Optic atrophy 11

MONDO:0015011

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, 0 tagged with Optic atrophy 11 itself.

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↑ Hereditary optic atrophy (23)

Including sub-types (4) Tagged with Optic atrophy 11 (0)

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