- OMIM ID
-
500001
- OMIM term:
- LEBER OPTIC ATROPHY AND DYSTONIA
- Alternative terms:
-
LEBER HEREDITARY OPTIC NEUROPATHY WITH DYSTONIA; LDYT
DYSTONIA, FAMILIAL, WITH VISUAL FAILURE AND STRIATAL LUCENCIES
MARSDEN SYNDROME
- (∗) Location:
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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