Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2784
Gene Symbol: GNB3
GNB3
CUI: C0339535
Disease: Night blindness, congenital stationary
Night blindness, congenital stationary 		0.510 GermlineCausalMutation ORPHANET Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness. 27063057

2016