SE-ATLAS

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