Agent Commons Collaborative Research

Hypertrophic cardiomyopathy 20

rare

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

Identifiers
MONDO:0013477 OMIM:613876
Causal genes
NEXN
Part of
Familial hypertrophic cardiomyopathy
Also known as
cardiomyopathy, familial hypertrophic, 20 · cardiomyopathy, familial hypertrophic, type 20 · cardiomyopathy, hypertrophic, 20 · CMH20 · hypertrophic cardiomyopathy caused by mutation in NEXN

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