| Disease Information | ||||||
|---|---|---|---|---|---|---|
| Disease Name | Gene Name | Type | UMLS | Association Type | Score | Source |
| Albuminuria | ACE | phenotype | C0001925 | GeneticVariation | 0.51 | disgenet |
| Albuminuria | ACE | phenotype | C0001925 | Therapeutic | 0.51 | disgenet |
| Albuminuria | ACE | phenotype | C0001925 | Biomarker | 0.51 | disgenet |
| Albuminuria | INS | phenotype | C0001925 | Biomarker | 0.5 | disgenet |
| Albuminuria | PTGS2 | phenotype | C0001925 | Biomarker | 0.3 | disgenet |
| Albuminuria | GNAQ | phenotype | C0001925 | Biomarker | 0.3 | disgenet |
| Albuminuria | SOD2 | phenotype | C0001925 | Biomarker | 0.3 | disgenet |
| Albuminuria | IL6 | phenotype | C0001925 | Biomarker | 0.3 | disgenet |
| Albuminuria | NPHS1 | phenotype | C0001925 | Biomarker | 0.3 | disgenet |
| Albuminuria | NCK2 | phenotype | C0001925 | Biomarker | 0.3 | disgenet |
| Albuminuria | MIR155 | phenotype | C0001925 | Biomarker | 0.3 | disgenet |
| Albuminuria | AGT | phenotype | C0001925 | Biomarker | 0.3 | disgenet |
| Albuminuria | PYCARD | phenotype | C0001925 | Biomarker | 0.3 | disgenet |
| Albuminuria | MIR424 | phenotype | C0001925 | Biomarker | 0.3 | disgenet |
| Albuminuria | MIR130A | phenotype | C0001925 | Biomarker | 0.3 | disgenet |
| Albuminuria | NCK1 | phenotype | C0001925 | Biomarker | 0.3 | disgenet |
| Albuminuria | GPC5 | phenotype | C0001925 | Therapeutic | 0.3 | disgenet |
| Albuminuria | LEPR | phenotype | C0001925 | Biomarker | 0.3 | disgenet |
| Albuminuria | CP | phenotype | C0001925 | Biomarker | 0.3 | disgenet |
| Albuminuria | TNF | phenotype | C0001925 | Biomarker | 0.3 | disgenet |
| Albuminuria | MIR145 | phenotype | C0001925 | Biomarker | 0.3 | disgenet |
| Albuminuria | CASP1 | phenotype | C0001925 | Biomarker | 0.3 | disgenet |
| Albuminuria | CD38 | phenotype | C0001925 | Biomarker | 0.3 | disgenet |
| Albuminuria | REN | phenotype | C0001925 | Biomarker | 0.3 | disgenet |
| Albuminuria | TSLP | phenotype | C0001925 | Biomarker | 0.3 | disgenet |
| Albuminuria | NPHS2 | phenotype | C0001925 | Biomarker | 0.3 | disgenet |
| Albuminuria | TRPC3 | phenotype | C0001925 | Biomarker | 0.2 | disgenet |
| Albuminuria | ALB | phenotype | C0001925 | Biomarker | 0.2 | disgenet |
| Albuminuria | SH2B3 | phenotype | C0001925 | Biomarker | 0.2 | disgenet |
| Albuminuria | LRP2 | phenotype | C0001925 | Biomarker | 0.2 | disgenet |
| Albuminuria | AGER | phenotype | C0001925 | Therapeutic | 0.2 | disgenet |
| Albuminuria | CSF1 | phenotype | C0001925 | Therapeutic | 0.2 | disgenet |
| Albuminuria | SPP1 | phenotype | C0001925 | Biomarker | 0.2 | disgenet |
| Albuminuria | CTSB | phenotype | C0001925 | Biomarker | 0.2 | disgenet |
| Albuminuria | CYP11B1 | phenotype | C0001925 | Biomarker | 0.2 | disgenet |
| Albuminuria | CASR | phenotype | C0001925 | Biomarker | 0.2 | disgenet |
| Albuminuria | CTSL | phenotype | C0001925 | Biomarker | 0.2 | disgenet |
| Albuminuria | RAB38 | phenotype | C0001925 | Biomarker | 0.2 | disgenet |
| Albuminuria | EDN1 | phenotype | C0001925 | Biomarker | 0.2 | disgenet |
| Albuminuria | TRPC6 | phenotype | C0001925 | Biomarker | 0.2 | disgenet |
| Albuminuria | PDPN | phenotype | C0001925 | Biomarker | 0.2 | disgenet |
| Albuminuria | FBXL20 | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | FUT1 | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | HOTTIP | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | NMU | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | SBF2 | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | PEX1 | phenotype | C0001925 | Biomarker | 0.1 | disgenet |
| Albuminuria | LINC00862 | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | USP3 | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | CHD7 | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | GALT | phenotype | C0001925 | Biomarker | 0.1 | disgenet |
| Albuminuria | ARL15 | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | CCT2 | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | CWC27 | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | LRMDA | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | CPS1 | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | AK5 | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | ICA1L | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | BAHCC1 | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | ADO | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | SNX17 | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | AQP7 | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | NRXN1 | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | COL4A4 | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | LINC02752 | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | SPATA5L1 | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | AHR | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | C2orf83 | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | SHROOM3 | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | CUBN | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | MYL3 | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | MAPKBP1 | phenotype | C0001925 | GeneticVariation | 0.1 | disgenet |
| Albuminuria | VEGFA | phenotype | C0001925 | Biomarker | 0.01 | disgenet |
| Albuminuria | DCN | phenotype | C0001925 | GeneticVariation | 0.01 | disgenet |
| Albuminuria | ADD1 | phenotype | C0001925 | GeneticVariation | 0.01 | disgenet |
| Albuminuria | CCL2 | phenotype | C0001925 | AlteredExpression | 0.01 | disgenet |
| Albuminuria | CCL5 | phenotype | C0001925 | GeneticVariation | 0.01 | disgenet |
| Albuminuria | SELP | phenotype | C0001925 | GeneticVariation | 0.01 | disgenet |
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