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ICD-10-CM Current in FY 2027

E71.51

Disorders of peroxisome biogenesis

Release
FY 2027
Effective
Official source (opens in a new tab)

Hierarchy

Where E71.51 sits in the official hierarchy. Each level is the code it is classified under.

  1. E71 Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
  2. E71.5 Parent Peroxisomal disorders
  3. E71.51 This code Disorders of peroxisome biogenesis

Official Coding Notes

Reproduced verbatim from the FY 2027 ICD-10-CM files. Notes labelled as inherited are declared on a parent code and apply here too.

Inclusion Terms

Group 1 peroxisomal disorders

Excludes1

Schilder's disease ( G37.0 )

Inherited from E71.5 — Peroxisomal disorders

Excludes1

Refsum's disease ( G60.1 )

More Specific Codes

3 codes under E71.51

Version History

How E71.51 appears in each release imported from the official files, newest first.

  1. FY 2027 Effective

    Current

    Disorders of peroxisome biogenesis

  2. FY 2026 Effective

    Unchanged

    Disorders of peroxisome biogenesis

Related Codes

Other codes under E71.5

Data Source

Code information on this page is derived from the FY 2027 ICD-10-CM files published by CDC NCHS and CMS.

Release
FY 2027
Effective
Source file
icd10cm-code-descriptions-2027.zip

Official ICD-10-CM source files (opens in a new tab)

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