Diflunisal

Basic Information

Item Value
DrugBank ID DB00861
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 72

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 spondyloarthropathy, susceptibility to KG + DL
4 myosclerosis KG + DL
5 ankylosing spondylitis KG + DL
6 brachyolmia KG + DL
7 hypermobility of coccyx KG + DL
8 rheumatoid vasculitis KG + DL
9 colobomatous microphthalmia-rhizomelic dysplasia syndrome KG + DL
10 inflammatory spondylopathy KG + DL
11 brachydactyly-syndactyly syndrome KG + DL
12 polyarticular juvenile rheumatoid arthritis KG + DL
13 Kummell disease KG + DL
14 pseudoachondroplasia KG + DL
15 vertebral disease KG + DL
16 WHIM syndrome KG + DL
17 juvenile arthritis due to defect in LACC1 KG + DL
18 juvenile idiopathic arthritis KG + DL
19 rheumatoid nodulosis KG + DL
20 rheumatoid factor-positive polyarticular juvenile idiopathic arthritis KG + DL
21 juvenile chronic polyarthritis KG + DL
22 spondyloarthropathy KG + DL
23 avascular necrosis of femoral head, primary KG + DL
24 mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency KG + DL
25 Czech dysplasia, metatarsal type KG + DL
26 spondyloepimetaphyseal dysplasia, Handigodu type KG + DL
27 platyspondylic dysplasia, Torrance type KG + DL
28 combined immunodeficiency due to moesin deficiency KG + DL
29 Stickler syndrome, type I, nonsyndromic ocular KG + DL
30 spondylometaphyseal dysplasia, Schmidt type KG + DL
31 mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis KG + DL
32 megaepiphyseal dwarfism KG + DL
33 spondyloperipheral dysplasia-short ulna syndrome KG + DL
34 tenosynovitis KG + DL
35 ankylosis (disease) KG + DL
36 vertebral joint disease KG + DL
37 transient arthropathy KG + DL
38 spondyloepiphyseal dysplasia, Reardon type KG + DL
39 articular cartilage disease KG + DL
40 ganglion or cyst of synovium/tendon/bursa KG + DL
41 Behcet syndrome arthropathy KG + DL
42 shoulder impingement syndrome KG + DL
43 de Quervain disease KG + DL
44 brachydactylous dwarfism, Mseleni type KG + DL
45 progressive pseudorheumatoid arthropathy of childhood KG + DL
46 gout KG + DL
47 bursitis KG + DL
48 spondylo-megaepiphyseal-metaphyseal dysplasia KG + DL
49 spondyloepimetaphyseal dysplasia, Genevieve type KG + DL
50 spondyloepimetaphyseal dysplasia-abnormal dentition syndrome KG + DL

(Showing top 50 of 72 predictions)

Disclaimer

These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.


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