WT1, WT1 transcription factor, 7490

N. diseases: 446; N. variants: 61
Disease: Abnormality of the diaphragm ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1848873
Disease: Abnormality of the diaphragm
Abnormality of the diaphragm 		0.010 GeneticVariation phenotype BEFREE These results exclude WT1 gene mutations as a major etiological factor for the isolated diaphragmatic defect. 8811558 1996