SE-ATLAS

Spinale Muskelatrophie, proximale, Typ 1 Emery-Dreifuss Muskeldystrophie Gliedergürtelmuskeldystrophie, autosomal-dominante, Typ 1A Calpain-3-assoziierte Gliedergürtelmuskeldystrophie R1 Dysferlin-assoziierte Gliedergürtelmuskeldystrophie R2 Muskeldystrophie, fazio-skapulo-humerale Muskeldystrophie, okulopharyngeale Myotone Dystrophie Steinert Carnitin-Palmitoyl-Transferase II-Mangel Carnitin-Mangel, primärer systemischer Amyotrophe Lateralsklerose Mitochondriale Myopathie - Laktatazidose - Schwerhörigkeit Paralyse, normokaliämische periodische Paralyse, hypokaliämische periodische Paralyse, hyperkaliämische periodische Paramyotonia congenita Eulenburg Hereditäre spastische Paraplegie 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 Chronic inflammatory demyelinating polyneuropathy Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy Proximal spinal muscular atrophy type 4 Nemaline myopathy Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5 Lipid storage disease 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