3-methylcrotonyl CoA carboxylase deficiency

3-甲基巴豆酰CoA羧化酶缺乏症,β-甲基巴豆酰甘氨酸尿症

Medical Chinese dictionary (湘雅医学词典). 2013.

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  • 3-Methylcrotonyl-CoA carboxylase deficiency — Classification and external resources Methylcrotonyl CoA OMIM 210200 …   Wikipedia

  • 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

  • Methylcrotonyl-CoA-Carboxylase — Methylcrotonoyl CoA Carboxylase 1 (α Untereinheit) Größe 725 AA Kofaktor Biotin Bezeichner …   Deutsch Wikipedia

  • Methylcrotonyl-CoA carboxylase — methylcrotonoyl Coenzyme A carboxylase 1 (alpha) Identifiers Symbol MCCC1 Entrez 56922 HUGO …   Wikipedia

  • Methylcrotonoyl-CoA-Carboxylase — 1 (α Untereinheit) Masse/Länge Primärstruktur 725 AA …   Deutsch Wikipedia

  • Methylmalonyl-CoA mutase deficiency — Classification and external resources OMIM 251000 DiseasesDB 29509 Methylmalonyl CoA mutase deficiency ( MUT ) is an inborn error of organ …   Wikipedia

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  • methylcrotonoyl-CoA carboxylase — meth·yl·cro·ton·o·yl CoA car·box·y·lase (meth″əl kro tonґo əl ko aґ kahr bokґsə lās) [EC 6.4.1.4] a biotin containing enzyme of the ligase class that catalyzes the ATP driven carboxylation of 1. 3 methylcrotonyl CoA to… …   Medical dictionary

  • 3-methylcrotonyl-CoA — An intermediate in the degradation of l leucine; accumulates in a deficiency of M. carboxylase. 3 methylcrotonyl CoA carboxylase a biotin dependent enzyme in the pathway of l leucine degradation that catalyzes the reaction of M. with CO2, ATP,… …   Medical dictionary

  • Ornithine transcarbamylase deficiency — Classification and external resources Ornithine ICD 10 E …   Wikipedia

  • Glutathione synthetase deficiency — Classification and external resources Glutathione OMIM 266130 …   Wikipedia

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