x

Share
Share

Search for a classification

return to list of classifications

Orphanet classification of rare genetic diseases

Rare genetic disease ORPHA:98053
- Rare genetic skin disease ORPHA:68346
  - Genetic epidermal appendage anomaly ORPHA:183447
    - Ectodermal dysplasia syndrome ORPHA:79373
      - Anonychia with flexural pigmentation ORPHA:69125

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
      - Anonychia with flexural pigmentation ORPHA:69125

Rare genetic disease ORPHA:98053
- Rare genetic skin disease ORPHA:68346
  - Genetic epidermal appendage anomaly ORPHA:183447
    - Genetic nail anomaly ORPHA:183454
      - Syndromic nail anomaly ORPHA:79370
        
        Anonychia with flexural pigmentation ORPHA:69125

return to list of classifications

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.