Okülorenal defektli Joubert sendromu
ORPHA:2318· ICD-10 Q04.3· Joubert syndrome with oculorenal defect
- Yaygınlık
- <1 / 1 000 000
- Kalıtım
- Autosomal recessive
- Başlangıç yaşı
- Infancy, Neonatal
ORPHA:2318· ICD-10 Q04.3· Joubert syndrome with oculorenal defect