SE-ATLAS

Myopathie distale de l'adulte due à des mutations de VCP Myosite parasitaire Myopathie inflammatoire idiopathique juvénile Myosite bactérienne Myosite fongique Myopathie précoce avec cardiomyopathie létale Myopathie avec surcharge en myosine Rhabdomyosarcome Neuropathie motrice distale héréditaire de l'adulte jeune Syndrome de Richieri-Costa-da Silva Dystrophie musculaire congénitale due à une dystroglycanopathie 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 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 Myopathie avec surcharge en desmine et inclusions de corps de Mallory Amyotrophie spinale proximale autosomique dominante de l'enfance associée à DYNC1H1 Myopathie vacuolaire avec agrégation de protéines du réticulum sarcoplasmique Myopathie létale congénitale type Compton-North Neuropathie motrice distale héréditaire autosomique dominante Sclérose latérale amyotrophique Dystrophie musculaire congénitale liée à la sous-unité alpha 2 de la laminine Dystrophie musculaire d'Emery-Dreifuss Syndrome d'Isaacs Syndrome d'atrophie spinale-ophtalmoplégie-syndrome pyramidal Dystrophie musculaire de Duchenne et Becker Myopathie à corps réducteurs Rippling muscle disease Myopathie amérindienne Myopathie distale précoce associée à KLHL9 Paralysie périodique thyrotoxique Amyotrophie spinale proximale type 1 Syndrome de Morvan Dystrophie musculaire Myopathie congénitale Dystrophie musculaire oculo-pharyngée Skeletal muscle disease Rigid spine syndrome Infantile myofibromatosis Hyperkalemic periodic paralysis Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome Paramyotonia congenita of Von Eulenburg Ullrich congenital muscular dystrophy Acquired skeletal muscle disease Finnish upper limb-onset distal myopathy Progressive muscular dystrophy Distal myopathy with early respiratory muscle involvement Hereditary myopathy with lactic acidosis due to ISCU deficiency Distal spinal muscular atrophy type 3 Hereditary continuous muscle fiber activity Brody myopathy Autosomal dominant distal myopathy Congenital myopathy with excess of thin filaments Distal nebulin myopathy Alpha-crystallinopathy Cap myopathy Late-onset distal myopathy, Markesbery-Griggs type Motor neuron disease Non-dystrophic myopathy with collagen 6 anomaly Distal myotilinopathy Eosinophilic fasciitis Miyoshi myopathy Congenital myopathy with cores Presynaptic congenital myasthenic syndromes Myotonia permanens Acquired motor neuron disease Inclusion myopathy Acetazolamide-responsive myotonia Hereditary inclusion body myopathy type 4 Idiopathic eosinophilic myositis Autosomal recessive myogenic arthrogryposis multiplex congenita Congenital myasthenic syndrome Myofibrillar myopathy Juvenile myasthenia gravis Muscular glycogenosis Adult-onset myasthenia gravis Central core disease Distal myopathy Infantile-onset X-linked spinal muscular atrophy Inclusion body myopathy with Paget disease of bone and frontotemporal dementia Fetal akinesia-cerebral and retinal hemorrhage syndrome Congenital myopathy, Paradas type X-linked myopathy with postural muscle atrophy Proximal myotonic myopathy Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Nemaline myopathy Bethlem muscular dystrophy Inclusion body myositis Myotonic syndrome Potassium-aggravated myotonia Infantile-onset ascending hereditary spastic paralysis Bulbospinal muscular atrophy Proximal spinal muscular atrophy Kennedy disease Overlap myositis Bulbospinal muscular atrophy of adult Muscular dystrophy, Selcen type Rippling muscle disease with myasthenia gravis Cyprus facial-neuromusculoskeletal syndrome Proximal spinal muscular atrophy type 4 Muscular lipidosis Distal hereditary motor neuropathy type 1 Myotonia