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 +
 C16.320.565.580.554 Lysosomal Storage Diseases, Nervous System D020140 +
 C16.320.565.580.554.295 Fucosidosis D005645 
 C16.320.565.580.554.340 Glycogen Storage Disease Type II D006009 
 C16.320.565.580.554.590 Mucolipidoses D009081 
 C16.320.565.580.554.825 Sphingolipidoses D013106 +
 C16.320.565.580.554.810 Sialic Acid Storage Disease D029461