night blindness, congenital stationary (complete), 1d, autosomal recessive Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/613830
Similar Terms
Downloads & Tools

Genes

1 genes associated with the night blindness, congenital stationary (complete), 1d, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SLC24A1 solute carrier family 24 (sodium/potassium/calcium exchanger), member 1