Piroxicam
DrugBank ID: DB00554
Summary
| Metric | Value |
|---|---|
| Total Predictions | 50 |
| KG+DL (Dual Validated) | 1 |
| DL Only | 49 |
| KG Only | 0 |
Predictions
| Indication | Score | Source |
|---|---|---|
| osteoarthritis susceptibility | 1.0000 | DL |
| rheumatoid arthritis | 1.0000 | DL |
| osteoarthritis | 1.0000 | DL |
| colobomatous microphthalmia-rhizomelic dysplasia syndrome | 1.0000 | DL |
| brachydactyly-syndactyly syndrome | 1.0000 | DL |
| acromesomelic dysplasia, Hunter-Thompson type | 1.0000 | DL |
| brachyolmia-amelogenesis imperfecta syndrome | 1.0000 | DL |
| myosclerosis | 0.9999 | DL |
| brachyolmia | 0.9999 | DL |
| arthropathy | 0.9999 | KG+DL |
| pseudoachondroplasia | 0.9999 | DL |
| WHIM syndrome | 0.9996 | DL |
| rheumatoid nodulosis | 0.9993 | DL |
| juvenile idiopathic arthritis | 0.9993 | DL |
| rheumatoid factor-positive polyarticular juvenile idiopathic arthritis | 0.9993 | DL |
| juvenile arthritis due to defect in LACC1 | 0.9991 | DL |
| spondyloarthropathy, susceptibility to | 0.9991 | DL |
| juvenile chronic polyarthritis | 0.9990 | DL |
| ankylosing spondylitis | 0.9956 | DL |
| combined immunodeficiency due to moesin deficiency | 0.9950 | DL |
| spondyloarthropathy | 0.9936 | DL |
| rheumatoid vasculitis | 0.9934 | DL |
| hypermobility of coccyx | 0.9932 | DL |
| vertebral disease | 0.9927 | DL |
| polyarticular juvenile rheumatoid arthritis | 0.9923 | DL |
| Kummell disease | 0.9921 | DL |
| inflammatory spondylopathy | 0.9921 | DL |
| Behr syndrome | 0.9817 | DL |
| frozen shoulder | 0.9802 | DL |
| avascular necrosis of femoral head, primary | 0.9695 | DL |
| leukoplakia | 0.9672 | DL |
| mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency | 0.9661 | DL |
| psoriasis-related juvenile idiopathic arthritis | 0.9459 | DL |
| ankylosis (disease) | 0.9432 | DL |
| vertebral joint disease | 0.9351 | DL |
| Czech dysplasia, metatarsal type | 0.9320 | DL |
| Stickler syndrome, type I, nonsyndromic ocular | 0.9314 | DL |
| spondyloepimetaphyseal dysplasia, Handigodu type | 0.9302 | DL |
| platyspondylic dysplasia, Torrance type | 0.9299 | DL |
| spondylometaphyseal dysplasia, Schmidt type | 0.9257 | DL |
| intracranial embolism | 0.9245 | DL |
| bursitis | 0.9231 | DL |
| megaepiphyseal dwarfism | 0.9204 | DL |
| mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis | 0.9183 | DL |
| transient arthropathy | 0.9182 | DL |
| contracture | 0.9152 | DL |
| hypotrichosis simplex of the scalp | 0.9144 | DL |
| spondyloperipheral dysplasia-short ulna syndrome | 0.9130 | DL |
| articular cartilage disease | 0.9120 | DL |
| Behcet syndrome arthropathy | 0.9104 | 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.