osteogenesis imperfecta type 5
MeSH: C536046ORPHA: 216828
Overview
osteogenesis imperfecta that has material basis in mutation in the IFITM5 gene on chromosome 11p15
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C536046Orphanet Code
ORPHA:216828osteogenesis imperfecta type 5
| MeSH | C536046 |
| Orphanet | ORPHA:216828 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO