Susoctocog Alfa
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB11606 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 67 |
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 | hemophilia | KG + DL |
| 5 | acquired coagulation factor deficiency | KG + DL |
| 6 | Scott syndrome | KG + DL |
| 7 | bleeding diathesis due to a collagen receptor defect | KG + DL |
| 8 | hemorrhagic disorder due to a constitutional thrombocytopenia | KG + DL |
| 9 | congenital factor XIII deficiency | KG + DL |
| 10 | adenosine deaminase deficiency | KG + DL |
| 11 | factor XIII, A subunit, deficiency | KG + DL |
| 12 | prothrombin deficiency | KG + DL |
| 13 | congenital factor VII deficiency | KG + DL |
| 14 | reticular dysgenesis | KG + DL |
| 15 | hemorrhagic disorder due to a platelet anomaly | KG + DL |
| 16 | severe combined immunodeficiency due to LCK deficiency | KG + DL |
| 17 | platelet-type bleeding disorder | KG + DL |
| 18 | fetal and neonatal alloimmune thrombocytopenia | KG + DL |
| 19 | hemophilia A with vascular abnormality | KG + DL |
| 20 | factor XI deficiency | KG + DL |
| 21 | factor X deficiency | KG + DL |
| 22 | factor VII deficiency | KG + DL |
| 23 | coagulation protein disease | KG + DL |
| 24 | Ehlers-Danlos syndrome, fibronectinemic type | KG + DL |
| 25 | flood factor deficiency | KG + DL |
| 26 | hereditary thrombocytosis with transverse limb defect | KG + DL |
| 27 | familial thrombomodulin anomalies | KG + DL |
| 28 | hepatic infarction | KG + DL |
| 29 | congenital factor V deficiency | KG + DL |
| 30 | purine nucleoside phosphorylase deficiency | KG + DL |
| 31 | esophageal varices with bleeding | KG + DL |
| 32 | esophageal varices without bleeding | KG + DL |
| 33 | syndrome with combined immunodeficiency | KG + DL |
| 34 | factor XIII deficiency | KG + DL |
| 35 | severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive | KG + DL |
| 36 | Tatsumi factor deficiency | KG + DL |
| 37 | alpha-2-plasmin inhibitor deficiency | KG + DL |
| 38 | methylcobalamin deficiency type cblG | KG + DL |
| 39 | Steel syndrome | KG + DL |
| 40 | combined deficiency of factor V and factor VIII | KG + DL |
| 41 | multiple intestinal atresia | KG + DL |
| 42 | peliosis hepatis | KG + DL |
| 43 | multiple sclerosis-ichthyosis-factor VIII deficiency syndrome | KG + DL |
| 44 | hypoplasminogenemia | KG + DL |
| 45 | Arts syndrome | KG + DL |
| 46 | autosomal dominant familial periodic fever | KG + DL |
| 47 | lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome | KG + DL |
| 48 | varicose disease | KG + DL |
| 49 | disease of catalytic activity | KG + DL |
| 50 | hemorrhagic disorder due to a coagulation factors defect | KG + DL |
(Showing top 50 of 67 predictions)
Disclaimer
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.