Phthalylsulfathiazole
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB13248 |
| 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 | gout | KG + DL |
| 2 | allergic asthma | KG + DL |
| 3 | intrinsic asthma | KG + DL |
| 4 | diabetic nephropathy | KG + DL |
| 5 | brain small vessel disease 1 with or without ocular anomalies | KG + DL |
| 6 | autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome | KG + DL |
| 7 | type 1 diabetes mellitus | KG + DL |
| 8 | Raynaud disease | KG + DL |
| 9 | autoimmune oophoritis | KG + DL |
| 10 | chronic kidney disease | KG + DL |
| 11 | congestive heart failure | KG + DL |
| 12 | Prinzmetal angina | KG + DL |
| 13 | end stage renal failure | KG + DL |
| 14 | asthma | KG + DL |
| 15 | asthma-related traits, susceptibility to | KG + DL |
| 16 | exostosis | KG + DL |
| 17 | acute pulmonary heart disease | KG + DL |
| 18 | bronchitis | KG + DL |
| 19 | chronic pulmonary heart disease | KG + DL |
| 20 | pulmonary hypertension with unclear multifactorial mechanism | KG + DL |
| 21 | pulmonary hypertension owing to lung disease and/or hypoxia | KG + DL |
| 22 | malignant hypertensive renal disease | KG + DL |
| 23 | malignant renovascular hypertension | KG + DL |
| 24 | osteoarthritis | KG + DL |
| 25 | hypertensive disorder | KG + DL |
| 26 | myocardial infarction | KG + DL |
| 27 | Braddock syndrome | KG + DL |
| 28 | hemoglobinopathy | KG + DL |
| 29 | osteoarthritis susceptibility | KG + DL |
| 30 | posterolateral myocardial infarction | KG + DL |
| 31 | posteroinferior myocardial infarction | KG + DL |
| 32 | benign prostatic hyperplasia (disease) | KG + DL |
| 33 | chronic renal failure syndrome | KG + DL |
| 34 | septal myocardial infarction | KG + DL |
| 35 | diabetes mellitus (disease) | KG + DL |
| 36 | pseudoachondroplasia | KG + DL |
| 37 | Lesch-Nyhan syndrome | KG + DL |
| 38 | disorder of O-xylosylglycan synthesis | KG + DL |
| 39 | iris disease | KG + DL |
| 40 | partial deletion of the short arm of chromosome 16 | KG + DL |
| 41 | beta-thalassemia with other manifestations | KG + DL |
| 42 | high output heart failure | KG + DL |
| 43 | exostoses, multiple, | KG + DL |
| 44 | thiamine-responsive dysfunction syndrome | KG + DL |
| 45 | pyropoikilocytosis, hereditary | KG + DL |
| 46 | opsismodysplasia | KG + DL |
| 47 | classic stiff person syndrome | KG + DL |
| 48 | focal stiff limb syndrome | KG + DL |
| 49 | acromesomelic dysplasia, Hunter-Thompson type | KG + DL |
| 50 | symptomatic heart failure | 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.