Troxerutin

Basic Information

Item Value
DrugBank ID DB13124
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 58

Predicted Indications (TxGNN)

The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.

# Indication Source
1 hemoglobinopathy KG + DL
2 myocardial infarction KG + DL
3 partial deletion of the short arm of chromosome 16 KG + DL
4 beta-thalassemia with other manifestations KG + DL
5 hemolytic anemia due to glucophosphate isomerase deficiency KG + DL
6 pyruvate kinase deficiency of red cells KG + DL
7 posteroinferior myocardial infarction KG + DL
8 posterolateral myocardial infarction KG + DL
9 septal myocardial infarction KG + DL
10 coronary thrombosis KG + DL
11 pyropoikilocytosis, hereditary KG + DL
12 rheumatoid arthritis KG + DL
13 myocardial infarction (disease) KG + DL
14 coronary stenosis KG + DL
15 thrombotic disease KG + DL
16 congenital coronary artery anomaly KG + DL
17 gout KG + DL
18 colobomatous microphthalmia-rhizomelic dysplasia syndrome KG + DL
19 postoperative ventricular dysfunction KG + DL
20 autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome KG + DL
21 brachydactyly-syndactyly syndrome KG + DL
22 brain small vessel disease 1 with or without ocular anomalies KG + DL
23 diabetic nephropathy KG + DL
24 interventricular septum aneurysm KG + DL
25 pulmonary valve disease KG + DL
26 Jeune syndrome situs inversus KG + DL
27 heart disease KG + DL
28 Pierre Robin syndrome associated with a chromosomal anomaly KG + DL
29 orofacial clefting syndrome KG + DL
30 partial deletion of the long arm of chromosome 7 KG + DL
31 partial deletion of the long arm of chromosome 22 KG + DL
32 bronchitis KG + DL
33 disorder of fucoglycosan synthesis KG + DL
34 genetic syndromic Pierre Robin syndrome KG + DL
35 Laubry-Pezzi syndrome KG + DL
36 mitral valve disease KG + DL
37 vein disease KG + DL
38 Prinzmetal angina KG + DL
39 cavernous sinus thrombosis KG + DL
40 lateral sinus thrombosis KG + DL
41 angiodysplasia KG + DL
42 venous thromboembolism KG + DL
43 fibrocartilaginous embolism KG + DL
44 non-inflammatory vasculopathy KG + DL
45 myositis fibrosa KG + DL
46 idiopathic granulomatous myositis KG + DL
47 laryngotracheitis KG + DL
48 heparin cofactor 2 deficiency KG + DL
49 renal osteodystrophy KG + DL
50 tendinitis KG + DL

(Showing top 50 of 58 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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