Allopurinol

DrugBank ID: DB00437

Summary

Metric	Value
Total Predictions	50
KG+DL (Dual Validated)	3
DL Only	47
KG Only	0

Predictions

Indication	Score	Source
hepatic porphyria	0.9995	DL
early-onset familial noncirrhotic portal hypertension	0.9994	DL
hepatoportal sclerosis	0.9994	DL
hepatopulmonary syndrome	0.9994	DL
idiopathic copper-associated cirrhosis	0.9994	DL
primitive portal vein thrombosis	0.9994	DL
disorder of phenylalanine metabolism	0.9989	DL
gout	0.9988	KG+DL
immune-mediated necrotizing myopathy	0.9986	DL
antisynthetase syndrome	0.9985	DL
idiopathic eosinophilic myositis	0.9985	DL
inflammatory myopathy with abundant macrophages	0.9985	DL
focal myositis	0.9985	DL
glycogen storage disease due to hepatic glycogen synthase deficiency	0.9983	DL
G6PD deficiency	0.9983	DL
disorder of tyrosine metabolism	0.9981	DL
teratogenic Pierre Robin syndrome	0.9978	DL
selective IgG immunodeficiency	0.9978	DL
Lesch-Nyhan syndrome	0.9977	DL
tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria	0.9976	DL
obsolete hyperuricemia (disease)	0.9976	KG+DL
galactosemia	0.9974	DL
hypouricemia, renal	0.9973	DL
sclerosing cholangitis	0.9969	DL
granulomatous disease, chronic, X-linked	0.9966	DL
anemia, nonspherocytic hemolytic, due to G6PD deficiency	0.9961	DL
selective IgG subclass deficiency	0.9961	DL
dermatomyositis	0.9958	DL
mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies	0.9958	DL
genetic otorhinolaryngological malformation	0.9956	DL
cystinosis	0.9955	DL
acute urate nephropathy	0.9949	KG+DL
recurrent infections associated with rare immunoglobulin isotypes deficiency	0.9947	DL
neonatal epileptic encephalopathy due to glutaminase deficiency	0.9947	DL
galactokinase deficiency	0.9947	DL
idiopathic bilateral vestibulopathy	0.9944	DL
semicircular canal dehiscence syndrome	0.9944	DL
juvenile nasopharyngeal angiofibroma (disease)	0.9943	DL
familial nasal acilia	0.9942	DL
silent sinus syndrome	0.9942	DL
inborn disorder of histidine metabolism	0.9941	DL
tetrahydrobiopterin metabolic process disease	0.9940	DL
cerebral creatine deficiency syndrome	0.9940	DL
inborn disorder of phenylalanin or tyrosine metabolism	0.9939	DL
hypoxanthine guanine phosphoribosyltransferase partial deficiency	0.9939	DL
3-hydroxyisobutyryl-CoA hydrolase deficiency	0.9938	DL
phenylketonuria	0.9937	DL
paraplegia	0.9936	DL
inborn disorder of ornithine metabolism	0.9936	DL
renal tubular acidosis	0.9935	DL

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