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 +
    C16.320.565.556 Lipid Metabolism, Inborn Errors D008052 +
     C16.320.565.556.641 Lipoidosis D008064 +
       C16.320.565.556.641.391 Lipoidproteinosis D008065 
       C16.320.565.556.641.509 Neuronal Ceroid-Lipofuscinosis D009472 
       C16.320.565.556.641.643 Refsum Disease D012035 
       C16.320.565.556.641.803 Sphingolipidoses D013106 +
       C16.320.565.556.641.201 Cholesterol Ester Storage Disease D015217 
       C16.320.565.556.641.923 Wolman Disease D015223 
       C16.320.565.556.641.723 Sjogren-Larsson Syndrome D016111 
 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 +
       C18.452.648.556.641.391 Lipoidproteinosis D008065 
       C18.452.648.556.641.509 Neuronal Ceroid-Lipofuscinosis D009472 
       C18.452.648.556.641.643 Refsum Disease D012035 
       C18.452.648.556.641.803 Sphingolipidoses D013106 +
       C18.452.648.556.641.201 Cholesterol Ester Storage Disease D015217 
       C18.452.648.556.641.923 Wolman Disease D015223 
       C18.452.648.556.641.723 Sjogren-Larsson Syndrome D016111