Riluzole

DrugBank ID: DB00740

Summary

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

Predictions

Indication	Score	Source
bilateral parasagittal parieto-occipital polymicrogyria	0.9999	DL
amyotrophic lateral sclerosis	0.9999	KG+DL
axial spondylometaphyseal dysplasia	0.9999	DL
lower motor neuron syndrome with late-adult onset	0.9999	DL
trichomegaly-retina pigmentary degeneration-dwarfism syndrome	0.9999	DL
lethal arthrogryposis-anterior horn cell disease syndrome	0.9999	DL
monomelic amyotrophy	0.9999	DL
Mills syndrome	0.9998	DL
amyotrophic lateral sclerosis, susceptibility to	0.9998	DL
autosomal dominant mitochondrial myopathy with exercise intolerance	0.9998	DL
amyotrohpic lateral sclerosis type 22	0.9998	DL
polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis	0.9970	DL
hydranencephaly (disease)	0.9967	DL
congenital disorder of glycosylation with defective fucosylation	0.9967	DL
schizophrenia	0.9966	DL
retinal dystrophy with or without extraocular anomalies	0.9964	DL
atypical glycine encephalopathy	0.9962	DL
Charcot-Marie-Tooth disease, demyelinating, type 1G	0.9959	DL
myopia 26, X-linked, female-limited	0.9955	DL
syndromic myopia	0.9954	DL
myopia X-linked	0.9947	DL
proximal spinal muscular atrophy	0.9864	DL
acute intermittent porphyria	0.9797	DL
PLA2G6-associated neurodegeneration	0.9794	DL
renal pelvis carcinoma	0.9767	DL
paralysis agitans, juvenile, of Hunt	0.9766	DL
short rib-polydactyly syndrome, Majewski type	0.9764	DL
renal cell carcinoma (disease)	0.9749	DL
lethal infantile mitochondrial myopathy	0.9727	DL
febrile infection-related epilepsy syndrome	0.9715	DL
Lennox-Gastaut syndrome	0.9700	DL
dermatofibrosarcoma protuberans	0.9699	DL
Parkinson disease	0.9681	DL
hereditary coproporphyria	0.9671	DL
perioral myoclonia with absences	0.9646	DL
rhabdoid tumor	0.9619	DL
atypical childhood epilepsy with centrotemporal spikes	0.9617	DL
cryptogenic late-onset epileptic spasms	0.9617	DL
photosensitive occipital lobe epilepsy	0.9617	DL
adolescent/adult-onset epilepsy syndrome	0.9611	DL
neuronopathy, distal hereditary motor	0.9600	DL
distal 17p13.3 microdeletion syndrome	0.9591	DL
familial encephalopathy with neuroserpin inclusion bodies	0.9577	DL
infantile neuronal ceroid lipofuscinosis	0.9569	DL
frontotemporal neurodegeneration with movement disorder	0.9569	DL
poliomyelitis	0.9566	DL
adolescence-adult electroclinical syndrome	0.9561	DL
gastrocutaneous syndrome	0.9553	DL
myoclonic epilepsy, juvenile, susceptibility to	0.9549	DL
familial generalized lentiginosis	0.9536	DL

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