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Orphanet classification of rare neurological diseases

Rare neurologic disease ORPHA:98006
- Rare peripheral neuropathy ORPHA:98496
  - Genetic peripheral neuropathy ORPHA:98497
    - Distal hereditary motor neuropathy ORPHA:53739
      - Autosomal dominant distal hereditary motor neuropathy ORPHA:140465
        
        Autosomal dominant congenital benign spinal muscular atrophy ORPHA:1216
        
        Autosomal dominant distal axonal motor neuropathy-myofibrillar myopathy syndrome ORPHA:476093
        
        Autosomal dominant spastic paraplegia type 17 ORPHA:100998
        
        Distal hereditary motor neuropathy type 1 ORPHA:139518
        
        Distal hereditary motor neuropathy type 2 ORPHA:139525
        
        Distal hereditary motor neuropathy type 5 ORPHA:139536
        
        Distal hereditary motor neuropathy type 7 ORPHA:139589
        
        Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome ORPHA:397744

Rare neurologic disease ORPHA:98006
- Neuromuscular disease ORPHA:68381
  - Motor neuron disease ORPHA:98503
    - Genetic motor neuron disease ORPHA:98505
      - Distal hereditary motor neuropathy ORPHA:53739
        
        Autosomal dominant distal hereditary motor neuropathy ORPHA:140465
        
        Autosomal dominant congenital benign spinal muscular atrophy ORPHA:1216
        
        Autosomal dominant distal axonal motor neuropathy-myofibrillar myopathy syndrome ORPHA:476093
        
        Autosomal dominant spastic paraplegia type 17 ORPHA:100998
        
        Distal hereditary motor neuropathy type 1 ORPHA:139518
        
        Distal hereditary motor neuropathy type 2 ORPHA:139525
        
        Distal hereditary motor neuropathy type 5 ORPHA:139536
        
        Distal hereditary motor neuropathy type 7 ORPHA:139589
        
        Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome ORPHA:397744

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