SE-ATLAS

Tyrosinemia type 3 Isovaleric acidemia Mucopolysaccharidosis type 1 Phenylketonuria Mucopolysaccharidosis type 2 Propionic acidemia Mucopolysaccharidosis type 3 Mucopolysaccharidosis type 4 Mucopolysaccharidosis type 6 Mucopolysaccharidosis type 7 Citrullinemia Fabry disease Alpha-mannosidosis Tyrosinemia type 1 Galactosemia Wolman disease GM1 gangliosidosis Gaucher disease Argininemia Glycogen storage disease due to acid maltase deficiency Infantile neurovisceral acid sphingomyelinase deficiency GM2 gangliosidosis Chronic visceral acid sphingomyelinase deficiency Maple syrup urine disease Niemann-Pick disease type C, severe perinatal form Niemann-Pick disease type C, juvenile neurologic onset Beta-mannosidosis Ornithine transcarbamylase deficiency Niemann-Pick disease type C, adult neurologic onset Glycine encephalopathy Niemann-Pick disease type E Tyrosinemia type 2 Niemann-Pick disease type D Mucopolysaccharidosis Glycogen storage disease due to glucose-6-phosphatase deficiency