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Hereditary xanthinuria

Just diagnosed with Hereditary xanthinuria?

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 →

Overview

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

Find care for Hereditary xanthinuria

Authoritative references for Hereditary xanthinuria

Common questions

I was just diagnosed with Hereditary xanthinuria — what should I do first?

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.

Where can I find a specialist for Hereditary xanthinuria?

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

Are there clinical trials for Hereditary xanthinuria?

Tomeko shows live, recruiting studies for Hereditary xanthinuria 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