Nabumetone
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB00461 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 56 |
Predicted Indications (TxGNN)
The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.
| # | Indication | Source |
|---|---|---|
| 1 | acromesomelic dysplasia, Hunter-Thompson type | KG + DL |
| 2 | brachyolmia-amelogenesis imperfecta syndrome | KG + DL |
| 3 | myosclerosis | KG + DL |
| 4 | colobomatous microphthalmia-rhizomelic dysplasia syndrome | KG + DL |
| 5 | brachyolmia | KG + DL |
| 6 | brachydactyly-syndactyly syndrome | KG + DL |
| 7 | pseudoachondroplasia | KG + DL |
| 8 | spondyloarthropathy, susceptibility to | KG + DL |
| 9 | WHIM syndrome | KG + DL |
| 10 | rheumatoid nodulosis | KG + DL |
| 11 | juvenile idiopathic arthritis | KG + DL |
| 12 | rheumatoid factor-positive polyarticular juvenile idiopathic arthritis | KG + DL |
| 13 | juvenile arthritis due to defect in LACC1 | KG + DL |
| 14 | juvenile chronic polyarthritis | KG + DL |
| 15 | ankylosing spondylitis | KG + DL |
| 16 | hypermobility of coccyx | KG + DL |
| 17 | vertebral disease | KG + DL |
| 18 | rheumatoid vasculitis | KG + DL |
| 19 | inflammatory spondylopathy | KG + DL |
| 20 | combined immunodeficiency due to moesin deficiency | KG + DL |
| 21 | Kummell disease | KG + DL |
| 22 | polyarticular juvenile rheumatoid arthritis | KG + DL |
| 23 | spondyloarthropathy | KG + DL |
| 24 | avascular necrosis of femoral head, primary | KG + DL |
| 25 | ankylosis (disease) | KG + DL |
| 26 | bursitis | KG + DL |
| 27 | vertebral joint disease | KG + DL |
| 28 | leukoplakia | KG + DL |
| 29 | mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency | KG + DL |
| 30 | transient arthropathy | KG + DL |
| 31 | frozen shoulder | KG + DL |
| 32 | shoulder impingement syndrome | KG + DL |
| 33 | ganglion or cyst of synovium/tendon/bursa | KG + DL |
| 34 | de Quervain disease | KG + DL |
| 35 | Behcet syndrome arthropathy | KG + DL |
| 36 | articular cartilage disease | KG + DL |
| 37 | Behr syndrome | KG + DL |
| 38 | Stickler syndrome, type I, nonsyndromic ocular | KG + DL |
| 39 | Czech dysplasia, metatarsal type | KG + DL |
| 40 | platyspondylic dysplasia, Torrance type | KG + DL |
| 41 | trigeminal autonomic cephalalgia | KG + DL |
| 42 | spondyloepimetaphyseal dysplasia, Handigodu type | KG + DL |
| 43 | spondylometaphyseal dysplasia, Schmidt type | KG + DL |
| 44 | mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis | KG + DL |
| 45 | hypotrichosis simplex of the scalp | KG + DL |
| 46 | megaepiphyseal dwarfism | KG + DL |
| 47 | spondyloperipheral dysplasia-short ulna syndrome | KG + DL |
| 48 | headache disorder | KG + DL |
| 49 | congenital hypotrichosis milia | KG + DL |
| 50 | psoriasis-related juvenile idiopathic arthritis | KG + DL |
(Showing top 50 of 56 predictions)
Disclaimer
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.