Global Variome shared LOVD

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Phenotype #0000361835 Individual ID 00477225 Associated disease OCA2 Phenotype details Visual impairment and foveal hypoplasia 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 2026-04-25 00:59:32 +02:00 (CEST) Date last edited 2026-04-29 09:13:02 +02:00 (CEST)

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