Hereditary Central Nervous System Demyelinating Diseases
"Hereditary Central Nervous System Demyelinating Diseases" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Inherited conditions characterized by a loss of MYELIN in the central nervous system.
Descriptor ID |
D020279
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MeSH Number(s) |
C10.228.140.163.100.362 C10.228.140.695.625 C10.314.400 C10.574.500.494 C16.320.400.367 C16.320.565.189.362 C18.452.132.100.362 C18.452.648.189.362
|
Concept/Terms |
Hereditary Central Nervous System Demyelinating Diseases- Hereditary Central Nervous System Demyelinating Diseases
- Central Nervous System Demyelinating Hereditary Diseases
- Hereditary Demyelinating Diseases, Central Nervous System
- Demyelinating Central Nervous System Diseases, Hereditary
- Demyelinating Diseases, Central Nervous System, Hereditary
- Central Nervous System Demyelinating Diseases, Hereditary
- Central Nervous System Hereditary Demyelinating Diseases
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Below are MeSH descriptors whose meaning is more general than "Hereditary Central Nervous System Demyelinating Diseases".
- Diseases [C]
- 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]
- Hereditary Central Nervous System Demyelinating Diseases [C10.228.140.163.100.362]
- Leukoencephalopathies [C10.228.140.695]
- Hereditary Central Nervous System Demyelinating Diseases [C10.228.140.695.625]
- Demyelinating Diseases [C10.314]
- Hereditary Central Nervous System Demyelinating Diseases [C10.314.400]
- Neurodegenerative Diseases [C10.574]
- Heredodegenerative Disorders, Nervous System [C10.574.500]
- Hereditary Central Nervous System Demyelinating Diseases [C10.574.500.494]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Heredodegenerative Disorders, Nervous System [C16.320.400]
- Hereditary Central Nervous System Demyelinating Diseases [C16.320.400.367]
- Metabolism, Inborn Errors [C16.320.565]
- Brain Diseases, Metabolic, Inborn [C16.320.565.189]
- Hereditary Central Nervous System Demyelinating Diseases [C16.320.565.189.362]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- Brain Diseases, Metabolic [C18.452.132]
- Brain Diseases, Metabolic, Inborn [C18.452.132.100]
- Hereditary Central Nervous System Demyelinating Diseases [C18.452.132.100.362]
- Metabolism, Inborn Errors [C18.452.648]
- Brain Diseases, Metabolic, Inborn [C18.452.648.189]
- Hereditary Central Nervous System Demyelinating Diseases [C18.452.648.189.362]
Below are MeSH descriptors whose meaning is more specific than "Hereditary Central Nervous System Demyelinating Diseases".
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