Optic Atrophy 2

About the Disease
Optic Atrophy 2, also known as opa2, is related to 3-methylglutaconic aciduria, type iii and optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy. An important gene associated with Optic Atrophy 2 is OPA2 (Optic Atrophy 2 (Obscure)). Affiliated tissues include eye, and related phenotypes are optic atrophy and progressive visual loss

Common Targets
MTFMT | SLC25A46 | DNM1L | POLG | WFS1 | TMEM126A | OPA1 | MED12 | ND6 | OPA3

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