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Proximal 16p11.2 microdeletion syndrome

Just diagnosed with Proximal 16p11.2 microdeletion syndrome?

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

Open the full Proximal 16p11.2 microdeletion syndrome hub →

Overview

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

Identifiers: ORPHA:261197 · OMIM 611913 · ICD-10 Q93.5 · GARD 0010740

Find care for Proximal 16p11.2 microdeletion syndrome

Authoritative references for Proximal 16p11.2 microdeletion syndrome

Common questions

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

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

Where can I find a specialist for Proximal 16p11.2 microdeletion syndrome?

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

Are there clinical trials for Proximal 16p11.2 microdeletion syndrome?

Tomeko shows live, recruiting studies for Proximal 16p11.2 microdeletion 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