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Orphanet classification of rare genetic diseases

Rare genetic disease ORPHA:98053
- Rare genetic developmental defect during embryogenesis ORPHA:183530
  - Genetic vascular anomaly ORPHA:211240
    - Primary lymphedema ORPHA:77240
      - Primary lymphedema without systemic or visceral involvement ORPHA:568041
        
        Congenital primary lymphedema without systemic or visceral involvement ORPHA:2416
        
        Congenital primary lymphedema of Gordon ORPHA:569821
        
        German syndrome ORPHA:2077
        
        Microcephaly-lymphedema-chorioretinopathy syndrome ORPHA:2526
        
        Milroy disease ORPHA:79452

Rare genetic disease ORPHA:98053
- Rare genetic skin disease ORPHA:68346
  - Primary lymphedema ORPHA:77240
    - Primary lymphedema without systemic or visceral involvement ORPHA:568041
      - Congenital primary lymphedema without systemic or visceral involvement ORPHA:2416
        
        Congenital primary lymphedema of Gordon ORPHA:569821
        
        German syndrome ORPHA:2077
        
        Microcephaly-lymphedema-chorioretinopathy syndrome ORPHA:2526
        
        Milroy disease ORPHA:79452

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