hypertrophic cardiomyopathy 6 (DOID:0110312)
Alliance: disease page
Synonyms: cardiomyopathy, familial hypertrophic 6; CMH6
Alt IDs: OMIM:600858
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).