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Orphanet classification of rare neurological diseases

Rare neurologic disease ORPHA:98006
- Neuromuscular disease ORPHA:68381
  - Motor neuron disease ORPHA:98503
    - Genetic motor neuron disease ORPHA:98505
      - Bulbospinal muscular atrophy ORPHA:206701
        
        Bulbospinal muscular atrophy of adult ORPHA:206707
        
        Bulbospinal muscular atrophy of childhood ORPHA:206704
        
        Generalized bulbospinal muscular atrophy ORPHA:206710
        
        Spinal muscular atrophy associated with central nervous system anomaly ORPHA:207012

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