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List of amino acid metabolism disorders : ウィキペディア英語版 | Congenital disorders of amino acid metabolism
Inborn errors of amino acid metabolism are metabolic disorders which impair the synthesis and degradation of amino acids. Types include: *Alkaptonuria *Aspartylglucosaminuria *Methylmalonic acidemia *Maple syrup urine disease *Homocystinuria *Tyrosinemia *Trimethylaminuria *Hartnup disease *Biotinidase deficiency *Ornithine carbamoyltransferase deficiency *Carbamoyl-phosphate synthase I deficiency disease *Citrullinemia *Hyperargininemia *Hyperhomocysteinemia *Hypermethioninemia *Hyperlysinemias *Nonketotic hyperglycinemia *Propionic acidemia *Hyperprolinemia ==Amino acid transport disorders==
*Cystinuria *Dicarboxylic aminoaciduria *Hartnup disease
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「Congenital disorders of amino acid metabolism」の詳細全文を読む
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