Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
CUI: C1858805
Disease: Vohwinkel Syndrome, Variant Form
Vohwinkel Syndrome, Variant Form
0.010 AlteredExpression BEFREE Thus, this study suggests that VEGF release and the subsequent activation of VEGF receptor 2 link loricrin gene mutations to rapid cell proliferation in a cellular model of loricrin keratoderma. 20236940

2010