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Orphanet classification of rare genetic diseases

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Rare genetic intellectual disability ORPHA:183757
    - Rare genetic syndromic intellectual disability ORPHA:183763
      - Rare syndromic intellectual disability without multiple congenital anomalies/dysmorphic syndrome ORPHA:611314
        
        Alström syndrome ORPHA:64

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
        
        Alström syndrome ORPHA:64

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
        
        Alström syndrome ORPHA:64

Rare genetic disease ORPHA:98053
- Rare genetic developmental defect during embryogenesis ORPHA:183530
  - Genetic overgrowth/obesity syndrome ORPHA:183573
    - Genetic obesity ORPHA:77828
      - Syndromic obesity ORPHA:240371
        
        Alström syndrome ORPHA:64

Rare genetic disease ORPHA:98053
- Rare genetic endocrine disease ORPHA:156638
  - Genetic obesity ORPHA:77828
    - Syndromic obesity ORPHA:240371
      - Alström syndrome ORPHA:64

Rare genetic disease ORPHA:98053
- Rare genetic cardiac disease ORPHA:98054
  - Familial dilated cardiomyopathy ORPHA:217607
    - Syndrome associated with dilated cardiomyopathy ORPHA:217619
      - Alström syndrome ORPHA:64

Rare genetic disease ORPHA:98053
- Rare genetic endocrine disease ORPHA:156638
  - Rare genetic diabetes mellitus ORPHA:183625
    - Alström syndrome ORPHA:64

Rare genetic disease ORPHA:98053
- Rare genetic renal disease ORPHA:98056
  - Genetic renal tubular disease ORPHA:183592
    - Alström syndrome ORPHA:64

Rare genetic disease ORPHA:98053
- Ciliopathy ORPHA:363250
  - Retinal ciliopathy ORPHA:156165
    - Alström syndrome ORPHA:64

Rare genetic disease ORPHA:98053
- Ciliopathy ORPHA:363250
  - Renal ciliopathy ORPHA:156162
    - Alström syndrome ORPHA:64

Rare genetic disease ORPHA:98053
- Genetic otorhinolaryngologic disease ORPHA:466084
  - Rare genetic deafness ORPHA:96210
    - Syndromic genetic deafness ORPHA:90642
      - Alström syndrome ORPHA:64

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