Global Variome shared LOVD

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Phenotype #0000299889 Individual ID 00407756 Associated disease - Phenotype details congenital severe and progressive rod-cone dystrophy form of the disease Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite Leber congenital amaurosis Age/Examination - 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 2022-04-08 10:07:02 +02:00 (CEST) Date last edited N/A

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