3-methylglutaconic aciduria type 3

From BugSigDB


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