Phenotype #0000303739

Individual ID 00411712
Associated disease -
Phenotype details Decreased VA: 0.1; Relative central scotoma in HFA (30–2); OCT Abnormality, EZ: blurred fovea, blurred parafovea; Slight ring-shaped hyperfluorescence
Diagnosis/Initial occult macular dystrophy (OMD)
Inheritance Unknown
Diagnosis/Definite -
Age/Examination 19y (19 years)
Age/Diagnosis -
Age/Onset 11y
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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