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Primary hyperoxaluria, type I

Just diagnosed with Primary hyperoxaluria, type I?

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

Open the full Primary hyperoxaluria, type I hub →

Overview

Primary hyperoxaluria, type I is a rare condition. Also known as Glycolic aciduria, Peroxisomal alanine-glyoxylate aminotransferase deficiency. Tomeko brings together the specialists, research, clinical trials, treatments and community for Primary hyperoxaluria, type I so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:93598 · OMIM 259900 · ICD-10 E74.8 · GARD 0002835

Find care for Primary hyperoxaluria, type I

Authoritative references for Primary hyperoxaluria, type I

Common questions

I was just diagnosed with Primary hyperoxaluria, type I — what should I do first?

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

Where can I find a specialist for Primary hyperoxaluria, type I?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Primary hyperoxaluria, type I, filtered to your area.

Are there clinical trials for Primary hyperoxaluria, type I?

Tomeko shows live, recruiting studies for Primary hyperoxaluria, type I 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