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.


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