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Rare Disease Database

2 Search Results for: AGU

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...