Peginterferon alfa-2a
DrugBank ID: DB00008
Summary
| Metric | Value |
|---|---|
| Total Predictions | 50 |
| KG+DL (Dual Validated) | 3 |
| DL Only | 47 |
| KG Only | 0 |
Predictions
| Indication | Score | Source |
|---|---|---|
| chronic hepatitis C virus infection | 0.9999 | KG+DL |
| hepatitis B virus infection | 0.9994 | DL |
| hepatitis C virus infection | 0.9991 | KG+DL |
| hepatitis E virus infection | 0.9983 | DL |
| hepatitis A virus infection | 0.9982 | DL |
| hepatitis, viral, animal | 0.9982 | DL |
| Omsk hemorrhagic fever | 0.9982 | DL |
| chronic hepatitis B virus infection | 0.9981 | KG+DL |
| Kyasanur forest disease | 0.9981 | DL |
| heart conduction disease | 0.9950 | DL |
| heart neoplasm | 0.9937 | DL |
| heart valve disease | 0.9936 | DL |
| congenital anomaly of ventricular septum | 0.9923 | DL |
| pericardium disease | 0.9913 | DL |
| carcinoid heart disease | 0.9903 | DL |
| cardiac anomalies-heterotaxy syndrome | 0.9903 | DL |
| cor biloculare | 0.9903 | DL |
| heart aneurysm | 0.9903 | DL |
| myocardial rupture | 0.9903 | DL |
| white forelock with malformations | 0.9868 | DL |
| microcephaly-cardiac defect-lung malsegmentation syndrome | 0.9867 | DL |
| patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome | 0.9862 | DL |
| cardiac ventricle disease | 0.9831 | DL |
| aortopulmonary window | 0.9823 | DL |
| cardiovascular disease | 0.9678 | DL |
| tarp syndrome | 0.9585 | DL |
| cardiac disease with cataract | 0.9580 | DL |
| myocardial disorder | 0.9570 | DL |
| hereditary thrombocytopenia with normal platelets | 0.9513 | DL |
| marcothrombocytopenia with mitral valve insufficiency | 0.9507 | DL |
| transient neonatal thrombocytopenia | 0.9459 | DL |
| dense granule disease | 0.9429 | DL |
| early-onset familial noncirrhotic portal hypertension | 0.9314 | DL |
| hepatoportal sclerosis | 0.9314 | DL |
| hepatopulmonary syndrome | 0.9314 | DL |
| idiopathic copper-associated cirrhosis | 0.9314 | DL |
| primitive portal vein thrombosis | 0.9314 | DL |
| thrombocytopenia | 0.9212 | DL |
| disorder of tyrosine metabolism | 0.9185 | DL |
| Ledderhose disease | 0.9140 | DL |
| teratogenic Pierre Robin syndrome | 0.9139 | DL |
| HIV infectious disease | 0.9126 | DL |
| hepatic porphyria | 0.9085 | DL |
| tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria | 0.8966 | DL |
| relapsing-remitting multiple sclerosis | 0.8953 | DL |
| infantile digital fibromatosis | 0.8953 | DL |
| disorder of phenylalanine metabolism | 0.8940 | DL |
| commissural lip fistula | 0.8939 | DL |
| feline acquired immunodeficiency syndrome | 0.8934 | DL |
| simian immunodeficiency virus infection | 0.8934 | DL |
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Disclaimer
Predictions are for research purposes only and do not constitute medical advice.
Predictions are for research purposes only and do not constitute medical advice.