Levocarnitine

Basic Information

Item Value
DrugBank ID DB00583
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 autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome KG + DL
2 brain small vessel disease 1 with or without ocular anomalies KG + DL
3 diabetic nephropathy KG + DL
4 rheumatoid arthritis KG + DL
5 sclerosing cholangitis KG + DL
6 gout KG + DL
7 brachydactyly-syndactyly syndrome KG + DL
8 colobomatous microphthalmia-rhizomelic dysplasia syndrome KG + DL
9 congestive heart failure KG + DL
10 hypoalphalipoproteinemia KG + DL
11 pulmonary hypertension KG + DL
12 homozygous familial hypercholesterolemia KG + DL
13 acute pulmonary heart disease KG + DL
14 kyphoscoliotic heart disease KG + DL
15 chronic renal failure syndrome KG + DL
16 chronic kidney disease KG + DL
17 chronic pulmonary heart disease KG + DL
18 end stage renal failure KG + DL
19 malignant renovascular hypertension KG + DL
20 malignant hypertensive renal disease KG + DL
21 hypertensive disorder KG + DL
22 pulmonary hypertension owing to lung disease and/or hypoxia KG + DL
23 pulmonary hypertension with unclear multifactorial mechanism KG + DL
24 Prinzmetal angina KG + DL
25 intracerebral hemorrhage KG + DL
26 Braddock syndrome KG + DL
27 osteoarthritis susceptibility KG + DL
28 cor pulmonale KG + DL
29 paratenonitis KG + DL
30 methemoglobinemia, alpha type KG + DL
31 calcific tendinitis KG + DL
32 hemoglobinopathy KG + DL
33 obsolete hyperuricemia (disease) KG + DL
34 obsolete familial combined hyperlipidemia KG + DL
35 hyperthyroidism KG + DL
36 Lesch-Nyhan syndrome KG + DL
37 myositis KG + DL
38 conjunctivitis KG + DL
39 methemoglobin reductase deficiency KG + DL
40 resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta KG + DL
41 methemoglobinemia KG + DL
42 partial deletion of the short arm of chromosome 16 KG + DL
43 multiple endocrine neoplasia KG + DL
44 beta-thalassemia with other manifestations KG + DL
45 WHIM syndrome KG + DL
46 pyropoikilocytosis, hereditary KG + DL
47 hemolytic anemia due to glucophosphate isomerase deficiency KG + DL
48 peripheral arterial disease KG + DL
49 Graves disease KG + DL
50 peripheral vascular disease 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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