oligosacchariduria Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Increased urinary excretion of oligosaccharides (low molecular weight carbohydrate chains composed of at least three monosaccharide subunits), derived from a partial degradation of glycoproteins. (Human Phenotype Ontology, HP_0010471)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010471
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Genes

4 genes associated with the oligosacchariduria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FUCA1 fucosidase, alpha-L- 1, tissue
MANBA mannosidase, beta A, lysosomal
NEU1 sialidase 1 (lysosomal sialidase)
OCRL oculocerebrorenal syndrome of Lowe