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Illness finder is a diagnostic medicine tool for educational purpose that looks up your patients' health conditions or symptoms and diagnosis and find diseases or illnesses based on chosen gender, age, risk factors, illness, signs, symptoms and prevalence. Illnessfinder is inspired by Evidence based medicine (EMB) and healthcare that aims to apply the best (most reliable) knowledge that is available at decision time. Illnessfinder aims to free up time for the therapeutic dialogue and ensure quality at the evidence based practice, uniting proven medical findings and clinical evidence with systematised data technology.
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| Multiple Acyl Coenzyme A Dehydrogenase Deficiency | Legal notice |
Other terms
Ethylmalonic-Adipicaciduria,Ethylmalonic Adipicaciduria,Electron Transfer Flavoprotein Deficiency,MADD (Multiple Acyl-CoA Dehydrogenase Deficiency),MADD (Multiple Acyl CoA Dehydrogenase Deficiency),MADDs (Multiple Acyl-CoA Dehydrogenase Deficiency),Glutaric Aciduria Type II,Ethylmalonic-Adipic Aciduria,Aciduria, Ethylmalonic-Adipic,Acidurias, Ethylmalonic-Adipic,Ethylmalonic Adipic Aciduria,Ethylmalonic-Adipic Acidurias,Multiple Acyl-CoA Dehydrogenase Deficiency,Multiple Acyl CoA Dehydrogenase Deficiency,Glutaric Aciduria II,Glutaric Aciduria Type 2,Glutaric Aciduria IIB,ETFB Deficiency,ETFB Deficiencies,Electron Transfer Flavoprotein Beta Subunit Deficiency,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
Description
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).
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