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Summary Literature (0)
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 Disease Ontology (on Monarch Initiative):
MONDO:0008682 - Denys-Drash syndrome

OMIM:
OMIM:194080 - DENYS-DRASH SYNDROME; DDS

Other Model Organisms: AGR, 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)