| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzymes galactose 6-sulfate sulfatase (Type A) or beta-galactosidase (Type B) needed to break down the keratan sulfate sugar chain. (Human Disease Ontology, DOID_12804) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D009085 |
| Similar Terms | |
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2 genes/proteins associated with the disease Mucopolysaccharidosis IV from the curated CTD Gene-Disease Associations dataset.
