Bemiparin

DrugBank ID: DB09258

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	0.9871	DL
Glanzmann thrombasthenia	0.9866	DL
pseudo-von Willebrand disease	0.9829	DL
hemorrhagic disorder due to a constitutional thrombocytopenia	0.9486	DL
bleeding diathesis due to a collagen receptor defect	0.9481	DL
Scott syndrome	0.9380	DL
fetal and neonatal alloimmune thrombocytopenia	0.9254	DL
platelet-type bleeding disorder	0.9024	DL
pulmonary embolism (disease)	0.8792	DL
autosomal dominant macrothrombocytopenia	0.8721	DL
hereditary thrombocytosis with transverse limb defect	0.8638	DL
familial thrombomodulin anomalies	0.8631	DL
flood factor deficiency	0.8631	DL
Ehlers-Danlos syndrome, fibronectinemic type	0.8602	DL
inherited thrombophilia	0.8535	DL
thrombotic thrombocytopenic purpura	0.8404	DL
methylcobalamin deficiency type cblG	0.7741	DL
congenital factor V deficiency	0.7537	DL
hemoglobinopathy	0.7295	DL
thrombophilia	0.7202	DL
hemophilia	0.7068	DL
partial deletion of the short arm of chromosome 16	0.7068	DL
acquired coagulation factor deficiency	0.7032	DL
thromboangiitis obliterans	0.6992	DL
hemolytic anemia due to glucophosphate isomerase deficiency	0.6951	DL
cholecystolithiasis	0.6951	DL
purpura fulminans	0.6924	DL
beta-thalassemia with other manifestations	0.6880	DL
antithrombin deficiency type 2	0.6870	DL
heparin cofactor 2 deficiency	0.6836	DL
Ledderhose disease	0.6745	DL
factor 5 excess with spontaneous thrombosis	0.6738	DL
pyropoikilocytosis, hereditary	0.6575	DL
infantile digital fibromatosis	0.6489	DL
autoimmune thrombocytopenic	0.6460	DL
cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder	0.6419	DL
palmar fibromatosis	0.6274	DL
hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency	0.6255	DL
familial hypodysfibrinogenemia	0.6229	DL
thrombocytopenic purpura	0.6225	DL
pyruvate kinase deficiency of red cells	0.6183	DL
penile fibromatosis	0.6103	DL
filariasis	0.6096	DL
complement factor I deficiency	0.6026	DL
neuropathy, painful	0.5956	DL
coronary thrombosis	0.5839	DL
scalp dermatosis	0.5815	DL
atypical hemolytic-uremic syndrome with thrombomodulin anomaly	0.5742	DL
non-syndromic esophageal malformation	0.5721	DL
congenital coronary artery anomaly	0.5719	DL

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