Pholcodine
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB09209 |
| 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 | obsolete hyperuricemia (disease) | KG + DL |
| 2 | primitive portal vein thrombosis | KG + DL |
| 3 | early-onset familial noncirrhotic portal hypertension | KG + DL |
| 4 | hepatoportal sclerosis | KG + DL |
| 5 | hepatopulmonary syndrome | KG + DL |
| 6 | idiopathic copper-associated cirrhosis | KG + DL |
| 7 | hypouricemia, renal | KG + DL |
| 8 | hepatic porphyria | KG + DL |
| 9 | hypoxanthine guanine phosphoribosyltransferase partial deficiency | KG + DL |
| 10 | gastroduodenitis | KG + DL |
| 11 | ocular tuberculosis | KG + DL |
| 12 | peptic ulcer disease | KG + DL |
| 13 | common cold | KG + DL |
| 14 | glycogen storage disease due to hepatic glycogen synthase deficiency | KG + DL |
| 15 | guttate psoriasis | KG + DL |
| 16 | corneal pigmentation | KG + DL |
| 17 | congenital temporomandibular joint ankylosis | KG + DL |
| 18 | sunburn | KG + DL |
| 19 | obsolete pathologic fracture | KG + DL |
| 20 | anuria | KG + DL |
| 21 | obsolete superimposed infection | KG + DL |
| 22 | myringitis bullosa hemorrhagica | KG + DL |
| 23 | methylcobalamin deficiency type cblDv1 | KG + DL |
| 24 | arteriosclerosis obliterans | KG + DL |
| 25 | cholangiocarcinoma, susceptibility to | KG + DL |
| 26 | primary hereditary glaucoma | KG + DL |
| 27 | polydipsia | KG + DL |
| 28 | hypermobility syndrome | KG + DL |
| 29 | atrial flutter (disease) | KG + DL |
| 30 | non-specific granulomatous orchitis | KG + DL |
| 31 | obsolete left bundle branch block | KG + DL |
| 32 | valvar pulmonary stenosis | KG + DL |
| 33 | muscular disease | KG + DL |
| 34 | sudden arrhythmia death syndrome | KG + DL |
| 35 | distal monosomy 7p | KG + DL |
| 36 | aphasia | KG + DL |
| 37 | mixed receptive-expressive language disorder | KG + DL |
| 38 | paranasal sinus disease | KG + DL |
| 39 | acute pulmonary heart disease | KG + DL |
| 40 | paramedian facial cleft | KG + DL |
| 41 | open-angle glaucoma | KG + DL |
| 42 | partial duplication of the short arm of chromosome X | KG + DL |
| 43 | Tay-Sachs disease, b variant | KG + DL |
| 44 | disorder of beta and omega amino acid metabolism | KG + DL |
| 45 | partial deletion of the long arm of chromosome 12 | KG + DL |
| 46 | congenital cystic eye multiple ocular and intracranial anomalies | KG + DL |
| 47 | glycerol kinase deficiency, juvenile form | KG + DL |
| 48 | glycerol kinase deficiency, adult form | KG + DL |
| 49 | non-hereditary degenerative ataxia | KG + DL |
| 50 | uniparental disomy of chromosome X | 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.