You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Hereditary xanthinuria type 1, look for clinical trials, and connect with others living with it — all in one place.
Open the full Hereditary xanthinuria type 1 hub →Hereditary xanthinuria type 1 is a rare condition. Also known as XDH deficiency, XO deficiency, XOR deficiency, Xanthine dehydrogenase deficiency, Xanthine oxidase deficiency, Xanthine oxidoreductase deficiency. Tomeko brings together the specialists, research, clinical trials, treatments and community for Hereditary xanthinuria type 1 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:93601 · OMIM 278300 · ICD-10 E79.8 · GARD 0005621
Start by learning the basics from an authoritative source, find a specialist or center that sees Hereditary xanthinuria type 1, 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 Hereditary xanthinuria type 1, filtered to your area.
Tomeko shows live, recruiting studies for Hereditary xanthinuria type 1 from ClinicalTrials.gov on the hub.