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.
Open the full interactive Maternal uniparental disomy of chromosome 13 hub →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
Research & market landscape for Maternal uniparental disomy of chromosome 13
Following Maternal uniparental disomy of chromosome 13 for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Maternal uniparental disomy of chromosome 13 — the real-world landscape behind the condition, in one place.
- Latest Maternal uniparental disomy of chromosome 13 research on PubMed ↗
- Recruiting Maternal uniparental disomy of chromosome 13 trials on ClinicalTrials.gov ↗
- Explore the Maternal uniparental disomy of chromosome 13 research & specialist footprint on Tomeko
Researchers, patient organizations & industry: Tomeko provides de-identified, no-PHI demand and engagement signal, trial awareness, and a labeled, editorially-firewalled presence for Maternal uniparental disomy of chromosome 13 and every rare condition. See how Tomeko works with industry →
Common questions
What is Maternal uniparental disomy of chromosome 13?
Maternal uniparental disomy of chromosome 13 is a rare condition. Also known as UPD(13)mat. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Maternal uniparental disomy of chromosome 13 together in one place.
What are the symptoms of Maternal uniparental disomy of chromosome 13?
Symptoms of Maternal uniparental disomy of chromosome 13 vary from person to person. For a reviewed, plain-language overview see the authoritative references below (NIH GARD, Orphanet), and discuss your own symptoms with a clinician who treats Maternal uniparental disomy of chromosome 13.
How is Maternal uniparental disomy of chromosome 13 treated?
Treatment for Maternal uniparental disomy of chromosome 13 depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Maternal uniparental disomy of chromosome 13, and review current options with them.
What causes Maternal uniparental disomy of chromosome 13 — is it genetic?
The cause and inheritance of Maternal uniparental disomy of chromosome 13 are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Maternal uniparental disomy of chromosome 13 can explain what it means for you and your family.
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.
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