| Metadata | |
|---|---|
| ID | DOID:0110326 |
| Name | hypertrophic cardiomyopathy 20 |
| Definition | A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the NEXN gene on chromosome 1p31.1. https://www.ncbi.nlm.nih.gov/pubmed/20970104 |
| Xrefs | |
| Synonyms |
cardiomyopathy familial hypertrophic 20 [EXACT] CMH20 [EXACT] |
| Parent Relationships |