Wilms tumor 1

An autosomal disorder due to pathogenic variants in the WT1 gene leading to an increased risk Wilms tumor and genitourinary abnormalities incorporating Denys-Drash syndrome and Frasier syndrome.

Also known as: Wilms' tumor, Wilms' tumour, renal Wilms tumor, renal Wilms tumour, WT1-related Wilms tumor predisposition, Wilms tumor 1, Wilms tumor type 1, Wilms tumor, autosomal dominant, somatic mutation

2733 clinical trials for this condition and its sub-types, 4 tagged with Wilms tumor 1 itself.