. . . . . . . . . . . . "[Patients carrying mutations in the retinal guanylate cyclase (GUCY2D) gene were reported to be constantly affected with a particular form of Leber congenital amaurosis (LCA) defined as a 'congenital stationary cone-rod dystrophy with high hypermetropia, panretinal degeneration and highly reduced visual acuity'.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2015-02-27"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2015-08-25T14:41:58+02:00"^^ . . . . . . . . . . . "v3.0.0.0" . "v3.0.0" .