SE-ATLAS

Distale Myopathie durch VCP-Genmutation mit Beginn im Erwachsenenalter Myosklerose Myositis, fokale Myositis, parasitäre Myopathie, idiopathische inflammatorische, juvenile Form Lateralsklerose, primäre Myositis, bakterielle Kamptokormie, idiopathische Myositis bei Pilzerkrankungen Myopathie mit fataler Kardiomyopathie, früh-beginnende Form Myosin-Speicher-Myopathie Rhabdomyosarkom Neuropathie, distale kongenitale motorische, des jungen Erwachsenen Kongenitale Muskeldystrophie durch Dystroglykanopathie Richieri-Costa-da-Silva-Syndrom Kongenitale Muskeldystrophie-infantile Katarakt-Hyogonadismus-Syndrom Myositis-Overlap-Syndrom, juveniles Proximale spinale Muskelatrophie mit Beginn im Kindesalter, autosomal-dominant Muskeldystrophie - Spongiosis der weissen Gehirnmasse Dermatomyositis, juvenile Alpha-B Crystallin-abhängige spät beginnende Myopathie Spinale Muskelatrophie mit assoziierten Anomalien des Zentralnervensystems Amyotrophe Lateralsklerose Typ 4 Myopathie, benigne, Typ Samariter Myopathie, kongenitale, mit Fasertyp-Disproportion Untere Vorderhornerkrankung mit Beginn im späten Erwachsenenalter Myopathie, metabolische, durch Laktat-Transporter-Defekt BICD2-assoziierte proximale spinale Muskelatrophie mit Beginn im Kindesalter, autosomal-dominant Proximale spinale Muskelatrophie mit Beginn im Erwachsenenalter, autosomal-dominante Motoneuron-Krankheit Madras DYNC1H1-assoziierte autosomal-dominante im Kindesalter beginnende proximale spinale Muskelatrophie Desmin-abhängige Myopathie mit Mallory Körperchen-ähnlichen Einschlüssen Vakuoläre Myopathie mit Proteinaggregaten des sarkoplasmatischen Retikulums Schwartz-Jampel-Syndrom Muskeldystrophie, megakoniale kongenitale Neuropathy, motorische, distale, hereditäre, autosomal-rezessive Myopathie, letale, kongenitale, Typ Compton-North Riboflavin-Transporter-Defizienz Sphäroidkörper-Myopathie Neuropathy, motorische, distale, hereditäre, autosomal-dominante Ionenkanalkrankheit, muskuläre Amyotrophe Lateralsklerose Muskeldystrophie, kongenitale, Typ 1A Hereditäre Einschlusskörperchenmyopathie - Gelenkkontrakturen - Ophthalmoplegie Fingerprint-Body-Myopathie Distale Myopathie mit Beteiligung der posterioren Bein- und anterioren Handmuskulatur Neuropathie, distale hereditäre motorische, Typ 1 Emery-Dreifuss Muskeldystrophie Kongenitale benigne spinale Muskelatrophie, autosomal-dominante Form O'Sullivan-McLeod-Syndrom Duchenne- und Becker-Muskeldystrophie Spinale Atrophie-Ophthalmoplegie-Pyramidenbahn-Symptomatik-Syndrom Isaacs-Syndrom Gliedergürtelmuskeldystrophie Reducing-Body-Myopathie Rippling-Muskel-Krankheit Native-American-Myopathie Zebra-Körperchen-Myopathie Corpus callosum-Agenesie-Neuropathie-Syndrom KLHL9-abhängige distale Myopathie mit Beginn in der Kindheit Paralyse, periodische thyreotoxische Muskeldystrophie, fazio-skapulo-humerale Spinale Muskelatrophie, proximale, Typ 1 Muskeldystrophie, kongenitale Morvan-Syndrom Muskeldystrophie Myxofibrosarkom Muskeldystrophie, okulopharyngeale Myopathie, kongenitale Skelettmuskel-Krankheit Rigid-Spine-Syndrom Neuropathie, distale hereditäre motorische, Typ 2 Paralyse, hypokaliämische periodische Filaminopathie, muskuläre Myofibromatose, infantile Steinert myotonic dystrophy Hyperkalemic periodic paralysis Genetic skeletal muscle disease Tubular aggregate myopathy Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome Paramyotonia congenita of Von Eulenburg Distal myopathy with anterior tibial onset Juvenile amyotrophic lateral sclerosis Juvenile polymyositis Ullrich congenital muscular dystrophy Acquired skeletal muscle disease Finnish upper limb-onset distal myopathy Congenital muscular dystrophy type 1B Progressive muscular dystrophy Idiopathic inflammatory myopathy Distal hereditary motor neuropathy type 5 Metabolic myopathy Oculopharyngodistal myopathy Myotonic dystrophy Congenital muscular dystrophy with integrin alpha-7 deficiency Malignant hyperthermia of anesthesia Distal myopathy with early respiratory muscle involvement Hereditary myopathy with lactic acidosis due to ISCU deficiency Distal spinal muscular atrophy type 3 Autosomal recessive