet:73229 Orphanet:477765 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendency MONDO:0012727 mucocutaneous lymph node syndrome MONDO:0015489 Orphanet:2331 Orphanet:156143 obsolete predominantly medium-vessel vasculitis MONDO:0012734 SERKAL syndrome MONDO:0017965 Orphanet:139466 Orphanet:325109 obsolete syndrome with 46,XX disorder of sex development MONDO:0012734 SERKAL syndrome MONDO:8000032 Orphanet:139466 Orphanet:377789 obsolete malformation syndrome @@ -5408,6 +5415,7 @@ MONDO:0012824 hypomyelinating leukodystrophy 4 MONDO:8000031 Orphanet:280288 Orp MONDO:0012830 chromosome 10q23 deletion syndrome MONDO:8000032 Orphanet:276413 Orphanet:377789 obsolete malformation syndrome MONDO:0012833 Crouzon syndrome-acanthosis nigricans syndrome MONDO:0020254 Orphanet:93262 Orphanet:98684 obsolete craniostenosis associated with a strabismus MONDO:0012833 Crouzon syndrome-acanthosis nigricans syndrome MONDO:8000032 Orphanet:93262 Orphanet:377789 obsolete malformation syndrome +MONDO:0012839 pyogenic bacterial infections due to MyD88 deficiency MONDO:0015979 Orphanet:183713 Orphanet:183710 obsolete hereditary predisposition to infections MONDO:0012853 Fontaine progeroid syndrome MONDO:0020253 Orphanet:2963 Orphanet:98683 obsolete syndrome with a symptomatic strabismus MONDO:0012853 Fontaine progeroid syndrome MONDO:0043008 Orphanet:2095 Orphanet:330206 obsolete genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability MONDO:0012853 Fontaine progeroid syndrome MONDO:8000032 Orphanet:2095 Orphanet:377789 obsolete malformation syndrome @@ -5704,12 +5712,13 @@ MONDO:0013394 porencephaly-microcephaly-bilateral congenital cataract syndrome M MONDO:0013394 porencephaly-microcephaly-bilateral congenital cataract syndrome MONDO:8000032 Orphanet:306547 Orphanet:377789 obsolete malformation syndrome MONDO:0013396 chromosome 1p32-p31 deletion syndrome MONDO:0035863 Orphanet:401986 Orphanet:611327 obsolete genetic multiple congenital anomalies/dysmorphic syndrome-intellectual disability MONDO:0013396 chromosome 1p32-p31 deletion syndrome MONDO:8000032 Orphanet:401986 Orphanet:377789 obsolete malformation syndrome -MONDO:0013400 Congenital adrenal insuffiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency MONDO:0019595 Orphanet:168558 Orphanet:90786 obsolete 46,XY disorder of sex development due to adrenal and testicular steroidogenesis defect -MONDO:0013400 Congenital adrenal insuffiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency MONDO:0020999 Orphanet:168558 Orphanet:101960 obsolete genetic chronic primary adrenal insufficiency +MONDO:0013400 Congenital adrenal insufficiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency MONDO:0019595 Orphanet:168558 Orphanet:90786 obsolete 46,XY disorder of sex development due to adrenal and testicular steroidogenesis defect +MONDO:0013400 Congenital adrenal insufficiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency MONDO:0020999 Orphanet:168558 Orphanet:101960 obsolete genetic chronic primary adrenal insufficiency MONDO:0013404 hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase MONDO:0035863 Orphanet:88618 Orphanet:611327 obsolete genetic multiple congenital anomalies/dysmorphic syndrome-intellectual disability MONDO:0013408 FADD-related immunodeficiency MONDO:0015709 Orphanet:306550 Orphanet:169355 obsolete immunodeficiency syndrome with autoimmunity MONDO:0013424 3p- syndrome MONDO:8000032 Orphanet:1620 Orphanet:377789 obsolete malformation syndrome MONDO:0013426 aneurysm-osteoarthritis syndrome MONDO:0017311 Orphanet:284984 Orphanet:285014 obsolete rare disease with thoracic aortic aneurysm and aortic dissection +MONDO:0013427 immunodeficiency 31B MONDO:0015979 Orphanet:391311 Orphanet:183710 obsolete hereditary predisposition to infections MONDO:0013440 autosomal recessive limb-girdle muscular dystrophy type 2P MONDO:0018283 Orphanet:280333 Orphanet:371040 obsolete primary qualitative or quantitative defects of alpha-dystroglycan MONDO:0013440 autosomal recessive limb-girdle muscular dystrophy type 2P MONDO:0018284 Orphanet:280333 Orphanet:371047 obsolete congenital disorder of glycosylation with neurological involvement MONDO:0013440 autosomal recessive limb-girdle muscular dystrophy type 2P MONDO:0035862 Orphanet:280333 Orphanet:611314 obsolete rare syndromic intellectual disability without multiple congenital anomalies/dysmorphic syndrome @@ -5774,6 +5783,7 @@ MONDO:0013587 glycogen storage disease due to lactate dehydrogenase H-subunit de MONDO:0013595 hyperbiliverdinemia MONDO:0015507 Orphanet:276405 Orphanet:156601 obsolete rare genetic hepatic disease MONDO:0013595 hyperbiliverdinemia MONDO:0018928 Orphanet:276405 Orphanet:57146 obsolete rare hepatic disease MONDO:0013599 autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome MONDO:0015709 Orphanet:391487 Orphanet:169355 obsolete immunodeficiency syndrome with autoimmunity +MONDO:0013599 autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome MONDO:0015979 Orphanet:391487 Orphanet:183710 obsolete hereditary predisposition to infections MONDO:0013599 autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome MONDO:0026209 Orphanet:391487 Orphanet:183643 obsolete genetic polyendocrinopathy MONDO:0013607 monocytopenia with susceptibility to infections MONDO:0015133 Orphanet:228423 Orphanet:101985 obsolete quantitative and/or qualitative congenital phagocyte defect MONDO:0013614 hypertelorism-preauricular sinus-punctual pits-deafness syndrome MONDO:0019589 Orphanet:293958 Orphanet:90642 obsolete syndromic genetic hearing loss @@ -5884,7 +5894,7 @@ MONDO:0013858 pontine tegmental cap dysplasia MONDO:8000030 Orphanet:269229 Orph MONDO:0013863 combined immunodeficiency due to LRBA deficiency MONDO:0026209 Orphanet:445018 Orphanet:183643 obsolete genetic polyendocrinopathy MONDO:0013865 mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency MONDO:0016327 Orphanet:314637 Orphanet:217587 obsolete mitochondrial disease with hypertrophic cardiomyopathy MONDO:0013865 mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency MONDO:0018157 Orphanet:314637 Orphanet:35696 obsolete mitochondrial disorder due to a defect in mitochondrial protein synthesis -MONDO:0013867 brown-Vialetto-van Laere syndrome 2 MONDO:8000031 Orphanet:572550 Orphanet:557494 obsolete subtype of a disorder +MONDO:0013867 Brown-Vialetto-van Laere syndrome 2 MONDO:8000031 Orphanet:572550 Orphanet:557494 obsolete subtype of a disorder MONDO:0013869 adenine phosphoribosyltransferase deficiency MONDO:0019743 Orphanet:976 Orphanet:93593 obsolete nephropathy secondary to a storage or other metabolic disease MONDO:0013870 TMEM165-congenital disorder of glycosylation MONDO:0018284 Orphanet:314667 Orphanet:371047 obsolete congenital disorder of glycosylation with neurological involvement MONDO:0013870 TMEM165-congenital disorder of glycosylation MONDO:0018288 Orphanet:314667 Orphanet:371157 obsolete congenital disorder of glycosylation with hepatic involvement @@ -6837,6 +6847,7 @@ MONDO:0015273 complete atrioventricular canal MONDO:8000030 Orphanet:1329 Orphan MONDO:0015275 partial atrioventricular canal MONDO:8000030 Orphanet:1330 Orphanet:377791 obsolete morphological anomaly MONDO:0015278 familial pancreatic carcinoma MONDO:0015618 Orphanet:1333 Orphanet:165661 obsolete genetic pancreatic disease MONDO:0015278 familial pancreatic carcinoma MONDO:0016314 Orphanet:1333 Orphanet:217074 obsolete rare carcinoma of pancreas +MONDO:0015279 chronic mucocutaneous candidiasis MONDO:0015979 Orphanet:1334 Orphanet:183710 obsolete hereditary predisposition to infections MONDO:0015279 chronic mucocutaneous candidiasis MONDO:0019305 Orphanet:1334 Orphanet:79391 obsolete immune deficiency with skin involvement MONDO:0015279 chronic mucocutaneous candidiasis MONDO:0026166 Orphanet:1334 Orphanet:183494 obsolete genetic immune deficiency with skin involvement MONDO:0015280 cardiofaciocutaneous syndrome MONDO:0026989 Orphanet:1340 Orphanet:217595 obsolete syndrome associated with hypertrophic cardiomyopathy @@ -7174,7 +7185,6 @@ MONDO:0015530 trigeminal autonomic cephalalgia MONDO:0020011 Orphanet:157843 Orp MONDO:0015531 non-Langerhans cell histiocytosis MONDO:0017368 Orphanet:157987 Orphanet:290836 obsolete systemic disease with skin involvement MONDO:0015540 hemophagocytic syndrome MONDO:0020008 Orphanet:158032 Orphanet:98004 obsolete rare immune disease MONDO:0015541 hereditary hemophagocytic lymphohistiocytosis MONDO:0015144 Orphanet:540 Orphanet:102005 obsolete brain inflammatory disease -MONDO:0015541 hereditary hemophagocytic lymphohistiocytosis MONDO:0015710 Orphanet:158038 Orphanet:169361 obsolete immune dysregulation disease with immunodeficiency MONDO:0015544 acquired hemophagocytic lymphohistiocytosis associated with malignant disease MONDO:0032014 Orphanet:158057 Orphanet:377793 obsolete particular clinical situation in a disease or syndrome MONDO:0015545 macrophage activation syndrome MONDO:0032013 Orphanet:158061 Orphanet:377792 obsolete clinical syndrome MONDO:0015546 non-distal monosomy 10q MONDO:0020253 Orphanet:1581 Orphanet:98683 obsolete syndrome with a symptomatic strabismus @@ -7594,7 +7604,7 @@ MONDO:0015976 obsolete hyper-IgM syndrome without susceptibility to opportunisti MONDO:0015976 obsolete hyper-IgM syndrome without susceptibility to opportunistic infections MONDO:0018040 Orphanet:183666 Orphanet:331240 obsolete immunodeficiency with severe reduction in serum IgG and IgA with normal/elevated IgM and normal number of B-cells MONDO:0015977 agammaglobulinemia MONDO:0015132 Orphanet:183669 Orphanet:101977 obsolete immunodeficiency predominantly affecting antibody production MONDO:0015978 functional neutrophil defect MONDO:0015133 Orphanet:183681 Orphanet:101985 obsolete quantitative and/or qualitative congenital phagocyte defect -MONDO:0015979 hereditary predisposition to infections MONDO:0015135 Orphanet:183710 Orphanet:101988 obsolete primary immunodeficiency due to a genetic defect in innate immunity +MONDO:0015979 obsolete hereditary predisposition to infections MONDO:0015135 Orphanet:183710 Orphanet:101988 obsolete primary immunodeficiency due to a genetic defect in innate immunity MONDO:0015980 obsolete rare genetic gynecological and obstetrical diseases MONDO:0021198 Orphanet:183731 Orphanet:98053 obsolete rare genetic disease MONDO:0015981 obsolete inherited gynecological tumor MONDO:0019041 Orphanet:183734 Orphanet:68336 obsolete rare genetic inherited tumor MONDO:0015982 obsolete rare genetic intellectual disability MONDO:0019117 Orphanet:183757 Orphanet:71859 obsolete genetic nervous system disorder @@ -9637,7 +9647,6 @@ MONDO:0018038 obsolete immunodeficiency with isotype or light chain deficiencies MONDO:0018039 selective IgM deficiency MONDO:0018038 Orphanet:331235 Orphanet:331232 obsolete immunodeficiency with isotype or light chain deficiencies with normal number of B-cells MONDO:0018040 obsolete immunodeficiency with severe reduction in serum IgG and IgA with normal/elevated IgM and normal number of B-cells MONDO:0015132 Orphanet:331240 Orphanet:101977 obsolete immunodeficiency predominantly affecting antibody production MONDO:0018041 obsolete other immunodeficiency syndrome with predominantly antibody defects MONDO:0015132 Orphanet:331244 Orphanet:101977 obsolete immunodeficiency predominantly affecting antibody production -MONDO:0018042 obsolete immunodeficiency syndrome with abnormal pigmentation MONDO:0015541 Orphanet:331249 Orphanet:158038 hereditary hemophagocytic lymphohistiocytosis MONDO:0018043 Thomas syndrome MONDO:0015335 Orphanet:3316 Orphanet:139039 obsolete Mendelian syndromes with cleft lip/palate MONDO:0018043 Thomas syndrome MONDO:0015506 Orphanet:3316 Orphanet:156532 obsolete rare syndrome with cardiac malformations MONDO:0018043 Thomas syndrome MONDO:0019721 Orphanet:3316 Orphanet:93547 obsolete syndromic renal or urinary tract malformation @@ -10024,7 +10033,6 @@ MONDO:0018346 ferro-cerebro-cutaneous syndrome MONDO:0015114 Orphanet:397922 Orp MONDO:0018346 ferro-cerebro-cutaneous syndrome MONDO:0015115 Orphanet:397922 Orphanet:101940 obsolete rare genetic metabolic liver disease MONDO:0018346 ferro-cerebro-cutaneous syndrome MONDO:0015508 Orphanet:397922 Orphanet:156604 obsolete hereditary parenchymatous liver disease MONDO:0018346 ferro-cerebro-cutaneous syndrome MONDO:0015918 Orphanet:397922 Orphanet:182070 obsolete rare neurodegenerative disease -MONDO:0018347 severe intellectual disability-progressive postnatal microcephaly- midline stereotypic hand movements syndrome MONDO:0035862 Orphanet:397933 Orphanet:611314 obsolete rare syndromic intellectual disability without multiple congenital anomalies/dysmorphic syndrome MONDO:0018349 MAN1B1-congenital disorder of glycosylation MONDO:0018284 Orphanet:397941 Orphanet:371047 obsolete congenital disorder of glycosylation with neurological involvement MONDO:0018349 MAN1B1-congenital disorder of glycosylation MONDO:0035862 Orphanet:397941 Orphanet:611314 obsolete rare syndromic intellectual disability without multiple congenital anomalies/dysmorphic syndrome MONDO:0018353 refractory celiac disease MONDO:0015245 Orphanet:398063 Orphanet:117569 obsolete rare intestinal disease @@ -10525,8 +10533,8 @@ MONDO:0018784 pediatric multiple sclerosis MONDO:0016428 Orphanet:477738 Orphane MONDO:0018787 obsolete genetic cerebral small vessel disease MONDO:0015953 Orphanet:477754 Orphanet:183503 obsolete genetic central nervous system and retinal vascular disease MONDO:0018787 obsolete genetic cerebral small vessel disease MONDO:0019110 Orphanet:477754 Orphanet:71281 obsolete rare central nervous system or retinal vascular disease MONDO:0018788 obsolete COL4A1 or COL4A2-related cerebral small vessel disease MONDO:0018787 Orphanet:477759 Orphanet:477754 obsolete genetic cerebral small vessel disease -MONDO:0018789 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with ischemic tendancy MONDO:0018788 Orphanet:477762 Orphanet:477759 obsolete COL4A1 or COL4A2-related cerebral small vessel disease -MONDO:0018790 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendancy MONDO:0018788 Orphanet:477765 Orphanet:477759 obsolete COL4A1 or COL4A2-related cerebral small vessel disease +MONDO:0018789 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with ischemic tendency MONDO:0018788 Orphanet:477762 Orphanet:477759 obsolete COL4A1 or COL4A2-related cerebral small vessel disease +MONDO:0018790 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendency MONDO:0018788 Orphanet:477765 Orphanet:477759 obsolete COL4A1 or COL4A2-related cerebral small vessel disease MONDO:0018791 obsolete Moyomoya angiopathy MONDO:0019110 Orphanet:477768 Orphanet:71281 obsolete rare central nervous system or retinal vascular disease MONDO:0018792 obsolete Moyamoya syndrome MONDO:0015953 Orphanet:477771 Orphanet:183503 obsolete genetic central nervous system and retinal vascular disease MONDO:0018792 obsolete Moyamoya syndrome MONDO:0018791 Orphanet:477771 Orphanet:477768 obsolete Moyomoya angiopathy @@ -10588,7 +10596,7 @@ MONDO:0018827 familial chilblain lupus MONDO:0015948 Orphanet:481662 Orphanet:18 MONDO:0018827 familial chilblain lupus MONDO:0018792 Orphanet:481662 Orphanet:477771 obsolete Moyamoya syndrome MONDO:0018828 pseudo-TORCH syndrome 2 MONDO:0019117 Orphanet:481665 Orphanet:71859 obsolete genetic nervous system disorder MONDO:0018828 pseudo-TORCH syndrome 2 MONDO:0020009 Orphanet:481665 Orphanet:98006 obsolete rare neurologic disease -MONDO:0018829 familial schizencephaly MONDO:0018790 Orphanet:481986 Orphanet:477765 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendancy +MONDO:0018829 familial schizencephaly MONDO:0018790 Orphanet:481986 Orphanet:477765 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendency MONDO:0018829 familial schizencephaly MONDO:8000031 Orphanet:481986 Orphanet:557494 obsolete subtype of a disorder MONDO:0018831 obsolete HTRA1-related cerebral small vessel disease MONDO:0015547 Orphanet:482072 Orphanet:158124 hereditary dementia MONDO:0018831 obsolete HTRA1-related cerebral small vessel disease MONDO:0018787 Orphanet:482072 Orphanet:477754 obsolete genetic cerebral small vessel disease @@ -10987,6 +10995,7 @@ MONDO:0019142 inherited porphyria MONDO:0019743 Orphanet:738 Orphanet:93593 obso MONDO:0019143 angiostrongyliasis MONDO:0015577 Orphanet:74 Orphanet:163588 obsolete rare parasitic disease MONDO:0019144 hereditary thrombophilia due to congenital protein S deficiency MONDO:0016320 Orphanet:743 Orphanet:217454 obsolete rare hereditary thrombophilia MONDO:0019145 hereditary thrombophilia due to congenital protein C deficiency MONDO:0016320 Orphanet:745 Orphanet:217454 obsolete rare hereditary thrombophilia +MONDO:0019146 inherited susceptibility to mycobacterial diseases MONDO:0015979 Orphanet:748 Orphanet:183710 obsolete hereditary predisposition to infections MONDO:0019147 myiasis MONDO:0015577 Orphanet:75110 Orphanet:163588 obsolete rare parasitic disease MONDO:0019148 Wolman disease MONDO:0015115 Orphanet:75233 Orphanet:101940 obsolete rare genetic metabolic liver disease MONDO:0019148 Wolman disease MONDO:8000031 Orphanet:75233 Orphanet:557494 obsolete subtype of a disorder @@ -12103,7 +12112,6 @@ MONDO:0020315 obsolete unclassified myelodysplastic syndrome MONDO:0000001 Orpha MONDO:0020315 obsolete unclassified myelodysplastic syndrome MONDO:0019453 Orphanet:98827 Orphanet:86836 myelodysplastic syndrome with multilineage dysplasia MONDO:0020316 acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22) MONDO:0020078 Orphanet:98829 Orphanet:98277 obsolete acute myeloid leukemia with recurrent genetic anomaly MONDO:0020317 acute myeloid leukemia with 11q23 abnormalities MONDO:0020078 Orphanet:98831 Orphanet:98277 obsolete acute myeloid leukemia with recurrent genetic anomaly -MONDO:0020327 classic Hodgkin lymphoma, nodular sclerosis type MONDO:8000031 Orphanet:98843 Orphanet:557494 obsolete subtype of a disorder MONDO:0020336 autosomal dominant Emery-Dreifuss muscular dystrophy MONDO:0029810 Orphanet:98853 Orphanet:300755 obsolete laminopathy with striated muscle involvement MONDO:0020336 autosomal dominant Emery-Dreifuss muscular dystrophy MONDO:8000031 Orphanet:98853 Orphanet:557494 obsolete subtype of a disorder MONDO:0020339 obsolete X-linked complex spastic paraplegia MONDO:0015150 Orphanet:98888 Orphanet:102013 complex hereditary spastic paraplegia @@ -12288,7 +12296,7 @@ MONDO:0020494 oculootodental syndrome MONDO:0015336 Orphanet:99806 Orphanet:1390 MONDO:0020494 oculootodental syndrome MONDO:0026190 Orphanet:99806 Orphanet:183580 obsolete genetic malformation syndrome with odontal and/or periodontal component MONDO:0020494 oculootodental syndrome MONDO:8000032 Orphanet:99806 Orphanet:377789 obsolete malformation syndrome MONDO:0020495 PEHO-like syndrome MONDO:0035471 Orphanet:99807 Orphanet:568047 obsolete disorder with multisystemic involvement and primary lymphedema -MONDO:0020496 familial porencephaly MONDO:0018790 Orphanet:99810 Orphanet:477765 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendancy +MONDO:0020496 familial porencephaly MONDO:0018790 Orphanet:99810 Orphanet:477765 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendency MONDO:0020496 familial porencephaly MONDO:8000031 Orphanet:99810 Orphanet:557494 obsolete subtype of a disorder MONDO:0020497 Turcot syndrome with polyposis MONDO:0016756 Orphanet:99818 Orphanet:252190 obsolete inherited nervous system cancer-predisposing syndrome MONDO:0020497 Turcot syndrome with polyposis MONDO:8000031 Orphanet:99818 Orphanet:557494 obsolete subtype of a disorder @@ -12313,7 +12321,6 @@ MONDO:0020544 streptococcal toxic-shock syndrome MONDO:8000031 Orphanet:99918 Or MONDO:0020545 staphylococcal toxic-shock syndrome MONDO:8000031 Orphanet:99919 Orphanet:557494 obsolete subtype of a disorder MONDO:0020546 acute graft versus host disease MONDO:8000031 Orphanet:99920 Orphanet:557494 obsolete subtype of a disorder MONDO:0020547 chronic graft versus host disease MONDO:8000031 Orphanet:99921 Orphanet:557494 obsolete subtype of a disorder -MONDO:0020548 ocular pemphigoid MONDO:0020198 Orphanet:99922 Orphanet:98610 obsolete rare conjunctival disease MONDO:0020553 secondary pulmonary hemosiderosis MONDO:0017034 Orphanet:99930 Orphanet:264944 obsolete secondary interstitial lung disease in childhood and adulthood MONDO:0020554 Heiner syndrome MONDO:8000031 Orphanet:99932 Orphanet:557494 obsolete subtype of a disorder MONDO:0020555 pleuropulmonary blastoma type 1 MONDO:8000031 Orphanet:99933 Orphanet:557494 obsolete subtype of a disorder @@ -12608,7 +12615,7 @@ MONDO:0032780 hypotonia, hypoventilation, impaired intellectual development, dys MONDO:0032780 hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities MONDO:0018557 Orphanet:656273 Orphanet:434786 obsolete rare genetic autonomic nervous system disorder MONDO:0032780 hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities MONDO:0032013 Orphanet:656273 Orphanet:377792 obsolete clinical syndrome MONDO:0032780 hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities MONDO:0035862 Orphanet:656273 Orphanet:611314 obsolete rare syndromic intellectual disability without multiple congenital anomalies/dysmorphic syndrome -MONDO:0032814 microangiopathy and leukoencephalopathy, pontine, autosomal dominant MONDO:0018789 Orphanet:477749 Orphanet:477762 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with ischemic tendancy +MONDO:0032814 microangiopathy and leukoencephalopathy, pontine, autosomal dominant MONDO:0018789 Orphanet:477749 Orphanet:477762 obsolete COL4A1 or COL4A2-related cerebral small vessel disease with ischemic tendency MONDO:0032830 snijders blok-fisher syndrome MONDO:0035863 Orphanet:656135 Orphanet:611327 obsolete genetic multiple congenital anomalies/dysmorphic syndrome-intellectual disability MONDO:0032831 pontocerebellar hypoplasia, type 13 MONDO:0035863 Orphanet:613267 Orphanet:611327 obsolete genetic multiple congenital anomalies/dysmorphic syndrome-intellectual disability MONDO:0032831 pontocerebellar hypoplasia, type 13 MONDO:8000032 Orphanet:613267 Orphanet:377789 obsolete malformation syndrome @@ -13623,6 +13630,9 @@ MONDO:0958352 true myeloschisis MONDO:8000031 Orphanet:645401 Orphanet:557494 ob MONDO:0968955 hypocalcified amelogenesis imperfecta MONDO:8000031 Orphanet:100032 Orphanet:557494 obsolete subtype of a disorder MONDO:0968959 isolated arhinencephaly MONDO:0016054 Orphanet:268936 Orphanet:199633 obsolete cerebral malformation MONDO:0968959 isolated arhinencephaly MONDO:8000030 Orphanet:268936 Orphanet:377791 obsolete morphological anomaly +MONDO:0968986 chaotic conus spinal cord lipoma MONDO:8000030 Orphanet:645285 Orphanet:377791 obsolete morphological anomaly +MONDO:0968987 extramedullary conus spinal cord lipoma MONDO:8000030 Orphanet:645297 Orphanet:377791 obsolete morphological anomaly +MONDO:0968989 non-saccular limited dorsal myeloschisis MONDO:8000030 Orphanet:645343 Orphanet:377791 obsolete morphological anomaly MONDO:8000006 WHIM syndrome 1 MONDO:0018032 Orphanet:51636 Orphanet:331184 obsolete constitutional neutropenia with extra-hematopoietic manifestations MONDO:8000006 WHIM syndrome 1 MONDO:0018033 Orphanet:51636 Orphanet:331193 obsolete other immunodeficiency syndromes due to defects in innate immunity MONDO:8000008 Martsolf syndrome 1 MONDO:0015890 Orphanet:1387 Orphanet:181387 obsolete rare disorder with congenital hypogonadotropic hypogonadism diff --git a/src/ontology/reports/ordo.subclass.added.robot.tsv b/src/ontology/reports/ordo.subclass.added.robot.tsv index 1bad5357..7dd1af06 100644 --- a/src/ontology/reports/ordo.subclass.added.robot.tsv +++ b/src/ontology/reports/ordo.subclass.added.robot.tsv @@ -28,7 +28,6 @@ MONDO:0005035 ganglioneuroblastoma MONDO:0016713 Orphanet:251877 Orphanet:251870 MONDO:0005048 pancreatic insulin-producing neuroendocrine tumor MONDO:0023206 Orphanet:97279 Orphanet:506060 functional pancreatic neuroendocrine tumor MONDO:0005072 neuroblastoma MONDO:0016713 Orphanet:635 Orphanet:251870 central nervous system Ewing sarcoma/peripheral primitive neuroectodermal tumor MONDO:0005100 systemic sclerosis MONDO:0016345 Orphanet:90291 Orphanet:217720 non-familial restrictive cardiomyopathy -MONDO:0005116 Whipple disease MONDO:0015979 Orphanet:3452 Orphanet:183710 hereditary predisposition to infections MONDO:0005164 fibrosarcoma MONDO:0021054 Orphanet:2030 Orphanet:223727 bone sarcoma MONDO:0005272 myelodysplastic syndrome with single lineage dysplasia MONDO:0019453 Orphanet:98826 Orphanet:86836 myelodysplastic syndrome with multilineage dysplasia MONDO:0005502 dengue disease MONDO:0018093 Orphanet:99828 Orphanet:344 arbovirus fever @@ -438,6 +437,7 @@ MONDO:0010641 X-linked diffuse leiomyomatosis-Alport syndrome MONDO:0018965 Orph MONDO:0010650 Melnick-Needles syndrome MONDO:0015161 Orphanet:2484 Orphanet:102285 multiple congenital anomalies/dysmorphic syndrome without intellectual disability MONDO:0010652 X-linked intellectual disability-seizures-psoriasis syndrome MONDO:0015159 Orphanet:3052 Orphanet:102283 multiple congenital anomalies/dysmorphic syndrome-intellectual disability MONDO:0010653 Renpenning syndrome MONDO:0015159 Orphanet:3242 Orphanet:102283 multiple congenital anomalies/dysmorphic syndrome-intellectual disability +MONDO:0010656 intellectual disability, X-linked 1 MONDO:0015653 Orphanet:397933 Orphanet:166472 monogenic epilepsy MONDO:0010661 severe X-linked intellectual disability, Gustavson type MONDO:0015159 Orphanet:3078 Orphanet:102283 multiple congenital anomalies/dysmorphic syndrome-intellectual disability MONDO:0010662 paraplegia-intellectual disability-hyperkeratosis syndrome MONDO:0015159 Orphanet:2824 Orphanet:102283 multiple congenital anomalies/dysmorphic syndrome-intellectual disability MONDO:0010664 syndromic X-linked intellectual disability Snyder type MONDO:0015159 Orphanet:3063 Orphanet:102283 multiple congenital anomalies/dysmorphic syndrome-intellectual disability @@ -583,7 +583,6 @@ MONDO:0012423 MORM syndrome MONDO:0022410 Orphanet:75858 Orphanet:156165 retinal MONDO:0012436 neonatal diabetes mellitus with congenital hypothyroidism MONDO:0019741 Orphanet:79118 Orphanet:93587 familial cystic renal disease MONDO:0012496 Koolen-de Vries syndrome MONDO:0015338 Orphanet:96169 Orphanet:139393 syndromic craniosynostosis MONDO:0012517 Gaucher disease due to saposin C deficiency MONDO:0018150 Orphanet:309252 Orphanet:355 Gaucher disease -MONDO:0012521 herpes simplex encephalitis MONDO:0015979 Orphanet:1930 Orphanet:183710 hereditary predisposition to infections MONDO:0012526 hereditary angioedema type 3 MONDO:0100567 Orphanet:100054 Orphanet:528647 hereditary angioedema with normal C1Inh MONDO:0012574 Potocki-Lupski syndrome MONDO:0015159 Orphanet:1713 Orphanet:102283 multiple congenital anomalies/dysmorphic syndrome-intellectual disability MONDO:0012589 Pitt-Hopkins syndrome MONDO:0015653 Orphanet:2896 Orphanet:166472 monogenic epilepsy @@ -593,7 +592,6 @@ MONDO:0012611 polyhydramnios, megalencephaly, and symptomatic epilepsy MONDO:001 MONDO:0012634 craniofacial dysplasia - osteopenia syndrome MONDO:0015159 Orphanet:314555 Orphanet:102283 multiple congenital anomalies/dysmorphic syndrome-intellectual disability MONDO:0012638 microphthalmia-brain atrophy syndrome MONDO:0015159 Orphanet:77299 Orphanet:102283 multiple congenital anomalies/dysmorphic syndrome-intellectual disability MONDO:0012650 Cernunnos-XLF deficiency MONDO:0018814 Orphanet:169079 Orphanet:480549 non-SCID combined immunodeficiency -MONDO:0012682 immunodeficiency 35 MONDO:0000001 Orphanet:331226 Orphanet:377788 disease MONDO:0012687 familial cavitary optic disk anomaly MONDO:0850010 Orphanet:464760 Orphanet:519333 congenital optic disk excavation MONDO:0012721 progressive myoclonic epilepsy type 3 MONDO:0019261 Orphanet:263516 Orphanet:79263 infantile neuronal ceroid lipofuscinosis MONDO:0012735 Temple-Baraitser syndrome MONDO:0015159 Orphanet:420561 Orphanet:102283 multiple congenital anomalies/dysmorphic syndrome-intellectual disability @@ -601,7 +599,6 @@ MONDO:0012739 microtia-eye coloboma-imperforation of the nasolacrimal duct syndr MONDO:0012747 glycogen storage disease due to aldolase A deficiency MONDO:0002412 Orphanet:57 Orphanet:79201 disorder of glycogen metabolism MONDO:0012794 ANE syndrome MONDO:0004907 Orphanet:157954 Orphanet:79364 alopecia MONDO:0012817 Ewing sarcoma MONDO:0021054 Orphanet:319 Orphanet:223727 bone sarcoma -MONDO:0012839 pyogenic bacterial infections due to MyD88 deficiency MONDO:0000001 Orphanet:183713 Orphanet:377788 disease MONDO:0012853 Fontaine progeroid syndrome MONDO:0019303 Orphanet:2963 Orphanet:79389 premature aging syndrome MONDO:0012864 chromosome 2q32-q33 deletion syndrome MONDO:0015159 Orphanet:251019 Orphanet:102283 multiple congenital anomalies/dysmorphic syndrome-intellectual disability MONDO:0012873 Ehlers-Danlos syndrome, spondylocheirodysplastic type MONDO:0034021 Orphanet:157965 Orphanet:536471 spondylodysplastic Ehlers-Danlos syndrome @@ -628,13 +625,11 @@ MONDO:0013357 chromosome 17q11.2 deletion syndrome, 1.4Mb MONDO:0019716 Orphanet MONDO:0013387 developmental and epileptic encephalopathy, 7 MONDO:0015653 Orphanet:439218 Orphanet:166472 monogenic epilepsy MONDO:0013396 chromosome 1p32-p31 deletion syndrome MONDO:0015159 Orphanet:401986 Orphanet:102283 multiple congenital anomalies/dysmorphic syndrome-intellectual disability MONDO:0013404 hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase MONDO:0015159 Orphanet:88618 Orphanet:102283 multiple congenital anomalies/dysmorphic syndrome-intellectual disability -MONDO:0013427 immunodeficiency 31B MONDO:0000001 Orphanet:391311 Orphanet:377788 disease MONDO:0013523 Nestor-Guillermo progeria syndrome MONDO:0020087 Orphanet:280576 Orphanet:98305 hereditary lipodystrophy MONDO:0013531 PSPH deficiency MONDO:0035004 Orphanet:79350 Orphanet:583595 serine biosynthesis pathway deficiency, infantile/juvenile form MONDO:0013541 complex cortical dysplasia with other brain malformations 1 MONDO:0015159 Orphanet:300570 Orphanet:102283 multiple congenital anomalies/dysmorphic syndrome-intellectual disability MONDO:0013572 Keppen-Lubinsky syndrome MONDO:0015159 Orphanet:435628 Orphanet:102283 multiple congenital anomalies/dysmorphic syndrome-intellectual disability MONDO:0013574 cutis laxa - Marfanoid syndrome MONDO:0017310 Orphanet:171719 Orphanet:284993 Marfan and Marfan-related disorder -MONDO:0013599 autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome MONDO:0015979 Orphanet:391487 Orphanet:183710 hereditary predisposition to infections MONDO:0013673 Wolfram-like syndrome MONDO:0015967 Orphanet:411590 Orphanet:183625 monogenic diabetes MONDO:0013686 distal myopathy, Tateyama type MONDO:0016146 Orphanet:488650 Orphanet:207078 caveolinopathy MONDO:0013743 autosomal systemic lupus erythematosus type 16 MONDO:0700264 Orphanet:300345 Orphanet:477647 type 1 interferonopathy @@ -741,7 +736,6 @@ MONDO:0015240 digitotalar dysmorphism MONDO:0957111 Orphanet:1146 Orphanet:98738 MONDO:0015248 ataxia-photosensitivity-short stature syndrome MONDO:0100309 Orphanet:1184 Orphanet:183518 hereditary ataxia MONDO:0015253 Diamond-Blackfan anemia MONDO:0019236 Orphanet:124 Orphanet:79191 inborn disorder of purine metabolism MONDO:0015267 Feingold syndrome MONDO:0015159 Orphanet:1305 Orphanet:102283 multiple congenital anomalies/dysmorphic syndrome-intellectual disability -MONDO:0015279 chronic mucocutaneous candidiasis MONDO:0015979 Orphanet:1334 Orphanet:183710 hereditary predisposition to infections MONDO:0015285 Carney complex MONDO:0015079 Orphanet:1359 Orphanet:100094 multiple polyglandular tumor MONDO:0015285 Carney complex MONDO:0019289 Orphanet:1359 Orphanet:79375 hyperpigmentation of the skin MONDO:0015285 Carney complex MONDO:0021227 Orphanet:1359 Orphanet:100091 adrenal gland neoplasm @@ -753,7 +747,6 @@ MONDO:0015431 ring chromosome 10 MONDO:0015159 Orphanet:1438 Orphanet:102283 mul MONDO:0015452 Coffin-Siris syndrome MONDO:0015338 Orphanet:1465 Orphanet:139393 syndromic craniosynostosis MONDO:0015518 infantile bilateral striatal necrosis MONDO:0024237 Orphanet:1576 Orphanet:183500 inherited neurodegenerative disorder MONDO:0015538 indeterminate dendritic cell tumor MONDO:0020082 Orphanet:158019 Orphanet:98289 dendritic cell tumor -MONDO:0015541 hereditary hemophagocytic lymphohistiocytosis MONDO:0015541 Orphanet:540 Orphanet:158038 hereditary hemophagocytic lymphohistiocytosis MONDO:0015552 acral dystrophic epidermolysis bullosa MONDO:0035349 Orphanet:158673 Orphanet:595356 localized dystrophic epidermolysis bullosa MONDO:0015553 dystrophic epidermolysis bullosa, nails only MONDO:0035349 Orphanet:158676 Orphanet:595356 localized dystrophic epidermolysis bullosa MONDO:0015564 Castleman disease MONDO:0015757 Orphanet:160 Orphanet:171898 lymphoid hemopathy @@ -915,7 +908,6 @@ MONDO:0018320 primary microcephaly-mild intellectual disability-young-onset diab MONDO:0018320 primary microcephaly-mild intellectual disability-young-onset diabetes syndrome MONDO:0015967 Orphanet:391408 Orphanet:183625 monogenic diabetes MONDO:0018341 3q27.3 microdeletion syndrome MONDO:0016902 Orphanet:397695 Orphanet:262019 partial deletion of the long arm of chromosome 3 MONDO:0018346 ferro-cerebro-cutaneous syndrome MONDO:0017748 Orphanet:397922 Orphanet:309515 inborn disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation -MONDO:0018347 severe intellectual disability-progressive postnatal microcephaly- midline stereotypic hand movements syndrome MONDO:0015653 Orphanet:397933 Orphanet:166472 monogenic epilepsy MONDO:0018354 Prader-Willi-like syndrome MONDO:0015159 Orphanet:398073 Orphanet:102283 multiple congenital anomalies/dysmorphic syndrome-intellectual disability MONDO:0018419 autosomal recessive spastic paraplegia type 67 MONDO:0017748 Orphanet:401820 Orphanet:309515 inborn disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation MONDO:0018448 clear cell papillary renal cell carcinoma MONDO:0005005 Orphanet:404511 Orphanet:319276 clear cell renal carcinoma diff --git a/src/ontology/reports/ordo.subclass.confirmed.robot.tsv b/src/ontology/reports/ordo.subclass.confirmed.robot.tsv index 40671ff4..93cb259f 100644 --- a/src/ontology/reports/ordo.subclass.confirmed.robot.tsv +++ b/src/ontology/reports/ordo.subclass.confirmed.robot.tsv @@ -56,6 +56,7 @@ MONDO:0004604 Hodgkin's lymphoma, lymphocytic-histiocytic predominance MONDO:000 MONDO:0004620 Hodgkin's lymphoma, lymphocytic depletion MONDO:0009348 Orphanet:98846 Orphanet:391 classic Hodgkin lymphoma MONDO:0004633 Hodgkin's lymphoma, mixed cellularity MONDO:0009348 Orphanet:98844 Orphanet:391 classic Hodgkin lymphoma MONDO:0004653 atypical chronic myeloid leukemia, BCR-ABL1 negative MONDO:0020077 Orphanet:98824 Orphanet:98275 myelodysplastic/myeloproliferative disease +MONDO:0004665 nodular sclerosis classical Hodgkin lymphoma MONDO:0009348 Orphanet:98843 Orphanet:391 classic Hodgkin lymphoma MONDO:0004684 plantar fibromatosis MONDO:0016037 Orphanet:199251 Orphanet:199257 superficial Fibromatosis MONDO:0004739 urea cycle disorder MONDO:0019189 Orphanet:79167 Orphanet:79062 inborn disorder of amino acid and other organic acid metabolism MONDO:0004907 alopecia MONDO:0019278 Orphanet:79364 Orphanet:79363 hair anomaly @@ -652,7 +653,6 @@ MONDO:0008896 campomelia, Cumming type MONDO:0019698 Orphanet:1318 Orphanet:9343 MONDO:0008898 camptodactyly syndrome, Guadalajara type 1 MONDO:0015161 Orphanet:1327 Orphanet:102285 multiple congenital anomalies/dysmorphic syndrome without intellectual disability MONDO:0008899 camptodactyly syndrome, Guadalajara type 2 MONDO:0015161 Orphanet:1326 Orphanet:102285 multiple congenital anomalies/dysmorphic syndrome without intellectual disability MONDO:0008900 camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia MONDO:0015159 Orphanet:1321 Orphanet:102283 multiple congenital anomalies/dysmorphic syndrome-intellectual disability -MONDO:0008905 predisposition to invasive fungal disease due to CARD9 deficiency MONDO:0015979 Orphanet:457088 Orphanet:183710 hereditary predisposition to infections MONDO:0008907 PMM2-congenital disorder of glycosylation MONDO:0017740 Orphanet:79318 Orphanet:309347 disorder of protein N-glycosylation MONDO:0008908 MGAT2-congenital disorder of glycosylation MONDO:0017740 Orphanet:79329 Orphanet:309347 disorder of protein N-glycosylation MONDO:0008917 heart defects-limb shortening syndrome MONDO:0015161 Orphanet:1354 Orphanet:102285 multiple congenital anomalies/dysmorphic syndrome without intellectual disability @@ -1291,7 +1291,6 @@ MONDO:0010621 CHILD syndrome MONDO:0015161 Orphanet:139 Orphanet:102285 multiple MONDO:0010621 CHILD syndrome MONDO:0017269 Orphanet:139 Orphanet:281210 X-linked ichthyosis syndrome MONDO:0010621 CHILD syndrome MONDO:0019240 Orphanet:139 Orphanet:79195 sterol biosynthesis disorder MONDO:0010621 CHILD syndrome MONDO:0019701 Orphanet:139 Orphanet:93442 chondrodysplasia punctata -MONDO:0010627 X-linked lymphoproliferative syndrome MONDO:0015541 Orphanet:2442 Orphanet:158038 hereditary hemophagocytic lymphohistiocytosis MONDO:0010627 X-linked lymphoproliferative syndrome MONDO:0016537 Orphanet:2442 Orphanet:238510 lymphoproliferative syndrome MONDO:0010631 incontinentia pigmenti MONDO:0019287 Orphanet:464 Orphanet:79373 ectodermal dysplasia syndrome MONDO:0010641 X-linked diffuse leiomyomatosis-Alport syndrome MONDO:0017007 Orphanet:1018 Orphanet:263756 partial deletion of the long arm of chromosome X @@ -1600,7 +1599,6 @@ MONDO:0011874 neonatal ichthyosis-sclerosing cholangitis syndrome MONDO:0018646 MONDO:0011883 Curly hair - acral keratoderma - caries syndrome MONDO:0019287 Orphanet:307766 Orphanet:79373 ectodermal dysplasia syndrome MONDO:0011884 hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome MONDO:0019287 Orphanet:307936 Orphanet:79373 ectodermal dysplasia syndrome MONDO:0011886 torsion dystonia 13 MONDO:0015990 Orphanet:98807 Orphanet:1866 focal, segmental or multifocal dystonia -MONDO:0011888 immunodeficiency 67 MONDO:0015979 Orphanet:70592 Orphanet:183710 hereditary predisposition to infections MONDO:0011889 Charcot-Marie-Tooth disease type 2I MONDO:0018993 Orphanet:99942 Orphanet:64746 Charcot-Marie-Tooth disease type 2 MONDO:0011890 Charcot-Marie-Tooth disease type 1D MONDO:0019011 Orphanet:101084 Orphanet:65753 Charcot-Marie-Tooth disease type 1 MONDO:0011894 Charcot-Marie-Tooth disease type 2E MONDO:0018993 Orphanet:99939 Orphanet:64746 Charcot-Marie-Tooth disease type 2 @@ -1801,7 +1799,6 @@ MONDO:0012824 hypomyelinating leukodystrophy 4 MONDO:0017226 Orphanet:280288 Orp MONDO:0012825 extraskeletal myxoid chondrosarcoma MONDO:0018078 Orphanet:209916 Orphanet:3394 soft tissue sarcoma MONDO:0012830 chromosome 10q23 deletion syndrome MONDO:0016909 Orphanet:276413 Orphanet:262083 partial monosomy of the long arm of chromosome 10 MONDO:0012833 Crouzon syndrome-acanthosis nigricans syndrome MONDO:0015338 Orphanet:93262 Orphanet:139393 syndromic craniosynostosis -MONDO:0012839 pyogenic bacterial infections due to MyD88 deficiency MONDO:0015979 Orphanet:183713 Orphanet:183710 hereditary predisposition to infections MONDO:0012853 Fontaine progeroid syndrome MONDO:0015161 Orphanet:2095 Orphanet:102285 multiple congenital anomalies/dysmorphic syndrome without intellectual disability MONDO:0012853 Fontaine progeroid syndrome MONDO:0019287 Orphanet:2095 Orphanet:79373 ectodermal dysplasia syndrome MONDO:0012858 primary CD59 deficiency MONDO:0020127 Orphanet:169464 Orphanet:98497 hereditary peripheral neuropathy @@ -1927,7 +1924,6 @@ MONDO:0013393 distal 7q11.23 microdeletion syndrome MONDO:0016906 Orphanet:25435 MONDO:0013396 chromosome 1p32-p31 deletion syndrome MONDO:0016883 Orphanet:401986 Orphanet:261857 partial deletion of the short arm of chromosome 1 MONDO:0013424 3p- syndrome MONDO:0016885 Orphanet:1620 Orphanet:261875 partial deletion of the short arm of chromosome 3 MONDO:0013424 3p- syndrome MONDO:0017393 Orphanet:1620 Orphanet:293642 blepharophimosis - intellectual disability syndrome -MONDO:0013427 immunodeficiency 31B MONDO:0015979 Orphanet:391311 Orphanet:183710 hereditary predisposition to infections MONDO:0013433 primary sclerosing cholangitis MONDO:0018646 Orphanet:171 Orphanet:447771 sclerosing cholangitis MONDO:0013439 congenital bile acid synthesis defect 3 MONDO:0018841 Orphanet:79302 Orphanet:485631 congenital bile acid synthesis defect MONDO:0013440 autosomal recessive limb-girdle muscular dystrophy type 2P MONDO:0015152 Orphanet:280333 Orphanet:102015 autosomal recessive limb-girdle muscular dystrophy @@ -2004,7 +2000,7 @@ MONDO:0013837 deafness-encephaloneuropathy-obesity-valvulopathy syndrome MONDO:0 MONDO:0013840 encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome MONDO:0018151 Orphanet:319678 Orphanet:35656 coenzyme Q10 deficiency MONDO:0013847 chromosome 16p11.2 duplication syndrome MONDO:0016949 Orphanet:370079 Orphanet:262794 partial duplication of the short arm of chromosome 16 MONDO:0013851 autosomal dominant aplasia and myelodysplasia MONDO:0001713 Orphanet:314399 Orphanet:68383 inherited aplastic anemia -MONDO:0013867 brown-Vialetto-van Laere syndrome 2 MONDO:0008891 Orphanet:572550 Orphanet:97229 riboflavin transporter deficiency +MONDO:0013867 Brown-Vialetto-van Laere syndrome 2 MONDO:0008891 Orphanet:572550 Orphanet:97229 riboflavin transporter deficiency MONDO:0013869 adenine phosphoribosyltransferase deficiency MONDO:0019236 Orphanet:976 Orphanet:79191 inborn disorder of purine metabolism MONDO:0013870 TMEM165-congenital disorder of glycosylation MONDO:0017740 Orphanet:314667 Orphanet:309347 disorder of protein N-glycosylation MONDO:0013875 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome MONDO:0017359 Orphanet:352328 Orphanet:289902 3-methylglutaconic aciduria @@ -2443,7 +2439,6 @@ MONDO:0015536 papular xanthoma MONDO:0015531 Orphanet:158008 Orphanet:157987 non MONDO:0015537 necrobiotic xanthogranuloma MONDO:0015531 Orphanet:158011 Orphanet:157987 non-Langerhans cell histiocytosis MONDO:0015538 indeterminate dendritic cell tumor MONDO:0015531 Orphanet:158019 Orphanet:157987 non-Langerhans cell histiocytosis MONDO:0015539 progressive nodular histiocytosis MONDO:0015531 Orphanet:158022 Orphanet:157987 non-Langerhans cell histiocytosis -MONDO:0015541 hereditary hemophagocytic lymphohistiocytosis MONDO:0015540 Orphanet:158038 Orphanet:158032 hemophagocytic syndrome MONDO:0015542 secondary hemophagocytic lymphohistiocytosis MONDO:0015540 Orphanet:158041 Orphanet:158032 hemophagocytic syndrome MONDO:0015544 acquired hemophagocytic lymphohistiocytosis associated with malignant disease MONDO:0015542 Orphanet:158057 Orphanet:158041 secondary hemophagocytic lymphohistiocytosis MONDO:0015545 macrophage activation syndrome MONDO:0015542 Orphanet:158061 Orphanet:158041 secondary hemophagocytic lymphohistiocytosis @@ -3852,7 +3847,6 @@ MONDO:0019133 visceral neuropathy-brain anomalies-facial dysmorphism-development MONDO:0019141 porokeratosis of Mibelli MONDO:0006602 Orphanet:735 Orphanet:79358 porokeratosis MONDO:0019142 inherited porphyria MONDO:0015951 Orphanet:738 Orphanet:183490 hereditary photodermatosis MONDO:0019142 inherited porphyria MONDO:0017754 Orphanet:738 Orphanet:309813 inborn disorder of porphyrin metabolism -MONDO:0019146 inherited susceptibility to mycobacterial diseases MONDO:0015979 Orphanet:748 Orphanet:183710 hereditary predisposition to infections MONDO:0019148 Wolman disease MONDO:0800449 Orphanet:75233 Orphanet:275761 lysosomal acid lipase deficiency MONDO:0019149 cholesteryl ester storage disease MONDO:0800449 Orphanet:75234 Orphanet:275761 lysosomal acid lipase deficiency MONDO:0019153 brain malformation-congenital heart disease-postaxial polydactyly syndrome MONDO:0015159 Orphanet:75389 Orphanet:102283 multiple congenital anomalies/dysmorphic syndrome-intellectual disability @@ -4304,7 +4298,6 @@ MONDO:0020321 acute undifferentiated leukemia MONDO:0019460 Orphanet:98835 Orpha MONDO:0020323 primary mediastinal large B-cell lymphoma MONDO:0018905 Orphanet:98838 Orphanet:544 diffuse large B-cell lymphoma MONDO:0020324 intravascular large B-cell lymphoma MONDO:0018905 Orphanet:98839 Orphanet:544 diffuse large B-cell lymphoma MONDO:0020326 lymphomatoid papulosis MONDO:0018897 Orphanet:98842 Orphanet:541 primary cutaneous CD30+ T-cell lymphoproliferative disease -MONDO:0020327 classic Hodgkin lymphoma, nodular sclerosis type MONDO:0009348 Orphanet:98843 Orphanet:391 classic Hodgkin lymphoma MONDO:0020331 indolent systemic mastocytosis MONDO:0016586 Orphanet:98848 Orphanet:2467 systemic mastocytosis MONDO:0020332 systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease MONDO:0016586 Orphanet:98849 Orphanet:2467 systemic mastocytosis MONDO:0020333 aggressive systemic mastocytosis MONDO:0016586 Orphanet:98850 Orphanet:2467 systemic mastocytosis @@ -4763,5 +4756,10 @@ MONDO:0958353 intermediate collagen VI-related muscular dystrophy MONDO:0958077 MONDO:0958356 primary central precocious puberty in male MONDO:0958270 Orphanet:650087 Orphanet:649929 central precocious puberty in male MONDO:0958357 secondary central precocious puberty in male MONDO:0958270 Orphanet:650092 Orphanet:649929 central precocious puberty in male MONDO:0968955 hypocalcified amelogenesis imperfecta MONDO:0019507 Orphanet:100032 Orphanet:88661 amelogenesis imperfecta +MONDO:0968986 chaotic conus spinal cord lipoma MONDO:0958350 Orphanet:645285 Orphanet:645367 conus spinal cord lipoma +MONDO:0968987 extramedullary conus spinal cord lipoma MONDO:0958350 Orphanet:645297 Orphanet:645367 conus spinal cord lipoma +MONDO:0968988 saccular spinal dysraphism with a stalk to the dome MONDO:0017069 Orphanet:645319 Orphanet:268744 spina bifida cystica +MONDO:0968988 saccular spinal dysraphism with a stalk to the dome MONDO:0958345 Orphanet:645319 Orphanet:645196 limited dorsal myeloschisis +MONDO:0968989 non-saccular limited dorsal myeloschisis MONDO:0958345 Orphanet:645343 Orphanet:645196 limited dorsal myeloschisis MONDO:8000008 Martsolf syndrome 1 MONDO:0015159 Orphanet:1387 Orphanet:102283 multiple congenital anomalies/dysmorphic syndrome-intellectual disability MONDO:8000011 visceral neuropathy, familial, 1, autosomal recessive MONDO:0017574 Orphanet:99811 Orphanet:2978 chronic intestinal pseudoobstruction diff --git a/src/ontology/reports/ordo_exclusion_reasons.robot.template.tsv b/src/ontology/reports/ordo_exclusion_reasons.robot.template.tsv index 30275332..4160eac2 100644 --- a/src/ontology/reports/ordo_exclusion_reasons.robot.template.tsv +++ b/src/ontology/reports/ordo_exclusion_reasons.robot.template.tsv @@ -250,6 +250,7 @@ Orphanet:324953 MONDO:excludeGrouping Orphanet:324960 MONDO:excludeGrouping Orphanet:325713 MONDO:excludeGrouping Orphanet:357506 MONDO:excludeGrouping +Orphanet:522514 MONDO:excludeGrouping Orphanet:523000 MONDO:excludeGrouping Orphanet:641343 MONDO:excludeGrouping Orphanet:650182 MONDO:excludeGrouping @@ -315,6 +316,7 @@ Orphanet:269550 MONDO:excludeGroupingOriginGenetic Orphanet:522534 MONDO:excludeGroupingOriginGenetic Orphanet:522540 MONDO:excludeGroupingOriginGenetic Orphanet:522560 MONDO:excludeGroupingOriginGenetic +Orphanet:522562 MONDO:excludeGroupingOriginGenetic Orphanet:622914 MONDO:excludeGroupingOriginGenetic Orphanet:98495 MONDO:excludeGroupingOriginGenetic Orphanet:98737 MONDO:excludeGroupingOriginGenetic @@ -349,6 +351,9 @@ Orphanet:269567 MONDO:excludeGroupingPhenotype Orphanet:269570 MONDO:excludeGroupingPhenotype Orphanet:289825 MONDO:excludeGroupingPhenotype Orphanet:404574 MONDO:excludeGroupingPhenotype +Orphanet:519337 MONDO:excludeGroupingPhenotype +Orphanet:522520 MONDO:excludeGroupingPhenotype +Orphanet:522530 MONDO:excludeGroupingPhenotype Orphanet:525677 MONDO:excludeGroupingPhenotype Orphanet:564178 MONDO:excludeGroupingPhenotype Orphanet:567556 MONDO:excludeGroupingPhenotype diff --git a/src/ontology/reports/ordo_mapping_status.tsv b/src/ontology/reports/ordo_mapping_status.tsv index 0105c32f..613aed6f 100644 --- a/src/ontology/reports/ordo_mapping_status.tsv +++ b/src/ontology/reports/ordo_mapping_status.tsv @@ -37,22 +37,13 @@ Orphanet:409978 6-9 / 10 000 False False False Orphanet:409979 <1 / 1 000 000 False False False Orphanet:409980 >1 / 1000 False False False Orphanet:409981 Unknown_epidemiological_range False False False -Orphanet:519337 Disorder with optic nerve compression False False False -Orphanet:522514 Congenital optic disc excavation of genetic origin False False False -Orphanet:522520 Syndromic genetic disorder with strabismus False False False -Orphanet:522530 Rare genetic disorder with entropion False False False -Orphanet:522562 Genetic superficial corneal dystrophy False False False Orphanet:557495 category False False False -Orphanet:645285 Chaotic conus spinal cord lipoma False False False Orphanet:645288 Terminal extramedullary conus spinal cord lipoma False False False Orphanet:645291 Transitional extramedullary conus spinal cord lipoma False False False Orphanet:645294 Posterior extramedullary conus spinal cord lipoma False False False -Orphanet:645297 Extramedullary conus spinal cord lipoma False False False Orphanet:645300 Lipomatous non-saccular limited dorsal myeloschisis False False False Orphanet:645310 Fibroneural non-saccular limited dorsal myeloschisis False False False -Orphanet:645319 Saccular spinal dysraphism with a stalk to the dome False False False Orphanet:645337 Terminal myelocystocele False False False -Orphanet:645343 Non-saccular limited dorsal myeloschisis False False False Orphanet:645354 Saccular limited dorsal myeloschisis False False False Orphanet:645378 Myelic limited dorsal malformation False False False Orphanet:650097 Genetic central precocious puberty in male False False False @@ -1636,6 +1627,7 @@ Orphanet:140541 RPGRIP1 like False True False Orphanet:140560 ATP binding cassette subfamily A member 3 False True False Orphanet:140567 MAF bZIP transcription factor False True False Orphanet:156077 NK2 homeobox 1 False True False +Orphanet:158038 Primary hemophagocytic lymphohistiocytosis False True False Orphanet:158048 Hemophagocytic syndrome associated with an infection False True False Orphanet:158065 aspartyl-tRNA synthetase 2, mitochondrial False True False Orphanet:158072 pyruvate dehydrogenase phosphatase catalytic subunit 1 False True False @@ -4149,6 +4141,7 @@ Orphanet:519319 Isolated stationary inherited retinal disorder False True False Orphanet:519321 Syndromic chorioretinal dystrophy False True False Orphanet:519323 Syndromic macular dystrophy False True False Orphanet:519329 Rare disorder involving multiple structures of the eye False True False +Orphanet:519337 Disorder with optic nerve compression False True False Orphanet:519345 Rare disorder with optic disc malformation False True False Orphanet:519347 Rare neuromuscular disorder with ocular motility/alignment anomaly False True False Orphanet:519351 Rare optic nerve disorder False True False @@ -4170,12 +4163,15 @@ Orphanet:522506 Rare genetic brainstem or cerebellar disorder with ophthalmic in Orphanet:522508 Rare genetic ophthalmic disorder with cortical involvement False True False Orphanet:522510 Rare genetic ophthalmic disorder with cranial nerve involvement False True False Orphanet:522512 Rare genetic optic nerve disorder False True False +Orphanet:522514 Congenital optic disc excavation of genetic origin False True False Orphanet:522516 Rare genetic ocular motility/alignment disorder False True False Orphanet:522518 Rare genetic disorder with strabismus False True False +Orphanet:522520 Syndromic genetic disorder with strabismus False True False Orphanet:522522 Rare genetic neuromuscular disorder with ocular motility/alignment anomaly False True False Orphanet:522524 Rare genetic disorder of the ocular adnexa False True False Orphanet:522526 Rare genetic palpebral disorder False True False Orphanet:522528 Rare genetic eyelid malposition disorder False True False +Orphanet:522530 Rare genetic disorder with entropion False True False Orphanet:522532 Rare genetic disorder of the lacrimal apparatus False True False Orphanet:522534 Lacrimal drainage system anomaly of genetic origin False True False Orphanet:522536 Structural developmental eye defect of genetic origin False True False @@ -4190,6 +4186,7 @@ Orphanet:522554 Syndromic genetic ectopia lentis False True False Orphanet:522556 Rare genetic corneal disorder False True False Orphanet:522558 Rare genetic disorder with corneal involvement as a major feature False True False Orphanet:522560 Genetic corneal dystrophy False True False +Orphanet:522562 Genetic superficial corneal dystrophy False True False Orphanet:522564 Syndromic genetic keratoconus False True False Orphanet:522566 Rare genetic inflammatory/autoimmune corneal disorder False True False Orphanet:522568 Rare genetic disorder of the pupil False True False @@ -12617,10 +12614,14 @@ Orphanet:645196 Limited dorsal myeloschisis True False False Orphanet:645202 Closed spinal dysraphism True False False Orphanet:645273 Dysraphic spinal cord lipoma True False False Orphanet:645276 Spinal cord lipoma True False False +Orphanet:645285 Chaotic conus spinal cord lipoma True False False +Orphanet:645297 Extramedullary conus spinal cord lipoma True False False +Orphanet:645319 Saccular spinal dysraphism with a stalk to the dome True False False Orphanet:645322 Isolated transitional filum lipoma True False False Orphanet:645325 Isolated filum lipoma True False False Orphanet:645334 Retained medullary cord True False False Orphanet:645340 Non-terminal myelocystocele True False False +Orphanet:645343 Non-saccular limited dorsal myeloschisis True False False Orphanet:645350 Segmental arterial mediolysis True False False Orphanet:645359 Intramedullary non-dysraphic spinal cord lipoma True False False Orphanet:645362 Dorsal spinal cord lipoma True False False @@ -14966,7 +14967,6 @@ Orphanet:108971 Non-syndromic visceral malformation True True False Orphanet:117573 Syndromic anorectal malformation True True False Orphanet:1303 Bronchiolitis obliterans True True False Orphanet:156152 Anti-neutrophil cytoplasmic antibody-associated vasculitis True True False -Orphanet:158038 Primary hemophagocytic lymphohistiocytosis True True False Orphanet:163631 Bile acid synthesis defect with cholestasis and malabsorption True True False Orphanet:164823 Rare acquired aplastic anemia True True False Orphanet:165704 Non-syndromic urogenital tract malformation True True False diff --git a/src/ontology/reports/ordo_term_exclusions.txt b/src/ontology/reports/ordo_term_exclusions.txt index 0b392a5f..83c14950 100644 --- a/src/ontology/reports/ordo_term_exclusions.txt +++ b/src/ontology/reports/ordo_term_exclusions.txt @@ -5126,6 +5126,7 @@ Orphanet:519321 Orphanet:519323 Orphanet:519329 Orphanet:519335 +Orphanet:519337 Orphanet:519345 Orphanet:519347 Orphanet:519351 @@ -5152,12 +5153,15 @@ Orphanet:522506 Orphanet:522508 Orphanet:522510 Orphanet:522512 +Orphanet:522514 Orphanet:522516 Orphanet:522518 +Orphanet:522520 Orphanet:522522 Orphanet:522524 Orphanet:522526 Orphanet:522528 +Orphanet:522530 Orphanet:522532 Orphanet:522534 Orphanet:522536 @@ -5173,6 +5177,7 @@ Orphanet:522554 Orphanet:522556 Orphanet:522558 Orphanet:522560 +Orphanet:522562 Orphanet:522564 Orphanet:522566 Orphanet:522568 diff --git a/src/ontology/reports/ordo_unmapped_terms.tsv b/src/ontology/reports/ordo_unmapped_terms.tsv index 96100619..a7d221ff 100644 --- a/src/ontology/reports/ordo_unmapped_terms.tsv +++ b/src/ontology/reports/ordo_unmapped_terms.tsv @@ -5,22 +5,13 @@ Orphanet:409977 1-9 / 100 000 Orphanet:409978 6-9 / 10 000 Orphanet:409979 <1 / 1 000 000 Orphanet:409980 >1 / 1000 -Orphanet:645285 Chaotic conus spinal cord lipoma -Orphanet:522514 Congenital optic disc excavation of genetic origin -Orphanet:519337 Disorder with optic nerve compression -Orphanet:645297 Extramedullary conus spinal cord lipoma Orphanet:645310 Fibroneural non-saccular limited dorsal myeloschisis Orphanet:650097 Genetic central precocious puberty in male -Orphanet:522562 Genetic superficial corneal dystrophy Orphanet:645300 Lipomatous non-saccular limited dorsal myeloschisis Orphanet:645378 Myelic limited dorsal malformation Orphanet:650102 Non-genetic central precocious puberty in male -Orphanet:645343 Non-saccular limited dorsal myeloschisis Orphanet:645294 