Altrenogest

Basic Information

Item Value
DrugBank ID DB11372
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 100

Predicted Indications (TxGNN)

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

# Indication Source
1 orofacial clefting syndrome KG + DL
2 interventricular septum aneurysm KG + DL
3 Jeune syndrome situs inversus KG + DL
4 Pierre Robin syndrome associated with a chromosomal anomaly KG + DL
5 genetic syndromic Pierre Robin syndrome 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 partial deletion of the long arm of chromosome 22 KG + DL
10 pulmonary valve disease KG + DL
11 hemoglobinopathy KG + DL
12 heart disease KG + DL
13 mitral valve disease KG + DL
14 partial deletion of the short arm of chromosome 16 KG + DL
15 myocardial infarction KG + DL
16 beta-thalassemia with other manifestations KG + DL
17 hemolytic anemia due to glucophosphate isomerase deficiency KG + DL
18 postoperative ventricular dysfunction KG + DL
19 pyruvate kinase deficiency of red cells KG + DL
20 posteroinferior myocardial infarction KG + DL
21 posterolateral myocardial infarction KG + DL
22 pyropoikilocytosis, hereditary KG + DL
23 septal myocardial infarction KG + DL
24 epiglottitis KG + DL
25 coronary thrombosis KG + DL
26 tendinitis KG + DL
27 heart valve disease KG + DL
28 coronary stenosis KG + DL
29 myositis fibrosa KG + DL
30 idiopathic granulomatous myositis KG + DL
31 antithrombin deficiency type 2 KG + DL
32 myocardial disorder KG + DL
33 heparin cofactor 2 deficiency KG + DL
34 factor 5 excess with spontaneous thrombosis KG + DL
35 heart neoplasm KG + DL
36 heart conduction disease KG + DL
37 malignant pleural mesothelioma KG + DL
38 congenital anomaly of ventricular septum KG + DL
39 laryngitis KG + DL
40 pericardium disease KG + DL
41 bronchitis KG + DL
42 patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome KG + DL
43 fibromyalgia KG + DL
44 congenital coronary artery anomaly KG + DL
45 myocardial infarction (disease) KG + DL
46 thrombophilia KG + DL
47 gout KG + DL
48 rheumatoid arthritis KG + DL
49 white forelock with malformations KG + DL
50 cardiac anomalies-heterotaxy syndrome KG + DL

(Showing top 50 of 100 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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