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 Déficit en hyaluronidase Maladie de stockage des esters du cholestérol Mucopolysaccharidose type 6, forme rapidement progressive Mucopolysaccharidose type 6, forme lentement progressive Maladie de Gaucher type 1 Maladie de Tay-Sachs, forme adulte Glycogénose par déficit en maltase acide à début infantile Maladie de Gaucher type 2 Maladie de Salla Fucosidose Galactosialidose Mucolipidose Gangliosidose à GM2 variant AB Mucopolysaccharidose type 2, forme sévère