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 +
      C10.228.140.163.100.725 Pyruvate Carboxylase Deficiency Disease D015324 
 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 +
     C16.320.565.150.725 Pyruvate Carboxylase Deficiency Disease D015324 
 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
  C16.320 Genetic Diseases, Inborn D030342 +
   C16.320.565 Metabolism, Inborn Errors D008661 +
    C16.320.565.202 Carbohydrate Metabolism, Inborn Errors D002239 +
     C16.320.565.202.810 Pyruvate Metabolism, Inborn Errors D015323 +
      C16.320.565.202.810.666 Pyruvate Carboxylase Deficiency Disease D015324 
 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 +
     C18.452.100.100.725 Pyruvate Carboxylase Deficiency Disease D015324 
 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 +
     C18.452.648.151.725 Pyruvate Carboxylase Deficiency Disease D015324 
 C18 Nutritional and Metabolic Diseases D009750 +
  C18.452 Metabolic Diseases D008659 +
   C18.452.648 Metabolism, Inborn Errors D008661 +
    C18.452.648.202 Carbohydrate Metabolism, Inborn Errors D002239 +
     C18.452.648.202.810 Pyruvate Metabolism, Inborn Errors D015323 +
      C18.452.648.202.810.666 Pyruvate Carboxylase Deficiency Disease D015324 
 C18 Nutritional and Metabolic Diseases D009750 +
  C18.452 Metabolic Diseases D008659 +
   C18.452.660 Mitochondrial Diseases D028361 +
    C18.452.660.705 Pyruvate Carboxylase Deficiency Disease D015324