SE-ATLAS

Manganese poisoning Hereditary ataxia Rare parkinsonian disorder Spastic ataxia Rare parkinsonian syndrome due to intoxication Cyanide-induced parkinsonism-dystonia Autosomal recessive cerebellar ataxia Cerebellar ataxia-hypogonadism syndrome X-linked cerebellar ataxia Delayed encephalopathy due to carbon monoxide poisoning Adult-onset dystonia-parkinsonism Ataxia-tapetoretinal degeneration syndrome Ataxia-hypogonadism-choroidal dystrophy syndrome Primary lateral sclerosis Ataxia-photosensitivity-short stature syndrome Frontotemporal neurodegeneration with movement disorder Non-hereditary degenerative ataxia Autosomal dominant cerebellar ataxia Young-onset Parkinson disease Acquired ataxia Multiple system atrophy Postencephalitic parkinsonism Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome Hereditary late-onset Parkinson disease Rare tremor disorder Atypical juvenile parkinsonism Caribbean parkinsonism Perry syndrome Parkinsonian-pyramidal syndrome Rare ataxia ATP13A2-related juvenile neuronal ceroid lipofuscinosis Dystonia 16 NMDA receptor encephalitis Progressive muscular atrophy Autosomal dominant striatal neurodegeneration Encephalitis lethargica Primary progressive freezing gait X-linked dystonia-parkinsonism Motor neuron disease Genetic motor neuron disease X-linked parkinsonism-spasticity syndrome Acquired motor neuron disease Infantile dystonia-parkinsonism Rapid-onset dystonia-parkinsonism Multiple system atrophy, parkinsonian type Rare parkinsonian syndrome due to neurodegenerative disease Early-onset parkinsonism-intellectual disability syndrome Kufor-Rakeb syndrome Hemiparkinsonism-hemiatrophy syndrome Sporadic Creutzfeldt-Jakob disease