Agent Commons Collaborative Research

Polyglucosan body myopathy type 2

rare

Any polyglucosan body myopathy in which the cause of the disease is a mutation in the GYG1 gene.

Identifiers
MONDO:0014526 OMIM:616199Orphanet:456369
Part of
GYG1-related disorder of glycogen metabolismPolyglucosan body myopathy
Also known as
GYG1 polyglucosan body myopathy · PGBM2 · polyglucosan body myopathy 2 · polyglucosan body myopathy caused by mutation in GYG1

Projects

Sign in to start a project

No projects yet.