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Hereditary Central Nervous System Demyelinating Diseases
Inherited conditions characterized by a loss of MYELIN in the central nervous system.
推出的年份: 2000
副标题
blood
cerebrospinal fluid
chemically induced
classification
complications
diagnosis
diagnostic imaging
diet therapy
drug therapy
economics
embryology
enzymology
epidemiology
ethnology
etiology
genetics
history
immunology
metabolism
microbiology
mortality
nursing
parasitology
pathology
physiopathology
prevention and control
psychology
radiotherapy
rehabilitation
surgery
therapy
urine
veterinary
virology
树号:
C10.228.140.163.100.362, C10.228.140.695.625, C10.314.400, C10.574.500.490, C16.320.400.367, C16.320.565.189.362, C18.452.132.100.362, C18.452.648.189.362
MeSH 单一 ID:
D020279
进入的组:
Demyelinating Central Nervous System Diseases, Hereditary
Hereditary Demyelinating Diseases, Central Nervous System
Central Nervous System Demyelinating Hereditary Diseases
Central Nervous System Hereditary Demyelinating Diseases
Central Nervous System Demyelinating Diseases, Hereditary
Demyelinating Diseases, Central Nervous System, Hereditary
All MeSH Categories
Diseases Category
Nervous System Diseases [C10]
Central Nervous System Diseases [C10.228]
Brain Diseases [C10.228.140]
Brain Diseases, Metabolic [C10.228.140.163]
Brain Diseases, Metabolic, Inborn [C10.228.140.163.100]
Adrenoleukodystrophy [C10.228.140.163.100.084]
Cerebral Amyloid Angiopathy, Familial [C10.228.140.163.100.168]
Galactosemias [C10.228.140.163.100.320]
Hartnup Disease [C10.228.140.163.100.355]
Hepatolenticular Degeneration [C10.228.140.163.100.360]
Hereditary Central Nervous System Demyelinating Diseases [C10.228.140.163.100.362]
Adrenoleukodystrophy [C10.228.140.163.100.362.250]
Alexander Disease [C10.228.140.163.100.362.312]
Canavan Disease [C10.228.140.163.100.362.375]
Leukodystrophy, Globoid Cell [C10.228.140.163.100.362.500]
Leukodystrophy, Metachromatic [C10.228.140.163.100.362.550]
Pelizaeus-Merzbacher Disease [C10.228.140.163.100.362.775]
Homocystinuria [C10.228.140.163.100.365]
Hyperglycinemia, Nonketotic [C10.228.140.163.100.375]
Hyperlysinemias [C10.228.140.163.100.380]
Leigh Disease [C10.228.140.163.100.412]
Lesch-Nyhan Syndrome [C10.228.140.163.100.425]
Lysosomal Storage Diseases, Nervous System [C10.228.140.163.100.435]
add_circle
Maple Syrup Urine Disease [C10.228.140.163.100.520]
MELAS Syndrome [C10.228.140.163.100.535]
Menkes Kinky Hair Syndrome [C10.228.140.163.100.540]
MERRF Syndrome [C10.228.140.163.100.545]
Mevalonate Kinase Deficiency [C10.228.140.163.100.593]
Oculocerebrorenal Syndrome [C10.228.140.163.100.640]
Phenylketonurias [C10.228.140.163.100.687]
add_circle
Pyruvate Carboxylase Deficiency Disease [C10.228.140.163.100.725]
Pyruvate Dehydrogenase Complex Deficiency Disease [C10.228.140.163.100.750]
Refsum Disease [C10.228.140.163.100.813]
Refsum Disease, Infantile [C10.228.140.163.100.844]
Tyrosinemias [C10.228.140.163.100.875]
Urea Cycle Disorders, Inborn [C10.228.140.163.100.937]
add_circle
Zellweger Syndrome [C10.228.140.163.100.968]
All MeSH Categories
Diseases Category
Nervous System Diseases [C10]
