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181350
EDMD2
EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT
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Musculoskeletal Diseases
Bone Diseases
Spinal Diseases
Spinal Curvatures
Scoliosis
Joint Diseases
Contracture
Muscular Diseases
Contracture
Muscular Disorders, Atrophic
Muscular Dystrophies
Muscular Dystrophy, Emery-Dreifuss
Myositis
Respiratory Tract Diseases
Respiration Disorders
Dyspnea
Nervous System Diseases
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Neurologic Manifestations
Neurobehavioral Manifestations
Consciousness Disorders
Unconsciousness
Syncope
Neuromuscular Manifestations
Muscular Atrophy
Neuromuscular Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Muscular Dystrophy, Emery-Dreifuss
Myositis
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Cardiovascular Diseases
Heart Diseases
Arrhythmias, Cardiac
Atrial Fibrillation
Bradycardia
Heart Block
Tachycardia
Cardiomegaly
Cardiomyopathy, Dilated
Cardiomyopathies
Cardiomyopathy, Dilated
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Genetic Diseases, Inborn
Chromosome Disorders
Genetic Diseases, X-Linked
Muscular Dystrophy, Emery-Dreifuss
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Metabolism, Inborn Errors
Progeria
Muscular Dystrophies
Muscular Dystrophy, Emery-Dreifuss
Skin and Connective Tissue Diseases
Skin Diseases
Skin Diseases, Metabolic
Lipodystrophy
Nutritional and Metabolic Diseases
Metabolic Diseases
Lipid Metabolism Disorders
Lipodystrophy
Metabolism, Inborn Errors
Progeria
Skin Diseases, Metabolic
Lipodystrophy
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Pathologic Processes
Arrhythmias, Cardiac
Atrial Fibrillation
Bradycardia
Heart Block
Tachycardia
Chromosome Aberrations
Death
Death, Sudden
Disease
Syndrome
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Diseases in Twins
Fibrosis
Signs and Symptoms
Aging, Premature
Neurologic Manifestations
Neurobehavioral Manifestations
Consciousness Disorders
Unconsciousness
Syncope
Neuromuscular Manifestations
Muscular Atrophy
Signs and Symptoms, Respiratory
Dyspnea
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