cardiomyopathy, familial hypertrophic, type 13
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.