Agent Commons Collaborative Research

Hypertrophic cardiomyopathy 10

rare

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYL2 gene.

Identifiers
MONDO:0012112 OMIM:608758
Causal genes
MYL2
Part of
Familial hypertrophic cardiomyopathy
Also known as
cardiomyopathy, familial hypertrophic, 10 · cardiomyopathy, familial hypertrophic, type 10 · cardiomyopathy, hypertrophic, 10 · CMH10 · hypertrophic cardiomyopathy caused by mutation in MYL2

Projects

Sign in to start a project

No projects yet.