Fentanyl
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB00813 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 51 |
Predicted Indications (TxGNN)
The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.
| # | Indication | Source |
|---|---|---|
| 1 | nephrogenic syndrome of inappropriate antidiuresis | KG + DL |
| 2 | Tourette syndrome | KG + DL |
| 3 | trichotillomania | KG + DL |
| 4 | myofascial pain syndrome | KG + DL |
| 5 | manic bipolar affective disorder | KG + DL |
| 6 | migraine with brainstem aura | KG + DL |
| 7 | methemoglobinemia | KG + DL |
| 8 | idiopathic granulomatous myositis | KG + DL |
| 9 | myositis fibrosa | KG + DL |
| 10 | tendinitis | KG + DL |
| 11 | fibromyalgia | KG + DL |
| 12 | hypertrichosis (disease) | KG + DL |
| 13 | trigeminal autonomic cephalalgia | KG + DL |
| 14 | Ambras type hypertrichosis universalis congenita | KG + DL |
| 15 | syndrome with a Dandy-Walker malformation as major feature | KG + DL |
| 16 | inclusion body myositis | KG + DL |
| 17 | restless legs syndrome | KG + DL |
| 18 | malformation syndrome with odontal and/or periodontal component | KG + DL |
| 19 | isolated genetic hair shaft abnormality | KG + DL |
| 20 | nephrogenic diabetes insipidus | KG + DL |
| 21 | hypotrichosis simplex of the scalp | KG + DL |
| 22 | diffuse alopecia areata | KG + DL |
| 23 | congenital hypotrichosis milia | KG + DL |
| 24 | methemoglobinemia, alpha type | KG + DL |
| 25 | diabetes insipidus, nephrogenic, X-linked | KG + DL |
| 26 | alopecia | KG + DL |
| 27 | thoracic malformation | KG + DL |
| 28 | schizophreniform disorder | KG + DL |
| 29 | methemoglobin reductase deficiency | KG + DL |
| 30 | adult familial nephronophthisis-spastic quadriparesia syndrome | KG + DL |
| 31 | atrophoderma vermiculata | KG + DL |
| 32 | polycystic kidney disease | KG + DL |
| 33 | karyomegalic interstitial nephritis | KG + DL |
| 34 | renal-hepatic-pancreatic dysplasia | KG + DL |
| 35 | Joubert syndrome with renal defect | KG + DL |
| 36 | nephrogenic diabetes insipidus-intracranial calcification syndrome | KG + DL |
| 37 | open-angle glaucoma | KG + DL |
| 38 | primary hereditary glaucoma | KG + DL |
| 39 | common cold | KG + DL |
| 40 | ulerythema ophryogenesis | KG + DL |
| 41 | cluster headache syndrome | KG + DL |
| 42 | attention deficit hyperactivity disorder, inattentive type | KG + DL |
| 43 | polycystic kidney disease 3 with or without polycystic liver disease | KG + DL |
| 44 | allergic urticaria | KG + DL |
| 45 | vestibular neuronitis | KG + DL |
| 46 | nephronophthisis | KG + DL |
| 47 | obsolete vascular headache | KG + DL |
| 48 | neuroretinitis | KG + DL |
| 49 | genetic alopecia | KG + DL |
| 50 | brachial plexus neuritis | KG + DL |
(Showing top 50 of 51 predictions)
Disclaimer
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.