Methylprednisolone
DrugBank ID: DB00959
Summary
| Metric | Value |
|---|---|
| Total Predictions | 138 |
| KG+DL (Dual Validated) | 18 |
| DL Only | 32 |
| KG Only | 88 |
Predictions
| Indication | Score | Source |
|---|---|---|
| alopecia areata | 0.9999 | DL |
| alopecia mucinosa | 0.9999 | DL |
| telogen effluvium | 0.9999 | DL |
| Quinquaud's folliculitis decalvans | 0.9999 | DL |
| alopecia antibody deficiency | 0.9999 | DL |
| hereditary hypotrichosis with recurrent skin vesicles | 0.9999 | DL |
| alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome | 0.9999 | DL |
| atrichia with papular lesions | 0.9995 | DL |
| granulomatous slack skin disease | 0.9972 | KG+DL |
| tenosynovitis | 0.9971 | KG+DL |
| alopecia universalis onychodystrophy vitiligo | 0.9970 | DL |
| familial adrenal hypoplasia with absent pituitary luteinizing hormone | 0.9963 | DL |
| nephrotic syndrome | 0.9956 | KG+DL |
| acquired thrombocytopenia | 0.9956 | KG+DL |
| Addison disease | 0.9951 | KG+DL |
| miliary tuberculosis | 0.9947 | KG+DL |
| adrenocortical insufficiency | 0.9941 | KG+DL |
| idiopathic steroid-sensitive nephrotic syndrome | 0.9939 | DL |
| autoimmune hemolytic anemia | 0.9935 | DL |
| sporadic idiopathic steroid-resistant nephrotic syndrome | 0.9934 | DL |
| PAGOD syndrome | 0.9927 | DL |
| disorder of GPI anchor biosynthesis | 0.9913 | DL |
| fetal erythroblastosis | 0.9912 | KG+DL |
| persistent polyclonal B-cell lymphocytosis | 0.9909 | DL |
| 46,XY disorder of sex development | 0.9908 | DL |
| spondyloarthropathy, susceptibility to | 0.9902 | KG+DL |
| hemoglobinuria | 0.9899 | DL |
| acquired aplastic anemia | 0.9897 | DL |
| necrobiosis lipoidica | 0.9893 | DL |
| heparin-induced thrombocytopenia (disease) | 0.9889 | KG+DL |
| acute lymphoblastic leukemia (disease) | 0.9888 | KG+DL |
| gout | 0.9888 | KG+DL |
| rheumatic heart disease | 0.9881 | KG+DL |
| articular cartilage disease | 0.9878 | DL |
| transient arthropathy | 0.9876 | DL |
| BENTA disease | 0.9876 | DL |
| Stevens-Johnson syndrome | 0.9874 | KG+DL |
| severe combined immunodeficiency due to CARD11 deficiency | 0.9873 | DL |
| Behcet syndrome arthropathy | 0.9873 | DL |
| de Quervain disease | 0.9873 | DL |
| ganglion or cyst of synovium/tendon/bursa | 0.9873 | DL |
| shoulder impingement syndrome | 0.9873 | DL |
| Hodgkins lymphoma | 0.9867 | KG+DL |
| pemphigus | 0.9864 | KG+DL |
| mantle cell lymphoma | 0.9862 | KG+DL |
| ankylosis (disease) | 0.9860 | DL |
| inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency | 0.9859 | DL |
| prolapse of lacrimal gland | 0.9859 | DL |
| leukemia, lymphocytic, susceptibility to | 0.9855 | KG+DL |
| adrenomyodystrophy | 0.9854 | DL |
Showing top 50 of 138 predictions.
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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.