Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Night Blindness, Congenital Stationary, Type 1B GRM6 disease C1850362 GeneticVariation 0.91 disgenet
Night Blindness, Congenital Stationary, Type 1B GRM6 disease C1850362 Biomarker 0.91 disgenet
Night Blindness, Congenital Stationary, Type 1B GRM6 disease C1850362 CausalMutation 0.91 disgenet
Night Blindness, Congenital Stationary, Type 1B PDE6B disease C1850362 Biomarker 0.3 disgenet
Night Blindness, Congenital Stationary, Type 1B SAG disease C1850362 Biomarker 0.3 disgenet
Night Blindness, Congenital Stationary, Type 1B SLC24A1 disease C1850362 Biomarker 0.3 disgenet
Night Blindness, Congenital Stationary, Type 1B NYX disease C1850362 Biomarker 0.3 disgenet
Night Blindness, Congenital Stationary, Type 1B GPR179 disease C1850362 Biomarker 0.3 disgenet
Night Blindness, Congenital Stationary, Type 1B RHO disease C1850362 Biomarker 0.3 disgenet
Night Blindness, Congenital Stationary, Type 1B GNB3 disease C1850362 Biomarker 0.3 disgenet
Night Blindness, Congenital Stationary, Type 1B TRPM1 disease C1850362 Biomarker 0.3 disgenet
Night Blindness, Congenital Stationary, Type 1B LRIT3 disease C1850362 Biomarker 0.3 disgenet
Night Blindness, Congenital Stationary, Type 1B GNAT1 disease C1850362 Biomarker 0.3 disgenet
Night Blindness, Congenital Stationary, Type 1B CACNA1F disease C1850362 Biomarker 0.3 disgenet
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