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:
Amyotrophic lateral sclerosis Anaplastic astrocytoma Angiocentric glioma Astroblastoma Astrocytoma Atypical papilloma of choroid plexus Atypical teratoid rhabdoid tumor Autosomal recessive cerebellar ataxia Autosomal recessive cerebelloparenchymal disorder type 3 Benign schwannoma CLIPPERS Central neurocytoma Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy Chordoid glioma Choroid plexus carcinoma Classic stiff person syndrome Congenital myotonia Cowden syndrome Craniopharyngioma Diffuse astrocytoma Diffuse intrinsic pontine glioma Duchenne and Becker muscular dystrophy Dysembryoplastic neuroepithelial tumor Ependymoma Focal stiff limb syndrome Fragile X-associated tremor/ataxia syndrome Full NF2-related schwannomatosis Full schwannomatosis Gangliocytoma Ganglioglioma Glial tumor Glioblastoma Hereditary hyperekplexia Hereditary spastic paraplegia Hyperkalemic periodic paralysis Lambert-Eaton myasthenic syndrome Langerhans cell histiocytosis Li-Fraumeni syndrome Malignant peripheral nerve sheath tumor Medulloblastoma Meningioma Multifocal motor neuropathy Multiple system atrophy Muscular dystrophy Myotonic dystrophy Neurofibroma Neurofibromatosis type 1 Non-functioning paraganglioma Oligodendroglioma Pilocytic astrocytoma Pilomyxoid astrocytoma Pineoblastoma Pituicytoma Pituitary adenoma Pleomorphic xanthoastrocytoma Primary angiitis of the central nervous system Primary central nervous system lymphoma Progressive encephalomyelitis with rigidity and myoclonus Progressive supranuclear palsy Prolactinoma Proximal myotonic myopathy Rare dystonia Rosette-forming glioneuronal tumor Stiff person spectrum disorder Subependymal giant cell astrocytoma Subependymoma Superficial siderosis Susac syndrome Unclassified autosomal dominant spinocerebellar ataxia