Methylprednisolone Aceponate

Basic Information

Item Value
DrugBank ID DB14643
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 97

Predicted Indications (TxGNN)

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

# Indication Source
1 gout KG + DL
2 Raynaud disease KG + DL
3 allergic asthma KG + DL
4 diabetic nephropathy KG + DL
5 brain small vessel disease 1 with or without ocular anomalies KG + DL
6 intrinsic asthma KG + DL
7 autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome KG + DL
8 congestive heart failure KG + DL
9 pulmonary hypertension owing to lung disease and/or hypoxia KG + DL
10 pulmonary hypertension with unclear multifactorial mechanism KG + DL
11 benign prostatic hyperplasia (disease) KG + DL
12 hypertensive disorder KG + DL
13 Prinzmetal angina KG + DL
14 malignant hypertensive renal disease KG + DL
15 malignant renovascular hypertension KG + DL
16 type 1 diabetes mellitus KG + DL
17 chronic pulmonary heart disease KG + DL
18 Braddock syndrome KG + DL
19 chronic kidney disease KG + DL
20 acute pulmonary heart disease KG + DL
21 autoimmune oophoritis KG + DL
22 end stage renal failure KG + DL
23 osteoarthritis KG + DL
24 myocardial infarction KG + DL
25 exostosis KG + DL
26 osteoarthritis susceptibility KG + DL
27 posteroinferior myocardial infarction KG + DL
28 posterolateral myocardial infarction KG + DL
29 hypotensive disorder KG + DL
30 chronic renal failure syndrome KG + DL
31 septal myocardial infarction KG + DL
32 asthma KG + DL
33 hemoglobinopathy KG + DL
34 asthma-related traits, susceptibility to KG + DL
35 alopecia KG + DL
36 pseudoachondroplasia KG + DL
37 acromesomelic dysplasia, Hunter-Thompson type KG + DL
38 brachyolmia KG + DL
39 heart failure KG + DL
40 hypotrichosis simplex of the scalp KG + DL
41 exostoses, multiple, KG + DL
42 brachyolmia-amelogenesis imperfecta syndrome KG + DL
43 arthropathy KG + DL
44 myosclerosis KG + DL
45 congenital hypotrichosis milia KG + DL
46 partial deletion of the short arm of chromosome 16 KG + DL
47 beta-thalassemia with other manifestations KG + DL
48 disorder of O-xylosylglycan synthesis KG + DL
49 pyropoikilocytosis, hereditary KG + DL
50 bronchitis KG + DL

(Showing top 50 of 97 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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