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ontobot.yaml
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[Merge] MONDO:0957426 autosomal recessive hyper-IgE syndrome into MONDO:0032654 hyper-IgE recurrent infection syndrome 3, autosomal recessive Create new pull request #2451: Issue #8401 opened by twhetzel
November 14, 2024 23:13 13s
November 14, 2024 23:13 13s
Update autosomal recessive hyper-IgE syndrome due to ZNF341 deficiency Create new pull request #2450: Issue comment #8387 (comment) created by twhetzel
November 14, 2024 23:08 17s
November 14, 2024 23:08 17s
keratoconus Create new pull request #2449: Issue comment #8068 (comment) created by sabrinatoro
November 14, 2024 22:48 13s
November 14, 2024 22:48 13s
ClinGen request to relabel MONDO:0013069 Create new pull request #2448: Issue comment #8185 (comment) created by katiermullen
November 14, 2024 22:46 11s
November 14, 2024 22:46 11s
keratoconus Create new pull request #2447: Issue comment #8068 (comment) created by sabrinatoro
November 14, 2024 22:45 11s
November 14, 2024 22:45 11s
MONDO:0957426 autosomal recessive hyper-IgE syndrome Create new pull request #2446: Issue comment #7844 (comment) created by twhetzel
November 14, 2024 22:42 12s
November 14, 2024 22:42 12s
Update porphyria due to ALA dehydratase deficiency Create new pull request #2445: Issue comment #8394 (comment) created by sabrinatoro
November 14, 2024 22:13 18s
November 14, 2024 22:13 18s
MONDO hasExactSyn axiom DbXref points to an ORCID ID Create new pull request #2444: Issue comment #8089 (comment) created by katiermullen
November 14, 2024 22:01 13s
November 14, 2024 22:01 13s
MONDO_0017579 Baraitser-Winter cerebrofrontofacial syndrome reference to an ExactSynonym to an non-exist MONDO ID Create new pull request #2443: Issue comment #8085 (comment) created by katiermullen
November 14, 2024 21:46 13s
November 14, 2024 21:46 13s
Subclasses of injury are not always injuries Create new pull request #2442: Issue comment #8067 (comment) created by katiermullen
November 14, 2024 21:17 13s
November 14, 2024 21:17 13s
Update autosomal recessive hyper-IgE syndrome due to ZNF341 deficiency Create new pull request #2441: Issue comment #8387 (comment) created by sabrinatoro
November 14, 2024 19:57 14s
November 14, 2024 19:57 14s
Update Trimethylaminuria Classification Create new pull request #2440: Issue comment #8385 (comment) created by sabrinatoro
November 14, 2024 19:46 12s
November 14, 2024 19:46 12s
Revise subclass relationship of "hypertensive nephropathy" Create new pull request #2439: Issue comment #8010 (comment) created by twhetzel
November 14, 2024 19:35 13s
November 14, 2024 19:35 13s
Hemihydranencephaly Create new pull request #2438: Issue comment #8311 (comment) created by galyea123
November 14, 2024 19:28 16s
November 14, 2024 19:28 16s
Request for new synonym: Krabbe disease Create new pull request #2437: Issue comment #8028 (comment) created by katiermullen
November 14, 2024 18:56 12s
November 14, 2024 18:56 12s
GNB1-Related Disorder Create new pull request #2436: Issue comment #8167 (comment) created by sabrinatoro
November 14, 2024 18:15 11s
November 14, 2024 18:15 11s
Incorrect ICD10 mapping for undifferentiated carcinoma of the corpus uteri Create new pull request #2435: Issue comment #7998 (comment) created by katiermullen
November 14, 2024 18:15 13s
November 14, 2024 18:15 13s
SPATA5L1-related complex neurodevelopmental disorder with motor features and hearing loss Create new pull request #2434: Issue comment #7975 (comment) edited by twhetzel
November 14, 2024 18:10 12s
November 14, 2024 18:10 12s
SPATA5L1-related complex neurodevelopmental disorder with motor features and hearing loss Create new pull request #2433: Issue comment #7975 (comment) edited by twhetzel
November 14, 2024 18:09 13s
November 14, 2024 18:09 13s
SPATA5L1-related complex neurodevelopmental disorder with motor features and hearing loss Create new pull request #2432: Issue comment #7975 (comment) edited by twhetzel
November 14, 2024 18:08 12s
November 14, 2024 18:08 12s
SPATA5L1-related complex neurodevelopmental disorder with motor features and hearing loss Create new pull request #2431: Issue comment #7975 (comment) edited by twhetzel
November 14, 2024 18:08 18s
November 14, 2024 18:08 18s
SPATA5L1-related complex neurodevelopmental disorder with motor features and hearing loss Create new pull request #2430: Issue comment #7975 (comment) edited by twhetzel
November 14, 2024 18:07 23s
November 14, 2024 18:07 23s
SPATA5L1-related complex neurodevelopmental disorder with motor features and hearing loss Create new pull request #2429: Issue comment #7975 (comment) created by twhetzel
November 14, 2024 18:06 18s
November 14, 2024 18:06 18s
MONDO:0014606- Spelling Error in Definition Create new pull request #2428: Issue comment #7964 (comment) created by katiermullen
November 14, 2024 17:51 14s
November 14, 2024 17:51 14s
FOXG1 syndrome/Disorder; Rett syndrome, congenital variant [Merge] Create new pull request #2427: Issue comment #7850 (comment) created by katiermullen
November 14, 2024 17:39 12s
November 14, 2024 17:39 12s