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

C536047

Orphanet Code

ORPHA:216812
osteogenesis imperfecta type 6
MeSHC536047
OrphanetORPHA:216812
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO