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Orphanet classification of rare genetic diseases

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 metabolic disease with peripheral neuropathy ORPHA:207018
        
        Mitochondrial disease with peripheral neuropathy ORPHA:225703
        
        Coenzyme Q10 deficiency ORPHA:35656
        
        Autosomal recessive ataxia due to ubiquinone deficiency ORPHA:139485

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Rare genetic epilepsy ORPHA:183512
    - Metabolic diseases with epilepsy ORPHA:166481
      - Energy metabolism disorder with epilepsy ORPHA:225696
        
        Mitochondrial disease with epilepsy ORPHA:225700
        
        Coenzyme Q10 deficiency ORPHA:35656
        
        Autosomal recessive ataxia due to ubiquinone deficiency ORPHA:139485

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Neurometabolic disease ORPHA:68385
    - Coenzyme Q10 deficiency ORPHA:35656
      - Autosomal recessive ataxia due to ubiquinone deficiency ORPHA:139485

Rare genetic disease ORPHA:98053
- Rare inborn errors of metabolism ORPHA:68367
  - Disorder of energy metabolism ORPHA:79200
    - Mitochondrial disease ORPHA:68380
      - Mitochondrial oxidative phosphorylation disorder ORPHA:223713
        
        Mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies ORPHA:2443
        
        Coenzyme Q10 deficiency ORPHA:35656
        
        Autosomal recessive ataxia due to ubiquinone deficiency ORPHA:139485

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Rare hereditary ataxia ORPHA:183518
    - Autosomal recessive cerebellar ataxia ORPHA:1172
      - Autosomal recessive ataxia due to ubiquinone deficiency ORPHA:139485

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 ataxia due to ubiquinone deficiency ORPHA:139485

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 ataxia due to ubiquinone deficiency ORPHA:139485

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