| Health / Medical Topics |
Acyl-CoA Dehydrogenase, Medium-Chain Deficiency
A genetic disorder characterized by deficiency of the enzyme medium-chain acyl-coenzyme A dehydrogenase that metabolizes medium-chain fatty acids. Signs and symptoms appear in infancy or childhood and may be triggered during fasting or illness. They include vomiting, hypoglycemia and lethargy. (NCI Thesaurus)
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