Eribulin
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB08871 |
| 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 | autosomal recessive familial Mediterranean fever | KG + DL |
| 2 | dermatofibrosarcoma protuberans | KG + DL |
| 3 | pleural mesothelioma | KG + DL |
| 4 | malignant peritoneal mesothelioma | KG + DL |
| 5 | ovarian myxoid liposarcoma | KG + DL |
| 6 | pleural adenomatoid tumor | KG + DL |
| 7 | pleural biphasic mesothelioma | KG + DL |
| 8 | fibroblastic neoplasm | KG + DL |
| 9 | pleural epithelioid mesothelioma | KG + DL |
| 10 | heart fibrosarcoma | KG + DL |
| 11 | well differentiated papillary mesothelioma | KG + DL |
| 12 | conventional fibrosarcoma | KG + DL |
| 13 | pericardium cancer | KG + DL |
| 14 | pleural sarcomatoid mesothelioma | KG + DL |
| 15 | kidney fibrosarcoma | KG + DL |
| 16 | lymphohistiocytoid mesothelioma | KG + DL |
| 17 | low grade fibromyxoid sarcoma | KG + DL |
| 18 | benign PEComa | KG + DL |
| 19 | uterine corpus perivascular epithelioid cell tumor | KG + DL |
| 20 | lymphangiomyoma | KG + DL |
| 21 | situs inversus | KG + DL |
| 22 | familial Mediterranean fever, autosomal dominant | KG + DL |
| 23 | iminoglycinuria | KG + DL |
| 24 | familial caudal dysgenesis | KG + DL |
| 25 | Marfan syndrome | KG + DL |
| 26 | heart position anomaly | KG + DL |
| 27 | laterality defects, autosomal dominant | KG + DL |
| 28 | neonatal Marfan syndrome | KG + DL |
| 29 | cryptogenic organizing pneumonia | KG + DL |
| 30 | tuberous sclerosis | KG + DL |
| 31 | obsolete Marfan syndrome type 2 | KG + DL |
| 32 | Loeys-Dietz syndrome | KG + DL |
| 33 | familial Mediterranean fever | KG + DL |
| 34 | diaphragmatic or abdominal wall malformation | KG + DL |
| 35 | male infertility with teratozoospermia due to single gene mutation | KG + DL |
| 36 | situs ambiguus | KG + DL |
| 37 | cutis laxa - Marfanoid syndrome | KG + DL |
| 38 | malformation syndrome with hamartosis | KG + DL |
| 39 | lung PEComa | KG + DL |
| 40 | heterotaxy, visceral, 1, X-linked | KG + DL |
| 41 | visceral heterotaxy | KG + DL |
| 42 | external auditory canal aplasia/hypoplasia | KG + DL |
| 43 | liver fibrosarcoma | KG + DL |
| 44 | paralytic facial malformation | KG + DL |
| 45 | cutaneous leiomyosarcoma (disease) | KG + DL |
| 46 | desquamative interstitial pneumonia | KG + DL |
| 47 | lymphoid interstitial pneumonia | KG + DL |
| 48 | EDICT syndrome | KG + DL |
| 49 | digestive tract malformation | KG + DL |
| 50 | facial cleft | 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.