Add nomenclature synonym to nemaline myopathy 3

Author: csbjohnson

src/ontology/doid-edit.owl

@@ -55112,8 +55112,8 @@ AnnotationAssertion(oboInOwl:created_by obo:DOID_0080102 "lschriml")
 AnnotationAssertion(oboInOwl:creation_date obo:DOID_0080102 "2015-11-10T17:27:15Z")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080102 "MIM:255310")
 AnnotationAssertion(Annotation(oboInOwl:hasSynonymType obo:OMO_0003012) oboInOwl:hasExactSynonym obo:DOID_0080102 "CFTD")
-AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0080102 "congenital fiber-type disproportion")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0080102 "autosomal dominant congenital myopathy 4A")
+AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0080102 "congenital fiber-type disproportion")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0080102 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0080102 "DOID:0080102")
 AnnotationAssertion(rdfs:label obo:DOID_0080102 "congenital myopathy 4A")
@@ -80941,14 +80941,14 @@ AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110633 "classic MmD")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110633 "classic multiminicore disease")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110633 "classic multiminicore myopathy")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110633 "congenital merosin-positive muscular dystrophy with early spine rigidity")
+AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110633 "congenital myopathy 3 with rigid spine")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110633 "desmin-related myopathy with Mallory bodies")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110633 "desmin-related myopathy with Mallory body-like inclusions")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110633 "early-onset desmin-related myopathy")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110633 "rigid spine syndrome")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110633 "severe classic form minicore myopathy")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110633 "severe classic form multicore myopathy")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110633 "severe classic form multiminicore disease")
-AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110633 "congenital myopathy 3 with rigid spine")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0110633 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0110633 "DOID:0110633")
 AnnotationAssertion(oboInOwl:inSubset obo:DOID_0110633 doid:DO_rare_slim)
@@ -84969,9 +84969,9 @@ AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasD
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0110926 "MESH:C538348")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0110926 "MIM:609284")
 AnnotationAssertion(Annotation(oboInOwl:hasSynonymType obo:OMO_0003012) oboInOwl:hasExactSynonym obo:DOID_0110926 "NEM1")
+AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110926 "autosomal recessive congenital myopathy 4B")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110926 "congenital myopathy 4B")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110926 "nemaline myopathy 1, autosomal dominant or recessive")
-AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110926 "autosomal recessive congenital myopathy 4B")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0110926 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0110926 "DOID:0110926")
 AnnotationAssertion(rdfs:label obo:DOID_0110926 "nemaline myopathy 1")
@@ -84986,6 +84986,7 @@ AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0110927 "MIM:161800")
 AnnotationAssertion(Annotation(oboInOwl:hasSynonymType obo:OMO_0003012) oboInOwl:hasExactSynonym obo:DOID_0110927 "NEM3")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110927 "congenital myopathy 2A")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110927 "nemaline myopathy 3, autosomal dominant or recessive")
+AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110927 "autosomal dominant typical congenital myopathy 2A")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0110927 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0110927 "DOID:0110927")
 AnnotationAssertion(rdfs:label obo:DOID_0110927 "nemaline myopathy 3")