G37.0 ICD-10-CM Code: Diffuse sclerosis of central nervous system
Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.
Coding at a Glance
- Tabular directives
- 2 inclusion terms · 1 Excludes1
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 058 — MULTIPLE SCLEROSIS AND CEREBELLAR ATAXIA WITH MCC (MDC 01)
- MS-DRG 059 — MULTIPLE SCLEROSIS AND CEREBELLAR ATAXIA WITH CC (MDC 01)
- MS-DRG 060 — MULTIPLE SCLEROSIS AND CEREBELLAR ATAXIA WITHOUT CC/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 198 — Multiple Sclerosis
Other models: CMS-HCC V22 HCC 77 · RxHCC V08 HCC 159
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 G37.0 in the official ICD-10-CM tabular list, quoted as published.
Source: CMS/CDC — ICD-10-CM Tabular ListRelease: FY2027Effective: October 1, 2026
Inclusion Terms
Alternative terms the tabular list files under this code.
- Periaxial encephalitis
- Schilder's disease
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).
- X linked adrenoleukodystrophy (E71.52-) Compare G37.0 vs E71.52 →
Coder workflow for G37.0
MedCoder structured workflow — derived from this code’s own official record
Before you code G37.0
- Check the Excludes1 note: if the documentation supports a condition named there, do not simply proceed with G37.0. 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 a condition named in G37.0’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.ReviewE71.52
Consider G37.0. 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).
- Acuity
- Acute or chronic as documented; when both are documented and separate codes exist, both are reported with the acute code first (Guidelines I.B.8).
Official instructions as workflow
Excludes1 — check before selecting G37.0(1 note)
Coding workflow: If the documentation supports a condition named in this note, do not simply proceed with G37.0: the two are not reported together. The one exception is when the record shows the two conditions are unrelated to each other.
CompareE71.52
See the official tabular notes · Guidelines I.A.12.a
Coding decision scenarios
Pattern scenarios for this code’s structure — decision rules, not clinical cases
Documentation: Both the condition G37.0 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).
ReviewE71.52
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.
Indexed Clinical Terms (6)
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.
- Encephalitis (chronic) (hemorrhagic) (idiopathic) (nonepidemic) (spurious) (subacute), periaxial
- Encephalopathy (acute), centrolobar progressive (Schilder)
- Flatau-Schilder disease
- Schilderdisease (-Flatau)
- Sclerosis, sclerotic, brain (generalized) (lobular), diffuse
- Sclerosis, sclerotic, diffuse (brain) (spinal cord)
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 G37.0 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 2 Excludes1 notes: E71.3 — Disorders of fatty-acid metabolism, E71.5 — Peroxisomal disorders.
These codes’ tabular lists mark this diagnosis as mutually exclusive — not reported together unless the conditions are documented as unrelated.
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 13 clinically related codes on its CMS exclusion list.
Named in the grouper logic of 3 MS-DRGs: DRG 058 (MDC 01), DRG 059 (MDC 01), DRG 060 (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):NVS020 — Other nervous system disorders (neither hereditary nor 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.
A92.30 — West Nile virus infection, unspecified, A92.31 — West Nile virus infection with encephalitis, A92.32 — West Nile virus infection with other neurologic manifestation, A92.39 — West Nile virus infection with other complications, 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
Same CMS-HCC risk category (V28)
CMS maps these diagnoses to the same Hierarchical Condition Category (Multiple Sclerosis) for risk-adjusted payment.
