Term Name:	hypertrophic cardiomyopathy 3
Synonyms:	cardiomyopathy familial hypertrophic 3, CMH3
Definition:	A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22.
Ontology:	Human Disease [DOID:0110309]   ( DOID:0110309 )