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Orphanet classification of rare genetic diseases

Rare genetic disease ORPHA:98053
- Rare chromosomal anomaly ORPHA:68335
  - Autosomal anomaly ORPHA:98127
    - Autosomal monosomy ORPHA:102020
      - Partial autosomal monosomy ORPHA:98142
        
        Partial deletion of the long arm of chromosome 15 ORPHA:262119
        
        15q11.2 microdeletion syndrome ORPHA:261183
        
        15q13.3 microdeletion syndrome ORPHA:199318
        
        15q14 microdeletion syndrome ORPHA:261190
        
        15q24 microdeletion syndrome ORPHA:94065
        
        Angelman syndrome due to maternal 15q11q13 deletion ORPHA:98794
        
        Deafness-infertility syndrome ORPHA:94064
        
        Distal monosomy 15q ORPHA:1596
        
        Prader-Willi syndrome due to paternal 15q11q13 deletion ORPHA:98793

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