SE-ATLAS

Ullrich congenital muscular dystrophy Proximal spinal muscular atrophy Glycogen storage disease due to muscle beta-enolase deficiency Morvan syndrome Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome Infantile myofibromatosis Tubular aggregate myopathy Juvenile amyotrophic lateral sclerosis Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Congenital muscular dystrophy type 1B Myasthenia gravis Congenital myasthenic syndrome Oculopharyngodistal myopathy Macrophagic myofasciitis Myofibrillar myopathy Centronuclear myopathy Distal myopathy Vocal cord and pharyngeal distal myopathy Congenital myopathy with excess of thin filaments GNE myopathy Distal myopathy, Welander type Megaconial congenital muscular dystrophy Young adult-onset distal hereditary motor neuropathy Infantile-onset X-linked spinal muscular atrophy Myotonic syndrome Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency Viral myositis Infectious, fungal or parasitic myopathy Bacterial myositis Monomelic amyotrophy Parasitic myositis Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Neurogenic scapuloperoneal syndrome, Kaeser type Fungal myositis Juvenile overlap myositis Desmin-related myopathy with Mallory body-like inclusions Juvenile idiopathic inflammatory myopathy Spinal muscular atrophy associated with central nervous system anomaly Muscular dystrophy Skeletal muscle disease Isaacs syndrome Idiopathic inflammatory myopathy Autosomal recessive distal hereditary motor neuropathy Muscular channelopathy Neuromuscular junction disease Acquired neuromuscular junction disease Autosomal dominant congenital benign spinal muscular atrophy Spinal atrophy-ophthalmoplegia-pyramidal syndrome Genetic motor neuron disease Acquired motor neuron disease Pontocerebellar hypoplasia type 1 Inclusion body myopathy with Paget disease of bone and frontotemporal dementia Tel Hashomer camptodactyly syndrome Distal myopathy with anterior tibial onset Congenital lethal myopathy, Compton-North type Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome Distal hereditary motor neuropathy type 1 Thyrotoxic periodic paralysis Laminin subunit alpha 2-related congenital muscular dystrophy Emery-Dreifuss muscular dystrophy Distal hereditary motor neuropathy type 2 Limb-girdle muscular dystrophy Congenital muscular dystrophy due to dystroglycanopathy Facioscapulohumeral dystrophy Oculopharyngeal muscular dystrophy Distal hereditary motor neuropathy type 5 Congenital muscular dystrophy due to LMNA mutation Hereditary myopathy with early respiratory failure Distal hereditary motor neuropathy, Jerash type X-linked distal spinal muscular atrophy type 3 Idiopathic camptocormia Congenital fibrosis of extraocular muscles Infantile-onset ascending hereditary spastic paralysis Congenital muscular dystrophy with hyperlaxity Distal hereditary motor neuropathy type 7 Juvenile myasthenia gravis Transient neonatal myasthenia gravis Glycogen storage disease due to acid maltase deficiency Glycogen storage disease due to muscle glycogen phosphorylase deficiency Glycogen storage disease due to muscle phosphofructokinase deficiency Intellectual disability-developmental delay-contractures syndrome Lambert-Eaton myasthenic syndrome Miyoshi myopathy Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency Myotonia fluctuans Acetazolamide-responsive myotonia Embryonal rhabdomyosarcoma Muscle filaminopathy Proximal spinal muscular atrophy type 3 Pontocerebellar hypoplasia type 2 Kennedy disease Desminopathy Proximal myotonic myopathy Distal myotilinopathy Nemaline myopathy Alpha-crystallinopathy Postsynaptic congenital myasthenic syndromes Myosclerosis Late-onset distal myopathy, Markesbery-Griggs type Tibial muscular dystrophy Bethlem muscular dystrophy Synaptic congenital myasthenic syndromes Presynaptic congenital myasthenic syndromes Inclusion body myositis Potassium-aggravated myotonia Early-onset myopathy with fatal cardiomyopathy Thomsen and Becker disease Spinal muscular atrophy with respiratory distress type 1 Cyprus facial-neuromusculoskeletal syndrome Polyglucosan body myopathy type 1 O'Sullivan-McLeod syndrome Native American myopathy Autosomal recessive limb-girdle muscular dystrophy Autosomal dominant limb-girdle muscular dystrophy Autosomal dominant spastic paraplegia type 17 Madras motor neuron disease Congenital myopathy, Paradas type Metabolic myopathy due to lactate transporter defect Hypokalemic