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
| Organization | |
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Organic Acidemia Association (OAA) |
| Overviews | |
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What Are Organic Acidemias?:OAA |
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The Organic Acidemias: An Overview:GeneReviews |
| 2-HGA: 2-Hydroxyglutaric Aciduria | |
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2-Hydroxyglutaric Aciduria:Genetics Home Reference, NLM |
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D-2 Hydroxyglutaric Aciduria:OAA |
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L-2 Hydroxyglutaric Aciduria:OAA |
| 2M3HBA: 2-Methyl-3-Hydroxy Butyric Aciduria | |
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2-Methyl-3-Hydroxybutyryl CoA Dehydrogenase Deficiency:Vanderbilt Medical Center [PDF] |
| 2MBCD: 2-Methylbutyryl-CoA Dehydrogenase | |
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2-Methylbutyryl-CoA Dehydrogenase Deficiency (2MBCD Deficiency):STAR-G Project |
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2-Methylbutyryl-Coenzyme A Dehydrogenase Deficiency:Genetics Home Reference |
| 3MGA: 3-Methylglutaconic Aciduria | |
| 3MGA, Overview | |
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3-Methylglutaconic Aciduria:Genetics Home Reference, NLM |
| 3MGA, Type I | |
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3-Methylglutaconic Aciduria Type I:Genetic and Rare Diseases Information Center |
| 3MGA, Type II (Barth Syndrome) | |
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3-Methylglutaconic Aciduria Type II:Oregon Dept of Human Services [PDF] |
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3MGA, Type III (Costeff Syndrome) |
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3-Methylglutaconic Aciduria Type 3:GeneReviews |
| 3MGA, Type IV | |
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3-Methylglutaconic Aciduria Type IV:Genetic and Rare Diseases Information Center |
| 5-OXO: 5-Oxoprolinuria (Glutathione Synthetase Deficiency) | |
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5-oxoprolinemia - Glutathione Synethtase Deficiency:OAA |
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Glutathione Synthetase Deficiency:Genetics Home Reference, NLM |
| BKT: Beta Ketothiolase | |
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Beta Ketothiolase Deficiency:STAR-G Project |
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Beta Ketothiolase Deficiency:Genetics Home Reference, NLM |
| HMG: 3-Hydroxy-3-Methylglutaryl-CoA Lyase | |
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3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency:STAR-G Project |
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3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency:Genetics Home Reference, NLM |
| IBD: Isobutyryl-CoA Dehydrogenase | |
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Isobutyryl-CoA Dehydrogenase Deficiency (IBD Deficiency):STAR-G Project |
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Isobutyryl-Coenzyme A Dehydrogenase Deficiency:Genetics Home Reference, NLM |
| IVA: Isovaleric Acidemia | |
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Isovaleric Acidemia:STAR-G Project |
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Isovaleric Acidemia:OAA |
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Isovaleric Acidemia:Genetics Home Reference, NLM |
| MCD: Multiple Carboxylase (Holocarboxylase Synthetase) | |
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Holocarboxylase Synthetase Deficiency (Multiple Carboxylase Deficiency):STAR-G Project |
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Holocarboxylase Synthetase Deficiency:Genetics Home Reference, NLM |
