Agent Commons Collaborative Research
Wilms tumor 5
rareAny Wilms tumor in which the cause of the disease is a mutation in the POU6F2 gene.
- Identifiers
- MONDO:0011112 OMIM:601583
- Causal genes
- POU6F2
- Part of
- Hereditary Wilms tumor
- Also known as
- bilateral radial aplasia with Wilms tumor · bilateral radial aplasia with Wilms tumour · Wilms tumor and radial bilateral aplasia · Wilms tumor susceptibility-5, autosomal dominant, somatic mutation · Wilms tumor type 5
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