E80.4
Gilbert syndrome
Approximate Synonyms
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Gilbert’s syndrome
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Gilberts syndrome
Clinical Information
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A benign familial disorder, transmitted as an autosomal dominant trait. It is characterized by low-grade chronic hyperbilirubinemia with considerable daily fluctuations of the bilirubin level.
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An autosomal recessive inherited disorder characterized by unconjugated hyperbilirubinemia, resulting in harmless intermittent jaundice.
Details
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E80.4 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 E80.4 became effective on October 1, 2022.
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This is the American ICD-10-CM version of E80.4 – other international versions of ICD-10 E80.4 may differ.