Mapping of Health Care Providers
for People with Rare Diseases

In the following you will find the diseases that are treated in this facility:
ATTRV30M amyloidosis Acetazolamide-responsive myotonia Acquired motor neuron disease Acquired neuromuscular junction disease Acquired skeletal muscle disease Acute disseminated encephalomyelitis Adult-onset distal myopathy due to VCP mutation Adult-onset myasthenia gravis Alpha-B crystallin-related late-onset myopathy Alpha-crystallinopathy Alveolar rhabdomyosarcoma Amyloidosis Amyotrophic lateral sclerosis Amyotrophic lateral sclerosis type 4 Andersen-Tawil syndrome Antisynthetase syndrome Arthrogryposis due to muscular dystrophy Atypical progressive supranuclear palsy syndrome Autosomal dominant adult-onset proximal spinal muscular atrophy Autosomal dominant childhood-onset proximal spinal muscular atrophy Autosomal dominant congenital benign spinal muscular atrophy Autosomal dominant distal hereditary motor neuropathy Autosomal dominant distal myopathy Autosomal dominant proximal spinal muscular atrophy Autosomal dominant spastic paraplegia type 17 Autosomal recessive distal hereditary motor neuropathy Autosomal recessive distal myopathy Autosomal recessive lower motor neuron disease with childhood onset Autosomal recessive myogenic arthrogryposis multiplex congenita BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy Bacterial myositis Baló concentric sclerosis Behavioral variant of frontotemporal dementia Benign Samaritan congenital myopathy Bethlem myopathy Brain inflammatory disease Brody myopathy Bulbospinal muscular atrophy Bulbospinal muscular atrophy of adult Bulbospinal muscular atrophy of childhood CANOMAD syndrome CLIPPERS Cap myopathy Centronuclear myopathy Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Chronic inflammatory demyelinating polyneuropathy Classic progressive supranuclear palsy syndrome Congenital fiber-type disproportion myopathy Congenital fibrosis of extraocular muscles Congenital lethal myopathy, Compton-North type Congenital muscular dystrophy Congenital muscular dystrophy due to LMNA mutation Congenital muscular dystrophy due to dystroglycanopathy Congenital muscular dystrophy type 1B Congenital muscular dystrophy with hyperlaxity Congenital muscular dystrophy with integrin alpha-7 deficiency Congenital muscular dystrophy, Ullrich type Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome Congenital myasthenic syndrome Congenital myasthenic syndromes with glycosylation defect Congenital myopathy Congenital myopathy with cores Congenital myopathy with excess of thin filaments Congenital myopathy, Paradas type Congenital myotonia Corpus callosum agenesis-neuronopathy syndrome Cylindrical spirals myopathy Cyprus facial-neuromusculoskeletal syndrome DYNC1H1-related autosomal dominant childhood-onset proximal spinal muscular atrophy Dermatomyositis Desmin-related myopathy with Mallory body-like inclusions Desminopathy Distal anoctaminopathy 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 Distal myopathy Distal myopathy with anterior tibial onset Distal myopathy with early respiratory muscle involvement Distal myopathy with posterior leg and anterior hand involvement Distal myopathy, Welander type Distal myotilinopathy Distal nebulin myopathy Distal spinal muscular atrophy type 3 Duchenne and Becker muscular dystrophy Early-onset autosomal dominant Alzheimer disease Early-onset myopathy with fatal cardiomyopathy Embryonal rhabdomyosarcoma Emery-Dreifuss muscular dystrophy Encephalitis Eosinophilic fasciitis Facioscapulohumeral dystrophy Familial hemophagocytic lymphohistiocytosis Fatal post-viral neurodegenerative disorder Fetal akinesia-cerebral and retinal hemorrhage syndrome Fingerprint body myopathy Finnish upper limb-onset distal myopathy Focal myositis Friedreich ataxia Frontotemporal degeneration with dementia Frontotemporal dementia Frontotemporal dementia with motor neuron disease Frontotemporal dementia, right temporal atrophy variant Fungal myositis GNE myopathy Generalized bulbospinal muscular atrophy Genetic motor neuron disease Genetic neuromuscular junction disease Genetic periodic paralysis Genetic skeletal muscle disease Griscelli syndrome type 1 Guillain-Barré syndrome Hereditary continuous muscle fiber activity Hereditary inclusion body myopathy type 4 Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome Hereditary myopathy with early respiratory failure Hereditary myopathy with lactic acidosis due to ISCU deficiency Hereditary spastic paraplegia Huntington disease Hyaline body myopathy Hyperkalemic periodic paralysis Hypokalemic periodic paralysis Idiopathic camptocormia Idiopathic eosinophilic myositis Idiopathic inflammatory myopathy