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Multiple Acyl Coenzyme A Dehydrogenase Deficiency

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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).      Other names Multiple Acyl CoA Dehydrogenase Deficiency; MADDs (Multiple Acyl-CoA Dehydrogenase Deficiency); MADD (Multiple Acyl CoA Dehydrogenase Deficiency); Ethylmalonic-Adipic Acidurias; Ethylmalonic Adipicaciduria; Ethylmalonic Adipic Aciduria; ETFDH Deficiencies; ETFB Deficiencies; ETFA Deficiencies; Acidurias, Ethylmalonic-Adipic; Aciduria, Ethylmalonic-Adipic; Multiple Acyl-CoA Dehydrogenase Deficiency; MADD (Multiple Acyl-CoA Dehydrogenase Deficiency); Glutaric Aciduria Type II; Glutaric Aciduria Type 2; Glutaric Aciduria IIC; Glutaric Aciduria IIB; Glutaric Aciduria IIA; Ethylmalonic-Adipicaciduria; Ethylmalonic-Adipic Aciduria
 
SubstanceCAS Registry & nameCategoriesSource
Glutaric aciduria 2  0   *Multiple Acyl Coenzyme A Dehydrogenase Deficiency.

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012
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