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

Preferred term

Multiple Acyl Coenzyme A Dehydrogenase Deficiency  

Type

  • Topical Descriptor

Broader concept

Entry terms

  • Aciduria, Ethylmalonic-Adipic
  • Acidurias, Ethylmalonic-Adipic
  • Electron Transfer Flavoprotein Deficiency
  • Ethylmalonic Adipic Aciduria
  • Ethylmalonic Adipicaciduria
  • Ethylmalonic-Adipic Aciduria
  • Ethylmalonic-Adipicaciduria
  • Ethylmalonic-Adipic Acidurias
  • Glutaric Acidemia, Type 2
  • Glutaric Acidemia Type II
  • Glutaric Aciduria II
  • Glutaric Aciduria Type 2
  • Glutaric Aciduria, Type 2
  • Glutaric Aciduria Type II
  • MADD (Multiple Acyl CoA Dehydrogenase Deficiency)
  • MADD (Multiple Acyl-CoA Dehydrogenase Deficiency)
  • MADDs (Multiple Acyl-CoA Dehydrogenase Deficiency)
  • Multiple Acyl CoA Dehydrogenase Deficiency
  • Multiple Acyl-CoA Dehydrogenase Deficiency
  • Multiple FAD Dehydrogenase Deficiency

Scope note

  • 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).

History note

  • 2008

In other languages

URI

http://www.yso.fi/onto/mesh/D054069

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