Search for a classification

Orphanet classification of rare developmental anomalies during embryogenesis

Rare developmental defect during embryogenesis ORPHA:93890
- Disorder of sex development ORPHA:90771
  - 46,XX disorder of sex development ORPHA:2982
    - Syndrome with 46,XX disorder of sex development ORPHA:325109
      - Müllerian aplasia and hyperandrogenism ORPHA:247768

Rare developmental defect during embryogenesis ORPHA:93890
- Urogenital tract malformation ORPHA:83001
  - Non-syndromic urogenital tract malformation ORPHA:165704
    - Non-syndromic urogenital tract malformation of female ORPHA:182117
      - Non-syndromic uterovaginal malformation ORPHA:180065
        
        Müllerian aplasia ORPHA:73217
        
        Partial bilateral aplasia of the Müllerian ducts ORPHA:180068
        
        Müllerian aplasia and hyperandrogenism ORPHA:247768

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.