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Orphanet classification of rare genetic diseases

Rare genetic disease ORPHA:98053
- Rare genetic eye disease ORPHA:101435
  - Rare genetic disorder of the visual organs ORPHA:522504
    - Genetic neuro-ophthalmological disease ORPHA:183616
      - Rare genetic brainstem or cerebellar disorder with ophthalmic involvement as a major feature ORPHA:522506
        
        Friedreich ataxia ORPHA:95

Rare genetic disease ORPHA:98053
- Rare genetic cardiac disease ORPHA:98054
  - Rare familial disorder with hypertrophic cardiomyopathy ORPHA:99739
    - Syndrome associated with hypertrophic cardiomyopathy ORPHA:217595
      - Friedreich ataxia ORPHA:95

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Genetic peripheral neuropathy ORPHA:98497
    - Rare hereditary disease with peripheral neuropathy ORPHA:207015
      - Rare hereditary neurologic disease with peripheral neuropathy ORPHA:207025
        
        Cerebellar ataxia with peripheral neuropathy ORPHA:207028
        
        Friedreich ataxia ORPHA:95

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Hereditary ataxia ORPHA:183518
    - Autosomal recessive cerebellar ataxia ORPHA:1172
      - Autosomal recessive degenerative and progressive cerebellar ataxia ORPHA:98098
        
        Friedreich ataxia ORPHA:95

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Genetic neurodegenerative disease ORPHA:183500
    - Genetic neurodegenerative disease with dementia ORPHA:276058
      - Ataxia with dementia ORPHA:98538
        
        Early-onset ataxia with dementia ORPHA:98539
        
        Autosomal recessive cerebellar ataxia ORPHA:1172
        
        Autosomal recessive degenerative and progressive cerebellar ataxia ORPHA:98098
        
        Friedreich ataxia ORPHA:95

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Genetic dementia ORPHA:158124
    - Genetic neurodegenerative disease with dementia ORPHA:276058
      - Ataxia with dementia ORPHA:98538
        
        Early-onset ataxia with dementia ORPHA:98539
        
        Autosomal recessive cerebellar ataxia ORPHA:1172
        
        Autosomal recessive degenerative and progressive cerebellar ataxia ORPHA:98098
        
        Friedreich ataxia ORPHA:95

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Neurometabolic disease ORPHA:68385
    - Friedreich ataxia ORPHA:95

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