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Orphanet classification of rare developmental anomalies during embryogenesis

Rare developmental defect during embryogenesis ORPHA:93890
- Rare bone development disorder ORPHA:139012
  - Dysostosis ORPHA:364559
    - Craniosynostosis ORPHA:1531
      - Syndromic craniosynostosis ORPHA:139393
        
        Shprintzen-Goldberg syndrome ORPHA:2462

Rare developmental defect during embryogenesis ORPHA:93890
- Cranial malformation ORPHA:98038
  - Craniosynostosis ORPHA:1531
    - Syndromic craniosynostosis ORPHA:139393
      - Shprintzen-Goldberg syndrome ORPHA:2462

Rare developmental defect during embryogenesis ORPHA:93890
- Multiple congenital anomalies/dysmorphic syndrome ORPHA:68341
  - Multiple congenital anomalies/dysmorphic syndrome-intellectual disability ORPHA:102283
    - Shprintzen-Goldberg syndrome ORPHA:2462

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