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Human Disease and Mouse Model Detail
Human Disease Leigh Syndrome, French Canadian Type; LSFC
OMIM ID: 220111
Human Phenotype Ontology associations
Synonyms Cox Deficiency, French Canadian Type; Cox Deficiency, Saguenay-Lac-Saint-Jean Type; Cytochrome C Oxidase Deficiency, French Canadian Type; Leigh Syndrome; Leigh Syndrome, Saguenay-Lac-Saint-Jean Type
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     LRPPRC* Lrpprc   HomoloGene and HGNC

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory