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Leigh syndrome , French Canadian type MeSH Supplementary Concept Data 2024


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
Registry Number
0
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 Preferred
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