leber congenital amaurosis 2 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/204100
Similar Terms
Downloads & Tools


1 genes associated with the leber congenital amaurosis 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
RPE65 retinal pigment epithelium-specific protein 65kDa