fluctuans Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome Andersen-Tawil syndrome Autosomal recessive lower motor neuron disease with childhood onset Myopathy with hexagonally cross-linked tubular arrays Generalized bulbospinal muscular atrophy Congenital muscular dystrophy Congenital myotonia Bulbospinal muscular atrophy of childhood Congenital myasthenic syndromes with glycosylation defect Megaconial congenital muscular dystrophy Autosomal dominant proximal spinal muscular atrophy Periodic paralysis Viral myositis Idiopathic inflammatory myopathy Metabolic myopathy Neuromuscular junction disease Acquired neuromuscular junction disease Genetic motor neuron disease Tel Hashomer camptodactyly syndrome Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome Distal hereditary motor neuropathy type 2 Facioscapulohumeral dystrophy X-linked distal spinal muscular atrophy type 3 Congenital muscular dystrophy with hyperlaxity Distal hereditary motor neuropathy type 7 Transient neonatal myasthenia gravis Intellectual disability-developmental delay-contractures syndrome Lambert-Eaton myasthenic syndrome Embryonal rhabdomyosarcoma Muscle filaminopathy Proximal spinal muscular atrophy type 3 Tubular aggregate myopathy Myasthenia gravis Vocal cord and pharyngeal distal myopathy GNE myopathy Desminopathy Postsynaptic congenital myasthenic syndromes Tibial muscular dystrophy Congenital muscular dystrophy with integrin alpha-7 deficiency Non-dystrophic myopathy Spheroid body myopathy Antisynthetase syndrome Arthrogryposis due to muscular dystrophy Muscular tumor Neurogenic scapuloperoneal syndrome, Kaeser type Autosomal recessive distal hereditary motor neuropathy Muscular channelopathy Genetic neuromuscular junction disease Autosomal dominant congenital benign spinal muscular atrophy Dermatomyositis Myxofibrosarcoma Limb-girdle muscular dystrophy Steinert myotonic dystrophy Distal hereditary motor neuropathy type 5 Congenital muscular dystrophy due to LMNA mutation Hereditary myopathy with early respiratory failure X-linked myopathy with excessive autophagy Juvenile polymyositis King-Denborough syndrome Alveolar rhabdomyosarcoma Corpus callosum agenesis-neuronopathy syndrome Proximal spinal muscular atrophy type 2 Juvenile amyotrophic lateral sclerosis Congenital muscular dystrophy type 1B Macrophagic myofasciitis Centronuclear myopathy Distal myopathy, Welander type Synaptic congenital myasthenic syndromes Spinal muscular atrophy with respiratory distress type 1 Madras motor neuron disease Hypokalemic periodic paralysis Trichinellosis Poliomyelitis Myosclerosis Thomsen and Becker disease O'Sullivan-McLeod syndrome Autosomal dominant spastic paraplegia type 17 Postpoliomyelitis syndrome Inflammatory myopathy with abundant macrophages Polymyositis Laing early-onset distal myopathy Schwartz-Jampel syndrome Distal myopathy with posterior leg and anterior hand involvement Genetic periodic paralysis Distal anoctaminopathy Focal myositis Genetic skeletal muscle disease Myotonic dystrophy Juvenile primary lateral sclerosis Autosomal recessive distal myopathy Zebra body myopathy Benign Samaritan congenital myopathy Primary lateral sclerosis Cylindrical spirals myopathy Lower motor neuron syndrome with late-adult onset Congenital fiber-type disproportion myopathy Intellectual disability-myopathy-short stature-endocrine defect syndrome Riboflavin transporter deficiency Infectious, fungal or parasitic myopathy Monomelic amyotrophy Idiopathic camptocormia Distal myopathy with anterior tibial onset Distal hereditary motor neuropathy, Jerash type Congenital fibrosis of extraocular muscles Oculopharyngodistal myopathy Immune-mediated necrotizing myopathy Neuromuscular disease Fingerprint body myopathy