Dataset | HuGE Navigator Gene-Phenotype Associations |
Category | disease or phenotype associations |
Type | phenotype |
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) |
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2 genes associated with the Denys-Drash Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.