Holoprozensefali
ORPHA:2162· ICD-10 Q04.2· Holoprosencephaly
- Yaygınlık
- Unknown
- Kalıtım
- Autosomal recessive, Multigenic/multifactorial, Not applicable, Oligogenic, X-linked dominant
- Başlangıç yaşı
- Antenatal, Neonatal
ORPHA:2162· ICD-10 Q04.2· Holoprosencephaly