MeSH Treeview
Query OMIM entry list
609260
CMT2A2
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2
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Musculoskeletal Diseases
Foot Deformities
Foot Deformities, Acquired
Nervous System Diseases
Autoimmune Diseases of the Nervous System
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Movement Disorders
Demyelinating Diseases
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Hereditary Sensory and Autonomic Neuropathies
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Hereditary Sensory and Autonomic Neuropathies
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
Pyruvate Dehydrogenase Complex Deficiency Disease
Neuromuscular Manifestations
Muscular Atrophy
Neuromuscular Diseases
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Hereditary Sensory and Autonomic Neuropathies
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Hereditary Sensory and Autonomic Neuropathies
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Pyruvate Dehydrogenase Complex Deficiency Disease
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Hereditary Sensory and Autonomic Neuropathies
Mental Retardation, X-Linked
Pyruvate Dehydrogenase Complex Deficiency Disease
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Mitochondrial Diseases
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Immune System Diseases
Autoimmune Diseases
Autoimmune Diseases of the Nervous System
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Pathologic Processes
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Nerve Degeneration
Signs and Symptoms
Neurologic Manifestations
Neuromuscular Manifestations
Muscular Atrophy
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