Hemin
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB03404 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 100 |
Predicted Indications (TxGNN)
The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.
| # | Indication | Source |
|---|---|---|
| 1 | thrombocytopenic purpura | KG + DL |
| 2 | hemophilia | KG + DL |
| 3 | C1 inhibitor deficiency | KG + DL |
| 4 | acquired coagulation factor deficiency | KG + DL |
| 5 | serpinopathy with toxic serpin polymerization | KG + DL |
| 6 | hereditary angioedema with C1Inh deficiency | KG + DL |
| 7 | inherited thrombophilia | KG + DL |
| 8 | symptomatic form of hemophilia in female carriers | KG + DL |
| 9 | hereditary von Willebrand disease | KG + DL |
| 10 | congenital factor XI deficiency | KG + DL |
| 11 | inherited prekallikrein deficiency | KG + DL |
| 12 | pancreatitis | KG + DL |
| 13 | flood factor deficiency | KG + DL |
| 14 | thrombotic thrombocytopenic purpura | KG + DL |
| 15 | von Willebrand disease | KG + DL |
| 16 | Von Willebrand disease, X-linked form | KG + DL |
| 17 | Scott syndrome | KG + DL |
| 18 | immune-mediated necrotizing myopathy | KG + DL |
| 19 | antisynthetase syndrome | KG + DL |
| 20 | focal myositis | KG + DL |
| 21 | familial thrombomodulin anomalies | KG + DL |
| 22 | hereditary thrombocytosis with transverse limb defect | KG + DL |
| 23 | methylcobalamin deficiency type cblG | KG + DL |
| 24 | inflammatory myopathy with abundant macrophages | KG + DL |
| 25 | idiopathic eosinophilic myositis | KG + DL |
| 26 | juvenile nasopharyngeal angiofibroma (disease) | KG + DL |
| 27 | familial nasal acilia | KG + DL |
| 28 | indomethacin embryofetopathy | KG + DL |
| 29 | silent sinus syndrome | KG + DL |
| 30 | branchial cleft anomaly | KG + DL |
| 31 | craniorhiny | KG + DL |
| 32 | velo-facial-skeletal syndrome | KG + DL |
| 33 | maternal hyperthermia induced birth defects | KG + DL |
| 34 | fetal trimethadione syndrome | KG + DL |
| 35 | Pick disease | KG + DL |
| 36 | fetal minoxidil syndrome | KG + DL |
| 37 | familial apolipoprotein C-II deficiency | KG + DL |
| 38 | phenobarbital embryopathy | KG + DL |
| 39 | cleft lip/palate-intestinal malrotation-cardiopathy syndrome | KG + DL |
| 40 | cocaine embryofetopathy | KG + DL |
| 41 | Bencze syndrome | KG + DL |
| 42 | mandibulofacial dysostosis-macroblepharon-macrostomia syndrome | KG + DL |
| 43 | diabetic embryopathy | KG + DL |
| 44 | hemophilia A with vascular abnormality | KG + DL |
| 45 | primary hyperoxaluria | KG + DL |
| 46 | genetic otorhinolaryngological malformation | KG + DL |
| 47 | aminopterin/methotrexate embryofetopathy | KG + DL |
| 48 | bleeding diathesis due to a collagen receptor defect | KG + DL |
| 49 | osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome | KG + DL |
| 50 | toluene embryopathy | KG + DL |
(Showing top 50 of 100 predictions)
Disclaimer
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.