Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Night blindness, congenital stationary
0.510 GermlineCausalMutation disease ORPHANET Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness. 27063057 2016
Night blindness, congenital stationary
0.510 Biomarker disease BEFREE Homozygosity mapping ruled out most known CSNB candidates as well as CACNA2D4 and GNB3. 26368928 2015
Night blindness, congenital stationary
0.510 Biomarker disease CTD_human