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Results 1 - 6 of 6 for Childhood kidney cell carcinoma
  1. WT1 gene 
    ... and is named for its main features: a childhood kidney cancer known as Wilms tumor (described below), an eye problem called anirida, genitourinary anomalies, and intellectual disability. This deletion affects one copy of the WT1 gene in each cell. The loss of this gene is responsible for ...
    https://medlineplus.gov/genetics/gene/wt1 - Genetics
  2. TRIP13 gene 
    ... MVA) syndrome. This condition is typically characterized by cells with ... called Wilms tumor in childhood. They may also grow slowly and have an ...
    https://medlineplus.gov/genetics/gene/trip13 - Genetics
  3. PAX6 gene 
    ... and is named for its main features: a childhood kidney cancer known as ... copy of the PAX6 gene in each cell. A loss of the PAX6 gene is associated ...
    https://medlineplus.gov/genetics/gene/pax6 - Genetics
  4. BDNF gene 
    ... and is named for its main features: a childhood kidney cancer known as Wilms tumor, an eye problem called anirida, genitourinary anomalies, and intellectual disability (formerly ... that begins in childhood in people with WAGRO syndrome.People with WAGRO ...
    https://medlineplus.gov/genetics/gene/bdnf - Genetics
  5. SDHB gene 
    ... in a small number of people with renal cell carcinoma, which is a type of kidney cancer. SDHB gene mutations have also been identified in people with both renal cell cancer and paraganglioma (described above). An inherited SDHB ...
    https://medlineplus.gov/genetics/gene/sdhb - Genetics
  6. EXT2 gene 
    ... has a role in the spread (metastasis) of cancer cells. About 220 mutations in the EXT2 gene have ...
    https://medlineplus.gov/genetics/gene/ext2 - Genetics