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:
Organic Acidemia

Organic Acidemia Association (OAA)

What Are Organic Acidemias?:OAA
The Organic Acidemias: An Overview:GeneReviews

2-HGA: 2-Hydroxyglutaric Aciduria
2-Hydroxyglutaric Aciduria:Genetics Home Reference, NLM
D-2 Hydroxyglutaric Aciduria:OAA
L-2 Hydroxyglutaric Aciduria:OAA

2M3HBA: 2-Methyl-3-Hydroxy Butyric Aciduria
2-Methyl-3-Hydroxybutyryl CoA Dehydrogenase Deficiency:Vanderbilt Medical Center [PDF]

2MBCD: 2-Methylbutyryl-CoA Dehydrogenase
2-Methylbutyryl-CoA Dehydrogenase Deficiency (2MBCD Deficiency):STAR-G Project
2-Methylbutyryl-Coenzyme A Dehydrogenase Deficiency:Genetics Home Reference

3MCC: 3-Methylcrotonyl-CoA Carboxylase
3-Methylcrotonyl-CoA Carboxylase Deficiency STAR-G Project
Parents' Guide to 3MCC Deficiency:California Dept of Health Services [PDF]
3-Methylcrotonyl-CoA Carboxylase Deficiency (3-MCC):OAA
3-Methylcrotonyl-CoA carboxylase Deficiency:Genetics Home Reference, NLM

3MGA: 3-Methylglutaconic Aciduria
3MGA, Overview
3-Methylglutaconic Aciduria:Genetics Home Reference, NLM
3MGA, Type I
3-Methylglutaconic Aciduria Type I:Genetic and Rare Diseases Information Center
3MGA, Type II (Barth Syndrome)
3-Methylglutaconic Aciduria Type II:Oregon Dept of Human Services [PDF]
3MGA, Type III (Costeff Syndrome)
3-Methylglutaconic Aciduria Type 3:GeneReviews
3MGA, Type IV
3-Methylglutaconic Aciduria Type IV:Genetic and Rare Diseases Information Center

5-OXO: 5-Oxoprolinuria (Glutathione Synthetase Deficiency)
5-oxoprolinemia - Glutathione Synethtase Deficiency:OAA
Glutathione Synthetase Deficiency:Genetics Home Reference, NLM

BKT: Beta Ketothiolase
Beta Ketothiolase Deficiency:STAR-G Project
Beta Ketothiolase Deficiency:Genetics Home Reference, NLM

GA-I: Glutaric Acidemia Type I
Glutaric Acidemia Type I:STAR-G Project
Parents' Guide to GA-1:California Dept of Health Services [PDF]
Glutaric Acidemia Type 1:OAA
Glutaric Acidemia Type I:Genetics Home Reference, NLM

HMG: 3-Hydroxy-3-Methylglutaryl-CoA Lyase
3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency:STAR-G Project
3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency:Genetics Home Reference, NLM

IBD: Isobutyryl-CoA Dehydrogenase
Isobutyryl-CoA Dehydrogenase Deficiency (IBD Deficiency):STAR-G Project
Isobutyryl-Coenzyme A Dehydrogenase Deficiency:Genetics Home Reference, NLM

IVA: Isovaleric Acidemia
Isovaleric Acidemia:STAR-G Project
Isovaleric Acidemia:OAA
Isovaleric Acidemia:Genetics Home Reference, NLM

MCD: Multiple Carboxylase (Holocarboxylase Synthetase)
Holocarboxylase Synthetase Deficiency (Multiple Carboxylase Deficiency):STAR-G Project
Holocarboxylase Synthetase Deficiency:Genetics Home Reference, NLM

MMA (MUT): Methylmalonic Acidemia (Methylmalonyl-CoA Mutase )
Methylmalonic Acidemia:STAR-G Project
Parents' Guide to MMA:California Dept of Health Services [PDF]
Methylmalonic Acidemia:OAA
Methylmalonic Acidemia with Homocystinuria:STAR-G Project
Methylmalonic Acidemia:Genetics Home Reference, NLM
Methylmalonic Acidemia:GeneReviews
Disorders of Intracellular Cobalamin Metabolism:GeneReviews

PROP: Propionic Acidemia
Propionic Acidemia:STAR-G Project
FAQ:Propionic Acidemia Foundation
Parents' Guide to PA:California Dept of Health Services [PDF]
Propionic Acidemia:OAA
Propionic Acidemia:Genetics Home Reference, NLM

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