Global Variome shared LOVD

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Phenotype #0000361833 Individual ID 00477223 Associated disease OCA2 Phenotype details Retinal dystrophy, central scotoma, visual impairment, nonprogressive visual loss and reduced visual acuity Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite Oculocutaneous albinism Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Mohammed A.M Derar Database submission license Creative Commons Attribution-NonCommercial 4.0 International Created by Mohammed A.M Derar Date created 2026-04-24 23:47:50 +02:00 (CEST) Date last edited 2026-04-29 09:07:23 +02:00 (CEST)

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