Type 1

Type 2

von Gierke disease or hepatorenal glycogenosis

Pompe disease

Type 3

Forbes-Cori disease or limit dextrinosis

Type 4

amylopectinosis or Andersen disease

Type 5

McArdle disease

glucose-6-phosphatase (G6Pase)
alpha-1,4-glucosidase (acid maltase)

mutations in G6PC and SLC37A4, cause GSDI

glycogen debranching enzyme

Mutations in the AGL gene cause GSDIII

Mutations in the GBE1 gene cause GSD IV
Mutations in the PYGM gene cause GSDV

Muscle phosphorylase / myophosphorylase

mutation in GAA

4, cause GSDI

e GSD IV
se GSDV