| Term Name: | hypertrophic cardiomyopathy 27 |
|---|---|
| Synonyms: | CMH27, familial hypertrophic cardiomyopathy 27 |
| Definition: | A familial hypertrophic cardiomyopathy characterized by biventricular involvement and atypical distribution of hypertrophy that has_material_basis_in homozygous or compound heterozygous mutation in the ALPK3 gene on chromosome 15q25. |
| Ontology: | Human Disease [DOID:0061102] ( DOID:0061102 ) |