All

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 C10 Nervous System Diseases D009422 +
  C10.228 Central Nervous System Diseases D002493 +
   C10.228.140 Brain Diseases D001927 +
    C10.228.140.163 Brain Diseases, Metabolic D001928 +
     C10.228.140.163.100 Brain Diseases, Metabolic, Inborn D020739 +
      C10.228.140.163.100.680 Peroxisomal Disorders D018901 +
       C10.228.140.163.100.680.100 Adrenoleukodystrophy D000326 
 C10 Nervous System Diseases D009422 +
  C10.314 Demyelinating Diseases D003711 +
   C10.314.400 Hereditary Central Nervous System Demyelinating Diseases D020279 +
    C10.314.400.250 Adrenoleukodystrophy D000326 
 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 
 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 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 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
  C16.320 Genetic Diseases, Inborn D030342 +
   C16.320.565 Metabolism, Inborn Errors D008661 +
    C16.320.565.150 Brain Diseases, Metabolic, Inborn D020739 +
     C16.320.565.150.680 Peroxisomal Disorders D018901 +
      C16.320.565.150.680.100 Adrenoleukodystrophy D000326 
 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
  C16.320 Genetic Diseases, Inborn D030342 +
   C16.320.565 Metabolism, Inborn Errors D008661 +
    C16.320.565.556 Lipid Metabolism, Inborn Errors D008052 +
     C16.320.565.556.750 Peroxisomal Disorders D018901 +
      C16.320.565.556.750.112 Adrenoleukodystrophy D000326 
 C18 Nutritional and Metabolic Diseases D009750 +
  C18.452 Metabolic Diseases D008659 +
   C18.452.100 Brain Diseases, Metabolic D001928 +
    C18.452.100.100 Brain Diseases, Metabolic, Inborn D020739 +
     C18.452.100.100.680 Peroxisomal Disorders D018901 +
      C18.452.100.100.680.100 Adrenoleukodystrophy D000326 
 C18 Nutritional and Metabolic Diseases D009750 +
  C18.452 Metabolic Diseases D008659 +
   C18.452.648 Metabolism, Inborn Errors D008661 +
    C18.452.648.151 Brain Diseases, Metabolic, Inborn D020739 +
     C18.452.648.151.680 Peroxisomal Disorders D018901 +
      C18.452.648.151.680.100 Adrenoleukodystrophy D000326 
 C18 Nutritional and Metabolic Diseases D009750 +
  C18.452 Metabolic Diseases D008659 +
   C18.452.648 Metabolism, Inborn Errors D008661 +
    C18.452.648.556 Lipid Metabolism, Inborn Errors D008052 +
     C18.452.648.556.750 Peroxisomal Disorders D018901 +
      C18.452.648.556.750.112 Adrenoleukodystrophy D000326 
 C19 Endocrine Diseases D004700 +
  C19.053 Adrenal Gland Diseases D000307 +
   C19.053.264 Adrenal Gland Hypofunction D000309 +
    C19.053.264.270 Adrenoleukodystrophy D000326