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・ 2-Polyprenyl-6-hydroxyphenyl methylase
・ 2-pop
・ 2-Hydroxy-5-methoxybenzaldehyde
・ 2-hydroxy-6-oxo-6-(2-aminophenyl)hexa-2,4-dienoate hydrolase
・ 2-hydroxy-6-oxo-6-phenylhexa-2,4-dienoate reductase
・ 2-hydroxy-6-oxonona-2,4-dienedioate hydrolase
・ 2-hydroxy-dATP diphosphatase
・ 2-Hydroxyacylsphingosine 1-beta-galactosyltransferase
・ 2-hydroxybiphenyl 3-monooxygenase
・ 2-Hydroxybutyric acid
・ 2-hydroxychromene-2-carboxylate isomerase
・ 2-hydroxycyclohexanone 2-monooxygenase
・ 2-hydroxyethylphosphonate dioxygenase
・ 2-hydroxyglutarate dehydrogenase
・ 2-hydroxyglutarate synthase
2-Hydroxyglutaric aciduria
・ 2-hydroxyhexa-2,4-dienoate hydratase
・ 2-Hydroxyisocaproic acid
・ 2-hydroxyisoflavanone dehydratase
・ 2-hydroxymethylglutarate dehydrogenase
・ 2-Hydroxymuconate semialdehyde
・ 2-hydroxymuconate tautomerase
・ 2-Hydroxymuconate-6-semialdehyde dehydrogenase
・ 2-hydroxymuconate-semialdehyde hydrolase
・ 2-hydroxyphytanoyl-CoA lyase
・ 2-hydroxypropyl-CoM lyase
・ 2-hydroxypyridine 5-monooxygenase
・ 2-hydroxyquinoline 5,6-dioxygenase
・ 2-hydroxyquinoline 8-monooxygenase
・ 2-Imidazoline


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2-Hydroxyglutaric aciduria : ウィキペディア英語版
2-Hydroxyglutaric aciduria

2-hydroxyglutaric aciduria is a group of rare neurometabolic disorders characterized by the significantly elevated levels of hydroxyglutaric acid in ones urine. It is either autosomal recessive or autosomal dominant.
==Classification==

2-hydroxyglutaric aciduria is an organic aciduria, and because of the stereoisomeric property of 2-hydroxyglutarate different variants of this disorder are distinguished:

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
ウィキペディアで「2-Hydroxyglutaric aciduria」の詳細全文を読む



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