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DOID:0111433 - optic atrophy 3
Disease Ontology Definition:An optic atrophy characterized by optic atrophy and cataract that has_material_basis_in heterozygous mutation in the OPA3 gene on chromosome 19q13.32.
Synonyms: ADOAC, OPA3, autosomal dominant optic atrophy 3, autosomal dominant optic atrophy and cataract, autosomal dominant optic atrophy type 3, optic atrophy 3 with cataract,
Xenbase Genes : opa3
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee