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:
Fatty Oxidation Disorders

Organization
FOD Family Support Group (FODFSG)


Overviews
FODs Defined:FODFSG
Index to Descriptions of Disorders:FODFSG


CACT: Carnitine-Acylcarnitine Translocase Deficiency
Carnitine Acylcarnitine Translocase Deficiency:STAR-G Project
Carnitine-Acylcarnitine Translocase Deficiency:Genetics Home Reference


CPT: Carnitine Palmityl Transferase Deficiencies
General Information
Matter Over Mind: The Realities of a Common Muscle Disease:FODFSG
Carnitine Palmityl Transferase Deficiency:Muscular Dystrophy Association
CPT Type 1
Carnitine Palmitoyl Transferase Deficiency, Type 1A:STAR-G Project
Carnitine Palmitoyltransferase I Deficiency:Genetics Home Reference
Carnitine Palmitoyltransferase 1A Deficiency:GeneReviews
CPT Type 2
Carnitine Palmitoyl Transferase Deficiency. Type 2:STAR-G Project
Carnitine Palmitoyltransferase II Deficiency:Genetics Home Reference
Carnitine Palmitoyltransferase II Deficiency:GeneReviews


CUD: Carnitine Uptake Defect (Carnitine Transporter Deficiency)
Carnitine Deficiency:Muscular Dystrophy Association
Carnitine Transporter Deficiency:STAR-G Project
Primary Carnitine Deficiency:Genetics Home Reference, NLM


De-Red: Dienoyl-CoA Reductase
2,4 Dienoyl CoA Reductase Deficiency:Pediatrix Medical Group


EMA: Ethylmalonic Aciduria
Ethylmalonic Encephalopathy:Genetics Home Reference, NLM


GA-II: Glutaric Acidemia, Type 2
Glutaric Acidemia II (GA2):FODFSG
Glutaric Acidemia, Type 2:STAR-G Project
Parents' Guide to GA-2:California Dept of Health Services [PDF]
Glutaric Acidemia Type II:Genetics Home Reference, NLM


LCHAD Deficiency
LCHAD: Long-Chain 3 Hydroxyacyl CoA Dehydrogenase:FODFSG
Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency:STAR-G Project
Long-Chain 3-Hydroxyacyl-Coenzyme A Dehydrogenase Deficiency:Genetics Home Reference, NLM


MAL: Malonyl-CoA Decarboxylase Deficiency
Malonyl-CoA Decarboxylase Deficiency:Genetics Home Reference, NLM


MCAD Deficiency
MCAD: Medium Chain acyl CoA Dehydrogenase - Information for Families:FODFSG
Medium Chain Acyl-CoA Dehydrogenase Deficiency:STAR-G Project
Parents' Guide to MCADD:California Dept of Health Services [PDF]
Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency:Genetics Home Reference, NLM
Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency:GeneReviews


MCKAT Deficiency
Medium Chain 3-Ketoacyl-Coenzyme A Thiolase Deficiency:OMIM, NCBI


SCAD Deficiency
Short Chain Acyl-CoA Dehydrogenase Deficiency:STAR-G Project
Parents' Guide to SCADD:California Dept of Health Services [PDF]
Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency:Genetics Home Reference, NLM


SCHAD Deficiency
Short Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency:STAR-G Project
3-Hydroxyacyl-Coenzyme A Dehydrogenase Deficiency:Genetics Home Reference, NLM


TFP: Trifunctional Protein Deficiency
Trifunctional Protein Deficiency:STAR-G Project
Mitochondrial Trifunctional Protein Deficiency:Genetics Home Reference, NLM


VLCAD Deficiency
Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency:STAR-G Project
Parents' Guide to VLCADD:California Dept of Health Services [PDF]
Very Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency:Genetics Home Reference:NLM


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