ICD-10/E83.00

E83.00 ICD 2026 Code: Disorder of copper metabolism, unspecified

E83.00 is the authoritative medical code for Disorder of copper metabolism, unspecified. This classification is used in medical billing and clinical recording to specify the clinical criteria for disorder of copper metabolism, unspecified (ICD-10-CM E83.00), ensuring healthcare documentation aligns with 2026 federal coding standards.

Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.

Official Registry Overview & Definition

Disorder of copper metabolism, unspecified is a billable ICD-10-CM diagnosis code E83.00. Excludes1 (not coded here): dietary mineral deficiency E58-E61; parathyroid disorders E20-E21; vitamin D deficiency E55.-; androgen insensitivity syndrome E34.5-; congenital adrenal hyperplasia E25.0; hemolytic anemias attributable to enzyme disorders D55.-; Marfan syndrome Q87.4-; 5-alpha-reductase deficiency E29.1. Excludes2 (not included here): Ehlers-Danlos syndromes Q79.6-.

Official Tabular Instructional Notes

Sequencing, inclusion, and exclusion notes published for E83.00 in the official ICD-10-CM tabular list.

Excludes1 — Not Coded Here

Conditions that can never be reported with this code; the two are mutually exclusive.

  • dietary mineral deficiency E58-E61
  • parathyroid disorders E20-E21
  • vitamin D deficiency E55.-
  • androgen insensitivity syndrome E34.5-
  • congenital adrenal hyperplasia E25.0
  • hemolytic anemias attributable to enzyme disorders D55.-
  • Marfan syndrome Q87.4-
  • 5-alpha-reductase deficiency E29.1

Excludes2 — Not Included Here

Conditions not covered by this code, but which may be reported alongside it when both are present.

  • Ehlers-Danlos syndromes Q79.6-

Frequently Asked Questions (FAQ) & Clinical Guidance

What can't be coded together with E83.00?

Per Excludes1 instructions, E83.00 must not be reported with: dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); androgen insensitivity syndrome (E34.5-).

Can E83.00 be reported alongside related conditions?

Per Excludes2 instructions, E83.00 and the following may both be reported when both are present: Ehlers-Danlos syndromes (Q79.6-).

Codes in This Family (39)

Official ICD-10-CM classifications in the same code family as E83.00, with their registry titles.

  • E83 — Disorders of mineral metabolism
  • E83.0 — Disorders of copper metabolism
  • E83.01 — Wilson's disease
  • E83.09 — Other disorders of copper metabolism
  • E83.1 — Disorders of iron metabolism
  • E83.10 — Disorder of iron metabolism, unspecified
  • E83.11 — Hemochromatosis
  • E83.110 — Hereditary hemochromatosis
  • E83.111 — Hemochromatosis due to repeated red blood cell transfusions
  • E83.118 — Other hemochromatosis
  • E83.119 — Hemochromatosis, unspecified
  • E83.19 — Other disorders of iron metabolism
  • E83.2 — Disorders of zinc metabolism
  • E83.3 — Disorders of phosphorus metabolism and phosphatases
  • 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
  • E83.4 — Disorders of magnesium metabolism
  • E83.40 — Disorders of magnesium metabolism, unspecified
  • E83.41 — Hypermagnesemia
  • E83.42 — Hypomagnesemia
  • E83.49 — Other disorders of magnesium metabolism
  • E83.5 — Disorders of calcium metabolism
  • E83.50 — Unspecified disorder of calcium metabolism
  • E83.51 — Hypocalcemia
  • E83.52 — Hypercalcemia
  • E83.59 — Other disorders of calcium metabolism
  • E83.8 — Other disorders of mineral metabolism
  • E83.81 — Hungry bone syndrome
  • E83.82 — Disorders of pyrophosphate metabolism
  • 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
  • E83.89 — Other disorders of mineral metabolism
  • E83.9 — Disorder of mineral metabolism, unspecified

Indexed Clinical Terms (1)

Clinical term phrases from the official ICD-10-CM Index to Diseases and Injuries that map to this code.

  • Disorder (of), metabolism NOS, copper

Related Codes & Numerical Sequence (Crawl Map)

Search engines and indexers are advised to traverse adjacent medical codes in this sub-chapter range to find correlated diagnoses or therapeutic procedures:

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