SE-ATLAS

Duchenne- und Becker-Muskeldystrophie Gliedergürtelmuskeldystrophie Gliedergürtelmuskeldystrophie, autosomale-dominante Gliedergürtelmuskeldystrophie, autosomale-rezessive Paramyotonia congenita Eulenburg Muskeldystrophie Typ Duchenne Muskeldystrophie Typ Becker Myotone Dystrophie Symptomatische Form der Muskeldystrophie Duchenne und Becker in weiblichen Trägerinnen Myotonie, kongenitale Myotonie, Kalium-sensitive Myotones Syndrom Morvan-Syndrom Neuromuskuläre Krankheit Spinale Muskelatrophie-progressive Myoklonusepilepsie-Syndrom Amyotrophe Lateralsklerose Kamptokormie, idiopathische Genetisch bedingte Krankheit der Skelettmuskeln Erworbene Krankheit der Skelettmuskeln Hereditäre Spastische Paralyse, aufsteigende, des frühen Kindesalters Progressive muscular atrophy Juvenile primary lateral sclerosis Progressive muscular dystrophy Juvenile amyotrophic lateral sclerosis Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Non-dystrophic myopathy Proximal spinal muscular atrophy Macrophagic myofasciitis Muscular dystrophy-white matter spongiosis syndrome Distal myopathy Autosomal dominant proximal spinal muscular atrophy Poliomyelitis Thomsen and Becker disease Bulbospinal muscular atrophy Cyprus facial-neuromusculoskeletal syndrome Infantile-onset X-linked spinal muscular atrophy Intellectual disability-developmental delay-contractures syndrome Muscular tumor Infectious, fungal or parasitic myopathy Monomelic amyotrophy Myotonia fluctuans Neurogenic scapuloperoneal syndrome, Kaeser type Muscular dystrophy Hypokalemic periodic paralysis Hyperkalemic periodic paralysis Isaacs syndrome Autosomal dominant childhood-onset proximal spinal muscular atrophy Amyotrophic lateral sclerosis type 4 Neuromuscular junction disease Genetic neuromuscular junction disease Motor neuron disease Acquired motor neuron disease Congenital muscular dystrophy Tel Hashomer camptodactyly syndrome Distal hereditary motor neuropathy Postpoliomyelitis syndrome Periodic paralysis Madras motor neuron disease Idiopathic dropped head syndrome Scapuloperoneal spinal muscular atrophy Myotonia permanens Acetazolamide-responsive myotonia Malignant hyperthermia of anesthesia Skeletal muscle disease Andersen-Tawil syndrome Idiopathic inflammatory myopathy Muscular channelopathy Periodic paralysis with transient compartment-like syndrome Acquired neuromuscular junction disease Genetic motor neuron disease Congenital myopathy Juvenile dermatomyositis Genetic periodic paralysis