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Orphanet classification of rare skin diseases

Rare skin disease ORPHA:89826
- Epidermal disease ORPHA:79353
  - 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 skin disease ORPHA:89826
- Pigmentation anomaly of the skin ORPHA:79374
  - Hyperpigmentation of the skin ORPHA:79375
    - Naegeli-Franceschetti-Jadassohn syndrome ORPHA:69087

Rare skin disease ORPHA:89826
- Epidermal appendage anomaly ORPHA:79362
  - Ectodermal dysplasia syndrome ORPHA:79373
    - Naegeli-Franceschetti-Jadassohn syndrome ORPHA:69087

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