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16p13.11 microduplication syndrome

Just diagnosed with 16p13.11 microduplication syndrome?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees 16p13.11 microduplication syndrome, look for clinical trials, and connect with others living with it — all in one place.

Open the full 16p13.11 microduplication syndrome hub →

Overview

16p13.11 microduplication syndrome is a rare condition. Also known as Dup(16)(p13.11), Trisomy 16p13.11. Tomeko brings together the specialists, research, clinical trials, treatments and community for 16p13.11 microduplication syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:261243 · ICD-10 Q92.3 · GARD 0020775

Find care for 16p13.11 microduplication syndrome

Authoritative references for 16p13.11 microduplication syndrome

Common questions

I was just diagnosed with 16p13.11 microduplication syndrome — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees 16p13.11 microduplication syndrome, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for 16p13.11 microduplication syndrome?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat 16p13.11 microduplication syndrome, filtered to your area.

Are there clinical trials for 16p13.11 microduplication syndrome?

Tomeko shows live, recruiting studies for 16p13.11 microduplication 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