Central Nervous System Diseases [C10.228]
Brain Diseases [C10.228.140]
Leukoencephalopathies [C10.228.140.695]
Dementia, Vascular [C10.228.140.695.500]
Demyelinating Autoimmune Diseases, CNS [C10.228.140.695.562]
add_circle
Hereditary Central Nervous System Demyelinating Diseases [C10.228.140.695.625]
Adrenoleukodystrophy [C10.228.140.695.625.250]
Alexander Disease [C10.228.140.695.625.312]
Canavan Disease [C10.228.140.695.625.375]
Leukodystrophy, Globoid Cell [C10.228.140.695.625.500]
Leukodystrophy, Metachromatic [C10.228.140.695.625.550]
Pelizaeus-Merzbacher Disease [C10.228.140.695.625.775]
Leukoencephalopathy, Progressive Multifocal [C10.228.140.695.750]
Posterior Leukoencephalopathy Syndrome [C10.228.140.695.875]
All MeSH Categories
Diseases Category
Nervous System Diseases [C10]
Demyelinating Diseases [C10.314]
Demyelinating Autoimmune Diseases, CNS [C10.314.350]
add_circle
Hereditary Central Nervous System Demyelinating Diseases [C10.314.400]
Adrenoleukodystrophy [C10.314.400.250]
Alexander Disease [C10.314.400.312]
Canavan Disease [C10.314.400.375]
Leukodystrophy, Globoid Cell [C10.314.400.500]
Leukodystrophy, Metachromatic [C10.314.400.550]
Pelizaeus-Merzbacher Disease [C10.314.400.775]
Leukoencephalopathy, Progressive Multifocal [C10.314.450]
Marchiafava-Bignami Disease [C10.314.475]
Myelinolysis, Central Pontine [C10.314.500]
Ophthalmoplegic Migraine [C10.314.687]
Polyradiculoneuropathy [C10.314.750]
add_circle
Subacute Combined Degeneration [C10.314.875]
All MeSH Categories
Diseases Category
Nervous System Diseases [C10]
Neurodegenerative Diseases [C10.574]
Heredodegenerative Disorders, Nervous System [C10.574.500]
Alexander Disease [C10.574.500.024]
Amyloid Neuropathies, Familial [C10.574.500.050]
Bulbo-Spinal Atrophy, X-Linked [C10.574.500.175]
Canavan Disease [C10.574.500.300]
Cockayne Syndrome [C10.574.500.362]
Dystonia Musculorum Deformans [C10.574.500.393]
Gerstmann-Straussler-Scheinker Disease [C10.574.500.425]
Hepatolenticular Degeneration [C10.574.500.487]
Hereditary Central Nervous System Demyelinating Diseases [C10.574.500.490]
Hereditary Sensory and Autonomic Neuropathies [C10.574.500.493]
add_circle
Hereditary Sensory and Motor Neuropathy [C10.574.500.495]
add_circle
Huntington Disease [C10.574.500.497]
Lafora Disease [C10.574.500.529]
Myotonia Congenita [C10.574.500.545]
Myotonic Dystrophy [C10.574.500.547]
Neurofibromatoses [C10.574.500.549]
add_circle
Neuronal Ceroid-Lipofuscinoses [C10.574.500.550]
Optic Atrophies, Hereditary [C10.574.500.662]
add_circle
Pantothenate Kinase-Associated Neurodegeneration [C10.574.500.700]
Spinal Muscular Atrophies of Childhood [C10.574.500.812]
Spinocerebellar Degenerations [C10.574.500.825]
add_circle
Tourette Syndrome [C10.574.500.850]
Tuberous Sclerosis [C10.574.500.865]
Unverricht-Lundborg Syndrome [C10.574.500.875]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Heredodegenerative Disorders, Nervous System [C16.320.400]
Alexander Disease [C16.320.400.024]
Amyloid Neuropathies, Familial [C16.320.400.050]
Bulbo-Spinal Atrophy, X-Linked [C16.320.400.100]
Canavan Disease [C16.320.400.150]
Cockayne Syndrome [C16.320.400.200]
