Brakitelahalanji-dismorphizm-Kallmann sendromu
ORPHA:1295· ICD-10 Q87.0· Brachytelephalangy-dysmorphism-Kallmann syndrome
- Yaygınlık
- <1 / 1 000 000
- Kalıtım
- Autosomal dominant
- Başlangıç yaşı
- Neonatal
ORPHA:1295· ICD-10 Q87.0· Brachytelephalangy-dysmorphism-Kallmann syndrome