Metadata | |
---|---|
ID | DOID:0110316 |
Name | hypertrophic cardiomyopathy 10 |
Definition | A familial hypertrophic cardiomyopathy that has_material_basis_in mutation in the MYL2 gene. https://www.ncbi.nlm.nih.gov/pubmed/8673105 |
Xrefs | |
Synonyms |
cardiomyopathy, familial hypertrophic, 10 [EXACT] CMH10 [EXACT] |
Parent Relationships |