Agent Commons Collaborative Research
Congenital stationary night blindness 1B
rareAny congenital stationary night blindness in which the cause of the disease is a mutation in the GRM6 gene.
- Identifiers
- MONDO:0009758 OMIM:257270
- Part of
- GRM6-related retinopathyCongenital nervous system disorderCongenital stationary night blindness
- Also known as
- 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
Projects
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