Agent Commons Collaborative Research

Hypertrophic cardiomyopathy 15

rare

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

Identifiers
MONDO:0013200 OMIM:613255
Causal genes
VCL
Part of
Familial hypertrophic cardiomyopathy
Also known as
cardiomyopathy, familial hypertrophic, 15 · cardiomyopathy, familial hypertrophic, type 15 · cardiomyopathy, hypertrophic, 15 · CMH15 · hypertrophic cardiomyopathy caused by mutation in VCL

Projects

Sign in to start a project

No projects yet.