DO_rare_slim late-onset retinal degeneration disease_ontology A retinal degeneration characterized by autosomal dominant inheritance of night blindness and drusen deposits, progressing to severe central and peripheral degeneration, with choroidal neovascularization and chorioretinal atrophy with onset in the fifth to sixth decade of life that has_material_basis_in heterozygous mutation in the C1QTNF5 gene on chromosome 11q23. LORD ORDO:67042 MESH:C565309 GARD:4357 MIM:605670 DOID:0060869 autosomal dominant late-onset retinal degeneration retinal degeneration