All
 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