SE-ATLAS

17q11 microdeletion syndrome Amyotrophic lateral sclerosis Amyotrophic lateral sclerosis type 4 Atypical progressive supranuclear palsy syndrome Autosomal recessive distal hereditary motor neuropathy Behavioral variant of frontotemporal dementia Cerebral sinovenous thrombosis Classic progressive supranuclear palsy syndrome Corticobasal syndrome Encephalitis Familial cerebral saccular aneurysm Foix-Chavany-Marie syndrome Frontotemporal degeneration with dementia Frontotemporal dementia Frontotemporal dementia, right temporal atrophy variant Full NF2-related schwannomatosis Huntington disease ITM2B amyloidosis Infectious encephalitis Juvenile amyotrophic lateral sclerosis Juvenile primary lateral sclerosis Kennedy disease Leigh syndrome Logopenic progressive aphasia MELAS Madras motor neuron disease Monosomy 22q13.3 Motor neuron disease Moyamoya disease Moyamoya disease with early-onset achalasia Multiple system atrophy, cerebellar type Multiple system atrophy, parkinsonian type Neurofibromatosis type 1 Neuromyelitis optica spectrum disorder Neuronal intranuclear inclusion disease PLA2G6-associated neurodegeneration Parkinson-dementia complex of Guam Posterior cortical atrophy Primary angiitis of the central nervous system Primary lateral sclerosis Primary progressive aphasia Progressive muscular atrophy Progressive non-fluent aphasia Progressive supranuclear palsy Progressive supranuclear palsy-corticobasal syndrome Progressive supranuclear palsy-parkinsonism syndrome Progressive supranuclear palsy-progressive non-fluent aphasia syndrome Progressive supranuclear palsy-pure akinesia with gait freezing syndrome Reversible cerebral vasoconstriction syndrome Semantic dementia Subacute sclerosing leukoencephalitis Susac syndrome