Krabbe disease
ORPHA:487Acatalasemia
ORPHA:926Alpha-N-acetylgalactosaminidase deficiency
ORPHA:3137B4GALT1-CDG
ORPHA:79332Beta-mannosidosis
ORPHA:118Biotinidase deficiency
ORPHA:79241Classic galactosemia
ORPHA:79239Erythrocyte galactose epimerase deficiency
ORPHA:308473Fabry disease
ORPHA:324Farber disease
ORPHA:333Fructose-1,6-bisphosphatase deficiency
ORPHA:348Fucosidosis
ORPHA:349Galactokinase deficiency
ORPHA:79237Galactose epimerase deficiency
ORPHA:79238Galactosialidosis
ORPHA:351Gaucher disease
ORPHA:355Generalized galactose epimerase deficiency
ORPHA:308487Glycogen storage disease due to acid maltase deficiency
ORPHA:365Glycogen storage disease due to glycogen debranching enzyme deficiency
ORPHA:366GM1 gangliosidosis
ORPHA:354Guanidinoacetate methyltransferase deficiency
ORPHA:382Histidinemia
ORPHA:2157Hyaluronidase deficiency
ORPHA:67041MOGS-CDG
ORPHA:79330Mucopolysaccharidosis type 4A
ORPHA:309297Mucopolysaccharidosis type 4B
ORPHA:309310Prolidase deficiency
ORPHA:742Purine nucleoside phosphorylase deficiency
ORPHA:760Trehalase deficiency
ORPHA:103909