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606483
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CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE A
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Nervous System Diseases
Central Nervous System Diseases
Spinal Cord Diseases
Muscular Atrophy, Spinal
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
Motor Neuron Disease
Muscular Atrophy, Spinal
Neurologic Manifestations
Neuromuscular Manifestations
Muscular Atrophy
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
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Signs and Symptoms
Neurologic Manifestations
Neuromuscular Manifestations
Muscular Atrophy
Database Center for Life Science