Dystonia Musculorum Deformans [C16.320.400.330]
Gerstmann-Straussler-Scheinker Disease [C16.320.400.350]
Hepatolenticular Degeneration [C16.320.400.361]
Hereditary Central Nervous System Demyelinating Diseases [C16.320.400.367]
Hereditary Sensory and Autonomic Neuropathies [C16.320.400.415]
add_circle
Hereditary Sensory and Motor Neuropathy [C16.320.400.375]
add_circle
Huntington Disease [C16.320.400.430]
Lafora Disease [C16.320.400.480]
Mental Retardation, X-Linked [C16.320.400.525]
add_circle
Myotonia Congenita [C16.320.400.540]
Myotonic Dystrophy [C16.320.400.542]
Neuroacanthocytosis [C16.320.400.550]
Neurofibromatoses [C16.320.400.560]
add_circle
Neuronal Ceroid-Lipofuscinoses [C16.320.400.600]
Optic Atrophies, Hereditary [C16.320.400.630]
add_circle
Pantothenate Kinase-Associated Neurodegeneration [C16.320.400.650]
Spinal Muscular Atrophies of Childhood [C16.320.400.765]
Spinocerebellar Degenerations [C16.320.400.780]
add_circle
Tourette Syndrome [C16.320.400.820]
Tuberous Sclerosis [C16.320.400.880]
Unverricht-Lundborg Syndrome [C16.320.400.940]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Metabolism, Inborn Errors [C16.320.565]
Brain Diseases, Metabolic, Inborn [C16.320.565.189]
Adrenoleukodystrophy [C16.320.565.189.084]
Cerebral Amyloid Angiopathy, Familial [C16.320.565.189.168]
Galactosemias [C16.320.565.189.320]
Hartnup Disease [C16.320.565.189.355]
Hepatolenticular Degeneration [C16.320.565.189.360]
Hereditary Central Nervous System Demyelinating Diseases [C16.320.565.189.362]
Adrenoleukodystrophy [C16.320.565.189.362.250]
Alexander Disease [C16.320.565.189.362.312]
Canavan Disease [C16.320.565.189.362.375]
Leukodystrophy, Globoid Cell [C16.320.565.189.362.500]
Leukodystrophy, Metachromatic [C16.320.565.189.362.550]
Pelizaeus-Merzbacher Disease [C16.320.565.189.362.775]
Homocystinuria [C16.320.565.189.365]
Hyperglycinemia, Nonketotic [C16.320.565.189.375]
Hyperlysinemias [C16.320.565.189.380]
Leigh Disease [C16.320.565.189.412]
Lesch-Nyhan Syndrome [C16.320.565.189.425]
Lysosomal Storage Diseases, Nervous System [C16.320.565.189.435]
add_circle
Maple Syrup Urine Disease [C16.320.565.189.520]
MELAS Syndrome [C16.320.565.189.535]
Menkes Kinky Hair Syndrome [C16.320.565.189.540]
MERRF Syndrome [C16.320.565.189.545]
Mevalonate Kinase Deficiency [C16.320.565.189.593]
Oculocerebrorenal Syndrome [C16.320.565.189.640]
Phenylketonurias [C16.320.565.189.687]
add_circle
Pyruvate Carboxylase Deficiency Disease [C16.320.565.189.725]
Pyruvate Dehydrogenase Complex Deficiency Disease [C16.320.565.189.750]
Refsum Disease [C16.320.565.189.813]
Refsum Disease, Infantile [C16.320.565.189.844]
Tyrosinemias [C16.320.565.189.875]
Urea Cycle Disorders, Inborn [C16.320.565.189.937]
add_circle
Zellweger Syndrome [C16.320.565.189.968]
All MeSH Categories
Diseases Category
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Brain Diseases, Metabolic [C18.452.132]
Brain Diseases, Metabolic, Inborn [C18.452.132.100]
Adrenoleukodystrophy [C18.452.132.100.084]
Cerebral Amyloid Angiopathy, Familial [C18.452.132.100.168]
Galactosemias [C18.452.132.100.320]
Hartnup Disease [C18.452.132.100.355]
Hepatolenticular Degeneration [C18.452.132.100.360]
