SE-ATLAS

Myopathie distale de l'adulte due à des mutations de VCP Myosclérose Myosite focale Myosite parasitaire Myopathie inflammatoire idiopathique juvénile Sclérose latérale primitive Myosite bactérienne Camptocormie idiopathique Myosite fongique Myopathie précoce avec cardiomyopathie létale Myopathie avec surcharge en myosine Rhabdomyosarcome Neuropathie motrice distale héréditaire de l'adulte jeune Dystrophie musculaire congénitale due à une dystroglycanopathie Syndrome de Richieri-Costa-da Silva Syndrome de dystrophie musculaire congénitale-cataracte infantile-hypogonadisme Myosite de chevauchement juvénile Amyotrophie spinale proximale autosomique dominante de l'enfance Syndrome de dystrophie musculaire-substance blanche cérébrale spongieuse Dermatomyosite juvénile Myopathie tardive associée à l'alpha-B cristalline Amyotrophie spinale associée à une malformation du système nerveux central Sclérose latérale amyotrophique type 4 Myopathie congénitale bénigne des Samaritains Myopathie congénitale avec disproportion des types de fibres musculaires Syndrome du motoneurone inférieur, forme tardive de l'adulte Myopathie métabolique par défaut de transport du lactate Amyotrophie spinale proximale autosomique dominante de l'enfance associée à BICD2 Amyotrophie spinale proximale autosomique dominante de l'adulte Maladie du motoneurone type Madras Amyotrophie spinale proximale autosomique dominante de l'enfance associée à DYNC1H1 Myopathie avec surcharge en desmine et inclusions de corps de Mallory Myopathie vacuolaire avec agrégation de protéines du réticulum sarcoplasmique Syndrome de Schwartz-Jampel Dystrophie musculaire congénitale mégaconiale Neuropathie motrice distale héréditaire autosomique récessive Myopathie létale congénitale type Compton-North Déficit en transporteur de la riboflavine Myopathie à corps sphéroïdes Neuropathie motrice distale héréditaire autosomique dominante Canalopathie musculaire Sclérose latérale amyotrophique Dystrophie musculaire congénitale liée à la sous-unité alpha 2 de la laminine Syndrome héréditaire de myopathie à corps d'inclusions-contractures articulaires-ophtalmoplégie Myopathie à empreintes digitales Myopathie distale avec atteinte des muscles postérieurs des jambes et des muscles antérieurs des mains Neuropathie motrice distale héréditaire type 1 Dystrophie musculaire d'Emery-Dreifuss Amyotrophie spinale bénigne congénitale autosomique dominante Syndrome d'O'Sullivan-McLeod Dystrophie musculaire de Duchenne et Becker Syndrome d'atrophie spinale-ophtalmoplégie-syndrome pyramidal Syndrome d'Isaacs Dystrophie musculaire des ceintures Myopathie à corps réducteurs Rippling muscle disease Myopathie amérindienne Myopathie à corps zébrés Syndrome d'agénesie du corps calleux-neuropathie Myopathie distale précoce associée à KLHL9 Paralysie périodique thyrotoxique Dystrophie facio-scapulo-humérale Amyotrophie spinale proximale type 1 Dystrophie musculaire congénitale Syndrome de Morvan Dystrophie musculaire Myxofibrosarcome Dystrophie musculaire oculo-pharyngée Myopathie congénitale Skeletal muscle disease Rigid spine syndrome Distal hereditary motor neuropathy type 2 Hypokalemic periodic paralysis Muscle filaminopathy Infantile myofibromatosis Steinert myotonic dystrophy Hyperkalemic periodic paralysis Genetic skeletal muscle disease Tubular aggregate myopathy Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome Paramyotonia congenita of Von Eulenburg Distal myopathy with anterior tibial onset Juvenile amyotrophic lateral sclerosis Juvenile polymyositis Ullrich congenital muscular dystrophy Acquired skeletal muscle disease Finnish upper limb-onset distal myopathy Congenital muscular dystrophy type 1B Progressive muscular dystrophy Idiopathic inflammatory myopathy Distal hereditary motor neuropathy type 5 Metabolic myopathy Oculopharyngodistal myopathy Myotonic dystrophy Congenital muscular dystrophy with integrin alpha-7 deficiency Malignant hyperthermia of anesthesia Distal myopathy with early respiratory muscle involvement Hereditary myopathy with lactic acidosis due to ISCU deficiency Distal spinal muscular atrophy type 3 Autosomal