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160150
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MYOPATHY, CENTRONUCLEAR, AUTOSOMAL DOMINANT
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Musculoskeletal Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Muscular Dystrophy, Duchenne
Myotonic Dystrophy
Myopathies, Structural, Congenital
Myotonic Disorders
Myotonic Dystrophy
Nervous System Diseases
Cranial Nerve Diseases
Ocular Motility Disorders
Ophthalmoplegia
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Myotonic Dystrophy
Neurologic Manifestations
Neuromuscular Manifestations
Muscular Atrophy
Paralysis
Ophthalmoplegia
Neuromuscular Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Muscular Dystrophy, Duchenne
Myotonic Dystrophy
Myopathies, Structural, Congenital
Myotonic Disorders
Myotonic Dystrophy
Eye Diseases
Eye Abnormalities
Eyelid Diseases
Blepharoptosis
Ocular Motility Disorders
Ophthalmoplegia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Eye Abnormalities
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Muscular Dystrophy, Duchenne
Heredodegenerative Disorders, Nervous System
Myotonic Dystrophy
Muscular Dystrophies
Muscular Dystrophy, Duchenne
Myotonic Dystrophy
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Signs and Symptoms
Fatigue
Neurologic Manifestations
Neuromuscular Manifestations
Muscular Atrophy
Paralysis
Ophthalmoplegia
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