MeSH Browser

MeSH Supplementary: Leigh syndrome , French Canadian type
Unique ID: C537004
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537004
Entry Term(s): Cox Deficiency, French-Canadian Type; Cox Deficiency, Saguenay-Lac Saint-Jean Type; Cox deficiency, French Canadian type; Cox deficiency, Saguenay Lac saint Jean type; Cytochrome C Oxidase Deficiency, French-Canadian Type; Cytochrome c oxidase deficiency, French Canadian type; Leigh Syndrome, French-Canadian Type; Leigh Syndrome, Saguenay-Lac Saint-Jean Type; Leigh syndrome, Saguenay Lac saint Jean type
Heading Mapped to: *Leigh Disease; *Cytochrome-c Oxidase Deficiency
Frequency: 10
Date of Entry: 2010/08/25
Revision Date: 2012/12/03

Leigh syndrome , French Canadian type MeSH Supplementary Concept Data 2024