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