SE-ATLAS

Syndrome myasthénique congénital Trichinellose Myofasciite à macrophages Lipidose musculaire Myopathie myofibrillaire Poliomyélite Myopathie centronucléaire Polymyosite Myasthénie auto-immune de l'adulte Myopathie distale Amyotrophie spinale infantile liée à l'X Myopathie distale avec faiblesse des cordes vocales Rhabdomyosarcome alvéolaire Myopathie autosomique récessive avec ophtalmoplégie externe de l'enfant Myasthénie auto-immune transitoire du nouveau-né Myopathie liée à GNE Glycogénose musculaire Myopathie distale type Welander Myasthénie auto-immune juvénile Myopathie congénitale type Paradas Myopathie myotonique proximale Myopathie à némaline Myopathie héréditaire avec atteinte respiratoire précoce Dystrophie musculaire tibiale Syndrome myotonique Dystrophie musculaire de Bethlem Myopathie avec autophagie excessive liée à l'X Myosite à inclusions Syndrome d'akinésie foetale-hémorragies cérébrales et rétiniennes Myotonie aggravée par le potassium Amyotrophie bulbospinale Paralysie spastique infantile ascendante héréditaire Myotonie congénitale de Thomsen et Becker Paraplégie spastique autosomique dominante type 17 Amyotrophie spinale proximale Amyotrophie bulbospinale de l'adulte Dystrophie musculaire type Selcen Myopathie nécrosante à médiation auto-immune Hypoplasie pontocérébelleuse type 1 Amyotrophie bulbospinale de l'enfant Paralysie périodique Tumeur musculaire Fibrose congénitale des muscles oculo-moteurs Amyotrophie spinale généralisée Syndromes myasthéniques congénitaux par défaut de glycosylation Syndrome post-poliomyélite Amyotrophie monomélique Myopathie infectieuse, fongique ou parasitaire Syndrome des antisynthétases Rippling muscle disease avec myasthenia gravis Syndrome neuro-musculo-squelettique type chypriote Amyotrophie spinale proximale type 3 Myosite virale Dermatomyosite Amyotrophie spinale proximale type 4 Myopathie distale de l'adulte due à des mutations de VCP Myosite focale Myosclérose Sclérose latérale primitive Camptocormie idiopathique Myosite fongique Myosite parasitaire Myopathie précoce avec cardiomyopathie létale Myosite de chevauchement juvénile Amyotrophie spinale proximale autosomique dominante de l'enfance Rhabdomyosarcome Neuropathie motrice distale héréditaire de l'adulte jeune Syndrome de dystrophie musculaire congénitale-cataracte infantile-hypogonadisme Syndrome de dystrophie musculaire-substance blanche cérébrale spongieuse Amyotrophie spinale associée à une malformation du système nerveux central Dermatomyosite juvénile Dystrophie musculaire congénitale due à une dystroglycanopathie Amyotrophie spinale proximale autosomique dominante de l'adulte Maladie du motoneurone type Madras BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy Metabolic myopathy due to lactate transporter defect DYNC1H1-related autosomal dominant childhood-onset proximal spinal muscular atrophy Desmin-related myopathy with Mallory body-like inclusions Spheroid body myopathy Congenital lethal myopathy, Compton-North type Riboflavin transporter deficiency Megaconial congenital muscular dystrophy Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome Autosomal dominant distal hereditary motor neuropathy Amyotrophic lateral sclerosis 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 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 Distal hereditary motor neuropathy type 2 Juvenile amyotrophic lateral sclerosis Corpus callosum agenesis-neuronopathy syndrome Skeletal muscle disease Rigid spine syndrome Facioscapulohumeral dystrophy Morvan syndrome Distal myopathy with anterior tibial onset Muscular dystrophy Hypokalemic periodic paralysis Infantile myofibromatosis Hyperkalemic periodic paralysis Myxofibrosarcoma Steinert