Multiple Acyl Coenzyme A Dehydrogenase Deficiency

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).

Also Known As:

ETFA Deficiency; ETFB Deficiency; ETFDH Deficiency; Electron Transfer Flavoprotein Alpha Subunit Deficiency; Electron Transfer Flavoprotein Beta Subunit Deficiency; Electron Transfer Flavoprotein Deficiency; Electron Transfer Flavoprotein Dehydrogenase Deficiency; Ethylmalonic-Adipic Aciduria; Ethylmalonic-Adipicaciduria; Glutaric Acidemia Type II; Glutaric Acidemia, Type 2; Glutaric Aciduria II; Glutaric Aciduria IIA; Glutaric Aciduria IIB; Glutaric Aciduria IIC; Glutaric Aciduria Type 2; Glutaric Aciduria Type II; Glutaric Aciduria, Type 2; MADD (Multiple Acyl-CoA Dehydrogenase Deficiency); Multiple Acyl-CoA Dehydrogenase Deficiency; Multiple FAD Dehydrogenase Deficiency; Aciduria, Ethylmalonic-Adipic; Acidurias, Ethylmalonic-Adipic; ETFA Deficiencies; ETFB Deficiencies; ETFDH Deficiencies; Ethylmalonic Adipic Aciduria; Ethylmalonic Adipicaciduria; Ethylmalonic-Adipic Acidurias; MADD (Multiple Acyl CoA Dehydrogenase Deficiency); MADDs (Multiple Acyl-CoA Dehydrogenase Deficiency); Multiple Acyl CoA Dehydrogenase Deficiency

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Inborn Errors Metabolism: 1162
    - Inborn Errors Amino Acid Metabolism: 1
      - Multiple Acyl Coenzyme A Dehydrogenase Deficiency: 323
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10142
  - Mitochondrial Diseases: 21919
    - Multiple Acyl Coenzyme A Dehydrogenase Deficiency: 323
  - Inborn Errors Metabolism: 1162
    - Inborn Errors Amino Acid Metabolism: 1
      - Multiple Acyl Coenzyme A Dehydrogenase Deficiency: 323

Sara Volta Selected Research

Sara Volta Research Topics

Disease

Drug/Important Bio-Agent (IBA)