Denys-Drash syndrome

Summary

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:

In OMIM:

OMIM:194080 - DENYS-DRASH SYNDROME; DDS

OMIM:194080 - DENYS-DRASH SYNDROME; DDS

In Mondo Disease Ontology:

MONDO:0008682 - Denys-Drash syndrome

MONDO:0008682 - Denys-Drash syndrome

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: wt1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Parent(s): autosomal dominant disease (is_a), syndrome (is_a)