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Osteogenesis imperfecta

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 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

Common questions

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.

Informational only — not medical advice. Always consult a qualified clinician. Provider and reference data from public sources (NIH GARD, Orphanet, OMIM, HPO, MONDO, ClinicalTrials.gov, CMS NPPES). © Tomeko · tomekohealth.com