E71.312
Short chain acyl CoA dehydrogenase deficiency
Applicable To
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SCAD
Approximate Synonyms
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Deficiency of butyryl-coa dehydrogenase
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Fatty acid oxidation disorder, scadd
Clinical Information
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A genetic disorder characterized by deficiency of the enzyme short-chain acyl-coenzyme a dehydrogenase that metabolizes short-chain fatty acids. Signs and symptoms appear in infancy or childhood and may be triggered during fasting or illness. They include vomiting, hypoglycemia, lethargy, hypotonia and failure to thrive.
Details
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E71.312 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
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The 2023 edition of ICD-10-CM E71.312 became effective on October 1, 2022.
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This is the American ICD-10-CM version of E71.312 – other international versions of ICD-10 E71.312 may differ.