SE-ATLAS

Mucopolysaccharidosis type 1 Mucopolysaccharidosis type 2 Mucopolysaccharidosis type 3 Mucopolysaccharidosis type 4 Mucopolysaccharidosis type 6 Mucopolysaccharidosis type 7 Fabry disease Alpha-mannosidosis Wolman disease GM1 gangliosidosis Gaucher disease Glycogen storage disease due to acid maltase deficiency Infantile neurovisceral acid sphingomyelinase deficiency GM2 gangliosidosis Chronic visceral acid sphingomyelinase deficiency Niemann-Pick disease type C, severe perinatal form Niemann-Pick disease type C, juvenile neurologic onset Beta-mannosidosis Niemann-Pick disease type C, adult neurologic onset Atypical Gaucher disease due to saposin C deficiency Chronic neurovisceral acid sphingomyelinase deficiency Mucopolysaccharidosis type 2, attenuated form Niemann-Pick disease type C Niemann-Pick disease type C, severe early infantile neurologic onset Niemann-Pick disease type C, late infantile neurologic onset GM1 gangliosidosis type 1 GM1 gangliosidosis type 3 Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome GM1 gangliosidosis type 2 Acid sphingomyelinase deficiency Gangliosidosis Sandhoff disease Hurler syndrome Scheie syndrome Sanfilippo syndrome type A Hurler-Scheie syndrome Sanfilippo syndrome type C Alpha-mannosidosis, infantile form Sandhoff disease, infantile form Sanfilippo syndrome type B Sialidosis Alpha-mannosidosis, adult form Sialidosis type 1 Sandhoff disease, juvenile form Sandhoff disease, adult form Mucopolysaccharidosis type 4A Mucopolysaccharidosis type 4B Tay-Sachs disease, infantile form Mucolipidosis type II Alpha-N-acetylgalactosaminidase deficiency Mucolipidosis type III Mucolipidosis type IV Tay-Sachs disease, juvenile form Sialidosis type 2 Multiple sulfatase deficiency Glycogen storage disease due to acid maltase deficiency, late-onset Gaucher disease type 3 Tay-Sachs disease Farber disease Fetal Gaucher disease Aspartylglucosaminuria Hyaluronidase deficiency Cholesteryl ester storage disease Mucopolysaccharidosis type 6, rapidly progressing Mucopolysaccharidosis type 6, slowly progressing Gaucher disease type 1 Tay-Sachs disease, adult form Glycogen storage disease due to acid maltase deficiency, infantile onset Gaucher disease type 2 Salla disease Fucosidosis Galactosialidosis Mucolipidosis GM2 gangliosidosis, AB variant Mucopolysaccharidosis type 2, severe form