嗅觉正常先天性低促性腺激素性性腺功能减退症
ORPHA:432· ICD-10 E23.0· Normosmic congenital hypogonadotropic hypogonadism
- 遗传方式
- Autosomal dominant, Autosomal recessive, Multigenic/multifactorial, X-linked recessive
- 发病年龄
- Infancy, Neonatal
ORPHA:432· ICD-10 E23.0· Normosmic congenital hypogonadotropic hypogonadism