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Polyglucosan body myopathy type 2

MONDO:0014526

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, PGBM2, polyglucosan body myopathy 2

4 clinical trials for this condition and its sub-types, 1 tagged with Polyglucosan body myopathy type 2 itself.

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Including sub-types (4) Tagged with Polyglucosan body myopathy type 2 (1)

Trials to join now! 1

Scientists launch Largest-Ever study of Ultra-Rare GSDs

Knowledge-focused Recruiting now

This study tracks 200 people with ultra-rare glycogen storage diseases (GSDs) like types 0a, 0b, VII, X, XII, XIII, XV, PRKAG2 syndrome, and Danon disease. Researchers will collect medical records and other data to see how these conditions progress over time. No treatments or dru…

Sponsor: Duke University • Aim: Knowledge-focused

Last updated Jun 27, 2026 08:08 UTC

Polyglucosan body myopathy type 2

Where it sits in the disease tree

Scientists launch Largest-Ever study of Ultra-Rare GSDs