Global Variome shared LOVD

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Phenotype #0000282118 Individual ID 00388578 Associated disease - Phenotype details Non‐syndrom Diagnosis/Initial Nystagmus and visual deficit Inheritance Familial, autosomal recessive Diagnosis/Definite Leber congenital amaurosis type 10 Age/Examination - Age/Diagnosis 3m Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2021-11-04 19:02:37 +01:00 (CET) Date last edited N/A

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