Add myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis 1

Author: csbjohnson

src/ontology/doid-edit.owl

@@ -2214,6 +2214,7 @@ Declaration(Class(obo:DOID_0061179))
 Declaration(Class(obo:DOID_0061180))
 Declaration(Class(obo:DOID_0061181))
 Declaration(Class(obo:DOID_0061182))
+Declaration(Class(obo:DOID_0061183))
 Declaration(Class(obo:DOID_0070000))
 Declaration(Class(obo:DOID_0070001))
 Declaration(Class(obo:DOID_0070002))
@@ -44691,6 +44692,17 @@ AnnotationAssertion(rdfs:label obo:DOID_0061182 "familial hypercholanemia 2")
 SubClassOf(obo:DOID_0061182 obo:DOID_1701)
 SubClassOf(obo:DOID_0061182 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000148))
 
+# Class: obo:DOID_0061183 (myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis 1)
+
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007637) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/34935254/") obo:IAO_0000115 obo:DOID_0061183 "A muscular disease characterized by the onset of muscle cramping and stiffness on exertion in infancy or early childhood, although later (even adult) onset has also been reported that has_material_basis_in homozygous or compound heterozygous mutation in the MLIP gene on chromosome 6p12.")
+AnnotationAssertion(oboInOwl:created_by obo:DOID_0061183 "claudiasbj")
+AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0061183 "MIM:620138")
+AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0061183 "disease_ontology")
+AnnotationAssertion(oboInOwl:id obo:DOID_0061183 "DOID:0061183")
+AnnotationAssertion(rdfs:label obo:DOID_0061183 "myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis 1")
+SubClassOf(obo:DOID_0061183 obo:DOID_0080000)
+SubClassOf(obo:DOID_0061183 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.")