Term Name:	hypertrophic cardiomyopathy 1
Synonyms:	cardiomyopathy, familial hypertrophic 1, CMH1, hypertrophic cardiomyopathy 19
Definition:	A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the MYH7 gene on chromosome 14q12.
Ontology:	Human Disease [DOID:0110307]   ( DOID:0110307 )