You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Osteogenesis imperfecta type I, look for clinical trials, and connect with others living with it — all in one place.
Open the full Osteogenesis imperfecta type I hub →Osteogenesis imperfecta type I is a rare condition. Also known as Non-deforming osteogenesis imperfecta, OI type 1, Van der Hoeve syndrome, Adair-Dighton syndrome, Mild osteogenesis imperfecta. Tomeko brings together the specialists, research, clinical trials, treatments and community for Osteogenesis imperfecta type I so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:216796 · OMIM 166200, 166230 · ICD-10 Q78.0 · GARD 0008694
Start by learning the basics from an authoritative source, find a specialist or center that sees Osteogenesis imperfecta type I, and connect with a patient organization. Tomeko brings these together on one hub.
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Osteogenesis imperfecta type I, filtered to your area.
Tomeko shows live, recruiting studies for Osteogenesis imperfecta type I from ClinicalTrials.gov on the hub.