| Term Name: | hypertrophic cardiomyopathy 10 |
|---|---|
| Synonyms: | cardiomyopathy, familial hypertrophic, 10, CMH10 |
| Definition: | A familial hypertrophic cardiomyopathy that has_material_basis_in mutation in the MYL2 gene. |
| Ontology: | Human Disease [DOID:0110316] ( DOID:0110316 ) |