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Nume Myotonia
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Boli A-Z Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Al-Raqad Syndrome Aminoaciduria Androgen Insensitivity Syndrome, Mild Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Apraxia Apraxia of Eyelid Opening Arthrochalasia Ehlers-Danlos Syndrome Aspiration Pneumonia Benign Familial Infantile Epilepsy Blepharophimosis Blepharospasm Blood Group--Ahonen Blood Group, I System Blood Group, Vel System Cataract Cenani-Lenz Syndactyly Syndrome Centronuclear Myopathy Charcot-Marie-Tooth Disease Conn's Syndrome Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis Creatine Phosphokinase, Elevated Serum Cyanosis, Transient Neonatal Dilated Cardiomyopathy Dysphagia Dystonia Encephalitis Epilepsy Familial Periodic Paralyses Familial Periodic Paralysis Gas Gangrene Glycogen Storage Disease Ii Head Injury Helix Syndrome Hepatic Adenomas, Familial Hyperkalemic Periodic Paralysis Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypertrophic Pyloric Stenosis Hypokalemic Periodic Paralysis, Type 2 Hypoparathyroidism Infertility Limbic Encephalitis Major Affective Disorder 2 Malignant Hyperthermia Mitochondrial Disorders Multicentric Reticulohistiocytosis Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Muscle Hypertrophy Muscle Tissue Disease Muscular Atrophy Muscular Dystrophy Muscular Dystrophy, Duchenne Type Myasthenia Gravis Myoclonus Myoglobinuria Myoglobinuria, Acute Recurrent, Autosomal Recessive Myopathy Myositis Myotonia Atrophica Myotonia Congenita Myotonia Congenita, Autosomal Dominant Myotonia Congenita, Autosomal Recessive Myotonia, Potassium-Aggravated Myotonic Disease Myotonic Dystrophy Myotonic Dystrophy 1 Myotonic Dystrophy 2 Myxedema Nephrolithiasis Nephrolithiasis, X-Linked Recessive, with Renal Failure Neuromuscular Disease Neuronitis Neuropathy, Hereditary Sensory and Autonomic, Type Iii Nondystrophic Myotonia Normokalemic Periodic Paralysis Paramyotonia Congenita of Von Eulenburg Periodic Paralyses Pilomatrixoma Pneumonia Polymyositis Prinzmetal's Variant Angina Pseudomyotonia Ptosis Pyle Disease Retinitis Retinitis Pigmentosa Sarcoidosis 2 Schwartz-Jampel Syndrome, Type 1 Scoliosis Seizures, Benign Familial Neonatal, 1 Spinal Muscular Atrophy Strabismus Syncope Thyroiditis Tooth Disease Undifferentiated Pleomorphic Sarcoma Wolff-Parkinson-White Syndrome