Iron
DrugBank ID: DB01592
Summary
| Metric | Value |
|---|---|
| Total Predictions | 50 |
| KG+DL (Dual Validated) | 6 |
| DL Only | 44 |
| KG Only | 0 |
Predictions
| Indication | Score | Source |
|---|---|---|
| deficiency anemia | 0.9996 | KG+DL |
| iron deficiency anemia | 0.9991 | KG+DL |
| vitamin B12- and folate-independent constitutional megaloblastic anemia | 0.9989 | DL |
| Plummer-Vinson syndrome | 0.9989 | DL |
| non-syndromic esophageal malformation | 0.9986 | DL |
| biotin metabolic disease | 0.9974 | DL |
| vitamin deficiency disorder | 0.9968 | DL |
| esophageal disease | 0.9942 | DL |
| injury | 0.9856 | DL |
| microcytic anemia | 0.9837 | KG+DL |
| florid cemento-osseous dysplasia | 0.9804 | DL |
| perinatal disease | 0.9804 | DL |
| segmental odontomaxillary dysplasia | 0.9804 | DL |
| radiation or chemically induced disorder | 0.9802 | DL |
| disease by subcellular system affected | 0.9801 | DL |
| iatrogenic disease | 0.9786 | DL |
| cell proliferation disorder | 0.9780 | DL |
| regional odontodysplasia | 0.9766 | DL |
| anemia of prematurity | 0.9728 | KG+DL |
| folic acid deficiency anemia | 0.9714 | KG+DL |
| Keshan disease | 0.9692 | DL |
| steatitis | 0.9685 | DL |
| ariboflavinosis | 0.9673 | DL |
| choline deficiency disease | 0.9670 | DL |
| potassium deficiency | 0.9670 | DL |
| swayback | 0.9670 | DL |
| esophageal ulcer | 0.9642 | DL |
| protein-energy malnutrition | 0.9642 | DL |
| inborn error of biotin metabolism | 0.9632 | DL |
| magnesium deficiency | 0.9607 | DL |
| IRIDA syndrome | 0.9268 | DL |
| vitamin A deficiency (disease) | 0.9221 | DL |
| filariasis | 0.9048 | DL |
| esotropia | 0.8993 | DL |
| severe nonproliferative diabetic retinopathy | 0.8950 | DL |
| ascorbic acid deficiency | 0.8869 | DL |
| acquired amyloid peripheral neuropathy | 0.8753 | DL |
| dermis disease | 0.8703 | DL |
| primary amyloidosis | 0.8645 | DL |
| cerebral folate deficiency | 0.8591 | DL |
| hypochromic anemia | 0.8537 | KG+DL |
| primary release disorder of platelets | 0.8505 | DL |
| inborn disorder of pyridoxine metabolism | 0.8492 | DL |
| constitutional megaloblastic anemia due to folate metabolism disorder | 0.8461 | DL |
| infantile digital fibromatosis | 0.8425 | DL |
| palmar fibromatosis | 0.8413 | DL |
| amyloidosis cutis dyschromia | 0.8404 | DL |
| macular amyloidosis | 0.8404 | DL |
| nodular cutaneous amyloidosis | 0.8404 | DL |
| penile fibromatosis | 0.8313 | 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.