Turoctocog alfa

DrugBank ID: DB09109

Summary

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

Predictions

Indication	Score	Source
primary release disorder of platelets	0.9999	DL
pseudo-von Willebrand disease	0.9999	DL
Glanzmann thrombasthenia	0.9999	DL
hemophilia	0.9997	DL
Scott syndrome	0.9995	DL
acquired coagulation factor deficiency	0.9995	DL
bleeding diathesis due to a collagen receptor defect	0.9991	DL
hemorrhagic disorder due to a constitutional thrombocytopenia	0.9991	DL
flood factor deficiency	0.9961	DL
thrombotic thrombocytopenic purpura	0.9954	DL
hereditary thrombocytosis with transverse limb defect	0.9952	DL
familial thrombomodulin anomalies	0.9952	DL
fetal and neonatal alloimmune thrombocytopenia	0.9947	DL
inherited thrombophilia	0.9935	DL
platelet-type bleeding disorder	0.9930	DL
symptomatic form of hemophilia in female carriers	0.9924	DL
methylcobalamin deficiency type cblG	0.9920	DL
Ehlers-Danlos syndrome, fibronectinemic type	0.9880	DL
thrombocytopenic purpura	0.9745	DL
hemorrhagic disorder due to a platelet anomaly	0.9738	DL
hemophilia A with vascular abnormality	0.9714	DL
congenital factor V deficiency	0.9683	DL
congenital factor XIII deficiency	0.9671	DL
factor XIII, A subunit, deficiency	0.9669	DL
factor XI deficiency	0.9603	DL
inherited prekallikrein deficiency	0.9602	DL
congenital factor XI deficiency	0.9536	DL
Tatsumi factor deficiency	0.9475	DL
multiple sclerosis-ichthyosis-factor VIII deficiency syndrome	0.9427	DL
hemorrhagic disorder due to a coagulation factors defect	0.9163	DL
prothrombin deficiency	0.9061	DL
acquired hemophilia	0.8988	DL
C1 inhibitor deficiency	0.8985	DL
serpinopathy with toxic serpin polymerization	0.8862	DL
Ledderhose disease	0.8665	DL
infantile digital fibromatosis	0.8601	DL
von Willebrand disease (hereditary or acquired)	0.8577	DL
autosomal dominant macrothrombocytopenia	0.8526	DL
palmar fibromatosis	0.8331	DL
factor X deficiency	0.8330	DL
Peyronie disease	0.8125	DL
penile fibromatosis	0.8063	DL
congenital vitamin K-dependent coagulation factors deficiency	0.8009	DL
hypoplasminogenemia	0.7996	DL
congenital plasminogen activator inhibitor type 1 deficiency	0.7959	DL
factor XIII deficiency	0.7928	DL
Von Willebrand disease, X-linked form	0.7793	DL
thrombophilia, X-linked, due to factor 9 defect	0.7544	DL
von Willebrand disease	0.7530	DL
disease of catalytic activity	0.7382	DL

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