WT1, WT1 transcription factor, 7490

N. diseases: 54; N. variants: 44
Disease: Deletion 11p13 ×
Source: CURATED ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2931803
Disease: Deletion 11p13
Deletion 11p13 		0.300 ChromosomalRearrangement disease ORPHANET The modifier effect of the BDNF gene in the phenotype of the WAGRO syndrome. 23266638 2013