Posterior extramedullary conus spinal cord lipoma -Orphanet:522530 Rare genetic disorder with entropion Orphanet:645354 Saccular limited dorsal myeloschisis -Orphanet:645319 Saccular spinal dysraphism with a stalk to the dome -Orphanet:522520 Syndromic genetic disorder with strabismus Orphanet:645288 Terminal extramedullary conus spinal cord lipoma Orphanet:645337 Terminal myelocystocele Orphanet:645291 Transitional extramedullary conus spinal cord lipoma diff --git a/src/ontology/reports/sync-subClassOf.direct-in-mondo-only.tsv b/src/ontology/reports/sync-subClassOf.direct-in-mondo-only.tsv index 42ded4e1..dc0ac3ea 100644 --- a/src/ontology/reports/sync-subClassOf.direct-in-mondo-only.tsv +++ b/src/ontology/reports/sync-subClassOf.direct-in-mondo-only.tsv @@ -1356,7 +1356,6 @@ MONDO:0001890 MONDO:0002325 True pulp erosion tooth erosion, non-bacterial UNSUP MONDO:0001892 MONDO:0002571 True spinal cord lymphoma primary central nervous system lymphoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0001892 MONDO:0003544 True spinal cord lymphoma spinal cord cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0001893 MONDO:0003544 True spinal cord melanoma spinal cord cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED -MONDO:0001893 MONDO:0016747 True spinal cord melanoma primary melanoma of the central nervous system UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0001894 MONDO:0002217 True spinal cord sarcoma central nervous system sarcoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0001894 MONDO:0003544 True spinal cord sarcoma spinal cord cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0001896 MONDO:0001150 True obstructive hydrocephalus hydrocephalus SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -2518,7 +2517,7 @@ MONDO:0002934 MONDO:0006646 True intravascular angioleiomyoma angioleiomyoma UNS MONDO:0002935 MONDO:0005341 True penis basal cell carcinoma skin basal cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0002936 MONDO:0005341 True scrotum basal cell carcinoma skin basal cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0002937 MONDO:0005341 True nodular basal cell carcinoma skin basal cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED -MONDO:0002938 MONDO:0005341 True metatypical basal cell carcinoma skin basal cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED +MONDO:0002938 MONDO:0005341 True metatypical basal cell carcinoma skin basal cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0002939 MONDO:0005341 True skin pigmented basal cell carcinoma skin basal cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0002940 MONDO:0005341 True anal margin basal cell carcinoma skin basal cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0002941 MONDO:0002656 True anal margin carcinoma skin carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS @@ -2529,7 +2528,7 @@ MONDO:0002944 MONDO:0002038 True external ear carcinoma head and neck carcinoma MONDO:0002944 MONDO:0003574 True external ear carcinoma external ear cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0002945 MONDO:0005341 True micronodular basal cell carcinoma skin basal cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0002946 MONDO:0002263 True gynatresia female reproductive system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED -MONDO:0002947 MONDO:0005341 True adamantinoid basal cell epithelioma skin basal cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED +MONDO:0002947 MONDO:0005341 True adamantinoid basal cell epithelioma skin basal cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0002948 MONDO:0005341 True skin fibroepithelial basal cell carcinoma skin basal cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0002949 MONDO:0005341 True morpheaform basal cell carcinoma skin basal cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0002950 MONDO:0005341 True skin clear cell basal cell carcinoma skin basal cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -2762,7 +2761,6 @@ MONDO:0003165 MONDO:0002913 True cerebellar astrocytoma cerebellar neoplasm UNSU MONDO:0003165 MONDO:0021631 True cerebellar astrocytoma brain astrocytoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0003168 MONDO:0003165 True cerebellar pilocytic astrocytoma cerebellar astrocytoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0003168 MONDO:0016691 True cerebellar pilocytic astrocytoma pilocytic astrocytoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS -MONDO:0003168 MONDO:0021499 True cerebellar pilocytic astrocytoma benign neoplasm of cerebellum UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0003169 MONDO:0002786 True diencephalic astrocytomas diencephalic cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0003169 MONDO:0021631 True diencephalic astrocytomas brain astrocytoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0003170 MONDO:0021636 True gliofibroma astrocytic tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -2826,7 +2824,6 @@ MONDO:0003219 MONDO:0006181 True gastroesophageal junction adenocarcinoma digest MONDO:0003220 MONDO:0005411 True gallbladder carcinoma gallbladder cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0003220 MONDO:0006181 True gallbladder carcinoma digestive system carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003222 MONDO:0002714 True central nervous system melanocytic neoplasm central nervous system cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED -MONDO:0003222 MONDO:0021143 True central nervous system melanocytic neoplasm melanocytic neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0003223 MONDO:0005094 True meninges hemangiopericytoma hemangiopericytoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0003225 MONDO:0005570 True bone marrow disorder hematologic disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0003227 MONDO:0005638 True prosopagnosia agnosia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -3084,9 +3081,6 @@ MONDO:0003421 MONDO:0021043 True mixed cell adenoma mixed neoplasm UNSUPPORTED-M MONDO:0003422 MONDO:0002732 True lung adenoma lung benign neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0003422 MONDO:0004972 True lung adenoma adenoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0003422 MONDO:0036976 True lung adenoma benign epithelial neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0003423 MONDO:0004972 True middle ear adenoma adenoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS -MONDO:0003423 MONDO:0021482 True middle ear adenoma benign neoplasm of middle ear UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0003423 MONDO:0036976 True middle ear adenoma benign epithelial neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0003424 MONDO:0004972 True oncocytic adenoma adenoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003424 MONDO:0010795 True oncocytic adenoma oncocytic neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0003425 MONDO:0001584 True ophthalmoplegia ocular motility disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -3305,7 +3299,6 @@ MONDO:0003626 MONDO:0002741 True uterine ligament serous adenocarcinoma uterine MONDO:0003627 MONDO:0000603 True rheumatic pulmonary valve disease autoimmune disorder of cardiovascular system UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0003627 MONDO:0003628 True rheumatic pulmonary valve disease pulmonary valve disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0003628 MONDO:0002869 True pulmonary valve disorder heart valve disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED -MONDO:0003629 MONDO:0006003 True uterine corpus serous adenocarcinoma uterine corpus cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0003630 MONDO:0002810 True pancreatic serous cystadenocarcinoma pancreatic serous cystic neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003630 MONDO:0002867 True pancreatic serous cystadenocarcinoma pancreatic cystadenocarcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0003630 MONDO:0024621 True pancreatic serous cystadenocarcinoma serous cystadenocarcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -3484,7 +3477,6 @@ MONDO:0003759 MONDO:0020577 True childhood ovarian yolk sac tumor childhood gona MONDO:0003760 MONDO:0003751 True pediatric ovarian germ cell tumor childhood germ cell tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003760 MONDO:0011366 True pediatric ovarian germ cell tumor ovarian germ cell tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0003761 MONDO:0003762 True leptomeningeal melanoma malignant leptomeningeal tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED -MONDO:0003761 MONDO:0016747 True leptomeningeal melanoma primary melanoma of the central nervous system UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0003762 MONDO:0016642 True malignant leptomeningeal tumor meningioma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0003762 MONDO:0021322 True malignant leptomeningeal tumor malignant tumor of meninges UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0003763 MONDO:0005618 True acute stress disorder anxiety disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -3621,7 +3613,7 @@ MONDO:0003864 MONDO:0004948 True chronic lymphocytic leukemia/small lymphocytic MONDO:0003865 MONDO:0005012 True acral lentiginous melanoma cutaneous melanoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0003866 MONDO:0002397 True liver extraskeletal osteosarcoma liver sarcoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003866 MONDO:0002621 True liver extraskeletal osteosarcoma extraosseous osteosarcoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS -MONDO:0003867 MONDO:0003222 True diffuse meningeal melanocytosis central nervous system melanocytic neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED +MONDO:0003867 MONDO:0003222 True diffuse meningeal melanocytosis central nervous system melanocytic neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0003868 MONDO:0003109 True anterior foramen magnum meningioma foramen magnum meningioma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0003869 MONDO:0002911 True childhood brain stem glioma brain stem glioma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003869 MONDO:0002914 True childhood brain stem glioma childhood brain stem neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -3996,7 +3988,7 @@ MONDO:0004134 MONDO:0002531 True benign dermal neurilemmoma skin neoplasm UNSUPP MONDO:0004136 MONDO:0005183 True ovarian endometrioid cystadenoma ovarian cystadenoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0004139 MONDO:0002280 True normocytic anemia anemia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0004140 MONDO:0003514 True intermediate malignant teratoma malignant teratoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED -MONDO:0004141 MONDO:0005105 True melanomatosis melanoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED +MONDO:0004141 MONDO:0005105 True melanomatosis melanoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0004142 MONDO:0003960 True lung combined large cell neuroendocrine carcinoma pulmonary large cell neuroendocrine carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0004142 MONDO:0006167 True lung combined large cell neuroendocrine carcinoma combined lung carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0004143 MONDO:0016642 True psammomatous meningioma meningioma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -4105,8 +4097,6 @@ MONDO:0004220 MONDO:0006192 True endometrial endometrioid adenocarcinoma with sp MONDO:0004221 MONDO:0006359 True uterine corpus perivascular epithelioid cell tumor neoplasm with perivascular epithelioid cell differentiation UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0004222 MONDO:0002702 True ovarian clear cell cystadenocarcinoma ovarian cystadenocarcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0004222 MONDO:0006045 True ovarian clear cell cystadenocarcinoma ovarian clear cell adenocarcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS -MONDO:0004223 MONDO:0005079 True polyp of middle ear polyp UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0004223 MONDO:0021366 True polyp of middle ear neoplasm of middle ear UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0004224 MONDO:0003335 True chronic metabolic polyneuropathy chronic polyneuropathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0004227 MONDO:0004230 True epididymal adenomatoid tumor adenomatoid tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0004227 MONDO:0021473 True epididymal adenomatoid tumor benign neoplasm of epididymis UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -4459,9 +4449,7 @@ MONDO:0004487 MONDO:0003238 True endometrial type cervical adenomyoma cervical a MONDO:0004488 MONDO:0003238 True cervical atypical polypoid adenomyoma cervical adenomyoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0004489 MONDO:0006206 True fallopian tube gestational choriocarcinoma fallopian tube carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0004489 MONDO:0020550 True fallopian tube gestational choriocarcinoma gestational choriocarcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED -MONDO:0004490 MONDO:0004491 True gestational uterine corpus choriocarcinoma uterine corpus choriocarcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED -MONDO:0004490 MONDO:0020550 True gestational uterine corpus choriocarcinoma gestational choriocarcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED -MONDO:0004491 MONDO:0005207 True uterine corpus choriocarcinoma choriocarcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED +MONDO:0004491 MONDO:0020550 True uterine corpus choriocarcinoma gestational choriocarcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0004493 MONDO:0003402 True testicular yolk sac tumor, papillary pattern testicular yolk sac tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0004494 MONDO:0003402 True testicular yolk sac tumor, hepatoid pattern testicular yolk sac tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0004495 MONDO:0005129 True myotonic cataract cataract UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -4482,9 +4470,6 @@ MONDO:0004508 MONDO:0005076 True periapical periodontitis periodontitis UNSUPPOR MONDO:0004509 MONDO:0003455 True intrahepatic biliary papillomatosis bile duct papillary neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0004510 MONDO:0006097 True inflammatory liposarcoma atypical lipomatous tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0004511 MONDO:0003908 True lower clivus meningioma clivus meningioma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED -MONDO:0004512 MONDO:0004141 True meningeal melanomatosis melanomatosis UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS -MONDO:0004512 MONDO:0016747 True meningeal melanomatosis primary melanoma of the central nervous system UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0004512 MONDO:0021322 True meningeal melanomatosis malignant tumor of meninges UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0004513 MONDO:0017386 True adult pleomorphic rhabdomyosarcoma pleomorphic rhabdomyosarcoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0004514 MONDO:0003014 True chronic rhinitis rhinitis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0004516 MONDO:0004197 True bulbomembranous urethral cancer male urethral cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -4639,7 +4624,7 @@ MONDO:0004662 MONDO:0004664 True heterophyiasis helminthiasis UNSUPPORTED-MISSIN MONDO:0004663 MONDO:0002032 True colon carcinoma in situ colon carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0004663 MONDO:0004698 True colon carcinoma in situ intestine carcinoma in situ UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0004664 MONDO:0005135 True helminthiasis parasitic infectious disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED -MONDO:0004665 MONDO:0009348 True nodular sclerosis classical Hodgkin lymphoma classic Hodgkin lymphoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0004665 MONDO:0009348 True nodular sclerosis classical Hodgkin lymphoma classic Hodgkin lymphoma UNSUPPORTED-MISSING SUPPORTED SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0004666 MONDO:0004664 True metagonimiasis helminthiasis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0004667 MONDO:0021242 True sublingual gland cancer sublingual gland neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0004667 MONDO:0044743 True sublingual gland cancer major salivary gland cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -5060,7 +5045,6 @@ MONDO:0005100 MONDO:0019340 True systemic sclerosis scleroderma UNSUPPORTED-MISS MONDO:0005101 MONDO:0005292 True ulcerative colitis colitis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0005102 MONDO:0002397 True undifferentiated (embryonal) sarcoma liver sarcoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005103 MONDO:0005060 True well-differentiated liposarcoma liposarcoma UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0005104 MONDO:0005089 True aJCC grade 1 sarcoma sarcoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005105 MONDO:0021143 True melanoma melanocytic neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005106 MONDO:0044983 True lipoma benign lipomatous neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005108 MONDO:0005550 True viral infectious disease infectious disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -5212,7 +5196,6 @@ MONDO:0005358 MONDO:0005502 True Dengue hemorrhagic fever dengue disease UNSUPPO MONDO:0005361 MONDO:0001409 True eosinophilic esophagitis esophagitis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0005362 MONDO:0002134 True erectile dysfunction physiological sexual disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0005367 MONDO:0005530 True heroin dependence opiate dependence UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED -MONDO:0005369 MONDO:0019496 True carcinoid tumor neuroendocrine neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005372 MONDO:0003150 True male infertility male reproductive system disorder SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0005374 MONDO:0002334 True bone marrow neoplasm hematopoietic and lymphoid system neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0005374 MONDO:0003225 True bone marrow neoplasm bone marrow disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -5635,7 +5618,6 @@ MONDO:0006035 MONDO:0005036 True gastric tubular adenocarcinoma gastric adenocar MONDO:0006035 MONDO:0005606 True gastric tubular adenocarcinoma tubular adenocarcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0006036 MONDO:0006055 True granulosa cell tumor sex cord-stromal tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0006037 MONDO:0006025 True hydrolethalus syndrome autosomal recessive disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED -MONDO:0006041 MONDO:0005369 True lung carcinoid tumor carcinoid tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006041 MONDO:0005454 True lung carcinoid tumor lung neuroendocrine neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006043 MONDO:0006256 True metaplastic breast carcinoma invasive breast carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006045 MONDO:0000548 True ovarian clear cell adenocarcinoma ovarian clear cell cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS @@ -5684,7 +5666,6 @@ MONDO:0006091 MONDO:0015066 True appendix neuroendocrine tumor G1 neuroendocrine MONDO:0006092 MONDO:0006088 True appendix villous adenoma appendix adenoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006093 MONDO:0006155 True ascending colon neuroendocrine tumor G1 colon neuroendocrine tumor G1 UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006094 MONDO:0018271 True Askin tumor peripheral primitive neuroectodermal tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0006095 MONDO:0005369 True atypical carcinoid tumor carcinoid tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006097 MONDO:0021354 True atypical lipomatous tumor tumor of adipose tissue UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006098 MONDO:0002486 True atypical lobular breast hyperplasia lobular neoplasia UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006098 MONDO:0005043 True atypical lobular breast hyperplasia hyperplasia UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -5790,7 +5771,8 @@ MONDO:0006191 MONDO:0005004 True endometrial clear cell adenocarcinoma clear cel MONDO:0006191 MONDO:0005461 True endometrial clear cell adenocarcinoma endometrium adenocarcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0006192 MONDO:0005026 True endometrial endometrioid adenocarcinoma endometrioid adenocarcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006195 MONDO:0004701 True endometrial polyp uterine polyp UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0006196 MONDO:0005278 True endometrial serous adenocarcinoma serous adenocarcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0006196 MONDO:0005278 True endometrial serous adenocarcinoma serous adenocarcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS +MONDO:0006196 MONDO:0006003 True endometrial serous adenocarcinoma uterine corpus cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0006197 MONDO:0000402 True endometrial small cell carcinoma small cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0006197 MONDO:0002447 True endometrial small cell carcinoma endometrial carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0006198 MONDO:0002447 True endometrial squamous cell carcinoma endometrial carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -5834,7 +5816,6 @@ MONDO:0006223 MONDO:0018905 True gastric diffuse large B-cell lymphoma diffuse l MONDO:0006225 MONDO:0018876 True gastric mantle cell lymphoma mantle cell lymphoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006226 MONDO:0007650 True gastric mucosa-associated lymphoid tissue lymphoma MALT lymphoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006226 MONDO:0042493 True gastric mucosa-associated lymphoid tissue lymphoma gastric non-hodgkin lymphoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0006227 MONDO:0005369 True gastric neuroendocrine tumor G1 carcinoid tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006227 MONDO:0015062 True gastric neuroendocrine tumor G1 gastric neuroendocrine tumor, well differentiated, low or intermediate grade UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006228 MONDO:0002512 True gastric papillary adenocarcinoma papillary adenocarcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0006228 MONDO:0005036 True gastric papillary adenocarcinoma gastric adenocarcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -6015,7 +5996,6 @@ MONDO:0006380 MONDO:0006407 True pleural sarcomatoid mesothelioma sarcomatoid me MONDO:0006381 MONDO:0017795 True plexiform ameloblastoma ameloblastoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006382 MONDO:0004970 True poorly differentiated thyroid gland carcinoma adenocarcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006383 MONDO:0018905 True primary cutaneous diffuse large B-cell lymphoma, Leg type diffuse large B-cell lymphoma UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0006385 MONDO:0010150 True primary intraosseous squamous cell carcinoma head and neck squamous cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006386 MONDO:0015686 True primary peritoneal serous adenocarcinoma primary peritoneal carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006387 MONDO:0018905 True primary pulmonary diffuse large B-cell lymphoma diffuse large B-cell lymphoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006387 MONDO:0020644 True primary pulmonary diffuse large B-cell lymphoma lung non-Hodgkin lymphoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -6211,7 +6191,7 @@ MONDO:0006576 MONDO:0005230 True Ludwig's angina cellulitis UNSUPPORTED-MISSING MONDO:0006577 MONDO:0001735 True maxillary sinus cholesteatoma paranasal sinus disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0006577 MONDO:0006530 True maxillary sinus cholesteatoma cholesteatoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0006578 MONDO:0006574 True mediastinal lipomatosis lipomatosis UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED -MONDO:0006579 MONDO:0008420 True melanoacanthoma seborrheic keratosis UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED +MONDO:0006579 MONDO:0008420 True melanoacanthoma seborrheic keratosis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0006580 MONDO:0006615 True miliaria sweat gland disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0006581 MONDO:0006580 True miliaria rubra miliaria UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0006582 MONDO:0005093 True mongolian spot skin disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -7399,7 +7379,7 @@ MONDO:0008300 MONDO:0015770 True Prader-Willi syndrome congenital hypogonadotrop MONDO:0008300 MONDO:0019040 True Prader-Willi syndrome chromosomal disorder UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0008301 MONDO:0002254 True Guttmacher syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0008301 MONDO:0003847 True Guttmacher syndrome hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED -MONDO:0008302 MONDO:0019165 True centra precocious puberty 1 central precocious puberty UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED +MONDO:0008302 MONDO:0019165 True central precocious puberty 1 central precocious puberty UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0008303 MONDO:0003847 True familial male-limited precocious puberty hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0008303 MONDO:0015791 True familial male-limited precocious puberty peripheral precocious puberty UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0008305 MONDO:0002254 True Currarino triad syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -7840,7 +7820,6 @@ MONDO:0008901 MONDO:0020120 True Tel Hashomer camptodactyly syndrome skeletal mu MONDO:0008903 MONDO:0000376 True lung cancer respiratory system cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0008903 MONDO:0003274 True lung cancer thoracic cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0008903 MONDO:0021117 True lung cancer lung neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0008905 MONDO:0015979 True predisposition to invasive fungal disease due to CARD9 deficiency hereditary predisposition to infections UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0008907 MONDO:0005500 True PMM2-congenital disorder of glycosylation congenital disorder of glycosylation type I UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0008907 MONDO:0017740 True PMM2-congenital disorder of glycosylation disorder of protein N-glycosylation UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0008908 MONDO:0005501 True MGAT2-congenital disorder of glycosylation congenital disorder of glycosylation type II UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED @@ -7880,7 +7859,6 @@ MONDO:0008955 MONDO:0008926 True cerebrooculofacioskeletal syndrome 1 COFS syndr MONDO:0008958 MONDO:0001029 True Klippel-Feil syndrome 2, autosomal recessive Klippel-Feil syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0008961 MONDO:0018995 True Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4 UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0008962 MONDO:0018306 True Griscelli syndrome type 1 Griscelli syndrome UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED -MONDO:0008963 MONDO:0015541 True Chediak-Higashi syndrome hereditary hemophagocytic lymphohistiocytosis UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING MONDO:0008963 MONDO:0017305 True Chediak-Higashi syndrome syndromic oculocutaneous albinism UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0008963 MONDO:0017739 True Chediak-Higashi syndrome disorder of lysosomal-related organelles UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0008963 MONDO:0020127 True Chediak-Higashi syndrome hereditary peripheral neuropathy UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -7899,7 +7877,7 @@ MONDO:0008977 MONDO:0005089 True chondrosarcoma sarcoma UNSUPPORTED-MISSING UNSU MONDO:0008978 MONDO:0002597 True chordoma notochordal tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0008980 MONDO:0015770 True ataxia-hypogonadism-choroidal dystrophy syndrome congenital hypogonadotropic hypogonadism UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0008980 MONDO:0100309 True ataxia-hypogonadism-choroidal dystrophy syndrome hereditary ataxia UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS -MONDO:0008988 MONDO:0015991 True citrullinemia type I citrullinemia UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED +MONDO:0008988 MONDO:0015991 True citrullinemia type I citrullinemia UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0008991 MONDO:0015161 True Verloove Vanhorick-Brubakk syndrome multiple congenital anomalies/dysmorphic syndrome without intellectual disability UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0008992 MONDO:0015161 True Juberg-Hayward syndrome multiple congenital anomalies/dysmorphic syndrome without intellectual disability UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0008995 MONDO:0002254 True Yunis-Varon syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -8464,7 +8442,7 @@ MONDO:0009677 MONDO:0016143 True autosomal recessive limb-girdle muscular dystro MONDO:0009677 MONDO:0016333 True autosomal recessive limb-girdle muscular dystrophy type 2C familial dilated cardiomyopathy UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING MONDO:0009678 MONDO:0000171 True muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4 muscular dystrophy-dystroglycanopathy, type A UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-SUBCLASS MONDO:0009680 MONDO:0019950 True congenital muscular dystrophy-infantile cataract-hypogonadism syndrome congenital muscular dystrophy UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0009681 MONDO:0000355 True Ullrich congenital muscular dystrophy 1A Ullrich congenital muscular dystrophy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING +MONDO:0009681 MONDO:0000355 True Ullrich congenital muscular dystrophy 1A Ullrich congenital muscular dystrophy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0009683 MONDO:0015152 True autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0009683 MONDO:0016153 True autosomal recessive limb-girdle muscular dystrophy type 2H qualitative or quantitative defects of TRIM32 UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0009685 MONDO:0018949 True Miyoshi myopathy distal myopathy UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS SUPPORTED @@ -8586,6 +8564,7 @@ MONDO:0009843 MONDO:0017226 True hypomyelinating leukodystrophy 3 Pelizaeus-Merz MONDO:0009845 MONDO:0018234 True pelviscapular dysplasia dysostosis UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0009845 MONDO:0019054 True pelviscapular dysplasia congenital limb malformation UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0009848 MONDO:0019296 True dissecting cellulitis of the scalp subcutaneous tissue disorder UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0009849 MONDO:0005046 True hyperimmunoglobulinemia D with periodic fever immune system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0009849 MONDO:0017708 True hyperimmunoglobulinemia D with periodic fever mevalonate kinase deficiency UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0009852 MONDO:0000424 True hereditary intrinsic factor deficiency inborn vitamin B12 deficiency UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0009852 MONDO:0016624 True hereditary intrinsic factor deficiency inherited deficiency anemia UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -9268,7 +9247,6 @@ MONDO:0010622 MONDO:0020605 True recessive X-linked ichthyosis X-linked recessiv MONDO:0010626 MONDO:0000425 True hyper-IgM syndrome type 1 X-linked disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0010626 MONDO:0003947 True hyper-IgM syndrome type 1 hyper-IgM syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0010627 MONDO:0000425 True X-linked lymphoproliferative syndrome X-linked disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED -MONDO:0010627 MONDO:0015541 True X-linked lymphoproliferative syndrome hereditary hemophagocytic lymphohistiocytosis UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0010627 MONDO:0016537 True X-linked lymphoproliferative syndrome lymphoproliferative syndrome UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0010631 MONDO:0019287 True incontinentia pigmenti ectodermal dysplasia syndrome UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-SUBCLASS MONDO:0010632 MONDO:0100062 True developmental and epileptic encephalopathy, 1 developmental and epileptic encephalopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED @@ -9285,7 +9263,7 @@ MONDO:0010651 MONDO:0017762 True Menkes disease disorder of copper metabolism UN MONDO:0010653 MONDO:0020119 True Renpenning syndrome X-linked syndromic intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0010654 MONDO:0020119 True Partington syndrome X-linked syndromic intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0010655 MONDO:0015159 True X-linked intellectual disability with marfanoid habitus multiple congenital anomalies/dysmorphic syndrome-intellectual disability UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0010656 MONDO:0019181 True intellectual disability, X-linked 1 non-syndromic X-linked intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED +MONDO:0010656 MONDO:0019181 True intellectual disability, X-linked 1 non-syndromic X-linked intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0010657 MONDO:0016826 True methylmalonic acidemia with homocystinuria, type cblX methylmalonic aciduria and homocystinuria UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0010657 MONDO:0019181 True methylmalonic acidemia with homocystinuria, type cblX non-syndromic X-linked intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-SUBCLASS MONDO:0010658 MONDO:0020119 True syndromic X-linked intellectual disability 12 X-linked syndromic intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED @@ -10124,7 +10102,6 @@ MONDO:0011868 MONDO:0017436 True lethal congenital contracture syndrome 2 lethal MONDO:0011871 MONDO:0017014 True Niemann-Pick disease type B interstitial lung disease specific to childhood UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0011871 MONDO:0020127 True Niemann-Pick disease type B hereditary peripheral neuropathy UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0011872 MONDO:0015134 True Griscelli syndrome type 2 constitutional neutropenia UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0011872 MONDO:0015541 True Griscelli syndrome type 2 hereditary hemophagocytic lymphohistiocytosis UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING MONDO:0011872 MONDO:0018306 True Griscelli syndrome type 2 Griscelli syndrome UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0011874 MONDO:0015947 True neonatal ichthyosis-sclerosing cholangitis syndrome inherited ichthyosis UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0011874 MONDO:0018646 True neonatal ichthyosis-sclerosing cholangitis syndrome sclerosing cholangitis UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -10138,7 +10115,6 @@ MONDO:0011883 MONDO:0019287 True Curly hair - acral keratoderma - caries syndrom MONDO:0011884 MONDO:0017672 True hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome focal palmoplantar keratoderma UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0011884 MONDO:0019287 True hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome ectodermal dysplasia syndrome UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING MONDO:0011886 MONDO:0015990 True torsion dystonia 13 focal, segmental or multifocal dystonia UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0011888 MONDO:0015979 True immunodeficiency 67 hereditary predisposition to infections UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0011888 MONDO:0021094 True immunodeficiency 67 immunodeficiency disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0011889 MONDO:0018993 True Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2 UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0011890 MONDO:0019011 True Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1 UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -10222,7 +10198,6 @@ MONDO:0011992 MONDO:0015150 True hereditary spastic paraplegia 25 complex heredi MONDO:0011994 MONDO:0019587 True autosomal dominant nonsyndromic hearing loss 41 autosomal dominant nonsyndromic hearing loss UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0011996 MONDO:0004643 True chronic myelogenous leukemia, BCR-ABL1 positive myeloid leukemia UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0011997 MONDO:0015134 True Hermansky-Pudlak syndrome 2 constitutional neutropenia UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0011997 MONDO:0015541 True Hermansky-Pudlak syndrome 2 hereditary hemophagocytic lymphohistiocytosis UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING MONDO:0011997 MONDO:0019312 True Hermansky-Pudlak syndrome 2 Hermansky-Pudlak syndrome UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0011999 MONDO:0005349 True otosclerosis 3 otosclerosis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0012000 MONDO:0003699 True specific phobia phobic disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -10483,7 +10458,7 @@ MONDO:0012353 MONDO:0001115 True erythrocytosis, familial, 3 familial polycythem MONDO:0012354 MONDO:0000009 True platelet-type bleeding disorder 8 inherited bleeding disorder, platelet-type UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0012354 MONDO:0021181 True platelet-type bleeding disorder 8 inherited blood coagulation disorder UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012355 MONDO:0019588 True autosomal recessive nonsyndromic hearing loss 28 hearing loss, autosomal recessive UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED -MONDO:0012360 MONDO:0000045 True congenital nongoitrous hypothryoidism 3 hypothyroidism, congenital, nongoitrous UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING +MONDO:0012360 MONDO:0000045 True congenital nongoitrous hypothyroidism 3 hypothyroidism, congenital, nongoitrous UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0012362 MONDO:0016333 True dilated cardiomyopathy 1P familial dilated cardiomyopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0012363 MONDO:0019200 True retinitis pigmentosa 32 retinitis pigmentosa UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0012364 MONDO:0016333 True dilated cardiomyopathy 1Q familial dilated cardiomyopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING @@ -10723,7 +10698,7 @@ MONDO:0012678 MONDO:0018054 True atrial fibrillation, familial, 5 familial atria MONDO:0012679 MONDO:0019026 True autosomal recessive osteopetrosis 6 autosomal recessive osteopetrosis UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0012680 MONDO:0019005 True nephronophthisis 7 nephronophthisis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0012681 MONDO:0000032 True febrile seizures, familial, 7 febrile seizures, familial UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED -MONDO:0012682 MONDO:0015979 True immunodeficiency 35 hereditary predisposition to infections UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0012682 MONDO:0021094 True immunodeficiency 35 immunodeficiency disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0012683 MONDO:0016387 True pontocerebellar hypoplasia type 6 mitochondrial oxidative phosphorylation disorder UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012683 MONDO:0020135 True pontocerebellar hypoplasia type 6 pontocerebellar hypoplasia UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0012684 MONDO:0016342 True arrhythmogenic right ventricular dysplasia 12 familial isolated arrhythmogenic right ventricular dysplasia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING @@ -10840,7 +10815,7 @@ MONDO:0012833 MONDO:0000426 True Crouzon syndrome-acanthosis nigricans syndrome MONDO:0012833 MONDO:0015338 True Crouzon syndrome-acanthosis nigricans syndrome syndromic craniosynostosis UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012837 MONDO:0005265 True inflammatory bowel disease 15 inflammatory bowel disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0012838 MONDO:0005265 True inflammatory bowel disease 16 inflammatory bowel disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED -MONDO:0012839 MONDO:0015979 True pyogenic bacterial infections due to MyD88 deficiency hereditary predisposition to infections UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0012839 MONDO:0021094 True pyogenic bacterial infections due to MyD88 deficiency immunodeficiency disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0012840 MONDO:0005265 True inflammatory bowel disease 17 inflammatory bowel disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0012841 MONDO:0005265 True inflammatory bowel disease 18 inflammatory bowel disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0012842 MONDO:0024462 True melanoma, cutaneous malignant, susceptibility to, 7 susceptibility to familial cutaneous melanoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING @@ -11280,9 +11255,9 @@ MONDO:0013396 MONDO:0003847 True chromosome 1p32-p31 deletion syndrome hereditar MONDO:0013396 MONDO:0016883 True chromosome 1p32-p31 deletion syndrome partial deletion of the short arm of chromosome 1 UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013397 MONDO:0024516 True acne inversa, familial, 2 familial acne inversa UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0013398 MONDO:0024516 True acne inversa, familial, 3 familial acne inversa UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING -MONDO:0013400 MONDO:0003847 True Congenital adrenal insuffiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED -MONDO:0013400 MONDO:0005495 True Congenital adrenal insuffiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency adrenal gland disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED -MONDO:0013400 MONDO:0020040 True Congenital adrenal insuffiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency 46,XY disorder of sex development UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0013400 MONDO:0003847 True Congenital adrenal insufficiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED +MONDO:0013400 MONDO:0005495 True Congenital adrenal insufficiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency adrenal gland disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED +MONDO:0013400 MONDO:0020040 True Congenital adrenal insufficiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency 46,XY disorder of sex development UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013401 MONDO:0019064 True hereditary spastic paraplegia 51 hereditary spastic paraplegia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0013402 MONDO:0019200 True retinitis pigmentosa 27 retinitis pigmentosa UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0013403 MONDO:0018677 True heterotaxy, visceral, 4, autosomal visceral heterotaxy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING @@ -11303,7 +11278,8 @@ MONDO:0013424 MONDO:0016885 True 3p- syndrome partial deletion of the short arm MONDO:0013424 MONDO:0017393 True 3p- syndrome blepharophimosis - intellectual disability syndrome UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013425 MONDO:0019200 True retinitis pigmentosa 20 retinitis pigmentosa UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0013426 MONDO:0018954 True aneurysm-osteoarthritis syndrome Loeys-Dietz syndrome UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED -MONDO:0013427 MONDO:0015979 True immunodeficiency 31B hereditary predisposition to infections UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0013427 MONDO:0006025 True immunodeficiency 31B autosomal recessive disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED +MONDO:0013427 MONDO:0021094 True immunodeficiency 31B immunodeficiency disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0013428 MONDO:0016817 True Meier-Gorlin syndrome 2 Meier-Gorlin syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0013429 MONDO:0019200 True retinitis pigmentosa 40 retinitis pigmentosa UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0013430 MONDO:0016817 True Meier-Gorlin syndrome 3 Meier-Gorlin syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED @@ -11565,7 +11541,7 @@ MONDO:0013754 MONDO:0019572 True cutis laxa, autosomal recessive, type 1B autoso MONDO:0013755 MONDO:0017569 True PYCR1-related de Barsy syndrome de Barsy syndrome UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0013755 MONDO:0100237 True PYCR1-related de Barsy syndrome inherited cutis laxa UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0013756 MONDO:0016620 True hypertrophic osteoarthropathy, primary, autosomal recessive, 2 primary hypertrophic osteoarthropathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING -MONDO:0013757 MONDO:0000045 True congenital nongoitrous hypothryoidism 6 hypothyroidism, congenital, nongoitrous UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING +MONDO:0013757 MONDO:0000045 True congenital nongoitrous hypothyroidism 6 hypothyroidism, congenital, nongoitrous UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0013758 MONDO:0019548 True Charcot-Marie-Tooth disease dominant intermediate E autosomal dominant intermediate Charcot-Marie-Tooth disease UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013759 MONDO:0024462 True melanoma, cutaneous malignant, susceptibility to, 8 susceptibility to familial cutaneous melanoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0013760 MONDO:0018117 True congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome disorder of phospholipids, sphingolipids and fatty acids biosynthesis UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -11665,7 +11641,7 @@ MONDO:0013862 MONDO:0015517 True immunodeficiency, common variable, 7 common var MONDO:0013863 MONDO:0015517 True combined immunodeficiency due to LRBA deficiency common variable immunodeficiency UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0013864 MONDO:0016033 True Cornelia de Lange syndrome 4 Cornelia de Lange syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0013865 MONDO:0000732 True mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency combined oxidative phosphorylation deficiency UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED -MONDO:0013867 MONDO:0008891 True brown-Vialetto-van Laere syndrome 2 riboflavin transporter deficiency UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED +MONDO:0013867 MONDO:0008891 True Brown-Vialetto-van Laere syndrome 2 riboflavin transporter deficiency UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0013869 MONDO:0019236 True adenine phosphoribosyltransferase deficiency inborn disorder of purine metabolism UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013870 MONDO:0005501 True TMEM165-congenital disorder of glycosylation congenital disorder of glycosylation type II UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0013870 MONDO:0017740 True TMEM165-congenital disorder of glycosylation disorder of protein N-glycosylation UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -12358,7 +12334,7 @@ MONDO:0014650 MONDO:0005115 True familial temporal lobe epilepsy 8 temporal lobe MONDO:0014651 MONDO:0018237 True acrofacial dysostosis Cincinnati type acrofacial dysostosis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0014652 MONDO:0019516 True exudative vitreoretinopathy 6 exudative vitreoretinopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0014653 MONDO:0019200 True retinitis pigmentosa 72 retinitis pigmentosa UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED -MONDO:0014654 MONDO:0000355 True Ullrich congenital muscular dystrophy 2 Ullrich congenital muscular dystrophy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING +MONDO:0014654 MONDO:0000355 True Ullrich congenital muscular dystrophy 2 Ullrich congenital muscular dystrophy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0014656 MONDO:0000090 True progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2 progressive external ophthalmoplegia with mitochondrial DNA deletions UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0014657 MONDO:0016575 True primary ciliary dyskinesia 32 primary ciliary dyskinesia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0014658 MONDO:0000426 True severe achondroplasia-developmental delay-acanthosis nigricans syndrome autosomal dominant disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -12373,7 +12349,7 @@ MONDO:0014665 MONDO:0018993 True Charcot-Marie-Tooth disease axonal type 2V Char MONDO:0014666 MONDO:0019046 True hypomyelinating leukodystrophy 11 leukodystrophy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0014667 MONDO:0015487 True cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3 fatal infantile encephalocardiomyopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0014668 MONDO:0015487 True cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4 fatal infantile encephalocardiomyopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED -MONDO:0014669 MONDO:0015993 True cone-rod dystrophy 21 cone-rod dystrophy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING +MONDO:0014669 MONDO:0015993 True cone-rod dystrophy 21 cone-rod dystrophy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0014670 MONDO:0017436 True lethal congenital contracture syndrome 9 lethal congenital contracture syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0014674 MONDO:0018911 True maturity-onset diabetes of the young type 14 maturity-onset diabetes of the young UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS SUPPORTED MONDO:0014675 MONDO:0019588 True autosomal recessive nonsyndromic hearing loss 104 hearing loss, autosomal recessive UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED @@ -13672,9 +13648,6 @@ MONDO:0016742 MONDO:0002714 True mixed germ cell tumor of central nervous system MONDO:0016742 MONDO:0003000 True mixed germ cell tumor of central nervous system central nervous system germ cell tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016743 MONDO:0006130 True tumor of meninges central nervous system neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016745 MONDO:0016743 True diffuse leptomeningeal melanocytosis tumor of meninges UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0016746 MONDO:0003222 True meningeal melanocytoma central nervous system melanocytic neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS -MONDO:0016747 MONDO:0003222 True primary melanoma of the central nervous system central nervous system melanocytic neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0016747 MONDO:0006320 True primary melanoma of the central nervous system non-cutaneous melanoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016750 MONDO:0015159 True microcephaly-cleft palate syndrome multiple congenital anomalies/dysmorphic syndrome-intellectual disability UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016751 MONDO:0021089 True malignant perineurioma peripheral nervous system cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016752 MONDO:0016749 True benign peripheral nerve sheath tumor tumor of cranial and spinal nerves UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -14340,8 +14313,6 @@ MONDO:0017895 MONDO:0015447 True familial papillary or follicular thyroid carcin MONDO:0017895 MONDO:0017896 True familial papillary or follicular thyroid carcinoma familial nonmedullary thyroid carcinoma UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017896 MONDO:0015075 True familial nonmedullary thyroid carcinoma thyroid gland carcinoma UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017900 MONDO:0019146 True autosomal recessive Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency inherited susceptibility to mycobacterial diseases UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0017901 MONDO:0015979 True autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency hereditary predisposition to infections UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0017902 MONDO:0015979 True autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency hereditary predisposition to infections UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017903 MONDO:0019146 True autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency inherited susceptibility to mycobacterial diseases UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017905 MONDO:0019146 True X-linked Mendelian susceptibility to mycobacterial diseases inherited susceptibility to mycobacterial diseases UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017906 MONDO:0015301 True amyloidosis cutis dyschromia primary cutaneous amyloidosis UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -15138,7 +15109,6 @@ MONDO:0019142 MONDO:0015951 True inherited porphyria hereditary photodermatosis MONDO:0019142 MONDO:0017754 True inherited porphyria inborn disorder of porphyrin metabolism UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019143 MONDO:0004664 True angiostrongyliasis helminthiasis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0019144 MONDO:0002304 True hereditary thrombophilia due to congenital protein S deficiency protein S deficiency UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED -MONDO:0019146 MONDO:0015979 True inherited susceptibility to mycobacterial diseases hereditary predisposition to infections UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019147 MONDO:0002875 True myiasis parasitic ectoparasitic infectious disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0019148 MONDO:0800449 True Wolman disease lysosomal acid lipase deficiency UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0019149 MONDO:0800449 True cholesteryl ester storage disease lysosomal acid lipase deficiency UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED @@ -15190,8 +15160,6 @@ MONDO:0019203 MONDO:0002429 True acute interstitial pneumonia idiopathic interst MONDO:0019204 MONDO:0002429 True respiratory bronchiolitis-interstitial lung disease syndrome idiopathic interstitial pneumonia UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019205 MONDO:0019287 True trichodysplasia-amelogenesis imperfecta syndrome ectodermal dysplasia syndrome UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019210 MONDO:0002120 True cutaneous neuroendocrine carcinoma neuroendocrine carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0019210 MONDO:0002656 True cutaneous neuroendocrine carcinoma skin carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0019210 MONDO:0003363 True cutaneous neuroendocrine carcinoma malignant dermis tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019210 MONDO:0017341 True cutaneous neuroendocrine carcinoma virus associated tumor UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019211 MONDO:0019284 True isolated congenital anonychia inherited isolated nail anomaly UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019212 MONDO:0006602 True disseminated superficial actinic porokeratosis porokeratosis UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -15784,7 +15752,6 @@ MONDO:0020323 MONDO:0018905 True primary mediastinal large B-cell lymphoma diffu MONDO:0020324 MONDO:0018905 True intravascular large B-cell lymphoma diffuse large B-cell lymphoma UNSUPPORTED-MISSING SUPPORTED SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0020325 MONDO:0000430 True anaplastic large cell