Disease Information | ||||||
---|---|---|---|---|---|---|
Disease Name | Gene Name | Type | UMLS | Association Type | Score | Source |
Affective Symptom | BDNF | phenotype | C0001726 | GeneticVariation | 0.03 | disgenet |
Affective Symptom | BDNF | phenotype | C0001726 | AlteredExpression | 0.03 | disgenet |
Affective Symptom | PCDH19 | phenotype | C0001726 | Biomarker | 0.02 | disgenet |
Affective Symptom | COMT | phenotype | C0001726 | GeneticVariation | 0.02 | disgenet |
Affective Symptom | PCDH19 | phenotype | C0001726 | GeneticVariation | 0.02 | disgenet |
Affective Symptom | COMT | phenotype | C0001726 | Biomarker | 0.02 | disgenet |
Affective Symptom | FTO | phenotype | C0001726 | GeneticVariation | 0.01 | disgenet |
Affective Symptom | FKBP5 | phenotype | C0001726 | AlteredExpression | 0.01 | disgenet |
Affective Symptom | HTR1A | phenotype | C0001726 | Biomarker | 0.01 | disgenet |
Affective Symptom | TACR1 | phenotype | C0001726 | Biomarker | 0.01 | disgenet |
Affective Symptom | OXTR | phenotype | C0001726 | Biomarker | 0.01 | disgenet |
Affective Symptom | KCNK5 | phenotype | C0001726 | Biomarker | 0.01 | disgenet |
Affective Symptom | SLC6A3 | phenotype | C0001726 | GeneticVariation | 0.01 | disgenet |
Affective Symptom | TRIM32 | phenotype | C0001726 | GeneticVariation | 0.01 | disgenet |
Affective Symptom | CD28 | phenotype | C0001726 | GeneticVariation | 0.01 | disgenet |
Affective Symptom | APOE | phenotype | C0001726 | GeneticVariation | 0.01 | disgenet |
Affective Symptom | SLC6A4 | phenotype | C0001726 | GeneticVariation | 0.01 | disgenet |
Affective Symptom | MCIDAS | phenotype | C0001726 | GeneticVariation | 0.01 | disgenet |
Affective Symptom | KCNK3 | phenotype | C0001726 | Biomarker | 0.01 | disgenet |
Affective Symptom | OPN1SW | phenotype | C0001726 | Biomarker | 0.01 | disgenet |
Affective Symptom | EBI3 | phenotype | C0001726 | GeneticVariation | 0.01 | disgenet |
Affective Symptom | CRP | phenotype | C0001726 | Biomarker | 0.01 | disgenet |
Affective Symptom | ACE | phenotype | C0001726 | Biomarker | 0.01 | disgenet |
Affective Symptom | MIR137 | phenotype | C0001726 | GeneticVariation | 0.01 | disgenet |
Affective Symptom | PRKG2 | phenotype | C0001726 | GeneticVariation | 0.01 | disgenet |
Affective Symptom | CTLA4 | phenotype | C0001726 | GeneticVariation | 0.01 | disgenet |
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