3-methylglutaconic aciduria type 3

Also known as Costeff syndrome, MGA3, Iraqi-Jewish optic atrophy plus, Costeff optic atrophy syndrome, infantile optic atrophy with chorea and spastic paraplegia, autosomal recessive optic atrophy plus syndrome, autosomal recessive optic atrophy type 3, 3-methylglutaconic aciduria type III

3-methylglutaconic aciduria that has material basis in mutation in the OPA3 gene