cytochrome P450 17α-hydroxylase deficiency

P45017α欠損症

WordNet

1. (biochemistry) a class of hemoprotein whose principal biological function is electron transfer (especially in cellular respiration)

PrepTutorEJDIC

1. 〈U〉〈C〉(…の)(量・額などの)不足,欠乏《+『of』(『in』)+『名』》 / 〈C〉不足分,不足量,不足額 / 〈C〉(精神・肉体などの)欠陥

UpToDate Contents

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• 1. 副腎ステロイド生合成 adrenal steroid biosynthesis
• 2. 小児における原発性副腎不全の原因および臨床症状 causes and clinical manifestations of primary adrenal insufficiency in children
• 3. 原発性無月経の病因、診断、および治療 etiology diagnosis and treatment of primary amenorrhea
• 4. Uncommon congenital adrenal hyperplasias
• 5. Congenital lipoid adrenal hyperplasia

Japanese Journal

• Combined 17α-hydroxylase/17,20-lyase deficiency caused by heterogeneous stop codons in the cytochrome p450 17α-hydroxylase gene.

• RUMSY G.
• Clin Endocrinol 39, 483-485, 1993
• NAID 30035799469

Related Links

• Two-step biochemical differential diagnosis of classic 21 ...

1. Clin Chem. 2012 Apr;58(4):741-7. doi: 10.1373/clinchem.2011.173286. Epub 2012 Jan 24. Two-step biochemical differential diagnosis of classic 21-hydroxylase deficiency and cytochrome P450 oxidoreductase deficiency in ...

• Two-Step Biochemical Differential Diagnosis of Classic 21 ...

Two-Step Biochemical Differential Diagnosis of Classic 21-Hydroxylase Deficiency and Cytochrome P450 Oxidoreductase Deficiency in Japanese ... BACKGROUND: The clinical differential diagnosis of classic 21-hydroxylase ...

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★リンクテーブル★

リンク元	「P45017α欠損症」
関連記事	「deficiency」

「P45017α欠損症」

　　[★]

英

cytochrome P450 17α-hydroxylase deficiency

関

P450

「deficiency」

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• n.

• 不足、欠乏、欠失、欠如、欠損、不十分。栄養不足、栄養素欠乏、欠乏症。(遺伝子)(染色体内の)遺伝子欠失
• 欠けているもの、不足している物。不足分。不完全なもの、欠点のあるもの

関

absence, agenesis, dearth, defect, defective, deficient, deficit, delete, deletion, deletional, depletion, deprivation, deprive, lack, miss, missing, morphological defect, paucity, scarce, scarcity, starve