Sennosides
DrugBank ID: DB11365
Summary
| Metric | Value |
|---|---|
| Total Predictions | 50 |
| KG+DL (Dual Validated) | 0 |
| DL Only | 50 |
| KG Only | 0 |
Predictions
| Indication | Score | Source |
|---|---|---|
| hypotrichosis simplex of the scalp | 0.9929 | DL |
| congenital hypotrichosis milia | 0.9923 | DL |
| diffuse alopecia areata | 0.9912 | DL |
| open-angle glaucoma | 0.9911 | DL |
| primary hereditary glaucoma | 0.9910 | DL |
| alopecia | 0.9910 | DL |
| glaucoma 1, open angle | 0.9670 | DL |
| open angle glaucoma | 0.9649 | DL |
| esophageal varices with bleeding | 0.9529 | DL |
| esophageal varices without bleeding | 0.9529 | DL |
| endolymphatic hydrops | 0.9502 | DL |
| active cochlear Meniere disease | 0.9404 | DL |
| active cochleovestibular Meniere disease | 0.9404 | DL |
| active vestibular Meniere disease | 0.9404 | DL |
| varicose disease | 0.9397 | DL |
| vertigo, benign recurrent, 2 | 0.9362 | DL |
| pulmonary hypertension | 0.9352 | DL |
| idiopathic bronchiectasis | 0.9328 | DL |
| enterocolitis (disease) | 0.9320 | DL |
| kyphoscoliotic heart disease | 0.9303 | DL |
| 46,XY disorder of gonadal development | 0.9186 | DL |
| male infertility due to gonadal dysgenesis | 0.9183 | DL |
| Meniere disease | 0.9177 | DL |
| pulmonary hypertension, primary, autosomal recessive | 0.9111 | DL |
| dermatitis | 0.9071 | DL |
| renal tubular acidosis | 0.9062 | DL |
| gonadal dysgenesis | 0.9038 | DL |
| acrodermatitis chronica atrophicans | 0.9009 | DL |
| restless legs syndrome | 0.8970 | DL |
| peripheral vertigo | 0.8966 | DL |
| androgenetic alopecia | 0.8961 | DL |
| gastroenteritis | 0.8955 | DL |
| age-related hearing impairment | 0.8941 | DL |
| osteoarthritis | 0.8939 | DL |
| obsolete patella aplasia, coxa vara, and tarsal synostosis | 0.8919 | DL |
| otosclerosis | 0.8918 | DL |
| respiratory failure | 0.8879 | DL |
| neonatal dermatomyositis | 0.8875 | DL |
| pulmonary arterial hypertension | 0.8863 | DL |
| hydroa vacciniforme, familial | 0.8860 | DL |
| secondary interstitial lung disease specific to childhood associated with a connective tissue disease | 0.8857 | DL |
| Axenfeld anomaly | 0.8837 | DL |
| pulmonary hypertension, primary | 0.8837 | DL |
| pregnancy associated osteoporosis | 0.8798 | DL |
| amyopathic dermatomyositis | 0.8796 | DL |
| postmenopausal osteoporosis | 0.8795 | DL |
| idiopathic pulmonary arterial hypertension | 0.8793 | DL |
| autosomal dominant neovascular inflammatory vitreoretinopathy | 0.8790 | DL |
| pseudopelade of Brocq | 0.8788 | DL |
| combined immunodeficiency due to moesin deficiency | 0.8748 | DL |
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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.