Polyglucosan body myopathy type 2

Definition

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

Also known as GYG1 polyglucosan body myopathy, polyglucosan body myopathy caused by mutation in GYG1, polyglucosan body myopathy type 2 — per MONDO

Also identified as

• OMIM 616199 per MONDO
• Orphanet 456369 per MONDO
• UMLS C4015452 per MONDO