L-Histidine
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB00117 |
| 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 | gastroparesis (disease) | KG + DL |
| 2 | sclerosing cholangitis | KG + DL |
| 3 | congenital prothrombin deficiency | KG + DL |
| 4 | familial visceral myopathy | KG + DL |
| 5 | potassium deficiency disease | KG + DL |
| 6 | dyspepsia | KG + DL |
| 7 | myopathic intestinal pseudoobstruction | KG + DL |
| 8 | unclassified intestinal pseudoobstruction | KG + DL |
| 9 | primary aldosteronism | KG + DL |
| 10 | intestinal obstruction | KG + DL |
| 11 | neuronal intestinal dysplasia, type B | KG + DL |
| 12 | acne (disease) | KG + DL |
| 13 | Bartter disease | KG + DL |
| 14 | obsolete vitamin D deficiency | KG + DL |
| 15 | hyperaldosteronism | KG + DL |
| 16 | stomach disease | KG + DL |
| 17 | albinism-deafness syndrome | KG + DL |
| 18 | Liddle syndrome | KG + DL |
| 19 | renal tubular acidosis | KG + DL |
| 20 | dry eye syndrome | KG + DL |
| 21 | postmenopausal osteoporosis | KG + DL |
| 22 | intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked | KG + DL |
| 23 | primary hereditary glaucoma | KG + DL |
| 24 | open-angle glaucoma | KG + DL |
| 25 | neuronal intestinal pseudoobstruction | KG + DL |
| 26 | angle-closure glaucoma | KG + DL |
| 27 | postgastrectomy syndrome | KG + DL |
| 28 | hypophosphatemic rickets | KG + DL |
| 29 | closed-angle glaucoma | KG + DL |
| 30 | Werner syndrome | KG + DL |
| 31 | pregnancy associated osteoporosis | KG + DL |
| 32 | sebaceous gland anomaly | KG + DL |
| 33 | autosomal dominant neovascular inflammatory vitreoretinopathy | KG + DL |
| 34 | autosomal recessive hydrocephalus due to congenital stenosis of aqueduct of Sylvius | KG + DL |
| 35 | Worth syndrome | KG + DL |
| 36 | succinyl-CoA:3-ketoacid CoA transferase deficiency | KG + DL |
| 37 | Alstrom syndrome | KG + DL |
| 38 | aqueous misdirection | KG + DL |
| 39 | traumatic glaucoma | KG + DL |
| 40 | obsolete CFM1 | KG + DL |
| 41 | glaucomatous atrophy of optic disc | KG + DL |
| 42 | neovascular glaucoma | KG + DL |
| 43 | Pendred syndrome | KG + DL |
| 44 | vitamin deficiency disorder | KG + DL |
| 45 | oculodentodigital dysplasia, autosomal recessive | KG + DL |
| 46 | multiple endocrine neoplasia | KG + DL |
| 47 | autosomal recessive nonsyndromic deafness | KG + DL |
| 48 | HELIX syndrome | KG + DL |
| 49 | leukocyte adhesion deficiency | KG + DL |
| 50 | hypermanganesemia with dystonia | 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.