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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 trisomy ORPHA:98130
      - Partial autosomal trisomy/tetrasomy ORPHA:98132
        
        Partial duplication of chromosome 17 ORPHA:262677
        
        Partial duplication of the long arm of chromosome 17 ORPHA:262968
        
        17q11.2 microduplication syndrome ORPHA:139474

Rare developmental defect during embryogenesis ORPHA:93890
- Multiple congenital anomalies/dysmorphic syndrome ORPHA:68341
  - Multiple congenital anomalies/dysmorphic syndrome-intellectual disability ORPHA:102283
    - 17q11.2 microduplication syndrome ORPHA:139474

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