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11p partial monosomy syndrome

Just diagnosed with 11p partial monosomy syndrome?

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

Open the full 11p partial monosomy syndrome hub →

Overview

11p partial monosomy syndrome is a rare condition. Also known as Del(11)(p13), Deletion 11p13, Monosomy 11p13, Wilms tumor-aniridia-genitourinary anomalies-intellectual disability syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for 11p partial monosomy syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:893 · OMIM 194072, 612469 · ICD-10 C64 · GARD 0005528

Find care for 11p partial monosomy syndrome

Authoritative references for 11p partial monosomy syndrome

Common questions

I was just diagnosed with 11p partial monosomy syndrome — what should I do first?

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

Where can I find a specialist for 11p partial monosomy syndrome?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat 11p partial monosomy syndrome, filtered to your area.

Are there clinical trials for 11p partial monosomy syndrome?

Tomeko shows live, recruiting studies for 11p partial monosomy 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