Belimumab

Basic Information

Item Value
DrugBank ID DB08879
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 40

Predicted Indications (TxGNN)

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

# Indication Source
1 primary release disorder of platelets KG + DL
2 pseudo-von Willebrand disease KG + DL
3 Glanzmann thrombasthenia KG + DL
4 fetal and neonatal alloimmune thrombocytopenia KG + DL
5 severe nonproliferative diabetic retinopathy KG + DL
6 autosomal dominant macrothrombocytopenia KG + DL
7 granulomatous disease, chronic, autosomal recessive, 5 KG + DL
8 anus disease KG + DL
9 inflammatory bowel disease KG + DL
10 granulomatous disease with defect in neutrophil chemotaxis KG + DL
11 Scott syndrome KG + DL
12 functional neutrophil defect KG + DL
13 congenital hypotrichosis with juvenile macular dystrophy KG + DL
14 systemic sclerosis KG + DL
15 psoriasis KG + DL
16 bleeding diathesis due to a collagen receptor defect KG + DL
17 hemorrhagic disorder due to a constitutional thrombocytopenia KG + DL
18 Crohn disease of the esophagus KG + DL
19 ulcerative colitis (disease) KG + DL
20 cyclic hematopoiesis KG + DL
21 platelet-type bleeding disorder KG + DL
22 adult idiopathic neutropenia KG + DL
23 X-linked severe congenital neutropenia KG + DL
24 Ehlers-Danlos syndrome, fibronectinemic type KG + DL
25 peeling skin syndrome KG + DL
26 pityriasis lichenoides KG + DL
27 congenital neutropenia-myelofibrosis-nephromegaly syndrome KG + DL
28 autosomal recessive severe congenital neutropenia due to JAGN1 deficiency KG + DL
29 autosomal recessive severe congenital neutropenia due to CSF3R deficiency KG + DL
30 parapsoriasis KG + DL
31 diabetic retinopathy KG + DL
32 psoriasis 14, pustular KG + DL
33 C1 inhibitor deficiency KG + DL
34 autosomal recessive severe congenital neutropenia due to CXCR2 deficiency KG + DL
35 pustulosis palmaris et plantaris KG + DL
36 acute lichenoid pityriasis KG + DL
37 serpinopathy with toxic serpin polymerization KG + DL
38 Peyronie disease KG + DL
39 thrombotic thrombocytopenic purpura KG + DL
40 heparin cofactor 2 deficiency 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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