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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, Costeff optic atrophy syndrome, Costeff syndrome, Iraqi-Jewish optic atrophy plus, MGA3, autosomal recessive optic atrophy plus syndrome, autosomal recessive optic atrophy type 3, infantile optic atrophy with chorea and spastic paraplegia

In OMIM:
OMIM:258501 - 3-METHYLGLUTACONIC ACIDURIA, TYPE III; MGCA3

In Mondo Disease Ontology:
MONDO:0009787 - 3-methylglutaconic aciduria type 3

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : opa3, micos13

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): 3-methylglutaconic aciduria (is_a)