LD2A.3
睾酮代谢缺陷引起的46,XY性发育障碍
46,XY disorder of sex development due to a defect in testosterone metabolism
- 上级条目
- LD2A 性发育畸形
- 层级
- 4 级
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跨章引用 同一概念在其他章节另有编码
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- 睾酮代谢缺陷引起的46,XY性发育障碍
- 睾酮代谢缺陷引起的46,XY DSD性发育障碍
- 17-β-羟类固醇脱氢酶3型缺乏引起的46,XY性发育障碍
- 17-β-羟类固醇脱氢酶3型缺乏引起的男性假两性畸形
- 17-β-羟类固醇脱氢酶3型缺乏症
- 17-酮类固醇还原酶缺乏症
- 17-酮还原酶缺乏症
- 17-β-羟类固醇脱氢酶3型缺乏引起的46,XY DSD
- 5-α-还原酶2型缺乏引起的46,XY性发育障碍
- 5-α-还原酶2型缺乏引起的46,XY DSD
- 5-α-还原酶2型缺乏Y引起的男性假两性畸形
- 孤立性17,20裂解酶缺乏引起的46,XY性发育障碍
- 孤立性17,20裂解酶缺乏引起的46,XY DSD
- Leydig细胞发育不全
- LH（黄体生成素）缺陷引起的46,XY性发育障碍
- LH（黄体生成素）受体失活引起的LH（黄体生成素）抵抗
- LH（黄体生成素）缺陷引起的46,XY DSD
- LH（黄体生成素）缺陷引起的男性假两性畸形
- 睾丸间质细胞发育不全
- 完全LH（黄体生成素）受体失活引起的LH（黄体生成素）抵抗
- 部分LH（黄体生成素）受体失活引起的LH（黄体生成素）抵抗
英文词条（20）
- 46,XY disorder of sex development due to a defect in testosterone metabolism
- 46,XY DSD due to a defect in testosterone metabolism
- 46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency
- 17-beta-hydroxysteroid dehydrogenase 3 deficiency
- 17-ketoreductase deficiency
- 17-ketosteroidreductase deficiency
- 46,XY DSD due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency
- Male pseudohermaphroditism due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency
- 46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency
- 46,XY DSD due to 5-alpha-reductase 2 deficiency
- Male pseudohermaphroditism due to 5-alpha-reductase 2 deficiency
- 46,XY disorder of sex development due to isolated 17, 20 lyase deficiency
- 46,XY DSD due to isolated 17, 20 lyase deficiency
- Leydig cell hypoplasia
- 46,XY DSD due to LH defects
- 46,XY disorder of sex development due to LH defects
- LH resistance due to LH receptor inactivation
- Male pseudohermaphrodism due to LH defects
- LH resistance due to complete LH receptor inactivation
- LH resistance due to partial LH receptor inactivation
后组配轴 Postcoordination
该条目未定义后组配轴，直接使用上面的编码即可。后组配是在主干编码之后追加侧别、具体解剖部位、严重程度、病因等细节的可选组合方式，不是必填项。