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Results 1 - 10 of 22 for Wilms tumor 2
  1. Wilms tumor 
    ... of chromosome 11 are also associated with developing Wilms tumor. Two genes in this area, IGF2 and H19, are ... Testing Registry: Wilms tumor 1 Genetic Testing Registry: Wilms tumor 2 Genetic Testing Registry: Wilms tumor 4 Genetic Testing ...
    https://medlineplus.gov/genetics/condition/wilms-tumor - Genetics
  2. AMER1 gene 
    ... similarity 123B FLJ39827 OSCS protein FAM123B RP11-403E24.2 Wilms tumor gene on the X chromosome protein Wilms tumor ...
    https://medlineplus.gov/genetics/gene/amer1 - Genetics
  3. IGF2 gene 
    ... PubMed Al-Hussain T, Ali A, Akhtar M. Wilms tumor: an update. Adv Anat Pathol. 2014 May;21(3):166-73. doi: 10.1097/PAP.0000000000000017. Citation on PubMed Bergman D, Halje M, Nordin M, Engstrom W. Insulin-like growth factor 2 in development and disease: a mini-review. Gerontology. ...
    https://medlineplus.gov/genetics/gene/igf2 - Genetics
  4. WT1 gene 
    ... they are part of a spectrum and not two distinct conditions. More About This Health Condition Variants in the WT1 gene can cause Wilms tumor, a rare form of kidney cancer that occurs ...
    https://medlineplus.gov/genetics/gene/wt1 - Genetics
  5. Denys-Drash syndrome 
    ... normal WT1 protein increases the risk of developing Wilms tumor in affected individuals.Denys-Drash syndrome has features similar to another condition called Frasier syndrome, which is also caused by mutations in the WT1 gene. Because these two conditions share a genetic cause and have overlapping ...
    https://medlineplus.gov/genetics/condition/denys-drash-syndrome - Genetics
  6. Mosaic variegated aneuploidy syndrome 
    ... is characterized by a high risk of developing Wilms tumor. Individuals with this form may also have other ... type 1, CEP57 gene mutations cause MVA syndrome type 2, and TRIP13 gene mutations cause the other form ...
    https://medlineplus.gov/.../mosaic-variegated-aneuploidy-syndrome - Genetics
  7. WAGR syndrome 
    ... retardation and autism. Cytogenet Genome Res. 2008;122(2):181-7. doi: 10.1159/000172086. Epub 2008 Dec 18. Erratum In: Cytogenet Genome Res. 2009;124(1):112. Citation on PubMed
    https://medlineplus.gov/genetics/condition/wagr-syndrome - Genetics
  8. 2q37 deletion syndrome 
    ... develop a rare form of kidney cancer called Wilms tumor. ... from a specific region in the long (q) arm of chromosome 2. The deletions occur near the end of the ...
    https://medlineplus.gov/genetics/condition/2q37-deletion-syndrome - Genetics
  9. TRIP13 gene 
    ... although the exact mechanism is unclear. ... a form of kidney cancer called Wilms tumor in childhood. They may also grow slowly and ...
    https://medlineplus.gov/genetics/gene/trip13 - Genetics
  10. H19 gene 
    ... have also been found in some cases of Wilms tumor, a rare form of kidney cancer that occurs almost exclusively in children.In some people with Wilms tumor, the maternally inherited copy of the IC1 region ...
    https://medlineplus.gov/genetics/gene/h19 - Genetics
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