Cyanocobalamin

Basic Information

Item Value
DrugBank ID DB00115
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 37

Predicted Indications (TxGNN)

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

# Indication Source
1 biotin metabolic disease KG + DL
2 inborn error of biotin metabolism KG + DL
3 non-syndromic esophageal malformation KG + DL
4 inflammatory myopathy with abundant macrophages KG + DL
5 idiopathic eosinophilic myositis KG + DL
6 immune-mediated necrotizing myopathy KG + DL
7 antisynthetase syndrome KG + DL
8 proteinuria KG + DL
9 focal myositis KG + DL
10 primary CD59 deficiency KG + DL
11 neonatal autoimmune hemolytic anemia KG + DL
12 primary release disorder of platelets KG + DL
13 mixed-type autoimmune hemolytic anemia KG + DL
14 pseudo-von Willebrand disease KG + DL
15 drug-induced autoimmune hemolytic anemia KG + DL
16 cold agglutinin disease KG + DL
17 paroxysmal nocturnal hemoglobinuria KG + DL
18 Glanzmann thrombasthenia KG + DL
19 constitutional megaloblastic anemia due to folate metabolism disorder KG + DL
20 esophageal disease KG + DL
21 infantile digital fibromatosis KG + DL
22 cerebral folate deficiency KG + DL
23 inborn disorder of pyridoxine metabolism KG + DL
24 acquired amyloid peripheral neuropathy KG + DL
25 Ledderhose disease KG + DL
26 C1 inhibitor deficiency KG + DL
27 primary amyloidosis KG + DL
28 penile fibromatosis KG + DL
29 palmar fibromatosis KG + DL
30 dermis disease KG + DL
31 serpinopathy with toxic serpin polymerization KG + DL
32 nodular cutaneous amyloidosis KG + DL
33 amyloidosis cutis dyschromia KG + DL
34 macular amyloidosis KG + DL
35 amyloidosis (disease) KG + DL
36 dermatomyositis KG + DL
37 selective IgG immunodeficiency 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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