Sulpiride

DrugBank ID: DB00391

Summary

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

Predictions

Indication	Score	Source
schizophrenia	0.9996	DL
retinal dystrophy with or without extraocular anomalies	0.9995	DL
hydranencephaly (disease)	0.9993	DL
polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis	0.9992	DL
Charcot-Marie-Tooth disease, demyelinating, type 1G	0.9992	DL
myopia X-linked	0.9992	DL
congenital disorder of glycosylation with defective fucosylation	0.9992	DL
myopia 26, X-linked, female-limited	0.9992	DL
syndromic myopia	0.9991	DL
atypical glycine encephalopathy	0.9990	DL
distal 17p13.3 microdeletion syndrome	0.9224	DL
hydrops-lactic acidosis-sideroblastic anemia-multisystemic failure syndrome	0.8900	DL
manic bipolar affective disorder	0.8515	DL
schizophreniform disorder	0.7399	DL
bipolar disorder	0.6724	DL
early-onset schizophrenia	0.6452	DL
treatment-refractory schizophrenia	0.6252	DL
psychotic disorder	0.5902	DL
fetal growth restriction	0.5890	DL
atrial flutter (disease)	0.5771	DL
REM sleep behavior disorder	0.5763	DL
major affective disorder	0.5758	DL
paralysis agitans, juvenile, of Hunt	0.5756	DL
cholangiocarcinoma, susceptibility to	0.5716	DL
mitral valve prolapse, myxomatous	0.5513	DL
epidural abscess	0.5504	DL
conduct disorder	0.5488	DL
GCGR-related hyperglucagonemia	0.5454	DL
syncope, familial vasovagal	0.5446	DL
monoclonal gammopathy of uncertain significance	0.5405	DL
nonarteritic anterior ischemic optic neuropathy, susceptibility to	0.5378	DL
psychosexual disorder	0.5354	DL
lethal infantile mitochondrial myopathy	0.5345	DL
hypospadias 3, autosomal	0.5316	DL
sella turcica, bridged	0.5316	DL
triphalangeal thumb, Nonopposable	0.5316	DL
intraductal tubulopapillary neoplasm of pancreas	0.5314	DL
celiac artery stenosis from compression by median arcuate ligament of diaphragm	0.5308	DL
ergotism	0.5303	DL
placenta disease	0.5285	DL
paramedian facial cleft	0.5255	DL
metachromatic leukodystrophy, adult-onset, with normal arylsulfatase A	0.5222	DL
hypermobility syndrome	0.5218	DL
tremor, hereditary essential, and idiopathic normal pressure hydrocephalus	0.5216	DL
pancreas, dorsal, agenesis of	0.5216	DL
placenta accreta	0.5208	DL
perineural cyst	0.5207	DL
familial chronic myelocytic leukemia-like syndrome	0.5205	DL
psoriatic arthritis, susceptibility to, 1	0.5197	DL
hypercarotenemia and vitamin A deficiency, autosomal recessive	0.5186	DL

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