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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,
Xenbase Genes
:
opa3,
micos13
| MONDO:0009787 - 3-methylglutaconic aciduria type 3 |
| OMIM:258501 - 3-METHYLGLUTACONIC ACIDURIA, TYPE III; MGCA3 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
3-methylglutaconic aciduria (is_a)