Term Name:	hypertrophic cardiomyopathy 17
Synonyms:	cardiomyopathy familial hypertrophic 17, CMH17
Definition:	A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the junctophilin gene (JPH2) on chromosome 20q12.
Ontology:	Human Disease [DOID:0110323]   ( DOID:0110323 )