lymphoma mature T-cell and NK-cell non-Hodgkin lymphoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0020326 MONDO:0018897 True lymphomatoid papulosis primary cutaneous CD30+ T-cell lymphoproliferative disease UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0020327 MONDO:0009348 True classic Hodgkin lymphoma, nodular sclerosis type classic Hodgkin lymphoma UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0020331 MONDO:0016586 True indolent systemic mastocytosis systemic mastocytosis UNSUPPORTED-MISSING SUPPORTED SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0020332 MONDO:0016586 True systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease systemic mastocytosis UNSUPPORTED-MISSING SUPPORTED SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0020333 MONDO:0016586 True aggressive systemic mastocytosis systemic mastocytosis UNSUPPORTED-MISSING SUPPORTED SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -15998,6 +15965,7 @@ MONDO:0020641 MONDO:0005070 True respiratory tract neoplasm neoplasm UNSUPPORTED MONDO:0020641 MONDO:0005087 True respiratory tract neoplasm respiratory system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0020644 MONDO:0003987 True lung non-Hodgkin lymphoma lung lymphoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0020644 MONDO:0018908 True lung non-Hodgkin lymphoma non-Hodgkin lymphoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0020646 MONDO:0005586 True ocular adnexal lymphoma head and neck neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0020646 MONDO:0018908 True ocular adnexal lymphoma non-Hodgkin lymphoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0020649 MONDO:0020656 True warty carcinoma of the penis human papillomavirus-related penile squamous cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0020653 MONDO:0001704 True vaginal adenocarcinoma vaginal glandular neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -16416,8 +16384,6 @@ MONDO:0021390 MONDO:0005079 True polyp of ureter polyp UNSUPPORTED-MISSING UNSUP MONDO:0021390 MONDO:0021111 True polyp of ureter ureter neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021394 MONDO:0005079 True polyp of vagina polyp SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021396 MONDO:0005079 True polyp of vulva polyp SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0021402 MONDO:0005079 True polyp of external auditory canal polyp UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0021402 MONDO:0021235 True polyp of external auditory canal external ear neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021424 MONDO:0005094 True hemangiopericytoma of skin hemangiopericytoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021427 MONDO:0021333 True squamous cell carcinoma of lip carcinoma of lip UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021429 MONDO:0004958 True squamous cell carcinoma of floor of mouth oral cavity squamous cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -16574,10 +16540,8 @@ MONDO:0021532 MONDO:0005167 True fibroma of prostate fibroma UNSUPPORTED-MISSING MONDO:0021532 MONDO:0021510 True fibroma of prostate benign neoplasm of prostate UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021533 MONDO:0000386 True intestinal neuroendocrine tumor G1 digestive system neuroendocrine tumor, grade 1/2 UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021533 MONDO:0002883 True intestinal neuroendocrine tumor G1 intestinal neuroendocrine neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0021533 MONDO:0005369 True intestinal neuroendocrine tumor G1 carcinoid tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021534 MONDO:0006162 True rectal neuroendocrine tumor G1 colorectal neuroendocrine tumor G1 UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021534 MONDO:0015068 True rectal neuroendocrine tumor G1 neuroendocrine tumor of rectum, well differentiated, low or intermediate grade UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0021535 MONDO:0005369 True pancreatic neuroendocrine tumor G1 carcinoid tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021535 MONDO:0019954 True pancreatic neuroendocrine tumor G1 pancreatic neuroendocrine tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021537 MONDO:0015459 True undifferentiated carcinoma of nasopharynx nasopharyngeal carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021538 MONDO:0004958 True verrucous carcinoma of oral cavity oral cavity squamous cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -16643,7 +16607,6 @@ MONDO:0022513 MONDO:0021154 True atrophoderma of Pierini and Pasini dermis disor MONDO:0022519 MONDO:0004496 True autoimmune myocarditis myocarditis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0022529 MONDO:0005784 True BK-virus nephropathy hantavirus hemorrhagic fever with renal syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0022578 MONDO:0004986 True childhood bladder carcinoma urinary bladder carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0022642 MONDO:0005369 True childhood carcinoid tumor carcinoid tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0022642 MONDO:0021079 True childhood carcinoid tumor childhood neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0022697 MONDO:0006497 True athetoid cerebral palsy cerebral palsy SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0022742 MONDO:0004979 True occupational asthma asthma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -16677,6 +16640,8 @@ MONDO:0023670 MONDO:0015229 True Bardet-Biedl syndrome 20 Bardet-Biedl syndrome MONDO:0023671 MONDO:0025193 True oculopharyngodistal myopathy 3 oculopharyngodistal myopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0023682 MONDO:0006239 True tympanic paraganglioma head and neck paraganglioma UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0023691 MONDO:0009563 True maple syrup urine disease type 1A maple syrup urine disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING +MONDO:0023692 MONDO:0009563 True maple syrup urine disease type 1B maple syrup urine disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING +MONDO:0023693 MONDO:0009563 True maple syrup urine disease type 2 maple syrup urine disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0023726 MONDO:0005744 True mediastinal yolk sac tumor yolk sac tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0023726 MONDO:0006298 True mediastinal yolk sac tumor mediastinal malignant germ cell tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0024182 MONDO:0006676 True dry beriberi beriberi UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED @@ -17054,7 +17019,7 @@ MONDO:0030436 MONDO:0020099 True anemia, sideroblastic, 5 inherited sideroblasti MONDO:0030437 MONDO:0005501 True congenital disorder of glycosylation, type IIw congenital disorder of glycosylation type II UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0030438 MONDO:0020135 True pontocerebellar hypoplasia, type 16 pontocerebellar hypoplasia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0030439 MONDO:0004983 True spermatogenic failure 57 spermatogenic failure UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED -MONDO:0030440 MONDO:0015993 True cone-rod dystrophy 22 cone-rod dystrophy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING +MONDO:0030440 MONDO:0015993 True cone-rod dystrophy 22 cone-rod dystrophy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0030448 MONDO:0021094 True immunodeficiency 86 immunodeficiency disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0030449 MONDO:0019588 True hearing loss, autosomal recessive 118, with cochlear aplasia hearing loss, autosomal recessive UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0030453 MONDO:0100062 True developmental and epileptic encephalopathy 97 developmental and epileptic encephalopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED @@ -17303,7 +17268,7 @@ MONDO:0031068 MONDO:0015626 True Charcot-Marie-Tooth disease, axonal, IIa 2II Ch MONDO:0031071 MONDO:0015253 True Diamond-Blackfan anemia 21 Diamond-Blackfan anemia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0031077 MONDO:0004983 True spermatogenic failure 76 spermatogenic failure UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0031083 MONDO:0004983 True spermatogenic failure 77 spermatogenic failure UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING -MONDO:0031084 MONDO:0019507 True amelogenesis imperfecta, IIa 1K amelogenesis imperfecta UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING +MONDO:0031084 MONDO:0019507 True amelogenesis imperfecta, IIa 1K amelogenesis imperfecta UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0031329 MONDO:0002254 True craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0031332 MONDO:0100326 True Glanzmann thrombasthenia 1 Glanzmann thrombasthenia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0031421 MONDO:0019272 True Olmsted syndrome hereditary palmoplantar keratoderma UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -17672,7 +17637,6 @@ MONDO:0033862 MONDO:0019787 True primary autoimmune enteropathy autoimmune enter MONDO:0033946 MONDO:0019623 True hereditary angioedema with C1Inh deficiency hereditary angioedema UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0033946 MONDO:0027749 True hereditary angioedema with C1Inh deficiency serpinopathy UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0033948 MONDO:0019624 True acquired angioedema with C1Inh deficiency acquired angioedema UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0033954 MONDO:0005570 True monoclonal mast cell activation syndrome hematologic disorder UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0033968 MONDO:0003778 True immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections-lymphopenia syndrome inborn error of immunity UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0033969 MONDO:0003778 True inflammatory bowel disease-recurrent sinopulmonary infections syndrome inborn error of immunity UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0033980 MONDO:0003266 True RELA fusion-positive ependymoma ependymal tumor UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -18179,6 +18143,7 @@ MONDO:0060455 MONDO:0003689 True X-linked congenital hemolytic anemia familial h MONDO:0060486 MONDO:0015168 True arthrogryposis multiplex congenita 1, neurogenic, with myelin defect arthrogryposis multiplex congenita UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0060489 MONDO:0100249 True 46,XX sex reversal 4 46,XX testicular disorder of sex development UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0060502 MONDO:0015159 True neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies multiple congenital anomalies/dysmorphic syndrome-intellectual disability UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0060533 MONDO:0003847 True microcephaly, short stature, and limb abnormalities hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0060549 MONDO:0003847 True congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0060554 MONDO:0020831 True vertebral, cardiac, renal, and limb defects syndrome 1 congenital vertebral-cardiac-renal anomalies syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0060555 MONDO:0020831 True vertebral, cardiac, renal, and limb defects syndrome 2 congenital vertebral-cardiac-renal anomalies syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING @@ -18549,6 +18514,7 @@ MONDO:0859006 MONDO:0018234 True proximal femoral focal deficiency dysostosis UN MONDO:0859007 MONDO:0019289 True mosaic Legius syndrome hyperpigmentation of the skin UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0859008 MONDO:0015356 True neurofibromatosis/schwannomatosis hereditary neoplastic syndrome UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0859086 MONDO:0019181 True intellectual developmental disorder, X-linked 110 non-syndromic X-linked intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING +MONDO:0859139 MONDO:0003847 True blepharophimosis-impaired intellectual development syndrome hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0859160 MONDO:0033885 True mitochondrial complex IV deficiency, nuclear type 22 mitochondrial complex IV deficiency, nuclear-type UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0859171 MONDO:0003847 True Luo-Schoch-Yamamoto syndrome hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0859175 MONDO:0019005 True nephronophthisis-like nephropathy 2 nephronophthisis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING @@ -18705,7 +18671,7 @@ MONDO:0957228 MONDO:0100172 True intellectual developmental disorder, autosomal MONDO:0957229 MONDO:0021094 True hatipoglu immunodeficiency syndrome immunodeficiency disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0957230 MONDO:0014769 True oocyte/zygote/embryo maturation arrest 18 inherited oocyte maturation defect UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0957231 MONDO:0014769 True oocyte/zygote/embryo maturation arrest 19 inherited oocyte maturation defect UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING -MONDO:0957240 MONDO:0015993 True cone-rod dystrophy 24 cone-rod dystrophy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING +MONDO:0957240 MONDO:0015993 True cone-rod dystrophy 24 cone-rod dystrophy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0957247 MONDO:0019952 True congenital myopathy 22A, classic congenital myopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0957248 MONDO:0100062 True developmental and epileptic encephalopathy 31B developmental and epileptic encephalopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0957249 MONDO:0004983 True spermatogenic failure 82 spermatogenic failure UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING @@ -18894,8 +18860,8 @@ MONDO:0958230 MONDO:0015375 True orofaciodigital syndrome 20 orofaciodigital syn MONDO:0958232 MONDO:0019587 True hearing loss, autosomal dominant 90 autosomal dominant nonsyndromic hearing loss UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0958233 MONDO:0008029 True Bethlem myopathy 1B Bethlem myopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0958234 MONDO:0008029 True Bethlem myopathy 1C Bethlem myopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING -MONDO:0958235 MONDO:0000355 True Ullrich congenital muscular dystrophy 1B Ullrich congenital muscular dystrophy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING -MONDO:0958236 MONDO:0000355 True Ullrich congenital muscular dystrophy 1C Ullrich congenital muscular dystrophy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING +MONDO:0958235 MONDO:0000355 True Ullrich congenital muscular dystrophy 1B Ullrich congenital muscular dystrophy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED +MONDO:0958236 MONDO:0000355 True Ullrich congenital muscular dystrophy 1C Ullrich congenital muscular dystrophy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED MONDO:0958239 MONDO:0000170 True microphthalmia/coloboma 11 microphthalmia, isolated, with coloboma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0958241 MONDO:0024573 True cardiomyopathy, familial hypertrophic, 30, atrial familial hypertrophic cardiomyopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0958242 MONDO:0004983 True spermatogenic failure 90 spermatogenic failure UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING @@ -18907,6 +18873,15 @@ MONDO:0958270 MONDO:0019165 True central precocious puberty in male central prec MONDO:0958273 MONDO:0958091 True cleft palate-congenital heart defect-intellectual disability syndrome due to MEIS2 mutation cleft palate-congenital heart defect-intellectual disability syndrome UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0958274 MONDO:0958110 True benign atrophic papulosis atrophic papulosis UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0958277 MONDO:0019588 True hearing loss, autosomal recessive 123 hearing loss, autosomal recessive UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING +MONDO:0958295 MONDO:0958159 True BCOR ITD sarcoma sarcoma with BCOR genetic alterations UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED +MONDO:0958296 MONDO:0958159 True BCOR-CCNB3 sarcoma sarcoma with BCOR genetic alterations UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED +MONDO:0958297 MONDO:0958159 True childhood sarcoma with BCOR genetic alterations sarcoma with BCOR genetic alterations UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED +MONDO:0958298 MONDO:0958160 True childhood round cell sarcoma with EWSR1-non-ETS fusion round cell sarcoma with EWSR1-non-ETS fusion UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED +MONDO:0958299 MONDO:0958160 True round cell sarcoma with EWSR1-NFATC2 gene fusion round cell sarcoma with EWSR1-non-ETS fusion UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED +MONDO:0958300 MONDO:0958160 True round cell sarcoma with EWSR1-PATZ1 gene fusion round cell sarcoma with EWSR1-non-ETS fusion UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED +MONDO:0958301 MONDO:0958160 True round cell sarcoma with FUS-NFATC2 gene fusion round cell sarcoma with EWSR1-non-ETS fusion UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED +MONDO:0958302 MONDO:0017886 True TFEB-rearranged renal cell carcinoma MIT family translocation renal cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED +MONDO:0958303 MONDO:0017886 True childhood renal cell carcinoma with MiT translocations MIT family translocation renal cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED MONDO:0958322 MONDO:0020119 True intellectual developmental disorder, x-linked, syndromic 37 X-linked syndromic intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0958324 MONDO:0018214 True generalized epilepsy with febrile seizures plus, type 12 generalized epilepsy with febrile seizures plus UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0958325 MONDO:0100241 True thrombocytopenia 12 with or without myopathy inherited thrombocytopenia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING @@ -18926,9 +18901,19 @@ MONDO:0958354 MONDO:0019165 True genetic central precocious puberty in female ce MONDO:0958355 MONDO:0019165 True secondary central precocious puberty in female central precocious puberty UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0958356 MONDO:0958270 True primary central precocious puberty in male central precocious puberty in male UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0958357 MONDO:0958270 True secondary central precocious puberty in male central precocious puberty in male UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0968944 MONDO:0019502 True intellectual developmental disorder, autosomal recessive 82 autosomal recessive non-syndromic intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING +MONDO:0968944 MONDO:0019502 True intellectual developmental disorder, autosomal recessive 82 autosomal recessive non-syndromic intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED SUPPORTED +MONDO:0968946 MONDO:0100062 True developmental and epileptic encephalopathy 115 developmental and epileptic encephalopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:0968955 MONDO:0019507 True hypocalcified amelogenesis imperfecta amelogenesis imperfecta UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0968959 MONDO:0020022 True isolated arhinencephaly central nervous system malformation UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0968974 MONDO:0004095 True large B-cell lymphoma B-cell neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED +MONDO:0968980 MONDO:0005349 True otosclerosis 12 otosclerosis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING +MONDO:0968981 MONDO:0019588 True autosomal recessive nonsyndromic hearing loss 124 hearing loss, autosomal recessive UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING +MONDO:0968983 MONDO:0009726 True proteasome-associated autoinflammatory syndrome 6 proteosome-associated autoinflammatory syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING +MONDO:0968986 MONDO:0958350 True chaotic conus spinal cord lipoma conus spinal cord lipoma UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0968987 MONDO:0958350 True extramedullary conus spinal cord lipoma conus spinal cord lipoma UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0968988 MONDO:0017069 True saccular spinal dysraphism with a stalk to the dome spina bifida cystica UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0968988 MONDO:0958345 True saccular spinal dysraphism with a stalk to the dome limited dorsal myeloschisis UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0968989 MONDO:0958345 True non-saccular limited dorsal myeloschisis limited dorsal myeloschisis UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:8000006 MONDO:0015134 True WHIM syndrome 1 constitutional neutropenia UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:8000006 MONDO:0023880 True WHIM syndrome 1 WHIM syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING MONDO:8000008 MONDO:0015159 True Martsolf syndrome 1 multiple congenital anomalies/dysmorphic syndrome-intellectual disability UNSUPPORTED-MISSING SUPPORTED UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -18962,7 +18947,7 @@ MONDO:0000045 MONDO:0018612 False hypothyroidism, congenital, nongoitrous congen MONDO:0000050 MONDO:0013099 False isolated congenital growth hormone deficiency combined pituitary hormone deficiencies, genetic form UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING MONDO:0000062 MONDO:0003847 False isolated microphthalmia hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0000065 MONDO:0020573 False microvascular complications of diabetes, susceptibility inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0000070 MONDO:0015979 False Mycobacterium tuberculosis, susceptibility hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0000070 MONDO:0020573 False Mycobacterium tuberculosis, susceptibility inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0000078 MONDO:0019796 False acrocephalopolysyndactyly acrocephalosyndactyly UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0000079 MONDO:0005298 False nephrolithiasis/osteoporosis, hypophosphatemic osteoporosis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-SUBCLASS MONDO:0000082 MONDO:0005039 False pelvic organ prolapse reproductive system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -18973,7 +18958,7 @@ MONDO:0000090 MONDO:0005181 False progressive external ophthalmoplegia with mito MONDO:0000104 MONDO:0000387 False anemia, hypochromic microcytic with iron overload hypochromic microcytic anemia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0000104 MONDO:0003847 False anemia, hypochromic microcytic with iron overload hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0000107 MONDO:0007500 False auriculocondylar syndrome ear malformation UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING -MONDO:0000108 MONDO:0015979 False bacteremia, susceptibility hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0000108 MONDO:0020573 False bacteremia, susceptibility inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0000110 MONDO:0024623 False bifid nose otorhinolaryngologic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0000115 MONDO:0003847 False Chiari malformation hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0000118 MONDO:0019288 False reticulate pigment disorder skin pigmentation disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -19690,6 +19675,7 @@ MONDO:0001881 MONDO:0002254 False toxic shock syndrome syndromic disease UNSUPPO MONDO:0001887 MONDO:0045043 False Allen-Masters syndrome disorder of uterine broad ligament UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0001888 MONDO:0002166 False anus lymphoma rectum lymphoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0001890 MONDO:0003394 False pulp erosion dental pulp disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS +MONDO:0001893 MONDO:0016747 False spinal cord melanoma primary melanoma of the central nervous system UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0001895 MONDO:0020683 False acute retrobulbar neuritis acute disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0001895 MONDO:0024335 False acute retrobulbar neuritis retrobulbar neuritis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0001898 MONDO:0005552 False optic choroid disorder ocular vascular disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -19751,6 +19737,7 @@ MONDO:0002083 MONDO:0021058 False Richter syndrome neoplastic syndrome UNSUPPORT MONDO:0002083 MONDO:0024882 False Richter syndrome secondary neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0002089 MONDO:0020672 False retinal vascular occlusion vascular occlusion disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0002102 MONDO:0021166 False cheilitis inflammatory disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0002109 MONDO:0002149 False pituitary cancer reproductive system cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0002109 MONDO:0003766 False pituitary cancer thalamic cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0002112 MONDO:0002373 False benign peritoneal mesothelioma benign mesothelioma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0002118 MONDO:0700096 False urinary system disorder human disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -20057,6 +20044,7 @@ MONDO:0003154 MONDO:0003241 False hemangioma of peripheral nerve central nervous MONDO:0003155 MONDO:0002334 False cavernous hemangioma hematopoietic and lymphoid system neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003159 MONDO:0005385 False vascular hemostatic disease vascular disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003168 MONDO:0000638 False cerebellar pilocytic astrocytoma benign glioma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0003168 MONDO:0021499 False cerebellar pilocytic astrocytoma benign neoplasm of cerebellum UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0003169 MONDO:0005499 False diencephalic astrocytomas brain glioma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003171 MONDO:0003169 False pineal gland astrocytoma diencephalic astrocytomas UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003177 MONDO:0005082 False prostate adenoid cystic carcinoma prostate adenocarcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS @@ -20074,6 +20062,7 @@ MONDO:0003199 MONDO:0044937 False anal carcinoma rectal carcinoma UNSUPPORTED-MI MONDO:0003205 MONDO:0005086 False renal pelvis adenocarcinoma renal cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003208 MONDO:0004953 False breast secretory carcinoma invasive ductal breast carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003210 MONDO:0001487 False intrahepatic cholangiocarcinoma intrahepatic bile duct cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS +MONDO:0003222 MONDO:0021143 False central nervous system melanocytic neoplasm melanocytic neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0003223 MONDO:0021322 False meninges hemangiopericytoma malignant tumor of meninges UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0003225 MONDO:0005046 False bone marrow disorder immune system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003225 MONDO:0005172 False bone marrow disorder skeletal system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -20125,6 +20114,7 @@ MONDO:0003350 MONDO:0003349 False granular cell leiomyosarcoma central nervous s MONDO:0003358 MONDO:0003379 False anus leiomyosarcoma rectum leiomyosarcoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003362 MONDO:0005058 False cutaneous leiomyosarcoma leiomyosarcoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003377 MONDO:0003378 False extrahepatic bile duct leiomyosarcoma liver leiomyosarcoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS +MONDO:0003381 MONDO:0005039 False pituitary gland disorder reproductive system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003381 MONDO:0005560 False pituitary gland disorder brain disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003382 MONDO:0000462 False eyelid disorder eye adnexa disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0003382 MONDO:0005328 False eyelid disorder eye disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS @@ -20142,6 +20132,9 @@ MONDO:0003411 MONDO:0021100 False breast hemangiopericytoma breast neoplasm UNSU MONDO:0003412 MONDO:0024645 False retroperitoneal hemangiopericytoma retroperitoneal neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0003420 MONDO:0002369 False bile duct cystadenoma cystadenoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003420 MONDO:0006108 False bile duct cystadenoma bile duct adenoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS +MONDO:0003423 MONDO:0004972 False middle ear adenoma adenoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS +MONDO:0003423 MONDO:0021482 False middle ear adenoma benign neoplasm of middle ear UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0003423 MONDO:0036976 False middle ear adenoma benign epithelial neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0003425 MONDO:0006496 False ophthalmoplegia palsy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0003429 MONDO:0003604 False functioning pituitary gland adenoma functioning pituitary gland neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003430 MONDO:0017611 False prolactin producing pituitary tumor pituitary tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -20209,8 +20202,6 @@ MONDO:0003619 MONDO:0000922 False salpingitis pelvic inflammatory disease UNSUPP MONDO:0003624 MONDO:0004953 False acinic cell breast carcinoma invasive ductal breast carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003626 MONDO:0003631 False uterine ligament serous adenocarcinoma cervical serous adenocarcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003627 MONDO:0005554 False rheumatic pulmonary valve disease rheumatic disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS -MONDO:0003629 MONDO:0005213 False uterine corpus serous adenocarcinoma uterine carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0003629 MONDO:0005278 False uterine corpus serous adenocarcinoma serous adenocarcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003632 MONDO:0021166 False endocervicitis inflammatory disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0003638 MONDO:0021322 False lung meningioma malignant tumor of meninges UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0003640 MONDO:0005236 False verruciform xanthoma of skin xanthoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -20239,6 +20230,7 @@ MONDO:0003746 MONDO:0004188 False ciliary body spindle cell melanoma iris spindl MONDO:0003749 MONDO:0044991 False esophageal disorder upper digestive tract disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0003754 MONDO:0002254 False Brown-Sequard syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003757 MONDO:0006496 False paraplegia palsy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0003761 MONDO:0016747 False leptomeningeal melanoma primary melanoma of the central nervous system UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0003763 MONDO:0020683 False acute stress disorder acute disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0003764 MONDO:0003057 False pediatric leptomeningeal melanoma pediatric meningioma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0003764 MONDO:0042494 False pediatric leptomeningeal melanoma childhood malignant melanoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -20348,6 +20340,8 @@ MONDO:0004207 MONDO:0040676 False pulmonary artery leiomyosarcoma great vessel c MONDO:0004208 MONDO:0003032 False superior vena cava leiomyosarcoma superior vena cava angiosarcoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0004215 MONDO:0024295 False cutaneous anthrax skin disease caused by bacterial infection UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0004221 MONDO:0004526 False uterine corpus perivascular epithelioid cell tumor mixed endometrial stromal and smooth muscle tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS +MONDO:0004223 MONDO:0005079 False polyp of middle ear polyp UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0004223 MONDO:0021366 False polyp of middle ear neoplasm of middle ear UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0004225 MONDO:0004960 False monoclonal gammopathy of uncertain significance monoclonal gammopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0004226 MONDO:0021098 False diffuse intraductal papillomatosis papillomatosis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0004227 MONDO:0002373 False epididymal adenomatoid tumor benign mesothelioma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS @@ -20420,11 +20414,12 @@ MONDO:0004496 MONDO:0024636 False myocarditis inflammation of heart layer UNSUPP MONDO:0004496 MONDO:0024643 False myocarditis myocardial disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0004504 MONDO:0001325 False penile urethral cancer penile cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0004510 MONDO:0005103 False inflammatory liposarcoma well-differentiated liposarcoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0004512 MONDO:0004141 False meningeal melanomatosis melanomatosis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS +MONDO:0004512 MONDO:0016747 False meningeal melanomatosis primary melanoma of the central nervous system UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0004512 MONDO:0021322 False meningeal melanomatosis malignant tumor of meninges UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0004517 MONDO:0005247 False ureter tuberculosis bacterial urinary tract infection UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0004522 MONDO:0043786 False peritonitis serositis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0004525 MONDO:0021201 False scabies skin infection UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0004527 MONDO:0002320 False congenital granular cell tumor congenital nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS -MONDO:0004527 MONDO:0006235 False congenital granular cell tumor granular cell tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0004528 MONDO:0024339 False lymph node palisaded myofibroblastoma lymph node neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0004531 MONDO:0003725 False sclerosing adenosis of breast breast adenosis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0004546 MONDO:0001829 False lumbar plexus neoplasm lumbosacral plexus lesion UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS @@ -20597,7 +20592,7 @@ MONDO:0004934 MONDO:0021166 False periostitis inflammatory disease UNSUPPORTED-M MONDO:0004940 MONDO:0020683 False acute female pelvic peritonitis acute disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0004947 MONDO:0015759 False B-cell acute lymphoblastic leukemia B-cell non-Hodgkin lymphoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0004948 MONDO:0004967 False B-cell chronic lymphocytic leukemia acute lymphoblastic leukemia UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS -MONDO:0004951 MONDO:0015979 False susceptibility to HIV infection hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0004951 MONDO:0020573 False susceptibility to HIV infection inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0004957 MONDO:0020596 False mucinous adenocarcinoma mucin-producing carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0004960 MONDO:0005570 False monoclonal gammopathy hematologic disorder UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0004963 MONDO:0005525 False T-cell acute lymphoblastic leukemia T-cell leukemia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -20672,6 +20667,7 @@ MONDO:0005098 MONDO:0011057 False stroke disorder cerebrovascular disorder UNSUP MONDO:0005099 MONDO:0005560 False subarachnoid hemorrhage brain disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005099 MONDO:0043218 False subarachnoid hemorrhage neurovascular disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005100 MONDO:0005093 False systemic sclerosis skin disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS +MONDO:0005104 MONDO:0005089 False aJCC grade 1 sarcoma sarcoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005109 MONDO:0021682 False HIV infectious disease viral sexually transmitted disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005109 MONDO:0022034 False HIV infectious disease lentivirus infection UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005110 MONDO:0004994 False idiopathic cardiomyopathy cardiomyopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -20827,6 +20823,7 @@ MONDO:0005364 MONDO:0005397 False Graves disease goiter UNSUPPORTED-MISSING UNSU MONDO:0005364 MONDO:0005623 False Graves disease autoimmune thyroid disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005365 MONDO:0021945 False hearing loss disorder hearing disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005366 MONDO:0005344 False chronic hepatitis B virus infection hepatitis B virus infection UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0005369 MONDO:0019496 False carcinoid tumor neuroendocrine neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005371 MONDO:0005084 False mood disorder mental disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005372 MONDO:0005047 False male infertility infertility disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0005373 MONDO:0005113 False meningococcal infection bacterial infectious disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -20971,8 +20968,6 @@ MONDO:0005634 MONDO:0001214 False acute hemorrhagic conjunctivitis acute conjunc MONDO:0005634 MONDO:0043541 False acute hemorrhagic conjunctivitis viral conjunctivitis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005638 MONDO:0024417 False agnosia perceptual disorders UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005639 MONDO:0005109 False AIDS related complex HIV infectious disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0005641 MONDO:0025371 False aleutian mink disease Parvoviridae infectious disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0005641 MONDO:0100329 False aleutian mink disease primary viral infectious disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005642 MONDO:0005551 False atopic conjunctivitis eye allergy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005643 MONDO:0005985 False Alphavirus infectious disease Togaviridae infectious disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005645 MONDO:0005943 False ancylostomiasis Rhabditida infectious disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -21002,9 +20997,6 @@ MONDO:0005671 MONDO:0005644 False Blastocystis infectious disease amebiasis UNSU MONDO:0005671 MONDO:0024270 False Blastocystis infectious disease parasitic intestinal disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005673 MONDO:0020598 False blind loop syndrome malabsorption syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005675 MONDO:0024985 False border disease sheep disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0005676 MONDO:0005156 False borna disease encephalomyelitis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS -MONDO:0005676 MONDO:0005856 False borna disease Mononegavirales infectious disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0005676 MONDO:0024318 False borna disease viral infection of central nervous system UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005678 MONDO:0024913 False bovine respiratory disease complex cattle disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005678 MONDO:0700104 False bovine respiratory disease complex respiratory system disorder, non-human animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0005679 MONDO:0024913 False bovine virus diarrhea-mucosal disease cattle disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -21285,7 +21277,7 @@ MONDO:0006011 MONDO:0100329 False viral hepatitis primary viral infectious disea MONDO:0006012 MONDO:0024352 False viral pneumonia viral respiratory tract infection UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006012 MONDO:0100329 False viral pneumonia primary viral infectious disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006013 MONDO:0024985 False visna disease sheep disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0006013 MONDO:0700049 False visna disease infectious disease, non-human animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0006013 MONDO:0700053 False visna disease viral infectious disease, non-human animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006014 MONDO:0000879 False vulvovaginal candidiasis cutaneous candidiasis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0006014 MONDO:0007019 False vulvovaginal candidiasis vulvovaginitis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0006014 MONDO:0023557 False vulvovaginal candidiasis infective vaginitis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -21302,6 +21294,7 @@ MONDO:0006038 MONDO:0005292 False indeterminate colitis colitis UNSUPPORTED-MISS MONDO:0006039 MONDO:0005292 False infectious colitis colitis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006039 MONDO:0043424 False infectious colitis digestive system infectious disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006040 MONDO:0005066 False lactic acidosis metabolic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0006041 MONDO:0005369 False lung carcinoid tumor carcinoid tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006042 MONDO:0000271 False meningeal tuberculosis tuberculous salpingitis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006042 MONDO:0005696 False meningeal tuberculosis central nervous system tuberculosis UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006042 MONDO:0006670 False meningeal tuberculosis bacterial meningitis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -21330,6 +21323,7 @@ MONDO:0006090 MONDO:0056798 False appendix hyperplastic polyp disorder of append MONDO:0006091 MONDO:0006126 False appendix neuroendocrine tumor G1 cecum neuroendocrine tumor G1 UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006092 MONDO:0000525 False appendix villous adenoma cecum villous adenoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006094 MONDO:0003274 False Askin tumor thoracic cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS +MONDO:0006095 MONDO:0005369 False atypical carcinoid tumor carcinoid tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006096 MONDO:0000931 False atypical endometrial hyperplasia endometrial disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006096 MONDO:0005043 False atypical endometrial hyperplasia hyperplasia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006098 MONDO:0000653 False atypical lobular breast hyperplasia integumentary system cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -21376,6 +21370,7 @@ MONDO:0006173 MONDO:0010150 False conjunctival squamous cell carcinoma head and MONDO:0006188 MONDO:0004805 False EBV-positive T-cell lymphoproliferative disorder of childhood leukocyte disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006193 MONDO:0005043 False endometrial hyperplasia without atypia hyperplasia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006195 MONDO:0000931 False endometrial polyp endometrial disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0006196 MONDO:0005213 False endometrial serous adenocarcinoma uterine carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006202 MONDO:0003549 False extrahepatic bile duct adenosquamous carcinoma adenosquamous bile duct carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006202 MONDO:0006203 False extrahepatic bile duct adenosquamous carcinoma extrahepatic bile duct squamous cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006203 MONDO:0003500 False extrahepatic bile duct squamous cell carcinoma squamous cell bile duct carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -21390,6 +21385,7 @@ MONDO:0006225 MONDO:0000621 False gastric mantle cell lymphoma immune system can MONDO:0006225 MONDO:0042493 False gastric mantle cell lymphoma gastric non-hodgkin lymphoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006226 MONDO:0005966 False gastric mucosa-associated lymphoid tissue lymphoma spleen cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006226 MONDO:0018502 False gastric mucosa-associated lymphoid tissue lymphoma hereditary gastric cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0006227 MONDO:0005369 False gastric neuroendocrine tumor G1 carcinoid tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006231 MONDO:0006499 False gastrointestinal hamartoma hamartoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006231 MONDO:0021223 False gastrointestinal hamartoma digestive system neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006231 MONDO:0024292 False gastrointestinal hamartoma gastrointestinal polyp UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -21447,6 +21443,7 @@ MONDO:0006366 MONDO:0006224 False Peutz-Jeghers polyp of the stomach gastric ham MONDO:0006366 MONDO:0006365 False Peutz-Jeghers polyp of the stomach Peutz-Jeghers polyp UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006372 MONDO:0002109 False pituicytoma pituitary cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0006372 MONDO:0003169 False pituicytoma diencephalic astrocytomas UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS +MONDO:0006385 MONDO:0010150 False primary intraosseous squamous cell carcinoma head and neck squamous cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006386 MONDO:0003195 False primary peritoneal serous adenocarcinoma peritoneal serous adenocarcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006387 MONDO:0000621 False primary pulmonary diffuse large B-cell lymphoma immune system cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0006388 MONDO:0003430 False prolactin-producing pituitary gland carcinoma prolactin producing pituitary tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -22393,7 +22390,6 @@ MONDO:0007841 MONDO:0018230 False coxopodopatellar syndrome skeletal dysplasia U MONDO:0007842 MONDO:0020066 False joint laxity, familial Ehlers-Danlos syndrome UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING MONDO:0007844 MONDO:0018800 False hypogonadotropic hypogonadism 2 with or without anosmia Kallmann syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0007845 MONDO:0015356 False Kaposi sarcoma, susceptibility to hereditary neoplastic syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0007845 MONDO:0015979 False Kaposi sarcoma, susceptibility to hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0007846 MONDO:0000508 False KBG syndrome syndromic intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0007846 MONDO:0002320 False KBG syndrome congenital nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0007846 MONDO:0100545 False KBG syndrome hereditary neurological disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -22622,7 +22618,7 @@ MONDO:0008103 MONDO:0003847 False noduli Cutanei, multiple, with urinary tract a MONDO:0008105 MONDO:0003847 False nose, anomalous shape of hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0008107 MONDO:0005712 False nystagmus, hereditary vertical congenital nystagmus UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING MONDO:0008108 MONDO:0100545 False oculocerebrocutaneous syndrome hereditary neurological disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0008109 MONDO:0018746 False ocular cicatricial pemphigoid mucous membrane pemphigoid UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0008109 MONDO:0018746 False ocular cicatricial pemphigoid mucous membrane pemphigoid UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0008111 MONDO:0005328 False oculodentodigital dysplasia eye disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0008111 MONDO:0015160 False oculodentodigital dysplasia multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0008113 MONDO:0002254 False Schilbach-Rott syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -23280,6 +23276,7 @@ MONDO:0008899 MONDO:0000111 False camptodactyly syndrome, Guadalajara type 2 cam MONDO:0008900 MONDO:0006025 False camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia autosomal recessive disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0008902 MONDO:0003847 False camptodactyly-ichthyosis syndrome hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0008904 MONDO:0002254 False camptomelic syndrome, long-limb type syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0008905 MONDO:0020573 False predisposition to invasive fungal disease due to CARD9 deficiency inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0008908 MONDO:0100547 False MGAT2-congenital disorder of glycosylation cardiogenetic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0008909 MONDO:0003847 False congenital disorder of glycosylation, type i/IIx hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0008911 MONDO:0010771 False cardiac lipidosis, familial histiocytoid cardiomyopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING @@ -23335,6 +23332,7 @@ MONDO:0008961 MONDO:0012014 False Charcot-Marie-Tooth disease type 4A Charcot-Ma MONDO:0008962 MONDO:0100545 False Griscelli syndrome type 1 hereditary neurological disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0008963 MONDO:0002320 False Chediak-Higashi syndrome congenital nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0008963 MONDO:0015134 False Chediak-Higashi syndrome constitutional neutropenia UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0008963 MONDO:0015541 False Chediak-Higashi syndrome hereditary hemophagocytic lymphohistiocytosis UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING MONDO:0008964 MONDO:0045032 False congenital secretory chloride diarrhea 1 congenital secretory diarrhea UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0008965 MONDO:0015160 False CHARGE syndrome multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0008965 MONDO:0021635 False CHARGE syndrome neurocristopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -23777,7 +23775,7 @@ MONDO:0009497 MONDO:0003847 False Kifafa seizure disorder hereditary disease UNS MONDO:0009498 MONDO:0005516 False lethal Kniest-like dysplasia osteochondrodysplasia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0009499 MONDO:0004884 False Krabbe disease eye degenerative disorder UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0009499 MONDO:0020127 False Krabbe disease hereditary peripheral neuropathy UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0009500 MONDO:0015979 False kuru, susceptibility to hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0009500 MONDO:0020573 False kuru, susceptibility to inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0009501 MONDO:0700223 False metabolic myopathy due to lactate transporter defect hereditary skeletal muscle disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0009504 MONDO:0006040 False mitochondrial DNA depletion syndrome 9 lactic acidosis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0009505 MONDO:0017688 False lactic aciduria due to D-lactic acid disorder of glycolysis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -23790,7 +23788,7 @@ MONDO:0009511 MONDO:0100547 False Larsen-like syndrome, B3GAT3 type cardiogeneti MONDO:0009513 MONDO:0002254 False laryngo-onycho-cutaneous syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0009513 MONDO:0005087 False laryngo-onycho-cutaneous syndrome respiratory system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0009516 MONDO:0003847 False absence deformity of leg-cataract syndrome hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0009518 MONDO:0015979 False leprosy, susceptibility to, 3 hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0009518 MONDO:0020573 False leprosy, susceptibility to, 3 inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0009519 MONDO:0017025 False letterer-Siwe disease Langerhans cell histiocytosis specific to childhood UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0009521 MONDO:0003847 False leukemia, acute myelocytic, with polyposis coli and colon cancer hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0009521 MONDO:0020683 False leukemia, acute myelocytic, with polyposis coli and colon cancer acute disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -23874,7 +23872,7 @@ MONDO:0009615 MONDO:0002012 False methylmalonic acidemia due to methylmalonyl-Co MONDO:0009616 MONDO:0002254 False microcephalic primordial dwarfism, Toriello type syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0009616 MONDO:0800063 False microcephalic primordial dwarfism, Toriello type primordial dwarfism and slender bone disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0009617 MONDO:0100200 False microcephaly 1, primary, autosomal recessive microcephaly with intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0009619 MONDO:0003847 False microcephaly-micromelia syndrome hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0009619 MONDO:0003847 False microcephaly-micromelia syndrome hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0009620 MONDO:0002254 False Say-Barber-Miller syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0009622 MONDO:0003847 False Jawad syndrome hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0009623 MONDO:0015327 False Nijmegen breakage syndrome developmental anomaly of metabolic origin UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -24059,7 +24057,6 @@ MONDO:0009845 MONDO:0019713 False pelviscapular dysplasia non-syndromic limb red MONDO:0009846 MONDO:0019231 False pentosuria inborn disorder of pentose phosphate metabolism UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0009847 MONDO:0001370 False pericardial effusion, chronic pericardial effusion UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0009847 MONDO:0100547 False pericardial effusion, chronic cardiogenetic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0009849 MONDO:0005046 False hyperimmunoglobulinemia D with periodic fever immune system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0009850 MONDO:0003847 False periodontitis, chronic, adult hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0009850 MONDO:0005593 False periodontitis, chronic, adult chronic periodontitis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0009851 MONDO:0003847 False peripheral neuropathy, ataxia, focal necrotizing encephalopathy, and spongy degeneration of brain hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -24799,7 +24796,7 @@ MONDO:0010843 MONDO:0020573 False dyslexia, susceptibility to, 2 inherited disea MONDO:0010850 MONDO:0015824 False Tessier number 4 facial cleft oculomaxillofacial dysostosis UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0010851 MONDO:0005328 False Lowry-MacLean syndrome eye disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0010852 MONDO:0016907 False chromosome 8Q12.1-q21.2 deletion syndrome partial deletion of the long arm of chromosome 8 UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0010853 MONDO:0015979 False Helicobacter pylori infection, susceptibility to hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0010853 MONDO:0020573 False Helicobacter pylori infection, susceptibility to inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0010857 MONDO:0015059 False semantic dementia progressive non-fluent aphasia UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0010857 MONDO:0017160 False semantic dementia behavioral variant of frontotemporal dementia UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0010858 MONDO:0002320 False macrocephaly-spastic paraplegia-dysmorphism syndrome congenital nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -24942,8 +24939,8 @@ MONDO:0011047 MONDO:0003847 False deafness-epiphyseal dysplasia-short stature sy MONDO:0011050 MONDO:0005267 False microcephaly-cardiac defect-lung malsegmentation syndrome heart disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0011052 MONDO:0002254 False amelia cleft lip palate hydrocephalus iris coloboma syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0011052 MONDO:0003847 False amelia cleft lip palate hydrocephalus iris coloboma hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0011053 MONDO:0000508 False intellectual disability-sparse hair-brachydactyly syndrome syndromic intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0011053 MONDO:0002320 False intellectual disability-sparse hair-brachydactyly syndrome congenital nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0011053 MONDO:0000508 False intellectual disability-sparse hair-brachydactyly syndrome syndromic intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS +MONDO:0011053 MONDO:0002320 False intellectual disability-sparse hair-brachydactyly syndrome congenital nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0011053 MONDO:0100545 False intellectual disability-sparse hair-brachydactyly syndrome hereditary neurological disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0011053 MONDO:0700120 False intellectual disability-sparse hair-brachydactyly syndrome BAFopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0011054 MONDO:0006025 False autosomal recessive amelia autosomal recessive disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -25170,7 +25167,7 @@ MONDO:0011370 MONDO:0019353 False Stargardt disease 4 Stargardt disease UNSUPPOR MONDO:0011371 MONDO:0018024 False hydroa vacciniforme, familial hydroa vacciniforme UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0011371 MONDO:0100118 False hydroa vacciniforme, familial hereditary skin disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0011372 MONDO:0016660 False microcephaly with simplified gyral pattern autosomal recessive primary microcephaly UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING -MONDO:0011373 MONDO:0015979 False urinary tract infections, recurrent, susceptibility to hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0011373 MONDO:0020573 False urinary tract infections, recurrent, susceptibility to inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0011374 MONDO:0037748 False hypercholesterolemia, familial, 4 hyperlipoproteinemia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0011375 MONDO:0019019 False brittle bone disorder osteogenesis imperfecta UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING MONDO:0011376 MONDO:0100234 False ventricular fibrillation, paroxysmal familial, type 1 paroxysmal familial ventricular fibrillation UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -25204,7 +25201,7 @@ MONDO:0011422 MONDO:0006025 False autosomal recessive proximal renal tubular aci MONDO:0011422 MONDO:0019052 False autosomal recessive proximal renal tubular acidosis inborn errors of metabolism UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0011424 MONDO:0021058 False Carney triad neoplastic syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0011426 MONDO:0004884 False aceruloplasminemia eye degenerative disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS -MONDO:0011427 MONDO:0015979 False Ascaris lumbricoides infection, susceptibility to hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0011427 MONDO:0020573 False Ascaris lumbricoides infection, susceptibility to inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0011429 MONDO:0005554 False juvenile idiopathic arthritis rheumatic disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0011429 MONDO:0700007 False juvenile idiopathic arthritis idiopathic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0011431 MONDO:0016663 False MASS syndrome overlapping connective tissue disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -25485,6 +25482,7 @@ MONDO:0011869 MONDO:0015550 False epidermolysis bullosa simplex superficialis su MONDO:0011870 MONDO:0020702 False annular epidermolytic ichthyosis autosomal dominant epidermolytic ichthyosis UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0011871 MONDO:0006025 False Niemann-Pick disease type B autosomal recessive disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0011871 MONDO:0100464 False Niemann-Pick disease type B acid sphingomyelinase deficiency UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0011872 MONDO:0015541 False Griscelli syndrome type 2 hereditary hemophagocytic lymphohistiocytosis UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING MONDO:0011873 MONDO:0018982 False Niemann-Pick disease, type C2 Niemann-Pick disease type C UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0011874 MONDO:0002254 False neonatal ichthyosis-sclerosing cholangitis syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0011879 MONDO:0015355 False neuronopathy, distal hereditary motor, type 7B distal hereditary motor neuropathy type 7 UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS @@ -25561,6 +25559,7 @@ MONDO:0011989 MONDO:0100120 False leishmaniasis vector-borne disease UNSUPPORTED MONDO:0011993 MONDO:0003847 False aspirin resistance hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0011995 MONDO:0021147 False cataract - congenital heart disease - neural tube defect syndrome disorder of development or morphogenesis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0011996 MONDO:0023603 False chronic myelogenous leukemia, BCR-ABL1 positive hereditary disorder of connective tissue UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0011997 MONDO:0015541 False Hermansky-Pudlak syndrome 2 hereditary hemophagocytic lymphohistiocytosis UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING MONDO:0011998 MONDO:0015358 False autosomal dominant slowed nerve conduction velocity hereditary motor and sensory neuropathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012000 MONDO:0100545 False specific phobia hereditary neurological disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012001 MONDO:0003847 False mandibulofacial dysostosis with ptosis, autosomal dominant hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -25592,7 +25591,7 @@ MONDO:0012048 MONDO:0100545 False endogenous depression hereditary neurological MONDO:0012050 MONDO:0020573 False major depressive disorder 1 inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012051 MONDO:0005593 False periodontitis, aggressive, 2 chronic periodontitis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012056 MONDO:0800101 False Leber congenital amaurosis 9 NMNAT1-related retinopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0012057 MONDO:0015979 False legionnaire disease, susceptibility to hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0012057 MONDO:0020573 False legionnaire disease, susceptibility to inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012058 MONDO:0020573 False myocardial infarction, susceptibility to, 2 inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012059 MONDO:0019673 False polydactyly, postaxial, type A4 postaxial polydactyly type A UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012061 MONDO:0001823 False familial sick sinus syndrome sick sinus syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -25660,7 +25659,7 @@ MONDO:0012155 MONDO:0018751 False choanal atresia hereditary otorhinolaryngologi MONDO:0012156 MONDO:0011088 False myasthenic syndrome, congenital, 1B, fast-channel congenital myasthenic syndrome 1A UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-SUBCLASS MONDO:0012157 MONDO:0020344 False congenital myasthenic syndrome 4C postsynaptic congenital myasthenic syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012159 MONDO:0015356 False lung cancer susceptibility 1 hereditary neoplastic syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0012161 MONDO:0015979 False susceptibility to respiratory infections associated with CD8alpha chain mutation hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0012161 MONDO:0020573 False susceptibility to respiratory infections associated with CD8alpha chain mutation inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012163 MONDO:0044200 False immunodeficiency 104 T-B+ severe combined immunodeficiency UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012164 MONDO:0002254 False Meacham syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012164 MONDO:0003847 False Meacham syndrome hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -25736,7 +25735,7 @@ MONDO:0012288 MONDO:0003847 False iridogoniodysgenesis and skeletal anomalies he MONDO:0012289 MONDO:0002320 False myofibrillar myopathy 5 congenital nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0012289 MONDO:0100545 False myofibrillar myopathy 5 hereditary neurological disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012291 MONDO:0001341 False immunoglobulin A deficiency 2 selective IgA deficiency disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0012292 MONDO:0015979 False hepatitis C virus, susceptibility to hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0012292 MONDO:0020573 False hepatitis C virus, susceptibility to inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012295 MONDO:0000015 False complement component 5 deficiency classic complement early component deficiency UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012295 MONDO:0015700 False complement component 5 deficiency immunodeficiency due to a late component of complement deficiency UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012296 MONDO:0018075 False lipomyelomeningocele neural tube defect UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -25767,9 +25766,9 @@ MONDO:0012349 MONDO:0010180 False spondylocostal dysostosis 3, autosomal recessi MONDO:0012350 MONDO:0005334 False complement factor H deficiency hereditary nephritis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012350 MONDO:0018013 False complement factor H deficiency non-immunoglobulin-mediated membranoproliferative glomerulonephritis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012352 MONDO:0003847 False vasculitis, lymphocytic, cutaneous small vessel hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0012358 MONDO:0015979 False leprosy, susceptibility to, 1 hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0012358 MONDO:0020573 False leprosy, susceptibility to, 1 inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012359 MONDO:0017855 False combined immunodeficiency due to partial RAG1 deficiency T-B- severe combined immunodeficiency UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0012360 MONDO:0019995 False congenital nongoitrous hypothryoidism 3 peripheral resistance to thyroid hormones UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0012360 MONDO:0019995 False congenital nongoitrous hypothyroidism 3 peripheral resistance to thyroid hormones UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012361 MONDO:0020573 False systemic lupus erythematosus, susceptibility to, 5 inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012367 MONDO:0700233 False retinitis pigmentosa 31 TOPORS-related retinopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012368 MONDO:0004736 False aminoacylase 1 deficiency inborn disorder of amino acid metabolism UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -25842,7 +25841,7 @@ MONDO:0012476 MONDO:0700055 False hereditary spastic paraplegia 30 KIF1A related MONDO:0012477 MONDO:0800098 False retinitis pigmentosa 33 SNRNP200-related dominant retinopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012480 MONDO:0020525 False diabetes mellitus, transient neonatal, 2 transient neonatal diabetes mellitus UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012481 MONDO:0005328 False mevalonic aciduria eye disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS -MONDO:0012482 MONDO:0015979 False West Nile virus, susceptibility to hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0012482 MONDO:0020573 False West Nile virus, susceptibility to inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012484 MONDO:0003227 False prosopagnosia, hereditary prosopagnosia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012484 MONDO:0100545 False prosopagnosia, hereditary hereditary neurological disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012486 MONDO:0003847 False preauricular tag, isolated, autosomal dominant, 1 hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -25854,7 +25853,7 @@ MONDO:0012494 MONDO:0003847 False testicular microlithiasis hereditary disease U MONDO:0012496 MONDO:0003847 False Koolen-de Vries syndrome hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012497 MONDO:0002320 False congenital stationary night blindness autosomal dominant 3 congenital nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0012498 MONDO:0002320 False congenital stationary night blindness autosomal dominant 1 congenital nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS -MONDO:0012499 MONDO:0015979 False Buruli ulcer, susceptibility to hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0012499 MONDO:0020573 False Buruli ulcer, susceptibility to inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012500 MONDO:0700256 False chilblain lupus 1 TREX1-related type 1 interferonopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012502 MONDO:0019052 False normophosphatemic familial tumoral calcinosis inborn errors of metabolism UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0012507 MONDO:0015993 False retinal cone dystrophy 4 cone-rod dystrophy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-SUBCLASS @@ -25920,7 +25919,7 @@ MONDO:0012593 MONDO:0002254 False brain-lung-thyroid syndrome syndromic disease MONDO:0012593 MONDO:0005151 False brain-lung-thyroid syndrome endocrine system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012593 MONDO:0005395 False brain-lung-thyroid syndrome movement disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012593 MONDO:0100545 False brain-lung-thyroid syndrome hereditary neurological disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0012595 MONDO:0015979 False leprosy, susceptibility to, 4 hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0012595 MONDO:0020573 False leprosy, susceptibility to, 4 inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012597 MONDO:0023122 False prostate cancer, hereditary, 9 familial prostate carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING MONDO:0012599 MONDO:0020573 False hypertension, essential, susceptibility to, 8 inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012604 MONDO:0016764 False isolated microphthalmia 3 isolated anophthalmia-microphthalmia syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -25951,8 +25950,8 @@ MONDO:0012650 MONDO:0017855 False Cernunnos-XLF deficiency T-B- severe combined MONDO:0012655 MONDO:0020573 False myoclonic epilepsy, juvenile, susceptibility to, 4 inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012657 MONDO:0003847 False Mungan syndrome hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012658 MONDO:0100521 False brachydactyly type B2 NOG-related symphalangism spectrum disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0012660 MONDO:0015979 False susceptibility to visceral leishmaniasis, 2 hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0012661 MONDO:0015979 False susceptibility to visceral leishmaniasis, 3 hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0012660 MONDO:0020573 False susceptibility to visceral leishmaniasis, 2 inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0012661 MONDO:0020573 False susceptibility to visceral leishmaniasis, 3 inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0012665 MONDO:0011060 False cataract 33 early-onset non-syndromic cataract UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING MONDO:0012666 MONDO:0010940 False asthma-related traits, susceptibility to, 6 inherited susceptibility to asthma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING MONDO:0012668 MONDO:0003847 False Tented eyebrows hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -26267,7 +26266,7 @@ MONDO:0013180 MONDO:0010940 False asthma-related traits, susceptibility to, 8 in MONDO:0013181 MONDO:0015048 False amelogenesis imperfecta hypomaturation type 2A3 amelogenesis imperfecta type 2 UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013183 MONDO:0800402 False congenital stationary night blindness 1C TRPM1-related retinopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013184 MONDO:0045032 False congenital diarrhea 5 with tufting enteropathy congenital secretory diarrhea UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0013185 MONDO:0015979 False leprosy, susceptibility to, 5 hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0013185 MONDO:0020573 False leprosy, susceptibility to, 5 inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013187 MONDO:0018029 False factor XIII, A subunit, deficiency of congenital factor XIII deficiency UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013187 MONDO:0021181 False factor XIII, A subunit, deficiency of inherited blood coagulation disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013189 MONDO:0003847 False trichotillomania hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS @@ -26308,7 +26307,7 @@ MONDO:0013246 MONDO:0020573 False fatty liver disease, nonalcoholic, susceptibil MONDO:0013247 MONDO:0007600 False Fanconi renotubular syndrome 2 primary Fanconi syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013251 MONDO:0003847 False Birbeck granule deficiency hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013254 MONDO:0001149 False microcephaly, seizures, and developmental delay microcephaly UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS -MONDO:0013257 MONDO:0015979 False leprosy, susceptibility to, 6 hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0013257 MONDO:0020573 False leprosy, susceptibility to, 6 inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013259 MONDO:0019152 False Oguchi disease-2 Oguchi disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013260 MONDO:0003847 False esophagitis, eosinophilic, 2 hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013260 MONDO:0005361 False esophagitis, eosinophilic, 2 eosinophilic esophagitis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -26453,7 +26452,7 @@ MONDO:0013557 MONDO:0016502 False Hermansky-Pudlak syndrome 5 Hermansky-Pudlak s MONDO:0013558 MONDO:0016502 False Hermansky-Pudlak syndrome 6 Hermansky-Pudlak syndrome without pulmonary fibrosis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013561 MONDO:0000226 False chondrodysplasia with joint dislocations, gPAPP type mineral metabolism disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013561 MONDO:0019052 False chondrodysplasia with joint dislocations, gPAPP type inborn errors of metabolism UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS -MONDO:0013562 MONDO:0015979 False aspergillosis, susceptibility to hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0013562 MONDO:0020573 False aspergillosis, susceptibility to inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013564 MONDO:0003847 False anhaptoglobinemia hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013568 MONDO:0020573 False sick sinus syndrome 3, susceptibility to inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013571 MONDO:0100306 False acatalasia disorder of defective peroxisome oxidative status UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -26535,7 +26534,7 @@ MONDO:0013696 MONDO:0016884 False chromosome 2p16.3 deletion syndrome partial de MONDO:0013696 MONDO:0100545 False chromosome 2p16.3 deletion syndrome hereditary neurological disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013700 MONDO:0002356 False pancreatic triacylglycerol lipase deficiency pancreas disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013705 MONDO:0019502 False intellectual disability, autosomal recessive 19 autosomal recessive non-syndromic intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING -MONDO:0013713 MONDO:0015979 False dengue virus, susceptibility to hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0013713 MONDO:0020573 False dengue virus, susceptibility to inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013715 MONDO:0017593 False amyotrophic lateral sclerosis type 16 juvenile amyotrophic lateral sclerosis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013720 MONDO:0000015 False complement component 4b deficiency classic complement early component deficiency UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013720 MONDO:0015699 False complement component 4b deficiency immunodeficiency due to a classical component pathway complement deficiency UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -26560,7 +26559,7 @@ MONDO:0013745 MONDO:0009480 False Joubert syndrome 14 Joubert syndrome with ocul MONDO:0013745 MONDO:0016364 False Joubert syndrome 14 Joubert syndrome with ocular defect UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013746 MONDO:0100009 False ventricular septal defect 1 structural congenital heart disease, multiple types - GATA4 UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013747 MONDO:0100009 False atrioventricular septal defect 4 structural congenital heart disease, multiple types - GATA4 UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0013757 MONDO:0019995 False congenital nongoitrous hypothryoidism 6 peripheral resistance to thyroid hormones UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0013757 MONDO:0019995 False congenital nongoitrous hypothyroidism 6 peripheral resistance to thyroid hormones UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013760 MONDO:0015905 False congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome syndromic dyslipidemia UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013763 MONDO:0016364 False Joubert syndrome 15 Joubert syndrome with ocular defect UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013764 MONDO:0009480 False Joubert syndrome 16 Joubert syndrome with oculorenal defect UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING @@ -26600,7 +26599,7 @@ MONDO:0013843 MONDO:0003847 False intestinal obstruction in the newborn due to g MONDO:0013843 MONDO:0021189 False intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency intestinal motility disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013843 MONDO:0054868 False intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency meconium ileus UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013846 MONDO:0020573 False peripartum cardiomyopathy, susceptibility to inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0013855 MONDO:0015979 False influenza, severe, susceptibility to hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0013855 MONDO:0020573 False influenza, severe, susceptibility to inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013856 MONDO:0003847 False hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, intellectual disability, and recurrent inflammatory episodes hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013857 MONDO:0003847 False alar cleft, isolated hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013859 MONDO:0011060 False cataract 38 early-onset non-syndromic cataract UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING @@ -26634,14 +26633,14 @@ MONDO:0013906 MONDO:0015048 False amelogenesis imperfecta hypomaturation type 2A MONDO:0013907 MONDO:0018764 False bilateral generalized polymicrogyria microcephalic primordial dwarfism due to RTTN deficiency UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013907 MONDO:0100545 False bilateral generalized polymicrogyria hereditary neurological disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013908 MONDO:0020573 False thyrotoxic periodic paralysis, susceptibility to, 3 inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0013909 MONDO:0015979 False human herpesvirus 8, susceptibility to hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0013909 MONDO:0020573 False human herpesvirus 8, susceptibility to inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013910 MONDO:0018800 False hypogonadotropic hypogonadism 8 with or without anosmia Kallmann syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0013911 MONDO:0018800 False hypogonadotropic hypogonadism 9 with or without anosmia Kallmann syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0013913 MONDO:0018800 False hypogonadotropic hypogonadism 11 with or without anosmia Kallmann syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0013917 MONDO:0017842 False nephronophthisis 15 Senior-Loken syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-SUBCLASS MONDO:0013919 MONDO:0020573 False epilepsy, idiopathic generalized, susceptibility to, 12 inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0013920 MONDO:0015979 False herpes simplex encephalitis, susceptibility to, 3 hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0013921 MONDO:0015979 False herpes simplex encephalitis, susceptibility to, 4 hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0013920 MONDO:0020573 False herpes simplex encephalitis, susceptibility to, 3 inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0013921 MONDO:0020573 False herpes simplex encephalitis, susceptibility to, 4 inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013926 MONDO:0018800 False hypogonadotropic hypogonadism 14 with or without anosmia Kallmann syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0013927 MONDO:0100266 False peroxisome biogenesis disorder 3A (Zellweger) peroxisome biogenesis disorder due to PEX12 defect UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013930 MONDO:0100263 False peroxisome biogenesis disorder 4A (Zellweger) peroxisome biogenesis disorder due to PEX6 defect UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -26657,7 +26656,7 @@ MONDO:0013941 MONDO:0005172 False metaphyseal chondromatosis with D-2-hydroxyglu MONDO:0013942 MONDO:0100269 False peroxisome biogenesis disorder 8A (Zellweger) peroxisome biogenesis disorder due to PEX16 defect UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013943 MONDO:0100269 False peroxisome biogenesis disorder 8B peroxisome biogenesis disorder due to PEX16 defect UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013944 MONDO:0023603 False autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation hereditary disorder of connective tissue UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0013945 MONDO:0019609 False peroxisome biogenesis disorder 9B Zellweger spectrum disorders UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0013945 MONDO:0019609 False peroxisome biogenesis disorder 9B Zellweger spectrum disorders UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0013946 MONDO:0018800 False hypogonadotropic hypogonadism 15 with or without anosmia Kallmann syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0013948 MONDO:0100261 False peroxisome biogenesis disorder 10A (Zellweger) peroxisome biogenesis disorder due to PEX3 defect UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0013949 MONDO:0100267 False peroxisome biogenesis disorder 11A (Zellweger) peroxisome biogenesis disorder due to PEX13 defect UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -26704,6 +26703,7 @@ MONDO:0014034 MONDO:0002320 False severe intellectual disability-poor language-s MONDO:0014035 MONDO:0000508 False severe intellectual disability-progressive spastic diplegia syndrome syndromic intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0014035 MONDO:0002320 False severe intellectual disability-progressive spastic diplegia syndrome congenital nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0014035 MONDO:0100172 False severe intellectual disability-progressive spastic diplegia syndrome intellectual disability, autosomal dominant UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING +MONDO:0014035 MONDO:0100571 False severe intellectual disability-progressive spastic diplegia syndrome CTNNB1-related neurodevelopmental disorder and/or vitreoretinopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014038 MONDO:0015356 False colorectal cancer, susceptibility to, 12 hereditary neoplastic syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014043 MONDO:0018230 False microcephalic primordial dwarfism due to ZNF335 deficiency skeletal dysplasia UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014044 MONDO:0015160 False dysmorphism-conductive hearing loss-heart defect syndrome multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -26802,7 +26802,7 @@ MONDO:0014249 MONDO:0000620 False multiple fibroadenoma of the breast breast ben MONDO:0014249 MONDO:0003847 False multiple fibroadenoma of the breast hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014250 MONDO:0005804 False familial hyperprolactinemia hyperprolactinemia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014250 MONDO:0100545 False familial hyperprolactinemia hereditary neurological disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0014251 MONDO:0015979 False melioidosis, susceptibility to hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0014251 MONDO:0020573 False melioidosis, susceptibility to inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014255 MONDO:0003847 False complement factor b deficiency hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014257 MONDO:0019006 False nephrotic syndrome, type 9 familial idiopathic steroid-resistant nephrotic syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014258 MONDO:0002254 False congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -26885,6 +26885,7 @@ MONDO:0014404 MONDO:0003847 False Webb-Dattani syndrome hereditary disease UNSUP MONDO:0014405 MONDO:0005385 False STING-associated vasculopathy with onset in infancy vascular disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0014405 MONDO:0021166 False STING-associated vasculopathy with onset in infancy inflammatory disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014405 MONDO:0023603 False STING-associated vasculopathy with onset in infancy hereditary disorder of connective tissue UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0014407 MONDO:0800485 False megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2 AKT3-related overgrowth spectrum UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014412 MONDO:0015905 False hyperlipoproteinemia, type 1D syndromic dyslipidemia UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014414 MONDO:0002334 False STAT3-related early-onset multisystem autoimmune disease hematopoietic and lymphoid system neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014415 MONDO:0003847 False kallikrein, decreased urinary activity of hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -26922,7 +26923,7 @@ MONDO:0014487 MONDO:0002254 False congenital sideroblastic anemia-B-cell immunod MONDO:0014487 MONDO:0005046 False congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome immune system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0014488 MONDO:0005148 False diabetes mellitus, noninsulin-dependent, 5 type 2 diabetes mellitus UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING MONDO:0014488 MONDO:0015967 False diabetes mellitus, noninsulin-dependent, 5 monogenic diabetes UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0014493 MONDO:0017979 False autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency autoimmune lymphoproliferative syndrome UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0014493 MONDO:0017979 False autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency autoimmune lymphoproliferative syndrome UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014494 MONDO:0100171 False psoriasis 15, pustular, susceptibility to psoriasis, susceptibility to UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014495 MONDO:0002254 False retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014495 MONDO:0003847 False retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -27041,7 +27042,7 @@ MONDO:0014676 MONDO:0021106 False Emery-Dreifuss muscular dystrophy 3, autosomal MONDO:0014677 MONDO:0100447 False achromatopsia 7 ATF6-related retinopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014679 MONDO:0020340 False polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis bilateral perisylvian polymicrogyria UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014679 MONDO:0100545 False polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis hereditary neurological disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0014680 MONDO:0015979 False herpes simplex encephalitis, susceptibility to, 7 hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0014680 MONDO:0020573 False herpes simplex encephalitis, susceptibility to, 7 inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014681 MONDO:0005034 False thyroid cancer, nonmedullary, 4 thyroid gland follicular carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014681 MONDO:0017895 False thyroid cancer, nonmedullary, 4 familial papillary or follicular thyroid carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014682 MONDO:0005034 False thyroid cancer, nonmedullary, 5 thyroid gland follicular carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -27052,6 +27053,7 @@ MONDO:0014686 MONDO:0005151 False short stature, microcephaly, and endocrine dys MONDO:0014686 MONDO:0800063 False short stature, microcephaly, and endocrine dysfunction primordial dwarfism and slender bone disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014688 MONDO:0018342 False short-rib thoracic dysplasia 14 with polydactyly Joubert syndrome with Jeune asphyxiating thoracic dystrophy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014690 MONDO:0005570 False dyskeratosis congenita, autosomal dominant 6 hematologic disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS +MONDO:0014690 MONDO:0100569 False dyskeratosis congenita, autosomal dominant 6 ACD-related short telomere syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014694 MONDO:0010180 False spondylocostal dysostosis 6, autosomal recessive autosomal recessive spondylocostal dysostosis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014698 MONDO:0003847 False microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0014698 MONDO:0005328 False microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome eye disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -27295,7 +27297,6 @@ MONDO:0015167 MONDO:0018230 False amniotic band syndrome skeletal dysplasia UNSU MONDO:0015169 MONDO:0044751 False chronic diarrhea due to glucoamylase deficiency chronic diarrheal disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015170 MONDO:0000824 False congenital sodium diarrhea congenital diarrhea UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015171 MONDO:0005020 False congenital enterocyte heparan sulfate deficiency intestinal disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0015174 MONDO:0019787 False autoimmune enteropathy type 3 autoimmune enteropathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015175 MONDO:0000588 False autoimmune pancreatitis autoimmune disorder of gastrointestinal tract UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0015175 MONDO:0004982 False autoimmune pancreatitis pancreatitis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0015175 MONDO:0017287 False autoimmune pancreatitis IgG4-related disease UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS @@ -27329,7 +27330,6 @@ MONDO:0015249 MONDO:0003767 False mitral atresia disorder mitral valve disorder MONDO:0015249 MONDO:0005453 False mitral atresia disorder congenital heart disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015252 MONDO:0002320 False severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome congenital nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015254 MONDO:0100120 False schistosomiasis vector-borne disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0015257 MONDO:0007263 False sino-auricular heart block cardiac rhythm disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015260 MONDO:0042488 False diphyllobothriasis Cestode infectious disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015263 MONDO:0002254 False Brugada syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0015263 MONDO:0100547 False Brugada syndrome cardiogenetic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -27426,12 +27426,9 @@ MONDO:0015411 MONDO:0023369 False facial cleft disorder of facial skeleton UNSUP MONDO:0015414 MONDO:0008866 False paramedian nasal cleft bifid nose, autosomal recessive UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015420 MONDO:0000358 False cleft lip and alveolus orofacial cleft UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015420 MONDO:0021147 False cleft lip and alveolus disorder of development or morphogenesis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0015424 MONDO:0005516 False lethal chondrodysplasia, Moerman type osteochondrodysplasia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0015424 MONDO:0018230 False lethal chondrodysplasia, Moerman type skeletal dysplasia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015425 MONDO:0003847 False lethal recessive chondrodysplasia hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015425 MONDO:0022723 False lethal recessive chondrodysplasia chondrodysplasia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015426 MONDO:0003847 False Desbuquois dysplasia hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS -MONDO:0015429 MONDO:0019118 False choroideremia-hypopituitarism syndrome inherited retinal dystrophy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015430 MONDO:0700008 False ring chromosome 1 chromosome 1 disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015430 MONDO:0700091 False ring chromosome 1 ring chromosome disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015431 MONDO:0002254 False ring chromosome 10 syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -27469,7 +27466,6 @@ MONDO:0015455 MONDO:0006668 False gonococcal conjunctivitis bacterial conjunctiv MONDO:0015457 MONDO:0002254 False corpus callosum agenesis-double urinary collecting system syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015461 MONDO:0002254 False short rib-polydactyly syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015465 MONDO:0042973 False craniometaphyseal dysplasia familial osteosclerosis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0015468 MONDO:0015338 False craniosynostosis-cataract syndrome syndromic craniosynostosis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015469 MONDO:0003847 False craniosynostosis hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0015474 MONDO:0024270 False cryptosporidiosis parasitic intestinal disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015476 MONDO:0024623 False cysts and fistulae of the face and oral cavity otorhinolaryngologic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -27491,6 +27487,8 @@ MONDO:0015518 MONDO:0005559 False infantile bilateral striatal necrosis neurodeg MONDO:0015519 MONDO:0002320 False congenital or early infantile CACH syndrome congenital nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015524 MONDO:0004335 False hyperplastic polyposis syndrome digestive system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015525 MONDO:0003847 False congenital pseudoarthrosis of the limbs hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0015528 MONDO:0002320 False congenital epulis congenital nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS +MONDO:0015528 MONDO:0006235 False congenital epulis granular cell tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0015528 MONDO:0006424 False congenital epulis soft tissue neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015528 MONDO:0006499 False congenital epulis hamartoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015528 MONDO:0021086 False congenital epulis gingival neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -27595,7 +27593,6 @@ MONDO:0015743 MONDO:0700007 False idiopathic bilateral vestibulopathy idiopathic MONDO:0015745 MONDO:0021147 False microcephaly-polymicrogyria-corpus callosum agenesis syndrome disorder of development or morphogenesis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015748 MONDO:0005073 False hereditary mucosal leukokeratosis melanocytic nevus UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015748 MONDO:0100118 False hereditary mucosal leukokeratosis hereditary skin disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0015752 MONDO:0002254 False intellectual disability-cataracts-kyphosis syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015753 MONDO:0100084 False cap myopathy alpha-actinopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015753 MONDO:0100108 False cap myopathy TPM3-related myopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015756 MONDO:0002334 False myeloid hemopathy hematopoietic and lymphoid system neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -27653,7 +27650,6 @@ MONDO:0015855 MONDO:0002657 False isolated congenital breast hypoplasia/aplasia MONDO:0015855 MONDO:0003847 False isolated congenital breast hypoplasia/aplasia hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015856 MONDO:0002657 False syndromic breast hypoplasia/aplasia breast disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015863 MONDO:0003578 False polyembryoma extragonadal nonseminomatous germ cell tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0015874 MONDO:0021100 False benign ductal tumor of breast breast neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015884 MONDO:0000426 False autosomal dominant hypohidrotic ectodermal dysplasia autosomal dominant disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015892 MONDO:0002254 False growth hormone insensitivity syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015898 MONDO:0005495 False adrenogenital syndrome adrenal gland disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -27683,13 +27679,11 @@ MONDO:0015962 MONDO:0100191 False inherited renal tubular disease inherited kidn MONDO:0015967 MONDO:0005015 False monogenic diabetes diabetes mellitus UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015967 MONDO:0019052 False monogenic diabetes inborn errors of metabolism UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015978 MONDO:0004805 False functional neutrophil defect leukocyte disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0015979 MONDO:0020573 False hereditary predisposition to infections inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015985 MONDO:0018230 False bone dysplasia, Azouz type skeletal dysplasia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015987 MONDO:0002254 False scimitar syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015987 MONDO:0017705 False scimitar syndrome congenital pulmonary venous return anomaly UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015988 MONDO:0002473 False multicystic dysplastic kidney cystic kidney disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015988 MONDO:0021147 False multicystic dysplastic kidney disorder of development or morphogenesis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0015994 MONDO:0020120 False muscular dystrophy-white matter spongiosis syndrome skeletal muscle disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015997 MONDO:0001176 False ectopia lentis-chorioretinal dystrophy-myopia syndrome lens disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015997 MONDO:0019118 False ectopia lentis-chorioretinal dystrophy-myopia syndrome inherited retinal dystrophy UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0015999 MONDO:0003847 False primary pigmented nodular adrenocortical disease hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS @@ -27922,7 +27916,6 @@ MONDO:0016416 MONDO:0003150 False diphallia male reproductive system disorder UN MONDO:0016416 MONDO:0021147 False diphallia disorder of development or morphogenesis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016417 MONDO:0002254 False congenital ichthyosis-microcephalus-tetraplegia syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016419 MONDO:0003847 False hereditary breast carcinoma hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0016420 MONDO:0020242 False familial flecked retinopathy hereditary macular dystrophy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016421 MONDO:0029000 False toxic oil syndrome poisoning UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016425 MONDO:0002254 False Hughes-Stovin syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016429 MONDO:0005301 False Marburg acute multiple sclerosis multiple sclerosis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -28006,7 +27999,6 @@ MONDO:0016554 MONDO:0005151 False neonatal iodine exposure endocrine system diso MONDO:0016558 MONDO:0002320 False familial congenital mirror movements congenital nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0016558 MONDO:0100545 False familial congenital mirror movements hereditary neurological disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016559 MONDO:0009633 False glaucoma secondary to spherophakia/ectopia lentis and megalocornea microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0016560 MONDO:0015159 False ptosis-syndactyly-learning difficulties syndrome multiple congenital anomalies/dysmorphic syndrome-intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016568 MONDO:0002254 False Lowe-Kohn-Cohen syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016568 MONDO:0021147 False Lowe-Kohn-Cohen syndrome disorder of development or morphogenesis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016571 MONDO:0002320 False macrocephaly-short stature-paraplegia syndrome congenital nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -28071,7 +28063,6 @@ MONDO:0016682 MONDO:0002501 False giant cell glioblastoma brain glioblastoma UNS MONDO:0016683 MONDO:0005499 False gliomatosis cerebri brain glioma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0016685 MONDO:0019781 False low-grade astrocytoma astrocytoma (excluding glioblastoma) UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016685 MONDO:0021638 False low-grade astrocytoma low grade astrocytic tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0016697 MONDO:0016698 False low grade ependymoma ependymoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016703 MONDO:0016702 False anaplastic oligoastrocytoma oligoastrocytoma UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016706 MONDO:0002786 False chordoid glioma of the third ventricle diencephalic cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0016706 MONDO:0005499 False chordoid glioma of the third ventricle brain glioma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS @@ -28079,6 +28070,9 @@ MONDO:0016706 MONDO:0021639 False chordoid glioma of the third ventricle grade I MONDO:0016715 MONDO:0016713 False ependymoblastoma central nervous system Ewing sarcoma/peripheral primitive neuroectodermal tumor UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016734 MONDO:0016733 False anaplastic ganglioglioma ganglioglioma UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016742 MONDO:0000524 False mixed germ cell tumor of central nervous system mixed extragonadal germ cell cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0016746 MONDO:0003222 False meningeal melanocytoma central nervous system melanocytic neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS +MONDO:0016747 MONDO:0003222 False primary melanoma of the central nervous system central nervous system melanocytic neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0016747 MONDO:0006320 False primary melanoma of the central nervous system non-cutaneous melanoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016748 MONDO:0000648 False hemangioblastoma nervous system benign neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0016748 MONDO:0002407 False hemangioblastoma capillary hemangioma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0016748 MONDO:0043218 False hemangioblastoma neurovascular disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -28115,14 +28109,12 @@ MONDO:0016818 MONDO:0002254 False Mikati-Najjar-Sahli syndrome syndromic disease MONDO:0016819 MONDO:0008006 False Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome Mobius syndrome UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016819 MONDO:0100545 False Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome hereditary neurological disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016820 MONDO:0100545 False Moyamoya disease hereditary neurological disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0016821 MONDO:0002254 False shoulder and girdle defects-familial intellectual disability syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016822 MONDO:0005554 False myalgia-eosinophilia syndrome associated with tryptophan rheumatic disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016823 MONDO:0019296 False mycetoma subcutaneous tissue disorder UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016824 MONDO:0023603 False infantile myofibromatosis hereditary disorder of connective tissue UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016824 MONDO:0044335 False infantile myofibromatosis benign soft tissue neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016826 MONDO:0002012 False methylmalonic aciduria and homocystinuria methylmalonic acidemia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016826 MONDO:0004737 False methylmalonic aciduria and homocystinuria homocystinuria UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0016827 MONDO:0002254 False myopathy-growth delay-intellectual disability-hypospadias syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016828 MONDO:0006025 False autosomal recessive sideroblastic anemia autosomal recessive disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016829 MONDO:0020754 False familial visceral myopathy visceral myopathy 1 UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016829 MONDO:0021189 False familial visceral myopathy intestinal motility disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -28139,10 +28131,6 @@ MONDO:0016853 MONDO:0700091 False ring chromosome Y ring chromosome disorder UNS MONDO:0016854 MONDO:0700027 False 49,XXXYY syndrome chromosome X disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016854 MONDO:0700028 False 49,XXXYY syndrome chromosome Y disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016854 MONDO:0700064 False 49,XXXYY syndrome aneuploidy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0016857 MONDO:0007201 False blepharophimosis-epicanthus inversus-ptosis due to 3q23 rearrangement syndrome blepharophimosis, ptosis, and epicanthus inversus syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0016857 MONDO:0016902 False blepharophimosis-epicanthus inversus-ptosis due to 3q23 rearrangement syndrome partial deletion of the long arm of chromosome 3 UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0016858 MONDO:0007201 False blepharophimosis-epicanthus inversus-ptosis due to a point mutation syndrome blepharophimosis, ptosis, and epicanthus inversus syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0016859 MONDO:0007201 False blepharophimosis-epicanthus inversus-ptosis due to copy number variations blepharophimosis, ptosis, and epicanthus inversus syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016866 MONDO:0000761 False partial deletion of chromosome 1 syndrome caused by partial chromosomal deletion UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016866 MONDO:0700008 False partial deletion of chromosome 1 chromosome 1 disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016867 MONDO:0000761 False partial deletion of chromosome 2 syndrome caused by partial chromosomal deletion UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -28216,7 +28204,6 @@ MONDO:0016964 MONDO:0000762 False partial duplication of the long arm of chromos MONDO:0016965 MONDO:0000762 False partial duplication of the long arm of chromosome 15 syndrome caused by partial chromosomal duplication UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016972 MONDO:0000762 False partial duplication of the long arm of chromosome 22 syndrome caused by partial chromosomal duplication UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016974 MONDO:0004805 False thymoma type B leukocyte disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS -MONDO:0016980 MONDO:0020119 False ATR-X-related syndrome X-linked syndromic intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016983 MONDO:0015231 False Bartter syndrome with hypocalcemia Bartter syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016984 MONDO:0005073 False nevus of Ota melanocytic nevus UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0016985 MONDO:0005073 False nevus of Ito melanocytic nevus UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -28265,7 +28252,6 @@ MONDO:0017103 MONDO:0005560 False encephaloclastic disorder brain disorder UNSUP MONDO:0017123 MONDO:0008823 False arthrogryposis-renal dysfunction-cholestasis syndrome arthrogryposis multiplex congenita 2, neurogenic type UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-SUBCLASS MONDO:0017123 MONDO:0015327 False arthrogryposis-renal dysfunction-cholestasis syndrome developmental anomaly of metabolic origin UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017124 MONDO:0005113 False noma bacterial infectious disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS -MONDO:0017126 MONDO:0002254 False oculo-skeletal-renal syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017135 MONDO:0002254 False olivopontocerebellar atrophy-deafness syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017137 MONDO:0005943 False onchocerciasis Rhabditida infectious disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017137 MONDO:0100120 False onchocerciasis vector-borne disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -28463,24 +28449,8 @@ MONDO:0017474 MONDO:0021147 False macrodactyly of fingers disorder of developmen MONDO:0017475 MONDO:0021147 False macrodactyly of toes disorder of development or morphogenesis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017476 MONDO:0021147 False upper limb hypertrophy disorder of development or morphogenesis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017477 MONDO:0021147 False lower limb hypertrophy disorder of development or morphogenesis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0017490 MONDO:0010144 False tibial hemimelia, unilateral tibial hemimelia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0017491 MONDO:0010144 False tibial hemimelia, bilateral tibial hemimelia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017503 MONDO:0017445 False acheiria, bilateral acheiria UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017514 MONDO:0017450 False split foot, bilateral split foot UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0017519 MONDO:0015516 False symbrachydactyly of hand and foot, unilateral symbrachydactyly of hands and feet UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0017520 MONDO:0015516 False symbrachydactyly of hand and foot, bilateral symbrachydactyly of hands and feet UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0017523 