2023

  1. ICD-10-CM Codes
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  2. E00-E89
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  3. E70-E88
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  4. E71-
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  5. 2023 ICD-10-CM Diagnosis Code E71.528

2023 ICD-10-CM Diagnosis Code E71.528

Other X-linked adrenoleukodystrophy

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
  • E71.528 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
  • The 2023 edition of ICD-10-CM E71.528 became effective on October 1, 2022.
  • This is the American ICD-10-CM version of E71.528 - other international versions of ICD-10 E71.528 may differ.
Applicable To
  • Addison only phenotype adrenoleukodystrophy
  • Addison-Schilder adrenoleukodystrophy
The following code(s) above E71.528 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
  • Applicable To annotations, or
  • Code Also annotations, or
  • Code First annotations, or
  • Excludes1 annotations, or
  • Excludes2 annotations, or
  • Includes annotations, or
  • Note annotations, or
  • Use Additional annotations
that may be applicable to E71.528:
  • E00-E89
    2023 ICD-10-CM Range E00-E89

    Endocrine, nutritional and metabolic diseases

    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.
    Type 1 Excludes
    • transitory endocrine and metabolic disorders specific to newborn (P70-P74)
    Endocrine, nutritional and metabolic diseases
  • E70-E88
    2023 ICD-10-CM Range E70-E88

    Metabolic disorders

    Type 1 Excludes
    • androgen insensitivity syndrome (E34.5-)
    • congenital adrenal hyperplasia (E25.0)
    • hemolytic anemias attributable to enzyme disorders (D55.-)
    • Marfan's syndrome (Q87.4)
    • 5-alpha-reductase deficiency (E29.1)
    Type 2 Excludes
    • Ehlers-Danlos syndromes (Q79.6-)
    Metabolic disorders
  • E71.5
    ICD-10-CM Diagnosis Code E71.5

    Peroxisomal disorders

      2016 2017 2018 2019 2020 2021 2022 2023 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • Schilder's disease (G37.0)
    Peroxisomal disorders
ICD-10-CM E71.528 is grouped within Diagnostic Related Group(s) (MS-DRG v40.0):
  • 642 Inborn and other disorders of metabolism

Convert E71.528 to ICD-9-CM

Code History
  • 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
  • 2017 (effective 10/1/2016): No change
  • 2018 (effective 10/1/2017): No change
  • 2019 (effective 10/1/2018): No change
  • 2020 (effective 10/1/2019): No change
  • 2021 (effective 10/1/2020): No change
  • 2022 (effective 10/1/2021): No change
  • 2023 (effective 10/1/2022): No change
Code annotations containing back-references to E71.528:
  • Type 1 Excludes: E27.1
    , E27.4
    , E75.2
    ICD-10-CM Diagnosis Code E27.1

    Primary adrenocortical insufficiency

      2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
    Applicable To
    • Addison's disease
    • Autoimmune adrenalitis
    Type 1 Excludes
    • Addison only phenotype adrenoleukodystrophy (E71.528)
    • amyloidosis (E85.-)
    • tuberculous Addison's disease (A18.7)
    • Waterhouse-Friderichsen syndrome (A39.1)
    ICD-10-CM Diagnosis Code E27.4

    Other and unspecified adrenocortical insufficiency

      2016 2017 2018 2019 2020 2021 2022 2023 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • adrenoleukodystrophy [Addison-Schilder] (E71.528)
    • Waterhouse-Friderichsen syndrome (A39.1)
    ICD-10-CM Diagnosis Code E75.2

    Other sphingolipidosis

      2016 2017 2018 2019 2020 2021 2022 2023 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • adrenoleukodystrophy [Addison-Schilder] (E71.528)

Diagnosis Index entries containing back-references to E71.528:
  • Addison-Schilder complex E71.528
  • Adrenoleukodystrophy E71.529
    ICD-10-CM Diagnosis Code E71.529

    X-linked adrenoleukodystrophy, unspecified type

      2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
    • X-linked E71.529
      ICD-10-CM Diagnosis Code E71.529

      X-linked adrenoleukodystrophy, unspecified type

        2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
      • Addison only phenotype E71.528
      • Addison-Schilder E71.528
      • other specified E71.528
  • Complex
    • Addison-Schilder E71.528
    • Schilder-Addison E71.528
  • Disorder (of) - see also Disease
    • peroxisomal E71.50
      ICD-10-CM Diagnosis Code E71.50

      Peroxisomal disorder, unspecified

        2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
      • X-linked adrenoleukodystrophy E71.529
        ICD-10-CM Diagnosis Code E71.529

        X-linked adrenoleukodystrophy, unspecified type

          2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
        • specified form NEC E71.528

ICD-10-CM Codes Adjacent To E71.528
E71.5 Peroxisomal disorders
E71.50 Peroxisomal disorder, unspecified
E71.51 Disorders of peroxisome biogenesis
E71.510 Zellweger syndrome
E71.511 Neonatal adrenoleukodystrophy
E71.518 Other disorders of peroxisome biogenesis
E71.52 X-linked adrenoleukodystrophy
E71.520 Childhood cerebral X-linked adrenoleukodystrophy
E71.521 Adolescent X-linked adrenoleukodystrophy
E71.522 Adrenomyeloneuropathy
E71.528 Other X-linked adrenoleukodystrophy
E71.529 …… unspecified type
E71.53 Other group 2 peroxisomal disorders
E71.54 Other peroxisomal disorders
E71.540 Rhizomelic chondrodysplasia punctata
E71.541 Zellweger-like syndrome
E71.542 Other group 3 peroxisomal disorders
E71.548 Other peroxisomal disorders
E72 Other disorders of amino-acid metabolism
E72.0 Disorders of amino-acid transport
E72.00 …… unspecified

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.

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