Wilms tumor 5

MONDO:0011112

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

2456 clinical trials for this condition and its sub-types.

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