SE-ATLAS

Proximal spinal muscular atrophy type 1 Emery-Dreifuss muscular dystrophy Autosomal dominant limb-girdle muscular dystrophy type 1A Calpain-3-related limb-girdle muscular dystrophy R1 Dysferlin-related limb-girdle muscular dystrophy R2 Facioscapulohumeral dystrophy Oculopharyngeal muscular dystrophy Steinert myotonic dystrophy Carnitine palmitoyltransferase II deficiency Systemic primary carnitine deficiency Amyotrophic lateral sclerosis Mitochondrial myopathy-lactic acidosis-deafness syndrome Normokalemic periodic paralysis Hypokalemic periodic paralysis Hyperkalemic periodic paralysis Paramyotonia congenita of Von Eulenburg Hereditary spastic paraplegia Pediatric multiple sclerosis 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 Centronuclear myopathy DNAJB6-related limb-girdle muscular dystrophy D1 Central core disease Distal myopathy Delta-sarcoglycan-related limb-girdle muscular dystrophy R6 Polymyositis Proximal myotonic myopathy Friedreich ataxia Kennedy disease Inclusion body myositis Thomsen and Becker disease Immune-mediated necrotizing myopathy Glycogen storage disease due to acid maltase deficiency Glycogen storage disease due to glycogen branching enzyme deficiency Polyradiculonévrite inflammatoire démyélinisante chronique Ophtalmoplégie externe progressive chronique de l'adulte avec myopathie mitochondriale Amyotrophie spinale proximale type 4 Myopathie à némaline Dystrophie musculaire des ceintures liée au gamma-sarcoglycane R5 Maladie de surchage lipidique Amyotrophie spinale avec détresse respiratoire type 1 Glycogénose par déficit en glucose-6-phosphatase Glycogénose par déficit en enzyme débranchante Glycogénose par déficit en glycogène phosphorylase musculaire Dystrophie musculaire des ceintures liée au bêta-sarcoglycane R4