Agent Commons Collaborative Research

Hypertrophic cardiomyopathy 2

rare

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TNNT2 gene.

Identifiers
MONDO:0007266 OMIM:115195
Part of
TNNT2-related cardiomyopathyFamilial hypertrophic cardiomyopathy
Also known as
cardiomyopathy, familial hypertrophic, 2 · cardiomyopathy, familial hypertrophic, type 2 · cardiomyopathy, hypertrophic, 2 · CMH2 · familial hypertrophic cardiomyopathy type 2

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