myotonic dystrophy Tubular aggregate myopathy Acquired skeletal muscle disease Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome Paramyotonia congenita of Von Eulenburg Ullrich congenital muscular dystrophy Congenital muscular dystrophy type 1B Finnish upper limb-onset distal myopathy Distal hereditary motor neuropathy type 5 Metabolic myopathy Myotonic dystrophy Distal anoctaminopathy Congenital muscular dystrophy with integrin alpha-7 deficiency Oculopharyngodistal myopathy Distal myopathy with early respiratory muscle involvement Hereditary myopathy with lactic acidosis due to ISCU deficiency Distal spinal muscular atrophy type 3 Brody myopathy Hereditary continuous muscle fiber activity Tel Hashomer camptodactyly syndrome Genetic neuromuscular junction disease Congenital myopathy with excess of thin filaments Acquired neuromuscular junction disease Lambert-Eaton myasthenic syndrome Autosomal recessive distal myopathy Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome Non-dystrophic myopathy with collagen 6 anomaly Congenital muscular dystrophy with hyperlaxity Distal myotilinopathy Alpha-crystallinopathy Distal nebulin myopathy Distal hereditary motor neuropathy, Jerash type Non-dystrophic myopathy Desminopathy Eosinophilic fasciitis Late-onset distal myopathy, Markesbery-Griggs type Synaptic congenital myasthenic syndromes Acquired motor neuron disease Cap myopathy Miyoshi myopathy X-linked distal spinal muscular atrophy type 3 Presynaptic congenital myasthenic syndromes Genetic motor neuron disease Myotonia permanens Myotonia fluctuans Congenital myopathy with cores Congenital muscular dystrophy due to LMNA mutation Acetazolamide-responsive myotonia Cylindrical spirals myopathy Autosomal dominant proximal spinal muscular atrophy Neurogenic scapuloperoneal syndrome, Kaeser type Spinal muscular atrophy with respiratory distress type 1 Hereditary inclusion body myopathy type 4 Idiopathic eosinophilic myositis King-Denborough syndrome Genetic periodic paralysis Myasthenia gravis Neuromuscular disease X-linked myopathy with postural muscle atrophy Schwartz-Jampel syndrome Genetic skeletal muscle disease Juvenile primary lateral sclerosis Progressive muscular dystrophy Autosomal dominant distal myopathy Inclusion myopathy Distal hereditary motor neuropathy type 7 Autosomal recessive myogenic arthrogryposis multiplex congenita Myopathy with hexagonally cross-linked tubular arrays Postsynaptic congenital myasthenic syndromes Congenital myotonia Arthrogryposis due to muscular dystrophy Bacterial myositis Juvenile idiopathic inflammatory myopathy Andersen-Tawil syndrome Idiopathic inflammatory myopathy Amyotrophic lateral sclerosis type 4 Neuromuscular junction disease Motor neuron disease Inclusion body myopathy with Paget disease of bone and frontotemporal dementia Alpha-B crystallin-related late-onset myopathy Overlap myositis KLHL9-related early-onset distal myopathy Autosomal recessive lower motor neuron disease with childhood onset Laing early-onset distal myopathy Laminin subunit alpha 2-related congenital muscular dystrophy Duchenne and Becker muscular dystrophy Oculopharyngeal muscular dystrophy Intellectual disability-developmental delay-contractures syndrome Juvenile polymyositis Proximal spinal muscular atrophy type 1 Inflammatory myopathy with abundant macrophages Embryonal rhabdomyosarcoma Muscle filaminopathy Myosin storage myopathy Lower motor neuron syndrome with late-adult onset Proximal spinal muscular atrophy type 2 Pontocerebellar hypoplasia type 2 Kennedy disease Congenital myopathy Congenital fiber-type disproportion myopathy Intellectual disability-myopathy-short stature-endocrine defect syndrome Benign Samaritan congenital myopathy