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Methylcrotonyl-CoA carboxylase deficiency

Just diagnosed with Methylcrotonyl-CoA carboxylase deficiency?

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

Open the full Methylcrotonyl-CoA carboxylase deficiency hub →

Overview

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

Identifiers: ORPHA:6 · OMIM 210200, 210210 · ICD-10 E71.1 · GARD 0010954

Find care for Methylcrotonyl-CoA carboxylase deficiency

Authoritative references for Methylcrotonyl-CoA carboxylase deficiency

Common questions

I was just diagnosed with Methylcrotonyl-CoA carboxylase deficiency — what should I do first?

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

Where can I find a specialist for Methylcrotonyl-CoA carboxylase deficiency?

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

Are there clinical trials for Methylcrotonyl-CoA carboxylase deficiency?

Tomeko shows live, recruiting studies for Methylcrotonyl-CoA carboxylase 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