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3 Search Results for: AGU

Rare Disease Information

NORD Rare Disease Database


Aspartylglycosaminuria is a very rare genetic disorder that is concentrated among persons of Finnish decent, but is also found, even more rarely, in other populations...

Also known as: AGA, AGU, Aspartylglucosaminidase Deficiency, Glycosylasparaginase Deficiency

NIH GARD Information


Aspartylglycosaminuria is a very rare lysosomal storage disease that causes a progressive decline in mental functioning. Infants with aspartylglycosaminuria...

Organizations Results

Rare Trait Hope Fund

Rare Trait Hope Fund mission is to fund treatment and cure and to support development of treatment and cure for Aspartylglucosaminuria (AGU), and to be the resource for...