Piribedil
DrugBank ID: DB12478
Summary
| Metric | Value |
|---|---|
| Total Predictions | 50 |
| KG+DL (Dual Validated) | 1 |
| DL Only | 49 |
| KG Only | 0 |
Predictions
| Indication | Score | Source |
|---|---|---|
| Parkinson disease | 0.9943 | DL |
| retinal dystrophy with or without extraocular anomalies | 0.9934 | DL |
| paralysis agitans, juvenile, of Hunt | 0.9934 | DL |
| polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis | 0.9912 | DL |
| PLA2G6-associated neurodegeneration | 0.9907 | DL |
| juvenile onset Parkinson disease 19A | 0.9901 | DL |
| lethal infantile mitochondrial myopathy | 0.9900 | DL |
| myopia 26, X-linked, female-limited | 0.9894 | DL |
| congenital disorder of glycosylation with defective fucosylation | 0.9894 | DL |
| myopia X-linked | 0.9886 | DL |
| atypical glycine encephalopathy | 0.9885 | DL |
| Charcot-Marie-Tooth disease, demyelinating, type 1G | 0.9882 | DL |
| hydranencephaly (disease) | 0.9865 | DL |
| syndromic myopia | 0.9865 | DL |
| hereditary late onset Parkinson disease | 0.9853 | DL |
| schizophrenia | 0.9844 | DL |
| atypical juvenile parkinsonism | 0.9786 | DL |
| X-linked parkinsonism-spasticity syndrome | 0.9725 | DL |
| progressive supranuclear palsy-corticobasal syndrome | 0.9703 | DL |
| parkinsonian disorder | 0.9691 | KG+DL |
| Rasmussen subacute encephalitis | 0.9678 | DL |
| myelitis | 0.9657 | DL |
| Lewy body dementia | 0.9632 | DL |
| parkinsonian-pyramidal syndrome | 0.9563 | DL |
| transaldolase deficiency | 0.9525 | DL |
| hemiparkinsonism-hemiatrophy syndrome | 0.9500 | DL |
| fructose-1,6-bisphosphatase deficiency | 0.9432 | DL |
| autosomal recessive Parkinson disease | 0.9372 | DL |
| acute intermittent porphyria | 0.9304 | DL |
| early-onset parkinsonism-intellectual disability syndrome | 0.9208 | DL |
| dystonia | 0.8887 | DL |
| X-linked intellectual disability-cerebellar hypoplasia syndrome | 0.8872 | DL |
| X-linked intellectual disability-ataxia-apraxia syndrome | 0.8845 | DL |
| X-linked spasticity-intellectual disability-epilepsy syndrome | 0.8818 | DL |
| torsion dystonia | 0.8683 | DL |
| CLCN4-related X-linked intellectual disability syndrome | 0.8658 | DL |
| NAA10-related syndrome | 0.8629 | DL |
| glaucoma | 0.8613 | DL |
| lissencephaly type 1 due to doublecortin gene mutation | 0.8610 | DL |
| X-linked intellectual disability-precocious puberty-obesity syndrome | 0.8562 | DL |
| MED12-related intellectual disability syndrome | 0.8556 | DL |
| X-linked intellectual disability-spastic quadriparesis syndrome | 0.8548 | DL |
| intellectual disability, X-linked, syndromic | 0.8514 | DL |
| syndromic X-linked intellectual disability Chudley-Schwartz type | 0.8511 | DL |
| X-linked cerebral-cerebellar-coloboma syndrome syndrome | 0.8486 | DL |
| intellectual developmental disorder, X-linked, syndromic, Hackmann-Di Donato type | 0.8486 | DL |
| Prieto syndrome | 0.8479 | DL |
| Paganini-Miozzo syndrome | 0.8469 | DL |
| X-linked intellectual disability-hypotonia-movement disorder syndrome | 0.8467 | DL |
| X-linked intellectual disability, Stocco dos Santos type | 0.8458 | 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.