: MeSH: Multiple Acyl Coenzyme A Dehydrogenase Deficiency

Nutritional and Metabolic Diseases > Metabolic Diseases > Mitochondrial Diseases > Multiple Acyl Coenzyme A Dehydrogenase Deficiency

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Amino Acid Metabolism, Inborn Errors > Multiple Acyl Coenzyme A Dehydrogenase Deficiency

Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Amino Acid Metabolism, Inborn Errors > Multiple Acyl Coenzyme A Dehydrogenase Deficiency

Multiple Acyl Coenzyme A Dehydrogenase Deficiency

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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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