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Summary Literature (0)
DOID:0110004 - 3-methylglutaconic aciduria type 3

Disease Ontology Definition:A 3-methylglutaconic aciduria that has_material_basis_in mutation in the OPA3 gene.

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

Xenbase Genes : opa3, micos13

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009787 - 3-methylglutaconic aciduria type 3


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): 3-methylglutaconic aciduria (is_a), autosomal recessive disease (is_a)