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Xanthinuria type II

Just diagnosed with Xanthinuria type II?

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

Open the full Xanthinuria type II hub →

Overview

Xanthinuria type II is a rare condition. Also known as XDH and AOX dual deficiency, Xanthine dehydrogenase and xanthine aldehyde oxidase dual deficiency. Tomeko brings together the specialists, research, clinical trials, treatments and community for Xanthinuria type II so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:93602 · OMIM 603592 · ICD-10 E79.8 · GARD 0005620

Find care for Xanthinuria type II

Authoritative references for Xanthinuria type II

Common questions

I was just diagnosed with Xanthinuria type II — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Xanthinuria type II, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Xanthinuria type II?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Xanthinuria type II, filtered to your area.

Are there clinical trials for Xanthinuria type II?

Tomeko shows live, recruiting studies for Xanthinuria type II 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