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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: autosomal recessive optic atrophy type 3, 3-methylglutaconic aciduria type III, autosomal recessive optic atrophy plus syndrome, 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

MIM:
MIM:258501 - 3-METHYLGLUTACONIC ACIDURIA, TYPE III; MGCA3

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

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