Trazodone
DrugBank ID: DB00656
Summary
| Metric | Value |
|---|---|
| Total Predictions | 50 |
| KG+DL (Dual Validated) | 0 |
| DL Only | 50 |
| KG Only | 0 |
Predictions
| Indication | Score | Source |
|---|---|---|
| obsessive-compulsive disorder | 0.9995 | DL |
| histrionic personality disorder (disease) | 0.9992 | DL |
| paranoid personality disorder | 0.9992 | DL |
| schizoid personality disorder | 0.9992 | DL |
| schizotypal personality disorder | 0.9992 | DL |
| anxiety disorder | 0.9990 | DL |
| benign paroxysmal torticollis of infancy | 0.9983 | DL |
| agoraphobia | 0.9981 | DL |
| endogenous depression | 0.9978 | DL |
| major depressive disorder | 0.9968 | DL |
| dysthymic disorder | 0.9948 | DL |
| unipolar depression | 0.9947 | DL |
| phobic disorder | 0.9945 | DL |
| Ohdo syndrome and variants | 0.9928 | DL |
| melancholia | 0.9907 | DL |
| neurotic depression | 0.9905 | DL |
| blepharophimosis - intellectual disability syndrome, Ohdo type | 0.9904 | DL |
| childhood apraxia of speech | 0.9903 | DL |
| dependent personality disorder | 0.9874 | DL |
| mixed anxiety and depressive disorder | 0.9872 | DL |
| Keppen-Lubinsky syndrome | 0.9860 | DL |
| narcissistic personality disorder | 0.9858 | DL |
| surfactant metabolism dysfunction, pulmonary | 0.9851 | DL |
| schizophrenia | 0.9847 | DL |
| ligneous conjunctivitis | 0.9842 | DL |
| neurotic disorder | 0.9802 | DL |
| congenital isolated adrenocorticotropic hormone deficiency (disease) | 0.9792 | DL |
| attention deficit-hyperactivity disorder | 0.9788 | DL |
| avoidant personality disorder | 0.9743 | DL |
| major affective disorder | 0.9741 | DL |
| chromosome 15q26-qter deletion syndrome | 0.9727 | DL |
| autosomal dominant slowed nerve conduction velocity | 0.9695 | DL |
| retinal dystrophy with or without extraocular anomalies | 0.9656 | DL |
| post-traumatic stress disorder | 0.9645 | DL |
| faciodigitogenital syndrome | 0.9643 | DL |
| bipolar disorder | 0.9634 | DL |
| vitamin B12-responsive methylmalonic acidemia | 0.9630 | DL |
| congenital disorder of glycosylation with defective fucosylation | 0.9620 | DL |
| syndromic myopia | 0.9614 | DL |
| hydranencephaly (disease) | 0.9597 | DL |
| myopia X-linked | 0.9581 | DL |
| Charcot-Marie-Tooth disease, demyelinating, type 1G | 0.9546 | DL |
| polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis | 0.9536 | DL |
| chondromyxoid fibroma | 0.9535 | DL |
| myopia 26, X-linked, female-limited | 0.9529 | DL |
| distal 17p13.3 microdeletion syndrome | 0.9506 | DL |
| atypical glycine encephalopathy | 0.9497 | DL |
| manic bipolar affective disorder | 0.9475 | DL |
| attention deficit hyperactivity disorder, inattentive type | 0.9257 | DL |
| hydrops-lactic acidosis-sideroblastic anemia-multisystemic failure syndrome | 0.9019 | DL |
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Disclaimer
Predictions are for research purposes only and do not constitute medical advice.
Predictions are for research purposes only and do not constitute medical advice.