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Odontochondrodysplasia 1

Just diagnosed with Odontochondrodysplasia 1?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Odontochondrodysplasia 1, look for clinical trials, and connect with others living with it — all in one place.

Open the full Odontochondrodysplasia 1 hub →

Overview

Odontochondrodysplasia 1 is a rare condition. Also known as Chondrodysplasia-dentinogenesis imperfecta-joint laxity syndrome, Goldblatt chondrodysplasia, Goldblatt syndrome, ODCD. Tomeko brings together the specialists, research, clinical trials, treatments and community for Odontochondrodysplasia 1 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:166272 · OMIM 184260 · ICD-10 Q78.8 · GARD 0008717

Find care for Odontochondrodysplasia 1

Authoritative references for Odontochondrodysplasia 1

Common questions

I was just diagnosed with Odontochondrodysplasia 1 — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Odontochondrodysplasia 1, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Odontochondrodysplasia 1?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Odontochondrodysplasia 1, filtered to your area.

Are there clinical trials for Odontochondrodysplasia 1?

Tomeko shows live, recruiting studies for Odontochondrodysplasia 1 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