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Orphanet classification of rare neurological diseases

Rare neurologic disease ORPHA:98006
- Rare intellectual disability ORPHA:87277
  - Rare syndromic intellectual disability ORPHA:102369
    - Rare syndromic intellectual disability without multiple congenital anomalies/dysmorphic syndrome ORPHA:611314
      - Ataxia-telangiectasia ORPHA:100

Rare neurologic disease ORPHA:98006
- Inherited nervous system cancer-predisposing syndrome ORPHA:252190
  - Ataxia-telangiectasia ORPHA:100

Rare neurologic disease ORPHA:98006
- Rare ataxia ORPHA:102002
  - Hereditary ataxia ORPHA:183518
    - Autosomal recessive cerebellar ataxia ORPHA:1172
      - Autosomal recessive cerebellar ataxia due to a DNA repair defect ORPHA:98097
        
        Ataxia-telangiectasia ORPHA:100

Rare neurologic disease ORPHA:98006
- Rare neurodegenerative disease ORPHA:182070
  - Neurodegenerative disease with dementia ORPHA:98534
    - Ataxia with dementia ORPHA:98538
      - Early-onset ataxia with dementia ORPHA:98539
        
        Autosomal recessive cerebellar ataxia ORPHA:1172
        
        Autosomal recessive cerebellar ataxia due to a DNA repair defect ORPHA:98097
        
        Ataxia-telangiectasia ORPHA:100

Rare neurologic disease ORPHA:98006
- Rare neurologic disease with psychiatric involvement ORPHA:98033
  - Rare dementia ORPHA:89043
    - Neurodegenerative disease with dementia ORPHA:98534
      - Ataxia with dementia ORPHA:98538
        
        Early-onset ataxia with dementia ORPHA:98539
        
        Autosomal recessive cerebellar ataxia ORPHA:1172
        
        Autosomal recessive cerebellar ataxia due to a DNA repair defect ORPHA:98097
        
        Ataxia-telangiectasia ORPHA:100

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