Erdosteine

Basic Information

Item Value
DrugBank ID DB05057
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 marcothrombocytopenia with mitral valve insufficiency KG + DL
2 hereditary thrombocytopenia with normal platelets KG + DL
3 thrombocytopenia KG + DL
4 dense granule disease KG + DL
5 transient neonatal thrombocytopenia KG + DL
6 platelet storage pool deficiency KG + DL
7 Ledderhose disease KG + DL
8 penile fibromatosis KG + DL
9 respiratory syncytial virus infectious disease KG + DL
10 infantile digital fibromatosis KG + DL
11 anaphylaxis KG + DL
12 palmar fibromatosis KG + DL
13 food-dependent exercise-induced anaphylaxis KG + DL
14 glaucoma KG + DL
15 familial Dupuytren contracture KG + DL
16 hyperplasia KG + DL
17 dry eye syndrome KG + DL
18 selective pituitary resistance to thyroid hormone KG + DL
19 toxic diffuse goiter KG + DL
20 subacute lymphocytic thyroiditis KG + DL
21 suppurative thyroiditis KG + DL
22 subacute thyroiditis KG + DL
23 autoimmune hemolytic anemia KG + DL
24 thyroid crisis (disease) KG + DL
25 skin disease KG + DL
26 diffuse cutaneous mucinosis KG + DL
27 scleredema adultorum KG + DL
28 cutaneous focal mucinosis KG + DL
29 drug-induced osteoporosis KG + DL
30 erythema palmare hereditarium KG + DL
31 keratolytic winter erythema KG + DL
32 genetic nail anomaly KG + DL
33 lichen myxedematosus KG + DL
34 bone Paget disease KG + DL
35 zinc-responsive necrolytic acral erythema KG + DL
36 congenital erosive and vesicular dermatosis KG + DL
37 warty dyskeratoma KG + DL
38 congenital lethal erythroderma KG + DL
39 hyperkeratosis lenticularis perstans (disease) KG + DL
40 Fox-Fordyce disease KG + DL
41 nail anomaly KG + DL
42 hereditary poikiloderma KG + DL
43 acrokeratoderma KG + DL
44 open-angle glaucoma KG + DL
45 decubitus ulcer KG + DL
46 ulcer of lower limbs KG + DL
47 primary hereditary glaucoma KG + DL
48 reticulate pigment disorder KG + DL
49 secondary catabolic mucinosis of skin KG + DL
50 genetic hair anomaly 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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