recessive distal myopathy Brody myopathy Hereditary continuous muscle fiber activity Neuromuscular junction disease Autosomal dominant distal myopathy Tel Hashomer camptodactyly syndrome Acquired neuromuscular junction disease Distal anoctaminopathy Lambert-Eaton myasthenic syndrome Distal hereditary motor neuropathy, Jerash type Congenital myopathy with excess of thin filaments Genetic neuromuscular junction disease Non-dystrophic myopathy Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome Distal nebulin myopathy Alpha-crystallinopathy Desminopathy Cap myopathy X-linked distal spinal muscular atrophy type 3 Late-onset distal myopathy, Markesbery-Griggs type Motor neuron disease Non-dystrophic myopathy with collagen 6 anomaly Distal myotilinopathy Congenital muscular dystrophy with hyperlaxity Eosinophilic fasciitis Genetic motor neuron disease Miyoshi myopathy Congenital myopathy with cores Congenital muscular dystrophy due to LMNA mutation Presynaptic congenital myasthenic syndromes Postsynaptic congenital myasthenic syndromes Inflammatory myopathy with abundant macrophages Cylindrical spirals myopathy Myotonia permanens Myotonia fluctuans Acquired motor neuron disease Inclusion myopathy Synaptic congenital myasthenic syndromes Myopathy with hexagonally cross-linked tubular arrays Acetazolamide-responsive myotonia Spinal muscular atrophy with respiratory distress type 1 King-Denborough syndrome Hereditary inclusion body myopathy type 4 Autosomal dominant proximal spinal muscular atrophy Neurogenic scapuloperoneal syndrome, Kaeser type Idiopathic eosinophilic myositis Myasthenia gravis Autosomal recessive myogenic arthrogryposis multiplex congenita Intellectual disability-developmental delay-contractures syndrome Congenital myasthenic syndrome Trichinellosis Andersen-Tawil syndrome Genetic periodic paralysis Macrophagic myofasciitis Myofibrillar myopathy Poliomyelitis Juvenile myasthenia gravis Muscular lipidosis Centronuclear myopathy Polymyositis Neuromuscular disease Juvenile primary lateral sclerosis Muscular glycogenosis Adult-onset myasthenia gravis Central core disease Alveolar rhabdomyosarcoma Distal myopathy Infantile-onset X-linked spinal muscular atrophy Vocal cord and pharyngeal distal myopathy Embryonal rhabdomyosarcoma Inclusion body myopathy with Paget disease of bone and frontotemporal dementia GNE myopathy Fetal akinesia-cerebral and retinal hemorrhage syndrome Distal myopathy, Welander type Transient neonatal myasthenia gravis Congenital myopathy, Paradas type X-linked myopathy with postural muscle atrophy Proximal myotonic myopathy Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Nemaline myopathy Distal hereditary motor neuropathy type 7 Tibial muscular dystrophy Arthrogryposis due to muscular dystrophy Bethlem muscular dystrophy Inclusion body myositis Myotonic syndrome X-linked myopathy with excessive autophagy Potassium-aggravated myotonia Hereditary myopathy with early respiratory failure Periodic paralysis Intellectual disability-myopathy-short stature-endocrine defect syndrome Infantile-onset ascending hereditary spastic paralysis Autosomal dominant spastic paraplegia type 17 Bulbospinal muscular atrophy of childhood Thomsen and Becker disease Pontocerebellar hypoplasia type 2 Bulbospinal muscular atrophy Proximal spinal muscular atrophy Congenital myotonia Kennedy disease Pontocerebellar hypoplasia type 1 Overlap myositis Bulbospinal muscular atrophy of adult Muscular dystrophy, Selcen type Immune-mediated necrotizing myopathy Congenital fibrosis of extraocular muscles Laing early-onset distal myopathy Postpoliomyelitis syndrome Rippling muscle disease with myasthenia gravis Generalized bulbospinal muscular atrophy Monomelic amyotrophy Congenital myasthenic syndromes with glycosylation defect Muscular tumor Autosomal recessive lower motor neuron disease with childhood onset Antisynthetase syndrome Infectious, fungal or parasitic myopathy Cyprus facial-neuromusculoskeletal syndrome Proximal spinal muscular atrophy type 3 Proximal spinal muscular atrophy type 2 Dermatomyositis Proximal spinal muscular atrophy type 4 Viral myositis