Category:Inborn errors of metabolism

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For more information, see the article about [[{{{1|Inborn errors of metabolism}}}]].

Articles in category "Inborn errors of metabolism"

There are 25 articles in this category.

Inborn error of metabolism A Adenosine deaminase deficiency B Beta-ketothiolase deficiency C Citrullinemia G Gaucher's disease Glycogen storage disease Glycogen storage disease type I Glycogen storage disease type II

G cont. Glycogen storage disease type V H Holocarboxylase synthetase deficiency 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-coenzyme A dehydrogenase deficiency Menkes disease

M cont. Myoadenylate deaminase deficiency P Phenylketonuria Propionic acidemia S Sly syndrome Smith-Lemli-Opitz syndrome T Trimethylaminuria W Wolman's disease Z Zellweger's syndrome