Structured Summary
Abstract
Inherited conditions characterized by a loss of MYELIN in the central nervous system.
MeSH Record
Classification
Related Concepts
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MeSH Record
Synonyms
6 entry terms
- Central Nervous System Demyelinating Diseases, Hereditary
- Central Nervous System Demyelinating Hereditary Diseases
- Central Nervous System Hereditary Demyelinating Diseases
- Demyelinating Central Nervous System Diseases, Hereditary
- Demyelinating Diseases, Central Nervous System, Hereditary
- Hereditary Demyelinating Diseases, Central Nervous System
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings 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 & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2000
MeSH Hierarchy
Tree Numbers
MeSH Record
NLM Classification
WL 350
AMA Style
References
- National Library of Medicine. Hereditary Central Nervous System Demyelinating Diseases. Medical Subject Headings (MeSH). 2026. Unique ID D020279. http://id.nlm.nih.gov/mesh/2026/D020279
- Hereditary Central Nervous System Demyelinating Diseases. In: Wikipedia. https://en.wikipedia.org/wiki/Hereditary_CNS_demyelinating_disease
- Hereditary Central Nervous System Demyelinating Diseases. In: Wikidata. https://www.wikidata.org/wiki/Q17048613