All
 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
 C16.320 Genetic Diseases, Inborn D030342 +
 C16.320.565 Metabolism, Inborn Errors D008661 +
 C16.320.565.150 Brain Diseases, Metabolic, Inborn D020739 +
 C16.320.565.150.435 Lysosomal Storage Diseases, Nervous System D020140 +
 C16.320.565.150.435.825 Sphingolipidoses D013106 +
 C16.320.565.150.435.825.200 Fabry Disease D000795