ICD-10-CM 2027
ICD-10 code for xanthinuria
From the official ICD-10-CM alphabetic index entry “Xanthinuria, hereditary”. Page updated September 29, 2026.
About coding xanthinuria
The ICD-10-CM code for xanthinuria is E79.82 (Hereditary xanthinuria).
Within E79.8 (other disorders of purine and pyrimidine metabolism), E79.82 is specifically for hereditary xanthinuria. Related codes cover Aicardi-Goutieres syndrome (E79.81) and other specified disorders of purine and pyrimidine metabolism (E79.89).
As a secondary diagnosis it is a CC (complication or comorbidity), which can move an inpatient stay into the "with CC" MS-DRG of its family, unless the principal diagnosis excludes it.
In MS-DRG v44.0, it is part of the grouping logic for DRG 642 (Inborn and Other Disorders of Metabolism, relative weight 1.3219), in MDC 10 (Endocrine, Nutritional and Metabolic Diseases and Disorders), as a principal or secondary diagnosis. The DRG a claim lands in depends on the principal diagnosis, procedures and any CC/MCC secondary diagnoses.
Common questions about xanthinuria ICD-10 codes
What is the ICD-10 code for xanthinuria?
- E79.82 — Hereditary xanthinuria.
Is E79.82 billable?
- Yes. E79.82 is a billable/specific ICD-10-CM code valid for FY2027 (October 1, 2026 – September 30, 2027).
Can E79.82 be used as a principal diagnosis?
- Yes. The Medicare Code Editor doesn't restrict E79.82 as a principal diagnosis.
Is E79.82 a CC or MCC?
- E79.82 is a CC (complication or comorbidity) under MS-DRG v44.0, unless excluded by the principal diagnosis.