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 interactive 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
Research & market landscape for Hereditary xanthinuria
Following Hereditary xanthinuria for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Hereditary xanthinuria — the real-world landscape behind the condition, in one place.
- Latest Hereditary xanthinuria research on PubMed ↗
- Recruiting Hereditary xanthinuria trials on ClinicalTrials.gov ↗
- Explore the Hereditary xanthinuria research & specialist footprint on Tomeko
Researchers, patient organizations & industry: Tomeko provides de-identified, no-PHI demand and engagement signal, trial awareness, and a labeled, editorially-firewalled presence for Hereditary xanthinuria and every rare condition. See how Tomeko works with industry →
Common questions
What is Hereditary xanthinuria?
Hereditary xanthinuria is a rare condition. Also known as Classic xanthinuria, Xanthic urolithiasis, Xanthine stone disease. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Hereditary xanthinuria together in one place.
What are the symptoms of Hereditary xanthinuria?
Symptoms of Hereditary xanthinuria vary from person to person. For a reviewed, plain-language overview see the authoritative references below (NIH GARD, Orphanet), and discuss your own symptoms with a clinician who treats Hereditary xanthinuria.
How is Hereditary xanthinuria treated?
Treatment for Hereditary xanthinuria depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Hereditary xanthinuria, and review current options with them.
What causes Hereditary xanthinuria — is it genetic?
The cause and inheritance of Hereditary xanthinuria are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Hereditary xanthinuria can explain what it means for you and your family.
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.
Related conditions
Other conditions on Tomeko you may be looking for:
- 2-aminoadipic 2-oxoadipic aciduria
- 3 beta-Hydroxysteroid dehydrogenase deficiency
- 3-hydroxy-3-methylglutaryl-CoA synthase deficiency
- 3-Hydroxyisobutyric aciduria
- 3-hydroxyisobutyryl-CoA hydrolase deficiency
- 3-methylglutaconic aciduria type 1
- 3-Methylglutaconic aciduria type 2
- 3-Methylglutaconic aciduria type 3