Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
ADH Syndrome, Inappropriate AVP phenotype C0021141 Biomarker 0.37 disgenet
ADH Syndrome, Inappropriate AVP phenotype C0021141 AlteredExpression 0.37 disgenet
ADH Syndrome, Inappropriate HMBS phenotype C0021141 CausalMutation 0.11 disgenet
ADH Syndrome, Inappropriate HMBS phenotype C0021141 GeneticVariation 0.11 disgenet
ADH Syndrome, Inappropriate SP110 phenotype C0021141 Biomarker 0.1 disgenet
ADH Syndrome, Inappropriate AQP2 phenotype C0021141 Biomarker 0.03 disgenet
ADH Syndrome, Inappropriate AQP2 phenotype C0021141 GeneticVariation 0.03 disgenet
ADH Syndrome, Inappropriate AQP4 phenotype C0021141 Biomarker 0.02 disgenet
ADH Syndrome, Inappropriate TUBA1A phenotype C0021141 GeneticVariation 0.01 disgenet
ADH Syndrome, Inappropriate CYP2D6 phenotype C0021141 GeneticVariation 0.01 disgenet
ADH Syndrome, Inappropriate IL6 phenotype C0021141 Biomarker 0.01 disgenet
ADH Syndrome, Inappropriate ACE phenotype C0021141 Biomarker 0.01 disgenet
ADH Syndrome, Inappropriate SLC5A2 phenotype C0021141 Biomarker 0.01 disgenet
ADH Syndrome, Inappropriate COMT phenotype C0021141 GeneticVariation 0.01 disgenet
ADH Syndrome, Inappropriate PPOX phenotype C0021141 GeneticVariation 0.01 disgenet
ADH Syndrome, Inappropriate POMC phenotype C0021141 Biomarker 0.01 disgenet
ADH Syndrome, Inappropriate AVPR2 phenotype C0021141 Biomarker 0.01 disgenet
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