osteogenesis imperfecta type 16
ORPHA: 216812
Overview
osteogenesis imperfecta that has material basis in contiguous gene deletion on chromosome 11p11
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
Orphanet Code
ORPHA:216812osteogenesis imperfecta type 16
| Orphanet | ORPHA:216812 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO