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

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/615058
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Genes

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

Symbol Name
LRIT3 leucine-rich repeat, immunoglobulin-like and transmembrane domains 3