Catridecacog
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB09310 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 46 |
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 | congenital factor XIII deficiency | KG + DL |
| 5 | hemophilia | KG + DL |
| 6 | Scott syndrome | KG + DL |
| 7 | acquired coagulation factor deficiency | KG + DL |
| 8 | bleeding diathesis due to a collagen receptor defect | KG + DL |
| 9 | hemorrhagic disorder due to a constitutional thrombocytopenia | KG + DL |
| 10 | acquired hemophilia | KG + DL |
| 11 | fetal and neonatal alloimmune thrombocytopenia | KG + DL |
| 12 | thrombotic thrombocytopenic purpura | KG + DL |
| 13 | thrombophilia, X-linked, due to factor 9 defect | KG + DL |
| 14 | thrombocytopenic purpura | KG + DL |
| 15 | inherited thrombophilia | KG + DL |
| 16 | platelet-type bleeding disorder | KG + DL |
| 17 | autosomal dominant macrothrombocytopenia | KG + DL |
| 18 | flood factor deficiency | KG + DL |
| 19 | hemophilia A with vascular abnormality | KG + DL |
| 20 | hereditary thrombocytosis with transverse limb defect | KG + DL |
| 21 | familial thrombomodulin anomalies | KG + DL |
| 22 | heparin cofactor 2 deficiency | KG + DL |
| 23 | factor XI deficiency | KG + DL |
| 24 | Ehlers-Danlos syndrome, fibronectinemic type | KG + DL |
| 25 | methylcobalamin deficiency type cblG | KG + DL |
| 26 | malignant peritoneal mesothelioma | KG + DL |
| 27 | congenital factor V deficiency | KG + DL |
| 28 | monosomy X | KG + DL |
| 29 | thrombomodulin-related bleeding disorder | KG + DL |
| 30 | pleural mesothelioma | KG + DL |
| 31 | inherited prekallikrein deficiency | KG + DL |
| 32 | congenital factor XI deficiency | KG + DL |
| 33 | congenital fibrinogen deficiency | KG + DL |
| 34 | pleural adenomatoid tumor | KG + DL |
| 35 | pleural biphasic mesothelioma | KG + DL |
| 36 | symptomatic form of hemophilia in female carriers | KG + DL |
| 37 | lymphohistiocytoid mesothelioma | KG + DL |
| 38 | well differentiated papillary mesothelioma | KG + DL |
| 39 | factor 5 excess with spontaneous thrombosis | KG + DL |
| 40 | hemorrhagic disorder due to a platelet anomaly | KG + DL |
| 41 | acquired von willebrand syndrome | KG + DL |
| 42 | pleural epithelioid mesothelioma | KG + DL |
| 43 | pleural sarcomatoid mesothelioma | KG + DL |
| 44 | pericardium cancer | KG + DL |
| 45 | iminoglycinuria | KG + DL |
| 46 | pseudoachondroplasia | KG + DL |
Disclaimer
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.