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78 workflow run results
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Early March 2025 Release DOID CI #1401: Commit e436b3b pushed by allenbaron
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Add doid-diff to post-release reports DOID CI #1400: Commit 839b5e0 pushed by allenbaron
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Merge in viral infectious disease revisions DOID CI #1399: Commit 52a60d4 pushed by allenbaron
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Bulk replace Merriam Webster definition source URLs DOID CI #1398: Commit 1ceb10b pushed by allenbaron
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Add hypertrophic cardiomyopathy 27 DOID CI #1397: Commit 949b97f pushed by csbjohnson
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Add Cowden syndrome 6 synonym DOID CI #1396: Commit 8068dbb pushed by csbjohnson
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Add immunodeficiency 132A DOID CI #1395: Commit 5c4902f pushed by csbjohnson
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xref update DOID CI #1394: Commit b6989d3 pushed by csbjohnson
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Fix xref format DOID CI #1393: Commit c8798c9 pushed by csbjohnson
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Update "Henoch-Schoenlein purpura" to "IgA vasculitis" DOID CI #1392: Commit bb9d3a6 pushed by allenbaron
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Update SCA4 (DOID:0050957) DOID CI #1391: Commit 56a4d51 pushed by allenbaron
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Remove empty xref field DOID CI #1390: Commit d37aec4 pushed by csbjohnson
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Merge branch 'main' of https://github.com/DiseaseOntology/HumanDiseas… DOID CI #1389: Commit f491deb pushed by lschriml
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Merge branch 'main' of https://github.com/DiseaseOntology/HumanDiseas… DOID CI #1388: Commit 8c52869 pushed by csbjohnson
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updated epilepsy classification DOID CI #1387: Commit bcab373 pushed by lschriml
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updating nomenclature DOID CI #1386: Commit dd0db9d pushed by lschriml
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Update definition of primary autosomal recessive microcephaly 9 DOID CI #1385: Commit 4b437fc pushed by csbjohnson
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Add inheritance axiom and update definition of Seckel syndrome 2 DOID CI #1384: Commit dad8f14 pushed by csbjohnson
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Add inheritance axiom and update definition of Bardet-Biedl syndrome 7 DOID CI #1383: Commit 4f3a496 pushed by csbjohnson
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Update definition Cornelia de Lange syndrome 1 DOID CI #1382: Commit 71b8a70 pushed by csbjohnson
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Add gene and update mitochondrial DNA depletion syndrome 15 DOID CI #1381: Commit caf1f1d pushed by csbjohnson
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nomenclature updates DOID CI #1380: Commit 588be5d pushed by lschriml
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added subtypes congenital disorder of glycosylation type II DOID CI #1379: Commit 8ddfe4e pushed by lschriml
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Add immunodeficiency 132B DOID CI #1378: Commit 8ef54dd pushed by csbjohnson
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Add Perrault syndrome 7 DOID CI #1377: Commit 5543da9 pushed by csbjohnson
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