3-methylcrotonyl-CoA carboxylase deficiency

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Disease Overview

3-methylcrotonyl-CoA carboxylase deficiency (3-MCCD) is an inherited disorder of leucine metabolism characterized by a highly variable clinical picture ranging from metabolic crisis in infancy to asymptomatic adults.


Synonyms

  • 3-MCC deficiency
  • 3-methylcrotonyl-CoA carboxylase deficiency
  • 3-methylcrotonylglycinuria
  • 3MCC deficiency
  • BMCC deficiency
  • MCC deficiency
  • MCCD
  • Methylcrotonyl-CoA carboxylase deficiency
  • methylcrotonylglycinuria3-MCC deficiency
  • 3-methylcrotonyl-CoA carboxylase deficiency
  • 3-methylcrotonylglycinuria
  • 3MCC deficiency
  • BMCC deficiency
  • MCC deficiency
  • MCCD
  • Methylcrotonyl-CoA carboxylase deficiency
  • methylcrotonylglycinuria