MONDO:0008269 False polydactyly of a biphalangeal thumb, unilateral polydactyly of a biphalangeal thumb UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0017524 MONDO:0008269 False polydactyly of a biphalangeal thumb, bilateral polydactyly of a biphalangeal thumb UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0017525 MONDO:0008270 False polydactyly of a triphalangeal thumb, unilateral polydactyly of a triphalangeal thumb UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0017526 MONDO:0008270 False polydactyly of a triphalangeal thumb, bilateral polydactyly of a triphalangeal thumb UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0017527 MONDO:0008271 False polydactyly of an index finger, unilateral polydactyly of an index finger UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0017528 MONDO:0008271 False polydactyly of an index finger, bilateral polydactyly of an index finger UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0017529 MONDO:0008272 False polysyndactyly, unilateral polysyndactyly 4 UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0017530 MONDO:0008272 False polysyndactyly, bilateral polysyndactyly 4 UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0017531 MONDO:0019673 False postaxial polydactyly type A, unilateral postaxial polydactyly type A UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0017532 MONDO:0019673 False postaxial polydactyly type A, bilateral postaxial polydactyly type A UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0017533 MONDO:0019674 False postaxial polydactyly type B, unilateral postaxial polydactyly type B UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0017534 MONDO:0019674 False postaxial polydactyly type B, bilateral postaxial polydactyly type B UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017571 MONDO:0002051 False Proteus-like syndrome integumentary system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017572 MONDO:0025294 False tick-borne encephalitis tick-borne infectious disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017573 MONDO:0002254 False 46,XX disorder of sex development-anorectal anomalies syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -28505,6 +28475,7 @@ MONDO:0017593 MONDO:0005144 False juvenile amyotrophic lateral sclerosis familia MONDO:0017604 MONDO:0036696 False marginal zone lymphoma spleen neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017609 MONDO:0005240 False renal tubular dysgenesis kidney disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017611 MONDO:0002082 False pituitary tumor endocrine gland neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0017611 MONDO:0006054 False pituitary tumor reproductive system neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017611 MONDO:0006799 False pituitary tumor hypothalamic neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017614 MONDO:0002320 False X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome congenital nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017614 MONDO:0020119 False X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome X-linked syndromic intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -28521,7 +28492,6 @@ MONDO:0017639 MONDO:0021095 False carbon monoxide-induced parkinsonism parkinson MONDO:0017639 MONDO:0800373 False carbon monoxide-induced parkinsonism carbon monoxide poisoning UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017640 MONDO:0021095 False cyanide-induced parkinsonism parkinsonian disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017640 MONDO:0029000 False cyanide-induced parkinsonism poisoning UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0017642 MONDO:0002254 False intellectual disability-microcephaly-phalangeal-facial abnormalities syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017648 MONDO:0005071 False Sydenham chorea nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017649 MONDO:0003441 False hemidystonia-hemiatrophy syndrome dystonic disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017658 MONDO:0005395 False hyperekplexia movement disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -28641,6 +28611,8 @@ MONDO:0017882 MONDO:0005763 False Omsk hemorrhagic fever Flaviviridae infectious MONDO:0017882 MONDO:0025294 False Omsk hemorrhagic fever tick-borne infectious disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017893 MONDO:0023603 False inherited acute myeloid leukemia hereditary disorder of connective tissue UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017896 MONDO:0003847 False familial nonmedullary thyroid carcinoma hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0017901 MONDO:0020573 False autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0017902 MONDO:0020573 False autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017904 MONDO:0005066 False steroid dehydrogenase deficiency-dental anomalies syndrome metabolic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017904 MONDO:0021147 False steroid dehydrogenase deficiency-dental anomalies syndrome disorder of development or morphogenesis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0017907 MONDO:0003454 False primary lymphoma of the conjunctiva conjunctival cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -28772,7 +28744,6 @@ MONDO:0018108 MONDO:0700007 False idiopathic disseminated cytomegalovirus infect MONDO:0018109 MONDO:0002251 False fulminant viral hepatitis hepatitis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0018115 MONDO:0002254 False epidermal nevus syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0018116 MONDO:0005328 False galactosemia eye disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS -MONDO:0018122 MONDO:0002254 False digital anomalies-intellectual disability-short stature syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0018123 MONDO:0002254 False intellectual disability-obesity-brain malformations-facial dysmorphism syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0018124 MONDO:0001068 False Oncogenic osteomalacia osteomalacia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0018124 MONDO:0700252 False Oncogenic osteomalacia parneoplastic endocrine syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -28881,7 +28852,6 @@ MONDO:0018341 MONDO:0000761 False 3q27.3 microdeletion syndrome syndrome caused MONDO:0018341 MONDO:0002320 False 3q27.3 microdeletion syndrome congenital nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0018343 MONDO:0100546 False periodic paralysis with later-onset distal motor neuropathy hereditary neuromuscular disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0018346 MONDO:0002254 False ferro-cerebro-cutaneous syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0018347 MONDO:0002254 False severe intellectual disability-progressive postnatal microcephaly- midline stereotypic hand movements syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0018353 MONDO:0005020 False refractory celiac disease intestinal disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0018354 MONDO:0002320 False Prader-Willi-like syndrome congenital nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0018354 MONDO:0015160 False Prader-Willi-like syndrome multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -28904,7 +28874,6 @@ MONDO:0018383 MONDO:0003847 False osteonecrosis of genetic origin hereditary dis MONDO:0018383 MONDO:0005380 False osteonecrosis of genetic origin osteonecrosis UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0018394 MONDO:0005372 False male infertility with teratozoospermia due to single gene mutation male infertility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0018408 MONDO:0044346 False cystic echinococcosis echinococcus granulosus infectious disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0018420 MONDO:0015150 False autosomal recessive spastic paraplegia type 68 complex hereditary spastic paraplegia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0018424 MONDO:0037858 False inherited lipoic acid biosynthesis defect inherited fatty acid metabolism disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0018424 MONDO:0045022 False inherited lipoic acid biosynthesis defect disorder of organic acid metabolism UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0018424 MONDO:0056803 False inherited lipoic acid biosynthesis defect sulfur metabolism disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -28947,7 +28916,6 @@ MONDO:0018493 MONDO:0100546 False malignant hyperthermia of anesthesia hereditar MONDO:0018500 MONDO:0005135 False cutaneous larva migrans parasitic infectious disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0018502 MONDO:0003847 False hereditary gastric cancer hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0018502 MONDO:0004950 False hereditary gastric cancer gastric carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0018503 MONDO:0004950 False carcinoma of stomach, salivary gland type gastric carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0018506 MONDO:0004251 False mesenchymal tumor of small intestine small intestine neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0018507 MONDO:0002254 False microcephaly-complex motor and sensory axonal neuropathy syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0018507 MONDO:0100545 False microcephaly-complex motor and sensory axonal neuropathy syndrome hereditary neurological disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -29374,6 +29342,7 @@ MONDO:0019140 MONDO:0029000 False acute ackee fruit intoxication poisoning UNSUP MONDO:0019142 MONDO:0037939 False inherited porphyria porphyria UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019144 MONDO:0100240 False hereditary thrombophilia due to congenital protein S deficiency inherited thrombophilia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019145 MONDO:0100240 False hereditary thrombophilia due to congenital protein C deficiency inherited thrombophilia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0019146 MONDO:0020573 False inherited susceptibility to mycobacterial diseases inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019154 MONDO:0003847 False androgen insensitivity syndrome hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0019156 MONDO:0002254 False angioosteohypotrophic syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019156 MONDO:0005497 False angioosteohypotrophic syndrome bone development disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -29420,6 +29389,8 @@ MONDO:0019203 MONDO:0020683 False acute interstitial pneumonia acute disease UNS MONDO:0019207 MONDO:0100164 False DEND syndrome permanent neonatal diabetes mellitus UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019208 MONDO:0020068 False Bickerstaff brainstem encephalitis postinfectious encephalitis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019209 MONDO:0020601 False Japanese encephalitis mosquito-borne viral encephalitis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0019210 MONDO:0002656 False cutaneous neuroendocrine carcinoma skin carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0019210 MONDO:0003363 False cutaneous neuroendocrine carcinoma malignant dermis tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019210 MONDO:0005872 False cutaneous neuroendocrine carcinoma nervous system cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019210 MONDO:0021635 False cutaneous neuroendocrine carcinoma neurocristopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019214 MONDO:0037792 False inborn carbohydrate metabolic disorder carbohydrate metabolism disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -29546,7 +29517,6 @@ MONDO:0019414 MONDO:0002254 False BRESEK syndrome syndromic disease UNSUPPORTED- MONDO:0019415 MONDO:0002243 False fetal and neonatal alloimmune thrombocytopenia hemorrhagic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019416 MONDO:0002320 False X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome congenital nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019416 MONDO:0020119 False X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome X-linked syndromic intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0019417 MONDO:0020119 False X-linked intellectual disability-precocious puberty-obesity syndrome X-linked syndromic intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019418 MONDO:0002320 False X-linked intellectual disability-epilepsy-progressive joint contractures-dysmorphism syndrome congenital nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019418 MONDO:0020119 False X-linked intellectual disability-epilepsy-progressive joint contractures-dysmorphism syndrome X-linked syndromic intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019419 MONDO:0020119 False X-linked intellectual disability-macrocephaly-macroorchidism syndrome X-linked syndromic intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -29684,14 +29654,6 @@ MONDO:0019638 MONDO:0021147 False renal dysplasia disorder of development or mor MONDO:0019639 MONDO:0005240 False congenital megacalycosis kidney disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019641 MONDO:0002462 False Pauci-immune glomerulonephritis glomerulonephritis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019642 MONDO:0024299 False vitamin D-dependent rickets, type 2 vitamin D-dependent rickets UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0019649 MONDO:0019067 False idiopathic steroid-sensitive nephrotic syndrome with focal segmental hyalinosis idiopathic steroid-sensitive nephrotic syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0019650 MONDO:0019067 False idiopathic steroid-sensitive nephrotic syndrome with minimal change idiopathic steroid-sensitive nephrotic syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0019651 MONDO:0019067 False idiopathic steroid-sensitive nephrotic syndrome with diffuse mesangial proliferation idiopathic steroid-sensitive nephrotic syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0019652 MONDO:0019006 False familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation familial idiopathic steroid-resistant nephrotic syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0019653 MONDO:0019006 False familial idiopathic steroid-resistant nephrotic syndrome with minimal changes familial idiopathic steroid-resistant nephrotic syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0019654 MONDO:0019006 False familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis familial idiopathic steroid-resistant nephrotic syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0019655 MONDO:0019401 False sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis sporadic idiopathic steroid-resistant nephrotic syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0019656 MONDO:0019401 False sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis sporadic idiopathic steroid-resistant nephrotic syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019666 MONDO:0000226 False spondyloepimetaphyseal dysplasia, PAPSS2 type mineral metabolism disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019666 MONDO:0019052 False spondyloepimetaphyseal dysplasia, PAPSS2 type inborn errors of metabolism UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0019668 MONDO:0004972 False adenoma of pancreas adenoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -29715,8 +29677,6 @@ MONDO:0019734 MONDO:0019127 False juvenile polymyositis polymyositis UNSUPPORTED MONDO:0019735 MONDO:0002254 False polymyalgia rheumatica syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0019735 MONDO:0005554 False polymyalgia rheumatica rheumatic disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0019737 MONDO:0001531 False thrombotic microangiopathy blood coagulation disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0019738 MONDO:0009335 False atypical hemolytic-uremic syndrome with H factor anomaly hemolytic uremic syndrome, atypical, susceptibility to, 1 UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0019738 MONDO:0016244 False atypical hemolytic-uremic syndrome with H factor anomaly atypical hemolytic-uremic syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019739 MONDO:0009335 False atypical hemolytic-uremic syndrome with anti-factor H antibodies hemolytic uremic syndrome, atypical, susceptibility to, 1 UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019740 MONDO:0001198 False acquired thrombotic thrombocytopenic purpura acquired thrombocytopenia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019741 MONDO:0002473 False familial cystic renal disease cystic kidney disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -29724,10 +29684,8 @@ MONDO:0019741 MONDO:0100191 False familial cystic renal disease inherited kidney MONDO:0019742 MONDO:0019232 False late-onset nephronophthisis inborn disorder of peptide metabolism UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019751 MONDO:0002254 False autoinflammatory syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019751 MONDO:0005554 False autoinflammatory syndrome rheumatic disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0019752 MONDO:0015564 False pediatric Castleman disease Castleman disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019755 MONDO:0021147 False developmental defect during embryogenesis disorder of development or morphogenesis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019760 MONDO:0015167 False terminal transverse defects of arm amniotic band syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0019770 MONDO:0016160 False X-linked dominant intellectual disability-epilepsy syndrome X-linked intellectual disability-epilepsy syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019780 MONDO:0024623 False anotia otorhinolaryngologic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019782 MONDO:0001411 False humero-ulnar synostosis synostosis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019787 MONDO:0000588 False autoimmune enteropathy autoimmune disorder of gastrointestinal tract UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -29875,7 +29833,6 @@ MONDO:0019977 MONDO:0001627 False parkinsonism with dementia of Guadeloupe demen MONDO:0019977 MONDO:0021095 False parkinsonism with dementia of Guadeloupe parkinsonian disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019978 MONDO:0015160 False Robinow syndrome multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019983 MONDO:0021163 False multiloculated renal cyst kidney neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0019986 MONDO:0019401 False sporadic idiopathic steroid-resistant nephrotic syndrome with collapsing glomerulopathy sporadic idiopathic steroid-resistant nephrotic syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019991 MONDO:0002462 False immunotactoid glomerulopathy glomerulonephritis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019993 MONDO:0005240 False congenital renal artery stenosis kidney disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0019993 MONDO:0005385 False congenital renal artery stenosis vascular disorder UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -29925,12 +29882,9 @@ MONDO:0020153 MONDO:0003382 False cryptophthalmia eyelid disorder UNSUPPORTED-MI MONDO:0020159 MONDO:0001519 False congenital entropion entropion UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0020161 MONDO:0002043 False congenital ectropion ectropion UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0020172 MONDO:0002235 False palpebral epidermal tumor eyelid neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0020173 MONDO:0020172 False benign tumor of palpebral epidermis palpebral epidermal tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0020173 MONDO:0021605 False benign tumor of palpebral epidermis benign eyelid neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0020175 MONDO:0020172 False malignant tumor of palpebral epidermis palpebral epidermal tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0020175 MONDO:0021313 False malignant tumor of palpebral epidermis eyelid cancer UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0020179 MONDO:0020173 False palpebral nevus benign tumor of palpebral epidermis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0020183 MONDO:0002235 False neurogenic palpebral tumor eyelid neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0020242 MONDO:0019118 False hereditary macular dystrophy inherited retinal dystrophy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0020246 MONDO:0005283 False inherited vitreoretinopathy retinal disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0020246 MONDO:0100545 False inherited vitreoretinopathy hereditary neurological disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -30052,7 +30006,6 @@ MONDO:0020541 MONDO:0021069 False maligant granulosa cell tumor of ovary maligna MONDO:0020542 MONDO:0036595 False malignant Sertoli-Leydig cell tumor of ovary ovarian Sertoli-Leydig cell tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0020544 MONDO:0021680 False streptococcal toxic-shock syndrome streptococcal infection UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0020546 MONDO:0020683 False acute graft versus host disease acute disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0020548 MONDO:0005328 False ocular pemphigoid eye disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0020550 MONDO:0003578 False gestational choriocarcinoma extragonadal nonseminomatous germ cell tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0020559 MONDO:0011224 False O'Sullivan-McLeod syndrome monomelic amyotrophy UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0020560 MONDO:0002217 False atypical teratoid rhabdoid tumor central nervous system sarcoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS @@ -30104,7 +30057,6 @@ MONDO:0020642 MONDO:0019741 False polycystic kidney disease familial cystic rena MONDO:0020645 MONDO:0000426 False autosomal dominant osteopetrosis autosomal dominant disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0020645 MONDO:0017198 False autosomal dominant osteopetrosis osteopetrosis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0020646 MONDO:0000462 False ocular adnexal lymphoma eye adnexa disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0020646 MONDO:0005586 False ocular adnexal lymphoma head and neck neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0020647 MONDO:0003847 False microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0020648 MONDO:0020068 False rubella encephalitis postinfectious encephalitis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0020648 MONDO:0021674 False rubella encephalitis post-viral disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -30274,13 +30226,13 @@ MONDO:0021009 MONDO:0044964 False salivary gland mucoepidermoid carcinoma oral c MONDO:0021010 MONDO:0002656 False skin lymphangiosarcoma skin carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021011 MONDO:0001595 False hereditary progressive chorea without dementia choreatic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021011 MONDO:0100545 False hereditary progressive chorea without dementia hereditary neurological disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0021012 MONDO:0015979 False susceptibility to visceral leishmaniasis, 1 hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0021012 MONDO:0020573 False susceptibility to visceral leishmaniasis, 1 inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021019 MONDO:0020605 False X-linked recessive ocular albinism X-linked recessive disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021019 MONDO:0043209 False X-linked recessive ocular albinism albinism UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021019 MONDO:0700230 False X-linked recessive ocular albinism GPR143-related foveal hypoplasia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021021 MONDO:0015465 False craniodiaphyseal dysplasia, autosomal dominant craniometaphyseal dysplasia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-SUBCLASS MONDO:0021022 MONDO:0100545 False hereditary hyperekplexia hereditary neurological disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0021024 MONDO:0015979 False malaria, susceptibility to hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0021024 MONDO:0020573 False malaria, susceptibility to inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021025 MONDO:0007329 False cirrhosis, familial, with antigenemia cirrhosis, familial UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING MONDO:0021026 MONDO:0005093 False hereditary epidermal appendage anomaly skin disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021032 MONDO:0003382 False herpes zoster with dermatitis of eyelid eyelid disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -30467,6 +30419,8 @@ MONDO:0021398 MONDO:0001593 False polyp of rectum rectal disorder UNSUPPORTED-MI MONDO:0021398 MONDO:0021392 False polyp of rectum polyp of large intestine UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021400 MONDO:0003409 False polyp of colon colonic disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021400 MONDO:0021392 False polyp of colon polyp of large intestine UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0021402 MONDO:0005079 False polyp of external auditory canal polyp UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0021402 MONDO:0021235 False polyp of external auditory canal external ear neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021404 MONDO:0001735 False polyp of sphenoidal sinus paranasal sinus disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021404 MONDO:0005079 False polyp of sphenoidal sinus polyp UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021404 MONDO:0023369 False polyp of sphenoidal sinus disorder of facial skeleton UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -30484,6 +30438,7 @@ MONDO:0021420 MONDO:0004382 False polyp of vocal cord laryngeal disorder UNSUPPO MONDO:0021420 MONDO:0005079 False polyp of vocal cord polyp UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021424 MONDO:0002531 False hemangiopericytoma of skin skin neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021427 MONDO:0004958 False squamous cell carcinoma of lip oral cavity squamous cell carcinoma UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0021439 MONDO:0000383 False benign neoplasm of pituitary gland benign reproductive system neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0021439 MONDO:0000631 False benign neoplasm of pituitary gland bone benign neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0021440 MONDO:0000652 False benign neoplasm of skin integumentary system benign neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021444 MONDO:0024634 False benign neoplasm of large intestine large intestine disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -30536,6 +30491,8 @@ MONDO:0021515 MONDO:0000633 False benign neoplasm of ethmoidal sinus sensory org MONDO:0021517 MONDO:0000382 False benign neoplasm of trachea respiratory system benign neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021522 MONDO:0021580 False benign neoplasm of lower jaw bone neoplasm of jaw UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021527 MONDO:0000628 False benign neoplasm of meninges central nervous system organ benign neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0021533 MONDO:0005369 False intestinal neuroendocrine tumor G1 carcinoid tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0021535 MONDO:0005369 False pancreatic neuroendocrine tumor G1 carcinoid tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021537 MONDO:0005617 False undifferentiated carcinoma of nasopharynx undifferentiated carcinoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021539 MONDO:0002297 False hamartoma of skin appendage epidermal appendage tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0021539 MONDO:0006499 False hamartoma of skin appendage hamartoma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -30788,7 +30745,7 @@ MONDO:0022612 MONDO:0002254 False Brunsting-Perry syndrome syndromic disease UNS MONDO:0022618 MONDO:0006687 False burning mouth syndrome type 3 burning mouth syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0022633 MONDO:0002254 False camptodactyly joint contractures and facial skeletal dysplasia syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0022634 MONDO:0002254 False camptodactyly vertebral fusion syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0022648 MONDO:0002254 False cardiomyopathy and deafness due to tRNA lysine gene mutation syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0022642 MONDO:0005369 False childhood carcinoid tumor carcinoid tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0022654 MONDO:0002254 False cardiomyopathy hypogonadism collagenoma syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0022673 MONDO:0022672 False autosomal dominant non-nuclear cataract autosomal dominant cataract UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0022687 MONDO:0002427 False cerebellar degeneration cerebellar disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS @@ -30869,7 +30826,6 @@ MONDO:0023094 MONDO:0001910 False exogenous ochronosis ochronosis disorder UNSUP MONDO:0023106 MONDO:0005516 False Fairbank disease osteochondrodysplasia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0023111 MONDO:0002254 False familial capillaro-venous leptomeningeal angiomatosis syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0023119 MONDO:0009692 False familial myelofibrosis primary myelofibrosis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0023121 MONDO:0003847 False familial partial paralysis hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0023122 MONDO:0003847 False familial prostate carcinoma hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0023133 MONDO:0002254 False Faye-Petersen-Ward-Carey syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0023134 MONDO:0024250 False febrile ulceronecrotic Mucha-Habermann disease acute lichenoid pityriasis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -30982,8 +30938,6 @@ MONDO:0023679 MONDO:0005093 False hematohidrosis skin disorder UNSUPPORTED-MISSI MONDO:0023682 MONDO:0015071 False tympanic paraganglioma middle ear neuroendocrine tumor UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0023682 MONDO:0018751 False tympanic paraganglioma hereditary otorhinolaryngologic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0023682 MONDO:0037940 False tympanic paraganglioma inherited auditory system disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0023692 MONDO:0009563 False maple syrup urine disease type 1B maple syrup urine disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING -MONDO:0023693 MONDO:0009563 False maple syrup urine disease type 2 maple syrup urine disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING MONDO:0023696 MONDO:0002254 False Marinesco-Sjogren-like syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0023696 MONDO:0003847 False Marinesco-Sjogren-like syndrome hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0023699 MONDO:0007041 False Maroteaux Fonfria syndrome Apert syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -31084,7 +31038,6 @@ MONDO:0024335 MONDO:0005885 False retrobulbar neuritis optic neuritis UNSUPPORTE MONDO:0024340 MONDO:0021231 False retinal neuroblastoma retina neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0024343 MONDO:0006547 False pityriasis simplex exanthem UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0024344 MONDO:0006547 False pityriasis folliculorum exanthem UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0024345 MONDO:0006547 False pityriasis streptogenes exanthem UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0024346 MONDO:0006547 False pityriasis amiantacea exanthem UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0024349 MONDO:0006547 False pityriasis alba exanthem UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0024350 MONDO:0006547 False pityriasis steatoides exanthem UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -31181,7 +31134,7 @@ MONDO:0024539 MONDO:0100441 False choroidal dystrophy, central areolar, 1 GUCY2D MONDO:0024545 MONDO:0016145 False Miyoshi muscular dystrophy 1 qualitative or quantitative defects of dysferlin UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0024551 MONDO:0020605 False X-linked lymphoproliferative disease due to SH2D1A deficiency X-linked recessive disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0024561 MONDO:0011979 False vitelliform macular dystrophy 3 adult-onset foveomacular vitelliform dystrophy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0024563 MONDO:0015979 False herpes simplex encephalitis, susceptibility to, 1 hereditary predisposition to infections UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0024563 MONDO:0020573 False herpes simplex encephalitis, susceptibility to, 1 inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0024566 MONDO:0100545 False febrile seizures, familial, 11 hereditary neurological disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0024569 MONDO:0014720 False optic atrophy 8 autosomal dominant optic atrophy plus syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:0024570 MONDO:0015027 False hyperparathyroidism 4 familial isolated hyperparathyroidism UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -31369,15 +31322,15 @@ MONDO:0025385 MONDO:0700095 False bluetongue Reoviridae infectious disease, non- MONDO:0025389 MONDO:0024913 False brucellosis, bovine cattle disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025389 MONDO:0700050 False brucellosis, bovine bacterial infectious disease, non-human animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025397 MONDO:0024919 False canine distemper dog disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0025397 MONDO:0700049 False canine distemper infectious disease, non-human animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0025397 MONDO:0700053 False canine distemper viral infectious disease, non-human animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025404 MONDO:0025113 False coronaviral enteritis of turkeys poultry disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0025404 MONDO:0700049 False coronaviral enteritis of turkeys infectious disease, non-human animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0025404 MONDO:0700053 False coronaviral enteritis of turkeys viral infectious disease, non-human animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025412 MONDO:0024912 False feline panleukopenia cat disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025412 MONDO:0700206 False feline panleukopenia Parvoviridae infectious disease, non-human animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025417 MONDO:0024905 False fowlpox bird disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025419 MONDO:0024934 False furunculosis fish disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025420 MONDO:0024990 False gastroenteritis, transmissible, of swine swine disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0025420 MONDO:0700049 False gastroenteritis, transmissible, of swine infectious disease, non-human animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0025420 MONDO:0700053 False gastroenteritis, transmissible, of swine viral infectious disease, non-human animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025425 MONDO:0024919 False hepatitis, infectious canine dog disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025425 MONDO:0025085 False hepatitis, infectious canine hepatitis, viral, animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025431 MONDO:0024913 False keratoconjunctivitis, infectious cattle disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -31396,7 +31349,7 @@ MONDO:0025483 MONDO:0700098 False mammary neoplasms, animal neoplasm, non-human MONDO:0025484 MONDO:0025102 False simian acquired immunodeficiency syndrome monkey disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025484 MONDO:0700106 False simian acquired immunodeficiency syndrome immune system disorder, non-human animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025485 MONDO:0024912 False feline acquired immunodeficiency syndrome cat disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0025485 MONDO:0700049 False feline acquired immunodeficiency syndrome infectious disease, non-human animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0025485 MONDO:0700053 False feline acquired immunodeficiency syndrome viral infectious disease, non-human animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025485 MONDO:0700106 False feline acquired immunodeficiency syndrome immune system disorder, non-human animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025487 MONDO:0024981 False murine acquired immunodeficiency syndrome rodent disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025487 MONDO:0700106 False murine acquired immunodeficiency syndrome immune system disorder, non-human animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -31404,12 +31357,12 @@ MONDO:0025488 MONDO:0700100 False leukemia, feline leukemia, non-human animal UN MONDO:0025488 MONDO:0700175 False leukemia, feline feline neoplasm UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025489 MONDO:0700135 False enzootic bovine leukosis bovine leukemia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025491 MONDO:0024912 False feline infectious peritonitis cat disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0025491 MONDO:0700049 False feline infectious peritonitis infectious disease, non-human animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0025491 MONDO:0700053 False feline infectious peritonitis viral infectious disease, non-human animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025494 MONDO:0024990 False porcine reproductive and respiratory syndrome swine disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0025494 MONDO:0700049 False porcine reproductive and respiratory syndrome infectious disease, non-human animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0025494 MONDO:0700053 False porcine reproductive and respiratory syndrome viral infectious disease, non-human animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025505 MONDO:0700206 False mink viral enteritis Parvoviridae infectious disease, non-human animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025506 MONDO:0024990 False porcine postweaning multisystemic wasting syndrome swine disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0025506 MONDO:0700049 False porcine postweaning multisystemic wasting syndrome infectious disease, non-human animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0025506 MONDO:0700053 False porcine postweaning multisystemic wasting syndrome viral infectious disease, non-human animal UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025513 MONDO:0005492 False autoimmune urticaria urticaria UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025513 MONDO:0007179 False autoimmune urticaria autoimmune disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0025514 MONDO:0005093 False livedoid vasculopathy skin disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS @@ -31748,6 +31701,7 @@ MONDO:0032938 MONDO:0700007 False basal ganglia calcification, idiopathic, 8, au MONDO:0032939 MONDO:0015802 False intellectual developmental disorder, autosomal dominant 63, with macrocephaly autosomal dominant non-syndromic intellectual disability UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0032942 MONDO:0100500 False neurodevelopmental disorder with microcephaly and dysmorphic facies Mendelian neurodevelopmental disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0032943 MONDO:0100500 False neurodevelopmental disorder with relative macrocephaly and with or without cardiac or endocrine anomalies Mendelian neurodevelopmental disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0033123 MONDO:0100571 False exudative vitreoretinopathy 7 CTNNB1-related neurodevelopmental disorder and/or vitreoretinopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0033169 MONDO:0029000 False curariform drugs toxicity poisoning UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0033170 MONDO:0029000 False statin toxicity poisoning UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0033181 MONDO:0029000 False phenytoin or carbamazepine toxicity poisoning UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -31819,7 +31773,7 @@ MONDO:0033926 MONDO:0005351 False prepubertal anorexia nervosa anorexia nervosa MONDO:0033938 MONDO:0002254 False acute radiation syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0033938 MONDO:0020683 False acute radiation syndrome acute disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0033954 MONDO:0002254 False monoclonal mast cell activation syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0033954 MONDO:0005046 False monoclonal mast cell activation syndrome immune system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0033954 MONDO:0100004 False monoclonal mast cell activation syndrome mast cell activation syndrome UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0033968 MONDO:0006025 False immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections-lymphopenia syndrome autosomal recessive disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0034041 MONDO:0002320 False congenital axonal neuropathy with encephalopathy congenital nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0034041 MONDO:0004183 False congenital axonal neuropathy with encephalopathy axonal neuropathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -32501,9 +32455,6 @@ MONDO:0044742 MONDO:0007239 False autosomal recessive epidermolytic ichthyosis e MONDO:0044744 MONDO:0001531 False prekallikrein deficiency blood coagulation disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0044745 MONDO:0005071 False nervous system injury nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0044745 MONDO:0021178 False nervous system injury injury UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0044749 MONDO:0000425 False X-linked congenital stationary night blindness X-linked disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0044749 MONDO:0002320 False X-linked congenital stationary night blindness congenital nervous system disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0044749 MONDO:0016293 False X-linked congenital stationary night blindness congenital stationary night blindness UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0044750 MONDO:0005650 False lassa virus infectious disease Arenaviridae infectious disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0044751 MONDO:0001673 False chronic diarrheal disease diarrheal disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0044753 MONDO:0005965 False lumbar spinal stenosis spinal stenosis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -32651,7 +32602,6 @@ MONDO:0060507 MONDO:0003847 False retinal dystrophy with or without macular stap MONDO:0060510 MONDO:0003847 False Cohen-Gibson syndrome hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0060527 MONDO:0003847 False maleylacetoacetate isomerase deficiency hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0060532 MONDO:0003847 False congenital heart defects and skeletal malformations syndrome hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0060533 MONDO:0003847 False microcephaly, short stature, and limb abnormalities hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0060550 MONDO:0019673 False polydactyly, postaxial, type a7 postaxial polydactyly type A UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0060551 MONDO:0003847 False cerebellar atrophy, developmental delay, and seizures hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0060556 MONDO:0002254 False joint laxity, short stature, and myopia syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -33178,7 +33128,6 @@ MONDO:0859083 MONDO:0007915 False systemic lupus erythematosus 17 systemic lupus MONDO:0859085 MONDO:0700092 False neurodevelopmental disorder with gait disturbance, dysmorphic facies, and behavioral abnormalities, X-linked neurodevelopmental disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0859136 MONDO:0700092 False Alzahrani-Kuwahara syndrome neurodevelopmental disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0859137 MONDO:0700092 False neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia neurodevelopmental disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0859139 MONDO:0003847 False blepharophimosis-impaired intellectual development syndrome hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0859141 MONDO:0700092 False neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia neurodevelopmental disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0859142 MONDO:0700092 False Hiatt-Neu-Cooper neurodevelopmental syndrome neurodevelopmental disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0859143 MONDO:0003847 False Radio-Tartaglia syndrome hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -33391,6 +33340,7 @@ MONDO:0957400 MONDO:0003847 False cataracts, hearing impairment, nephrotic syndr MONDO:0957403 MONDO:0015137 False periodic fever syndrome of childhood periodic fever syndrome UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0957405 MONDO:0019751 False granulomatous autoinflammatory syndrome of childhood autoinflammatory syndrome UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0957408 MONDO:0700264 False type 1 interferonopathy of childhood type 1 interferonopathy UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0957421 MONDO:0005856 False borna virus encephalitis Mononegavirales infectious disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0957423 MONDO:0021156 False immunotherapy induced hypophysitis hypophysitis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0957427 MONDO:0004947 False B-lymphoblastic leukemia/lymphoma with t(7;9)(q11.2;p13.2) B-cell acute lymphoblastic leukemia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0957428 MONDO:0004947 False B-lymphoblastic leukemia/lymphoma with t(17;19) B-cell acute lymphoblastic leukemia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING @@ -33513,10 +33463,14 @@ MONDO:0958342 MONDO:0002135 False isolated optic nerve aplasia optic nerve disor MONDO:0958346 MONDO:0958260 False isolated transitional filum lipoma dysraphic spinal cord lipoma UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0958347 MONDO:0958260 False isolated filum lipoma dysraphic spinal cord lipoma UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0968945 MONDO:0100500 False neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder Mendelian neurodevelopmental disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING -MONDO:0968946 MONDO:0100062 False developmental and epileptic encephalopathy 115 developmental and epileptic encephalopathy UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING MONDO:0968947 MONDO:0100500 False neurodevelopmental disorder plus optic atrophy Mendelian neurodevelopmental disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0968949 MONDO:0019272 False palmoplantar keratoderma, epidermolytic hereditary palmoplantar keratoderma UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:0968951 MONDO:0009071 False hypouricemia, renal hereditary renal hypouricemia UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0968976 MONDO:0700092 False neurodevelopmental disorder with progressive movement abnormalities neurodevelopmental disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0968977 MONDO:0008947 False basal ganglia calcification, idiopathic, 9, autosomal recessive bilateral striopallidodentate calcinosis UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING +MONDO:0968978 MONDO:0002254 False aplasia cutis-enamel dysplasia syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0968979 MONDO:0700092 False neurodevelopmental disorder with hypotonia and seizures neurodevelopmental disorder UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING +MONDO:0968982 MONDO:0003847 False autoinflammation with episodic fever and immune dysregulation hereditary disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:1030001 MONDO:0020573 False epilepsy, juvenile absence, susceptibility to inherited disease susceptibility UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING MONDO:8000010 MONDO:0002254 False antiphospholipid syndrome syndromic disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-SUBCLASS MONDO:8000014 MONDO:0000426 False familial antiphospholipid syndrome autosomal dominant disease UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING UNSUPPORTED-MISSING diff --git a/src/ontology/slurp/doid.tsv b/src/ontology/slurp/doid.tsv index 02d8b4f2..9a34e2aa 100644 --- a/src/ontology/slurp/doid.tsv +++ b/src/ontology/slurp/doid.tsv @@ -1,58 +1,10 @@ mondo_id mondo_label xref xref_source original_label definition parents ID LABEL A oboInOwl:hasDbXref >A oboInOwl:source SPLIT=| A IAO:0000115 SC % MONDO:0958281 mitochondrial complex v (atp synthase) deficiency nuclear type 4 DOID:0060333 MONDO:equivalentTo mitochondrial complex V (ATP synthase) deficiency nuclear type 4 MONDO:0014471 -MONDO:0958282 dystonia 28, childhood-onset DOID:0060936 MONDO:equivalentTo dystonia 28, childhood-onset MONDO:0003441|MONDO:0000426 -MONDO:0958283 dystonia 30 DOID:0060937 MONDO:equivalentTo dystonia 30 MONDO:0003441|MONDO:0000426 -MONDO:0958284 dystonia 31 DOID:0060938 MONDO:equivalentTo dystonia 31 MONDO:0003441|MONDO:0006025 -MONDO:0958285 dystonia 32 DOID:0060939 MONDO:equivalentTo dystonia 32 MONDO:0003441|MONDO:0006025 -MONDO:0958286 dystonia 33 DOID:0060940 MONDO:equivalentTo dystonia 33 MONDO:0003441|MONDO:0006025|MONDO:0000426 -MONDO:0958287 ullrich congenital muscular dystrophy 2 DOID:0060944 MONDO:equivalentTo Ullrich congenital muscular dystrophy 2 MONDO:0000355 -MONDO:0958288 dystonia 35, childhood-onset DOID:0060955 MONDO:equivalentTo dystonia 35, childhood-onset MONDO:0003441|MONDO:0006025 -MONDO:0958289 dystonia 37, early-onset with striatal lesions DOID:0060956 MONDO:equivalentTo dystonia 37, early-onset with striatal lesions MONDO:0003441|MONDO:0006025 -MONDO:0958290 myoclonic dystonia 34 DOID:0060957 MONDO:equivalentTo myoclonic dystonia 34 MONDO:0003441|MONDO:0000426 -MONDO:0958291 dystonia, dopa-responsive DOID:0060963 MONDO:equivalentTo dystonia, DOPA-responsive MONDO:0006025|MONDO:0003441|MONDO:0000426 -MONDO:0958292 dystonia 22, juvenile-onset DOID:0060966 MONDO:equivalentTo dystonia 22, juvenile-onset MONDO:0003441|MONDO:0006025 -MONDO:0958293 dystonia 22, adult-onset DOID:0060967 MONDO:equivalentTo dystonia 22, adult-onset MONDO:0003441|MONDO:0006025 -MONDO:0958294 halperin-birk syndrome DOID:0070539 MONDO:equivalentTo Halperin-Birk syndrome MONDO:0006025|MONDO:0002254 -MONDO:0958295 bcor itd sarcoma DOID:0081403 MONDO:equivalentTo BCOR ITD sarcoma A sarcoma with BCOR genetic alterations that is characterized by the presence of BCOR internal tandem duplication. MONDO:0958159 -MONDO:0958296 bcor-ccnb3 sarcoma DOID:0081404 MONDO:equivalentTo BCOR-CCNB3 sarcoma A sarcoma with BCOR genetic alterations that is characterized by the presence of BCOR-CCNB3 fusion gene. MONDO:0958159 -MONDO:0958297 childhood sarcoma with bcor genetic alterations DOID:0081405 MONDO:equivalentTo childhood sarcoma with BCOR genetic alterations A sarcoma with BCOR genetic alterations that occurs during childhood. MONDO:0958159 -MONDO:0958298 childhood round cell sarcoma with ewsr1-non-ets fusion DOID:0081407 MONDO:equivalentTo childhood round cell sarcoma with EWSR1-non-ETS fusion A round cell sarcoma with EWSR1-non-ETS fusion that is characterized by EWSR1-non-ETS fusion that occurs during childhood. MONDO:0958160 -MONDO:0958299 round cell sarcoma with ewsr1-nfatc2 gene fusion DOID:0081408 MONDO:equivalentTo round cell sarcoma with EWSR1-NFATC2 gene fusion A round cell sarcoma with EWSR1-non-ETS fusion that is characterized by the presence of EWSR1-NFATC2 gene fusion. MONDO:0958160 -MONDO:0958300 round cell sarcoma with ewsr1-patz1 gene fusion DOID:0081409 MONDO:equivalentTo round cell sarcoma with EWSR1-PATZ1 gene fusion A round cell sarcoma with EWSR1-non-ETS fusion that is characterized by the presence of EWSR1-PATZ1 gene fusion. MONDO:0958160 -MONDO:0958301 round cell sarcoma with fus-nfatc2 gene fusion DOID:0081410 MONDO:equivalentTo round cell sarcoma with FUS-NFATC2 gene fusion A round cell sarcoma with EWSR1-non-ETS fusion that is characterized by the presence of FUS-NFATC2 gene fusion. MONDO:0958160 -MONDO:0958302 tfeb-rearranged renal cell carcinoma DOID:0081414 MONDO:equivalentTo TFEB-rearranged renal cell carcinoma A renal cell carcinoma with MiT translocations that is characterized by the presence of the chromosomal translocation t(6;11) which fuses the TFEB transcription factor gene, located on chromosome 6, with the MALAT1 gene, located on chromosome 11. MONDO:0017886 -MONDO:0958303 childhood renal cell carcinoma with mit translocations DOID:0081416 MONDO:equivalentTo childhood renal cell carcinoma with MiT translocations A renal cell carcinoma with MiT translocations that is characterized by a TFE3 or TFEB-rearranged renal cell carcinoma that occurs during childhood. MONDO:0017886 -MONDO:0958304 microcephaly, short stature, and limb abnormalities DOID:0081431 MONDO:equivalentTo microcephaly, short stature, and limb abnormalities An osteochondrodysplasia that is characterized by intrauterine growth retardation, microcephaly, variable short stature, and limb abnormalities mainly affecting the upper limb and radial ray and that has_material_basis_in homozygous or compound heterozygous mutation in the DONSON gene on chromosome 21q22. Biallelic mutation in the DONSON gene can also cause microcephaly-micromelia syndrome, a more severe disorder that usually results in intrauterine or perinatal death. MONDO:0005516|MONDO:0006025 -MONDO:0958305 microcephaly-micromelia syndrome DOID:0081432 MONDO:equivalentTo microcephaly-micromelia syndrome A syndrome that is characterized by intrauterine growth retardation (IUGR), marked microcephaly, craniosynostosis, and severe malformation of the limbs, especially the arms and that has_material_basis_in homozygous mutation in the DONSON gene on chromosome 21q22. Biallelic mutation in the DONSON gene can also cause microcephaly, short stature, and limb abnormalities, a less severe disorder. MONDO:0002254 -MONDO:0958306 peroxisome biogenesis disorder 4b DOID:0081433 MONDO:equivalentTo Peroxisome biogenesis disorder 4B MONDO:0019234|MONDO:0006025|MONDO:0000426 -MONDO:0958307 peroxisome biogenesis disorder 5b DOID:0081434 MONDO:equivalentTo Peroxisome biogenesis disorder 5B MONDO:0019234|MONDO:0006025 -MONDO:0958308 peroxisome biogenesis disorder 6b DOID:0081435 MONDO:equivalentTo Peroxisome biogenesis disorder 6B MONDO:0019234|MONDO:0006025 -MONDO:0958309 peroxisome biogenesis disorder 7b DOID:0081436 MONDO:equivalentTo Peroxisome biogenesis disorder 7B MONDO:0019234|MONDO:0006025 -MONDO:0958310 peroxisome biogenesis disorder 8b DOID:0081437 MONDO:equivalentTo Peroxisome biogenesis disorder 8B MONDO:0019234|MONDO:0006025 -MONDO:0958311 peroxisome biogenesis disorder 9b DOID:0081438 MONDO:equivalentTo Peroxisome biogenesis disorder 9B MONDO:0019234|MONDO:0006025 -MONDO:0958312 peroxisome biogenesis disorder 11b DOID:0081439 MONDO:equivalentTo Peroxisome biogenesis disorder 11B MONDO:0019234|MONDO:0006025 -MONDO:0958313 peroxisome biogenesis disorder 10b DOID:0081440 MONDO:equivalentTo Peroxisome biogenesis disorder 10B MONDO:0019234|MONDO:0006025 -MONDO:0958314 nicolaides-baraitser syndrome DOID:0081441 MONDO:equivalentTo Nicolaides-Baraitser syndrome A syndrome