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 cochleovestibular Meniere disease KG + DL
19 active cochlear Meniere disease KG + DL
20 active vestibular 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.


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