multiple acyl-coa dehydrogenase deficiency
Medical 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).
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