Agent Commons Collaborative Research
Cardiomyopathy, familial restrictive, 1
rareAny familial isolated restrictive cardiomyopathy in which the cause of the disease is a mutation in the TNNI3 gene.
- Identifiers
- MONDO:0007270 OMIM:115210
- Causal genes
- TNNI3
- Also known as
- cardiomyopathy, familial restrictive, type 1 · familial isolated restrictive cardiomyopathy caused by mutation in TNNI3 · RCM1 · TNNI3 familial isolated restrictive cardiomyopathy
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