Sulfinpyrazone

Basic Information

Item Value
DrugBank ID DB01138
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 64

Predicted Indications (TxGNN)

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

# Indication Source
1 hypouricemia, renal KG + DL
2 hypoxanthine guanine phosphoribosyltransferase partial deficiency KG + DL
3 Lesch-Nyhan syndrome KG + DL
4 neonatal epileptic encephalopathy due to glutaminase deficiency KG + DL
5 genetic otorhinolaryngological malformation KG + DL
6 disorder of phenylalanine metabolism KG + DL
7 semicircular canal dehiscence syndrome KG + DL
8 idiopathic bilateral vestibulopathy KG + DL
9 familial nasal acilia KG + DL
10 juvenile nasopharyngeal angiofibroma (disease) KG + DL
11 silent sinus syndrome KG + DL
12 inborn disorder of phenylalanin or tyrosine metabolism KG + DL
13 maternal hyperthermia induced birth defects KG + DL
14 tetrahydrobiopterin metabolic process disease KG + DL
15 fetal trimethadione syndrome KG + DL
16 cleft lip/palate-intestinal malrotation-cardiopathy syndrome KG + DL
17 phenobarbital embryopathy KG + DL
18 fetal minoxidil syndrome KG + DL
19 Bencze syndrome KG + DL
20 velo-facial-skeletal syndrome KG + DL
21 diabetic embryopathy KG + DL
22 mandibulofacial dysostosis-macroblepharon-macrostomia syndrome KG + DL
23 branchial cleft anomaly KG + DL
24 craniorhiny KG + DL
25 propylthiouracil embryofetopathy KG + DL
26 indomethacin embryofetopathy KG + DL
27 disorder of tyrosine metabolism KG + DL
28 teratogenic Pierre Robin syndrome KG + DL
29 cocaine embryofetopathy KG + DL
30 phenylketonuria KG + DL
31 tibial aplasia-ectrodactyly syndrome KG + DL
32 aminopterin/methotrexate embryofetopathy KG + DL
33 toluene embryopathy KG + DL
34 tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria KG + DL
35 hepatopulmonary syndrome KG + DL
36 primitive portal vein thrombosis KG + DL
37 idiopathic copper-associated cirrhosis KG + DL
38 early-onset familial noncirrhotic portal hypertension KG + DL
39 hepatoportal sclerosis KG + DL
40 hepatic porphyria KG + DL
41 cerebral creatine deficiency syndrome KG + DL
42 3-hydroxyisobutyryl-CoA hydrolase deficiency KG + DL
43 cholelithiasis KG + DL
44 glycogen storage disease due to hepatic glycogen synthase deficiency KG + DL
45 inborn disorder of amino acid and other organic acid metabolism KG + DL
46 inborn disorder of ornithine metabolism KG + DL
47 inborn disorder of gamma-aminobutyric acid metabolism KG + DL
48 inborn disorder of histidine metabolism KG + DL
49 inborn disorder of serine family metabolism KG + DL
50 inborn disorder of aspartate family metabolism KG + DL

(Showing top 50 of 64 predictions)

Disclaimer

These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.


← Back to Drug Search


Copyright © 2026 藥提醒科技有限公司 (yao.care). This report is for research purposes only and does not constitute medical advice.

This site uses Just the Docs, a documentation theme for Jekyll.