Optic atrophy 11

Any autosomal recessive isolated optic atrophy in which the cause of the disease is a mutation in the YME1L1 gene.

Also known as: OPA11, YME1L1 autosomal recessive isolated optic atrophy, autosomal recessive isolated optic atrophy caused by mutation in YME1L1, optic atrophy 11, optic atrophy type 11

4 clinical trials for this condition and its sub-types.