睾丸17,20-碳链裂解酶缺乏所致的46,XY 性发育障碍
ORPHA:443087· ICD-10 E29.1· 46,XY difference of sex development due to testicular 17,20-desmolase deficiency
- 患病率
- <1 / 1 000 000
- 遗传方式
- Autosomal recessive
- 发病年龄
- Neonatal
ORPHA:443087· ICD-10 E29.1· 46,XY difference of sex development due to testicular 17,20-desmolase deficiency