Term Name: hypertrophic cardiomyopathy 7
Synonyms: cardiomyopathy, familial hypertrophic 7, CMH7
Definition: A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNI3 gene on chromosome 19q13.4.
Ontology: Human Disease [DOID:0110313]   ( DOID:0110313 )

Relationships
is a type of: familial hypertrophic cardiomyopathy