WT1, WT1 transcription factor, 7490

N. diseases: 446; N. variants: 61
Disease: Congenital ptosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0266573
Disease: Congenital ptosis
Congenital ptosis 		0.010 Biomarker disease BEFREE The patient is examined in light of other reported patients with deletions and/or translocations involving the regions between 11p12 --> 11p14 including patients with WAGR + obesity (WAGRO) as well as with other reported patients with aniridia and congenital ptosis. 16646034 2006