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Multiple acyl-CoA dehydrogenase deficiency

Just diagnosed with Multiple acyl-CoA dehydrogenase deficiency?

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

Open the full Multiple acyl-CoA dehydrogenase deficiency hub →

Overview

Multiple acyl-CoA dehydrogenase deficiency is a rare condition. Also known as Glutaric acidemia type 2, Glutaric aciduria type 2, MAD deficiency, MADD. Tomeko brings together the specialists, research, clinical trials, treatments and community for Multiple acyl-CoA dehydrogenase deficiency so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:26791 · OMIM 231680 · ICD-10 E71.3 · GARD 0006523

Find care for Multiple acyl-CoA dehydrogenase deficiency

Authoritative references for Multiple acyl-CoA dehydrogenase deficiency

Common questions

I was just diagnosed with Multiple acyl-CoA dehydrogenase deficiency — what should I do first?

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

Where can I find a specialist for Multiple acyl-CoA dehydrogenase deficiency?

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

Are there clinical trials for Multiple acyl-CoA dehydrogenase deficiency?

Tomeko shows live, recruiting studies for Multiple acyl-CoA dehydrogenase 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