孤立型17，20-裂解酶缺乏男性假两性畸形
ORPHA:90796· ICD-10 E29.1· 46,XY difference of sex development due to isolated 17,20-lyase deficiency
- 患病率
- <1 / 1 000 000
- 遗传方式
- Autosomal recessive
- 发病年龄
- Neonatal
ORPHA:90796· ICD-10 E29.1· 46,XY difference of sex development due to isolated 17,20-lyase deficiency