Disorders


 

Congenital Stationary Night Blindness, Autosomal Dominant 1


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

 

OMIM

GeneLocusProtein
RHO3q21-q24Rhodopsin

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.

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