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Maternal uniparental disomy of chromosome 13

Just diagnosed with Maternal uniparental disomy of chromosome 13?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Maternal uniparental disomy of chromosome 13, look for clinical trials, and connect with others living with it — all in one place.

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Overview

Maternal uniparental disomy of chromosome 13 is a rare condition. Also known as UPD(13)mat. Tomeko brings together the specialists, research, clinical trials, treatments and community for Maternal uniparental disomy of chromosome 13 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:97678 · ICD-10 Q99.8 · GARD 0019382

Find care for Maternal uniparental disomy of chromosome 13

Authoritative references for Maternal uniparental disomy of chromosome 13

Common questions

I was just diagnosed with Maternal uniparental disomy of chromosome 13 — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Maternal uniparental disomy of chromosome 13, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Maternal uniparental disomy of chromosome 13?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Maternal uniparental disomy of chromosome 13, filtered to your area.

Are there clinical trials for Maternal uniparental disomy of chromosome 13?

Tomeko shows live, recruiting studies for Maternal uniparental disomy of chromosome 13 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