CHD3-related developmental delay-speech delay-intellectual disability-abnormalities of vision-facial dysmorphism syndrome
ORPHA:599082· ICD-10 Q87.0
- Yaygınlık
- <1 / 1 000 000
- Kalıtım
- Autosomal dominant
- Başlangıç yaşı
- Infancy, Neonatal
ORPHA:599082· ICD-10 Q87.0