Disease-gene associations mined from literature

Human genes for Denys-Drash syndrome

Denys-Drash syndrome [DOID:3764]

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).

Synonyms:  Denys-Drash syndrome,  DOID:3764,  DenysDrash syndrome,  Denys-Drash disease,  Denys-Drash disorder ...

Linkouts:  OMIM