cardiomyopathy, familial hypertrophic, type 13

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cardiomyopathy, familial hypertrophic, type 13

A cardiomyopathy (OMIM:613243) characterised by ventricular dilation and impaired systolic function, resulting in congestive heart failure (CHF), arrhythmia and premature death.

Molecular pathology
Caused by defects of TNNC1, which encodes a troponin C protein.