Tilmicosin

Basic Information

Item Value
DrugBank ID DB11471
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 37

Predicted Indications (TxGNN)

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

# Indication Source
1 Jeune syndrome situs inversus KG + DL
2 interventricular septum aneurysm KG + DL
3 heart disease KG + DL
4 partial deletion of the long arm of chromosome 22 KG + DL
5 Pierre Robin syndrome associated with a chromosomal anomaly KG + DL
6 Laubry-Pezzi syndrome KG + DL
7 disorder of fucoglycosan synthesis KG + DL
8 partial deletion of the long arm of chromosome 7 KG + DL
9 genetic syndromic Pierre Robin syndrome KG + DL
10 pulmonary valve disease KG + DL
11 orofacial clefting syndrome KG + DL
12 mitral valve disease KG + DL
13 heart conduction disease KG + DL
14 rheumatoid arthritis KG + DL
15 heart valve disease KG + DL
16 heart neoplasm KG + DL
17 female breast carcinoma KG + DL
18 congenital anomaly of ventricular septum KG + DL
19 pericardium disease KG + DL
20 cardiac ventricle disease KG + DL
21 patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome KG + DL
22 white forelock with malformations KG + DL
23 microcephaly-cardiac defect-lung malsegmentation syndrome KG + DL
24 carcinoid heart disease KG + DL
25 myocardial rupture KG + DL
26 cardiac anomalies-heterotaxy syndrome KG + DL
27 heart aneurysm KG + DL
28 cor biloculare KG + DL
29 cardiovascular disease KG + DL
30 aortopulmonary window KG + DL
31 colobomatous microphthalmia-rhizomelic dysplasia syndrome KG + DL
32 myocardial disorder KG + DL
33 brachydactyly-syndactyly syndrome KG + DL
34 defect in conserved oligomeric Golgi complex KG + DL
35 tarp syndrome KG + DL
36 myocardial ischemia KG + DL
37 malformation syndrome with short stature KG + DL

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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