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Aspartylglucosaminuria:
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Category Description:
Includes informational sites about Aspartylglucosaminuria (AGU), an inherited disease that is part of a group of disorders called Lysosomal storage diseases.
See Also:
Health: Conditions and Illness: Genetic_Disorders
Geneva Foundation for Medical Education and Research
- GFMER gives brief clinical information about aspartylglucosaminuria and offers pictures.
International Advocate for Glycoprotein Storage Diseases
- ISMRD offers a description of aspartylglucosaminuria (AGU). Includes the clinical features, and testing.
Lysosomal Learning
- Find information about the metabolic defect, aspartylglucosaminidase deficiency. Includes the symptoms, and a clinical description.
National Organization for Rare Disorders - AGA
- NORD provides a general description of Aspartylglycosaminuria, gives the alternate names and a list of related organizations.
Online Mendelian Inheritance in Man
- OMIM gives a clinical synopsis and a gene map of Aspartylglucosaminuria, a lysosomal disease. Also gives the alternative names.
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