Term Name:	hypertrophic cardiomyopathy 6
Synonyms:	cardiomyopathy, familial hypertrophic 6, CMH6
Definition:	A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the gene encoding the gamma-2 regulatory subunit of AMP-activated protein kinase (PRKAG2).
Ontology:	Human Disease [DOID:0110312]   ( DOID:0110312 )