Desmopressin Acetate
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB00035 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 50 |
Predicted Indications (TxGNN)
The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.
| # | Indication | Source |
|---|---|---|
| 1 | congenital prothrombin deficiency | KG + DL |
| 2 | inherited thrombophilia | KG + DL |
| 3 | Glanzmann thrombasthenia | KG + DL |
| 4 | primary release disorder of platelets | KG + DL |
| 5 | pseudo-von Willebrand disease | KG + DL |
| 6 | Scott syndrome | KG + DL |
| 7 | flood factor deficiency | KG + DL |
| 8 | thrombocytopenic purpura | KG + DL |
| 9 | bleeding diathesis due to a collagen receptor defect | KG + DL |
| 10 | hereditary thrombocytosis with transverse limb defect | KG + DL |
| 11 | familial thrombomodulin anomalies | KG + DL |
| 12 | acquired prothrombin deficiency | KG + DL |
| 13 | hemorrhagic disorder due to a constitutional thrombocytopenia | KG + DL |
| 14 | Von Willebrand disease, X-linked form | KG + DL |
| 15 | inherited prekallikrein deficiency | KG + DL |
| 16 | esophageal varices without bleeding | KG + DL |
| 17 | esophageal varices with bleeding | KG + DL |
| 18 | varicose disease | KG + DL |
| 19 | acquired coagulation factor deficiency | KG + DL |
| 20 | methylcobalamin deficiency type cblG | KG + DL |
| 21 | thrombotic thrombocytopenic purpura | KG + DL |
| 22 | congenital factor XI deficiency | KG + DL |
| 23 | trigeminal autonomic cephalalgia | KG + DL |
| 24 | acquired von willebrand syndrome | KG + DL |
| 25 | glaucoma | KG + DL |
| 26 | congenital factor V deficiency | KG + DL |
| 27 | venous insufficiency (disease) | KG + DL |
| 28 | headache disorder | KG + DL |
| 29 | Ehlers-Danlos syndrome, fibronectinemic type | KG + DL |
| 30 | platelet-type bleeding disorder | KG + DL |
| 31 | fetal and neonatal alloimmune thrombocytopenia | KG + DL |
| 32 | hypotrichosis simplex of the scalp | KG + DL |
| 33 | congenital hypotrichosis milia | KG + DL |
| 34 | hemorrhagic disorder due to a coagulation factors defect | KG + DL |
| 35 | phlebitis | KG + DL |
| 36 | Tatsumi factor deficiency | KG + DL |
| 37 | multiple sclerosis-ichthyosis-factor VIII deficiency syndrome | KG + DL |
| 38 | small bowel Crohn disease | KG + DL |
| 39 | glomus jugulare neoplasm | KG + DL |
| 40 | superior vena cava angiosarcoma | KG + DL |
| 41 | diffuse alopecia areata | KG + DL |
| 42 | gastritis | KG + DL |
| 43 | respiratory failure | KG + DL |
| 44 | multiple intestinal atresia | KG + DL |
| 45 | acrorenal syndrome, autosomal recessive | KG + DL |
| 46 | autosomal recessive Alport syndrome | KG + DL |
| 47 | skin fragility-woolly hair-palmoplantar keratoderma syndrome | KG + DL |
| 48 | autosomal recessive humeroradial synostosis | KG + DL |
| 49 | immune-mediated necrotizing myopathy | KG + DL |
| 50 | bifid nose, autosomal recessive | KG + DL |
Disclaimer
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.