MeSH Treeview
Query OMIM entry list
601472
CMT2D
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D
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Nervous System Diseases
Autoimmune Diseases of the Nervous System
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Central Nervous System Diseases
Spinal Cord Diseases
Muscular Atrophy, Spinal
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
Motor Neuron Disease
Muscular Atrophy, Spinal
Neuromuscular Diseases
Motor Neuron Disease
Muscular Atrophy, Spinal
Muscular Atrophy, Spinal
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
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Hereditary Sensory and Autonomic Neuropathies
Immune System Diseases
Autoimmune Diseases
Autoimmune Diseases of the Nervous System
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
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