SE-ATLAS

Distal myopathy Thomsen and Becker disease Hypokalemic periodic paralysis Hyperkalemic periodic paralysis Paramyotonia congenita of Von Eulenburg Dysferlin-related limb-girdle muscular dystrophy R2 Oculopharyngeal muscular dystrophy Steinert myotonic dystrophy Carnitine palmitoyltransferase II deficiency Systemic primary carnitine deficiency Mitochondrial myopathy-lactic acidosis-deafness syndrome Normokalemic periodic paralysis Glycogen storage disease due to aldolase A deficiency Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3 Spinocerebellar ataxia type 3 Spinocerebellar ataxia type 6 Fragile X-associated tremor/ataxia syndrome Myasthenia gravis Becker muscular dystrophy Duchenne muscular dystrophy FKRP-related limb-girdle muscular dystrophy R9 Emery-Dreifuss muscular dystrophy Autosomal dominant limb-girdle muscular dystrophy type 1A Calpain-3-related limb-girdle muscular dystrophy R1 Central core disease Polymyositis Nemaline myopathy Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5 Lipid storage disease Immune-mediated necrotizing myopathy Glycogen storage disease due to acid maltase deficiency Glycogen storage disease due to glycogen branching enzyme deficiency Chronic inflammatory demyelinating polyneuropathy Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy Proximal spinal muscular atrophy type 1 Facioscapulohumeral dystrophy Amyotrophic lateral sclerosis Hereditary spastic paraplegia Pediatric multiple sclerosis Centronuclear myopathy DNAJB6-related limb-girdle muscular dystrophy D1 Delta-sarcoglycan-related limb-girdle muscular dystrophy R6 Dermatomyositis Proximal spinal muscular atrophy type 4 Proximal myotonic myopathy Friedreich ataxia Kennedy disease Inclusion body myositis Spinal muscular atrophy with respiratory distress type 1 Glycogen storage disease due to glucose-6-phosphatase deficiency Glycogen storage disease due to glycogen debranching enzyme deficiency Glycogen storage disease due to muscle glycogen phosphorylase deficiency Beta-sarcoglycan-related limb-girdle muscular dystrophy R4