3-methylglutaconic aciduria type 3

3-methylglutaconic aciduria type III (MGA III) is an organic aciduria characterised by the association of optic atrophy and choreoathetosis with 3-methylglutaconic aciduria.

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Aliases

• 3-alpha methylglutaconic aciduria type III
• 3-methylglutaconic aciduria caused by mutation in OPA3
• 3-methylglutaconic aciduria type 3
• 3-methylglutaconic aciduria type III
• 3-methylglutaconic aciduria, type 3
• 3-methylglutaconic aciduria, type III
• Autosomal recessive optic atrophy plus syndrome
• autosomal recessive optic atrophy plus syndrome
• Autosomal recessive optic atrophy type 3
• autosomal recessive optic atrophy type 3
• Costeff optic atrophy syndrome
• Costeff syndrome
• Infantile optic atrophy with chorea and spastic paraplegia
• infantile optic atrophy with chorea and spastic paraplegia
• Iraqi Jewish optic atrophy plus
• Iraqi-Jewish 'optic atrophy plus'
• Iraqi-Jewish optic atrophy plus
• MGA type III
• MGA, type 3
• MGA3
• MGCA3
• OPA3 3-methylglutaconic aciduria
• OPA3 defect
• OPA3, autosomal recessive
• optic atrophy 3, autosomal recessive
• optic atrophy infantile with chorea and spastic paraplegia
• optic atrophy plus syndrome
• optic atrophy, infantile, with chorea and spastic paraplegia