Pentetic Acid

Basic Information

Item Value
DrugBank ID DB14007
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 74

Predicted Indications (TxGNN)

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

# Indication Source
1 thrombocytopenic purpura KG + DL
2 hepatic porphyria KG + DL
3 benign recurrent intrahepatic cholestasis KG + DL
4 early-onset familial noncirrhotic portal hypertension KG + DL
5 hepatopulmonary syndrome KG + DL
6 idiopathic copper-associated cirrhosis KG + DL
7 hepatoportal sclerosis KG + DL
8 primitive portal vein thrombosis KG + DL
9 peliosis hepatis KG + DL
10 hepatic infarction KG + DL
11 hereditary North American Indian childhood cirrhosis KG + DL
12 sclerosing cholangitis KG + DL
13 rheumatoid arthritis KG + DL
14 inborn disorder of bilirubin metabolism KG + DL
15 congenital hypotrichosis milia KG + DL
16 diffuse alopecia areata KG + DL
17 syndrome with combined immunodeficiency KG + DL
18 osteoarthritis susceptibility KG + DL
19 hypotrichosis simplex of the scalp KG + DL
20 familial intrahepatic cholestasis KG + DL
21 hepatic veno-occlusive disease KG + DL
22 bilirubin metabolism disease KG + DL
23 bronchitis KG + DL
24 cholestasis KG + DL
25 microvillus inclusion disease KG + DL
26 gout KG + DL
27 drug-induced liver injury KG + DL
28 Smouldering systemic mastocytosis KG + DL
29 osteoarthritis KG + DL
30 systemic mastocytosis KG + DL
31 dermatitis KG + DL
32 mitochondrial DNA depletion syndrome, hepatocerebral form KG + DL
33 nevus of Ito KG + DL
34 hydroa vacciniforme, familial KG + DL
35 lymphoadenopathic mastocytosis with eosinophilia KG + DL
36 thrombotic thrombocytopenic purpura KG + DL
37 liver angiosarcoma KG + DL
38 myositis KG + DL
39 acrodermatitis chronica atrophicans KG + DL
40 malignant peritoneal mesothelioma KG + DL
41 secondary interstitial lung disease specific to childhood associated with a connective tissue disease KG + DL
42 neonatal dermatomyositis KG + DL
43 adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency KG + DL
44 selective IgG subclass deficiency KG + DL
45 alopecia KG + DL
46 oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies KG + DL
47 oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies KG + DL
48 immune-mediated necrotizing myopathy KG + DL
49 colobomatous microphthalmia-rhizomelic dysplasia syndrome KG + DL
50 Ledderhose disease KG + DL

(Showing top 50 of 74 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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