SE-ATLAS

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