D81.819
Biotin-dependent carboxylase deficiency unspecified
Applicable To
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Multiple carboxylase deficiency, unspecified
Approximate Synonyms
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Biotin dependent carboxylase deficiency
Clinical Information
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A deficiency in the activities of biotin-dependent enzymes propionyl-coa carboxylase, methylcrotonyl-coa carboxylase, and pyruvate carboxylase) due to one of two defects in biotin metabolism. The neonatal form is due to holocarboxylase synthetase deficiency. The late-onset form is due to biotinidase deficiency.
Details
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D81.819 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 D81.819 became effective on October 1, 2022.
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This is the American ICD-10-CM version of D81.819 – other international versions of ICD-10 D81.819 may differ.