Terazosin
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB01162 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 69 |
Predicted Indications (TxGNN)
The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.
| # | Indication | Source |
|---|---|---|
| 1 | hypotrichosis simplex of the scalp | KG + DL |
| 2 | congenital hypotrichosis milia | KG + DL |
| 3 | diffuse alopecia areata | KG + DL |
| 4 | alopecia | KG + DL |
| 5 | migraine disorder | KG + DL |
| 6 | migraine with brainstem aura | KG + DL |
| 7 | Raynaud disease | KG + DL |
| 8 | Ambras type hypertrichosis universalis congenita | KG + DL |
| 9 | manic bipolar affective disorder | KG + DL |
| 10 | kyphoscoliotic heart disease | KG + DL |
| 11 | pulmonary hypertension | KG + DL |
| 12 | malformation syndrome with odontal and/or periodontal component | KG + DL |
| 13 | hypertrichosis (disease) | KG + DL |
| 14 | syndrome with a Dandy-Walker malformation as major feature | KG + DL |
| 15 | primary hereditary glaucoma | KG + DL |
| 16 | isolated genetic hair shaft abnormality | KG + DL |
| 17 | respiratory failure | KG + DL |
| 18 | open-angle glaucoma | KG + DL |
| 19 | pulmonary hypertension owing to lung disease and/or hypoxia | KG + DL |
| 20 | pulmonary hypertension with unclear multifactorial mechanism | KG + DL |
| 21 | transient ischemic attack (disease) | KG + DL |
| 22 | variably protease-sensitive prionopathy | KG + DL |
| 23 | pseudopelade of Brocq | KG + DL |
| 24 | malignant hypertensive renal disease | KG + DL |
| 25 | malignant renovascular hypertension | KG + DL |
| 26 | Braddock syndrome | KG + DL |
| 27 | cerebrovascular disorder | KG + DL |
| 28 | spinal cord ischemia | KG + DL |
| 29 | atrophoderma vermiculata | KG + DL |
| 30 | Prinzmetal angina | KG + DL |
| 31 | sinoatrial node disease | KG + DL |
| 32 | obsolete patella aplasia, coxa vara, and tarsal synostosis | KG + DL |
| 33 | arterial thoracic outlet syndrome | KG + DL |
| 34 | venous thoracic outlet syndrome | KG + DL |
| 35 | ulerythema ophryogenesis | KG + DL |
| 36 | sinoatrial block | KG + DL |
| 37 | pulmonary hypertension, primary, autosomal recessive | KG + DL |
| 38 | familial isolated trichomegaly | KG + DL |
| 39 | major affective disorder | KG + DL |
| 40 | headache disorder | KG + DL |
| 41 | neurogenic thoracic outlet syndrome | KG + DL |
| 42 | familial clubfoot due to 17q23.1q23.2 microduplication | KG + DL |
| 43 | glaucoma 1, open angle | KG + DL |
| 44 | essential hypertension, genetic | KG + DL |
| 45 | attention deficit-hyperactivity disorder | KG + DL |
| 46 | trigeminal autonomic cephalalgia | KG + DL |
| 47 | faciodigitogenital syndrome | KG + DL |
| 48 | vascular disease | KG + DL |
| 49 | angiodysplasia of stomach | KG + DL |
| 50 | idiopathic spontaneous coronary artery dissection | KG + DL |
(Showing top 50 of 69 predictions)
Disclaimer
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.