GSD 0 (Lewis’ disease), Glycogen synthase, (Muscle GYS1 / Liver GYS2)
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GSD I / GSD 1 (von Gierke’s disease), Glucose-6-phosphatase / Glucose-6-phosphate translocase, (G6PC / SLC37A4 /SLC17A3)
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GSD II / GSD 2 (Pompe disease, formerly GSD-IIa), Acid alpha-glucosidase, (GAA)
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Danon disease (formerly GSD-IIb), Lysosome-associated membrane protein 2,(LAMP2)
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GSD III / GSD 3,(Cori’s disease or Forbes’ disease), Glycogen debranching enzyme
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GSD IV / GSD 4, (Andersen’s disease), Glycogen branching enzyme, (GBE1)
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GSD V / GSD 5, (McArdle’s disease), Muscle glycogen phosphorylase, (PYGM)
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GSD VI / GSD 6 (Hers’ disease), Liver glycogen phosphorylase, (PYGL)
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GSD VII / GSD 7 (Tarui’s disease), Muscle phosphofructokinase, (PFKM)
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GSD IX / GSD 9 Phosphorylase kinase, (PHKA2 / PHKB / PHKG2 / PHKA1)
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GSD X / GSD 10 Muscle Phosphoglycerate mutase(PGAM2)
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GSD XI / GSD 11 Muscle lactate dehydrogenase, (LDHA), Fanconi-Bickel syndrome, formerly GSD XI / GSD 11, no longer considered a GSD. Glucose transporter (GLUT2)
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GSD XII / GSD 12 (Aldolase A deficiency), Aldolase A, (ALDOA)
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GSD XIII / GSD 13, β-enolase, (ENO3)
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CDG1T (formally GSD XIV / GSD 14), Phosphoglucomutase-1(PGM1)
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GSD XV / GSD 15, Glycogenin-1, (GYG1)
