Orlistat

DrugBank ID: DB01083

Summary

Metric	Value
Total Predictions	50
KG+DL (Dual Validated)	2
DL Only	48
KG Only	0

Predictions

Indication	Score	Source
obesity disorder	0.9946	KG+DL
hypervitaminosis	0.9942	DL
proximal 16p11.2 microdeletion syndrome	0.9887	DL
obsolete hypertelorism (disease)	0.9775	DL
frontorhiny	0.9664	DL
hypoalphalipoproteinemia	0.9647	DL
monogenic obesity	0.9445	KG+DL
obsolete susceptibility to ischemic stroke	0.9200	DL
ABri amyloidosis	0.8567	DL
fatty liver disease	0.8526	DL
homozygous familial hypercholesterolemia	0.7984	DL
amenorrhea (disease)	0.7789	DL
non-alcoholic steatohepatitis	0.7714	DL
hypercarotenemia and vitamin A deficiency, autosomal recessive	0.7103	DL
lethal polymalformative syndrome, Boissel type	0.6851	DL
duodenogastric reflux	0.6839	DL
pentosuria	0.6826	DL
duodenal obstruction	0.6811	DL
fibrosis of extraocular muscles, congenital, with synergistic divergence	0.6692	DL
mitral valve prolapse, myxomatous	0.6679	DL
hypospadias 3, autosomal	0.6645	DL
sella turcica, bridged	0.6645	DL
triphalangeal thumb, Nonopposable	0.6645	DL
hyperparathyroidism, primary, caused by water clear cell hyperplasia	0.6491	DL
cholangiocarcinoma, susceptibility to	0.6445	DL
pancreas, dorsal, agenesis of	0.6396	DL
lymphopenic hypergammaglobulinemia, antibody deficiency, autoimmune hemolytic anemia, and glomerulonephritis	0.6334	DL
diarrhea 11, malabsorptive, congenital	0.6258	DL
corneal degeneration, band-shaped spheroid	0.6235	DL
glaucoma with elevated episcleral venous pressure	0.6235	DL
hyperemesis gravidarum (disease)	0.6226	DL
hemangiomas of small intestine	0.6216	DL
duodenal ulcer (disease)	0.6206	DL
retinal aplasia	0.6179	DL
familial chronic myelocytic leukemia-like syndrome	0.6166	DL
sclerocornea, autosomal dominant	0.6161	DL
abdominal obesity-metabolic syndrome quantitative trait locus 2	0.6149	DL
prostate cancer, hereditary, X-linked	0.6139	DL
lattice degeneration of retina leading to retinal detachment	0.6108	DL
Tristichiasis	0.6092	DL
melanoma, malignant familial intraocular	0.6085	DL
ear folding	0.6080	DL
ear malformation	0.6080	DL
macular dystrophy, fenestrated sheen type	0.6070	DL
hereditary persistence of alpha-fetoprotein	0.6060	DL
ocular cicatricial pemphigoid	0.6057	DL
cornea plana 1, autosomal dominant	0.6042	DL
musk, inability to smell	0.6042	DL
polyhydramnios, chronic idiopathic	0.6042	DL
factor VII and Factor VIII, combined deficiency of	0.6039	DL

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