G11 ICD-10-CM Code: Hereditary ataxia
Billing Status: NO. This is a clinician non-billable / parent hierarchy grouping in the ICD-10-CM system.
Coding at a Glance
- Tabular directives
- 3 Excludes2
Coding instructions
Official Tabular Instructional Notes: the inclusion, exclusion and sequencing notes published for G11 in the official ICD-10-CM tabular list, quoted as published.
Source: CMS/CDC — ICD-10-CM Tabular ListRelease: FY2026Effective: October 1, 2025
Excludes2 — Not Included Here
Conditions not covered by this code, but which may be reported alongside it when both are present.
- cerebral palsy (G80.-) Compare G11 vs G80 →
- hereditary and idiopathic neuropathy (G60.-) Compare G11 vs G60 →
- metabolic disorders (E70-E88) Compare G11 vs E70 →
Coder workflow for G11
MedCoder structured workflow — derived from this code’s own official record
Before you code G11
- G11 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).
ReviewG11.0, G11.1, G11.2, G11.3, G11.4, G11.5, G11.6, G11.8, G11.9
See the relationships section · Guide: How to choose an ICD-10-CM code →
Choose the right path
- Does the documentation support one of the more specific codes beneath G11?
Yes → Select that code and continue the checks below on its own page.
No → G11 cannot be reported as written; query for the specificity its subcategory needs.ReviewG11.0, G11.1, G11.2, G11.3, G11.4, G11.5, G11.6, G11.8, G11.9
Consider G11. 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
Excludes2 — not part of G11(3 notes)
Coding workflow: The conditions named in this note are not included in G11. When the record documents both, both may be reported; the note is a boundary, not a prohibition.
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.
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
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 G11 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: R26 — Abnormalities of gait and mobility, R27 — Other lack of coordination.
These codes’ tabular lists mark this diagnosis as mutually exclusive — not reported together unless the conditions are documented as unrelated.
Contextual Map
Every relationship of G11 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 G11 with these 10 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
- G10-G14 — Systemic atrophies primarily affecting the central nervous system[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
Excludes2 (19)
- E70 — Disorders of aromatic amino-acid metabolism[Excludes2]: “metabolic disorders (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- E71 — Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism[Excludes2]: “metabolic disorders (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- E72 — Other disorders of amino-acid metabolism[Excludes2]: “metabolic disorders (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- E73 — Lactose intolerance[Excludes2]: “metabolic disorders (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- E74 — Other disorders of carbohydrate metabolism[Excludes2]: “metabolic disorders (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- E75 — Disorders of sphingolipid metabolism and other lipid storage disorders[Excludes2]: “metabolic disorders (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- E76 — Disorders of glycosaminoglycan metabolism[Excludes2]: “metabolic disorders (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- E77 — Disorders of glycoprotein metabolism[Excludes2]: “metabolic disorders (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- and 11 more
Referenced by Excludes1 notes
- R26 — Abnormalities of gait and mobility[Excludes1]: “hereditary ataxia (G11.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- R27 — Other lack of coordination[Excludes1]: “hereditary ataxia (G11.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Nearest codes (12)
- G11.0 — Congenital nonprogressive ataxia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- G11.1 — Early-onset cerebellar ataxia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- G11.10 — Early-onset cerebellar ataxia, unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- G11.11 — Friedreich ataxia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- G11.19 — Other early-onset cerebellar ataxia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- G11.2 — Late-onset cerebellar ataxia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- G11.3 — Cerebellar ataxia with defective DNA repair[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- G11.4 — Hereditary spastic paraplegia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- and 4 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 G11 be billed directly?
No. G11 (Hereditary ataxia) 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. "G11 — Hereditary ataxia." ICD-10-CM FY2026. https://medcoder.ai/icd10/code/g11-hereditary-ataxia
Change history
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionHereditary ataxia
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 G11 in its code family, with their registry titles.
- G11.0 — Congenital nonprogressive ataxia
- G11.1 — Early-onset cerebellar ataxia
- G11.10 — Early-onset cerebellar ataxia, unspecified
- G11.11 — Friedreich ataxia
- G11.19 — Other early-onset cerebellar ataxia
- G11.2 — Late-onset cerebellar ataxia
- G11.3 — Cerebellar ataxia with defective DNA repair
- G11.4 — Hereditary spastic paraplegia
- G11.5 — Hypomyelination - hypogonadotropic hypogonadism - hypodontia
- G11.6 — Leukodystrophy with vanishing white matter disease
- G11.8 — Other hereditary ataxias
- G11.9 — Hereditary ataxia, unspecified