WT1, WT1 transcription factor, 7490

N. diseases: 446; N. variants: 61
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.060 AlteredExpression disease BEFREE High prognostic value of pre-allogeneic stem cell transplantation minimal residual disease detection by WT1 gene expression in AML transplanted in cytologic complete remission. 29096332 2017
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.060 Biomarker disease BEFREE MN, PNET, CCSK and AML were negative for WT1. 27748279 2016
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.060 GeneticVariation disease BEFREE The single nucleotide polymorphism (SNP) rs16754 of the WT1 gene has been previously described as a possible prognostic marker in normal karyotype acute myeloid leukemia (AML) patients. 23070125 2012
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.060 Biomarker disease BEFREE Wilms' tumor protein 1 (WT1) peptide vaccination in AML patients: predominant TCR CDR3β sequence associated with remission in one patient is detectable in other vaccinated patients. 21898091 2012
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.060 GeneticVariation disease BEFREE To analyze the prevalence and clinical implications of Wilms' tumor 1 (WT1) single nucleotide polymorphism (SNP) rs16754 in the context of other prognostic markers in pediatric acute myeloid leukemia (AML). 21189390 2011
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
0.060 GeneticVariation disease BEFREE Wilms tumor 1 (WT1) mutations have recently been identified in approximately 10% of adult acute myeloid leukemia (AML) with normal cytogenetics (CN-AML) and are associated with poor outcome. 19171881 2009