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Query OMIM entry list
300401
PLP1
PROTEOLIPID PROTEIN 1
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Nervous System Diseases
Autoimmune Diseases of the Nervous System
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Multiple Sclerosis
Multiple Sclerosis, Relapsing-Remitting
Central Nervous System Diseases
Brain Diseases
Brain Damage, Chronic
Cerebral Palsy
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Pelizaeus-Merzbacher Disease
Cerebellar Diseases
Diffuse Cerebral Sclerosis of Schilder
Leukoencephalopathies
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Hereditary Central Nervous System Demyelinating Diseases
Pelizaeus-Merzbacher Disease
Leukoencephalopathies
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Hereditary Central Nervous System Demyelinating Diseases
Pelizaeus-Merzbacher Disease
Demyelinating Diseases
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Multiple Sclerosis
Multiple Sclerosis, Relapsing-Remitting
Hereditary Central Nervous System Demyelinating Diseases
Pelizaeus-Merzbacher Disease
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Spastic Paraplegia, Hereditary
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Central Nervous System Demyelinating Diseases
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Spastic Paraplegia, Hereditary
Neurologic Manifestations
Dyskinesias
Ataxia
Paralysis
Paraplegia
Neuromuscular Diseases
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Spastic Paraplegia, Hereditary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Spastic Paraplegia, Hereditary
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Pelizaeus-Merzbacher Disease
Heredodegenerative Disorders, Nervous System
Hereditary Central Nervous System Demyelinating Diseases
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Spastic Paraplegia, Hereditary
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
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Multiple Sclerosis
Multiple Sclerosis, Relapsing-Remitting
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Chromosome Breakage
Chromosome Inversion
Translocation, Genetic
Disease Attributes
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Inflammation
Nerve Degeneration
Wallerian Degeneration
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Paralysis
Paraplegia
Database Center for Life Science
