SE-ATLAS

Ullrich congenital muscular dystrophy Proximal spinal muscular atrophy Megaconial congenital muscular dystrophy Young adult-onset distal hereditary motor neuropathy Infantile-onset X-linked spinal muscular atrophy Myotonic syndrome Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency Viral myositis Infectious, fungal or parasitic myopathy Bacterial myositis Monomelic amyotrophy Parasitic myositis Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Fungal myositis Juvenile overlap myositis Desmin-related myopathy with Mallory body-like inclusions Juvenile idiopathic inflammatory myopathy Spinal muscular atrophy associated with central nervous system anomaly Muscular dystrophy Skeletal muscle disease Isaacs syndrome Idiopathic inflammatory myopathy Autosomal recessive distal hereditary motor neuropathy Muscular channelopathy Neuromuscular junction disease Autosomal dominant congenital benign spinal muscular atrophy Spinal atrophy-ophthalmoplegia-pyramidal syndrome Genetic motor neuron disease Acquired motor neuron disease Inclusion body myopathy with Paget disease of bone and frontotemporal dementia Tel Hashomer camptodactyly syndrome Distal myopathy with anterior tibial onset Congenital lethal myopathy, Compton-North type Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome Distal hereditary motor neuropathy type 1 Thyrotoxic periodic paralysis Laminin subunit alpha 2-related congenital muscular dystrophy Distal hereditary motor neuropathy type 2 Limb-girdle muscular dystrophy Congenital muscular dystrophy due to dystroglycanopathy Facioscapulohumeral dystrophy Oculopharyngeal muscular dystrophy Distal hereditary motor neuropathy type 5 Congenital muscular dystrophy due to LMNA mutation Hereditary myopathy with early respiratory failure Distal hereditary motor neuropathy, Jerash type X-linked distal spinal muscular atrophy type 3 Idiopathic camptocormia Congenital fibrosis of extraocular muscles Congenital muscular dystrophy with hyperlaxity Distal hereditary motor neuropathy type 7 Juvenile myasthenia gravis Transient neonatal myasthenia gravis Glycogen storage disease due to acid maltase deficiency Glycogen storage disease due to muscle glycogen phosphorylase deficiency Glycogen storage disease due to muscle phosphofructokinase deficiency Intellectual disability-developmental delay-contractures syndrome Lambert-Eaton myasthenic syndrome Miyoshi myopathy Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency Myotonia fluctuans Embryonal rhabdomyosarcoma Muscle filaminopathy Proximal spinal muscular atrophy type 3 Kennedy disease Glycogen storage disease due to muscle beta-enolase deficiency Morvan syndrome Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome Infantile myofibromatosis Tubular aggregate myopathy Juvenile amyotrophic lateral sclerosis Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Congenital muscular dystrophy type 1B Congenital myasthenic syndrome Oculopharyngodistal myopathy Macrophagic myofasciitis Myofibrillar myopathy Centronuclear myopathy Distal myopathy Vocal cord and pharyngeal distal myopathy Congenital myopathy with excess of thin filaments GNE myopathy Distal myopathy, Welander type Desminopathy Proximal myotonic myopathy Nemaline myopathy Alpha-crystallinopathy Postsynaptic congenital myasthenic syndromes Myosclerosis Late-onset distal myopathy, Markesbery-Griggs type Early-onset myopathy with fatal cardiomyopathy Thomsen and Becker disease Spinal muscular atrophy with respiratory distress type 1 Cyprus facial-neuromusculoskeletal syndrome Polyglucosan body myopathy type 1 O'Sullivan-McLeod syndrome Native American myopathy Autosomal recessive limb-girdle muscular dystrophy Autosomal dominant limb-girdle muscular dystrophy Autosomal dominant spastic paraplegia type 17 Madras motor neuron disease Congenital myopathy, Paradas type Metabolic myopathy due to lactate transporter defect Hypokalemic periodic paralysis Motor neuron disease Myxofibrosarcoma Duchenne and Becker muscular dystrophy Steinert myotonic dystrophy Distal spinal muscular atrophy type 3 X-linked myopathy with postural muscle atrophy Adult-onset myasthenia gravis Glycogen storage disease due to glycogen debranching enzyme deficiency Glycogen storage disease due to glycogen branching enzyme deficiency X-linked myopathy with excessive autophagy Juvenile polymyositis Myotonia permanens King-Denborough syndrome Autosomal dominant adult-onset proximal