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- C-11羟化酶缺乏 C11-hydroxylase deficiency
- 11β-羟化酶缺乏 11 beta-hydroxylase deficiency
- 四氢生物蝶呤反应性苯丙氨酸羟化酶缺乏症的临床和基因检测 Clinical and gene detection of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency
- 苯丙酮酸尿症是一种由于苯丙氨酸羟化酶缺乏,苯丙氨酸转变成酪氨酸的过程被削弱的病。 Phenylketonuria is a condition in which phenylalanine to tyrosine conversion is diminished because the enzyme phenylalanine hydroxylaze is deficient.
- 苯丙酮酸尿症是一种由于苯丙氨酸羟化酶缺乏，苯丙氨酸转变成酪氨酸的过程被削弱的病。 Phenylketonuria is a condition in which phenylalanine to tyrosine conversion is diminished because the enzyme phenylalanine hydroxylaze is deficient
- 柔红霉素C-14羟化酶 daunorubicin C-14 hydroxylase
- 磷酸化酶缺乏 phosphorylase deficiency
- 甾类11-β-羟化酶 steroid-11-β-hydroxylase
- 21－羟化酶基因缺陷与先天性肾上腺皮质增生症临床类型相关性的研究 A STUDY ON CORRELATION BETWEEN21-HYDROXYLASE GENE DEFECTS ANDCLINICAL TYPES BY USING PCR-ASO TECH-NIQUE
- 柔红霉素C-14羟化酶基因 Daunorubiein C-14 hydroxylase gene
- 18-羟化皮质酮脱氢酶缺乏 18-Hydroxycorticosterone dehydrogenase deficiency
- 黄体酮11α-羟化酶 Progesterone 11alpha-hydroxylase
- 3β-羟化类固醇脱氢酶缺乏 3 beta-Hydroxysteroid dehydrogenase deficiency
- 苯丙氨酸羟化酶 phenylalanine hydroxylase
- 羟化酶 hydroxylase
- 脂羟化酶 butyrinase
- 18-羟化类固醇脱氢酶缺乏致醛固酮缺乏 Aldosterone deficiency due to 18-hydroxysteroid dehydrogenase deficiency
- 17-羟化酶 17-hydroxylase
- 21-羟化酶 21-hydroxylase
- 24-羟化酶 24-hydroxylase
