Optic atrophy 9

MONDO:0014571

Also known as: ACO2 autosomal recessive isolated optic atrophy, autosomal recessive isolated optic atrophy caused by mutation in ACO2, optic atrophy 9, OPA9

17 clinical trials for this condition and its sub-types, 0 tagged with Optic atrophy 9 itself.

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Including sub-types (17) Tagged with Optic atrophy 9 (0)

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