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 +
 C16.320.565.580.803.350 Gangliosidoses D005733 +
 C16.320.565.580.803.350.300 Gangliosidoses GM2 D020143 +
 C16.320.565.580.803.350.300.700 Sandhoff Disease D012497