Potassium Citrate

Basic Information

Item Value
DrugBank ID DB09125
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 85

Predicted Indications (TxGNN)

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

# Indication Source
1 familial visceral myopathy KG + DL
2 mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies KG + DL
3 Pendred syndrome KG + DL
4 nephrolithiasis KG + DL
5 cystinosis KG + DL
6 nephrolithiasis susceptibility caused by SLC26A1 KG + DL
7 autosomal recessive nonsyndromic deafness KG + DL
8 exocrine pancreatic insufficiency KG + DL
9 leukocyte adhesion deficiency KG + DL
10 adult Fanconi syndrome KG + DL
11 Fraser syndrome KG + DL
12 Alstrom syndrome KG + DL
13 temtamy preaxial brachydactyly syndrome KG + DL
14 human HOXA1 syndromes KG + DL
15 dyspepsia KG + DL
16 glycogen storage disease due to GLUT2 deficiency KG + DL
17 myopathic intestinal pseudoobstruction KG + DL
18 unclassified intestinal pseudoobstruction KG + DL
19 neuronal intestinal dysplasia, type B KG + DL
20 exercise-induced malignant hyperthermia KG + DL
21 primary Fanconi syndrome KG + DL
22 intestinal obstruction KG + DL
23 congenital short bowel syndrome 1 KG + DL
24 osteopetrosis KG + DL
25 HELIX syndrome KG + DL
26 combined oxidative phosphorylation defect KG + DL
27 deafness dystonia syndrome KG + DL
28 malignant hyperthermia, susceptibility to KG + DL
29 calcium-alkali syndrome KG + DL
30 King-Denborough syndrome KG + DL
31 urolithiasis KG + DL
32 intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked KG + DL
33 primary bone dysplasia KG + DL
34 obsolete CFM1 KG + DL
35 central core myopathy KG + DL
36 neuronal intestinal pseudoobstruction KG + DL
37 renal hypomagnesemia KG + DL
38 congenital multicore myopathy with external ophthalmoplegia KG + DL
39 moderate multiminicore disease with hand involvement KG + DL
40 primary bone dysplasia with defective bone mineralization KG + DL
41 immune-mediated necrotizing myopathy KG + DL
42 antisynthetase syndrome KG + DL
43 cytochrome-c oxidase deficiency disease KG + DL
44 inflammatory myopathy with abundant macrophages KG + DL
45 idiopathic eosinophilic myositis KG + DL
46 X-linked centronuclear myopathy KG + DL
47 focal myositis KG + DL
48 Jervell and Lange-Nielsen syndrome KG + DL
49 X-linked distal spinal muscular atrophy type 3 KG + DL
50 distal spinal muscular atrophy type 3 KG + DL

(Showing top 50 of 85 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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