Term Name:	hypertrophic cardiomyopathy 13
Synonyms:	cardiomyopathy familial hypertrophic 13, CMH13
Definition:	A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNC1 gene on chromosome 3p21.
Ontology:	Human Disease [DOID:0110319]   ( DOID:0110319 )