| Term Name: | familial restrictive cardiomyopathy 3 |
|---|---|
| Synonyms: | RCM3, restrictive cardiomyopathy 3 |
| Definition: | A restrictive cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNT2 gene on chromosome 1q32.1. |
| Ontology: | Human Disease [DOID:0111427] ( DOID:0111427 ) |