SE-ATLAS

Andersen-Tawil syndrome Congenital myasthenic syndrome Trichinellosis Macrophagic myofasciitis Muscular lipidosis Myofibrillar myopathy Poliomyelitis Centronuclear myopathy Polymyositis Neuromuscular disease Adult-onset myasthenia gravis Distal myopathy Embryonal rhabdomyosarcoma Infantile-onset X-linked spinal muscular atrophy Vocal cord and pharyngeal distal myopathy Alveolar rhabdomyosarcoma Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Transient neonatal myasthenia gravis GNE myopathy Juvenile primary lateral sclerosis Muscular glycogenosis Inclusion body myopathy with Paget disease of bone and frontotemporal dementia Distal myopathy, Welander type Juvenile myasthenia gravis Congenital myopathy, Paradas type Distal hereditary motor neuropathy type 7 X-linked myopathy with postural muscle atrophy Proximal myotonic myopathy Nemaline myopathy Hereditary myopathy with early respiratory failure Tibial muscular dystrophy Myotonic syndrome Arthrogryposis due to muscular dystrophy Bethlem muscular dystrophy X-linked myopathy with excessive autophagy Inclusion body myositis Fetal akinesia-cerebral and retinal hemorrhage syndrome Potassium-aggravated myotonia Bulbospinal muscular atrophy Intellectual disability-myopathy-short stature-endocrine defect syndrome Infantile-onset ascending hereditary spastic paralysis Congenital myotonia Thomsen and Becker disease Autosomal dominant spastic paraplegia type 17 Pontocerebellar hypoplasia type 2 Proximal spinal muscular atrophy Bulbospinal muscular atrophy of adult Muscular dystrophy, Selcen type Immune-mediated necrotizing myopathy Pontocerebellar hypoplasia type 1 Kennedy disease Bulbospinal muscular atrophy of childhood Periodic paralysis Muscular tumor Congenital fibrosis of extraocular muscles Generalized bulbospinal muscular atrophy Laing early-onset distal myopathy Congenital myasthenic syndromes with glycosylation defect Overlap myositis Postpoliomyelitis syndrome Monomelic amyotrophy Infectious, fungal or parasitic myopathy Antisynthetase syndrome Rippling muscle disease with myasthenia gravis Cyprus facial-neuromusculoskeletal syndrome Proximal spinal muscular atrophy type 3 Proximal spinal muscular atrophy type 2 Viral myositis Dermatomyositis Proximal spinal muscular atrophy type 4 Autosomal recessive lower motor neuron disease with childhood onset Adult-onset distal myopathy due to VCP mutation Focal myositis Bacterial myositis Juvenile idiopathic inflammatory myopathy Myosclerosis Primary lateral sclerosis Idiopathic camptocormia Fungal myositis Parasitic myositis Early-onset myopathy with fatal cardiomyopathy Juvenile overlap myositis Myosin storage myopathy Autosomal dominant childhood-onset proximal spinal muscular atrophy Rhabdomyosarcoma Young adult-onset distal hereditary motor neuropathy Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome Muscular dystrophy-white matter spongiosis syndrome Spinal muscular atrophy associated with central nervous system anomaly Juvenile dermatomyositis Congenital muscular dystrophy due to dystroglycanopathy Autosomal dominant adult-onset proximal spinal muscular atrophy Benign Samaritan congenital myopathy Madras motor neuron disease BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy Lower motor neuron syndrome with late-adult onset Congenital fiber-type disproportion myopathy Amyotrophic lateral sclerosis type 4 Metabolic myopathy due to lactate transporter defect DYNC1H1-related autosomal dominant childhood-onset proximal spinal muscular atrophy Spheroid body myopathy Desmin-related myopathy with Mallory body-like inclusions Congenital lethal myopathy, Compton-North type Riboflavin transporter deficiency Alpha-B crystallin-related late-onset myopathy Megaconial congenital muscular dystrophy Schwartz-Jampel syndrome Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome Autosomal dominant distal hereditary motor neuropathy Amyotrophic lateral sclerosis Laminin subunit alpha 2-related congenital muscular dystrophy Muscular channelopathy