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Multiple Acyl Coenzyme A Dehydrogenase Deficiency MeSH Descriptor Data 2025
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).
Entry Term(s)
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
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).