Term Name:	hypertrophic cardiomyopathy 2
Synonyms:	cardiomyopathy familial hypertrophic 2, CMH2
Definition:	A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the cardiac troponin-T2 gene (TNNT2).
Ontology:	Human Disease [DOID:0110308]   ( DOID:0110308 )