Global Variome shared LOVD

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Phenotype #0000361834 Individual ID 00477224 Associated disease OCA2 Phenotype details Nonprogressive visual loss, central scotoma, visual impairment, macular atrophy 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 23:57:59 +02:00 (CEST) Date last edited 2026-04-29 09:09:29 +02:00 (CEST)

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