Add 'autosomal dominant polycystic kidney disease' synonym and xref

DiseaseOntology · Jan 30, 2024 · 64a8b22 · 64a8b22
1 parent 781d6ee
commit 64a8b22
Showing 1 changed file with 2 additions and 1 deletion.
diff --git a/src/ontology/doid-edit.owl b/src/ontology/doid-edit.owl
@@ -197993,7 +197993,7 @@ AnnotationAssertion(owl:deprecated obo:DOID_8979 "true"^^xsd:boolean)
 
 # Class: obo:DOID_898 (autosomal dominant polycystic kidney disease)
 
-AnnotationAssertion(Annotation(dc:type obo:ECO_0007637) Annotation(dc:type obo:ECO_0007638) Annotation(oboInOwl:hasDbXref "url:https://en.wikipedia.org/wiki/Ciliopathy#cite_note-davenport2008-4") Annotation(oboInOwl:hasDbXref "url:https://rarediseases.info.nih.gov/diseases/10413/autosomal-dominant-polycystic-kidney-disease") obo:IAO_0000115 obo:DOID_898 "A polycystic kidney disease characterized by the presence of multiple cysts located_in the kidney resulting from ciliopathy that disrupts the function of primary cilium, inherited in an autosomal dominant fashion.")
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007637) Annotation(dc:type obo:ECO_0007638) Annotation(oboInOwl:hasDbXref "url:https://en.wikipedia.org/wiki/Ciliopathy#cite_note-davenport2008-4") Annotation(oboInOwl:hasDbXref "url:https://rarediseases.info.nih.gov/diseases/10413/autosomal-dominant-polycystic-kidney-disease") Annotation(oboInOwl:hasDbXref "url:https://www.genome.gov/Genetic-Disorders/Autosomal-Polycystic-Kidney-Disease") obo:IAO_0000115 obo:DOID_898 "A polycystic kidney disease characterized by the presence of multiple cysts located_in the kidney resulting from ciliopathy that disrupts the function of primary cilium, inherited in an autosomal dominant fashion.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_898 "GARD:7419")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_898 "ICD10CM:Q61.3")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_898 "ICD9CM:753.12")
@@ -198004,6 +198004,7 @@ AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_898 "SNOMEDCT_US_2023_03_01:2049
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_898 "UMLS_CUI:C0022680")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_898 "Congenital biliary ectasias"@en)
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_898 "POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1"@en)
+AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_898 "ADPKD")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_898 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_898 "DOID:898")
 AnnotationAssertion(oboInOwl:inSubset obo:DOID_898 doid:DO_rare_slim)