Multiple Acyl Coenzyme A Dehydrogenase Deficiency

**Definition:** 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).

**Tree numbers:** - C16.320.565.100.614 - C18.452.648.100.614 - C18.452.660.612

**Synonyms:** - Glutaric Aciduria Type II - Glutaric Aciduria, Type 2 - MADD (Multiple Acyl-CoA Dehydrogenase Deficiency) - Multiple Acyl-CoA Dehydrogenase Deficiency - Multiple FAD Dehydrogenase Deficiency - Electron Transfer Flavoprotein Deficiency - Ethylmalonic-Adipic Aciduria - Ethylmalonic-Adipicaciduria - Glutaric Acidemia Type II - Glutaric Acidemia, Type 2 - Glutaric Aciduria Type 2 - Glutaric Aciduria II