Safinamide

DrugBank ID: DB06654

Summary

Metric	Value
Total Predictions	50
KG+DL (Dual Validated)	5
DL Only	45
KG Only	0

Predictions

Indication	Score	Source
juvenile onset Parkinson disease 19A	0.9993	DL
hereditary late onset Parkinson disease	0.9972	DL
atypical juvenile parkinsonism	0.9967	KG+DL
Rasmussen subacute encephalitis	0.9963	DL
X-linked parkinsonism-spasticity syndrome	0.9951	KG+DL
myelitis	0.9946	DL
PLA2G6-associated neurodegeneration	0.9922	DL
parkinsonian-pyramidal syndrome	0.9909	KG+DL
transaldolase deficiency	0.9894	DL
hemiparkinsonism-hemiatrophy syndrome	0.9890	KG+DL
Parkinson disease	0.9880	DL
fructose-1,6-bisphosphatase deficiency	0.9879	DL
paralysis agitans, juvenile, of Hunt	0.9876	DL
Lewy body dementia	0.9843	DL
early-onset parkinsonism-intellectual disability syndrome	0.9826	KG+DL
X-linked intellectual disability-ataxia-apraxia syndrome	0.9793	DL
lethal infantile mitochondrial myopathy	0.9788	DL
X-linked intellectual disability-cerebellar hypoplasia syndrome	0.9768	DL
CLCN4-related X-linked intellectual disability syndrome	0.9731	DL
hydrocephaly-cerebellar agenesis syndrome	0.9713	DL
progressive supranuclear palsy-corticobasal syndrome	0.9711	DL
X-linked intellectual disability-spastic quadriparesis syndrome	0.9706	DL
X-linked spasticity-intellectual disability-epilepsy syndrome	0.9705	DL
intellectual disability, X-linked, syndromic	0.9696	DL
syndromic X-linked intellectual disability Chudley-Schwartz type	0.9692	DL
Paganini-Miozzo syndrome	0.9692	DL
X-linked cerebral-cerebellar-coloboma syndrome syndrome	0.9689	DL
X-linked intellectual disability-hypotonia-movement disorder syndrome	0.9688	DL
X-linked intellectual disability, Stocco dos Santos type	0.9683	DL
polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis	0.9680	DL
Prieto syndrome	0.9678	DL
intellectual developmental disorder, X-linked, syndromic, Hackmann-Di Donato type	0.9676	DL
Basilicata-Akhtar syndrome	0.9673	DL
NAA10-related syndrome	0.9673	DL
MED12-related intellectual disability syndrome	0.9670	DL
X-linked intellectual disability with hypopituitarism	0.9666	DL
lissencephaly type 1 due to doublecortin gene mutation	0.9665	DL
X-linked intellectual disability-craniofacioskeletal syndrome	0.9660	DL
X-linked intellectual disability-precocious puberty-obesity syndrome	0.9654	DL
holoprosencephaly 13, X-linked	0.9650	DL
X-linked intellectual disability-acromegaly-hyperactivity syndrome	0.9639	DL
atypical glycine encephalopathy	0.9599	DL
Charcot-Marie-Tooth disease, demyelinating, type 1G	0.9596	DL
congenital disorder of glycosylation with defective fucosylation	0.9575	DL
retinal dystrophy with or without extraocular anomalies	0.9558	DL
myopia X-linked	0.9505	DL
myopia 26, X-linked, female-limited	0.9484	DL
syndromic myopia	0.9429	DL
hydranencephaly (disease)	0.9402	DL
Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome	0.9297	DL

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