|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
4 genes/proteins associated with the disease Mucopolysaccharidosis III from the curated CTD Gene-Disease Associations dataset.