MeSH Browser

MeSH Supplementary: Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant
Unique ID: C566813
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566813
Entry Term(s): Multiple Sclerosis-Like Disorder; Pelizaeus-Merzbacher Disease, Autosomal Dominant Or Late-Onset Type
Registry Numbers: 0
Heading Mapped to: *Pelizaeus-Merzbacher Disease
Frequency: 18
Note: A hereditary, autosomal dominant form of Pelizaeus-Merzbacher Disease, a MULTIPLE SCLEROSIS - like syndrome, that is associated with duplication of the LAMIN B -1 (LMNB1) gene. OMIM: 169500
Date of Entry: 2012/11/05
Revision Date: 2016/09/29

Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant MeSH Supplementary Concept Data 2025