Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition A rare retinal dystrophy characterized by photophobia, progressive loss of visual acuity, nystagmus, visual field abnormalities, abnormal color vision, and psychophysical and electrophysiological evidence of abnormal cone function. Progressive cone dystrophy usually presents in childhood or early adult life, and patients tend to develop rod photoreceptor dysfunction in later life. Disease data Classification Disease Synonyms Cone dystrophy Dystrofia stożka ORPHA code 1871 OMIM code 613093 ICD10 code H35.5 ICD11 code 9B70 *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl