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Orphanet classification of rare genetic diseases

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Genetic neuromuscular disease ORPHA:183497
    - Genetic neurological muscular channelopathy ORPHA:98737
      - Neurological muscular channelopathy due to a genetic ryanodine receptor defect ORPHA:98742
        
        Benign Samaritan congenital myopathy ORPHA:324581

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Genetic neuromuscular disease ORPHA:183497
    - Genetic skeletal muscle disease ORPHA:206634
      - Non-dystrophic myopathy ORPHA:206656
        
        Congenital myopathy ORPHA:97245
        
        Benign Samaritan congenital myopathy ORPHA:324581

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