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Disease Ontology Browser
bradyopsia 1 (DOID:0070363)
Alliance: disease page
Synonyms: prolonged electroretinal response suppression 1
Alt IDs: OMIM:608415
Definition: A braydopsia that has_material_basis_in homozygous or compound heterozygous mutation in the RGS9 gene on chromosome 17q24.

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
12/10/2024
MGI 6.24 		The Jackson Laboratory