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159440
MPZ
MYELIN PROTEIN ZERO
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Neoplasms
Neoplasms by Histologic Type
Neoplasms, Connective and Soft Tissue
Neoplasms, Connective Tissue
Neoplasms, Bone Tissue
Osteosarcoma
Sarcoma
Osteosarcoma
Neoplasms, Germ Cell and Embryonal
Neuroectodermal Tumors
Neoplasms, Neuroepithelial
Glioma
Neoplasms, Glandular and Epithelial
Neoplasms, Neuroepithelial
Glioma
Neoplasms, Nerve Tissue
Neuroectodermal Tumors
Neoplasms, Neuroepithelial
Glioma
Neoplasms by Site
Bone Neoplasms
Nervous System Neoplasms
Central Nervous System Neoplasms
Brain Neoplasms
Musculoskeletal Diseases
Bone Diseases
Bone Neoplasms
Spinal Diseases
Spinal Curvatures
Scoliosis
Muscular Diseases
Muscle Weakness
Digestive System Diseases
Gastrointestinal Diseases
Intestinal Diseases
Colonic Diseases
Colonic Diseases, Functional
Irritable Bowel Syndrome
Respiratory Tract Diseases
Respiration Disorders
Cough
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Hearing Loss, Sensorineural
Nervous System Diseases
Autoimmune Diseases of the Nervous System
Demyelinating Autoimmune Diseases, CNS
Multiple Sclerosis
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Autonomic Nervous System Diseases
Adie Syndrome
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Brain Neoplasms
Leukoencephalopathies
Hereditary Central Nervous System Demyelinating Diseases
Leukoencephalopathies
Hereditary Central Nervous System Demyelinating Diseases
Cranial Nerve Diseases
Oculomotor Nerve Diseases
Adie Syndrome
Demyelinating Diseases
Demyelinating Autoimmune Diseases, CNS
Multiple Sclerosis
Hereditary Central Nervous System 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
Nervous System Neoplasms
Central Nervous System Neoplasms
Brain Neoplasms
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Central Nervous System Demyelinating Diseases
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Hereditary Sensory and Autonomic Neuropathies
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Hypotonia
Muscle Weakness
Muscular Atrophy
Pain
Paresis
Pupil Disorders
Tonic Pupil
Reflex, Abnormal
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Hearing Loss, Sensorineural
Somatosensory Disorders
Hyperalgesia
Hypesthesia
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
Sleep Disorders
Dyssomnias
Sleep Disorders, Intrinsic
Restless Legs Syndrome
Parasomnias
Restless Legs Syndrome
Eye Diseases
Ocular Motility Disorders
Oculomotor Nerve Diseases
Adie Syndrome
Pupil Disorders
Tonic Pupil
Adie Syndrome
Male Urogenital Diseases
Genital Diseases, Male
Sexual Dysfunction, Physiological
Erectile Dysfunction
Urologic Diseases
Urination Disorders
Urinary Incontinence
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Urination Disorders
Urinary Incontinence
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
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
Anemia, Hemolytic, Congenital
Chromosome Disorders
Heredodegenerative Disorders, Nervous System
Hereditary Central Nervous System Demyelinating Diseases
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
Skin and Connective Tissue Diseases
Skin Diseases
Hair Diseases
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Immune System Diseases
Autoimmune Diseases
Autoimmune Diseases of the Nervous System
Demyelinating Autoimmune Diseases, CNS
Multiple Sclerosis
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Hypertrophy
Pathologic Processes
Chromosome Aberrations
Disease
Syndrome
Disease Attributes
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Diseases in Twins
Muscle Weakness
Nerve Degeneration
Retrograde Degeneration
Signs and Symptoms
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Hypotonia
Muscle Weakness
Muscular Atrophy
Pain
Paresis
Pupil Disorders
Tonic Pupil
Reflex, Abnormal
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Hearing Loss, Sensorineural
Somatosensory Disorders
Hyperalgesia
Hypesthesia
Pain
Signs and Symptoms, Respiratory
Cough
Urological Manifestations
Lower Urinary Tract Symptoms
Urinary Incontinence
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