Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Preferred term
Hereditary Central Nervous System Demyelinating Diseases
Type
-
Topical Descriptor
Broader concept
Narrower concepts
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
Scope note
- Inherited conditions characterized by a loss of MYELIN in the central nervous system.
History note
- 2000
In other languages
URI
http://www.yso.fi/onto/mesh/D020279
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