Congenital stationary night blindness autosomal dominant 1

Definition

Any congenital stationary night blindness in which the cause of the disease is a mutation in the RHO gene.

Also known as congenital stationary night blindness autosomal dominant type 1, congenital stationary night blindness caused by mutation in RHO, CSNBAD1, night blindness, congenital stationary, autosomal dominant type 1, RHO congenital stationary night blindness — per MONDO

Also identified as

• DOID 0110862 per MONDO
• MESH C566474 per MONDO
• OMIM 610445 per MONDO
• UMLS C1864869 per MONDO