SE-ATLAS

Foix-Chavany-Marie syndrome Progressive supranuclear palsy-pure akinesia with gait freezing syndrome Corticobasal syndrome Progressive supranuclear palsy-corticobasal syndrome Dubowitz syndrome Leigh syndrome Distal hereditary motor neuropathy type 2 Infantile-onset ascending hereditary spastic paralysis Cockayne syndrome Classic progressive supranuclear palsy syndrome Distal hereditary motor neuropathy type 1 Progressive muscular atrophy Multiple system atrophy, cerebellar type Distal hereditary motor neuropathy type 5 Progressive supranuclear palsy-parkinsonism syndrome Neuronal intranuclear inclusion disease Infantile neuroaxonal dystrophy Distal hereditary motor neuropathy, Jerash type Distal hereditary motor neuropathy type 7 Huntington disease Motor neuron disease Frontotemporal degeneration with dementia MELAS Susac syndrome Amyotrophic lateral sclerosis type 4 Kennedy disease Progressive supranuclear palsy-progressive non-fluent aphasia syndrome Noonan syndrome Aarskog-Scott syndrome Subacute sclerosing leukoencephalitis Moyamoya disease Seckel syndrome Progressive supranuclear palsy Amyotrophic lateral sclerosis Robinow syndrome Multiple system atrophy, parkinsonian type Madras motor neuron disease Logopenic progressive aphasia ITM2B amyloidosis Smith-Lemli-Opitz syndrome Frontotemporal dementia, right temporal atrophy variant Primary lateral sclerosis Young adult-onset distal hereditary motor neuropathy Spinal atrophy-ophthalmoplegia-pyramidal syndrome Moyamoya disease with early-onset achalasia X-linked distal hereditary motor neuropathy HERNS syndrome Watson syndrome Primary angiitis of the central nervous system Primary progressive aphasia Semantic dementia Autosomal recessive lower motor neuron disease with childhood onset Neuromyelitis optica spectrum disorder 17q11 microdeletion syndrome Autosomal recessive distal hereditary motor neuropathy Monosomy 22q13.3 Atypical progressive supranuclear palsy syndrome Juvenile primary lateral sclerosis Juvenile amyotrophic lateral sclerosis Sporadic infantile bilateral striatal necrosis Behavioral variant of frontotemporal dementia Progressive non-fluent aphasia Guam-Parkinson-Demenz-Komplex Enzephalitis, infektiöse Reversibles zerebrales Vasokonstriktionssyndrom Familiäres zerebrales sakkuläres Aneurysma Zerebrale Sinus- und Venenthrombose Striatale Nekrose, infantile Striatale Nekrose, infantile familiäre Frontotemporale Demenz Legius-Syndrom Hereditäre spastische Paraplegie Atrophie, kortikale posteriore Enzephalitis Neurofibromatose Typ 1 Schwannomatose, NF2-assoziierte