E83 Disorders of mineral metabolism

Non-Billable/Non-Specific

Type 1 Excludes

dietary mineral deficiency (E58-E61)
parathyroid disorders (E20-E21)
vitamin D deficiency (E55.-)

Codes

E83.0Disorders of copper metabolism
- E83.00Disorder of copper metabolism, unspecified
- E83.01Wilson's disease
- E83.09Other disorders of copper metabolism
E83.1Disorders of iron metabolism
- E83.10Disorder of iron metabolism, unspecified
- E83.11Hemochromatosis
  E83.110Hereditary hemochromatosis
  E83.111Hemochromatosis due to repeated red blood cell transfusions
  E83.118Other hemochromatosis
  E83.119Hemochromatosis, unspecified
- E83.19Other disorders of iron metabolism
E83.2Disorders of zinc metabolism
E83.3Disorders of phosphorus metabolism and phosphatases
- E83.30Disorder of phosphorus metabolism, unspecified
- E83.31Familial hypophosphatemia
- E83.32Hereditary vitamin D-dependent rickets (type 1) (type 2)
- E83.39Other disorders of phosphorus metabolism
E83.4Disorders of magnesium metabolism
- E83.40Disorders of magnesium metabolism, unspecified
- E83.41Hypermagnesemia
- E83.42Hypomagnesemia
- E83.49Other disorders of magnesium metabolism
E83.5Disorders of calcium metabolism
- E83.50Unspecified disorder of calcium metabolism
- E83.51Hypocalcemia
- E83.52Hypercalcemia
- E83.59Other disorders of calcium metabolism
E83.8Other disorders of mineral metabolism
- E83.81Hungry bone syndrome
- E83.82Disorders of pyrophosphate metabolism
  E83.820Generalized arterial calcification of infancy with unspecified genetic causality
  E83.821ENPP1 deficiency causing generalized arterial calcification of infancy
  E83.822ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2
  E83.823ABCC6 deficiency causing generalized arterial calcification of infancy
  E83.824ABCC6 deficiency causing pseudoxanthoma elasticum
  E83.825CD73 deficiency causing arterial calcification
- E83.89Other disorders of mineral metabolism
E83.9Disorder of mineral metabolism, unspecified