that is characterized by severely impaired intellectual development, early-onset seizures, short stature, dysmorphic facial features, and sparse hair and that has_material_basis_in heterozygous mutation in the SMARCA2 gene on chromosome 9p24. MONDO:0000426|MONDO:0002254 -MONDO:0958315 blepharophimosis-impaired intellectual development syndrome DOID:0081442 MONDO:equivalentTo blepharophimosis-impaired intellectual development syndrome A syndrome that is characterized by a distinct facial appearance with blepharophimosis and global development delay and that has_material_basis_in heterozygous mutation in the SMARCA2 gene on chromosome 9p24. MONDO:0002254|MONDO:0000426 -MONDO:0958316 stolerman neurodevelopmental syndrome DOID:0081443 MONDO:equivalentTo Stolerman neurodevelopmental syndrome A syndrome that is characterized by developmental delay, often with motor and speech delay, mildly impaired intellectual development (in most patients), learning difficulties, and behavioral abnormalities, including autism spectrum disorder and that has_material_basis_in heterozygous mutation in the KDM6B gene on chromosome 17p13. MONDO:0002254 -MONDO:0958317 neurodevelopmental disorder with poor growth and behavioral abnormalities DOID:0081444 MONDO:equivalentTo neurodevelopmental disorder with poor growth and behavioral abnormalities An autosomal recessive intellectual developmental disorder that is characterized by global developmental delay, moderately to severely impaired intellectual development, often with absent speech, and behavioral abnormalities, including hyperactivity, short attention span, and ADHD and that has_material_basis_in homozygous or compound heterozygous mutation in the ATP9A gene on chromosome 20q13. MONDO:0019502 MONDO:0958318 chronic inflammatory demyelinating polyneuritis DOID:2536 MONDO:equivalentTo chronic inflammatory demyelinating polyneuritis MONDO:0002336 MONDO:0958319 congenital kyphosis DOID:4668 MONDO:equivalentTo congenital kyphosis MONDO:0958320 postural kyphosis DOID:9373 MONDO:equivalentTo postural kyphosis MONDO:0958359 childhood spinal muscular atrophy DOID:0060160 MONDO:equivalentTo childhood spinal muscular atrophy MONDO:0001516 MONDO:0958360 cholesterol-ester transfer protein deficiency DOID:0111368 MONDO:equivalentTo cholesterol-ester transfer protein deficiency MONDO:0002525 -MONDO:0968961 interstitial lung disease 1 DOID:0060941 MONDO:equivalentTo interstitial lung disease 1 MONDO:0000426|MONDO:0015925|MONDO:0006025 -MONDO:0968962 ullrich congenital muscular dystrophy 1b DOID:0060942 MONDO:equivalentTo Ullrich congenital muscular dystrophy 1B MONDO:0000355 -MONDO:0968963 ullrich congenital muscular dystrophy 1c DOID:0060943 MONDO:equivalentTo Ullrich congenital muscular dystrophy 1C MONDO:0000355 -MONDO:0968964 amelogenesis imperfecta type 1k DOID:0060945 MONDO:equivalentTo amelogenesis imperfecta type 1K MONDO:0019507 -MONDO:0968965 ullrich congenital muscular dystrophy 1a DOID:0060946 MONDO:equivalentTo Ullrich congenital muscular dystrophy 1A An Ullrich congenital muscular dystrophy characterized by generalized muscle weakness and striking hypermobility of distal joints in conjunction with variable contractures of more proximal joints and normal intelligence that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the COL6A1 gene on chromosome 21q22. MONDO:0000355 -MONDO:0968966 autosomal recessive intellectual developmental disorder 82 DOID:0060947 MONDO:equivalentTo autosomal recessive intellectual developmental disorder 82 An autosomal recessive intellectual developmental disorder characterized by global developmental delay with motor and speech delay, variably impaired intellectual development, and behavioral abnormalities has_material_basis_in homozygous mutation in the NSUN6 gene on chromosome 10p12. MONDO:0019502 -MONDO:0968967 sickle cell disease DOID:0081445 MONDO:equivalentTo sickle cell disease A blood protein disease that is characterized by chronic hemolytic anemia and intermittent vaso-occlusive events that result in tissue ischemia leading to acute and chronic pain as well as organ damage that can affect any organ system, resulting from the replacement of one of the beta-globin subunits in hemoglobin with atypical hemoglobin molecules called hemoglobin S which can distort red blood cells into a sickle or crescent shape. Sickle cell disease subtypes should include a detailed genotypic description for the hemoglobin molecules (e.g., Hb S/S, Hb S/C, Hb S/β0-thalassemia). MONDO:0003804 -MONDO:0968968 dimethylglycine dehydrogenase deficiency DOID:0081446 MONDO:equivalentTo dimethylglycine dehydrogenase deficiency An amino acid metabolic disorder that is characterized by a fish-like odor, chronic fatigue, and increased level of the muscle form of creatine kinase in serum and that has_material_basis_in homozygous mutation in the DMGDH on chromosome 5q14. MONDO:0004736|MONDO:0006025 -MONDO:0968969 cone-rod dystrophy 21 DOID:0081447 MONDO:equivalentTo cone-rod dystrophy 21 A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the DRAM2 gene on chromosome 1p13. MONDO:0006025|MONDO:0015993 -MONDO:0968970 cone-rod dystrophy 22 DOID:0081448 MONDO:equivalentTo cone-rod dystrophy 22 A cone-rod dystrophy that is characterized by loss of central vision due to cone photoreceptor degeneration, with onset of symptoms ranging from the first to fifth decades of life and that has_material_basis_in homozygous mutation in the TLCD3B gene on chromosome 16p11. MONDO:0006025|MONDO:0015993 -MONDO:0968971 cone-rod dystrophy 24 DOID:0081449 MONDO:equivalentTo cone-rod dystrophy 24 A cone-rod dystrophy that is characterized by night blindness, defective color vision, and reduced visual acuity and that has_material_basis_in heterozygous mutation in the UNC119 gene on chromosome 17q11. MONDO:0000426|MONDO:0015993 -MONDO:0968972 hyperimmunoglobulinemia d periodic fever syndrome DOID:0081450 MONDO:equivalentTo hyperimmunoglobulinemia D periodic fever syndrome A hyperimmunoglobulin syndrome that is characterized as periodic fever from early infancy accompanied by elevated serum C-reactive protein and that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding mevalonate kinase (MVK) on chromosome 12q24. MONDO:0002468 -MONDO:0968973 pfapa syndrome DOID:0081451 MONDO:equivalentTo PFAPA syndrome An autoimmune disease that is characterized by recurrent febrile episodes associated with aphthous stomatitis, pharyngitis and cervical adenitis. MONDO:0007179 -MONDO:0968974 large b-cell lymphoma DOID:0081452 MONDO:equivalentTo large B-cell lymphoma A B-cell lymphoma that is characterized by large lymphoid cells of the B-cell lineage that by definition form sheets or clusters. MONDO:0004095 +MONDO:0968993 aleutian mink disease DOID:2934 MONDO:equivalentTo aleutian mink disease MONDO:0005108 +MONDO:0968994 borna disease DOID:5154 MONDO:equivalentTo borna disease MONDO:0005108|MONDO:0002602 diff --git a/src/ontology/slurp/ncit.tsv b/src/ontology/slurp/ncit.tsv index 15427860..f15ec2da 100644 --- a/src/ontology/slurp/ncit.tsv +++ b/src/ontology/slurp/ncit.tsv @@ -1,6 +1,5 @@ mondo_id mondo_label xref xref_source original_label definition parents ID LABEL A oboInOwl:hasDbXref >A oboInOwl:source SPLIT=| A IAO:0000115 SC % -MONDO:0853205 conjunctival melanocytic intraepithelial neoplasia NCIT:C100054 MONDO:equivalentTo Conjunctival Melanocytic Intraepithelial Neoplasia MONDO:0020204 MONDO:0853241 primary central nervous system neoplasm NCIT:C102871 MONDO:equivalentTo Primary Central Nervous System Neoplasm MONDO:0006130 MONDO:0853254 adrenal cortical carcinoma by ensat stage NCIT:C104030 MONDO:equivalentTo Adrenal Cortical Carcinoma by ENSAT Stage MONDO:0006639 MONDO:0853255 ovarian high grade serous adenocarcinoma NCIT:C105555 MONDO:equivalentTo Ovarian High Grade Serous Adenocarcinoma MONDO:0005211 @@ -49,8 +48,6 @@ MONDO:0853501 intermediate chondrogenic neoplasm NCIT:C121846 MONDO:equivalentTo MONDO:0853502 chondrosarcoma, grade 2 NCIT:C121870 MONDO:equivalentTo Chondrosarcoma, Grade 2 MONDO:0008977 MONDO:0853503 chondrosarcoma, grade 3 NCIT:C121871 MONDO:equivalentTo Chondrosarcoma, Grade 3 MONDO:0008977 MONDO:0853504 benign notochordal cell tumor NCIT:C121901 MONDO:equivalentTo Benign Notochordal Cell Tumor MONDO:0002597|MONDO:0000631 -MONDO:0853505 ivory exostosis NCIT:C121923 MONDO:equivalentTo Ivory Exostosis MONDO:0005166 -MONDO:0853506 enostosis NCIT:C121924 MONDO:equivalentTo Enostosis MONDO:0005166 MONDO:0853507 intermediate osteogenic neoplasm NCIT:C121925 MONDO:equivalentTo Intermediate Osteogenic Neoplasm MONDO:0045053 MONDO:0853508 intermediate bone neoplasm NCIT:C121926 MONDO:equivalentTo Intermediate Bone Neoplasm MONDO:0019060 MONDO:0853510 primary bone non-hodgkin lymphoma NCIT:C121930 MONDO:equivalentTo Primary Bone Non-Hodgkin Lymphoma MONDO:0017814|MONDO:0018908 @@ -89,7 +86,6 @@ MONDO:0853738 fallopian tube lymphoma NCIT:C126464 MONDO:equivalentTo Fallopian MONDO:0853742 broad ligament serous adenocarcinoma NCIT:C126479 MONDO:equivalentTo Broad Ligament Serous Adenocarcinoma MONDO:0002741|MONDO:0005278 MONDO:0853743 oropharyngeal poorly differentiated carcinoma NCIT:C126750 MONDO:equivalentTo Oropharyngeal Poorly Differentiated Carcinoma MONDO:0044704 MONDO:0853745 endometrial dedifferentiated carcinoma NCIT:C126769 MONDO:equivalentTo Endometrial Dedifferentiated Carcinoma MONDO:0002447 -MONDO:0853747 uterine corpus neuroendocrine tumor g1 NCIT:C126773 MONDO:equivalentTo Uterine Corpus Neuroendocrine Tumor G1 MONDO:0005369|MONDO:0021650 MONDO:0853748 uterine corpus hydropic leiomyoma NCIT:C126975 MONDO:equivalentTo Uterine Corpus Hydropic Leiomyoma MONDO:0007886 MONDO:0853749 uterine corpus high grade endometrial stromal sarcoma NCIT:C126998 MONDO:equivalentTo Uterine Corpus High Grade Endometrial Stromal Sarcoma MONDO:0002923 MONDO:0853751 benign uterine corpus pecoma NCIT:C127071 MONDO:equivalentTo Benign Uterine Corpus PEComa MONDO:0004221|MONDO:0021525|MONDO:0020581 @@ -101,9 +97,8 @@ MONDO:0853776 ovarian cancer by ajcc v6 and v7 stage NCIT:C128106 MONDO:equivale MONDO:0853779 vaginal germ cell tumor NCIT:C128112 MONDO:equivalentTo Vaginal Germ Cell Tumor MONDO:0005040|MONDO:0021050 MONDO:0853781 vulvar squamous intraepithelial lesion, hpv-associated NCIT:C128142 MONDO:equivalentTo Vulvar Squamous Intraepithelial Lesion, HPV-Associated MONDO:0005198 MONDO:0853784 vulvar adenocarcinoma of mammary gland type NCIT:C128162 MONDO:equivalentTo Vulvar Adenocarcinoma of Mammary Gland Type MONDO:0024336 -MONDO:0853787 vulvar adenocarcinoma, intestinal-type NCIT:C128166 MONDO:equivalentTo Vulvar Adenocarcinoma, Intestinal-Type MONDO:0024336|MONDO:0006254|MONDO:0004957 +MONDO:0853787 vulvar mucinous adenocarcinoma, intestinal-type NCIT:C128166 MONDO:equivalentTo Vulvar Mucinous Adenocarcinoma, Intestinal-Type MONDO:0024336|MONDO:0006254|MONDO:0004957 MONDO:0853788 vulvar keratoacanthoma NCIT:C128167 MONDO:equivalentTo Vulvar Keratoacanthoma MONDO:0024609|MONDO:0002527 -MONDO:0853793 vulvar merkel cell carcinoma NCIT:C128247 MONDO:equivalentTo Vulvar Merkel Cell Carcinoma MONDO:0019210|MONDO:0056816 MONDO:0853797 vulvar germ cell tumor NCIT:C128294 MONDO:equivalentTo Vulvar Germ Cell Tumor MONDO:0005040|MONDO:0021049 MONDO:0853835 b acute lymphoblastic leukemia, philadelphia chromosome negative NCIT:C128629 MONDO:equivalentTo B Acute Lymphoblastic Leukemia, Philadelphia Chromosome Negative MONDO:0020511 MONDO:0853837 nk-cell lymphoma, unclassifiable NCIT:C128697 MONDO:equivalentTo NK-Cell Lymphoma, Unclassifiable MONDO:0000430 @@ -198,9 +193,6 @@ MONDO:0854066 lung non-keratinizing squamous cell carcinoma NCIT:C136714 MONDO:e MONDO:0854067 lung non-mucinous adenocarcinoma in situ NCIT:C136716 MONDO:equivalentTo Lung Non-Mucinous Adenocarcinoma In Situ MONDO:0000503 MONDO:0854068 lung mucinous adenocarcinoma in situ NCIT:C136717 MONDO:equivalentTo Lung Mucinous Adenocarcinoma In Situ MONDO:0000503 MONDO:0854069 lung squamous cell carcinoma in situ NCIT:C136719 MONDO:equivalentTo Lung Squamous Cell Carcinoma In Situ MONDO:0005097|MONDO:0004693 -MONDO:0854071 atypical spitz nevus NCIT:C136825 MONDO:equivalentTo Atypical Spitz Nevus MONDO:0005073|MONDO:0021583 -MONDO:0854072 merkel cell carcinoma by ajcc v7 stage NCIT:C136869 MONDO:equivalentTo Merkel Cell Carcinoma by AJCC v7 Stage MONDO:0019210 -MONDO:0854073 merkel cell carcinoma by ajcc v8 stage NCIT:C136870 MONDO:equivalentTo Merkel Cell Carcinoma by AJCC v8 Stage MONDO:0019210 MONDO:0854075 cutaneous melanoma by ajcc v8 stage NCIT:C137645 MONDO:equivalentTo Cutaneous Melanoma by AJCC v8 Stage MONDO:0005012 MONDO:0854076 occult breast carcinoma NCIT:C137674 MONDO:equivalentTo Occult Breast Carcinoma MONDO:0004989 MONDO:0854077 breast pleomorphic lobular carcinoma in situ NCIT:C137839 MONDO:equivalentTo Breast Pleomorphic Lobular Carcinoma In Situ MONDO:0006270 @@ -273,7 +265,6 @@ MONDO:0854249 recurrent lymphoproliferative disorder NCIT:C147861 MONDO:equivale MONDO:0854250 oropharyngeal p16ink4a-negative squamous cell carcinoma NCIT:C147906 MONDO:equivalentTo Oropharyngeal p16INK4a-Negative Squamous Cell Carcinoma MONDO:0044704 MONDO:0854251 central nervous system b-cell non-hodgkin lymphoma NCIT:C147948 MONDO:equivalentTo Central Nervous System B-Cell Non-Hodgkin Lymphoma MONDO:0015759|MONDO:0044887 MONDO:0854253 refractory melanoma NCIT:C147983 MONDO:equivalentTo Refractory Melanoma MONDO:0036501|MONDO:0005105 -MONDO:0854257 unresectable craniopharyngioma NCIT:C148076 MONDO:equivalentTo Unresectable Craniopharyngioma MONDO:0018907 MONDO:0854268 refractory round cell liposarcoma NCIT:C148299 MONDO:equivalentTo Refractory Round Cell Liposarcoma MONDO:0005238 MONDO:0854269 metastatic round cell liposarcoma NCIT:C148300 MONDO:equivalentTo Metastatic Round Cell Liposarcoma MONDO:0005238 MONDO:0854270 refractory sarcoma NCIT:C148301 MONDO:equivalentTo Refractory Sarcoma MONDO:0005089|MONDO:0036501 @@ -334,8 +325,6 @@ MONDO:0854492 mixed gangliocytoma-pituitary neuroendocrine tumor NCIT:C155767 MO MONDO:0854495 ependymal pituicytoma NCIT:C155774 MONDO:equivalentTo Ependymal Pituicytoma MONDO:0003257 MONDO:0854496 sellar meningioma NCIT:C155776 MONDO:equivalentTo Sellar Meningioma MONDO:0002998|MONDO:0002720 MONDO:0854500 sellar solitary fibrous tumor NCIT:C155784 MONDO:equivalentTo Sellar Solitary Fibrous Tumor MONDO:0002720|MONDO:0003223 -MONDO:0854504 pituitary gland non-hodgkin lymphoma NCIT:C155796 MONDO:equivalentTo Pituitary Gland Non-Hodgkin Lymphoma MONDO:0002109|MONDO:0044887 -MONDO:0854506 sellar germ cell tumor NCIT:C155801 MONDO:equivalentTo Sellar Germ Cell Tumor MONDO:0003000|MONDO:0002720 MONDO:0854518 metastatic malignant pancreatic neoplasm NCIT:C155852 MONDO:equivalentTo Metastatic Malignant Pancreatic Neoplasm MONDO:0009831|MONDO:0024880 MONDO:0854521 chest wall sarcoma NCIT:C155873 MONDO:equivalentTo Chest Wall Sarcoma MONDO:0005089|MONDO:0021323 MONDO:0854523 unresectable desmoid fibromatosis NCIT:C155877 MONDO:equivalentTo Unresectable Desmoid Fibromatosis MONDO:0007608 @@ -346,7 +335,6 @@ MONDO:0854530 chromophobe renal cell carcinoma associated with birt-hogg-dube sy MONDO:0854531 uterine ligament papillary cystadenoma NCIT:C155952 MONDO:equivalentTo Uterine Ligament Papillary Cystadenoma MONDO:0021091|MONDO:0020582 MONDO:0854533 thyroid gland spindle cell follicular adenoma NCIT:C155957 MONDO:equivalentTo Thyroid Gland Spindle Cell Follicular Adenoma MONDO:0005032 MONDO:0854534 thyroid gland black follicular adenoma NCIT:C155958 MONDO:equivalentTo Thyroid Gland Black Follicular Adenoma MONDO:0005032 -MONDO:0854544 third ventricle pilocytic astrocytoma NCIT:C156037 MONDO:equivalentTo Third Ventricle Pilocytic Astrocytoma MONDO:0021631|MONDO:0016691 MONDO:0854545 hypothalamic-chiasmatic pilomyxoid astrocytoma NCIT:C156038 MONDO:equivalentTo Hypothalamic-Chiasmatic Pilomyxoid Astrocytoma MONDO:0016692 MONDO:0854546 fourth ventricle medulloblastoma NCIT:C156039 MONDO:equivalentTo Fourth Ventricle Medulloblastoma MONDO:0007959 MONDO:0854547 third ventricle germinoma NCIT:C156040 MONDO:equivalentTo Third Ventricle Germinoma MONDO:0002214 @@ -363,11 +351,7 @@ MONDO:0854599 bladder alveolar soft part sarcoma NCIT:C156277 MONDO:equivalentTo MONDO:0854600 cellular nerve sheath myxoma NCIT:C156278 MONDO:equivalentTo Cellular Nerve Sheath Myxoma MONDO:0006317 MONDO:0854601 colon liposarcoma NCIT:C156279 MONDO:equivalentTo Colon Liposarcoma MONDO:0003352|MONDO:0005060 MONDO:0854608 thyroid gland schwannoma NCIT:C156340 MONDO:equivalentTo Thyroid Gland Schwannoma MONDO:0004820|MONDO:0006107 -MONDO:0854609 thyroid gland malignant peripheral nerve sheath tumor NCIT:C156341 MONDO:equivalentTo Thyroid Gland Malignant Peripheral Nerve Sheath Tumor MONDO:0003028|MONDO:0017827 -MONDO:0854613 thyroid gland leiomyoma NCIT:C156346 MONDO:equivalentTo Thyroid Gland Leiomyoma MONDO:0006107|MONDO:0001572 -MONDO:0854614 thyroid gland leiomyosarcoma NCIT:C156347 MONDO:equivalentTo Thyroid Gland Leiomyosarcoma MONDO:0003028|MONDO:0005058 MONDO:0854616 thyroid gland solitary fibrous tumor NCIT:C156349 MONDO:equivalentTo Thyroid Gland Solitary Fibrous Tumor MONDO:0016238|MONDO:0015074 -MONDO:0854625 brain ependymoma NCIT:C156462 MONDO:equivalentTo Brain Ependymoma MONDO:0016698|MONDO:0021632 MONDO:0854631 metastatic neuroendocrine neoplasm NCIT:C156485 MONDO:equivalentTo Metastatic Neuroendocrine Neoplasm MONDO:0019496|MONDO:0024880 MONDO:0854639 malignant abdominal neoplasm NCIT:C156714 MONDO:equivalentTo Malignant Abdominal Neoplasm MONDO:0004992 MONDO:0854640 malignant pelvic neoplasm NCIT:C156715 MONDO:equivalentTo Malignant Pelvic Neoplasm MONDO:0004992 @@ -450,7 +434,7 @@ MONDO:0854911 metastatic malignant digestive system neoplasm NCIT:C162255 MONDO: MONDO:0854912 hypermutated colorectal carcinoma NCIT:C162256 MONDO:equivalentTo Hypermutated Colorectal Carcinoma MONDO:0024331 MONDO:0854925 thymic neuroendocrine neoplasm NCIT:C162460 MONDO:equivalentTo Thymic Neuroendocrine Neoplasm MONDO:0018079|MONDO:0019496 MONDO:0854927 intratubular large cell hyalinizing sertoli cell neoplasia NCIT:C162466 MONDO:equivalentTo Intratubular Large Cell Hyalinizing Sertoli Cell Neoplasia MONDO:0003125 -MONDO:0854928 primary diffuse large b-cell lymphoma of the testis NCIT:C162467 MONDO:equivalentTo Primary Diffuse Large B-Cell Lymphoma of the Testis MONDO:0018905|MONDO:0001472 +MONDO:0854928 testicular diffuse large b-cell lymphoma NCIT:C162467 MONDO:equivalentTo Testicular Diffuse Large B-Cell Lymphoma MONDO:0018905|MONDO:0001472 MONDO:0854929 testicular nasal type extranodal nk/t-cell lymphoma NCIT:C162468 MONDO:equivalentTo Testicular Nasal Type Extranodal NK/T-Cell Lymphoma MONDO:0001472|MONDO:0019472 MONDO:0854930 testicular myeloid sarcoma NCIT:C162469 MONDO:equivalentTo Testicular Myeloid Sarcoma MONDO:0005447|MONDO:0006861 MONDO:0854931 testicular plasmacytoma NCIT:C162470 MONDO:equivalentTo Testicular Plasmacytoma MONDO:0005447|MONDO:0002754 @@ -471,16 +455,14 @@ MONDO:0854984 refractory childhood malignant neoplasm NCIT:C162703 MONDO:equival MONDO:0854998 asph-positive head and neck squamous cell carcinoma NCIT:C162770 MONDO:equivalentTo ASPH-Positive Head and Neck Squamous Cell Carcinoma MONDO:0010150 MONDO:0855003 parapharyngeal neoplasm NCIT:C162820 MONDO:equivalentTo Parapharyngeal Neoplasm MONDO:0021351 MONDO:0855006 retropharyngeal neoplasm NCIT:C162825 MONDO:equivalentTo Retropharyngeal Neoplasm MONDO:0021351 -MONDO:0855011 digital papillary adenoma NCIT:C162848 MONDO:equivalentTo Digital Papillary Adenoma MONDO:0024247 MONDO:0855015 non-invasive cribriform carcinoma NCIT:C162973 MONDO:equivalentTo Non-Invasive Cribriform Carcinoma MONDO:0006176 MONDO:0855016 malignant brain glioma NCIT:C162993 MONDO:equivalentTo Malignant Brain Glioma MONDO:0100342|MONDO:0001657|MONDO:0021632 -MONDO:0855017 unresectable meningioma NCIT:C163006 MONDO:equivalentTo Unresectable Meningioma MONDO:0016642 MONDO:0855028 micropapillary carcinoma NCIT:C164144 MONDO:equivalentTo Micropapillary Carcinoma MONDO:0006509 MONDO:0855034 aggressive prostate adenocarcinoma NCIT:C164185 MONDO:equivalentTo Aggressive Prostate Adenocarcinoma MONDO:0005082 MONDO:0855035 head and neck sarcoma NCIT:C164198 MONDO:equivalentTo Head and Neck Sarcoma MONDO:0005089|MONDO:0005627 MONDO:0855040 warty carcinoma NCIT:C164248 MONDO:equivalentTo Warty Carcinoma MONDO:0002979 MONDO:0855041 differentiated intraepithelial neoplasia NCIT:C164249 MONDO:equivalentTo Differentiated Intraepithelial Neoplasia MONDO:0024474 -MONDO:0855042 human papillomavirus-negative squamous cell carcinoma NCIT:C164250 MONDO:equivalentTo Human Papillomavirus-Negative Squamous Cell Carcinoma MONDO:0005096 +MONDO:0855042 human papillomavirus-independent squamous cell carcinoma NCIT:C164250 MONDO:equivalentTo Human Papillomavirus-Independent Squamous Cell Carcinoma MONDO:0005096 MONDO:0855043 invasive sarcomatoid urothelial carcinoma NCIT:C164252 MONDO:equivalentTo Invasive Sarcomatoid Urothelial Carcinoma MONDO:0002837|MONDO:0040678 MONDO:0855044 mixed neuroendocrine non-neuroendocrine neoplasm NCIT:C164255 MONDO:equivalentTo Mixed Neuroendocrine Non-Neuroendocrine Neoplasm MONDO:0021043|MONDO:0005626 MONDO:0855047 nf1-associated malignant peripheral nerve sheath tumor NCIT:C164313 MONDO:equivalentTo NF1-Associated Malignant Peripheral Nerve Sheath Tumor MONDO:0017827 @@ -490,19 +472,14 @@ MONDO:0855058 soft tissue sarcoma of the trunk and extremities NCIT:C165190 MOND MONDO:0855059 metastatic malignant mesothelioma NCIT:C165252 MONDO:equivalentTo Metastatic Malignant Mesothelioma MONDO:0006292|MONDO:0024880 MONDO:0855079 skin verrucous carcinoma NCIT:C165465 MONDO:equivalentTo Skin Verrucous Carcinoma MONDO:0002529|MONDO:0006006 MONDO:0855080 skin squamous cell carcinoma with osteoclast-like giant cells NCIT:C165466 MONDO:equivalentTo Skin Squamous Cell Carcinoma with Osteoclast-Like Giant Cells MONDO:0002529 -MONDO:0855081 skin lymphoepithelioma-like carcinoma NCIT:C165467 MONDO:equivalentTo Skin Lymphoepithelioma-Like Carcinoma MONDO:0002529|MONDO:0003572 +MONDO:0855081 skin lymphoepithelial carcinoma NCIT:C165467 MONDO:equivalentTo Skin Lymphoepithelial Carcinoma MONDO:0002529|MONDO:0003572 MONDO:0855082 skin squamous cell carcinoma with sarcomatoid differentiation NCIT:C165468 MONDO:equivalentTo Skin Squamous Cell Carcinoma with Sarcomatoid Differentiation MONDO:0002529|MONDO:0002928 MONDO:0855085 lichen planus-like keratosis NCIT:C165485 MONDO:equivalentTo Lichen Planus-Like Keratosis MONDO:0002093 -MONDO:0855087 spitz melanoma NCIT:C165497 MONDO:equivalentTo Spitz Melanoma MONDO:0005012 -MONDO:0855088 pigmented epithelioid melanocytoma NCIT:C165498 MONDO:equivalentTo Pigmented Epithelioid Melanocytoma MONDO:0021583 -MONDO:0855092 bap1-inactivated skin melanocytic neoplasm NCIT:C165522 MONDO:equivalentTo BAP1-Inactivated Skin Melanocytic Neoplasm MONDO:0021583 MONDO:0855094 combined nevus NCIT:C165529 MONDO:equivalentTo Combined Nevus MONDO:0044794 MONDO:0855104 proximal gastric adenocarcinoma NCIT:C165628 MONDO:equivalentTo Proximal Gastric Adenocarcinoma MONDO:0005036 -MONDO:0855106 high-csd melanoma NCIT:C165659 MONDO:equivalentTo High-CSD Melanoma MONDO:0005012 MONDO:0855113 mixed carcinoma NCIT:C165723 MONDO:equivalentTo Mixed Carcinoma MONDO:0005853|MONDO:0004993 MONDO:0855116 hormone receptor-negative breast carcinoma NCIT:C165743 MONDO:equivalentTo Hormone Receptor-Negative Breast Carcinoma MONDO:0004988 MONDO:0855127 musculoskeletal neoplasm NCIT:C166354 MONDO:equivalentTo Musculoskeletal Neoplasm MONDO:0044334|MONDO:0002081 -MONDO:0855130 mucosal nodular melanoma NCIT:C166405 MONDO:equivalentTo Mucosal Nodular Melanoma MONDO:0000544 MONDO:0855132 pancreatobiliary carcinoma NCIT:C166418 MONDO:equivalentTo Pancreatobiliary Carcinoma MONDO:0006181 MONDO:0855139 acute myeloid leukemia with ram immunophenotype NCIT:C167089 MONDO:equivalentTo Acute Myeloid Leukemia with RAM Immunophenotype MONDO:0004996 MONDO:0855140 obesity-related malignant neoplasm NCIT:C167168 MONDO:equivalentTo Obesity-Related Malignant Neoplasm MONDO:0004992 @@ -549,7 +526,6 @@ MONDO:0855346 refractory myeloid neoplasm NCIT:C172281 MONDO:equivalentTo Refrac MONDO:0855368 skin ewing sarcoma NCIT:C172634 MONDO:equivalentTo Skin Ewing Sarcoma MONDO:0018270|MONDO:0006414 MONDO:0855377 oxyntic gland adenoma NCIT:C172655 MONDO:equivalentTo Oxyntic Gland Adenoma MONDO:0006221 MONDO:0855378 gastroblastoma NCIT:C172659 MONDO:equivalentTo Gastroblastoma MONDO:0001056 -MONDO:0855379 digestive system neuroendocrine tumor g3 NCIT:C172660 MONDO:equivalentTo Digestive System Neuroendocrine Tumor G3 MONDO:0000386 MONDO:0855386 colorectal conventional adenoma NCIT:C172680 MONDO:equivalentTo Colorectal Conventional Adenoma MONDO:0005484 MONDO:0855389 colorectal poorly cohesive adenocarcinoma NCIT:C172694 MONDO:equivalentTo Colorectal Poorly Cohesive Adenocarcinoma MONDO:0005008 MONDO:0855390 colorectal adenoma-like adenocarcinoma NCIT:C172699 MONDO:equivalentTo Colorectal Adenoma-Like Adenocarcinoma MONDO:0005008|MONDO:0003204 @@ -565,35 +541,24 @@ MONDO:0855408 pancreatic poorly cohesive adenocarcinoma NCIT:C172811 MONDO:equiv MONDO:0855409 pancreatic undifferentiated carcinoma with rhabdoid cells NCIT:C172812 MONDO:equivalentTo Pancreatic Undifferentiated Carcinoma with Rhabdoid Cells MONDO:0006478 MONDO:0855413 conventional follicular dendritic cell sarcoma NCIT:C172846 MONDO:equivalentTo Conventional Follicular Dendritic Cell Sarcoma MONDO:0005764 MONDO:0855418 digestive system soft tissue neoplasm NCIT:C172852 MONDO:equivalentTo Digestive System Soft Tissue Neoplasm MONDO:0006424|MONDO:0021223 -MONDO:0855432 sinonasal spindle cell squamous cell carcinoma NCIT:C173079 MONDO:equivalentTo Sinonasal Spindle Cell Squamous Cell Carcinoma MONDO:0044787|MONDO:0021663 +MONDO:0855432 sinonasal spindle cell squamous carcinoma NCIT:C173079 MONDO:equivalentTo Sinonasal Spindle Cell Squamous Carcinoma MONDO:0044787|MONDO:0021663 MONDO:0855433 sinonasal lymphoepithelial carcinoma NCIT:C173080 MONDO:equivalentTo Sinonasal Lymphoepithelial Carcinoma MONDO:0002831|MONDO:0003572 MONDO:0855435 head and neck nut carcinoma NCIT:C173087 MONDO:equivalentTo Head and Neck NUT Carcinoma MONDO:0005563|MONDO:0002038 MONDO:0855439 malignant sinonasal neoplasm NCIT:C173097 MONDO:equivalentTo Malignant Sinonasal Neoplasm MONDO:0056820|MONDO:0005627 -MONDO:0855449 sinonasal soft tissue neoplasm NCIT:C173117 MONDO:equivalentTo Sinonasal Soft Tissue Neoplasm MONDO:0056820|MONDO:0006424 MONDO:0855471 peritoneal implant NCIT:C173164 MONDO:equivalentTo Peritoneal Implant MONDO:0006901 MONDO:0855472 sinonasal ameloblastoma NCIT:C173166 MONDO:equivalentTo Sinonasal Ameloblastoma MONDO:0056820 MONDO:0855481 microsatellite stable colorectal carcinoma NCIT:C173324 MONDO:equivalentTo Microsatellite Stable Colorectal Carcinoma MONDO:0024331 MONDO:0855487 nasopharyngeal adenoid cystic carcinoma NCIT:C173340 MONDO:equivalentTo Nasopharyngeal Adenoid Cystic Carcinoma MONDO:0006367|MONDO:0015459 MONDO:0855489 ectopic pituitary neuroendocrine tumor NCIT:C173345 MONDO:equivalentTo Ectopic Pituitary Neuroendocrine Tumor MONDO:0006373 -MONDO:0855491 pharyngeal lymphoma NCIT:C173354 MONDO:equivalentTo Pharyngeal Lymphoma MONDO:0005517|MONDO:0017207 -MONDO:0855495 neuroendocrine carcinoma, excluding head and neck NCIT:C173385 MONDO:equivalentTo Neuroendocrine Carcinoma, Excluding Head and Neck MONDO:0002120 -MONDO:0855498 laryngeal soft tissue neoplasm NCIT:C173397 MONDO:equivalentTo Laryngeal Soft Tissue Neoplasm MONDO:0006424|MONDO:0021071 +MONDO:0855495 cutaneous merkel cell carcinoma NCIT:C173385 MONDO:equivalentTo Cutaneous Merkel Cell Carcinoma MONDO:0019210|MONDO:0002656 MONDO:0855506 laryngeal chondroma NCIT:C173406 MONDO:equivalentTo Laryngeal Chondroma MONDO:0002360|MONDO:0002354 MONDO:0855507 laryngeal chondrosarcoma NCIT:C173407 MONDO:equivalentTo Laryngeal Chondrosarcoma MONDO:0002448|MONDO:0008977 -MONDO:0855516 oral verruca vulgaris NCIT:C173475 MONDO:equivalentTo Oral Verruca Vulgaris MONDO:0001209 -MONDO:0855518 oral cavity soft tissue neoplasm NCIT:C173479 MONDO:equivalentTo Oral Cavity Soft Tissue Neoplasm MONDO:0021245|MONDO:0006424 -MONDO:0855523 head and neck histiocytic and dendritic cell neoplasm NCIT:C173485 MONDO:equivalentTo Head and Neck Histiocytic and Dendritic Cell Neoplasm MONDO:0006247|MONDO:0005586 MONDO:0855526 head and neck melanocytic neoplasm NCIT:C173488 MONDO:equivalentTo Head and Neck Melanocytic Neoplasm MONDO:0021143|MONDO:0005586 -MONDO:0855527 oral cavity myeloid sarcoma NCIT:C173489 MONDO:equivalentTo Oral Cavity Myeloid Sarcoma MONDO:0005515|MONDO:0006861 MONDO:0855532 refractory primitive neuroectodermal tumor NCIT:C173565 MONDO:equivalentTo Refractory Primitive Neuroectodermal Tumor MONDO:0005462|MONDO:0036501 MONDO:0855540 head and neck heterotopia-associated carcinoma NCIT:C173588 MONDO:equivalentTo Head and Neck Heterotopia-Associated Carcinoma MONDO:0002038 MONDO:0855551 salivary gland poorly differentiated carcinoma NCIT:C173649 MONDO:equivalentTo Salivary Gland Poorly Differentiated Carcinoma MONDO:0000521 MONDO:0855553 salivary gland lymphadenoma NCIT:C173659 MONDO:equivalentTo Salivary Gland Lymphadenoma MONDO:0021460 -MONDO:0855556 salivary gland hemangioma NCIT:C173680 MONDO:equivalentTo Salivary Gland Hemangioma MONDO:0021460|MONDO:0006500 -MONDO:0855557 salivary gland lipoma NCIT:C173681 MONDO:equivalentTo Salivary Gland Lipoma MONDO:0021460|MONDO:0005106 MONDO:0855558 sialolipoma NCIT:C173682 MONDO:equivalentTo Sialolipoma MONDO:0021460 -MONDO:0855561 salivary gland nodular fasciitis NCIT:C173687 MONDO:equivalentTo Salivary Gland Nodular Fasciitis MONDO:0021460|MONDO:0004187 -MONDO:0855563 salivary gland lymphoma NCIT:C173690 MONDO:equivalentTo Salivary Gland Lymphoma MONDO:0017207|MONDO:0004669 MONDO:0855575 appendix disorder NCIT:C173799 MONDO:equivalentTo Appendix Disorder MONDO:0855576 retroperitoneal undifferentiated pleomorphic sarcoma NCIT:C173808 MONDO:equivalentTo Retroperitoneal Undifferentiated Pleomorphic Sarcoma MONDO:0001501|MONDO:0002142 MONDO:0855577 lung alveolar soft part sarcoma NCIT:C173809 MONDO:equivalentTo Lung Alveolar Soft Part Sarcoma MONDO:0002426|MONDO:0011655 @@ -607,13 +572,13 @@ MONDO:0855616 conjunctival oncocytoma NCIT:C174388 MONDO:equivalentTo Conjunctiv MONDO:0855617 conjunctival keratoacanthoma NCIT:C174390 MONDO:equivalentTo Conjunctival Keratoacanthoma MONDO:0006173|MONDO:0002527 MONDO:0855618 conjunctival spindle cell carcinoma NCIT:C174398 MONDO:equivalentTo Conjunctival Spindle Cell Carcinoma MONDO:0006173|MONDO:0021663 MONDO:0855620 conjunctival carcinoma NCIT:C174403 MONDO:equivalentTo Conjunctival Carcinoma MONDO:0002466|MONDO:0003454 -MONDO:0855625 conjunctival subepithelial nevus NCIT:C174426 MONDO:equivalentTo Conjunctival Subepithelial Nevus MONDO:0006172 +MONDO:0855625 conjunctival subepithelial (stromal) nevus NCIT:C174426 MONDO:equivalentTo Conjunctival Subepithelial (Stromal) Nevus MONDO:0006172 MONDO:0855630 conjunctival blue nevus NCIT:C174452 MONDO:equivalentTo Conjunctival Blue Nevus MONDO:0006172 MONDO:0855631 atypical ewing sarcoma NCIT:C174456 MONDO:equivalentTo Atypical Ewing Sarcoma MONDO:0012817 MONDO:0855633 conjunctival spitz nevus NCIT:C174493 MONDO:equivalentTo Conjunctival Spitz Nevus MONDO:0006172 MONDO:0855634 metastatic malignant neoplasm in the conjunctiva NCIT:C174496 MONDO:equivalentTo Metastatic Malignant Neoplasm in the Conjunctiva MONDO:0044913|MONDO:0003454 MONDO:0855635 iris epithelioid cell melanoma NCIT:C174498 MONDO:equivalentTo Iris Epithelioid Cell Melanoma MONDO:0004064|MONDO:0006200 -MONDO:0855640 iris mixed cell melanoma NCIT:C174506 MONDO:equivalentTo Iris Mixed Cell Melanoma MONDO:0004064|MONDO:0003910 +MONDO:0855640 iris mixed epithelioid and spindle cell melanoma NCIT:C174506 MONDO:equivalentTo Iris Mixed Epithelioid and Spindle Cell Melanoma MONDO:0004064|MONDO:0003910 MONDO:0855641 metastatic malignant neoplasm in the uvea NCIT:C174507 MONDO:equivalentTo Metastatic Malignant Neoplasm in the Uvea MONDO:0002659|MONDO:0044913 MONDO:0855646 retinal astrocytoma NCIT:C174539 MONDO:equivalentTo Retinal Astrocytoma MONDO:0024649|MONDO:0021231 MONDO:0855649 adenoma of the retinal pigment epithelium NCIT:C174550 MONDO:equivalentTo Adenoma of the Retinal Pigment Epithelium MONDO:0021453|MONDO:0004972 @@ -632,7 +597,7 @@ MONDO:0855677 benign lacrimal system neoplasm NCIT:C175307 MONDO:equivalentTo Be MONDO:0855678 malignant lacrimal system neoplasm NCIT:C175308 MONDO:equivalentTo Malignant Lacrimal System Neoplasm MONDO:0002460|MONDO:0002236 MONDO:0855679 lacrimal drainage system neoplasm NCIT:C175316 MONDO:equivalentTo Lacrimal Drainage System Neoplasm MONDO:0002460 MONDO:0855684 lacrimal drainage system non-keratinizing squamous cell carcinoma NCIT:C175335 MONDO:equivalentTo Lacrimal Drainage System Non-Keratinizing Squamous Cell Carcinoma MONDO:0003492 -MONDO:0855694 conjunctival non-hodgkin lymphoma NCIT:C175432 MONDO:equivalentTo Conjunctival Non-Hodgkin Lymphoma MONDO:0020646|MONDO:0003454 +MONDO:0855694 conjunctival non-hodgkin lymphoma NCIT:C175432 MONDO:equivalentTo Conjunctival Non-Hodgkin Lymphoma MONDO:0004034|MONDO:0003454 MONDO:0855700 primary uveal non-hodgkin lymphoma NCIT:C175451 MONDO:equivalentTo Primary Uveal Non-Hodgkin Lymphoma MONDO:0004351|MONDO:0002659|MONDO:0017594 MONDO:0855708 conjunctival myxoma NCIT:C175495 MONDO:equivalentTo Conjunctival Myxoma MONDO:0044784|MONDO:0006105 MONDO:0855710 conjunctival hemangioma NCIT:C175497 MONDO:equivalentTo Conjunctival Hemangioma MONDO:0006105|MONDO:0006500 @@ -658,11 +623,10 @@ MONDO:0855757 male breast carcinoma in situ NCIT:C176503 MONDO:equivalentTo Male MONDO:0855758 invasive male breast carcinoma NCIT:C176504 MONDO:equivalentTo Invasive Male Breast Carcinoma MONDO:0006256|MONDO:0005628 MONDO:0855763 invasive female breast carcinoma NCIT:C176579 MONDO:equivalentTo Invasive Female Breast Carcinoma MONDO:0006256|MONDO:0004379 MONDO:0855764 female breast carcinoma in situ NCIT:C176580 MONDO:equivalentTo Female Breast Carcinoma In Situ MONDO:0004658|MONDO:0004379 -MONDO:0855783 functioning lung carcinoid tumor NCIT:C176705 MONDO:equivalentTo Functioning Lung Carcinoid Tumor MONDO:0021120|MONDO:0006041 -MONDO:0855784 non-functioning lung carcinoid tumor NCIT:C176706 MONDO:equivalentTo Non-Functioning Lung Carcinoid Tumor MONDO:0021119|MONDO:0006041 +MONDO:0855783 functioning lung neuroendocrine tumor NCIT:C176705 MONDO:equivalentTo Functioning Lung Neuroendocrine Tumor MONDO:0021120|MONDO:0006041 +MONDO:0855784 non-functioning lung neuroendocrine tumor NCIT:C176706 MONDO:equivalentTo Non-Functioning Lung Neuroendocrine Tumor MONDO:0021119|MONDO:0006041 MONDO:0855809 metastatic malignant thoracic neoplasm NCIT:C176862 MONDO:equivalentTo Metastatic Malignant Thoracic Neoplasm MONDO:0024880|MONDO:0003274 MONDO:0855811 psammocarcinoma NCIT:C176887 MONDO:equivalentTo Psammocarcinoma MONDO:0004970 -MONDO:0855812 unresectable glioma NCIT:C176889 MONDO:equivalentTo Unresectable Glioma MONDO:0021042 MONDO:0855859 infantile myofibromatosis 1 NCIT:C176943 MONDO:equivalentTo Infantile Myofibromatosis 1 MONDO:0016824 MONDO:0855860 infantile myofibromatosis 2 NCIT:C176944 MONDO:equivalentTo Infantile Myofibromatosis 2 MONDO:0016824 MONDO:0855861 lipoma-like atypical lipomatous tumor/well differentiated liposarcoma NCIT:C176979 MONDO:equivalentTo Lipoma-Like Atypical Lipomatous Tumor/Well Differentiated Liposarcoma MONDO:0006097 @@ -675,7 +639,6 @@ MONDO:0855885 epithelioid myxofibrosarcoma NCIT:C177414 MONDO:equivalentTo Epith MONDO:0855891 bladder flat urothelial carcinoma NCIT:C177531 MONDO:equivalentTo Bladder Flat Urothelial Carcinoma MONDO:0005611 MONDO:0855897 epithelioid hemangioendothelioma with wwtr1-camta1 gene fusion NCIT:C177552 MONDO:equivalentTo Epithelioid Hemangioendothelioma with WWTR1-CAMTA1 Gene Fusion MONDO:0015523 MONDO:0855898 epithelioid hemangioendothelioma with yap1-tfe3 gene fusion NCIT:C177553 MONDO:equivalentTo Epithelioid Hemangioendothelioma with YAP1-TFE3 Gene Fusion MONDO:0015523 -MONDO:0855901 sigmoid colon carcinoma NCIT:C177680 MONDO:equivalentTo Sigmoid Colon Carcinoma MONDO:0002032 MONDO:0855909 who grade 1 glioma NCIT:C177797 MONDO:equivalentTo WHO Grade 1 Glioma MONDO:0021637 MONDO:0855911 poorly differentiated chordoma NCIT:C177898 MONDO:equivalentTo Poorly Differentiated Chordoma MONDO:0008978 MONDO:0855914 ebv-associated smooth muscle tumor NCIT:C178217 MONDO:equivalentTo EBV-Associated Smooth Muscle Tumor MONDO:0006975 @@ -743,7 +706,6 @@ MONDO:0856106 major salivary gland squamous cell carcinoma NCIT:C181161 MONDO:eq MONDO:0856110 lung rhabdomyosarcoma NCIT:C181201 MONDO:equivalentTo Lung Rhabdomyosarcoma MONDO:0002426|MONDO:0005212 MONDO:0856111 lung hodgkin lymphoma NCIT:C181205 MONDO:equivalentTo Lung Hodgkin Lymphoma MONDO:0004952|MONDO:0003987 MONDO:0856112 primary bone hodgkin lymphoma NCIT:C181207 MONDO:equivalentTo Primary Bone Hodgkin Lymphoma MONDO:0004952|MONDO:0017814 -MONDO:0856113 thyroid gland hodgkin lymphoma NCIT:C181209 MONDO:equivalentTo Thyroid Gland Hodgkin Lymphoma MONDO:0004952|MONDO:0019962 MONDO:0856114 cervical cancer by ajcc v9 stage NCIT:C181562 MONDO:equivalentTo Cervical Cancer by AJCC v9 Stage MONDO:0005131 MONDO:0856117 epiglottic squamous cell carcinoma NCIT:C181714 MONDO:equivalentTo Epiglottic Squamous Cell Carcinoma MONDO:0004293|MONDO:0004473 MONDO:0856124 vulvar squamous cell carcinoma, not otherwise specified NCIT:C181902 MONDO:equivalentTo Vulvar Squamous Cell Carcinoma, Not Otherwise Specified MONDO:0024609 @@ -755,7 +717,6 @@ MONDO:0856139 vulvar ewing sarcoma NCIT:C181977 MONDO:equivalentTo Vulvar Ewing MONDO:0856154 bronchiolar adenoma/ciliated muconodular papillary tumor NCIT:C183045 MONDO:equivalentTo Bronchiolar Adenoma/Ciliated Muconodular Papillary Tumor MONDO:0003422 MONDO:0856155 invasive lung non-mucinous adenocarcinoma NCIT:C183109 MONDO:equivalentTo Invasive Lung Non-Mucinous Adenocarcinoma MONDO:0040677|MONDO:0005061 MONDO:0856156 thoracic smarca4-deficient undifferentiated tumor NCIT:C183115 MONDO:equivalentTo Thoracic SMARCA4-Deficient Undifferentiated Tumor MONDO:0003274 -MONDO:0856157 lung hyalinizing clear cell carcinoma NCIT:C183116 MONDO:equivalentTo Lung Hyalinizing Clear Cell Carcinoma MONDO:0005138 MONDO:0856158 lung intravascular large b-cell lymphoma NCIT:C183121 MONDO:equivalentTo Lung Intravascular Large B-Cell Lymphoma MONDO:0006387|MONDO:0020324 MONDO:0856161 pleural mesothelioma in situ NCIT:C183134 MONDO:equivalentTo Pleural Mesothelioma In Situ MONDO:0003308 MONDO:0856165 cardiac diffuse large b-cell lymphoma NCIT:C183146 MONDO:equivalentTo Cardiac Diffuse Large B-Cell Lymphoma MONDO:0018905|MONDO:0003917 @@ -793,11 +754,10 @@ MONDO:0856257 pituitary neuroendocrine tumor without distinct lineage differenti MONDO:0856258 pituitary neuroendocrine tumor, not otherwise specified NCIT:C187135 MONDO:equivalentTo Pituitary Neuroendocrine Tumor, Not Otherwise Specified MONDO:0006373 MONDO:0856267 thyroid gland follicular adenoma with papillary architecture NCIT:C187261 MONDO:equivalentTo Thyroid Gland Follicular Adenoma with Papillary Architecture MONDO:0005032 MONDO:0856268 low risk thyroid gland neoplasm NCIT:C187273 MONDO:equivalentTo Low Risk Thyroid Gland Neoplasm MONDO:0015074 -MONDO:0856271 platinum-sensitive endometrial serous adenocarcinoma NCIT:C187374 MONDO:equivalentTo Platinum-Sensitive Endometrial Serous Adenocarcinoma MONDO:0006196 MONDO:0856272 invasive breast lobular carcinoma with extracellular mucin NCIT:C187405 MONDO:equivalentTo Invasive Breast Lobular Carcinoma with Extracellular Mucin MONDO:0005051 MONDO:0856275 thyroid gland follicular carcinoma, signet ring cell variant NCIT:C187643 MONDO:equivalentTo Thyroid Gland Follicular Carcinoma, Signet Ring Cell Variant MONDO:0005034 MONDO:0856276 classic thyroid gland papillary carcinoma NCIT:C187644 MONDO:equivalentTo Classic Thyroid Gland Papillary Carcinoma MONDO:0005075 -MONDO:0856277 follicular-derived thyroid gland carcinoma, high grade NCIT:C187645 MONDO:equivalentTo Follicular-Derived Thyroid Gland Carcinoma, High Grade MONDO:0024622 +MONDO:0856277 high grade follicular cell-derived non-anaplastic thyroid gland carcinoma NCIT:C187645 MONDO:equivalentTo High Grade Follicular Cell-Derived Non-Anaplastic Thyroid Gland Carcinoma MONDO:0024622 MONDO:0856285 thyroid gland secretory carcinoma NCIT:C187994 MONDO:equivalentTo Thyroid Gland Secretory Carcinoma MONDO:0024622 MONDO:0856286 thyroblastoma NCIT:C187995 MONDO:equivalentTo Thyroblastoma MONDO:0002108|MONDO:0005564 MONDO:0856287 teratoma with endocrine differentiation NCIT:C188013 MONDO:equivalentTo Teratoma with Endocrine Differentiation MONDO:0002601 @@ -814,7 +774,6 @@ MONDO:0856310 retroperitoneal rhabdomyosarcoma NCIT:C188071 MONDO:equivalentTo R MONDO:0856312 retroperitoneal malignant peripheral nerve sheath tumor NCIT:C188073 MONDO:equivalentTo Retroperitoneal Malignant Peripheral Nerve Sheath Tumor MONDO:0001501|MONDO:0017827 MONDO:0856313 rectal epithelioid cell melanoma NCIT:C188079 MONDO:equivalentTo Rectal Epithelioid Cell Melanoma MONDO:0002167|MONDO:0002973 MONDO:0856316 lung anaplastic large cell lymphoma NCIT:C188082 MONDO:equivalentTo Lung Anaplastic Large Cell Lymphoma MONDO:0020644|MONDO:0020325 -MONDO:0856318 middle ear embryonal rhabdomyosarcoma NCIT:C188115 MONDO:equivalentTo Middle Ear Embryonal Rhabdomyosarcoma MONDO:0009993|MONDO:0003275 MONDO:0856325 adrenal cortical myxoid carcinoma NCIT:C188182 MONDO:equivalentTo Adrenal Cortical Myxoid Carcinoma MONDO:0006639 MONDO:0856326 adrenal cortical high grade carcinoma NCIT:C188183 MONDO:equivalentTo Adrenal Cortical High Grade Carcinoma MONDO:0006639 MONDO:0856327 adrenal cortical melanoma NCIT:C188185 MONDO:equivalentTo Adrenal Cortical Melanoma MONDO:0021312|MONDO:0006320 @@ -859,7 +818,7 @@ MONDO:0856472 conventional extraskeletal myxoid chondrosarcoma NCIT:C27501 MONDO MONDO:0856473 intra-abdominal lymphangioma NCIT:C27508 MONDO:equivalentTo Intra-Abdominal Lymphangioma MONDO:0002013 MONDO:0856474 angiosarcoma associated with lymphedema NCIT:C27512 MONDO:equivalentTo Angiosarcoma Associated with Lymphedema MONDO:0016982 MONDO:0856475 desmoplastic fibroblastoma NCIT:C27515 MONDO:equivalentTo Desmoplastic Fibroblastoma MONDO:0005167 -MONDO:0856477 desmoplastic trichoepithelioma NCIT:C27524 MONDO:equivalentTo Desmoplastic Trichoepithelioma MONDO:0020593 +MONDO:0856477 columnar trichoblastoma NCIT:C27524 MONDO:equivalentTo Columnar Trichoblastoma MONDO:0020593 MONDO:0856478 tubular apocrine adenoma NCIT:C27527 MONDO:equivalentTo Tubular Apocrine Adenoma MONDO:0002804 MONDO:0856479 primary cutaneous mucinous carcinoma NCIT:C27533 MONDO:equivalentTo Primary Cutaneous Mucinous Carcinoma MONDO:0005524|MONDO:0004957 MONDO:0856501 oral cavity disorder NCIT:C27641 MONDO:equivalentTo Oral Cavity Disorder @@ -898,7 +857,7 @@ MONDO:0856599 biliary system disorder NCIT:C2899 MONDO:equivalentTo Biliary Syst MONDO:0856602 enchondroma NCIT:C3007 MONDO:equivalentTo Enchondroma MONDO:0002360|MONDO:0000631 MONDO:0856604 pancreatic glucagon-producing neuroendocrine tumor NCIT:C3062 MONDO:equivalentTo Pancreatic Glucagon-Producing Neuroendocrine Tumor MONDO:0019954 MONDO:0856606 chronic phase chronic myeloid leukemia, bcr-abl1 positive NCIT:C3175 MONDO:equivalentTo Chronic Phase Chronic Myeloid Leukemia, BCR-ABL1 Positive MONDO:0001014|MONDO:0011996 -MONDO:0856607 myeloid leukemia, philadelphia- negative NCIT:C3176 MONDO:equivalentTo Myeloid Leukemia, Philadelphia- Negative MONDO:0004643 +MONDO:0856607 myeloid leukemia, philadelphia-negative NCIT:C3176 MONDO:equivalentTo Myeloid Leukemia, Philadelphia-Negative MONDO:0004643 MONDO:0856608 neoplasm by site NCIT:C3263 MONDO:equivalentTo Neoplasm by Site MONDO:0005070 MONDO:0856610 osteochondroma NCIT:C3295 MONDO:equivalentTo Osteochondroma MONDO:0000631|MONDO:0024470 MONDO:0856611 extra-adrenal paraganglioma NCIT:C3309 MONDO:equivalentTo Extra-Adrenal Paraganglioma MONDO:0000448 @@ -911,7 +870,7 @@ MONDO:0856691 uterine corpus degenerated leiomyoma NCIT:C3511 MONDO:equivalentTo MONDO:0856703 eyelid vascular disorder NCIT:C35198 MONDO:equivalentTo Eyelid Vascular Disorder MONDO:0856706 placental polyp NCIT:C3521 MONDO:equivalentTo Placental Polyp MONDO:0021498|MONDO:0005079 MONDO:0856715 chondromatosis NCIT:C35259 MONDO:equivalentTo Chondromatosis MONDO:0024470 -MONDO:0856716 malignant submandibular gland neoplasm NCIT:C3526 MONDO:equivalentTo Malignant Submandibular Gland Neoplasm MONDO:0044743|MONDO:0021244 +MONDO:0856716 malignant submandibular gland neoplasm NCIT:C3526 MONDO:equivalentTo Malignant Submandibular Gland Neoplasm MONDO:0021244|MONDO:0044743 MONDO:0856723 malignant palate neoplasm NCIT:C3530 MONDO:equivalentTo Malignant Palate Neoplasm MONDO:0005515|MONDO:0005286 MONDO:0856758 malignant neoplasm of multiple primary sites NCIT:C35427 MONDO:equivalentTo Malignant Neoplasm of Multiple Primary Sites MONDO:0004992 MONDO:0856764 behavioral disorder NCIT:C35470 MONDO:equivalentTo Behavioral Disorder @@ -919,7 +878,6 @@ MONDO:0856772 lung kaposi sarcoma NCIT:C3551 MONDO:equivalentTo Lung Kaposi Sarc MONDO:0856784 malignant exocervical neoplasm NCIT:C3554 MONDO:equivalentTo Malignant Exocervical Neoplasm MONDO:0002974 MONDO:0856786 malignant uterine corpus neoplasm NCIT:C3556 MONDO:equivalentTo Malignant Uterine Corpus Neoplasm MONDO:0021254|MONDO:0002715 MONDO:0856787 complex endometrial hyperplasia with atypia NCIT:C35560 MONDO:equivalentTo Complex Endometrial Hyperplasia with Atypia MONDO:0006169 -MONDO:0856809 ocular adnexal mucosa-associated lymphoid tissue lymphoma NCIT:C35689 MONDO:equivalentTo Ocular Adnexal Mucosa-Associated Lymphoid Tissue Lymphoma MONDO:0020646|MONDO:0007650 MONDO:0856810 mixed tumor of the salivary gland NCIT:C35691 MONDO:equivalentTo Mixed Tumor of the Salivary Gland MONDO:0021043|MONDO:0021357 MONDO:0856811 posterior pharyngeal wall carcinoma NCIT:C35692 MONDO:equivalentTo Posterior Pharyngeal Wall Carcinoma MONDO:0021345 MONDO:0856812 benign uvula neoplasm NCIT:C35698 MONDO:equivalentTo Benign Uvula Neoplasm MONDO:0021480 @@ -970,7 +928,7 @@ MONDO:0856906 chronic lymphocytic leukemia with unmutated immunoglobulin heavy c MONDO:0856907 high grade b-cell lymphoma with blastoid morphologic features NCIT:C37209 MONDO:equivalentTo High Grade B-Cell Lymphoma with Blastoid Morphologic Features MONDO:0044889 MONDO:0856911 benign kidney mixed epithelial and stromal tumor NCIT:C37264 MONDO:equivalentTo Benign Kidney Mixed Epithelial and Stromal Tumor MONDO:0002513|MONDO:0002386 MONDO:0856912 atypical small acinar proliferation of the prostate gland NCIT:C37268 MONDO:equivalentTo Atypical Small Acinar Proliferation of the Prostate Gland MONDO:0021259 -MONDO:0856914 head and neck basaloid carcinoma NCIT:C37290 MONDO:equivalentTo Head and Neck Basaloid Carcinoma MONDO:0003486|MONDO:0010150 +MONDO:0856914 head and neck basaloid squamous cell carcinoma NCIT:C37290 MONDO:equivalentTo Head and Neck Basaloid Squamous Cell Carcinoma MONDO:0003486|MONDO:0010150 MONDO:0856915 mixed mesodermal (mullerian) tumor NCIT:C3730 MONDO:equivalentTo Mixed Mesodermal (Mullerian) Tumor MONDO:0021148|MONDO:0021043 MONDO:0856917 abdominal (mesenteric) fibromatosis NCIT:C3741 MONDO:equivalentTo Abdominal (Mesenteric) Fibromatosis MONDO:0007608 MONDO:0856918 adenomatous polyp NCIT:C3764 MONDO:equivalentTo Adenomatous Polyp MONDO:0006180|MONDO:0021075 @@ -1005,7 +963,7 @@ MONDO:0856969 pleomorphic variant mantle cell lymphoma NCIT:C39747 MONDO:equival MONDO:0856970 type ii endometrial adenocarcinoma NCIT:C39749 MONDO:equivalentTo Type II Endometrial Adenocarcinoma MONDO:0005461 MONDO:0856971 glioblastoma, idh-wildtype NCIT:C39750 MONDO:equivalentTo Glioblastoma, IDH-Wildtype MONDO:0018177 MONDO:0856972 secondary glioblastoma NCIT:C39751 MONDO:equivalentTo Secondary Glioblastoma MONDO:0018177 -MONDO:0856973 solid/multicystic ameloblastoma NCIT:C39755 MONDO:equivalentTo Solid/Multicystic Ameloblastoma MONDO:0017795 +MONDO:0856973 conventional ameloblastoma NCIT:C39755 MONDO:equivalentTo Conventional Ameloblastoma MONDO:0017795 MONDO:0856974 unicystic ameloblastoma NCIT:C39756 MONDO:equivalentTo Unicystic Ameloblastoma MONDO:0021077|MONDO:0017795 MONDO:0856975 renal cell carcinoma with constitutional chromosome 3 translocations NCIT:C39790 MONDO:equivalentTo Renal Cell Carcinoma with Constitutional Chromosome 3 Translocations MONDO:0003008 MONDO:0856976 renal cell carcinoma associated with inv(x)(p11;q12) NCIT:C39802 MONDO:equivalentTo Renal Cell Carcinoma Associated with inv(X)(p11;q12) MONDO:0006397 @@ -1053,7 +1011,7 @@ MONDO:0857040 cervical glandular neoplasm NCIT:C40210 MONDO:equivalentTo Cervica MONDO:0857041 cervical soft tissue neoplasm NCIT:C40216 MONDO:equivalentTo Cervical Soft Tissue Neoplasm MONDO:0006424|MONDO:0021230 MONDO:0857043 cervical mixed epithelial and mesenchymal neoplasm NCIT:C40226 MONDO:equivalentTo Cervical Mixed Epithelial and Mesenchymal Neoplasm MONDO:0021043|MONDO:0021230 MONDO:0857045 vaginal keratinizing squamous cell carcinoma NCIT:C40243 MONDO:equivalentTo Vaginal Keratinizing Squamous Cell Carcinoma MONDO:0005056|MONDO:0006490 -MONDO:0857046 vaginal basaloid carcinoma NCIT:C40245 MONDO:equivalentTo Vaginal Basaloid Carcinoma MONDO:0003486|MONDO:0006490 +MONDO:0857046 vaginal basaloid squamous cell carcinoma NCIT:C40245 MONDO:equivalentTo Vaginal Basaloid Squamous Cell Carcinoma MONDO:0003486|MONDO:0006490 MONDO:0857047 vaginal endometrioid adenocarcinoma NCIT:C40251 MONDO:equivalentTo Vaginal Endometrioid Adenocarcinoma MONDO:0020653|MONDO:0005026 MONDO:0857048 vaginal mucinous adenocarcinoma NCIT:C40252 MONDO:equivalentTo Vaginal Mucinous Adenocarcinoma MONDO:0020653|MONDO:0004957 MONDO:0857049 vaginal mesonephric adenocarcinoma NCIT:C40253 MONDO:equivalentTo Vaginal Mesonephric Adenocarcinoma MONDO:0020653|MONDO:0005613 @@ -1115,20 +1073,19 @@ MONDO:0857132 junctional nevus NCIT:C4231 MONDO:equivalentTo Junctional Nevus M MONDO:0857133 melanoma in junctional nevus NCIT:C4232 MONDO:equivalentTo Melanoma in Junctional Nevus MONDO:0005012 MONDO:0857134 type a spindle cell melanoma NCIT:C4238 MONDO:equivalentTo Type A Spindle Cell Melanoma MONDO:0006427 MONDO:0857135 type b spindle cell melanoma NCIT:C4239 MONDO:equivalentTo Type B Spindle Cell Melanoma MONDO:0006427 -MONDO:0857136 melanoma arising from blue nevus NCIT:C4240 MONDO:equivalentTo Melanoma Arising from Blue Nevus MONDO:0005012 +MONDO:0857136 melanoma arising in blue nevus NCIT:C4240 MONDO:equivalentTo Melanoma Arising in Blue Nevus MONDO:0005012 MONDO:0857137 cellular blue nevus NCIT:C4241 MONDO:equivalentTo Cellular Blue Nevus MONDO:0006680 MONDO:0857138 fibrolipoma NCIT:C4249 MONDO:equivalentTo Fibrolipoma MONDO:0005106 MONDO:0857139 fibromyxolipoma NCIT:C4251 MONDO:equivalentTo Fibromyxolipoma MONDO:0005106 MONDO:0857140 lipoblastomatosis NCIT:C4255 MONDO:equivalentTo Lipoblastomatosis MONDO:0044983 MONDO:0857141 sporadic retinoblastoma NCIT:C42596 MONDO:equivalentTo Sporadic Retinoblastoma MONDO:0008380 -MONDO:0857142 low grade endometrioid stromal sarcoma NCIT:C4263 MONDO:equivalentTo Low Grade Endometrioid Stromal Sarcoma MONDO:0006745 MONDO:0857144 acute myelomonocytic leukemia without abnormal eosinophils NCIT:C42779 MONDO:equivalentTo Acute Myelomonocytic Leukemia without Abnormal Eosinophils MONDO:0018871 MONDO:0857145 pericardial solitary fibrous tumor NCIT:C4281 MONDO:equivalentTo Pericardial Solitary Fibrous Tumor MONDO:0016238|MONDO:0021381 MONDO:0857146 benign hemangiopericytoma NCIT:C4300 MONDO:equivalentTo Benign Hemangiopericytoma MONDO:0005094 MONDO:0857147 benign odontogenic neoplasm NCIT:C4306 MONDO:equivalentTo Benign Odontogenic Neoplasm MONDO:0021445|MONDO:0021192 MONDO:0857152 pure cutaneous mastocytosis NCIT:C43277 MONDO:equivalentTo Pure Cutaneous Mastocytosis MONDO:0019023 MONDO:0857155 germinative follicular epithelium neoplasm NCIT:C43311 MONDO:equivalentTo Germinative Follicular Epithelium Neoplasm MONDO:0003413|MONDO:0021634 -MONDO:0857156 mixed epithelial and mesenchymal hair follicle neoplasm NCIT:C43312 MONDO:equivalentTo Mixed Epithelial and Mesenchymal Hair Follicle Neoplasm MONDO:0003413|MONDO:0021043 +MONDO:0857156 adamantinoid trichoblastoma NCIT:C43312 MONDO:equivalentTo Adamantinoid Trichoblastoma MONDO:0020593 MONDO:0857160 outer hair sheath and infundibulum neoplasm NCIT:C43324 MONDO:equivalentTo Outer Hair Sheath and Infundibulum Neoplasm MONDO:0003413 MONDO:0857163 superficial epithelioma with sebaceous differentiation NCIT:C43334 MONDO:equivalentTo Superficial Epithelioma with Sebaceous Differentiation MONDO:0021490 MONDO:0857164 sebaceoma NCIT:C43336 MONDO:equivalentTo Sebaceoma MONDO:0021490 @@ -1139,7 +1096,7 @@ MONDO:0857168 ductal eccrine carcinoma with spindle cell elements NCIT:C43346 MO MONDO:0857169 squamoid eccrine ductal carcinoma NCIT:C43347 MONDO:equivalentTo Squamoid Eccrine Ductal Carcinoma MONDO:0024245 MONDO:0857170 ductal eccrine carcinoma with abundant fibromyxoid stroma NCIT:C43349 MONDO:equivalentTo Ductal Eccrine Carcinoma with Abundant Fibromyxoid Stroma MONDO:0024245 MONDO:0857171 sporadic cylindroma NCIT:C43351 MONDO:equivalentTo Sporadic Cylindroma MONDO:0021812 -MONDO:0857172 classical poroma NCIT:C43353 MONDO:equivalentTo Classical Poroma MONDO:0006738 +MONDO:0857172 classic poroma NCIT:C43353 MONDO:equivalentTo Classic Poroma MONDO:0006738 MONDO:0857173 porocarcinoma in situ NCIT:C43354 MONDO:equivalentTo Porocarcinoma In Situ MONDO:0006189 MONDO:0857174 aleukemic lymphoid leukemia NCIT:C4343 MONDO:equivalentTo Aleukemic Lymphoid Leukemia MONDO:0005402|MONDO:0003730 MONDO:0857175 sporadic gastric adenocarcinoma NCIT:C43527 MONDO:equivalentTo Sporadic Gastric Adenocarcinoma MONDO:0005036 @@ -1167,7 +1124,6 @@ MONDO:0857200 gallbladder flat biliary intraepithelial neoplasia NCIT:C43607 MON MONDO:0857201 gallbladder papillary biliary intraepithelial neoplasia NCIT:C43609 MONDO:equivalentTo Gallbladder Papillary Biliary Intraepithelial Neoplasia MONDO:0006218 MONDO:0857202 pleomorphic hepatocellular carcinoma NCIT:C43625 MONDO:equivalentTo Pleomorphic Hepatocellular Carcinoma MONDO:0007256 MONDO:0857203 sarcomatoid hepatocellular carcinoma NCIT:C43627 MONDO:equivalentTo Sarcomatoid Hepatocellular Carcinoma MONDO:0007256 -MONDO:0857205 cherry hemangioma of lip NCIT:C4372 MONDO:equivalentTo Cherry Hemangioma of Lip MONDO:0002323|MONDO:0021496 MONDO:0857206 accessory urethral gland neoplasm NCIT:C4378 MONDO:equivalentTo Accessory Urethral Gland Neoplasm MONDO:0021239 MONDO:0857208 clear cell intrahepatic cholangiocarcinoma NCIT:C43848 MONDO:equivalentTo Clear Cell Intrahepatic Cholangiocarcinoma MONDO:0005004|MONDO:0003210 MONDO:0857210 anogenital papillomaviral intraepithelial neoplasia NCIT:C4394 MONDO:equivalentTo Anogenital Papillomaviral Intraepithelial Neoplasia MONDO:0024475 @@ -1180,7 +1136,7 @@ MONDO:0857217 cutaneous neural neoplasm NCIT:C4479 MONDO:equivalentTo Cutaneous MONDO:0857219 malignant skin hemangiopericytoma NCIT:C4493 MONDO:equivalentTo Malignant Skin Hemangiopericytoma MONDO:0021424|MONDO:0009330 MONDO:0857220 cockade nevus NCIT:C4495 MONDO:equivalentTo Cockade Nevus MONDO:0044794 MONDO:0857222 common blue nevus NCIT:C4496 MONDO:equivalentTo Common Blue Nevus MONDO:0006680 -MONDO:0857223 nevus spilus NCIT:C4498 MONDO:equivalentTo Nevus Spilus MONDO:0044794 +MONDO:0857223 nevus spilus NCIT:C4498 MONDO:equivalentTo Nevus Spilus MONDO:0044792 MONDO:0857224 benign ovarian epithelial tumor NCIT:C4510 MONDO:equivalentTo Benign Ovarian Epithelial Tumor MONDO:0002229|MONDO:0036976|MONDO:0000646 MONDO:0857229 classical low grade fibromyxoid sarcoma NCIT:C45210 MONDO:equivalentTo Classical Low Grade Fibromyxoid Sarcoma MONDO:0006272 MONDO:0857233 cutaneous hematopoietic and lymphoid cell neoplasm NCIT:C45240 MONDO:equivalentTo Cutaneous Hematopoietic and Lymphoid Cell Neoplasm MONDO:0002531|MONDO:0044881 @@ -1195,8 +1151,7 @@ MONDO:0857251 lung basaloid squamous cell carcinoma NCIT:C45507 MONDO:equivalent MONDO:0857252 lung spindle cell carcinoma NCIT:C45541 MONDO:equivalentTo Lung Spindle Cell Carcinoma MONDO:0006279 MONDO:0857253 lung pleomorphic carcinoma NCIT:C45542 MONDO:equivalentTo Lung Pleomorphic Carcinoma MONDO:0006279|MONDO:0003573 MONDO:0857254 lung carcinosarcoma NCIT:C45543 MONDO:equivalentTo