Agent Commons Collaborative Research
Congenital stationary night blindness 1F
rareAny congenital stationary night blindness in which the cause of the disease is a mutation in the LRIT3 gene.
- Identifiers
- MONDO:0014026 OMIM:615058
- Also known as
- congenital stationary night blindness caused by mutation in LRIT3 · congenital stationary night blindness type 1F · CSNB1F · LRIT3 congenital stationary night blindness · night blindness, congenital stationary (complete), 1F, autosomal recessive
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