Sulfadimethoxine Sodium

Basic Information

Item Value
DrugBank ID DB06150
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 78

Predicted Indications (TxGNN)

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

# Indication Source
1 rheumatoid arthritis KG + DL
2 gout KG + DL
3 Jeune syndrome situs inversus KG + DL
4 heart disease KG + DL
5 Pierre Robin syndrome associated with a chromosomal anomaly KG + DL
6 partial deletion of the long arm of chromosome 22 KG + DL
7 disorder of fucoglycosan synthesis KG + DL
8 interventricular septum aneurysm KG + DL
9 pulmonary valve disease KG + DL
10 Laubry-Pezzi syndrome KG + DL
11 orofacial clefting syndrome KG + DL
12 partial deletion of the long arm of chromosome 7 KG + DL
13 genetic syndromic Pierre Robin syndrome KG + DL
14 mitral valve disease KG + DL
15 Prinzmetal angina KG + DL
16 colobomatous microphthalmia-rhizomelic dysplasia syndrome KG + DL
17 brachydactyly-syndactyly syndrome KG + DL
18 high output heart failure KG + DL
19 osteoarthritis KG + DL
20 symptomatic heart failure KG + DL
21 pseudoachondroplasia KG + DL
22 myositis fibrosa KG + DL
23 idiopathic granulomatous myositis KG + DL
24 female breast carcinoma KG + DL
25 allergic asthma KG + DL
26 tendinitis KG + DL
27 coronary artery disease KG + DL
28 kyphoscoliotic heart disease KG + DL
29 heart valve disease KG + DL
30 heart conduction disease KG + DL
31 pulmonary hypertension KG + DL
32 osteoarthritis susceptibility KG + DL
33 intrinsic asthma KG + DL
34 intracranial arteriosclerosis KG + DL
35 anomalous left coronary artery from the pulmonary artery KG + DL
36 myocardial ischemia KG + DL
37 hemoglobinopathy KG + DL
38 myocardial disorder KG + DL
39 fibromyalgia KG + DL
40 inclusion body myositis KG + DL
41 postoperative ventricular dysfunction KG + DL
42 intermittent vascular claudication KG + DL
43 genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability KG + DL
44 brain small vessel disease 1 with or without ocular anomalies KG + DL
45 autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome KG + DL
46 acromesomelic dysplasia, Hunter-Thompson type KG + DL
47 diabetic nephropathy KG + DL
48 beta-thalassemia with other manifestations KG + DL
49 cardiac ventricle disease KG + DL
50 congenital anomaly of ventricular septum KG + DL

(Showing top 50 of 78 predictions)

Disclaimer

These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.


← Back to Drug Search


Copyright © 2026 藥提醒科技有限公司 (yao.care). 本報告僅供研究參考,不構成醫療建議。

This site uses Just the Docs, a documentation theme for Jekyll.