Axitinib

Basic Information

Item Value
DrugBank ID DB06626
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 renal cell carcinoma associated with Xp11.2 translocations/TFE3 gene fusions KG + DL
2 unclassified renal cell carcinoma KG + DL
3 renal cell carcinoma associated with neuroblastoma KG + DL
4 childhood kidney cell carcinoma KG + DL
5 liposarcoma KG + DL
6 renal carcinoma KG + DL
7 ovarian myxoid liposarcoma KG + DL
8 angiolipoma KG + DL
9 collecting duct carcinoma KG + DL
10 familial spontaneous pneumothorax KG + DL
11 endocrine-cerebro-osteodysplasia syndrome KG + DL
12 renal pelvis carcinoma KG + DL
13 chromophobe renal cell carcinoma KG + DL
14 sarcomatoid renal cell carcinoma KG + DL
15 adenocarcinoma of liver and intrahepatic biliary tract KG + DL
16 spindle cell liposarcoma KG + DL
17 undifferentiated carcinoma of liver and intrahepatic biliary tract KG + DL
18 extrahepatic bile duct adenocarcinoma KG + DL
19 kidney medullary carcinoma KG + DL
20 acquired cystic disease-associated renal cell carcinoma KG + DL
21 cystic renal cell carcinoma KG + DL
22 amyotrophic lateral sclerosis KG + DL
23 multilocular clear cell renal cell carcinoma KG + DL
24 paroxysmal dyskinesia KG + DL
25 vulva sarcoma KG + DL
26 breast fibroadenoma KG + DL
27 renal pelvis adenocarcinoma KG + DL
28 Mills syndrome KG + DL
29 amyotrophic lateral sclerosis, susceptibility to KG + DL
30 amyotrohpic lateral sclerosis type 22 KG + DL
31 bilateral parasagittal parieto-occipital polymicrogyria KG + DL
32 axial spondylometaphyseal dysplasia KG + DL
33 Wolffian duct adenocarcinoma KG + DL
34 X-linked hydrocephalus with stenosis of the aqueduct of Sylvius KG + DL
35 glycogen storage disease due to lactate dehydrogenase H-subunit deficiency KG + DL
36 X-linked complicated corpus callosum dysgenesis KG + DL
37 heart fibrosarcoma KG + DL
38 pyruvate dehydrogenase E1-beta deficiency KG + DL
39 3M syndrome KG + DL
40 classic variant of chromophobe renal cell carcinoma KG + DL
41 uterine corpus perivascular epithelioid cell tumor KG + DL
42 kidney fibrosarcoma KG + DL
43 fibroblastic neoplasm KG + DL
44 trichomegaly-retina pigmentary degeneration-dwarfism syndrome KG + DL
45 benign PEComa KG + DL
46 autosomal dominant mitochondrial myopathy with exercise intolerance KG + DL
47 lymphangiomyoma KG + DL
48 familial rhabdoid tumor KG + DL
49 monomelic amyotrophy KG + DL
50 childhood malignant kidney neoplasm 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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