Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Night Blindness, Congenital Stationary, Type 2A CACNA1F disease C1848172 GeneticVariation 1 disgenet
Night Blindness, Congenital Stationary, Type 2A CACNA1F disease C1848172 AlteredExpression 1 disgenet
Night Blindness, Congenital Stationary, Type 2A CACNA1F disease C1848172 Biomarker 1 disgenet
Night Blindness, Congenital Stationary, Type 2A CACNA1F disease C1848172 CausalMutation 1 disgenet
Night Blindness, Congenital Stationary, Type 2A NYX disease C1848172 GeneticVariation 0.4 disgenet
Night Blindness, Congenital Stationary, Type 2A NYX disease C1848172 Biomarker 0.4 disgenet
Night Blindness, Congenital Stationary, Type 2A NYX disease C1848172 AlteredExpression 0.4 disgenet
Night Blindness, Congenital Stationary, Type 2A LRIT3 disease C1848172 Biomarker 0.3 disgenet
Night Blindness, Congenital Stationary, Type 2A SAG disease C1848172 Biomarker 0.3 disgenet
Night Blindness, Congenital Stationary, Type 2A RHO disease C1848172 Biomarker 0.3 disgenet
Night Blindness, Congenital Stationary, Type 2A SLC24A1 disease C1848172 Biomarker 0.3 disgenet
Night Blindness, Congenital Stationary, Type 2A PDE6B disease C1848172 Biomarker 0.3 disgenet
Night Blindness, Congenital Stationary, Type 2A GNAT1 disease C1848172 Biomarker 0.3 disgenet
Night Blindness, Congenital Stationary, Type 2A TRPM1 disease C1848172 Biomarker 0.3 disgenet
Night Blindness, Congenital Stationary, Type 2A GRM6 disease C1848172 Biomarker 0.3 disgenet
Night Blindness, Congenital Stationary, Type 2A GPR179 disease C1848172 Biomarker 0.3 disgenet
Night Blindness, Congenital Stationary, Type 2A GNB3 disease C1848172 Biomarker 0.3 disgenet
Night Blindness, Congenital Stationary, Type 2A OTC disease C1848172 Biomarker 0.02 disgenet
Night Blindness, Congenital Stationary, Type 2A OTC disease C1848172 GeneticVariation 0.02 disgenet
Night Blindness, Congenital Stationary, Type 2A TIMP1 disease C1848172 Biomarker 0.02 disgenet
Night Blindness, Congenital Stationary, Type 2A TIMP1 disease C1848172 GeneticVariation 0.02 disgenet
Night Blindness, Congenital Stationary, Type 2A RP2 disease C1848172 GeneticVariation 0.01 disgenet
Night Blindness, Congenital Stationary, Type 2A DMD disease C1848172 GeneticVariation 0.01 disgenet
Night Blindness, Congenital Stationary, Type 2A SEC16B disease C1848172 GeneticVariation 0.01 disgenet
Night Blindness, Congenital Stationary, Type 2A MYBPC1 disease C1848172 GeneticVariation 0.01 disgenet
Night Blindness, Congenital Stationary, Type 2A CNGA3 disease C1848172 GeneticVariation 0.01 disgenet
Night Blindness, Congenital Stationary, Type 2A MAPRE3 disease C1848172 GeneticVariation 0.01 disgenet
Night Blindness, Congenital Stationary, Type 2A RPGR disease C1848172 GeneticVariation 0.01 disgenet
Night Blindness, Congenital Stationary, Type 2A CABP4 disease C1848172 Biomarker 0.01 disgenet
Night Blindness, Congenital Stationary, Type 2A NR2E3 disease C1848172 GeneticVariation 0.01 disgenet
Night Blindness, Congenital Stationary, Type 2A DYNLT3 disease C1848172 GeneticVariation 0.01 disgenet
Night Blindness, Congenital Stationary, Type 2A CRB1 disease C1848172 GeneticVariation 0.01 disgenet
Night Blindness, Congenital Stationary, Type 2A PLXNA2 disease C1848172 Biomarker 0.01 disgenet
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