| Disease Aliases (24) | Cox deficiency, french canadian type Cox deficiency, saguenay-lac-saint-jean type Cox deficiency Cox deficiency, french-canadian type Cytochrome c oxidase deficiency, french canadian type Cox deficiency, saguenay-lac saint-jean type Cox deficiency, saguenay lac saint jean type Cytochrome c oxidase deficiency, french-canadian type Cytochrome c oxidase deficiency Cytochrome oxidase deficiency Cytochrome oxidase deficiency, saguenay-lac-saint-jean type French-canadian type Leigh syndrome, french canadian type Leigh syndrome, saguenay-lac-saint-jean type Lsfc Leigh syndrome, french-canadian type Leigh syndrome, saguenay-lac saint-jean type Leigh syndrome, french canadian type; lsfc Leigh syndrome, saguenay lac saint jean type Mc4dn5 Slsj-cox deficiency Saguenay-lac-saint-jean type Congenital lactic acidosis, saguenay-lac-saint-jean type |
Associated Genes (1) NCBI-RefSeq: LRPPRC (Leucine rich pentatricopeptide repeat containing) External Links: gnomAD browser Ensembl GeneCards
| |||||||
| Cross-references of Leigh syndrome | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |