Term Name: | hypertrophic cardiomyopathy 15 |
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Synonyms: | cardiomyopathy familial hypertrophic 15, CMH15 |
Definition: | A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the vinculin gene (VCL) on chromosome 10q22. |
Ontology: | Human Disease [DOID:0110321] ( DOID:0110321 ) |