Polidocanol

DrugBank ID: DB06811

Summary

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

Predictions

Indication	Score	Source
esophageal varices with bleeding	0.9995	DL
esophageal varices without bleeding	0.9995	DL
varicose disease	0.9991	KG+DL
Immunoerythromyeloid hypoplasia	0.9978	DL
pigmented paravenous retinochoroidal atrophy	0.9973	DL
progressive bifocal chorioretinal atrophy	0.9969	DL
X-linked retinal dysplasia	0.9968	DL
monosomy X	0.9967	DL
cone dystrophy	0.9966	DL
oligocone trichromacy	0.9965	DL
retinoschisis of fovea	0.9965	DL
MRCS syndrome	0.9965	DL
helicoid peripapillary chorioretinal degeneration	0.9964	DL
ectopia lentis-chorioretinal dystrophy-myopia syndrome	0.9963	DL
lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome	0.9963	DL
reticular dysgenesis	0.9962	DL
familial benign flecked retina	0.9962	DL
mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies	0.9962	DL
retinal dystrophy in systemic or cerebroretinal lipidoses	0.9961	DL
familial flecked retinopathy	0.9961	DL
Aland island eye disease	0.9960	DL
T-B+ severe combined immunodeficiency due to gamma chain deficiency	0.9958	DL
non-severe combined immunodeficiency	0.9957	DL
genetic macular dystrophy	0.9957	DL
retinal drusen	0.9957	DL
retinoschisis	0.9956	DL
Blessig's cysts	0.9955	DL
pseudoretinitis pigmentosa	0.9955	DL
senile reticular retinal degeneration	0.9955	DL
exocrine pancreatic insufficiency	0.9953	DL
macular degeneration	0.9951	DL
cystoid macular retinal degeneration	0.9946	DL
hole retinal cyst	0.9946	DL
preretinal fibrosis	0.9946	DL
toxic maculopathy	0.9946	DL
T-B+ severe combined immunodeficiency due to CD45 deficiency	0.9944	DL
combined immunodeficiency, X-linked	0.9937	DL
adenosine deaminase deficiency	0.9936	DL
familial apolipoprotein C-II deficiency	0.9936	DL
severe combined immunodeficiency due to LCK deficiency	0.9930	DL
syndrome with combined immunodeficiency	0.9902	DL
severe combined immunodeficiency (disease)	0.9896	DL
Steel syndrome	0.9892	DL
late-onset retinal degeneration	0.9885	DL
Omenn syndrome	0.9871	DL
severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive	0.9867	DL
adenosine monophosphate deaminase deficiency	0.9857	DL
hypophosphatasia	0.9852	DL
purine nucleoside phosphorylase deficiency	0.9848	DL
hepatic infarction	0.9840	DL

External Links

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