osteogenesis imperfecta type 9
MeSH: C564921ORPHA: 216804
Overview
osteogenesis imperfecta that has material basis in mutation in the PPIB gene on chromosome 15q22
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C564921Orphanet Code
ORPHA:216804osteogenesis imperfecta type 9
| MeSH | C564921 |
| Orphanet | ORPHA:216804 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO