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Disease Ontology Browser
Denys-Drash syndrome (DOID:3764)
Alliance: disease page
Alt IDs: OMIM:194080, MESH:D030321, NCI:C84668, UMLS_CUI:C0950121
Definition: 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).

Disease References using Mouse Models (5)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.11
The Jackson Laboratory