| Human Disease |
Term: Leigh Syndrome, French Canadian Type; LSFC
OMIM ID: 220111
|
| Synonyms |
Cox Deficiency, French Canadian Type; Cox Deficiency, Saguenay-Lac-Saint-Jean Type; Cytochrome C Oxidase Deficiency, French Canadian Type; Leigh Syndrome, Saguenay-Lac-Saint-Jean Type |
| Associated Genes |
Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.
Mouse Gene |
Human Gene |
|
Characteristics of this human disease are associated with mutations in... |
| |
|
|
|
|
 ...the human gene.
MGI data currently do not associate this disease with mutations in the orthologous mouse gene. |
| |
|
|
|
Analysis Tools