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Orphanet classification of rare neurological diseases

Rare neurologic disease ORPHA:98006
- Rare epilepsy ORPHA:101998
  - 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 neurologic disease ORPHA:98006
- Rare epilepsy ORPHA:101998
  - 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 neurologic disease ORPHA:98006
- Rare epilepsy ORPHA:101998
  - 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 neurologic disease ORPHA:98006
- Rare epilepsy ORPHA:101998
  - 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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