Rasagiline
DrugBank ID: DB01367
Summary
| Metric | Value |
|---|---|
| Total Predictions | 50 |
| KG+DL (Dual Validated) | 0 |
| DL Only | 50 |
| KG Only | 0 |
Predictions
| Indication | Score | Source |
|---|---|---|
| hereditary late onset Parkinson disease | 0.9990 | DL |
| juvenile onset Parkinson disease 19A | 0.9989 | DL |
| X-linked parkinsonism-spasticity syndrome | 0.9974 | DL |
| atypical juvenile parkinsonism | 0.9972 | DL |
| PLA2G6-associated neurodegeneration | 0.9971 | DL |
| Rasmussen subacute encephalitis | 0.9956 | DL |
| Parkinson disease | 0.9940 | DL |
| parkinsonian-pyramidal syndrome | 0.9934 | DL |
| myelitis | 0.9932 | DL |
| paralysis agitans, juvenile, of Hunt | 0.9925 | DL |
| transaldolase deficiency | 0.9919 | DL |
| hemiparkinsonism-hemiatrophy syndrome | 0.9915 | DL |
| polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis | 0.9901 | DL |
| congenital disorder of glycosylation with defective fucosylation | 0.9884 | DL |
| Lewy body dementia | 0.9883 | DL |
| fructose-1,6-bisphosphatase deficiency | 0.9882 | DL |
| retinal dystrophy with or without extraocular anomalies | 0.9881 | DL |
| early-onset parkinsonism-intellectual disability syndrome | 0.9879 | DL |
| lethal infantile mitochondrial myopathy | 0.9871 | DL |
| Charcot-Marie-Tooth disease, demyelinating, type 1G | 0.9869 | DL |
| myopia X-linked | 0.9858 | DL |
| atypical glycine encephalopathy | 0.9849 | DL |
| schizophrenia | 0.9847 | DL |
| syndromic myopia | 0.9833 | DL |
| myopia 26, X-linked, female-limited | 0.9828 | DL |
| progressive supranuclear palsy-corticobasal syndrome | 0.9818 | DL |
| X-linked intellectual disability-ataxia-apraxia syndrome | 0.9814 | DL |
| hydranencephaly (disease) | 0.9801 | DL |
| X-linked intellectual disability-cerebellar hypoplasia syndrome | 0.9783 | DL |
| CLCN4-related X-linked intellectual disability syndrome | 0.9750 | DL |
| NAA10-related syndrome | 0.9733 | DL |
| X-linked intellectual disability-spastic quadriparesis syndrome | 0.9732 | DL |
| MED12-related intellectual disability syndrome | 0.9726 | DL |
| hydrocephaly-cerebellar agenesis syndrome | 0.9719 | DL |
| syndromic X-linked intellectual disability Chudley-Schwartz type | 0.9712 | DL |
| intellectual disability, X-linked, syndromic | 0.9711 | DL |
| X-linked cerebral-cerebellar-coloboma syndrome syndrome | 0.9710 | DL |
| X-linked intellectual disability-precocious puberty-obesity syndrome | 0.9707 | DL |
| X-linked intellectual disability-hypotonia-movement disorder syndrome | 0.9707 | DL |
| Paganini-Miozzo syndrome | 0.9706 | DL |
| X-linked intellectual disability, Stocco dos Santos type | 0.9703 | DL |
| lissencephaly type 1 due to doublecortin gene mutation | 0.9702 | DL |
| X-linked intellectual disability with hypopituitarism | 0.9699 | DL |
| Prieto syndrome | 0.9698 | DL |
| intellectual developmental disorder, X-linked, syndromic, Hackmann-Di Donato type | 0.9694 | DL |
| Basilicata-Akhtar syndrome | 0.9689 | DL |
| X-linked intellectual disability-craniofacioskeletal syndrome | 0.9685 | DL |
| holoprosencephaly 13, X-linked | 0.9683 | DL |
| X-linked spasticity-intellectual disability-epilepsy syndrome | 0.9680 | DL |
| X-linked intellectual disability-acromegaly-hyperactivity syndrome | 0.9637 | 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.