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).
Year introduced: 2008
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Subheadings:
Tree Number(s): C16.320.565.100.614, C18.452.648.100.614, C18.452.660.612
MeSH Unique ID: D054069
Entry Terms:
- Glutaric Aciduria Type II
- Glutaric Aciduria, Type 2
- 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
- Electron Transfer Flavoprotein Deficiency
- Ethylmalonic-Adipic Aciduria
- Aciduria, Ethylmalonic-Adipic
- Acidurias, Ethylmalonic-Adipic
- Ethylmalonic Adipic Aciduria
- Ethylmalonic-Adipic Acidurias
- Ethylmalonic-Adipicaciduria
- Ethylmalonic Adipicaciduria
- Glutaric Acidemia Type II
- Glutaric Acidemia, Type 2
- Glutaric Aciduria Type 2
- Glutaric Aciduria II
- Glutaric Aciduria IIA
- Electron Transfer Flavoprotein Alpha Subunit Deficiency
- ETFA Deficiency
- ETFA Deficiencies
- Glutaric Aciduria IIB
- Electron Transfer Flavoprotein Beta Subunit Deficiency
- ETFB Deficiency
- ETFB Deficiencies
- Glutaric Aciduria IIC
- Electron Transfer Flavoprotein Dehydrogenase Deficiency
- ETFDH Deficiency
- ETFDH Deficiencies