osteogenesis imperfecta type 8
MeSH: C536049ORPHA: 216804
Overview
osteogenesis imperfecta that has material basis in mutation in the P3H1 gene on chromosome 1p34.2
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C536049Orphanet Code
ORPHA:216804osteogenesis imperfecta type 8
| MeSH | C536049 |
| Orphanet | ORPHA:216804 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO