bn:03354141n
Noun Concept
Categories: Autosomal recessive disorders, Fatty-acid metabolism disorders
EN
Medium-chain acyl-coenzyme A dehydrogenase deficiency  medium chain acyl-CoA dehydrogenase deficiency  Medium chain acyl CoA dehydrogenase deficiency  Acadm Deficiency  ACADMD
EN
Medium-chain acyl-CoA dehydrogenase deficiency is a disorder of fatty acid oxidation that impairs the body's ability to break down medium-chain fatty acids into acetyl-CoA. Wikipedia
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EN
Medium-chain acyl-CoA dehydrogenase deficiency is a disorder of fatty acid oxidation that impairs the body's ability to break down medium-chain fatty acids into acetyl-CoA. Wikipedia
Caused by mutations in the ACADM gene Wikipedia Disambiguation
Lipid metabolism disorder that is characterized by a deficiency of the enzyme medium chain acyl-CoA dehydrogenase that results in the inability to convert medium chain fatty acids to energy, particularly during fasting Wikidata