Lung Carcinosarcoma MONDO:0006279|MONDO:0002928 -MONDO:0857255 lung typical carcinoid tumor NCIT:C45550 MONDO:equivalentTo Lung Typical Carcinoid Tumor MONDO:0006041 -MONDO:0857256 lung atypical carcinoid tumor NCIT:C45551 MONDO:equivalentTo Lung Atypical Carcinoid Tumor MONDO:0006041|MONDO:0006095 +MONDO:0857256 lung neuroendocrine tumor g2 NCIT:C45551 MONDO:equivalentTo Lung Neuroendocrine Tumor G2 MONDO:0006041|MONDO:0006095 MONDO:0857259 ciliary body malignant medulloepithelioma NCIT:C4557 MONDO:equivalentTo Ciliary Body Malignant Medulloepithelioma MONDO:0017050|MONDO:0002969 MONDO:0857260 lung squamous papilloma NCIT:C45573 MONDO:equivalentTo Lung Squamous Papilloma MONDO:0006278|MONDO:0001825 MONDO:0857262 bronchial glandular papilloma NCIT:C45601 MONDO:equivalentTo Bronchial Glandular Papilloma MONDO:0006278|MONDO:0021078 @@ -1286,7 +1241,7 @@ MONDO:0857379 androgen-producing adrenal cortical adenoma NCIT:C48454 MONDO:equi MONDO:0857380 estrogen-producing adrenal cortical adenoma NCIT:C48456 MONDO:equivalentTo Estrogen-Producing Adrenal Cortical Adenoma MONDO:0006408 MONDO:0857382 invasive prostate carcinoma NCIT:C48596 MONDO:equivalentTo Invasive Prostate Carcinoma MONDO:0040677|MONDO:0005159 MONDO:0857383 minimal deviation melanoma NCIT:C48612 MONDO:equivalentTo Minimal Deviation Melanoma MONDO:0005012 -MONDO:0857384 melanoma in congenital melanocytic nevus NCIT:C48613 MONDO:equivalentTo Melanoma in Congenital Melanocytic Nevus MONDO:0005012 +MONDO:0857384 melanoma arising in congenital melanocytic nevus NCIT:C48613 MONDO:equivalentTo Melanoma Arising in Congenital Melanocytic Nevus MONDO:0005012 MONDO:0857385 desmoplastic neurotropic melanoma NCIT:C48614 MONDO:equivalentTo Desmoplastic Neurotropic Melanoma MONDO:0044785 MONDO:0857386 mucosal lentiginous melanoma NCIT:C48622 MONDO:equivalentTo Mucosal Lentiginous Melanoma MONDO:0000544 MONDO:0857388 metastatic malignant neoplasm in the trachea NCIT:C4887 MONDO:equivalentTo Metastatic Malignant Neoplasm in the Trachea MONDO:0001407|MONDO:0024880 @@ -1321,8 +1276,8 @@ MONDO:0857477 invasive breast cribriform carcinoma NCIT:C5142 MONDO:equivalentTo MONDO:0857478 malignant breast adenomyoepithelioma NCIT:C5143 MONDO:equivalentTo Malignant Breast Adenomyoepithelioma MONDO:0007254|MONDO:0002066 MONDO:0857479 infratentorial glioblastoma NCIT:C5148 MONDO:equivalentTo Infratentorial Glioblastoma MONDO:0003107|MONDO:0002501 MONDO:0857480 supratentorial glioblastoma NCIT:C5149 MONDO:equivalentTo Supratentorial Glioblastoma MONDO:0002071|MONDO:0002501 -MONDO:0857482 high grade breast mucoepidermoid carcinoma NCIT:C5167 MONDO:equivalentTo High Grade Breast Mucoepidermoid Carcinoma MONDO:0003087 -MONDO:0857483 low grade breast mucoepidermoid carcinoma NCIT:C5168 MONDO:equivalentTo Low Grade Breast Mucoepidermoid Carcinoma MONDO:0003087 +MONDO:0857482 breast high grade mucoepidermoid carcinoma NCIT:C5167 MONDO:equivalentTo Breast High Grade Mucoepidermoid Carcinoma MONDO:0003087 +MONDO:0857483 breast low grade mucoepidermoid carcinoma NCIT:C5168 MONDO:equivalentTo Breast Low Grade Mucoepidermoid Carcinoma MONDO:0003087 MONDO:0857486 breast non-hodgkin lymphoma NCIT:C5181 MONDO:equivalentTo Breast Non-Hodgkin Lymphoma MONDO:0003661|MONDO:0018908 MONDO:0857487 breast complex fibroadenoma NCIT:C5194 MONDO:equivalentTo Breast Complex Fibroadenoma MONDO:0002056 MONDO:0857488 benign nipple neoplasm NCIT:C5197 MONDO:equivalentTo Benign Nipple Neoplasm MONDO:0002482|MONDO:0000620 @@ -1350,11 +1305,9 @@ MONDO:0857528 malignant pulmonary artery neoplasm NCIT:C5380 MONDO:equivalentTo MONDO:0857529 malignant pulmonary vein neoplasm NCIT:C5383 MONDO:equivalentTo Malignant Pulmonary Vein Neoplasm MONDO:0040676 MONDO:0857532 leiomyosarcoma of vessels NCIT:C5387 MONDO:equivalentTo Leiomyosarcoma of Vessels MONDO:0005058 MONDO:0857533 benign atrial neoplasm NCIT:C5389 MONDO:equivalentTo Benign Atrial Neoplasm MONDO:0021450 -MONDO:0857534 parotid gland lymphangioma NCIT:C5393 MONDO:equivalentTo Parotid Gland Lymphangioma MONDO:0002013|MONDO:0021494 MONDO:0857535 solitary adult fibroma NCIT:C5394 MONDO:equivalentTo Solitary Adult Fibroma MONDO:0005167 MONDO:0857536 fibrous histiocytoma of bone NCIT:C53963 MONDO:equivalentTo Fibrous Histiocytoma of Bone MONDO:0000631|MONDO:0002989 MONDO:0857537 bone leiomyoma NCIT:C53964 MONDO:equivalentTo Bone Leiomyoma MONDO:0001572 -MONDO:0857541 undifferentiated stromal sarcoma NCIT:C53994 MONDO:equivalentTo Undifferentiated Stromal Sarcoma MONDO:0037742|MONDO:0044337|MONDO:0001416 MONDO:0857542 benign gastrointestinal stromal tumor NCIT:C53998 MONDO:equivalentTo Benign Gastrointestinal Stromal Tumor MONDO:0044335|MONDO:0011719 MONDO:0857543 malignant gastrointestinal stromal tumor NCIT:C53999 MONDO:equivalentTo Malignant Gastrointestinal Stromal Tumor MONDO:0011719|MONDO:0044337 MONDO:0857546 region 17p13 allelic loss associated medulloblastoma NCIT:C5402 MONDO:equivalentTo Region 17p13 Allelic Loss Associated Medulloblastoma MONDO:0007959 @@ -1365,16 +1318,15 @@ MONDO:0857550 malignant central nervous system germ cell tumor NCIT:C54099 MONDO MONDO:0857552 breast columnar cell lesion NCIT:C54180 MONDO:equivalentTo Breast Columnar Cell Lesion MONDO:0021100 MONDO:0857556 head and neck keratinizing squamous cell carcinoma NCIT:C54283 MONDO:equivalentTo Head and Neck Keratinizing Squamous Cell Carcinoma MONDO:0005056|MONDO:0010150 MONDO:0857559 metastasizing ameloblastoma NCIT:C54297 MONDO:equivalentTo Metastasizing Ameloblastoma MONDO:0024883|MONDO:0017795 -MONDO:0857561 primary intraosseous squamous cell carcinoma derived from keratocystic odontogenic tumor NCIT:C54303 MONDO:equivalentTo Primary Intraosseous Squamous Cell Carcinoma Derived From Keratocystic Odontogenic Tumor MONDO:0006385|MONDO:0024878 MONDO:0857562 lipomatosis of nerve NCIT:C5431 MONDO:equivalentTo Lipomatosis of Nerve MONDO:0000648|MONDO:0001406|MONDO:0006574 MONDO:0857564 laryngeal papillary squamous cell carcinoma NCIT:C54335 MONDO:equivalentTo Laryngeal Papillary Squamous Cell Carcinoma MONDO:0002979|MONDO:0005595 -MONDO:0857565 laryngeal squamous cell carcinoma, spindle cell variant NCIT:C54336 MONDO:equivalentTo Laryngeal Squamous Cell Carcinoma, Spindle Cell Variant MONDO:0005595|MONDO:0021663 +MONDO:0857565 laryngeal spindle cell squamous carcinoma NCIT:C54336 MONDO:equivalentTo Laryngeal Spindle Cell Squamous Carcinoma MONDO:0005595|MONDO:0021663 MONDO:0857566 laryngeal acantholytic squamous cell carcinoma NCIT:C54337 MONDO:equivalentTo Laryngeal Acantholytic Squamous Cell Carcinoma MONDO:0003487|MONDO:0005595 MONDO:0857567 laryngeal adenosquamous carcinoma NCIT:C54338 MONDO:equivalentTo Laryngeal Adenosquamous Carcinoma MONDO:0002358|MONDO:0006074 MONDO:0857568 laryngeal undifferentiated carcinoma NCIT:C54339 MONDO:equivalentTo Laryngeal Undifferentiated Carcinoma MONDO:0002358|MONDO:0005617 MONDO:0857570 kadish stage c olfactory neuroblastoma NCIT:C5435 MONDO:equivalentTo Kadish Stage C Olfactory Neuroblastoma MONDO:0006329 MONDO:0857571 drop metastasis in the spinal cord NCIT:C5439 MONDO:equivalentTo Drop Metastasis in the Spinal Cord MONDO:0044912 -MONDO:0857572 nasopharyngeal papillary adenocarcinoma NCIT:C54400 MONDO:equivalentTo Nasopharyngeal Papillary Adenocarcinoma MONDO:0015459|MONDO:0002512 +MONDO:0857572 nasopharyngeal low grade papillary adenocarcinoma NCIT:C54400 MONDO:equivalentTo Nasopharyngeal Low Grade Papillary Adenocarcinoma MONDO:0015459|MONDO:0002512 MONDO:0857574 meningeal gliomatosis NCIT:C5446 MONDO:equivalentTo Meningeal Gliomatosis MONDO:0100342|MONDO:0021322 MONDO:0857575 invasive breast apocrine carcinoma NCIT:C5457 MONDO:equivalentTo Invasive Breast Apocrine Carcinoma MONDO:0006256|MONDO:0003934 MONDO:0857576 breast nevus NCIT:C54658 MONDO:equivalentTo Breast Nevus MONDO:0044794|MONDO:0000620 @@ -1382,7 +1334,6 @@ MONDO:0857577 acral nevus NCIT:C54659 MONDO:equivalentTo Acral Nevus MONDO:0044 MONDO:0857578 flexural skin nevus NCIT:C54660 MONDO:equivalentTo Flexural Skin Nevus MONDO:0044794 MONDO:0857580 nevoid melanoma NCIT:C54662 MONDO:equivalentTo Nevoid Melanoma MONDO:0005012 MONDO:0857581 signet ring melanoma NCIT:C54663 MONDO:equivalentTo Signet Ring Melanoma MONDO:0005012 -MONDO:0857582 skin keratotic basal cell carcinoma NCIT:C54665 MONDO:equivalentTo Skin Keratotic Basal Cell Carcinoma MONDO:0005341 MONDO:0857583 invasive breast lobular carcinoma, signet ring variant NCIT:C54691 MONDO:equivalentTo Invasive Breast Lobular Carcinoma, Signet Ring Variant MONDO:0005051|MONDO:0002671 MONDO:0857587 central nervous system dermoid cyst NCIT:C5508 MONDO:equivalentTo Central Nervous System Dermoid Cyst MONDO:0002378|MONDO:0003733 MONDO:0857589 appendix mucinous cystadenoma NCIT:C5510 MONDO:equivalentTo Appendix Mucinous Cystadenoma MONDO:0006088|MONDO:0006859 @@ -1411,7 +1362,6 @@ MONDO:0857648 oral cavity adenocarcinoma NCIT:C5914 MONDO:equivalentTo Oral Cavi MONDO:0857660 minor salivary gland mucoepidermoid carcinoma NCIT:C5953 MONDO:equivalentTo Minor Salivary Gland Mucoepidermoid Carcinoma MONDO:0045069|MONDO:0021009 MONDO:0857661 minor salivary gland small cell neuroendocrine carcinoma NCIT:C5956 MONDO:equivalentTo Minor Salivary Gland Small Cell Neuroendocrine Carcinoma MONDO:0045069|MONDO:0006405 MONDO:0857663 minor salivary gland squamous cell carcinoma NCIT:C5959 MONDO:equivalentTo Minor Salivary Gland Squamous Cell Carcinoma MONDO:0044740|MONDO:0045069 -MONDO:0857665 ear polyp NCIT:C5971 MONDO:equivalentTo Ear Polyp MONDO:0021474|MONDO:0021075 MONDO:0857671 oropharyngeal polyp NCIT:C5988 MONDO:equivalentTo Oropharyngeal Polyp MONDO:0021479|MONDO:0005079 MONDO:0857679 lung mature b-cell neoplasm NCIT:C60310 MONDO:equivalentTo Lung Mature B-Cell Neoplasm MONDO:0021117|MONDO:0004949 MONDO:0857682 nasopharyngeal polyp NCIT:C6034 MONDO:equivalentTo Nasopharyngeal Polyp MONDO:0021478|MONDO:0005079 @@ -1419,7 +1369,6 @@ MONDO:0857683 stage 0 nasopharyngeal undifferentiated carcinoma ajcc v6, v7, and MONDO:0857685 nasopharyngeal squamous papilloma NCIT:C6037 MONDO:equivalentTo Nasopharyngeal Squamous Papilloma MONDO:0001825|MONDO:0021478 MONDO:0857686 oropharyngeal squamous papilloma NCIT:C6038 MONDO:equivalentTo Oropharyngeal Squamous Papilloma MONDO:0021479|MONDO:0001825 MONDO:0857687 stage 0 oropharyngeal squamous cell carcinoma ajcc v6 and v7 NCIT:C6039 MONDO:equivalentTo Stage 0 Oropharyngeal Squamous Cell Carcinoma AJCC v6 and v7 MONDO:0044704|MONDO:0021298 -MONDO:0857688 thyroid gland non-hodgkin lymphoma NCIT:C6044 MONDO:equivalentTo Thyroid Gland Non-Hodgkin Lymphoma MONDO:0019962|MONDO:0018908 MONDO:0857689 stage 0 hypopharyngeal squamous cell carcinoma ajcc v6, v7, and v8 NCIT:C6048 MONDO:equivalentTo Stage 0 Hypopharyngeal Squamous Cell Carcinoma AJCC v6, v7, and v8 MONDO:0021288|MONDO:0044638 MONDO:0857690 stage 0 oral cavity squamous cell carcinoma ajcc v6 and v7 NCIT:C6052 MONDO:equivalentTo Stage 0 Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7 MONDO:0004958|MONDO:0000371|MONDO:0004693 MONDO:0857692 anterior tongue neoplasm NCIT:C6062 MONDO:equivalentTo Anterior Tongue Neoplasm MONDO:0021240 @@ -1454,8 +1403,8 @@ MONDO:0857753 penile kaposi sarcoma NCIT:C6377 MONDO:equivalentTo Penile Kaposi MONDO:0857758 orbit paraganglioma NCIT:C6408 MONDO:equivalentTo Orbit Paraganglioma MONDO:0006239|MONDO:0024611 MONDO:0857759 laryngeal paraganglioma NCIT:C6409 MONDO:equivalentTo Laryngeal Paraganglioma MONDO:0015070|MONDO:0006239|MONDO:0021052 MONDO:0857760 intrathoracic paravertebral paraganglioma NCIT:C6411 MONDO:equivalentTo Intrathoracic Paravertebral Paraganglioma MONDO:0000550|MONDO:0021350 -MONDO:0857763 foregut neuroendocrine tumor g1 NCIT:C6421 MONDO:equivalentTo Foregut Neuroendocrine Tumor G1 MONDO:0005369 -MONDO:0857765 hindgut neuroendocrine tumor g1 NCIT:C6423 MONDO:equivalentTo Hindgut Neuroendocrine Tumor G1 MONDO:0005369 +MONDO:0857763 foregut neuroendocrine tumor NCIT:C6421 MONDO:equivalentTo Foregut Neuroendocrine Tumor MONDO:0000386 +MONDO:0857765 hindgut neuroendocrine tumor NCIT:C6423 MONDO:equivalentTo Hindgut Neuroendocrine Tumor MONDO:0000386 MONDO:0857767 malignant mediastinal nongerminomatous germ cell tumor NCIT:C6439 MONDO:equivalentTo Malignant Mediastinal Nongerminomatous Germ Cell Tumor MONDO:0003578|MONDO:0006298 MONDO:0857768 gastric germ cell tumor NCIT:C6448 MONDO:equivalentTo Gastric Germ Cell Tumor MONDO:0018201|MONDO:0021085 MONDO:0857769 benign germ cell tumor NCIT:C6449 MONDO:equivalentTo Benign Germ Cell Tumor MONDO:0005040|MONDO:0005165 @@ -1506,7 +1455,7 @@ MONDO:0857822 adenocarcinoma with neuroendocrine differentiation NCIT:C66745 MON MONDO:0857823 testicular sex cord-stromal tumor, not otherwise specified NCIT:C66748 MONDO:equivalentTo Testicular Sex Cord-Stromal Tumor, Not Otherwise Specified MONDO:0003125 MONDO:0857824 ovarian stromal tumor with minor sex cord elements NCIT:C66749 MONDO:equivalentTo Ovarian Stromal Tumor with Minor Sex Cord Elements MONDO:0021657 MONDO:0857825 adult granulosa cell tumor NCIT:C66750 MONDO:equivalentTo Adult Granulosa Cell Tumor MONDO:0006036 -MONDO:0857826 malignant melanoma in precancerous melanosis NCIT:C66753 MONDO:equivalentTo Malignant Melanoma in Precancerous Melanosis MONDO:0005012 +MONDO:0857826 melanoma in precancerous melanosis NCIT:C66753 MONDO:equivalentTo Melanoma in Precancerous Melanosis MONDO:0005012 MONDO:0857827 small congenital melanocytic nevus NCIT:C66754 MONDO:equivalentTo Small Congenital Melanocytic Nevus MONDO:0044792 MONDO:0857828 proliferative nodules in congenital melanocytic nevus NCIT:C66755 MONDO:equivalentTo Proliferative Nodules in Congenital Melanocytic Nevus MONDO:0044792 MONDO:0857829 periosteal fibroma NCIT:C66761 MONDO:equivalentTo Periosteal Fibroma MONDO:0000631|MONDO:0005167 @@ -1538,8 +1487,6 @@ MONDO:0857862 stromal neoplasm NCIT:C6781 MONDO:equivalentTo Stromal Neoplasm M MONDO:0857864 benign apocrine neoplasm NCIT:C6799 MONDO:equivalentTo Benign Apocrine Neoplasm MONDO:0003686|MONDO:0021489 MONDO:0857866 benign external ear neoplasm NCIT:C6807 MONDO:equivalentTo Benign External Ear Neoplasm MONDO:0021474|MONDO:0021235 MONDO:0857867 prostate ductal adenocarcinoma NCIT:C6813 MONDO:equivalentTo Prostate Ductal Adenocarcinoma MONDO:0005082 -MONDO:0857870 high grade paranasal sinus sarcoma NCIT:C6850 MONDO:equivalentTo High Grade Paranasal Sinus Sarcoma MONDO:0001758 -MONDO:0857871 low grade paranasal sinus sarcoma NCIT:C6851 MONDO:equivalentTo Low Grade Paranasal Sinus Sarcoma MONDO:0001758 MONDO:0857872 kadish stage a olfactory neuroblastoma NCIT:C6853 MONDO:equivalentTo Kadish Stage A Olfactory Neuroblastoma MONDO:0006329 MONDO:0857873 kadish stage b olfactory neuroblastoma NCIT:C6854 MONDO:equivalentTo Kadish Stage B Olfactory Neuroblastoma MONDO:0006329 MONDO:0857874 oropharyngeal undifferentiated carcinoma NCIT:C68610 MONDO:equivalentTo Oropharyngeal Undifferentiated Carcinoma MONDO:0044704|MONDO:0003572 @@ -1550,7 +1497,7 @@ MONDO:0857882 adrenal cortical sarcomatoid carcinoma NCIT:C68644 MONDO:equivalen MONDO:0857884 hodgkin lymphoma by clinical course NCIT:C68666 MONDO:equivalentTo Hodgkin Lymphoma by Clinical Course MONDO:0004952 MONDO:0857892 adult gliosarcoma NCIT:C68701 MONDO:equivalentTo Adult Gliosarcoma MONDO:0020690|MONDO:0016681 MONDO:0857893 adult giant cell glioblastoma NCIT:C68702 MONDO:equivalentTo Adult Giant Cell Glioblastoma MONDO:0020690|MONDO:0016682 -MONDO:0857895 pancreatic mixed acinar-neuroendocrine carcinoma NCIT:C6878 MONDO:equivalentTo Pancreatic Mixed Acinar-Neuroendocrine Carcinoma MONDO:0044727 +MONDO:0857895 pancreatic mixed acinar carcinoma-neuroendocrine carcinoma NCIT:C6878 MONDO:equivalentTo Pancreatic Mixed Acinar Carcinoma-Neuroendocrine Carcinoma MONDO:0044727 MONDO:0857896 cellular fibroma NCIT:C6892 MONDO:equivalentTo Cellular Fibroma MONDO:0005167 MONDO:0857897 malignant solitary fibrous tumor NCIT:C6894 MONDO:equivalentTo Malignant Solitary Fibrous Tumor MONDO:0016238|MONDO:0004992 MONDO:0857899 atypical burkitt/burkitt-like lymphoma NCIT:C6917 MONDO:equivalentTo Atypical Burkitt/Burkitt-Like Lymphoma MONDO:0007243 @@ -1563,7 +1510,6 @@ MONDO:0857906 anaplastic kidney wilms tumor NCIT:C6952 MONDO:equivalentTo Anapla MONDO:0857907 simple endometrial hyperplasia with atypia NCIT:C6991 MONDO:equivalentTo Simple Endometrial Hyperplasia with Atypia MONDO:0006410 MONDO:0857910 central nervous system kaposi sarcoma NCIT:C7006 MONDO:equivalentTo Central Nervous System Kaposi Sarcoma MONDO:0005055|MONDO:0002217 MONDO:0857913 central nervous system inflammatory myofibroblastic tumor NCIT:C7020 MONDO:equivalentTo Central Nervous System Inflammatory Myofibroblastic Tumor MONDO:0015798|MONDO:0003244 -MONDO:0857914 refractory multiple myeloma NCIT:C7024 MONDO:equivalentTo Refractory Multiple Myeloma MONDO:0004816|MONDO:0009693 MONDO:0857918 meningioma by site NCIT:C7051 MONDO:equivalentTo Meningioma by Site MONDO:0016642 MONDO:0857919 mature b-cell non-hodgkin lymphoma NCIT:C7056 MONDO:equivalentTo Mature B-Cell Non-Hodgkin Lymphoma MONDO:0015759|MONDO:0004949 MONDO:0857921 neoplasm by special category NCIT:C7062 MONDO:equivalentTo Neoplasm by Special Category MONDO:0005070 @@ -1572,7 +1518,6 @@ MONDO:0857926 prostate cancer by whitmore-jewett stage NCIT:C7079 MONDO:equivale MONDO:0857931 metastatic non-cutaneous melanoma NCIT:C7092 MONDO:equivalentTo Metastatic Non-Cutaneous Melanoma MONDO:0005191|MONDO:0006320 MONDO:0857935 teratoid hepatoblastoma NCIT:C7098 MONDO:equivalentTo Teratoid Hepatoblastoma MONDO:0003650 MONDO:0857937 adult pilocytic astrocytoma NCIT:C71016 MONDO:equivalentTo Adult Pilocytic Astrocytoma MONDO:0002503|MONDO:0016691 -MONDO:0857938 adult subependymal giant cell astrocytoma NCIT:C71017 MONDO:equivalentTo Adult Subependymal Giant Cell Astrocytoma MONDO:0002503|MONDO:0016693 MONDO:0857940 liver non-epithelial neoplasm NCIT:C7107 MONDO:equivalentTo Liver Non-Epithelial Neoplasm MONDO:0024477 MONDO:0857943 stage i liver cancer NCIT:C7116 MONDO:equivalentTo Stage I Liver Cancer MONDO:0018531 MONDO:0857944 stage ii liver cancer NCIT:C7117 MONDO:equivalentTo Stage II Liver Cancer MONDO:0018531 @@ -1629,25 +1574,21 @@ MONDO:0858029 invasive papillary adenocarcinoma NCIT:C7438 MONDO:equivalentTo In MONDO:0858030 benign myoepithelioma NCIT:C7442 MONDO:equivalentTo Benign Myoepithelioma MONDO:0044335|MONDO:0002380 MONDO:0858036 pure erythroid leukemia NCIT:C7467 MONDO:equivalentTo Pure Erythroid Leukemia MONDO:0017858 MONDO:0858037 anal extramucosal (perianal) adenocarcinoma NCIT:C7474 MONDO:equivalentTo Anal Extramucosal (Perianal) Adenocarcinoma MONDO:0002652 -MONDO:0858041 primary intraosseous squamous cell carcinoma-solid type NCIT:C7491 MONDO:equivalentTo Primary Intraosseous Squamous Cell Carcinoma-Solid Type MONDO:0006385 MONDO:0858042 ameloblastic carcinoma-primary type NCIT:C7493 MONDO:equivalentTo Ameloblastic Carcinoma-Primary Type MONDO:0006079 MONDO:0858043 ameloblastic carcinoma-secondary type (dedifferentiated) NCIT:C7496 MONDO:equivalentTo Ameloblastic Carcinoma-Secondary Type (Dedifferentiated) MONDO:0006079|MONDO:0024878 MONDO:0858044 ameloblastic carcinoma derived from odontogenic cyst NCIT:C7497 MONDO:equivalentTo Ameloblastic Carcinoma Derived From Odontogenic Cyst MONDO:0006079|MONDO:0024878 -MONDO:0858045 primary intraosseous squamous cell carcinoma derived from odontogenic cyst NCIT:C7500 MONDO:equivalentTo Primary Intraosseous Squamous Cell Carcinoma Derived From Odontogenic Cyst MONDO:0006385|MONDO:0024878 +MONDO:0858045 primary intraosseous carcinoma, not otherwise specified, derived from odontogenic cyst NCIT:C7500 MONDO:equivalentTo Primary Intraosseous Carcinoma, Not Otherwise Specified, Derived from Odontogenic Cyst MONDO:0006385 MONDO:0858049 metastatic malignant neoplasm in the breast NCIT:C7511 MONDO:equivalentTo Metastatic Malignant Neoplasm in the Breast MONDO:0007254|MONDO:0024880 MONDO:0858050 malignant esophageal neoplasm by anatomic region NCIT:C7512 MONDO:equivalentTo Malignant Esophageal Neoplasm by Anatomic Region MONDO:0007576 MONDO:0858051 malignant esophageal neoplasm by topographic region NCIT:C7513 MONDO:equivalentTo Malignant Esophageal Neoplasm by Topographic Region MONDO:0007576 MONDO:0858052 kidney and ureter neoplasm NCIT:C7514 MONDO:equivalentTo Kidney and Ureter Neoplasm MONDO:0021066 MONDO:0858059 atypical adenoma NCIT:C7559 MONDO:equivalentTo Atypical Adenoma MONDO:0004972 MONDO:0858060 eccrine hidrocystoma NCIT:C7565 MONDO:equivalentTo Eccrine Hidrocystoma MONDO:0024247|MONDO:0006787 -MONDO:0858062 deep penetrating nevus NCIT:C7576 MONDO:equivalentTo Deep Penetrating Nevus MONDO:0044794 -MONDO:0858064 nevus of female genitalia NCIT:C7578 MONDO:equivalentTo Nevus of Female Genitalia MONDO:0005073|MONDO:0021148 MONDO:0858066 regressing nevus NCIT:C7603 MONDO:equivalentTo Regressing Nevus MONDO:0044794 MONDO:0858068 cerebral non-hodgkin lymphoma NCIT:C7609 MONDO:equivalentTo Cerebral Non-Hodgkin Lymphoma MONDO:0003655|MONDO:0044887 MONDO:0858069 malignant thymoma NCIT:C7612 MONDO:equivalentTo Malignant Thymoma MONDO:0002586|MONDO:0006456 MONDO:0858070 cutaneous lymphoproliferative disorder NCIT:C7614 MONDO:equivalentTo Cutaneous Lymphoproliferative Disorder MONDO:0858074 bilateral malignant neoplasm NCIT:C7627 MONDO:equivalentTo Bilateral Malignant Neoplasm MONDO:0004992 -MONDO:0858078 regional malignant urethral neoplasm NCIT:C7639 MONDO:equivalentTo Regional Malignant Urethral Neoplasm MONDO:0004192 MONDO:0858080 intermediate soft tissue neoplasm NCIT:C7653 MONDO:equivalentTo Intermediate Soft Tissue Neoplasm MONDO:0006424 MONDO:0858081 carcinoma in a polyp NCIT:C7682 MONDO:equivalentTo Carcinoma in a Polyp MONDO:0004993 MONDO:0858082 invasive breast ductal carcinoma and lobular carcinoma in situ NCIT:C7689 MONDO:equivalentTo Invasive Breast Ductal Carcinoma and Lobular Carcinoma In Situ MONDO:0005050 @@ -1656,7 +1597,6 @@ MONDO:0858086 adult hodgkin lymphoma NCIT:C7702 MONDO:equivalentTo Adult Hodgkin MONDO:0858087 adult non-hodgkin lymphoma NCIT:C7704 MONDO:equivalentTo Adult Non-Hodgkin Lymphoma MONDO:0003660|MONDO:0018908 MONDO:0858088 childhood non-hodgkin lymphoma NCIT:C7706 MONDO:equivalentTo Childhood Non-Hodgkin Lymphoma MONDO:0003659|MONDO:0018908 MONDO:0858089 adult soft tissue sarcoma NCIT:C7707 MONDO:equivalentTo Adult Soft Tissue Sarcoma MONDO:0018078 -MONDO:0858090 digestive system neuroendocrine tumor g1 NCIT:C7709 MONDO:equivalentTo Digestive System Neuroendocrine Tumor G1 MONDO:0000386|MONDO:0005369 MONDO:0858091 adult liver carcinoma NCIT:C7711 MONDO:equivalentTo Adult Liver Carcinoma MONDO:0018531 MONDO:0858092 childhood hodgkin lymphoma NCIT:C7714 MONDO:equivalentTo Childhood Hodgkin Lymphoma MONDO:0004952|MONDO:0003659 MONDO:0858094 gingival carcinoma NCIT:C7721 MONDO:equivalentTo Gingival Carcinoma MONDO:0005507|MONDO:0044925 @@ -1684,10 +1624,10 @@ MONDO:0858170 testicular mixed embryonal carcinoma and yolk sac tumor NCIT:C8001 MONDO:0858171 testicular mixed yolk sac tumor and teratoma NCIT:C8002 MONDO:equivalentTo Testicular Mixed Yolk Sac Tumor and Teratoma MONDO:0003120|MONDO:0003403 MONDO:0858172 testicular mixed yolk sac tumor and teratoma with seminoma NCIT:C8003 MONDO:equivalentTo Testicular Mixed Yolk Sac Tumor and Teratoma with Seminoma MONDO:0003120 MONDO:0858173 pancreatic somatostatin-producing neuroendocrine tumor NCIT:C8006 MONDO:equivalentTo Pancreatic Somatostatin-Producing Neuroendocrine Tumor MONDO:0006976|MONDO:0002994 -MONDO:0858174 low grade salivary gland carcinoma NCIT:C8012 MONDO:equivalentTo Low Grade Salivary Gland Carcinoma MONDO:0000521 +MONDO:0858174 salivary gland low grade carcinoma NCIT:C8012 MONDO:equivalentTo Salivary Gland Low Grade Carcinoma MONDO:0000521 MONDO:0858175 lip basal cell carcinoma NCIT:C8014 MONDO:equivalentTo Lip Basal Cell Carcinoma MONDO:0005341|MONDO:0021333 -MONDO:0858176 intermediate grade salivary gland mucoepidermoid carcinoma NCIT:C8017 MONDO:equivalentTo Intermediate Grade Salivary Gland Mucoepidermoid Carcinoma MONDO:0021009 -MONDO:0858177 high grade salivary gland carcinoma NCIT:C8018 MONDO:equivalentTo High Grade Salivary Gland Carcinoma MONDO:0000521 +MONDO:0858176 salivary gland intermediate grade mucoepidermoid carcinoma NCIT:C8017 MONDO:equivalentTo Salivary Gland Intermediate Grade Mucoepidermoid Carcinoma MONDO:0021009 +MONDO:0858177 salivary gland high grade carcinoma NCIT:C8018 MONDO:equivalentTo Salivary Gland High Grade Carcinoma MONDO:0000521 MONDO:0858178 salivary gland adenocarcinoma NCIT:C8021 MONDO:equivalentTo Salivary Gland Adenocarcinoma MONDO:0000521|MONDO:0004970 MONDO:0858179 salivary gland poorly differentiated squamous cell carcinoma NCIT:C8022 MONDO:equivalentTo Salivary Gland Poorly Differentiated Squamous Cell Carcinoma MONDO:0044740 MONDO:0858180 salivary gland undifferentiated carcinoma NCIT:C8024 MONDO:equivalentTo Salivary Gland Undifferentiated Carcinoma MONDO:0000521|MONDO:0005617 @@ -1757,7 +1697,6 @@ MONDO:0858365 stage iii t lymphoblastic leukemia/lymphoma NCIT:C8699 MONDO:equiv MONDO:0858366 stage iv t lymphoblastic leukemia/lymphoma NCIT:C8700 MONDO:equivalentTo Stage IV T Lymphoblastic Leukemia/Lymphoma MONDO:0003537 MONDO:0858370 metastatic malignant hemangiopericytoma NCIT:C8709 MONDO:equivalentTo Metastatic Malignant Hemangiopericytoma MONDO:0009330 MONDO:0858371 primary malignant hemangiopericytoma NCIT:C8710 MONDO:equivalentTo Primary Malignant Hemangiopericytoma MONDO:0009330 -MONDO:0858372 regional malignant ureter neoplasm NCIT:C8716 MONDO:equivalentTo Regional Malignant Ureter Neoplasm MONDO:0008627 MONDO:0858381 stage i ovarian choriocarcinoma NCIT:C8730 MONDO:equivalentTo Stage I Ovarian Choriocarcinoma MONDO:0003507 MONDO:0858382 stage ii ovarian choriocarcinoma NCIT:C8731 MONDO:equivalentTo Stage II Ovarian Choriocarcinoma MONDO:0003507 MONDO:0858383 stage iii ovarian choriocarcinoma NCIT:C8732 MONDO:equivalentTo Stage III Ovarian Choriocarcinoma MONDO:0003507 @@ -1775,9 +1714,7 @@ MONDO:0858472 malignant mastocytosis NCIT:C8991 MONDO:equivalentTo Malignant Mas MONDO:0858473 benign adrenal cortical neoplasm NCIT:C9004 MONDO:equivalentTo Benign Adrenal Cortical Neoplasm MONDO:0021511|MONDO:0036591 MONDO:0858474 acute myelomonocytic leukemia with abnormal eosinophils NCIT:C9020 MONDO:equivalentTo Acute Myelomonocytic Leukemia with Abnormal Eosinophils MONDO:0018871 MONDO:0858475 sarcoma by fnclcc grade NCIT:C9023 MONDO:equivalentTo Sarcoma by FNCLCC Grade MONDO:0005089 -MONDO:0858476 low grade malignant peripheral nerve sheath tumor NCIT:C9026 MONDO:equivalentTo Low Grade Malignant Peripheral Nerve Sheath Tumor MONDO:0017827 MONDO:0858477 atypical cartilaginous tumor/chondrosarcoma, grade 1 NCIT:C9027 MONDO:equivalentTo Atypical Cartilaginous Tumor/Chondrosarcoma, Grade 1 MONDO:0008977 -MONDO:0858478 high grade malignant peripheral nerve sheath tumor NCIT:C9030 MONDO:equivalentTo High Grade Malignant Peripheral Nerve Sheath Tumor MONDO:0017827 MONDO:0858479 renal cell cancer by ajcc v6 stage NCIT:C90343 MONDO:equivalentTo Renal Cell Cancer by AJCC v6 Stage MONDO:0005549 MONDO:0858480 bladder cancer by ajcc v6 stage NCIT:C90344 MONDO:equivalentTo Bladder Cancer by AJCC v6 Stage MONDO:0004986 MONDO:0858481 vulvar cancer by ajcc v6 stage NCIT:C90345 MONDO:equivalentTo Vulvar Cancer by AJCC v6 Stage MONDO:0005215 @@ -1827,7 +1764,6 @@ MONDO:0858536 invasive breast carcinoma of no special type with predominant intr MONDO:0858537 invasive breast lobular carcinoma with predominant in situ component NCIT:C9136 MONDO:equivalentTo Invasive Breast Lobular Carcinoma with Predominant In Situ Component MONDO:0005051 MONDO:0858538 adult acute myeloid leukemia NCIT:C9154 MONDO:equivalentTo Adult Acute Myeloid Leukemia MONDO:0018874 MONDO:0858543 testicular mixed embryonal carcinoma and yolk sac tumor with seminoma NCIT:C9172 MONDO:equivalentTo Testicular Mixed Embryonal Carcinoma and Yolk Sac Tumor with Seminoma MONDO:0003120 -MONDO:0858544 middle ear carcinoma in situ NCIT:C91741 MONDO:equivalentTo Middle Ear Carcinoma In Situ MONDO:0003190|MONDO:0004647 MONDO:0858546 good prognosis metastatic gestational trophoblastic tumor NCIT:C9177 MONDO:equivalentTo Good Prognosis Metastatic Gestational Trophoblastic Tumor MONDO:0018944 MONDO:0858547 poor prognosis metastatic gestational trophoblastic tumor NCIT:C9178 MONDO:equivalentTo Poor Prognosis Metastatic Gestational Trophoblastic Tumor MONDO:0018944 MONDO:0858549 intraocular schwannoma NCIT:C92182 MONDO:equivalentTo Intraocular Schwannoma MONDO:0021454|MONDO:0004820 @@ -1845,13 +1781,11 @@ MONDO:0858584 lymphocyte-depleted classic hodgkin lymphoma NCIT:C9283 MONDO:equi MONDO:0858585 central nervous system histiocytic and dendritic cell neoplasm NCIT:C92944 MONDO:equivalentTo Central Nervous System Histiocytic and Dendritic Cell Neoplasm MONDO:0006247|MONDO:0003641 MONDO:0858588 peritoneal malignant mesothelioma NCIT:C9350 MONDO:equivalentTo Peritoneal Malignant Mesothelioma MONDO:0006292|MONDO:0002087|MONDO:0006362 MONDO:0858595 combined lung small cell carcinoma and lung adenocarcinoma NCIT:C9379 MONDO:equivalentTo Combined Lung Small Cell Carcinoma and Lung Adenocarcinoma MONDO:0003438 -MONDO:0858596 sarcoma by nci grade NCIT:C9387 MONDO:equivalentTo Sarcoma by NCI Grade MONDO:0005089 MONDO:0858597 well differentiated malignant hemangiopericytoma NCIT:C9392 MONDO:equivalentTo Well Differentiated Malignant Hemangiopericytoma MONDO:0009330 MONDO:0858598 malignant hemangiopericytoma nci grade 2 NCIT:C9393 MONDO:equivalentTo Malignant Hemangiopericytoma NCI Grade 2 MONDO:0002789 MONDO:0858599 malignant hemangiopericytoma nci grade 3 NCIT:C9394 MONDO:equivalentTo Malignant Hemangiopericytoma NCI Grade 3 MONDO:0002789 MONDO:0858600 round cell liposarcoma nci grade 2 NCIT:C9401 MONDO:equivalentTo Round Cell Liposarcoma NCI Grade 2 MONDO:0005238 MONDO:0858601 round cell liposarcoma nci grade 3 NCIT:C9402 MONDO:equivalentTo Round Cell Liposarcoma NCI Grade 3 MONDO:0005238 -MONDO:0858602 sarcoma by ajcc grade NCIT:C9416 MONDO:equivalentTo Sarcoma by AJCC Grade MONDO:0005089 MONDO:0858603 childhood hematopoietic and lymphoid cell neoplasm NCIT:C9431 MONDO:equivalentTo Childhood Hematopoietic and Lymphoid Cell Neoplasm MONDO:0021079|MONDO:0044881 MONDO:0858619 grade 1 colorectal adenocarcinoma NCIT:C9446 MONDO:equivalentTo Grade 1 Colorectal Adenocarcinoma MONDO:0005008 MONDO:0858620 grade 2 colorectal adenocarcinoma NCIT:C9447 MONDO:equivalentTo Grade 2 Colorectal Adenocarcinoma MONDO:0005008 @@ -1880,7 +1814,7 @@ MONDO:0858658 pancreatic well differentiated ductal adenocarcinoma NCIT:C95426 M MONDO:0858659 pancreatic moderately differentiated ductal adenocarcinoma NCIT:C95427 MONDO:equivalentTo Pancreatic Moderately Differentiated Ductal Adenocarcinoma MONDO:0005184 MONDO:0858660 pancreatic poorly differentiated ductal adenocarcinoma NCIT:C95428 MONDO:equivalentTo Pancreatic Poorly Differentiated Ductal Adenocarcinoma MONDO:0005184 MONDO:0858661 pancreatic mixed acinar-ductal carcinoma NCIT:C95458 MONDO:equivalentTo Pancreatic Mixed Acinar-Ductal Carcinoma MONDO:0006047 -MONDO:0858662 pancreatic mixed acinar-ductal neuroendocrine carcinoma NCIT:C95460 MONDO:equivalentTo Pancreatic Mixed Acinar-Ductal Neuroendocrine Carcinoma MONDO:0044727 +MONDO:0858662 pancreatic mixed ductal adenocarcinoma-acinar carcinoma-neuroendocrine carcinoma NCIT:C95460 MONDO:equivalentTo Pancreatic Mixed Ductal Adenocarcinoma-Acinar Carcinoma-Neuroendocrine Carcinoma MONDO:0044727 MONDO:0858663 pancreatic hepatoid adenocarcinoma NCIT:C95465 MONDO:equivalentTo Pancreatic Hepatoid Adenocarcinoma MONDO:0005184|MONDO:0006243 MONDO:0858664 pancreatic medullary carcinoma NCIT:C95466 MONDO:equivalentTo Pancreatic Medullary Carcinoma MONDO:0005184 MONDO:0858665 pancreatic serous adenoma NCIT:C95470 MONDO:equivalentTo Pancreatic Serous Adenoma MONDO:0021441|MONDO:0002810|MONDO:0036976 @@ -1907,7 +1841,7 @@ MONDO:0858702 intestinal neuroendocrine tumor NCIT:C96062 MONDO:equivalentTo Int MONDO:0858703 small intestinal mixed adenoneuroendocrine carcinoma NCIT:C96066 MONDO:equivalentTo Small Intestinal Mixed Adenoneuroendocrine Carcinoma MONDO:0006182|MONDO:0005522 MONDO:0858705 colorectal neuroendocrine neoplasm NCIT:C96152 MONDO:equivalentTo Colorectal Neuroendocrine Neoplasm MONDO:0002883|MONDO:0005335 MONDO:0858706 colorectal mixed adenoneuroendocrine carcinoma NCIT:C96158 MONDO:equivalentTo Colorectal Mixed Adenoneuroendocrine Carcinoma MONDO:0006182|MONDO:0024331 -MONDO:0858707 digestive system neuroendocrine tumor g2 NCIT:C96166 MONDO:equivalentTo Digestive System Neuroendocrine Tumor G2 MONDO:0000386 +MONDO:0858707 digestive system neuroendocrine tumor g2 NCIT:C96166 MONDO:equivalentTo Digestive System Neuroendocrine Tumor G2 MONDO:0000386|MONDO:0006095 MONDO:0858715 serrated lesions and polyps NCIT:C96414 MONDO:equivalentTo Serrated Lesions and Polyps MONDO:0006180 MONDO:0858717 appendix enterochromaffin cell serotonin-producing neuroendocrine tumor NCIT:C96424 MONDO:equivalentTo Appendix Enterochromaffin Cell Serotonin-Producing Neuroendocrine Tumor MONDO:0015066 MONDO:0858721 rectal serrated lesions and polyps NCIT:C96465 MONDO:equivalentTo Rectal Serrated Lesions and Polyps MONDO:0006164|MONDO:0000530|MONDO:0021398 @@ -1958,7 +1892,6 @@ MONDO:0858789 invasive breast lobular carcinoma, pleomorphic variant NCIT:C97051 MONDO:0858790 invasive breast lobular carcinoma, solid variant NCIT:C97052 MONDO:equivalentTo Invasive Breast Lobular Carcinoma, Solid Variant MONDO:0005051 MONDO:0858791 invasive breast lobular carcinoma, tubulolobular variant NCIT:C97053 MONDO:equivalentTo Invasive Breast Lobular Carcinoma, Tubulolobular Variant MONDO:0005051 MONDO:0858792 mixed congenital mesoblastic nephroma NCIT:C97058 MONDO:equivalentTo Mixed Congenital Mesoblastic Nephroma MONDO:0017043|MONDO:0005853 -MONDO:0858804 sclerosing polycystic adenosis NCIT:C97135 MONDO:equivalentTo Sclerosing Polycystic Adenosis MONDO:0021460 MONDO:0858851 contralateral breast carcinoma NCIT:C99390 MONDO:equivalentTo Contralateral Breast Carcinoma MONDO:0003982 MONDO:0859471 neoplastic medium-sized lymphocyte NCIT:C37004 MONDO:equivalentTo Neoplastic Medium-Sized Lymphocyte MONDO:0859472 neoplastic b-lymphocyte NCIT:C38640 MONDO:equivalentTo Neoplastic B-Lymphocyte @@ -1986,7 +1919,7 @@ MONDO:0860056 tobacco use disorder NCIT:C35074 MONDO:equivalentTo Tobacco Use Di MONDO:0860057 sternal disorder NCIT:C35744 MONDO:equivalentTo Sternal Disorder MONDO:0860058 chest wall disorder NCIT:C35745 MONDO:equivalentTo Chest Wall Disorder MONDO:0860059 axillary disorder NCIT:C35746 MONDO:equivalentTo Axillary Disorder -MONDO:0860060 hematopoietic and lymphoid system disorder NCIT:C35814 MONDO:equivalentTo Hematopoietic and Lymphoid System Disorder +MONDO:0860060 hematopoietic and lymphatic system disorder NCIT:C35814 MONDO:equivalentTo Hematopoietic and Lymphatic System Disorder MONDO:0860062 anal precancerous condition NCIT:C7407 MONDO:equivalentTo Anal Precancerous Condition MONDO:0860063 esophageal precancerous condition NCIT:C7423 MONDO:equivalentTo Esophageal Precancerous Condition MONDO:0860064 gastric precancerous condition NCIT:C7424 MONDO:equivalentTo Gastric Precancerous Condition @@ -2023,7 +1956,6 @@ MONDO:0957639 childhood low grade fibromyxoid sarcoma NCIT:C188970 MONDO:equival MONDO:0957640 extragonadal teratoma NCIT:C189045 MONDO:equivalentTo Extragonadal Teratoma MONDO:0018201|MONDO:0002601 MONDO:0957641 testicular teratoma, postpubertal-type NCIT:C189057 MONDO:equivalentTo Testicular Teratoma, Postpubertal-Type MONDO:0003510|MONDO:0018193 MONDO:0957642 kidney carcinoma molecular subtypes NCIT:C189241 MONDO:equivalentTo Kidney Carcinoma Molecular Subtypes MONDO:0005206 -MONDO:0957643 eosinophilic solid and cystic renal cell carcinoma NCIT:C189254 MONDO:equivalentTo Eosinophilic Solid and Cystic Renal Cell Carcinoma MONDO:0005549 MONDO:0957644 ovarian sertoli-leydig cell tumor molecular subtypes NCIT:C189319 MONDO:equivalentTo Ovarian Sertoli-Leydig Cell Tumor Molecular Subtypes MONDO:0036595 MONDO:0957645 mullerian papilloma NCIT:C189336 MONDO:equivalentTo Mullerian Papilloma MONDO:0021078 MONDO:0957646 childhood breast neoplasm NCIT:C189338 MONDO:equivalentTo Childhood Breast Neoplasm MONDO:0021079|MONDO:0021100 @@ -2103,7 +2035,6 @@ MONDO:0957719 acute myeloid leukemia with myelodysplasia-related cytogenetic abn MONDO:0957720 low grade endometrioid adenocarcinoma NCIT:C199146 MONDO:equivalentTo Low Grade Endometrioid Adenocarcinoma MONDO:0005026 MONDO:0957721 high grade endometrioid adenocarcinoma NCIT:C199149 MONDO:equivalentTo High Grade Endometrioid Adenocarcinoma MONDO:0005026 MONDO:0957722 early t precursor lymphoblastic leukemia/lymphoma NCIT:C199170 MONDO:equivalentTo Early T Precursor Lymphoblastic Leukemia/Lymphoma MONDO:0003537 -MONDO:0957723 early t precursor acute lymphoblastic leukemia with bcl11b rearrangement NCIT:C199171 MONDO:equivalentTo Early T Precursor Acute Lymphoblastic Leukemia with BCL11B Rearrangement MONDO:0100291 MONDO:0957724 early t precursor acute lymphoblastic leukemia, not otherwise specified NCIT:C199172 MONDO:equivalentTo Early T Precursor Acute Lymphoblastic Leukemia, Not Otherwise Specified MONDO:0100291 MONDO:0957725 t lymphoblastic leukemia/lymphoma, not otherwise specified NCIT:C199173 MONDO:equivalentTo T Lymphoblastic Leukemia/Lymphoma, Not Otherwise Specified MONDO:0003537 MONDO:0957726 b acute lymphoblastic leukemia with recurrent genetic abnormalities NCIT:C199202 MONDO:equivalentTo B Acute Lymphoblastic Leukemia with Recurrent Genetic Abnormalities MONDO:0020511|MONDO:0035605 @@ -2145,7 +2076,7 @@ MONDO:0957761 ebv-negative burkitt lymphoma NCIT:C200688 MONDO:equivalentTo EBV- MONDO:0957762 plasma cell neoplasm with associated paraneoplastic syndrome NCIT:C200738 MONDO:equivalentTo Plasma Cell Neoplasm with Associated Paraneoplastic Syndrome MONDO:0004959 MONDO:0957763 who grade 4 glioma NCIT:C200758 MONDO:equivalentTo WHO Grade 4 Glioma MONDO:0100342 MONDO:0957764 primary cutaneous peripheral t-cell lymphoma, not otherwise specified NCIT:C201080 MONDO:equivalentTo Primary Cutaneous Peripheral T-Cell Lymphoma, Not Otherwise Specified MONDO:0000607 -MONDO:0957765 cribriform comedo-type adenocarcinoma NCIT:C201124 MONDO:equivalentTo Cribriform Comedo-Type Adenocarcinoma MONDO:0003575 +MONDO:0957765 cribriform comedo-type adenocarcinoma NCIT:C201124 MONDO:equivalentTo Cribriform Comedo-Type Adenocarcinoma MONDO:0003575|MONDO:0006176 MONDO:0957766 aleukemic myeloid leukemia NCIT:C201127 MONDO:equivalentTo Aleukemic Myeloid leukemia MONDO:0003730|MONDO:0004643 MONDO:0957767 solid pseudopapillary neoplasm NCIT:C201136 MONDO:equivalentTo Solid Pseudopapillary Neoplasm MONDO:0004992 MONDO:0957768 endemic burkitt lymphoma NCIT:C27122 MONDO:equivalentTo Endemic Burkitt Lymphoma MONDO:0007243 @@ -2176,3 +2107,105 @@ MONDO:0957866 stage m2 pineoblastoma NCIT:C186570 MONDO:equivalentTo Stage M2 Pi MONDO:0957867 stage m3 pineoblastoma NCIT:C186571 MONDO:equivalentTo Stage M3 Pineoblastoma MONDO:0016722 MONDO:0957868 stage m4 pineoblastoma NCIT:C186572 MONDO:equivalentTo Stage M4 Pineoblastoma MONDO:0016722 MONDO:0958220 colorectal perineurioma NCIT:C96513 MONDO:equivalentTo Colorectal Perineurioma MONDO:0015031|MONDO:0021444 +MONDO:0968996 platinum-resistant primary peritoneal carcinoma NCIT:C157622 MONDO:equivalentTo Platinum-Resistant Primary Peritoneal Carcinoma MONDO:0015686 +MONDO:0968997 platinum-resistant malignant female reproductive system neoplasm NCIT:C169021 MONDO:equivalentTo Platinum-Resistant Malignant Female Reproductive System Neoplasm MONDO:0001416 +MONDO:0968998 extracutaneous merkel cell carcinoma NCIT:C173586 MONDO:equivalentTo Extracutaneous Merkel Cell Carcinoma MONDO:0019210 +MONDO:0968999 non-neoplastic tonsillar disorder NCIT:C173798 MONDO:equivalentTo Non-Neoplastic Tonsillar Disorder +MONDO:0969000 swi/snf complex-deficient sinonasal carcinoma NCIT:C201634 MONDO:equivalentTo SWI/SNF Complex-Deficient Sinonasal Carcinoma MONDO:0056819 +MONDO:0969001 tracheal verrucous carcinoma NCIT:C201742 MONDO:equivalentTo Tracheal Verrucous Carcinoma MONDO:0001419|MONDO:0006006 +MONDO:0969002 hypopharyngeal verrucous carcinoma NCIT:C201743 MONDO:equivalentTo Hypopharyngeal Verrucous Carcinoma MONDO:0044638|MONDO:0006006 +MONDO:0969003 hypopharyngeal papillary squamous cell carcinoma NCIT:C201748 MONDO:equivalentTo Hypopharyngeal Papillary Squamous Cell Carcinoma MONDO:0002979|MONDO:0044638 +MONDO:0969004 hypopharyngeal spindle cell squamous carcinoma NCIT:C201749 MONDO:equivalentTo Hypopharyngeal Spindle Cell Squamous Carcinoma MONDO:0044638|MONDO:0021663 +MONDO:0969005 parotid gland keratocystoma NCIT:C201770 MONDO:equivalentTo Parotid Gland Keratocystoma MONDO:0021460 +MONDO:0969006 hyalinizing clear cell carcinoma NCIT:C201821 MONDO:equivalentTo Hyalinizing Clear Cell Carcinoma MONDO:0004993 +MONDO:0969007 tongue verrucous carcinoma NCIT:C201878 MONDO:equivalentTo Tongue Verrucous Carcinoma MONDO:0021538|MONDO:0000500 +MONDO:0969008 palatine tonsil hamartomatous polyp NCIT:C201900 MONDO:equivalentTo Palatine Tonsil Hamartomatous Polyp +MONDO:0969009 transformed chronic lymphocytic leukemia to hodgkin lymphoma NCIT:C201960 MONDO:equivalentTo Transformed Chronic Lymphocytic Leukemia to Hodgkin Lymphoma MONDO:0004948 +MONDO:0969010 pineoblastoma molecular subtypes NCIT:C201966 MONDO:equivalentTo Pineoblastoma Molecular Subtypes MONDO:0016722 +MONDO:0969011 spinal cord pilocytic astrocytoma NCIT:C201976 MONDO:equivalentTo Spinal Cord Pilocytic Astrocytoma MONDO:0003174|MONDO:0016691 +MONDO:0969012 brain low grade glioma NCIT:C201977 MONDO:equivalentTo Brain Low Grade Glioma MONDO:0021632|MONDO:0021637 +MONDO:0969013 clear cell calcifying epithelial odontogenic tumor NCIT:C202057 MONDO:equivalentTo Clear Cell Calcifying Epithelial Odontogenic Tumor MONDO:0022057 +MONDO:0969014 cystic/microcystic calcifying epithelial odontogenic tumor NCIT:C202058 MONDO:equivalentTo Cystic/Microcystic Calcifying Epithelial Odontogenic Tumor MONDO:0022057 +MONDO:0969015 non-calcifying/langerhans cell-rich calcifying epithelial odontogenic tumor NCIT:C202059 MONDO:equivalentTo Non-Calcifying/Langerhans Cell-Rich Calcifying Epithelial Odontogenic Tumor MONDO:0022057 +MONDO:0969016 adenoid ameloblastoma NCIT:C202061 MONDO:equivalentTo Adenoid Ameloblastoma MONDO:0017795 +MONDO:0969017 egfr-positive lung non-small cell carcinoma NCIT:C202131 MONDO:equivalentTo EGFR-Positive Lung Non-Small Cell Carcinoma MONDO:0005233 +MONDO:0969018 juvenile trabecular ossifying fibroma NCIT:C202205 MONDO:equivalentTo Juvenile Trabecular Ossifying Fibroma MONDO:0002119 +MONDO:0969019 psammomatoid ossifying fibroma NCIT:C202209 MONDO:equivalentTo Psammomatoid Ossifying Fibroma MONDO:0002119 +MONDO:0969020 surface osteoma NCIT:C202252 MONDO:equivalentTo Surface Osteoma MONDO:0005166 +MONDO:0969021 central osteoma NCIT:C202253 MONDO:equivalentTo Central Osteoma MONDO:0005166 +MONDO:0969022 rhabdomyosarcoma with tfcp2 rearrangement NCIT:C202263 MONDO:equivalentTo Rhabdomyosarcoma with TFCP2 Rearrangement MONDO:0005212 +MONDO:0969023 non-clear cell renal cell carcinoma NCIT:C202497 MONDO:equivalentTo Non-Clear Cell Renal Cell Carcinoma MONDO:0005549 +MONDO:0969024 middle ear papilloma NCIT:C202582 MONDO:equivalentTo Middle Ear Papilloma MONDO:0021078|MONDO:0021482 +MONDO:0969025 external auditory canal squamous cell carcinoma NCIT:C202594 MONDO:equivalentTo External Auditory Canal Squamous Cell Carcinoma MONDO:0003501 +MONDO:0969026 orbit solitary fibrous tumor NCIT:C202620 MONDO:equivalentTo Orbit Solitary Fibrous Tumor MONDO:0016238|MONDO:0024611 +MONDO:0969027 head and neck soft tissue neoplasm NCIT:C202623 MONDO:equivalentTo Head and Neck Soft Tissue Neoplasm MONDO:0006424|MONDO:0005586 +MONDO:0969028 proximal colon carcinoma NCIT:C202633 MONDO:equivalentTo Proximal Colon Carcinoma MONDO:0002032 +MONDO:0969029 distal colon carcinoma NCIT:C202634 MONDO:equivalentTo Distal Colon Carcinoma MONDO:0002032 +MONDO:0969030 oral cavity neurofibroma NCIT:C202860 MONDO:equivalentTo Oral Cavity Neurofibroma MONDO:0021445|MONDO:0016755 +MONDO:0969031 oral cavity schwannoma NCIT:C202876 MONDO:equivalentTo Oral Cavity Schwannoma MONDO:0021445|MONDO:0004820 +MONDO:0969032 head and neck phosphaturic mesenchymal tumor NCIT:C202879 MONDO:equivalentTo Head and Neck Phosphaturic Mesenchymal Tumor MONDO:0006368|MONDO:0005586 +MONDO:0969033 appendicular skeleton phosphaturic mesenchymal tumor NCIT:C202880 MONDO:equivalentTo Appendicular Skeleton Phosphaturic Mesenchymal Tumor MONDO:0019060|MONDO:0006368 +MONDO:0969034 poorly differentiated synovial sarcoma NCIT:C202883 MONDO:equivalentTo Poorly Differentiated Synovial Sarcoma MONDO:0010434 +MONDO:0969035 primary cd30-positive t-cell lymphoproliferative disorder NCIT:C202952 MONDO:equivalentTo Primary CD30-Positive T-Cell Lymphoproliferative Disorder MONDO:0005169 +MONDO:0969036 head and neck hematopoietic and lymphoid cell neoplasm NCIT:C202954 MONDO:equivalentTo Head and Neck Hematopoietic and Lymphoid Cell Neoplasm MONDO:0005586|MONDO:0044881 +MONDO:0969037 head and neck germ cell tumor NCIT:C202977 MONDO:equivalentTo Head and Neck Germ Cell Tumor MONDO:0018201|MONDO:0005586 +MONDO:0969038 cecum neuroendocrine tumor NCIT:C203386 MONDO:equivalentTo Cecum Neuroendocrine Tumor MONDO:0005694|MONDO:0015067 +MONDO:0969039 ascending colon neuroendocrine tumor NCIT:C203387 MONDO:equivalentTo Ascending Colon Neuroendocrine Tumor MONDO:0015067 +MONDO:0969040 descending colon neuroendocrine tumor NCIT:C203388 MONDO:equivalentTo Descending Colon Neuroendocrine Tumor MONDO:0015067 +MONDO:0969041 sigmoid colon neuroendocrine tumor NCIT:C203389 MONDO:equivalentTo Sigmoid Colon Neuroendocrine Tumor MONDO:0015067 +MONDO:0969042 transverse colon neuroendocrine tumor NCIT:C203390 MONDO:equivalentTo Transverse Colon Neuroendocrine Tumor MONDO:0015067 +MONDO:0969043 histiocytic disorder NCIT:C203422 MONDO:equivalentTo Histiocytic Disorder +MONDO:0969044 myelodysplastic chronic myelomonocytic leukemia NCIT:C203443 MONDO:equivalentTo Myelodysplastic Chronic Myelomonocytic Leukemia MONDO:0020311 +MONDO:0969045 myeloproliferative chronic myelomonocytic leukemia NCIT:C203444 MONDO:equivalentTo Myeloproliferative Chronic Myelomonocytic Leukemia MONDO:0020311 +MONDO:0969046 t acute lymphoblastic leukemia with recurrent genetic abnormalities NCIT:C203469 MONDO:equivalentTo T Acute Lymphoblastic Leukemia with Recurrent Genetic Abnormalities MONDO:0004963 +MONDO:0969047 esophageal and gastroesophageal junction carcinoma NCIT:C203673 MONDO:equivalentTo Esophageal and Gastroesophageal Junction Carcinoma MONDO:0006181 +MONDO:0969048 low grade mucinous carcinoma peritonei NCIT:C203946 MONDO:equivalentTo Low Grade Mucinous Carcinoma Peritonei MONDO:0017048 +MONDO:0969049 high grade mucinous carcinoma peritonei NCIT:C203948 MONDO:equivalentTo High Grade Mucinous Carcinoma Peritonei MONDO:0017048 +MONDO:0969050 merkel cell polyoma virus-positive merkel cell carcinoma NCIT:C204383 MONDO:equivalentTo Merkel Cell Polyoma Virus-Positive Merkel Cell Carcinoma MONDO:0019210 +MONDO:0969051 merkel cell polyoma virus-negative merkel cell carcinoma NCIT:C204385 MONDO:equivalentTo Merkel Cell Polyoma Virus-Negative Merkel Cell Carcinoma MONDO:0019210 +MONDO:0969052 lentiginous melanocytic nevus NCIT:C204482 MONDO:equivalentTo Lentiginous Melanocytic Nevus MONDO:0044794 +MONDO:0969053 mitf pathway-activated melanocytic tumor NCIT:C204739 MONDO:equivalentTo MITF Pathway-Activated Melanocytic Tumor MONDO:0021583 +MONDO:0969054 dermal spitz nevus NCIT:C204789 MONDO:equivalentTo Dermal Spitz Nevus MONDO:0006813|MONDO:0044793 +MONDO:0969055 spitz tumor NCIT:C204790 MONDO:equivalentTo Spitz Tumor MONDO:0021583 +MONDO:0969056 melanoma in intermittently sun-exposed skin NCIT:C204840 MONDO:equivalentTo Melanoma in Intermittently Sun-Exposed Skin MONDO:0005012 +MONDO:0969057 low-csd melanoma, superficial spreading melanoma subtype NCIT:C204843 MONDO:equivalentTo Low-CSD Melanoma, Superficial Spreading Melanoma Subtype MONDO:0020638 +MONDO:0969058 melanoma in chronically sun-exposed skin NCIT:C204864 MONDO:equivalentTo Melanoma in Chronically Sun-Exposed Skin MONDO:0005012 +MONDO:0969059 mucosal nevus NCIT:C204907 MONDO:equivalentTo Mucosal Nevus MONDO:0005073 +MONDO:0969060 dendritic blue nevus NCIT:C204910 MONDO:equivalentTo Dendritic Blue Nevus MONDO:0006680 +MONDO:0969061 intermediate congenital melanocytic nevus NCIT:C204976 MONDO:equivalentTo Intermediate Congenital Melanocytic Nevus MONDO:0044792 +MONDO:0969062 conjunctival melanocytic neoplasm NCIT:C204977 MONDO:equivalentTo Conjunctival Melanocytic Neoplasm MONDO:0021143|MONDO:0020204 +MONDO:0969063 uveal melanocytic neoplasm NCIT:C205057 MONDO:equivalentTo Uveal Melanocytic Neoplasm MONDO:0021143|MONDO:0021225 +MONDO:0969064 nodular melanoma NCIT:C205125 MONDO:equivalentTo Nodular Melanoma MONDO:0005105 +MONDO:0969065 dermal melanoma NCIT:C205129 MONDO:equivalentTo Dermal Melanoma MONDO:0005012 +MONDO:0969066 metastatic melanoma in the lymph nodes NCIT:C205131 MONDO:equivalentTo Metastatic Melanoma in the Lymph Nodes MONDO:0005191|MONDO:0005438 +MONDO:0969067 platinum-sensitive endometrial carcinoma NCIT:C205187 MONDO:equivalentTo Platinum-Sensitive Endometrial Carcinoma MONDO:0002447 +MONDO:0969068 early stage cervical carcinoma NCIT:C205287 MONDO:equivalentTo Early Stage Cervical Carcinoma MONDO:0005131 +MONDO:0969069 early stage clear cell renal cell carcinoma NCIT:C205289 MONDO:equivalentTo Early Stage Clear Cell Renal Cell Carcinoma MONDO:0005005 +MONDO:0969070 early stage colorectal carcinoma NCIT:C205290 MONDO:equivalentTo Early Stage Colorectal Carcinoma MONDO:0024331 +MONDO:0969071 early stage endometrial carcinoma NCIT:C205295 MONDO:equivalentTo Early Stage Endometrial Carcinoma MONDO:0002447 +MONDO:0969072 early stage esophageal carcinoma NCIT:C205298 MONDO:equivalentTo Early Stage Esophageal Carcinoma MONDO:0019086 +MONDO:0969073 early stage hepatocellular carcinoma NCIT:C205301 MONDO:equivalentTo Early Stage Hepatocellular Carcinoma MONDO:0007256 +MONDO:0969074 early stage lung non-small cell carcinoma NCIT:C205303 MONDO:equivalentTo Early Stage Lung Non-Small Cell Carcinoma MONDO:0005233 +MONDO:0969075 early stage malignant skin neoplasm NCIT:C205307 MONDO:equivalentTo Early Stage Malignant Skin Neoplasm MONDO:0002898 +MONDO:0969076 primary cutaneous nut adnexal carcinoma NCIT:C205357 MONDO:equivalentTo Primary Cutaneous NUT Adnexal Carcinoma MONDO:0005563|MONDO:0006973 +MONDO:0969077 trichogerminoma NCIT:C205371 MONDO:equivalentTo Trichogerminoma MONDO:0020593 +MONDO:0969078 apocrine cystadenoma NCIT:C205459 MONDO:equivalentTo Apocrine Cystadenoma MONDO:0002804|MONDO:0002369 +MONDO:0969079 eccrine poroma NCIT:C205462 MONDO:equivalentTo Eccrine Poroma MONDO:0006738|MONDO:0024247 +MONDO:0969080 hidroacanthoma simplex NCIT:C205475 MONDO:equivalentTo Hidroacanthoma Simplex MONDO:0006738 +MONDO:0969081 solid cystic hidradenoma NCIT:C205539 MONDO:equivalentTo Solid Cystic Hidradenoma MONDO:0002805 +MONDO:0969082 sialoblastoma NCIT:C35837 MONDO:equivalentTo Sialoblastoma MONDO:0004669 +MONDO:0969083 cribriform trichoblastoma NCIT:C43322 MONDO:equivalentTo Cribriform Trichoblastoma MONDO:0020593 +MONDO:0969084 lung neuroendocrine carcinoma NCIT:C45569 MONDO:equivalentTo Lung Neuroendocrine Carcinoma MONDO:0005454|MONDO:0005138|MONDO:0002120 +MONDO:0969085 branchioma NCIT:C53595 MONDO:equivalentTo Branchioma MONDO:0021455 +MONDO:0969086 ear carcinoma NCIT:C54262 MONDO:equivalentTo Ear Carcinoma MONDO:0003277|MONDO:0002038 +MONDO:0969087 intracranial melanoma NCIT:C5442 MONDO:equivalentTo Intracranial Melanoma MONDO:0003761|MONDO:0001657|MONDO:0021632 +MONDO:0969088 meckel diverticulum neuroendocrine tumor g1 NCIT:C6424 MONDO:equivalentTo Meckel Diverticulum Neuroendocrine Tumor G1 MONDO:0021533 +MONDO:0969089 duodenal neuroendocrine tumor g1 NCIT:C6425 MONDO:equivalentTo Duodenal Neuroendocrine Tumor G1 MONDO:0000540|MONDO:0015063 +MONDO:0969090 intracranial myeloid sarcoma NCIT:C7008 MONDO:equivalentTo Intracranial Myeloid Sarcoma MONDO:0003641|MONDO:0001657|MONDO:0006861|MONDO:0021632 +MONDO:0969091 hamartomatous polyp NCIT:C8372 MONDO:equivalentTo Hamartomatous Polyp +MONDO:0969092 well differentiated fibrosarcoma NCIT:C9025 MONDO:equivalentTo Well Differentiated Fibrosarcoma MONDO:0005164 +MONDO:0969093 poorly differentiated angiosarcoma NCIT:C9031 MONDO:equivalentTo Poorly Differentiated Angiosarcoma MONDO:0016982 +MONDO:0969094 well differentiated leiomyosarcoma NCIT:C9389 MONDO:equivalentTo Well Differentiated Leiomyosarcoma MONDO:0005058 +MONDO:0969095 poorly differentiated fibrosarcoma NCIT:C9404 MONDO:equivalentTo Poorly Differentiated Fibrosarcoma MONDO:0005164 +MONDO:0969096 low grade sarcoma NCIT:C9417 MONDO:equivalentTo Low Grade Sarcoma MONDO:0005089 +MONDO:0969097 high grade sarcoma NCIT:C9418 MONDO:equivalentTo High Grade Sarcoma MONDO:0005089 diff --git a/src/ontology/slurp/omim.tsv b/src/ontology/slurp/omim.tsv index 1fa75226..ed322813 100644 --- a/src/ontology/slurp/omim.tsv +++ b/src/ontology/slurp/omim.tsv @@ -1,12 +1,7 @@ mondo_id mondo_label xref xref_source original_label definition parents ID LABEL A oboInOwl:hasDbXref >A oboInOwl:source SPLIT=| A IAO:0000115 SC % -MONDO:0968950 li-fraumeni syndrome OMIMPS:151623 MONDO:equivalentTo Li-Fraumeni syndrome -MONDO:0968976 neurodevelopmental disorder with progressive movement abnormalities OMIM:620785 MONDO:equivalentTo neurodevelopmental disorder with progressive movement abnormalities -MONDO:0968977 basal ganglia calcification, idiopathic, 9, autosomal recessive OMIM:620786 MONDO:equivalentTo basal ganglia calcification, idiopathic, 9, autosomal recessive -MONDO:0968978 aplasia cutis-enamel dysplasia syndrome OMIM:620789 MONDO:equivalentTo aplasia cutis-enamel dysplasia syndrome -MONDO:0968979 neurodevelopmental disorder with hypotonia and seizures OMIM:620790 MONDO:equivalentTo neurodevelopmental disorder with hypotonia and seizures -MONDO:0968980 otosclerosis 12 OMIM:620792 MONDO:equivalentTo otosclerosis 12 MONDO:0005349 -MONDO:0968981 deafness, autosomal recessive 124 OMIM:620794 MONDO:equivalentTo deafness, autosomal recessive 124 MONDO:0019588 -MONDO:0968982 autoinflammation with episodic fever and immune dysregulation OMIM:620795 MONDO:equivalentTo autoinflammation with episodic fever and immune dysregulation -MONDO:0968983 proteasome-associated autoinflammatory syndrome 6 OMIM:620796 MONDO:equivalentTo proteasome-associated autoinflammatory syndrome 6 MONDO:0009726 -MONDO:0968984 citrullinemia OMIMPS:215700 MONDO:equivalentTo Citrullinemia +MONDO:0969099 leigh syndrome, mitochondrial OMIM:500017 MONDO:equivalentTo leigh syndrome, mitochondrial +MONDO:0969100 developmental and epileptic encephalopathy 116 OMIM:620806 MONDO:equivalentTo developmental and epileptic encephalopathy 116 MONDO:0100062 +MONDO:0969101 rothmund-thomson syndrome, type 4 OMIM:620819 MONDO:equivalentTo rothmund-thomson syndrome, type 4 MONDO:0010002 +MONDO:0969102 el hayek-chahrour neurodevelopmental syndrome OMIM:620820 MONDO:equivalentTo el hayek-chahrour neurodevelopmental syndrome +MONDO:0969103 neuroocular syndrome OMIMPS:619539 MONDO:equivalentTo Neuroocular syndrome diff --git a/src/ontology/slurp/ordo.tsv b/src/ontology/slurp/ordo.tsv index f28dc071..89670d61 100644 --- a/src/ontology/slurp/ordo.tsv +++ b/src/ontology/slurp/ordo.tsv @@ -1,13 +1,12 @@ mondo_id mondo_label xref xref_source original_label definition parents ID LABEL A oboInOwl:hasDbXref >A oboInOwl:source SPLIT=| A IAO:0000115 SC % -MONDO:0958337 disorder with optic nerve compression Orphanet:519337 MONDO:equivalentTo Disorder with optic nerve compression MONDO:8000033 -MONDO:0958338 congenital optic disc excavation of genetic origin Orphanet:522514 MONDO:equivalentTo Congenital optic disc excavation of genetic origin MONDO:8000033|MONDO:0026186 -MONDO:0958339 syndromic genetic disorder with strabismus Orphanet:522520 MONDO:equivalentTo Syndromic genetic disorder with strabismus MONDO:8000033 -MONDO:0958340 rare genetic disorder with entropion Orphanet:522530 MONDO:equivalentTo Rare genetic disorder with entropion MONDO:8000033 -MONDO:0958341 genetic superficial corneal dystrophy Orphanet:522562 MONDO:equivalentTo Genetic superficial corneal dystrophy MONDO:8000033 -MONDO:0968986 chaotic conus spinal cord lipoma Orphanet:645285 MONDO:equivalentTo