Diagnosis Code: G11.19

Short Description: Other early-onset cerebellar ataxia

Long Description: Other early-onset cerebellar ataxia

The code G11.19 is VALID for claim submission

Code Classification:

• Diseases of the nervous system (G00–G99)
  • Systemic atrophies primarily affecting the central nervous system (G10-G14)
    • Hereditary ataxia (G11)
      • G11.19 Other early-onset cerebellar ataxia

Code Version: 2022 ICD-10-CM

Synonyms

• Autosomal recessive posterior column ataxia and retinitis pigmentosa
• Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia
• Dyssynergia cerebellaris myoclonica
• Early onset cerebellar ataxia with essential tremor
• Early onset cerebellar ataxia with hypogonadism
• Early onset cerebellar ataxia with myoclonus
• Early onset cerebellar ataxia with retained tendon reflexes
• Early onset cerebellar ataxia with retinitis pigmentosa and optic atrophy
• Infantile onset spinocerebellar ataxia
• Infantile-onset autosomal recessive non progressive cerebellar ataxia
• Primary cerebellar degeneration
• Progressive cerebellar tremor
• Progressive spinocerebellar ataxia with retained tendon reflexes
• Spectrin-associated autosomal recessive cerebellar ataxia
• Vestibulocerebellar ataxia
• X chromosome-linked sideroblastic anemia
• X-linked intellectual disability with ataxia and apraxia syndrome
• X-linked sideroblastic anemia with spinocerebellar ataxia
• X-linked spinocerebellar ataxia type 3
• X-linked spinocerebellar ataxia type 4

References to Index of Diseases and Injuries

The code G11.19 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • 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

Similar Codes

This page was last updated on: 10/1/2023

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