Osteogenesis imperfecta, typ 5
ORPHA:216828· ICD-10 Q78.0· Osteogenesis imperfecta type 5
- Prevalence
- <1 / 1 000 000
- Dědičnost
- Autosomal dominant, Autosomal recessive
- Věk nástupu
- Infancy, Neonatal
ORPHA:216828· ICD-10 Q78.0· Osteogenesis imperfecta type 5