Nicergoline
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB00699 |
| 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 | syndrome with a Dandy-Walker malformation as major feature | KG + DL |
| 5 | benign prostatic hyperplasia (disease) | KG + DL |
| 6 | isolated genetic hair shaft abnormality | KG + DL |
| 7 | nephrogenic syndrome of inappropriate antidiuresis | KG + DL |
| 8 | migraine disorder | KG + DL |
| 9 | subarachnoid hemorrhage (disease) | KG + DL |
| 10 | migraine with brainstem aura | KG + DL |
| 11 | pulmonary hypertension | KG + DL |
| 12 | open-angle glaucoma | KG + DL |
| 13 | primary hereditary glaucoma | KG + DL |
| 14 | kyphoscoliotic heart disease | KG + DL |
| 15 | migraine with or without aura, susceptibility to | KG + DL |
| 16 | headache disorder | KG + DL |
| 17 | chronic tic disorder | KG + DL |
| 18 | phaeochromocytoma | KG + DL |
| 19 | benign shuddering attacks | KG + DL |
| 20 | extrapyramidal and movement disease | KG + DL |
| 21 | psychogenic movement disorders | KG + DL |
| 22 | acquired aneurysmal subarachnoid hemorrhage | KG + DL |
| 23 | multiple system atrophy | KG + DL |
| 24 | benign paroxysmal tonic upgaze of childhood with ataxia | KG + DL |
| 25 | trigeminal autonomic cephalalgia | KG + DL |
| 26 | primary orthostatic tremor | KG + DL |
| 27 | tremor-nystagmus-duodenal ulcer syndrome | KG + DL |
| 28 | lingual-facial-buccal dyskinesia | KG + DL |
| 29 | pulmonary hypertension, primary, autosomal recessive | KG + DL |
| 30 | atrophoderma vermiculata | KG + DL |
| 31 | variably protease-sensitive prionopathy | KG + DL |
| 32 | ulerythema ophryogenesis | KG + DL |
| 33 | obsolete patella aplasia, coxa vara, and tarsal synostosis | KG + DL |
| 34 | common cold | KG + DL |
| 35 | venous thoracic outlet syndrome | KG + DL |
| 36 | arterial thoracic outlet syndrome | KG + DL |
| 37 | genetic alopecia | KG + DL |
| 38 | vascular disease | KG + DL |
| 39 | neurogenic thoracic outlet syndrome | KG + DL |
| 40 | chromosome 17q23.1-q23.2 deletion syndrome | KG + DL |
| 41 | pulmonary arterial hypertension | KG + DL |
| 42 | familial clubfoot due to 17q23.1q23.2 microduplication | KG + DL |
| 43 | visceral calciphylaxis | KG + DL |
| 44 | glaucoma 1, open angle | KG + DL |
| 45 | Raynaud disease | KG + DL |
| 46 | coxopodopatellar syndrome | KG + DL |
| 47 | allergic urticaria | KG + DL |
| 48 | small intestine cancer | KG + DL |
| 49 | idiopathic spontaneous coronary artery dissection | KG + DL |
| 50 | angiodysplasia of stomach | 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.