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Glycogen storage disease
Overview
Classification Glycogen storage disease type I Glycogen storage disease type II Glycogen storage disease type III Glycogen storage disease type IV Glycogen storage disease type V Glycogen storage disease type VI Glycogen storage disease type VII
Pathophysiology
Differentiating Glycogen storage disease

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Anmol Pitliya, M.B.B.S. M.D.[2]

Glycogen storage disease

Glycogen storage disease		Enzyme deficiency	Genetics	Inheritence	Hypoglycemia	Muscle weakness	Hepatomegaly	Cardiomegaly	Elevated CK
Glycogen storage disease type I	Von Gierke's disease	Glucose-6-phosphatase
Glycogen storage disease type II	Pompe disease	Alpha acid-glucosidase
Glycogen storage disease type III	Cori disease	Debranching enzyme
Glycogen storage disease type IV	Andersen's disease	Branching enzyme
Glycogen storage disease type V	McArdle disease	Muscle glycogen phosphorylase
Glycogen storage disease type VI	Hers' disease	Liver glycogen phosphorylase
Glycogen storage disease type VII	Tauri's disease	Muscle phosphofruktokinase
Glycogen storage disease type IX		Phosphorylase b kinase
Glycogen storage disease type X		Phosphoglycerate mutase
Glycogen storage disease type XI	Fanconi-Bickel syndrome	Glucose transporter 2
Glycogen storage disease type XII	Aldolase A deficiency	Aldolase A
Glycogen storage disease type XIII		Beta-enolase
Glycogen storage disease type XIV		Phosphoglucomutase type 2
Glycogen storage disease type 0	Lewis' disease	Hepatic glycogen synthase