MeSH Browser

MeSH Supplementary: Leukodystrophy, Hypomyelinating, 4
Unique ID: C567390
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567390
Entry Term(s): Mitochondrial Hsp60 Chaperonopathy
Registry Numbers: 0
Heading Mapped to: *Hereditary Central Nervous System Demyelinating Diseases; *Mitochondrial Diseases
Frequency: 8
Note: mutation in HSPD1
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Leukodystrophy, Hypomyelinating, 4 MeSH Supplementary Concept Data 2025