Nomenclature review of nephrotic syndrome type 14

Author: csbjohnson

src/ontology/doid-edit.owl

@@ -57087,13 +57087,14 @@ AnnotationAssertion(rdfs:label obo:DOID_0080264 "exudative vitreoretinopathy 7")
 SubClassOf(obo:DOID_0080264 obo:DOID_0050535)
 SubClassOf(obo:DOID_0080264 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000147))
 
-# Class: obo:DOID_0080265 (nephrotic syndrome type 14)
+# Class: obo:DOID_0080265 (RENI syndrome)
 
 AnnotationAssertion(Annotation(dc:type obo:ECO_0007636) Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/28165343") Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/30683667") Annotation(oboInOwl:hasDbXref "url:https://www.omim.org/entry/617575") obo:IAO_0000115 obo:DOID_0080265 "A familial nephrotic syndrome that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the sphingosine-1-phosphate lyase 1 (SGPL1) gene on chromosome 10q21.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080265 "MIM:617575")
+AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0080265 "nephrotic syndrome type 14")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0080265 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0080265 "DOID:0080265")
-AnnotationAssertion(rdfs:label obo:DOID_0080265 "nephrotic syndrome type 14")
+AnnotationAssertion(rdfs:label obo:DOID_0080265 "RENI syndrome")
 SubClassOf(obo:DOID_0080265 obo:DOID_2590)
 SubClassOf(obo:DOID_0080265 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000148))