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Multiple Acyl Coenzyme A Dehydrogenase Deficiency

An autosomal recessive disorder of fatty acid oxidation, and branched chain amino acids (AMINO ACIDS, BRANCHED-CHAIN); LYSINE; and CHOLINE catabolism, that is due to defects in either subunit of ELECTRON TRANSFER FLAVOPROTEIN or its dehydrogenase, electron transfer flavoprotein-ubiquinone oxidoreductase (EC 1.5.5.1).

Year introduced: 2008

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Tree Number(s): C16.320.565.100.614, C18.452.648.100.614, C18.452.660.612

MeSH Unique ID: D054069

Entry Terms:

  • Ethylmalonic-Adipic Aciduria
  • Aciduria, Ethylmalonic-Adipic
  • Acidurias, Ethylmalonic-Adipic
  • Ethylmalonic Adipic Aciduria
  • Ethylmalonic-Adipic Acidurias
  • Ethylmalonic-Adipicaciduria
  • Ethylmalonic Adipicaciduria
  • Glutaric Acidemia Type II
  • Glutaric Acidemia, Type 2
  • Glutaric Aciduria II
  • Glutaric Aciduria Type II
  • Glutaric Aciduria, Type 2
  • MADD (Multiple Acyl-CoA Dehydrogenase Deficiency)
  • MADD (Multiple Acyl CoA Dehydrogenase Deficiency)
  • MADDs (Multiple Acyl-CoA Dehydrogenase Deficiency)
  • Multiple Acyl-CoA Dehydrogenase Deficiency
  • Multiple Acyl CoA Dehydrogenase Deficiency
  • Multiple FAD Dehydrogenase Deficiency
  • Electron Transfer Flavoprotein Deficiency
  • Glutaric Aciduria Type 2
  • Glutaric Aciduria IIC
  • ETFDH Deficiency
  • ETFDH Deficiencies
  • Electron Transfer Flavoprotein Dehydrogenase Deficiency
  • Glutaric Aciduria IIA
  • ETFA Deficiency
  • ETFA Deficiencies
  • Electron Transfer Flavoprotein Alpha Subunit Deficiency
  • Glutaric Aciduria IIB
  • Electron Transfer Flavoprotein Beta Subunit Deficiency
  • ETFB Deficiency
  • ETFB Deficiencies

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