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302800
CMTX1
CHARCOT-MARIE-TOOTH DISEASE, X-LINKED, 1
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Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
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
Hereditary Central Nervous System Demyelinating Diseases
Pelizaeus-Merzbacher Disease
Encephalitis
Encephalomyelitis
Headache Disorders
Headache Disorders, Primary
Migraine Disorders
Migraine with Aura
Leukoencephalopathies
Hereditary Central Nervous System Demyelinating Diseases
Pelizaeus-Merzbacher Disease
Central Nervous System Infections
Encephalomyelitis
Encephalomyelitis
Leukoencephalopathies
Hereditary Central Nervous System Demyelinating Diseases
Pelizaeus-Merzbacher Disease
Spinal Cord Diseases
Muscular Atrophy, Spinal
Demyelinating Diseases
Hereditary Central Nervous System Demyelinating Diseases
Pelizaeus-Merzbacher Disease
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
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Neuromuscular Manifestations
Muscular Atrophy
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
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
Eye Diseases
Retinal Diseases
Retinal Degeneration
Uveal Diseases
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Fetal Diseases
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Hereditary Sensory and Autonomic Neuropathies
Fetal Diseases
Genetic Diseases, Inborn
Chromosome Disorders
Genetic Diseases, X-Linked
Pelizaeus-Merzbacher Disease
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Hereditary Sensory and Autonomic Neuropathies
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Pelizaeus-Merzbacher Disease
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Pelizaeus-Merzbacher Disease
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Pelizaeus-Merzbacher 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
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Sex Chromosome Aberrations
Disease
Syndrome
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Diseases in Twins
Recurrence
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Neuromuscular Manifestations
Muscular Atrophy
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
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