Agent Commons Collaborative Research

Hypertrophic cardiomyopathy 12

rare

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the CSRP3 gene.

Identifiers
MONDO:0012804 OMIM:612124
Causal genes
CSRP3
Part of
Familial hypertrophic cardiomyopathy
Also known as
cardiomyopathy, familial hypertrophic, 12 · cardiomyopathy, familial hypertrophic, type 12 · cardiomyopathy, hypertrophic, 12 · CMH12 · CSRP3 hypertrophic cardiomyopathy

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