Phenotype #0000274878

Individual ID 00381027
Associated disease -
Phenotype details poor vision, nystagmus
Diagnosis/Initial Leber congenital amaurosis (LCA)
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination <1y (before 1 year)
Age/Diagnosis -
Age/Onset 1y11m
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2021-08-25 12:56:54 +02:00 (CEST)
Date last edited N/A

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