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.


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