Sulfasalazine
DrugBank ID: DB00795
Summary
| Metric | Value |
|---|---|
| Total Predictions | 50 |
| KG+DL (Dual Validated) | 6 |
| DL Only | 44 |
| KG Only | 0 |
Predictions
| Indication | Score | Source |
|---|---|---|
| rheumatoid arthritis | 0.9997 | KG+DL |
| brachydactyly-syndactyly syndrome | 0.9994 | DL |
| colobomatous microphthalmia-rhizomelic dysplasia syndrome | 0.9994 | DL |
| osteoarthritis susceptibility | 0.9988 | DL |
| ulcerative colitis (disease) | 0.9981 | KG+DL |
| congenital hypotrichosis with juvenile macular dystrophy | 0.9966 | DL |
| osteoarthritis | 0.9964 | DL |
| WHIM syndrome | 0.9962 | DL |
| acromesomelic dysplasia, Hunter-Thompson type | 0.9961 | DL |
| spondyloarthropathy, susceptibility to | 0.9953 | DL |
| brachyolmia-amelogenesis imperfecta syndrome | 0.9949 | DL |
| myosclerosis | 0.9943 | DL |
| gout | 0.9940 | DL |
| brachyolmia | 0.9938 | DL |
| arthropathy | 0.9934 | DL |
| ankylosing spondylitis | 0.9933 | DL |
| inflammatory bowel disease | 0.9922 | KG+DL |
| rheumatoid factor-positive polyarticular juvenile idiopathic arthritis | 0.9918 | DL |
| rheumatoid nodulosis | 0.9916 | DL |
| pseudoachondroplasia | 0.9916 | DL |
| juvenile chronic polyarthritis | 0.9906 | DL |
| juvenile idiopathic arthritis | 0.9903 | KG+DL |
| rheumatoid vasculitis | 0.9895 | DL |
| granulomatous disease with defect in neutrophil chemotaxis | 0.9889 | DL |
| granulomatous disease, chronic, autosomal recessive, 5 | 0.9888 | DL |
| anus disease | 0.9880 | DL |
| hypermobility of coccyx | 0.9879 | DL |
| inflammatory spondylopathy | 0.9878 | DL |
| Kummell disease | 0.9875 | DL |
| functional neutrophil defect | 0.9874 | DL |
| vertebral disease | 0.9863 | DL |
| Crohn disease of the esophagus | 0.9861 | DL |
| polyarticular juvenile rheumatoid arthritis | 0.9857 | DL |
| juvenile arthritis due to defect in LACC1 | 0.9830 | KG+DL |
| tenosynovitis | 0.9809 | DL |
| avascular necrosis of femoral head, primary | 0.9793 | DL |
| seborrheic dermatitis | 0.9793 | DL |
| exostosis | 0.9790 | DL |
| spondyloepimetaphyseal dysplasia, Handigodu type | 0.9770 | DL |
| ankylosis (disease) | 0.9763 | DL |
| platyspondylic dysplasia, Torrance type | 0.9755 | DL |
| Czech dysplasia, metatarsal type | 0.9751 | DL |
| spondyloarthropathy | 0.9749 | KG+DL |
| seborrheic keratosis | 0.9749 | DL |
| Stickler syndrome, type I, nonsyndromic ocular | 0.9745 | DL |
| spondylometaphyseal dysplasia, Schmidt type | 0.9744 | DL |
| mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis | 0.9713 | DL |
| megaepiphyseal dwarfism | 0.9713 | DL |
| vertebral joint disease | 0.9708 | DL |
| transient arthropathy | 0.9707 | 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.