Hydroxocobalamin

Basic Information

Item Value
DrugBank ID DB00200
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 32

Predicted Indications (TxGNN)

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

# Indication Source
1 esophageal varices with bleeding KG + DL
2 esophageal varices without bleeding KG + DL
3 varicose disease KG + DL
4 immune-mediated necrotizing myopathy KG + DL
5 antisynthetase syndrome KG + DL
6 focal myositis KG + DL
7 inflammatory myopathy with abundant macrophages KG + DL
8 idiopathic eosinophilic myositis KG + DL
9 vitamin deficiency disorder KG + DL
10 congenital prothrombin deficiency KG + DL
11 biotin metabolic disease KG + DL
12 osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome KG + DL
13 C1 inhibitor deficiency KG + DL
14 maternally-inherited mitochondrial myopathy KG + DL
15 maternally-inherited mitochondrial dystonia KG + DL
16 primary optic atrophy KG + DL
17 hypophosphatasia KG + DL
18 serpinopathy with toxic serpin polymerization KG + DL
19 Steel syndrome KG + DL
20 Leber hereditary optic neuropathy KG + DL
21 pyridoxine deficiency anemia KG + DL
22 dermatomyositis KG + DL
23 maternally-inherited Leigh syndrome KG + DL
24 leukocyte adhesion deficiency KG + DL
25 osteopetrosis KG + DL
26 multiple intestinal atresia KG + DL
27 selective IgG immunodeficiency KG + DL
28 hereditary angioedema with C1Inh deficiency KG + DL
29 autosomal recessive Alport syndrome KG + DL
30 acrorenal syndrome, autosomal recessive KG + DL
31 Pendred syndrome KG + DL
32 Immunoerythromyeloid hypoplasia 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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