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: C0950121
Disease: Denys-Drash Syndrome
Denys-Drash Syndrome 		1.000 Biomarker disease GENOMICS_ENGLAND
CUI: C0950121
Disease: Denys-Drash Syndrome
Denys-Drash Syndrome 		1.000 Biomarker disease GENOMICS_ENGLAND
CUI: C0950121
Disease: Denys-Drash Syndrome
Denys-Drash Syndrome 		1.000 Biomarker disease CTD_human
CUI: C0950121
Disease: Denys-Drash Syndrome
Denys-Drash Syndrome 		1.000 Biomarker disease GENOMICS_ENGLAND
CUI: C0027708
Disease: Nephroblastoma
Nephroblastoma 		0.800 Biomarker disease HPO
CUI: C0027708
Disease: Nephroblastoma
Nephroblastoma 		0.800 CausalMutation disease CGI
CUI: C0027708
Disease: Nephroblastoma
Nephroblastoma 		0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C0027708
Disease: Nephroblastoma
Nephroblastoma 		0.800 SusceptibilityMutation disease ORPHANET
CUI: C0027708
Disease: Nephroblastoma
Nephroblastoma 		0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C0027708
Disease: Nephroblastoma
Nephroblastoma 		0.800 SomaticCausalMutation disease ORPHANET
CUI: C0027708
Disease: Nephroblastoma
Nephroblastoma 		0.800 GenomicAlterations disease CGI
CUI: C0206115
Disease: WAGR Syndrome
WAGR Syndrome 		0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C0206115
Disease: WAGR Syndrome
WAGR Syndrome 		0.800 Biomarker disease CTD_human
CUI: C0950122
Disease: Frasier Syndrome
Frasier Syndrome 		0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C0950122
Disease: Frasier Syndrome
Frasier Syndrome 		0.800 Biomarker disease CTD_human
CUI: C0950122
Disease: Frasier Syndrome
Frasier Syndrome 		0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C0950122
Disease: Frasier Syndrome
Frasier Syndrome 		0.800 GeneticVariation disease CLINVAR
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 CausalMutation disease CGI
CUI: C1837026
Disease: MEACHAM SYNDROME (disorder)
MEACHAM SYNDROME (disorder) 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C1837026
Disease: MEACHAM SYNDROME (disorder)
MEACHAM SYNDROME (disorder) 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C1837026
Disease: MEACHAM SYNDROME (disorder)
MEACHAM SYNDROME (disorder) 		0.700 Biomarker disease CTD_human
CUI: C1837026
Disease: MEACHAM SYNDROME (disorder)
MEACHAM SYNDROME (disorder) 		0.700 CausalMutation disease CLINVAR
CUI: C3151568
Disease: NEPHROTIC SYNDROME, TYPE 4
NEPHROTIC SYNDROME, TYPE 4 		0.700 Biomarker disease CTD_human
CUI: C3151568
Disease: NEPHROTIC SYNDROME, TYPE 4
NEPHROTIC SYNDROME, TYPE 4 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C3151568
Disease: NEPHROTIC SYNDROME, TYPE 4
NEPHROTIC SYNDROME, TYPE 4 		0.700 GeneticVariation disease CLINVAR