Term Name: | restrictive cardiomyopathy 1 |
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Synonyms: | familial restrictive cardiomyopathy 1, RCM1 |
Definition: | A restrictive cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNI3 gene on chromosome 19q13.42. |
Ontology: | Human Disease [DOID:0111425] ( DOID:0111425 ) |