E71.52 ICD-10-CM Code: X-linked adrenoleukodystrophy
Billing Status: NO. This is a clinician non-billable / parent hierarchy grouping in the ICD-10-CM system.
Coding at a Glance
- Tabular directives
- 6 Excludes1 · 1 Excludes2
Coding instructions
Official Tabular Instructional Notes: the inclusion, exclusion and sequencing notes published for E71.52 in the official ICD-10-CM tabular list, quoted as published.
Source: CMS/CDC — ICD-10-CM Tabular ListRelease: FY2026Effective: October 1, 2025
Notes without a marker are published on E71.52 itself; “inherited from” names the category or block whose note applies here.
Excludes1 — Not Coded Here
Conditions generally not reported together with this code (Excludes1) -- an error unless the two conditions are documented as unrelated to each other (ICD-10-CM Official Guidelines, Section I.A.12.a).
- Schilder's disease (G37.0) inherited from E71.5Compare E71.52 vs G37.0 →
- androgen insensitivity syndrome (E34.5-) inherited from E70-E88Compare E71.52 vs E34.5 →
- congenital adrenal hyperplasia (E25.0) inherited from E70-E88Compare E71.52 vs E25.0 →
- hemolytic anemias attributable to enzyme disorders (D55.-) inherited from E70-E88Compare E71.52 vs D55 →
- Marfan syndrome (Q87.4-) inherited from E70-E88Compare E71.52 vs Q87.4 →
- 5-alpha-reductase deficiency (E29.1) inherited from E70-E88Compare E71.52 vs E29.1 →
Excludes2 — Not Included Here
Conditions not covered by this code, but which may be reported alongside it when both are present.
- Ehlers-Danlos syndromes (Q79.6-) Compare E71.52 vs Q79.6 →
Source: inherited from E70-E88
Coder workflow for E71.52
MedCoder structured workflow — derived from this code’s own official record
Before you code E71.52
- E71.52 is not reportable as written. Select the more specific code beneath it that the documentation supports. Codes are reported to the highest level of specificity the classification provides (Guidelines I.B.2).
ReviewE71.520, E71.521, E71.522, E71.528, E71.529
See the relationships section · Guide: How to choose an ICD-10-CM code →
- Check the Excludes1 note: if the documentation supports a condition named there, do not simply proceed with E71.52. Excludes1 conditions are not reported together with this code unless the record shows they are unrelated (Guidelines I.A.12.a).
Choose the right path
- Does the documentation support one of the more specific codes beneath E71.52?
Yes → Select that code and continue the checks below on its own page.
No → E71.52 cannot be reported as written; query for the specificity its subcategory needs. - Does the documentation support a condition named in E71.52’s Excludes1 note?
Yes → Do not simply proceed: review the excluded code. Both are reported only when the record shows the two conditions are unrelated.
No → Continue.
Consider E71.52. Then confirm the code is valid for the date of service in the Verify section.
Documentation check
- The provider’s diagnostic statement
- Codes are assigned from the provider’s documented diagnosis, not from clinical criteria, test values or a medication list (Guidelines I.A.19).
Official instructions as workflow
Excludes1 — check before selecting E71.52(6 notes)
Coding workflow: If the documentation supports a condition named in this note, do not simply proceed with E71.52: the two are not reported together. The one exception is when the record shows the two conditions are unrelated to each other.
CompareG37.0, E34.5, E25.0, D55, Q87.4, E29.1
See the official tabular notes · Guidelines I.A.12.a
Excludes2 — not part of E71.52(1 note)
Coding workflow: The conditions named in this note are not included in E71.52. When the record documents both, both may be reported; the note is a boundary, not a prohibition.
CompareQ79.6
See the official tabular notes · Guidelines I.A.12.b
Coding decision scenarios
Pattern scenarios for this code’s structure — decision rules, not clinical cases
Documentation: Both the condition E71.52 describes and a condition named in its Excludes1 note are documented for the same encounter.
Coding question: Can both codes be reported?
Path: Review the Excludes1 note and the excluded code, and look for a provider statement on whether the two conditions are related.
Reason: Excludes1 means the two are not coded together; the exception is when the record shows the conditions are unrelated to each other (Guidelines I.A.12.a).
