SE-ATLAS

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