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214400
CMT4A
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A
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Musculoskeletal Diseases
Bone Diseases
Spinal Diseases
Spinal Curvatures
Muscular Diseases
Muscle Weakness
Nervous System Diseases
Demyelinating 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
Neuromuscular Manifestations
Muscle Weakness
Muscular Atrophy
Neuromuscular Diseases
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
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
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Nutritional and Metabolic Diseases
Metabolic Diseases
Mitochondrial Diseases
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Pathologic Processes
Chromosome Aberrations
Disease
Syndrome
Disease Attributes
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Muscle Weakness
Signs and Symptoms
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Weakness
Muscular Atrophy
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