Every row is derived from this code’s own record — its title, tabular notes, 7th-character family and same-category siblings — with fixed MedCoder wording; nothing is inferred about a patient. The official notes and guideline text are in the sections each row links to, and they control.
Code Overview
MedCoder summary Summary composed by MedCoder from this code's official ICD-10-CM record. The tabular instructional notes themselves appear verbatim below.
Verify Before Coding
- Not billable as written — a more specific code is required: E71.520, E71.521, E71.522, E71.528, E71.529.
From the code registry, the Medicare Code Editor, and the MS-DRG Definitions Manual. Check it against a full claim in Claim Check.
Relationships & Classification
MedCoder structured relationships — computed from published CMS and AHRQ datasets
Other codes that name E71.52 or its code family, from the CMS ICD-10-CM tabular instructional notes. Tabular-note edges are stored at the code family level that carries each note.
Referenced by 8 Excludes1 notes across 3 chapters: G37.0 — Diffuse sclerosis of central nervous system, P59 — Neonatal jaundice from other and unspecified causes (via E71.-), R79 — Other abnormal findings of blood chemistry (via E71.-), R79.83 — Abnormal findings of blood amino-acid level (via E71.-), R80 — Proteinuria (via E71.-), R80-R82 — Abnormal findings on examination of urine, without diagnosis (R80-R82) (via E71.-), R81 — Glycosuria (via E71.-), R82 — Other and unspecified abnormal findings in urine (via E71.-).
These codes’ tabular lists mark this diagnosis as mutually exclusive — not reported together unless the conditions are documented as unrelated.
Referenced by 4 Excludes2 notes across 2 chapters: G11 — Hereditary ataxia (via E71.-), G71 — Primary disorders of muscles (via E71.-), N25.0 — Renal osteodystrophy (via E71.-), N25.81 — Secondary hyperparathyroidism of renal origin (via E71.-).
These codes’ tabular lists name this diagnosis as distinct — both may be reported when both are documented.
Referenced by 2 Code First instructions across 2 chapters: G63 — Polyneuropathy in diseases classified elsewhere (via E71.-), H42 — Glaucoma in diseases classified elsewhere (via E71.-).
Each of these codes carries a Code First note naming this condition — when that code is reported, THIS code is sequenced first, ahead of it.
Related Codes
Same Index main term, other category
The ICD-10-CM Index to Diseases and Injuries files this code under the main term “Aciduria”; these codes share that main term but sit in a different category of the Tabular List.
D53.0 — Protein deficiency anemia (orotic, anemia), E72.22 — Arginosuccinic aciduria (argininosuccinic), E72.3 — Disorders of lysine and hydroxylysine metabolism (glutaric), E72.81 — Disorders of gamma aminobutyric acid metabolism (4-hydroxybutyric), E79.89 — Other specified disorders of purine and pyrimidine metabolism (orotic)
Contextual Map
Every relationship of E71.52 in one view: hierarchy, official tabular instructions in both directions, clinical classification, risk adjustment, MS-DRG participation, index terms and change history — each edge carrying the CMS source it derives from.
