Tramadol
DrugBank ID: DB00193
Summary
| Metric | Value |
|---|---|
| Total Predictions | 50 |
| KG+DL (Dual Validated) | 0 |
| DL Only | 50 |
| KG Only | 0 |
Predictions
| Indication | Score | Source |
|---|---|---|
| osteoarthritis susceptibility | 1.0000 | DL |
| osteoarthritis | 0.9999 | DL |
| acromesomelic dysplasia, Hunter-Thompson type | 0.9999 | DL |
| brachyolmia-amelogenesis imperfecta syndrome | 0.9999 | DL |
| myosclerosis | 0.9999 | DL |
| brachyolmia | 0.9999 | DL |
| pseudoachondroplasia | 0.9998 | DL |
| arthropathy | 0.9998 | DL |
| spondyloarthropathy, susceptibility to | 0.9997 | DL |
| juvenile idiopathic arthritis | 0.9992 | DL |
| juvenile arthritis due to defect in LACC1 | 0.9992 | DL |
| rheumatoid nodulosis | 0.9992 | DL |
| rheumatoid factor-positive polyarticular juvenile idiopathic arthritis | 0.9990 | DL |
| juvenile chronic polyarthritis | 0.9988 | DL |
| ankylosing spondylitis | 0.9986 | DL |
| WHIM syndrome | 0.9984 | DL |
| rheumatoid arthritis | 0.9982 | DL |
| myofascial pain syndrome | 0.9980 | DL |
| brachydactyly-syndactyly syndrome | 0.9980 | DL |
| hypermobility of coccyx | 0.9975 | DL |
| rheumatoid vasculitis | 0.9975 | DL |
| colobomatous microphthalmia-rhizomelic dysplasia syndrome | 0.9974 | DL |
| inflammatory spondylopathy | 0.9972 | DL |
| Kummell disease | 0.9972 | DL |
| polyarticular juvenile rheumatoid arthritis | 0.9971 | DL |
| vertebral disease | 0.9966 | DL |
| obsolete vascular headache | 0.9964 | DL |
| Behr syndrome | 0.9949 | DL |
| spondyloarthropathy | 0.9945 | DL |
| avascular necrosis of femoral head, primary | 0.9934 | DL |
| combined immunodeficiency due to moesin deficiency | 0.9921 | DL |
| atherosclerosis susceptibility | 0.9886 | DL |
| ankylosis (disease) | 0.9886 | DL |
| 14q32 duplication syndrome | 0.9879 | DL |
| bursitis | 0.9876 | DL |
| otitis media, susceptibility to | 0.9875 | DL |
| bulimia nervosa, susceptibility to | 0.9871 | DL |
| Czech dysplasia, metatarsal type | 0.9868 | DL |
| orofacial cleft 6, susceptibility to | 0.9867 | DL |
| Stickler syndrome, type I, nonsyndromic ocular | 0.9865 | DL |
| spondyloepimetaphyseal dysplasia, Handigodu type | 0.9864 | DL |
| vertebral joint disease | 0.9863 | DL |
| platyspondylic dysplasia, Torrance type | 0.9863 | DL |
| aortic aneurysm, familial thoracic 11, susceptibility to | 0.9860 | DL |
| atrioventricular septal defect, susceptibility to, 2 | 0.9857 | DL |
| transient arthropathy | 0.9851 | DL |
| spondylometaphyseal dysplasia, Schmidt type | 0.9849 | DL |
| systemic lupus erythematosus, susceptibility to | 0.9848 | DL |
| scoliosis, isolated, susceptibility to | 0.9847 | DL |
| dysplastic nevus syndrome | 0.9846 | 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.