MeSH Browser

MeSH Supplementary: Pelizaeus-Merzbacher-like disease, autosomal recessive, 2
Unique ID: C536319
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536319
Entry Term(s): Leukodystrophy, Hypomyelinating, 3; Perinatal Sudanophilic leukodystrophy
Registry Number: 0
Heading Mapped to: Diffuse Cerebral Sclerosis of Schilder / *congenital
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Pelizaeus-Merzbacher-like disease, autosomal recessive, 2 MeSH Supplementary Concept Data 2024