Rivastigmine
DrugBank ID: DB00989
Summary
| Metric | Value |
|---|---|
| Total Predictions | 51 |
| KG+DL (Dual Validated) | 2 |
| DL Only | 48 |
| KG Only | 1 |
Predictions
| Indication | Score | Source |
|---|---|---|
| glaucoma | 0.9927 | DL |
| acute intermittent porphyria | 0.9823 | DL |
| psychogenic movement disorders | 0.9816 | DL |
| primary orthostatic tremor | 0.9801 | DL |
| tremor-nystagmus-duodenal ulcer syndrome | 0.9798 | DL |
| benign shuddering attacks | 0.9787 | DL |
| extrapyramidal and movement disease | 0.9787 | DL |
| benign paroxysmal tonic upgaze of childhood with ataxia | 0.9786 | DL |
| chronic tic disorder | 0.9781 | DL |
| Pick disease | 0.9756 | KG+DL |
| primary hereditary glaucoma | 0.9688 | DL |
| lingual-facial-buccal dyskinesia | 0.9661 | DL |
| open-angle glaucoma | 0.9608 | DL |
| myoclonic dystonia | 0.9522 | DL |
| myoclonus-dystonia syndrome | 0.9506 | DL |
| focal hand dystonia | 0.9447 | DL |
| torsion dystonia | 0.9282 | DL |
| early-onset generalized dystonia | 0.9277 | DL |
| Alzheimer disease | 0.9222 | DL |
| parkinsonian disorder | 0.9202 | DL |
| X-linked dystonia-parkinsonism | 0.9190 | DL |
| torsion dystonia with onset in infancy | 0.9083 | DL |
| lethal infantile mitochondrial myopathy | 0.9076 | DL |
| Axenfeld anomaly | 0.8988 | DL |
| porphyria | 0.8978 | DL |
| Parkinson disease | 0.8944 | DL |
| glaucoma 1, open angle | 0.8928 | DL |
| paralysis agitans, juvenile, of Hunt | 0.8864 | DL |
| cerebrovascular dementia | 0.8853 | DL |
| isolated dystonia | 0.8755 | DL |
| persistent combined dystonia | 0.8710 | DL |
| cyclic hematopoiesis | 0.8692 | DL |
| generalized dystonia | 0.8678 | DL |
| focal dystonia | 0.8634 | DL |
| dementia pugilistica | 0.8606 | DL |
| combined dystonia | 0.8529 | DL |
| dystonia | 0.8386 | DL |
| spasmodic dystonia | 0.8353 | DL |
| cerebellar degeneration | 0.8304 | KG+DL |
| oromandibular dystonia | 0.8279 | DL |
| glaucoma 3, primary infantile, B | 0.8254 | DL |
| autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | 0.8117 | DL |
| retinal dystrophy with or without extraocular anomalies | 0.8091 | DL |
| mitochondrial proton-transporting ATP synthase complex deficiency | 0.7985 | DL |
| primary immunodeficiency syndrome due to p14 deficiency | 0.7944 | DL |
| mitochondrial complex V (ATP synthase) deficiency, nuclear | 0.7929 | DL |
| polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis | 0.7861 | DL |
| obsolete rare pulmonary disease | 0.7852 | DL |
| dystonia, focal, task-specific | 0.7837 | DL |
| PUM1-associated developmental disability-ataxia-seizure syndrome | 0.7813 | DL |
Showing top 50 of 51 predictions.
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Disclaimer
Predictions are for research purposes only and do not constitute medical advice.
Predictions are for research purposes only and do not constitute medical advice.