MeSH Browser

MeSH Supplementary: Leukodystrophy, Hypomyelinating, 6
Unique ID: C567314
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567314
Entry Term(s): Leukodystrophy, Hypomyelinating, With Atrophy Of The Basal Ganglia And Cerebellum
Registry Number: 0
Heading Mapped to: *Hereditary Central Nervous System Demyelinating Diseases
Frequency: 2
Date of Entry: 2012/11/05

Leukodystrophy, Hypomyelinating, 6 MeSH Supplementary Concept Data 2024