AutoICD API

E80

Non-billable

Disorders of porphyrin and bilirubin metabolism

Disorders of porphyrin and bilirubin metabolism

This is a header/category code. For billing purposes, use a more specific child code from the list below.

Status

Non-billable / Header

Block

E70-E88

Child Codes

8

Coding Notes

Includes

Conditions included under this code

  • defects of catalase and peroxidase

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

  • transitory endocrine and metabolic disorders specific to newborn (P70-P74)
  • 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

Conditions not included here, but the patient may have both

  • Ehlers-Danlos syndromes (Q79.6-)

Child Codes (8)

E80.0

Hereditary erythropoietic porphyria

BillableE80.1

Porphyria cutanea tarda

BillableE80.2

Other and unspecified porphyria

E80.3

Defects of catalase and peroxidase

BillableE80.4

Gilbert syndrome

BillableE80.5

Crigler-Najjar syndrome

BillableE80.6

Other disorders of bilirubin metabolism

BillableE80.7

Disorder of bilirubin metabolism, unspecified

Billable

Also Known As / Clinical Terms

UMLS

Frequently Asked Questions

What is ICD-10 code E80?

ICD-10-CM code E80 represents "Disorders of porphyrin and bilirubin metabolism". It is a non-billable header code — use a more specific child code for billing purposes.

Is E80 a billable code?

No, E80 is a non-billable header code. You need to use one of its more specific child codes for billing. There are 8 child codes under E80.

What chapter is E80 in?

E80 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E80?

E80 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 3 more.

What are the subcategories under E80?

E80 has 8 child codes, including: E80.0 (Hereditary erythropoietic porphyria), E80.1 (Porphyria cutanea tarda), E80.2 (Other and unspecified porphyria), E80.3 (Defects of catalase and peroxidase), and 4 more.

What are the UMLS CUIs for E80?

E80 is linked to 2 UMLS Concept Unique Identifiers: C0494349, C0494347. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.