Search Ontology:
Human Disease

3-methylglutaconic aciduria type 3

Term ID
DOID:0110004
Synonyms
  • 3-methylglutaconic aciduria type III
  • autosomal recessive optic atrophy plus syndrome
  • autosomal recessive optic atrophy type 3
  • Costeff optic atrophy syndrome
  • Costeff syndrome
  • infantile optic atrophy with chorea and spastic paraplegia
  • Iraqi-Jewish optic atrophy plus
  • MGA3
Definition
A 3-methylglutaconic aciduria that has_material_basis_in mutation in the OPA3 gene. (2)
References
Ontology
Human Disease   ( DOID:0110004 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models