SE-ATLAS

Lower motor neuron syndrome with late-adult onset Progressive muscular atrophy Alpha-B crystallin-related late-onset myopathy Desmin-related myopathy with Mallory body-like inclusions Schwartz-Jampel syndrome Scapuloperoneal spinal muscular atrophy Riboflavin transporter deficiency Amyotrophic lateral sclerosis Distal myopathy with posterior leg and anterior hand involvement Spheroid body myopathy Duchenne and Becker muscular dystrophy Autosomal dominant congenital benign spinal muscular atrophy Emery-Dreifuss muscular dystrophy Limb-girdle muscular dystrophy Isaacs syndrome Rippling muscle disease Facioscapulohumeral dystrophy Muscular dystrophy Distal myopathy with anterior tibial onset Distal hereditary motor neuropathy Steinert myotonic dystrophy Paramyotonia congenita of Von Eulenburg Becker muscular dystrophy Progressive muscular dystrophy Duchenne muscular dystrophy Myotonic dystrophy Hereditary continuous muscle fiber activity Brody myopathy Distal anoctaminopathy Lambert-Eaton myasthenic syndrome Alpha-crystallinopathy Desminopathy Late-onset distal myopathy, Markesbery-Griggs type X-linked distal spinal muscular atrophy type 3 Distal myotilinopathy Inclusion myopathy Miyoshi myopathy Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Myotonia fluctuans Idiopathic eosinophilic myositis Acetazolamide-responsive myotonia Myotonia permanens Adult-onset myasthenia gravis Myasthenia gravis Autosomal dominant proximal spinal muscular atrophy Macrophagic myofasciitis Myofibrillar myopathy Juvenile myasthenia gravis Transient neonatal myasthenia gravis Proximal myotonic myopathy Myotonic syndrome Bethlem muscular dystrophy Inclusion body myositis Myopathie mit exzessiver Autophagie, X-chromosomal Myotonie, kongenitale Myotonie, Kalium-sensitive Myotonia congenita Typ Thomsen und Becker Spinale Muskelatrophie, proximale Muskeldystrophie Typ Selcen Kennedy-Krankheit Pyomyositis Myositis, virale Myopathie bei infektiösen und parasitären Krankheiten Spinale Muskelatrophie, proximale, Typ 4 Myositis, fokale Myositis bei Pilzerkrankungen Lateralsklerose, primäre Myositis, parasitäre Myopathie mit fataler Kardiomyopathie, früh-beginnende Form Distale Myopathie durch VCP-Genmutation mit Beginn im Erwachsenenalter Myosklerose