spinal muscular atrophy Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome DYNC1H1-related autosomal dominant childhood-onset proximal spinal muscular atrophy Myosin storage myopathy Corpus callosum agenesis-neuronopathy syndrome Proximal spinal muscular atrophy type 2 Hyperkalemic periodic paralysis Muscular dystrophy, Selcen type Amyotrophic lateral sclerosis type 4 Polyglucosan body myopathy type 2 Glycogen storage disease due to phosphoglycerate kinase 1 deficiency Alpha-B crystallin-related late-onset myopathy Distal anoctaminopathy Laing early-onset distal myopathy Adult-onset distal myopathy due to VCP mutation Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency Focal myositis Hereditary inclusion body myopathy type 4 Glycogen storage disease due to LAMP-2 deficiency Neuromuscular disease Schwartz-Jampel syndrome Myotonic dystrophy Progressive muscular dystrophy Autosomal dominant distal myopathy Non-dystrophic myopathy Trichinellosis Spheroid body myopathy Primary lateral sclerosis Bulbospinal muscular atrophy Bulbospinal muscular atrophy of adult Generalized bulbospinal muscular atrophy Autosomal dominant childhood-onset proximal spinal muscular atrophy Congenital myopathy with cores Hereditary continuous muscle fiber activity Juvenile dermatomyositis Congenital muscular dystrophy with integrin alpha-7 deficiency Distal nebulin myopathy Rhabdomyosarcoma Amyotrophic lateral sclerosis Distal myopathy with posterior leg and anterior hand involvement Juvenile primary lateral sclerosis Autosomal recessive distal myopathy Non-dystrophic myopathy with collagen 6 anomaly Inclusion myopathy Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome Autosomal recessive myogenic arthrogryposis multiplex congenita Poliomyelitis Cap myopathy Cylindrical spirals myopathy Myopathy with hexagonally cross-linked tubular arrays Bulbospinal muscular atrophy of childhood Postpoliomyelitis syndrome Fetal akinesia-cerebral and retinal hemorrhage syndrome Inflammatory myopathy with abundant macrophages Idiopathic eosinophilic myositis Fingerprint body myopathy Glykogenose durch Phosphoglycerat-Mutase-Mangel Muskeldystrophie, kongenitale Rigid-Spine-Syndrom Myopathie, kongenitale, mit Fasertyp-Disproportion Myotone Dystrophie Steinert, juvenile Form Antisynthetase-Syndrom Fasziitis, eosinophile Hereditäre Myopathie mit Laktatazidose durch ISCU-Mangel Glykogenose, muskuläre Myotonie, kongenitale Arthrogrypose infolge Muskeldystrophie Neuropathy, motorische, distale, hereditäre, autosomal-dominante Glykogenose durch muskulären Phosphorylasekinase-Mangel Genetisch bedingte Krankheit der Skelettmuskeln BICD2-assoziierte proximale spinale Muskelatrophie mit Beginn im Kindesalter, autosomal-dominant Riboflavin-Transporter-Defizienz Untere Vorderhornerkrankung mit Beginn im späten Erwachsenenalter Zebra-Körperchen-Myopathie Myopathie, kongenitale Myopathie, benigne, Typ Samariter Intelligenzminderung-Myopathie-Kleinwuchs-endokrine Störung-Syndrom Myasthenische Syndrome, kongenitale, mit Glykosylierungsdefekt Spinale Muskelatrophie, proximale, autosomal-dominante Brody-Myopathie Lipidose, muskuläre Periodische Paralyse Muskeltumor Neurogenes scapulo-peroneales Syndrom Typ Kaeser Myopathie, metabolische Neuromuskuläre Übertragungsstörung, genetisch bedingte Neuromuskuläre Übertragungsstörung, erworbene Dermatomyositis Emery-Dreifuss Muskeldystrophie Spinale Muskelatrophie, proximale, Typ 1 Myotilinopathie, distale Muskeldystrophie, tibiale Myasthenische Syndrome, kongenitale synpatische Einschlusskörper-Myositis Paramyotonia congenita Eulenburg Andersen-Tawil-Syndrom Myopathie, distale, mit früher Beteiligung der Atemmuskulatur Distale Myopathie der obere Extremitäten mit Beginn im Erwachsenenalter, Finnischer Typ Rippling-Muskel-Krankheit mit Myasthenia gravis Myositis-Overlap-Syndrom Vorderhornerkrankung, autosomal-rezessive, des Kindes Muskeldystrophie - Spongiosis der weissen Gehirnmasse Reducing-Body-Myopathie Rippling-Muskel-Krankheit Hereditäre Spastische Paralyse, aufsteigende, des frühen Kindesalters Myotonia congenita, Azetazolamidempfindliche Rhabdomyosarkom, alveoläres Spinale Muskelatrophie, proximale, Typ 4 Myasthenia gravis Bethlem-Myopathie Myasthenische Syndrome, kongenitale präsynaptische Myotonie, Kalium-sensitive Polymyositis Immunvermittelte nekrotisierende Myopathie Periodische Paralyse, genetisch bedingte KLHL9-abhängige distale Myopathie mit Beginn in der Kindheit