Wilms Tumor 1 Gene Syndromes

**Semantic type:** Disease or Syndrome

**Definition:** A group of syndromes caused by autosomal dominant mutation(s) in the WT1 gene, encoding Wilms tumor protein. Patients with this mutation may have a predisposition to developing Wilms tumors.

**Synonyms:** - WT1 Gene Syndromes - WT1 Gene Syndromes - WT1 Syndromes