All
 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
 C16.320 Genetic Diseases, Inborn D030342 +
 C16.320.565 Metabolism, Inborn Errors D008661 +
 C16.320.565.580 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 +