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G23.0 ICD-10-CM Code: Hallervorden-Spatz disease

Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.

Coding at a Glance

Tabular directives
1 inclusion term · 1 Excludes2
Risk adjustment
CMS-HCC V28: 1 category · CMS-HCC V22 category 78 · RxHCC V08 category 161

Inpatient Payment Groups (MS-DRG)

Potential MS-DRG participation — not a DRG assignment.

MS-DRGs this diagnosis helps define, as principal or secondary, per the CMS ICD-10-CM/PCS MS-DRG Definitions Manual v44, Appendix B.

  • MS-DRG 056 — DEGENERATIVE NERVOUS SYSTEM DISORDERS WITH MCC (MDC 01)
  • MS-DRG 057 — DEGENERATIVE NERVOUS SYSTEM DISORDERS WITHOUT MCC (MDC 01)

A diagnosis appearing in a group's logic does not by itself determine the DRG assigned to a stay; the grouper uses the full claim.

Risk Adjustment (CMS-HCC)

Payment categories this diagnosis maps to under CMS-HCC V28, payment year 2026.

  • HCC 199 — Parkinson and Other Degenerative Disease of Basal Ganglia

Other models: CMS-HCC V22 HCC 78 · RxHCC V08 HCC 161

Risk scores depend on the enrollee's full accepted diagnosis set and segment; a category mapping alone does not determine payment.

Coding instructions

Official Tabular Instructional Notes: the inclusion, exclusion and sequencing notes published for G23.0 in the official ICD-10-CM tabular list, quoted as published.

Source: CMS/CDC — ICD-10-CM Tabular ListRelease: FY2027Effective: October 1, 2026

Trace:FY2027 changesChange historyRelease, file and checksum

Notes without a marker are published on G23.0 itself; “inherited from” names the category or block whose note applies here.

Inclusion Terms

Alternative terms the tabular list files under this code.

  • Pigmentary pallidal degeneration

Excludes2 — Not Included Here

Conditions not covered by this code, but which may be reported alongside it when both are present.

Source: inherited from G23

Coder workflow for G23.0

MedCoder structured workflow — derived from this code’s own official record

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

  • Excludes2 — not part of G23.0(1 note)

    Coding workflow: The conditions named in this note are not included in G23.0. When the record documents both, both may be reported; the note is a boundary, not a prohibition.

    CompareG90.3

    See the official tabular notes · Guidelines I.A.12.b

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.

Don’t confuse G23.0 with…

MedCoder analysis — pairs from this code’s official notes, distinctions written by MedCoder

The codes most likely to be picked instead of G23.0 — named in its own official notes, or sharing its laterality or encounter family — with what separates them and which documentation moves the case. Each links to the full comparison.

  • G23.9— Specificity relationship (Review)

    Overlapping diagnoses in the same category.

    Overlapping codes in the same category — the documentation decides which is the more specific fit.

    What moves you there: A record that documents no more than “Degenerative disease of basal ganglia, unspecified” takes G23.9; specificity in the record moves it back here.

    Full comparison: G23.0 vs G23.9 →

  • G90.3— Excludes2 relationship (Informational)

    Distinct conditions — both may be reported.

    A distinct condition — both may be reported when both are documented.

    What moves you there: Documentation of multi-system degeneration of the autonomic nervous system adds G90.3; it is not part of this code and both may be reported when both are documented.

    Full comparison: G23.0 vs G90.3 →

Relationships are read from this code's own official notes, its laterality siblings and its encounter family; the wording of each distinction is MedCoder editorial, and the documentation named in each “what moves you there” line is the official note phrase or sibling title itself. Source: CMS ICD-10-CM tabular instructional notes; ICD-10-CM Official Guidelines, Section I.A.12.a.

Code Overview

Hallervorden-Spatz disease is a billable ICD-10-CM diagnosis code (G23.0).

MedCoder summary Summary composed by MedCoder from this code's official ICD-10-CM record. The tabular instructional notes themselves appear verbatim below.

Indexed Clinical Terms (4)

Official source data — entries quoted as published, in the Index’s own lookup phrasing

Clinical term phrases from the official ICD-10-CM Index to Diseases and Injuries that map to this code. These are alphabetic-index entries shown as the Index writes them — lookup phrasing, not necessarily the wording of a final diagnosis.

Verify Before Coding

  • CC as a secondary diagnosis (FY2027). Can raise the stay's MS-DRG severity tier.

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 G23.0 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 1 Excludes1 note: R25 — Abnormal involuntary movements (via G23.-).

