Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C3151568
Disease: NEPHROTIC SYNDROME, TYPE 4
NEPHROTIC SYNDROME, TYPE 4 		0.700 GeneticVariation UNIPROT Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome. 20798252

2010
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C3151568
Disease: NEPHROTIC SYNDROME, TYPE 4
NEPHROTIC SYNDROME, TYPE 4 		0.700 GeneticVariation UNIPROT Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome. 15253707

2004
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C3151568
Disease: NEPHROTIC SYNDROME, TYPE 4
NEPHROTIC SYNDROME, TYPE 4 		0.700 GeneticVariation UNIPROT Constitutional WT1 correlate with clinical features in children with progressive nephropathy. 11182928

2000
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C3151568
Disease: NEPHROTIC SYNDROME, TYPE 4
NEPHROTIC SYNDROME, TYPE 4 		0.700 GeneticVariation UNIPROT Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database. 9529364

1998
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C3151568
Disease: NEPHROTIC SYNDROME, TYPE 4
NEPHROTIC SYNDROME, TYPE 4 		0.700 GeneticVariation UNIPROT Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations. 9607189

1998