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 (A - C)

(Jump to: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z )

	Acid Lipase Disease
	Acid Lipase Disease:NINDS
	Wolman Disease:Gale Encyclopedia of Genetic Disorders
	Wolman Disease:Genetics Home Reference, NLM
	Cholesterol Ester Storage Disease:Genetics Home Reference, NLM

	Acrodermatitis Enteropathica
	Acrodermatitis Enteropathica:NORD
	Acrodermatitis Enteropathica:New Zealand Dermatological Society

	Alkaptonuria
	What is AKU?:Alkaptonuria Society
	Alkaptonuria:Genetics Home Reference, NLM
	Alkaptonuria:GeneReviews

	Amino Acid Metabolism
	Overview
	Amino Acid Metabolism:Merck Manual, Home Edition

	Index to Specific Amino Acid Disorders
	Albinism		Hyperprolinemia
	Alkaptonuria		Maple Syrup Urine Disease
	Hartnup Disease		Nonketotic Hyperglycinemia
	Homocystinuria		Phenylketonuria
	Hyperhomcysteinemia		Tyrosinemia
	Hypermethioninemia		Urea Cycle Disorders

	Amyloidosis
	Amyloidosis:Mayo Clinic
	What is Amyloidosis?:Amyloidosis Support Network
	PLWC Guide to Amyloidosis:American Society of Clinical Oncology
	Treament Options:Amyloidosis Support Network
	Amyloidosis and Kidney Disease:NIDDK
	Amyloid Treatment and Research Program:Boston Medical Center
	Transthyretin Amyloidosis:GeneReviews

	Batten Disease
	Batten Disease Fact Sheet:NINDS
	Batten Disease General Information:Batten Disease Support & Research Foundation
	Neuronal Ceroid-Lipofuscinoses:GeneReviews

	Biotinidase Deficiency
	Biotinidase Deficiency:Madisons Foundation
	Biotinidase Deficiency: A Booklet for Families and Professionals:Connecticut Children's Medical Center
	Biotinidase Deficiency:Genetics Home Reference, NLM
	Biotinidase Deficiency:GeneReviews

	Carbohydrate Metabolism
	Overview
	Carbohydrate Metabolism:Merck Manual, Home Edition

	Index to Specific Carbohydrate Disorders
	Congenital Disorders of Glycosylation		Hyperoxaluria
	Galactosemia		Lactose Intolerance
	Glycogen Storage Diseases		Mucolipidosis
	Hereditary Fructose Intolerance		Mucopolysaccharidosis

	Congenital Disorders of Glycosylation
	Congenital Disorders of Glycosylation Type Ia:NORD
	About CDG:CDG Family Network
	Congenital Disorders of Glycosylation Overview:GeneReviews
	Congenital Disorder of Glycosylation Type 1a:GeneReviews

	Copper Transport Disorders
	Overview
	ATP7A-Related Copper Transport Disorders:GeneReviews
	Menkes Kinky Hair Disease
	Menkes Disease:NINDS
	Menkes Disease:Madisons Foundation
	Menkes Syndrome:Genetics Home Reference, NLM
	Occipital Horn Syndrome
	Occipital Horn Syndrome:Madisons Foundation

	Cystinosis
	About Cystinosis:Cystinosis Research Network
	Facts About Cystinosis:The Cystinosis Foundation
	Cystinosis:Genetics Home Reference, NLM
	Cystinosis:GeneReviews

	Cystinuria
	Cystinuria:Merck Manual, Home Edition
	What is Cystinuria?:Cystinuria Support Network
	A Stone Owners Manual:Cystinuria Support Network [PDF]
	Cystinuria:Genetics Home Reference, NLM

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