Mycophenolic acid

DrugBank ID: DB01024

Summary

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

Predictions

Indication	Score	Source
hemoglobinopathy	0.9960	DL
migraine disorder	0.9957	DL
migraine with brainstem aura	0.9947	DL
partial deletion of the short arm of chromosome 16	0.9935	DL
beta-thalassemia with other manifestations	0.9933	DL
pyropoikilocytosis, hereditary	0.9928	DL
hemolytic anemia due to glucophosphate isomerase deficiency	0.9925	DL
pyruvate kinase deficiency of red cells	0.9919	DL
rheumatoid arthritis	0.9918	DL
antithrombin deficiency type 2	0.9916	DL
heparin cofactor 2 deficiency	0.9912	DL
myocardial infarction	0.9912	DL
tendinitis	0.9908	DL
factor 5 excess with spontaneous thrombosis	0.9907	DL
idiopathic granulomatous myositis	0.9906	DL
myositis fibrosa	0.9906	DL
fibromyalgia	0.9901	DL
thrombophilia	0.9884	DL
inclusion body myositis	0.9873	DL
homozygous familial hypercholesterolemia	0.9872	DL
myocardial infarction (disease)	0.9872	DL
coronary thrombosis	0.9863	DL
septal myocardial infarction	0.9856	DL
autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome	0.9856	DL
gout	0.9855	DL
brain small vessel disease 1 with or without ocular anomalies	0.9852	DL
posteroinferior myocardial infarction	0.9851	DL
posterolateral myocardial infarction	0.9851	DL
migraine with or without aura, susceptibility to	0.9842	DL
colobomatous microphthalmia-rhizomelic dysplasia syndrome	0.9842	DL
coronary stenosis	0.9833	DL
diabetic nephropathy	0.9833	DL
brachydactyly-syndactyly syndrome	0.9832	DL
atrophoderma vermiculata	0.9827	DL
ulerythema ophryogenesis	0.9807	DL
obsolete familial combined hyperlipidemia	0.9766	DL
congenital coronary artery anomaly	0.9759	DL
Prinzmetal angina	0.9740	DL
paratenonitis	0.9740	DL
calcific tendinitis	0.9736	DL
HIV infectious disease	0.9720	DL
myositis	0.9683	DL
myelodysplastic syndrome	0.9643	DL
bone Paget disease	0.9642	DL
feline acquired immunodeficiency syndrome	0.9621	DL
simian immunodeficiency virus infection	0.9621	DL
neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter	0.9615	DL
exostosis	0.9614	DL
refractory cytopenia of childhood	0.9591	DL
partial deletion of the long arm of chromosome 5	0.9587	DL

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