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Results 1 - 4 of 4 for "Acyl-CoA" oxidase deficiency
  1. Peroxisomal acyl-CoA oxidase deficiency 
    ... not show signs and symptoms of the condition. Acyl-coenzyme A oxidase deficiency Pseudo-NALD Pseudoadrenoleukodystrophy Pseudoneonatal adrenoleukodystrophy Straight-chain acyl- ...
    https://medlineplus.gov/.../peroxisomal-acyl-coa-oxidase-deficiency - Genetics
  2. ACOX1 gene 
    ... HR. Clinical, biochemical, and mutational spectrum of peroxisomal acyl-coenzyme A oxidase deficiency. Hum Mutat. 2007 Sep;28(9):904-12. ... Besley GT, Wanders RJ, King MD. Straight-chain acyl-CoA oxidase deficiency presenting with dysmorphia, neurodevelopmental autistic-type regression and ...
    https://medlineplus.gov/genetics/gene/acox1 - Genetics
  3. ETFDH gene 
    ... as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency. ... oxidoreductase (ETF-QO) to human chromosome 4q33 by fluorescence ...
    https://medlineplus.gov/genetics/gene/etfdh - Genetics
  4. Glutaric acidemia type II 
    ... and mutations of the electron transfer flavoprotein:ubiquinone oxidoreductase (ETF:QO) ... acyl-CoA dehydrogenation deficiency. Hum Mutat. 2003 Jul;22(1):12-23. ...
    https://medlineplus.gov/genetics/condition/glutaric-acidemia-type-ii - Genetics