Global Variome shared LOVD

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Phenotype #0000210720 Individual ID 00276130 Associated disease neuropathy, optic Phenotype details Optic atrophy (HP:0000648) Diagnosis/Initial - Diagnosis/Definite - Inheritance Familial, autosomal dominant Age/Examination 33y (33 years) Age/Diagnosis 15y Age/Onset - Phenotype/Onset - Protein - Owner name Khadidja Guehlouz Database submission license No license selected Created by Khadidja Guehlouz Date created 2020-01-28 14:16:36 +01:00 (CET) Date last edited 2020-08-25 21:27:59 +02:00 (CEST)

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