Lonoctocog alfa

DrugBank ID: DB13998

Summary

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

Predictions

Indication	Score	Source
pseudo-von Willebrand disease	0.9985	DL
primary release disorder of platelets	0.9984	DL
Glanzmann thrombasthenia	0.9976	DL
Scott syndrome	0.9944	DL
symptomatic form of hemophilia in female carriers	0.9931	DL
hemophilia	0.9927	DL
acquired coagulation factor deficiency	0.9885	DL
bleeding diathesis due to a collagen receptor defect	0.9871	DL
hemorrhagic disorder due to a constitutional thrombocytopenia	0.9864	DL
esophageal varices with bleeding	0.9841	DL
esophageal varices without bleeding	0.9841	DL
thrombotic thrombocytopenic purpura	0.9813	DL
hemophilia A with vascular abnormality	0.9771	DL
varicose disease	0.9763	DL
factor XI deficiency	0.9712	DL
familial apolipoprotein C-II deficiency	0.9651	DL
fetal and neonatal alloimmune thrombocytopenia	0.9649	DL
primary immunodeficiency syndrome due to p14 deficiency	0.9611	DL
flood factor deficiency	0.9603	DL
hemorrhagic disorder due to a platelet anomaly	0.9575	DL
methylcobalamin deficiency type cblG	0.9555	DL
inherited thrombophilia	0.9550	DL
Ehlers-Danlos syndrome, fibronectinemic type	0.9531	DL
familial thrombomodulin anomalies	0.9512	DL
hereditary thrombocytosis with transverse limb defect	0.9512	DL
platelet-type bleeding disorder	0.9500	DL
primary CD59 deficiency	0.9496	DL
primary hyperoxaluria	0.9496	DL
severe congenital neutropenia	0.9477	DL
congenital Horner syndrome (disease)	0.9419	DL
cold agglutinin disease	0.9408	DL
ptosis-strabismus-ectopic pupils syndrome	0.9408	DL
mixed-type autoimmune hemolytic anemia	0.9404	DL
ptosis-vocal cord paralysis syndrome	0.9390	DL
camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye	0.9388	DL
jaw-winking syndrome	0.9381	DL
cyclic hematopoiesis	0.9375	DL
drug-induced autoimmune hemolytic anemia	0.9374	DL
congenital entropion	0.9356	DL
epiblepharon	0.9346	DL
congenital ectropion	0.9329	DL
congenital factor XIII deficiency	0.9328	DL
X-linked severe congenital neutropenia	0.9326	DL
Barth syndrome	0.9308	DL
proteinuria	0.9308	DL
ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome	0.9306	DL
Charcot-Marie-Tooth disease	0.9303	DL
C1 inhibitor deficiency	0.9296	DL
autosomal recessive severe congenital neutropenia due to CSF3R deficiency	0.9264	DL
neonatal autoimmune hemolytic anemia	0.9260	DL

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