Candesartan

Basic Information

Item Value
DrugBank ID DB13919
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 migraine disorder KG + DL
2 migraine with brainstem aura KG + DL
3 migraine with or without aura, susceptibility to KG + DL
4 pulmonary hypertension KG + DL
5 Prinzmetal angina KG + DL
6 kyphoscoliotic heart disease KG + DL
7 atrophoderma vermiculata KG + DL
8 ulerythema ophryogenesis KG + DL
9 benign prostatic hyperplasia (disease) KG + DL
10 alopecia KG + DL
11 hypotrichosis simplex of the scalp KG + DL
12 Raynaud disease KG + DL
13 congenital hypotrichosis milia KG + DL
14 diffuse alopecia areata KG + DL
15 peripheral vascular disease KG + DL
16 intermittent vascular claudication KG + DL
17 intracranial arteriosclerosis KG + DL
18 pulmonary hypertension, primary, autosomal recessive KG + DL
19 homozygous familial hypercholesterolemia KG + DL
20 headache disorder KG + DL
21 Monckeberg arteriosclerosis KG + DL
22 rheumatoid arthritis KG + DL
23 obsolete patella aplasia, coxa vara, and tarsal synostosis KG + DL
24 tendinitis KG + DL
25 trigeminal autonomic cephalalgia KG + DL
26 fibromyalgia KG + DL
27 hypertrichosis (disease) KG + DL
28 myositis fibrosa KG + DL
29 idiopathic granulomatous myositis KG + DL
30 peripheral arterial disease KG + DL
31 cor pulmonale KG + DL
32 familial clubfoot due to 17q23.1q23.2 microduplication KG + DL
33 chromosome 17q23.1-q23.2 deletion syndrome KG + DL
34 coxopodopatellar syndrome KG + DL
35 inclusion body myositis KG + DL
36 Ambras type hypertrichosis universalis congenita KG + DL
37 myocardial infarction KG + DL
38 nephrogenic syndrome of inappropriate antidiuresis KG + DL
39 idiopathic pulmonary arterial hypertension KG + DL
40 idiopathic and/or familial pulmonary arterial hypertension KG + DL
41 malformation syndrome with odontal and/or periodontal component KG + DL
42 brachydactyly-syndactyly syndrome KG + DL
43 syndrome with a Dandy-Walker malformation as major feature KG + DL
44 pseudopelade of Brocq KG + DL
45 pulmonary hypertension, primary KG + DL
46 isolated genetic hair shaft abnormality KG + DL
47 obsolete susceptibility to ischemic stroke KG + DL
48 colobomatous microphthalmia-rhizomelic dysplasia syndrome KG + DL
49 subarachnoid hemorrhage (disease) KG + DL
50 gastrointestinal hamartoma 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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