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Results 1 - 4 of 4 for "Methylcrotonyl-CoA" carboxylase deficiency
  1. 3-methylcrotonyl-CoA carboxylase deficiency 
    3-methylcrotonyl-CoA carboxylase deficiency (also called MCC deficiency) is an inherited disorder in which the body is unable to process certain proteins. ...
    https://medlineplus.gov/...methylcrotonyl-coa-carboxylase-deficiency - Genetics
  2. MCCC2 gene 
    ... gene have been identified in people with 3-methylcrotonyl-CoA carboxylase deficiency (also called MCC deficiency). MCC deficiency is an ... Valle D. The molecular basis of human 3-methylcrotonyl-CoA carboxylase deficiency. J Clin Invest. 2001 Feb;107(4):495- ...
    https://medlineplus.gov/genetics/gene/mccc2 - Genetics
  3. MCCC1 gene 
    ... gene have been identified in people with 3-methylcrotonyl-CoA carboxylase deficiency (also called MCC deficiency). MCC deficiency is an ... Valle D. The molecular basis of human 3-methylcrotonyl-CoA carboxylase deficiency. J Clin Invest. 2001 Feb;107(4):495- ...
    https://medlineplus.gov/genetics/gene/mccc1 - Genetics
  4. CA5A gene 
    ... in the liver. Propionyl-CoA carboxylase and 3-methylcrotonyl-CoA carboxylase help break down ... carbonic anhydrase VA deficiency. This inherited disorder is characterized by potentially life- ...
    https://medlineplus.gov/genetics/gene/ca5a - Genetics