Gemfibrozil
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB01241 |
| 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 | rheumatoid arthritis | KG + DL |
| 2 | multiple endocrine neoplasia | KG + DL |
| 3 | HIV infectious disease | KG + DL |
| 4 | hypoalphalipoproteinemia | KG + DL |
| 5 | brachydactyly-syndactyly syndrome | KG + DL |
| 6 | colobomatous microphthalmia-rhizomelic dysplasia syndrome | KG + DL |
| 7 | methemoglobinemia, alpha type | KG + DL |
| 8 | obsolete familial combined hyperlipidemia | KG + DL |
| 9 | sclerosing cholangitis | KG + DL |
| 10 | methemoglobin reductase deficiency | KG + DL |
| 11 | neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter | KG + DL |
| 12 | homozygous familial hypercholesterolemia | KG + DL |
| 13 | feline acquired immunodeficiency syndrome | KG + DL |
| 14 | simian immunodeficiency virus infection | KG + DL |
| 15 | gout | KG + DL |
| 16 | bone Paget disease | KG + DL |
| 17 | methemoglobinemia | KG + DL |
| 18 | blindness (disorder) | KG + DL |
| 19 | congestive heart failure | KG + DL |
| 20 | methemoglobinemia due to deficiency of methemoglobin reductase | KG + DL |
| 21 | hemoglobinopathy | KG + DL |
| 22 | autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome | KG + DL |
| 23 | brain small vessel disease 1 with or without ocular anomalies | KG + DL |
| 24 | meningococcal infection | KG + DL |
| 25 | chronic pulmonary heart disease | KG + DL |
| 26 | acute pulmonary heart disease | KG + DL |
| 27 | malignant renovascular hypertension | KG + DL |
| 28 | malignant hypertensive renal disease | KG + DL |
| 29 | Prinzmetal angina | KG + DL |
| 30 | pulmonary hypertension owing to lung disease and/or hypoxia | KG + DL |
| 31 | pulmonary hypertension with unclear multifactorial mechanism | KG + DL |
| 32 | diabetic nephropathy | KG + DL |
| 33 | pyropoikilocytosis, hereditary | KG + DL |
| 34 | Braddock syndrome | KG + DL |
| 35 | beta-thalassemia with other manifestations | KG + DL |
| 36 | myocardial infarction | KG + DL |
| 37 | hypertensive disorder | KG + DL |
| 38 | partial deletion of the short arm of chromosome 16 | KG + DL |
| 39 | hypolipoproteinemia (disease) | KG + DL |
| 40 | hemolytic anemia due to glucophosphate isomerase deficiency | KG + DL |
| 41 | AIDS | KG + DL |
| 42 | posteroinferior myocardial infarction | KG + DL |
| 43 | posterolateral myocardial infarction | KG + DL |
| 44 | septal myocardial infarction | KG + DL |
| 45 | familial hyperlipidemia | KG + DL |
| 46 | pyruvate kinase deficiency of red cells | KG + DL |
| 47 | chronic renal failure syndrome | KG + DL |
| 48 | cerebral infarction | KG + DL |
| 49 | paratenonitis | KG + DL |
| 50 | calcific tendinitis | 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.