DISEASES

Disease-gene associations mined from literature

Human genes for bradyopsia

Bradyopsia [DOID:0050335]

A retinal disease characterized by the slower than usual adaptation of the eyes to changing light conditions; can have material basis in mutations in the RGS9 or the R9AP genes.

Synonyms:  bradyopsia,  DOID:0050335,  bradyopsias,  prolonged electroretinal response suppression,  prolonged electroretinal response suppressions

Linkouts:  OMIM