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DOID:3764 - Denys-Drash syndrome
Disease Ontology Definition:A syndrome 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).
Synonyms:
Xenbase Genes
:
wt1
| MONDO:0008682 - Denys-Drash syndrome |
| MIM:194080 - DENYS-DRASH SYNDROME; DDS |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal dominant disease (is_a),
syndrome (is_a)