Medical dictionary. 2011.
3-methylcrotonyl CoA carboxylase deficiency — 3 meth·yl·cro·to·nyl CoA car·box·y·lase de·fi·cien·cy (meth″əl kroґtə nil″ ko aґ kahr bokґsə lās) an autosomal recessive aminoacidopathy due to deficiency of methylcrotonoyl CoA carboxylase, which can result from… … Medical dictionary
β-methylcrotonylglycinuria — β meth·yl·cro·to·nyl·gly·cin·u·ria (meth″əl kro″to nəl gli″sĭ nuґre ə) 3 methylcrotonyl CoA carboxylase deficiency. 2. excretion of 3 methylcrotonylglycine in the urine, as occurs in 3 methylcrotonyl CoA … Medical dictionary
