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Query OMIM entry list
118220
CMT1A
CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A
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Neoplasms
Neoplasms by Histologic Type
Lymphoma
Hodgkin Disease
Neoplasms, Germ Cell and Embryonal
Teratoma
Neoplasms, Nerve Tissue
Nerve Sheath Neoplasms
Neurofibroma
Neurofibromatoses
Neurofibromatosis 1
Neoplasms by Site
Endocrine Gland Neoplasms
Testicular Neoplasms
Urogenital Neoplasms
Genital Neoplasms, Male
Testicular Neoplasms
Neoplastic Syndromes, Hereditary
Neurofibromatoses
Neurofibromatosis 1
Musculoskeletal Diseases
Bone Diseases
Spinal Diseases
Spinal Curvatures
Scoliosis
Muscular Diseases
Muscle Weakness
Respiratory Tract Diseases
Respiration Disorders
Apnea
Sleep Apnea Syndromes
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Nervous System Diseases
Autoimmune Diseases of the Nervous System
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Central Nervous System Diseases
Brain Diseases
Diffuse Cerebral Sclerosis of Schilder
Leukoencephalopathies
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Leukoencephalopathies
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Spinal Cord Diseases
Muscular Atrophy, Spinal
Spinal Cord Compression
Demyelinating Diseases
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Hereditary Sensory and Autonomic Neuropathies
Neurocutaneous Syndromes
Neurofibromatoses
Neurofibromatosis 1
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Hereditary Sensory and Autonomic Neuropathies
Neurofibromatoses
Neurofibromatosis 1
Motor Neuron Disease
Muscular Atrophy, Spinal
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Intellectual Disability
Neuromuscular Manifestations
Muscle Weakness
Muscular Atrophy
Paralysis
Paraplegia
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Somatosensory Disorders
Paresthesia
Neuromuscular Diseases
Motor Neuron Disease
Muscular Atrophy, Spinal
Muscular Atrophy, Spinal
Peripheral Nervous System Diseases
Mononeuropathies
Sciatic Neuropathy
Nerve Compression Syndromes
Neurofibromatosis 1
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Hereditary Sensory and Autonomic Neuropathies
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Sleep Disorders
Dyssomnias
Sleep Disorders, Intrinsic
Sleep Apnea Syndromes
Male Urogenital Diseases
Genital Diseases, Male
Genital Neoplasms, Male
Testicular Neoplasms
Urogenital Neoplasms
Genital Neoplasms, Male
Testicular Neoplasms
Hemic and Lymphatic Diseases
Lymphatic Diseases
Lymphoproliferative Disorders
Lymphoma
Hodgkin Disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Chromosome Disorders
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Hereditary Sensory and Autonomic Neuropathies
Genetic Diseases, Inborn
Chromosome Disorders
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Hereditary Sensory and Autonomic Neuropathies
Neurofibromatoses
Neurofibromatosis 1
Neoplastic Syndromes, Hereditary
Neurofibromatoses
Neurofibromatosis 1
Endocrine System Diseases
Endocrine Gland Neoplasms
Testicular Neoplasms
Gonadal Disorders
Testicular Diseases
Testicular Neoplasms
Immune System Diseases
Autoimmune Diseases
Autoimmune Diseases of the Nervous System
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Immunoproliferative Disorders
Lymphoproliferative Disorders
Lymphoma
Hodgkin Disease
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Hypertrophy
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Trisomy
Chromosome Breakage
Chromosome Duplication
Trisomy
Translocation, Genetic
Disease Attributes
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Muscle Weakness
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Intellectual Disability
Neuromuscular Manifestations
Muscle Weakness
Muscular Atrophy
Paralysis
Paraplegia
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Somatosensory Disorders
Paresthesia
Sleep Disorders
Wounds and Injuries
Spinal Cord Injuries
Spinal Cord Compression
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