Congenital stationary night blindness 1B

Definition

Any congenital stationary night blindness in which the cause of the disease is a mutation in the GRM6 gene.

Also known as congenital stationary night blindness 1B, congenital stationary night blindness caused by mutation in GRM6, congenital stationary night blindness type 1B, CSNB1B, GRM6 congenital stationary night blindness, night blindness, congenital stationary (complete), 1B, autosomal recessive — per MONDO

Also identified as

• DOID 0110865 per MONDO
• OMIM 257270 per MONDO
• UMLS C1850362 per MONDO