Congenital stationary night blindness 1E

Definition

Any congenital stationary night blindness in which the cause of the disease is a mutation in the GPR179 gene.

Also known as congenital stationary night blindness 1E, congenital stationary night blindness caused by mutation in GPR179, congenital stationary night blindness type 1E, CSNB1E, GPR179 congenital stationary night blindness, night blindness, congenital stationary (complete), 1E, autosomal recessive — per MONDO

Also identified as

• DOID 0110869 per MONDO
• OMIM 614565 per MONDO
• UMLS C3281215 per MONDO