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).
推出的年份: 2008
树号: C16.320.565.100.614, C18.452.648.100.614, C18.452.660.612
MeSH 单一 ID: D054069
进入的组:
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 II
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
Glutaric Aciduria Type 2
Glutaric Aciduria IIC
ETFDH Deficiency
ETFDH Deficiencies
Electron Transfer Flavoprotein Dehydrogenase Deficiency
Glutaric Aciduria IIA
ETFA Deficiency
ETFA Deficiencies
Electron Transfer Flavoprotein Alpha Subunit Deficiency
Glutaric Aciduria IIB
Electron Transfer Flavoprotein Beta Subunit Deficiency
ETFB Deficiency
ETFB Deficiencies
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