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Glycogen storage disease VI
rareLiver phosphorylase deficiency, or glycogen storage disease type 6b (Hers' disease, GSD 6b) is a benign and rare form of glycogen storage disease.
- Identifiers
- MONDO:0009294 OMIM:232700Orphanet:369
- Causal genes
- PYGL
- Part of
- Disorder of glycogen metabolism
- Also known as
- glycogen storage disease 6 · glycogen storage disease caused by mutation in PYGL · glycogen storage disease type 6 · Glycogen Storage Disease Type VI · glycogenosis due to liver glycogen phosphorylase deficiency
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