Leber Congenital Amaurosis 10 (LCA10)

Leber Congenital Amaurosis 10, also known as lca10, is related to retinal disease and fundus dystrophy. An important gene associated with Leber Congenital Amaurosis 10 is CEP290 (Centrosomal Protein 290), and among its related pathways/superpathways are Visual phototransduction and Ciliary landscape. Affiliated tissues include retina and eye, and related phenotypes are seizure and visual impairment