Global Variome shared LOVD

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Phenotype #0000297737 Individual ID 00405188 Associated disease - Phenotype details - Diagnosis/Initial X-linked congenital stationary night blindness (CSNB1A) Inheritance Familial, X-linked Diagnosis/Definite - Age/Examination 6y (6 years) Age/Diagnosis - Age/Onset - Phenotype/Onset non-progressive stable severe night blindness since early childhood and moderate to high myopia Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Julia Lopez Date created 2022-03-16 13:42:42 +01:00 (CET) Date last edited N/A

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