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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 deletion ORPHA:98142
        
        Partial deletion of chromosome 17 ORPHA:261831
        
        Partial deletion of the long arm of chromosome 17 ORPHA:262137
        
        17q12 microdeletion syndrome ORPHA:261265

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