Pentetic acid
DrugBank ID: DB14007
Summary
| Metric | Value |
|---|---|
| Total Predictions | 50 |
| KG+DL (Dual Validated) | 0 |
| DL Only | 50 |
| KG Only | 0 |
Predictions
| Indication | Score | Source |
|---|---|---|
| thrombocytopenic purpura | 0.9725 | DL |
| hepatic porphyria | 0.9672 | DL |
| benign recurrent intrahepatic cholestasis | 0.9614 | DL |
| early-onset familial noncirrhotic portal hypertension | 0.9600 | DL |
| hepatoportal sclerosis | 0.9600 | DL |
| hepatopulmonary syndrome | 0.9600 | DL |
| idiopathic copper-associated cirrhosis | 0.9600 | DL |
| primitive portal vein thrombosis | 0.9600 | DL |
| peliosis hepatis | 0.9584 | DL |
| hepatic infarction | 0.9566 | DL |
| hereditary North American Indian childhood cirrhosis | 0.9557 | DL |
| sclerosing cholangitis | 0.9525 | DL |
| rheumatoid arthritis | 0.9523 | DL |
| inborn disorder of bilirubin metabolism | 0.9436 | DL |
| congenital hypotrichosis milia | 0.9401 | DL |
| diffuse alopecia areata | 0.9386 | DL |
| syndrome with combined immunodeficiency | 0.9376 | DL |
| osteoarthritis susceptibility | 0.9374 | DL |
| hypotrichosis simplex of the scalp | 0.9361 | DL |
| familial intrahepatic cholestasis | 0.9347 | DL |
| hepatic veno-occlusive disease | 0.9339 | DL |
| bilirubin metabolism disease | 0.9330 | DL |
| bronchitis | 0.9329 | DL |
| cholestasis | 0.9328 | DL |
| microvillus inclusion disease | 0.9321 | DL |
| gout | 0.9313 | DL |
| drug-induced liver injury | 0.9311 | DL |
| Smouldering systemic mastocytosis | 0.9306 | DL |
| osteoarthritis | 0.9304 | DL |
| systemic mastocytosis | 0.9285 | DL |
| dermatitis | 0.9246 | DL |
| mitochondrial DNA depletion syndrome, hepatocerebral form | 0.9217 | DL |
| nevus of Ito | 0.9214 | DL |
| hydroa vacciniforme, familial | 0.9205 | DL |
| lymphoadenopathic mastocytosis with eosinophilia | 0.9194 | DL |
| thrombotic thrombocytopenic purpura | 0.9182 | DL |
| liver angiosarcoma | 0.9155 | DL |
| myositis | 0.9149 | DL |
| acrodermatitis chronica atrophicans | 0.9138 | DL |
| malignant peritoneal mesothelioma | 0.9126 | DL |
| secondary interstitial lung disease specific to childhood associated with a connective tissue disease | 0.9123 | DL |
| neonatal dermatomyositis | 0.9123 | DL |
| adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency | 0.9115 | DL |
| selective IgG subclass deficiency | 0.9114 | DL |
| alopecia | 0.9114 | DL |
| oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies | 0.9107 | DL |
| oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies | 0.9107 | DL |
| immune-mediated necrotizing myopathy | 0.9107 | DL |
| colobomatous microphthalmia-rhizomelic dysplasia syndrome | 0.9103 | DL |
| Ledderhose disease | 0.9100 | DL |
External Links
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.