G35 — Multiple sclerosis, G35.A — Relapsing-remitting multiple sclerosis, G35.B0 — Primary progressive multiple sclerosis, unspecified, G35.B1 — Active primary progressive multiple sclerosis, G35.B2 — Non-active primary progressive multiple sclerosis, G35.C0 — Secondary progressive multiple sclerosis, unspecified, G35.C1 — Active secondary progressive multiple sclerosis, G35.C2 — Non-active secondary progressive multiple sclerosis, G35.D — Multiple sclerosis, unspecified, G36.0 — Neuromyelitis optica [Devic], G36.1 — Acute and subacute hemorrhagic leukoencephalitis [Hurst], G36.8 — Other specified acute disseminated demyelination, G36.9 — Acute disseminated demyelination, unspecified, G37.1 — Central demyelination of corpus callosum, G37.2 — Central pontine myelinolysis, G37.5 — Concentric sclerosis [Balo] of central nervous system, G37.81 — Myelin oligodendrocyte glycoprotein antibody disease, G37.89 — Other specified demyelinating diseases of central nervous system, G37.9 — Demyelinating disease of central nervous system, unspecified
Same clinical category (CCSR)
AHRQ's Clinical Classifications Software groups these diagnoses under the same clinical category (Other nervous system disorders (neither hereditary nor degenerative)).
E13.44 — Other specified diabetes mellitus with diabetic amyotrophy, G08 — Intracranial and intraspinal phlebitis and thrombophlebitis, G13.0 — Paraneoplastic neuromyopathy and neuropathy, G13.1 — Other systemic atrophy primarily affecting central nervous system in neoplastic disease, G13.2 — Systemic atrophy primarily affecting the central nervous system in myxedema, G13.8 — Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere, G36.0 — Neuromyelitis optica [Devic], G36.1 — Acute and subacute hemorrhagic leukoencephalitis [Hurst], G36.8 — Other specified acute disseminated demyelination, G36.9 — Acute disseminated demyelination, unspecified, G37.1 — Central demyelination of corpus callosum, G37.2 — Central pontine myelinolysis, G37.3 — Acute transverse myelitis in demyelinating disease of central nervous system, G37.4 — Subacute necrotizing myelitis of central nervous system, G37.5 — Concentric sclerosis [Balo] of central nervous system, G37.8 — Other specified demyelinating diseases of central nervous system, G37.81 — Myelin oligodendrocyte glycoprotein antibody disease, G37.89 — Other specified demyelinating diseases of central nervous system, G37.9 — Demyelinating disease of central nervous system, unspecified, G46.0 — Middle cerebral artery syndrome, +97 more
Same Index main term, other category
The ICD-10-CM Index to Diseases and Injuries files this code under the main terms “Sclerosis, sclerotic”, “Encephalitis”, “Encephalopathy”; these codes share that main term but sit in a different category of the Tabular List.
G31.82 — Leigh's disease (necrotizing, subacute), G32.89 — Other specified degenerative disorders of nervous system in diseases classified elsewhere (degenerative, in specified disease NEC), G35.A — Relapsing-remitting multiple sclerosis (multiple, relapsing-remitting), G35.B0 — Primary progressive multiple sclerosis, unspecified (multiple, progressive, primary), G35.B1 — Active primary progressive multiple sclerosis (multiple, progressive, primary, active), G35.B2 — Non-active primary progressive multiple sclerosis (multiple, progressive, primary, non-active), G35.C0 — Secondary progressive multiple sclerosis, unspecified (multiple, progressive, secondary), G35.C1 — Active secondary progressive multiple sclerosis (multiple, progressive, secondary, active), G35.C2 — Non-active secondary progressive multiple sclerosis (multiple, progressive, secondary, non-active), G35.D — Multiple sclerosis, unspecified (dorsal), G61.0 — Guillain-Barre syndrome (spinal, ascending), G92.8 — Other toxic encephalopathy (toxic NEC), G92.9 — Unspecified toxic encephalopathy (toxic), G93.40 — Encephalopathy, unspecified, G93.41 — Metabolic encephalopathy (septic), G93.45 — Developmental and epileptic encephalopathy (early infantile epileptic), G93.49 — Other encephalopathy (specified NEC), G93.81 — Temporal sclerosis (temporal), G93.89 — Other specified disorders of brain (postradiation), G95.89 — Other specified diseases of spinal cord (spinal), +129 more
Contextual Map
Every relationship of G37.0 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 G37.0 with these 3 related codes in Claim Check
Hierarchy
