Desmopressin

DrugBank ID: DB00035

Summary

Metric	Value
Total Predictions	50
KG+DL (Dual Validated)	0
DL Only	50
KG Only	0

Predictions

Indication	Score	Source
congenital prothrombin deficiency	0.9970	DL
hereditary von Willebrand disease	0.9946	DL
inherited thrombophilia	0.9944	DL
Glanzmann thrombasthenia	0.9930	DL
primary release disorder of platelets	0.9926	DL
pseudo-von Willebrand disease	0.9916	DL
Scott syndrome	0.9916	DL
flood factor deficiency	0.9915	DL
thrombocytopenic purpura	0.9895	DL
bleeding diathesis due to a collagen receptor defect	0.9895	DL
hereditary thrombocytosis with transverse limb defect	0.9895	DL
familial thrombomodulin anomalies	0.9894	DL
acquired prothrombin deficiency	0.9892	DL
hemorrhagic disorder due to a constitutional thrombocytopenia	0.9891	DL
Von Willebrand disease, X-linked form	0.9870	DL
inherited prekallikrein deficiency	0.9863	DL
esophageal varices with bleeding	0.9855	DL
esophageal varices without bleeding	0.9855	DL
von Willebrand disease	0.9847	DL
hemophilia	0.9846	DL
varicose disease	0.9838	DL
acquired coagulation factor deficiency	0.9828	DL
methylcobalamin deficiency type cblG	0.9828	DL
thrombotic thrombocytopenic purpura	0.9804	DL
congenital factor XI deficiency	0.9800	DL
trigeminal autonomic cephalalgia	0.9668	DL
acquired von willebrand syndrome	0.9661	DL
glaucoma	0.9635	DL
congenital factor V deficiency	0.9595	DL
venous insufficiency (disease)	0.9581	DL
headache disorder	0.9571	DL
Ehlers-Danlos syndrome, fibronectinemic type	0.9563	DL
platelet-type bleeding disorder	0.9561	DL
fetal and neonatal alloimmune thrombocytopenia	0.9548	DL
hypotrichosis simplex of the scalp	0.9503	DL
congenital hypotrichosis milia	0.9426	DL
hemorrhagic disorder due to a coagulation factors defect	0.9360	DL
phlebitis	0.9359	DL
Tatsumi factor deficiency	0.9305	DL
multiple sclerosis-ichthyosis-factor VIII deficiency syndrome	0.9285	DL
small bowel Crohn disease	0.9281	DL
glomus jugulare neoplasm	0.9278	DL
superior vena cava angiosarcoma	0.9236	DL
diffuse alopecia areata	0.9231	DL
gastritis	0.9224	DL
respiratory failure	0.9122	DL
multiple intestinal atresia	0.9101	DL
symptomatic form of hemophilia in female carriers	0.9081	DL
acrorenal syndrome, autosomal recessive	0.9069	DL
autosomal recessive Alport syndrome	0.9056	DL

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Disclaimer
Predictions are for research purposes only and do not constitute medical advice.