mid October release

DOreports/DO-equivalentClass.tsv

@@ -293,7 +293,7 @@ DOID:175	vascular cancer	cancer and ('disease has location' some 'vascular syste
 DOID:1756	facial nerve disease	disease and ('disease has location' some 'facial nerve')
 DOID:176	cardiovascular cancer	cancer and ('disease has location' some 'cardiovascular system')
 DOID:178	vascular disease	disease and ('disease has location' some 'vascular system')
-DOID:1781	thyroid gland cancer	cancer and ('disease has location' some 'thyroid gland')
+DOID:1781	thyroid cancer	cancer and ('disease has location' some 'thyroid gland')
 DOID:1785	pituitary cancer	cancer and ('disease has location' some 'pituitary gland')
 DOID:1790	malignant mesothelioma	cancer and (('derives from' some 'epithelioid macrophage') and ('disease has location' some mesothelium))
 DOID:1793	pancreatic cancer	cancer and ('disease has location' some pancreas)
@@ -402,6 +402,7 @@ DOID:3168	squamous cell neoplasm	'benign neoplasm' and ((('disease has location'
 DOID:3181	oligodendroglioma	cancer and (('derives from' some 'glial cell') and ('derives from' some oligodendrocyte))
 DOID:3185	spinal cord glioma	cancer and (('derives from' some 'glial cell') and ('disease has location' some 'spinal cord'))
 DOID:319	spinal cord disease	disease and ('disease has location' some 'spinal cord')
+DOID:3192	neurilemmoma	'benign neoplasm' and ('derives from' some 'Schwann cell')
 DOID:3197	schwannoma of twelfth cranial nerve	neurilemmoma and ('disease has location' some 'hypoglossal nerve')
 DOID:3225	tracheal disease	disease and ('disease has location' some trachea)
 DOID:3277	thymus cancer	cancer and ('disease has location' some thymus)
@@ -584,7 +585,7 @@ DOID:6112	cerebral meningioma	meningioma and ('disease has location' some cerebr
 DOID:6115	lateral ventricle meningioma	meningioma and ('disease has location' some 'telencephalic ventricle')
 DOID:612	primary immunodeficiency disease	disease and ('has phenotype' some 'Abnormality of immune system physiology')
 DOID:6148	nasal cavity carcinoma in situ	'in situ carcinoma' and ('disease has location' some 'nasal cavity')
-DOID:6175	mediastinal neurilemmoma	'benign neoplasm' and ('disease has location' some mediastinum)
+DOID:6175	mediastinal neurilemmoma	neurilemmoma and ('disease has location' some mediastinum)
 DOID:6198	corneal intraepithelial neoplasm	'pre-malignant neoplasm' and ('disease has location' some cornea)
 DOID:6199	cornea cancer	cancer and ('disease has location' some cornea)
 DOID:62	aortic valve disease	disease and ('disease has location' some 'aortic valve')