- G00-G99 — Chapter 6: Diseases of the Nervous System (G00-G99) (G00-G99)[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- G35-G37 — Demyelinating diseases of the central nervous system[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
Excludes1
- E71.52 — X-linked adrenoleukodystrophy[Excludes1]: “X linked adrenoleukodystrophy (E71.52-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Referenced by Excludes1 notes
- E71.3 — Disorders of fatty-acid metabolism[Excludes1]: “Schilder's disease (G37.0)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- E71.5 — Peroxisomal disorders[Excludes1]: “Schilder's disease (G37.0)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Clinical classification (CCSR)
- NVS020 — Other nervous system disorders (neither hereditary nor degenerative)[CCSR]— AHRQ CCSR for ICD-10-CM Diagnoses (HCUP)
Risk adjustment (CMS-HCC)
- HCC 198 — Multiple Sclerosis [CMS-HCC]— CMS-HCC V28 · 2026
MS-DRG Grouper
- CC — Complication or Comorbidity [MS-DRG severity]: “As a secondary diagnosis this code can raise the stay's MS-DRG severity tier (CC).”— CMS MS-DRG Definitions Manual (Appendix C) · FY2027
- DRG 058 — MULTIPLE SCLEROSIS AND CEREBELLAR ATAXIA WITH MCC[MS-DRG]: “MULTIPLE SCLEROSIS AND CEREBELLAR ATAXIA WITH MCC (MDC 01)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2027
- DRG 059 — MULTIPLE SCLEROSIS AND CEREBELLAR ATAXIA WITH CC[MS-DRG]: “MULTIPLE SCLEROSIS AND CEREBELLAR ATAXIA WITH CC (MDC 01)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2027
- DRG 060 — MULTIPLE SCLEROSIS AND CEREBELLAR ATAXIA WITHOUT CC/MCC[MS-DRG]: “MULTIPLE SCLEROSIS AND CEREBELLAR ATAXIA WITHOUT CC/MCC (MDC 01)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2027
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
- Encephalitis (chronic) (hemorrhagic) (idiopathic) (nonepidemic) (spurious) (subacute), periaxial[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Encephalopathy (acute), centrolobar progressive (Schilder)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Flatau-Schilder disease[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Schilderdisease (-Flatau)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Sclerosis, sclerotic, brain (generalized) (lobular), diffuse[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Sclerosis, sclerotic, diffuse (brain) (spinal cord)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
Nearest codes (10)
- G37 — Other demyelinating diseases of central nervous system[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- G37.1 — Central demyelination of corpus callosum[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- G37.2 — Central pontine myelinolysis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- G37.3 — Acute transverse myelitis in demyelinating disease of central nervous system[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- G37.4 — Subacute necrotizing myelitis of central nervous system[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- G37.5 — Concentric sclerosis [Balo] of central nervous system[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- G37.8 — Other specified demyelinating diseases of central nervous system[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- G37.81 — Myelin oligodendrocyte glycoprotein antibody disease[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- and 2 more
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. "G37.0 — Diffuse sclerosis of central nervous system." ICD-10-CM FY2027. https://medcoder.ai/icd10/code/g37.0-diffuse-sclerosis-of-central-nervous-system
Change history
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionDiffuse sclerosis of central nervous system
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 G37.0 in its code family, with their registry titles.
- G37 — Other demyelinating diseases of central nervous system
- G37.1 — Central demyelination of corpus callosum
- G37.2 — Central pontine myelinolysis
- G37.3 — Acute transverse myelitis in demyelinating disease of central nervous system
- G37.4 — Subacute necrotizing myelitis of central nervous system
- G37.5 — Concentric sclerosis [Balo] of central nervous system
- G37.8 — Other specified demyelinating diseases of central nervous system
- G37.81 — Myelin oligodendrocyte glycoprotein antibody disease
- G37.89 — Other specified demyelinating diseases of central nervous system
- G37.9 — Demyelinating disease of central nervous system, unspecified