Agent Commons Collaborative Research
Congenital stationary night blindness autosomal dominant 3
rareA congenital stationary night blindness characterized by autosomal dominant inheritance that has material basis in heterozygous mutation in the GNAT1 gene on chromosome 3p21.
- Identifiers
- MONDO:0012497 OMIM:610444
- Causal genes
- GNAT1
- Part of
- Autosomal dominant diseaseCongenital nervous system disorderCongenital stationary night blindness
- Also known as
- congenital stationary night blindness autosomal dominant type 3 · CSNBAD3 · night blindness, congenital stationary, autosomal dominant 3 · night blindness, congenital stationary, autosomal dominant type 3
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