Phenotype #0000057838

Individual ID 00078063
Associated disease STGD1
Phenotype details Stargardt disease, severe; y46, visual acuity OD: <20/400, OS: <20/400. y31: Severe chorioretinal atrophy, macula up to periphery; macula most affected.
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 7y
Phenotype/Onset unknown
Protein -
Owner name Stéphanie Cornelis
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Stéphanie Cornelis
Date created 2016-02-22 12:22:09 +01:00 (CET)
Date last edited N/A

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