Term Name:	hypertrophic cardiomyopathy 12
Synonyms:	cardiomyopathy familial hypertrophic 12, CMH12
Definition:	A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the CSRP3 gene on chromosome 11p15.
Ontology:	Human Disease [DOID:0110318]   ( DOID:0110318 )