Daptomycin

Basic Information

Item Value
DrugBank ID DB00080
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 osteoarthritis KG + DL
2 rheumatoid arthritis KG + DL
3 osteoarthritis susceptibility KG + DL
4 gout KG + DL
5 pseudoachondroplasia KG + DL
6 acromesomelic dysplasia, Hunter-Thompson type KG + DL
7 brachyolmia KG + DL
8 brachydactyly-syndactyly syndrome KG + DL
9 colobomatous microphthalmia-rhizomelic dysplasia syndrome KG + DL
10 brachyolmia-amelogenesis imperfecta syndrome KG + DL
11 myosclerosis KG + DL
12 arthropathy KG + DL
13 congestive heart failure KG + DL
14 acute pulmonary heart disease KG + DL
15 chronic pulmonary heart disease KG + DL
16 pulmonary hypertension with unclear multifactorial mechanism KG + DL
17 pulmonary hypertension owing to lung disease and/or hypoxia KG + DL
18 malignant renovascular hypertension KG + DL
19 malignant hypertensive renal disease KG + DL
20 hypertensive disorder KG + DL
21 hepatic porphyria KG + DL
22 Braddock syndrome KG + DL
23 female breast carcinoma KG + DL
24 idiopathic copper-associated cirrhosis KG + DL
25 hepatopulmonary syndrome KG + DL
26 hepatoportal sclerosis KG + DL
27 primitive portal vein thrombosis KG + DL
28 early-onset familial noncirrhotic portal hypertension KG + DL
29 paratenonitis KG + DL
30 calcific tendinitis KG + DL
31 myositis KG + DL
32 hemoglobinopathy KG + DL
33 disorder of phenylalanine metabolism KG + DL
34 subarachnoid hemorrhage (disease) KG + DL
35 cerebral infarction KG + DL
36 suppurative cholangitis KG + DL
37 beta-thalassemia with other manifestations KG + DL
38 breast fibrocystic disease KG + DL
39 disorder of tyrosine metabolism KG + DL
40 WHIM syndrome KG + DL
41 hypoalphalipoproteinemia KG + DL
42 pyruvate kinase deficiency of red cells KG + DL
43 partial deletion of the short arm of chromosome 16 KG + DL
44 teratogenic Pierre Robin syndrome KG + DL
45 hypotrichosis simplex of the scalp KG + DL
46 pyropoikilocytosis, hereditary KG + DL
47 IgG4-related pachymeningitis KG + DL
48 obsolete familial combined hyperlipidemia KG + DL
49 tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria KG + DL
50 hemolytic anemia due to glucophosphate isomerase deficiency 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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