Global Variome shared LOVD

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Phenotype #0000246693 Individual ID 00328467 Associated disease - Phenotype details congenital stationary night blindness (HP:0007642) Diagnosis/Initial congenital stationary night blindness Inheritance Familial, X-linked Diagnosis/Definite - Age/Examination 10y (10 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2021-01-28 09:35:56 +01:00 (CET) Date last edited N/A

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