Update definition of primary ovarian insufficiency 3

Author: csbjohnson

src/ontology/doid-edit.owl

@@ -62235,7 +62235,7 @@ SubClassOf(obo:DOID_0080859 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_000014
 
 # Class: obo:DOID_0080860 (primary ovarian insufficiency 3)
 
-AnnotationAssertion(Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/12149404/") obo:IAO_0000115 obo:DOID_0080860 "A primary ovarian insufficiency that has_material_basis_in heterozygous mutation in the FOXL2 gene on chromosome 3q22.")
+AnnotationAssertion(Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/12149404/") obo:IAO_0000115 obo:DOID_0080860 "A primary ovarian insufficiency characterized by the cessation of ovarian function before the age of 40 years, with amenorrhea, hypoestrogenism, and elevated serum gonadotropin concentrations that has_material_basis_in heterozygous mutation in the FOXL2 gene on chromosome 3q22.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080860 "MIM:608996")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0080860 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0080860 "DOID:0080860")