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 Moyamoya disease MELAS Noonan syndrome Progressive supranuclear palsy Amyotrophic lateral sclerosis type 4 Subacute sclerosing leukoencephalitis Seckel syndrome Susac syndrome Aarskog-Scott syndrome Kennedy disease Progressive supranuclear palsy-progressive non-fluent aphasia syndrome Moyamoya disease with early-onset achalasia X-linked distal hereditary motor neuropathy Robinow syndrome Young adult-onset distal hereditary motor neuropathy Multiple system atrophy, parkinsonian type Madras motor neuron disease Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion Spinal atrophy-ophthalmoplegia-pyramidal syndrome Amyotrophic lateral sclerosis Smith-Lemli-Opitz syndrome Primary lateral sclerosis Logopenic progressive aphasia ITM2B amyloidosis Frontotemporal dementia, right temporal atrophy variant Monosomy 22q13.3 Neuromyelitis optica spectrum disorder Autosomal recessive distal hereditary motor neuropathy Primary angiitis of the central nervous system Primary progressive aphasia Semantic dementia Autosomal recessive lower motor neuron disease with childhood onset HERNS syndrome Watson syndrome 17q11 microdeletion syndrome Atypical progressive supranuclear palsy syndrome 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 Sporadic infantile bilateral striatal necrosis Familial infantile bilateral striatal necrosis Behavioral variant of frontotemporal dementia Parkinson-dementia complex of Guam Infectious encephalitis Neurofibromatosis type 1 Full NF2-related schwannomatosis Hereditary spastic paraplegia Frontotemporal dementia Legius syndrome Posterior cortical atrophy Encephalitis