Add myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis 2

Author: csbjohnson

src/ontology/doid-edit.owl

@@ -2215,6 +2215,7 @@ Declaration(Class(obo:DOID_0061180))
 Declaration(Class(obo:DOID_0061181))
 Declaration(Class(obo:DOID_0061182))
 Declaration(Class(obo:DOID_0061183))
+Declaration(Class(obo:DOID_0061184))
 Declaration(Class(obo:DOID_0070000))
 Declaration(Class(obo:DOID_0070001))
 Declaration(Class(obo:DOID_0070002))
@@ -44703,6 +44704,17 @@ AnnotationAssertion(rdfs:label obo:DOID_0061183 "myopathy with myalgia, increase
 SubClassOf(obo:DOID_0061183 obo:DOID_0080000)
 SubClassOf(obo:DOID_0061183 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000148))
 
+# Class: obo:DOID_0061184 (myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis 2)
+
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007637) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/36799992/") obo:IAO_0000115 obo:DOID_0061184 "A muscular disease characterized by myalgia, muscle cramps, exercise intolerance, and increased serum creatine kinase with onset between the first and fourth decades of life that has_material_basis_in heterozygous mutation in the DTNA gene on chromosome 18q12.")
+AnnotationAssertion(oboInOwl:created_by obo:DOID_0061184 "claudiasbj")
+AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0061184 "MIM:620971")
+AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0061184 "disease_ontology")
+AnnotationAssertion(oboInOwl:id obo:DOID_0061184 "DOID:0061184")
+AnnotationAssertion(rdfs:label obo:DOID_0061184 "myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis 2")
+SubClassOf(obo:DOID_0061184 obo:DOID_0080000)
+SubClassOf(obo:DOID_0061184 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000147))
+
 # 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.")