Mucopolysaccharidosis III Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme resulting in incomplete breakdown of the heparan sulfate sugar chain. (Human Disease Ontology, DOID_12801)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D009084
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Genes

4 genes/proteins associated with the disease Mucopolysaccharidosis III from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
HGSNAT heparan-alpha-glucosaminide N-acetyltransferase 2.88009
GNS glucosamine (N-acetyl)-6-sulfatase 2.88009
SGSH N-sulfoglucosamine sulfohydrolase 2.88009
NAGLU N-acetylglucosaminidase, alpha 2.88009