You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Paternal uniparental disomy of chromosome 13, look for clinical trials, and connect with others living with it — all in one place.
Open the full Paternal uniparental disomy of chromosome 13 hub →Paternal uniparental disomy of chromosome 13 is a rare condition. Also known as UPD(13)pat. Tomeko brings together the specialists, research, clinical trials, treatments and community for Paternal uniparental disomy of chromosome 13 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:99324 · ICD-10 Q99.8 · GARD 0019678
Start by learning the basics from an authoritative source, find a specialist or center that sees Paternal uniparental disomy of chromosome 13, and connect with a patient organization. Tomeko brings these together on one hub.
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Paternal uniparental disomy of chromosome 13, filtered to your area.
Tomeko shows live, recruiting studies for Paternal uniparental disomy of chromosome 13 from ClinicalTrials.gov on the hub.