IgG4-related pachymeningitis Immune-mediated necrotizing myopathy Inclusion body myopathy with Paget disease of bone and frontotemporal dementia Inclusion body myositis Inclusion myopathy Infantile myofibromatosis Infantile-onset X-linked spinal muscular atrophy Infantile-onset ascending hereditary spastic paralysis Infectious, fungal or parasitic myopathy Inflammatory myopathy with abundant macrophages Intellectual disability-developmental delay-contractures syndrome Intellectual disability-myopathy-short stature-endocrine defect syndrome Isaac syndrome Juvenile amyotrophic lateral sclerosis Juvenile dermatomyositis Juvenile idiopathic inflammatory myopathy Juvenile myasthenia gravis Juvenile overlap myositis Juvenile polymyositis Juvenile primary lateral sclerosis KLHL9-related early-onset distal myopathy Kennedy disease King-Denborough syndrome Laing early-onset distal myopathy Lambert-Eaton myasthenic syndrome Laminin subunit alpha 2-related congenital muscular dystrophy Late-onset distal myopathy, Markesbery-Griggs type Limb-girdle muscular dystrophy Logopenic progressive aphasia Lower motor neuron syndrome with late-adult onset Macrophagic myofasciitis Madras motor neuron disease Malignant hyperthermia of anesthesia Marburg acute multiple sclerosis Megaconial congenital muscular dystrophy Metabolic myopathy Metabolic myopathy due to lactate transporter defect Miyoshi myopathy Monomelic amyotrophy Morvan syndrome Motor neuron disease Multiple sclerosis variant Muscle filaminopathy Muscular channelopathy Muscular dystrophy Muscular dystrophy, Selcen type Muscular dystrophy-white matter spongiosis syndrome Muscular glycogenosis Muscular lipidosis Muscular tumor Myasthenia gravis Myofibrillar myopathy Myopathy with hexagonally cross-linked tubular arrays Myosclerosis Myotonia fluctuans Myotonia permanens Myotonic dystrophy Myotonic syndrome Myxofibrosarcoma Native American myopathy Nemaline myopathy Neurogenic scapuloperoneal syndrome, Kaeser type Neuromuscular disease Neuromuscular junction disease Neuromyelitis optica spectrum disorder Niemann-Pick disease type C Niemann-Pick disease type C, adult neurologic onset Niemann-Pick disease type C, juvenile neurologic onset Niemann-Pick disease type C, late infantile neurologic onset Niemann-Pick disease type C, severe early infantile neurologic onset Niemann-Pick disease type C, severe perinatal form Non-dystrophic myopathy Non-dystrophic myopathy with collagen 6 anomaly Oculopharyngeal muscular dystrophy Oculopharyngodistal myopathy Opsoclonus-myoclonus syndrome Overlap myositis Paramyotonia congenita of Von Eulenburg Parasitic myositis Parkinson-dementia complex of Guam Periodic paralysis Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome Poliomyelitis Polymyositis Polyneuropathy associated with IgM monoclonal gammapathy with anti-MAG Pontocerebellar hypoplasia type 1 Pontocerebellar hypoplasia type 2 Posterior cortical atrophy Postpoliomyelitis syndrome Postsynaptic congenital myasthenic syndromes Potassium-aggravated myotonia Presynaptic congenital myasthenic syndromes Primary lateral sclerosis Primary progressive aphasia Progressive hemifacial atrophy Progressive muscular dystrophy 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 Proximal myotonic myopathy Proximal spinal muscular atrophy Proximal spinal muscular atrophy type 1 Proximal spinal muscular atrophy type 2 Proximal spinal muscular atrophy type 3 Proximal spinal muscular atrophy type 4 Rare dystonia Rare neuroinflammatory or neuroimmunological disease Reducing body myopathy Rhabdomyosarcoma Riboflavin transporter deficiency Rigid spine syndrome Rippling muscle disease Rippling muscle disease with myasthenia gravis Schilder disease Schwartz-Jampel syndrome Semantic dementia Skeletal muscle disease Spheroid body myopathy Spinal atrophy-ophthalmoplegia-pyramidal syndrome Spinal muscular atrophy associated with central nervous system anomaly Spinal muscular atrophy with respiratory distress type 1 Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome Sporadic Creutzfeldt-Jakob disease Steinert myotonic dystrophy Stiff person spectrum disorder Synaptic congenital myasthenic syndromes Tel Hashomer camptodactyly syndrome Thomsen and Becker disease Thyrotoxic periodic paralysis Tibial muscular dystrophy Transient neonatal myasthenia gravis Trichinellosis Tubular aggregate myopathy Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Viral myositis Vocal cord and pharyngeal distal myopathy Vogt-Koyanagi-Harada disease X-linked distal spinal muscular atrophy type 3 X-linked myopathy with excessive autophagy X-linked myopathy with postural muscle atrophy Young adult-onset distal hereditary motor neuropathy Zebra body myopathy