SE-ATLAS

Spinocerebellar ataxia type 2 Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome Friedreich ataxia Hereditary spastic paraplegia Rare genetic parkinsonian disorder Multiple system atrophy, cerebellar type Spinocerebellar ataxia type 1 Spinocerebellar ataxia type 3 Leukodystrophy Early-onset cerebellar ataxia with retained tendon reflexes Multiple system atrophy, parkinsonian type Hereditary episodic ataxia Benign hereditary chorea Hereditary ataxia Rare parkinsonian disorder Autosomal recessive cerebellar ataxia Behavioral variant of frontotemporal dementia Frontotemporal dementia with motor neuron disease Frontotemporal neurodegeneration with movement disorder Non-hereditary degenerative ataxia Progressive non-fluent aphasia Acquired ataxia Multiple system atrophy Neurodegenerative disease with chorea Rare tremor disorder Rare movement disorder Amyotrophic lateral sclerosis Huntington disease Huntington disease-like 1 Progressive supranuclear palsy