Mecobalamin
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB03614 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 79 |
Predicted Indications (TxGNN)
The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.
| # | Indication | Source |
|---|---|---|
| 1 | sclerosing cholangitis | KG + DL |
| 2 | multiple endocrine neoplasia | KG + DL |
| 3 | bone Paget disease | KG + DL |
| 4 | gastroparesis (disease) | KG + DL |
| 5 | juvenile Paget disease | KG + DL |
| 6 | acne (disease) | KG + DL |
| 7 | osteomesopyknosis | KG + DL |
| 8 | obsolete vitamin D deficiency | KG + DL |
| 9 | choledocholithiasis | KG + DL |
| 10 | colorectal cancer | KG + DL |
| 11 | dry eye syndrome | KG + DL |
| 12 | fetal erythroblastosis | KG + DL |
| 13 | familial isolated hypoparathyroidism due to impaired PTH secretion | KG + DL |
| 14 | Paget disease of bone | KG + DL |
| 15 | myopathy due to myoadenylate deaminase deficiency | KG + DL |
| 16 | Sjogren syndrome | KG + DL |
| 17 | Paget disease of bone 2, early-onset | KG + DL |
| 18 | ectodermal dysplasia, hypohidrotic/hair/nail/tooth type | KG + DL |
| 19 | acromesomelic dysplasia, Campailla Martinelli type | KG + DL |
| 20 | isolated Dandy-Walker malformation | KG + DL |
| 21 | hypertrophic osteoarthropathy, primary | KG + DL |
| 22 | autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome | KG + DL |
| 23 | myoglobinuria, acute recurrent, autosomal recessive | KG + DL |
| 24 | neurodegeneration, childhood-onset, with cerebellar atrophy | KG + DL |
| 25 | cephalocele (disease) | KG + DL |
| 26 | craniofacial conodysplasia | KG + DL |
| 27 | Dahlberg-Borer-Newcomer syndrome | KG + DL |
| 28 | rectosigmoid junction cancer | KG + DL |
| 29 | brain small vessel disease 1 with or without ocular anomalies | KG + DL |
| 30 | autosomal recessive cutis laxa type 2, classic type | KG + DL |
| 31 | X-linked diffuse leiomyomatosis-Alport syndrome | KG + DL |
| 32 | rectum lymphoma | KG + DL |
| 33 | hypoparathyroidism | KG + DL |
| 34 | gingival fibromatosis-hypertrichosis syndrome | KG + DL |
| 35 | atypical hemolytic-uremic syndrome with MCP/CD46 anomaly | KG + DL |
| 36 | ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis | KG + DL |
| 37 | diabetic nephropathy | KG + DL |
| 38 | phosphorus metabolism disease | KG + DL |
| 39 | Pyle disease | KG + DL |
| 40 | measles | KG + DL |
| 41 | hypercalcemia disease | KG + DL |
| 42 | prolapse of lacrimal gland | KG + DL |
| 43 | Compton-North congenital myopathy | KG + DL |
| 44 | potassium-aggravated myotonia | KG + DL |
| 45 | calcium-alkali syndrome | KG + DL |
| 46 | fingerprint body myopathy | KG + DL |
| 47 | cylindrical spirals myopathy | KG + DL |
| 48 | myopathy with hexagonally cross-linked tubular arrays | KG + DL |
| 49 | hyaline body myopathy | KG + DL |
| 50 | primary bone dysplasia with defective bone mineralization | KG + DL |
(Showing top 50 of 79 predictions)
Disclaimer
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.