Lonoctocog Alfa
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB13998 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 63 |
Predicted Indications (TxGNN)
The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.
| # | Indication | Source |
|---|---|---|
| 1 | pseudo-von Willebrand disease | KG + DL |
| 2 | primary release disorder of platelets | KG + DL |
| 3 | Glanzmann thrombasthenia | KG + DL |
| 4 | Scott syndrome | KG + DL |
| 5 | acquired coagulation factor deficiency | KG + DL |
| 6 | bleeding diathesis due to a collagen receptor defect | KG + DL |
| 7 | hemorrhagic disorder due to a constitutional thrombocytopenia | KG + DL |
| 8 | esophageal varices without bleeding | KG + DL |
| 9 | esophageal varices with bleeding | KG + DL |
| 10 | thrombotic thrombocytopenic purpura | KG + DL |
| 11 | hemophilia A with vascular abnormality | KG + DL |
| 12 | varicose disease | KG + DL |
| 13 | factor XI deficiency | KG + DL |
| 14 | familial apolipoprotein C-II deficiency | KG + DL |
| 15 | fetal and neonatal alloimmune thrombocytopenia | KG + DL |
| 16 | primary immunodeficiency syndrome due to p14 deficiency | KG + DL |
| 17 | flood factor deficiency | KG + DL |
| 18 | hemorrhagic disorder due to a platelet anomaly | KG + DL |
| 19 | methylcobalamin deficiency type cblG | KG + DL |
| 20 | inherited thrombophilia | KG + DL |
| 21 | Ehlers-Danlos syndrome, fibronectinemic type | KG + DL |
| 22 | familial thrombomodulin anomalies | KG + DL |
| 23 | hereditary thrombocytosis with transverse limb defect | KG + DL |
| 24 | platelet-type bleeding disorder | KG + DL |
| 25 | primary CD59 deficiency | KG + DL |
| 26 | primary hyperoxaluria | KG + DL |
| 27 | severe congenital neutropenia | KG + DL |
| 28 | congenital Horner syndrome (disease) | KG + DL |
| 29 | cold agglutinin disease | KG + DL |
| 30 | ptosis-strabismus-ectopic pupils syndrome | KG + DL |
| 31 | mixed-type autoimmune hemolytic anemia | KG + DL |
| 32 | ptosis-vocal cord paralysis syndrome | KG + DL |
| 33 | camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye | KG + DL |
| 34 | jaw-winking syndrome | KG + DL |
| 35 | cyclic hematopoiesis | KG + DL |
| 36 | drug-induced autoimmune hemolytic anemia | KG + DL |
| 37 | congenital entropion | KG + DL |
| 38 | epiblepharon | KG + DL |
| 39 | congenital ectropion | KG + DL |
| 40 | congenital factor XIII deficiency | KG + DL |
| 41 | X-linked severe congenital neutropenia | KG + DL |
| 42 | Barth syndrome | KG + DL |
| 43 | proteinuria | KG + DL |
| 44 | ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome | KG + DL |
| 45 | Charcot-Marie-Tooth disease | KG + DL |
| 46 | C1 inhibitor deficiency | KG + DL |
| 47 | autosomal recessive severe congenital neutropenia due to CSF3R deficiency | KG + DL |
| 48 | neonatal autoimmune hemolytic anemia | KG + DL |
| 49 | Steel syndrome | KG + DL |
| 50 | congenital factor V deficiency | KG + DL |
(Showing top 50 of 63 predictions)
Disclaimer
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.