osteogenesis imperfecta type 6
MeSH: C536047ORPHA: 216812
Overview
osteogenesis imperfecta that has material basis in mutation in the SERPINF1 gene on chromosome 17p13.3
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C536047Orphanet Code
ORPHA:216812osteogenesis imperfecta type 6
| MeSH | C536047 |
| Orphanet | ORPHA:216812 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO