Congenital stationary night blindness 1H

Definition

Any congenital stationary night blindness in which the cause of the disease is a mutation in the GNB3 gene.

Also known as congenital stationary night blindness caused by mutation in GNB3, congenital stationary night blindness type 1H, CSNB1H, GNB3 congenital stationary night blindness, night blindness, congenital stationary, type 1H — per MONDO

Also identified as

• DOID 0110866 per MONDO
• OMIM 617024 per MONDO
• UMLS C4310758 per MONDO