WT1, WT1 transcription factor, 7490

N. diseases: 446; N. variants: 61
Disease: Congenital hemihypertrophy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0332890
Disease: Congenital hemihypertrophy
Congenital hemihypertrophy 		0.010 AlteredExpression disease BEFREE There is no known association between CMN and WT1 gene expression and the association of hemihypertrophy and CMN is not well known. 19011477 2008