Tildrakizumab

Basic Information

Item Value
DrugBank ID DB14004
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 47

Predicted Indications (TxGNN)

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

# Indication Source
1 severe nonproliferative diabetic retinopathy KG + DL
2 diabetic retinopathy KG + DL
3 diabetic cataract KG + DL
4 drug-induced osteoporosis KG + DL
5 nuclear senile cataract KG + DL
6 cortical cataract KG + DL
7 senile cataract KG + DL
8 mature cataract KG + DL
9 craniostenosis cataract KG + DL
10 immature cataract KG + DL
11 diabetes mellitus type 2 associated cataract KG + DL
12 tetanic cataract KG + DL
13 dermatitis KG + DL
14 neonatal dermatomyositis KG + DL
15 amyopathic dermatomyositis KG + DL
16 acrodermatitis chronica atrophicans KG + DL
17 secondary interstitial lung disease specific to childhood associated with a connective tissue disease KG + DL
18 acne keloid KG + DL
19 hydroa vacciniforme, familial KG + DL
20 acne (disease) KG + DL
21 psoriasis KG + DL
22 primary release disorder of platelets KG + DL
23 pseudo-von Willebrand disease KG + DL
24 Glanzmann thrombasthenia KG + DL
25 pityriasis lichenoides KG + DL
26 cholestasis KG + DL
27 benign recurrent intrahepatic cholestasis KG + DL
28 hemorrhagic disease of newborn KG + DL
29 zinc, elevated plasma KG + DL
30 non-syndromic visceral malformation KG + DL
31 biliary atresia intrahepatic KG + DL
32 familial intrahepatic cholestasis KG + DL
33 HER2 positive breast carcinoma KG + DL
34 nevus of Ito KG + DL
35 Mirizzi syndrome KG + DL
36 microvillus inclusion disease KG + DL
37 mitochondrial DNA depletion syndrome, hepatocerebral form KG + DL
38 inborn disorder of bilirubin metabolism KG + DL
39 bilirubin metabolism disease KG + DL
40 progesterone-receptor positive breast cancer KG + DL
41 normal breast-like subtype of breast carcinoma KG + DL
42 breast tumor luminal A or B KG + DL
43 parapsoriasis KG + DL
44 progesterone-receptor negative breast cancer KG + DL
45 adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency KG + DL
46 hereditary North American Indian childhood cirrhosis KG + DL
47 chromosome 17q12 deletion syndrome KG + DL

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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