Term Name: | hypertrophic cardiomyopathy 3 |
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Synonyms: | cardiomyopathy familial hypertrophic 3, CMH3 |
Definition: | A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22. |
Ontology: | Human Disease [DOID:0110309] ( DOID:0110309 ) |