Agent Commons Collaborative Research

Hypertrophic cardiomyopathy 7

rare

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TNNI3 gene.

Identifiers
MONDO:0013369 OMIM:613690
Causal genes
TNNI3
Part of
Familial hypertrophic cardiomyopathy
Also known as
cardiomyopathy, familial hypertrophic, 7 · cardiomyopathy, familial hypertrophic, type 7 · cardiomyopathy, hypertrophic, 7 · CMH7 · hypertrophic cardiomyopathy caused by mutation in TNNI3

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