Toripalimab

Basic Information

Item Value
DrugBank ID DB15043
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 31

Predicted Indications (TxGNN)

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

# Indication Source
1 mixed-type autoimmune hemolytic anemia KG + DL
2 idiopathic aplastic anemia KG + DL
3 dermatitis KG + DL
4 paroxysmal nocturnal hemoglobinuria KG + DL
5 drug-induced autoimmune hemolytic anemia KG + DL
6 proteinuria KG + DL
7 acne keloid KG + DL
8 neonatal autoimmune hemolytic anemia KG + DL
9 primary CD59 deficiency KG + DL
10 amyopathic dermatomyositis KG + DL
11 neonatal dermatomyositis KG + DL
12 cold agglutinin disease KG + DL
13 hydroa vacciniforme, familial KG + DL
14 secondary interstitial lung disease specific to childhood associated with a connective tissue disease KG + DL
15 acrodermatitis chronica atrophicans KG + DL
16 hepatic veno-occlusive disease-immunodeficiency syndrome KG + DL
17 pancytopenia due to IKZF1 mutations KG + DL
18 chromhidrosis KG + DL
19 adult idiopathic neutropenia KG + DL
20 congenital neutropenia-myelofibrosis-nephromegaly syndrome KG + DL
21 Dowling-Degos disease KG + DL
22 autosomal recessive severe congenital neutropenia due to JAGN1 deficiency KG + DL
23 psoriasis KG + DL
24 X-linked severe congenital neutropenia KG + DL
25 autosomal recessive severe congenital neutropenia due to CXCR2 deficiency KG + DL
26 cyclic hematopoiesis KG + DL
27 autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis KG + DL
28 thrombocytopenia due to immune destruction KG + DL
29 combined immunodeficiency due to CRAC channel dysfunction KG + DL
30 hidradenitis KG + DL
31 facial dysmorphism-immunodeficiency-livedo-short stature 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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