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optic atrophy 9 | RareConnect | RareConnect.io

/ACO2-related optic atrophy with or without extraocular features

/optic atrophy 9

optic atrophy 9

Rare Disease

MONDO:0014571

Also Known As

ACO2 autosomal recessive isolated optic atrophyautosomal recessive isolated optic atrophy caused by mutation in ACO2optic atrophy 9OPA9

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:616289 ↗

GARD

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