DOreports/DO-subClassOf-anonymous.tsv

@@ -477,6 +477,7 @@ DOID:0060189	ileitis	'disease has location' some ileum|'has symptom' some 'right
 DOID:0060190	ileocolitis	'disease has location' some ileum|'has symptom' some 'right lower quadrant abdominal pain'|'has symptom' some 'weight loss'|'has symptom' some diarrhea|'has symptom' some inflammation
 DOID:0060191	gastroduodenal Crohn's disease	'disease has feature' some duodenitis|'has symptom' some 'loss of appetite'|'has symptom' some 'weight loss'|'has symptom' some inflammation|'has symptom' some nausea|'has symptom' some vomiting
 DOID:0060192	Crohn's colitis	'disease has feature' some 'anal fistula'|'disease has feature' some 'ulcer of anus and rectum'|'has symptom' some 'anal abscess'|'has symptom' some 'skin lesion'|'has symptom' some abscess|'has symptom' some bleeding|'has symptom' some diarrhea|'has symptom' some inflammation
+DOID:0060193	amyotrophic lateral sclerosis type 1	'has material basis in' some 'autosomal dominant inheritance'|'has material basis in' some 'autosomal recessive inheritance'
 DOID:0060216	Cogan syndrome	'has symptom' some fatigue|'has symptom' some fever
 DOID:0060224	atrial fibrillation	'has symptom' some 'chest pain'|'has symptom' some arrhythmia|'has symptom' some confusion|'has symptom' some dizziness|'has symptom' some dyspnea|'has symptom' some fatigue|'has symptom' some lightheadedness|'has symptom' some palpitation|'has symptom' some weakness
 DOID:0060225	3MC syndrome	'has material basis in' some 'autosomal recessive inheritance'|'has symptom' some ptosis
@@ -1098,6 +1099,12 @@ DOID:0070467	carpal tunnel syndrome 2	'has material basis in' some 'autosomal do
 DOID:0070468	Yoon-Bellen neurodevelopmental syndrome	'has material basis in' some 'autosomal recessive inheritance'
 DOID:0070471	early-onset epilepsy 2	'existence starts during' some ('Infantile onset' or 'Neonatal onset' or 'Childhood onset')|'has material basis in' some 'autosomal dominant inheritance'
 DOID:0070472	early-onset epilepsy 3	'existence starts during' some ('Infantile onset' or 'Childhood onset')|'has material basis in' some 'autosomal dominant inheritance'
+DOID:0070475	renal medullary carcinoma	'disease has location' some 'renal medulla'
+DOID:0070476	diphthamide deficiency syndrome	'has material basis in' some 'autosomal recessive inheritance'|'has phenotype' some 'Global developmental delay'|'has phenotype' some 'Short stature'|'has phenotype' some 'Sparse hair'
+DOID:0070479	neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties	'has phenotype' some 'Absent speech'|'has phenotype' some 'Delayed ability to walk'|'has phenotype' some 'Difficulty walking'|'has phenotype' some 'Feeding difficulties'
+DOID:0070482	spinal neurofibromatosis	'disease has location' some 'spinal nerve root'
+DOID:0070483	Watson syndrome	'has material basis in' some 'autosomal dominant inheritance'
+DOID:0070484	Legius syndrome	'has material basis in' some 'autosomal dominant inheritance'
 DOID:0080007	bone deterioration disease	'disease has location' some 'bone element'
 DOID:0080010	bone structure disease	'has phenotype' some 'Abnormal bone structure'
 DOID:0080020	Jansen's metaphyseal chondrodysplasia	'has material basis in' some 'autosomal dominant inheritance'|'has phenotype' some 'Disproportionate short-limb short stature'
@@ -1807,6 +1814,11 @@ DOID:0081373	disabling pansclerotic morphea	'existence starts during' some 'Chil
 DOID:0081374	nemaline myopathy 5B	'existence starts during' some 'Childhood onset'|'has material basis in' some 'autosomal recessive inheritance'
 DOID:0081375	nemaline myopathy 5C	'has material basis in' some 'autosomal dominant inheritance'
 DOID:0081376	sorbitol dehydrogenase deficiency with peripheral neuropathy	'has material basis in' some 'autosomal recessive inheritance'
+DOID:0081378	amyotrophic lateral sclerosis type 24	'existence starts during' some 'Adult onset'|'has material basis in' some 'autosomal dominant inheritance'
+DOID:0081379	amyotrophic lateral sclerosis type 25	'has material basis in' some 'autosomal dominant inheritance'
+DOID:0081380	amyotrophic lateral sclerosis type 26	'existence starts during' some 'Adult onset'|'has material basis in' some 'autosomal dominant inheritance'
+DOID:0081381	juvenile amyotrophic lateral sclerosis type 27	'existence starts during' some 'Juvenile onset'|'has material basis in' some 'autosomal dominant inheritance'
+DOID:0081382	amyotrophic lateral sclerosis type 28	'existence starts during' some 'Adult onset'|'has material basis in' some 'autosomal dominant inheritance'|'has material basis in' some trinucleotide_repeat_expansion
 DOID:0090001	Fraser syndrome	'has material basis in' some 'autosomal recessive inheritance'
 DOID:0090002	Tietz syndrome	'has material basis in' some 'autosomal dominant inheritance'
 DOID:0090003	agenesis of the corpus callosum with peripheral neuropathy	'has material basis in' some 'autosomal recessive inheritance'
@@ -2635,7 +2647,7 @@ DOID:0111248	cerebrocostomandibular syndrome	'has material basis in' some 'autos
 DOID:0111249	uveal coloboma-cleft lip and palate-intellectual disability	'has material basis in' some 'autosomal dominant inheritance'
 DOID:0111250	Parkinson's disease 3	'has material basis in' some 'autosomal dominant inheritance'
 DOID:0111251	Parkinson's disease 21	'has material basis in' some 'autosomal dominant inheritance'
-DOID:0111252	neurofibromatosis 2	'has material basis in' some 'autosomal dominant inheritance'
+DOID:0111252	vestibular schwannomatosis	'has material basis in' some 'autosomal dominant inheritance'
 DOID:0111253	neurofibromatosis 1	'has material basis in' some 'autosomal dominant inheritance'
 DOID:0111254	glutaric acidemia I	'has material basis in' some 'autosomal recessive inheritance'
 DOID:0111255	McKusick-Kaufman syndrome	'has material basis in' some 'autosomal recessive inheritance'
@@ -4289,6 +4301,7 @@ DOID:3183	childhood oligodendroglioma	'existence starts during' some 'Childhood
 DOID:3184	spinal cord oligodendroglioma	'derives from' some 'glial cell'|'derives from' some oligodendrocyte
 DOID:3186	adult oligodendroglioma	'existence starts during' some 'Adult onset'
 DOID:3191	nemaline myopathy	'has symptom' some 'muscle weakness'
+DOID:3204	schwannomatosis	'has material basis in' some 'autosomal dominant inheritance'
 DOID:321	tropical spastic paraparesis	'disease has location' some 'spinal cord'|'has material basis in' some 'Human T-cell leukemia virus type I'|'has symptom' some 'muscle weakness'|'has symptom' some 'sensory disturbance'|'transmitted by' some ('contact transmission' or 'vehicle-borne ingestion transmission')
 DOID:3210	Pelizaeus-Merzbacher disease	'has material basis in' some 'X-linked recessive inheritance'
 DOID:322	myelitis	'has symptom' some inflammation

