SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases


In the following you will find the diseases that are treated in this facility:
17q11 microdeletion syndrome Aarskog-Scott syndrome Amyotrophic lateral sclerosis Atrophie multisystématisée type cérébelleux Atrophie musculaire progressive 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 Dystrophie neuroaxonale infantile Dégénérescence fronto-temporale avec démence Encephalitis Familial cerebral saccular aneurysm Familial infantile bilateral striatal necrosis Frontotemporal dementia Frontotemporal dementia, right temporal atrophy variant Full NF2-related schwannomatosis HERNS syndrome Hereditary spastic paraplegia ITM2B amyloidosis Infantile bilateral striatal necrosis Infectious encephalitis Juvenile amyotrophic lateral sclerosis Juvenile primary lateral sclerosis Legius syndrome Logopenic progressive aphasia MELAS Madras motor neuron disease Maladie de Huntington Maladie de Kennedy Maladie des inclusions intranucléaires neuronales Maladie du motoneurone Monosomy 22q13.3 Moyamoya disease Moyamoya disease with early-onset achalasia Multiple system atrophy, parkinsonian type Neurofibromatosis type 1 Neuromyelitis optica spectrum disorder Neuropathie motrice distale héréditaire type 1 Neuropathie motrice distale héréditaire type 2 Neuropathie motrice distale héréditaire type 5 Neuropathie motrice distale héréditaire type 7 Neuropathie motrice distale héréditaire type Jerash Noonan syndrome Paralysie spastique infantile ascendante héréditaire Parkinson-dementia complex of Guam Posterior cortical atrophy Primary angiitis of the central nervous system Primary lateral sclerosis Primary progressive aphasia Progressive non-fluent aphasia Progressive supranuclear palsy Reversible cerebral vasoconstriction syndrome Robinow syndrome Sclérose latérale amyotrophique type 4 Seckel syndrome Semantic dementia Smith-Lemli-Opitz syndrome Spinal atrophy-ophthalmoplegia-pyramidal syndrome Sporadic infantile bilateral striatal necrosis Subacute sclerosing leukoencephalitis Syndrome corticobasal Syndrome de Cockayne Syndrome de Dubowitz Syndrome de Foix-Chavany-Marie Syndrome de Leigh Syndrome de Susac Syndrome de paralysie supranucléaire progressive classique Syndrome de paralysie supranucléaire progressive-akinésie pure avec freezing de la marche Syndrome de paralysie supranucléaire progressive-aphasie progressive non fluente Syndrome de paralysie supranucléaire progressive-parkinsonisme Syndrome de paralysie supranucléaire progressive-syndrome corticobasal Watson syndrome X-linked distal hereditary motor neuropathy Young adult-onset distal hereditary motor neuropathy