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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
National Ophthalmic Genotyping and Phenotyping Network (eyeGENE (Registered Trademark)), Stage 3 - Expansion of DNA and Data Repositories for Rare Inherited Ophthalmic DiseasesCongenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Abnormalities, Eye Diseases, Hereditary, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, albinism, aniridia, blue cone monochromacy, corneal disorder, corneal dystrophy, eye disorder, hereditary disease, hereditary skin disorder, hypopigmentation of the skin, inborn disorder of amino acid metabolism, inborn errors of metabolism, iris disorder, macular degeneration, metabolic disease, retinal degeneration, retinal disorder, skin disorder, skin pigmentation disorder, uveal disorder, vitelliform macular dystrophy, vitiligoRecruitingNot stated2026-06-09NCT06491615

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OrganizationsLinked trials
National Eye Institute (NEI)122

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Research sitesCityCountryLinked trials
National Eye Institute (NEI)BethesdaUnited States2
National Institutes of Health Clinical CenterBethesdaUnited States800