Sodium Lactate

Basic Information

Item Value
DrugBank ID DB09395
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 100

Predicted Indications (TxGNN)

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

# Indication Source
1 congenital prothrombin deficiency KG + DL
2 epiglottitis KG + DL
3 urinary tract infection (disease) KG + DL
4 sclerosing cholangitis KG + DL
5 Ureaplasma urethritis KG + DL
6 gonococcal urethritis KG + DL
7 dyspepsia KG + DL
8 uterine inflammatory disease KG + DL
9 gastroparesis (disease) KG + DL
10 xanthogranulomatous pyelonephritis KG + DL
11 IgG4-related pachymeningitis KG + DL
12 IgG4-related mesenteritis KG + DL
13 eosinophilic angiocentric fibrosis KG + DL
14 IgG4-related aortitis KG + DL
15 IgG4-related mediastinitis KG + DL
16 laryngitis KG + DL
17 IgG4-related retroperitoneal fibrosis KG + DL
18 myopathic intestinal pseudoobstruction KG + DL
19 unclassified intestinal pseudoobstruction KG + DL
20 neuronal intestinal dysplasia, type B KG + DL
21 IgG4-related hepatopathy KG + DL
22 congestive heart failure KG + DL
23 intestinal obstruction KG + DL
24 acute pulmonary heart disease KG + DL
25 vitamin deficiency disorder KG + DL
26 stomach disease KG + DL
27 toxocariasis KG + DL
28 non-syndromic esophageal malformation KG + DL
29 type I complement component 8 deficiency KG + DL
30 autosomal recessive hydrocephalus due to congenital stenosis of aqueduct of Sylvius KG + DL
31 Alstrom syndrome KG + DL
32 renal tubular acidosis KG + DL
33 HELIX syndrome KG + DL
34 Senior-Loken syndrome KG + DL
35 primary hereditary glaucoma KG + DL
36 bone Paget disease KG + DL
37 esophageal disease KG + DL
38 primary aldosteronism KG + DL
39 autosomal recessive extra-oral halitosis KG + DL
40 CoQ-responsive OXPHOS deficiency KG + DL
41 autosomal recessive Ehlers-Danlos syndrome, vascular type KG + DL
42 open-angle glaucoma KG + DL
43 suppurative cholangitis KG + DL
44 urogenital tuberculosis KG + DL
45 pyridoxine deficiency anemia KG + DL
46 autosomal recessive humeroradial synostosis KG + DL
47 hyperphenylalaninemia due to tetrahydrobiopterin deficiency KG + DL
48 fibular hypoplasia and complex brachydactyly KG + DL
49 autosomal recessive axonal hereditary motor and sensory neuropathy KG + DL
50 acrorenal syndrome, autosomal recessive KG + DL

(Showing top 50 of 100 predictions)

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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