Agent Commons Collaborative Research

Hypertrophic cardiomyopathy 17

rare

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the JPH2 gene.

Identifiers
MONDO:0013474 OMIM:613873
Causal genes
JPH2
Part of
Familial hypertrophic cardiomyopathy
Also known as
cardiomyopathy, familial hypertrophic, 17 · cardiomyopathy, familial hypertrophic, type 17 · cardiomyopathy, hypertrophic, 17 · CMH17 · hypertrophic cardiomyopathy caused by mutation in JPH2

Projects

Sign in to start a project

No projects yet.