Varenicline
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB01273 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 100 |
Predicted Indications (TxGNN)
The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.
| # | Indication | Source |
|---|---|---|
| 1 | migraine disorder | KG + DL |
| 2 | migraine with brainstem aura | KG + DL |
| 3 | congenital hypotrichosis milia | KG + DL |
| 4 | hypotrichosis simplex of the scalp | KG + DL |
| 5 | diffuse alopecia areata | KG + DL |
| 6 | alopecia | KG + DL |
| 7 | open-angle glaucoma | KG + DL |
| 8 | primary hereditary glaucoma | KG + DL |
| 9 | headache disorder | KG + DL |
| 10 | pulmonary hypertension | KG + DL |
| 11 | atrophoderma vermiculata | KG + DL |
| 12 | trigeminal autonomic cephalalgia | KG + DL |
| 13 | ulerythema ophryogenesis | KG + DL |
| 14 | kyphoscoliotic heart disease | KG + DL |
| 15 | restless legs syndrome | KG + DL |
| 16 | hypotrichosis of eyelid | KG + DL |
| 17 | atypical coarctation of aorta | KG + DL |
| 18 | migraine with or without aura, susceptibility to | KG + DL |
| 19 | pseudopelade of Brocq | KG + DL |
| 20 | pulmonary hypertension, primary, autosomal recessive | KG + DL |
| 21 | genetic alopecia | KG + DL |
| 22 | obsolete patella aplasia, coxa vara, and tarsal synostosis | KG + DL |
| 23 | pulmonary arterial hypertension | KG + DL |
| 24 | cryptorchidism (disease) | KG + DL |
| 25 | methemoglobinemia | KG + DL |
| 26 | aortic malformation | KG + DL |
| 27 | erectile dysfunction (disease) | KG + DL |
| 28 | familial clubfoot due to 17q23.1q23.2 microduplication | KG + DL |
| 29 | acne (disease) | KG + DL |
| 30 | urethral obstruction sequence | KG + DL |
| 31 | chromosome 17q23.1-q23.2 deletion syndrome | KG + DL |
| 32 | glaucoma 1, open angle | KG + DL |
| 33 | sciatic neuropathy | KG + DL |
| 34 | methemoglobinemia, alpha type | KG + DL |
| 35 | amenorrhea (disease) | KG + DL |
| 36 | endolymphatic hydrops | KG + DL |
| 37 | Tourette syndrome | KG + DL |
| 38 | Ambras type hypertrichosis universalis congenita | KG + DL |
| 39 | phaeochromocytoma | KG + DL |
| 40 | pulmonary arterial hypertension associated with congenital heart disease | KG + DL |
| 41 | nicotine dependence | KG + DL |
| 42 | trichotillomania | KG + DL |
| 43 | coxopodopatellar syndrome | KG + DL |
| 44 | respiratory failure | KG + DL |
| 45 | Nager acrofacial dysostosis | KG + DL |
| 46 | pulmonary arteriovenous malformation (disease) | KG + DL |
| 47 | malformation syndrome with odontal and/or periodontal component | KG + DL |
| 48 | small intestine cancer | KG + DL |
| 49 | hypertrichosis (disease) | KG + DL |
| 50 | nocturnal enuresis | KG + DL |
(Showing top 50 of 100 predictions)
Disclaimer
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.