Orphanet: Classifications

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Orphanet classification of rare developmental anomalies during embryogenesis

Rare developmental defect during embryogenesis ORPHA:93890
- Rare chromosomal anomaly ORPHA:68335
  - Autosomal anomaly ORPHA:98127
    - Autosomal monosomy ORPHA:102020
      - Partial autosomal monosomy ORPHA:98142
        
        Partial deletion of chromosome 11 ORPHA:261816
        
        Partial deletion of the short arm of chromosome 11 ORPHA:261947
        
        WAGR syndrome ORPHA:893

Rare developmental defect during embryogenesis ORPHA:93890
- Overgrowth/obesity syndrome ORPHA:139024
  - Syndromic obesity ORPHA:240371
    - WAGR syndrome ORPHA:893

Rare developmental defect during embryogenesis ORPHA:93890
- Multiple congenital anomalies/dysmorphic syndrome ORPHA:68341
  - Multiple congenital anomalies/dysmorphic syndrome-intellectual disability ORPHA:102283
    - WAGR syndrome ORPHA:893

Rare developmental defect during embryogenesis ORPHA:93890
- Developmental defect of the eye ORPHA:98553
  - Anterior segment developmental anomaly ORPHA:88632
    - Anterior segment developmental abnormality with extraocular manifestations ORPHA:519276
      - Syndromic aniridia ORPHA:98557
        
        WAGR syndrome ORPHA:893

Rare developmental defect during embryogenesis ORPHA:93890
- Disorder of sex development ORPHA:90771
  - 46,XY disorder of sex development ORPHA:98085
    - Syndrome with 46,XY disorder of sex development ORPHA:98087
      - WAGR syndrome ORPHA:893

Rare developmental defect during embryogenesis ORPHA:93890
- Renal or urinary tract malformation ORPHA:93545
  - Syndromic renal or urinary tract malformation ORPHA:93547
    - WAGR syndrome ORPHA:893

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