E80.2

Other and unspecified porphyria

Non-billable header

E80.2 is a non-billable header code. Use one of the more specific codes below.

Inclusion terms

Includes (from E80)

  • defects of catalase and peroxidase
  • Note: 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.

Excludes1

Not coded here — never report together with this code.

  • transitory endocrine and metabolic disorders specific to newborn (P70-P74) (from E80)
  • androgen insensitivity syndrome (E34.5-) (from E80)
  • congenital adrenal hyperplasia (E25.0) (from E80)
  • hemolytic anemias attributable to enzyme disorders (D55.-) (from E80)
  • Marfan syndrome (Q87.4-) (from E80)
  • 5-alpha-reductase deficiency (E29.1) (from E80)

Excludes2

Not included here — may be reported together when both conditions exist.

  • Ehlers-Danlos syndromes (Q79.6-) (from E80)

Parent code

  • E80Disorders of porphyrin and bilirubin metabolismHeader

More specific codes E80.2

  • E80.20Unspecified porphyriaBillable
  • E80.21Acute intermittent (hepatic) porphyriaBillable
  • E80.29Other porphyriaBillable

Related codes

  • E80.0Hereditary erythropoietic porphyriaBillable
  • E80.1Porphyria cutanea tardaBillable
  • E80.3Defects of catalase and peroxidaseBillable
  • E80.4Gilbert syndromeBillable
  • E80.5Crigler-Najjar syndromeBillable
  • E80.6Other disorders of bilirubin metabolismBillable
  • E80.7Disorder of bilirubin metabolism, unspecifiedBillable

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