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Osteogenesis imperfecta type III

Just diagnosed with Osteogenesis imperfecta type III?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Osteogenesis imperfecta type III, look for clinical trials, and connect with others living with it — all in one place.

Open the full Osteogenesis imperfecta type III hub →

Overview

Osteogenesis imperfecta type III is a rare condition. Also known as OI type 3, Progressive deforming osteogenesis imperfecta, Severe osteogenesis imperfecta. Tomeko brings together the specialists, research, clinical trials, treatments and community for Osteogenesis imperfecta type III so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:216812 · OMIM 259420, 259440, 610682 · ICD-10 Q78.0 · GARD 0008695

Find care for Osteogenesis imperfecta type III

Authoritative references for Osteogenesis imperfecta type III

Common questions

I was just diagnosed with Osteogenesis imperfecta type III — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Osteogenesis imperfecta type III, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Osteogenesis imperfecta type III?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Osteogenesis imperfecta type III, filtered to your area.

Are there clinical trials for Osteogenesis imperfecta type III?

Tomeko shows live, recruiting studies for Osteogenesis imperfecta type III 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