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 | — |
| E83.0 | Disorders of copper metabolism | — |
| E83.00 | Disorder of copper metabolism, unspecified | ✓ |
| E83.00 | Disorder of copper metabolism, unspecified | ✓ |
| E83.01 | Wilson's disease | ✓ |
| E83.01 | Wilson's disease | ✓ |
| E83.1 | Disorders of iron metabolism | — |
| E83.1 | Disorders of iron metabolism | — |
| E83.2 | Disorders of zinc metabolism | ✓ |
| E83.2 | Disorders of zinc metabolism | ✓ |
| E83.3 | Disorders of phosphorus metabolism and phosphatases | — |
| E83.3 | Disorders of phosphorus metabolism and phosphatases | — |
| E83.4 | Disorders of magnesium metabolism | — |
| E83.4 | Disorders of magnesium metabolism | — |
| E83.5 | Disorders of calcium metabolism | — |
| E83.5 | Disorders of calcium metabolism | — |
| E83.8 | Other disorders of mineral metabolism | — |
| E83.8 | Other disorders of mineral metabolism | — |
| E83.09 | Other disorders of copper metabolism | ✓ |
| E83.09 | Other disorders of copper metabolism | ✓ |
| E83.9 | Disorder of mineral metabolism, unspecified | ✓ |
| E83.9 | Disorder of mineral metabolism, unspecified | ✓ |
| E83.10 | Disorder of iron metabolism, unspecified | ✓ |
| E83.10 | Disorder of iron metabolism, unspecified | ✓ |
| E83.11 | Hemochromatosis | — |
| E83.11 | Hemochromatosis | — |
| E83.19 | Other disorders of iron metabolism | ✓ |
| E83.19 | Other disorders of iron metabolism | ✓ |
| E83.30 | Disorder of phosphorus metabolism, unspecified | ✓ |
| E83.30 | Disorder of phosphorus metabolism, unspecified | ✓ |
| E83.31 | Familial hypophosphatemia | ✓ |
| E83.31 | Familial hypophosphatemia | ✓ |
| E83.32 | Hereditary vitamin D-dependent rickets (type 1) (type 2) | ✓ |
| E83.32 | Hereditary vitamin D-dependent rickets (type 1) (type 2) | ✓ |
| E83.39 | Other disorders of phosphorus metabolism | ✓ |
| E83.39 | Other disorders of phosphorus metabolism | ✓ |
| E83.40 | Disorders of magnesium metabolism, unspecified | ✓ |
| E83.40 | Disorders of magnesium metabolism, unspecified | ✓ |
| E83.41 | Hypermagnesemia | ✓ |
| E83.41 | Hypermagnesemia | ✓ |
| E83.42 | Hypomagnesemia | ✓ |
| E83.42 | Hypomagnesemia | ✓ |
| E83.49 | Other disorders of magnesium metabolism | ✓ |
| E83.49 | Other disorders of magnesium metabolism | ✓ |
| E83.50 | Unspecified disorder of calcium metabolism | ✓ |
| E83.50 | Unspecified disorder of calcium metabolism | ✓ |
| E83.51 | Hypocalcemia | ✓ |
| E83.51 | Hypocalcemia | ✓ |
| E83.52 | Hypercalcemia | ✓ |
| E83.52 | Hypercalcemia | ✓ |
| E83.59 | Other disorders of calcium metabolism | ✓ |
| E83.59 | Other disorders of calcium metabolism | ✓ |
| E83.81 | Hungry bone syndrome | ✓ |
| E83.81 | Hungry bone syndrome | ✓ |
| E83.82 | Disorders of pyrophosphate metabolism | — |
| E83.82 | Disorders of pyrophosphate metabolism | — |
| E83.89 | Other disorders of mineral metabolism | ✓ |
| E83.89 | Other disorders of mineral metabolism | ✓ |
| E83.110 | Hereditary hemochromatosis | ✓ |
| E83.110 | Hereditary hemochromatosis | ✓ |
| E83.111 | Hemochromatosis due to repeated red blood cell transfusions | ✓ |
| E83.111 | Hemochromatosis due to repeated red blood cell transfusions | ✓ |
| E83.118 | Other hemochromatosis | ✓ |
| E83.118 | Other hemochromatosis | ✓ |
| E83.119 | Hemochromatosis, unspecified | ✓ |
| E83.119 | Hemochromatosis, unspecified | ✓ |
| E83.820 | Generalized arterial calcification of infancy with unspecified genetic causality | ✓ |
| E83.820 | Generalized arterial calcification of infancy with unspecified genetic causality | ✓ |
| E83.821 | ENPP1 deficiency causing generalized arterial calcification of infancy | ✓ |
| E83.821 | ENPP1 deficiency causing generalized arterial calcification of infancy | ✓ |
| E83.822 | ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2 | ✓ |
| E83.822 | ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2 | ✓ |
| E83.823 | ABCC6 deficiency causing generalized arterial calcification of infancy | ✓ |
| E83.823 | ABCC6 deficiency causing generalized arterial calcification of infancy | ✓ |
| E83.824 | ABCC6 deficiency causing pseudoxanthoma elasticum | ✓ |
| E83.824 | ABCC6 deficiency causing pseudoxanthoma elasticum | ✓ |
| E83.825 | CD73 deficiency causing arterial calcification | ✓ |
| E83.825 | CD73 deficiency causing arterial calcification | ✓ |
Frequently asked questions
What is ICD-10-CM code E83?
E83 is an ICD-10-CM category covering Disorders of mineral metabolism. It contains 78 more specific diagnosis codes, 62 of which are billable.
Is E83 a billable code?
No — E83 is a category header and isn't billable on its own. Code to the highest level of specificity using one of its subcodes (for example E83.0 — Disorders of copper metabolism). 62 of the 78 codes under E83 are billable.
What codes fall under E83?
E83 includes E83.0, E83.0, E83.00, E83.00, E83.01, plus 73 more. See the full list with descriptions and billable status above.
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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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