All

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 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 +
       C10.597.606.643.455.124 Adrenoleukodystrophy D000326 
       C10.597.606.643.455.500 Fragile X Syndrome D005600 
       C10.597.606.643.455.687 Menkes Kinky Hair Syndrome D007706 
       C10.597.606.643.455.625 Lesch-Nyhan Syndrome D007926 
       C10.597.606.643.455.875 Pyruvate Dehydrogenase Complex Deficiency Disease D015325 
       C10.597.606.643.455.937 Rett Syndrome D015518 
       C10.597.606.643.455.750 Mucopolysaccharidosis II D016532 
       C10.597.606.643.455.249 Coffin-Lowry Syndrome D038921 
 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 +
      C16.320.322.500.124 Adrenoleukodystrophy D000326 
      C16.320.322.500.500 Fragile X Syndrome D005600 
      C16.320.322.500.687 Menkes Kinky Hair Syndrome D007706 
      C16.320.322.500.625 Lesch-Nyhan Syndrome D007926 
      C16.320.322.500.875 Pyruvate Dehydrogenase Complex Deficiency Disease D015325 
      C16.320.322.500.937 Rett Syndrome D015518 
      C16.320.322.500.750 Mucopolysaccharidosis II D016532 
      C16.320.322.500.249 Coffin-Lowry Syndrome D038921 
 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 +
      C16.320.400.525.124 Adrenoleukodystrophy D000326 
      C16.320.400.525.500 Fragile X Syndrome D005600 
      C16.320.400.525.687 Menkes Kinky Hair Syndrome D007706 
      C16.320.400.525.625 Lesch-Nyhan Syndrome D007926 
      C16.320.400.525.875 Pyruvate Dehydrogenase Complex Deficiency Disease D015325 
      C16.320.400.525.937 Rett Syndrome D015518 
      C16.320.400.525.750 Mucopolysaccharidosis II D016532 
      C16.320.400.525.249 Coffin-Lowry Syndrome D038921