osteogenesis imperfecta type 12
ORPHA: 216820
Overview
osteogenesis imperfecta that has material basis in mutation in the SP7 gene on chromosome 12q13
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
Orphanet Code
ORPHA:216820osteogenesis imperfecta type 12
| Orphanet | ORPHA:216820 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO