Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 338917
Gene Symbol: VSX2
VSX2
CUI: C0026010
Disease: Microphthalmos
Microphthalmos 		0.200 CausalMutation CLINVAR Targeted resequencing identifies PTCH1 as a major contributor to ocular developmental anomalies and extends the SOX2 regulatory network. 26893459

2016