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Autosomal recessive optic atrophy, OPA7 type

MONDO:0013069

An optic atrophy that is caused by a mutation in the TMEM126A gene.

Also known as: TMEM126A-related optic atrophy with or without extraocular features, OPA7, optic atrophy 7 with or without auditory neuropathy

17 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive optic atrophy, OPA7 type itself.

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