All

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 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
  C16.131 Abnormalities D000013 +
   C16.131.260 Chromosome Disorders D025063 +
    C16.131.260.800 Sex Chromosome Disorders D025064 +
      C16.131.260.800.240 Ectodermal Dysplasia D004476 +
      C16.131.260.800.300 Fragile X Syndrome D005600 
      C16.131.260.800.345 Gonadal Dysgenesis, Mixed D006060 
      C16.131.260.800.340 Gonadal Dysgenesis, 46,XY D006061 
      C16.131.260.800.490 Klinefelter Syndrome D007713 
      C16.131.260.800.670 Orofaciodigital Syndromes D009958 
      C16.131.260.800.870 Turner Syndrome D014424 
 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
  C16.320 Genetic Diseases, Inborn D030342 +
   C16.320.180 Chromosome Disorders D025063 +
    C16.320.180.800 Sex Chromosome Disorders D025064 +
      C16.320.180.800.240 Ectodermal Dysplasia D004476 +
      C16.320.180.800.300 Fragile X Syndrome D005600 
      C16.320.180.800.345 Gonadal Dysgenesis, Mixed D006060 
      C16.320.180.800.340 Gonadal Dysgenesis, 46,XY D006061 
      C16.320.180.800.490 Klinefelter Syndrome D007713 
      C16.320.180.800.670 Orofaciodigital Syndromes D009958 
      C16.320.180.800.870 Turner Syndrome D014424