Osteogenesis imperfecta, typ 4
ORPHA:216820· ICD-10 Q78.0· Osteogenesis imperfecta type 4
- Prevalence
- Unknown
- Dědičnost
- Autosomal dominant, Autosomal recessive, X-linked recessive
- Věk nástupu
- Infancy, Neonatal
ORPHA:216820· ICD-10 Q78.0· Osteogenesis imperfecta type 4