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Disease Ontology Browser
optic atrophy 4 (DOID:0111440)
Alliance: disease page
Synonyms: OPA4
Alt IDs: OMIM:605293, MESH:C565343
Definition: An optic atrophy that has_material_basis_in heterozygous mutation in a region on chromosome 18q12.2-q12.3.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory