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 →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
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.
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Xanthinuria type II, filtered to your area.
Tomeko shows live, recruiting studies for Xanthinuria type II from ClinicalTrials.gov on the hub.