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 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
  C16.320 Genetic Diseases, Inborn D030342 +
   C16.320.322 Genetic Diseases, X-Linked D040181 +
     C16.320.322.124 Fabry Disease D000795 
     C16.320.322.360 Hemophilia B D002836 
     C16.320.322.186 Focal Dermal Hypoplasia D005489 
     C16.320.322.217 Glycogen Storage Disease Type VIII D006015 
     C16.320.322.233 Granulomatous Disease, Chronic D006105 
     C16.320.322.750 Oculocerebrorenal Syndrome D009800 
     C16.320.322.061 Androgen-Insensitivity Syndrome D013734 
     C16.320.322.937 Wiskott-Aldrich Syndrome D014923 
     C16.320.322.092 Choroideremia D015794 
     C16.320.322.241 Ichthyosis, X-Linked D016114 
     C16.320.322.480 Kallmann Syndrome D017436 
     C16.320.322.108 Dyskeratosis Congenita D019871 
     C16.320.322.906 Pelizaeus-Merzbacher Disease D020371 
     C16.320.322.562 Muscular Dystrophy, Duchenne D020388 
     C16.320.322.625 Muscular Dystrophy, Emery-Dreifuss D020389 
     C16.320.322.500 Mental Retardation, X-Linked D038901 +