Bosentan

Basic Information

Item Value
DrugBank ID DB00559
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 62

Predicted Indications (TxGNN)

The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.

# Indication Source
1 rheumatoid arthritis KG + DL
2 brachydactyly-syndactyly syndrome KG + DL
3 limited systemic sclerosis KG + DL
4 colobomatous microphthalmia-rhizomelic dysplasia syndrome KG + DL
5 pseudoxanthoma elasticum, forme fruste KG + DL
6 kyphoscoliotic heart disease KG + DL
7 elastoma KG + DL
8 gout KG + DL
9 hypertrichosis (disease) KG + DL
10 Ambras type hypertrichosis universalis congenita KG + DL
11 uterine polyp KG + DL
12 malformation syndrome with odontal and/or periodontal component KG + DL
13 epulis KG + DL
14 syndrome with a Dandy-Walker malformation as major feature KG + DL
15 diffuse cutaneous systemic sclerosis KG + DL
16 polyp of vocal cord KG + DL
17 polyp of middle ear KG + DL
18 fibroepithelial polyp KG + DL
19 polyp of frontal sinus KG + DL
20 polyp of ureter KG + DL
21 neoplastic polyp KG + DL
22 polyp of vulva KG + DL
23 polyp of external auditory canal KG + DL
24 subarachnoid hemorrhage (disease) KG + DL
25 isolated genetic hair shaft abnormality KG + DL
26 autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome KG + DL
27 brain small vessel disease 1 with or without ocular anomalies KG + DL
28 peeling skin syndrome KG + DL
29 nephrogenic syndrome of inappropriate antidiuresis KG + DL
30 limited cutaneous systemic sclerosis KG + DL
31 pulmonary hypertension, primary, autosomal recessive KG + DL
32 diabetic nephropathy KG + DL
33 pneumocystosis KG + DL
34 Raynaud disease KG + DL
35 cor pulmonale KG + DL
36 obsolete patella aplasia, coxa vara, and tarsal synostosis KG + DL
37 hypocomplementemic urticarial vasculitis KG + DL
38 idiopathic pulmonary arterial hypertension KG + DL
39 familial clubfoot due to 17q23.1q23.2 microduplication KG + DL
40 chromosome 17q23.1-q23.2 deletion syndrome KG + DL
41 coxopodopatellar syndrome KG + DL
42 obsolete susceptibility to ischemic stroke KG + DL
43 paratenonitis KG + DL
44 calcific tendinitis KG + DL
45 pulmonary hypertension, primary KG + DL
46 trigeminal autonomic cephalalgia KG + DL
47 tropical endomyocardial fibrosis KG + DL
48 idiopathic and/or familial pulmonary arterial hypertension KG + DL
49 cardiac sarcoidosis KG + DL
50 headache disorder KG + DL

(Showing top 50 of 62 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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