Urofollitropin
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB00094 |
| 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 | migraine disorder | KG + DL |
| 2 | migraine with brainstem aura | KG + DL |
| 3 | cauda equina syndrome | KG + DL |
| 4 | His bundle tachycardia | KG + DL |
| 5 | restless legs syndrome | KG + DL |
| 6 | obsolete neurogenic bladder (disease) | KG + DL |
| 7 | multifocal atrial tachycardia (disease) | KG + DL |
| 8 | postural orthostatic tachycardia syndrome | KG + DL |
| 9 | migraine with or without aura, susceptibility to | KG + DL |
| 10 | Raynaud disease | KG + DL |
| 11 | atrophoderma vermiculata | KG + DL |
| 12 | idiopathic neonatal atrial flutter | KG + DL |
| 13 | ulerythema ophryogenesis | KG + DL |
| 14 | sinoatrial node dysfunction and deafness | KG + DL |
| 15 | erectile dysfunction (disease) | KG + DL |
| 16 | progressive familial heart block | KG + DL |
| 17 | Johanson-Blizzard syndrome | KG + DL |
| 18 | brachydactyly-long thumb syndrome | KG + DL |
| 19 | pulmonary hypertension | KG + DL |
| 20 | adrenal gland hyperfunction | KG + DL |
| 21 | autosomal dominant cardiac arrhythmia (Kuhn) | KG + DL |
| 22 | amenorrhea (disease) | KG + DL |
| 23 | torsade-de-pointes syndrome with short coupling interval | KG + DL |
| 24 | sino-auricular heart block | KG + DL |
| 25 | atrial conduction disease | KG + DL |
| 26 | esophageal disease | KG + DL |
| 27 | atrioventricular block | KG + DL |
| 28 | obsolete heart block | KG + DL |
| 29 | histiocytoid cardiomyopathy | KG + DL |
| 30 | atrioventricular block (disease) | KG + DL |
| 31 | kyphoscoliotic heart disease | KG + DL |
| 32 | Ambras type hypertrichosis universalis congenita | KG + DL |
| 33 | X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome | KG + DL |
| 34 | non-syndromic esophageal malformation | KG + DL |
| 35 | sciatic neuropathy | KG + DL |
| 36 | hypertrichosis (disease) | KG + DL |
| 37 | atrioventricular dissociation (disease) | KG + DL |
| 38 | ventricular tachycardia, familial | KG + DL |
| 39 | atypical coarctation of aorta | KG + DL |
| 40 | familial sick sinus syndrome | KG + DL |
| 41 | malformation syndrome with odontal and/or periodontal component | KG + DL |
| 42 | acne (disease) | KG + DL |
| 43 | isolated genetic hair shaft abnormality | KG + DL |
| 44 | oligospermia | KG + DL |
| 45 | spermatogenic failure, Y-linked | KG + DL |
| 46 | syndrome with a Dandy-Walker malformation as major feature | KG + DL |
| 47 | esophageal ulcer | KG + DL |
| 48 | mutism (disease) | KG + DL |
| 49 | ventricular tachycardia | KG + DL |
| 50 | obsolete bundle branch block | 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.