Hereditary Central Nervous System Demyelinating Diseases [C18.452.132.100.362]
Adrenoleukodystrophy [C18.452.132.100.362.250]
Alexander Disease [C18.452.132.100.362.312]
Canavan Disease [C18.452.132.100.362.375]
Leukodystrophy, Globoid Cell [C18.452.132.100.362.500]
Leukodystrophy, Metachromatic [C18.452.132.100.362.550]
Pelizaeus-Merzbacher Disease [C18.452.132.100.362.775]
Homocystinuria [C18.452.132.100.365]
Hyperglycinemia, Nonketotic [C18.452.132.100.375]
Hyperlysinemias [C18.452.132.100.380]
Leigh Disease [C18.452.132.100.412]
Lesch-Nyhan Syndrome [C18.452.132.100.425]
Lysosomal Storage Diseases, Nervous System [C18.452.132.100.435]
add_circle
Maple Syrup Urine Disease [C18.452.132.100.520]
MELAS Syndrome [C18.452.132.100.535]
Menkes Kinky Hair Syndrome [C18.452.132.100.540]
MERRF Syndrome [C18.452.132.100.545]
Mevalonate Kinase Deficiency [C18.452.132.100.593]
Oculocerebrorenal Syndrome [C18.452.132.100.640]
Phenylketonurias [C18.452.132.100.687]
add_circle
Pyruvate Carboxylase Deficiency Disease [C18.452.132.100.725]
Pyruvate Dehydrogenase Complex Deficiency Disease [C18.452.132.100.750]
Refsum Disease [C18.452.132.100.813]
Refsum Disease, Infantile [C18.452.132.100.844]
Tyrosinemias [C18.452.132.100.875]
Urea Cycle Disorders, Inborn [C18.452.132.100.937]
add_circle
Zellweger Syndrome [C18.452.132.100.968]
All MeSH Categories
Diseases Category
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Metabolism, Inborn Errors [C18.452.648]
Brain Diseases, Metabolic, Inborn [C18.452.648.189]
Adrenoleukodystrophy [C18.452.648.189.084]
Cerebral Amyloid Angiopathy, Familial [C18.452.648.189.168]
Galactosemias [C18.452.648.189.320]
Hartnup Disease [C18.452.648.189.355]
Hepatolenticular Degeneration [C18.452.648.189.360]
Hereditary Central Nervous System Demyelinating Diseases [C18.452.648.189.362]
Adrenoleukodystrophy [C18.452.648.189.362.250]
Alexander Disease [C18.452.648.189.362.312]
Canavan Disease [C18.452.648.189.362.375]
Leukodystrophy, Globoid Cell [C18.452.648.189.362.500]
Leukodystrophy, Metachromatic [C18.452.648.189.362.550]
Pelizaeus-Merzbacher Disease [C18.452.648.189.362.775]
Homocystinuria [C18.452.648.189.365]
Hyperglycinemia, Nonketotic [C18.452.648.189.375]
Hyperlysinemias [C18.452.648.189.380]
Leigh Disease [C18.452.648.189.412]
Lesch-Nyhan Syndrome [C18.452.648.189.425]
Lysosomal Storage Diseases, Nervous System [C18.452.648.189.435]
add_circle
Maple Syrup Urine Disease [C18.452.648.189.520]
MELAS Syndrome [C18.452.648.189.535]
Menkes Kinky Hair Syndrome [C18.452.648.189.540]
MERRF Syndrome [C18.452.648.189.545]
Mevalonate Kinase Deficiency [C18.452.648.189.593]
Oculocerebrorenal Syndrome [C18.452.648.189.640]
Phenylketonurias [C18.452.648.189.687]
add_circle
Pyruvate Carboxylase Deficiency Disease [C18.452.648.189.725]
Pyruvate Dehydrogenase Complex Deficiency Disease [C18.452.648.189.750]
Refsum Disease [C18.452.648.189.813]
Refsum Disease, Infantile [C18.452.648.189.844]
Tyrosinemias [C18.452.648.189.875]
Urea Cycle Disorders, Inborn [C18.452.648.189.937]
add_circle
Zellweger Syndrome [C18.452.648.189.968]
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