Midodrine Hcl
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB00211 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 57 |
Predicted Indications (TxGNN)
The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.
| # | Indication | Source |
|---|---|---|
| 1 | variably protease-sensitive prionopathy | KG + DL |
| 2 | faciodigitogenital syndrome | KG + DL |
| 3 | attention deficit-hyperactivity disorder | KG + DL |
| 4 | hypotensive disorder | KG + DL |
| 5 | attention deficit hyperactivity disorder, inattentive type | KG + DL |
| 6 | sinoatrial node disease | KG + DL |
| 7 | monogenic obesity | KG + DL |
| 8 | specific developmental disorder | KG + DL |
| 9 | obsolete hypertelorism (disease) | KG + DL |
| 10 | sinoatrial block | KG + DL |
| 11 | obsolete neurogenic bladder (disease) | KG + DL |
| 12 | chondromyxoid fibroma | KG + DL |
| 13 | insomnia (disease) | KG + DL |
| 14 | frontorhiny | KG + DL |
| 15 | obesity disorder | KG + DL |
| 16 | proximal 16p11.2 microdeletion syndrome | KG + DL |
| 17 | peripheral motor neuropathy-dysautonomia syndrome | KG + DL |
| 18 | hypervitaminosis | KG + DL |
| 19 | Ambras type hypertrichosis universalis congenita | KG + DL |
| 20 | restless legs syndrome | KG + DL |
| 21 | trichotillomania | KG + DL |
| 22 | Meniere disease | KG + DL |
| 23 | otosclerosis | KG + DL |
| 24 | cauda equina syndrome | KG + DL |
| 25 | malformation syndrome with odontal and/or periodontal component | KG + DL |
| 26 | esophageal varices with bleeding | KG + DL |
| 27 | esophageal varices without bleeding | KG + DL |
| 28 | syndrome with a Dandy-Walker malformation as major feature | KG + DL |
| 29 | hypotrichosis simplex of the scalp | KG + DL |
| 30 | hypertrichosis (disease) | KG + DL |
| 31 | progressive familial heart block | KG + DL |
| 32 | isolated genetic hair shaft abnormality | KG + DL |
| 33 | peripheral vertigo | KG + DL |
| 34 | age-related hearing impairment | KG + DL |
| 35 | congenital hypotrichosis milia | KG + DL |
| 36 | endolymphatic hydrops | KG + DL |
| 37 | blepharospasm | KG + DL |
| 38 | active vestibular Meniere disease | KG + DL |
| 39 | active cochlear Meniere disease | KG + DL |
| 40 | active cochleovestibular Meniere disease | KG + DL |
| 41 | sleep disorder, initiating and maintaining sleep | KG + DL |
| 42 | primary hereditary glaucoma | KG + DL |
| 43 | diffuse alopecia areata | KG + DL |
| 44 | disorder of peroxisomal alpha-, beta- and omega-oxidation | KG + DL |
| 45 | miscellaneous movement disorder due to genetic neurodegenerative disease | KG + DL |
| 46 | major affective disorder | KG + DL |
| 47 | vertigo, benign recurrent, 2 | KG + DL |
| 48 | idiopathic bronchiectasis | KG + DL |
| 49 | myopia X-linked | KG + DL |
| 50 | X-linked adrenoleukodystrophy | KG + DL |
(Showing top 50 of 57 predictions)
Disclaimer
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.