SE-ATLAS

Acetazolamide-responsive myotonia Adult-onset distal myopathy due to VCP mutation Adult-onset myasthenia gravis Alpha-B crystallin-related late-onset myopathy Alpha-crystallinopathy Amyotrophic lateral sclerosis Autosomal dominant congenital benign spinal muscular atrophy Autosomal dominant proximal spinal muscular atrophy Becker muscular dystrophy Bethlem muscular dystrophy Brody myopathy Congenital myotonia Desmin-related myopathy with Mallory body-like inclusions Desminopathy Distal anoctaminopathy Distal hereditary motor neuropathy Distal myopathy with anterior tibial onset Distal myopathy with posterior leg and anterior hand involvement Distal myotilinopathy Duchenne and Becker muscular dystrophy Duchenne muscular dystrophy Early-onset myopathy with fatal cardiomyopathy Emery-Dreifuss muscular dystrophy Facioscapulohumeral dystrophy Focal myositis Fungal myositis Hereditary continuous muscle fiber activity Idiopathic eosinophilic myositis Inclusion body myositis Inclusion myopathy Infectious, fungal or parasitic myopathy Isaacs syndrome Juvenile myasthenia gravis Kennedy disease Lambert-Eaton myasthenic syndrome Late-onset distal myopathy, Markesbery-Griggs type Limb-girdle muscular dystrophy Lower motor neuron syndrome with late-adult onset Macrophagic myofasciitis Miyoshi myopathy Muscular dystrophy Muscular dystrophy, Selcen type Myasthenia gravis Myofibrillar myopathy Myosclerosis Myotonia fluctuans Myotonia permanens Myotonic dystrophy Myotonic syndrome Paramyotonia congenita of Von Eulenburg Parasitic myositis Potassium-aggravated myotonia Primary lateral sclerosis Progressive muscular atrophy Progressive muscular dystrophy Proximal myotonic myopathy Proximal spinal muscular atrophy Proximal spinal muscular atrophy type 4 Pyomyositis Riboflavin transporter deficiency Rippling muscle disease Scapuloperoneal spinal muscular atrophy Schwartz-Jampel syndrome Spheroid body myopathy Steinert myotonic dystrophy Thomsen and Becker disease Transient neonatal myasthenia gravis Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Viral myositis X-linked distal spinal muscular atrophy type 3 X-linked myopathy with excessive autophagy