has material basis in germline mutation in POU6F2 hereditary Wilms tumor Wilms tumor 5 https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/wilms_tumor_5 bilateral radial aplasia with Wilms tumor GARD:0015336 Wilms tumor 5 Wilms tumor, susceptibility to Any Wilms tumor in which the cause of the disease is a mutation in the POU6F2 gene. Wilms tumour type 5 MESH:C536707 OMIM:601583 Wilms tumour and radial bilateral aplasia MEDGEN:316905 Wilms tumor and radial bilateral aplasia Wilms tumour susceptibility-5, autosomal dominant, somatic mutation bilateral radial aplasia with Wilms tumour UMLS:C1832099 Wilms tumor susceptibility-5, autosomal dominant, somatic mutation MONDO:0011112 Wilms tumor type 5 WT5