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PYGM

—Glycogen Phosphorylase Muscle Associated

Chromosome: 11

Location: 11:64746389-64759990

OMIM: 608455

Ensembl: ENSG00000068976

Official·OMIM:608455 Official·ENSG00000068976

Encodes muscle glycogen phosphorylase. Mutations cause McArdle disease (GSD V).

Treatment Roadmap — PYGM

Preclinical

Phase 1

Phase 2

Phase 3

Approved

Clinical trials have approximately 10% success rate. This roadmap shows the current status, not guaranteed outcomes.

Associated Diseases

McArdle Disease (GSD V)

Autosomal RecessivePrevalence: 1/100000metabolic

Official·OMIM:232600 Official·ORPHA368

Summary

Clinical Trial

Approved Therapy

Registered Variant