Aspartylglucosaminuria

Aspartylglycosaminuria (AGU) is an autosomal recessive lysosomal storage disease belonging to the oligosaccharidosis group (also called glycoproteinosis).

Also known as: Aspartylglycosaminuria, aspartylglucosaminidase deficiency, aspartylglucosaminuria, aspartylglycosaminuria, glycosylasparaginase deficiency, AGU, Aga deficiency, Aspartylglucosamidase (AGA) deficiency

68 clinical trials for this condition and its sub-types.