SE-ATLAS

17q11 microdeletion syndrome Aarskog-Scott syndrome Amyotrophic lateral sclerosis Amyotrophic lateral sclerosis type 4 Atypical progressive supranuclear palsy syndrome Autosomal recessive distal hereditary motor neuropathy Autosomal recessive lower motor neuron disease with childhood onset Behavioral variant of frontotemporal dementia Cerebral sinovenous thrombosis Classic progressive supranuclear palsy syndrome Cockayne syndrome Corticobasal syndrome Distal hereditary motor neuropathy type 1 Distal hereditary motor neuropathy type 2 Distal hereditary motor neuropathy type 5 Distal hereditary motor neuropathy type 7 Distal hereditary motor neuropathy, Jerash type Dubowitz syndrome Encephalitis Familial cerebral saccular aneurysm Familial infantile bilateral striatal necrosis Foix-Chavany-Marie syndrome Frontotemporal degeneration with dementia Frontotemporal dementia Frontotemporal dementia, right temporal atrophy variant Full NF2-related schwannomatosis HERNS syndrome Hereditary spastic paraplegia Huntington disease ITM2B amyloidosis Infantile bilateral striatal necrosis Infantile neuroaxonal dystrophy Infantile-onset ascending hereditary spastic paralysis Infectious encephalitis Juvenile amyotrophic lateral sclerosis Juvenile primary lateral sclerosis Kennedy disease Legius syndrome 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 Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion Neuromyelitis optica spectrum disorder Neuronal intranuclear inclusion disease Noonan syndrome Parkinson-dementia complex of Guam Posterior cortical atrophy Prader-Willi syndrome 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 Robinow syndrome Seckel syndrome Semantic dementia Smith-Lemli-Opitz syndrome Spinal atrophy-ophthalmoplegia-pyramidal syndrome Sporadic infantile bilateral striatal necrosis Subacute sclerosing leukoencephalitis Susac syndrome Watson syndrome X-linked distal hereditary motor neuropathy Young adult-onset distal hereditary motor neuropathy