L-Tryptophan
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB00150 |
| 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 | restless legs syndrome | KG + DL |
| 2 | primary hereditary glaucoma | KG + DL |
| 3 | open-angle glaucoma | KG + DL |
| 4 | insomnia (disease) | KG + DL |
| 5 | methemoglobinemia | KG + DL |
| 6 | methemoglobinemia, alpha type | KG + DL |
| 7 | methemoglobin reductase deficiency | KG + DL |
| 8 | congenital prothrombin deficiency | KG + DL |
| 9 | acne (disease) | KG + DL |
| 10 | pregnancy associated osteoporosis | KG + DL |
| 11 | endolymphatic hydrops | KG + DL |
| 12 | postmenopausal osteoporosis | KG + DL |
| 13 | autosomal dominant neovascular inflammatory vitreoretinopathy | KG + DL |
| 14 | sleep disorder, initiating and maintaining sleep | KG + DL |
| 15 | dyspepsia | KG + DL |
| 16 | preeclampsia | KG + DL |
| 17 | gastroparesis (disease) | KG + DL |
| 18 | active cochlear Meniere disease | KG + DL |
| 19 | active vestibular Meniere disease | KG + DL |
| 20 | active cochleovestibular Meniere disease | KG + DL |
| 21 | Worth syndrome | KG + DL |
| 22 | succinyl-CoA:3-ketoacid CoA transferase deficiency | KG + DL |
| 23 | vertigo, benign recurrent, 2 | KG + DL |
| 24 | glaucoma 1, open angle | KG + DL |
| 25 | Meniere disease | KG + DL |
| 26 | neurohypophyseal diabetes insipidus | KG + DL |
| 27 | cauda equina syndrome | KG + DL |
| 28 | irritable bowel syndrome | KG + DL |
| 29 | methemoglobinemia due to deficiency of methemoglobin reductase | KG + DL |
| 30 | open angle glaucoma | KG + DL |
| 31 | blindness (disorder) | KG + DL |
| 32 | exercise-induced malignant hyperthermia | KG + DL |
| 33 | peripheral vertigo | KG + DL |
| 34 | otosclerosis | KG + DL |
| 35 | age-related hearing impairment | KG + DL |
| 36 | parkinsonian disorder | KG + DL |
| 37 | primary aldosteronism | KG + DL |
| 38 | ascorbic acid deficiency | KG + DL |
| 39 | X-linked deafness | KG + DL |
| 40 | headache disorder | KG + DL |
| 41 | Wernicke-Korsakoff syndrome | KG + DL |
| 42 | blepharospasm | KG + DL |
| 43 | substance abuse/dependence | KG + DL |
| 44 | postgastrectomy syndrome | KG + DL |
| 45 | sebaceous gland anomaly | KG + DL |
| 46 | ochronosis disorder | KG + DL |
| 47 | inherited vitreous-retinal disease | KG + DL |
| 48 | manic bipolar affective disorder | KG + DL |
| 49 | retinal ciliopathy | KG + DL |
| 50 | channelopathy-associated congenital insensitivity to pain, autosomal recessive | 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.