The information on this page is for informational purposes only and does not constitute medical advice. Consult your genetic counselor or specialist physician for treatment decisions.

Congenital Stationary Night Blindness

Prevalence: 1/30000

ophthalmologic

Official·OMIM:310500 Official·ORPHA215

Non-progressive night blindness due to NYX, GRM6, and other gene mutations.

Associated Genes

No gene records found associated with this disease.