Guselkumab

Basic Information

Item Value
DrugBank ID DB11834
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 drug-induced osteoporosis KG + DL
2 severe nonproliferative diabetic retinopathy KG + DL
3 psoriasis KG + DL
4 diabetic retinopathy KG + DL
5 renal osteodystrophy KG + DL
6 ulcerative colitis (disease) KG + DL
7 congenital hypotrichosis with juvenile macular dystrophy KG + DL
8 primary release disorder of platelets KG + DL
9 Glanzmann thrombasthenia KG + DL
10 non-renal secondary hyperparathyroidism KG + DL
11 pseudo-von Willebrand disease KG + DL
12 impaired renal function disease KG + DL
13 gout KG + DL
14 benign recurrent intrahepatic cholestasis KG + DL
15 hyperparathyroidism, transient neonatal KG + DL
16 familial intrahepatic cholestasis KG + DL
17 diabetic cataract KG + DL
18 pityriasis lichenoides KG + DL
19 bone remodeling disease KG + DL
20 cholestasis KG + DL
21 dermatitis KG + DL
22 nuclear senile cataract KG + DL
23 cortical cataract KG + DL
24 senile cataract KG + DL
25 monosomy X KG + DL
26 diabetes mellitus type 2 associated cataract KG + DL
27 craniostenosis cataract KG + DL
28 tetanic cataract KG + DL
29 mature cataract KG + DL
30 immature cataract KG + DL
31 inborn disorder of bilirubin metabolism KG + DL
32 acrodermatitis chronica atrophicans KG + DL
33 neonatal dermatomyositis KG + DL
34 amyopathic dermatomyositis KG + DL
35 nevus of Ito KG + DL
36 secondary interstitial lung disease specific to childhood associated with a connective tissue disease KG + DL
37 bilirubin metabolism disease KG + DL
38 gonadal dysgenesis KG + DL
39 parapsoriasis KG + DL
40 microvillus inclusion disease KG + DL
41 biliary atresia intrahepatic KG + DL
42 mitochondrial DNA depletion syndrome, hepatocerebral form KG + DL
43 non-syndromic visceral malformation KG + DL
44 acne keloid KG + DL
45 psoriasis 14, pustular KG + DL
46 46,XY disorder of gonadal development KG + DL
47 hydroa vacciniforme, familial KG + DL
48 male infertility due to gonadal dysgenesis KG + DL
49 adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency KG + DL
50 Navajo neurohepatopathy 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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