These codes’ tabular lists mark this diagnosis as mutually exclusive — not reported together unless the conditions are documented as unrelated.

Referenced by 1 Excludes2 note: F98.4 — Stereotyped movement disorders (via G23.-).

These codes’ tabular lists name this diagnosis as distinct — both may be reported when both are documented.

MS-DRG Grouper Relationships (FY2027)

Potential MS-DRG participation — not a DRG assignment.

FY2027 MS-DRG: CC — Complication or Comorbidity. Reported as a secondary diagnosis, this code raises the stay's MS-DRG severity tier — except when the principal diagnosis is one of 23 clinically related codes on its CMS exclusion list.

Named in the grouper logic of 2 MS-DRGs: DRG 056 (MDC 01), DRG 057 (MDC 01).

From the CMS MS-DRG Definitions Manual (Appendices B and C). Actual DRG assignment depends on the complete claim.

Clinical classification (AHRQ CCSR):NVS006 — Other nervous system disorders (often hereditary or degenerative) (default).

Clinical Classifications Software Refined (CCSR) for ICD-10-CM Diagnoses. Healthcare Cost and Utilization Project (HCUP), Agency for Healthcare Research and Quality.

Related Codes

Same clinical process (MS-DRG)

Acts as CC — raises the severity of other admissions. CMS groups these diagnoses into one MS-DRG principal-diagnosis exclusion process — a CC/MCC on this list never raises severity when the principal diagnosis is also on it.

G20.B1 — Parkinson's disease with dyskinesia, without mention of fluctuations, G20.B2 — Parkinson's disease with dyskinesia, with fluctuations, G20.C — Parkinsonism, unspecified, G21.11 — Neuroleptic induced parkinsonism, G21.19 — Other drug induced secondary parkinsonism, G21.2 — Secondary parkinsonism due to other external agents, G21.3 — Postencephalitic parkinsonism, G21.4 — Vascular parkinsonism, G21.8 — Other secondary parkinsonism, G21.9 — Secondary parkinsonism, unspecified, G90.01 — Carotid sinus syncope, G90.09 — Other idiopathic peripheral autonomic neuropathy, G93.40 — Encephalopathy, unspecified, G93.41 — Metabolic encephalopathy, G93.42 — Megalencephalic leukoencephalopathy with subcortical cysts, G93.43 — Leukoencephalopathy with calcifications and cysts, G93.44 — Adult-onset leukodystrophy with axonal spheroids, G93.45 — Developmental and epileptic encephalopathy, G93.49 — Other encephalopathy, I67.83 — Posterior reversible encephalopathy syndrome, +2 more

Same CMS-HCC risk category (V28)

CMS maps these diagnoses to the same Hierarchical Condition Category (Parkinson and Other Degenerative Disease of Basal Ganglia) for risk-adjusted payment.

G20.A1 — Parkinson's disease without dyskinesia, without mention of fluctuations, G20.A2 — Parkinson's disease without dyskinesia, with fluctuations, G20.B1 — Parkinson's disease with dyskinesia, without mention of fluctuations, G20.B2 — Parkinson's disease with dyskinesia, with fluctuations, G20.C — Parkinsonism, unspecified, G21.3 — Postencephalitic parkinsonism, G21.4 — Vascular parkinsonism, G21.8 — Other secondary parkinsonism, G21.9 — Secondary parkinsonism, unspecified, G23.1 — Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski], G23.2 — Striatonigral degeneration, G23.3 — Hypomyelination with atrophy of the basal ganglia and cerebellum, G23.8 — Other specified degenerative diseases of basal ganglia, G23.9 — Degenerative disease of basal ganglia, unspecified, G90.3 — Multi-system degeneration of the autonomic nervous system

Same clinical category (CCSR)

AHRQ's Clinical Classifications Software groups these diagnoses under the same clinical category (Other nervous system disorders (often hereditary or degenerative)).

G12.8 — Other spinal muscular atrophies and related syndromes, G12.9 — Spinal muscular atrophy, unspecified, G21.0 — Malignant neuroleptic syndrome, G21.11 — Neuroleptic induced parkinsonism, G21.19 — Other drug induced secondary parkinsonism, G21.2 — Secondary parkinsonism due to other external agents, G21.3 — Postencephalitic parkinsonism, G21.4 — Vascular parkinsonism, G21.8 — Other secondary parkinsonism, G21.9 — Secondary parkinsonism, unspecified, G23.1 — Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski], G23.2 — Striatonigral degeneration, G23.3 — Hypomyelination with atrophy of the basal ganglia and cerebellum, G23.8 — Other specified degenerative diseases of basal ganglia, G23.9 — Degenerative disease of basal ganglia, unspecified, G24.01 — Drug induced subacute dyskinesia, G24.02 — Drug induced acute dystonia, G24.09 — Other drug induced dystonia, G24.1 — Genetic torsion dystonia, G24.2 — Idiopathic nonfamilial dystonia, +83 more

Same Index main term, other category

The ICD-10-CM Index to Diseases and Injuries files this code under the main term “Degeneration, degenerative”; these codes share that main term but sit in a different category of the Tabular List.

