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Diseases

Genetic and Rare Diseases Information Center (GARD)

3-methylcrotonyl-CoA carboxylase deficiency


Other Names for this Disease
  • 3MCC
  • 3-MCC deficiency
  • 3-methylcrotonylglycinuria
  • Isolated 3-methylcrotonyl-CoA carboxylase deficiency
  • MCC deficiency
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.

Tests & Diagnosis

On this page

Testing

  • The Genetic Testing Registry (GTR) provides information about the genetic tests for this condition. The intended audience for the GTR is health care providers and researchers. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.
  • Orphanet lists international laboratories offering diagnostic testing for this condition.

Newborn Screening

  • Baby's First Test is the nation's newborn screening education center for families and providers. This site provides information and resources about screening at the local, state, and national levels and serves as the Clearinghouse for newborn screening information.
Other Names for this Disease
  • 3MCC
  • 3-MCC deficiency
  • 3-methylcrotonylglycinuria
  • Isolated 3-methylcrotonyl-CoA carboxylase deficiency
  • MCC deficiency
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.