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Orphanet classification of rare genetic diseases

Rare genetic disease ORPHA:98053
- Rare genetic skin disease ORPHA:68346
  - Genetic pigmentation anomaly of the skin ORPHA:183463
    - Genetic hyperpigmentation of the skin ORPHA:183466
      - Naegeli-Franceschetti-Jadassohn syndrome ORPHA:69087

Rare genetic disease ORPHA:98053
- Rare genetic skin disease ORPHA:68346
  - Genetic epidermal disorder ORPHA:183426
    - Hereditary palmoplantar keratoderma ORPHA:79357
      - Diffuse palmoplantar keratoderma ORPHA:307141
        
        Disease with diffuse palmoplantar keratoderma as a major feature ORPHA:307711
        
        Autosomal dominant disease with diffuse palmoplantar keratoderma as a major feature ORPHA:98352
        
        Naegeli-Franceschetti-Jadassohn syndrome ORPHA:69087

Rare genetic disease ORPHA:98053
- Rare genetic skin disease ORPHA:68346
  - Genetic epidermal appendage anomaly ORPHA:183447
    - Ectodermal dysplasia syndrome ORPHA:79373
      - Naegeli-Franceschetti-Jadassohn syndrome ORPHA:69087

Rare genetic disease ORPHA:98053
- Rare genetic developmental defect during embryogenesis ORPHA:183530
  - Rare developmental defect with skin/mucosae involvement ORPHA:139027
    - Ectodermal dysplasia syndrome ORPHA:79373
      - Naegeli-Franceschetti-Jadassohn syndrome ORPHA:69087

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