Turoctocog Alfa Pegol

Basic Information

Item Value
DrugBank ID DB14738
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 31

Predicted Indications (TxGNN)

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

# Indication Source
1 primary release disorder of platelets KG + DL
2 pseudo-von Willebrand disease KG + DL
3 Glanzmann thrombasthenia KG + DL
4 acquired coagulation factor deficiency KG + DL
5 Scott syndrome KG + DL
6 bleeding diathesis due to a collagen receptor defect KG + DL
7 hemorrhagic disorder due to a constitutional thrombocytopenia KG + DL
8 flood factor deficiency KG + DL
9 hereditary thrombocytosis with transverse limb defect KG + DL
10 fetal and neonatal alloimmune thrombocytopenia KG + DL
11 familial thrombomodulin anomalies KG + DL
12 thrombotic thrombocytopenic purpura KG + DL
13 platelet-type bleeding disorder KG + DL
14 inherited thrombophilia KG + DL
15 methylcobalamin deficiency type cblG KG + DL
16 Ehlers-Danlos syndrome, fibronectinemic type KG + DL
17 hemophilia A with vascular abnormality KG + DL
18 hemorrhagic disorder due to a platelet anomaly KG + DL
19 factor XIII, A subunit, deficiency KG + DL
20 congenital factor V deficiency KG + DL
21 factor XI deficiency KG + DL
22 congenital factor XIII deficiency KG + DL
23 thrombocytopenic purpura KG + DL
24 inherited prekallikrein deficiency KG + DL
25 congenital factor XI deficiency KG + DL
26 Tatsumi factor deficiency KG + DL
27 multiple sclerosis-ichthyosis-factor VIII deficiency syndrome KG + DL
28 hemorrhagic disorder due to a coagulation factors defect KG + DL
29 prothrombin deficiency KG + DL
30 acquired hemophilia KG + DL
31 autosomal dominant macrothrombocytopenia 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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