Larotrectinib

Basic Information

Item Value
DrugBank ID DB14723
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 HER2 positive breast carcinoma KG + DL
3 cytomegalovirus infection KG + DL
4 malignant catarrh KG + DL
5 infectious bovine rhinotracheitis KG + DL
6 progesterone-receptor negative breast cancer KG + DL
7 progesterone-receptor positive breast cancer KG + DL
8 normal breast-like subtype of breast carcinoma KG + DL
9 breast tumor luminal A or B KG + DL
10 thrombocytopenia KG + DL
11 pulmonary hypertension KG + DL
12 marcothrombocytopenia with mitral valve insufficiency KG + DL
13 hereditary thrombocytopenia with normal platelets KG + DL
14 transient neonatal thrombocytopenia KG + DL
15 dense granule disease KG + DL
16 amyotrophic lateral sclerosis KG + DL
17 kyphoscoliotic heart disease KG + DL
18 homozygous familial hypercholesterolemia KG + DL
19 amenorrhea (disease) KG + DL
20 hyperthyroidism KG + DL
21 female breast carcinoma KG + DL
22 thrombotic disease KG + DL
23 amyotrohpic lateral sclerosis type 22 KG + DL
24 amyotrophic lateral sclerosis, susceptibility to KG + DL
25 axial spondylometaphyseal dysplasia KG + DL
26 Mills syndrome KG + DL
27 resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta KG + DL
28 trichomegaly-retina pigmentary degeneration-dwarfism syndrome KG + DL
29 lethal arthrogryposis-anterior horn cell disease syndrome KG + DL
30 bilateral parasagittal parieto-occipital polymicrogyria KG + DL
31 neuroblastoma KG + DL
32 lower motor neuron syndrome with late-adult onset KG + DL
33 adrenal gland hyperfunction KG + DL
34 platelet storage pool deficiency KG + DL
35 secondary dysgenetic glaucoma associated with neural crest cell migration anomaly KG + DL
36 Prinzmetal angina KG + DL
37 myeloid leukemia KG + DL
38 monomelic amyotrophy KG + DL
39 ganglioneuroblastoma (disease) KG + DL
40 vertebral anomalies and variable endocrine and T-cell dysfunction KG + DL
41 stroke disorder KG + DL
42 collagenopathy KG + DL
43 lymphocytic hypereosinophilic syndrome KG + DL
44 retroperitoneal neoplasm KG + DL
45 hereditary neuroendocrine tumor of small intestine KG + DL
46 HIV infectious disease KG + DL
47 vein disease KG + DL
48 autosomal dominant mitochondrial myopathy with exercise intolerance KG + DL
49 Leydig cell hypoplasia due to LH resistance KG + DL
50 46,XY disorder of sex development due to impaired androgen production 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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