Stanford Health Library

Nutritional & Metabolic Diseases

Use these links to jump directly to your topic of interest in Nutritional & Metabolic Diseases:

Nutrition: General Nutrition | Dietary Recommendations | Dietary Supplements | Caffeine | Carbohydrates | Fats | Fiber | Food Additives | Functional Foods | Minerals | Protein | Sugars and Sweeteners | Vitamins | Acid-Base Balance | Water Balance

Nutritional Disease: Malnutrition | Obesity

Metabolic Disease: General Metabolic Disease | Specific Diseases: A-C, D-G, H-L, M-P, R-Z


Metabolic Diseases:
Glycogen Storage Diseases

(Jump to: Organization | Overview | GSD 0 | GSD 1 | GSD 2 | GSD 3 | GSD 4 | GSD 5 | GSD 6 | GSD 7 | GSD 9 | GSD 10 | GSD 11 )

Organization
Association for Glycogen Storage Disease (ASGD)


Overview
What Is Glycogen Storage Disease?:ASGD


GSD 0 (Glycogen Synthetase Deficiency
Type 0 Glycogen Storage Disease:ASGD


GSD I (von Gierke Disease, Glycogenosis)
Type I Glycogen Storage Disease:ASGD
Glycogen Storage Disease Type 1a:Madisons Foundation
Glycogen Storage Disease Type 1b:Madisons Foundation
Glycogen Storage Disease Type I:GeneReviews


GSD II (Pompe Disease, Acid Maltase Deficiency)
Type II Glycogen Storage Disease:ASGD
Pompe Disease:NINDS
Acid Maltase Deficiency:Muscular Dystrophy Association
Acid Maltase Deficiency Association
Pompe Disease:Genetics Home Reference, NLM
Glycogen Storage Disease Type II (Pompe Disease):GeneReviews


GSD III (Cori Disease, Forbes Disease, Debrancher Enzyme Deficiency)
Type III Glycogen Storage Disease:ASGD
Glycogen Storage Disease Type 3:Madisons Foundation
Debrancher Enzyme Deficiency:Muscular Dystrophy Association


GSD IV (Andersen Disease, Brancher Deficiency, Amylopectinosis)
Type IV Glycogen Storage Disease:ASGD


GSD V (McArdle Disease, Phosphorylase Deficiency)
Type V Glycogen Storage Disease:ASGD
Phosphorylase Deficiency:Muscular Dystrophy Association
Glycogen Storage Disease Type V:GeneReviews


GSD VI (Hers Disease, Liver Phosphorylase Deficiency)
Type VI Glycogen Storage Disease:AGSD
Glycogen Storage Disease Type VI:Madisons Foundation


GSD VII (Tarui Disease, Muscle Phosphofructokinase Deficiency)
Type VII Glycogen Storage Disease:AGSD
Phosphofructokinase Deficiency:Muscular Dystrophy Association


GSD IX (Phosphoglycerate Kinase Deficiency)
Type IX Glycogen Storage Disease:AGSD
Phosphoglycerate Kinase Deficiency:Muscular Dystrophy Association


GSD X (Phosphoglycerate Mutase Deficiency)
Phosphoglycerate Mutase Deficiency:Muscular Dystrophy Association


GSD XI (Lactate Dehydrogenase Deficiency)
Lactate Dehydrogenase Deficiency:Muscular Dystrophy Association


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