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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 ocular motility/alignment disorder ORPHA:522516
        
        Rare genetic disorder with strabismus ORPHA:522518
        
        Syndromic genetic disorder with strabismus ORPHA:522520
        
        Neonatal adrenoleukodystrophy ORPHA:44

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Rare genetic epilepsy ORPHA:183512
    - Metabolic diseases with epilepsy ORPHA:166481
      - Peroxisomal disease with epilepsy ORPHA:225686
        
        Neonatal adrenoleukodystrophy ORPHA:44

Rare genetic disease ORPHA:98053
- Rare genetic endocrine disease ORPHA:156638
  - Rare genetic adrenal disease ORPHA:183637
    - Genetic chronic primary adrenal insufficiency ORPHA:101960
      - Neonatal adrenoleukodystrophy ORPHA:44

Rare genetic disease ORPHA:98053
- Rare genetic eye disease ORPHA:101435
  - Rare genetic disorder of the visual organs ORPHA:522504
    - Rare genetic disorder of the anterior segment of the eye ORPHA:522538
      - Genetic lens and zonula anomaly ORPHA:183607
        
        Rare genetic disorder with lens opacification ORPHA:522546
        
        Syndromic genetic cataract ORPHA:522548
        
        Metabolic disease with cataract ORPHA:98644
        
        Neonatal adrenoleukodystrophy ORPHA:44

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
        
        Peroxisome biogenesis disorder ORPHA:79189
        
        Neonatal adrenoleukodystrophy ORPHA:44

Rare genetic disease ORPHA:98053
- Rare genetic hepatic disease ORPHA:156601
  - Rare metabolic liver disease ORPHA:101940
    - Peroxisome biogenesis disorder ORPHA:79189
      - Neonatal adrenoleukodystrophy ORPHA:44

Rare genetic disease ORPHA:98053
- Rare genetic eye disease ORPHA:101435
  - Rare genetic disorder of the visual organs ORPHA:522504
    - Rare genetic disorder of the posterior segment of the eye ORPHA:522570
      - Rare genetic retinal disorder ORPHA:522572
        
        Inherited retinal disorder ORPHA:71862
        
        Syndromic inherited retinal disorder ORPHA:519325
        
        Syndromic rod-cone dystrophy ORPHA:98661
        
        Peroxisome biogenesis disorder ORPHA:79189
        
        Neonatal adrenoleukodystrophy ORPHA:44

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Neurometabolic disease ORPHA:68385
    - Peroxisome biogenesis disorder ORPHA:79189
      - Neonatal adrenoleukodystrophy ORPHA:44

Rare genetic disease ORPHA:98053
- Rare inborn errors of metabolism ORPHA:68367
  - Peroxisomal disease ORPHA:68373
    - Peroxisome biogenesis disorder ORPHA:79189
      - Neonatal adrenoleukodystrophy ORPHA:44

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Leukodystrophy ORPHA:68356
    - Peroxisome biogenesis disorder ORPHA:79189
      - Neonatal adrenoleukodystrophy ORPHA:44

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