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Primary hyperoxaluria, type II

Just diagnosed with Primary hyperoxaluria, type II?

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

Open the full Primary hyperoxaluria, type II hub →

Overview

Primary hyperoxaluria, type II is a rare condition. Also known as D-glycerate dehydrogenase deficiency, L-glyceric aciduria. Tomeko brings together the specialists, research, clinical trials, treatments and community for Primary hyperoxaluria, type II so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:93599 · OMIM 260000 · ICD-10 E74.8 · GARD 0002836

Find care for Primary hyperoxaluria, type II

Authoritative references for Primary hyperoxaluria, type II

Common questions

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

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

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

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

Are there clinical trials for Primary hyperoxaluria, type II?

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