the Wilms Tumor 1 (WT1) or Wilms Tumor 2 (WT2) genes, and the tumor presents with a group of other signs and symptoms. Non-syndromic Wilms' tumor is not...

Wilms tumor protein (WT33) is a protein that in humans is encoded by the WT1 gene on chromosome 11p. This gene encodes a transcription factor that contains...

and Wilms' tumor. Clinically, Denys–Drash is characterized by the triad of pseudohermaphroditism, mesangial renal sclerosis, and Wilms' tumor. The condition...

Wilms tumor-4 is a phenotype that in humans is associated with a genetic locus 17q12-q21 on chromosome 17. "Human PubMed Reference:". National Center...

syndrome (PS), also known as nephroblastomatosis-fetal ascites-macrosomia-Wilms tumor syndrome, is a rare overgrowth syndrome caused by autosomal recessive...

WAGR syndrome (also known as WAGR complex, Wilms tumour-aniridia syndrome, aniridia-Wilms tumour syndrome) is a rare genetic syndrome in which affected...

atypical teratoid rhabdoid tumor. Other, less common childhood cancer types are: Neuroblastoma (6%, nervous system) Wilms tumor (5%, kidney) Non-Hodgkin...

treatment protocols by the National Wilms Tumor Study Group resulted in a 90% survival rate in children with Wilms' tumors by the end of the century. In 1939...

cancer are renal cell cancer (RCC), transitional cell cancer (TCC), and Wilms' tumor. RCC makes up approximately 80% of kidney cancers, and TCC accounts for...

Omphalocele (also called exomphalos) or umbilical hernia Embryonal tumor (e.g., Wilms tumor, hepatoblastoma, neuroblastoma, rhabdomyosarcoma) in childhood...