osteogenesis imperfecta type 10
ORPHA: 216812
Overview
osteogenesis imperfecta that has material basis in mutation in the SERPINH gene on chromosome 11q13
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 10
| Orphanet | ORPHA:216812 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO