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Summary Literature (0)
DOID:0070363 - bradyopsia 1

Disease Ontology Definition:A braydopsia that has_material_basis_in homozygous or compound heterozygous mutation in the RGS9 gene on chromosome 17q24.

Synonyms: prolonged electroretinal response suppression 1

Xenbase Genes : rgs9bp, rgs9bpl, rgs9



Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): bradyopsia (is_a)