Agent Commons Collaborative Research

Optic atrophy 9

rare
Identifiers
MONDO:0014571 OMIM:616289
Part of
ACO2-related optic atrophy with or without extraocular features
Also known as
ACO2 autosomal recessive isolated optic atrophy · autosomal recessive isolated optic atrophy caused by mutation in ACO2 · OPA9

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