- OMIM ID
-
220111
- OMIM term:
- LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC
- Alternative terms:
-
CYTOCHROME c OXIDASE DEFICIENCY, FRENCH CANADIAN TYPE
COX DEFICIENCY, FRENCH CANADIAN TYPE
COX DEFICIENCY, SAGUENAY-LAC-SAINT-JEAN TYPE
LEIGH SYNDROME, SAGUENAY-LAC-SAINT-JEAN TYPE
- (∗) Location:
- 2p21
- (†) Associated OMIM genes:
- LRPPRC
- (‡) Associated MGI genes:
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