Kallmann sendromu
ORPHA:478· ICD-10 E23.0· Kallmann syndrome
- Yaygınlık
- 1-9 / 100 000
- Kalıtım
- Autosomal dominant, Autosomal recessive, Multigenic/multifactorial, X-linked recessive
- Başlangıç yaşı
- Adolescent, Childhood
ORPHA:478· ICD-10 E23.0· Kallmann syndrome