Vigabatrin

DrugBank ID: DB01080

Summary

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

Predictions

Indication	Score	Source
West syndrome	0.9909	KG+DL
intellectual disability, X-linked, with or without seizures, arx-related	0.9866	DL
episodic kinesigenic dyskinesia	0.9726	DL
developmental and epileptic encephalopathy	0.9718	KG+DL
1q44 microdeletion syndrome	0.9671	DL
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation	0.9656	DL
DK1-CDG	0.9647	DL
microtriplication 11q24.1	0.9631	DL
CCDC115-CDG	0.9627	DL
neonatal period electroclinical syndrome	0.9625	DL
genetic lethal multiple congenital anomalies/dysmorphic syndrome	0.9622	DL
COG2-CDG	0.9620	DL
colobomatous microphthalmia - obesity - hypogenitalism - intellectual disability syndrome	0.9609	DL
X-linked dominant intellectual disability-epilepsy syndrome	0.9602	DL
male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome	0.9601	DL
Jawad syndrome	0.9600	DL
muscular hypertrophy-hepatomegaly-polyhydramnios syndrome	0.9599	DL
infancy electroclinical syndrome	0.9598	DL
neonatal epileptic encephalopathy	0.9591	DL
craniofaciofrontodigital syndrome	0.9591	DL
blepharophimosis - intellectual disability syndrome, MKB type	0.9590	DL
pancreatic agenesis-holoprosencephaly syndrome	0.9587	DL
ALG12-CDG	0.9585	DL
microcephaly-intellectual disability-phalangeal and neurological anomalies syndrome	0.9585	DL
defect in V-ATPase	0.9584	DL
myoclonic epilepsy, Hartung type	0.9576	DL
Crane-Heise syndrome	0.9575	DL
faciocardiorenal syndrome	0.9573	DL
X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome	0.9569	DL
XYLT1-CDG	0.9567	DL
arachnodactyly-abnormal ossification-intellectual disability syndrome	0.9566	DL
telecanthus-hypertelorism-strabismus-pes cavus syndrome	0.9564	DL
malignant migrating partial seizures of infancy	0.9563	DL
macrocephaly-short stature-paraplegia syndrome	0.9561	DL
microcephaly-short stature-intellectual disability-facial dysmorphism syndrome	0.9559	DL
trigeminal nerve neoplasm	0.9532	DL
pseudoachondroplasia	0.9478	DL
epilepsy of infancy with migrating focal seizures	0.9353	DL
myoclonic encephalopathy in non-progressive disorder	0.9353	DL
self-limited familial and non-familial neonatal/infantile seizures	0.9353	DL
adolescent/adult onset autosomal dominant epilepsy with auditory features	0.9328	DL
restless legs syndrome	0.9242	DL
osteoarthritis	0.9209	DL
myoclonic-atonic epilepsy	0.9066	DL
guanidinoacetate methyltransferase deficiency	0.9058	DL
epilepsy with generalized tonic-clonic seizures	0.8948	DL
beta-ketothiolase deficiency	0.8934	DL
neonatal/infantile epilepsy syndrome	0.8902	DL
monosomy X	0.8900	DL
reading seizures	0.8836	DL

External Links

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