Phenotype #0000283562

Individual ID 00390022
Associated disease STGD
Phenotype details Fndus: macular atrophy, hyper-reflective deposition, thinning of the retina in the macular area
Diagnosis/Initial Stargardt disease
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination 25y (25 years)
Age/Diagnosis -
Age/Onset 15y
Phenotype/Onset -
Protein -
Owner name Anna Tracewska
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2021-11-08 11:09:25 +01:00 (CET)
Date last edited N/A

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