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Atelosteogenesis type I

Just diagnosed with Atelosteogenesis type I?

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

Open the full Atelosteogenesis type I hub →

Overview

Atelosteogenesis type I is a rare condition. Also known as AO1, AOI, Atelosteogenesis type 1, Giant cell chondrodysplasia, Spondylo-humero-femoral dysplasia. Tomeko brings together the specialists, research, clinical trials, treatments and community for Atelosteogenesis type I so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:1190 · OMIM 108720 · ICD-10 Q78.8 · GARD 0009287

Find care for Atelosteogenesis type I

Authoritative references for Atelosteogenesis type I

Common questions

I was just diagnosed with Atelosteogenesis type I — what should I do first?

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

Where can I find a specialist for Atelosteogenesis type I?

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

Are there clinical trials for Atelosteogenesis type I?

Tomeko shows live, recruiting studies for Atelosteogenesis type I 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