Donepezil

DrugBank ID: DB00843

Summary

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

Predictions

Indication	Score	Source
psychogenic movement disorders	0.9923	DL
chronic tic disorder	0.9919	DL
primary orthostatic tremor	0.9917	DL
benign shuddering attacks	0.9916	DL
extrapyramidal and movement disease	0.9916	DL
tremor-nystagmus-duodenal ulcer syndrome	0.9915	DL
benign paroxysmal tonic upgaze of childhood with ataxia	0.9912	DL
lingual-facial-buccal dyskinesia	0.9902	DL
acute intermittent porphyria	0.9875	DL
glaucoma	0.9828	DL
primary hereditary glaucoma	0.9766	DL
open-angle glaucoma	0.9720	DL
porphyria	0.9613	DL
Pick disease	0.9562	DL
cerebellar degeneration	0.9329	DL
X-linked parkinsonism-spasticity syndrome	0.9321	DL
hereditary late onset Parkinson disease	0.9201	DL
miscellaneous movement disorder due to neurodegenerative disease	0.9143	DL
PUM1-associated developmental disability-ataxia-seizure syndrome	0.9084	DL
GRID2-related autosomal dominant spinocerebellar ataxia	0.9079	DL
ataxia with dementia	0.9079	DL
Alzheimer disease without neurofibrillary tangles	0.9073	DL
Reye syndrome	0.8967	DL
mitochondrial proton-transporting ATP synthase complex deficiency	0.8944	DL
erythropoietic uroporphyria associated with myeloid malignancy	0.8939	DL
Axenfeld anomaly	0.8887	DL
hereditary photodermatosis	0.8781	DL
glaucoma 1, open angle	0.8777	DL
mitochondrial complex V (ATP synthase) deficiency, nuclear	0.8721	DL
drug-induced dyskinesia	0.8567	DL
porphyria due to ALA dehydratase deficiency	0.8488	DL
hemiparkinsonism-hemiatrophy syndrome	0.8460	DL
trigeminal autonomic cephalalgia	0.8450	DL
myoclonic dystonia	0.8417	DL
learning disability	0.8399	DL
PLA2G6-associated neurodegeneration	0.8372	DL
kleptomania	0.8302	DL
myoclonus-dystonia syndrome	0.8198	DL
obsolete rare pulmonary disease	0.8174	DL
glaucoma 3, primary infantile, B	0.8173	DL
early-onset parkinsonism-intellectual disability syndrome	0.8157	DL
X-linked intellectual disability-ataxia-apraxia syndrome	0.8153	DL
open angle glaucoma	0.8152	DL
progeria-short stature-pigmented nevi syndrome	0.8108	DL
frontotemporal dementia	0.8076	DL
Lewy body dementia	0.8062	DL
headache disorder	0.8014	DL
hereditary coproporphyria	0.8004	DL
X-linked spasticity-intellectual disability-epilepsy syndrome	0.7969	DL
acquired lactic acidosis	0.7920	DL

External Links

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