E80.1
Porphyria cutanea tarda
Clinical Information
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An autosomal dominant or acquired porphyria due to a deficiency of uroporphyrinogen decarboxylase in the liver. It is characterized by photosensitivity and cutaneous lesions with little or no neurologic symptoms. Type i is the acquired form and is strongly associated with liver diseases and hepatic toxicities caused by alcohol or estrogenic steroids. Type ii is the familial form.
Details
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E80.1 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 E80.1 became effective on October 1, 2022.
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This is the American ICD-10-CM version of E80.1 – other international versions of ICD-10 E80.1 may differ.