All
 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 +
 C18.452.648.595.803 Sphingolipidoses D013106 +
 C18.452.648.595.803.300 Fabry Disease D000795 
 C18.452.648.595.803.350 Gangliosidoses D005733 +
 C18.452.648.595.803.441 Gaucher Disease D005776 
 C18.452.648.595.803.585 Leukodystrophy, Globoid Cell D007965 
 C18.452.648.595.803.594 Leukodystrophy, Metachromatic D007966 
 C18.452.648.595.803.730 Niemann-Pick Diseases D009542 
 C18.452.648.595.803.850 Sea-Blue Histiocyte Syndrome D012618