Eluxadoline
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB09272 |
| 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 | gastroduodenitis | KG + DL |
| 2 | primary hereditary glaucoma | KG + DL |
| 3 | open-angle glaucoma | KG + DL |
| 4 | peptic ulcer disease | KG + DL |
| 5 | acute intermittent porphyria | KG + DL |
| 6 | familial porphyria cutanea tarda | KG + DL |
| 7 | methemoglobin reductase deficiency | KG + DL |
| 8 | methemoglobinemia, alpha type | KG + DL |
| 9 | nephrogenic syndrome of inappropriate antidiuresis | KG + DL |
| 10 | restless legs syndrome | KG + DL |
| 11 | methemoglobinemia | KG + DL |
| 12 | porphyria | KG + DL |
| 13 | enterocolitis (disease) | KG + DL |
| 14 | open angle glaucoma | KG + DL |
| 15 | methemoglobinemia due to deficiency of methemoglobin reductase | KG + DL |
| 16 | trigeminal autonomic cephalalgia | KG + DL |
| 17 | headache disorder | KG + DL |
| 18 | glaucoma 1, open angle | KG + DL |
| 19 | non-syndromic esophageal malformation | KG + DL |
| 20 | common cold | KG + DL |
| 21 | nasal cavity disease | KG + DL |
| 22 | gastroenteritis | KG + DL |
| 23 | esophageal disease | KG + DL |
| 24 | inborn disorder of porphyrin metabolism | KG + DL |
| 25 | porphyria due to ALA dehydratase deficiency | KG + DL |
| 26 | erythropoietic uroporphyria associated with myeloid malignancy | KG + DL |
| 27 | bronchitis | KG + DL |
| 28 | myoclonus, familial | KG + DL |
| 29 | acute laryngopharyngitis | KG + DL |
| 30 | substance abuse/dependence | KG + DL |
| 31 | channelopathy-associated congenital insensitivity to pain, autosomal recessive | KG + DL |
| 32 | pharyngitis | KG + DL |
| 33 | mesial temporal lobe epilepsy with hippocampal sclerosis | KG + DL |
| 34 | progressive encephalopathy with leukodystrophy due to DECR deficiency | KG + DL |
| 35 | hereditary photodermatosis | KG + DL |
| 36 | mitochondrial membrane transport disorder | KG + DL |
| 37 | early myoclonic encephalopathy | KG + DL |
| 38 | neonatal dermatomyositis | KG + DL |
| 39 | acrodermatitis chronica atrophicans | KG + DL |
| 40 | amyopathic dermatomyositis | KG + DL |
| 41 | dermatitis | KG + DL |
| 42 | secondary interstitial lung disease specific to childhood associated with a connective tissue disease | KG + DL |
| 43 | parkinsonian disorder | KG + DL |
| 44 | insomnia (disease) | KG + DL |
| 45 | large intestine disease | KG + DL |
| 46 | hydroa vacciniforme, familial | KG + DL |
| 47 | HELIX syndrome | KG + DL |
| 48 | methemoglobinemia type 4 | KG + DL |
| 49 | Senior-Loken syndrome | KG + DL |
| 50 | hereditary renal hypouricemia | 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.