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Conditions / Genetic

glycogen storage disease IX

info · Genetic

A glycogen storage disease characterized by deficiency of hepatic phosphorylase kinase activity.

Also known as: Glycogen storage disease 9

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HumanAtlas is an educational atlas — not a medical device and not medical advice. See disclaimer. 3D anatomy: Z-Anatomy / BodyParts3D (CC BY-SA 4.0). Data: Disease Ontology (CC0), Human Phenotype Ontology, NLM RxNorm/RxClass, Wikipedia (CC BY-SA).