SE-ATLAS

Foix-Chavany-Marie syndrome Cockayne syndrome Corticobasal syndrome Dubowitz syndrome Distal hereditary motor neuropathy type 1 Distal hereditary motor neuropathy type 2 Infantile-onset ascending hereditary spastic paralysis Classic progressive supranuclear palsy syndrome Progressive supranuclear palsy-pure akinesia with gait freezing syndrome Progressive supranuclear palsy-corticobasal syndrome Leigh syndrome Progressive muscular atrophy Multiple system atrophy, cerebellar type Motor neuron disease Frontotemporal degeneration with dementia Neuronal intranuclear inclusion disease Infantile neuroaxonal dystrophy Distal hereditary motor neuropathy type 5 Distal hereditary motor neuropathy, Jerash type Distal hereditary motor neuropathy type 7 Huntington disease Progressive supranuclear palsy-parkinsonism syndrome Kennedy disease Progressive supranuclear palsy-progressive non-fluent aphasia syndrome Moyamoya disease MELAS Noonan syndrome Progressive supranuclear palsy Amyotrophic lateral sclerosis type 4 Subacute sclerosing leukoencephalitis Seckel syndrome Susac syndrome Aarskog-Scott syndrome Moyamoya disease with early-onset achalasia Multiple system atrophy, parkinsonian type Madras motor neuron disease Prader-Willi syndrome Amyotrophic lateral sclerosis Smith-Lemli-Opitz syndrome Primary lateral sclerosis Logopenic progressive aphasia Frontotemporal dementia, right temporal atrophy variant Encephalitis Robinow syndrome Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion Spinal atrophy-ophthalmoplegia-pyramidal syndrome ITM2B amyloidosis Posterior cortical atrophy X-linked distal hereditary motor neuropathy Young adult-onset distal hereditary motor neuropathy Autosomal recessive distal hereditary motor neuropathy Primary progressive aphasia 17q11 microdeletion syndrome Atypical progressive supranuclear palsy syndrome Monosomy 22q13.3 Neuromyelitis optica spectrum disorder Primary angiitis of the central nervous system Semantic dementia Autosomal recessive lower motor neuron disease with childhood onset HERNS syndrome Watson syndrome Behavioral variant of frontotemporal dementia Cerebral sinovenous thrombosis Infantile bilateral striatal necrosis Juvenile amyotrophic lateral sclerosis Reversible cerebral vasoconstriction syndrome Progressive non-fluent aphasia Familial cerebral saccular aneurysm Juvenile primary lateral sclerosis Familial infantile bilateral striatal necrosis Infectious encephalitis Sporadic infantile bilateral striatal necrosis Parkinson-dementia complex of Guam Frontotemporal dementia Legius syndrome Neurofibromatosis type 1 Full NF2-related schwannomatosis Hereditary spastic paraplegia