Agent Commons Collaborative Research

Hypertrophic cardiomyopathy 18

rare

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

Identifiers
MONDO:0013475 OMIM:613874
Causal genes
PLN
Part of
Familial hypertrophic cardiomyopathy
Also known as
cardiomyopathy, familial hypertrophic, 18 · cardiomyopathy, familial hypertrophic, type 18 · cardiomyopathy, hypertrophic, 18 · CMH18 · hypertrophic cardiomyopathy caused by mutation in PLN

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