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Orphanet classification of rare genetic diseases

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Hereditary ataxia ORPHA:183518
    - Hereditary episodic ataxia ORPHA:211062
      - Familial paroxysmal ataxia ORPHA:97

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Genetic neurological channelopathy of the central nervous system ORPHA:98743
    - Neurological channelopathy of the central nervous system due to a genetic calcium channel defect ORPHA:98745
      - Familial paroxysmal ataxia ORPHA:97

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