Disease Information | ||||||
---|---|---|---|---|---|---|
Disease Name | Gene Name | Type | UMLS | Association Type | Score | Source |
Scleroses | IL1RN | phenotype | C0036429 | Therapeutic | 0.3 | disgenet |
Scleroses | PRNP | phenotype | C0036429 | GeneticVariation | 0.02 | disgenet |
Scleroses | IL1B | phenotype | C0036429 | GeneticVariation | 0.02 | disgenet |
Scleroses | CCL26 | phenotype | C0036429 | AlteredExpression | 0.01 | disgenet |
Scleroses | ITGB1 | phenotype | C0036429 | AlteredExpression | 0.01 | disgenet |
Scleroses | LAMB2 | phenotype | C0036429 | Biomarker | 0.01 | disgenet |
Scleroses | ADM | phenotype | C0036429 | Biomarker | 0.01 | disgenet |
Scleroses | AOC3 | phenotype | C0036429 | AlteredExpression | 0.01 | disgenet |
Scleroses | ITGA3 | phenotype | C0036429 | AlteredExpression | 0.01 | disgenet |
Scleroses | WT1 | phenotype | C0036429 | AlteredExpression | 0.01 | disgenet |
Scleroses | HSPA4 | phenotype | C0036429 | AlteredExpression | 0.01 | disgenet |
Scleroses | TIMP1 | phenotype | C0036429 | Biomarker | 0.01 | disgenet |
Scleroses | NOS1 | phenotype | C0036429 | PosttranslationalModification | 0.01 | disgenet |
Scleroses | CDK5R1 | phenotype | C0036429 | Biomarker | 0.01 | disgenet |
Scleroses | TSC1 | phenotype | C0036429 | GeneticVariation | 0.01 | disgenet |
Scleroses | WRN | phenotype | C0036429 | AlteredExpression | 0.01 | disgenet |
Scleroses | GZMB | phenotype | C0036429 | AlteredExpression | 0.01 | disgenet |
Scleroses | EIF2S1 | phenotype | C0036429 | PosttranslationalModification | 0.01 | disgenet |
Scleroses | VTN | phenotype | C0036429 | Biomarker | 0.01 | disgenet |
Scleroses | CREB1 | phenotype | C0036429 | Biomarker | 0.01 | disgenet |
Scleroses | RPS6KA2 | phenotype | C0036429 | Biomarker | 0.01 | disgenet |
Scleroses | TSC2 | phenotype | C0036429 | GeneticVariation | 0.01 | disgenet |
Scleroses | CXCL9 | phenotype | C0036429 | AlteredExpression | 0.01 | disgenet |
Scleroses | PTGS2 | phenotype | C0036429 | Biomarker | 0.01 | disgenet |
Scleroses | POLR3B | NA | C0036429 | NA | NA | orphanet |
Scleroses | KLHDC8B | NA | C0036429 | NA | NA | orphanet |
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