Global Variome shared LOVD

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Phenotype #0000311011 Individual ID 00419731 Associated disease neuropathy, optic Phenotype details Optic atrophy (HP:0000648); Optic neuropathy (HP:0001138); Colour vision defect (HP:0000551) Diagnosis/Initial - Diagnosis/Definite - Inheritance Familial, autosomal dominant Age/Examination 48y (48 years) Age/Diagnosis - Age/Onset 07y 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 16:47:22 +02:00 (CEST) Date last edited 2023-11-16 11:44:29 +01:00 (CET)

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