You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Hereditary xanthinuria, look for clinical trials, and connect with others living with it — all in one place.
Open the full Hereditary xanthinuria hub →Hereditary xanthinuria is a rare condition. Also known as Classic xanthinuria, Xanthic urolithiasis, Xanthine stone disease. Tomeko brings together the specialists, research, clinical trials, treatments and community for Hereditary xanthinuria so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:3467 · OMIM 278300, 603592 · ICD-10 E79.8 · GARD 0016628
Start by learning the basics from an authoritative source, find a specialist or center that sees Hereditary xanthinuria, 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, filtered to your area.
Tomeko shows live, recruiting studies for Hereditary xanthinuria from ClinicalTrials.gov on the hub.