Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Sjogren-Larsson Syndrome ALDH3A2 disease C0037231 Biomarker 0.8 disgenet
Sjogren-Larsson Syndrome ALDH3A2 disease C0037231 GermlineCausalMutation 0.8 disgenet
Sjogren-Larsson Syndrome ALDH3A2 disease C0037231 AlteredExpression 0.8 disgenet
Sjogren-Larsson Syndrome ALDH3A2 disease C0037231 CausalMutation 0.8 disgenet
Sjogren-Larsson Syndrome ALDH3A2 disease C0037231 GeneticVariation 0.8 disgenet
Sjogren-Larsson Syndrome ADH5 disease C0037231 Biomarker 0.06 disgenet
Sjogren-Larsson Syndrome ADH5 disease C0037231 AlteredExpression 0.06 disgenet
Sjogren-Larsson Syndrome ADH5 disease C0037231 GeneticVariation 0.06 disgenet
Sjogren-Larsson Syndrome HSD17B6 disease C0037231 GeneticVariation 0.02 disgenet
Sjogren-Larsson Syndrome MRC1 disease C0037231 GeneticVariation 0.02 disgenet
Sjogren-Larsson Syndrome TXNRD1 disease C0037231 GeneticVariation 0.02 disgenet
Sjogren-Larsson Syndrome NPHP3 disease C0037231 GeneticVariation 0.01 disgenet
Sjogren-Larsson Syndrome MLH1 disease C0037231 GeneticVariation 0.01 disgenet
Sjogren-Larsson Syndrome POLD1 disease C0037231 GeneticVariation 0.01 disgenet
Sjogren-Larsson Syndrome FANCA disease C0037231 Biomarker 0.01 disgenet
Sjogren-Larsson Syndrome KRT18 disease C0037231 AlteredExpression 0.01 disgenet
Sjogren-Larsson Syndrome FAH disease C0037231 Biomarker 0.01 disgenet
Sjogren-Larsson Syndrome POLE disease C0037231 GeneticVariation 0.01 disgenet
Sjogren-Larsson Syndrome NXPH3 disease C0037231 GeneticVariation 0.01 disgenet
Sjogren-Larsson Syndrome CD59 disease C0037231 AlteredExpression 0.01 disgenet
Sjogren-Larsson Syndrome DNAJC13 disease C0037231 GeneticVariation 0.01 disgenet
Sjogren-Larsson Syndrome SCLT1 disease C0037231 GeneticVariation 0.01 disgenet
Sjogren-Larsson Syndrome IQCB1 disease C0037231 GeneticVariation 0.01 disgenet
Sjogren-Larsson Syndrome MSH2 disease C0037231 GeneticVariation 0.01 disgenet
Sjogren-Larsson Syndrome ALDH3A1 disease C0037231 GeneticVariation 0.01 disgenet
Sjogren-Larsson Syndrome WDR19 disease C0037231 GeneticVariation 0.01 disgenet
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