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Boli A-Z Achromatopsia Achromatopsia 3 Adie Pupil Aland Island Eye Disease Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Autosomal Dominant Congenital Stationary Night Blindness Autosomal Recessive Congenital Stationary Night Blindness Blood Group--Ahonen Blood Group, Dombrock System Choroideremia Chromosome 15q13.3 Deletion Syndrome Cone Dystrophy Cone-Rod Dystrophy 2 Cone-Rod Dystrophy 3 Cone-Rod Dystrophy 6 Degeneration of Macula and Posterior Pole Focal Chorioretinitis Fundus Albipunctatus Hepatic Adenomas, Familial Hereditary Night Blindness Hereditary Retinal Dystrophy Keratoconus Keratomalacia Leber Congenital Amaurosis Leber Congenital Amaurosis 1 Leber Congenital Amaurosis 12 Leber Congenital Amaurosis 4 Leber Congenital Amaurosis 9 Melanoma-Associated Retinopathy Muscular Dystrophy Myopia Night Blindness Night Blindness, Congenital Stationary, Autosomal Dominant 2 Night Blindness, Congenital Stationary, Type 1a Night Blindness, Congenital Stationary, Type 1b Night Blindness, Congenital Stationary, Type 1e Night Blindness, Congenital Stationary, Type 2a Prolonged Electroretinal Response Suppression Red-Green Color Blindness Retinal Degeneration Retinal Disease Retinitis Retinitis Pigmentosa Retinitis Pigmentosa 26 Retinitis Pigmentosa 3 Retinoschisis 1, X-Linked, Juvenile Rhyns Syndrome Scotoma Severe Early-Childhood-Onset Retinal Dystrophy Stargardt Disease Stargardt Disease 1 Stargardt Macular Degeneration Strabismus Usher Syndrome, Type Iid Van Der Woude Syndrome 1 X-Linked Congenital Stationary Night Blindness Yemenite Deaf-Blind Hypopigmentation Syndrome