Ссылки на запись Gene: [01p31/ACADM] acyl-CoA dehydrogenase M (medium straight-chain fa C4/C12); hypoglycemia, non-ketotic, and secondary carnitine deficiency; dicarboxylicaciduria (MCAD deficiency); Reye-like syndrome (fatty acids beta-oxidation familial d


  • Gene: [02q3/ACADL] acyl-CoA dehydrogenase L (fatty acid long straight-chain C8 to C16); hypoglycemia, intermittent non-ketotic (LCAD deficiency); dicarboxylicaciduria (LCAD deficiency);
  • Gene: [04q3/ETFDH] electron-transferring-flavoprotein dehydrogenase; glutaricaciduria IIC (ETF dehydrogenase deficiency);
  • Gene: [0X^/ACADX] acyl-CoA dehydrogenase X, multiple deficiency; glutaric aciduria II, neonatal form (GA IIA);
  • Gene: [12q2/ACADS] acyl-CoA dehydrogenase S (FA short straight-chain C2/C6); butyryl-CoA dehydrogenase (ethylen reductase); lipid-storage myopathy, secondary to SCADh deficiency;
  • Gene: [15q1/ACADI] isovaleryl coenzyme A dehydrogenase; isovalericacidemia;
  • Gene: [15q2/ETFA] electron-transferring-flavoprotein, alpha polypeptide; glutaricaciduria IIA (ETF-alpha deficiency); ethylmalonic-adipicaciduria (glutaric aciduria IIA); multiple acyl-CoA dehydrogenase deficiency (MADD); [GA2A EMA MADD ]
  • Gene: [17p11/ACADVL] acyl-Coenzyme A dehydrogenase, very long chain; hypoketotic hypoglycemia due to VLCAD deficiency;
  • Gene: [19p132/GCDH] glutaryl-CoA dehydrogenase; glutaricaciduria I (glutaryl-CoA dehydrogenase deficiency);
  • Gene: [19q134/ETFB] electron transfer flavoprotein, beta polypeptide; glutaricaciduria IIB (ETF-beta deficiency);
  • ацил-CoA-дегидрогеназа-HUGEN