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Chromosome 16p11.2 duplication syndrome

Just diagnosed with Chromosome 16p11.2 duplication syndrome?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Chromosome 16p11.2 duplication syndrome, look for clinical trials, and connect with others living with it — all in one place.

Open the full Chromosome 16p11.2 duplication syndrome hub →

Overview

Chromosome 16p11.2 duplication syndrome is a rare condition. Also known as Proximal dup(16)(p11.2), Proximal trisomy 16p11.2. Tomeko brings together the specialists, research, clinical trials, treatments and community for Chromosome 16p11.2 duplication syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:370079 · OMIM 614671 · ICD-10 Q92.3 · GARD 0012388

Find care for Chromosome 16p11.2 duplication syndrome

Authoritative references for Chromosome 16p11.2 duplication syndrome

Common questions

I was just diagnosed with Chromosome 16p11.2 duplication syndrome — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Chromosome 16p11.2 duplication syndrome, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Chromosome 16p11.2 duplication syndrome?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Chromosome 16p11.2 duplication syndrome, filtered to your area.

Are there clinical trials for Chromosome 16p11.2 duplication syndrome?

Tomeko shows live, recruiting studies for Chromosome 16p11.2 duplication 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