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8p11.2 deletion syndrome

Just diagnosed with 8p11.2 deletion syndrome?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees 8p11.2 deletion syndrome, look for clinical trials, and connect with others living with it — all in one place.

Open the full 8p11.2 deletion syndrome hub →

Overview

8p11.2 deletion syndrome is a rare condition. Also known as Del(8)(p11.2), Monosomy 8p11.2. Tomeko brings together the specialists, research, clinical trials, treatments and community for 8p11.2 deletion syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:251066 · ICD-10 Q93.5 · GARD 0020693

Find care for 8p11.2 deletion syndrome

Authoritative references for 8p11.2 deletion syndrome

Common questions

I was just diagnosed with 8p11.2 deletion syndrome — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees 8p11.2 deletion syndrome, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for 8p11.2 deletion syndrome?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat 8p11.2 deletion syndrome, filtered to your area.

Are there clinical trials for 8p11.2 deletion syndrome?

Tomeko shows live, recruiting studies for 8p11.2 deletion 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