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Smith-Magenis syndrome

Just diagnosed with Smith-Magenis syndrome?

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

Open the full Smith-Magenis syndrome hub →

Overview

Smith-Magenis syndrome is a rare condition. Also known as 17p11.2 microdeletion syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Smith-Magenis syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:819 · OMIM 182290 · ICD-10 Q93.5 · GARD 0008197

Find care for Smith-Magenis syndrome

Authoritative references for Smith-Magenis syndrome

Common questions

I was just diagnosed with Smith-Magenis syndrome — what should I do first?

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

Where can I find a specialist for Smith-Magenis syndrome?

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

Are there clinical trials for Smith-Magenis syndrome?

Tomeko shows live, recruiting studies for Smith-Magenis 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