Global Variome shared LOVD

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Phenotype #0000311009 Individual ID 00419729 Associated disease neuropathy, optic Phenotype details Optic atrophy (HP:0000648); Optic neuropathy (HP:0001138); Abnormal macular morphology (HP:0001103); Reduced visual acuity (HP:0007663); Abnormal foveal morphology (HP:0000493); Macular dystrophy (HP:0007754) Diagnosis/Initial - Diagnosis/Definite - Inheritance Familial, autosomal dominant Age/Examination 15y (15 years) Age/Diagnosis 05y Age/Onset - Phenotype/Onset - Protein - Owner name Mohamed Selhane Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Created by Mohamed Selhane Date created 2022-10-21 15:08:52 +02:00 (CEST) Date last edited 2024-09-09 17:30:22 +02:00 (CEST)

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