Category:Inborn errors of metabolism

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The main article for this category is Inborn errors of metabolism.

Subcategories

There is one subcategory to this category shown below (more may be shown on subsequent pages).

L

• Lysosomal storage diseases

Pages in category "Inborn errors of metabolism"

There are 72 pages in this section of this category.

Inborn error of metabolism * Newborn screening 2 2,4 Dienoyl-CoA reductase deficiency 2-Methylbutyryl-CoA dehydrogenase deficiency 3 3-Methylcrotonyl-CoA carboxylase deficiency 3-hydroxy-3-methylglutaryl-CoA lyase deficiency 4 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency A Acatalasia Acid lipase disease Adenosine deaminase deficiency List of amino acid metabolism disorders Analbuminaemia Arakawa's syndrome II Arginemia Argininosuccinic aciduria B Beta-ketothiolase deficiency C CDG syndrome Carbamoyl phosphate synthetase I deficiency Carnitine palmitoyltransferase I deficiency Carnitine palmitoyltransferase II deficiency Carnitine-acylcarnitine translocase deficiency Cholesteryl ester storage disease Citrullinemia Crigler-Najjar syndrome

F List of fatty acid metabolism disorders Fucosidosis G Glutaric acidemia type 1 Glutaric acidemia type 2 Glycine encephalopathy Glycogen storage disease Glycogen storage disease type I Glycogen storage disease type II Glycogen storage disease type III Glycogen storage disease type V H Holocarboxylase synthetase deficiency I Idiosyncrasy Isobutyryl-coenzyme A dehydrogenase deficiency Isovaleric acidemia K Krabbe disease L Lecithin cholesterol acyltransferase deficiency Lesch-Nyhan syndrome Lipid storage disorder Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Lysinuric protein intolerance Lysosomal storage disease M Malonyl-CoA decarboxylase deficiency Maple syrup urine disease Medium-chain acyl-coenzyme A dehydrogenase deficiency Menkes disease

M cont. Mevalonic aciduria Mitochondrial trifunctional protein deficiency Myoadenylate deaminase deficiency N N-Acetylglutamate synthase deficiency O Ornithine transcarbamylase deficiency P Phenylketonuria Primary carnitine deficiency Propionic acidemia Pyruvate carboxylase deficiency R Refsum's disease Rotor syndrome S Sarcosinemia Short-chain acyl-coenzyme A dehydrogenase deficiency Sly syndrome Smith-Lemli-Opitz syndrome T Tangier disease Tetrahydrobiopterin deficiency Trimethylaminuria Tyrosinemia V Very long-chain acyl-coenzyme A dehydrogenase deficiency W Wolman disease X X-linked ichthyosis Z Zellweger syndrome

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Categories: Pediatrics | Endocrinology | Metabolic disorders | Metabolism

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• This page was last modified 19:41, 8 June 2005 by Anonymous user(s) of Wikipedia. Based on work by Wikipedia user(s) Cacycle, Neutrality, Bryan Derksen and Jfdwolff.
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