Congenital stationary night blindness 1D

Definition

Any congenital stationary night blindness in which the cause of the disease is a mutation in the SLC24A1 gene.

Also known as congenital stationary night blindness 1D, congenital stationary night blindness caused by mutation in SLC24A1, congenital stationary night blindness type 1D, CSNB1D, night blindness, congenital stationary (complete), 1D, autosomal recessive, SLC24A1 congenital stationary night blindness — per MONDO

Also identified as

• DOID 0110868 per MONDO
• OMIM 613830 per MONDO
• UMLS C3151193 per MONDO