Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Motion Sickness LINC01241 disease C0026603 GeneticVariation 0.1 disgenet
Motion Sickness LRP1B disease C0026603 GeneticVariation 0.1 disgenet
Motion Sickness CELF2 disease C0026603 GeneticVariation 0.1 disgenet
Motion Sickness SDK1 disease C0026603 GeneticVariation 0.1 disgenet
Motion Sickness LINC01243 disease C0026603 GeneticVariation 0.1 disgenet
Motion Sickness HOXD3 disease C0026603 GeneticVariation 0.1 disgenet
Motion Sickness POU6F2 disease C0026603 GeneticVariation 0.1 disgenet
Motion Sickness NLGN1 disease C0026603 GeneticVariation 0.1 disgenet
Motion Sickness MAP2K5 disease C0026603 GeneticVariation 0.1 disgenet
Motion Sickness AUTS2 disease C0026603 GeneticVariation 0.1 disgenet
Motion Sickness PRDM16 disease C0026603 GeneticVariation 0.1 disgenet
Motion Sickness GPD2 disease C0026603 GeneticVariation 0.1 disgenet
Motion Sickness PDZRN4 disease C0026603 GeneticVariation 0.1 disgenet
Motion Sickness LINC02607 disease C0026603 GeneticVariation 0.1 disgenet
Motion Sickness LINC00924 disease C0026603 GeneticVariation 0.1 disgenet
Motion Sickness LINC01440 disease C0026603 GeneticVariation 0.1 disgenet
Motion Sickness ST18 disease C0026603 GeneticVariation 0.1 disgenet
Motion Sickness HOXB-AS3 disease C0026603 GeneticVariation 0.1 disgenet
Motion Sickness LINC02641 disease C0026603 GeneticVariation 0.1 disgenet
Motion Sickness HOXB3 disease C0026603 GeneticVariation 0.1 disgenet
Motion Sickness CPNE4 disease C0026603 GeneticVariation 0.1 disgenet
Motion Sickness TRPV1 disease C0026603 Biomarker 0.01 disgenet
Motion Sickness SMS disease C0026603 Biomarker 0.01 disgenet
Motion Sickness COPE disease C0026603 GeneticVariation 0.01 disgenet
Motion Sickness CREB1 disease C0026603 Biomarker 0.01 disgenet
Motion Sickness CNR2 disease C0026603 AlteredExpression 0.01 disgenet
Motion Sickness GHSR disease C0026603 AlteredExpression 0.01 disgenet
Motion Sickness CNR1 disease C0026603 Biomarker 0.01 disgenet
Motion Sickness MAPK3 disease C0026603 Biomarker 0.01 disgenet
Motion Sickness HNMT disease C0026603 AlteredExpression 0.01 disgenet
Motion Sickness HRH1 disease C0026603 AlteredExpression 0.01 disgenet
Motion Sickness EFHD2 disease C0026603 Biomarker 0.01 disgenet
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