Benzbromarone

DrugBank ID: DB12319

Summary

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

Predictions

Indication	Score	Source
obsolete hyperuricemia (disease)	0.9921	KG+DL
hypouricemia, renal	0.9907	DL
Lesch-Nyhan syndrome	0.9838	DL
hypoxanthine guanine phosphoribosyltransferase partial deficiency	0.9815	DL
homozygous familial hypercholesterolemia	0.9768	DL
glycogen storage disease	0.9669	DL
glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form	0.9649	DL
glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form	0.9649	DL
tricarboxylic acid cycle disorder	0.9639	DL
early-onset familial noncirrhotic portal hypertension	0.9627	DL
hepatoportal sclerosis	0.9627	DL
hepatopulmonary syndrome	0.9627	DL
idiopathic copper-associated cirrhosis	0.9627	DL
primitive portal vein thrombosis	0.9627	DL
hepatic porphyria	0.9611	DL
adult polyglucosan body disease	0.9607	DL
disease of transporter activity	0.9603	DL
glycogen storage disease due to hepatic glycogen synthase deficiency	0.9599	DL
pyruvate metabolism disorder	0.9558	DL
hereditary renal hypouricemia	0.9538	DL
inborn disorder of fatty acid oxidation and ketone body metabolism	0.9525	DL
familial hyperlipidemia	0.9489	DL
glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form	0.9481	DL
glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form	0.9481	DL
glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form	0.9481	DL
glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form	0.9481	DL
glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form	0.9481	DL
inborn disorder of bilirubin metabolism	0.9292	DL
benign recurrent intrahepatic cholestasis	0.9260	DL
gout	0.9189	DL
hereditary North American Indian childhood cirrhosis	0.9175	DL
bilirubin metabolism disease	0.9084	DL
familial intrahepatic cholestasis	0.9010	DL
porphyria due to ALA dehydratase deficiency	0.9002	DL
nevus of Ito	0.8811	DL
microvillus inclusion disease	0.8804	DL
nephrogenic syndrome of inappropriate antidiuresis	0.8743	DL
drug-induced liver injury	0.8686	DL
psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome	0.8609	DL
familial hypobetalipoproteinemia	0.8588	DL
galactosemia	0.8545	DL
hyperbiliverdinemia	0.8539	DL
hypoalphalipoproteinemia	0.8528	DL
acute intermittent porphyria	0.8512	DL
mitochondrial DNA depletion syndrome, hepatocerebrorenal form	0.8500	DL
renal tubule disease	0.8466	DL
Senior-Boichis syndrome	0.8446	DL
familial apolipoprotein C-II deficiency	0.8445	DL
cranioectodermal dysplasia	0.8443	DL
Navajo neurohepatopathy	0.8415	DL

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