Rasburicase

DrugBank ID: DB00049

Summary

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

Predictions

Indication	Score	Source
obsolete hyperuricemia (disease)	0.9999	KG+DL
hypouricemia, renal	0.9999	DL
hypoxanthine guanine phosphoribosyltransferase partial deficiency	0.9997	DL
hepatic porphyria	0.9997	DL
early-onset familial noncirrhotic portal hypertension	0.9997	DL
hepatoportal sclerosis	0.9997	DL
hepatopulmonary syndrome	0.9997	DL
idiopathic copper-associated cirrhosis	0.9997	DL
primitive portal vein thrombosis	0.9997	DL
renal tubular acidosis	0.9985	DL
disorder of phenylalanine metabolism	0.9983	DL
disorder of tyrosine metabolism	0.9969	DL
teratogenic Pierre Robin syndrome	0.9968	DL
glycogen storage disease due to hepatic glycogen synthase deficiency	0.9958	DL
Lesch-Nyhan syndrome	0.9958	DL
tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria	0.9947	DL
G6PD deficiency	0.9900	DL
inborn disorder of gamma-aminobutyric acid metabolism	0.9773	DL
inborn disorder of ornithine metabolism	0.9768	DL
inborn disorder of amino acid and other organic acid metabolism	0.9766	DL
inborn disorder of histidine metabolism	0.9766	DL
inborn disorder of serine family metabolism	0.9765	DL
cerebral creatine deficiency syndrome	0.9762	DL
genetic otorhinolaryngological malformation	0.9750	DL
inborn disorder of aspartate family metabolism	0.9747	DL
neonatal epileptic encephalopathy due to glutaminase deficiency	0.9745	DL
inborn disorder of tryptophan metabolism	0.9742	DL
2-methylacetoacetyl CoA thiolase deficiency	0.9733	DL
idiopathic bilateral vestibulopathy	0.9725	DL
semicircular canal dehiscence syndrome	0.9725	DL
3-hydroxyisobutyryl-CoA hydrolase deficiency	0.9711	DL
inborn disorder of phenylalanin or tyrosine metabolism	0.9678	DL
familial nasal acilia	0.9654	DL
tetrahydrobiopterin metabolic process disease	0.9654	DL
juvenile nasopharyngeal angiofibroma (disease)	0.9649	DL
silent sinus syndrome	0.9645	DL
3-hydroxyisobutyric aciduria	0.9636	DL
maternal hyperthermia induced birth defects	0.9592	DL
mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies	0.9591	DL
cleft lip/palate-intestinal malrotation-cardiopathy syndrome	0.9584	DL
fetal trimethadione syndrome	0.9578	DL
craniorhiny	0.9565	DL
Bencze syndrome	0.9561	DL
phenobarbital embryopathy	0.9560	DL
fetal minoxidil syndrome	0.9556	DL
diabetic embryopathy	0.9555	DL
tibial aplasia-ectrodactyly syndrome	0.9555	DL
mandibulofacial dysostosis-macroblepharon-macrostomia syndrome	0.9538	DL
branchial cleft anomaly	0.9531	DL
galactokinase deficiency	0.9503	DL

External Links

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