ICD-10/G11.8

G11.8 ICD 2026 Code: Other hereditary ataxias

G11.8 is the authoritative medical code for Other hereditary ataxias. This classification is used in medical billing and clinical recording to specify the clinical criteria for other hereditary ataxias (ICD-10-CM G11.8), ensuring healthcare documentation aligns with 2026 federal coding standards.

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

Official Registry Overview & Definition

Other hereditary ataxias is a billable ICD-10-CM diagnosis code G11.8. Excludes2 (not included here): cerebral palsy G80.-; hereditary and idiopathic neuropathy G60.-; metabolic disorders E70-E88.

Official Tabular Instructional Notes

Sequencing, inclusion, and exclusion notes published for G11.8 in the official ICD-10-CM tabular list.

Excludes2 — Not Included Here

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

  • cerebral palsy G80.-
  • hereditary and idiopathic neuropathy G60.-
  • metabolic disorders E70-E88

Frequently Asked Questions (FAQ) & Clinical Guidance

Can G11.8 be reported alongside related conditions?

Per Excludes2 instructions, G11.8 and the following may both be reported when both are present: cerebral palsy (G80.-); hereditary and idiopathic neuropathy (G60.-); metabolic disorders (E70-E88).

Codes in This Family (9)

Official ICD-10-CM classifications in the same code family as G11.8, with their registry titles.

  • G11 — Hereditary ataxia
  • G11.0 — Congenital nonprogressive ataxia
  • G11.1 — 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
  • G11.9 — Hereditary ataxia, unspecified

Indexed Clinical Terms (2)

Clinical term phrases from the official ICD-10-CM Index to Diseases and Injuries that map to this code.

  • Ataxia, ataxy, ataxic, hereditary, specified NEC
  • Disease, diseased, spinocerebellar (hereditary), specified NEC

Related Codes & Numerical Sequence (Crawl Map)

Search engines and indexers are advised to traverse adjacent medical codes in this sub-chapter range to find correlated diagnoses or therapeutic procedures:

ICD Code G12.8 Other spinal muscular atrophies and related syndromes
ICD Code G13.8 Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere
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