AutoICD API

G11.19

Billable

Other early-onset cerebellar ataxia

Other early-onset cerebellar ataxia

Status

Billable / Specific

Block

G10-G14

Parent Code

G11.1

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Early-onset cerebellar ataxia with essential tremor
  • Early-onset cerebellar ataxia with myoclonus [Hunt's ataxia]
  • Early-onset cerebellar ataxia with retained tendon reflexes
  • X-linked recessive spinocerebellar ataxia

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(2)
G11.10

Early-onset cerebellar ataxia, unspecified

BillableG11.11

Friedreich ataxia

Billable
Also Known As / Clinical Terms(120)

SNOMED CT

UMLS

Clinical Terms

  • Early onset cerebellar ataxia with retinitis pigmentosa and optic atrophy
  • Infantile onset spinocerebellar ataxia
  • Early-onset cerebellar ataxia with retained tendon reflexes
  • X-linked sideroblastic anemia
  • Infantile-onset autosomal recessive nonprogressive cerebellar ataxia
  • Dyssynergia cerebellaris myoclonica
  • X-linked sideroblastic anaemia
  • X-linked sideroblastic anemia with spinocerebellar ataxia
  • Hunt's disease
  • Early onset cerebellar ataxia with myoclonus
  • Autosomal recessive spinocerebellar ataxia type 7
  • Ohaha syndrome
  • Progressive cerebellar tremor
  • Spectrin-associated autosomal recessive cerebellar ataxia
  • X chromosome-linked sideroblastic anemia
  • X-linked sideroblastic anaemia with spinocerebellar ataxia
  • Infantile-onset autosomal recessive non progressive cerebellar ataxia
  • Cerebellar ataxia early onset with retained tendon reflex
  • Non-progressive cerebellar ataxia
  • Harding ataxia
  • SCAR6 - autosomal recessive spinocerebellar ataxia type 6
  • Ramsay Hunt syndrome 1
  • Autosomal recessive spinocerebellar ataxia type 14
  • Autosomal recessive posterior column ataxia and retinitis pigmentosa
  • Vestibular ataxia
  • Autosomal recessive cerebellar ataxia, cognitive defect syndrome
  • X-linked spinocerebellar ataxia type 4
  • Cerebellar Ataxia, Early-Onset, with Retained Tendon Reflexes
  • EOCA
  • Early-onset cerebellar ataxia with essential tremor
  • X-linked intellectual disability with ataxia and apraxia syndrome
  • Progressive spinocerebellar ataxia with retained tendon reflexes
  • Early onset cerebellar ataxia with retained tendon reflexes (disorder)
  • Early onset cerebellar ataxia with essential tremor
  • Ophthalmoplegia, hypotonia, ataxia, hypoacusis, athetosis syndrome
  • X-linked spinocerebellar ataxia type 3
  • Autosomal recessive spinocerebellar ataxia type 6
  • Dentato-rubral atrophy syndrome
  • Dyssynergia cerebellaris progressiva
  • Dentate cerebellar ataxia
  • Early onset cerebellar ataxia with retained tendon reflexes
  • SCAR7 - autosomal recessive spinocerebellar ataxia type 7
  • Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia
  • X-linked ataxia deafness syndrome
  • Ramsay Hunt syndrome - ataxia
  • Spectrin-associated autosomal recessive cerebellar ataxia type 1
  • Primary cerebellar degeneration
  • Posterior column ataxia with retinitis pigmentosa syndrome
  • Vestibulocerebellar ataxia
  • X-linked recessive spinocerebellar ataxia
  • EOCA - Early onset cerebellar ataxia with retained tendon reflexes
  • Early onset cerebellar ataxia with essential tremor (disorder)
  • X-linked ataxia dementia syndrome
  • X chromosome-linked sideroblastic anaemia
  • Early-onset cerebellar ataxia with myoclonus [Hunt's ataxia]
  • Ataxia, harding type
  • Early onset cerebellar ataxia with hypogonadism
Frequently Asked Questions
What is the ICD-10 code for other early-onset cerebellar ataxia?

The ICD-10-CM code for other early-onset cerebellar ataxia is G11.19. The full clinical description is "Other early-onset cerebellar ataxia". G11.19 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code G11.19 mean?

ICD-10-CM code G11.19 represents “Other early-onset cerebellar ataxia”. It is classified under Chapter 6: Diseases of the Nervous System and is a billable/specific code that can be used on a claim.

Is G11.19 a billable code?

Yes, G11.19 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is G11.19 in?

G11.19 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).

What SNOMED CT codes does G11.19 map to?

G11.19 maps to 21 SNOMED CT concepts: 763351003, 724065003, 785300001, 785301002, 73495003, and 16 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for G11.19?

G11.19 is linked to 5 UMLS Concept Unique Identifiers: C0393520, C0393523, C5385211, C5384686, C2875046. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does G11.19 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other early-onset cerebellar ataxia affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of G11.19?

There is no direct ICD-11 mapping available for G11.19 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.