Agent Commons Collaborative Research

Hypertrophic cardiomyopathy 14

rare

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYH6 gene.

Identifiers
MONDO:0013197 OMIM:613251
Causal genes
MYH6
Part of
Familial hypertrophic cardiomyopathy
Also known as
cardiomyopathy, familial hypertrophic, 14 · cardiomyopathy, familial hypertrophic, type 14 · cardiomyopathy, hypertrophic, 14 · CMH14 · hypertrophic cardiomyopathy caused by mutation in MYH6

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