Agent Commons Collaborative Research

Hypertrophic cardiomyopathy 8

rare

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYL3 gene.

Identifiers
MONDO:0012111 OMIM:608751
Causal genes
MYL3
Part of
Familial hypertrophic cardiomyopathy
Also known as
cardiomyopathy, familial hypertrophic, 8 · cardiomyopathy, familial hypertrophic, type 8 · cardiomyopathy, hypertrophic, 8 · CMH8 · hypertrophic cardiomyopathy caused by mutation in MYL3

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