See Also: medium-chain acyl-CoA dehydrogenase(medicine)
short-chain acyl-CoA dehydrogenase(medicine)
long-chain-acyl-CoA dehydrogenase(medicine)
branched chain acyl-CoA oxidase(medicine)
acyl-ACP dehydrogenase(medicine)
acyl-CoA dehydrogenase(medicine)
long-chain-fatty-acyl-glutamate deacylase(medicine)
acyl-CoA dehydrogenase (NADPH-2b)(medicine)
N-acyl-D-mannosamine dehydrogenase(medicine)
long-chain-fatty-acid-(acyl-carrier-protein) ligase(medicine)

medium-chain acyl-CoA dehydrogenase (medicine)


medium-chain acyl-CoA dehydrogenase
<enzyme> Deficiency in mitochondrial beta oxidation of fatty acids gives a disorder frequently masquerading as reye syndrome or sudden infant death; leads to buildup of octanoyl carnitine in urine

Registry number: EC 1.3.-

Synonym: mcaca-dehydrogenase, medium-chain acyl-coenzyme a dehydrogenase, octanoyl-CoA dehydrogenase, mcad enzyme