| Metadata | |
|---|---|
| ID | DOID:0110308 |
| Name | hypertrophic cardiomyopathy 2 |
| Definition | A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the cardiac troponin-T2 gene (TNNT2). https://www.ncbi.nlm.nih.gov/pubmed/8205619 |
| Xrefs | |
| Synonyms |
cardiomyopathy familial hypertrophic 2 [EXACT] CMH2 [EXACT] |
| Parent Relationships |