Mycophenolate mofetil
DrugBank ID: DB00688
Summary
| Metric | Value |
|---|---|
| Total Predictions | 50 |
| KG+DL (Dual Validated) | 0 |
| DL Only | 50 |
| KG Only | 0 |
Predictions
| Indication | Score | Source |
|---|---|---|
| HIV infectious disease | 0.9986 | DL |
| neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter | 0.9976 | DL |
| bone Paget disease | 0.9974 | DL |
| feline acquired immunodeficiency syndrome | 0.9972 | DL |
| simian immunodeficiency virus infection | 0.9972 | DL |
| multiple sclerosis | 0.9954 | DL |
| hemosiderosis | 0.9952 | DL |
| Heiner syndrome | 0.9946 | DL |
| African iron overload | 0.9936 | DL |
| neonatal hemochromatosis | 0.9936 | DL |
| obsolete familial combined hyperlipidemia | 0.9935 | DL |
| chronic hepatitis C virus infection | 0.9932 | DL |
| hemosiderosis, pulmonary, with deficiency of gamma-a globulin | 0.9932 | DL |
| hereditary hemochromatosis | 0.9929 | DL |
| progressive relapsing multiple sclerosis | 0.9928 | DL |
| AIDS | 0.9925 | DL |
| gout | 0.9916 | DL |
| skin disease | 0.9889 | DL |
| psoriasis | 0.9880 | DL |
| obsolete rare hereditary hemochromatosis | 0.9879 | DL |
| rheumatoid arthritis | 0.9877 | DL |
| sclerosing cholangitis | 0.9870 | DL |
| hemochromatosis | 0.9862 | DL |
| AIDS related complex | 0.9861 | DL |
| congenital human immunodeficiency virus | 0.9861 | DL |
| reticulate pigment disorder | 0.9844 | DL |
| stromal corneal pigmentation | 0.9838 | DL |
| Judge Misch wright syndrome | 0.9836 | DL |
| cutaneous focal mucinosis | 0.9832 | DL |
| diffuse cutaneous mucinosis | 0.9832 | DL |
| scleredema adultorum | 0.9832 | DL |
| hereditary poikiloderma | 0.9830 | DL |
| chronic hepatitis B virus infection | 0.9829 | DL |
| acrokeratoderma | 0.9826 | DL |
| genetic nail anomaly | 0.9824 | DL |
| genetic hair anomaly | 0.9824 | DL |
| lichen myxedematosus | 0.9822 | DL |
| sweat gland neoplasm | 0.9820 | DL |
| congenital erosive and vesicular dermatosis | 0.9820 | DL |
| zinc-responsive necrolytic acral erythema | 0.9820 | DL |
| Fox-Fordyce disease | 0.9819 | DL |
| erythema palmare hereditarium | 0.9818 | DL |
| pityriasis lichenoides | 0.9818 | DL |
| decubitus ulcer | 0.9815 | DL |
| ulcer of lower limbs | 0.9815 | DL |
| nail anomaly | 0.9815 | DL |
| 20p12.3 microdeletion syndrome | 0.9813 | DL |
| warty dyskeratoma | 0.9813 | DL |
| secondary catabolic mucinosis of skin | 0.9812 | DL |
| fetal erythroblastosis | 0.9811 | 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.