Orphanet: Classifications

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Orphanet classification of rare genetic diseases

Rare genetic disease ORPHA:98053
- Rare genetic developmental defect during embryogenesis ORPHA:183530
  - Genetic overgrowth/obesity syndrome ORPHA:183573
    - Overgrowth syndrome ORPHA:93460
      - PIK3CA-related overgrowth syndrome ORPHA:530313
        
        CLOVES syndrome ORPHA:140944

Rare genetic disease ORPHA:98053
- Rare genetic developmental defect during embryogenesis ORPHA:183530
  - Rare genetic bone development disorder ORPHA:404584
    - Primary bone dysplasia ORPHA:364526
      - Overgrowth or tall stature syndrome with skeletal involvement ORPHA:498448
        
        CLOVES syndrome ORPHA:140944

Rare genetic disease ORPHA:98053
- Rare genetic bone disease ORPHA:183524
  - Primary bone dysplasia ORPHA:364526
    - Overgrowth or tall stature syndrome with skeletal involvement ORPHA:498448
      - CLOVES syndrome ORPHA:140944

Rare genetic disease ORPHA:98053
- Rare genetic developmental defect during embryogenesis ORPHA:183530
  - Genetic vascular anomaly ORPHA:211240
    - Genetic complex vascular malformation with associated anomalies ORPHA:459537
      - CLOVES syndrome ORPHA:140944

Rare genetic disease ORPHA:98053
- Rare genetic tumor ORPHA:68336
  - Genetic skin tumor ORPHA:183487
    - CLOVES syndrome ORPHA:140944

Rare genetic disease ORPHA:98053
- Rare genetic skin disease ORPHA:68346
  - Genetic subcutaneous tissue disorder ORPHA:183484
    - CLOVES syndrome ORPHA:140944

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