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Hereditary orotic aciduria

Just diagnosed with Hereditary orotic aciduria?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Hereditary orotic aciduria, look for clinical trials, and connect with others living with it — all in one place.

Open the full Hereditary orotic aciduria hub →

Overview

Hereditary orotic aciduria is a rare condition. Also known as Orotidylic decarboxylase deficiency, Uridine monophosphate synthetase deficiency. Tomeko brings together the specialists, research, clinical trials, treatments and community for Hereditary orotic aciduria so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:30 · OMIM 258900 · ICD-10 E79.8 · GARD 0005429

Find care for Hereditary orotic aciduria

Authoritative references for Hereditary orotic aciduria

Common questions

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

Start by learning the basics from an authoritative source, find a specialist or center that sees Hereditary orotic aciduria, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Hereditary orotic aciduria?

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

Are there clinical trials for Hereditary orotic aciduria?

Tomeko shows live, recruiting studies for Hereditary orotic aciduria 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