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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
        
        Hemihyperplasia-multiple lipomatosis syndrome ORPHA:276280

Rare genetic disease ORPHA:98053
- Rare genetic developmental defect during embryogenesis ORPHA:183530
  - Genetic vascular anomaly ORPHA:211240
    - Rare genetic capillary malformation ORPHA:459526
      - Rare capillary malformation with associated anomalies ORPHA:458830
        
        Hemihyperplasia-multiple lipomatosis syndrome ORPHA:276280

Rare genetic disease ORPHA:98053
- Rare genetic skin disease ORPHA:68346
  - Genetic skin tumor or hamartoma ORPHA:183487
    - Hemihyperplasia-multiple lipomatosis syndrome ORPHA:276280

Rare genetic disease ORPHA:98053
- Rare genetic tumor ORPHA:68336
  - Genetic skin tumor or hamartoma ORPHA:183487
    - Hemihyperplasia-multiple lipomatosis syndrome ORPHA:276280

Rare genetic disease ORPHA:98053
- Rare genetic developmental defect during embryogenesis ORPHA:183530
  - Malformation syndrome with hamartosis ORPHA:98196
    - Hemihyperplasia-multiple lipomatosis syndrome ORPHA:276280

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