Global Variome shared LOVD

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Phenotype #0000296830 Individual ID 00404241 Associated disease - Phenotype details - Diagnosis/Initial congenital stationary night blindness (XLCSNB) Inheritance Familial, X-linked recessive Diagnosis/Definite - Age/Examination 35y (35 years) Age/Diagnosis - Age/Onset - Phenotype/Onset nyctalopia and myopia Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Julia Lopez Date created 2022-02-28 03:03:50 +01:00 (CET) Date last edited N/A

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