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 +
 C16.320.565.580.803 Sphingolipidoses D013106 +
 C16.320.565.580.803.300 Fabry Disease D000795 
 C16.320.565.580.803.350 Gangliosidoses D005733 +
 C16.320.565.580.803.441 Gaucher Disease D005776 
 C16.320.565.580.803.585 Leukodystrophy, Globoid Cell D007965 
 C16.320.565.580.803.594 Leukodystrophy, Metachromatic D007966 
 C16.320.565.580.803.730 Niemann-Pick Diseases D009542 
 C16.320.565.580.803.850 Sea-Blue Histiocyte Syndrome D012618