Powered by

Up

All

 C10 Nervous System Diseases D009422 +
  C10.597 Neurologic Manifestations D009461 +
   C10.597.606 Neurobehavioral Manifestations D019954 +
    C10.597.606.643 Mental Retardation D008607 +
     C10.597.606.643.455 Mental Retardation, X-Linked D038901 +
      C10.597.606.643.455.500 Fragile X Syndrome D005600 

 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 +
     C16.131.260.800.300 Fragile X Syndrome D005600 

 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 +
     C16.320.180.800.300 Fragile X Syndrome D005600 

 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
  C16.320 Genetic Diseases, Inborn D030342 +
   C16.320.322 Genetic Diseases, X-Linked D040181 +
    C16.320.322.500 Mental Retardation, X-Linked D038901 +
     C16.320.322.500.500 Fragile X Syndrome D005600 

 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
  C16.320 Genetic Diseases, Inborn D030342 +
   C16.320.400 Heredodegenerative Disorders, Nervous System D020271 +
    C16.320.400.525 Mental Retardation, X-Linked D038901 +
     C16.320.400.525.500 Fragile X Syndrome D005600