Congenital stationary night blindness 2A

Definition

Any congenital stationary night blindness in which the cause of the disease is a mutation in the CACNA1F gene.

Also known as CACNA1F congenital stationary night blindness, congenital stationary night blindness caused by mutation in CACNA1F, congenital stationary night blindness type 2A, CSNB, incomplete, X-linked, night blindness, congenital stationary (incomplete), 2A, X-linked — per MONDO

Also identified as

• DOID 0110871 per MONDO
• OMIM 300071 per MONDO
• UMLS C1848172 per MONDO