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Multiple Acyl Coenzyme A Dehydrogenase Deficiency MeSH Descriptor Data 2023


MeSH Heading
Multiple Acyl Coenzyme A Dehydrogenase Deficiency
Tree Number(s)
C16.320.565.100.614
C18.452.648.100.614
C18.452.660.612
Unique ID
D054069
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D054069
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).
Entry Term(s)
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
Public MeSH Note
2008
History Note
2008
Date Established
2008/01/01
Date of Entry
2007/07/09
Revision Date
2013/07/08
Multiple Acyl Coenzyme A Dehydrogenase Deficiency Preferred
Glutaric Aciduria IIC Narrower
Glutaric Aciduria IIA Narrower
Glutaric Aciduria IIB Narrower
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