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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
      - Genetic multiple congenital anomalies/dysmorphic syndrome-intellectual disability ORPHA:611327
        
        Polymicrogyria ORPHA:35981
        
        Bilateral polymicrogyria ORPHA:268940
        
        Bilateral frontal polymicrogyria ORPHA:208444
        
        Bilateral frontoparietal polymicrogyria ORPHA:101070
        
        Bilateral generalized polymicrogyria ORPHA:208447
        
        Bilateral parasagittal parieto-occipital polymicrogyria ORPHA:208441
        
        Bilateral perisylvian polymicrogyria ORPHA:98889

Rare genetic disease ORPHA:98053
- Rare genetic developmental defect during embryogenesis ORPHA:183530
  - Genetic multiple congenital anomalies/dysmorphic syndrome ORPHA:183533
    - Genetic multiple congenital anomalies/dysmorphic syndrome-intellectual disability ORPHA:611327
      - Polymicrogyria ORPHA:35981
        
        Bilateral polymicrogyria ORPHA:268940
        
        Bilateral frontal polymicrogyria ORPHA:208444
        
        Bilateral frontoparietal polymicrogyria ORPHA:101070
        
        Bilateral generalized polymicrogyria ORPHA:208447
        
        Bilateral parasagittal parieto-occipital polymicrogyria ORPHA:208441
        
        Bilateral perisylvian polymicrogyria ORPHA:98889

Rare genetic disease ORPHA:98053
- Rare genetic developmental defect during embryogenesis ORPHA:183530
  - Genetic central nervous system malformation ORPHA:183506
    - Genetic non-syndromic central nervous system malformation ORPHA:269550
      - Genetic cerebral malformation ORPHA:269553
        
        Non-syndromic cerebral malformation due to abnormal neuronal migration ORPHA:163209
        
        Polymicrogyria ORPHA:35981
        
        Bilateral polymicrogyria ORPHA:268940
        
        Bilateral frontal polymicrogyria ORPHA:208444
        
        Bilateral frontoparietal polymicrogyria ORPHA:101070
        
        Bilateral generalized polymicrogyria ORPHA:208447
        
        Bilateral parasagittal parieto-occipital polymicrogyria ORPHA:208441
        
        Bilateral perisylvian polymicrogyria ORPHA:98889

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Genetic central nervous system malformation ORPHA:183506
    - Genetic non-syndromic central nervous system malformation ORPHA:269550
      - Genetic cerebral malformation ORPHA:269553
        
        Non-syndromic cerebral malformation due to abnormal neuronal migration ORPHA:163209
        
        Polymicrogyria ORPHA:35981
        
        Bilateral polymicrogyria ORPHA:268940
        
        Bilateral frontal polymicrogyria ORPHA:208444
        
        Bilateral frontoparietal polymicrogyria ORPHA:101070
        
        Bilateral generalized polymicrogyria ORPHA:208447
        
        Bilateral parasagittal parieto-occipital polymicrogyria ORPHA:208441
        
        Bilateral perisylvian polymicrogyria ORPHA:98889

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Rare genetic epilepsy ORPHA:183512
    - Cerebral malformation with epilepsy ORPHA:166478
      - Non-syndromic cerebral malformation due to abnormal neuronal migration ORPHA:163209
        
        Polymicrogyria ORPHA:35981
        
        Bilateral polymicrogyria ORPHA:268940
        
        Bilateral frontal polymicrogyria ORPHA:208444
        
        Bilateral frontoparietal polymicrogyria ORPHA:101070
        
        Bilateral generalized polymicrogyria ORPHA:208447
        
        Bilateral parasagittal parieto-occipital polymicrogyria ORPHA:208441
        
        Bilateral perisylvian polymicrogyria ORPHA:98889

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