Diseases and Disorders > 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:
Urea Cycle Disorders

	Organizations
	National Urea Cycle Disorders Foundation (NUCDF)
	Urea Cycle Disorders Consortium (UCDC)

	General Information
	What Is a Urea Cycle Disorder?:NUCDF
	What Are the Symptoms?:NUCDF
	What Are the Treatment Options?:NUCDF
	Frequently Asked Questions:NUCDF
	Disorder Definitions:UCDC
	Urea Cycle Disorders Overview:GeneReviews

	ARG: Arginase Deficiency (Argininemia)
	Arginemia / Arginase Deficiency:STAR-G Project
	Parents' Guide to Arginase Deficiency:California Dept of Health Services [PDF] [Order printed copy]
	Arginase Deficiency:Genetics Home Reference, NLM
	Arginase Deficiency:GeneReviews

	ASA: Argininosuccinic Aciduria (Argininosuccinic Acid Lyase Deficiency)
	Argininosuccinic Acid Lyase Deficiency:STAR-G Project
	Argininosuccinic Aciduria:Genetics Home Reference, NLM

	CPS: Carbamoyl Phosphate Synthetase Deficiency
	Carbamoyl Phosphate Synthetase One Deficiency:Madisons Foundation
	Carbamyl Phosphate Synthetase Deficiency, A Handbook for Parents:Pacific Northwest Regional Genetics Group [PDF]
	Carbamoyl Phosphate Synthetase I Deficiency:Genetics Home Reference, NLM

	Citrullinemia Type I (Argininosuccinate Synthetase Deficiency)
	Citrullinemia:STAR-G Project
	Citrullinemia:Genetics Home Reference, NLM
	Citrullinemia Type I:GeneReviews

	Citrullinemia Type II (Citrin Deficiency)
	Citrullinemia Type II:Oregon Dept of Human Services [PDF]
	Citrullinemia:Genetics Home Reference, NLM
	Citrin Deficiency:GeneReviews

	HHH: Hyperammonemia/Ornithinemia/Citrullinemia (Ornithine Transporter Defect)
	Ornithine Translocase Deficiency (HHH Syndrome):UCDC
	Ornithine Translocase Deficiency:Genetics Home Reference, NLM

	Lysinuric Protein Intolerance
	Lysinuric Protein Intolerance:Genetics Home Reference, NLM
	Lysinuric Protein Intolerance:GeneReviews

	NAGS: N-Acetylglutamate Synthetase Deficiency
	NAGS Deficiency:Madisons Foundation
	N-Acetylglutamate Synthase Deficiency:Genetics Home Reference, NLM

	OTC: Ornithine Transcarbamylase Deficiency
	Ornithine Transcarbamylase Deficiency (OTC):Madisons Foundation
	The Pediatrician's Guide to Ornithine Transcarbamylase Deficiency and Other Urea Cycle Disorders:NORD
	Ornithine Transcarbamylase Deficiency:Genetics Home Reference, NLM

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