Tocopherol

Basic Information

Item Value
DrugBank ID DB11251
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 sclerosing cholangitis KG + DL
2 pulmonary hypertension KG + DL
3 rheumatoid arthritis KG + DL
4 hypotrichosis simplex of the scalp KG + DL
5 congenital hypotrichosis milia KG + DL
6 kyphoscoliotic heart disease KG + DL
7 diffuse alopecia areata KG + DL
8 alopecia KG + DL
9 congestive heart failure KG + DL
10 peripheral vascular disease KG + DL
11 acute pulmonary heart disease KG + DL
12 Raynaud disease KG + DL
13 colobomatous microphthalmia-rhizomelic dysplasia syndrome KG + DL
14 primary hereditary glaucoma KG + DL
15 cor pulmonale KG + DL
16 pulmonary hypertension, primary, autosomal recessive KG + DL
17 open-angle glaucoma KG + DL
18 brachydactyly-syndactyly syndrome KG + DL
19 intermittent vascular claudication KG + DL
20 headache disorder KG + DL
21 trigeminal autonomic cephalalgia KG + DL
22 peripheral arterial disease KG + DL
23 intracranial arteriosclerosis KG + DL
24 migraine with brainstem aura KG + DL
25 blindness (disorder) KG + DL
26 migraine disorder KG + DL
27 potassium deficiency disease KG + DL
28 Monckeberg arteriosclerosis KG + DL
29 hypoalphalipoproteinemia KG + DL
30 hepatic porphyria KG + DL
31 chronic renal failure syndrome KG + DL
32 hepatopulmonary syndrome KG + DL
33 primitive portal vein thrombosis KG + DL
34 hepatoportal sclerosis KG + DL
35 idiopathic copper-associated cirrhosis KG + DL
36 early-onset familial noncirrhotic portal hypertension KG + DL
37 osteoarthritis KG + DL
38 postmenopausal osteoporosis KG + DL
39 congenital prothrombin deficiency KG + DL
40 gastroduodenitis KG + DL
41 pregnancy associated osteoporosis KG + DL
42 obsolete patella aplasia, coxa vara, and tarsal synostosis KG + DL
43 transient ischemic attack (disease) KG + DL
44 familial clubfoot due to 17q23.1q23.2 microduplication KG + DL
45 idiopathic and/or familial pulmonary arterial hypertension KG + DL
46 idiopathic pulmonary arterial hypertension KG + DL
47 chromosome 17q23.1-q23.2 deletion syndrome KG + DL
48 peptic ulcer disease KG + DL
49 autosomal dominant neovascular inflammatory vitreoretinopathy KG + DL
50 chronic pulmonary heart disease 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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