Search for a classification

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
      - Disorder with multisystemic involvement and primary lymphedema ORPHA:568047
      - Primary lymphedema without systemic or visceral involvement ORPHA:568041
      - Primary lymphedema with systemic or visceral involvement ORPHA:568044

Rare genetic disease ORPHA:98053
- Rare genetic skin disease ORPHA:68346
  - Primary lymphedema ORPHA:77240
    - Disorder with multisystemic involvement and primary lymphedema ORPHA:568047
    - Primary lymphedema without systemic or visceral involvement ORPHA:568041
    - Primary lymphedema with systemic or visceral involvement ORPHA:568044

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.