All
 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