osteogenesis imperfecta type 11
ORPHA: 216812
Overview
osteogenesis imperfecta that has material basis in mutation in the FKBP10 gene on chromosome 17q21
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 11
| Orphanet | ORPHA:216812 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO