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14-September-2008 10:43:22 - Metabolic disorders The main article for this category is Metabolic disorders. Contents Top · 0-9 · 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 previous 200 next 200 Subcategories This category has the following 2 subcategories, out of 4 total. D + Diabetes 8 I + Inborn errors of metabolism 1 Pages in category Metabolic disorders The following 198 pages are in this category, out of 316 total. This list may sometimes be slightly out of date learn more 2 2-Hydroxyglutaric aciduria 2-Methylbutyryl-CoA dehydrogenase deficiency 3 3-Methylcrotonyl-CoA carboxylase deficiency 3-hydroxy-3-methylglutaryl-CoA lyase deficiency 6 6-Pyruvoyltetrahydropterin synthase deficiency 6-phosphogluconate dehydrogenase deficiency A AA amyloidosis AL amyloidosis Abetalipoproteinemia Acatalasia Aceruloplasminemia Acid-base imbalance Acidosis Acrodermatitis enteropathica Activated protein C resistance Acute intermittent porphyria Adenine phosphoribosyltransferase deficiency Adenosine deaminase deficiency Adenylosuccinate lyase deficiency Adiposis dolorosa Adrenoleukodystrophy Age-Related Eye Disease Study Albinism Alcohol flush reaction Aldolase A deficiency Alkalosis Alkaptonuria Alpha 1-antitrypsin deficiency Alpha-mannosidosis Alzheimer's disease Amino acid transport disorder Amylin Amyloid Amyloid precursor protein Amyloid purpura Amyloidosis Antithrombin III deficiency Apolipoprotein B deficiency Argininemia Argininosuccinic aciduria Aspartylglucosaminuria Atransferrinemia B Barraquer-Simons syndrome Batten disease Beta amyloid Beta-2 microglobulin Beta-ketothiolase deficiency Beta-mannosidosis Biotinidase deficiency Blue diaper syndrome C Calcification Calcinosis Calcinosis cutis Calciphylaxis Carbamoyl phosphate synthetase I deficiency Cardiac amyloidosis Carnitine palmitoyltransferase I deficiency Carnitine palmitoyltransferase II deficiency Carnitine-acylcarnitine translocase deficiency Carnosinemia Cerebral amyloid angiopathy Cerebrotendineous xanthomatosis Cholesteryl ester storage disease Citrullinemia Combined hyperlipidemia Congenital disorder of glycosylation C cont. Congenital hyperinsulinism Crigler-Najjar syndrome Cystathioninuria Cystic fibrosis Cystinosis Cystinuria D D-Glyceric acidemia Dehydration Diagnostic fast Dihydropyrimidine dehydrogenase deficiency Disaccharidase Disorders of calcium metabolism Dubin-Johnson syndrome Dyslipidemia Dystrophic calcification E Endocrine system Erythropoietic protoporphyria Essential fructosuria F Fabry's disease Familial Merranean fever Familial amyloid neuropathy Familial hypercholesterolemia Familial renal amyloidosis Fanconi syndrome Farber disease Finnish type amyloidosis Fructose bisphosphatase deficiency Fructose malabsorption Fucosidosis Fumarase deficiency G GM1 gangliosidoses GM2 gangliosidoses GM2-gangliosidosis, AB variant Galactokinase deficiency Galactose epimerase deficiency Galactose-1-phosphate uridylyltransferase galactosemia Galactosemia Galactosemic cataract Galactosialidosis Gangliosidosis Gaucher's disease Gilbert's syndrome Glucose-6-phosphate dehydrogenase deficiency Glucose-galactose malabsorption Glutaric acidemia type 2 Glutaric aciduria type 1 Glutathione synthetase deficiency Glycogen storage disease Glycogen storage disease type 0 Glycogen storage disease type I Glycogen storage disease type II Glycogen storage disease type III Glycogen storage disease type IV Glycogen storage disease type IX Glycogen storage disease type V Glycogen storage disease type VI Glycoprotein Glycoproteinosis Glycosaminoglycan Gout Guanidinoacetate methyltransferase deficiency Gunther disease H Haemochromatosis Haemodialysis-associated amyloidosis Hartnup disease Hawkinsinuria Hemosiderosis H cont. Hepatic porphyria Hepatoerythropoietic porphyria Herary coproporphyria Herary fructose intolerance Herary hyperbilirubinemia Hermansky-Pudlak syndrome Histidinemia Holocarboxylase synthetase deficiency Homocystinuria Hunter syndrome Hurler syndrome Hyperammonemia Hypercalcaemia Hyperchloremia Hypercholesterolemia Hyperglycemia Hyperinsulinemic hypoglycemia Hyperkalemia Hyperlipidemia Hyperlysinemia Hypermagnesemia Hypermethioninemia Hypernatremia Hyperoxaluria Hyperphosphatemia Hyperprolinemia Hypertriglyceridemia Hyperuricemia Hypervalinemia Hypervolemia Hypoalphalipoproteinemia Hypobetalipoproteinemia Hypocalcaemia Hypochloremia Hypoglycemia List of causes of hypoglycemia Hypokalemia Hypolipoproteinemia Hypomagnesemia Hyponatremia Hypophosphatasia Hypophosphatemia Hypovolemia I I-cell disease ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases Inborn error of metabolism Inborn errors of amino acid metabolism Inborn errors of carbohydrate metabolism Inborn errors of lipid metabolism Inborn errors of purine-pyrimidine metabolism Inborn errors of renal tubular transport Infantile neuronal ceroid lipfuscinosis Iron metabolism disorder Iron overload disorder Isobutyryl-coenzyme A dehydrogenase deficiency Isovaleric acidemia J Jansky-Bielschowsky disease Juvenile hemochromatosis K Ketosis Ketotic hypoglycemia Krabbe disease L Lactic acidosis Lactose intolerance Lecithin cholesterol acyltransferase deficiency Lesch-Nyhan syndrome previous 200 next 200 Retrieved from http://en..org/wiki/Category:Metabolic_disorders Categories: Diseases | Endocrinology | Metabolism Views Category Discussion this page History Personal tools Log in / create account Navigation Main page Contents Featured content Current events Random article Search Go Search Interaction Community portal Recent changes Contact Donate to Help Toolbox What links here Related changes Upload file Special pages Printable version Permanent link Languages Deutsch Español Français í•œêµì–´ Bahasa Indonesia עברית Nederlands Polski Português SlovenÅ¡Ä?ina Suomi Türkçe Tiếng Việt This page was last modified on 26 August 2008, at 11:36
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