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Correct typo in immunodeficiency 17 for accuracy
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csbjohnson committed Jan 6, 2025
1 parent 8e67d93 commit 54d5711
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2 changes: 1 addition & 1 deletion src/ontology/doid-edit.owl
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Expand Up @@ -97363,7 +97363,7 @@ SubClassOf(obo:DOID_0111972 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_000014

# Class: obo:DOID_0111973 (immunodeficiency 17)

AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/1635567/") Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/17277165/") Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/8325321/") obo:IAO_0000115 obo:DOID_0111973 "A T cell deficiency characterized by partial T-cell lymphopenia with normal numbers of B and NK cells and highly variable clincal severity that has_material_basis_in homozygous or compound heterozygous mutation in the CD3G gene on chromosome 11q23.3."@en)
AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/1635567/") Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/17277165/") Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/8325321/") obo:IAO_0000115 obo:DOID_0111973 "A T cell deficiency characterized by partial T-cell lymphopenia with normal numbers of B and NK cells and highly variable clinical severity that has_material_basis_in homozygous or compound heterozygous mutation in the CD3G gene on chromosome 11q23.3."@en)
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111973 "MIM:615607")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111973 "UMLS_CUI:C3810107")
AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0111973 "CD3-gamma deficiency"@en)
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