WT1, WT1 transcription factor, 7490

N. diseases: 446; N. variants: 61
Disease: Diaphragmatic Hernia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0019284
Disease: Diaphragmatic Hernia
Diaphragmatic Hernia 		0.510 Biomarker phenotype CTD_human Genetic factors in congenital diaphragmatic hernia. 17436238 2007
CUI: C0019284
Disease: Diaphragmatic Hernia
Diaphragmatic Hernia 		0.510 Biomarker phenotype MGD Teratogen-induced, dietary and genetic models of congenital diaphragmatic hernia share a common mechanism of pathogenesis. 17071579 2006
CUI: C0019284
Disease: Diaphragmatic Hernia
Diaphragmatic Hernia 		0.510 Biomarker phenotype MGD The Wilms tumor suppressor gene wt1 is required for development of the spleen. 10469569 1999
CUI: C0019284
Disease: Diaphragmatic Hernia
Diaphragmatic Hernia 		0.510 AlteredExpression phenotype BEFREE The expression of the WT1 gene in pleural and abdominal mesothelium and the occurrence of diaphragmatic hernia in transgenic mice with a homozygous WT1 deletion strongly suggests that the diaphragmatic hernia in this patient is part of the malformation pattern caused by WT1 mutations. 7645607 1995