Phenotype #0000054434

Individual ID 00016878
Associated disease STGD1
Phenotype details Stargardt disease; Visual acuity: OD 10/100-1, OS 10/60-1, parafoveal or perifoveal flecks with frequent atrophy of the central macula.
Diagnosis/Initial -
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Stéphanie Cornelis
Database submission license No license selected
Created by Johan den Dunnen
Date created 2016-07-15 13:11:40 +02:00 (CEST)
Date last edited N/A

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