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