Wilms tumor 5

Any Wilms tumor in which the cause of the disease is a mutation in the POU6F2 gene.

Also known as: Wilms tumor 5, Wilms tumor susceptibility-5, autosomal dominant, somatic mutation, Wilms tumor type 5, Wilms tumour susceptibility-5, autosomal dominant, somatic mutation, Wilms tumour type 5, WT5, Wilms tumor and radial bilateral aplasia, Wilms tumor, susceptibility to

2729 clinical trials for this condition and its sub-types, 0 tagged with Wilms tumor 5 itself.