Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1837026
Disease: MEACHAM SYNDROME (disorder)
MEACHAM SYNDROME (disorder)
0.700 CausalMutation disease CLINVAR WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations. 17853480 2008
CUI: C1837026
Disease: MEACHAM SYNDROME (disorder)
MEACHAM SYNDROME (disorder)
0.700 GeneticVariation disease UNIPROT WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations. 17853480 2008
CUI: C1837026
Disease: MEACHAM SYNDROME (disorder)
MEACHAM SYNDROME (disorder)
0.700 CausalMutation disease CLINVAR Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations. 9607189 1998
CUI: C1837026
Disease: MEACHAM SYNDROME (disorder)
MEACHAM SYNDROME (disorder)
0.700 CausalMutation disease CLINVAR A clinical overview of WT1 gene mutations. 9090524 1997
CUI: C1837026
Disease: MEACHAM SYNDROME (disorder)
MEACHAM SYNDROME (disorder)
0.700 CausalMutation disease CLINVAR Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development. 1302008 1993
CUI: C1837026
Disease: MEACHAM SYNDROME (disorder)
MEACHAM SYNDROME (disorder)
0.700 CausalMutation disease CLINVAR Constitutional mutations in the WT1 gene in patients with Denys-Drash syndrome. 1338906 1993
CUI: C1837026
Disease: MEACHAM SYNDROME (disorder)
MEACHAM SYNDROME (disorder)
0.700 CausalMutation disease CLINVAR Inherited WT1 mutation in Denys-Drash syndrome. 1327525 1992
CUI: C1837026
Disease: MEACHAM SYNDROME (disorder)
MEACHAM SYNDROME (disorder)
0.700 CausalMutation disease CLINVAR Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome. 1655284 1991
CUI: C1837026
Disease: MEACHAM SYNDROME (disorder)
MEACHAM SYNDROME (disorder)
0.700 CausalMutation disease CLINVAR Glomerulonephritis associated with male pseudohermaphroditism and nephroblastoma. 6307071 1983
CUI: C1837026
Disease: MEACHAM SYNDROME (disorder)
MEACHAM SYNDROME (disorder)
0.700 GermlineCausalMutation disease ORPHANET
CUI: C1837026
Disease: MEACHAM SYNDROME (disorder)
MEACHAM SYNDROME (disorder)
0.700 Biomarker disease CTD_human