E72.530 Primary hyperoxaluria, type 1
Billable / valid for submission ICD10CM Release FY2026
Version history
| Release | Valid from | Valid to | Description | Billable |
|---|---|---|---|---|
| FY2026 | 2025-10-01 | current | Primary hyperoxaluria, type 1 | yes |
Related codes in E72
- E72 Other disorders of amino-acid metabolism
- E72.0 Disorders of amino-acid transport
- E72.00 Disorders of amino-acid transport, unspecified
- E72.01 Cystinuria
- E72.02 Hartnup's disease
- E72.03 Lowe's syndrome
- E72.04 Cystinosis
- E72.09 Other disorders of amino-acid transport
- E72.1 Disorders of sulfur-bearing amino-acid metabolism
- E72.10 Disorders of sulfur-bearing amino-acid metabolism, unspecified
- E72.11 Homocystinuria
- E72.12 Methylenetetrahydrofolate reductase deficiency
- E72.19 Other disorders of sulfur-bearing amino-acid metabolism
- E72.2 Disorders of urea cycle metabolism
- E72.20 Disorder of urea cycle metabolism, unspecified
- E72.21 Argininemia
- E72.22 Arginosuccinic aciduria
- E72.23 Citrullinemia
- E72.29 Other disorders of urea cycle metabolism
- E72.3 Disorders of lysine and hydroxylysine metabolism