- OMIM ID
-
308905
- OMIM term:
- LEBER OPTIC ATROPHY, SUSCEPTIBILITY TO
- Alternative terms:
-
LOAS
LEBER HEREDITARY OPTIC NEUROPATHY, MODIFIER OF
LHON, MODIFIER OF
- (∗) Location:
- Xp11
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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