Inclisiran
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB14901 |
| 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 | potassium deficiency disease | KG + DL |
| 2 | esophageal disease | KG + DL |
| 3 | atypical coarctation of aorta | KG + DL |
| 4 | migraine disorder | KG + DL |
| 5 | non-syndromic esophageal malformation | KG + DL |
| 6 | migraine with brainstem aura | KG + DL |
| 7 | migraine with or without aura, susceptibility to | KG + DL |
| 8 | aortic malformation | KG + DL |
| 9 | esophageal ulcer | KG + DL |
| 10 | Raynaud disease | KG + DL |
| 11 | peptic esophagitis | KG + DL |
| 12 | cauda equina syndrome | KG + DL |
| 13 | gastrin secretion abnormality | KG + DL |
| 14 | ulerythema ophryogenesis | KG + DL |
| 15 | irritable bowel syndrome | KG + DL |
| 16 | atrophoderma vermiculata | KG + DL |
| 17 | peptic ulcer disease | KG + DL |
| 18 | esophageal diverticulosis | KG + DL |
| 19 | phaeochromocytoma | KG + DL |
| 20 | dyskinesia of esophagus | KG + DL |
| 21 | esophageal atresia (disease) | KG + DL |
| 22 | esophageal leukoplakia (disease) | KG + DL |
| 23 | esophageal tuberculosis | KG + DL |
| 24 | lesion of sciatic nerve | KG + DL |
| 25 | intermittent vascular claudication | KG + DL |
| 26 | erectile dysfunction (disease) | KG + DL |
| 27 | postural orthostatic tachycardia syndrome | KG + DL |
| 28 | peripheral vascular disease | KG + DL |
| 29 | abnormality of glucagon secretion | KG + DL |
| 30 | esophageal malformation | KG + DL |
| 31 | purpura fulminans | KG + DL |
| 32 | endemic goiter | KG + DL |
| 33 | pulmonary hypertension | KG + DL |
| 34 | intracranial arteriosclerosis | KG + DL |
| 35 | gastroduodenitis | KG + DL |
| 36 | Monckeberg arteriosclerosis | KG + DL |
| 37 | symptomatic form of hemophilia in female carriers | KG + DL |
| 38 | hyperinsulinemic hypoglycemia, familial | KG + DL |
| 39 | idiopathic bronchiectasis | KG + DL |
| 40 | familial mitral valve prolapse | KG + DL |
| 41 | Smouldering systemic mastocytosis | KG + DL |
| 42 | thrombophilia due to protein C deficiency, autosomal recessive | KG + DL |
| 43 | esotropia | KG + DL |
| 44 | lymphoadenopathic mastocytosis with eosinophilia | KG + DL |
| 45 | autosomal dominant coarctation of aorta | KG + DL |
| 46 | congenital hypotrichosis milia | KG + DL |
| 47 | alopecia | KG + DL |
| 48 | pulmonary hypertension, primary, autosomal recessive | KG + DL |
| 49 | hypotrichosis simplex of the scalp | KG + DL |
| 50 | kyphoscoliotic heart disease | 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.