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:
Fatty Oxidation Disorders
| Organization | |
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FOD Family Support Group (FODFSG) |
| Overviews | |
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FODs Defined:FODFSG |
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Index to Descriptions of Disorders:FODFSG |
| CACT: Carnitine-Acylcarnitine Translocase Deficiency | |
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Carnitine Acylcarnitine Translocase Deficiency:STAR-G Project |
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Carnitine-Acylcarnitine Translocase Deficiency:Genetics Home Reference |
| CUD: Carnitine Uptake Defect (Carnitine Transporter Deficiency) | |
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Carnitine Deficiency:Muscular Dystrophy Association |
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Carnitine Transporter Deficiency:STAR-G Project |
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Primary Carnitine Deficiency:Genetics Home Reference, NLM |
| De-Red: Dienoyl-CoA Reductase | |
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2,4 Dienoyl CoA Reductase Deficiency:Pediatrix Medical Group |
| EMA: Ethylmalonic Aciduria | |
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Ethylmalonic Encephalopathy:Genetics Home Reference, NLM |
| MAL: Malonyl-CoA Decarboxylase Deficiency | |
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Malonyl-CoA Decarboxylase Deficiency:Genetics Home Reference, NLM |
| MCKAT Deficiency | |
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Medium Chain 3-Ketoacyl-Coenzyme A Thiolase Deficiency:OMIM, NCBI |
| SCHAD Deficiency | |
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Short Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency:STAR-G Project |
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3-Hydroxyacyl-Coenzyme A Dehydrogenase Deficiency:Genetics Home Reference, NLM |
| TFP: Trifunctional Protein Deficiency | |
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Trifunctional Protein Deficiency:STAR-G Project |
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Mitochondrial Trifunctional Protein Deficiency:Genetics Home Reference, NLM |
