WT1, WT1 transcription factor, 7490

N. diseases: 446; N. variants: 61
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C3151568
Disease: NEPHROTIC SYNDROME, TYPE 4
NEPHROTIC SYNDROME, TYPE 4
disease Disease or Syndrome 1 9 0.700 None 1.000 7 9 1992 2013
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia
disease Neoplastic Process 860 154 0.060 None 1.000 6 1 2006 2019
CUI: C1320468
Disease: Nephrogenic rest
Nephrogenic rest
disease Anatomical Abnormality 15 0.020 None 1.000 2 1996 2007
CUI: C2347748
Disease: Adult Erythroleukemia
Adult Erythroleukemia
disease Neoplastic Process 236 4 0.020 None 1.000 2 1994 1994
CUI: C4551835
Disease: Intralobar nephroblastomatosis
Intralobar nephroblastomatosis
disease Neoplastic Process 7 0.020 None 1.000 2 1991 2007
CUI: C0026985
Disease: Myelodysplasia
Myelodysplasia
disease Congenital Abnormality 181 4 0.010 None 1.000 1 2011 2011
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
phenotype Organism Attribute 565 1138 0.100 None 1.000 1 1 2019 2019
CUI: C0220810
Disease: Congenital defects
Congenital defects
group Congenital Abnormality 126 6 0.010 None 1.000 1 2009 2009
CUI: C0279068
Disease: Childhood Solid Neoplasm
Childhood Solid Neoplasm
phenotype Neoplastic Process 169 3 0.010 None 1.000 1 2010 2010
CUI: C0280099
Disease: Adult Solid Neoplasm
Adult Solid Neoplasm
group Neoplastic Process 163 3 0.010 None 1.000 1 2010 2010
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy
disease Disease or Syndrome 321 67 0.010 None 1.000 1 2018 2018
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
phenotype Clinical Attribute 843 1931 0.100 None 1.000 1 1 2019 2019
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
phenotype Neoplastic Process 6626 169 0.010 None 1.000 1 2018 2018
CUI: C1305904
Disease: Familial hematuria
Familial hematuria
disease Disease or Syndrome 23 7 0.010 None 1.000 1 2018 2018
CUI: C1319016
Disease: Nephrogenic rest, intralobar
Nephrogenic rest, intralobar
disease Congenital Abnormality 1 0.010 None 1.000 1 2010 2010
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
phenotype Neoplastic Process 1027 20 0.010 None 1.000 1 2005 2005
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
disease Disease or Syndrome 1075 276 0.010 None 1.000 1 1991 1991
CUI: C1848873
Disease: Abnormality of the diaphragm
Abnormality of the diaphragm
phenotype Anatomical Abnormality 12 2 0.010 None 1.000 1 1996 1996
CUI: C2826025
Disease: Mixed phenotype acute leukemia
Mixed phenotype acute leukemia
disease Neoplastic Process 37 0.010 None 1.000 1 1994 1994
CUI: C2931245
Disease: Bone Marrow failure syndromes
Bone Marrow failure syndromes
disease Disease or Syndrome 41 0.010 None 1.000 1 2018 2018
CUI: C2986658
Disease: Diffuse Intrinsic Pontine Glioma
Diffuse Intrinsic Pontine Glioma
disease Neoplastic Process 87 9 0.010 None 1.000 1 2019 2019
CUI: C3544205
Disease: Ovarian clear cell carcinoma
Ovarian clear cell carcinoma
disease Neoplastic Process 103 0.010 None 1.000 1 2015 2015
CUI: C3826743
Disease: Anemia in children
Anemia in children
disease Disease or Syndrome 9 0.010 None 1.000 1 2019 2019
Soluble Interleukin 6 Receptor Measurement
phenotype Laboratory Procedure 17 25 0.100 None 1.000 1 1 2018 2018
CUI: C3897752
Disease: Recurrent Childhood Glioblastoma
Recurrent Childhood Glioblastoma
disease Neoplastic Process 51 1 0.010 None 1.000 1 2014 2014