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 +
      C10.228.140.163.100.435 Lysosomal Storage Diseases, Nervous System D020140 +
       C10.228.140.163.100.435.825 Sphingolipidoses D013106 +
        C10.228.140.163.100.435.825.594 Leukodystrophy, Metachromatic D007966 
 C10 Nervous System Diseases D009422 +
  C10.314 Demyelinating Diseases D003711 +
   C10.314.400 Hereditary Central Nervous System Demyelinating Diseases D020279 +
    C10.314.400.550 Leukodystrophy, Metachromatic D007966 
 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 +
     C16.320.565.150.435 Lysosomal Storage Diseases, Nervous System D020140 +
      C16.320.565.150.435.825 Sphingolipidoses D013106 +
       C16.320.565.150.435.825.594 Leukodystrophy, Metachromatic D007966 
 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 +
     C16.320.565.556.641 Lipoidosis D008064 +
      C16.320.565.556.641.803 Sphingolipidoses D013106 +
       C16.320.565.556.641.803.594 Leukodystrophy, Metachromatic D007966 
 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
  C16.320 Genetic Diseases, Inborn D030342 +
   C16.320.565 Metabolism, Inborn Errors D008661 +
    C16.320.565.580 Lysosomal Storage Diseases D016464 +
     C16.320.565.580.554 Lysosomal Storage Diseases, Nervous System D020140 +
      C16.320.565.580.554.825 Sphingolipidoses D013106 +
       C16.320.565.580.554.825.594 Leukodystrophy, Metachromatic D007966 
 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
  C16.320 Genetic Diseases, Inborn D030342 +
   C16.320.565 Metabolism, Inborn Errors D008661 +
    C16.320.565.580 Lysosomal Storage Diseases D016464 +
     C16.320.565.580.803 Sphingolipidoses D013106 +
      C16.320.565.580.803.594 Leukodystrophy, Metachromatic D007966 
 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 +
     C18.452.100.100.435 Lysosomal Storage Diseases, Nervous System D020140 +
      C18.452.100.100.435.825 Sphingolipidoses D013106 +
       C18.452.100.100.435.825.594 Leukodystrophy, Metachromatic D007966 
 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 +
     C18.452.648.151.435 Lysosomal Storage Diseases, Nervous System D020140 +
      C18.452.648.151.435.825 Sphingolipidoses D013106 +
       C18.452.648.151.435.825.594 Leukodystrophy, Metachromatic D007966 
 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 +
     C18.452.648.151.825 Sphingolipidoses D013106 +
      C18.452.648.151.825.594 Leukodystrophy, Metachromatic D007966 
 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 +
     C18.452.648.556.641 Lipoidosis D008064 +
      C18.452.648.556.641.803 Sphingolipidoses D013106 +
       C18.452.648.556.641.803.594 Leukodystrophy, Metachromatic D007966 
 C18 Nutritional and Metabolic Diseases D009750 +
  C18.452 Metabolic Diseases D008659 +
   C18.452.648 Metabolism, Inborn Errors D008661 +
    C18.452.648.595 Lysosomal Storage Diseases D016464 +
     C18.452.648.595.554 Lysosomal Storage Diseases, Nervous System D020140 +
      C18.452.648.595.554.825 Sphingolipidoses D013106 +
       C18.452.648.595.554.825.594 Leukodystrophy, Metachromatic D007966 
 C18 Nutritional and Metabolic Diseases D009750 +
  C18.452 Metabolic Diseases D008659 +
   C18.452.648 Metabolism, Inborn Errors D008661 +
    C18.452.648.595 Lysosomal Storage Diseases D016464 +
     C18.452.648.595.803 Sphingolipidoses D013106 +
      C18.452.648.595.803.594 Leukodystrophy, Metachromatic D007966