Latanoprostene Bunod

Basic Information

Item Value
DrugBank ID DB11660
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 54

Predicted Indications (TxGNN)

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

# Indication Source
1 visceral calciphylaxis KG + DL
2 primary hereditary glaucoma KG + DL
3 venous thoracic outlet syndrome KG + DL
4 arterial thoracic outlet syndrome KG + DL
5 neurogenic thoracic outlet syndrome KG + DL
6 vascular disease KG + DL
7 idiopathic spontaneous coronary artery dissection KG + DL
8 angiodysplasia of stomach KG + DL
9 lymphangiectasis KG + DL
10 hemangioendothelioma KG + DL
11 blue toe syndrome KG + DL
12 atheroembolism of kidney KG + DL
13 arterial dissection-lentiginosis syndrome KG + DL
14 glaucoma 1, open angle KG + DL
15 respiratory failure KG + DL
16 subarachnoid hemorrhage (disease) KG + DL
17 tinea nigra KG + DL
18 open angle glaucoma KG + DL
19 hypotrichosis-lymphedema-telangiectasia syndrome (grouping) KG + DL
20 chylous ascites KG + DL
21 mullerian derivatives-lymphangiectasia-polydactyly syndrome KG + DL
22 lymphedema-cerebral arteriovenous anomaly syndrome KG + DL
23 microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability KG + DL
24 lymphedema-atrial septal defects-facial changes syndrome KG + DL
25 German syndrome KG + DL
26 podoconiosis KG + DL
27 congestive heart failure KG + DL
28 acute pulmonary heart disease KG + DL
29 Moyomoya angiopathy KG + DL
30 hepatic porphyria KG + DL
31 idiopathic macular telangiectasia KG + DL
32 vasoproliferative tumor of retina KG + DL
33 dermatophytosis KG + DL
34 primitive portal vein thrombosis KG + DL
35 hepatoportal sclerosis KG + DL
36 idiopathic copper-associated cirrhosis KG + DL
37 early-onset familial noncirrhotic portal hypertension KG + DL
38 hepatopulmonary syndrome KG + DL
39 non-syndromic esophageal malformation KG + DL
40 acquired aneurysmal subarachnoid hemorrhage KG + DL
41 androgen insensitivity syndrome KG + DL
42 benign choroid plexus neoplasm KG + DL
43 IRVAN syndrome KG + DL
44 cerebral visual impairment KG + DL
45 neonatal respiratory failure KG + DL
46 biotin metabolic disease KG + DL
47 homozygous familial hypercholesterolemia KG + DL
48 glaucoma KG + DL
49 esophageal disease KG + DL
50 vitamin deficiency disorder KG + DL

(Showing top 50 of 54 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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