SE-ATLAS

Rare dystonia Hereditary geniospasm Multiple system atrophy, parkinsonian type Rapid-onset dystonia-parkinsonism Rare parkinsonian syndrome due to neurodegenerative disease Primary orthostatic tremor Rare parkinsonian disorder Rare disorder with dystonia and other neurologic or systemic manifestation Sensorineural hearing loss-early graying-essential tremor syndrome Rare parkinsonian syndrome due to intoxication Tremor-nystagmus-duodenal ulcer syndrome Behavioral variant of frontotemporal dementia Wilson disease Frontotemporal dementia with motor neuron disease Frontotemporal neurodegeneration with movement disorder Progressive non-fluent aphasia Multiple system atrophy Rare tremor disorder Rare epilepsy Isolated dystonia Hemidystonia-hemiatrophy syndrome Progressive supranuclear palsy Combined dystonia Multiple system atrophy, cerebellar type Spinocerebellar ataxia type 1 Spinocerebellar ataxia type 3 Spinocerebellar ataxia type 2 Spinocerebellar ataxia type 27 Progressive supranuclear palsy-parkinsonism syndrome Myoclonus-dystonia syndrome Autosomal dominant cerebellar ataxia