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E83.82Non-billableSave

E83.82 - Disorders of pyrophosphate metabolism

ICD-10-CM Chapter 4: Endocrine, nutritional and metabolic diseases · E70-E88 Metabolic disorders (E70-E88) · Subcategory of E83.8 · FY2027

Coding Guidance

E83.82 is a non-billable heading. Report one of the 6 more specific codes below.

Includes, Excludes and Coding Notes

Excludes 1 — Not Coded HereFrom E83

Mutually exclusive: these conditions are never reported together with this code.

  • dietary mineral deficiency (E58-E61)
  • parathyroid disorders (E20-E21)
  • vitamin D deficiency (E55.-)
Excludes 1 — Not Coded HereFrom E70-E88 Metabolic disorders (E70-E88)

Mutually exclusive: these conditions are never reported together with this code.

  • 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)
Excludes 2 — Not Included HereFrom E70-E88 Metabolic disorders (E70-E88)

Not part of this code; report both codes when the patient has both conditions.

  • Ehlers-Danlos syndromes (Q79.6-)
Excludes 1 — Not Coded HereFrom Chapter E00-E89

Mutually exclusive: these conditions are never reported together with this code.

  • transitory endocrine and metabolic disorders specific to newborn (P70-P74)
NotesFrom Chapter E00-E89

Instructional notes from the ICD-10-CM tabular list.

  • All neoplasms, whether functionally active or not, are classified in Chapter 2. Appropriate codes in this chapter (i.e. E05.8, E07.0, E16-E31, E34.-) may be used as additional codes to indicate either functional activity by neoplasms and ectopic endocrine tissue or hyperfunction and hypofunction of endocrine glands associated with neoplasms and other conditions classified elsewhere.

More Specific Codes (6)

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→

Related condition guides

Documentation requirements, coding pitfalls and FAQs for conditions coded with E83.82.