Disorders

Congenital Stationary Night Blindness, Autosomal Dominant 1

Synonym(s): CSNBAD1, RHO-Related Autosomal Dominant Congenital Stationary Night Blindness

Gene	Locus	Protein
RHO	3q21-q24	Rhodopsin

Laboratory	Test Method	Prenatal	Carrier *
Centogene AG, Rare Disease Company - Rostock, Germany	• Sequence analysis of the entire coding region • Deletion/duplication analysis
GeneDx - Gaithersburg, MD, USA	• Sequence analysis of the entire coding region

^* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.