osteogenesis imperfecta type 14
ORPHA: 216820
Overview
osteogenesis imperfecta that has material basis in mutation in the TMEM38B gene on chromosome 9q31
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 14
| Orphanet | ORPHA:216820 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO