Nomenclature update of autosomal dominant Alport syndrome

Author: csbjohnson

src/ontology/doid-edit.owl

@@ -73394,16 +73394,18 @@ AnnotationAssertion(oboInOwl:inSubset obo:DOID_0110031 doid:DO_rare_slim)
 AnnotationAssertion(rdfs:label obo:DOID_0110031 "hemoglobin H disease")
 SubClassOf(obo:DOID_0110031 obo:DOID_1099)
 
-# Class: obo:DOID_0110032 (autosomal dominant Alport syndrome)
+# Class: obo:DOID_0110032 (autosomal dominant Alport syndrome 3A)
 
 AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/11044206") obo:IAO_0000115 obo:DOID_0110032 "An Alport syndrome that has_material_basis_in heterozygous mutation in the COL4A3 gene.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0110032 "GARD:624")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0110032 "MIM:104200")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0110032 "ORDO:88918")
+AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110032 "autosomal dominant Alport syndrome")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0110032 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0110032 "DOID:0110032")
 AnnotationAssertion(oboInOwl:inSubset obo:DOID_0110032 doid:DO_rare_slim)
-AnnotationAssertion(rdfs:label obo:DOID_0110032 "autosomal dominant Alport syndrome")
+AnnotationAssertion(rdfs:comment obo:DOID_0110032 "nomenclature update on Nov 2025 (claudiasbj)")
+AnnotationAssertion(rdfs:label obo:DOID_0110032 "autosomal dominant Alport syndrome 3A")
 SubClassOf(obo:DOID_0110032 obo:DOID_10983)
 SubClassOf(obo:DOID_0110032 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000147))