Ulipristal
DrugBank ID: DB08867
Summary
| Metric | Value |
|---|---|
| Total Predictions | 50 |
| KG+DL (Dual Validated) | 0 |
| DL Only | 50 |
| KG Only | 0 |
Predictions
| Indication | Score | Source |
|---|---|---|
| rheumatoid arthritis | 0.9031 | DL |
| primary release disorder of platelets | 0.8972 | DL |
| tendinitis | 0.8898 | DL |
| idiopathic granulomatous myositis | 0.8804 | DL |
| myositis fibrosa | 0.8804 | DL |
| pseudo-von Willebrand disease | 0.8717 | DL |
| Glanzmann thrombasthenia | 0.8699 | DL |
| brachydactyly-syndactyly syndrome | 0.8683 | DL |
| colobomatous microphthalmia-rhizomelic dysplasia syndrome | 0.8613 | DL |
| fibromyalgia | 0.8563 | DL |
| heart neoplasm | 0.8501 | DL |
| scalp dermatosis | 0.8464 | DL |
| thrombotic disease | 0.8382 | DL |
| indolent plasma cell myeloma | 0.8380 | DL |
| inclusion body myositis | 0.8353 | DL |
| amenorrhea (disease) | 0.8288 | DL |
| heart conduction disease | 0.8236 | DL |
| plasma cell myeloma | 0.8228 | DL |
| congenital anomaly of ventricular septum | 0.8211 | DL |
| conjunctivitis | 0.8205 | DL |
| heart valve disease | 0.8190 | DL |
| cholecystolithiasis | 0.8173 | DL |
| autosomal dominant macrothrombocytopenia | 0.8045 | DL |
| interventricular septum aneurysm | 0.8009 | DL |
| cardiovascular disease | 0.7988 | DL |
| pericardium disease | 0.7958 | DL |
| Laubry-Pezzi syndrome | 0.7956 | DL |
| vein disease | 0.7931 | DL |
| genetic syndromic Pierre Robin syndrome | 0.7887 | DL |
| patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome | 0.7876 | DL |
| Pierre Robin syndrome associated with a chromosomal anomaly | 0.7854 | DL |
| heart disease | 0.7849 | DL |
| orofacial clefting syndrome | 0.7837 | DL |
| marcothrombocytopenia with mitral valve insufficiency | 0.7812 | DL |
| partial deletion of the long arm of chromosome 7 | 0.7811 | DL |
| hereditary thrombocytopenia with normal platelets | 0.7803 | DL |
| Jeune syndrome situs inversus | 0.7802 | DL |
| disorder of fucoglycosan synthesis | 0.7797 | DL |
| white forelock with malformations | 0.7788 | DL |
| pulmonary valve disease | 0.7776 | DL |
| microcephaly-cardiac defect-lung malsegmentation syndrome | 0.7752 | DL |
| gout | 0.7743 | DL |
| partial deletion of the long arm of chromosome 22 | 0.7717 | DL |
| mitral valve disease | 0.7677 | DL |
| cardiac ventricle disease | 0.7677 | DL |
| carcinoid heart disease | 0.7672 | DL |
| cardiac anomalies-heterotaxy syndrome | 0.7672 | DL |
| cor biloculare | 0.7672 | DL |
| heart aneurysm | 0.7672 | DL |
| myocardial rupture | 0.7672 | 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.