Chondroitin Sulfate Sodium

Basic Information

Item Value
DrugBank ID DB09301
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 early-onset familial noncirrhotic portal hypertension KG + DL
2 primitive portal vein thrombosis KG + DL
3 idiopathic copper-associated cirrhosis KG + DL
4 hepatopulmonary syndrome KG + DL
5 hepatoportal sclerosis KG + DL
6 hepatic porphyria KG + DL
7 primary release disorder of platelets KG + DL
8 Glanzmann thrombasthenia KG + DL
9 pseudo-von Willebrand disease KG + DL
10 glycogen storage disease due to hepatic glycogen synthase deficiency KG + DL
11 Ledderhose disease KG + DL
12 congenital prothrombin deficiency KG + DL
13 congenital hypotrichosis milia KG + DL
14 hypotrichosis simplex of the scalp KG + DL
15 adenosine deaminase deficiency KG + DL
16 infantile digital fibromatosis KG + DL
17 Scott syndrome KG + DL
18 palmar fibromatosis KG + DL
19 obsolete hyperuricemia (disease) KG + DL
20 diffuse alopecia areata KG + DL
21 severe combined immunodeficiency due to LCK deficiency KG + DL
22 bleeding diathesis due to a collagen receptor defect KG + DL
23 hemorrhagic disorder due to a constitutional thrombocytopenia KG + DL
24 cholangiocarcinoma, susceptibility to KG + DL
25 lymphopenic hypergammaglobulinemia, antibody deficiency, autoimmune hemolytic anemia, and glomerulonephritis KG + DL
26 non-specific granulomatous orchitis KG + DL
27 epidural abscess KG + DL
28 hemoglobin C-beta-thalassemia syndrome KG + DL
29 ocular tuberculosis KG + DL
30 reticular dysgenesis KG + DL
31 hilar cholangiocarcinoma KG + DL
32 ergotism KG + DL
33 congenital cystic eye multiple ocular and intracranial anomalies KG + DL
34 Kozlowski Warren Fisher syndrome KG + DL
35 sunburn KG + DL
36 inherited thrombophilia KG + DL
37 paramedian facial cleft KG + DL
38 obsolete pathologic fracture KG + DL
39 giant neutrophil leukocytes KG + DL
40 penile fibromatosis KG + DL
41 craniofacial dystonia KG + DL
42 alpha granule disease KG + DL
43 guttate psoriasis KG + DL
44 mixed receptive-expressive language disorder KG + DL
45 aphasia KG + DL
46 muscular disease KG + DL
47 lymphatic malformation KG + DL
48 distal monosomy 7p KG + DL
49 anuria KG + DL
50 glycoprotein storage 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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