Category:Inborn errors of metabolism

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fr:Catégorie:Maladie métabolique congénitale

Articles in category "Inborn errors of metabolism"

There are 27 articles in this category.

Inborn error of metabolism 3 3-hydroxy-3-methylglutaryl-CoA lyase deficiency 3-methylcrotonyl-CoA carboxylase deficiency A Adenosine deaminase deficiency B Beta-ketothiolase deficiency C Citrullinemia G Gaucher's disease Glycogen storage disease H Holocarboxylase synthetase deficiency

H cont. Hunter syndrome I Isovaleric acidemia L Lesch-Nyhan syndrome Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency M Maple syrup urine disease Medium chain acyl dehydrogenase deficiency Menke's syndrome Mucopolysaccharidosis type VII Sly syndrome Myoadenylate deaminase deficiency P Phenylketonuria

P cont. Pompe's disease Primary carnitine deficiency Propionic acidemia S Smith-Lemli-Opitz syndrome T Trimethylaminuria Tyrosinemia V Von Gierke's disease Z Zellweger's syndrome

Wikipedia (http://en.wikipedia.org/wiki/Main_Page) Category:Inborn_errors_of_metabolism (http://en.wikipedia.org/wiki/Category:Inborn_errors_of_metabolism) version history (http://en.wikipedia.org/w/index.php?title=Category:Inborn_errors_of_metabolism&action=history) GNU Free Documentation Lizenz (http://en.wikipedia.org/wiki/Wikipedia:Text_of_the_GNU_Free_Documentation_License) CC-by-sa (http://creativecommons.org/licenses/by-sa/2.5/)

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