Iron sucrose

DrugBank ID: DB09146

Summary

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

Predictions

Indication	Score	Source
hyperphosphatemia (disease)	0.9963	KG+DL
primary hyperoxaluria	0.9882	DL
pancreatitis	0.9785	DL
tumoral calcinosis, hyperphosphatemic, familial	0.9784	DL
familial apolipoprotein C-II deficiency	0.9758	DL
esophageal varices with bleeding	0.9692	DL
esophageal varices without bleeding	0.9692	DL
familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome	0.9690	DL
hyperparathyroidism	0.9618	DL
hyperlipidemia	0.9606	DL
immune-mediated necrotizing myopathy	0.9603	DL
mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies	0.9589	DL
antisynthetase syndrome	0.9583	DL
hyperlipidemia due to hepatic triglyceride lipase deficiency	0.9564	DL
hypertriglyceridemia, familial	0.9550	DL
hyperlipoproteinemia	0.9528	DL
idiopathic eosinophilic myositis	0.9528	DL
inflammatory myopathy with abundant macrophages	0.9528	DL
focal myositis	0.9524	DL
lipase deficiency, combined	0.9520	DL
major hypertriglyceridemia	0.9480	DL
varicose disease	0.9469	DL
early-onset familial noncirrhotic portal hypertension	0.9376	DL
hepatoportal sclerosis	0.9376	DL
hepatopulmonary syndrome	0.9376	DL
idiopathic copper-associated cirrhosis	0.9376	DL
primitive portal vein thrombosis	0.9376	DL
hepatic porphyria	0.9180	DL
alcoholic cardiomyopathy	0.9172	DL
hereditary hypercarotenemia and vitamin A deficiency	0.9142	DL
nephrolithiasis susceptibility caused by SLC26A1	0.9023	DL
familial hypobetalipoproteinemia	0.8869	DL
cholesterol-ester transfer protein deficiency	0.8846	DL
progressive external ophthalmoplegia	0.8843	DL
MELAS syndrome	0.8823	DL
hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency	0.8817	DL
pernicious anemia	0.8798	DL
familial lipoprotein lipase deficiency	0.8747	DL
familial chylomicronemia syndrome	0.8650	DL
hyperalphalipoproteinemia	0.8613	DL
recurrent infections associated with rare immunoglobulin isotypes deficiency	0.8613	DL
exocrine pancreatic insufficiency	0.8571	DL
osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome	0.8558	DL
selective IgG immunodeficiency	0.8548	DL
maternally-inherited mitochondrial myopathy	0.8466	DL
disorder of vitamin and non-protein cofactor absorption and transport	0.8456	DL
primary optic atrophy	0.8389	DL
maternally-inherited mitochondrial dystonia	0.8316	DL
iron deficiency anemia	0.8282	DL
familial isolated deficiency of vitamin E	0.8252	DL

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