FOXE3, forkhead box E3, 2301

N. diseases: 118; N. variants: 11
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0152422
Disease: Congenital aphakia
Congenital aphakia
0.110 GeneticVariation disease BEFREE Lack of FOXE3 coding mutation in a case of congenital aphakia. 28805541 2018
CUI: C0152422
Disease: Congenital aphakia
Congenital aphakia
0.110 Biomarker disease HPO