Betahistine

DrugBank ID: DB06698

Summary

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

Predictions

Indication	Score	Source
restless legs syndrome	0.9851	DL
Meniere disease	0.9848	DL
endolymphatic hydrops	0.9842	DL
active cochlear Meniere disease	0.9834	DL
active cochleovestibular Meniere disease	0.9834	DL
active vestibular Meniere disease	0.9834	DL
otosclerosis	0.9819	DL
peripheral vertigo	0.9807	DL
age-related hearing impairment	0.9793	DL
vertigo, benign recurrent, 2	0.9778	DL
autosomal recessive hyperinsulinism due to Kir6.2 deficiency	0.9777	DL
hyperinsulinemic hypoglycemia, familial	0.9732	DL
variably protease-sensitive prionopathy	0.9727	DL
West syndrome	0.9727	DL
autosomal dominant hyperinsulinism due to Kir6.2 deficiency	0.9699	DL
autosomal recessive hyperinsulinism due to SUR1 deficiency	0.9675	DL
diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency	0.9675	DL
intellectual disability, X-linked, with or without seizures, arx-related	0.9667	DL
obsolete neurogenic bladder (disease)	0.9660	DL
cauda equina syndrome	0.9649	DL
episodic kinesigenic dyskinesia	0.9625	DL
multiple system atrophy	0.9605	DL
congenital hypotrichosis milia	0.9573	DL
hypotrichosis simplex of the scalp	0.9569	DL
congenital isolated hyperinsulinism	0.9554	DL
diffuse alopecia areata	0.9533	DL
developmental and epileptic encephalopathy	0.9529	DL
myoclonic epilepsy, Hartung type	0.9512	DL
genetic lethal multiple congenital anomalies/dysmorphic syndrome	0.9511	DL
neonatal period electroclinical syndrome	0.9507	DL
infancy electroclinical syndrome	0.9501	DL
colobomatous microphthalmia - obesity - hypogenitalism - intellectual disability syndrome	0.9473	DL
X-linked dominant intellectual disability-epilepsy syndrome	0.9462	DL
Jawad syndrome	0.9461	DL
CCDC115-CDG	0.9456	DL
defect in V-ATPase	0.9453	DL
1q44 microdeletion syndrome	0.9450	DL
muscular hypertrophy-hepatomegaly-polyhydramnios syndrome	0.9447	DL
COG2-CDG	0.9444	DL
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation	0.9440	DL
pancreatic agenesis-holoprosencephaly syndrome	0.9436	DL
neonatal epileptic encephalopathy	0.9435	DL
telecanthus-hypertelorism-strabismus-pes cavus syndrome	0.9431	DL
macrocephaly-short stature-paraplegia syndrome	0.9428	DL
microcephaly-short stature-intellectual disability-facial dysmorphism syndrome	0.9425	DL
craniofaciofrontodigital syndrome	0.9425	DL
male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome	0.9419	DL
blepharophimosis - intellectual disability syndrome, MKB type	0.9417	DL
osteoarthritis	0.9416	DL
Crane-Heise syndrome	0.9412	DL

External Links

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