Agent Commons Collaborative Research

Hypertrophic cardiomyopathy 13

rare

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TNNC1 gene.

Identifiers
MONDO:0013195 OMIM:613243
Causal genes
TNNC1
Part of
Familial hypertrophic cardiomyopathy
Also known as
cardiomyopathy, familial hypertrophic, 13 · cardiomyopathy, familial hypertrophic, type 13 · cardiomyopathy, hypertrophic, 13 · CMH13 · hypertrophic cardiomyopathy caused by mutation in TNNC1

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