- beta-methylcrotonyl-CoA carboxylase deficiency
- метилкротоновая ацидурия
Англо-русский медицинский словарь. 2012.
beta-methylcrotonyl-CoA carboxylase deficiency
Смотреть что такое "beta-methylcrotonyl-CoA carboxylase deficiency" в других словарях:
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
Propionyl-CoA carboxylase — PCCA redirects here. For other uses, see PCCA (disambiguation). Propionyl CoA carboxylase Identifiers EC number 6.4.1.3 CAS number … 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
Beta-ketothiolase deficiency — Classification and external resources Isoleucine OMIM 203750 … Wikipedia
Dopamine beta hydroxylase deficiency — Classification and external resources Dopamine beta hydroxylase is the enzyme responsible for converting dopamine (pictured) to norepinephrine. OMIM … Wikipedia
Ornithine transcarbamylase deficiency — Classification and external resources Ornithine ICD 10 E … Wikipedia
N-Acetylglutamate synthase deficiency — Classification and external resources N Acetylglutamic acid OMIM 237310 … Wikipedia
