SE-ATLAS

Acquired motor neuron disease Acquired neuromuscular junction disease Acquired skeletal muscle disease Amyotrophe Lateralsklerose Typ 4 Amyotrophic lateral sclerosis Andersen-Tawil syndrome Autosomal dominant proximal spinal muscular atrophy Bulbospinal muscular atrophy Congenital myasthenic syndrome Cyprus facial-neuromusculoskeletal syndrome Distal myopathy Genetic motor neuron disease Genetic neuromuscular junction disease Genetic periodic paralysis Genetic skeletal muscle disease Hyperkalemic periodic paralysis Hypokalemic periodic paralysis Idiopathic inflammatory myopathy Infantile-onset X-linked spinal muscular atrophy Infantile-onset ascending hereditary spastic paralysis Infectious, fungal or parasitic myopathy Intellectual disability-developmental delay-contractures syndrome Isaacs syndrome Juvenile amyotrophic lateral sclerosis Juvenile primary lateral sclerosis Kamptokormie, idiopathische Lambert-Eaton myasthenic syndrome Lateralsklerose, primäre Macrophagic myofasciitis Malignant hyperthermia of anesthesia Monomelic amyotrophy Morvan syndrome Motoneuron-Krankheit Madras Motor neuron disease Muscular channelopathy Muscular dystrophy Muscular tumor Muskeldystrophie - Spongiosis der weissen Gehirnmasse Myasthenia gravis Myotonic syndrome Neurogenic scapuloperoneal syndrome, Kaeser type Neuromuscular disease Neuromuscular junction disease Non-dystrophic myopathy Paramyotonia congenita of Von Eulenburg Periodic paralysis Poliomyelitis Postpoliomyelitis syndrome Potassium-aggravated myotonia Proximal spinal muscular atrophy Rippling muscle disease with myasthenia gravis Skeletal muscle disease Tel Hashomer camptodactyly syndrome Thomsen and Becker disease Vacuolar myopathy with sarcoplasmic reticulum protein aggregates