Informaţii despre

Nume Rigid Spine Muscular Dystrophy 1
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Congenital myopathies; Other primary disorders of muscles
Clasificare anatomică Malacards Boli musculare; Boli neuronale

Vezi şi

Boli A-Z Adie Pupil Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Anterior Compartment Syndrome Arthrochalasia Ehlers-Danlos Syndrome Atrial Standstill 1 Autosomal Recessive Limb-Girdle Muscular Dystrophy Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2b Axonal Neuropathy Bethlem Myopathy 1 Blood Group--Ahonen Cardiomyopathy, Dilated, 1b Cardiomyopathy, Dilated, 1d Cardioneuromyopathy with Hyaline Masses and Nemaline Rods Central Core Disease of Muscle Central Core Myopathy Centronuclear Myopathy Cerebritis Cervicitis Charcot-Marie-Tooth Disease Ciliary Dyskinesia, Primary, 1 Congenital Fiber-Type Disproportion Congenital Structural Myopathy Distal Muscular Dystrophy Dysferlinopathy Emerinopathy Emery-Dreifuss Muscular Dystrophy Foot Drop Glycogen Storage Disease Ii Hemophagocytic Lymphohistiocytosis, Familial, 1 Hepatic Adenomas, Familial Limb-Girdle Muscular Dystrophy Localized Lipodystrophy Minicore Myopathy with External Ophthalmoplegia Miyoshi Muscular Dystrophy 1 Multiminicore Disease Multiple Mitochondrial Dysfunctions Syndrome Muscle Tissue Disease Muscular Dystrophy Muscular Dystrophy, Becker Type Muscular Dystrophy, Congenital, 1b Muscular Dystrophy, Congenital, Lmna-Related Muscular Dystrophy, Congenital Merosin-Deficient, 1a Muscular Dystrophy, Congenital, Merosin-Positive Muscular Dystrophy, Duchenne Type Muscular Dystrophy-Dystroglycanopathy , Type a, 4 Muscular Dystrophy-Dystroglycanopathy , Type C, 5 Muscular Dystrophy, Limb-Girdle, Type 2a Muscular Dystrophy, Limb-Girdle, Type 2b Muscular Dystrophy, Limb-Girdle, Type 2c Muscular Dystrophy, Limb-Girdle, Type 2f Muscular Dystrophy, Limb-Girdle, Type 2h Muscular Dystrophy, Limb-Girdle, Type 2l Myofibrillar Myopathy Myopathy Myopathy, Congenital Myopathy, Congenital, with Fiber-Type Disproportion Myopathy, Myofibrillar, 1 Myopathy, Myofibrillar, 2 Myopathy, Spheroid Body Myopathy, X-Linked, with Excessive Autophagy Myositis Nemaline Myopathy Nervous System Disease Neuromuscular Disease Neuropathy Polyglucosan Body Myopathy 1 with or Without Immunodeficiency Pontocerebellar Hypoplasia, Type 2d Reducing Body Myopathy Respiratory Failure Robinow-Sorauf Syndrome Scapuloperoneal Myopathy Scoliosis Silver-Russell Syndrome Spondyloocular Syndrome Stormorken Syndrome Tooth Disease Ullrich Congenital Muscular Dystrophy 1