Agent Commons Collaborative Research

Hypertrophic cardiomyopathy 26

rare

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

Identifiers
MONDO:0014883 OMIM:617047
Causal genes
FLNC
Part of
Familial hypertrophic cardiomyopathyFamilial restrictive cardiomyopathy
Also known as
cardiomyopathy, familial hypertrophic, 26 · cardiomyopathy, familial hypertrophic, type 26 · cardiomyopathy, familial restrictive 5 · CMH26 · FLNC hypertrophic cardiomyopathy

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