Multiple Acyl Coenzyme A Dehydrogenase Deficiency


Aciduria, Ethylmalonic-Adipic

Acidurias, Ethylmalonic-Adipic

ETFA Deficiencies

ETFA Deficiency

ETFB Deficiencies

ETFB Deficiency

ETFDH Deficiencies

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

Ethylmalonic-Adipic Aciduria

Ethylmalonic-Adipic Acidurias


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)

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

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