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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease nephroblastoma
Comorbidity C1261473|sarcoma
Sentences 3
PubMedID- 24624323 This translocation fuses the ewing sarcoma gene (ews) with the wilms' tumor suppressor gene (wt1) to create a gene that likely acts as a transcriptional activator for pro-tumorigenic genes (fang et al., 2008).
PubMedID- 23922674 The hallmark of this disease is a ews-wt1 translocation resulting from apposition of the ewing's sarcoma (ews) gene with the wilms' tumor (wt1) gene.
PubMedID- 22439159 Extraocular retinoblastoma with central nervous system involvement, high-risk ewing's sarcoma family of tumors, high-risk relapsed wilm's tumor compared to conventional therapy (all three low strength).

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