21-羟化酶所致经典性先天性肾上腺皮质增生症
ORPHA:90794· ICD-10 E25.0· Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
- 患病率
- 1-9 / 100 000
- 遗传方式
- Autosomal recessive
- 发病年龄
- Adolescent, Adult, Antenatal, Childhood, Infancy, Neonatal
ORPHA:90794· ICD-10 E25.0· Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency