Hereditary Central Nervous System Demyelinating Diseases D020279

Related MeSH Hierarchy (8)

Diseases [C] » Nervous System Diseases [C10] » Central Nervous System Diseases » Brain Diseases » Brain Diseases, Metabolic » Brain Diseases, Metabolic, Inborn » Hereditary Central Nervous System Demyelinating Diseases

Diseases [C] » Nervous System Diseases [C10] » Central Nervous System Diseases » Brain Diseases » Leukoencephalopathies » Hereditary Central Nervous System Demyelinating Diseases

Diseases [C] » Nervous System Diseases [C10] » Demyelinating Diseases » Hereditary Central Nervous System Demyelinating Diseases

Diseases [C] » Nervous System Diseases [C10] » Neurodegenerative Diseases » Heredodegenerative Disorders, Nervous System » Hereditary Central Nervous System Demyelinating Diseases

Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Heredodegenerative Disorders, Nervous System » Hereditary Central Nervous System Demyelinating Diseases

Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Brain Diseases, Metabolic » Brain Diseases, Metabolic, Inborn » Hereditary Central Nervous System Demyelinating Diseases

Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Metabolism, Inborn Errors » Brain Diseases, Metabolic, Inborn » Hereditary Central Nervous System Demyelinating Diseases

Description

Inherited conditions characterized by a loss of MYELIN in the central nervous system.   MeSH

Hierarchy View

Subtype Terms (6)

Adrenoleukodystrophy
37 drugs (23 approved, 14 experimental)

Alexander Disease
1 experimental drug

Canavan Disease
6 drugs (3 approved, 3 experimental)

Leukodystrophy, Globoid Cell
19 drugs (12 approved, 7 experimental)

Leukodystrophy, Metachromatic
27 drugs (13 approved, 14 experimental)

Pelizaeus-Merzbacher Disease
3 drugs (1 approved, 2 experimental)

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UMLS Data


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