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 +
     C16.320.565.202.607 Mannosidase Deficiency Diseases D044904 +
      C16.320.565.202.607.500 alpha-Mannosidosis D008363 
 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 +
     C16.320.565.580.577 Mannosidase Deficiency Diseases D044904 +
      C16.320.565.580.577.500 alpha-Mannosidosis D008363 
 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 +
     C18.452.648.202.607 Mannosidase Deficiency Diseases D044904 +
      C18.452.648.202.607.500 alpha-Mannosidosis D008363 
 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 +
     C18.452.648.595.577 Mannosidase Deficiency Diseases D044904 +
      C18.452.648.595.577.500 alpha-Mannosidosis D008363