Febuxostat

DrugBank ID: DB04854

Summary

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

Predictions

Indication	Score	Source
obsolete hyperuricemia (disease)	1.0000	KG+DL
hypouricemia, renal	0.9999	DL
hypoxanthine guanine phosphoribosyltransferase partial deficiency	0.9998	DL
Lesch-Nyhan syndrome	0.9968	DL
early-onset familial noncirrhotic portal hypertension	0.9189	DL
hepatoportal sclerosis	0.9189	DL
hepatopulmonary syndrome	0.9189	DL
idiopathic copper-associated cirrhosis	0.9189	DL
primitive portal vein thrombosis	0.9189	DL
hepatic porphyria	0.9121	DL
disorder of phenylalanine metabolism	0.7904	DL
disorder of tyrosine metabolism	0.7722	DL
teratogenic Pierre Robin syndrome	0.7716	DL
cholelithiasis	0.7048	DL
Tay-Sachs disease, b variant	0.6526	DL
tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria	0.6400	DL
Wiskott-Aldrich syndrome 2	0.6335	DL
Tay-Sachs disease, B1 variant	0.6294	DL
anuria	0.6159	DL
alacrima, achalasia, and intellectual disability syndrome	0.6084	DL
glycogen storage disease due to hepatic glycogen synthase deficiency	0.5994	DL
genetic otorhinolaryngological malformation	0.5993	DL
Ramon syndrome	0.5978	DL
homozygous familial hypercholesterolemia	0.5957	DL
obsolete hypertension, diastolic, resistance to	0.5938	DL
hypermobility syndrome	0.5859	DL
obsolete left bundle branch block	0.5838	DL
transient infantile hypertriglyceridemia and hepatosteatosis	0.5825	DL
neonatal epileptic encephalopathy due to glutaminase deficiency	0.5786	DL
obsolete pathologic fracture	0.5782	DL
myopathy due to calsequestrin and SERCA1 protein overload	0.5768	DL
methylcobalamin deficiency type cblDv1	0.5716	DL
idiopathic bilateral vestibulopathy	0.5647	DL
semicircular canal dehiscence syndrome	0.5647	DL
childhood encephalopathy due to thiamine pyrophosphokinase deficiency	0.5637	DL
ocular tuberculosis	0.5635	DL
erythrocyte AMP deaminase deficiency	0.5629	DL
toxic labyrinthitis	0.5629	DL
guttate psoriasis	0.5627	DL
isolated tracheo-esophageal fistula	0.5619	DL
susceptibility to mononeuropathy of the median nerve, mild	0.5593	DL
sunburn	0.5587	DL
muscular disease	0.5568	DL
polydipsia	0.5563	DL
myopathy, proximal, and ophthalmoplegia	0.5549	DL
phosphohydroxylysinuria	0.5520	DL
cystic hygroma	0.5517	DL
maternal riboflavin deficiency	0.5496	DL
glomerulocystic kidney disease with hyperuricemia and isosthenuria	0.5452	DL
silent sinus syndrome	0.5446	DL

External Links

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