E79.82 Hereditary xanthinuria
Billable / valid for submission ICD10CM Release FY2026
Version history
| Release | Valid from | Valid to | Description | Billable |
|---|---|---|---|---|
| FY2026 | 2025-10-01 | current | Hereditary xanthinuria | yes |
Related codes in E79
- E79 Disorders of purine and pyrimidine metabolism
- E79.0 Hyperuricemia without signs of inflammatory arthritis and tophaceous disease
- E79.1 Lesch-Nyhan syndrome
- E79.2 Myoadenylate deaminase deficiency
- E79.8 Other disorders of purine and pyrimidine metabolism
- E79.81 Aicardi-Goutieres syndrome
- E79.89 Other specified disorders of purine and pyrimidine metabolism
- E79.9 Disorder of purine and pyrimidine metabolism, unspecified