Congenital stationary night blindness autosomal dominant 2

Definition

Any congenital stationary night blindness in which the cause of the disease is a mutation in the PDE6B gene.

Also known as congenital stationary night blindness autosomal dominant type 2, congenital stationary night blindness caused by mutation in PDE6B, CSNBAD2, night blindness, congenital stationary, autosomal dominant type 2, PDE6B congenital stationary night blindness — per MONDO

Also identified as

• DOID 0110863 per MONDO
• MESH C566869 per MONDO
• OMIM 163500 per MONDO
• UMLS C1876182 per MONDO