leber congenital amaurosis 16 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/614186
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1 genes associated with the leber congenital amaurosis 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
KCNJ13 potassium channel, inwardly rectifying subfamily J, member 13