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G11.2

Late-onset cerebellar ataxia

Billable FY2026 2025-10-01 → 2026-09-30 valid age >= 15
Exclusions 11 never code together
G11code
Excludes2
  • cerebral palsy (G80.-)G80.-
  • hereditary and idiopathic neuropathy (G60.-)G60.-
  • metabolic disorders (E70-E88)E70-E88
G00-G99chapter
Excludes2
  • certain conditions originating in the perinatal period (P04-P96)P04-P96
  • certain infectious and parasitic diseases (A00-B99)A00-B99
  • complications of pregnancy, childbirth and the puerperium (O00-O9A)O00-O9A
  • congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)Q00-Q99
  • endocrine, nutritional and metabolic diseases (E00-E88)E00-E88
  • injury, poisoning and certain other consequences of external causes (S00-T88)S00-T88
  • neoplasms (C00-D49)C00-D49
  • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)R00-R94

Excludes2 — not included here, but the patient may have both. Code both when documented.

Instructional notes

No further instructional notes apply.

Index entries leading here 3
  • Ataxia, ataxy, ataxic R27.0
    • cerebellar (hereditary) G11.9
      • late-onset (Marie's) G11.2
    • Marie's (cerebellar) (heredofamilial) (late- onset) G11.2
    • Sanger-Brown's (hereditary) G11.2
  • Marie's
    • cerebellar ataxia (late-onset) G11.2
  • Sanger-Brown ataxia G11.2
Alongside this code 8 same parent — G11
Medications 1

MED-RT files conditions by MeSH, which carves the world differently from ICD-10. These are name matches on this code's description, offered as candidates — not as an assertion that they are this code.

Additional references
AHA Coding Clinic® Licence required

Official coding advice for this code. Published by the American Hospital Association. Not included in this installation.

Risk adjustment

CMS22HCC72 CMS28HCC200 ESRD21HCC72 ESRD24HCC72

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This code

Billable
yes
Code set
FY2026
Parent
G11
Block
G10-G14
Siblings
8

Present FY2024–FY2027.