Update familial restrictive cardiomyopathy subtypes nomenclature

#1419
DiseaseOntology · Jan 8, 2025 · 82d4859 · 82d4859
1 parent a4c265b
commit 82d4859
Showing 1 changed file with 6 additions and 6 deletions.
diff --git a/src/ontology/doid-edit.owl b/src/ontology/doid-edit.owl
@@ -89080,37 +89080,37 @@ AnnotationAssertion(oboInOwl:id obo:DOID_0111424 "DOID:0111424")
 AnnotationAssertion(rdfs:label obo:DOID_0111424 "branchiootorenal syndrome 2"@en)
 SubClassOf(obo:DOID_0111424 obo:DOID_14702)
 
-# Class: obo:DOID_0111425 (restrictive cardiomyopathy 1)
+# Class: obo:DOID_0111425 (familial restrictive cardiomyopathy 1)
 
 AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/12531876") obo:IAO_0000115 obo:DOID_0111425 "A restrictive cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNI3 gene on chromosome 19q13.42."@en)
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111425 "MIM:115210")
 AnnotationAssertion(Annotation(oboInOwl:hasSynonymType obo:OMO_0003012) oboInOwl:hasExactSynonym obo:DOID_0111425 "RCM1"@en)
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0111425 "familial restrictive cardiomyopathy 1"@en)
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0111425 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0111425 "DOID:0111425")
-AnnotationAssertion(rdfs:label obo:DOID_0111425 "restrictive cardiomyopathy 1"@en)
+AnnotationAssertion(rdfs:label obo:DOID_0111425 "familial restrictive cardiomyopathy 1"@en)
 SubClassOf(obo:DOID_0111425 obo:DOID_397)
 
-# Class: obo:DOID_0111426 (restrictive cardiomyopathy 2)
+# Class: obo:DOID_0111426 (familial restrictive cardiomyopathy 2)
 
 AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/16061566") obo:IAO_0000115 obo:DOID_0111426 "A restrictive cardiomyopathy that has_material_basis_in variation in a region on chromosome 10q23.3."@en)
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111426 "MIM:609578")
 AnnotationAssertion(Annotation(oboInOwl:hasSynonymType obo:OMO_0003012) oboInOwl:hasExactSynonym obo:DOID_0111426 "RCM2"@en)
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0111426 "familial restrictive cardiomyopathy 2"@en)
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0111426 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0111426 "DOID:0111426")
-AnnotationAssertion(rdfs:label obo:DOID_0111426 "restrictive cardiomyopathy 2"@en)
+AnnotationAssertion(rdfs:label obo:DOID_0111426 "familial restrictive cardiomyopathy 2"@en)
 SubClassOf(obo:DOID_0111426 obo:DOID_397)
 
-# Class: obo:DOID_0111427 (restrictive cardiomyopathy 3)
+# Class: obo:DOID_0111427 (familial restrictive cardiomyopathy 3)
 
 AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/16651346") obo:IAO_0000115 obo:DOID_0111427 "A restrictive cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNT2 gene on chromosome 1q32.1."@en)
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111427 "MIM:612422")
 AnnotationAssertion(Annotation(oboInOwl:hasSynonymType obo:OMO_0003012) oboInOwl:hasExactSynonym obo:DOID_0111427 "RCM3"@en)
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0111427 "familial restrictive cardiomyopathy 3"@en)
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0111427 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0111427 "DOID:0111427")
-AnnotationAssertion(rdfs:label obo:DOID_0111427 "restrictive cardiomyopathy 3"@en)
+AnnotationAssertion(rdfs:label obo:DOID_0111427 "familial restrictive cardiomyopathy 3"@en)
 SubClassOf(obo:DOID_0111427 obo:DOID_397)
 
 # Class: obo:DOID_0111428 (essential tremor 1)