ICD-10-CM category
E83: Disorders of mineral metabolism
Codes under E83 (Disorders of mineral metabolism). A ✓ marks a billable (fully specified) code; category codes without a ✓ are not billable on their own.
| Code | Description | Billable |
|---|---|---|
| E83.0 | Disorders of copper metabolism | — |
| E83.00 | Disorder of copper metabolism, unspecified | ✓ |
| E83.01 | Wilson's disease | ✓ |
| E83.1 | Disorders of iron metabolism | — |
| E83.2 | Disorders of zinc metabolism | ✓ |
| E83.3 | Disorders of phosphorus metabolism and phosphatases | — |
| E83.4 | Disorders of magnesium metabolism | — |
| E83.5 | Disorders of calcium metabolism | — |
| E83.8 | Other disorders of mineral metabolism | — |
| E83.09 | Other disorders of copper metabolism | ✓ |
| E83.9 | Disorder of mineral metabolism, unspecified | ✓ |
| E83.10 | Disorder of iron metabolism, unspecified | ✓ |
| E83.11 | Hemochromatosis | — |
| E83.19 | Other disorders of iron metabolism | ✓ |
| E83.30 | Disorder of phosphorus metabolism, unspecified | ✓ |
| E83.31 | Familial hypophosphatemia | ✓ |
| E83.32 | Hereditary vitamin D-dependent rickets (type 1) (type 2) | ✓ |
| E83.39 | Other disorders of phosphorus metabolism | ✓ |
| E83.40 | Disorders of magnesium metabolism, unspecified | ✓ |
| E83.41 | Hypermagnesemia | ✓ |
| E83.42 | Hypomagnesemia | ✓ |
| E83.49 | Other disorders of magnesium metabolism | ✓ |
| E83.50 | Unspecified disorder of calcium metabolism | ✓ |
| E83.51 | Hypocalcemia | ✓ |
| E83.52 | Hypercalcemia | ✓ |
| E83.59 | Other disorders of calcium metabolism | ✓ |
| E83.81 | Hungry bone syndrome | ✓ |
| E83.82 | Disorders of pyrophosphate metabolism | — |
| E83.89 | Other disorders of mineral metabolism | ✓ |
| E83.110 | Hereditary hemochromatosis | ✓ |
| E83.111 | Hemochromatosis due to repeated red blood cell transfusions | ✓ |
| E83.118 | Other hemochromatosis | ✓ |
| E83.119 | Hemochromatosis, unspecified | ✓ |
| E83.820 | Generalized arterial calcification of infancy with unspecified genetic causality | ✓ |
| E83.821 | ENPP1 deficiency causing generalized arterial calcification of infancy | ✓ |
| E83.822 | ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2 | ✓ |
| E83.823 | ABCC6 deficiency causing generalized arterial calcification of infancy | ✓ |
| E83.824 | ABCC6 deficiency causing pseudoxanthoma elasticum | ✓ |
| E83.825 | CD73 deficiency causing arterial calcification | ✓ |
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Informational only, not coding or medical advice. Verify against the official ICD-10-CM (FY2026) and your payer's guidelines.
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