Remdesivir

Basic Information

Item Value
DrugBank ID DB14761
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 multiple endocrine neoplasia KG + DL
2 HIV infectious disease KG + DL
3 simian immunodeficiency virus infection KG + DL
4 feline acquired immunodeficiency syndrome KG + DL
5 neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter KG + DL
6 homozygous familial hypercholesterolemia KG + DL
7 Prinzmetal angina KG + DL
8 leprosy KG + DL
9 antithrombin deficiency type 2 KG + DL
10 cytomegalovirus infection KG + DL
11 factor 5 excess with spontaneous thrombosis KG + DL
12 heparin cofactor 2 deficiency KG + DL
13 infectious bovine rhinotracheitis KG + DL
14 malignant catarrh KG + DL
15 oral candidiasis KG + DL
16 hyperthyroidism KG + DL
17 hypoalphalipoproteinemia KG + DL
18 resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta KG + DL
19 conjunctivitis KG + DL
20 commissural lip fistula KG + DL
21 osteoradionecrosis of the mandible KG + DL
22 oral leukoedema KG + DL
23 burning mouth syndrome KG + DL
24 gastrin secretion abnormality KG + DL
25 acne (disease) KG + DL
26 rheumatoid arthritis KG + DL
27 hemoglobinopathy KG + DL
28 thrombophilia KG + DL
29 gout KG + DL
30 Smouldering systemic mastocytosis KG + DL
31 hereditary neuroendocrine tumor of small intestine KG + DL
32 beta-thalassemia with other manifestations KG + DL
33 partial deletion of the short arm of chromosome 16 KG + DL
34 lymphoadenopathic mastocytosis with eosinophilia KG + DL
35 colobomatous microphthalmia-rhizomelic dysplasia syndrome KG + DL
36 obsolete familial combined hyperlipidemia KG + DL
37 brachydactyly-syndactyly syndrome KG + DL
38 hemolytic anemia due to glucophosphate isomerase deficiency KG + DL
39 salivary gland disease KG + DL
40 pediatric systemic lupus erythematosus KG + DL
41 systemic mastocytosis KG + DL
42 pyropoikilocytosis, hereditary KG + DL
43 hyperthyroxinemia KG + DL
44 sclerosing cholangitis KG + DL
45 tongue disease KG + DL
46 conjunctivitis (disease) KG + DL
47 Graves disease KG + DL
48 pyruvate kinase deficiency of red cells KG + DL
49 autosomal recessive familial Mediterranean fever KG + DL
50 neoplasm of jaw 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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