Global Variome shared LOVD

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Phenotype #0000278860 Individual ID 00385076 Associated disease - Phenotype details no nyctalopia/photophobia, nystagmus, oculodigital sign, best corrected visual acuity right/left eye: NA Diagnosis/Initial Leber congenital amaurosis Inheritance Familial, autosomal dominant Diagnosis/Definite Leber congenital amaurosis Age/Examination 4y (4 years) Age/Diagnosis - Age/Onset 6m Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2021-10-06 17:52:46 +02:00 (CEST) Date last edited N/A

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