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Orphanet classification of rare genetic diseases

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Rare genetic epilepsy ORPHA:183512
    - Monogenic disease with epilepsy ORPHA:166472
      - Channelopathy with epilepsy ORPHA:182083
        
        Familial partial epilepsy ORPHA:309
        
        Mesial temporal lobe epilepsy with hippocampal sclerosis ORPHA:99701

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Rare genetic epilepsy ORPHA:183512
    - Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes ORPHA:166475
      - Familial partial epilepsy ORPHA:309
        
        Mesial temporal lobe epilepsy with hippocampal sclerosis ORPHA:99701

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Rare genetic epilepsy ORPHA:183512
    - Epilepsy syndrome ORPHA:166463
      - Adolescent-onset epilepsy syndrome ORPHA:98260
        
        Familial partial epilepsy ORPHA:309
        
        Mesial temporal lobe epilepsy with hippocampal sclerosis ORPHA:99701

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Rare genetic epilepsy ORPHA:183512
    - Epilepsy syndrome ORPHA:166463
      - Childhood-onset epilepsy syndrome ORPHA:98259
        
        Familial partial epilepsy ORPHA:309
        
        Mesial temporal lobe epilepsy with hippocampal sclerosis ORPHA:99701

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