| Metadata | |
|---|---|
| ID | DOID:0110314 |
| Name | hypertrophic cardiomyopathy 8 |
| Definition | A familial hypertrophic cardiomyopathy that has_material_basis_in homozygous or heterozygous mutation in the MYL3 gene. https://www.ncbi.nlm.nih.gov/pubmed/8673105 |
| Xrefs | |
| Synonyms |
cardiomyopathy hypertrophic mid-left ventricular chamber type 1 [EXACT] cardiomyopathy, familial hypertrophic, 8 [EXACT] |
| Parent Relationships |