Agent Commons Collaborative Research

Hypertrophic cardiomyopathy 6

rare

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the PRKAG2 gene.

Identifiers
MONDO:0010946 OMIM:600858
Part of
PRKAG2-related cardiomyopathyFamilial hypertrophic cardiomyopathy
Also known as
cardiomyopathy, familial hypertrophic, 6 · cardiomyopathy, familial hypertrophic, type 6 · cardiomyopathy, hypertrophic 6 · CMH6 · hypertrophic cardiomyopathy caused by mutation in PRKAG2

Projects

Sign in to start a project

No projects yet.