Just diagnosed with Osteogenesis imperfecta?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Osteogenesis imperfecta, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Osteogenesis imperfecta hub →Overview
Osteogenesis imperfecta is a rare condition. Also known as OI, Brittle bone disease, Glass bone disease, Lobstein disease. Tomeko brings together the specialists, research, clinical trials, treatments and community for Osteogenesis imperfecta so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:666 · OMIM 166200, 166210, 166220 · ICD-10 Q78.0 · GARD 0001017
Find care for Osteogenesis imperfecta
Authoritative references for Osteogenesis imperfecta
Research & market landscape for Osteogenesis imperfecta
Following Osteogenesis imperfecta for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Osteogenesis imperfecta — the real-world landscape behind the condition, in one place.
- Latest Osteogenesis imperfecta research on PubMed ↗
- Recruiting Osteogenesis imperfecta trials on ClinicalTrials.gov ↗
- Explore the Osteogenesis imperfecta research & specialist footprint on Tomeko
Researchers, patient organizations & industry: Tomeko provides de-identified, no-PHI demand and engagement signal, trial awareness, and a labeled, editorially-firewalled presence for Osteogenesis imperfecta and every rare condition. See how Tomeko works with industry →
Common questions
What is Osteogenesis imperfecta?
Osteogenesis imperfecta is a rare condition. Also known as OI, Brittle bone disease, Glass bone disease, Lobstein disease. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Osteogenesis imperfecta together in one place.
What are the symptoms of Osteogenesis imperfecta?
Symptoms of Osteogenesis imperfecta vary from person to person. For a reviewed, plain-language overview see the authoritative references below (NIH GARD, Orphanet), and discuss your own symptoms with a clinician who treats Osteogenesis imperfecta.
How is Osteogenesis imperfecta treated?
Treatment for Osteogenesis imperfecta depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Osteogenesis imperfecta, and review current options with them.
What causes Osteogenesis imperfecta — is it genetic?
The cause and inheritance of Osteogenesis imperfecta are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Osteogenesis imperfecta can explain what it means for you and your family.
I was just diagnosed with Osteogenesis imperfecta — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Osteogenesis imperfecta, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Osteogenesis imperfecta?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Osteogenesis imperfecta, filtered to your area.
Are there clinical trials for Osteogenesis imperfecta?
Tomeko shows live, recruiting studies for Osteogenesis imperfecta from ClinicalTrials.gov on the hub.
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