| OBO ID: DOID:3764 |
| Term Name: | Denys-Drash syndrome | Search Ontology: | |
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| 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). (2) | ||
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| Ontology: | Human Disease (DOID:3764) |
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