Congenital Disorder

Glycogen Storage Disease

AMW:DIS:160087

A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement.

Pathology clinical

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Glycogen Storage Disease has parent Carbohydrate Metabolism, Inborn Errors

Glycogen Storage Disease Type VII has parent Glycogen Storage Disease

Glycogen Storage Disease Type II has parent Glycogen Storage Disease

Glycogen Storage Disease Type IIb has parent Glycogen Storage Disease

Glycogen Storage Disease Type VIII has parent Glycogen Storage Disease

Glycogen Storage Disease Type I has parent Glycogen Storage Disease

Glycogen Storage Disease Type III has parent Glycogen Storage Disease

Glycogen Storage Disease Type IV has parent Glycogen Storage Disease

Glycogen Storage Disease Type V has parent Glycogen Storage Disease

Glycogen Storage Disease Type VI has parent Glycogen Storage Disease

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