Term Name:	hypertrophic cardiomyopathy 16
Synonyms:	cardiomyopathy familial hypertrophic 16, CMH16
Definition:	A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the MYOZ2 gene on chromosome 4q26.
Ontology:	Human Disease [DOID:0110322]   ( DOID:0110322 )