Global Variome shared LOVD

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Phenotype #0000299333 Individual ID 00406883 Associated disease - Phenotype details eye movement: roving, vitreous: clear, macula: minimal atrophy, white dots: equatorial, spiculation: none Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite Leber congenital amaurosi Age/Examination 6y (6 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2022-04-05 15:12:11 +02:00 (CEST) Date last edited N/A

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