1. Diseases
  2. Aspartylglucosaminuria

Aspartylglucosaminuria

Disease Export to PDF
Name:
Aspartylglucosaminuria
Description:
An autosomal recessive lysosomal storage disease belonging to the oligosaccharidosis group (also called glycoproteinosis).
ORPHAcode:
93
Synonyms:
Aspartylglucosaminidase deficiency
XREF(s):
Orphanet
MedDRA
ICD-10
OMIM
MeSH
MeSH
Analyte(s):
AGA
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14