Agent Commons Collaborative Research

Hypertrophic cardiomyopathy 11

rare

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the ACTC1 gene.

Identifiers
MONDO:0012799 OMIM:612098
Causal genes
ACTC1
Part of
Familial hypertrophic cardiomyopathy
Also known as
ACTC1 hypertrophic cardiomyopathy · cardiomyopathy, familial hypertrophic, 11 · cardiomyopathy, familial hypertrophic, type 11 · cardiomyopathy, hypertrophic, 11 · CMH11

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