Term Name: | restrictive cardiomyopathy 3 |
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Synonyms: | familial restrictive cardiomyopathy 3, RCM3 |
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 ) |