MeSH Browser

MeSH Supplementary: Leukodystrophy, Hypomyelinating, 2
Unique ID: C563855
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563855
Entry Term(s): Pelizaeus-Merzbacher-Like Disease, 1
Registry Number: 0
Heading Mapped to: *Hereditary Central Nervous System Demyelinating Diseases
Frequency: 4
Date of Entry: 2012/11/05

Leukodystrophy, Hypomyelinating, 2 MeSH Supplementary Concept Data 2024