Chaotic conus spinal cord lipoma A rare dysraphic spinal cord lipoma characterized by the lipomatous mass extending ventrally to the dorsal root entry zone, indicating a more severe malformation of the spinal cord. The diagnosis can be suggested on imaging but usually confirmed during surgery. MONDO:0958350|MONDO:8000034|MONDO:8000030 -MONDO:0968987 extramedullary conus spinal cord lipoma Orphanet:645297 MONDO:equivalentTo Extramedullary conus spinal cord lipoma A rare closed lipomatous, dysraphic malformation of the lower spinal cord characterized by extramedullary lipomatous mass attached to the conus region. The conus is dysplastic and poorly delineated. Various morphological subtypes are recognized. Possible symptoms include bowel and bladder dysfunction and neuro-orthopedic deformity of the lower limbs. MONDO:0958350|MONDO:8000034|MONDO:8000030 -MONDO:0968988 saccular spinal dysraphism with a stalk to the dome Orphanet:645319 MONDO:equivalentTo Saccular spinal dysraphism with a stalk to the dome A rare spinal dysraphism characterized by a meningocele, containing a stalk, that is attached to the inner surface of the meningocele. The stalk can be posteriorly fibroneural (saccular limited dorsal myeloschisis) or the spinal cord itself (myelic limited dorsal malformation). MONDO:0958345|MONDO:8000033|MONDO:0017069 -MONDO:0968989 non-saccular limited dorsal myeloschisis Orphanet:645343 MONDO:equivalentTo Non-saccular limited dorsal myeloschisis A rare form of limited dorsal myeloschisis (LDM), characterized by a non saccular cutaneous stigmata (midline skin abnormality classically dimple, pit or sometimes angioma), the stalk is attached to this cutaneous stigmata. Fibroneural stalk varies in thickness and complexity. MONDO:0958345|MONDO:8000030|MONDO:8000034 MONDO:0968990 genetic central precocious puberty in male Orphanet:650097 MONDO:equivalentTo Genetic central precocious puberty in male MONDO:8000031|MONDO:0958356 MONDO:0968991 non-genetic central precocious puberty in male Orphanet:650102 MONDO:equivalentTo Non-genetic central precocious puberty in male MONDO:0958356|MONDO:8000031 +MONDO:0969105 terminal extramedullary conus spinal cord lipoma Orphanet:645288 MONDO:equivalentTo Terminal extramedullary conus spinal cord lipoma A rare form of extramedullary conus region spinal cord lipoma characterized by its location, extending from the poorly delineated tip of the conus. MONDO:0968987|MONDO:8000031 +MONDO:0969106 transitional extramedullary conus spinal cord lipoma Orphanet:645291 MONDO:equivalentTo Transitional extramedullary conus spinal cord lipoma "A rare form of extramedullary conus region spinal cord lipoma characterized by a location at the posterior surface of the conus and its tip. i.e-""transitional"" between posterior and terminal conus region spinal cord lipoma." MONDO:0968987|MONDO:8000031 +MONDO:0969107 posterior extramedullary conus spinal cord lipoma Orphanet:645294 MONDO:equivalentTo Posterior extramedullary conus spinal cord lipoma A rare form of conus region spinal cord lipoma characterized by its location where the interface between the lipoma and the spinal cord is strictcly above the level of the tip of the conus. The tip of the conus is readily delineated. MONDO:0968987|MONDO:8000031 +MONDO:0969108 lipomatous non-saccular limited dorsal myeloschisis Orphanet:645300 MONDO:equivalentTo Lipomatous non-saccular limited dorsal myeloschisis A rare non-saccular limited dorsal myeloschisis histologically characterized by skin tissue with a jagged depression of squamous epithelium continued to subcutaneous mature adipose tissue with loose connective tissue. GFAP-immunopositive glial cells are embedded in the subcutaneous lipoma. The extradural and intradural stalk have cord-like fibrocollagenous tissue containing adipose tissue, peripheral nerve fibers, clusters of melanocytes, and skeletal muscle fibers. MONDO:0968989|MONDO:8000031 +MONDO:0969109 fibroneural non-saccular limited dorsal myeloschisis Orphanet:645310 MONDO:equivalentTo Fibroneural non-saccular limited dorsal myeloschisis A rare non-saccular limited dorsal myeloschisis, in which the stalk histology is characterized by skin tissue with dermo-epidermal epithelium in continuity with a subcutaneous fibrocollagenous tract containing various ectopic tissues. MONDO:8000031|MONDO:0968989 +MONDO:0969110 terminal myelocystocele Orphanet:645337 MONDO:equivalentTo Terminal myelocystocele A rare closed spinal dysraphism characterized by a myelocystocele at the termination of the spinal cord. It may be an isolated anomaly or be associated with other defects, including sacral agenesis, anorectal and genitourinary anomalies. The conus is not identifiable. The myelocystocele sac may have a significant lipomatous component (terminal lipomyelocystocele). MONDO:0968988|MONDO:8000034|MONDO:8000030|MONDO:0017077 +MONDO:0969111 saccular limited dorsal myeloschisis Orphanet:645354 MONDO:equivalentTo Saccular limited dorsal myeloschisis A rare form of limited dorsal myeloschisis (LDM), characterized by the stalk attached to the apex of a fully epithelialized meningocele. Chiari II malformation is not present. MONDO:0968988|MONDO:8000034|MONDO:8000030 +MONDO:0969112 myelic limited dorsal malformation Orphanet:645378 MONDO:equivalentTo Myelic limited dorsal malformation A rare intermediate form of open dysraphism between myelomeningocele and saccular limited dorsal myeloschisis without fulfilling the characteristics of one of these two diagnosis, characterized by stretched neurulated spinal cord attached at the dome of a sac. Partial cerebral signs of open dysraphism can be observed and the meningocele is usually poorly epithelialized. MONDO:0968988|MONDO:8000034|MONDO:8000030 diff --git a/src/ontology/unmapped/doid-unmapped.owl b/src/ontology/unmapped/doid-unmapped.owl index 1a47819c..950e2704 100644 --- a/src/ontology/unmapped/doid-unmapped.owl +++ b/src/ontology/unmapped/doid-unmapped.owl @@ -33,321 +33,33 @@ - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - + - + - + - + - + - + - + - + - + - + diff --git a/src/ontology/unmapped/ncit-unmapped.owl b/src/ontology/unmapped/ncit-unmapped.owl index 27c63372..1dbb834a 100644 --- a/src/ontology/unmapped/ncit-unmapped.owl +++ b/src/ontology/unmapped/ncit-unmapped.owl @@ -24,7 +24,7 @@ - + @@ -108,7 +108,6 @@ - @@ -237,6 +236,7 @@ + @@ -525,9 +525,9 @@ + + - - @@ -606,7 +606,11 @@ + + + + @@ -766,7 +770,7 @@ - + @@ -813,6 +817,7 @@ + @@ -853,6 +858,7 @@ + @@ -875,9 +881,9 @@ + - @@ -889,6 +895,7 @@ + @@ -1739,7 +1746,6 @@ - @@ -1777,8 +1783,7 @@ - - + @@ -1807,6 +1812,7 @@ + @@ -1841,7 +1847,6 @@ - @@ -1874,7 +1879,6 @@ - @@ -2040,8 +2044,8 @@ + - @@ -2055,6 +2059,7 @@ + @@ -2086,6 +2091,7 @@ + @@ -2106,6 +2112,7 @@ + @@ -2171,7 +2178,6 @@ - @@ -2229,14 +2235,8 @@ - - - - - - @@ -2325,8 +2325,8 @@ + - @@ -2463,8 +2463,8 @@ + - @@ -2571,6 +2571,7 @@ + @@ -2615,6 +2616,7 @@ + @@ -2791,8 +2793,7 @@ - - + @@ -2954,7 +2955,7 @@ - + @@ -3151,32 +3152,6 @@ - - - - - - - - - - - - - - - - - - - - - - - - - - @@ -3319,7 +3294,6 @@ - @@ -3331,7 +3305,6 @@ - @@ -3565,9 +3538,7 @@ - - - + @@ -3581,9 +3552,7 @@ - - - + @@ -3596,8 +3565,7 @@ - - + @@ -3610,8 +3578,7 @@ - - + @@ -3891,6 +3858,8 @@ + + @@ -3975,9 +3944,9 @@ + - @@ -4113,6 +4082,8 @@ + + @@ -4203,6 +4174,7 @@ + @@ -4341,7 +4313,6 @@ - @@ -4355,7 +4326,6 @@ - @@ -4504,7 +4474,7 @@ - + @@ -4672,8 +4642,8 @@ - + @@ -4681,6 +4651,7 @@ + @@ -4692,7 +4663,6 @@ - @@ -4790,7 +4760,6 @@ - @@ -5096,7 +5065,6 @@ - @@ -5108,7 +5076,6 @@ - @@ -5121,13 +5088,9 @@ - + - - - - @@ -5176,9 +5139,7 @@ - - - + @@ -5238,8 +5199,8 @@ + - @@ -5933,6 +5894,7 @@ + @@ -5947,6 +5909,7 @@ + @@ -6158,7 +6121,6 @@ - @@ -6202,9 +6164,9 @@ - + @@ -7287,8 +7249,8 @@ + - @@ -7298,6 +7260,7 @@ + @@ -7391,6 +7354,7 @@ + @@ -7597,6 +7561,7 @@ + @@ -7609,6 +7574,7 @@ + @@ -7924,7 +7890,7 @@ - + @@ -8955,6 +8921,7 @@ + @@ -8967,6 +8934,7 @@ + @@ -9763,7 +9731,6 @@ - @@ -10875,7 +10842,6 @@ - @@ -10918,7 +10884,6 @@ - @@ -10972,8 +10937,8 @@ - + @@ -10983,8 +10948,8 @@ - + @@ -11699,6 +11664,7 @@ + @@ -11791,6 +11757,8 @@ + + @@ -11806,6 +11774,7 @@ + @@ -11818,10 +11787,10 @@ - + @@ -12422,8 +12391,8 @@ - - + + @@ -12432,11 +12401,6 @@ - - - - - @@ -12445,11 +12409,6 @@ - - - - - @@ -13039,15 +12998,14 @@ - + - @@ -13056,15 +13014,14 @@ - + - @@ -14549,7 +14506,6 @@ - @@ -15482,8 +15438,8 @@ - + @@ -15560,7 +15516,6 @@ - @@ -15621,7 +15576,6 @@ - @@ -15737,6 +15691,7 @@ + @@ -15819,6 +15774,7 @@ + @@ -16421,7 +16377,6 @@ - @@ -16434,7 +16389,6 @@ - @@ -17303,7 +17257,6 @@ - @@ -17653,6 +17606,7 @@ + @@ -17666,6 +17620,7 @@ + @@ -17793,8 +17748,7 @@ - - + @@ -17873,6 +17827,7 @@ + @@ -17886,6 +17841,7 @@ + @@ -17960,9 +17916,7 @@ - - - + @@ -17975,10 +17929,8 @@ - + - - @@ -17990,6 +17942,7 @@ + @@ -18092,8 +18045,8 @@ - + @@ -18275,7 +18228,6 @@ - @@ -18350,7 +18302,6 @@ - @@ -18437,8 +18388,11 @@ - + + + + @@ -18650,6 +18604,7 @@ + @@ -18862,7 +18817,6 @@ - @@ -19253,6 +19207,7 @@ + @@ -19293,6 +19248,7 @@ + @@ -19304,6 +19260,7 @@ + @@ -19315,6 +19272,7 @@ + @@ -19327,6 +19285,7 @@ + @@ -19349,6 +19308,7 @@ + @@ -19823,7 +19783,6 @@ - @@ -20224,7 +20183,7 @@ - + @@ -20236,7 +20195,7 @@ - + @@ -20263,7 +20222,6 @@ - @@ -20315,7 +20273,6 @@ - @@ -20328,7 +20285,6 @@ - @@ -20376,7 +20332,6 @@ - @@ -20430,7 +20385,6 @@ - @@ -20503,6 +20457,7 @@ + @@ -20737,6 +20692,7 @@ + @@ -20746,7 +20702,7 @@ - + @@ -20791,8 +20747,7 @@ - - + @@ -20805,8 +20760,7 @@ - - + @@ -20820,8 +20774,7 @@ - - + @@ -20898,6 +20851,7 @@ + @@ -20925,7 +20879,6 @@ - @@ -21065,7 +21018,6 @@ - @@ -21100,7 +21052,7 @@ - + @@ -21407,15 +21359,6 @@ - - - - - - - - - @@ -21594,7 +21537,7 @@ - + @@ -21878,12 +21821,7 @@ - - - - - - + @@ -22141,6 +22079,7 @@ + @@ -22152,6 +22091,7 @@ + @@ -22380,6 +22320,7 @@ + @@ -22776,9 +22717,9 @@ - + @@ -22957,6 +22898,7 @@ + @@ -22971,6 +22913,7 @@ + @@ -22980,6 +22923,7 @@ + @@ -22992,6 +22936,7 @@ + @@ -23012,6 +22957,7 @@ + @@ -23026,6 +22972,7 @@ + @@ -23040,6 +22987,8 @@ + + @@ -23055,6 +23004,7 @@ + @@ -23091,6 +23041,7 @@ + @@ -23102,6 +23053,7 @@ + @@ -23214,8 +23166,8 @@ - + @@ -23416,12 +23368,7 @@ - - - - - - + @@ -23565,10 +23512,7 @@ - - - - + @@ -23608,6 +23552,7 @@ + @@ -23669,7 +23614,6 @@ - @@ -23743,7 +23687,6 @@ - @@ -23773,8 +23716,8 @@ + - @@ -23784,6 +23727,7 @@ + @@ -23796,6 +23740,7 @@ + @@ -24089,6 +24034,7 @@ + @@ -24101,6 +24047,7 @@ + @@ -24152,7 +24099,7 @@ - + @@ -24229,8 +24176,6 @@ - - @@ -24250,13 +24195,12 @@ + - - @@ -24272,8 +24216,6 @@ - - @@ -24314,10 +24256,7 @@ - - - - + @@ -24326,9 +24265,12 @@ + + + @@ -24485,11 +24427,12 @@ + + - @@ -24530,7 +24473,7 @@ - + @@ -24538,15 +24481,10 @@ - - - - + - - @@ -24555,13 +24493,12 @@ - - + + - @@ -24613,10 +24550,7 @@ - - - - + @@ -24624,8 +24558,8 @@ + - @@ -24690,8 +24624,8 @@ + - @@ -24789,21 +24723,12 @@ - - - - - - - - - - + @@ -24813,9 +24738,9 @@ - + @@ -24862,9 +24787,8 @@ - - + @@ -24904,10 +24828,8 @@ - - - + @@ -25790,8 +25712,10 @@ - + + + @@ -25799,7 +25723,10 @@ - + + + + @@ -26114,9 +26041,9 @@ - + @@ -26142,7 +26069,6 @@ - @@ -26252,12 +26178,9 @@ - - - + - @@ -26276,7 +26199,6 @@ - @@ -26444,6 +26366,7 @@ + @@ -26607,6 +26530,7 @@ + @@ -26790,7 +26714,6 @@ - @@ -26861,7 +26784,6 @@ - @@ -26928,7 +26850,7 @@ - + @@ -26993,7 +26915,6 @@ - @@ -27092,9 +27013,7 @@ - - @@ -27176,7 +27095,6 @@ - @@ -27460,8 +27378,6 @@ - - @@ -27475,9 +27391,7 @@ - - - + @@ -27491,9 +27405,7 @@ - - - + @@ -27840,8 +27752,6 @@ - - @@ -27853,8 +27763,6 @@ - - @@ -27913,7 +27821,6 @@ - @@ -27935,6 +27842,7 @@ + @@ -28061,7 +27969,6 @@ - @@ -28071,6 +27978,7 @@ + @@ -28114,6 +28022,7 @@ + @@ -28327,7 +28236,6 @@ - @@ -28737,6 +28645,7 @@ + @@ -28774,9 +28683,9 @@ - + @@ -28785,8 +28694,8 @@ - + @@ -29147,9 +29056,9 @@ - + @@ -29344,7 +29253,6 @@ - @@ -29574,8 +29482,6 @@ - - @@ -29652,7 +29558,7 @@ - + @@ -29792,14 +29698,8 @@ - - - - - - @@ -29966,8 +29866,6 @@ - - @@ -30075,6 +29973,8 @@ + + @@ -30104,6 +30004,7 @@ + @@ -30240,7 +30141,6 @@ - @@ -30417,7 +30317,6 @@ - @@ -30429,7 +30328,6 @@ - @@ -30468,13 +30366,10 @@ - - - + - @@ -30590,14 +30485,8 @@ - - - - - - @@ -30700,17 +30589,6 @@ - - - - - - - - - - - @@ -30818,6 +30696,7 @@ + @@ -30847,6 +30726,7 @@ + @@ -31029,7 +30909,6 @@ - @@ -31070,8 +30949,6 @@ - - @@ -31538,7 +31415,6 @@ - @@ -31716,7 +31592,6 @@ - @@ -31936,6 +31811,7 @@ + @@ -31948,15 +31824,7 @@ - - - - - - - - - + @@ -31964,8 +31832,7 @@ - - + @@ -31973,7 +31840,9 @@ - + + + @@ -31992,7 +31861,7 @@ - + @@ -32071,9 +31940,8 @@ - - + @@ -32188,9 +32056,7 @@ - - - + @@ -32340,7 +32206,6 @@ - @@ -32368,14 +32233,8 @@ - - - - - - @@ -32571,8 +32430,8 @@ + - @@ -32694,6 +32553,7 @@ + @@ -32709,8 +32569,7 @@ - - + @@ -32824,6 +32683,7 @@ + @@ -32835,6 +32695,7 @@ + @@ -33006,8 +32867,7 @@ - - + @@ -33034,9 +32894,8 @@ - - + @@ -33045,8 +32904,7 @@ - - + @@ -33264,7 +33122,6 @@ - @@ -33471,7 +33328,6 @@ - @@ -33878,6 +33734,7 @@ + @@ -33909,6 +33766,7 @@ + @@ -33930,6 +33788,7 @@ + @@ -33942,6 +33801,7 @@ + @@ -33973,7 +33833,8 @@ - + + @@ -34043,6 +33904,7 @@ + @@ -34239,8 +34101,6 @@ - - @@ -34470,7 +34330,6 @@ - @@ -34493,7 +34352,6 @@ - @@ -34517,7 +34375,6 @@ - @@ -35263,7 +35120,6 @@ - @@ -35277,7 +35133,6 @@ - @@ -35292,7 +35147,6 @@ - @@ -35341,10 +35195,7 @@ - - - - + @@ -35555,7 +35406,7 @@ - + @@ -35570,6 +35421,7 @@ + @@ -35975,12 +35827,7 @@ - - - - - - + @@ -36007,12 +35854,7 @@ - - - - - - + @@ -36033,8 +35875,8 @@ + - @@ -36055,6 +35897,7 @@ + @@ -36076,6 +35919,7 @@ + @@ -36302,6 +36146,7 @@ + @@ -36397,9 +36242,9 @@ - + @@ -36694,7 +36539,6 @@ - @@ -36846,6 +36690,7 @@ + @@ -36897,9 +36742,9 @@ - - + + @@ -36909,9 +36754,7 @@ - - @@ -36922,9 +36765,7 @@ - - @@ -37366,6 +37207,7 @@ + @@ -37380,6 +37222,7 @@ + @@ -37547,8 +37390,7 @@ - - + @@ -37663,6 +37505,7 @@ + @@ -37720,8 +37563,7 @@ - - + @@ -37753,8 +37595,8 @@ - + @@ -37762,13 +37604,8 @@ - - - - - - + @@ -37776,14 +37613,8 @@ - - - - - - - + @@ -37791,8 +37622,8 @@ - + @@ -37801,10 +37632,7 @@ - - - - + @@ -37813,12 +37641,7 @@ - - - - - - + @@ -37864,8 +37687,7 @@ - - + @@ -37875,10 +37697,7 @@ - - - - + @@ -37886,14 +37705,8 @@ - - - - - - - + @@ -37902,8 +37715,7 @@ - - + @@ -37964,6 +37776,7 @@ + @@ -38001,11 +37814,7 @@ - - - - - + @@ -38014,10 +37823,7 @@ - - - - + @@ -38026,10 +37832,7 @@ - - - - + @@ -38074,11 +37877,8 @@ - - - - - + + @@ -38088,10 +37888,7 @@ - - - - + @@ -38184,6 +37981,7 @@ + @@ -38245,10 +38043,9 @@ + - - @@ -38258,10 +38055,7 @@ - - - - + @@ -38270,10 +38064,7 @@ - - - - + @@ -38310,6 +38101,7 @@ + @@ -38330,6 +38122,7 @@ + @@ -38379,8 +38172,7 @@ - - + @@ -38392,11 +38184,9 @@ - - + - @@ -38405,8 +38195,7 @@ - - + @@ -38418,7 +38207,7 @@ - + @@ -38427,10 +38216,7 @@ - - - - + @@ -38542,6 +38328,7 @@ + @@ -38583,10 +38370,8 @@ - - + - @@ -38596,11 +38381,8 @@ - - + - - @@ -38611,6 +38393,7 @@ + @@ -38623,6 +38406,8 @@ + + @@ -38662,11 +38447,8 @@ + - - - - @@ -38782,7 +38564,9 @@ + + @@ -38793,15 +38577,6 @@ - - - - - - - - - @@ -38814,7 +38589,7 @@ - + @@ -39035,8 +38810,8 @@ + - @@ -39045,10 +38820,8 @@ - + - - @@ -39102,8 +38875,8 @@ + - @@ -39135,9 +38908,8 @@ + - - @@ -39147,10 +38919,7 @@ - - - - + @@ -39159,10 +38928,7 @@ - - - - + @@ -39171,9 +38937,7 @@ - - - + @@ -39192,7 +38956,7 @@ - + @@ -39210,7 +38974,7 @@ - + @@ -39286,6 +39050,12 @@ + + + + + + @@ -39325,8 +39095,6 @@ - - @@ -39353,8 +39121,11 @@ - - + + + + + @@ -39373,7 +39144,7 @@ - + @@ -39924,9 +39695,10 @@ + + - @@ -39935,9 +39707,10 @@ + + - @@ -39946,8 +39719,9 @@ + + - @@ -39973,8 +39747,9 @@ + + - @@ -40005,8 +39780,9 @@ + + - @@ -40024,6 +39800,7 @@ + @@ -40054,6 +39831,7 @@ + @@ -40082,6 +39860,7 @@ + @@ -40341,7 +40120,6 @@ - @@ -40815,7 +40593,9 @@ - + + + @@ -40854,8 +40634,8 @@ - + @@ -40951,10 +40731,7 @@ - - - - + @@ -41009,7 +40786,7 @@ - + @@ -41036,7 +40813,7 @@ - + @@ -41144,8 +40921,7 @@ - - + @@ -41269,7 +41045,6 @@ - @@ -41388,6 +41163,7 @@ + @@ -41737,6 +41513,7 @@ + @@ -41915,10 +41692,7 @@ - - - - + @@ -41927,9 +41701,9 @@ + - @@ -41937,9 +41711,9 @@ + - @@ -42061,6 +41835,7 @@ + @@ -42071,9 +41846,10 @@ - - + + + @@ -42095,6 +41871,7 @@ + @@ -42195,7 +41972,6 @@ - @@ -42298,11 +42074,11 @@ + + - - @@ -42310,7 +42086,7 @@ - + @@ -42320,11 +42096,11 @@ - + + - @@ -42374,7 +42150,6 @@ - @@ -42412,9 +42187,7 @@ - - - + @@ -42763,7 +42536,6 @@ - @@ -43200,6 +42972,7 @@ + @@ -43212,6 +42985,7 @@ + @@ -43229,7 +43003,6 @@ - @@ -43256,7 +43029,6 @@ - @@ -43283,7 +43055,6 @@ - @@ -43297,7 +43068,6 @@ - @@ -43311,7 +43081,6 @@ - @@ -43752,6 +43521,7 @@ + @@ -43824,7 +43594,6 @@ - @@ -43836,7 +43605,6 @@ - @@ -43950,8 +43718,7 @@ - - + @@ -43961,8 +43728,7 @@ - - + @@ -44000,8 +43766,8 @@ - + @@ -44486,8 +44252,8 @@ + - @@ -44522,7 +44288,7 @@ - + @@ -44531,6 +44297,7 @@ + @@ -44540,6 +44307,7 @@ + @@ -44644,6 +44412,7 @@ + @@ -45622,8 +45391,6 @@ - - @@ -45656,10 +45423,10 @@ + + - - @@ -45668,8 +45435,8 @@ + - @@ -46127,12 +45894,8 @@ - - + - - - @@ -46161,8 +45924,6 @@ - - @@ -46197,7 +45958,6 @@ - @@ -46211,7 +45971,6 @@ - @@ -46237,6 +45996,7 @@ + @@ -46279,8 +46039,6 @@ - - @@ -46302,8 +46060,6 @@ - - @@ -46416,6 +46172,7 @@ + @@ -46440,14 +46197,6 @@ - - - - - - - - @@ -46493,6 +46242,7 @@ + @@ -46680,9 +46430,7 @@ - - - + @@ -46691,12 +46439,9 @@ - - - + - @@ -46773,6 +46518,7 @@ + @@ -47380,6 +47126,7 @@ + @@ -47535,7 +47282,6 @@ - @@ -47571,7 +47317,7 @@ - + @@ -47621,6 +47367,7 @@ + @@ -47749,6 +47496,7 @@ + @@ -48300,6 +48048,7 @@ + @@ -48341,7 +48090,7 @@ - + @@ -48371,11 +48120,10 @@ - - + @@ -48463,7 +48211,7 @@ - + @@ -48474,7 +48222,7 @@ - + @@ -48765,21 +48513,11 @@ - - - - - - - - - - - + @@ -48787,9 +48525,8 @@ - - + @@ -48808,6 +48545,7 @@ + @@ -48919,8 +48657,8 @@ - + @@ -49141,8 +48879,6 @@ - - @@ -49167,7 +48903,6 @@ - @@ -49194,8 +48929,8 @@ + - @@ -49222,7 +48957,6 @@ - @@ -49314,9 +49048,6 @@ - - - @@ -49332,9 +49063,7 @@ - - @@ -49345,8 +49074,8 @@ + - @@ -49427,8 +49156,8 @@ + - @@ -49438,8 +49167,8 @@ + - @@ -49491,13 +49220,11 @@ + - - - @@ -49514,8 +49241,8 @@ - + @@ -49557,7 +49284,6 @@ - @@ -49570,7 +49296,6 @@ - @@ -49583,7 +49308,6 @@ - @@ -49728,6 +49452,7 @@ + @@ -49961,7 +49686,6 @@ - @@ -50255,6 +49979,7 @@ + @@ -50275,6 +50000,7 @@ + @@ -50305,6 +50031,7 @@ + @@ -50386,6 +50113,7 @@ + @@ -50410,6 +50138,7 @@ + @@ -50695,8 +50424,11 @@ - - + + + + + @@ -51081,7 +50813,6 @@ - @@ -51198,12 +50929,7 @@ - - - - - - + @@ -51256,10 +50982,8 @@ - - @@ -51301,7 +51025,6 @@ - @@ -51321,7 +51044,6 @@ - @@ -51330,7 +51052,6 @@ - @@ -51364,7 +51085,6 @@ - @@ -51550,7 +51270,6 @@ - @@ -51563,7 +51282,6 @@ - @@ -51710,8 +51428,8 @@ - + @@ -51793,7 +51511,6 @@ - @@ -51882,6 +51599,7 @@ + @@ -52018,8 +51736,7 @@ - - + @@ -52264,6 +51981,7 @@ + @@ -52325,8 +52043,12 @@ - + + + + + @@ -52335,6 +52057,7 @@ + @@ -52457,13 +52180,10 @@ - - - + - @@ -52472,12 +52192,7 @@ - - - - - - + @@ -52739,8 +52454,8 @@ - + @@ -52794,9 +52509,8 @@ - - + @@ -52847,6 +52561,7 @@ + @@ -54255,7 +53970,7 @@ - + @@ -54486,9 +54201,8 @@ - - + @@ -54496,9 +54210,8 @@ - - + @@ -54667,6 +54380,7 @@ + @@ -54784,6 +54498,7 @@ + @@ -54792,13 +54507,8 @@ - - + - - - - @@ -54852,8 +54562,6 @@ - - @@ -54862,7 +54570,7 @@ - + @@ -54879,6 +54587,7 @@ + @@ -56104,7 +55813,7 @@ - + @@ -56300,6 +56009,7 @@ + @@ -56598,7 +56308,8 @@ - + + @@ -56626,7 +56337,6 @@ - @@ -57200,6 +56910,7 @@ + @@ -57681,8 +57392,8 @@ + - @@ -58018,6 +57729,7 @@ + @@ -58097,271 +57809,3914 @@ - + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + - - - - - + + + - + - - - - - - - - + + - + - - - + + - + - - + + - + - - - - - + + - + - - - + - - + - - - - - + + - + - - - - - + + - + - - - - - + + - + - + - - - + - + + + - - + - + - - - - - + + - + - - - - + + - + - - - - + + + + + + - + - - - - + + + - + - - + + + + - + - - - - - + + + - + - - + + + + - + - - - - - - - - + + + - + - - - - - - - + + + - + - - + + + - + - - + - - + - - - + + - + - - - + + + - + - - - + + - + - - - + @@ -58369,287 +61724,343 @@ - + - - - - - - + + - - - - - + - - - - - + - + - - - + - - - - + + - + - - - - - - + + + + - + - - - + + + - + - - + + + + - + - - + + + + - + - - + + - + - - - + + + + - + - - - + + + + + + + - + - - + + + + - + - - + + + + - + - - + + + + - + - - + + + + + - + - - + + + + + + - + - - + - - - - - + - - - - + + + + + + - + - - - - + + + + + + + - + - - + + + + + + - + - - + + + - - + - - - + + + - + - - - + + + - - - + - + + + - + - + + + + + + + + + + + + + + + + + + + + + + + - + + + - + - - + + + + + - + - - + + + + + + - + - + + + + - + - - + + + + + + + + + - + - - + + + + + + + + + @@ -67368,8 +70779,8 @@ + - @@ -68215,9 +71626,7 @@ - - - + @@ -68230,9 +71639,7 @@ - - - + @@ -68662,6 +72069,7 @@ + @@ -69402,7 +72810,6 @@ - @@ -69663,13 +73070,10 @@ - - - + - @@ -69677,13 +73081,10 @@ - - - + - @@ -69691,13 +73092,10 @@ - - - + - @@ -69927,6 +73325,7 @@ + @@ -71141,13 +74540,8 @@ - - - - - - - + + @@ -71546,8 +74940,8 @@ - + @@ -71709,14 +75103,6 @@ - - - - - - - - @@ -73086,6 +76472,7 @@ + @@ -73416,7 +76803,6 @@ - @@ -73689,7 +77075,6 @@ - @@ -73698,7 +77083,6 @@ - @@ -73708,7 +77092,6 @@ - @@ -73719,7 +77102,6 @@ - @@ -73729,7 +77111,6 @@ - @@ -73779,7 +77160,6 @@ - @@ -73788,7 +77168,6 @@ - @@ -73797,7 +77176,6 @@ - @@ -73824,7 +77202,6 @@ - @@ -73834,7 +77211,6 @@ - @@ -73843,7 +77219,6 @@ - @@ -73882,7 +77257,6 @@ - @@ -73906,8 +77280,8 @@ + - @@ -74108,7 +77482,6 @@ - @@ -74137,7 +77510,6 @@ - @@ -74240,7 +77612,6 @@ - @@ -74253,7 +77624,6 @@ - @@ -74328,7 +77698,6 @@ - @@ -75446,7 +78815,6 @@ - @@ -75946,7 +79314,6 @@ - @@ -76011,7 +79378,6 @@ - @@ -76020,7 +79386,6 @@ - @@ -76031,7 +79396,6 @@ - @@ -76056,7 +79420,6 @@ - @@ -76252,6 +79615,7 @@ + @@ -76414,8 +79778,7 @@ - - + @@ -76474,8 +79837,7 @@ - - + @@ -76947,8 +80309,8 @@ - + @@ -77076,7 +80438,6 @@ - @@ -77089,7 +80450,6 @@ - @@ -77148,6 +80508,7 @@ + @@ -77362,9 +80723,7 @@ - - - + @@ -77834,6 +81193,7 @@ + @@ -77984,9 +81344,10 @@ + + - @@ -77997,7 +81358,6 @@ - @@ -78031,7 +81391,6 @@ - @@ -78171,7 +81530,6 @@ - @@ -78185,8 +81543,6 @@ - - @@ -78200,8 +81556,6 @@ - - @@ -78314,7 +81668,6 @@ - @@ -78328,8 +81681,6 @@ - - @@ -78343,8 +81694,6 @@ - - @@ -78430,6 +81779,7 @@ + @@ -78643,7 +81993,6 @@ - @@ -78657,8 +82006,6 @@ - - @@ -78672,8 +82019,6 @@ - - @@ -78688,8 +82033,6 @@ - - @@ -79229,7 +82572,7 @@ - + @@ -80119,9 +83462,7 @@ - - - + @@ -80716,7 +84057,6 @@ - @@ -81235,10 +84575,10 @@ + - @@ -81380,7 +84720,7 @@ - + @@ -81388,9 +84728,9 @@ + - @@ -81513,7 +84853,6 @@ - @@ -81573,9 +84912,9 @@ + - @@ -81984,7 +85323,9 @@ - + + + @@ -82181,8 +85522,8 @@ + - @@ -82251,6 +85592,7 @@ + @@ -82315,8 +85657,8 @@ + - @@ -82421,7 +85763,6 @@ - @@ -82520,13 +85861,7 @@ - - - - - - - + @@ -82738,9 +86073,12 @@ + - + + + @@ -82775,9 +86113,9 @@ + - @@ -82896,9 +86234,7 @@ - - - + @@ -84146,7 +87482,6 @@ - @@ -84169,7 +87504,6 @@ - @@ -84234,7 +87568,6 @@ - @@ -84615,14 +87948,8 @@ - - - - - - - + @@ -84631,10 +87958,7 @@ - - - - + @@ -85038,16 +88362,6 @@ - - - - - - - - - - @@ -85129,6 +88443,7 @@ + @@ -86566,10 +89881,10 @@ + + - - @@ -87438,11 +90753,8 @@ - + - - - @@ -87609,8 +90921,8 @@ + - @@ -88228,7 +91540,6 @@ - @@ -88419,9 +91730,9 @@ + - @@ -88493,9 +91804,8 @@ + - - @@ -88753,6 +92063,7 @@ + @@ -88839,7 +92150,6 @@ - @@ -91876,7 +95186,6 @@ - @@ -91894,6 +95203,8 @@ + + @@ -91902,7 +95213,7 @@ - + @@ -91911,6 +95222,8 @@ + + @@ -91918,7 +95231,6 @@ - @@ -91930,7 +95242,6 @@ - @@ -91940,8 +95251,8 @@ + - @@ -92025,8 +95336,8 @@ + - @@ -92199,7 +95510,7 @@ - + @@ -92284,15 +95595,6 @@ - - - - - - - - - @@ -93008,7 +96310,6 @@ - @@ -93710,7 +97011,6 @@ - @@ -93719,7 +97019,6 @@ - @@ -94330,7 +97629,6 @@ - @@ -95055,6 +98353,7 @@ + @@ -95066,6 +98365,7 @@ + @@ -95133,6 +98433,7 @@ + @@ -95156,6 +98457,7 @@ + @@ -95217,6 +98519,7 @@ + @@ -95252,7 +98555,6 @@ - @@ -95261,6 +98563,7 @@ + @@ -95276,7 +98579,6 @@ - @@ -95767,7 +99069,6 @@ - @@ -95931,10 +99232,12 @@ + - + + @@ -95979,6 +99282,7 @@ + @@ -95992,6 +99296,7 @@ + @@ -96051,14 +99356,6 @@ - - - - - - - - @@ -96172,7 +99469,7 @@ - + @@ -96339,8 +99636,11 @@ + + + @@ -96588,7 +99888,6 @@ - @@ -97036,6 +100335,7 @@ + @@ -97208,7 +100508,7 @@ - + @@ -97565,9 +100865,9 @@ + - @@ -97646,7 +100946,6 @@ - @@ -97689,7 +100988,6 @@ - @@ -98078,7 +101376,6 @@ - @@ -98455,13 +101752,7 @@ - - - - - - - + @@ -98497,7 +101788,6 @@ - @@ -98515,12 +101805,6 @@ - - - - - - @@ -98548,7 +101832,6 @@ - @@ -98852,9 +102135,7 @@ - - - + @@ -98874,7 +102155,7 @@ - + @@ -99116,8 +102397,8 @@ - - + + @@ -99153,7 +102434,6 @@ - @@ -99524,9 +102804,8 @@ - + - @@ -99561,7 +102840,6 @@ - @@ -99570,6 +102848,7 @@ + @@ -99599,8 +102878,9 @@ - + + @@ -100133,7 +103413,6 @@ - @@ -100784,7 +104063,6 @@ - @@ -100976,6 +104254,7 @@ + @@ -101169,10 +104448,8 @@ - + - - @@ -101185,10 +104462,8 @@ - + - - @@ -101201,9 +104476,8 @@ - + - @@ -101348,6 +104622,7 @@ + @@ -101359,6 +104634,7 @@ + @@ -101592,7 +104868,11 @@ + + + + @@ -102265,7 +105545,6 @@ - @@ -102279,8 +105558,6 @@ - - @@ -102913,6 +106190,7 @@ + @@ -102940,6 +106218,7 @@ + @@ -104242,6 +107521,12 @@ + + + + + + @@ -104265,6 +107550,7 @@ + @@ -104775,14 +108061,6 @@ - - - - - - - - @@ -105184,6 +108462,7 @@ + @@ -105567,6 +108846,7 @@ + @@ -105628,6 +108908,7 @@ + @@ -106582,9 +109863,8 @@ - - - + + @@ -107739,7 +111019,7 @@ - + @@ -107828,7 +111108,7 @@ - + @@ -107885,7 +111165,7 @@ - + @@ -107942,7 +111222,7 @@ - + @@ -107996,9 +111276,7 @@ - - - + @@ -108007,9 +111285,7 @@ - - - + @@ -108018,9 +111294,7 @@ - - - + @@ -108029,9 +111303,7 @@ - - - + @@ -108055,8 +111327,6 @@ - - @@ -108070,8 +111340,6 @@ - - @@ -108085,8 +111353,6 @@ - - @@ -108100,7 +111366,6 @@ - @@ -108114,7 +111379,6 @@ - @@ -108917,8 +112181,7 @@ - - + @@ -108932,7 +112195,6 @@ - @@ -108946,7 +112208,6 @@ - @@ -108960,7 +112221,6 @@ - @@ -109121,6 +112381,7 @@ + @@ -109150,6 +112411,7 @@ + @@ -109445,7 +112707,6 @@ - @@ -109461,7 +112722,6 @@ - @@ -111029,8 +114289,6 @@ - - @@ -111042,6 +114300,7 @@ + @@ -111080,6 +114339,7 @@ + @@ -111091,7 +114351,6 @@ - @@ -111288,7 +114547,6 @@ - @@ -111310,8 +114568,8 @@ + - @@ -111394,7 +114652,6 @@ - @@ -112022,7 +115279,6 @@ - @@ -112039,8 +115295,8 @@ + - @@ -112115,7 +115371,6 @@ - @@ -112308,8 +115563,7 @@ - - + @@ -112456,7 +115710,6 @@ - @@ -112488,9 +115741,8 @@ - + - @@ -113333,6 +116585,7 @@ + @@ -113519,8 +116772,8 @@ + - @@ -113566,9 +116819,7 @@ - - - + @@ -113590,8 +116841,6 @@ - - @@ -113599,12 +116848,6 @@ - - - - - - @@ -113613,12 +116856,6 @@ - - - - - - @@ -113727,8 +116964,6 @@ - - @@ -113768,12 +117003,6 @@ - - - - - - @@ -113782,12 +117011,6 @@ - - - - - - @@ -113796,10 +117019,6 @@ - - - - @@ -113808,10 +117027,6 @@ - - - - @@ -113820,10 +117035,6 @@ - - - - @@ -113832,10 +117043,6 @@ - - - - @@ -113849,9 +117056,9 @@ - + - + @@ -113859,34 +117066,12 @@ - - - - - - - - - - - - - - - - - - - - - - - - - + + + @@ -113894,7 +117079,7 @@ - + @@ -114053,7 +117238,6 @@ - @@ -114310,7 +117494,6 @@ - @@ -114322,7 +117505,6 @@ - @@ -114334,7 +117516,6 @@ - @@ -114346,7 +117527,6 @@ - @@ -114474,7 +117654,6 @@ - @@ -114776,6 +117955,7 @@ + @@ -114786,6 +117966,7 @@ + @@ -114796,6 +117977,7 @@ + @@ -114806,6 +117988,7 @@ + @@ -114836,8 +118019,8 @@ + - @@ -114859,6 +118042,7 @@ + @@ -114898,7 +118082,6 @@ - @@ -115056,7 +118239,6 @@ - @@ -115610,11 +118792,11 @@ - - + + @@ -115622,8 +118804,8 @@ - + @@ -116391,7 +119573,6 @@ - @@ -116533,7 +119714,6 @@ - @@ -116546,7 +119726,6 @@ - @@ -116559,7 +119738,6 @@ - @@ -116572,7 +119750,6 @@ - @@ -116585,7 +119762,6 @@ - @@ -116598,7 +119774,6 @@ - @@ -116610,7 +119785,6 @@ - @@ -116657,7 +119831,6 @@ - @@ -116990,8 +120163,7 @@ - - + diff --git a/src/ontology/unmapped/omim-unmapped.owl b/src/ontology/unmapped/omim-unmapped.owl index 93fa8de1..6609cc98 100644 --- a/src/ontology/unmapped/omim-unmapped.owl +++ b/src/ontology/unmapped/omim-unmapped.owl @@ -9895,12 +9895,6 @@ - - - - - - PML acute promyelocytic leukemia, inducer of myl @@ -12679,8 +12673,9 @@ + aortic arch anomaly with peculiar facies and impaired intellectual development aortic arch anomaly with peculiar facies and mental retardation - aortic arch anomaly with peculiar facies and mental retardation + aortic arch anomaly with peculiar facies and impaired intellectual development @@ -21654,7 +21649,7 @@ corneal hypesthesia with retinal abnormalities, sensorineural deafness, unusual facies, persistent ductus arteriosus, and mental retardation ramos-arroyo syndrome - corneal hypesthesia with retinal abnormalities, sensorineural deafness, unusual facies, persistent ductus arteriosus, and mental retardation + ramos-arroyo syndrome @@ -31218,10 +31213,16 @@ - + + + + + + + GLUL glutamate-ammonia ligase glutamate-ammonia ligase-like 1 @@ -33821,8 +33822,9 @@ + hirsutism, skeletal dysplasia, and impaired intellectual development hirsutism, skeletal dysplasia, and mental retardation - hirsutism, skeletal dysplasia, and mental retardation + hirsutism, skeletal dysplasia, and impaired intellectual development @@ -49120,8 +49122,17 @@ + + + + + + + + NOC2 + neuroocular syndrome 2, paroxysmal type paroxysmal tonic upgaze, benign childhood, with ataxia - paroxysmal tonic upgaze, benign childhood, with ataxia + neuroocular syndrome 2, paroxysmal type @@ -55193,6 +55204,31 @@ + + + + + + + + + + + + + + + + KDM5A + jumonji, at-rich interactive domain 1a + lysine demethylase 5a + lysine-specific demethylase 5a + retinoblastoma-binding protein 2 + KDM5A + + + + @@ -57331,8 +57367,9 @@ SPEMR + spastic paraplegia, epilepsy, and impaired intellectual development spastic paraplegia, epilepsy, and mental retardation - spastic paraplegia, epilepsy, and mental retardation + spastic paraplegia, epilepsy, and impaired intellectual development @@ -57340,8 +57377,9 @@ + spastic paraplegia, sensorineural deafness, impaired intellectual development, and progressive nephropathy spastic paraplegia, sensorineural deafness, mental retardation, and progressive nephropathy - spastic paraplegia, sensorineural deafness, mental retardation, and progressive nephropathy + spastic paraplegia, sensorineural deafness, impaired intellectual development, and progressive nephropathy @@ -65125,9 +65163,10 @@ + absent eyebrows and eyelashes with impaired intellectual development absent eyebrows and eyelashes with mental retardation pseudoprogeria syndrome - absent eyebrows and eyelashes with mental retardation + absent eyebrows and eyelashes with impaired intellectual development @@ -66030,7 +66069,8 @@ acd mental retardation syndrome alopecia-contractures-dwarfism mental retardation syndrome - alopecia-contractures-dwarfism mental retardation syndrome + intellectual developmental syndrome with alopecia, contractures, and dwarfism + intellectual developmental syndrome with alopecia, contractures, and dwarfism @@ -67419,8 +67459,9 @@ + aural atresia, multiple congenital anomalies, and impaired intellectual development aural atresia, multiple congenital anomalies, and mental retardation - aural atresia, multiple congenital anomalies, and mental retardation + aural atresia, multiple congenital anomalies, and impaired intellectual development @@ -67798,9 +67839,18 @@ brachymelic primordial dwarfism cephaloskeletal dysplasia low-birth-weight dwarfism with skeletal dysplasia + microcephalic osteodysplastic primordial dwarfism type i/iii + microcephalic osteodysplastic primordial dwarfism, caroline crachami type + microcephalic osteodysplastic primordial dwarfism, sicilian fairy type microcephalic osteodysplastic primordial dwarfism, type 1 + microcephalic osteodysplastic primordial dwarfism, type 3 mopd 1 + mopd 3 + mopd i/iii + mopd, caroline crachami type + mopd, sicilian fairy type osteodysplastic primordial dwarfism, type 1 + osteodysplastic primordial dwarfism, type 3 taybi-linder syndrome microcephalic osteodysplastic primordial dwarfism, type 1 @@ -67828,14 +67878,8 @@ - microcephalic osteodysplastic primordial dwarfism, caroline crachami type - microcephalic osteodysplastic primordial dwarfism, sicilian fairy type - microcephalic osteodysplastic primordial dwarfism, type 3 - mopd 3 - mopd, caroline crachami type - mopd, sicilian fairy type - osteodysplastic primordial dwarfism, type 3 - microcephalic osteodysplastic primordial dwarfism, type 3 + + true @@ -69378,8 +69422,9 @@ + choroid plexus calcification and impaired intellectual development choroid plexus calcification and mental retardation - choroid plexus calcification and mental retardation + choroid plexus calcification and impaired intellectual development @@ -70185,7 +70230,8 @@ craniosynostosis-mental retardation syndrome of 51n and gettig - craniosynostosis-mental retardation syndrome of 51n and gettig + lin-getting syndrome + lin-getting syndrome @@ -70193,8 +70239,9 @@ + craniosynostosis-impaired intellectual development-clefting syndrome craniosynostosis-mental retardation-clefting syndrome - craniosynostosis-mental retardation-clefting syndrome + craniosynostosis-impaired intellectual development-clefting syndrome @@ -70400,9 +70447,9 @@ - CVG/MR + cutis verticis gyrata and impaired intellectual development cutis verticis gyrata and mental retardation - cutis verticis gyrata and mental retardation + cutis verticis gyrata and impaired intellectual development @@ -70466,8 +70513,9 @@ + cystic fibrosis with helicobacter pylori gastritis, megaloblastic anemia, and impaired intellectual development cystic fibrosis with helicobacter pylori gastritis, megaloblastic anemia, and mental retardation - cystic fibrosis with helicobacter pylori gastritis, megaloblastic anemia, and mental retardation + cystic fibrosis with helicobacter pylori gastritis, megaloblastic anemia, and impaired intellectual development @@ -70655,8 +70703,9 @@ + dandy-walker malformation with impaired intellectual development, macrocephaly, myopia, and brachytelephalangy dandy-walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy - dandy-walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy + dandy-walker malformation with impaired intellectual development, macrocephaly, myopia, and brachytelephalangy @@ -71019,8 +71068,9 @@ + diabetes insipidus, nephrogenic, with impaired intellectual development and intracerebral calcification diabetes insipidus, nephrogenic, with mental retardation and intracerebral calcification - diabetes insipidus, nephrogenic, with mental retardation and intracerebral calcification + diabetes insipidus, nephrogenic, with impaired intellectual development and intracerebral calcification @@ -71441,7 +71491,7 @@ dwarfism, mental retardation, and eye abnormality mollica syndrome - dwarfism, mental retardation, and eye abnormality + mollica syndrome @@ -72129,8 +72179,9 @@ + epidermolysis bullosa, late-onset localized junctional, with impaired intellectual development epidermolysis bullosa, late-onset localized junctional, with mental retardation - epidermolysis bullosa, late-onset localized junctional, with mental retardation + epidermolysis bullosa, late-onset localized junctional, with impaired intellectual development @@ -72273,8 +72324,9 @@ + epilepsy, photogenic, with spastic diplegia and impaired intellectual development epilepsy, photogenic, with spastic diplegia and mental retardation - epilepsy, photogenic, with spastic diplegia and mental retardation + epilepsy, photogenic, with spastic diplegia and impaired intellectual development @@ -72492,8 +72544,9 @@ + facial abnormalities, kyphoscoliosis, and impaired intellectual development facial abnormalities, kyphoscoliosis, and mental retardation - facial abnormalities, kyphoscoliosis, and mental retardation + facial abnormalities, kyphoscoliosis, and impaired intellectual development @@ -74403,8 +74456,9 @@ + hair defect with photosensitivity and impaired intellectual development hair defect with photosensitivity and mental retardation - hair defect with photosensitivity and mental retardation + hair defect with photosensitivity and impaired intellectual development @@ -76143,8 +76197,9 @@ + hypospadias-impaired intellectual development syndrome hypospadias-mental retardation syndrome - hypospadias-mental retardation syndrome + hypospadias-impaired intellectual development syndrome @@ -76289,8 +76344,9 @@ + ichthyosis with alopecia, eclabium, ectropion, and impaired intellectual development ichthyosis with alopecia, eclabium, ectropion, and mental retardation - ichthyosis with alopecia, eclabium, ectropion, and mental retardation + ichthyosis with alopecia, eclabium, ectropion, and impaired intellectual development @@ -76307,8 +76363,9 @@ + ichthyosis, impaired intellectual development, dwarfism, and renal impairment ichthyosis, mental retardation, dwarfism, and renal impairment - ichthyosis, mental retardation, dwarfism, and renal impairment + ichthyosis, impaired intellectual development, dwarfism, and renal impairment @@ -76485,8 +76542,9 @@ + indolylacroyl glycinuria with impaired intellectual development indolylacroyl glycinuria with mental retardation - indolylacroyl glycinuria with mental retardation + indolylacroyl glycinuria with impaired intellectual development @@ -77403,8 +77461,9 @@ + leukomelanoderma, infantilism, impaired intellectual development, hypodontia, hypotrichosis leukomelanoderma, infantilism, mental retardation, hypodontia, hypotrichosis - leukomelanoderma, infantilism, mental retardation, hypodontia, hypotrichosis + leukomelanoderma, infantilism, impaired intellectual development, hypodontia, hypotrichosis @@ -77437,8 +77496,9 @@ + limb defects, distal transverse, with impaired intellectual development and spasticity limb defects, distal transverse, with mental retardation and spasticity - limb defects, distal transverse, with mental retardation and spasticity + limb defects, distal transverse, with impaired intellectual development and spasticity @@ -77969,8 +78029,9 @@ + mandibulofacial dysostosis with impaired intellectual development mandibulofacial dysostosis with mental retardation - mandibulofacial dysostosis with mental retardation + mandibulofacial dysostosis with impaired intellectual development @@ -78125,8 +78186,9 @@ + marfanoid impaired intellectual developmental syndrome, autosomal marfanoid mental retardation syndrome, autosomal - marfanoid mental retardation syndrome, autosomal + marfanoid impaired intellectual developmental syndrome, autosomal @@ -78354,8 +78416,9 @@ + intellectual developmental disorder, belgian type mental retardation syndrome, belgian type - mental retardation syndrome, belgian type + intellectual developmental disorder, belgian type @@ -78384,9 +78447,10 @@ + intellectual developmental disorder, buenos aires type mental retardation, buenos aires type mutchinick syndrome - mental retardation, buenos aires type + mutchinick syndrome @@ -79309,8 +79373,9 @@ MOCODA molybdenum cofactor deficiency, complementation group a + molybdenum cofactor deficiency, type a sulfite oxidase, xanthine dehydrogenase, and aldehyde oxidase, combined deficiency of - molybdenum cofactor deficiency, complementation group a + molybdenum cofactor deficiency, type a @@ -79327,7 +79392,8 @@ MOCODB molybdenum cofactor deficiency, complementation group B - molybdenum cofactor deficiency, complementation group B + molybdenum cofactor deficiency, type B + molybdenum cofactor deficiency, type B @@ -79788,7 +79854,7 @@ chudley syndrome multicore myopathy with mental retardation, short stature, and hypogonadotropic hypogonadism - multicore myopathy with mental retardation, short stature, and hypogonadotropic hypogonadism + chudley syndrome @@ -80449,8 +80515,9 @@ + myotonia with skeletal abnormalities and impaired intellectual development myotonia with skeletal abnormalities and mental retardation - myotonia with skeletal abnormalities and mental retardation + myotonia with skeletal abnormalities and impaired intellectual development @@ -80530,10 +80597,10 @@ - LS - leigh syndrome + NULS + leigh syndrome, nuclear necrotizing encephalopathy, infantile subacute, of leigh - leigh syndrome + leigh syndrome, nuclear @@ -83327,8 +83394,9 @@ + prune belly syndrome with pulmonic stenosis, impaired intellectual development, and deafness prune belly syndrome with pulmonic stenosis, mental retardation, and deafness - prune belly syndrome with pulmonic stenosis, mental retardation, and deafness + prune belly syndrome with pulmonic stenosis, impaired intellectual development, and deafness @@ -84324,8 +84392,9 @@ insulin-resistant diabetes with acanthosis nigricans, hypogonadism, pigmentary retinopathy, deafness, and mental retardation + retinitis pigmentosa, deafness, impaired intellectual development, and hypogonadism retinitis pigmentosa, deafness, mental retardation, and hypogonadism - retinitis pigmentosa, deafness, mental retardation, and hypogonadism + retinitis pigmentosa, deafness, impaired intellectual development, and hypogonadism @@ -85128,8 +85197,9 @@ + ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and impaired intellectual development ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and mental retardation - ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and mental retardation + ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and impaired intellectual development @@ -85255,8 +85325,9 @@ + spastic paresis, glaucoma, and impaired intellectual development spastic paresis, glaucoma, and mental retardation - spastic paresis, glaucoma, and mental retardation + spastic paresis, glaucoma, and impaired intellectual development @@ -85275,8 +85346,9 @@ + spastic quadriplegia, retinitis pigmentosa, and impaired intellectual development spastic quadriplegia, retinitis pigmentosa, and mental retardation - spastic quadriplegia, retinitis pigmentosa, and mental retardation + spastic quadriplegia, retinitis pigmentosa, and impaired intellectual development @@ -85320,8 +85392,9 @@ + spinal muscular atrophy with impaired intellectual development spinal muscular atrophy with mental retardation - spinal muscular atrophy with mental retardation + spinal muscular atrophy with impaired intellectual development @@ -85329,8 +85402,8 @@ - spinal muscular atrophy with microcephaly and mental subnormality - spinal muscular atrophy with microcephaly and mental subnormality + spinal muscular atrophy with microcephaly and impaired intellectual development + spinal muscular atrophy with microcephaly and impaired intellectual development @@ -85556,8 +85629,9 @@ sedt with mental retardation + spondyloepiphyseal dysplasia tarda with impaired intellectual development spondyloepiphyseal dysplasia tarda with mental retardation - spondyloepiphyseal dysplasia tarda with mental retardation + spondyloepiphyseal dysplasia tarda with impaired intellectual development @@ -86997,8 +87071,9 @@ mesomelia of the upper limbs, anonychia congenita, clubfeet, and mental retardation + ulnar hypoplasia with impaired intellectual development ulnar hypoplasia with mental retardation - ulnar hypoplasia with mental retardation + ulnar hypoplasia with impaired intellectual development @@ -87417,8 +87492,9 @@ + vitiligo, progressive, with impaired intellectual development and urethral duplication vitiligo, progressive, with mental retardation and urethral duplication - vitiligo, progressive, with mental retardation and urethral duplication + vitiligo, progressive, with impaired intellectual development and urethral duplication @@ -87601,7 +87677,8 @@ wolff mental retardation syndrome - wolff mental retardation syndrome + wolff syndrome + wolff syndrome @@ -88708,9 +88785,10 @@ + hyde-forster syndrome mental retardation, x-linked, hyde-forster type mental retardation, x-linked, with craniofacial dysmorphism - mental retardation, x-linked, with craniofacial dysmorphism + hyde-forster syndrome @@ -94313,6 +94391,7 @@ + XLHRR hypophosphatemic rickets, X-linked recessive hypophosphatemic rickets, X-linked recessive @@ -100430,8 +100509,9 @@ + cutis verticis gyrata, thyroid aplasia, and impaired intellectual development cutis verticis gyrata, thyroid aplasia, and mental retardation - cutis verticis gyrata, thyroid aplasia, and mental retardation + cutis verticis gyrata, thyroid aplasia, and impaired intellectual development @@ -101394,8 +101474,9 @@ + hypogonadism, male, with impaired intellectual development and skeletal anomalies hypogonadism, male, with mental retardation and skeletal anomalies - hypogonadism, male, with mental retardation and skeletal anomalies + hypogonadism, male, with impaired intellectual development and skeletal anomalies @@ -101436,7 +101517,7 @@ - XLHR + XLHRD hyp hypophosphatemia, X-linked hypophosphatemic rickets, X-linked dominant @@ -102087,8 +102168,9 @@ + impaired intellectual development and psoriasis mental retardation and psoriasis - mental retardation and psoriasis + impaired intellectual development and psoriasis @@ -102319,8 +102401,9 @@ + impaired intellectual development with spastic paraplegia and palmoplantar hyperkeratosis mental retardation with spastic paraplegia and palmoplantar hyperkeratosis - mental retardation with spastic paraplegia and palmoplantar hyperkeratosis + impaired intellectual development with spastic paraplegia and palmoplantar hyperkeratosis @@ -102452,10 +102535,11 @@ - MRSD + CHRS christian syndrome + impaired intellectual development, skeletal dysplasia, and abducens palsy mental retardation, skeletal dysplasia, and abducens palsy - mental retardation, skeletal dysplasia, and abducens palsy + christian syndrome @@ -103762,7 +103846,8 @@ choreoathetosis with mental retardation, X-linked schimke X-linked mental retardation syndrome - schimke X-linked mental retardation syndrome + schimke syndrome + schimke syndrome @@ -105320,6 +105405,16 @@ + + + + MILS + leigh syndrome, mitochondrial + leigh syndrome, mitochondrial + + + + @@ -106943,7 +107038,7 @@ male pseudohermaphroditism/mental retardation syndrome, verloes type verloes syndrome - male pseudohermaphroditism/mental retardation syndrome, verloes type + verloes syndrome @@ -107409,8 +107504,9 @@ + pterygium colli and impaired intellectual development with facial and digital anomalies pterygium colli and mental retardation with facial and digital anomalies - pterygium colli and mental retardation with facial and digital anomalies + pterygium colli and impaired intellectual development with facial and digital anomalies @@ -115676,8 +115772,9 @@ + ectodermal dysplasia with impaired intellectual development and syndactyly ectodermal dysplasia with mental retardation and syndactyly - ectodermal dysplasia with mental retardation and syndactyly + ectodermal dysplasia with impaired intellectual development and syndactyly @@ -117379,8 +117476,9 @@ + ichthyosis-impaired intellectual developmental syndrome with large keratohyalin granules 1n the skin ichthyosis-mental retardation syndrome with large keratohyalin granules 1n the skin - ichthyosis-mental retardation syndrome with large keratohyalin granules 1n the skin + ichthyosis-impaired intellectual developmental syndrome with large keratohyalin granules 1n the skin @@ -119250,8 +119348,9 @@ + alopecia-impaired intellectual developmental syndrome with convulsions and hypergonadotropic hypogonadism alopecia-mental retardation syndrome with convulsions and hypergonadotropic hypogonadism - alopecia-mental retardation syndrome with convulsions and hypergonadotropic hypogonadism + alopecia-impaired intellectual developmental syndrome with convulsions and hypergonadotropic hypogonadism @@ -120623,8 +120722,9 @@ + impaired intellectual development, microcephaly, epilepsy, and coarse face mental retardation, microcephaly, epilepsy, and coarse face - mental retardation, microcephaly, epilepsy, and coarse face + impaired intellectual development, microcephaly, epilepsy, and coarse face @@ -121624,6 +121724,7 @@ CFL2 cofilin 2 + cofilin, m-type cofilin, muscle CFL2 @@ -125858,8 +125959,9 @@ + coloboma-obesity-hypogenitalism-impaired intellectual development syndrome coloboma-obesity-hypogenitalism-mental retardation syndrome - coloboma-obesity-hypogenitalism-mental retardation syndrome + coloboma-obesity-hypogenitalism-impaired intellectual development syndrome @@ -126049,6 +126151,12 @@ + + + + + + DNA replication helicase 2, yeast, homolog of DNA replication helicase/nuclease 2 DNA2 @@ -132844,8 +132952,9 @@ + microcephaly, macrotia, and impaired intellectual development microcephaly, macrotia, and mental retardation - microcephaly, macrotia, and mental retardation + microcephaly, macrotia, and impaired intellectual development @@ -132908,8 +133017,9 @@ + emphysema, congenital, with deafness, penoscrotal web, and intellectual developmental disorder emphysema, congenital, with deafness, penoscrotal web, and mental retardation - emphysema, congenital, with deafness, penoscrotal web, and mental retardation + emphysema, congenital, with deafness, penoscrotal web, and intellectual developmental disorder @@ -133404,8 +133514,9 @@ + spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and impaired intellectual development spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and mental retardation - spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and mental retardation + spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and impaired intellectual development @@ -134215,9 +134326,9 @@ + intellectual developmental disorder with spasticity and pigmentary tapetoretinal degeneration mental retardation, severe, with spasticity and pigmentary tapetoretinal degeneration - mrst - mental retardation, severe, with spasticity and pigmentary tapetoretinal degeneration + intellectual developmental disorder with spasticity and pigmentary tapetoretinal degeneration @@ -137835,8 +137946,9 @@ + dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and impaired intellectual development dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and mental retardation - dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and mental retardation + dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and impaired intellectual development @@ -140694,7 +140806,7 @@ giuffre-tsukahara syndrome radioulnar synostosis with microcephaly, short stature, scoliosis, and mental retardation tsukahara syndrome - radioulnar synostosis with microcephaly, short stature, scoliosis, and mental retardation + tsukahara syndrome @@ -141874,8 +141986,9 @@ + microcephaly, facial abnormalities, micromelia, and impaired intellectual development microcephaly, facial abnormalities, micromelia, and mental retardation - microcephaly, facial abnormalities, micromelia, and mental retardation + microcephaly, facial abnormalities, micromelia, and impaired intellectual development @@ -145822,16 +145935,6 @@ - - - - ZNF106 - zinc finger protein 106 - zinc finger protein 106 - - - - @@ -148817,8 +148920,9 @@ + anemia, congenital hypoplastic, with multiple congenital anomalies/impaired intellectual development syndrome anemia, congenital hypoplastic, with multiple congenital anomalies/mental retardation syndrome - anemia, congenital hypoplastic, with multiple congenital anomalies/mental retardation syndrome + anemia, congenital hypoplastic, with multiple congenital anomalies/impaired intellectual development syndrome @@ -157734,8 +157838,9 @@ + fibromatosis, gingival, with hypertrichosis and impaired intellectual development fibromatosis, gingival, with hypertrichosis and mental retardation - fibromatosis, gingival, with hypertrichosis and mental retardation + fibromatosis, gingival, with hypertrichosis and impaired intellectual development @@ -164798,7 +164903,7 @@ kondoh syndrome mental retardation, microcephaly, growth retardation, joint contractures, and facial dysmorphism - mental retardation, microcephaly, growth retardation, joint contractures, and facial dysmorphism + kondoh syndrome @@ -170003,8 +170108,9 @@ + cree impaired intellectual development syndrome cree mental retardation syndrome - cree mental retardation syndrome + cree impaired intellectual development syndrome @@ -177099,9 +177205,9 @@ - spar + spastic paraplegia, ataxia, and impaired intellectual development spastic paraplegia, ataxia, and mental retardation - spastic paraplegia, ataxia, and mental retardation + spastic paraplegia, ataxia, and impaired intellectual development @@ -182347,8 +182453,9 @@ + lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones lipodystrophy, generalized, with mental retardation, deafness, short stature, and slender bones - lipodystrophy, generalized, with mental retardation, deafness, short stature, and slender bones + lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones @@ -183623,8 +183730,9 @@ + growth failure, microcephaly, impaired intellectual development, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy growth failure, microcephaly, mental retardation, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy - growth failure, microcephaly, mental retardation, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy + growth failure, microcephaly, impaired intellectual development, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy @@ -191008,8 +191116,9 @@ + intellectual developmental disorder with optic atrophy, facial dysmorphism, microcephaly, and short stature mental retardation with optic atrophy, facial dysmorphism, microcephaly, and short stature - mental retardation with optic atrophy, facial dysmorphism, microcephaly, and short stature + intellectual developmental disorder with optic atrophy, facial dysmorphism, microcephaly, and short stature @@ -194366,8 +194475,9 @@ + intellectual developmental disorder with keratoconus, febrile seizures, and sinoatrial block mental retardation, keratoconus, febrile seizures, and sinoatrial block - mental retardation, keratoconus, febrile seizures, and sinoatrial block + intellectual developmental disorder with keratoconus, febrile seizures, and sinoatrial block @@ -198908,12 +199018,7 @@ - - - - - - + GLND glutamine deficiency, congenital glutamine synthase deficiency, congenital systemic glutamine deficiency, congenital @@ -222379,8 +222484,9 @@ + stargardt macular degeneration, absent or hypoplastic corpus callosum, impaired intellectual development, and dysmorphic facial features stargardt macular degeneration, absent or hypoplastic corpus callosum, mental retardation, and dysmorphic facial features - stargardt macular degeneration, absent or hypoplastic corpus callosum, mental retardation, and dysmorphic facial features + stargardt macular degeneration, absent or hypoplastic corpus callosum, impaired intellectual development, and dysmorphic facial features @@ -229683,7 +229789,7 @@ brachydactyly, type a1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation tsukahara syndrome - brachydactyly, type a1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation + tsukahara syndrome @@ -234003,6 +234109,32 @@ + + + + + + + + + + + + + + + + DAGLA + dagl-alpha + dgl-alpha + dgla + diacylglycerol lipase, alpha + kiaa0659 + DAGLA + + + + @@ -241471,8 +241603,9 @@ + hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, mental retardation, and recurrent inflammatory episodes - hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, mental retardation, and recurrent inflammatory episodes + hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes @@ -249507,7 +249640,8 @@ MOCODC molybdenum cofactor deficiency, complementation group c - molybdenum cofactor deficiency, complementation group c + molybdenum cofactor deficiency, type c + molybdenum cofactor deficiency, type c @@ -252338,15 +252472,17 @@ + - SSMCF + RTS3 + rothmund-thomson syndrome, type 3 short stature with microcephaly and distinctive facies - short stature with microcephaly and distinctive facies + rothmund-thomson syndrome, type 3 @@ -286108,15 +286244,16 @@ + - NOC - neuroocular syndrome - neuroocular syndrome + NOC1 + neuroocular syndrome 1 + neuroocular syndrome 1 @@ -294733,6 +294870,7 @@ + @@ -294749,6 +294887,7 @@ + @@ -295343,6 +295482,7 @@ + DEE115 developmental and epileptic encephalopathy 115 developmental and epileptic encephalopathy 115 @@ -295485,6 +295625,45 @@ + + + + + DEE116 + developmental and epileptic encephalopathy 116 + developmental and epileptic encephalopathy 116 + + + + + + + + + RTS4 + rothmund-thomson syndrome, type 4 + rothmund-thomson syndrome, type 4 + + + + + + + + + + + + + + NEDEHC + el hayek-chahrour neurodevelopmental syndrome + neurodevelopmental disorder with absent speech, impaired intellectual development, and autism + el hayek-chahrour neurodevelopmental syndrome + + + + @@ -300097,6 +300276,14 @@ + + + + Neuroocular syndrome + + + +