SE-ATLAS

Congenital myasthenic syndrome Trichinellosis Macrophagic myofasciitis Muscular lipidosis Myofibrillar myopathy Poliomyelitis Centronuclear myopathy Polymyositis Adult-onset myasthenia gravis Distal myopathy Infantile-onset X-linked spinal muscular atrophy Vocal cord and pharyngeal distal myopathy Alveolar rhabdomyosarcoma Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Transient neonatal myasthenia gravis GNE myopathy Muscular glycogenosis Distal myopathy, Welander type Juvenile myasthenia gravis Congenital myopathy, Paradas type Proximal myotonic myopathy Nemaline myopathy Hereditary myopathy with early respiratory failure Tibial muscular dystrophy Myotonic syndrome Bethlem muscular dystrophy X-linked myopathy with excessive autophagy Inclusion body myositis Fetal akinesia-cerebral and retinal hemorrhage syndrome Potassium-aggravated myotonia Bulbospinal muscular atrophy Infantile-onset ascending hereditary spastic paralysis Thomsen and Becker disease Autosomal dominant spastic paraplegia type 17 Proximal spinal muscular atrophy Bulbospinal muscular atrophy of adult Muscular dystrophy, Selcen type Immune-mediated necrotizing myopathy Pontocerebellar hypoplasia type 1 Bulbospinal muscular atrophy of childhood Periodic paralysis Muscular tumor Congenital fibrosis of extraocular muscles Generalized bulbospinal muscular atrophy Congenital myasthenic syndromes with glycosylation defect Postpoliomyelitis syndrome Monomelic amyotrophy Infectious, fungal or parasitic myopathy Antisynthetase syndrome Rippling muscle disease with myasthenia gravis Cyprus facial-neuromusculoskeletal syndrome Proximal spinal muscular atrophy type 3 Viral myositis Dermatomyositis Proximal spinal muscular atrophy type 4 Adult-onset distal myopathy due to VCP mutation Focal myositis Myosclerosis Primary lateral sclerosis Idiopathic camptocormia Fungal myositis Parasitic myositis Early-onset myopathy with fatal cardiomyopathy Juvenile overlap myositis Autosomal dominant childhood-onset proximal spinal muscular atrophy Rhabdomyosarcoma Young adult-onset distal hereditary motor neuropathy Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome Muscular dystrophy-white matter spongiosis syndrome Spinal muscular atrophy associated with central nervous system anomaly Juvenile dermatomyositis Congenital muscular dystrophy due to dystroglycanopathy Autosomal dominant adult-onset proximal spinal muscular atrophy Madras motor neuron disease 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