Atomoxetine Hcl
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB00289 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 49 |
Predicted Indications (TxGNN)
The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.
| # | Indication | Source |
|---|---|---|
| 1 | specific developmental disorder | KG + DL |
| 2 | faciodigitogenital syndrome | KG + DL |
| 3 | chondromyxoid fibroma | KG + DL |
| 4 | trichotillomania | KG + DL |
| 5 | restless legs syndrome | KG + DL |
| 6 | manic bipolar affective disorder | KG + DL |
| 7 | Tourette syndrome | KG + DL |
| 8 | transient tic disorder | KG + DL |
| 9 | cerebellar ataxia | KG + DL |
| 10 | autosomal dominant cerebellar ataxia | KG + DL |
| 11 | variably protease-sensitive prionopathy | KG + DL |
| 12 | spinocerebellar degeneration with slow eye movements | KG + DL |
| 13 | tic disorder | KG + DL |
| 14 | communication disorder | KG + DL |
| 15 | developmental disorder of mental health | KG + DL |
| 16 | stereotypic movement disorder | KG + DL |
| 17 | fetal nicotine spectrum disorder | KG + DL |
| 18 | schizophrenia | KG + DL |
| 19 | congenital disorder of glycosylation with defective fucosylation | KG + DL |
| 20 | polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis | KG + DL |
| 21 | atypical glycine encephalopathy | KG + DL |
| 22 | retinal dystrophy with or without extraocular anomalies | KG + DL |
| 23 | myopia 26, X-linked, female-limited | KG + DL |
| 24 | myopia X-linked | KG + DL |
| 25 | Charcot-Marie-Tooth disease, demyelinating, type 1G | KG + DL |
| 26 | distal 17p13.3 microdeletion syndrome | KG + DL |
| 27 | syndromic myopia | KG + DL |
| 28 | hydranencephaly (disease) | KG + DL |
| 29 | focal, segmental or multifocal dystonia | KG + DL |
| 30 | Malan overgrowth syndrome | KG + DL |
| 31 | X-linked adrenoleukodystrophy | KG + DL |
| 32 | hydrops-lactic acidosis-sideroblastic anemia-multisystemic failure syndrome | KG + DL |
| 33 | disorder of peroxisomal alpha-, beta- and omega-oxidation | KG + DL |
| 34 | familial congenital mirror movements | KG + DL |
| 35 | essential tremor | KG + DL |
| 36 | CDKL5 disorder | KG + DL |
| 37 | obsolete diabetes insipidus, neurohypophyseal type, X-linked inheritance | KG + DL |
| 38 | X-linked intellectual disability-epilepsy syndrome | KG + DL |
| 39 | Balo concentric sclerosis | KG + DL |
| 40 | ACBD5 deficiency | KG + DL |
| 41 | tremor, hereditary essential | KG + DL |
| 42 | intermittent explosive disorder | KG + DL |
| 43 | channelopathy-associated congenital insensitivity to pain, autosomal recessive | KG + DL |
| 44 | striatal degeneration, autosomal dominant | KG + DL |
| 45 | Rett syndrome | KG + DL |
| 46 | parkinsonian disorder | KG + DL |
| 47 | arthrogryposis | KG + DL |
| 48 | dysthymic disorder | KG + DL |
| 49 | X-linked epilepsy-learning disabilities-behavior disorders syndrome | KG + DL |
Disclaimer
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.