distal myopathy Brody myopathy Hereditary continuous muscle fiber activity Neuromuscular junction disease Autosomal dominant distal myopathy Tel Hashomer camptodactyly syndrome Acquired neuromuscular junction disease Distal anoctaminopathy Lambert-Eaton myasthenic syndrome Distal hereditary motor neuropathy, Jerash type Congenital myopathy with excess of thin filaments Genetic neuromuscular junction disease Non-dystrophic myopathy Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome Distal nebulin myopathy Alpha-crystallinopathy Desminopathy Cap myopathy X-linked distal spinal muscular atrophy type 3 Late-onset distal myopathy, Markesbery-Griggs type Motor neuron disease Non-dystrophic myopathy with collagen 6 anomaly Distal myotilinopathy Congenital muscular dystrophy with hyperlaxity Eosinophilic fasciitis Genetic motor neuron disease Miyoshi myopathy Congenital myopathy with cores Congenital muscular dystrophy due to LMNA mutation Presynaptic congenital myasthenic syndromes Postsynaptic congenital myasthenic syndromes Inflammatory myopathy with abundant macrophages Cylindrical spirals myopathy Myotonia permanens Myotonia fluctuans Acquired motor neuron disease Inclusion myopathy Synaptic congenital myasthenic syndromes Myopathy with hexagonally cross-linked tubular arrays Acetazolamide-responsive myotonia Spinal muscular atrophy with respiratory distress type 1 King-Denborough syndrome Hereditary inclusion body myopathy type 4 Autosomal dominant proximal spinal muscular atrophy Neurogenic scapuloperoneal syndrome, Kaeser type Idiopathic eosinophilic myositis Myasthenia gravis Autosomal recessive myogenic arthrogryposis multiplex congenita Intellectual disability-developmental delay-contractures syndrome Congenital myasthenic syndrome Trichinellosis Andersen-Tawil syndrome Genetic periodic paralysis Macrophagic myofasciitis Myofibrillar myopathy Poliomyelitis Juvenile myasthenia gravis Muscular lipidosis Centronuclear myopathy Polymyositis Neuromuscular disease Juvenile primary lateral sclerosis Muscular glycogenosis Adult-onset myasthenia gravis Central core disease Alveolar rhabdomyosarcoma Distal myopathy Infantile-onset X-linked spinal muscular atrophy Vocal cord and pharyngeal distal myopathy Embryonal rhabdomyosarcoma Inclusion body myopathy with Paget disease of bone and frontotemporal dementia GNE myopathy Fetal akinesia-cerebral and retinal hemorrhage syndrome Distal myopathy, Welander type Transient neonatal myasthenia gravis Congenital myopathy, Paradas type X-linked myopathy with postural muscle atrophy Proximal myotonic myopathy Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Nemaline myopathy Distal hereditary motor neuropathy type 7 Tibial muscular dystrophy Arthrogryposis due to muscular dystrophy Bethlem muscular dystrophy Inclusion body myositis Myotonic syndrome X-linked myopathy with excessive autophagy Potassium-aggravated myotonia Hereditary myopathy with early respiratory failure Periodic paralysis Intellectual disability-myopathy-short stature-endocrine defect syndrome Infantile-onset ascending hereditary spastic paralysis Autosomal dominant spastic paraplegia type 17 Bulbospinal muscular atrophy of childhood Thomsen and Becker disease Pontocerebellar hypoplasia type 2 Bulbospinal muscular atrophy Proximal spinal muscular atrophy Congenital myotonia Kennedy disease Pontocerebellar hypoplasia type 1 Overlap myositis Bulbospinal muscular atrophy of adult Muscular dystrophy, Selcen type Immune-mediated necrotizing myopathy Congenital fibrosis of extraocular muscles Laing early-onset distal myopathy Postpoliomyelitis syndrome Rippling muscle disease with myasthenia gravis Generalized bulbospinal muscular atrophy Monomelic amyotrophy Congenital myasthenic syndromes with glycosylation defect Muscular tumor Autosomal recessive lower motor neuron disease with childhood onset Antisynthetase syndrome Infectious, fungal or parasitic myopathy Cyprus facial-neuromusculoskeletal syndrome Proximal spinal muscular atrophy type 3 Proximal spinal muscular atrophy type 2 Dermatomyositis Proximal spinal muscular atrophy type 4 Viral myositis