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 +
    C16.320.565.580 Lysosomal Storage Diseases D016464 +
      C16.320.565.580.600 Mucopolysaccharidoses D009083 +
      C16.320.565.580.803 Sphingolipidoses D013106 +
      C16.320.565.580.201 Cholesterol Ester Storage Disease D015217 
      C16.320.565.580.923 Wolman Disease D015223 
      C16.320.565.580.554 Lysosomal Storage Diseases, Nervous System D020140 +
      C16.320.565.580.577 Mannosidase Deficiency Diseases D044904 +
 C18 Nutritional and Metabolic Diseases D009750 +
  C18.452 Metabolic Diseases D008659 +
   C18.452.648 Metabolism, Inborn Errors D008661 +
    C18.452.648.595 Lysosomal Storage Diseases D016464 +
      C18.452.648.595.600 Mucopolysaccharidoses D009083 +
      C18.452.648.595.803 Sphingolipidoses D013106 +
      C18.452.648.595.201 Cholesterol Ester Storage Disease D015217 
      C18.452.648.595.923 Wolman Disease D015223 
      C18.452.648.595.554 Lysosomal Storage Diseases, Nervous System D020140 +
      C18.452.648.595.577 Mannosidase Deficiency Diseases D044904 +