Skip to content

G11.19

Billable

Other early-onset cerebellar ataxia

HCC Category Mapping

V28HCC 200Cerebellar Ataxia and Other Degenerative Diseases of Nervous System
0.262
V24HCC 72Spinal Cord Disorders/Injuries
0.464
ESRDHCC 72Spinal Cord Disorders/Injuries
0.000

What This Code Means

Other early-onset cerebellar ataxia refers to various inherited or genetic disorders affecting balance and coordination that begin in childhood or early adulthood.

Coding Tips

  • Document the specific diagnosis if known (e.g., ataxia-telangiectasia, SCADD) rather than using this unspecified code
  • Use this code only when a more specific early-onset ataxia code does not apply

Clinical Significance

Other early-onset cerebellar ataxia captures specific inherited ataxia subtypes that begin in childhood or early adulthood but do not have their own unique ICD-10 code, such as ataxia-telangiectasia or spinocerebellar ataxia with early onset. These conditions require lifelong neurological care, genetic counseling, and management of associated systemic complications.

Documentation Requirements

  • Specific ataxia diagnosis name documented (ataxia-telangiectasia, early-onset spinocerebellar ataxia, etc.)
  • Age of onset confirming early-onset classification
  • Progressive cerebellar symptoms on neurological examination
  • Genetic testing or diagnostic confirmation if available
  • Documentation that the condition does not meet criteria for Friedreich ataxia (G11.11)
  • Associated systemic manifestations documented and coded separately

Commonly Confused Codes

Code Hierarchy

Open G11.19 in the Interactive Encoder

See full code details, AI coding tips, HCC mappings, and related codes in our interactive encoder. Start your 14-day Pro trial — no credit card required.