Cabotegravir

Basic Information

Item Value
DrugBank ID DB11751
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 79

Predicted Indications (TxGNN)

The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.

# Indication Source
1 rheumatoid arthritis KG + DL
2 sclerosing cholangitis KG + DL
3 bronchitis KG + DL
4 colobomatous microphthalmia-rhizomelic dysplasia syndrome KG + DL
5 severe nonproliferative diabetic retinopathy KG + DL
6 brachydactyly-syndactyly syndrome KG + DL
7 diabetic retinopathy KG + DL
8 non-syndromic visceral malformation KG + DL
9 autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome KG + DL
10 brain small vessel disease 1 with or without ocular anomalies KG + DL
11 biliary atresia intrahepatic KG + DL
12 cholestasis KG + DL
13 colonic neoplasm KG + DL
14 Mirizzi syndrome KG + DL
15 diabetic nephropathy KG + DL
16 rectosigmoid junction neoplasm KG + DL
17 lipoma of colon KG + DL
18 colonic lymphangioma KG + DL
19 colon leiomyoma KG + DL
20 cavernous hemangioma of colon KG + DL
21 bronchial neoplasm (disease) KG + DL
22 cecum neuroendocrine tumor G1 KG + DL
23 cecum villous adenoma KG + DL
24 cecal disease KG + DL
25 benign neoplasm of cecum KG + DL
26 benign recurrent intrahepatic cholestasis KG + DL
27 pneumonia KG + DL
28 laryngotracheitis KG + DL
29 heparin cofactor 2 deficiency KG + DL
30 antithrombin deficiency type 2 KG + DL
31 nevus of Ito KG + DL
32 factor 5 excess with spontaneous thrombosis KG + DL
33 microvillus inclusion disease KG + DL
34 mitochondrial DNA depletion syndrome, hepatocerebral form KG + DL
35 drug-induced liver injury KG + DL
36 gout KG + DL
37 pyruvate kinase deficiency of red cells KG + DL
38 pyelonephritis KG + DL
39 hemoglobinopathy KG + DL
40 thrombophilia KG + DL
41 partial deletion of the short arm of chromosome 16 KG + DL
42 beta-thalassemia with other manifestations KG + DL
43 adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency KG + DL
44 hereditary North American Indian childhood cirrhosis KG + DL
45 hemolytic anemia due to glucophosphate isomerase deficiency KG + DL
46 familial intrahepatic cholestasis KG + DL
47 hyperbiliverdinemia KG + DL
48 pyropoikilocytosis, hereditary KG + DL
49 HIV infectious disease KG + DL
50 thrombotic disease KG + DL

(Showing top 50 of 79 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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