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medium-chain acyl-coa dehydrogenase deficiency

Medical Definition

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.
Related Codes (1)
Code
Description
Billable
Details
E71.311Medium chain acyl CoA dehydrogenase deficiency

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