Plecanatide
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB13170 |
| 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 | hypertrichosis (disease) | KG + DL |
| 2 | Ambras type hypertrichosis universalis congenita | KG + DL |
| 3 | malformation syndrome with odontal and/or periodontal component | KG + DL |
| 4 | isolated genetic hair shaft abnormality | KG + DL |
| 5 | syndrome with a Dandy-Walker malformation as major feature | KG + DL |
| 6 | idiopathic spontaneous coronary artery dissection | KG + DL |
| 7 | vascular disease | KG + DL |
| 8 | arterial thoracic outlet syndrome | KG + DL |
| 9 | venous thoracic outlet syndrome | KG + DL |
| 10 | phaeochromocytoma | KG + DL |
| 11 | exercise-induced malignant hyperthermia | KG + DL |
| 12 | neurogenic thoracic outlet syndrome | KG + DL |
| 13 | visceral calciphylaxis | KG + DL |
| 14 | blue toe syndrome | KG + DL |
| 15 | hemangioendothelioma | KG + DL |
| 16 | angiodysplasia of stomach | KG + DL |
| 17 | atheroembolism of kidney | KG + DL |
| 18 | alopecia | KG + DL |
| 19 | lymphangiectasis | KG + DL |
| 20 | allergic urticaria | KG + DL |
| 21 | arterial dissection-lentiginosis syndrome | KG + DL |
| 22 | respiratory failure | KG + DL |
| 23 | hypotrichosis simplex of the scalp | KG + DL |
| 24 | congenital hypotrichosis milia | KG + DL |
| 25 | familial periodic paralysis | KG + DL |
| 26 | diffuse alopecia areata | KG + DL |
| 27 | hypokalemic periodic paralysis | KG + DL |
| 28 | thyrotoxic periodic paralysis, susceptibility to | KG + DL |
| 29 | transient ischemic attack (disease) | KG + DL |
| 30 | benign prostatic hyperplasia (disease) | KG + DL |
| 31 | enterocolitis (disease) | KG + DL |
| 32 | congenital alveolar capillary dysplasia | KG + DL |
| 33 | thyrotoxic periodic paralysis | KG + DL |
| 34 | open-angle glaucoma | KG + DL |
| 35 | disorder of carbohydrate absorption and transport | KG + DL |
| 36 | sympathetic paraganglioma | KG + DL |
| 37 | malignant hyperthermia of anesthesia | KG + DL |
| 38 | hyperinsulinemic hypoglycemia | KG + DL |
| 39 | primary hereditary glaucoma | KG + DL |
| 40 | rhinitis | KG + DL |
| 41 | familial isolated trichomegaly | KG + DL |
| 42 | 16q24.1 microdeletion syndrome | KG + DL |
| 43 | primary interstitial lung disease specific to childhood | KG + DL |
| 44 | isolated pulmonary capillaritis | KG + DL |
| 45 | King-Denborough syndrome | KG + DL |
| 46 | adrenal gland pheochromocytoma | KG + DL |
| 47 | autosomal recessive hyperinsulinism due to SUR1 deficiency | KG + DL |
| 48 | diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency | KG + DL |
| 49 | small intestine cancer | KG + DL |
| 50 | hyperinsulinemic hypoglycemia, familial | 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.