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160565
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MYOPATHY, TUBULAR AGGREGATE
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Musculoskeletal Diseases
Muscular Diseases
Muscle Weakness
Myopathies, Structural, Congenital
Myotonic Disorders
Myotonia Congenita
Paralyses, Familial Periodic
Nervous System Diseases
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Myotonia Congenita
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Weakness
Pupil Disorders
Miosis
Reflex, Abnormal
Neuromuscular Diseases
Muscular Diseases
Myopathies, Structural, Congenital
Myotonic Disorders
Myotonia Congenita
Paralyses, Familial Periodic
Eye Diseases
Pupil Disorders
Miosis
Vision Disorders
Night Blindness
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Myotonia Congenita
Metabolism, Inborn Errors
Metal Metabolism, Inborn Errors
Paralyses, Familial Periodic
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Metal Metabolism, Inborn Errors
Paralyses, Familial Periodic
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Muscle Weakness
Signs and Symptoms
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Weakness
Pupil Disorders
Miosis
Reflex, Abnormal
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