Add synonym to congenital myopathy 2B

Author: csbjohnson

src/ontology/doid-edit.owl

@@ -68855,6 +68855,7 @@ SubClassOf(obo:DOID_0081338 obo:DOID_0080307)
 
 AnnotationAssertion(Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/25182138/") obo:IAO_0000115 obo:DOID_0081339 "A congenital myopathy that is characterized by severe hypotonia with lack of spontaneous movements and respiratory insufficiency, usually leading to death in infancy or early childhood and that has_material_basis_in homozygous or compound heterozygous mutation in the ACTA1 gene on chromosome 1q42.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0081339 "MIM:620265")
+AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0081339 "autosomal recessive congenital myopathy 2B")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0081339 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0081339 "DOID:0081339")
 AnnotationAssertion(rdfs:label obo:DOID_0081339 "congenital myopathy 2B")