AutoICD API

E71.5

Non-billable

Peroxisomal disorders

Peroxisomal disorders

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

Parent Code

E71

Child Codes

5

Coding Notes

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)
  • Schilder's disease (G37.0)

Excludes 2

Conditions not included here, but the patient may have both

  • Ehlers-Danlos syndromes (Q79.6-)

Child Codes (5)

E71.50

Peroxisomal disorder, unspecified

BillableE71.51

Disorders of peroxisome biogenesis

E71.52

X-linked adrenoleukodystrophy

E71.53

Other group 2 peroxisomal disorders

BillableE71.54

Other peroxisomal disorders

Also Known As / Clinical Terms

UMLS

Frequently Asked Questions

What is ICD-10 code E71.5?

ICD-10-CM code E71.5 represents "Peroxisomal disorders". It is a non-billable header code — use a more specific child code for billing purposes.

Is E71.5 a billable code?

No, E71.5 is a non-billable header code. You need to use one of its more specific child codes for billing. There are 5 child codes under E71.5.

What chapter is E71.5 in?

E71.5 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E71.5?

E71.5 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 4 more.

What are the subcategories under E71.5?

E71.5 has 5 child codes, including: E71.50 (Peroxisomal disorder, unspecified), E71.51 (Disorders of peroxisome biogenesis), E71.52 (X-linked adrenoleukodystrophy), E71.53 (Other group 2 peroxisomal disorders), and 1 more.

What are the UMLS CUIs for E71.5?

E71.5 is linked to 1 UMLS Concept Unique Identifier: C0282528. 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.