Leucovorin Calcium
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB00650 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 85 |
Predicted Indications (TxGNN)
The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.
| # | Indication | Source |
|---|---|---|
| 1 | primary hyperoxaluria | KG + DL |
| 2 | congenital intrinsic factor deficiency | KG + DL |
| 3 | immune-mediated necrotizing myopathy | KG + DL |
| 4 | antisynthetase syndrome | KG + DL |
| 5 | hereditary hemochromatosis | KG + DL |
| 6 | idiopathic eosinophilic myositis | KG + DL |
| 7 | inflammatory myopathy with abundant macrophages | KG + DL |
| 8 | focal myositis | KG + DL |
| 9 | primary amyloidosis | KG + DL |
| 10 | acquired amyloid peripheral neuropathy | KG + DL |
| 11 | dermis disease | KG + DL |
| 12 | amyloidosis (disease) | KG + DL |
| 13 | primary release disorder of platelets | KG + DL |
| 14 | pseudo-von Willebrand disease | KG + DL |
| 15 | hemochromatosis | KG + DL |
| 16 | macular amyloidosis | KG + DL |
| 17 | amyloidosis cutis dyschromia | KG + DL |
| 18 | nodular cutaneous amyloidosis | KG + DL |
| 19 | iron metabolism disease | KG + DL |
| 20 | microcytic anemia with liver iron overload | KG + DL |
| 21 | obsolete rare hereditary hemochromatosis | KG + DL |
| 22 | Wilson disease | KG + DL |
| 23 | chromosome 5q deletion syndrome | KG + DL |
| 24 | vitamin A deficiency (disease) | KG + DL |
| 25 | iron deficiency anemia | KG + DL |
| 26 | disorder of mineral absorption and transport | KG + DL |
| 27 | hypoglycemia | KG + DL |
| 28 | hemosiderosis | KG + DL |
| 29 | 20p12.3 microdeletion syndrome | KG + DL |
| 30 | TWIST1-related craniosynostosis | KG + DL |
| 31 | cold agglutinin disease | KG + DL |
| 32 | African iron overload | KG + DL |
| 33 | neonatal hemochromatosis | KG + DL |
| 34 | acute urate nephropathy | KG + DL |
| 35 | mixed-type autoimmune hemolytic anemia | KG + DL |
| 36 | familial benign copper deficiency | KG + DL |
| 37 | congenital dyserythropoietic anemia | KG + DL |
| 38 | autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | KG + DL |
| 39 | Glanzmann thrombasthenia | KG + DL |
| 40 | drug-induced autoimmune hemolytic anemia | KG + DL |
| 41 | mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies | KG + DL |
| 42 | hemosiderosis, pulmonary, with deficiency of gamma-a globulin | KG + DL |
| 43 | proteinuria | KG + DL |
| 44 | dermatomyositis | KG + DL |
| 45 | inborn vitamin B12 deficiency (disease) | KG + DL |
| 46 | Heiner syndrome | KG + DL |
| 47 | neonatal autoimmune hemolytic anemia | KG + DL |
| 48 | glaucoma | KG + DL |
| 49 | primary CD59 deficiency | KG + DL |
| 50 | retinal telangiectasia | KG + DL |
(Showing top 50 of 85 predictions)
Disclaimer
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.