| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | An autosomal dominant disease that is characterized by the association of diffuse mesangial sclerosis (DMS), male pseudohermaphroditism with a 46,XY karyotype, and nephroblastoma that derives_from an abnormality in the WT1 gene (Wilms' tumor suppressor gene). (Human Disease Ontology, DOID_3764) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D030321 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Denys-Drash Syndrome from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| WT1 | Wilms tumor 1 | 2.88009 |