DOreports/GARDinDO.tsv

@@ -476,6 +476,8 @@ id	label	xrefs
 "DOID:0070439"	"North Carolina macular dystrophy"	"GARD:9179"
 "DOID:0070452"	"xanthinuria type I"@en	"GARD:5621"
 "DOID:0070453"	"xanthinuria type II"@en	"GARD:5620"
+"DOID:0070475"	"renal medullary carcinoma"@en	"GARD:13175"
+"DOID:0070484"	"Legius syndrome"	"GARD:10714"
 "DOID:0080016"	"spina bifida"	"GARD:7673"
 "DOID:0080021"	"Schmid metaphyseal chondrodysplasia"	"GARD:7029"
 "DOID:0080028"	"spondyloepimetaphyseal dysplasia, Strudwick type"	"GARD:134"
@@ -883,7 +885,7 @@ id	label	xrefs
 "DOID:0111247"	"hypertension and brachydactyly syndrome"	"GARD:967"
 "DOID:0111248"	"cerebrocostomandibular syndrome"	"GARD:6026"
 "DOID:0111249"	"uveal coloboma-cleft lip and palate-intellectual disability"	"GARD:1440"
-"DOID:0111252"	"neurofibromatosis 2"	"GARD:7193"
+"DOID:0111252"	"vestibular schwannomatosis"	"GARD:7193"
 "DOID:0111254"	"glutaric acidemia I"	"GARD:6522"
 "DOID:0111255"	"McKusick-Kaufman syndrome"	"GARD:3427"
 "DOID:0111256"	"hyperferritinemia-cataract syndrome"	"GARD:2806"