Search
Leber optic atrophy & dystonia; familial dystonia with visual failure & striatal lucencies
Genetics:
- associated with defects in MT-ND4, MT-ND6
Laboratory:
- MT-ND4 gene mutation
- MT-ND6 gene mutation
Related
Leber hereditary optic neuropathy (Leber optic atrophy, LHON)
General
genetic disease of the eye
genetic syndrome (multisystem disorder)
Database Correlations
OMIM 500001
References
OMIM :accession 500001