Fingerprint body myopathy Autosomal recessive distal hereditary motor neuropathy Isaacs syndrome Emery-Dreifuss muscular dystrophy Distal myopathy with posterior leg and anterior hand involvement Autosomal dominant congenital benign spinal muscular atrophy Spinal atrophy-ophthalmoplegia-pyramidal syndrome Rippling muscle disease Duchenne and Becker muscular dystrophy O'Sullivan-McLeod syndrome Limb-girdle muscular dystrophy Native American myopathy Zebra body myopathy Distal hereditary motor neuropathy type 1 Reducing body myopathy Congenital muscular dystrophy Thyrotoxic periodic paralysis Proximal spinal muscular atrophy type 1 Distal hereditary motor neuropathy type 2 Juvenile amyotrophic lateral sclerosis Corpus callosum agenesis-neuronopathy syndrome Rigid spine syndrome Skeletal muscle disease Facioscapulohumeral dystrophy Morvan syndrome KLHL9-related early-onset distal myopathy Oculopharyngeal muscular dystrophy Genetic skeletal muscle disease Distal myopathy with anterior tibial onset Hypokalemic periodic paralysis Muscular dystrophy Infantile myofibromatosis Congenital myopathy Muscle filaminopathy Myxofibrosarcoma Hyperkalemic periodic paralysis Steinert myotonic dystrophy Tubular aggregate myopathy Acquired skeletal muscle disease Juvenile polymyositis Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome Paramyotonia congenita of Von Eulenburg Idiopathic inflammatory myopathy Ullrich congenital muscular dystrophy Congenital muscular dystrophy type 1B Myopathie distale avec atteinte initiale des membres supérieurs, type finlandais Neuropathie motrice distale héréditaire type 5 Dystrophie myotonique Myopathie d'origine métabolique Anoctaminopathie distale Dystrophie musculaire congénitale par déficit en intégrine alpha-7 Hyperthermie maligne de l'anesthésie Myopathie oculo-pharyngo-distale Myopathie distale avec atteinte respiratoire précoce Dystrophie musculaire progressive Myopathie héréditaire avec acidose lactique par déficit en ISCU Maladie de la jonction neuromusculaire Amyotrophie spinale distale type 3 Myopathie distale autosomique dominante Myopathie de Brody Activité continue familiale de la fibre musculaire Camptodactylie de Tel Hashomer Maladie génétique de la jonction neuromusculaire Myopathie congénitale avec excès de filaments fins Maladie acquise de la jonction neuromusculaire Syndrome myasthénique de Lambert-Eaton Syndrome de neuropathie périphérique-myopathie-raucité de la voix-surdité Myopathie distale autosomique récessive Myopathie non dystrophique avec anomalie du collag�ne 6 Dystrophie musculaire congénitale avec hyperlaxité Myotilinopathie distale Alpha-cristallinopathie Neuropathie motrice distale héréditaire type Jerash Myopathie distale précoce associée à la nébuline Myopathies non dystrophiques Desminopathie Myopathie inflammatoire avec abondance de macrophages Syndromes myasthéniques congénitaux post-synaptiques Maladie du motoneurone Fasciite à éosinophiles Myopathie distale tardive type Markesbery-Griggs Syndromes myasthéniques congénitaux synaptiques Myopathie à casquette Maladie acquise du motoneurone Myopathie distale type Miyoshi Myopathie à inclusion Atrophie musculaire spinale distale liée à l'X type 3 Maladie génétique du motoneurone Syndromes myasthéniques congénitaux pré-synaptiques Myotonie permanente Myotonie fluctuante Myopathie congénitale avec cores Dystrophie musculaire congénitale due à une mutation de LMNA Myotonie sensible à l'acétazolamide Myopathie à spirales cylindriques Syndrome scapulo-péronier neurogénique type Kaeser Amyotrophie spinale proximale autosomique dominante Amyotrophie spinale avec détresse respiratoire type 1 Myopathie à corps d'inclusion héréditaire type 4 Myopathie avec configuration hexagonale des tubules Myosite éosinophile idiopathique Syndrome de King-Denborough Paralysie périodique génétique Arthrogrypose multiple congénitale myogénique autosomique récessive Myasthénie auto-immune Syndrome de déficience intellectuelle-retard de développement-contractures