Diseases and Disorders > Nutritional & Metabolic Diseases

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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 Deficiency:RRTC/NMD
	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] [Order printed copy]
	Glutaric Acidemia Type II, A Guide for Parents:Pacific Northwest Regional Genetics Group [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:Oregon Dept of Human Services [PDF]
	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] [Order printed copy]
	MCAD, A Guide for Parents:Pacific Northwest Regional Genetics Group [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] [Order printed copy]
	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] [Order printed copy]
	Very Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency:Genetics Home Reference:NLM

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