| Metadata | |
|---|---|
| ID | DOID:0110309 |
| Name | hypertrophic cardiomyopathy 3 |
| Definition | A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22. https://www.ncbi.nlm.nih.gov/pubmed/8205619 |
| Xrefs | |
| Synonyms |
cardiomyopathy familial hypertrophic 3 [EXACT] CMH3 [EXACT] |
| Parent Relationships |