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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).

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We couldn't find any anagrams for the word multiple acyl coenzyme a dehydrogenase deficiency.

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multiphaser, multiphotography, multipinnate, multiplane, multiple, multiplepoinding, multiplet, multiplex, multipliable, multipliableness

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