Entacapone
DrugBank ID: DB00494
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 | 0.9995 | DL |
| hereditary late onset Parkinson disease | 0.9991 | DL |
| atypical juvenile parkinsonism | 0.9985 | KG+DL |
| X-linked parkinsonism-spasticity syndrome | 0.9980 | KG+DL |
| PLA2G6-associated neurodegeneration | 0.9976 | DL |
| Rasmussen subacute encephalitis | 0.9973 | DL |
| Parkinson disease | 0.9967 | DL |
| myelitis | 0.9963 | DL |
| paralysis agitans, juvenile, of Hunt | 0.9960 | DL |
| parkinsonian-pyramidal syndrome | 0.9955 | KG+DL |
| hemiparkinsonism-hemiatrophy syndrome | 0.9946 | KG+DL |
| transaldolase deficiency | 0.9943 | DL |
| early-onset parkinsonism-intellectual disability syndrome | 0.9929 | KG+DL |
| lethal infantile mitochondrial myopathy | 0.9928 | DL |
| Lewy body dementia | 0.9925 | DL |
| fructose-1,6-bisphosphatase deficiency | 0.9922 | DL |
| polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis | 0.9906 | DL |
| progressive supranuclear palsy-corticobasal syndrome | 0.9904 | DL |
| X-linked intellectual disability-ataxia-apraxia syndrome | 0.9896 | DL |
| congenital disorder of glycosylation with defective fucosylation | 0.9889 | DL |
| Charcot-Marie-Tooth disease, demyelinating, type 1G | 0.9882 | DL |
| retinal dystrophy with or without extraocular anomalies | 0.9881 | DL |
| X-linked intellectual disability-cerebellar hypoplasia syndrome | 0.9879 | DL |
| myopia X-linked | 0.9873 | DL |
| atypical glycine encephalopathy | 0.9867 | DL |
| CLCN4-related X-linked intellectual disability syndrome | 0.9862 | DL |
| X-linked spasticity-intellectual disability-epilepsy syndrome | 0.9855 | DL |
| X-linked intellectual disability-spastic quadriparesis syndrome | 0.9854 | DL |
| myopia 26, X-linked, female-limited | 0.9852 | DL |
| hydrocephaly-cerebellar agenesis syndrome | 0.9848 | DL |
| syndromic X-linked intellectual disability Chudley-Schwartz type | 0.9842 | DL |
| intellectual disability, X-linked, syndromic | 0.9842 | DL |
| X-linked cerebral-cerebellar-coloboma syndrome syndrome | 0.9840 | DL |
| X-linked intellectual disability-hypotonia-movement disorder syndrome | 0.9839 | DL |
| NAA10-related syndrome | 0.9839 | DL |
| Paganini-Miozzo syndrome | 0.9838 | DL |
| X-linked intellectual disability, Stocco dos Santos type | 0.9837 | DL |
| Prieto syndrome | 0.9834 | DL |
| intellectual developmental disorder, X-linked, syndromic, Hackmann-Di Donato type | 0.9834 | DL |
| X-linked intellectual disability with hypopituitarism | 0.9833 | DL |
| syndromic myopia | 0.9833 | DL |
| MED12-related intellectual disability syndrome | 0.9832 | DL |
| schizophrenia | 0.9831 | DL |
| X-linked intellectual disability-precocious puberty-obesity syndrome | 0.9830 | DL |
| Basilicata-Akhtar syndrome | 0.9828 | DL |
| X-linked intellectual disability-craniofacioskeletal syndrome | 0.9826 | DL |
| holoprosencephaly 13, X-linked | 0.9819 | DL |
| lissencephaly type 1 due to doublecortin gene mutation | 0.9818 | DL |
| X-linked intellectual disability-acromegaly-hyperactivity syndrome | 0.9794 | DL |
| hydranencephaly (disease) | 0.9791 | DL |
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Disclaimer
Predictions are for research purposes only and do not constitute medical advice.
Predictions are for research purposes only and do not constitute medical advice.