All

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 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 +
      C16.320.565.202.303 Fucosidosis D005645 
      C16.320.565.202.355 Galactosemias D005693 
      C16.320.565.202.449 Glycogen Storage Disease D006008 +
      C16.320.565.202.460 Hyperoxaluria, Primary D006960 
      C16.320.565.202.589 Lactose Intolerance D007787 
      C16.320.565.202.670 Mucolipidoses D009081 
      C16.320.565.202.715 Mucopolysaccharidoses D009083 +
      C16.320.565.202.720 Multiple Carboxylase Deficiency D009100 +
      C16.320.565.202.251 Fructose Metabolism, Inborn Errors D015318 +
      C16.320.565.202.810 Pyruvate Metabolism, Inborn Errors D015323 +
      C16.320.565.202.125 Carbohydrate-Deficient Glycoprotein Syndrome D018981 
      C16.320.565.202.765 Persistent Hyperinsulinemia Hypoglycemia of Infancy D044903 
      C16.320.565.202.607 Mannosidase Deficiency Diseases D044904 +
 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 +
      C18.452.648.202.303 Fucosidosis D005645 
      C18.452.648.202.355 Galactosemias D005693 
      C18.452.648.202.449 Glycogen Storage Disease D006008 +
      C18.452.648.202.460 Hyperoxaluria, Primary D006960 
      C18.452.648.202.589 Lactose Intolerance D007787 
      C18.452.648.202.670 Mucolipidoses D009081 
      C18.452.648.202.715 Mucopolysaccharidoses D009083 +
      C18.452.648.202.720 Multiple Carboxylase Deficiency D009100 +
      C18.452.648.202.251 Fructose Metabolism, Inborn Errors D015318 +
      C18.452.648.202.810 Pyruvate Metabolism, Inborn Errors D015323 +
      C18.452.648.202.125 Carbohydrate-Deficient Glycoprotein Syndrome D018981 
      C18.452.648.202.607 Mannosidase Deficiency Diseases D044904 +