Run E71.52 with these 14 related codes in Claim Check
Hierarchy
- E00-E89 — Chapter 4: Endocrine, Nutritional and Metabolic Diseases (E00-E89) (E00-E89)[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E70-E88 — Metabolic disorders[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
Referenced by Excludes1 notes
- G37.0 — Diffuse sclerosis of central nervous system[Excludes1]: “X linked adrenoleukodystrophy (E71.52-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- P59 — Neonatal jaundice from other and unspecified causes[Excludes1](via E71.-): “jaundice due to inborn errors of metabolism (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- R79 — Other abnormal findings of blood chemistry[Excludes1](via E71.-): “specific findings indicating disorder of amino-acid metabolism (E70-E72)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- R79.83 — Abnormal findings of blood amino-acid level[Excludes1](via E71.-): “disorders of amino-acid metabolism (E70-E72)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- R80 — Proteinuria[Excludes1](via E71.-): “specific findings indicating disorder of amino-acid metabolism (E70-E72)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- R80-R82 — Abnormal findings on examination of urine, without diagnosis (R80-R82)[Excludes1](via E71.-): “specific findings indicating disorder of amino-acid metabolism (E70-E72)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- R81 — Glycosuria[Excludes1](via E71.-): “specific findings indicating disorder of amino-acid metabolism (E70-E72)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- R82 — Other and unspecified abnormal findings in urine[Excludes1](via E71.-): “specific findings indicating disorder of amino-acid metabolism (E70-E72)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Referenced by Excludes2 notes
- G11 — Hereditary ataxia[Excludes2](via E71.-): “metabolic disorders (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- G71 — Primary disorders of muscles[Excludes2](via E71.-): “metabolic disorders (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- N25.0 — Renal osteodystrophy[Excludes2](via E71.-): “metabolic disorders classifiable to E70-E88”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- N25.81 — Secondary hyperparathyroidism of renal origin[Excludes2](via E71.-): “metabolic disorders classifiable to E70-E88”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Referenced by Code First instructions
- G63 — Polyneuropathy in diseases classified elsewhere[Code First](via E71.-): “metabolic diseases (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- H42 — Glaucoma in diseases classified elsewhere[Code First](via E71.-): “specified metabolic disorder (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Nearest codes (40)
- E71 — Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E71.121 — Propionic acidemia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E71.128 — Other disorders of propionate metabolism[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E71.19 — Other disorders of branched-chain amino-acid metabolism[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E71.2 — Disorder of branched-chain amino-acid metabolism, unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E71.3 — Disorders of fatty-acid metabolism[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E71.30 — Disorder of fatty-acid metabolism, unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E71.31 — Disorders of fatty-acid oxidation[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- and 32 more
Change history
- FY2016 — In the code set at ICD-10-CM adoption [Change history]— CMS release files (code change ledger) · icd10cm-fy2016
Common coding questions
Can E71.52 be billed directly?
No. E71.52 (X-linked adrenoleukodystrophy) is a non-billable ICD-10-CM category code. A more specific billable subcode must be selected based on clinical documentation.
Sources for this page
Codes, titles, notes, index terms and mappings on this page are transcribed from the datasets below. Relationships MedCoder computed and text MedCoder wrote are labelled where they appear.
- Code, title, tabular notes and index terms Official source data
- CMS/CDC ICD-10-CM FY2026 tabular list, index and tables, effective October 1, 2025 Release, file and checksum · Publisher’s page
- Claim edits Official source data
- CMS Definitions of Medicare Code Edits — v43.1 (April 2026) Release, file and checksum · Publisher’s page
- Change history and date-of-service validity Official source data
- CMS ICD-10-CM release addenda, ingested release by release into the change ledger Release, file and checksum · Publisher’s page
- Comparisons, relationships and the contextual map MedCoder structured relationship
- Computed by MedCoder from the tabular notes and tables above; every derived relationship is marked as derived where it appears
- Summary and FAQ answers MedCoder explanation
- Written by MedCoder to explain the sources above: drafted with AI assistance, checked by a person against the release files, and labelled as MedCoder text where it appears. Not official text.
Labels on this page: Official source data · MedCoder structured relationship · MedCoder explanation. How to read the labels · All data sources and release dates
Cite this page
Reference this page in a research guide, syllabus or article. The release is included because code content changes each year.
MedCoder.ai. "E71.52 — X-linked adrenoleukodystrophy." ICD-10-CM FY2026. https://medcoder.ai/icd10/code/e71.52-x-linked-adrenoleukodystrophy
Change history
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionX-linked adrenoleukodystrophy
No changes since FY2016 — additions, deletions, description changes and billable-status changes are tracked through FY2027 (effective October 1, 2026), and none are recorded for this code. Note changes are tracked from FY2027 only.
Nearest Codes in This Family
Official ICD-10-CM classifications closest to E71.52 in its code family, with their registry titles.
- 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
- E71.520 — Childhood cerebral X-linked adrenoleukodystrophy
- E71.521 — Adolescent X-linked adrenoleukodystrophy
- E71.522 — Adrenomyeloneuropathy
- E71.528 — Other X-linked adrenoleukodystrophy
- E71.529 — X-linked adrenoleukodystrophy, unspecified type