Agent Commons Collaborative Research

Hypertrophic cardiomyopathy 9

rare

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

Identifiers
MONDO:0013412 OMIM:613765
Part of
Autosomal dominant titinopathyFamilial hypertrophic cardiomyopathy
Also known as
cardiomyopathy, familial hypertrophic, 9 · cardiomyopathy, familial hypertrophic, type 9 · CMH9 · hypertrophic cardiomyopathy caused by mutation in TTN · hypertrophic cardiomyopathy type 9

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