E75.3 — Sphingolipidosis, unspecified (brain, in, sphingolipidosis), E75.4 — Neuronal ceroid lipofuscinosis (brain, in, lipidosis, cerebral), E75.6 — Lipid storage disorder, unspecified (brain, in, lipidosis, generalized), E76.1 — Mucopolysaccharidosis, type II (brain, in, Hunter's syndrome), E83.01 — Wilson's disease (lenticular), E85.4 — Organ-limited amyloidosis (skin, amyloid), E85.89 — Other amyloidosis (capillaries, amyloid), E85.9 — Amyloidosis, unspecified (amyloid), G11.9 — Hereditary ataxia, unspecified (cerebellar NOS, primary), G12.29 — Other motor neuron disease (anterior cornua, spinal cord), G25.9 — Extrapyramidal and movement disorder, unspecified (extrapyramidal), G31.1 — Senile degeneration of brain, not elsewhere classified (senile, brain), G31.2 — Degeneration of nervous system due to alcohol (brain, alcoholic), G31.81 — Alpers disease (grey matter), G31.85 — Corticobasal degeneration (corticobasal), G31.89 — Other specified degenerative diseases of nervous system (spinal), G31.9 — Degenerative disease of nervous system, unspecified (brain), G37.9 — Demyelinating disease of central nervous system, unspecified (myelin, central nervous system), G54.0 — Brachial plexus disorders (brachial plexus), G54.2 — Cervical root disorders, not elsewhere classified (cervical plexus), +116 more

Contextual Map

Every relationship of G23.0 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 G23.0 with these 2 related codes in Claim Check

Hierarchy

Referenced by Excludes1 notes

Referenced by Excludes2 notes

Clinical classification (CCSR)

Risk adjustment (CMS-HCC)

  • HCC 199 — Parkinson and Other Degenerative Disease of Basal Ganglia [CMS-HCC]— CMS-HCC V28 · 2026

MS-DRG Grouper

MDC crossing

  • MDC 01 — Diseases and Disorders of the Nervous System[MDC crossing]: “Diseases and Disorders of the Nervous System — the grouper's crossing between diagnoses and procedures: a principal diagnosis sets the MDC, and same-MDC procedures move the stay to its surgical DRGs. 8,919 same-MDC procedures group here; browse them on the MDC page.”— CMS MS-DRG Definitions Manual · FY2027

Index entries

  • Degeneration, degenerative, pallidal pigmentary (progressive)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
  • Degeneration, degenerative, pigmentary (diffuse) (general), pallidal (progressive)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
  • Hallervorden-Spatz disease[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
  • Syndrome, pigmentary pallidal degeneration (progressive)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026

Nearest codes

Change history

  • FY2016 — In the code set at ICD-10-CM adoption [Change history]— CMS release files (code change ledger) · icd10cm-fy2016

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 FY2027 tabular list, index and tables, effective October 1, 2026 Release, file and checksum · Publisher’s page
Claim edits Official source data
CMS Definitions of Medicare Code Edits — v44.0 (October 2026) Release, file and checksum · Publisher’s page
Inpatient payment groups Official source data
CMS MS-DRG Definitions Manual (incl. Appendix B diagnosis index, Appendix C CC/MCC list, Appendix E procedure index) and IPPS Final Rule tables — v44 Release, file and checksum · Publisher’s page
Risk adjustment Official source data
2026 Mid-Year Final ICD-10 Mappings + Model Software (cms.gov/files/zip/2026-midyear-final-icd-10-mappings.zip, 2026-midyear-final-model-software.zip) — CMS-HCC V28, PY2026 mid-year final release 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. "G23.0 — Hallervorden-Spatz disease." ICD-10-CM FY2027. https://medcoder.ai/icd10/code/g23.0-hallervorden-spatz-disease

Change history

  • FY2016 — October 1, 2015
    In the code set at ICD-10-CM adoption
    Hallervorden-Spatz disease

No changes since FY2016 — additions, deletions, description changes and billable-status changes are tracked through FY2027, 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 G23.0 in its code family, with their registry titles.

View all codes in the G23 family