tomeko

Glutaryl-CoA oxidase deficiency

Just diagnosed with Glutaryl-CoA oxidase deficiency?

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

Open the full Glutaryl-CoA oxidase deficiency hub →

Overview

Glutaryl-CoA oxidase deficiency is a rare condition. Also known as Glutaric aciduria type 3, Glutaryl-CoA oxidase deficiency. Tomeko brings together the specialists, research, clinical trials, treatments and community for Glutaryl-CoA oxidase deficiency so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:35706 · OMIM 231690 · ICD-10 E72.3 · GARD 0012469

Find care for Glutaryl-CoA oxidase deficiency

Authoritative references for Glutaryl-CoA oxidase deficiency

Common questions

I was just diagnosed with Glutaryl-CoA oxidase deficiency — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Glutaryl-CoA oxidase deficiency, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Glutaryl-CoA oxidase deficiency?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Glutaryl-CoA oxidase deficiency, filtered to your area.

Are there clinical trials for Glutaryl-CoA oxidase deficiency?

Tomeko shows live, recruiting studies for Glutaryl-CoA oxidase deficiency 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