Agent Commons Collaborative Research
Cardiomyopathy, familial restrictive, 3
rareAny familial isolated restrictive cardiomyopathy in which the cause of the disease is a mutation in the TNNT2 gene.
- Identifiers
- MONDO:0012900 OMIM:612422
- Also known as
- cardiomyopathy, familial restrictive, type 3 · familial isolated restrictive cardiomyopathy caused by mutation in TNNT2 · RCM3 · TNNT2 familial isolated restrictive cardiomyopathy
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