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168300	PMC	PARAMYOTONIA CONGENITA OF VON EULENBURG

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Musculoskeletal Diseases

Muscular Diseases

Muscle Rigidity

Muscular Disorders, Atrophic

Muscular Dystrophies

Myotonic Dystrophy

Myotonic Disorders

Myotonia Congenita

Myotonic Dystrophy

Paralyses, Familial Periodic

Hypokalemic Periodic Paralysis

Paralysis, Hyperkalemic Periodic

Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Genetic Diseases, Inborn

Heredodegenerative Disorders, Nervous System

Myotonia Congenita

Myotonic Dystrophy

Metabolism, Inborn Errors

Metal Metabolism, Inborn Errors

Paralyses, Familial Periodic

Hypokalemic Periodic Paralysis

Paralysis, Hyperkalemic Periodic

Muscular Dystrophies

Myotonic Dystrophy

Nutritional and Metabolic Diseases

Metabolic Diseases

Metabolism, Inborn Errors

Metal Metabolism, Inborn Errors

Paralyses, Familial Periodic

Hypokalemic Periodic Paralysis

Paralysis, Hyperkalemic Periodic

Water-Electrolyte Imbalance

Pathological Conditions, Signs and Symptoms

Signs and Symptoms

Neurologic Manifestations

Neuromuscular Manifestations

Muscle Hypertonia

Muscle Rigidity

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