Phenotype #0000317818

Individual ID 00426663
Associated disease -
Phenotype details VA: 20/400(RE) - 20/400(LE); Mild foveal pigment disruption with flecks.
Diagnosis/Initial Stargardt disease (adSTGD-like)
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination 68y (68 years)
Age/Diagnosis -
Age/Onset 63y
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2022-12-02 14:17:29 +01:00 (CET)
Date last edited N/A

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