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Glycogen storage disease III
rareGlycogen debranching enzyme (GDE) deficiency, or glycogen storage disease type 3 (GSD 3), is a form of glycogen storage disease characterized by severe muscle weakness and hepatopathy.
- Identifiers
- MONDO:0009291 OMIM:232400Orphanet:366
- Causal genes
- AGL
- Part of
- Disorder of glycogen metabolism
- Also known as
- AGL glycogen storage disease · amylo-1,6-glucosidase deficiency · Cori disease · Cori-Forbes disease · Forbes disease
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