Probenecid

DrugBank ID: DB01032

Summary

Metric	Value
Total Predictions	50
KG+DL (Dual Validated)	1
DL Only	49
KG Only	0

Predictions

Indication	Score	Source
obsolete hyperuricemia (disease)	0.9984	KG+DL
hypouricemia, renal	0.9973	DL
Lesch-Nyhan syndrome	0.9939	DL
hypoxanthine guanine phosphoribosyltransferase partial deficiency	0.9937	DL
cholelithiasis	0.9774	DL
early-onset familial noncirrhotic portal hypertension	0.9659	DL
hepatoportal sclerosis	0.9659	DL
hepatopulmonary syndrome	0.9659	DL
idiopathic copper-associated cirrhosis	0.9659	DL
primitive portal vein thrombosis	0.9659	DL
disorder of phenylalanine metabolism	0.9658	DL
hepatic porphyria	0.9643	DL
genetic otorhinolaryngological malformation	0.9619	DL
neonatal epileptic encephalopathy due to glutaminase deficiency	0.9592	DL
idiopathic bilateral vestibulopathy	0.9569	DL
semicircular canal dehiscence syndrome	0.9569	DL
juvenile nasopharyngeal angiofibroma (disease)	0.9556	DL
familial nasal acilia	0.9552	DL
gout	0.9547	DL
silent sinus syndrome	0.9534	DL
inborn disorder of phenylalanin or tyrosine metabolism	0.9513	DL
tetrahydrobiopterin metabolic process disease	0.9488	DL
maternal hyperthermia induced birth defects	0.9481	DL
disorder of tyrosine metabolism	0.9465	DL
cleft lip/palate-intestinal malrotation-cardiopathy syndrome	0.9458	DL
craniorhiny	0.9454	DL
fetal minoxidil syndrome	0.9452	DL
phenobarbital embryopathy	0.9445	DL
brain small vessel disease 1 with or without ocular anomalies	0.9442	DL
fetal trimethadione syndrome	0.9442	DL
Bencze syndrome	0.9436	DL
branchial cleft anomaly	0.9420	DL
velo-facial-skeletal syndrome	0.9418	DL
mandibulofacial dysostosis-macroblepharon-macrostomia syndrome	0.9415	DL
phenylketonuria	0.9400	DL
diabetic embryopathy	0.9400	DL
autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome	0.9392	DL
teratogenic Pierre Robin syndrome	0.9392	DL
hereditary renal hypouricemia	0.9292	DL
propylthiouracil embryofetopathy	0.9288	DL
indomethacin embryofetopathy	0.9272	DL
glycogen storage disease due to hepatic glycogen synthase deficiency	0.9222	DL
tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria	0.9215	DL
cocaine embryofetopathy	0.9201	DL
tibial aplasia-ectrodactyly syndrome	0.9147	DL
aminopterin/methotrexate embryofetopathy	0.9111	DL
toluene embryopathy	0.9104	DL
selective IgG subclass deficiency	0.8900	DL
obsolete familial combined hyperlipidemia	0.8890	DL
diabetic nephropathy	0.8833	DL

External Links

Disclaimer
Predictions are for research purposes only and do not constitute medical advice.