Any autosomal recessive isolated optic atrophy in which the cause of the disease is a mutation in the YME1L1 gene.
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
optic atrophy 13 with retinal and foveal abnormalities
MONDO:0008135
optic atrophy 6
MONDO:0009786
optic atrophy 2
MONDO:0010698
Leber hereditary optic neuropathy
MONDO:0010788
optic atrophy 4
MONDO:0011536
autosomal recessive optic atrophy, OPA7 type
MONDO:0013069