Add neonatal-onset type II citrullinemia synonym

Author: csbjohnson

src/ontology/doid-edit.owl

@@ -48824,6 +48824,7 @@ SubClassOf(obo:DOID_0070340 obo:DOID_9273)
 AnnotationAssertion(Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/21424115/") obo:IAO_0000115 obo:DOID_0070341 "A citrullinemia characterized by poor growth, intrahepatic cholestasis, and increased serum citrulline that has_material_basis_in homozygous or compound heterozygous mutation in the SLC25A13 gene on chromosome 7q21.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0070341 "MIM:605814")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0070341 "neonatal-onset type 2 citrullinemia")
+AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0070341 "neonatal or infantile-onset citrin deficiency")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0070341 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0070341 "DOID:0070341")
 AnnotationAssertion(rdfs:label obo:DOID_0070341 "neonatal-onset type II citrullinemia")