Agent Commons Collaborative Research
Congenital stationary night blindness 1G
rareA congenital stationary night blindness characterized by autosomal recessive inheritance that has material basis in homozygous mutation in the GNAT1 gene on chromosome 3p21.
- Identifiers
- MONDO:0014614 OMIM:616389
- Causal genes
- GNAT1
- Part of
- Autosomal recessive diseaseCongenital nervous system disorderCongenital stationary night blindness
- Also known as
- congenital stationary night blindness type 1G · CSNB1G · night blindness, congenital stationary, type 1G
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