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 (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: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
Cancer.Net Guide to Amyloidosis:ASCO
Treament Options:Amyloidosis Support Network
Amyloidosis and Kidney Disease:NIDDK
Transthyretin Amyloidosis:GeneReviews


Batten Disease
Batten Disease Fact Sheet:NINDS
About Batten Disease, NCL and History of the Disease:Batten Disease Support & Research Foundation


Biotinidase Deficiency
Biotinidase Deficiency:Madisons Foundation
Biotinidase Deficiency: eMedicine Pediatrics: Genetics and Metabolic Disease
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
Cystinosis Symptoms & Treatment: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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