| Disease Information | ||||||
|---|---|---|---|---|---|---|
| Disease Name | Gene Name | Type | UMLS | Association Type | Score | Source |
| Prodromal Symptom | SNCA | phenotype | C3494358 | GeneticVariation | 0.02 | disgenet |
| Prodromal Symptom | SNCA | phenotype | C3494358 | AlteredExpression | 0.02 | disgenet |
| Prodromal Symptom | ARHGEF7 | phenotype | C3494358 | Biomarker | 0.01 | disgenet |
| Prodromal Symptom | DAO | phenotype | C3494358 | Biomarker | 0.01 | disgenet |
| Prodromal Symptom | NFKB1 | phenotype | C3494358 | Biomarker | 0.01 | disgenet |
| Prodromal Symptom | CRP | phenotype | C3494358 | Biomarker | 0.01 | disgenet |
| Prodromal Symptom | PRKCD | phenotype | C3494358 | Biomarker | 0.01 | disgenet |
| Prodromal Symptom | DAOA | phenotype | C3494358 | Biomarker | 0.01 | disgenet |
| Prodromal Symptom | H3P40 | phenotype | C3494358 | Biomarker | 0.01 | disgenet |
| Prodromal Symptom | RTN4R | phenotype | C3494358 | GeneticVariation | 0.01 | disgenet |
| Prodromal Symptom | FGF9 | phenotype | C3494358 | Biomarker | 0.01 | disgenet |
| Prodromal Symptom | REM1 | phenotype | C3494358 | Biomarker | 0.01 | disgenet |
| Prodromal Symptom | GBA | phenotype | C3494358 | GeneticVariation | 0.01 | disgenet |
| Prodromal Symptom | CD40 | phenotype | C3494358 | Biomarker | 0.01 | disgenet |
| Prodromal Symptom | NMNAT2 | phenotype | C3494358 | GeneticVariation | 0.01 | disgenet |
| Prodromal Symptom | ASCC1 | phenotype | C3494358 | Biomarker | 0.01 | disgenet |
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