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Wilms tumor 1
rareAn 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.
- Identifiers
- MONDO:0008679 OMIM:194070
- Causal genes
- WT1
- Part of
- Hereditary Wilms tumor
- Also known as
- Wilms tumor type 1 · Wilms tumor, autosomal dominant, somatic mutation · Wilms tumor, somatic · Wilms tumor, type 1, autosomal dominant, somatic mutation · Wilms tumour type 1
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