Aripiprazole
DrugBank ID: DB01238
Summary
| Metric | Value |
|---|---|
| Total Predictions | 50 |
| KG+DL (Dual Validated) | 4 |
| DL Only | 46 |
| KG Only | 0 |
Predictions
| Indication | Score | Source |
|---|---|---|
| manic bipolar affective disorder | 0.9998 | KG+DL |
| bipolar disorder | 0.9972 | DL |
| autism spectrum disorder | 0.9968 | KG+DL |
| major affective disorder | 0.9962 | DL |
| autism susceptibility 1 | 0.9961 | KG+DL |
| gaze palsy, familial horizontal, with progressive scoliosis | 0.9960 | DL |
| schizophrenia | 0.9958 | DL |
| asperger syndrome, susceptibility to | 0.9952 | DL |
| Phelan-McDermid syndrome | 0.9944 | DL |
| amelocerebrohypohidrotic syndrome | 0.9934 | DL |
| distal 17p13.3 microdeletion syndrome | 0.9934 | DL |
| trichotillomania | 0.9926 | DL |
| Malan overgrowth syndrome | 0.9926 | DL |
| retinal dystrophy with or without extraocular anomalies | 0.9925 | DL |
| hydranencephaly (disease) | 0.9921 | DL |
| congenital disorder of glycosylation with defective fucosylation | 0.9917 | DL |
| polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis | 0.9901 | DL |
| myopia X-linked | 0.9900 | DL |
| syndromic myopia | 0.9898 | DL |
| myopia 26, X-linked, female-limited | 0.9895 | DL |
| hydrops-lactic acidosis-sideroblastic anemia-multisystemic failure syndrome | 0.9892 | DL |
| intellectual disability | 0.9890 | DL |
| Charcot-Marie-Tooth disease, demyelinating, type 1G | 0.9886 | DL |
| autism, susceptibility to | 0.9885 | DL |
| atypical glycine encephalopathy | 0.9876 | DL |
| chromosome 15q11.2 deletion syndrome | 0.9871 | DL |
| 16q24.3 microdeletion syndrome | 0.9866 | DL |
| occipital pachygyria and polymicrogyria | 0.9850 | DL |
| Tourette syndrome | 0.9839 | DL |
| epsilon-trimethyllysine hydroxylase deficiency | 0.9794 | DL |
| hypotonia, infantile, with psychomotor retardation and characteristic facies | 0.9777 | DL |
| autism (disease) | 0.9767 | KG+DL |
| childhood apraxia of speech | 0.9715 | DL |
| anxiety disorder | 0.9702 | DL |
| endogenous depression | 0.9606 | DL |
| benign paroxysmal torticollis of infancy | 0.9559 | DL |
| pyruvate carboxylase deficiency disease | 0.9539 | DL |
| major depressive disorder | 0.9436 | DL |
| agoraphobia | 0.9403 | DL |
| striatal degeneration, autosomal dominant | 0.9355 | DL |
| Ohdo syndrome and variants | 0.9329 | DL |
| pervasive developmental disorder - not otherwise specified | 0.9327 | DL |
| familial hypertryptophanemia | 0.9313 | DL |
| dysthymic disorder | 0.9284 | DL |
| phobic disorder | 0.9235 | DL |
| blepharophimosis - intellectual disability syndrome, Ohdo type | 0.9216 | DL |
| chromosome 2P16.3 deletion syndrome | 0.9203 | DL |
| attention deficit-hyperactivity disorder | 0.9134 | DL |
| melancholia | 0.9122 | DL |
| neurotic depression | 0.9118 | DL |
External Links
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.