periodic paralysis Hyperkalemic periodic paralysis Muscular dystrophy, Selcen type Andersen-Tawil syndrome Amyotrophic lateral sclerosis type 4 Polyglucosan body myopathy type 2 Glycogen storage disease due to phosphoglycerate kinase 1 deficiency Alpha-B crystallin-related late-onset myopathy Distal myopathy with early respiratory muscle involvement Polymyositis Finnish upper limb-onset distal myopathy Immune-mediated necrotizing myopathy Rippling muscle disease with myasthenia gravis Overlap myositis Autosomal recessive lower motor neuron disease with childhood onset Distal anoctaminopathy Laing early-onset distal myopathy Adult-onset distal myopathy due to VCP mutation Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency Focal myositis Hereditary inclusion body myopathy type 4 Glycogen storage disease due to LAMP-2 deficiency Neuromuscular disease Schwartz-Jampel syndrome Myotonic dystrophy Progressive muscular dystrophy Autosomal dominant distal myopathy Non-dystrophic myopathy Trichinellosis Spheroid body myopathy Primary lateral sclerosis Bulbospinal muscular atrophy Bulbospinal muscular atrophy of adult Generalized bulbospinal muscular atrophy Autosomal dominant childhood-onset proximal spinal muscular atrophy Congenital myopathy with cores Hereditary continuous muscle fiber activity Metabolic myopathy Motor neuron disease Dermatomyositis Myxofibrosarcoma Duchenne and Becker muscular dystrophy Steinert myotonic dystrophy Distal spinal muscular atrophy type 3 X-linked myopathy with postural muscle atrophy Adult-onset myasthenia gravis Glycogen storage disease due to glycogen debranching enzyme deficiency Glycogen storage disease due to glycogen branching enzyme deficiency X-linked myopathy with excessive autophagy Juvenile polymyositis Myotonia permanens King-Denborough syndrome Alveolar rhabdomyosarcoma Autosomal dominant adult-onset proximal spinal muscular atrophy Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome DYNC1H1-related autosomal dominant childhood-onset proximal spinal muscular atrophy Myosin storage myopathy Corpus callosum agenesis-neuronopathy syndrome Proximal spinal muscular atrophy type 2 Proximal spinal muscular atrophy type 4 Juvenile dermatomyositis Paramyotonia congenita of Von Eulenburg Congenital muscular dystrophy with integrin alpha-7 deficiency Genetic periodic paralysis KLHL9-related early-onset distal myopathy Distal nebulin myopathy Rhabdomyosarcoma Amyotrophic lateral sclerosis Distal myopathy with posterior leg and anterior hand involvement Juvenile primary lateral sclerosis Autosomal recessive distal myopathy Non-dystrophic myopathy with collagen 6 anomaly Inclusion myopathy Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome Autosomal recessive myogenic arthrogryposis multiplex congenita Poliomyelitis Cap myopathy Cylindrical spirals myopathy Myopathy with hexagonally cross-linked tubular arrays Bulbospinal muscular atrophy of childhood Postpoliomyelitis syndrome Fetal akinesia-cerebral and retinal hemorrhage syndrome Inflammatory myopathy with abundant macrophages Idiopathic eosinophilic myositis Fingerprint body myopathy Glycogen storage disease due to phosphoglycerate mutase deficiency Congenital muscular dystrophy Rigid spine syndrome Congenital fiber-type disproportion myopathy Juvenile-onset Steinert myotonic dystrophy Antisynthetase syndrome Eosinophilic fasciitis Hereditary myopathy with lactic acidosis due to ISCU deficiency Muscular glycogenosis Congenital myotonia Arthrogryposis due to muscular dystrophy Autosomal dominant distal hereditary motor neuropathy Glycogen storage disease due to muscle phosphorylase kinase deficiency Genetic skeletal muscle disease BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy Riboflavin transporter deficiency Syndrome du motoneurone inférieur, forme tardive de l'adulte Myopathie à corps zébrés Myopathie congénitale Myopathie congénitale bénigne des Samaritains Syndrome de déficience intellectuelle-myopathie-petite taille-défaut endocrinien Syndromes myasthéniques congénitaux par défaut de glycosylation Paralysie périodique Maladie génétique de la jonction neuromusculaire Amyotrophie spinale proximale autosomique dominante Myopathie de Brody Lipidose musculaire Tumeur musculaire Amyotrophie spinale proximale type 1 Syndrome de dystrophie musculaire-substance blanche cérébrale spongieuse Myopathie à corps réducteurs Rippling muscle disease