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
|
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".
This graph shows the total number of publications written about "Hereditary Central Nervous System Demyelinating Diseases" by people in this website by year, and whether "Hereditary Central Nervous System Demyelinating Diseases" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2017 | 1 | 1 | 2 |
| 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hereditary Central Nervous System Demyelinating Diseases" by people in Profiles.
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Expanding the clinical and genetic spectra of NKX6-2-related disorder. Clin Genet. 2018 05; 93(5):1087-1092.
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A Unique Mutational Spectrum of MLC1 in Korean Patients With Megalencephalic Leukoencephalopathy With Subcortical Cysts: p.Ala275Asp Founder Mutation and Maternal Uniparental Disomy of Chromosome 22. Ann Lab Med. 2017 Nov; 37(6):516-521.
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Down-regulation of the mitochondrial aspartate-glutamate carrier isoform 1 AGC1 inhibits proliferation and N-acetylaspartate synthesis in Neuro2A cells. Biochim Biophys Acta Mol Basis Dis. 2017 06; 1863(6):1422-1435.