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Williams syndrome

Just diagnosed with Williams syndrome?

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

Open the full Williams syndrome hub →

Overview

Williams syndrome is a rare condition. Also known as Deletion 7q11.23, Monosomy 7q11.23, Williams-Beuren syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Williams syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:904 · OMIM 194050 · ICD-10 Q93.8 · GARD 0007891

Find care for Williams syndrome

Authoritative references for Williams syndrome

Common questions

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

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

Where can I find a specialist for Williams syndrome?

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

Are there clinical trials for Williams syndrome?

Tomeko shows live, recruiting studies for Williams 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