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Cleidorhizomelic syndrome

Just diagnosed with Cleidorhizomelic syndrome?

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

Open the full Cleidorhizomelic syndrome hub →

Overview

Cleidorhizomelic syndrome is a rare condition. Also known as Rhizomelic shortness with clavicular defect, Wallis-Zieff-Goldblatt syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Cleidorhizomelic syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:1453 · OMIM 119650 · ICD-10 Q77.8 · GARD 0005532

Find care for Cleidorhizomelic syndrome

Authoritative references for Cleidorhizomelic syndrome

Common questions

I was just diagnosed with Cleidorhizomelic syndrome — what should I do first?

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

Where can I find a specialist for Cleidorhizomelic syndrome?

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

Are there clinical trials for Cleidorhizomelic syndrome?

Tomeko shows live, recruiting studies for Cleidorhizomelic syndrome 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