Add hypertrophic cardiomyopathy 27

Author: csbjohnson

src/ontology/doid-edit.owl

@@ -2134,6 +2134,7 @@ Declaration(Class(obo:DOID_0061098))
 Declaration(Class(obo:DOID_0061099))
 Declaration(Class(obo:DOID_0061100))
 Declaration(Class(obo:DOID_0061101))
+Declaration(Class(obo:DOID_0061102))
 Declaration(Class(obo:DOID_0070000))
 Declaration(Class(obo:DOID_0070001))
 Declaration(Class(obo:DOID_0070002))
@@ -43595,6 +43596,17 @@ AnnotationAssertion(rdfs:label obo:DOID_0061101 "immunodeficiency 132A")
 SubClassOf(obo:DOID_0061101 obo:DOID_612)
 SubClassOf(obo:DOID_0061101 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000147))
 
+# Class: obo:DOID_0061102 (hypertrophic cardiomyopathy 27)
+
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/26846950/") obo:IAO_0000115 obo:DOID_0061102 "A familial hypertrophic cardiomyopathy characterized by biventricular involvement and atypical distribution of hypertrophy that has_material_basis_in homozygous or compound heterozygous mutation in the ALPK3 gene on chromosome 15q25.")
+AnnotationAssertion(Annotation(oboInOwl:hasSynonymType obo:OMO_0003012) oboInOwl:hasExactSynonym obo:DOID_0061102 "CMH27")
+AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0061102 "familial hypertrophic cardiomyopathy 27")
+AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0061102 "disease_ontology")
+AnnotationAssertion(oboInOwl:id obo:DOID_0061102 "DOID:0061102")
+AnnotationAssertion(rdfs:label obo:DOID_0061102 "hypertrophic cardiomyopathy 27")
+SubClassOf(obo:DOID_0061102 obo:DOID_0080326)
+SubClassOf(obo:DOID_0061102 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000148))
+
 # Class: obo:DOID_0070000 (3-methylglutaconic aciduria type 8)
 
 AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/27208207") Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/27696117") obo:IAO_0000115 obo:DOID_0070000 "A 3-methylglutaconic aciduria that has_material_basis_in homozygous mutation in the HTRA2 gene on chromosome 2p13.")