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Paternal uniparental disomy of chromosome 1

Just diagnosed with Paternal uniparental disomy of chromosome 1?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Paternal uniparental disomy of chromosome 1, look for clinical trials, and connect with others living with it — all in one place.

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Overview

Paternal uniparental disomy of chromosome 1 is a rare condition. Also known as UPD(1)pat. Tomeko brings together the specialists, research, clinical trials, treatments and community for Paternal uniparental disomy of chromosome 1 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:251004 · ICD-10 Q99.8 · GARD 0020688

Find care for Paternal uniparental disomy of chromosome 1

Authoritative references for Paternal uniparental disomy of chromosome 1

Common questions

I was just diagnosed with Paternal uniparental disomy of chromosome 1 — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Paternal uniparental disomy of chromosome 1, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Paternal uniparental disomy of chromosome 1?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Paternal uniparental disomy of chromosome 1, filtered to your area.

Are there clinical trials for Paternal uniparental disomy of chromosome 1?

Tomeko shows live, recruiting studies for Paternal uniparental disomy of chromosome 1 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