| 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 |
| Similar Terms | |
| Downloads & Tools |
4 genes/proteins associated with the disease Mucopolysaccharidosis III from the curated CTD Gene-Disease Associations dataset.
