Phenotype #0000303742

Individual ID 00411715
Associated disease Healthy/Control
Phenotype details No visual symptoms, BCVA: R 1.0/ L 1.2; Relative paracentral scotoma in HFA (10–2); OCT Abnormality, EZ: mildly disrupted parafovea; OCT Abnormality, IZ: disappeared parafovea; Slight circular hyperfluorescence
Diagnosis/Initial Asymptomatic
Inheritance Unknown
Diagnosis/Definite -
Age/Examination 50y (50 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2022-06-18 03:05:08 +02:00 (CEST)
Date last edited N/A

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