L-Lysine
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB00123 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 64 |
Predicted Indications (TxGNN)
The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.
| # | Indication | Source |
|---|---|---|
| 1 | gastroparesis (disease) | KG + DL |
| 2 | congenital prothrombin deficiency | KG + DL |
| 3 | obsolete vitamin D deficiency | KG + DL |
| 4 | dyspepsia | KG + DL |
| 5 | familial visceral myopathy | KG + DL |
| 6 | vitamin deficiency disorder | KG + DL |
| 7 | hypophosphatemic rickets | KG + DL |
| 8 | renal tubular acidosis | KG + DL |
| 9 | biotin metabolic disease | KG + DL |
| 10 | postgastrectomy syndrome | KG + DL |
| 11 | albinism-deafness syndrome | KG + DL |
| 12 | postmenopausal osteoporosis | KG + DL |
| 13 | intestinal obstruction | KG + DL |
| 14 | unclassified intestinal pseudoobstruction | KG + DL |
| 15 | myopathic intestinal pseudoobstruction | KG + DL |
| 16 | stomach disease | KG + DL |
| 17 | neuronal intestinal dysplasia, type B | KG + DL |
| 18 | acne (disease) | KG + DL |
| 19 | familial isolated hypoparathyroidism due to impaired PTH secretion | KG + DL |
| 20 | hereditary hypophosphatemic rickets | KG + DL |
| 21 | pregnancy associated osteoporosis | KG + DL |
| 22 | acromesomelic dysplasia, Campailla Martinelli type | KG + DL |
| 23 | craniofacial conodysplasia | KG + DL |
| 24 | Dahlberg-Borer-Newcomer syndrome | KG + DL |
| 25 | autosomal dominant neovascular inflammatory vitreoretinopathy | KG + DL |
| 26 | sclerosing cholangitis | KG + DL |
| 27 | succinyl-CoA:3-ketoacid CoA transferase deficiency | KG + DL |
| 28 | Worth syndrome | KG + DL |
| 29 | osteomalacia (disease) | KG + DL |
| 30 | Donnai-Barrow syndrome | KG + DL |
| 31 | Pendred syndrome | KG + DL |
| 32 | osteoporosis | KG + DL |
| 33 | folic acid deficiency anemia | KG + DL |
| 34 | vitamin D-dependent rickets | KG + DL |
| 35 | potassium deficiency disease | KG + DL |
| 36 | non-syndromic esophageal malformation | KG + DL |
| 37 | hypoparathyroidism | KG + DL |
| 38 | hypermanganesemia with dystonia | KG + DL |
| 39 | intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked | KG + DL |
| 40 | autosomal recessive nonsyndromic deafness | KG + DL |
| 41 | NAD(P)HX dehydratase deficiency | KG + DL |
| 42 | Werner syndrome | KG + DL |
| 43 | leukocyte adhesion deficiency | KG + DL |
| 44 | Alstrom syndrome | KG + DL |
| 45 | autosomal recessive hydrocephalus due to congenital stenosis of aqueduct of Sylvius | KG + DL |
| 46 | human HOXA1 syndromes | KG + DL |
| 47 | neuronal intestinal pseudoobstruction | KG + DL |
| 48 | calcium-alkali syndrome | KG + DL |
| 49 | Fraser syndrome | KG + DL |
| 50 | rickets (disease) | KG + DL |
(Showing top 50 of 64 predictions)
Disclaimer
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.